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  • 1945-1949  (130,850)
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  • 1
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    Unknown
    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 212-217
    Publication Date: 2024-01-12
    Description: De hier besproken soorten zijn alle nieuw voor de Nederlandse fauna in zoverre, dat zij niet vermeld staan in de Catalogus Aranearum van VAN HASSELT. De collectie van deze araneoloog bevindt zich in het Rijksmuseum voor Natuurlijke Historie te Leiden en wordt daar momenteel gerevideerd, waarna een nieuwe naamlijst van Nederlandse spinnen zal worden samengesteld. In deze bijdrage wordt geen poging gedaan de twijfelachtige synoniemie van de Catalogus op te helderen, hetgeen zeker nog menige nieuwe soort voor ons land zal opleveren. Zij is slechts een tussentijds resultaat van het bewerken van de eigen collectie en van materiaal, dat mij van verschillende zijden ter bewerking werd toevertrouwd.\nDe gebruikte systematische indeling en de soortnamen zijn in hoofdzaak die uit de Katalog der Araneae Bd. I van ROEWER, waarbij echter enkele correcties op grond van nieuwere onderzoekingen werden aangebracht. Ook ben ik er toe overgegaan de namen van CLERCK te gebruiken.
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  • 2
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    Unknown
    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 308-314
    Publication Date: 2024-01-12
    Description: Weinig onderzoekingen hebben in zo wijde kring bekendheid verworven als die van onze landgenoot JAN SWAMMERDAM, die in zijn ,Ephemeri vita\xe2\x80\x99 (1675) en later in de ,Bybel der Natuur of Historie der insekten\xe2\x80\x99 (1737) de ontwikkelingsgeschiedenis beschreef van het beroemd geworden Oever-aas, Palingenia longicauda (Oliv.), de grootste palaearctische Ephemeride.\nDit allermerkwaardigst insect, dat \xe2\x80\x94 het zij terloops opgemerkt \xe2\x80\x94 reeds in 1634 door de Amsterdamse medicus AUGERIUS CLUTIUS was beschreven en afgebeeld \xc2\xb9), moet destijds in ons land alom de aandacht hebben getrokken wegens zijn massaal optreden gedurende een aantal warme dagen omstreeks het midden van de maand Juni. In Nederland echter is dit grote haft vermoedelijk reeds tegen het eind van de vorige eeuw uitgestorven. Thans leeft het nog in het stroomgebied der grote rivieren van Midden- en Oost-Europa (Oder, Weichsel en Wolga).
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  • 3
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 401-415
    Publication Date: 2024-01-12
    Description: Lower-Villafranchian landmammals lived in the South of the Netherlands when the coastline of the North Sea retired in northern direction during the Plio-Pleistocene transition period. In the province of Zealand their black remains have been fished out of the waters of the Scheldt in the depth of which littoral Poederlian deposits (Amstelian deposits are missing there in Zealand) occur and are eroded by the currents. Also borings in the provinces of Limburg and Guelderland have yielded black fossils of this fauna of which the following species could be stated in the Netherlands: Eucladoceros falconeri (Dawk.), Odobenus huxleyi (Lank.), Alachtherium spec., Anancus arvernensis (Croiz. et Job.), Archidiskodon planifrons (Falc. & Caut.), Gazella schreuderae Hooijer and Mustela erminea L. This Lower-Villafranchian fauna occurs also in the Red Crag of East-Anglia, in Pi\xc3\xa9mont (Villafranca) and in Auvergne (Perrier, etc.).\nThis fauna lived in the south of the Netherlands in the forests and along the coast of the North Sea which then was a deep quiet bay covering a strip of East-Anglia, te larger portion of the Netherlands and a small portion of Belgium along the Belgian-Dutch frontier from the North Sea coast to the east in the direction of the Meuse near Venlo. South of this coast-line a broad communication between England and the continent caused the identity of their mammals in that period.
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  • 4
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 97-105
    Publication Date: 2024-01-12
    Description: It is for me a pleasure to contribute the following descriptions of chosen rarities to the Jubilary Volume in honour of the highly esteemed Prof. Dr. L. F. DE BEAUFORT and Prof. Dr. J. E. W. IHLE, of the University of Amsterdam.\nI wish to express my gratitude to Dr. J. WILCKE, Wageningen, and to Mr. W. F. BREURKEN, Amsterdam, for the execution of the drawings.
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  • 5
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 466-471
    Publication Date: 2024-01-12
    Description: The most recent comprehensive treatment of this Indo-Pacific genus \xc2\xb9) is that of TESCH (1918, p. 78-82). Here seven species are recognised with the reservation that M. eydouxi H. Milne Edwards and M. thukuhar (Owen) are possibly not distinct.\nIn 1936 (TWEEDIE 1936, p. 49) I questioned the validity of the character used to separate M. latifrons (White) and M. maculatus H. M.-E., the relation of carapace length and breadth, and placed maculatus in the synonymy of latifrons.
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  • 6
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 149-152
    Publication Date: 2024-01-12
    Description: If you ask the layman: \xe2\x80\x9cWhat is a museum?\xe2\x80\x9d, he will answer. \xe2\x80\x9cA museum is a display of objects, that have an aesthetic value or scientific interest; the scope of a museum is to improve the taste of the visitor, is to give him, by visual means, aesthetic or intellectual enjoyment, to satisfy his curiosity, to show him the true and real things (a classic sculpture, an Indian weapon or a deepsea fish) instead of a documentary film, a radio report, or the descriptions and pictures in his books and magazines.\xe2\x80\x9d If an architect is in charge of designing a museum, he will see to it that the wallcases and the free-standing objects receive the right light and that the public and the conditioned air can circulate freely. He will design an entrance hall, an exhibition gallery, a director\xe2\x80\x99s room, and, perhaps, in the basement or on the top-floor a store-room for articles not on display \xc2\xb9).
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  • 7
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    Unknown
    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 477-504
    Publication Date: 2024-01-12
    Description: Our knowledge concerning the periodical movements in animals called migrations is chiefly based on observations on birds. By and by, however, a number of facts concerning migration in other animal groups have been assembled and it seems worth while to compare them with those known for birds. There is the more reason to do so here, because the victim of this jubilee is interested in birds and fishes alike. Though I shall not restrict myself to these two groups they will take more place than the rest.\nIn the following I shall deal with North to South and South to North migrations chiefly. In the hope to succeed and make my ideas comprehensible to those who are not specially acquainted with this particular field I shall begin with a very short description of the migration of some animals in the sea, which may be used as a starting point for the comparison which follows next. These animals are the cuttlefish ( Sepia officinalis L.), two species of fish: the anchovy ( Stolephorus encrasicholus (L.)) and the tunny ( Thunnus thynnus (L.)) and, finally, a mammal: the humpback (Megaptera novaeangliae (Borowski), one of the whales.
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  • 8
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    Unknown
    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 127-132
    Publication Date: 2024-01-12
    Description: After having collected the plankton samples in the Java Sea on which I have reported in Treubia XVII, 1939, I thought it desirable to gather similar samples from a more oceanic area of the East Indian seas, in order to be able to make a comparison between the two collections and to try to find out the characteristic differences between the two regions. It seemed to me interesting to choose in the first place Sunda Strait for this purpose, as it connects the shallow Java Sea with the deep Indian Ocean and, therefore, might offer all degrees of transition from the plankton of the former to that of the latter. The next year, then, in 1933, I made a cruise in Sunda Strait in the months of April-May, the transition months between the (wet) west monsoon and the (dry) east monsoon. The stations visited may be seen from the accompanying chart. The depth increases considerably in the direction Java Sea \xe2\x80\x94〉 Indian Ocean but is everywhere sufficient to allow the making of vertical hauls with the plankton net from 50 meters depth to the surface. For the sake of convenience, therefore, all the hauls in Sunda Strait have been made in this way. This was not possible the year before as at several stations in the Java Sea the depth is insufficient. The same net was used as the foregoing year: width of the mouth 1 1/3 m, length 4 m, Swiss plankton gauze nr. 3.\nIn the Sailor\'s Guide for the East-Indian Archipelago we read : ""This diurnal tidal stream (seil, in the Java Sea) is weakened towards the NE and strengthened towards the SW in the first place by a current to the SW starting from Bangka-Strait, which runs along the SE-coast of Sumatra and through Sunda Strait at the rate of more than 0.5 Mile per hour.
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  • 9
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    Unknown
    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 397-400
    Publication Date: 2024-01-12
    Description: Toen in 1881 door G. JANSE de Catalogus der Bibliotheek van het Koninklijk Zo\xc3\xb6logisch Genootschap Natura Artis Magistra werd samengesteld, werden daarin opgenomen onder: N\xc2\xb0 1202 Linnaei. C. Facsimile-reproductie van het vorige, (d.i. Systema Naturae sive Regna tria Naturae systematice proposita per Classes, Ordines, Genera et Species. Lugduni Batavorum. 1735. 7 bladen fol\xc2\xb0, max.) (Berlijn.) 12 bl. fol\xc2\xb0. max. N\xc2\xb0 1203 Linnaei C. Methodus juxta quam Physiologus accurate et f\xc3\xa9liciter concinnare potest Historiam cujuscunque Naturalis Subjecti sequentt. hisce Paragraphis comprehensa. I. Nomina. II. Theoria. III. Genus. IV. Species. V. Attributa. VI. Usus. VII. literaria. Lugduni Batavorum. 1736. 1 bl. fol\xc2\xb0 max. Facsimile-reproductie van de oorspronkelijke uitgave. Berlijn.
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  • 10
    Publication Date: 2024-01-12
    Description: 1. In Macroscelides (Elephantulus?) rozeti Duv., a North-African form, the pregnant uterus shows 3 swellings (sometimes this number is reduced to 1 or 2). The South-African form Elephantulus myurus Jamesoni, examined by prof. VAN DER HORST (Johannesburg) always shows two swellings, one in each half of the uterus horns. 2. The tuba is connected with a periovarial sac. 3. The eggs in the ampulla are naked and not surrounded by the zona pellucida. This causes sometimes the segmented cells to be set free. 4. The four-celled stage shows a tetrahedral arrangement. 5. In the uterus horn the unilaminar blastula is formed by the absorption of water. 6. In a stage of 120 cells the blastula-wall separates amoeboid cells into the interior forming a loose reticulum. Afterwards these cells concentrate at one side of the germinal vesicle and form the embryonic knot. 7. This organ separates an entodermal cell-layer at its base. 8. At the mesometrical side the germinal vesicle adheres to the uterine wall which is syncytial at this spot. 9. After the adhering of the germinal vesicle the mucosa uteri becomes very thick and the muscularis very thin. The small number of blood vessels in the mucosa is very remarkable. 10. There is a marked increase of the number and extent of the uterine glands. The image resembles that of the secretory phase in man. 11. In the following stage (N. 45) the trophoblast has become very thick and has penetrated into the mucosa uteri. The embryonic knot shows a large archamniotic cavity. 12. In N. 6 the embryonic region shows 7 \xc3\xa0 8 somites. A distinct pharynx is present. In the mid- and hindgut a large connection of enteron and yolk sac is present. Cloaca with allantoic evagination, a large, mesodermal, allantoic rudiment is present. The yolk sac forms about two thirds of the blastocyst, the remaining third part is formed by the exocoel and the amniotic cavity. A proamnion is present. Enlarged uterine glands surround the whole uterine cavity. A large ectoplacenta shows a toadstool-form and penetrates into the uterine wall forming a disc of foeto-maternal symplasma. Heart rudiment rather well developed. 13. N. 8. The embryo shows \xc2\xb1 25 somites. Allantois well developed, adhering to the ectoplacenta. The greater part of the blastocyst is formed by the exocoel. Three visceral pouches are present, the mouth plate is lacerated. The neural tube is completely closed. 14. In N. 1 30-35 somites and 12 nephric tubules are present. Rudiment of anterior extremity, 3-4 aortic arches. 15. In N. 3 the yolk sac is much smaller and its walls are shriveled. A yolk stalk may be seen but the connection between the lumina of gut and yolk sac has disappeared. The allantois surrounds the amniotic cavity and fills up the main part of the blastocyst. It shows four lobes. The ectoplacenta shows a thick layer of labyrinthic tissue at the embryonic side. The embryo is strongly coiled and possesses a distinct torsion. The kidney is well developed (with Malpighian corpuscula). Posterior extremities are present. In the anterior ones the rudiment of the skeleton may be noticed. 16. In the stages N. 45 and N. 1 a distinct mesoplacentarium consisting of numerous lamellae with bloodvessels is present at the mesometrical side of the uterine wall. As in the aguti (BECHER) this phenomenon may be in relation with the jumping propulsion.
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  • 11
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 144-148
    Publication Date: 2024-01-12
    Description: Depuis longtemps certain aspect larvaire de nombreuses formes p\xc3\xa9lagiques faisant partie du plancton permanent a retenu l\xe2\x80\x99attention des naturalistes et a conduit quelques-uns d\xe2\x80\x99entre eux \xc3\xa0 consid\xc3\xa9rer cette faune comme primitive. Si cette conclusion s\xe2\x80\x99est par la suite av\xc3\xa9r\xc3\xa9e inexacte et si l\xe2\x80\x99origine littorale de types planctoniques m\xc3\xaame les plus sp\xc3\xa9cialis\xc3\xa9s, comme les Siphonophores par exemple (W. GARSTANG, 1946), a pu \xc3\xaatre mise en \xc3\xa9vidence, il n\xe2\x80\x99en reste pas moins que cet aspect larvaire, qui avait frapp\xc3\xa9 les premiers observateurs, demeure dans bien des cas \xc3\xa9vident.\nSans doute, beaucoup de larves d\xe2\x80\x99esp\xc3\xa9ces benthiques m\xc3\xa8nent aussi, durant un temps plus ou moins long, une existence p\xc3\xa9lagique; et le fait que les constituants de ce plancton temporaire et du plancton permanent fr\xc3\xa9quentent ainsi un m\xc3\xaame milieu, qui a ses exigences propres, peut rendre compte de certains traits d\xe2\x80\x99organisation communs aux uns et aux autres. Mais il y a plus, et nous savons bien que la ressemblance entre Appendiculaires et larves d\xe2\x80\x99Ascidies n\xe2\x80\x99est pas seulement superficielle; que le Dactylactis Benedeni Gravier (1904) est bien une larve sexu\xc3\xa9e de C\xc3\xa9rianthe; que l\xe2\x80\x99 Amphioxides n\xe2\x80\x99est qu\xe2\x80\x99un Amphioxus continuant ind\xc3\xa9finiment sa vie en haute mer (R. GOLDSCHMIDT, 1933); que les Grimothea, dont les essaims innombrables colorent en rouge, par place, la surface des Mers du Sud, ne sont que des larves de Munida qui peuvent, sous certaines conditions, arriver en cet \xc3\xa9tat \xc3\xa0 maturit\xc3\xa9 (MATTHEWS, 1932); que ces Gobiid\xc3\xa9s, transparents comme le cristal, appartenant aux genres Aphya et Crystallogobius, issus, comme tous les membres de leur famille, d\xe2\x80\x99oeufs fix\xc3\xa9s sur les fonds littoraux, prolongent leur existence p\xc3\xa9lagique jusqu\xe2\x80\x99au moment o\xc3\xb9 ils reviennent \xc3\xa0 la c\xc3\xb4te pondre \xc3\xa0 leur tour et mourir. Sans parler des cas encore incompl\xc3\xa8tement \xc3\xa9lucid\xc3\xa9s des grands Glaucotho\xc3\xa9s, larves de Pagures (THOMPSON, 1943) et des Eryoneicus, larves de Polycheles (BOAS, 1939), que d\xe2\x80\x99exemples encore \xc3\xa0 citer d\xe2\x80\x99organismes planctoniques auxquels on peut, \xc3\xa0 bon droit, reconna\xc3\xaetre pour origine des larves de formes littorales n\xe2\x80\x99ayant pas accompli sur le fond la m\xc3\xa9tamorphose qui leur eut assur\xc3\xa9, comme \xc3\xa0 leurs cong\xc3\xa9n\xc3\xa8res, la persistance de la vie benthique. La connaissance des facteurs susceptibles de retarder cette m\xc3\xa9tamorphose est donc de premi\xc3\xa8re importance si l\xe2\x80\x99on veut comprendre les processus qui ont pu conduire \xc3\xa0 un tel r\xc3\xa9sultat.
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  • 12
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 449-452
    Publication Date: 2024-01-12
    Description: De eisen die de practijk stelt zijn voor de toegepaste wetenschap de stimulans, welke de vragen die de werkhypothese suggereert voor de zuivere wetenschap zijn. Is aan die eisen voldaan dan loopt het onderzoek dood \xe2\x80\x94 tenzij de practijk aan het resultaat der onderzoekingen nieuwe eisen ontleent: naar analogie van een nieuwe hypothese steunend op feiten die men, geleid door een oudere hypothese, al eerder had opgespoord. Ik wil hiervan een voorbeeld geven: zowel van het doodlopen ener reeks onderzoekingen, als van haar resuscitatie.\nHet eerste stuk van mijn voorbeeld is bekend. Ik zal daar slechts zoveel van in herinnering brengen als voor het tweede stuk nodig is.
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  • 13
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 416-448
    Publication Date: 2024-01-12
    Description: 1. A review is given of some phenomena concerning pregnancy and parturition of the Cetacea, depending on data in literature and on observations made in Antarctic Blue and Fin Whales on board the f.f. \xe2\x80\x9cWillem Barendsz\xe2\x80\x9d (1946\xe2\x80\x941947). 2. In Mystacoceti the frequency of twins appears to be less than in man and the big domestic animals. The majority of twins is born by females that are longer than the average female in the period of greatest sexual activity. This does not mean, however, that just as in man most twins are born at an elder age than that corresponding with the maximum of sexual activity. It may also be possible that, just as in the big domestic animals, the ages correspond, but that twins are mostly produced by the physically stronger developed females. 3. In Odontoceti the left ovary shows a very distinct morphological and functional prevalence. The foetus is exclusively found in the left uterine cornu. In Mystacoceti there is a prevalence of about 60 % of the right ovary and the right uterine cornu with regard to ovulation and pregnancy. The above described phenomena have also been observed in other uniparous Mammals, whereas in multiparous Mammals no distinct prevalence of a special side has been found. Transference of an ovum from the ovary of one side to the cornu of the other has been observed twice in Cetacea. 4. In Mystacoceti the number of cephalic presentations of the foetus very distinctly increases during the last months of pregnancy, just as in man and the big domestic animals. There is a great possibility that, just as the other uniparous Mammals, which give birth to comparatively large infants, in Mystacoceti a very high percentage of the young is born in cephalic presentation. In Odontoceti, on the contrary, a great number of foetuses is apparently delivered in tail-presentation. With regard to their shape and dimensions, such a birth in tail-presentation must be considered as an unfavourable event. An attempt has been made to explain these facts with the aid of the peristaltic uterine contractions. If these contractions act in the same way as in other Mammals, it might be expected that most of the Cetacea should be born in tailpresentation. So it is highly possible that in Mystacoceti some other factors are responsible for the high percentage of cephalic presentations. 5. In Cetacea the relative length of the umbilical cord (in % of the length of the foetus) decreases markedly during the second part of pregnancy. At birth its length is about 40 % of the total length of the calf and 57 % of its snout-anus length. As compared with other Mammals the cord of the Cetacea is rather short and this fact may have some influence on the way in which the connection between mother and calf is broken. This may occur by rupture of the cord immediately after birth as in Ungulates. On the other hand it appears to be also possible that, just as in Primates, Carnivores and Chiropteres, the placenta and the cord stick to the baby for some time after birth. 6. Some congenital anomalies of foetal Cetacea are described. Abortus probably may occur during chasing of the big whales or when they are struck by the harpoon. A case of fibromyoma uteri is described in an old female Blue Whale that showed an abnormal lactation. Probably the fibromyoma had caused an abortus some months ago, this abortus causing the lactation.
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  • 14
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    In:  Bijdragen tot de dierkunde vol. 28 no. 1, pp. 323-326
    Publication Date: 2024-01-12
    Description: Hoewel ik in het voorjaar van 1948 slechts korte tijd op Cura\xc3\xa7ao en Bonaire verbleef, deed ik hier naast waarnemingen, die een bevestiging zijn van die van RUTTEN (1931), ook een aantal aanvullende observaties. Ik wil deze gaarne publiceren in de feestbundel ter ere van Prof. Dr. J. E. W. IHLE en Prof. Dr. L. F. DE BEAUFORT, met wie ik gedurende vele jaren op verschillend gebied zo aangenaam samengewerkt heb.\nOver de vogels der Benedenwindse Eilanden is nog slechts weinig geschreven. Eigenlijk bestaat er slechts \xc3\xa9\xc3\xa9n goed artikel en wel dat van RUTTEN (1931), die hierin niet alleen oude mededelingen van HARTERT en van CORY verwerkte, maar ook tal van nieuwe, eigen waarnemingen, deels van veldornithologische aard, mededeelde. De lijst van DE JONG (1948) is min of meer een uittreksel van die van RUTTEN \xc2\xb9) en bevat slechts enkele eigen aanvullende gegevens.
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  • 15
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    In:  Zoologische Verhandelingen vol. 4 no. 1, pp. 1-44
    Publication Date: 2024-01-12
    Description: Opinions are divided in relation to what generical name has priority, Heliacus or Torinia. In proof of this I will quote, leaving aside those of many others, the opinions of two authorities.\nThiele [1918, p. 80 (114)] writes: "Bez\xc3\xbcglich des Namens Torinia bemerkt Iredale, dass ihm Heliacus Orbigny, weil \xc3\xa4lter, vorzuziehen sei; es mag sein, dass dieser Name ein wenig \xc3\xa4lter ist \xe2\x80\x94 nach Hermannsen von 1841, nach Iredale 1842, es scheint also die Zeit des Erscheinens nicht ganz festzustehen \xe2\x80\x94, w\xc3\xa4hrend Torinia von Gray 1842 auf die Beschaffenheit des Deckels hin begr\xc3\xbcndet worden ist".\nThe opinion of Tomlin (1928, p. 333), however, is quite different: "Gray in Proc. Zool. Soc., 1847, \xce\xa1\xc2\xb7 151, gives his own genus Torinia precedence, quoting it as of 1840 and 1842. These two references are to different editions of the \'Synopsis of the Contents of the British Museum\', and are fully explained by Iredale in Proc. Malac. Soc. (London), X, pp. 294-309.\nThe 1840 usage of Torinia is a nomen nudum; the 1842 edition gives a short comparative account of operculum only, quoted on p. 308. It hardly seems a sufficient diagnosis on which to found a genus, and the reasons for rejection given by Iredale on p. 301 may well be applied to this case at any rate".\nAs I mentioned already in a previous paper (1940, p. 223), I follow in this catalogue Thiele\'s "Handbuch der systematischen Weichtierkunde", in relation to the generic names and also as far as concerns the classification, but it is not my intention to state thereby hat I always completely agree with the opinions of his author.\nI wish to express here my heartiest thanks to the gentlemen who helped
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  • 16
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    In:  Zoologische Verhandelingen vol. 3 no. 1, pp. 1-58
    Publication Date: 2024-01-12
    Description: Au cours de l\'ann\xc3\xa9e 1935, le Directeur du Mus\xc3\xa9e de Prague a eu l\'amabilit\xc3\xa9 de m\'envoyer en communication les 3 syntypes de Synaptura lipophthalma Janos ; de son c\xc3\xb4t\xc3\xa9, M. Hardenberg, Directeur du Laboratoire oc\xc3\xa9anographique de Batavia (Laboratorium voor het Onderzoek der Zee), m\'a fait le don g\xc3\xa9n\xc3\xa9reux de 3 paratypes de son Typhlachirus caecus. C\'est avec joie que je saisis l\'occasion qui m\'est offerte ici de remercier ces deux savants de leur extr\xc3\xa8me courtoisie, gr\xc3\xa2ce \xc3\xa0 laquelle j\'ai pu examiner \xc3\xa0 loisir et comparer directement entre eux tous ces sp\xc3\xa9cimens.\nSommaire.\nI. \xe2\x80\x94 Revision du genre Typhla- Les \xc3\xa9piotiques......34\nchirus.........3 Le parasph\xc3\xa9no\xc3\xafde.....35\nRemarques .......21 Les prootiques......36\nII. \xe2\x80\x94 Esp\xc3\xa8ce dont il reste \xc3\xa0 pr\xc3\xa9ciser Les opisthotiques.....36\nla position syst\xc3\xa9matique . .22 Les pt\xc3\xa9rotiques......36\nIII. \xe2\x80\x94 Contribution \xc3\xa0 la morphologie Les sph\xc3\xa9notiques.....37\nanatomique de Typhlachirus L\'acrinioste.......37\nlipophthalmus......23 Les pari\xc3\xa9taux......38\nRemarques critiques relatives Les frontaux ......38\n\xc3\xa0 la nomenclature ost\xc3\xa9ologique Le parethmo\xc3\xafde nadiral . . 40 des T\xc3\xa9l\xc3\xa9ost\xc3\xa9ens .....23 Le parethmo\xc3\xafde z\xc3\xa9nithal . . 42 A. \xe2\x80\x94 L\'organe nasal z\xc3\xa9nithal ... 23 Le dermethmo\xc3\xafde.....42\nB. \xe2\x80\x94 Le clidoste.......24 Le vomer........43\nC. \xe2\x80\x94 Le neurocr\xc3\xa2ne......27 D. \xe2\x80\x94 Le rhachis abdominal .... 43\nCaract\xc3\xa8res g\xc3\xa9n\xc3\xa9raux .... 27 E. \xe2\x80\x94 L\'appareil digestif.....48\nLe basinioste ......32 F. \xe2\x80\x94 L\'appareil excr\xc3\xa9teur et l\'organe
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  • 17
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    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 5 no. 3, pp. 709-763
    Publication Date: 2024-01-12
    Description: Neuwiedia (sect. Euneuwiedia) Griffithii Rehb.f. Xenia Orch. II (1874), 215; Rolfe in Journ. Linn. Soc. XXV (1890), 235, 241, t. XLVIII, fig. 2\xe2\x80\x949; in Orch. Rev. II (1894), 276; IV (1896), 329; Hook. f. Fl. Br. Ind. VI (1890), 176; in Bot. Mag. CXXI (1895), t. 7425; Krzl. Orch. I (1897), 4; Pfitz. in Pflanzenr. IV. 50 (1903), 5; Ridl. in Journ. Linn. Soc. XXXII (1896), 416; Mat. Fl. Mal. Penins. I (1907), 231; Fl. Mal. Penins. IV (1924), 296.\nPlanta in genere parva. Caulis erectus, rigidus, teres, dilute viridis, c. 14 cm longus, 0.63 cm diam., c. 10-folius. Folia erecto-patentia, recurva, lanceolata, sensim longe et acutissime acuminata, basi acuta sensim in petioluin contracta, plicaita, nervis c. 7 subtus prominentibus, nervis tenuioribus alternantibus, papyracea, utrinque nitidule viridia, c. 18.5\xe2\x80\x94 22 cm longa, 4\xe2\x80\x945 cm lata, summa minora; petiolus latus, canaliculatus, 3-costatus, cum vagina tubulosa antice basi excepta rumpente c. 5.5\xe2\x80\x946.5 cm longus. Inflorescentia erecta, foliis multo brevior, subdense multiflora, cylindrica, pedunculo hirtello, atroviridi, c. 4 cm longo, nonnullis vaginulis in bracteas vergentibus donato, rachide angulato-cylindrica, patentissime hirtella, atroviridi, c. 6.5 cm longa. Bracteae patentes, incurvulae, e basi ovata sensim longe subulato-acuminatae, anguste obtusae, basi rachidem semiamplectentes, praesertim basi concavae, dorso et margine hirtellae, 3-nerviae, virides, ad c. 1.4 cm longae, superiores minores. Flores quaquaversi, parvuli, patentes, nutantes, sepalis dorso patentissime superne patenter strigillosis petalisque conniventibus, concavis, tenuibus, albis, pallide flavescenti-apiculatis. Sepalum dorsale ellipticum, apiculo tereti strigilloso, valde concavum, totum c. 0.83 cm longum, apiculo 0.05 cm, 0.4 cm latum. Sepala lateralia oblique ovato-elliptiea, apice cucullatoobtusa cum apiculo recto tereti-subulato strigilloso 0.08 cm longo, concava, costa media dorso convexo-incrassata, tota c. 0.87 cm longa, 0.375 cm lata. Petala late elliptico-obovata, obtusa, apice vix cucullata, basi margine antico vix unguiculato-contraeta, concava, costa media dorso valde incrassata strigosaque apice in apiculum brevem producta in praefloratione inter sepala prominente, c. 0.8 cm longa, 0.525 cm lata. Labellum a gynostemio subrectangule patens et recurvulum, supra basin obtusangule incurvum, stigma paululum superans, valde concavum, explanatum cuneato-angulato-obovatum, apice cucullato-obtusissimum, ungue cuneato excepto leviter crispulum et erosulum, basi intus valde convexoincrassatum, costa media dorso valde prominente et strigosa apice in apiculum incurvulum teretem hirtellum producta, fere 0.8 cm longum, mucrone 0.05 cm longo, 0.6 cm latum. Gynostemium totum c. 0.62 cm, usque ad apicem antherarum 0.4 cm longum. Stamina 3, glabra, inferne cum stylo in columnam rotundato-trigonam supra subtusque 2-sulcatum, c. 0.13 cm longam connata, superne divergentia, filamenti dorsalis pars libera a dorso compressa, oblonga, vix flavescenti-alba, c. 0.1 cm longa; filainentorum lateralium pars libera dorsali similis, 0.13 cm longa; antherae conniventes, fere basifixae, introrsae, praesertim dorsalis valde incurvae, cordatae, apicem versus paululum angustatae, late obtusae, lobis basilaribus obtusis, dorso valde convexae cum sulco levi longitudinali, crassae, vix flaveseenti-albae, dorsalis fere c. 2 cm longa, 0.14 cm lata, laterales bene 0.2 cm longae, 0.175 cm latae. Stylus undatus, teres, leviter clavatus, apice (stigmate) obtusus et papillosus, albus, basi dilute. sulphureus, totus c. 0.6 cm, parte libera 0.525 cm longus. Ovarium pedieellatum curvulum, rotundato-trigonum, patentissime strigillosum, pedicello apicem versus incrassato, pallide viridi, c. 0.33 cm longo, ovario trigono-ellipsoideo, viridi, c. 0.4 cm longo, fere 0.3 cm diam., apice in rostrum apice obliquum pallide viride dorso c. 0.275 cm longum contractum.
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  • 18
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    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 5 no. 3, pp. 700-708
    Publication Date: 2024-01-12
    Description: In Blumea V (1943), 316, I published a list of the Orchidaceae collected by Dr van Steenis in Atjeh. In this list a certain number of specimens were purposely omitted, on account of the fact that flowers had been preserved in alcohol, which material, however, was apparently not extant in Leiden. Under these conditions I have worked up the herbarium so far as possible from the dried specimens only.\nPeristylus goodyeroides (D. Don) Lndl. Gen. et Sp. Orch. (1835), 299; etc.
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  • 19
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    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 5 no. 3, pp. 600-640
    Publication Date: 2024-01-12
    Description: In one of his papers on Malaysian Orchids R. Schleehter (1911) expresses his surprise that the flora of Celebes, though promising so much from a phytogeographical point of view, is very little known in comparison with that of the Philippines and Java and even with that of Borneo. In 1926 E. D. Merrill repeated this assumption with little less emphasis, and it is, indeed, still holding good even nowadays. I am not able to tell the reason why Celebes has been so much neglected in this respect, though it has been given ample attention by zoogeographers.\nYet, botanical exploration has been carried out ever since the French scientific world cruises of the \xe2\x80\x9cAstrolabe\xe2\x80\x9d (1828) and the \xe2\x80\x9cAstrolabe\xe2\x80\x9d and the \xe2\x80\x9cZelee\xe2\x80\x9d (1839). The more important collections have been enumerated in the \xe2\x80\x9cAppendix\xe2\x80\x9d to the present paper and among these the most outstanding ones are those made by the Neth. \xe2\x80\x93 Indian Forestry Service and by such individual collectors as Forsten (1840, N), Zollinger (1847, SW and Salajar), Teysmann and De Vriese (1860, N), Teysmann (1877, SW and Salajar), Warburg (1888, SW), Koorders (1894\xe2\x80\x94\xe2\x80\x9995, N), P. and F. Sarasin (1893\xe2\x80\x94\xe2\x80\x9996 and 1902\xe2\x80\x94\xe2\x80\x9903, all parts), Elbert (1909, SE), Schleehter (1910, N), Van Vuuren (1912\xe2\x80\x94\xe2\x80\x9914, SW, C, SE), Docters van Leeuwen (1913, Salajar, etc.), Kaudern (1917\xe2\x80\x94\xe2\x80\x9920, SE, C, E, N), Bunnemeyer (1921, SW), Lam (1926, Talaud), Kjellberg (1929\xe2\x80\x94\xe2\x80\x9930, SW, SE), Eyma (1938, C, E) and Monod de Froideville (1937\xe2\x80\x94\xe2\x80\x9939, SW, C, SE).
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  • 20
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    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 6 no. 1, pp. 264-265
    Publication Date: 2024-01-12
    Description: The names Blumea intermedia Koster (syn. Bl. acutata DC. var. \xc3\x9f) and Blumea floresiana (Schultz-Bip.) Boerl. must be kept upright. Blumea humifusa (Miq.) Clarke var. monochasialis Koster has to be changed into Blumea tenella DC. var. monochasialis (Koster) Koster, for Blumea humifusa (Miq.) Clarke is a synonym of Blumea tenella DC.\nBlumea lacera (Burm.) DC. var. burmanni DC. is not a clearly distinguishable variety.\nBlumea runcinata DC. is a synonym of Blumea lacera (Burm.) DC.\nBlumea fasciculata DC. is a synonym of Blumea sessiliflora Decaisne, which is not a synonym of the closely related Blumea fistulosa (Roxb.) Kurz (syn. Bl. glomerata DC. and Bl. leptoclada DC.). Blumea chinensis (L.) DC. as well as Blumea semivestita DC. are a mixture of Blumea riparia (Bl.) DC. and Blumea bullata Koster.
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  • 21
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    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 6 no. 1, pp. 229-242
    Publication Date: 2024-01-12
    Description: The International Association of Wood Anatomists in the early years of its existence has undertaken to standardize the nomenclature used in describing woods. Later the classes of dimensions have been added thereinto.\nIn the same way it should be possible now to standardize one or two identification methods.\nUniversal schemes in the first place will fit for this purpose. In the introduction it is explained which requirements should be fulfilled in such schemes.\nThe advantages and drawbacks of an English and a Dutch identification method are compared mutually. It is suggested, that a procedure according to the Hollerith system will allow of a synthesis of both methods mentioned, thus combining advantages and eliminating their drawbacks. The restriction in the applicability of the Hollerith scheme is determined by the fact, that complicated devices are necessary the costs of which can only be justified, if they are constantly employed at full capacity. Thus the method can only be used in a central office. It will especially yield good results if a close international collaboration is established.\nA standardized codification and centralized multiplication and distribution of cards are indispensable requirements for realising this purpose. A short general survey is given of the Universal Decimal Classification and it is explained according to which principles wood species have been included in this scheme. The decimal codes of the U.D.C. can be used for indicating botanical and geographical data in the Hollerith identification. In this way, the great advantage is achieved, that a literature card index on wood species can be compiled with the same figure combinations. In doing so these figures get a wider field of application than when independant classifications are made for identification and documentation purposes.
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  • 22
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    Unknown
    In:  Blumea. Supplement vol. 3 no. 1, pp. 22-24
    Publication Date: 2024-01-12
    Description: On the 13th of October 1940 I found in the vicinity of a wool- and skinwork in Tilburg (The Netherlands, prov. N. Brabant) a sterile grasstuft, striking me by its peculiar habit. I transplanted it into my garden in Dordrecht and there it was flowering for the first time in June 1941, and in July it was collected to be dried. On the 4th of July 1941 I gathered one more fructifying specimen at the same locality in Tilburg. Doubtless the plant was a Deschampsia and my provisory identification was D. media R. et Sch.. Sending the material with this name to Dr P. Jansen in Amsterdam I got his reply: \xe2\x80\x9dCertainly not D. media. It is a species, unknown to me or, more probably, a variety of D. flexuosa\xe2\x80\x9c.\nThis conclusion, however, seemed unacceptable to me. The habit of the sterile as well as the fertile plant differs strongly from that of D. flexuosa. The tuft is denser and harder, with thicker and shorter leaves. The panicle is longer, wider and more diffuse, the branchlets less flexuous, the culms are relatively short, as long as the panicle or at most 1\xc2\xbd\xe2\x80\x942 times the length of the panicle (in D. flexuosa 4\xe2\x80\x945 times). The characteristics of the flower are decisive. The lower glume is 5 mm long, the upper one 6 mm, both of them overtop the lemma and palea of the enclosed flower (in D. flexuosa the glumes are little different in length and equaling or overtopped by the flowers). The stipe of the upper flower, remaining attached to the lower one, when the spikelet falls asunder, is densily pencilshapedly hirsute and 1.5 mm long (in D. flexuosa 0.6\xe2\x80\x940.8 mm). The upper flower bears a similar stipe of a fully rudimental third flower, in other words: the rachilla is produced behind the upper palea as a hairy bristle. These properties sooner recall D. setacea than D. flexuosa, but the anthers are very small, 0.3\xe2\x80\x940.5 mm long, on much longer filaments (D. setacea has anthers, 1.5 mm long, filaments 0.5 mm, D. flexuosa: anthers 1.8 mm, filaments very short). All this: the habit, the pale green spikelets without any touch of purple, brown or blue, and the small anthers on long filaments justifies a specific differentiation of the Tilburgian wooladventive. I propose to name it, in honour of Dr J. Th. Henrard, whom I owe so much in the field of adventives in general and of Gramineae in particular: Deschampsia Henrardii nov. spec.
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  • 23
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 25-41
    Publication Date: 2024-01-12
    Description: Urelytrum Henrardii Chippindall sp. nov.; ab U. agropyroidei Hack., cui e descriptione affine, culmis gracilibus, foliorum laminis non hirsutis, longe attenuatis, longioribus, racemis flavido-viridibus, spicularum sessilium gluma inferiore 5-nervi, arista breviore distinguendum \xe2\x80\x94 Fig. 1.\nGramen perenne caespitosum, usque ad 92 cm altum. Culmi erecti, simplices, graciles, pauci-nodes, glabri, racemos versus asperuli. Folia plerumque basalia; vaginae internodiis longiores, sublaxae, striatae, apicem versus carinatae, basales glabrae laevesque, superiores pilis patulis laxe pilosae, ore villoso-barbatae; ligulae scariosae, rotundato-obtusae, 0.8\xe2\x80\x941.25 mm longae; laminae lineares, apice tenuiter setaceae, planae vel leviter conduplicatae, usque ad 38 cm longae, 3\xe2\x80\x943.8 mm latae, marginibus scabridis, costis asperulis, pone ligulam pilis longis exceptis glabrae. Racemi ad culmi apicem solitarii, stricti, fragiles, subcylindrici, fere glabri, flavidi vel pallide flavido-virides, saltem 16 cm longi; articuli rhacheos compressi, infimo usque ad 2 cm longo, scaberuli, margine uno superne rigide ciliati, appendice membranacea inaequaliter dentata ciliolata; pedicelli articulis similes, sed appendice minore. Spiculae sessiles biflorae, anguste lanceolato-oblongae, 7.5\xe2\x80\x948.2 mm longae (callo excluso); callus crassus, rotundato-obtusus, basi barbatus. Glumae subaequales, minute punctatae; inferior spiculam aequans, coriacea, marginibus hyalinis, explanata lanceolata, subconvexa, subacuta, 5-nervis, dorso apicem versus parce spinuloso-ciliata, superne bicarnata, carinis angustissime alatis, alis spinuloso-ciliatis; superior inferiore paulo brevior, firme membranacea, marginibus hyalinis apice minute ciliolata, lanceolata, acuta, 3-nervis, superne carinata, carina anguste alata, ala spinuloso-ciliata. Anthoecium inferum \xe2\x99\x82: lemma tenuiter hyalinum, lanceolato-ovatum, 6\xe2\x80\x946.5 mm longum, 2-nerve, minute bidentatum, marginibus apicem versus minute ciliolatum; palea lemmati similis sed angustior et paulo longior; antherae 3 mm longae; lodiculae glabrae. Anthoecium superum \xe2\x99\x80: lemma lemmati anthoecii inferi simile sed 3-nerve, apice latius; palea angustior. Spiculae pedicellatae illis sessilibus absimiles, neutrae, ad glumas lemmaque redactae, sine arista 2\xe2\x80\x942.75 mm longae. Glumae coriaceae, marginibus hyalinis superne ciliolatae, minute punctatae; inferior spiculae aequilonga, lanceolata, 5-nervis, ad carinam superne angustissime alata, ala spinulosociliata, in aristam scabridam 9\xe2\x80\x9412.5 mm longam excurrente; superior inferiore paulo longior, apice integra, obtusa, superne carinata, carina anguste alata, ala spinuloso-ciliata, obscure 5-nervis. Lemma tenuiter hyalinum, parvum.
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  • 24
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 71-82
    Publication Date: 2024-01-12
    Description: In the following account the author of the present paper has endeavoured to compile all available information regarding this interesting member of the Gramineae-Zoysieae.\nAs the genus under consideration has in many cases been incorrectly described, it appeared highly desirable to amend the faults and inaccuracies committed by both the original author of the genus and various subsequent taxonomists. The results of these investigations are being put forward in the following pages.
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  • 25
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 113-119
    Publication Date: 2024-01-12
    Description: As my friend Dr J. Th. Henrard, when young, paid much attention to the adventitious species of Fumaria, I will give here an enumeration of the species found in our country. This genus has been somewhat neglected with us, mainly owing to the fact that the descriptions in our flora\xe2\x80\x99s are not exact, so that the determination was not always easy; the less so as the species are variable in several characters.\nAs I have not much space at my disposal, I will refrain from giving detailed descriptions, but the essential characters I will lay down into the key, so that a correct determination is possible. Minute descriptions are to be found in the splendid works of Mr H. W. Pugsley, which have been a great help to me.
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  • 26
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 1-3
    Publication Date: 2024-01-12
    Description: Fate has knocked at your door. It has reminded you that, as to the years of your life, you are no longer a young man, that your age will be sixty five on the day this little volume will be presented to you.\nTime and fate are inexorable powers. Sometimes the question has occurred to me, whether we have any right to speak of a \xe2\x80\x9cJubilee\xe2\x80\x9d, whether one\xe2\x80\x99s retirement from office or the attainment of high age is something to be gratulated upon, since these events are usually not exactly welcome to the person involved. Yet, I think there cannot be any doubt as to this. For, can there be ever more reason for deep satisfaction and gratitude than when a man may without self-reproach, look back upon an honest and successful life?
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  • 27
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 63-70
    Publication Date: 2024-01-12
    Description: A taxonomic study of the 6 species of Stipa that inhabit desert regions of the Puna de Atacama S. Bomani Haum., S. venusta Phil., S. obtusa [Nees et Mey.] Hitchc., S. rigidiseta [Pilg.] Hitchc., S. saltensis O. Kuntze, and the new species S. Henrardiana) indicates that they constitute a natural group which I designate Obtusae, using as type the species S. obtusa which is the one with priority. The group is characterised by setose leaves, with ligules 3 to 10 mm long, by glumes that are scarious, smooth, depressed and usually unequal, by the fusiform anthoecium with the palea as long as the lemma and by glabrous anthers. These characters reveal a close relationship with Orthachne Nees and Oryzopsis Michx. More detailed studies are necessary to decide the generic relationships.\nSome of the species studied ( S. Bomani and S. saltensis) contain cyanoglucosides in their vegetative organs and consequently are feared by the inhabitants of the Puna as being toxic to livestock.
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  • 28
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 44-44
    Publication Date: 2024-01-12
    Description: Dactyloctenium Henrardianum Bor spec. nov. quae ab omnibus aliis speciebus hujus generis inflorescentia racemosa haud digitata satis recedit.\nAn annual grass. Culms slender, 10\xe2\x80\x9430 cm tall, erect, smooth, glabrous, striate in robust specimens, terete, long-exserted from the uppermost leaf-sheath. Leaf-sheaths strongly keeled, loose, slipping from the culm, much shorter than the internode and leaf-blade, markedly striate, smooth and glabrous except for some bristles from bulbous bases sparsely arranged near the margins in the upper fourth; ligule a lacerate membrane not more than 2 mm long. Leaf-blades up to 10 cm long by 5 mm wide at the base, gradually narrowed into a fine point from the rounded base, very scabrid on the margins which also bear long bulbous-based bristles in the lower third; upper surface smooth; lower surface often with bulbous-based bristles; midrib strongly marked with 2\xe2\x80\x943 prominent parallel veins on either side.
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  • 29
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    In:  Blumea. Supplement vol. 3 no. 1, pp. 4-6
    Publication Date: 2024-01-12
    Description: On October 16th 1946 Dr J. Th. Henrard will have reached the pensionable age of sixty five years. In accordance with the legal prescriptions he is due to take leave officially as keeper of the \xe2\x80\x9dRijksherbarium\xe2\x80\x9c. The present director, Prof. Dr H. J. Lam, invited me to write a short biography of Dr Henrard on this occasion. Having been Henrard\xe2\x80\x99s eldest colleague till 1934 at the institution, I accepted willingly.\nJan Theodoor Henrard was born October 16th, 1881 at Maastricht, where his father, J. B. Henrard, was director of the Weight and Measures Office. There is a legend in the family that the Henrards originated from the Vend\xc3\xa9e (in France) as descendants of a Huguenot-refugee. Owing to this duties J. B. Henrard was often transferred with his family from one locality to the other; his children got their education in different towns of the country. Jan visited the elementary school at Maastricht. The secundary school he followed at Zwolle and Leeuwarden respectively. At Zwolle he made the acquaintance of two well-known Dutch florists, Lako, a teacher at the secundary school and Carmiggelt, an official at his fathers office. From them Jan gathered already an extensive knowledge of the Dutch flora. His final high school certificate he got at Sneek on August 10th, 1901 (Diploma H. B. S.).
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  • 30
    facet.materialart.
    Unknown
    In:  Blumea. Supplement vol. 3 no. 1, pp. 83-89
    Publication Date: 2024-01-12
    Description: Peculiarities in leaf anatomy support the opinion that the name Triodia R. Br. should be confined to the Australian species. The leaves of species of Plectrachne Henr. are quite different from those of Triraphis mollis, though formerly included in this genus, but are remarkably similar to those of Triodia.
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  • 31
    facet.materialart.
    Unknown
    In:  Blumea. Supplement vol. 3 no. 1, pp. 120-121
    Publication Date: 2024-01-12
    Description: A few years ago Prof. Dr W. Martin, at the time director of the Gallery of prints and drawings at Leyden, drew my attention to an oilpainting at Prof. J. N. Bakhuizen van den Brink\xe2\x80\x99s, 40 Rapenburg, Leyden. This painting (size 95 X 68 cm), which is owned by the Leyden University Fund, shows a peculiar group of flowering exotic plants, to which a few mushrooms, a snake, a lizard and some butterflies are added, and on the right side in the back-ground a view on a river or a lake. In the lower right hand corner the painting is signed Lau. Vinn. Prof. Martin concluded from this that it was one of the Haarlem painters Van der Vinne who made it. The most plausible inference seemed to look upon the senior Laurens van der Vinne (1658\xe2\x80\x941729), a well-known Dutch painter of flowers, as the maker. However, a closer investigation learnt that this was not correct.\nWhen Prof. Martin showed me the picture, I got the impression that I had seen a few of the drawings of the individual plants before. Looking through the plate collections of the \xe2\x80\x9cRijksherbarium\xe2\x80\x9d it appeared that this impression was right. These collections, namely, contain water-colours of the 4 species of Proteaceae figured in the painting and moreover a water-colour of the specimen of Sprekelia formosissima. All these once belonged to the Leyden professor Adriaan van Royen. The water-colour of Sprekelia formosissima is signed \xe2\x80\x9cLaurens van der Vinne Pinxcit 1736\xe2\x80\x9d. It is quite probable that this beautiful drawing, together with those of the Proteaceae, were used by Van der Vinne in composing his picture. Besides, it became evident that it was not the senior but the junior Van der Vinne who must be considered the painter, as the former died already in 1729 and the painting must have been made in 1736 or later.
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  • 32
    facet.materialart.
    Unknown
    In:  Blumea. Supplement vol. 3 no. 1, pp. 45-55
    Publication Date: 2024-01-12
    Description: According to general opinion the spikelets of Oryza consist, reckoned from their base upwards, of 2 sterile glumes, called hereafter I and II, one fertile glume (valvula inferior; lemma), called hereafter III, and the palea valvula superior) to this glume, called hereafter p3. The spikelets are placed singly on the very short ultimate branchlets, called hereafter pedicels, of a more or less strongly ramose panicle; the tips of the pedicels are broadened into a shallow infra-spicular cup, either distinctly 2-lobed or not; from the bottom of the cup arises a minute knob, on which the very distinct basal callus of the spikelet is jointed. When ripe, the spikelets of the wild species fall off as a whole, disarticulating at the joint (in dried specimens often long before maturity; hence in herbarium-specimens they are frequently lacking). In many cultivated forms they remain firmly attached to their pedicels, a property of very high economic value.\nThe spikelets are strongly laterally compressed. I and II are either 1-nerved or nerveless; as a rule they are many times shorter than the spikelet, sometimes even very minute. Only in O. Ridleyi they are comparatively well-developed, reaching about half the length of the spikelet, but very narrow. III is very rigid, usually conspicuously granulate, boatshaped, keeled, either awned or not, 5-nerved, with a strong midrib; it has the ultimate lateral nerves along the margins. P3 is likewise boatshaped, shortly cuspidate or not, with a narrow, rather rounded, less often faintly keeled back, 3-nerved; it is about as long as III, awn disregarded, and has the same rigid granulate structure, excepted the narrowly incurved thinly membranaceous smooth marginal parts (hidden by III). It might be taken for a fertile glume, but this view is inadmissible because of the averted position of the lodicules. It has a rather thin mid-nerve and strong lateral nerves, separating the rigid central part from the membranaceous borders. The well-developed lodicules are glabrous; the six stamens are free; there are 2 free shortish styles with large plumose white or violet stigmas which, during anthesis, stick out from the sides of the spikelet in or below its middle. The ripe fruit is oblong or lanceolate, usually angular; it is free from glume and palea but remains firmly incarcerated between them.
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  • 33
    facet.materialart.
    Unknown
    In:  Blumea. Supplement vol. 3 no. 1, pp. 6-9
    Publication Date: 2024-01-12
    Description: 1. (with G. H. H. ZANDVOORT) \xe2\x80\x94 Een voor Nederland nieuwe plant, Kentrophyllum lanatum DC. \xe2\x80\x94 De Levende Natuur XV, p. 376\xe2\x80\x94380, 4 fig.
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  • 34
    facet.materialart.
    Unknown
    In:  Blumea. Supplement vol. 3 no. 1, pp. 10-21
    Publication Date: 2024-01-12
    Description: Most classifications of the genera of the Gramineae have been on the structure and arrangement of their spikelets, for these organs provide a far greater variety of readily distinguishing characters than do other parts of the grass plant. Nevertheless it has not always been possible to decide from morphological studies alone whether marked similarities in structure point to a close affinity or are merely examples of parallel development. The modern taxonomist, endeavouring to arrange the grass genera in as natural a sequence as possible in order to emphasise relationships and evolutionary trends, sooner or later meets with difficulties in this respect, for examples of parallelism are of common occurrence in this family. He is more fortunate, however, than his predecessors, in that his own intensive morphological studies, based on a wider range of specimens, may be supplemented by additional data gleaned from the ecological, anatomical and cytological researches of contemporary workers. Thus aided by the more complete information at his disposal, it has been possible for him to rearrange certain groups, particularly the Festuceae and Hordeeae, in which parallel development has occasionally led to unrelated genera such as Lolium, Agropyron and Nardus, being too closely associated. In the following account an attempt has been made to provide a more natural classification for about eighteen species frequently referred to the genus Lepturus R. Br. by reason of their similar spicate inflorescences.
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  • 35
    facet.materialart.
    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta vol. 4 no. 1, pp. 43-44
    Publication Date: 2024-01-12
    Description: Floating aquatic herbs with dimorphic leaves, submerged ones opposite pinnatifid rootlike, apical ones in a rosette, rhomboid, dentate, with spongy often inflated petiole, arranged in leaf-mosaic; stipules 4-8, minute. Flowers bisexual, small, solitary, axillary, short-pedicelled, 4-merous, white or lilac. Petals imbricate. Disk present. Ovary half-inferior with 1 style and 2-4 persistent sepals turning often to thorns or horns. Fruit mostly 1-celled, 1-seeded, shell bone-hard; thorns after withering often set with barbs at the apex. Seed often producing 2-5 free germ-stalks.\nDistr. Several species in the Old World, but not known from Australia.
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  • 36
    facet.materialart.
    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta vol. 4 no. 1, pp. 601-631
    Publication Date: 2024-01-12
    Description: Suprageneric epiphels have been entered under the family name to which they belong preceded by the indication of their rank (tribes, e.g.).\nSupraspecific epithets have been entered under the generic name to which they belong preceded by the indication of their rank (sections, series).
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  • 37
    facet.materialart.
    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 5 no. 3, pp. 423-425
    Publication Date: 2024-01-12
    Description: We always have thoroughly detested the mentality of those scientific periodicals which deemed it proper to introduce politics into their columns. During the war we have repeatedly been offended by the unworthy attitude of the editorial staffs of certain botanical journals of \xe2\x80\x9cGreater Germany\xe2\x80\x9d who admitted \xe2\x80\x94 or possibly even deliberately furthered \xe2\x80\x94 perorations stating not only the marvellous achievements of nazi-methods and their amazing usefulness towards the particular field of science covered by the periodical in question, but the faith and the devotion of their persons towards the sacred cause of the nazi-system.\nWe have, as I say, not exactly admired this mentality in a scientific paper and we will not follow the example. However, too much has happened in the five long and hard years of bloody oppression by ruthless and barbarian enemies, both in Holland and in Indonesia, that this crucial moment in our national history could be passed without any comment even by a stolid and, allegedly, unemotional Hollander. For never more distinctly than in the past five years have we been enabled to state \xe2\x80\x94 or state again, as the case may be \xe2\x80\x94 how utterly different the Germans are from us, how fundamentally their mentality and their ideals differ from ours.
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  • 38
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 26 no. 10, pp. 271-280
    Publication Date: 2024-01-12
    Description: A revision of the material belonging to the genus Erebia Dalman in the Rijksmuseum van Natuurlijke Historie at Leiden, mainly based on the "Monograph of the genus Erebia" by B. C. S. Warren (London, 1936), induced me to describe a number of new subspecies and aberrations, and to make some remarks on forms already described.\nThe greater and most important part of the material is to be found in the Mezger collection, which is kept separate. It has always been indicated with the types, if they are to be found in that collection ; all other types are included in the general collection of Lepidoptera of the Rijksmuseum van Natuurlijke Historic Descriptions and remarks are following here in systematic order, according to Warren\'s system.\nErebia eriphyle (Frr.) subsp. tristis H.-S. ab. secundo-tertiopunctata nov. ab.\nThe typical eriphyle possesses two black spots on the forewing; specimens deviating in this respect were described as ab. tripunctata Hoffm. with three spots, and as ab. impunctata H\xc3\xb6fn. without black spots. One of the specimens in hand, from Reichenstein, Styria, and consequently belonging to the subsp. tristis H.-S., shows the two hindmost black spots of the ab. tripunctata Hoffm., but the foremost spot is lacking. I propose the name secundo-tertiopunctata nov. ab. for this aberration.\nHolotype: \xe2\x99\x82, Reichenstein, 15 VII 1923, in the Mezger collection.\nErebia manto (Schiff. & Dennis) subsp. osmanica Schaw. ab. subtuslutescens nov. ab., and ab. bubastis nov. ab.\nIn his excellent monograph of the genus Erebia Warren writes that the
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  • 39
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 26 no. 11, pp. 281-286
    Publication Date: 2024-01-12
    Description: When studying the European Caridea of the Rijksmuseum van Natuurlijke Historie at Leiden and of the Zoological Museum at Amsterdam, some specimens of the genus Pandalina came at hand, which proved to belong to a new species. These specimens had already been reported upon by Hoek (1882), who considered them to be Pandalina brevirostris (Rathke). Comparison with typical specimens of Pandalina brevirostris, however, showed various constant differences, which in my opinion justify the separation of Hoek\'s specimens as a distinct species.\nIn the present paper an enumeration of the specimens of both species of Pandalina present in the above mentioned Musea is given.\nPandalina profunda nov. spec. (fig. 1a-c) Pandalus brevirostris Hoek, 1882, Niederl. Arch. Zool., suppl. vol. 1 pt. 7, p. 22,pl. 1 fig. 10 (non Pandalus brevirostris Rathke, 1843).\nPandalus brevirostris A. Milne Edwards, 1883, Rec. Fig. Crust. nouv. peu conn., pl. 26 fig. 2.\nPandalina brevirostris Schellenberg, 1928, Tierw. Deutschl., vol. 10 pt. 2, fig. 7 (non p. 16, figs. 8, 9).\nMuseum Leiden: Barents Sea; 1878-1879; Willem Barents Expedition. \xe2\x80\x94 4 specimens 24-28 mm 1).\nBergen, Norway; 1907. \xe2\x80\x94 1 ovigerous \xe2\x99\x80 25 mm.\nDescription : The rostrum is short, it reaches to the middle of the second segment of the antennular peduncle ; it is straight or directed slightly upward at the apex. The upper margin is provided with eight to ten teeth; the anterior three or four of which are immovable, the posterior teeth articulate with the carapace. The lower margin of the rostrum is provided with three
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  • 40
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 26 no. 6, pp. 247-248
    Publication Date: 2024-01-12
    Description: In his key to the species of the genus Diploglossus, Boulenger (1885, p. 284) distinguishes between two groups of species, viz., one group in which the digits terminate in "a large compressed sheath, into which the claw may be entirely or nearly entirely retracted", while in the other group such a sheath is absent. Barbour (1910, p. 297) considers the presence or absence of an ungual sheath as a character of generic value ; he separates the species lacking such a sheath from the true Diploglossus, and revives the genus Celestus Gray for them 1). Burt & Burt (1931, pp. 241-242) also stress the importance of this character.\nIndeed the sheath is absent in Celestes occiduus (Shaw), of which Celestus striatus Gray (the type of the genus) is a synonym. Of the other species included in Celestus (Barbour, 1937, pp. 138-139) I have examined only Celestus de la sagra (Cocteau). Of the two specimens in our collection (Herp. reg. nos. 3626, 3634), one (no. 3626) is a cotype of Scincus (Diploglossus) de la sagra Cocteau (in Cocteau & Bibron, 1839, p. 180, pl. 20).\nIn both specimens the terminal scale on the upper surface of the digits forms a
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  • 41
    Publication Date: 2024-01-12
    Description: Besides the rather scanty material collected before 1900 the Phyllophorin\xd0\xb0\xd0\xb5 of the Leiden and the Amsterdam Museums consist of many of Karny\'s type specimens, and a number of specimens collected in New Guinea, especially by Van Kampen and by Versteeg.\nThough various authors (Kirby, 1899; Griffini, 1908) published papers of fundamental value concerning this subfamily of the Tettigoniidae, the general survey given by Caudell (1912) was little critical, in different genera even species are placed here of which the synonymy had already been established before (cf. Karny, 1924, pp. 19, 20). A modern revision of the subfamily was given by Karny (1924).\nThough Karny based his paper on a rather large number of specimens and a great deal of literature, it appears that there exist more species. The Leiden as well as the Amsterdam collections contain some specimens which could not be identified with the help of Karny\'s keys, and which did not fit in with the descriptions of the species already known. For that reason I feel justified to describe these as new species.\nAll specimens dealt with below, Karny\'s type specimens included, were carefully compared with the descriptions to avoid misinterpretations of Karny\'s view. In a few cases, however, I cannot agree with Karny\'s views concerning certain details in the keys as well as in the descriptions and I have given some additional notes when dealing with the genera or species under consideration.\nI abstained from giving a new key as that of Karny will do for the present when my remarks are taken into account.\nSasima Bol\xc3\xadvar
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  • 42
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 25 no. 5, pp. 36-38
    Publication Date: 2024-01-12
    Description: De Haan (1833, p. 22-23, tab. B (Eudora) tenax (mouthparts)) gives the following latin description of his subgenus Eudora: "Os quadratum. Max. 5arum articuli secundi paralleli, medio in longitudinem sulcati, apice truncati; articuli tertii dilatati, margine superiore emarginati; articuli apicales abbreviati1). Max. 3iarum laciniae externae supra medium, paulum dilatatae, apice emarginatae. Max. 2arum lobi interni in laciniis interioribus externis multo breviores. Thorax vix dimidio latior quam longior, dorso convexus. Chelae crassae, in utroque sexu inaequales, sinistra minor. Abdomen in utroque sexu 7-articulatum; in maribus angusto-parallelum; articulus tertius prioribus latior; articuli versus apicem sexti sinuato-angustiores; sextus quadratus; Septimus trigonus. In feminis oblongo-ovatum, a basi latescens; articulus sextus quinto duplo latior; septimus rotundatus. O c u l i vix tertia parte latitudinis thoracis distantes. Antennae oculorum canthis approximatae, flagello brevissimo.\nCANC. (EUDORA) TENAX Ruppell. \xe2\x80\x94 IMPRESSUS Lamarck n. 9. \xe2\x80\x94 INCISUS. n. sp. Mus. Reg. Bat." When studying the Xantho specimens of the Leiden Museum, I noticed among them in the dry collection, a \xe2\x99\x80 without mouthparts and a set of mouthparts from Mauritius, Museum Paris, both labelled Xantho (X.) impressus (Lam.) and both bearing an old label "Cancer (Eudora) impressus Lamarck, Isle de France, Mus. Gal." Now the presence of the set of mouthparts as well as the writing on the old label leave no doubt whatever to the fact that this is the specimen examined by De Haan and enumerated on page 23 of the Fauna Japonica. This specimen, however, is
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  • 43
    Publication Date: 2024-01-12
    Description: Professor I. Q. van Regteren Altena was zoo vriendelijk mij een aantal teekeningen ter beschikking te stellen, die eens aan het huis Plantijn moeten toebehoord hebben. Immers, sommige daarvan hebben gediend als voorbeeld voor houtsneden in den Herbarius von Dodonaeus van 1618, gedrukt \xe2\x80\x9et\'Antwerpen in de Plantynsche Druckerye van Balthasar Moretus" (zie Engel, in: Ned. Kruidk. Arch. 53, 1943, p. 46-55). Wanneer men de fraaie teekeningen vergelijkt met de reproducties in het Cruydtboeck, is het opvallend, dat de teekeningen losser, zwieriger en natuurlijker zijn, terwijl de houtsneden allerlei wijzigingen vertoonen, die klaarblijkelijk aangebracht werden ten einde de figuur in het formaat van het houtblok te doen passen. Toch komen beide tot in finesses overeen en, wat onze opvatting bevestigt, zij zijn elkanders spiegelbeeld. Behalve deze plantenafbeeldingen bevat de collectie nog een teekening van een vogel, Podiceps cristatus (L.), door mij beschreven en afgebeeld in Limosa, Orgaan der Club van Nederlandsche Vogelkundigen, XVI, 1-2, Juni 1943, p. 1-3, en verschillende figuren van visschen en lagere dieren.\nVoor deze dierenafbeeldingen is van belang een citaat uit: Max Rooses, Christophe Plantin, Imprimeur Anversois, 2me \xc3\xa9dition, Anvers, 1896, p. 325: \xe2\x80\x9ePlantin, qui avait retrouv\xc3\xa9 Dodoens en Hollande y renouva avec lui les liens d\'une ancienne amiti\xc3\xa9. Au moment du d\xc3\xa9c\xc3\xa8s du savant botaniste, l\'imprimeur rappelle, dans une de ses lettres, l\'affection qui les unissait et dit que Dodoens \xc3\xa0 la fin de sa vie avait commenc\xc3\xa9 une description des poissons et des oiseaux." Wij mogen er hier aan herinneren, hoe Dodoens in 1582 benoemd werd tot professor te Leiden, welke functie hij slechts korten tijd mocht ver-
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  • 44
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 27 no. 4, pp. 300-308
    Publication Date: 2024-01-12
    Description: During the time that I was stationed at Port Dickson (State of Negri Sembilan) on the west coast of the Malay Peninsula, a small zoological collection was made. The specimens were brought to me by the personnel of different units of the Royal Netherlands Forces, while I am also indebted to Major C. Rae, RASC, for some interesting specimens. Nearly all specimens belong to common species. However, this area has not been studied so very extensively and therefore, it seems worth while to place these species on record. Unless otherwise stated the specimens are from the strip of country along the coast road to the south of Port Dickson to about ten miles from the township. Where no unit is mentioned, the specimens have been collected by personnel of my own unit (NICA-NRX Detachment). The collection has been presented to the Rijksmuseum van Natuurlijke Historie, Leiden.\nBufo melanostictus Schn. 1 specimen, Major L. D. Brongersma, Herp. reg. no. 8488.\nBufo parvus Blgr. 1 \xe2\x99\x82 halfgrown, Herp. reg. no. 8486. 1 juv., among dry leaves in a rubber plantation, March 1946, Sergt.\nEveraarts, Herp. reg. no. 8487.\nI am indebted to Mr. H. W. Parker, London, for his advise that both these specimens should be referred to Bufo parvus Blgr.\nIn the male (length from snout to vent 33 mm), the cranial ridges are distinct. The supraorbital ridges are slightly divergent behind, while the short parietal ridges converge posteriorly; thus the whole of the ridge is somewhat curved. In a fullgrown Sumatran specimen these ridges are straight.
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  • 45
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 28 no. 7, pp. 267-270
    Publication Date: 2024-01-12
    Description: In 1776 beschreef P. L. S. M\xc3\xbcller (Syst. Nat. Suppl., p. 145) naar aanleiding van in Oost-Java verzameld materiaal de nominaatvorm dezer pitta onder de naam Turdus guajanus, terwijl de in West-Java levende ondersoort affinis als Myiothera affinis in 1821 door Horsfield (Trans. Linn. Soc.\nLondon, vol. 13, p. 154) werd beschreven op grond van in Bantam verkregen materiaal. In Cat. Birds Brit: Museum (vol. XIV, 1888, p. 445/6) vatte Sclater deze beide soorten samen onder de naam Eucichla cyanura.\nRobinson & Kloss (Treubia, vol. V, 1924, p. 279) noemden de OostJava vogels Eucichla c. cyanura en die van het Westen Eucichla cyanura affinis, welke naam ook door Bartels & Stresemann (1929) werd gebezigd. Later toonde Boden Kloss echter aan, dat de naam cyanura diende te worden gewijzigd in guajana (Journ. Mal. Br., Royal As. Soc., vol. IV, 1926, p. 161), terwijl Chasen in diens Handlist (1935) het geslacht Eucichla met Pitta vereenigde en deze brengt Pitta guajana guajana op voor OostJava en Bali en Pitta guajana affinis voor het Westen van dit eiland.\nDe oorspronkelijke beschrijving der beide ondersoorten hebben wij niet ter beschikking, maar Kuroda (Birds of the Island of Java, vol. I, 1933, p. 339) deelt ten aanzien van de nominaatvorm het volgende mede. ,,Characters: \xe2\x80\x94 Very similar to E. g. affinis of W. Java, but the blue gorget much more broader (10 mm in width in \xe2\x99\x82).\nAdult \xe2\x99\x82 (E. Java) \xe2\x80\x94 The ground-colour of underparts yellowish instead of brownish yellow as in affinis and the throat also whiter.\nAdult \xe2\x99\x80 (Bali) \xe2\x80\x94 "The ground-colour below of this female is not white as described in Cat. B. Brit. Mus. XIV. p. 446, but yellowish buff, and the throat is more white (HARTERT)."
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  • 46
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 28 no. 4, pp. 252-253
    Publication Date: 2024-01-12
    Description: In zijn laatste revisie van het genus Zosterops (Journ. f\xc3\xbcr Orn., vol. 87, 1939, p. 156-164) geeft Stresemann o.a. een schematische voorstelling van de horizontale en verticale verspreiding binnen deze Archipel van de vier voornaamste groepen van dit geslacht: montana, atricapilla, palpebrosa en chloris. Tot onze verwondering wordt hierin geen montana-vorm voor WestJava opgegeven, terwijl Siebers toch reeds in 1929 vogels van Goenoeng Tjerimai besprak, en afsplitste onder de naam Zosterops montana sindorensis (Treubia, vol. 11, 1929, p. 151). Deze ondersoort werd zoowel door Chasen (Handlist of Malaysian Birds, 1935, p. 266) als door Kuroda (Birds of the Island of Java, vol. 1, 1933, p. 127) geaccepteerd. De beide auteurs van \xe2\x80\x9eDe vogels van het Tenggergebergte" (De Tropische Natuur, jrg. 29, 1940, p. 93-101), de heer en mevrouw Van Bemmel, merken daarentegen weer op dat de soort Zosterops montana in West-Java ontbreekt, hetgeen echter in hetzelfde tijdschrift op p. 140 door den heer Bartels wordt herroepen, die melding maakt van het verzamelen van deze soort op de Papandajan. De laatste durft echter aan de hand van het geringe materiaal dat hem ter beschikking staat niet te zeggen tot welk ras de Papandajan-vogels behooren.\nHet Zoologisch Museum te Buitenzorg geraakte echter in 1941 in het bezit van negen balgen van dit brilvogeltje eveneens afkomstig van de Goenoeng Papandajan en aldaar verzameld op een hoogte van circa 2500 m door den heer A. de Vos. Deze balgen wijken in enkele opzichten z\xc3\xb3\xc3\xb3 belangrijk af van alle reeds bekende vormen, dat wij het alleszins verantwoord achten haar hieronder als nieuw te beschrijven.\nZosterops montana minor nov. subspec.
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  • 47
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 26 no. 2, pp. 139-210
    Publication Date: 2024-01-12
    Description: In Juli 1931 verscheen het overzicht van de gestrande Nederlandsche Cetacea van 808 tot en met 1930 (Van Deinse, 1931). De toen bekende 211 gevallen van aanspoeling op onze kust werden soort voor soort en een voor een behandeld.\nSedert zijn nu weer ettelijke jaren verloopen, waarin jaar na jaar aanteekening werd gehouden van de exemplaren die op onze kust te land kwamen en die zeer nabij die kust of in binnenwateren werden gevangen.\nTot en met 31 Dec. 1944, zijn er nu totaal reeds 379 gevallen van stranding bekend geworden en zijn er dus 168 bijgekomen na 1930, alzoo in 14 jaar.\nGemiddeld zijn er per jaar 12 dieren gemeld. In de afgeloopen jaren zijn natuurlijk ook aanvullingen en verbeteringen bekend geworden van oudere gevallen en die hoop ik hieronder in te voegen. In oude, soms zeer oude, literatuur zijn nog strandingen gevonden, die ik in 1931 niet kende en die mij door tal van belangstellende medewerkers werden opgegeven, terwijl ik er zelf ook enkele bij vond.\nZoo is onze kennis van de Nederlandsche Cetacea sedert 1931 zeer vermeerderd, is er belangstelling voor deze orde gewekt en zijn wij inderdaad sterk vooruitgegaan, niet het minst wat betreft geborgen materiaal, oude prenten, foto\'s enz.\nWaren er, in 1931, 17 soorten bekend van onze kust, nu is dat aantal tot 20 gestegen. De 3 soorten die er bij gevoegd konden worden zijn : 1. Pseudorca crassidens (Owen), in 1935, in 2 exemplaren. 2. Eschrichtius gibbosus (Erxleben), in 1935 en 1936, resp. in 1 en 2 exemplaren. 3. Delphinapterus leucas (Pallas), in 1936, in 1 exemplaar.
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  • 48
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 25 no. 7, pp. 41-42
    Publication Date: 2024-01-12
    Description: Falco peregrinus anatum Bonaparte Adult (evidently \xe2\x99\x80), Surinam.\nWing 363, tail 170, tarsus 53, culmen from cere 24 mm.\nTogether with other Surinam bird-skins, the specimen was sent to Harlem (Holland) in 1899 for exhibition at the "Koloniale Westindische Tentoonstelling". It is now in the collection of the Colonial Institution at Amsterdam.\nThe North-American Peregrine Falcon has not yet been recorded from all three Guyanas: Chubb (1916) does not mention it from the British Colony, nor the brothers Penard (1908) from Surinam, nor Von Berlepsch (1908) from Cayenne. As the bird has been recorded several times from Trinidad (off the coast of Venezuela) (cf. Roberts, 1934) and a juvenile specimen from Brazil is preserved in the Zoological Museum at Berlin (Kleinschmidt, 1927, p. 112: "Amazonasmundung"), occasional migratoryrecords do not come unexpected. Besides, Von Berlepsch lists the Peregrine Falcon among the Falconidae that are "not yet recorded from Cayenne", but are "likely to be found there" (p. 289).\nThe North-American Peregrine Falcon has a wide-spread winter-range and is recorded from several other localities in South-America (Ecuador, Matto Grosso; Chile?), but usually does not go farther south than Panama.\nCatoptrophorus semipalmatus inornatus (Brewster) In a relatively large collection of old stuffed birds, made in the Dutch Colony of Surinam, and received at Amsterdam in 1859, there are three specimens of the Willet (Catoptrophorus semipalmatus (Gm.)). All three birds are in winterdress. One of these birds shows remarkably large
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  • 49
    Publication Date: 2024-01-12
    Description: In the former Zuiderzee, the large brackish inland sea of the Netherlands, a species of crab was commonly met with, which species generally was considered to be endemic in the Dutch inland waters, and was named by most authors Heteropanope tridentata (Maitland). Examination of material and literature convinced us that the crab does not belong to the genus Heteropanope at all, but is a Rithropanopeus, while it is so closely related to the American Rithropanopeus harrisii (Gould), that we only can consider it to be a subspecies of that species.\nThe synonymy of the Dutch form is as follows: Pilumnus tridentatus Maitland, 1874, Tijdschr. Nederl. dierk. Ver., vol. 1, p. 232. non Pilumnus tridentatus Maitland, 1876, Tijdschr. Nederl. dierk. Ver., vol. 2, p. 11.\nPilumnus tridentatus Hoek, 1876, Tijdschr. Nederl. dierk. Ver., vol. 2, p. 243, pl. 14 fig. 12-16.\nPilumnus tridentatus Miers, 1886, Rep. Voy. Challenger, Zool., vol. 17, pp. 146, 149, 227.\nPilumnus tridentatus Hoek, 1887, Tijdschr. Nederl. dierk. Ver., ser. 2 vol. 1, p. 96.\nPilumnus tridentatus De Man, 1889, Zool. Jb. Syst, vol. 4, p. 422.\nHeteropanope tridentata De Man, 1892, Notes Leyden Mus., vol. 14, p. 228, pl. 7 figs. 1, 1a-1d.\nPilumnus tridentatus A. Milne Edwards & Bouvier, 1894, R\xc3\xa9s. Camp. sci. Monaco, vol. 7, p. 39.\nPilumnus tridentatus Maitland, 1897, Prodr. Faune Pays-Bas, p. 36.\nPilumnus tridentatus A. Milne Edwards & Bouvier, 1900, Exped. sci. Travailleur & Talisman, Crust. D\xc3\xa9cap., pt. 1, p. 72.\nPilumnus tridentatus Horst, 1903, Maandbl. Nederl. natuurk. Ver., vol. 2, p. 40.
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  • 50
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 25 no. 15, pp. 140-154
    Publication Date: 2024-01-12
    Description: I. Introduction.\nIn the Geological Institution of the University of Amsterdam there is a collection of recent shells as material for comparison with fossil Mollusca.\nFrom this collection the writer identified a lot of shells collected by Professor Dr. H. Gerth during his stay in Java from 1928 to 1929. These materials will be discussed here.\nThe writer is indebted to Prof. Dr. H. A. Brouwer (Amsterdam) for his permission to publish the results of these investigations on materials belonging to the Geological Institution, to Prof. Dr. H. Gerth for placing at his disposal the present collection and his field notes, and further to Dr. Ch. Bayer (Leiden), Mrs. W. S. S. van der Feen-van Benthem Jutting (Amsterdam), Mr. L. de Priester (Apeldoorn), Dr. F. A. Schilder (Naumburg-on-Saale), and Mr. J. R. le B. Tomlin (St Leonards-on-Sea) for their assistance in identifying the recorded species. 2. List of the localities.\nThe numbers in brackets refer to the sketch map (fig. 1). The remarks on local conditions have been borrowed from field notes by Prof. Gerth and from the labels of the samples. The localities have been classified from an ecological point of view by Prof. Gerth.\nA. Beaches with coral reefs.\nNorth coast: a) Thousand Islands (Duizend Eilanden) (7).\nThis is the only sample not collected by Prof. Gerth himself; it was collected by Prof. J. H. F. Umbgrove. The labels contain no particulars about the exact locality or localities from which the shells derive. According
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  • 51
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 25 no. 6, pp. 39-40
    Publication Date: 2024-01-12
    Description: Aulacocyclus laevipennis nov. spec. \nDescription. Lamellae of antennae rather short and stout. Labrum about twice as broad as long, with long, dark red hairs, strongly and closely punctured, anterior margin concave, angles rounded, sides slightly convergent behind. No groove between clypeus and frons. Central tubercle very robust, somewhat square in section, seen from the side its basal vertical part as broad as the whole hind half of the head, strongly elevated and regularly bent forward, excavated in front, seen from behind the base is a little narrower than the apex, the latter a little excavated. Surface of head and basal sides of central tubercle with coarse, hair-bearing punctures. Supra-orbital ridges straight, parallel, somewhat thickened in front. Mentum with a small, smooth, triangular central part, the rest coarsely punctured with dark red hairs. Mandibles with 3 terminal teeth, anterior lower tooth of the right mandible conical, pointed, that of the left mandible very broad, at the outer side with 3 teeth, at the inner side deeply excavated. \nThe angles of pronotum prominent and rounded. The median groove is deep but incomplete in front. The marginal grooves are narrow, scarcely punctured, the anterior marginal groove moderately broader and deeper behind the head. Scars are smooth, small and oval. Anterior part of scutellum coarsely punctured. \nElytrae smooth, glossy, only the grooves near the suture distinct, the other grooves towards the sides become more and more indistinct, the lateral grooves have disappeared and are only recognizable by the vaulting of the ribs and the rows of small, obscure punctures. Epipleurae densely
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  • 52
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 27 no. 2, pp. 205-252
    Publication Date: 2024-01-12
    Description: The Blattid fauna of Celebes, the Moluccas, and New Guinea, a region which from a zoogeographical point of view forms an important area of transition, is still insufficiently known. Moreover the literature on the Blattids of this region is scattered in various papers which made it desirable to give a general survey of the hitherto known species of the group from Celebes, the Moluccas, and New Guinea.\nThe present paper deals with the material of Blattidae from the region mentioned above contained in the Leiden and in the Amsterdam museums.\nI am indebted to Prof. Dr. H. Boschma and Dr. H. C. Bl\xc3\xb6te of the Rijksmuseum van Natuurlijke Historie at Leiden, and to Prof. Dr. L. F. de Beaufort and Mr. J. B. Corporaal of the Zoological Museum at Amsterdam for placing the material at my disposal. Further I should like to express my thanks to the board of Greshoff\'s Rumphiusfonds for a grant which enabled me to carry out the investigations.\nAs far as concerns our knowledge of the Blattidae in the region dealt with in the present paper, Celebes is the best known although the number of known species probably represents a part only of the existing forms. Hanitsch (1933) already came to this conclusion as he could state that few species only were caught by more than one collector. A survey of the most important collections from the region, with the names of the collectors and the authors who reported upon the material may be given here.\nBasler Naturhistorisches Museum, collectors P. and F. Sarasin (18931896 and 1902-1903), author R. Hanitsch.\nUniversity Museum Oxford, collector A. R. Wallace (1856-1859), author F. Walker (1868) ; collector W. Doherty (1896), author R. Shelford
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  • 53
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 30 no. 11, pp. 133-162
    Publication Date: 2024-01-12
    Description: In the first months of 1941, whilst engaged with the study of Hydroids occurring along the coasts of the Netherlands, I received a small collection of Hydroids from Jersey for identification. These Hydroids, which were kindly sent to me by Mrs. W. S. S. van der Feen n\xc3\xa9e van Benthem Jutting, curator at the Zo\xc3\xb6logisch Museum at Amsterdam, had been collected by the late Mr. R. Oppenheim, a very studious amateur-naturalist, during a prolonged stay at Jersey from 1914-1918. Before his death Mr. Oppenheim placed a large number of fine drawings of Hydroids at my disposal, which were made during his stay at Jersey, where he had ample time and opportunities to study an extensive number of living Hydroids. Both drawings and Hydroids are now in the collections of the Zo\xc3\xb6logisch Museum at Amsterdam; I wish to thank Mrs. W. S. S. van der Feen n\xc3\xa9e van Benthem Jutting for the loan of this small collection.\nAlthough the number of Hydroids in the collection from Jersey is small and the condition of the material generally bad, the drawings are very accurate and most species can be immediately recognized from the figures.\nMoreover, the drawings are accompanied by short notes on occurrence, presence of gonothecae, etc., which make them even more valuable. It seems desirable, therefore to publish a short report on this interesting collection.\nThe Hydroids of the Channel Islands are very badly known. Philbert 0935) published the results of short visits to the islands Lihou, Jethou, Sark, Herm and Guernsey, during which trips Hydroids were collected; a second paper on Channel Islands Hydroids (Philbert, 1935a) was not available to me. The Hydroid fauna of the north-west coast of France is known slightly better; Billard (1912) published a list of species collected
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  • 54
    facet.materialart.
    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 6 no. 1, pp. 310-336
    Publication Date: 2024-01-12
    Description: The \xe2\x80\x9cNotes on the Flora of Java\xe2\x80\x9d I and II published in Bull. Jard. hot. Buitenz., S\xc3\xa9r. III, Vol. XVI\xc2\xb2, 107\xe2\x80\x94110 (1939) and in Blumea V, No. 3, 490\xe2\x80\x94525 (1945).\nNext to these the present paper has two other precursors published under different titles but serving entirely the same purpose, which exists in the publishing of all the observations (including new species and nomenclatorial changes) made during the preparation of a Flora of Java under the direction of Dr C. A. Backer (see introduction to Notes II).
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  • 55
    facet.materialart.
    Unknown
    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 5 no. 3, pp. 641-685
    Publication Date: 2024-01-12
    Description: Tota breviter scabrido-pilosa. Radix multiceps. Caules 12\xe2\x80\x9420 cm alti, adscendentes vel erecti, interne microphyllini, demum defoliati, striati. Folia alterna, brevissime petiolata, intima circa 3 mm diametentia, firma, subtus purpurascentia, superiora sensim accrescentia, ad 1.5 cm longa, 12 mm lata, orbiculari-ovata, basi et apice obtusa, apiculata, firma; floralia sterilibus similia et vix majora. Umbellae radii 3\xe2\x80\x945. Cyathium pedunculo ad 2 mm longo suffultum, extus brevissime, intus longe pilosum ; lobi apice laciniati; glandulae 4, extus subtruncatae, supra concavae; bracteae florum \xe2\x99\x82 longe pilosae. Styli fere ad medium bilobi, cruribus apice capitatis. Capsula circa 3 mm longa, 5 mm lata, breviter pilosa. Semina circa 3 mm longa, dorso carinata, ecarunculata, grisea, rubro-maculata.\nComarapa, auf den h\xc3\xb6chsten Bergwiesen, 2600\xe2\x80\x942800 m alt., n. 1916.
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  • 56
    facet.materialart.
    Unknown
    In:  Leidse Geologische Mededelingen vol. 14 no. 2, pp. 1-257
    Publication Date: 2024-01-12
    Description: In the Bergamasc Alps we have observed one major unconformity between the Basement rock and the overlying Permian.\nThe total absence of any recognisable Palaeozoic sedimentary rocks accentuates this unconformity, and moreover this enormous hiatus makes the dating of any Palaeozoic event impossible. However, by comparison with the Central Alps and K\xc3\xa4rnten, we learned that the Asturian orogenitic phase precedes the deposition of the first volcanic sediments. In analogy with the Aar and Gotthard masses we presumed the intrusion of the less metamorphic ortho rocks of the Basement, the granodiorite and the gneiss chiaro, to be of Upper Carboniferous age. The close resemblance of the chemical composition and differentiation of the Permian volcanic rocks and the Upper Carboniferous intrusive rocks induces us to assemble this period of magmatic activity into one period of Permo-Carboniferous age. In long NE\xe2\x80\x94SW striking anticlinal zones these intrusives have penetrated into the old paraschists, causing some contact metamorphism. In the Lugano region where the volcanoes are better preserved and the differentiation of the lavas is more complete, we have seen 1) that the last feature of magmatic activity had been the pressing out of the granophyr, an acid igneous rock, in a very large dome-like structure. The chemical composition of this granophyr is so much like that of the gneiss chiaro or the granites of the Val Rossiga that there can be little doubt that they all belong to the same magmatic source. Also, the intrusive rocks of the Err-Bernina, Lower East-Alpine thrustsheets and their Permian porphyries have a similar chemical composition and must be closely related to our intrusive and volcanic rocks.\nHence the whole region of what Later became the Alpine geosyncline was in Permo-Carboniferous time the scene of extensive intrusion and extrusion of igneous rocks. In Permian time the topographical surface was above sea level in the Lugano region where erosion was active and the volcanoes were formed in a mountainous country, but it was mostly covered by shallow water further east. In the later stages of this period considerable tangential forces shaped long anticlines, pressed out the granophyr magma to the surface and formed the very deep central Permian trough and the Camonica uplift of the Bergamasc Alps (see Plate XLIII). Other structural features are indicated, but only these two latter structures, the Camonica uplift and the Permian trough, are clearly visible, and they may be the result of faulting instead of folding. The shape of the Permian trough with its steep flanks and flat bottom would indicate perhaps a fault trough rather than a syncline. This trough is flanked in the NW by the Averara ridge, which, however, is a more pronounced uplift in the Middle Triassic than in the Permian. Whether the Brinzio-Maroggio anticline of the Lugano district, along which the volcanoes are arranged, must also be regarded as a Permo-Carboniferous structure can not he ascertained.\nBoth the Lower Permian (Collio) and the Upper Permian (Verrucano) increase in thickness in eastern direction (compare fig. 16 and 17). In the Lugano region the Verrucano is only preserved in the small outcrops of the San Martino conglomerate at both sides of the Lugano lake. East of the Como lake it has a thickness of less than 50 m, but increases gradually to sonic 800 m in the eastern Bergamasc Alps. The Collio has a similar development of its thickness but is in the west a pure volcanic formation and is first observed round the Valsassina core as a sedimentary rock, further west only irregular patches of volcanic rocks have been deposited.\nIn the East Alpine thrustsheets the Verrucano is generally present but not in great thicknesses, except in the Campo sheet. The Permian in the Lower East Alpine sheets (Bernina sheet) consists of porphyries only. The western limit of the Permian is again observed in the Helvetian thrustsheets, where the most western Axen sheet does not contain any Permian, whilst the more eastern Glarner and M\xc3\xbcrtschen sheets contain thick Verrucano masses.\nThe same wedging out of the Permian towards the west is observed along the Tavetscher zone between the Gotthard and Aar massives.\nThe Triassic of the Lombardic Alps is its most interesting and best developped formation. The Werfenian of Lugano consists of a simple coarse sandstone, and the upper dolomitic member is encountered for the first time in the Valsassina. Through the whole Bergamasc Alps the Werfenian is rather sandy but becomes more and more shaly and calcareous towards the east, apparently we pass from a purely continental region in the west to a marine facies in the east. The same tendency was found in the Upper Permian where the Bellerophon horizon of South Tirol sets in above the Verrucano from the Brenta group eastwards. The development of the Middle Triassic as Anisian and Ladinian in distinct facies, in the Bergamasc Alps increasing in thickness in eastern direction, connects with the development of these stages on the Mt. Giorgio, where the Salvatore dolomite is already split in two by the Bituminous Horizon on the boundary between the two stages.\nThe Middle Triassic from Lugano, with its Salvatore dolomite where Anisian and Ladinian can hardly he distinguished, slowly develops in the Bergamasc facies of Ladinian Esino dolomite-limestone and Anisian Gracilisschists and Trinodosus horizon. We have seen that the northerly facies of the Ladinian contains mostly Buchensteiner and Wengener, in the southerly facies the Esino occupies the whole Ladinian. Over the Averara ridge both stages are much thinner and incomplete, and the Anisian increases in thickness towards the Val Camonica, whereas the Ladinian decreases. Here we find also the distinct Wengener splinter shale basin.\nOn the westerly border of the Camonica ridge many facies changes take place. FABER (lit. 21) pointed out that the wedging out of the Collio, the facies change from cavernous dolomite to Elto dolomite of the Upper Werfenian, and the rapid transition from Wengener shales to Esino dolomite all occur on approximately the same line, the one above the other.\nIn Southern Tirol the Middle Triassic has much the same development, the total thickness depending mostly on the presence of thick reef limestone (dolomite), e.g. the Schlern dolomite or Marmolata limestone.\nOne pecularity is, however, very striking in the region between the Pale San Martino and the Adamello and that is the disappearance of the Raibler as a distinct lithological horizon. The merging of Carnian and Ladinian dolomites sets in in the Val Camonica, in the Brenta group only occasionally some Upper Raibler mals are observed and the Raibler appears again north of the Pale San Martino. At the same time the Lower Ladinian facies of Buchensteiner and Wengener is also absent.\nElsewhere the Raibler, although very variable, has very much the same shallow water facies, with occasional tuffogenous intercalations. Is is much thinner in the Lugano region.\nThe Upper Triassic and Rhaetic are very different in the regions of Tirol, Bergamasc Alps and Lugano. In the east the two formations are developped as one dolomitic mass, the Dachstein dolomite; in the Bergamasc Alps we find a thick Norian Hauptdolomite and a complete series of well developped Rhaetic series, whereas in the Lugano region the Rhaetic is either absent or represented by the Upper member, the Conchodon dolomite. At the same time the Liassic rests here uncomformably on the Rhaetic or Norian with the typical transgressive Hierlatz facies.\nThe Liassic siliciferous limestones are very much the same from west to east, somewhat thicker in the west, specially in the large complex from the Mt. Generoso to the Como Lake.\nThe comparison of the three regions, Lugano, Bergamasc Alps and South Tirol has been summarized in a tabel. The boundaries between these geographical units are not constant though. The boundary between Tirol and Bergamasc Alps lies during the Norian-Rhetic in the Brenta group and in the Carnian-Ladinian and in the Permian west of Val Camonica. The Collio reappears even in a thick complex east of the Camonica ridge in the Val Trompia.\nThe boundary between the Lugano region and the Bergamasc Alps is even less fixed, it lies somewhere between the Generoso and the Alta Brianza Lecco region, but can not be determined much further as the Liassic limestones cover all the older formations between these two points.\nThe Averara ridge, altough very pronounced in the Permian, Lower and Middle Triassic is not a facies boundary, at both sides the facies is very similar.\nIt has always been known that the Lombardic Trias facies is very much alike that of the East Alpine thrustsheets. Both in the Helvetian and in the Pennine zones of the Alpine sedimentation basin the Triassic is very poorly developped, and can in no way be compared to that of the Southern and Eastern Alps. When we consider the conformity between the Lombardic and eastern Alps facies somewhat closer, we observe a great similarity between the Lugano region and the Lower East Alpine unit. Both have porphyries in the Permian and no Verrucano, in both the boundary between Ladinian and Anisian is very vague. The whole Triassic in the Err-Bernina sheets is much reduced as compared to the Triassic of Campo- and Silvretta thrustsheets. The Rhetic is much completer in the Err-Bernina than in the Lugano region, but both are again characterized by thick siliciferous Lias limestones, which is transgressive with a Hierlatz limestone facies on the Rhetic and Norian in both tectonical units.\nThe Middle East-Alpine thrustsheet, the Camposheet and its accessory units, is characterized in the M\xc3\xbcnster valley by a thick Verrucano series of some 600 m. with pebbles of quartzporphyry and granite. Porphyry sheets are lacking in this serie. The Triassic of the Camposheet as a whole is much thicker than that of the Lower East-Alpine sheets, but the Anisian is not very thick yet, much less than in the Upper East-Alpine sheets, and the Werfenian is hardly represented.\nLugano Bergamasc Alps South Tirol Liassic Siliciferous limestone 100\xe2\x80\x941000 m. Transgressive Hierlatz facies Siliciferous limestone 500\xe2\x80\x941000 m. Limestone 300\xe2\x80\x94400 m. Rhetic. Absent, or only Upper member Conchodon dolomite Complete from Alta Brianza to Brenta group 550\xe2\x80\x94800 m. Daehstein dolomite ;\' 1000 1400 m Norian Hauptdolomite 250 m. 1200 m. Hauptdolomite Carnian Series of shales, marl, dolomite 100\xe2\x80\x94350 m. Thick series of shales, marl, dolom. and sandstones 250\xe2\x80\x94700 m. Western facies Eastern facies Schlern dolomite porphyries, tufs etc. from Pale S. Martino 150 m shale Sst. dolomite Northern facies Southern facies Northern facies Southern facies Marmolata St. Cassian limestone Wengener Esino limestone Wengener sst. and sh. Buchensteiner chert, limestone 600\xe2\x80\x941200 Esino dolomite, limestone Wengener, splinter shale facies Ladinian Salvatore dolomite 300\xe2\x80\x94600 m Salvatore dot. Bituminous horizon Mendola dolomite Buchensteiner or Beitzi sch. Anisian Trinodosus hor. 50\xe2\x80\x94150 m. Gracilis Schists from W\xe2\x80\x94E 150\xe2\x80\x94450 m., Nodulous limest. Mendola dolomite Gracilis schists marls, dolom. """"Werfenian 50 m. sandstone Cavernous dolomite 200\xe2\x80\x94450 m. shale, marl, sst. Servino Campiler sch. 250 m. Gastropod, list. Seiser sch. 80 m. Permian absent or porphyries, tufs etc. basal congl. Verrucano from WE 50\xe2\x80\x94800 m. Collio, porph. vole. sst. tufs etc. central Collio shale basin 0\xe2\x80\x942000 m. Basal conglomerate Bellerophon hor. 0\xe2\x80\x94250 m. Ciavflpnn Sst 100 9.CV\\ m (Vermomnn} Bozener porphyries Basal conglomerate (Collio) The Ladinian is present as Wettersteindolomite (250\xe2\x80\x94600m) without the typical Partnach facies of the Upper East-Alpine thrustsheets. The Raibler is some 400 m thick, dolomites, shales, shaly limestones, rauhwacke and gypsum, porphyrites etc. The Norian is very thick, 500\xe2\x80\x942000m, and developed as typical Hauptdolomite, whereas the Rhetic is present in the facies of the K\xc3\xb6ssener schists, black and reddish shaly limestones and shales, which can be compared to the Lombardic facies of the Scisti neri.\nThe agreement with our western Bergamasc Alps is striking. Exeptionally thick Norian, Esinodolomite, thin Anisian, and thick Verrucano are the characteristics of the region between the Valsassina and the Val Seriana. The Werfenian is much completer in Lombardia, and the Collio of the central trough is absent in the Camposheet but in general the similarity is not less striking than that of the Err-Bernina sheet with the Lugano-Grigna region. The Averara ridge although not the boundary between the two facies, can possibly be correlated with the geoanticlinal ridge between the Lower and Upper East-Alpine sheets.\nThe Upper East-Alpine thrustsheets, (Lechtal, Silvretta) show a great similarity with the eastern Bergamasc Triassic. The Werfenian has an Upper Rauhwacke member, the Anisian shows the nodulous limestone (Reiflinger Knollenkalk), the Gracilis limestone, the brachiopod limestone etc. in exactly the same facies. The Ladinian is not identical to such a degree as the lower members of the Triassic, but the Arlberg Limestone and dolomite can be very well compared to the Esino limestone and the Partnachschichten to the Wengener shales (splinter-shales!). The Carnian again is very similar, rauhwacke, marls, gypsum, shales and sandstones, black limestones are present in both units.\nIn the Lechtal sheet the Norian Dachstein limestone and the Rhetic Dachstein corraline limestone are only separated by the \xe2\x80\x9eK\xc3\xb6ssenerschichten\xe2\x80\x9d, corraline limestone and shales of the Lower Rhetic. The Norian is reduced in comparison with that of the Camposheet.\nThe Carnian of the Ducan region is exeptionally thick, some 900 m, with an upper 300 m of Upper-Carnian dolomites 1). Such development of the southerly part of the Upper East Alpine thrustsheet can already be regarded as a transition to the Camonica facies where nearly the whole 700m thick Raibler is developped as dolomites.\nStriking as the agreement of the development of the sedimentary sequence in Lombardia and in the east Alpine thrustsheets may be, great differences can also be noted. First of all the Permian of the Bergamasc Alps with its central Permian trough with 1500\xe2\x80\x942000 m of Lower Permian Carona shales and volcanic rocks can not be found back in the Eastern Alpine thrustsheets. In the second place the typical development of the Lower Ladinian in Buchensteiner and Wengener facies is restricted to the Southern Alps and Tirol. Finally the \xe2\x80\x9eFlecken mergel\xe2\x80\x9d, (mottled marls), and Allg\xc3\xa4uschiefer of the Liassic of the eastern Alpine facies are not represented in Lombardia. On the other hand the abyssal facies of Upper Liassic, Dogger and Malm in Radiolarite and Aptici limestone and marl is present in both stratigraphical units.\nThat great differences exist between two regions, which in their original position in the geosyncline are widely separated although in the same basin, is quite logical. Lombardia is the southwesterly extension of a large basin, of which the East-Alpine thrustsheets occupy the centre and the north easterly end. Moreover the basin must have widened out considerably in NE direction. That the troughs and ridges opened fan-like in this direction from Lombardia follows from the fact that the E\xe2\x80\x94W distance from L. Maggiore to the Val Camonica is less than the combined breadth of the East Alpine thrustsheets. Moreover we must not forget that even in the small width of the Bergamasc Alps already considerable facies change from North to South could be demonstrated, both in the Ladinian and in the Anisian. The main differences are found, as mentioned above, in the Permian and in the Lower Liassic, particularly in the Middle and Upper East-Alpine sheets. The development of the Permian in the Bergamasc Alps is due to late Variscian movements which apparently are not parallel to the Alpine geosyncline, and therefore need not continue in similar facies in the direction of the Alpine geosyncline.\nThe Liassic Allg\xc3\xa4uschiefer of the East-Alpine facies can be regarded as a transition between the penninic B\xc3\xbcndnerschiefer facies and the Lombardic silieiferous limestone facies.\nThe Cretaceous of the East Alpine basins can in no way be compared to the Lombardic Majolica and Scaglia. This is due to the fact that in Upper Cretaceous time the Alpine orogeny attacked this northern part of the Alpine geosyncline, whereas Lombardia remained mostly undisturbed. The dividing line between the southern and eastern Alps originated with the folding of the East-Alpine sheets, and became accentuated when the Pennine sheets were folded in the Oligocene, and became still more pronounced when the uplift of the central folded system occurred in the post Oligocene Insubric phase.\nIn the tectonical part we have shown that the youngest Tertiary tectonical direction is purely W\xe2\x80\x94E. The Orobic thrustfault and its accessories cut off obliquely the older ENE\xe2\x80\x94WSW structures as for instance the Orobic anticline. This latter direction is mainly pronounced in the anticlinal structures, e.g. the Brinzio-Marroggio anticline, the Orobic anticline, the Cabianca-Trabuchello anticline, and the Cedegolo anticline, but also in some faults as the Clusone and Bondione faults. The great thrustmovements, the Grigna thrustsheets, the thrusting against the Valtorta and the Valcanale faults, further the Timogno and Ardesio thrusts, and the eastern thrusts of the Pzo Camino and the Palline Borno-Lozzio masses is all bound to the E\xe2\x80\x94W strike or the N\xe2\x80\x94S compression. The Insubric line, the boundary between the Southern Alps and the Central Alps, i.e. the division line between Pennine root zone and the Orobic zone, has also a W\xe2\x80\x94E strike from the Lago Maggiore to Dinaro. Therefore also this major tectonical line probably originated only in a later period of the folding process. This conclusion is in complete accordance with the views of the general conception of the Alpine orogeny, which places the origin of the Insubric line in the post Oligocene, older Insubric phase. In this phase the roots of the Pennine thrustsheets were tilted in a vertical position.\nThe Insubric phase, the tilting of the root zones is naturally a time of uplift, the Central Alps rose above their fore- and hinterland. This is also the origin of the several fault steps we could discern in the Bergamasc Alps. In the Younger Insubric phase (Pliocene) when the final compression took place, all the Bergamasc thrustsheets were formed, they were sheared of their substratum from a higher step and pushed over the lower step.\nThe N\xe2\x80\x94S faulting has a intermediate position, it is younger than the old anticlinal folding and older than the final thrust, and is probably connected with the older Insubric phase when the uplifting of the steps occurred.\nThe stratigraphic comparison has made it clear that the southern, the central and the eastern Alpine basins were portions of one geosyncline, separated from another probably by ridges, geanticlines, but still forming together one continuous unit. This connection was ruptured by the first severe Upper-Cretaceous Alpine orogenesis, the origin of the east-Alpine thrustsheets. At that moment an oblique line cut a southern minor portion from the rest. This rupture line later became the Insubric line. By its present position we can still follow its course in the original basin, because the southern Alps are only little changed in aspect compared to the more central parts. West of the Lago Maggiore it followed the ridge dividing the southern basins from the central Pennine ones, then, north of this lake it curves round to an E\xe2\x80\x94W strike thus cutting obliquely through the basin structures. It retains this diagonal coarse untill it had crossed or just reached the very important Camonica geanticline, it then swung back to its original direction parallel to this ridge along the so called Judicaria line. Finally it resumes its E\xe2\x80\x94W strike as the Pusteria line and limites southern Tirol to the North, separating this region from the East Alpine thrustsheets.\nThis early boundary line is not quite identical with the Insubric line, because the latter cuts occasionally with a very sharp angle through the root zones of the Pennine thrustsheets, but the two lines are sufficiently alike to identifie them for our purpose.\nThe remarkable wavy course of the Pusteria-Insubric line is thus due to the fact that the N\xe2\x80\x94S compressional direction necessitated an E\xe2\x80\x94W strike but the existing inhomogenities of the region indicated a NE\xe2\x80\x94SW strike, between those two influences the result alternated.\nThe ENE\xe2\x80\x94WSW anticlinal structures being older than the original Insubric line, belong therefore to a prae-Cretaceous or Cretaceous phase, a phase which also accounts for the totally different facies of the Cretaceous in East-Alpine and Lombardic sedimentary-basins. If this is true some erosion on the crests of the Cretaceous structures may have taken place before the much later, probably Pliocene, finial compression took place.\nRASSMUS 1) has thoroughly treated the Cretaceous folding phase of the Lombardic Alps. The Scaglia of the foothills, in which unfortunately no fossils of stratigraphic value have been found, belongs probably to the Cenomanian-Turonian and is a typical regressive facies with which the Alpine sedimentary cycle closes. In the thick Santonian gravels, which were deposited in the Po plain, the material is derived from Liassic and Jurassic rocks, but also of Triassic rocks and even of Permian porphyrites. This conglomerate can he regarded as a equivalent of the Gosau Schists of the northern Alps. The folding phase preceding the erosion can be put therefore in one of the subhercynic phases of Stille.\nUndoubtedly the final thrusting has therefore been preceded by erosion, and we may presume that some of the thrusting has the character of \xe2\x80\x9erelief\xc3\xbcberschietrangen\xe2\x80\x9d as advocated by AMPFERER 2). In general, however, our thrustsheets are of too small dimensions to allow the determination of the characteristics of this particular way of thrusting.\nThis phenomenon may to a certain extent account for the fact that the Grigna thrustsheets pass over the faulted and folded underground with plane thrustplanes without being affected in the least by these structures. I can not find much evidence in favour of such theory, though, because most of the structural features of the underground are of equally recent datum as the thrusting movement, or only very slightly older.\nThe Valtorta fault for instance is certainly older than the thrusting, both because the thrustplanes pass over the fault and because the Norian and Raibler of the southern limb have been pressed against it. But it is not as old as the Orobic anticline, although it is fairly parallel to this structure, because it certainly belongs to the phase of uplifting of the central Alps, the older Insubric phase, and therefore not to the Cretaceous phase of folding. Still, even between the Older and Younger Insubric phases some erosion may have taken place, that is between the Miocene and the Lower Pliocene, and the height differences along this fault may have been removed to some extent. The same is true for the Clusone fault in connection with the Presolana sheet and the Pilo fault in connection with the Lozio overthrust.\nLet us summarize the results of our deductions in a short tabel.\nExtensive denudation removing all palaeozoic sedimentary rocks.\nAsturian folding followed by extensive intrusion of acid magmas in long stretched NE\xe2\x80\x94SW zones.\nPermian. Erosion continues in the west. Magmatic intrusion is followed by widespread volcanic action. In the east deposition of large subaquatic volcanic sediments.\nSaalic compression, origin of central Permian Collio trough, Camonica uplift and extrusion of granophyr, Erosion in the western region continues, in the east deposition of Verrucano conglomerates.\nTriassic. Continuous sedimentation in the south-east Alpine basin of Triassic rocks.\nOlder Kimmeric phase uplift of the Arzo anticline followed by erosion and transgressive Hierlatz facies in the Lugano-Lower East Alpine region. In the Lugano region the movement started already in the Rhaetic.\nSedimentation of Liassic and of abyssal Dogger and Malm and bathyal Lower Cretaceous.\nAustrian or Subhercynic folding (\xe2\x80\x9eJuvavische phase\xe2\x80\x9d of R. Staub) origin of long ENE\xe2\x80\x94WSW anticlines. Only the first beginnings of the strong Cretaceous orogenesis of the East-Alpine sheets has effected Lombardia, later in this phase the eastern Alps were cut off along a diagonal line partly following the anticlinal ridges and were severely compressed in thrustsheets.\nThe major Pennine (Oligocene) phase of the folding of the Pennine sheets and further compression of the east Alpine sheets did not reach the southern alps. Insubric phases, lste phase. The central Alps were raised to considerable height, the roots were tilted in vertical position and the ,,steps"""" of the Lombardic Alps were formed. Origin of BNE\xe2\x80\x94WSW faults (Valtorta, Clusone, Valcanale faults). N\xe2\x80\x94S striking fault systems (Val Vedra fault trough, Manina fault troughs). Intrusion of Adamello tonalite. 2nd. phase. N"""" to S compression, the lower limbs of the ENB\xe2\x80\x94WSW faults were pressed against the fault, origin of Timogno and Ardesio thrusts. Origin of Tertiary dikes. 3rd. phase. Possibly some erosion. Strong N to S compression. Origin of Orobic thrust and accessory thrusts, (Jrigna thrustsheets, Arera thrust, Palline-Borno and Lozzio oventhrusts and the Presolana and (\'amino thrustsheets. Often renewed activity along existing faults (Clusone fault). The age of these Insubric phases can be judged by the fact that the Miocene inolasse has been folded, and that (the horizontal Pliocene has been deposited in fjords eroded in a strongly dissected landscape.
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  • 57
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    Unknown
    In:  Leidse Geologische Mededelingen vol. 14 no. 2, pp. 347-368
    Publication Date: 2024-01-12
    Description: Toen Cirillo Generelli in 1749 in de academic van Cremona een commentaar op de theorie van Lazzaro Moro (1687\xe2\x80\x941740) leverde, gaf hij te kennen, dat de geschiedenis der aarde zonder geweld, zonder verdichtsels, zonder veronderstellingen en zonder wonderen (\xe2\x80\x9esenza violenze, senza finzioni, senza supposti, senza miracoli\xe2\x80\x9d), maar uitsluitend met behulp der tegenwoordige gebeurtenissen op aarde verklaard kan worden (Lyell, 1853, p. 37). Hij zal toen wel niet vermoed hebben, dat het nog tachtig jaren zou duren, voordat deze nieuwe zienswijze het geologische denken zou gaan beheerschen. Want eerst kwam Cuvier de klok terugzetten door in 1812 in het \xe2\x80\x9eDiscours preliminaire\xe2\x80\x9d zijner \xe2\x80\x9eRecherches sur les ossements fossiles\xe2\x80\x9d (later gepubliceerd onder den naam \xe2\x80\x9eDiscours sur les revolutions du globe\xe2\x80\x9d) de theorie te verkondigen, die later de catastrophen-theorie genoemd is, waarin de ontwikkeling van het leven op aarde door catastrophes werd afgesneden, en telkens een nieuwe schepping weer leven op aarde bracht. Zijn volgeling Alcide d\'Orbigny telde in 1849 zelfs 27 vernietigingen der biosfeer, gevolgd door 27 scheppingen.\nHet was Charles Lyell (1797\xe2\x80\x941875) die aan Cuvier\'s theorie den nekslag toebracht door het uitgeven van zijn \xe2\x80\x9ePrinciples of Geology\xe2\x80\x9d, waarvan het eerste deel in 1830 verscheen en waarmede de denkwijze der catastrophen-theorie plaats begon te maken voor een andere, die reeds door Lazzaro Moro en Cirillo Generelli verkondigd was, maar in het vergeetboek geraakt was. Lyell\xe2\x80\x99s opvatting blijkt duidelijk uit den aanvankelijk bedoelden ondertitel: \xe2\x80\x9eBeing an Attempt to Explain the Former Changes of the Earth\xe2\x80\x99s Surface by Reference to Causes now in Operation\xe2\x80\x9d. In aantrekkelijken vorm gegoten en consequent doorgevoerd in zijn \xe2\x80\x9ePrinciples\xe2\x80\x9d, is deze denkwijze de geologische gedachtenwereld gaan be\xc3\xafnvloeden, en daarmede werd de moderne geologic ingeluid. Al spoedig werd in Engeland de naam van \xe2\x80\x9euniformitarianisme\xe2\x80\x9d hieraan gegeven, later in Duitschland door \xe2\x80\x9eactualisme\xe2\x80\x9d vervangen.
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  • 58
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 28 no. 5, pp. 254-260
    Publication Date: 2024-01-12
    Description: In 1823 heeft Temminck onder de naam Myiothera melanothorax (Pl.\nCol., pl. 185) Cyanoderma m. melanothorax voor het eerst voor Java vastgesteld naar aanleiding van in West-Java (zonder nadere plaatsaanduiding) verzameld materiaal. In 1930 (Orn. Monatsber., vol. 38, p. 148/9) noemt Stresemann vijf exemplaren van deze timelia, afkomstig van Goenoeng Gedeh (West-Java) typische vertegenwoordigers van de nominaatvorm.\nIn 1918 werd door Robinson (Journ. Fed. Mal. States Mus., vol. 7, p. 236) de ondersoort intermedia afgesplitst n.a.v. te Sodong Gerok (Idjen Geb., Oost-Java) verzameld materiaal, waarbij volgens Kuroda (Birds of the Island of Java, vol. I, p. 284/5) de volgende diagnose werd gegeven. \xe2\x80\x9eIntermediate between Stachyris (= Cyanoderma) m. melanothorax (Temm.) from Western Java and St. m. baliensis (Hartert) from Java (error for Bali). Differs from the former in having the middle of the breast sandy buff, uniform with the flanks, not white, and from the latter in having the chin and throat pure white, only very faintly tinged with buff. Outer webs of the primaries, decidedly richer brown than the back but not nearly so bright as the wing coverts".\nVergeleken met de later door Stresemann (l.c.) afgesplitste ondersoort albigula, zou intermedia hiervan afwijken door zand-isabella-kleurig in plaats van grijsachtig wit borst-centrum.\nDe diagnose van de ondersoort albigula, die in 1930 door Stresemann werd afgesplitst n.a.v. materiaal afkomstig van Goenoeng Papandajan (WestJava) luidt als volgt: \xe2\x80\x9eDrei Exemplare (1 \xe2\x99\x82, 2 \xe2\x99\x80\xe2\x99\x80) vom Papandajan wurden von mir in Berlin mit 1 Exemplar von G. Gedeh und von Mr. A. Goodson in Tring
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  • 59
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 30 no. 6, pp. 83-94
    Publication Date: 2024-01-12
    Description: When, in the fall of 1947, my predecessor, Dr. F. P. Koumans, suddenly withdrew from ichthyological research, some of the fossil fish-remains from Trinil, collected and partly examined by Prof. Dr. E. Dubois (1907; 1908), still remained to be investigated or re-examined. I gladly accepted the opportunity to complete the research on this interesting material.\nA considerable part of these fossil remains, labelled by Dr. Koumans (but not mentioned in his paper, 1948, p. 80) as "16 fragments of skullbones", which "probably belong to Ophicephalus spec." (no. 11640), still proved to be in a sufficient state of preservation to permit an accurate identification of the bones these fragments must represent, as well as of the kind of fish to which the greater part must have belonged, and its affinitie s.\nAlmost all identified bones or fragments obviously belong to an in my opinion extinct, Ophicephalid 1) species or form, and consequently have been compared most accurately with our material of that genus in the collection of fish-skeletons. However, I regret to have to state that this material was very small, consisting of but three specimens: one identified as Ophiocephalus striatus Bl., from Java, Kuhl & Van Hasselt, total length 21.5 cm (cat. a), in a rather bad condition; a second identified as O. micropeltis K. & v.\nH., from Java, Kuhl & Van Hasselt, 52.5 cm (cat. a) ; and a third identified as Ophiocephalus spec., also from Java, Van Raalte, 45 cm (cat. a). The latter two are in a fine condition.\nA close re-examination, moreover, quite convinced me that, especially on account of the locality, the dentification, and the numbers of finrays, the latter two specimens too probably must be regarded as representing the common recent O. striatus Bl., this making the material available for comparison
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  • 60
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 27 no. 5, pp. 309-311
    Publication Date: 2024-01-12
    Description: During the stay of the Nica-detachment at Port Dickson, Malaya, in March 1946, a small collection of fishes was made, which was presented by Major Dr. L. D. Brongersma to the Rijksmuseum van Natuurlijke Historie at Leiden. Besides these fishes from Malaya, two specimens of flying fishes from the Indian Ocean were presented.\nThe collection from Port Dickson was pretty small, 45 specimens in total, belonging to 25 species. It gives therefore by no means an idea of the fishfauna of Malaya. The fishfauna of the Westcoast of Malaya is still imperfectly known, so even this small collection can contribute to the knowledge of this fauna.\nThe species are arranged according to the system followed by M. Weber & L. F. de Beaufort in their Fishes of the Indo-Australian Archipelago.\nThe length of the specimens is the total length.\nPORT DICKSON, MALAYA, MARCH 1946 Stolephorus indicus (v. Hasselt) 2 specimens of 39 and 45 mm.\nPlotosus canius H.B. 1 specimen of 41 mm.\nMuraena (Gymnothorax) meleagris Shaw 1 specimen of 157 mm.\nSyngnathoides biaculeatus (Bl.) 4 specimens of 127-141 mm.\nHippocampus kuda Blkr. 1 specimen of 136 mm from tip of coronet to end of tail.\nZenarchopterus quadrimaculatus Mohr
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  • 61
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 26 no. 1, pp. 1-138
    Publication Date: 2024-01-12
    Description: Introduction........................ 1\nTerminology of the upper teeth of rhinoceros............ 3\nOn the recent occurrence of Rhinoceros sonda\xc3\xafcus Desmarest in Sumatra . . 6 On the distinguishing dental characters of Dicerorhinus sumatrensis (Fischer) and Rhinoceros sonda\xc3\xafcus Desmarest.............. 9\nDicerorhinus sumatrensis (Fischer)................ 12\nRhinoceros or Dicerorhinus spec.................. 29\nRhinoceros sonda\xc3\xafcus Desmarest................. 34\nRhinoceros unicornis L..................... 81\nRhinoceros kendengindicus Dubois................ 84\n"Aceratherium" boschi Von Koenigswald.............. 107\nRhinoceros spec....................... 108\nRhino\xd1\x81\xd0\xb5r\xd0\xbes karnuliensis Lydekker................. 112\nAceratherium perimense Falconer et Cautley............. 114\nLiterature......................... 117\nTables I-VIII........................ 123\nExplanation of the plates................... 135\n......... toutes mes d\xc3\xa9terminations d\'esp\xc3\xa8ces ont \xc3\xa9t\xc3\xa9 faites sur les os eux-m\xc3\xaames, ou sur de bonnes figures ; il s\'en faut au contraire beaucoup que j\'aie observ\xc3\xa9 par moi-m\xc3\xaame tous les lieux o\xc3\xb9 ces os ont \xc3\xa9t\xc3\xa9 d\xc3\xa9couverts.\nCUVIER, G., Discours sur les r\xc3\xa9volutions de la surface du globe, 3rd ed., 1825, p. 114/115.\n\nINTRODUCTION\nThe present paper contains descriptions of the subfossil remains of rhi-
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  • 62
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 28 no. 13, pp. 287-290
    Publication Date: 2024-01-12
    Description: Material collected by Mr. J. van der Drift and by myself in the National Park "De Hooge Veluwe", situated near Hoenderloo in the province Gelderland, led to some notes on the nomenclature and to supplementary descriptions of some Hahnia species.\nThe main works dealing with European Hahniidae are Dahl (1937) and Simon (1937).\nThe descriptions and figures in Dahl (1937) are very good and it is rather easy to recognise the species by the sexual organs. Unfortunately the nomenclature is partly wrong. Now the nomenclature in Simon (1937) for the greater part is correct, but the descriptions are sometimes incomplete.\nIn the following I tried to clear up some points.\nHahnia ononidum Simon, 1875 Hahnia mengei, M. Dahl, 1937, p. 105, figs. 6, 10, 19-21.\nHahnia ononidum, Simon, 1937, pp. 1029, 1045, figs. 1603-1605.\nHooge Veluwe, 13.XII.1946. \xe2\x80\x94 2 \xe2\x99\x82 \xe2\x99\x82 subadult.\nThis species did not yet occur on our faunal list. During my revision of the collection Van Hasselt I found one adult male between males of Hahnia nava (Blackwall). Our subadult males correspond close with the adult one. They show already the round spots near the petiolus.\nThe description in Simon (1937) makes the above-mentioned synonymy evident.\nHahnia cacuminata B\xc3\xb6senberg, 1902 Hahnia cacuminata, M. Dahl, 1937, p. 108, figs. 13, 24.\nHooge Veluwe (beechwood without herbaceous layer), 15. VIII. 1944. \xe2\x80\x94 2 \xe2\x99\x80 \xe2\x99\x80.\nSimon (1937, p. 1046) adds with a question-mark Hahnia cacuminata
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  • 63
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    In:  Zoologische Mededelingen vol. 30 no. 1, pp. 1-29
    Publication Date: 2024-01-12
    Description: Loveridge (1944) published a key to the species and subspecies belonging to the genus Maticora Gray. This author emphasized that a much larger material than he had at his disposal should be examined, and that all records from literature should be studied, if a clear picture of the subspecies and their ranges was to be obtained. This led me to study the forms of Maticora occurring in the Netherlands East Indies. In the present paper the subspecies of Maticora bivirgata (Boie) are discussed, and some notes on Bungarus flaviceps are given, as specimens of the latter species have been referred to Maticora by several authors.\nThe material examined by me consists of 110 specimens from the collections of the Rijksmuseum van Natuurlijke Historie, Leiden (67 specimens), from the Zoologisch Museum, Amsterdam (24 specimens), and from the Zoologisch Museum, Buitenzorg (19 specimens). Moreover I examined one specimen belonging to the Raffles Museum, Singapore. Mr. A. Loveridge kindly sent me data on 7 specimens in the Museum of Comparative Zo\xc3\xb6logy, Cambridge (Mass.). Thus data on 118 specimens have been included in the present paper.\nAlthough I tried to trace all references to Maticora bivirgata in literature, the synonymies are certainly not complete. Many of the references are incorporated in the synonymies of the subspecies only on the base of the localities recorded. In most cases, records in literature do not mention data on the lepidosis, coloration, and sex of the specimens, and this greatly reduces their value for studies as at present undertaken.\nH. Boie (in F. Boie, 1827, p. 556) described Elaps bivirgatus from Java, Cantor (1839, p. 33) described Elaps flaviceps from Malacca, and Bleeker
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  • 64
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    In:  Zoologische Mededelingen vol. 26 no. 12, pp. 287-351
    Publication Date: 2024-01-12
    Description: In the course of 1944, whilst engaged with the revision of the collections of Hydroids in the Rijksmuseum van Natuurlijke Historie at Leiden and the Zoological Museum at Amsterdam, I had the opportunity to study a considerable number of Hydroids from the tropical and subtropical parts of the three large oceans. No report has up to the present time been published on these Hydroids, although many specimens are of considerable interest. The present paper contains the results of the study of these samples, which were kindly put at my disposal by Prof. Dr. H. Boschma and Prof.\nDr. L. F. de Beaufort. I also wish the express my sincere thanks to Mrs.\nW. S. S. van der Feen n\xc3\xa9e van Benthem Jutting and Miss Dr. Jos. Th.\nKoster for their assistance in providing me with material.\nList of the species Tubulariidae : Tubularia larynx Ell. et Sol., 1786; Tubularia spec.\nHalocordylidae : Halocordyle disticha (Goldfuss, 1820) ; Halocordyle disticha (Goldfuss, 1820) var. australis (Bale, 1884).\nClavidae: Cordylophora caspia (Pall., 1771); Corydendrium parasiticum (L., 1767); Campaniclava clionis Vanh\xc3\xb6ffen, 1910; Campaniclava cleodorae (Gegenbaur, 1854).\nBougainvilliidae : Leuckartiara vestita (Wright, 1859) forma nana (Leloup, 1932).\nEudendriidae : Eudendrium capillare Aider, 1856.\nHaleciidae: Halecium halecinum (L., 1758); Halecium beanii (Johnst., 1838) ; Halecium liouvillei Billard, 1934.\nCampanulinidae : Stegolaria geniculata (Allman, 1888).\nLafoeidae : Lafoea benthophyla Ritchie, 1909 ; Hebella calcarata (L. Agas-
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  • 65
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    In:  Zoologische Mededelingen vol. 28 no. 6, pp. 261-266
    Publication Date: 2024-01-12
    Description: In 1923 splitsten Robinson en Kloss voor Oost-Java de ondersoort ablutum af naar aanleiding van twee huidjes verkregen nabij het langs het Idjen-gebergte gelegen Tamansari (Journ. Fed. Mal. States Mus., vol. II, 1923. P. 57), waarbij de volgende diagnose werd gepubliceerd. \xe2\x80\x9eMale. Like D. s. sanguinolentum Temm. of West Java; but with less red on the breast; throat and foreneck buffy, not suffused with red as in the typical race: in these respects intermediate between D. s. sanguinolentum and D. s. ignipectus (Hodgs.).\nFemale. Foreneck and breast grey washed with buff instead of buff washed with grey: rump and upper tail-coverts like the back (again as in D. s. ignipectus), not red as in D. s. sanguinolentum".\nIn 1929 gaven Bartels en Stresemann deze vorm echter in hun lijst van Java-vogels (Treubia, vol. 11, p. 142) met een vraagteeken op waarbij Stresemann de opmerking maakte: \xe2\x80\x9eDie Form bedarf der Best\xc3\xa4tigung".\nKuroda (Birds of the Island of Java, vol. I, p. 114) noemde deze vorm echter wel voor Java, terwijl Chasen in zijn \xe2\x80\x9eHandlist of Malaysian Birds" (1935, p. 268) hetzelfde deed. Rensch gaf in 1930 (Mitt. Zool. Mus. Berlin, vol. 16, 1930, p. 539) de ondersoort ablutum eveneens voor Bali op naar aanleiding van een door hem verzameld vrouwelijk exemplaar, abusievelijk door hem als een juveniel \xe2\x99\x82 beschouwd.\nHieromtrent deelt Rensch het volgende mede: \xe2\x80\x9eOffenbar liegt mit diesem St\xc3\xbccke das meines Wissens noch nicht beschriebene m\xc3\xa4nnliche Jugendkleid diesen Rassenkreises vor (die Gonaden und Nieren waren leider zerschossen). Die Oberseite ist dunkel stahlgrau, schwach schillernd, der B\xc3\xbcrzel leuchtend rot (aber dunkler als beim \xe2\x99\x80). Die Unterseite ist \xc3\xa4hnlich
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  • 66
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    In:  Zoologische Mededelingen vol. 25 no. 19, pp. 285-316
    Publication Date: 2024-01-12
    Description: TESSARATOMINAE\n\nONCOMERINI\nRhoecocoris sulciventris St\xc3\xa5l. 1. Australia, Felder.\nCumare nov. gen. Allied to Rhoecocoris Bergroth, the base of the venter with a blunt, depressed tubercle only, not spinous; the antennae fivejointed. Head flat above, eyes not very prominent. Antennae short, the first joint not reaching the apex of the head. Rostrum short, not reaching beyond the middle of the mesosternum. Orifices narrow, ending into an elevated thorn. Mesosternum anteriorly and posteriorly with elevated longitudinal keels, the medial line before the posterior keel narrowly furrowed. Type of the genus is: Cumare pallida nov. spec. (fig. 1). Pale greyish ochraceous throughout, only at both sides of the centre of the apical border of the sixth (seventh) ventral segment (in the \xe2\x99\x80) with a dark brown spot, and the apices of the claws black. Antennae orange yellow. Upper side very densely punctured, the pronotum with irregular transverse ridges, the punctures Fig. 1. Cumare pallida.\nX 31/3. not darkened. Prosternum with transverse ridges. Mesosterum smooth, with a narrow central furrow, which is bifur-
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  • 67
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    In:  Zoologische Mededelingen vol. 30 no. 15, pp. 227-255
    Publication Date: 2024-01-12
    Description: The present paper is based mainly on material collected at the Canary Islands during the spring of 1947 by Dr. G. Thorson of Universitetets Zoologiske Museum at Copenhagen and Dr. C. O. van Regteren Altena of the Rijksmuseum van Natuurlijke Historie at Leiden. Most of the specimens were collected by Dr. Thorson, who devoted almost all of his time to the study of the litoral fauna, while Dr. Van Regteren Altena studied the inland fauna and only made occasional visits to the sea shore.\nThe shrimp fauna of the Canary Islands is very poorly known. In 1839 Erulle, in the large work of Webb and Berthelot on the Natural History of the Canary Islands, listed 5 species of Caridea and since that time just two more species have been added to the list. The material collected by Dr. Thorson and Dr. Van Regteren Altena consists of 12 species, 9 of which have not been recorded previously from the Canary Islands, bringing the total number of Caridean species known from that archipelago up to 16.\nAs the very few data about the carcinological fauna of the region are scattered over several publications, I thought it useful to give here a compilation of all the information about the Canary Islands Caridea known to me. The deep-sea forms, which are collected some distance off the islands are not included.\nOne of the main reasons that the shrimps of the Canary Islands are so little known probably is the inaccessibility of the larger part of the shores, which makes collecting possible only at certain places and at certain times.\nIn most places the rocky shore rises steep and high from the sea and is heavily pounded by the surf. Only at a few localities there are small protected beaches, where some collecting may be done.
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  • 68
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    In:  Zoologische Mededelingen vol. 30 no. 14, pp. 205-226
    Publication Date: 2024-01-12
    Description: The fossil elephant remains recently discovered in S. Celebes by Mr. H.\nR. van Heekeren, and entrusted to me by Prof. Dr. A. J. Bernet Kempers, Head of the Archaeological Survey of the Dutch East Indies, belong to a small form of the genus Archidiskodon. These specimens, described and figured in the present paper, give the first evidence of the existence of Proboscidea in the island of Celebes. As stated already in earlier notes on the fossils in Mr. Van Heekeren\'s collection (Hooijer, 1948a, 1948b, 1948c) this elephant is associated with a fauna containing a peculiar suid (Celebochoerus heekereni Hooijer), a babirusa (Babyrousa babyrussa beruensis Hooijer), an anoa (Anoa depressicornis (Smith) subsp.), and a gigantic land-tortoise (Testudo margae Hooijer). None of the fossils has been found in situ, but one of the elephant molars was still embedded in the matrix, a note on which is given below because it may help to determine the exact stratigraphical position of the specimen when the geology of the site will have been studied.\nThe matrix of the unworn right M2 or M3 from Sompoh near Tjabeng\xc3\xa8 (Sopeng district), about 100 km N.E. of Macassar was kindly studied by Mr. L. J. Fick and is a river-laid sediment with volcanic material. The rock consists of detrital grains of lateritic sandstone, the interstices partly filled with amorphous limonitic silica and opaque components. There are some pieces of quartz and veins of rhombohedral calcite. The volcanic components consist for the greater part of diopside and a few crystals of alkaline felspar.\nArchidiskodon celebensis nov. spec.\nDiagnosis: Size small; about one-half as large as Archidiskodon plani-
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  • 69
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    In:  Zoologische Mededelingen vol. 29 no. 3, pp. 302-305
    Publication Date: 2024-01-12
    Description: Delage (1884) and Smith (1906), two authors who published extremely important contributions on Rhizocephala, largely differed in their views concerning the morphology of these parasites. Both regarded the surface of the parasites touching the thorax of the host as the left side, but in other respects they were of a quite different opinion.\nDelage\'s (1884) ideas on the morphology of Sacculina were, as he stated himself, different from those of previous authors. In his opinion the dorsal region of the parasite is on the left side of the host, the ventral region on the right side of the host. The left side of the parasite touches the sternum of the crab, the right side the abdomen. As a matter of fact then the region of the stalk must be regarded as the anterior (in Delage\'s terminology "superior") part of the parasite, the region of the mantle opening as the posterior (in Delage\'s terminology "inferior") part. According to Delage\'s views consequently the mesentery is found in the ventral region of the parasite.\nThe manner of orientation of Sacculina as proposed by Smith (1906) was largely based on comparison of the morphology with that of Peltogaster. According to Smith the mesentery determines the dorsal region.\nThe region of the stalk is the posterior part of the parasite, the region of the mantle opening the anterior part. Consequently the surface of the parasite which is in contact with the thorax of the crab is the left side, the surface which is lying against the abdomen is the right side.\nIn previous papers dealing with Sacculinidae I have followed Smith in distinguishing right and left side, dorsal and ventral region, anterior and posterior extremity of the parasites in exactly the same manner. In the
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  • 70
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    Unknown
    In:  Zoologische Mededelingen vol. 28 no. 11, pp. 280-284
    Publication Date: 2024-01-12
    Description: From his stay at Port Dickson on the Malay Peninsula at the beginning of 1946 Major Dr. L. D. Brongersma of the N I C A Detachment brought home several species of crabs. A list of this material which is now incorporated in the collections of the Museum of Natural History at Leiden is given below, while on some of the more interesting species some remarks are made.\nCoenobita cavipes Stimps. \xe2\x80\x94 26 specimens.\nClibanarius padavensis De Man. \xe2\x80\x94 1 specimen.\nClibanarius infraspinatus Hilg. \xe2\x80\x94 1 specimen.\nPetrolisthes speciosus (Dana). \xe2\x80\x94 1 \xe2\x99\x80.\nCamposcia retusa Latr. \xe2\x80\x94 2 \xe2\x99\x82\xe2\x99\x82, 1 \xe2\x99\x80.\nSchizophrys aspera (H. M. Edw.). \xe2\x80\x94 1 \xe2\x99\x82.\nNeptunus pelagicus L. \xe2\x80\x94 12 specimens, including 4 \xe2\x99\x82\xe2\x99\x82, 2 \xe2\x99\x80\xe2\x99\x80.\nCharybdis (Charybdis) helleri (A. M. Edw.). \xe2\x80\x94 1 \xe2\x99\x82.\nCharybdis (Charybdis) anisodon (De Haan). \xe2\x80\x94 1 \xe2\x99\x82.\nThalamita crenata Latr. \xe2\x80\x94 2 \xe2\x99\x82\xe2\x99\x82, 1 ovigerous \xe2\x99\x80.\nThalamita stimpsoni A. M. Edw. \xe2\x80\x94 1 \xe2\x99\x82, 1 \xe2\x99\x80, both young specimens.\nChlorodopsis pilumnoides (White). \xe2\x80\x94 1 juv. and a young Xanthid probably belonging here.\nOzius guttatus H. M. Edw. \xe2\x80\x94 1 \xe2\x99\x80.\nPilumnus vespertilio (Fabr.). \xe2\x80\x94 2 \xe2\x99\x82\xe2\x99\x82, 3 \xe2\x99\x80\xe2\x99\x80.\nPilumnus scabriusculus Ad. & White. \xe2\x80\x94 2 \xe2\x99\x82\xe2\x99\x82.\nPinnotheres borradailei Nob. \xe2\x80\x94 1 \xe2\x99\x80.\nOcypoda ceratophthalma (Pall.) \xe2\x80\x94 Many specimens.\nUca annulipes Latr. \xe2\x80\x94 2 \xe2\x99\x82\xe2\x99\x82.
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  • 71
    Publication Date: 2024-01-12
    Description: In Januari 1944 was ik in de gelegenheid om het Orthopteramateriaal, aanwezig in het Laboratorium voor Entomologie te Wageningen, te bestudeeren. Aan Prof. Dr. W. Roepke, directeur van genoemd Laboratorium, wil ik hier mijn dank brengen voor zijn medewerking en voor de in zijn laboratorium genoten gastvrijheid.\nBehalve het materiaal in de studiecollecties voor de toegepaste entomologie is thans ook tijdelijk de particuliere verzameling van Ir. P. A. Blijdorp in dit laboratorium ondergebracht. Vooral deze laatstgenoemde verzameling bevat mooi materiaal. Het is betrekkelijk nog pas kort geleden verzameld, voor het meerendeel door Mevr. M. E. Walsh, in W.-Java en Z.-Sumatra. Hoewel misschien de meeste soorten niet tot de groote zeldzaamheden behooren, is het vermelden toch de moeite waard, daar het aantal in de literatuur genoemde exemplaren en vindplaatsen tamelijk gering is. Ik heb het daarom nuttig geoordeeld om alle exemplaren van de Pterophyllinae uit de beide genoemde verzamelingen in de hier volgende lijst op te nemen.\nDe exemplaren van het Laboratorium voor Entomologie zijn met W. aangeduid, die uit de verzameling van Ir. Blijdorp met B.\n\nPTEROPHYLLINAE\n\nPSEUDOPHYLLINI\nChloracris prasina Pictet & Sauss., 1892 W.: 2 \xe2\x99\x80\xe2\x99\x80, vindplaats onbekend.\nB.: 1 \xe2\x99\x82, West-Java, 1935, leg. M. E. Walsh.\nChloracris brullei Pictet & Sauss., 1892 B.: 2 \xe2\x99\x80\xe2\x99\x80, Sumatra, Benkoelen, Kota, 3 I 1935 en III 1935, leg. F. W.
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  • 72
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    In:  Zoologische Mededelingen vol. 28 no. 14, pp. 291-333
    Publication Date: 2024-01-12
    Description: 1. Ramitrichophorus nov. subgen.\nMacrosiphoniella janckei B\xc3\xb6rner, 1939 (Arb. phys. angew. Entom., vol. VI, p. 83), found on Helichrysum arenarium, differs from all species of Macrosiphoniella which I have seen in the structure of its hairs, rostrum and cauda. The dorsal hairs and partly those on the legs and antennae are long and not thicker than in other Macrosiphoniella\'s but their apex is flattened and ramose, sometimes bifid. The ultimate rostral segment is Fig. 1. Ramitrichophorus janckei (B\xc3\xb6rner), apt. viv. fern.: a, siphunculus; b, cauda; c, last rostral segments. X 140. exceedingly long and narrow, about 1 2/3 times as long as second joint of hind tarsi and nearly 5/6 of the siphunculi. The hairs on this joint are very short and thin, while in typical Macrosiphoniella the longest hairs stand on basal half. The cauda is shortly triangular and acute. Scleroites are vaguely visible in the specimen which I received, and antesiphuncular sclerites are present. It seems desirable, with regard to the shape of the ultimate rostral segment, hairs and cauda, to erect a separate subgenus for this species, Ramitrichophorus nov. subgen., type Macrosiphoniella janckei B\xc3\xb6rner, 1939. 2. Macrosiphoniella chamomillae nov. spec.\nApterous viviparous female.\nMorphological characters. Body rather large, spindle-shaped, about 2.703.15 mm long. Hairs not on distinct scleroites, rather long; VIIIth abd. tergite with 6 hairs. Antesiphuncular sclerites absent or colourless. Head faintly dusky, with the sides between the bases of the antennae and the
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  • 73
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    In:  Zoologische Mededelingen vol. 30 no. 13, pp. 191-203
    Publication Date: 2024-01-12
    Description: Certain Rhizocephalan parasites of the crabs Xanthias lamarcki (H. M.\nE.), Lybia tesselata (Latr.), and Glyptoxanthus vermiculatus (Lam.) mutually so closely correspond in all their characters that undoubtedly they belong to the same species. When the characters of this species are defined it appears that these practically correspond with the characters of Sacculina carpiliae Gu\xc3\xa9r.-Gan. There are slight differences, not easily to define, and consequently not fit for a distinct specific description. Provisionally, therefore, the parasites of the crabs mentioned above are regarded as belonging to Sacculina carpiliae.\nThe present paper contains notes on some specimens which undoubtedly belong to Sacculina carpiliae (parasites of Carpilius convexus (R\xc3\xbcpp.)), so that the particulars of the parasites of the crabs mentioned may be compared to those of the typical representatives of Sacculina carpiliae.\nThe data of the material dealt with here are: Red Sea, Dr. Jousseaume leg. (collection Paris Museum), 1 specimen on Carpilius convexus (R\xc3\xbcpp.), holotype of Sacculina carpiliae Gu\xc3\xa9r.-Gan.\nZanzibar, Capt. F. R. Webb leg., February 1861 (collection Peabody Museum, New Haven, Conn.), 1 specimen on Carpilius convexus (R\xc3\xbcpp.).\nTamatave, Madagascar, W. Kaudern leg. (collection Stockholm Museum), 1 specimen on Carpilius convexus (R\xc3\xbcpp.).\nManin Island, C. Colm leg., 1912 (collection Munich Museum), 1 specimen on Xanthias lamarcki (H. M. E.).\nAranuka, Gilbert Islands, outer reef, S. Bock leg., November 3, 1917 (collection Stockholm Museum), 1 specimen on Lybia tesselata (Latr.).\nIndian Ocean, Salmin leg. (collection Munich Museum), 1 specimen on Glyptoxanthus
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  • 74
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    In:  Zoologische Mededelingen vol. 27 no. 6, pp. 312-322
    Publication Date: 2024-01-12
    Description: The study of the older literature on Crustacea, from Linnaeus (1758) to H. Milne Edwards (1837), has been much neglected by modern carcinologists. A result of this is that many wrong names at present are used, especially for European species. The European species namely were most extensively studied by the older authors, while moreover in the middle of the previous century handbooks on the carcinological fauna of several parts of Europe were published (for instance Bell\'s (1844-1853) "A History of the British stalk-eyed Crustacea", and Heller\'s (1863) " Die Crustaceen des s\xc3\xbcdlichen Europa"), which for many authors made a consultation of older works superfluous. It is astonishing to note how many names at present are used incorrectly for species of the group. The intention of the present paper is to deal with some of these nomenclatorial puzzles and to find the correct name for the species involved.\n\nPENAEIDAE\nPenaeus kerathurus (Forssk\xc3\xa5l) Cancer kerathurus Forssk\xc3\xa5l, 1775, Descr. Anim. It. orient., p. 95.\nPalaemon sulcatus Olivier, 1811, Encycl. m\xc3\xa9thod. Hist. nat., vol. 8, p. 661.\nPenaeus trisulcatus Leach, 1815, Trans. Linn. Soc. Lond., vol. 11, p. 347.\nAlpheus Caramote Risso, 1816, Hist. nat. Crust. Nice, p. 90.\nPenaeus sulcatus Lamarck, 1818, Hist. nat. Anim. s. Vert., vol. 5, p. 206.\nPeneus caramote Risso, 1826, Hist. nat. Europ. m\xc3\xa9rid., vol. 5, p. 67.\nPenaeus kerathurus Sharp, 1893, Proc. Acad. nat. Sci. Philad., 1893, p. 109.\nThe present species is best known under the name Penaeus caramote, though the name Penaeus trisulcatus also often is used for it. The species, however, was described for the first time neither in 1815 nor in 1816, but
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  • 75
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    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 6 no. 1, pp. 200-228
    Publication Date: 2024-01-12
    Description: Von den Arten der beiden Subsektionen Odorata und Sparsiflora wissen wir schon aus der Monographie, dass sie sich nicht scharf voneinander abgrenzen lassen. Damals wagte ich das nur vage auszusprechen, aus Zweifel, nicht gen\xc3\xbcgend Material gesehen zu haben und aus R\xc3\xbccksicht auf die vielen von \xc3\xa4ltern Autoren beschriebenen Arten, die ich dort nicht weiter als auf einen Drittel zu reduzieren wagte.\nDie erneuten Untersuchungen haben das Ineinanderfliessen aller Arten dieser beiden Subsektionen so vollkommen best\xc3\xa4tigt, dass ich mehr denn je von der Richtigkeit des in der Monographie eingesehlagenen Weges und der dort angedenteten Anffassung \xc3\xbcberzeugt bin.
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  • 76
    facet.materialart.
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    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 6 no. 1, pp. 266-273
    Publication Date: 2024-01-12
    Description: After a paper had been published i.a. on the species of Stevia of the collection mentioned in the heading\xc2\xb9) another Stevia from the same collection came into the author\xe2\x80\x99s hands. It proved to be new. The American genus Stevia has been treated in local revisions by B. L. Robinson (in Gray Herb. Harvard Univ. V, 90, 1930, 36\xe2\x80\x94159; 96, 1931, 28\xe2\x80\x9449; 100, 1932, 20\xe2\x80\x9469). Its floral characters are fairly uniform, but the pappus shows a great diversity. The 5 achenes in a head do not mature at the same time. The genus Stevia seems to have its greatest development in Bolivia, where it is represented by 44 species. The next representation is in Peru with 24 and in Argentina with 23 species.\nSection Eustevia, Robinson.
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  • 77
    facet.materialart.
    Unknown
    In:  Studies on the Fauna of Cura\xc3\xa7ao and other Caribbean Islands vol. 3 no. 1, pp. 29-77
    Publication Date: 2024-01-12
    Description: Whilst visiting the Leeward Group, in 1936\xe2\x80\x941937, I couldn\xe2\x80\x99t help being fascinated by the striking occurrence of representatives of the arachnid order Chelonethida on every island of this arid region which invited me to an investigation of its soil fauna. This first publication of a serial on a group in which so much taxonomical work has still to be done, may be considered as the inevitable aftereffect of these first-sight impressions.\nMy grateful thanks to JOSEPH C. CHAMBERLIN (Forest Grove, Oregon) and C. CLAYTON HOFF (Fort Collins, Colorado) for their interest in my work and to WILLIS J. GERTSCH and E. BROWNING for letting me have the loa.n of some material deposited in The American Museum of Natural History and the British Museum (Natural History).
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  • 78
    facet.materialart.
    Unknown
    In:  Leidse Geologische Mededelingen vol. 14 no. 2, pp. 258-346
    Publication Date: 2024-01-12
    Description: Pollen analytical and geological investigations of the Lower and Middle Pleistocene in the Northern Netherlands.\nThe Pleistocene deposits in the northern part of the Netherlands, form through their extreme thickness up to more than 300 m, a promising object for study from the stratigraphical point of view.\nThe boulder clay of the penultimate glaciation lies in the province of Drente at or near the surface, but in northerly and westerly directions it dips away beneath Upper Pleistocene and Holocene deposits. The Pleistocene deposits below this boulder clay form the subject of the present paper.\nIn the first chapter the existing opinions regarding the stratigraphy are briefly reviewed. Van Cappelle (1888, 1891, 1892a, 1892b) and Lori\xc3\xa9 (1887a, 1893, 1899) described several borings already in the last century. They found the boulder clay in general to be underlain by a fine grained sand below which a coarse sand occurred, containing many Scandinavian erratics. Both, Lori\xc3\xa9 and Van Cappelle considered the coarse sands as having been deposited under the simultaneous influence of southern rivers and northern fluvio-glacial streams. Therefore it was assumed that a Scandinavian ice-front was at that time not too far distant. Van Cappelle believed that this ice-front belonged to an older glaciation than that from which the boulder clay originated, since he found in the fine sediments some rare plant remains which indicated a temperate climate. Lori\xc3\xa9, however, took the ice-front to be a mere oscillation of the same glaciation which deposited the boulder clay. Later geologists agreed with Lori\xc3\xa9 (Tesch, 1934, 1937, 1947; Steenhuis, 1939), basing their opinion on a correlation with the central part of the Netherlands, where a coarse zone occurs above the Nede clay representing the Mindel-Riss Interglacial (Florsch\xc3\xbctz and Jonker, 1942). It is at present generally accepted that these coarse gravel containing sands form one continuous horizon which was deposited during the first cold stage of the Riss glaciation, whereas the boulder clay represents the second cold stage.\nHardly anything is known about deeper horizons in the northern Netherlands. According to Tesch and Steenhuis Mindel-Riss Interglacial deposits are lacking; the Mindel Glacial stage is perhaps represented by an other zone of coarse deposits overlying again a series of fine grained sediments. The base of the Pleistocene is formed by marine beds which, in the opinion of Tesch (1934, 1937), comprise in part, the G\xc3\xbcnz Glacial stage, since the molluscan fauna of the middle part bears a distinctly arctic character. Since the stratigraphy was based on lithological criteria alone it seemed desirable to investigate whether it could be confirmed on palaeontological grounds. For this purpose pollen analysis proved to be the most suitable method, since the sequence of sediments under review is accessible only in borings, which seldom yield macroscopic fossils.\nIn chapter II some technical aspects of the pollen analytical research are discussed. The material available consisted of samples of some rare peat beds, of samples of often thick clay beds and of lumps of clay and peat, which are found sometimes in sand samples. Such lumps probably originate from very thin peat beds, which were not differentiated in the sample as separate layers. This is proved by the similarity between the spectra of these lumps and the spectra of thin beds found in situ in nearby borings (table II and III, p. 272). In general very sandy samples were not analysed. unless they were very humic and nearly sandy peat in appearance (table IV, p. 273).\nThe samples investigated proved to be rich enough in pollen to furnish reliable counts. A number of absolute pollen frequencies of different materials are given in table I (p. 271). All the samples were prepared after the technique introduced by Erdtman (1943).\nSome spectra indicated pollen of tertiary genera, which became extinct in western Europe at the beginning of the Pleistocene period. These pollens are clearly derived from tertiary deposits, but the same may be the case with other pollen of less diagnostic character. The question thus arises to which extent the pollen content of the strata under study has been derived from older series.\nThe correction technique developed by Iversen (1936), who subtracted the clearly secondary pollen he found in a boulder clay from the spectrum he obtained in the complex overlying it, could not be applied in our case, where the sediments studied unfortunately underly the boulder clay.\nIt might be feasible to correct contaminated spectra by comparing them with pure spectra from nearly the same depth, so that possible climatic differences can be disregarded. Contaminated spectra were found in several thick clay complexes. In these cases intercalations of peat beds which could have yielded uncontaminated material for comparison do not occur. Therefore the amount of contamination could not be estimated and all spectra given are uncorrected. However, we have indicated in the diagrams the amount of typical tertiary pollen (T) and of Hystrix (H), expressed in percentages of the tree pollen.\nHowever, four arguments indicate that the amount of reworked pollen in general not great: 1. the low frequency of Hystrix, which proved to be a measure of the impurity in Iversen\xe2\x80\x99s material; 2. the absolute pollen frequencies of the impure spectra as compared with the pure ones; 3. the very small pollen content of the boulder clay; 4. the similarity of pure and impure spectra in corresponding zones of different diagrams.\nThe depth given for each spectrum in the diagrams corresponds with the average depth of top and bottom of the sample (in metres below N. A. P. = high water at Amsterdam).\nIn chapter III the results of the pollen analysis are discussed, whereas in chapter IV a stratigraphical interpretation is attempted after comparing the diagrams.\nThe number of Lower and Middle Pleistocene pollen diagrams from western Europe is still very limited. The most important diagrams are those from Quakenbr\xc3\xbcck (Wildvang, 1935; Jonas, 1937a) and Ummendorf (Selle, 1941), both from western Germany. The diagrams from Starup and Harreskov, published in the classical paper by Jessen and Milthers (1928), have not been used since it is quite uncertain whether the penultimate interglacial referred to by the authors can be correlated with the Mindel-Riss or the Riss-Warthe Interglacial.\nOf the borings investigated (for localities compare map, fig 1) Bantega yielded by far the best diagram. This boring has specially been carried out for this purpose and yielded a complete sequence of undisturbed cores. The diagram is found to be in close agreement with those of Quakenbr\xc3\xbcck and Ummendorf: during the hardwood phase the mixed oak forest reached its maximum at an early date (20.65\xe2\x80\x9420.85m); only afterwards Carpinus and Abies appeared and Picea had a distinct (double) maximum after the climatic optimum of the hardwood phase (18.54 and 17.94 m). There can be no doubt as to the Mindel-Riss Interglacial age of this diagram. The same interglacial epoch can, based on a smaller number of spectra still clearly be recognized in some other diagrams viz. Bergumerheide (41.60\xe2\x80\x9465.0 m), Sneek (24.0\xe2\x80\x9446.0 m), Spannenburg (20.40\xe2\x80\x9488.0 m), Lemsterland (15.58\xe2\x80\x94 54.47 m) and Gasselte (27.80\xe2\x80\x9462.65 m).\nFurthermore Bergumerheide (7.00 m) and Spannenburg (9.30 m) show a temperate spectrum close below the boulder clay, representing probably the Riss I/II Interstadial stage.\nThree deeper borings again show beneath the Mindel-Riss Interglacial a number of spectra with a temperate character. In a few of these pollen of Pterocarya occur (Spannenburg, 211.90 to and deeper; Lemsterland 153,40 m). Pterocarya has long been known from the Tegelen clay, but the age of this famous locality has not yet been determined with certainly. Tesch (1934, 1937) and Florsch\xc3\xbctz (1939) hold the view that it represents the G\xc3\xbcnz-Mindel Interglacial, but at present some authors consider the Tegelen clay as belonging to the G\xc3\xbcnz I/II Interstadial.\nOur palaeontological knowledge of the Lower Pleistocene is still too incomplete to solve the problem. We do not know whether some so-called tertiary relics (for inst. Tsuga, Pterocarya) which occur in the Tegelen clay, range upward into the first interglacial or not. In this respect we may remark that the diagrams from Spannenburg and Lemsterland possess no indications of cold spectra which could he interpreted as G\xc3\xbcnz II Glacial stage.\nAn equivalent of the Tegelen clay has probably been found at Bergumerheide. Florsch\xc3\xbctz (1938) mentioned Azolla tegeliensis (155\xe2\x80\x94157 m) which he suggested as a characteristic species of the zone of Tegelen. At Spannenburg another species (A. filiculoides) which is characteristic for the Nede clay (Mindel-Riss Interglacial) has been found between 25 and 40 m. A boring near Dordrecht however, yielded both species from the same bed. Bergumerheide shows between the horizon with A. tegeliensis and the Mindel-Riss Interglacial deposits a third zone with spectra of a temperate climate and without tertiary relics (88.0\xe2\x80\x94125.25 m). This strongly suggests that the zone of Tegelen belongs to the G\xc3\xbcnz I/II Interstadial and that the abovementioned horizon at Bergumerheide represents the G\xc3\xbcnz-Mindel Interglacial. Perhaps the spectra between 187.15 and 197.90 m of Spannenburg belong to the same horizon.\nAn entirely different picture is shown by the diagrams of Assen and Winschoten. Pinus predominates throughout the diagrams, but nearly all spectra are contaminated with tertiary pollen and with Hiystrix. As we do not know to which degree the percentages of certain genera are overrated, the diagrams are less valuable. The diagram of Assen is particularly monotonous. Winschoten shows rather high Alnus percentages in the lower part. The same has been observed in a thin peat bed of the boring Zuidbroek (93.17\xe2\x80\x9493.27 m, table V, p. 291), which possesses 2% Tsuga pollen. Since in this case we have no reason to believe that the sample is contaminated, it must be assumed that the entire pollen content is autochthonous and therefore the spectrum probably represents the (G\xc3\xbcnz I/II Interstadial. The same horizon can perhaps be recognized in the nearby boring at Winschoten.\nThe same picture as at Assen and Winschoten is shown by the diagram of Drouwen and the lower part of Sneek. We shall see later that geological considerations are of assistance in interpreting these profiles.\nIn chapter V further consideration is given to the Middle Pleistocene marine horizon and a new conclusion has been reached regarding the age of this deposit which has a hearing upon the general understanding of the glacial stratigraphy of the northern Netherlands.\nIn two borings the Middle Pleistocene sediments are partly developed in marine facies (Bergumerheide 46.00\xe2\x80\x9462.00 m; Sneek 31.00\xe2\x80\x9442.00 m). The marine deposits lie above a coarse fluviatile series which is generally held to be of early Riss Glacial age. The pollen diagrams prove the marine sediments to be deposited between the mixed oak forest phase and the Picea phase, i. e. in the second half, of the Mindel-Riss Interglacial. The underlying coarse deposits must therefore have been laid down during the first half of the same interglacial.\nA Mindel-Riss Interglacial transgression is known from England as well as from Germany. In East Anglia the Corton Sands (Baden-Powell and Reid Moir, 1942; Zeuner, 1945) and in N. W. Germany the sediments of the Holstein-See (Grahle, 1938) were deposited during this transgression. The molluscan fauna (Tesch, 1939) proves to be somewhat colder in character than the landflora which is understandable since the sea transgressed from the north and consequently introduced northern species. On the other hand free immigration from the south was possible by land. Reid (1890) has already pointed out that different conclusions may be reached regarding climatic conditions from a comparison of marine and terrestrial organisms.\nFurthermore several rivers are known to have had their main aggradation phases during interglacial times when the rising sea level decreased their transporting capacity and thus were forced to deposit their load. As Zeuner (1945) stated we have to distinguish between thallassostatic terraces in the lower and climatic terraces in the middle courses. All classic studies of river terraces have been made of climatic terraces with glacial aggradation and interglacial valley formation. The lower courses of two west European rivers have been studied from the eustatic point of view: the Somme (Commont, 1910; De Lamothe, 1918; Breuil and Koslowski, 1931/32) and the Thames (King and Oakley, 1936) and the results are briefly reviewed. It seems that the same conditions which obtained in the lower Somme and the lower Thames were present in the northern part of the Netherlands: the principal factors affecting the behaviour of the rivers were oscillations of the sealevel during glacial and interglacial times, although terraces in the morphological sense did not develop owing to the gradual subsidence of the North Sea basin. Since all relevant deposits are entirely covered by younger sediments we do not yet know where in this country the transition occurs from the type of sedimentation typical for the lower course of the rivers under predominant marine influence to the climatic terraces of their middle course.\nThree marine transgressions are known to have occurred in the Netherlands Pleistocene: 1\xc2\xb0 the Eemian, of Riss-W\xc3\xbcrm Interglacial age which has long been generally recognized; 2\xc2\xb0 the Middle Pleistocene transgression, the Mindel-Riss Interglacial age of which has now been proved by the pollen diagrams; and 3\xc2\xb0 the Lower Pleistocene transgression (Icenian), the exact age of which is still unknown. Therefore the question arises whether this oldest transgression might be connected with the first interglacial. This point is discussed in chapter VI. Tesch (1934, 1937) argued that the middle part of the marine Lower Pleistocene represents the G\xc3\xbcnz Glacial stage on the ground that its molluscan fauna is distinctly arctic in character. Unfortunately the oldest marine deposits occur in only one of the borings investigated (Lemsterland). A few spectra immediately above this horizon show a temperate character. Though the horizon from which the spectra are derived may possibly be separated from the marine deposits by a stratigraphical hiatus, we must consider the possibility that the marine Lower Pleistocene horizon has not been deposited under such cold conditions as would appear from the conclusions of Tesch. The lowermost spectrum shows a small amount of Pterocarya pollen, suggesting, in accordance with our present state of knowledge, a G\xc3\xbcnz I/II Interstadial age rather than a G\xc3\xbcnz-Mindel interglacial age. However, if Pterocarya would still prove to have occurred in G\xc3\xbcnz-Mindel Interglacial time, the marine Lower Pleistocene could be ascribed to a G\xc3\xbcnz-Mindel Interglacial age. Incidentally, during this epoch, a high sea-level has been observed all over the world.\nThe map (fig. 2) shows the location of all borings of more than 150 m deep, whereas some other important borings have been added in the southern part of the area. The following is an explanation of the figures shown on the map with each boring: if two figures are given the first means the depth to the top of the marine Lower Pleistocene in metres, whilst the second, in brackets, indicates the lowest level reached without penetrating this marine horizon. One figure in brackets indicates the greatest depth reached. In this case no marine Lower Pleistocene or older formations have been met with. A figure preceded by T means that the Tertiary has been reached at this depth without encountering marine Lower Pleistocene.\nThe map shows that the Lower Pleistocene in a marine facies is restricted to the western part of the area. Since the base of the marine beds has nowhere been reached we do not know whether it is transgressive, as it is in the southern Netherlands.\nComparing the figures of Zwartsluis, Vollenhove and Lemsterland with that of Spannenburg, there is a striking difference which suggests that the marine horizon has disappeared by erosion in the sub-soil of Spannenburg. The profile of Spannenburg gives no evidence of the relative age of the sediments present as compared with the marine deposits elswhere. It follows from the above that the Pleistocene of the area under investigation is not composed of a number of continuous horizons laid down one upon the other.\nUp to now it was assumed that coarse sediments represented cold or glacial periods, whereas finer deposits corresponded with wanner and intraglacial phases. However comparing the results of the Spannenburg and Lemsterland borings in this light, we are struck by the fact that the deposits of the Mindel Glacial phase at Lemsterland are composed of coarse grained sediments, whilst the equivalent interval at Spannenburg is fine grained. Both show, however, spectra indicating a cold climate. Furthermore at Bergumerheide a continuous coarse section is formed which shows a diagram containing successively warm, cold and again warm spectra, which correspond with the G\xc3\xbcnz-Mindel Interglacial, Mindel Glacial and Mindel-Riss Interglacial respectively. This demonstrates that grain size alone is not indicative of the climatic conditions prevailing during sedimentation.\nA number of borings have been investigated from a sedimentary penological viewpoint by Edelman (1933) and by B\xc3\xb6hmers (1937). From a stratigraphical viewpoint, the B-Scheemda group is most interesting. It is characterized by high percentages of para-metamorphic minerals, the amount of which decreases from east to west. Edelman therefore looked for their origin in an easterly direction. Later he suggested that this group might have been deposited during the Mindel glaciation, when the courses of German rivers were deflected through the northern Netherlands by the icefront (Edelman, 1939).\nIn the boring at Urk the most conspicuous B-Scheemda influence occurs between 66 and 99 m; in the Kippenburg boring between 66 and 92 m, whilst the nearest wells of Lemsterland and Spannenburg show spectra with a cold character at corresponding depths.\nIn the Suameer boring the B-Scheemda influence is, according to B\xc3\xb6hmers, most distinctly developed between 163 and 175 m. However, his mineralogical table (B\xc3\xb6hmers, 1937, p. 62) shows the presence of two more horizons with rather high percentages of para-metamorphic minerals, viz. between 122 and 142 m and between 70 and 80 m. The lowest interval could not be investigated for its pollen content. The 122\xe2\x80\x94142 m interval is unfortunately barren of pollen but the underlying and overlying beds contain a temperate flora. The uppermost zone (70\xe2\x80\x9480 m) is apparently equivalent to the Mindel Glacial interval as established at nearby Bergumerheide. Thus it is obvious that the B-Scheemda group or a mineral aggregate comparatively rich in parametamorphic minerals fluctuated at different times and that these fluctuations might correspond to periodic deflections of the Germanic rivers into the northern part of the Netherlands.\nA discussion of the considerable clay deposits, which puzzled Lori\xc3\xa9 already half a century ago, is given in chapter VII. These deposits are known from a limited number of localities. In general all fine grained sediments between the boulder clay and the upper coarse horizon have been considered to form one unit, comprising the Riss I/II Interstadial as well as the early fluvioglacial deposits. The pollen diagrams strongly indicate that this cannot be the case. The clay deposits of Bantega and the upper clay of Spannenburg are undoubtedly of Mindel-Riss Interglacial age. Assen and Winschoten, however, represent another, probably glacial type, also by their content of reworked pollen. Of further localities known to have very thick clay beds Dronrijp is the most interesting. Here the clay is clearly deposited in a valley cut in the marine Mindel-Riss Interglacial series and therefore is apparently younger. As the boulder clay shows hardly any depression above the clay, the valley must have been filled up before the Riss ice reached the region (pl. XLVI).\nAll localities with clay deposits thicker than 70 m, including occasionally fine sand beds, have been shown in black on the map (fig. 3). The two figures given indicate the top and bottom of the clay horizon, unless the second figure is in brackets, which means that at that depth the base has not been reached. Their distribution suggests that the localities belong to two valleys, one running from east to west and a second one from southeast to northwest. The thick clay deposits in the lower half of the Sneek boring correspond, from a pollen analytical point of view, to the clay deposits of Assen and Winschoten, which are of a post Mindel-Riss Interglacial age. The clay of Sneek however, is covered by the marine Mindel-Riss Interglacial beds and must therefore be older. This suggests that the thick clay beds of other localities might also have been deposited in two phases, although separating interglacial beds are lacking in most of the profiles. The clay itself is an unpromising medium for pollen analysis, but better results may be obtained from the border regions where intercalations of sands with peat might occur. The profiles (fig. 4) show a gradual thinning out of the coarse deposits in the direction of Assen. The profile at Drouwen, in the vicinity of Gasselte, yielded spectra with a cold character and with reworked pollen above (see plate XLV) as well as below (refer table, p. 290) the coarse horizon. Strong evidence therefore exists that thick clay beds were deposited twice in valleys of glacial age during the Lower and Middle Pleistocene. The older of the two deposits apparently correspond with the \xe2\x80\x9eLauenburger Ton\xe2\x80\x9d from northwestern Germany (Schucht, 1912).\nApart from the above discussed valley systems of Sneek and Dronrijp a still younger valley system is known to exist. It developed after the above mentioned two valley systems had been filled up and it still existed at the time the Riss ice arrived because we find a mantle of boulder clay deposited in the bottom as well as on the flanks of these valleys. Such valleys have been recognized below the present Overijselse Vecht and the Ems rivers.\nEssentially we have recognized three periods during which valleys were formed in Middle Pleistocene times. The first (Sneek) is pre Mindel-Riss Interglacial and therefore probably of Mindel Glacial age. The second (Dronrijp) and the third (Vecht-Ems) both occur between the Mindel-Riss Interglacial and the arrival of the Riss ice and therefore probably correspond with the two cold stages of the Riss Glacial. From this scheme it might be concluded that the Riss ice reached the Netherlands during the Riss II stage.\nChapter VIII summarizes in Dutch the sequence of events during the Lower and Middle Pleistocene and we refer to table (p. 333) for a chronological representation of most of the above described events.
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  • 79
    facet.materialart.
    Unknown
    In:  Studies on the Fauna of Cura\xc3\xa7ao and other Caribbean Islands vol. 3 no. 1, pp. 1-20
    Publication Date: 2024-01-12
    Description: The material on which the present paper is based was collected in fresh- and brackish-water habitats on the islands of the Leeward Group, West Indies, in 1936 and 1937. For completeness sake specimens from brackish water and from some isolated salt-water habitats \xe2\x80\x94 already studied by the author (K. STEPHENSEN, 1933a and 1933b) \xe2\x80\x94 were included. It seems highly probable that the greater part of the species treated below are also represented in the litoral fauna of the open sea.\nThe occurrence of the species on the various islands may be summarized as follows (see also Table 1.)
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  • 80
    facet.materialart.
    Unknown
    In:  Zoologische Mededelingen vol. 29 no. 1, pp. 1-174
    Publication Date: 2024-01-12
    Description: INTRODUCTION\nThe Blattid fauna of the Malayan subregion is very rich, accordingly since the earliest period of orthopterology students of Blattids have described and mentioned specimens from this region. Consequently the literature on Malayan Blattidae is greatly scattered, and though some of the authors did a considerable amount of work in compiling the most important contributions on the present subject, there is still much to be done in unravelling synonymy and distinguishing generic units and subfamilies.\nBrunner (1865) already described a great number of Malayan Blattidae.\nThe descriptions of new species by Walker (1868, 1869 and 1871) are very vague and full of mistakes, giving rise to a great deal of confusion.\nShelford largely restored the systematics of the group to good order by examining the species in the large collections which were at his disposal, including the types of Walker. After Shelford, Hanitsch published a large series of contributions on Malayan Blattidae, some of which (Hanitsch, 1915, 1923) contain a compilation of nearly the whole literature on this subject known at these times. In these and many other publications he also described numerous new species, but he scarcely made an attempt to arrange the unnatural aggregations of species into distinct, logical genera. Hebard (1929) on the other hand admirably succeeded in establishing numerous cases of synonymy and in describing new genera on a scientific base. Therefore it is largely due to him that the greater part of the confusion which occurred mainly in the Ectobiinae and Pseudomopinae has been cleared.\nIn the present paper an attempt has been made to continue the work along the principles put forward by Hebard.
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  • 81
    Publication Date: 2024-01-12
    Description: In De Tropische Natuur (jrg. 24, Juni 1935, p. 90/91) maakten wij, bij een goede foto der levende volgels, melding van een groote aalscholver door ons in 1935 waargenomen in de Brantas-delta, die later bleek Phalacrocorax sulcirostris territori te zijn en door ons onder dien naam werd gepubliceerd in Bull. Raffles Museum, no. 12, May 1936, p. 120. \xe2\x80\x9eIt is most curious\' schreven wij \xe2\x80\x9ethat there was no satisfactory formal record of this bird from Java when it breeds in hundreds in the eastern part of the island.", hetgeen echter niet geheel juist was, want Vorderman noemde deze aalscholver voor Java (Nat. Tijdschr. Ned. Ind., vol. 60, 1900, p. 99) naar aanleiding van Ogilvie Grant\'s opgave in Cat. Brit. Museum (vol. 26, p. 376) waar sprake is van een door Finsch als van Java afkomstig beschouwde vogel.\nAanleiding tot deze door ons gemaakte opmerking werd gevormd door het feit, dat het door Bartels en Stresemann in 1929 gepubliceerde systematische overzicht der Java-vogels (Treubia, vol. 11, Aug. 1929) de soort niet noemde, terwijl ook Peters in zijn in 1931 verschenen eerste deel der \xe2\x80\x9eChecklist of the birds of the world" Java niet indeelde bij het verspreidingsgebied dezer soort. Kuroda deelde waarschijnlijk de meening van Bartels, Stresemann en Peters, want ook de Japanner noemde de aalscholver aanvankelijk niet in zijn \xe2\x80\x9eBirds of the island of Java" (vol. II, 1936), maar gaf deze wel op in zijn in het slot van dit deel opgenomen \xe2\x80\x9eCorrigenda and addenda" (p. 769), vermoedelijk n.a.v. onze \xe2\x80\x9eontdekking". Ook Chasen noemde de soort weer voor Java in zijn Handlist of Malaysian birds (1935) na onderzoek van hem door ons toegezonden materiaal.\nOp p. 145 van de hierboven genoemde door Bartels en Stresemann ge-
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  • 82
    Publication Date: 2024-01-12
    Description: At present five species of Armadillidiidae, all belonging to the genus Armadillidium Brdt., are known from the Netherlands. These five species are Armadillidium vulgare (Latr.), A. nasutum B.-L., A. opacum (Koch), A. album Dollf., and A. pulchellum (Zenk.). The species will be dealt with in this order. Of every species, with the exception of A. vulgare, an enumeration is given here of the material present in the collection of the Rijksmuseum van Natuurlijke Historie at Leiden, the material collected in greenhouses excluded.\nArmadillidium (Armadillidium) vulgare (Latreille) This species, which is known also under the name Armadillidium cinereum (Zenk.), is the most common species of the genus from the Netherlands. It may be found throughout our country, and is often met in the neighbourhood of human settlements. It is therefore of no use to give here a list of the abundant Dutch material of this species present in the Rijksmuseum van Natuurlijke Historie at Leiden.\nArmadillidium (Pseudosphaerium) nasutum Budde-Lund Meerssen (southern part of the province Limburg); among Marchantia; June 10, 1927; leg. F. P. Koumans. \xe2\x80\x94 24 specimens 4-11 mm.\nThe specimens mentioned above were already reported upon by Koumans (1928), they are the only representatives of the species found up till now in the Netherlands in the open. The species is rather common in several Dutch greenhouses. Armadillidium nasutum occurs in Central and Northwest Italy, in Spain, in the western part of France, in Southern England and in the Netherlands; it attains in our country the northern limit of its range of distribution in the open.
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  • 83
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    In:  Zoologische Mededelingen vol. 30 no. 12, pp. 163-190
    Publication Date: 2024-01-12
    Description: The Isopod and Tanaidacean Crustacea of the Netherlands have not been treated as a whole since 1889, when Hoek published the second part of his Crustacea Neerlandica dealing with the Isopoda and Amphipoda. Hoek in this paper mentioned 25 species of Isopoda, 9 of which are marine forms, 1 a freshwater form and 15 terrestrial, no Dutch Tanaidacea were known to Hoek. At present we know 49 species of Dutch Isopoda, of which 20 are marine, 2 are freshwater forms and 27 are terrestrial, furthermore three species of Tanaidacea are known from this country.\nThe present paper is an enumeration of all Dutch species of the two above mentioned groups, with their distribution within our country and, if necessary, with remarks on their synonymy and ecology. A volume on the Isopoda and Tanaidacea for the series "Fauna van Nederland", written in the Dutch language is now ready for the press and will be published in the course of time; in this volume a complete bibliography of the Dutch Isopoda is given, so that in the present paper only the most necessary references are made.\nThe Isopoda found in Dutch greenhouses and those belonging to the family Armadillidiidae are treated here only summarily, as they have been dealt with more extensively in previous papers (Holthuis, 1946a, b).\nThe species Limnoria quadripunctata new species, Sphaeroma hookeri Leach, Dynamene bidentata (Adams), Idotea granulosa Rathke, Porcellium conspersum (Koch), Armadillidium pictum Brandt, Athelges paguri (Rathke) and Apseudes talpa (Mont.) are recorded here for the first time as belonging to the Dutch fauna.\nISOPODA
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  • 84
    Publication Date: 2024-01-12
    Description: ... there is one point which has delayed the right conception and understanding of the evolutionary process for a long time. This was the idea that the older the morphological age of the human form is, the more it must approach the living anthropoids.\nThis conclusion did not take into account that the big apes, too, must have undergone essential changes during the same period of time in which man evolved.\nWEIDENREICH, Apes, Giants, and Man, Chicago, 1946, p. 11/12.\n\nCONTENTS\nIntroduction . . . 175 Homo sapiens L. subsp . . . 182 Pongo pygmaeus palaeosumatrensis nov. subsp . . . 187 Incisors . . . 188 Canini . . . 199 Premolars . . . 208 Molars . . . 229 Milk dentition . . . 264 The prehistoric orang-utan population . . . 269 Pongo pygmaeus (Hoppius) subsp. from the Pleistocene of Java . . . 272 Pongo pygmaeus weidenreichi nov. subsp. from the Pleistocene of S. China . . . 280 Summary; the evolution of the dentition of Pongo pygmaeus (Hoppius) . . . 284\nINTRODUCTION\nMan\'s natural interest in his nearest relatives has built up an enormous
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  • 85
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    In:  Zoologische Mededelingen vol. 30 no. 5, pp. 77-82
    Publication Date: 2024-01-12
    Description: During his paleontological searches in Java, the late Prof. Eug. Dubois collected a number of fossil fish remains. His searches were instituted mainly in pleistocene deposits, and as far as I am aware these fish remains were the first of their kind to be collected in Java in strata of that age. This, and the fact that Dubois (1907, 1908) referred to these fish in two preliminary papers, gives this collection additional interest.\nIn the first of his preliminary papers, Dubois (1907, p. 455) mentions the following fish: Anabas microcephalus, Clarias magur, Ophiocephalus, Carcharias gangeticus.\nIn the second paper, Dubois (1908, p. 1239) mentions that at least seven species of freshwater fish are represented in his collection, viz., Anabas microcephalus, Clarias magur, and four other Silurids, several species of Ophiocephalids.\nA second collection was made in the Trinil beds by the Selenka Expedition, and the fish remains were described by Hennig (1911). This author identified the remains only to family or genus, and he did not succeed in identifying the species. Therefore, it is considered to be worth while to reexamine the remains collected by Dubois, and to check his identifications. In several cases it proved that the identifications by Dubois were correct.\nHowever, the names used by him prove to be synonyms of names now in use.\nComparisons were made with recent skeletons, as this not only is the
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  • 86
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    In:  Zoologische Mededelingen vol. 30 no. 4, pp. 73-76
    Publication Date: 2024-01-12
    Description: This paper contains the descriptions of one new genus, 3 new species and notes on three other species. The specimens are from the collections of the Rijksmuseum van Natuurlijke Historie and the Drake collection. The types are deposited as indicated beneath the descriptions of the new species.\n\nFAMILY PIESMIDAE\nMiespa, nov. gen.\nHead very broad, short; jugae and tylus subequal in length; eyes exserted; ocelli placed just in front of anterior margin of pronotum. Antennae moderately long, slender, the segments almost of equal lengths; I very stout, the others slender; antenniferous tubercles short, subconical, directed forward. Rostrum moderately long, placed in a shallow furrow, the sides of furrow raised on prosternum. Middle and hind coxae placed close together. Legs rather short, the femora moderately thickened. Pronotum subquadrate, transversely swollen through humeri, closely pitted, narrower in front; median carinae barely distinct or obselete; hind margin of pronotum broadly extended at middle; collar distinct, with anterior margin truncate; paranota wider and areolate in front, obsolete behind.\nScutellum small, exposed. Elytra narrowed apically, with distinct membrane; membrane with four oblique nervures, the first vein short; areas of elytra about the same as in Piesma.\nGenerotype, Mcatella reedi Drake from Chile. In this genus the head is very similar to Mcatella and the elytra to the genus Piesma. The membrane of elytra is present in the latter and absent in the former. The short-winged form is unknown.\nMiespa reedi (Drake)
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  • 87
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    In:  Zoologische Mededelingen vol. 30 no. 2, pp. 31-47
    Publication Date: 2024-01-12
    Description: In Dr. D. C. Geijskes\' collection of Surinam fishes, mentioned in my previous paper on this subject (Boeseman, 1948), I found six specimens belonging to the so-called "sting rays" (Dasyatidae), representing three different species, and all very interesting in some respects.\nI. Dasyatis schmardae (Werner).\nTrygon schmardae Werner, 1904, p. 298 (Jamaica).\nDasybatus schmardae, Garman, 1913, p. 386 (after Werner).\nDasybatus schmardae, Meek & Hildebrand, 1923, p. 81 (Toro Point & Mindi Cut, Panama Canal).\nDasyatis schmardae, Fowler, 1931, p. 391 (Vessigny River at Brighton, Trinidad).\nFour specimens, from Coppenam Point, Surinam, coll. Dr. D. C. Geijskes, Dec. 1942, 2 \xe2\x99\x82 \xe2\x99\x82 measuring 530 and 575 mm, 2 \xe2\x99\x80 \xe2\x99\x80 measuring 610 and 705 mm.\nThe condition of the specimens is excellent, even the tails, so often mutilated in these rays, are wholly undamaged. The agreement with the cited descriptions, especially the very extensive given by Meek & Hildebrand, is practically complete and, in my opinion, leaves no room for doubt as to the identification.\nAs far as I found in literature, this species hitherto never has been reported from the Guyanas, the most eastward report being Fowler\'s from Trinidad. Moreover, the previous literature on this species gives the impression of a very rare occurrence in its whole hitherto established geographical area: Werner (Jamaica) had but a single specimen, Meek & Hildebrand (Panama) two specimens, and Fowler again but one specimen at his disposal. Garman has not seen any specimens, and just quotes Werner. AH specimens hitherto reported were female.
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  • 88
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    In:  Zoologische Mededelingen vol. 25 no. 14, pp. 109-139
    Publication Date: 2024-01-12
    Description: I.\nINLEIDING\nTen behoeve van de N.V. Stoomschelpenzuiger- en schelpkalkbranderij te Brielle werd gedurende vele jaren schelpenmateriaal opgezogen in de Westerschelde ter hoogte van Ellewoudsdijk door den schelpenzuiger ,,Marie", eigendom van genoemde maatschappij.\nDit materiaal, hetwelk naast Mollusca ook resten van Bryozoa, Foraminifera, Selachii en Brachiopoda bevatte, werd in afwachting van de verwerking in de kalkbranderij opgeslagen op het terrein bij de kalkfabriek.\nNadere bijzonderheden over het bedrijf zijn reeds gepubliceerd door Dr. C.\nO. van Regteren Altena (1938).\nDank zij de welwillende medewerking van den Directeur, Ir. P. van der Wallen, zijn vele malacologen in de gelegenheid gesteld schelpenmateriaal te verzamelen op het terrein der kalkfabriek. Velen hebben dit gedaan, zij hebben op deze wijze mooie fossielen-collecties in hun bezit, echter met dit groote nadeel, dat het materiaal over diverse personen verspreid was.\nTeneinde dit bezwaar te ondervangen, werd het voorstel geopperd, alles samen te voegen tot \xc3\xa9\xc3\xa9n groote collectie, op welk voorstel ingegaan werd door de volgende personen (alfabetisch): A. Bloklander, J. Brouwer, P. H.\nCreutzberg, P. A. Florsch\xc3\xbctz, A. C. Geelhoed, H. van Haren, B. Immerzeel, H. Od\xc3\xa9, Mejuffrouw E. M. M. T. Postma, A. Slootweg.\nDe op deze wijze verkregen, uitgebreide collectie is tijdelijk ondergebracht in het Museum voor het Onderwijs te \'s-Gravenhage.\nEchter is nog niet alles bijeen, want veel materiaal berust nog bij de onderstaande personen: Dr. C. O. van Regteren Altena (in de collecties van het Zo\xc3\xb6logisch Museum, Amsterdam), D. Bakker, A. J. Dogterom, J.
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  • 89
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    In:  Zoologische Mededelingen vol. 26 no. 8, pp. 251-267
    Publication Date: 2024-01-12
    Description: Few fossil remains of rodents have been collected in Java until now, and they have received little attention. In the reports published during his paleontological researches in Java, Dubois twice records finds of Hystrix remains, viz., at Pati-Ajam in Japara (Anonymus, 1891, p. 12/13), and in the region between Bangle and Djeroek (Anonymus, 1893, p. 12). In a subsequent paper (Dubois, 1907, p. 454) we find mention of the presence of porcupines in the fossil fauna of Java, but in his review of the latter fauna Dubois (1908) bestows no words upon these rodents. The Selenka Expedition to Trinil secured one tooth, which was figured by Stremme (1911, p. 83, pl. XVI fig. 5) as a right M2 of a small species of Hystrix. Finally a tooth of Hystrix from Sangiran II was made mention of by Von Koenigswald (1934, p. 193).\nAmong the material from prehistoric caves in the Padang Highlands, in Central Sumatra, which were explored by Dubois in the years 1888 to 1890 (Anonymus, 1889-90) teeth of porcupines are prevalent, and almost every tooth or bone in the Sumatran collection bears evidence of the gnawing habits of these animals. We possess hundreds of isolated porcupine teeth, but also a number of rami with the teeth in situ, and a few bones referable to the same animals.\nThe recent porcupine of Java is regarded by modern authors as a subspecies of Acanthion brachyurus (L.) from the Malay Peninsula. The Sumatran form of Acanthion is intermediate in size, as in geographical position, between A. b. brachyurus (L.) and A. b. javanicum Cuvier; it is named Acanthion brachyurus longicaudum (Marsden) in the present paper.
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  • 90
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    In:  Zoologische Mededelingen vol. 25 no. 17, pp. 200-238
    Publication Date: 2024-01-12
    Description: Es war schon l\xc3\xa4ngst meine Absicht mich mit dieser Gattung zu befassen, weil sich im Leidener Museum eine grosse Sammlung befindet, welche durch Snellen van Vollenhoven damals von Holmgren k\xc3\xa4uflich erworben wurde. Die Tiere besitzen in meinen Augen einen paratypischen Wert. Erst heute bin ich imstande, das Ergebnis meiner Untersuchungen zu ver\xc3\xb6ffentlichen, wobei ich besonders den Herren Professoren Dr. H. Boschma, Direktor des Rijksmuseum van Natuurlijke Historic, Leiden, und Dr. W.\nRoepke, Direktor des Entomologischen Laboratorium der Landbouwhoogeschool, Wageningen, grossen Dank schulde f\xc3\xbcr die Bereitschaft, mit der sie das ihnen zuvertraute Material mir zur Verf\xc3\xbcgung gestellt haben. Den meisten Dank aber schulde ich Herrn Dr. A. Roman, den meist hervorragenden Ichneumonidenkenner unserer Zeit, der mich mit seinem Rat und dem Bestimmen von schwierigen Exemplaren zur Seite gegangen hat.\nBevor ich die Arten beschreibe, muss ich einige Bemerkungen machen, zuerst \xc3\xbcber die Farbe der Bauchfalte. Man muss die Bauchfalte mit der Lupe betrachten. Unter dem Mikroskop wird man bei k\xc3\xbcnstlicher Beleuchtung die Farbe zu hell einsch\xc3\xa4tzen. Die Bauchfalte nenne ich noch weiss, wenn einige Sterniten zum gr\xc3\xb6sstenteil weisslich sind. Wenn die Mitte dieser Sterniten br\xc3\xa4unlich wird, dann stelle man eine solche Art unter diejenigen mit dunkler Bauchfalte. Es wird also \xc3\xb6fters vorkommen, dass eine Art helle oder dunkle Bauchfalte haben kann. Bei der Beschreibung gebrauche ich einige neue Unterscheidungsmerkmale, deren Brauchbarkeit sich noch ausweisen muss. Ich meine in dem Verh\xc3\xa4ltnis der F\xc3\xbchlerglieder untereinander und mit den Hintertarsengliedern ein Merkmal f\xc3\xbcr die Schlankheit der F\xc3\xbchler gefunden zu haben. Die L\xc3\xa4nge des ersten Geissel-
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  • 91
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    In:  Zoologische Mededelingen vol. 25 no. 12, pp. 93-100
    Publication Date: 2024-01-12
    Description: In a previous paper (Hellebrekers, 1942) I stated my intention to give some more details on imperfectly known eggs, based on material of the collection of the Penard\'s. The description of these hitherto imperfectly known or incorrectly described eggs will be strongly aided by the coloured plate accompanying the present paper, this plate represents a number of eggs of four species of birds from Surinam, of each species such eggs are figured as to show the variation in shape and colour. Moreover I have the opportunity to give a number of corrections concerning some of the data given in my previous paper. When the latter appeared I sent a copy to Mr.\nM. Sch\xc3\xb6nwetter, one of the foremost living authorities in o\xc3\xb6logy, asking him for a critical comment on my paper. Mr. Sch\xc3\xb6nwetter kindly took a great deal of trouble to verify my statements and he could point out that among the data in my paper there are a number of mistakes and misprints regarding weights and measurements. Whilst in the following pages I give the necessary corrections to my previous paper I want to express my sincerest thanks to Mr. Sch\xc3\xb6nwetter for drawing my attention to these mistakes.\nIn all the cases where doubt might arise concerning the data in my previous paper I have taken new measurements and weights. Behind the name of each species dealt with below I have cited the page on which the species was mentioned in my previous paper.\nDendrocygna autumnalis discolor Scl. & Salv. (1. c, p. 241). I have already drawn attention to the fact that among these eggs there are a number which show a pronounced gloss whilst others are nearly glossless.\nThe different sets show the following data:
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  • 92
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    In:  Zoologische Mededelingen vol. 25 no. 13, pp. 101-108
    Publication Date: 2024-01-12
    Description: Some time ago Dr. L. D. Brongersma, curator of the Leiden Museum, entrusted me for examination some subfossil equine teeth, received from Mr. H. van Hoepen, who had found them between Glen and Mazelspoort, in Orange Free State. The teeth proved to belong all to one and the same individual, and to constitute the entire upper premolar-molar-series of the right side, almost undamaged. The importance of this find is evident, as most of the fossil or subfossil equine species from S. Africa are based on isolated teeth. An inner view of our specimen is given in pl. VI lower figure, the crown surfaces are represented in the upper figure of the same plate. It can be seen, that the P4 is the longest tooth, its height is 72 mm.\nThe mesostyle is prominent, and especially marked off anteriorly. The parastyle is well defined in P3 and P4, less so in the molars, especially in M1. Between these styles the ectoloph is almost straight in the premolars, and slightly concave in the molars. The posterior half of the ectoloph, however, is more concave in the premolars than in the molars, the latter having a less developed metastyle. The enamel pattern is comparatively simple, the pli protoloph 1) and the pli hypostyle are hardly or not developed. A slight trace of a pli prefossette is found in P4 only.\nA small pli postfossette is seen in the premolars, in the molars it is hardly indicated. The pli protoconule is present in all the teeth, though shorter in the molars than in the premolars. The groove between protocone and hypocone is sharply pointed towards the outer side, a pli caballin is absent.\nThe protocones are remarkable for the very slight development of their anterior lobe; they increase in length from before backward.\nFirst I compared the subfossil teeth with those of Equus quagga. Of
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  • 93
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    In:  Zoologische Mededelingen vol. 25 no. 9, pp. 55-64
    Publication Date: 2024-01-12
    Description: In 1944 Miss Dr. A. Schreuder sent me for identification a fossil horncore, which according to the accompanying letter came from a well-boring near Grubbenvorst (province of Limburg). It was found in a coarse sandy layer with gravel at a depth of 61.50 m below the surface; the topographic height of the latter is given as 24.53 m + N.A.P. (N.A.P. = sea-level at Amsterdam). Dr. J. F. Steenhuis, geologist to the Government Geological Foundation, informed me that deep borings for the water-supply of Central-Limburg have been made in the years 1918, 1919, and 1922 S. and S.E. of Grubbenvorst. Evidently we have to do with boring no. I of October 1918, which reached a depth of 83 m, the top being at 24.50 m + N.A.P. (Geological Foundation Index no. 695/4). The section is as follows (the denotations of the strata are those used by Tesch (1930)) : Laagterras II 8 from 24.50 m + to 15.50 m + N.A.P.\nMiddenterras (?) II 6 and Hoogterras II 1 from 15.50 m + to 4.\xe2\x80\x94 m + N.A.P.\nZone of the Teglian Clay, "Onderste Fijn" II o from 4.\xe2\x80\x94 m + to 2.50 m \xe2\x80\x94 N.A.P.\nMore or less coarse, mostly mudfree sand with gravel, alternating with rather fine sand with a variable mud and gravel content from 2.50 m \xe2\x80\x94 to 45.50 m \xe2\x80\x94 N.A.P.\nBelow 45.50 m \xe2\x80\x94 N.A.P. very fine micaceous sand containing much mud. The percentage of mud and mica increases with depth. The boring was finished at a depth of 58.50 m \xe2\x80\x94 N.A.P.
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  • 94
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    In:  Blumea: Biodiversity, Evolution and Biogeography of Plants vol. 5 no. 3, pp. 530-531
    Publication Date: 2024-01-12
    Description: Among a set of duplicates of Puccinellia, which I received through the courtesy of Dr C. Blom (Goteborg, Sweden), I found the following new species.
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  • 95
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    In:  Studies on the Fauna of Cura\xc3\xa7ao and other Caribbean Islands vol. 3 no. 1, pp. 21-28
    Publication Date: 2024-01-12
    Description: This small paper consists only of an enumeration of the specimens collected by Dr. HUMMELINCK in 1936 and 1937, together with the records of land and fresh water decapods from the articles by RATHBUN (1936) and SCHMITT (1936) on the collections made in 1930. Identifications of many of the brachyuran crabs were made by the late Dr. MARY J. RATHBUN (U.S. National Museum). The senior author is responsible for the identifications of the remainder of the crabs, as well as of the anomurans, while the junior author has determined the caridean species.\nThe material has been deposited in the U.S. National Museum, \'with the exception of the specimens of Coenobita, most of the Gecarcinus, and some of Macrobrachium faustinum, Cardisoma and Uca, which have been presented to the Rijksmuseum van Natuurlijke Historie at Leiden.
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  • 96
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    In:  Studies on the Fauna of Cura\xc3\xa7ao and other Caribbean Islands vol. 3 no. 1, pp. 87-88
    Publication Date: 2024-01-12
    Description: Two species of leeches only have been collected by dr HUMMELINCK in 1936\xe2\x80\x941937, but these are important as they evidently prove the occurrence in warm tropical waters of species hitherto only recorded from non-tropical areas.\nHelobdella scutifera is distinguished from H. stagnalis by AUTRUM, 1936, p. 26 and 34, though PAWLOWSKY (cf. AUTRUM 1939, Bronns Kl. u. Ordn., Hirudineae 2, p. 500) considered them synonymous. AUTRUM (l. c. p. 500 and footnote) remarks that H. stagnalis is not known from tropical localities, supposing the habitats in Ecuador, Brasil and Paraguay perhaps to be non-tropical because of their particular position. Our material, however, shows affinities to both species and tends to affirm the identity of H. stagnalis and H. scutifera. It is important to know that our habitat was really tropical, the temperature measured being 28\xc2\xb0\xe2\x80\x9431\xc2\xb0 C.
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  • 97
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    In:  Studies on the Fauna of Cura\xc3\xa7ao and other Caribbean Islands vol. 3 no. 1, pp. 78-86
    Publication Date: 2024-01-12
    Description: The smaller islands of the Caribbean Sea support relatively few species of ants. Even in the largest island in the West Indies, Cuba, there were in 1934 only about 90 forms (species, subspecies and \xe2\x80\x9evarieties\xe2\x80\x9d) known and this number has not been greatly increased since. During the 1930\xe2\x80\x99s there were recorded in the entire West Indies some 450 forms and at the present time the number can hardly much exceed 500. By way of comparison, the most recent enumeration of ants of the United States (1947) shows 742 kinds. The larger proportion of these West Indian ants occur on such islands as Hispaniola which offer varied and stable habitats. The small islands have relatively few species and these are in the large part common tropicopolitan forms which tend to drive out the endemic species. Few endemic species appear to remain in the Lesser Antilles, for example.\nAlthough dr HUMMELINCK told me he was not trying to gather representative material \xe2\x80\x94 especially on the islands of Cura\xc3\xa7ao, Aruba and Bonaire, in which collecting has been done in 1930 by dr H. J. MACGILLAVRY and the late dr L. W. J. VERMUNT \xe2\x80\x94 the present collection is of particular interest since it was made on many small islands whose ant fauna was hitherto completely unknown. A few records from the adjacent mainland and some other localities are also included (see Table 7). The value of the Caribbean records is enhanced by the fact that ant populations on small islands may tend to vary from time to time or to be replaced by populations of other species, not to speak of the possibility of speciation itself taking place in geographically isolated places. They also record the presence of specific cosmopolitan \xe2\x80\x9evagrants\xe2\x80\x9d on specific islands and some of these ants are still spreading.
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  • 98
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    In:  Studies on the Fauna of Cura\xc3\xa7ao and other Caribbean Islands vol. 3 no. 1, pp. 89-96
    Publication Date: 2024-01-12
    Description: The present notes deal with a small collection of frogs that was made by Dr. P. WAGENAAR HUMMELINCK during his visits to the islands of the Leeward Group, Venezuela and Eastern Colombia. I have included in this study the specimens of Pleurodema brachyops (Cope) already present in the Rijksmuseum van Natuurlijke Historie, Leiden, and in the Zoologisch Museum, Amsterdam.\nThe amphibian fauna of the Dutch Leeward Islands is very poor indeed. It consists of a single species Pleurodema brachyops (Cope)) that occurs in Aruba, Cura\xc3\xa7ao, Bonaire and Klein Bonaire. Bufo marinus (L.) has apparently been introduced into Aruba within the last few years (cf. p. 91). J. H. R. NEERVOORT VAN DE POLL, who visited Aruba in 1885, took a specimen of a Leptodactylus species. This has been mentioned by VAN LIDTH DE JEUDE (1887, p. 134) as ? Rana copii Blgr.\xe2\x80\x9d On the authority of Dr. G. A. BOULENGER the identification was changed into Leptodactylus albilabris (Gthr.), and as such it has been mentioned recently by BOSCHMA (1947, p. 42).
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  • 99
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    In:  Zoologische Mededelingen vol. 25 no. 16, pp. 155-199
    Publication Date: 2024-01-12
    Description: Inhoud: 1. Inleiding .... 155\n2. Materiaal .... 156\n3. Geologie van de vindplaats, met enkele opmerkingen over de brakwaterfauna van het veen op grootere diepte en de onderste holocene wadklei .... 157\n4. Beschrijving van de onderzochte mollusken .... 159\n5. Overzichtstabel van de onderzochte mollusken, hun oecologie en geographische verspreiding .... 183\n6. Algemeene beschouwingen en occologische conclusies .... 186\n7. Pleistocene land- and freshwatermollusca from the subsoil of Velzen (summary) .... 195\n8. Geciteerde literatuur .... 198\nI. Inleiding.\nHet bovenste plistoceen (\xe2\x80\x9elaagterras", II8 van de geologische kaart van Nederland) is te Velzen in een tweetal putten, gegraven voor den bouw van een tunnel onder het Noordzeekanaal, een tijdlang ontsloten geweest.\nDeze ontsluiting is door velen, die belang stellen in den geologischen bouw van Nederland, bezocht en ook de schrijvers dezer regelen prijzen zichzelf gelukkig het belangwekkende profiel te hebben aanschouwd en in de gelegenheid te zijn geweest ter plaatse mollusken te verzamelen. Hun buit en het materiaal, dat zij van andere zijde ter bewerking mochten ontvangen, bevat verscheidene vormen, die een publicatie over dit materiaal rechtvaardigen. Ook resten nog enkele problematica; hiervan is meer materiaal noodig om definitieve determinaties mogelijk te maken. Daarom hopen wij dat dit artikel een aansporing zal zijn tot verder onderzoek, wanneer
    Repository Name: National Museum of Natural History, Netherlands
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  • 100
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    In:  Zoologische Mededelingen vol. 28 no. 8, pp. 271-271
    Publication Date: 2024-01-12
    Description: Bartels & Stresemann noemen op p. 128 van hun \xe2\x80\x9eSystematische \xc3\x9cbersicht der bisher von Java nachgewiesenen V\xc3\xb6gel" (Treubia, vol. XI, 1929) Malacocincla abbotti baweana, waarbij de volgende aanteekening wordt gemaakt: \xe2\x80\x9eZwei Exemplare in U. S. Nat. Museum, gesammelt von Dr. W.\nL. Abbott. Uns nicht bekannt. \xe2\x80\x94" Aangezien Siebers in zijn aan dit overzicht toegevoegde \xe2\x80\x9eErg\xc3\xa4nzungen und Berichtigungen" geen melding maakt van tot deze soort behoorende vogels in de Museum-collectie te Buitenzorg, meenden wij, dat het van voldoende beteekenis was hier mededeeling te doen van enkele daar aanwezige balgen van deze timalia. Het gaat hier om twee \xe2\x99\x82\xe2\x99\x82 en twee \xe2\x99\x80\xe2\x99\x80, die op 13 Mei 1928, dus reeds voordat de hierboven genoemde lijst het licht zag, door Dammerman, destijds Hoofd van het Zo\xc3\xb6logisch Museum, werden verzameld in het Zuiden van Bawean.\nDeze exemplaren gelijken in vederkleed zeer veel op Malacocincla sepiaria, maar hebben iets minder bruin in het vederkleed van bovendeelen en vleugels, terwijl de olijfgrijsachtige bovenkop dezelfde tint heeft als de mantel, dus niet verschillend daarvan zooals bij sepiaria het geval pleegt te zijn. Bovendien geven de vrij goed zichtbare, lichte schachten der veertjes op de voorkop deze een zwak gestreept voorkomen, hetgeen bij sepiaria niet het geval is. Bovenstaartdekveeren en staartpennen hebben ongeveer dezelfde kleur als die van sepiaria.\nHet belangrijkste verschil tusschen beide soorten wordt echter gevormd door de grootere afmetingen van vleugel, staart en snavel, waardoor het \xe2\x99\x82 van abbotti op het eerste gezicht van sepiaria is te onderscheiden; de iets kleinere \xe2\x99\x80\xe2\x99\x80 zijn echter ongeveer even groot als \xe2\x99\x82\xe2\x99\x82 van sepiaria, zoodat
    Repository Name: National Museum of Natural History, Netherlands
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