ALBERT

Description: There comes a time in the history of nearly every genus when it becomes almost immoral to add new species without first having surveyed the genus as a whole. Dendrophthora has reached this state. From the time of its first recognition as a separate entity to the present, new species have been described, often on very tenuous grounds, and usually without an indication of infrageneric relationships, until today we are faced with a staggering mass of specific epithets in complete chaos. The genus has not been comprehensively studied for more than half a century, and no balanced attempt has as yet been made to establish natural divisions within. Having become interested in the morphology of this and the related genus Phoradendron (KUIJT, 1959), I was naturally led on to some taxonomic considerations. My stay in Europe in 1958-1959 enabled me to visit the major European herbaria, and the notes and sketches accumulated there soon pointed the way to the present work.

Description: 1. The chromosome numbers of 10 species of the genus Viola in the Netherlands were determined. 2. Viola riviniana has various chromosome numbers: 2n = 35, 40, 45, 46, 47 (most often 2n = 40). 3. It was not possible to find a correlation between the external morphology and the various chromosome numbers in V. riviniana. 4. Despite the variability of V. riviniana it proved impossible to divide the Dutch material into subspecies. 5. Some differential characters of V. riviniana and V. reichenbachiana are described. 6. V. canina is not variable in cytological respect in the Netherlands. 7. V. calaminaria is not related to V. lutea but to the V. tricolor complex.

Description: A. DE CANDOLLE’s (1830) treatment of the genus Campanula lists 137 species. Many new species were described since, so that the total number of species should be estimated to be at least twice that number. A new monograph of the genus is, therefore, highly desirable (CLIFFORD CROOK, 1951). Any classification into subgenera and sections, based on herbarium studies, is bound to meet considerable difficulties on account of the great uniformity among many floral characters of the various species. Cytological information may prove very valuable in order to arrive at a modern classification of the species within the genus.

Description: The bogs of S. E. Groningen are part of the great peat-marshes extending from S. E. Drente as far as N.W. Germany inclusive. So far as the territory of Westerwolde is concerned, people have begun digging off very early. According to the map by Krayenhoff in 1816 nearly the whole peat-marsh westward from the line Blijham—Termaarsch had already been reclaimed, only a few parts still being covered with the original peat-layer (cf. map, fig. 1). The digging off east of the above line commences at the beginning of the 19th century on the borderland of Groningen and Drente. Borings were performed in three places and the samples pollenanalytically and stratigraphically examined.

Description: E sectione Peltaea, Pavoniae speciosae H.B.K. proxima, sed forma folorium, indumento, involucri phyllis peltatis diversa. Suffrutex, caule minute stellato-piloso glabrescente, linea singula pilis simplicibus longioribus vestita in primo internodio ramulorum lateralium adaxiale notato. Folia breviter petiolata, petiolis tomentellis 2—4 mm longis, oblongo-elliptica, elliptica vel ellipticolanceolata, 3—5 cm longa, 1.25—1.5 cm lata trinervia basi acuta vel obtusa, superiora 5-nervia, basi subcordata, acutissima vel subacuminata, margine regulariter serrato-dentata, supra minute stellato-pilosa, oculo nudo glabra, infra dense sed minute stellatotomentella. Flores in axillis foliorum vel in apice ramulorum 2—3-glomeratis, bracteis ovato-triangularibus suffulti, plerumque subsessiles, interdum usque ad 4 mm pedicellati. Involucri phylla fere io linearia birta uniserialia, basi paullo connata, apice lamina foliacea peltata, id est supra basin affixa, anguste elliptica hirta, basi rotundata, apice acuta, appendiculata, 4 mm longa. Calyx cupuliformis, ultra medium incisus, 4—9 mm longus, lobis acutis hirtis, nervis trinis conspicuis, binis intermediis brevibus vel nullis. Petala 2.5—3 cm longa, teste collectore roseo-rubra, sicca rosea, basi atropurpurea. Stamina et styli more generis. Carpella 4 mm longa, mutica, dorso costa perpendiculari instructa, transverse nervosa, dense pubescentia.

Description: Culmi robusti, foliati. Folia lata, linearia, trinervia. Inflorescentia corymboso-paniculata, multispiculata. Spiculae (”spicae” multorum auctorum) parvae, multiflorae. Flores hermaphroditi (”spiculae androgynae” auctorum) perianthio utriculiformi, compresso, vix carinato, staminibus (”floribus masculinis monandris” auctorum) tribus, binis lateralibus tertio anteriore, ovario (”flore foemineo terminali nudo” auctorum) rostrato, basi angustato, haud stipitato, styli ramis ternis. Nux tri-costata, rugulosa. Generi Hypolytro L. C. Rich. proxima, a quo differt styli ramis tribus et nuce tri-costata. A Thoracostachyo et Paramapania, quibuscum stigmatum numero convenit, et structura florum et perianthio connato et nucis forma longe diversa, faciliter dignoscenda. Mapaniae potius affinis, sed ab omnibus speciebus huius generis inflorescentia a plerisque etiam perianthio connato discrepat.

Description: The genus Trymatococcus has been published in 1838 by Poeppig and Endlicher in Nova Genera ac Spec. Plant II. p. 30, and the genus was based on the species T. amazonicus. In 1876 Baillon added the species T. africanus to the genus. This gave a peculiar distribution for a genus with two species only: one in the Amazone region and one in West Africa. Later on several new species from Africa were described: three by Engler (T. kamerunianus, dorstenioides, and Conrauanus), one by De Wildeman (T. Gilletii) and one by Pellegrin (T. oligogyna). In 1922 (Archivos do Jardim Botanico Rio de Janeiro vol III. p. 22) Ducke described a second species from Amazonian Brazil (T. paraensis) and said in the notes to this new species that Lanessania turbinata Baill. should be transferred to the genus Trymatococcus and published a new combination (T. turbinatus Ducke). In 1925 (Archives IV. p. I) he emphasized his statements Trymatococcus and published a new combination (T. turbinatus as well as turbinatus and amazonicus have the stamens erect in the bud and not inflexed as was described in the former publications. He also emphasized that the place of Trymatococcus in the system has to be changed and the genus has to take the place taken up to this moment by Lanessania. Among the material of the Moraceae from Surinam which I am studying for the Flora of Surinam, I found also a Trymatococcus species. By the study of this genus I was struck by the peculiar geographic distribution of the genus, which fully supported my observations on the Euphorbiaceae (cf. Lanjouw, The Euphorbiaceae of Surinam pp. 70—84). For the preparation of a map of this distribution I studied the african species and after a careful examination I noted a number of important differences between the african species and the american ones. Part of these differences were never noticed before and no attention has ever been given to these facts. The first error in this case was made by Baillon. Most probably he had not seen T. amazonicus Poepp. et Endl. when he described his T. africanus. This is still more striking as he described in the same paper his genus Lanessania based on L. turbinata, which is a true Trymatococcus species. It is very curious that it was not possible for Baillonto observe his mistake because in his Histoire des Plantes (vol. VI. p. 199) he states „filamentis aestivatione inflexis vel nunc suberectis”. One can not understand why he did not observe that at least one of the species of Trymatococcus is the same as his genus Lanessania. After Baillon’s publication, we could say that we had got two type species, one american (Tr. amazonicus Poepp. et Endl.) and one african (Tr. africanus Baill.). Apparently Engler did not study exactly Tr. amazonicus Poepp. et Endl. when he described his new species though he states (Monogr. Afr. Pfl. fam. I. Morac. p. 28); ”Ein besonders auffallender Unterschied im Bau der Blüte und Frucht is nicht zu constatieren; bei der amerikanischen Art sind die männlichen Blüten dreimännig mit dreiteiliger Blütenhülle, bei den afrikanischen Arten sind sie zweimännig”. Likewise Ducke knew apparently only the american species when he pointed out the new place for this genus in the family. By these reasons only it is explained how confusion has crept into this genus. I have studied many specimens of Trymatococcus from the following herbaria: Berlin-Dahlem, British Museum (Natural History Museum), Kew, Leiden, Paris and Utrecht. I wish to express mv sincere thanks to the directors for their hospitality or fore sending the material on loan.

Description: Es handelt sich hier um ein grosses, zusammenhängendes Hochmoorgebiet, das sich nord-süd über 20 km, ost-west über 10 km ausdehnt. Im Süden und Westen ist es grösstenteils abgetorft. Die besonders im Zentrum und Osten noch erhaltenen Teile sind durch die intensive Trockenlegung meist verheidet; stellenweise, so in den „Engbertsdijkvenen”, wo grosse Flächen heute wenig entwässert sind, findet sich eine lebende Sphagnumdecke (Taf. III). (Lit. 5). Das Moor liegt auf pleistozänem Untergrunde (Fluvioglazial der Riss-Eiszeit und Niederterrasse der Würmeiszeit); im Osten und Westen stosst es an diluviale Rücken; im Nordwesten bildet die Niederterrasse der Vechte die Grenze. Im Südosten und Osten schliesst sich eine ausgedehnte Versumpfungszone an, während sich im Westen zwischen den Hügeln isolierte, ähnliche Bildungen vorfinden. Es handelt sich hier wahrscheinlich um ein Entwässerungsgebiet des Hochmoores. Ein prae-rissglazialer mit nördlichen Erratica bestreuter Rücken dringt vom Osten her, parallel dem Vechtetal, ungefähr bis in die Mitte, in das Moor vor. Für eine ausführliche Angabe der geologischen Verhältnisse verweisen wir auf die „Geologische Kaart van Nederland” vom „Rijks Geologische Dienst” (Blätter Almeloo I und II; Koevorden III und IV). Wir sammelten eine Anzahl Probenreihen. Die angeführten Analysen beziehen sich auf eine süd-nord gerichtete Profillinie im östlichen Teil des Gebietes (Paterswal 1 u. 2, Engbertsdijk, Bruine Haar) und ein Punktprofil im Nordwesten (Boerendijk), nahe dem Vechtetal.

Description: It is to be hoped, that the genus Pandanophyllum Hassk. never will revive, for it is based on a bad generic description and two nomina nuda, P. palustre Hassk. (Harassas tjaai) and P. humile Hassk., the first of which is supposed to indicate Mapania palustris (Steud.) Vill., while the other name has brought about much confusion, as it has been used for Hypolytrum humile (Steud.) Boeck. as well as for Mapania humilis (Miq., partly) Vill. The first validly published description of Pandanophyllum humile Hassk. nomen nudum in Cat. Pl. Hort. Bot. Bog. 1844, p. 297 has been given by Steudel in his Synopsis II (1855), p. 134 and is based upon a specimen collected in Java by Zollinger (n. 1511, Brit. Mus., Paris), belonging to the genus Hypolytrum. So this is the type-specimen of H. humile (Steud.) Boeck. in Linnaea XXXVII (1871—1873), p. 128. Bentham and Hooker, however, accepting the interpretation of Kurz in Journ. As. Soc. of Bengal XXXVIII, part 2 (1869), p. 82 and the revised opinion of Miquel in his Ill. Fl. Arch. Ind. (1871), p. 61, included both species in their section Pandanophyllum of Mapania (Gen. Pl. III, 1883, p. 1056). A quarter of a century later C. B. Clarke divided Benth. and Hooker’s section into two subgenera, viz. Pandanophyllum, including Mapania humilis Vill. and Halostemma (Wall.), including Mapania palustris (Steud.) Vill. Consequently our present section Pandanophyllum sensu Clarke probably excludes both species, which originally belonged to it. One might be inclined to rectify the mistake by changing the name of Halostemma into Pandanophyllum and coining a new name for the other subgenus, but the principal difficulty, caused by the ambiguity of Hasskarl’s generic description can not be solved in this manner. This description calls for a bifid style (perhaps referring to Hypolytrum humile Boeck.) and 3—5 spikelets (not appropriate to Mapania palustris Vill., highly improbable as to Mapania humilis Vill. and Hypolytrum humile Boeck.). The only way out of the difficulty is to reject the name Pandanophyllum as a nomen dubium in the sense of the rules of nomenclature (art. 63) and to rename the subgenus Pandanophyllum Benth. et Hook., sensu Clarke. I propose the name Pandanoscirpus.

Description: As Prof. Bremekamp has dealt with the genus Pleiocraterium from the taxonomic point of view, I intend to supplement his exposition here with some observations on the ecology of these remarkable additions to the Malaysian mountain flora. Some of these observations have been included already in a general report on the results of the Losir expedition published in Dutch. As a further illustration I am giving two photographs taken from one of the two Sumatran species in its natural habitat. Altitude. Both species were found on the highest parts of the mountains only, viz. Pl. gentianifolium just below the summit of Mt Goh Lembuh, and Pl. sumatranum between our camp at the base of the central Peak of Mt Losir at c. 3250 m. and the summit of the latter at 3460 m. These two mountains lie rather far apart: Mt Losir is the highest top of the Barisan Range proper, whereas Mt Goh Lembuh is a more isolated mountain, rising c. 50 km. NNE of Mt Losir and separated from the latter by a wide depression. The two mountains also differ geologically.

Description: La forme est le phénomène de la vie le plus important. Aussi on pourrait croire que toute étude biologique devait commencer par la forme. En effet aucune fonction n’est imaginable indépendante de la forme, tandis qu’on peut étudier la forme indépendemment de la fonction, par exemple à des objets morts. Cependant depuis Sachs le botaniste moderne est tellement possédé par les conceptions matérialistes et mécaniques, qu’il veut aussi expliquer causalement les formes organiques en oubliant que, même si toutes les formes sont matérielles, cela ne veut pas nécessairement dire que les lois physiques et chimiques qui dominent la matière sont capables d’expliquer la forme, c.à.d. l’organisation des êtres vivants. A l’aide de briques on peut bâtir des bâtiments les plus divers, mais on peut aussi bien construire ces mêmes bâtiments de bois ou de pierre naturelle: le matériel employé n’explique pas le projet de l’architecte. Ce n’est qu’en le contemplant et en le comparant à d’autres qu’on arrive à mieux le comprendre (von Veh, p. 139). La forme („type” ou „idée” dans la conception platonique) est indépendante de la matière. Elle est ce qui reste. C’est par la forme que passe le courant de la cause et de l’effet, comme l’eau passe par un endroit clair d’une rivière (Carus). La forme présente un des problèmes les plus difficiles de la biologie. Le physiologue et le morphologue (deux extrêmes psychologiques) commencent pour ainsi dire aux deux extrémités de la nature, chacun à sa manière (Troll, Meyer), l’un avec sa méthode physique et chimique, l’autre avec sa méthode comparative. Au domaine du premier appartient tout ce qui est dynamique: le métabolisme et la croissance, au domaine du second ce qui est statique: la forme. Que la feuille est la partie principale de la plante, sur cela les physiologues et les morphologues sont d’accord. Le premier la considère comme un organe qui a pour fonctions principales la CO2-assimilation et l’évaporation. Depuis Goethe le second considère tous les appendices de la tige, aussi bien les sépales que les pétales ainsi que les organes sexuels comme des feuilles métamorphosées. Même, sous l’impression de la phyllotaxie des frères Bravais, Nees d’Esenbeck croyait que „la plante n’est rien d’autre qu’une unité de feuilles reliées entre-elles par un ordre défini”. C’est pourquoi on peut aisément considérer la morphologie de la feuille comme le problème central de toute la morphologie. Il est intéressant de se rendre compte comment dans le courant des temps on a essayé d’approcher ce problème de divers côtés. Cela pourrait apporter quelque lumière sur les différentes tendances de l’étude scientifique et sur les manières de penser qui sont caractéristiques pour les différentes périodes.

Description: Notwithstanding the large amount of work spent by several botanists on this family, taxonomy does not appear very satisfactory, and a general agreement on generic limits has not yet been reached. The result has been a perplexing number of generic and sectional names. The present author apologizes for his adding to the number of interpretations. This study of American Sapotaceae, primarily undertaken in connection with the Flora of Surinam, could not have been completed without the generous loan of specimens by the herbaria at Brussels [B], Berlin—Dahlem [D], Kew [K], and Leyden [L]. In 1934 the author paid a short visit to the herbaria at Brussels [B] and at Paris [P]. The collections of this family at Paris are of special interest owing to the fact that they contain the material studied by Baillon, Pierre and Dubard, and bear numerous notes and analytical drawings, especially by Pierre, attached to the sheets. A number of British Guiana Sapotaceae from the Kew Herbarium was received for determination shortly afterwards. The author feels greatly indebted to the directors of the above mentioned Herbaria for their kind help, and particularly to Prof. Dr. A. Pulle, Utrecht, under whose direction this study was undertaken.

Description: Cytological studies on the Rubiaceae with special references to the genus Galium have been done by HOMEYER (1936) and FAGERLIND (1937). EHRENDORFER (1949, 1954, 1955, 1956) described the phylogeny of the section Leptogalium. More detailed cytological and cytotaxonomical investigations appeared by HANCOCK (1942) (Galium palustre L., Galium debile Desv. and Galium uliginosum L.), CLAPHAM (1949) ( Galium palustre L.), EHRENDORFER (1949, 1953) (Galium pumilum Murr.) 1955 (Galium rubrum L. and Galium pusillum L.) and of Galium boreale L. by Löve and Löve (1954) and more recently by RAHN (1961). FAGERLIND (1937) and, previous to him, HOMEYER (1936) determined the chromosome numbers of many Galium species. Later investigations by EHRENDORFER (1949, 1955, 1956, 1961), LÖVE and LÖVE (1954, 1956), PIOTROWICZ (1958), POUQUES (1949), RAHN (1960, 1961) and REESE (1957) confirmed and supplemented this list of chromosome numbers. Many investigators have paid attention to the genus Galium. However, their studies have concerned only with some critical species or groups. Many taxonomical problems remain concerning the genus. SCHUMANN (1891) in ENGLER and PRANTL „Die Natürlichen Pflanzenfamilien” divided the genus in 14 sections which are very distinct morphologically. However, within these sections it is often very difficult to define exactly the morphological differences between the species.

Description: The genus Pausandra Radlk. belongs to the Tribe Cluytieae of the Euphorbiaceae. It was described by Radlkofer in 1870 in Flora LIII pp. 79—95. The genus is based on Thouinia Morisiana of Casaretto. In his paper Radlkofer discussed at length that this species does not belong to the Sapindaceous genus Thouinia, but represents a new genus of the Euphorbiaceae. As at that time female flowers were unknown Radlkofer stated that the systematic position of the new genus was still doubtful, but that most probably it should belong to a new subtribe of the Jatropheae. Two new species were described in the genus in 1873 by Baillon, P. Trianae Baill. based on Pogonophora Trianae Müll. Arg. which was published in 1864, and P. Martinii Baill. based on very young material and erroneously described by Baillon as being 3-merous, as will be discussed below. He placed the genus in the affinity of Argithamnia Sw., which is certainly not right as this genus is quite different both in habit and in flowercharacters. A fourth species was added by Müller Arg. in 1874 in Flora Brasiliensis XI. II., where he inserted the genus in the same group as was suggested by Radlkofer. No more species had been described when Pax published in 1911 his monograph of the Tribe Cluytieae Pax in Engler, Das Pflanzenreich IV. 147. III. He inserted the genus Pausandra Radlk, with the genera Givotia Griff, and Ricinodendron Müll. Arg. in a new subtribe Ricinodendrinae Pax. I think that this is the right position for the genus, though it could be placed in a separate subtribe for its penninerved, glanduliferous leaves and the capsular fruits. It was a pity that Pax published this monograph without studying the original material. He now copied Baillon’s bad descriptions and the lack of a thorough study on the genus caused the publication of several superfluous species in recent years. P. quadriglandulosa Pax et K. Hoffm. and P. extorris Standley described in 1919 and 1929 are the same as P. Trianae (Müll. Arg.) Baill. P. flagellorhachis Lanj. is identic with P. Martinii Baill., while it was proved that the latter species is not trimerous. P. integrifolia Lanj. could not be maintained in the genus. Only the two new species published by Ducke in 1925 were truly new ones. Moreover three new species were recognized in the recent collections made by Krukoff in Brazil. It is for all these reasons that it seemed to me highly desirable to give a new treatment of this genus. Perhaps several of the old and new species can be united, as one can find often only small differences, but for the present I think it advisable to keep them separate. Pausandra Radlk, has been described to be dioecious, but recently it has been proved in some species that they are monoecious, so it is probable that most of them are under special cicumstances.

Description: Among the most remarkable finds made by Dr. van Steenis in the higher parts of the mountains of North Sumatra are a number of cushion plants. Two of these he recognized as Rubiaceae nearly related to Hedyotis verticillaris W. et A., a species occurring in similar habitats in the Nilgiri Hills, India, and in Ceylon. Hesitating, however, to express a definite opinion on their taxonomic position, he sent the material to me for further investigation. As I had occupied myself already for some time with the genus Hedyotis L. and its allies, this investigation offered me a Wellcome opportunity to test some of the principles which I had laid down for the subdivision of this group. Apart from the characters of the fruit I lay stress on the position of the inflorescence and on the form of the stipules. The name Hedyotis itself I wish to restrict to H. fruticosa L. and its nearest allies, i.e. to those species that are provided with terminal inflorescences, an ovary not distinctly produced beyond the insertion of the calyx, and fairly large drupes with apically and ventrally dehiscent pyrenes: to a group, therefore, which roughly agrees with Hedyotis section Diplophragma W. et A.

Description: This is the second paper dealing with Myxomycetes collected by me in the Netherlands, mostly in the neighbourhood of Doorwerth. Specimens of the species dealt with are preserved either in my private collection or in that of the Botanical Museum and Herbarium of the State University, Utrecht (in the last named case the numbers are followed by a “U”), or in both.

Description: Recent study of the copious material of Melastomaceae conserved in the Botanisch Museum en Herbarium at Utrecht has shown the existence of several undescribed species in Surinam and has given new ideas on the taxonomic status of a few other species. These results are presented below, in advance of the treatment of the family in the „Flora of Surinam”. Ernestia Pullei Gleason, sp. nov. Suffruticosa 4 dm. alta. Caulis purpureo-brunneus 4-angulatus dense glanduloso-pubescens, internodiis 10—15 mm. longis. Petioli graciles 5—10 mm. longi glanduloso-villosi. Laminae tenues ovatae usque ad 25 mm. longae 17 mm. latae acutae minutissime serrulatae basi cordulatae 5-nerviae, supra sparse minuteque glanduloso-pilosae, subtus dense cinereo-tomentellae. Paniculae magnae terminales ramosae 8—12 cm. longae multiflorae glanduloso-polisae, bracteis minimis oblongis. Florum 4- merorum non bene conservatorum structura difficiliter et fortasse non rite observanda. Hypanthium tubuloso-campanulatum 8-costatum dense glanduloso-pilosum. Sepala erecta triangularia acuta sparse glandulosa 1.6 mm. longa. Petala non visa. Stamina valde dimorpha. Filamenta glabra erecta gracilia 3-7 mm. longa. Antherae lineari-subulatae, staminum episepalorum horizontales 4.2 mm. longae, connectivo subtereti in semicirculum 1.5 mm. diam. curvato et supra insertionem filamenti in appendices 2 V-forme connatas dilatato, ad angulam externam appendicum inserto; appendicibus in angulo interno ad filamentum affixis, triangulari-subulatis 3.2 mm. longis, infra filamentum attenuatis in calcaria filiformia et interdum calcaribus similibus lateralibus 1 vel 2 ornatis; antherae staminum epipetalorum erectae 3.3 mm. longae, connectivo ad angulam 90° deflexo 1 mm. longo, infra insertionem filamenti calcaria 2 lineari-subulata erecta 1.7 mm. longa gerente. Ovarium superum, teste cl. Pulle in schedis 3-loculare, sed in uno dissecto distinctissime 4-loculare; stylo stigmateque non visis; seminibus cochleatis.

Description: Some months ago the first author published in his Studies in Moraceae II (Rec. trav. bot. néerl. XXXIII, 1936, pp. 254—276) a synopsis of the genus Clarisia R. & P. The second author traced in the Berlin Herbarium a specimen of this genus which had been described in 1821 as Excoecaria ilicifolia Spreng. As this species is identic with Clarisia strepitans (Fr. Allem.) Lanj., the name of the latter species has to be changed. As in addition some interesting specimens were kindly sent to Utrecht for determination by the Herbaria at Berlin-Dahlem (D), Geneva (G) and the Arnold Arboretum, Jamaica Plain (A), it seemed desirable to publish these notes.

Description: In the present study pollen morphology of the Euphorbeaceae is treated as an additional character in taxonomy. Besides the greater part of the genera occurring in the system of PAX and K. HOFFMANN (1931), most of the genera published after 1931 are studied. The pollen grains have been described with the aid of a terminology as simple as possible. In principle the terminology of IVERSEN and TROELS-SMITH has been followed, although in addition, many improvements of ERDTMAN have been used. One of the simplifications is the rejection of POTONIÉ’s term sculpture. All elements occurring on the endexine are called structure elements; all structure elements together form the structure of a pollen grain. For the sake of consequence endexine apertures and extexine apertures are discussed separately. Different pollen grains are placed in different pollen types. If the differences are of minor importance, the pollen grains are placed in subtypes. Several types can have some characters in common. To express the correspondences, these types are assembled in configurations. As the pollen types in Phyllanthoideae and Crotonoideae differ distinctly, the division of the Euphorbiaceae in these subfamilies is maintained in the discussion of the results. The Phyllanthodieae can be separated in three large groups of pollen types ( Antidesma configuration, Amanoa configuration and Aristogeitonia configuration), which agrees with the grouping of PAX in 1924. The remaining small configurations belong in taxonomic respect to the genera of the Antidesma configuration. In the Crotonoideae many genera possess pollen grains with a croton-pattern. These genera should be treated as a single group. Besides this natural group, the Plukenetiinae possess pollen grains which are clearly distinguished from other genera in the Crotonoideae. Pollen grains of Omphalea are similar to those in the Plukenetia configuration. This pollen-morphological result agrees with the opinion of CROIZAT. The remaining pollen grains in the Crotonoideae are less easy to differentiate in groups. One of the largest configurations is the Mallotus configuration, which includes most genera of the Acalypheae and several genera or other tribes. The Hippomane configuration is another large one. This configuration comprises the tribes Hippomaneae and Euphorbieae. The pollen grains of both tribes are very similar. The genus Pachystroma is pollen-morphologically as well as taxonomically related to the tribe Hippomaneae. Pera, treated as a separate tribe by PAX and K. HOFFMANN, is related by its pollen grains to some genera in the Acalypheae. Dalechampia is habitually related to the genera in the Plukenetiinae. Pollenmorphological data, however, do not support this relation. The pollen grains of Dalechampia are not similar to any other pollen type. The morphology of the pollen grains of the Stenolobeae is in agreement with the opinion of PAX, that any separation of these Australian genera is an artificial one.

Description: 1. The Orchids in the Netherlands have been subjected to a cytological investigation. 2. The division of the genera Orchis (L.) Klinge into two new genera: Orchis (L.) Vermln. and Dactylorchis (Kl.) Vermln. (Vermeulen, 1947), could be confirmed. 3. In Listera ovata (L.) R. Br. the diploid chromosome number is 34. Deviating numbers 2n = 35 and 2n = 36 were counted. Because aberations in chromosome number do not cause morphological differences these aberations seem to be unimportant. 4. Out of the material investigated it might be concluded that for the moment it does not seem to be correct to consider Dactylorchis fuchsii (Druce) Vermln, as a separate species besides Dactylorchis maculata (L.) Vermln. It seems more likely that D. fuchsii and D. maculata represent two types within a complex-species.

Description: Endlicheria Nees (non Presl) in Linnaea 8 (1833), p. 37; id., Progr. (1833), p. 16; id., Syst. (1836), p. 365; Endl., Gen. (1837), p. 321; id., Ench. (1841), p. 197; Dietrich, Synops. Pl. 2 (1840), p. 1332, 1350; Spach, Hist. nat. Végét. X (1841), p. 473; Steudel, Nomencl. ed. 2 (1841), p. 554; Meissn., Gen. I (1836—43), p. 326, II, p. 238; Orbigny, Dict. univ. (1846), p. 259; Lindl., Veg. kgd. (1846), p. 537; Meissn. in D.C., Prodr. XV, 1 (1864), p. 172; id. in Fl. Bras. V, 2 (1866), p. 281; Baillon, Hist. II (1870), p. 480 in adnot.; Pfeiffer, Nomencl. (1873), p. 1201; Benth. in Benth. & Hook., Gen. III (1880), p. 153; Durand, Index Gen. (1888), p. 348 sub Aydendron; Mez in Jahrb. Bot. Gart. Berl. V (1889), p. 111; Pax in Engl.-Prantl, Pfl. Fam. III, 2 (1889), p. 122; dalla Torre & Harms, Gen. (1900—07), p. 178 sub Aniba; Post & Kuntze, Lexicon (1904), p. 197; Lemée, Dict. 2 (1929), p. 857; Benoist in Arch. Bot. V (1931), p. 63; Kostermans in Meded. Bot. Mus. Utrecht 25 (1936), p. 41; id. in Pulle, F1. Surin. 2 (1936), p. 327. – Goeppertia Nees, Syst, l.c., p. 354, 365 (non alibi nec aliis); Endl., Gen., l.c., p. 321, n. 2051; id., Ench., l.c., p. 197; Dietrich, l.c., p. 1332, 1350; Spach., l.c., p. 473; Steudel, l.c., p. 697; Reichb., Nomencl. (1861), p. 70, n. 2659; Meissn., Gen. I, p. 326, II, p. 238; Orbigny, l.c., p. 259; Lindl., l.c., p. 537; Meissn. in D.C., l.c., p. 172; id. in Fl. Bras., l.c., p. 281; Baillon, l.c., p. 480; Pfeiffer, l.c., p. 1473; Benth., l.c., p. 153; Durand, l.c., p. 348 sub Aydendron; Mez, l.c.; Pax, l.c., p. 122; dalla Torre & Harms, l.c., p. 178 sub Aniba; Post & Kuntze, l.c., p. 253; Kosterm. in Meded., l.c. – Schauera Nees in Lindley, Nat. Syst. ed. 2 (1836), p. 202 in adnot. (non aliis nec alibi); Endl., l.c., p. 321; id., Ench., p. 197; Meissn., Gen. II, l.c., p. 238; Orbigny, l.c., p. 259; Lindl., Veg. kgd., l.c., p. 537; Benth., l.c., p. 153; Durand, l.c., p. 348 sub Aydendron; Mez, l.c.; Pfeiffer, l.c., p. 1071; dalla Torre & Harms, l.c., p. 178 sub Aniba; Post & Kuntze, l.c., p. 503; Lemée, l.c., p. 1006. – Schaueria Nees ex Meissn. in D.C., l.c., p. 172; id. in Fl. Bras., l.c., p. 281 (non aliis); Baillon, l.c., p. 480; Pax, l.c., p. 122. – Ampelodaphne Meissn. in D.C., l.c., p. 81; id. in Fl. Bras, l.c., p. 167; Baillon, l.c., p. 473; Pfeiffer, l.c., p. 1071; Benth., l.c., p. 153; Durand, l.c., p. 348 sub Aydendron; Pax, l.c., p. 122; dalla Torre & Harms, l.c., p. 178 n. 2812; Post & Kuntze, l.c., p. 24; Lemée, Dict., l.c., p. 210; Kosterm. in Meded., l.c. – Aydendron Griseb. (non Nees), p.p. in Fl. Brit. W. Ind. isl. (1860), p. 284; Benth., l.c., p. 153; Mez, l.c. – Huberodaphne Ducke in Arch. Jard. Rio de Janeiro 4 (1925), p. 191; Lemèe, Dict., l.c., 3 (1931), p. 661. Type species: Endlicheria hirsuta Nees.

Description: In the years 1954-1957 The Foundation for Biocenological Research (Stichting tot Onderzoek van Levensgemeenschappen, S.O.L.) carried out an extensive study on the vegetation of about 125 former river beds in the Netherlands. They were situated along the great rivers and their branches, viz. Meuse, Oude Maas (“Old Meuse”), Heusdense Maas (“Heusden Meuse”), Rhine, Lek, Merwede, Waal and IJsel. The work was made possible by a grant of the Netherlands Organisation for Pure Research (Nederlandse Organisatie voor Zuiver Wetenschappelijk Onderzoek, Z.W.O.). Dr. M. F. Mözer Bruijns proposed and supervised the investigation, and Dr. V. Westhoff took part in the interpretation of the results. The field work was carried out by A. J. Quené-Boterenbrood (1954-55), W. A. E. van Donselaar-ten Bokkel Huinink (1955-56), J. van Donselaar (1955— 57), Ir. L. G. Kop (1956-57), P. J. Schroevers (1954-55) and E. E. van der Voo (1954-57). Our study had several aims. The collected material had to contribute to our knowledge of a number of plant species and communities, especially of those playing a part in the hydrosere found in various kinds of water. With respect to the communities it should comprise their floristic composition as well as a definition of their habitat. Moreover, the former river beds should be classified according to their plant communities as well as to their abiotical properties. This classification should be useful as a basis for the choice of future naturereserves (see Gorter and Westhoff, 1952; Van Donselaar, 1956; Westhoff and Leentvaar, 1957).

Description: Anaueria Kosterm. in Chronica Botanica IV, 1 (1938), p. 14. Arbores brasilienses foliis sub-oppositis. Flores hermaphroditi ex-involucrati paniculati; tepalis sex tribus exterioribus minoribus. Stamina novem quorum sex exteriora fertilia filamentis in annulum ovarium cingentem connatis antheris liberis bilocellatis sub-introrsis; tria interiora sterilia staminodialia sub-aequilonga. Ovarium subglobosum tubo planiusculo insertum, stylo obtuso brevi stigmate inconspicuo. Staminodia seriei quartae nulla. Bacca magna ellipsoidea pedicello vix elongate cylindrico tepalis non incrassatis persistentibus insidens.

Description: Zu meiner Bearbeitung des surinamischen Materials der Gentianaceae für die von Pulle herausgegebene „Flora of Surinam” gehören nog einige kritische Bemerkungen. Ich muszte z.B. in einigen Fällen von der von Gilg in Engler und Prantl, Nat. Pflanzenfamilien gegebenen Einteilung der Gattungen und deren Umgrenzung abweichen. Auch stellte es sich heraus, dasz sich unter dem Material eine neue Art befand, deren Beschreibung und Abbildung unten folgen.

Description: Juniperus macropoda Boiss. Fl. Orient. V (1884) p. 709; Hooker Fl. Br. Ind. V (1890) p. 647. Umlung (Thalam-buti valley) 4200 m, 28 July no. 58. Big shrubs.

Description: This paper reports a palynological investigation of Lower Triassic rock salt samples from the eastern part of the Netherlands. Bisaccate pollen grains average 99 % in the spore-pollen complexes. Most important constituent is the group of non-striate pollen grains (about 91 %), whereas striate pollen grains occur only in a small number (about 8 %). 19 pollen species are recognized and described, of which 5 are new. Two new genera are described: Eridospollenites and Angustisulcites. The pollen assemblages are compared with Upper Permian and Lower Triassic assemblages from other localities.

Description: De in deze Jubileumserie van de „Mededeelingen van het Botanisch Museum en Herbarium te Utrecht” opgenomen artikelen zijn door de schrijvers ingezonden om Prof. Pulle, ter gelegenheid van zijn zilveren jubileum als hoogleeraar, hun waardeering te toonen. Een kort woord over den jubilaris moge hier als inleiding van deze bijdragen volgen. Op 10 Januari 1878, op den dag dat in verschillende plaatsen den Ioosten sterfdag van Linnaeus werd herdacht, werd August Adriaan Pulle te Arnhem geboren.

Description: Since the appearance of my „Notes on the Rubiaceae of Surinam” (in Rec. d. Trav. bot. néerl. XXXI, 1934, 248; also in Meded. Bot. Mus. Herb. Utrecht no. 11, 1934) a number of species and varieties new to the flora of that country have come to light. The majority have been collected by Mr. Rombouts during the 1935/36 expedition of the Boundary Commission who is surveying at present the border in the southern part of the colony; they were found along the River Corantyne and in the savannahs in the south-western part. One species was secured by Dr. Lanjouw, and has been mentioned already in his „Additions to Pulle’s Flora of Surinam I” (in Rec. d. Trav. bot. Néerl. XXXII, 1935, 258) and one, represented by a rather poor fruiting specimen collected years ago by the Forestry Bureau, was found among material provisionally consigned to another family. New to the flora of Surinam are the following twelve species: Alseis longifolia Ducke var. pentamera Brem. n. var., Sabicea cinerea Aubl., S. Romboutsii Brem. n. spec., S. surinamensis Brem. n. spec., Tocoyena surinamensis Brem. n. spec., Thieleodoxa nitidula Brem. n. spec., Guettarda Spruceana Müll. Arg., Psychotria Romboutsii Brem. n. spec., Declieuxia fruticosa (Willd. ex R. et S.) Kuntze, Diodia pulchristipula Brem. n. spec., Spermacoce guianensis Brem. n. spec, and Borreria verticillata (L.) G. F. W. Mey (the B. verticillata of the Flora of Surinam IV, 287 proved to be B. suaveolens G. F. W. Mey., under which name it had been recorded already by Miquel), and one variety: Sipanea pratensis Aubl. var. glaberrima Brem. n. var. Four of the ten genera to which these species belong, namely Alseis, Thieleodoxa, Declieuxia and Spermacoce, are also new to the flora of Surinam. Seven species and two varieties are entirely new, and will be described below. Before entering on this part of my task I will make a few remarks however on two of the species known already from elsewhere, namely on Guettarda Spruceana Müll. Arg. and on Borreria verticillata (L.) G. F. W. Mey, and on a third species, Coccocypselum guyanense (Aubl.) K. Sch., which is known since long from Surinam, but of which Mr. Rombouts collected a specimen differing somewhat from the older Surinam findings.

Description: Op 8 okt 1960 vond de heer J.C. Tanis, custos van het Biologisch Station “Schellingerland” op Terschelling, in de nabijheid van dit Station een bloeiend exemplaar van Erica cinerea L. Na opzending van een bloeiende tak via ondergetekenden naar het Rijksherbarium werd deze determinatie bevestigd. Deze opmerkelijke waarneming geeft aanleiding tot commentaar, temeer, daar men op het eerste gezicht geneigd is, hier enig verhand te zien met de ontdekking van twee andere, mediterraan-atlantische, Erica-soorten in dezelfde omgeving, te weten E. scoparia L. door Th.J. Reichgelt in 1952 (zie van Ooststroora en Reichgelt 1956) en E. ciliaris L. door P. Runge in 1955 (zie Runge 1956, van Ooststroom en Reichgelt 1956).

Description: In 1885 publiceerde J.D. Kobus een Flora van Wageningen en omgeving. Hij vermeldt hierin het voorkomen van Sambucus racemosa L. op de Wageningse Berg met het bijschrift; „aangeplant?” Of de soort aan de zuidelijke Veluwerand oorspronkelijk voorkomt is thans minder dan toentertijd uit te maken; ze is er nu zeker plaatselijk niet zeldzaam. Ook in het Zuidoosten van de provincie Utrecht wordt ze op tal van plaatsen aangetroffen. Zo groeit ze in groot aantal op en om de Grebbeberg, evenzo op en nabij het landgoed Remmerstein tussen Rhenen en Veenendaal. fan kunnen we de plant nog verspreid aantrffen te Eist (Utr.) en in de omgeving van Amerongen. Een wat ongewone en daardoor interessante vindplaats ligt in de gemeente Veenendaal. Hier vindt men in het laagste deel van het Griftgebied het natuurreservaat De Ho. open water met rietland er om heen. Als afsluiting heeft men na de laatste oorlog enkele el zenbosjes aangeplant. In deze elzenbosjes zijn verscheidene houtige gewassen spontaan verschenen: Ribes sylvestre, Ribes nigrum, Rubus, Sambucus nigra en ook Sambucus racemosa. He kiemplanten van Sambucus racemosa gaan veelal te gronde door te vochtig en schaduwrijk milieu, maar op enkele meer geschikte plaatsen hebben zich struiken weten te handhaven. Het rietland van De Hel is sinds jaar en dag een slaapplaats voor spreeuwen, die zich hier uit wijde ontrek verzamelen, waarschijnlijk uit een gebied met een straal van wel 15 km. Deze spreeuwen zijn stellig grotendeels oorzaak van het optreden van bovengenoende soorten.

Description: Abbayes, H. des: Lichens nouveaux ou intéressants du Vietnam (Rev. Bryol. & Lichénol. 32, 1963, 216-222, 1 pl.). Adams, H.H. & M.A. Reinikka: Calcareous Cypripediums of southern Asia (Orchid.) (Am. Orchid Soc. Bull. 1963, 182-186).

Description: This series of two or more volumes starts to be published in the summer of 1962; the page proofs of the first volume, which was sent to the press in May 1960, were received by Dr. E. Quisumbing at Manila where the volume is being printed, in March; its publication can be expected by July 1962. The series ”Pacific Plant Areas” means to give all that is already known about distribution of taxa of generic and lower level which centre round the Pacific Ocean, and also to add to our knowledge by giving new maps which have been carefully prepared by specialists. Hence the series consists of a bibliographic part and a cartographic part, preceded by an explanatory introduction. Volume I is mainly bibliographic, containing about 3200 references to maps and 26 newly prepared maps; volume II will be mainly cartographic, containing about 124 newly prepared maps, and will hopely be ready for the press by the end of 1962.

Description: 1. Introductory.--This project was to study fern specimens in certain herbaria in the U.S.A., especially of tree-ferns (Cyatheaceae), in connection with preparation of the Pteridophyte Series of Flora Malesiana, and to make contacts in the U.S.A. with a view to continued cooperation in this work. The family Cyatheaceae, on which I am at present engaged, is a particularly difficult one, comprising 350 described species in Malaysia, in a close alliance. Probably all should be regarded as belonging to one genus. Descriptions of species have on the whole been unsatisfactory, so that many identifications of specimens in herbaria are doubtful or erroneous. It is thus necessary to see all type specimens to establish the significance of names; and also, as the fronds are large so that only a part of one appears on each herbarium sheet, the different specimens of the same collection, distributed to different herbaria, often give complementary information, so that to see one is not enough. Furthermore, it is necessary to see as many collections as possible, to understand what variation is possible within a species. The material is bulky, and it is a physical impossibility to gather together in one place all that one needs to see for a proper understanding of the family. I had already spent more than a year on this study before going to the U.S.A., and had seen most of the type material in European herbaria.

Description: In de oudere jaargangen van Heukels’ flora staan aanvankelijk alleen Schouwen en Huisduinen genoemd als groeiplaatsen van Crithmum maritimum, in nieuwere drukken is er Vlissingen bijgekomen, nog later veranderd in Walcheren en thans prijkt Crithmum met vier groeiplaatsen, n.l. Huisduinen, Schouwen, Walcheren en West Zeeuws-Vlaanderen, Daaruit zoumen mogen concluderen.dat Crithmum, hoewel zeldzaam, niettemin in opmars is en zijn gebied uitbreidt. Een nauwkeurig volgen van de ontwikkeling op de bekende groeiplaatsen en een naarstig zoeken naar nieuwe gedurende een tijdvak van ongeveer 15 jaren hebben mij echter de overtuiging gebracht, dat de soort in Zeeland op zozeer kwetsbare plaatsen groeit, dat misschien wel van opmars doch geenszins van uitbreiding kan worden gesproken. Alle in die jaren gevonden planten groeiden aan zeeweringen op glooiingen van Vilvoordse steen en basalt, met slechts één uitzondering. Deze glooiingen staan enerzijds bloot aan zware aanvallen van de zee en behoeven anderzijds als gevolg van die aanvallen regelmatig te worden hersteld, vernieuwd of verzwaard. Vooral het herstel en verzwaren van die zeeweringen zijn de laatste jaren voor het voortbestaan van de soort bijna catastrophaal geworden, zoals uit het volgende relaas moge blijken. Het is mij niet bekend of de soort zich. in Huisduinen heeft kunnen handhaven, doch in Zeeland zijn de meeste gevonden groeiplaatsen na korter of langer tijd weer verdwenen, De groeiplaats in Vlissingen is mij nooit bekend geweest, maar er groeit in Vlissingen nu geen Crithmum meer. Op Schouwen was een groeiplaats op Vilvoordse steen in de omgeving van Flauwers met vrij veel, goed ontwikkelde planten, die konden bogen op een grote mate van inschikkelijkheid jegens haar door de Waterstaatsmensen – Zo zeer zelfs dat toen de glooiing versterkt moest worden en de ruimte tussen de stenen werd volgegoten met beton, de groeiplaats van Crithmum daarvan werd uitgezonderd om de planten te sparen, Na de ramp in 1953, waarbij de dijk en de planten ter plaatse intact bleven, moest de dijk zodanig worden verzwaard, dat het niet mogelijk bleek de planten nog langer te sparen. Zij zijn daar onder een laag klei van ongeveer twee meter dik begraven.

Description: As a student, I used to enjoy ’Karsten and Schenck’ propped up on the breakfast-table. With equal familiarity I treated ’Kerner’, 'Schimper', and other great picture-books of botany. The time came to translate the dreams of youth into vocation. ”Protista”, said the professor of zoology, ”are the pivot of biology”. I substituted my breakfast-reading with the Archiv für Protistenkunde, and hesitated at the coming call of biophysics. Ever since I have been rent, like the morning toast, by two forces which would make of me a student of the microcosm of protoplasm and a disciple of its greatness. They are the forces splitting biology into macromolecules and macro-organisms, and I do not know how this rift may be spanned. I cannot conceive what energy level, chemical bond, or carbon-grouping can decide whether it is insect-pollination or curiosity that will be inherited. But the pendulum has swung. The young botanist no longer looks at these books? he models molecules and chromosomes, and works very largely in vitro. Nevertheless, if biology is not to stand still, the pendulum will return and its amplitude will be the strength of those who have put their trust in the macrocosm. These were the thoughts which I vaguely entertained, when I found myself in the forests of Malaya and I measured my insignificance against the quiet majesty of the trees. All botanists should be humble. From trampling weeds and cutting lawns they should go where they are lost in the immense structure of the forest. It is built in surpassing beauty without any of the necessities of human endeavour; no muscle or machine, no sense-organ or instrument, no thought or blueprint has hoisted it up. It has grown by plant-nature to a stature and complexity exceeding any presentiment that can be gathered from books, and it is one of the most baffling problems of biology.

Description: Dr. J.A.R. Anderson, Kuching, will go on leave in October 1962. Mr P.S. Ashton, Cambridge (U.K.), has accepted the post of Forest Botanist at kuching, Sarawak, and will in September 1962 proceed to Borneo.

Description: Different trees have different sorts of hark, the variation is of two main kinds. The hark of an individual changes as it grows, and there are differences between mature trees of different species. The recognition of large trees in tropical forest depends on living as opposed to herbarium characters and amongst living characters baric is important. Botanists are slowly coming to realise that living characters are of importance to taxonomy and can supplement the characters visible on herbarium sheets but often hard to see in the forest (Corner 1940, Symington 1943, Henderson & Wyatt-Smith 1956). At present many living characters are used empirically if at all.

Description: The following is an author’s summary of the (as yet unpublished) thesis by Dr. J.A.R. Anderson of Kuching, Sarawak (see III. Personal news). Both the author and botanical science are to be congratulated with the completion of this important work, which we hope before long to see in print. The thesis embodies the results of botanical and ecological work on the coastal and deltaic peat swamp forests of Sarawak and Brunei undertaken intermittently over a period of ten years. Profiles of peat swamps have been prepared from the results of the level surveys and peat borings. A characteristic raised bog structure has been found in all swamps. A bog plain is usually present, and is most extensive on more inland swamps. The peat soils are markedly acidic and oligotrophia. Preliminary results from measurements of the stilted water table indicate that variations are more pronounced in the centre of swamps than near the margins. A comprehensive collection of botanical specimens of all flowering plants, ferns and fern allies has been made; 242 tree species have been recorded, and it is considered that knowledge on the representation of the arboreal flora is virtually complete.

Description: In papers and manuscripts on tropical phytography I find a growing tendency to ”overdo accuracy”, with the negative effect that accuracy is underdone. Tropical phytography operates, of necessity, at a different level of accuracy in details than does temperate botany, because the aim is wider and the materials and field knowledge scantier. But as often has been demonstrated, if the second and third storey are begun before the first storey has been completed, such a wing of the house of science is unfit for inhabitation. I see it therefore as the present task of the tropical botanist to finish the first storey of knowledge, and of accuracy, for all groups. With this in mind, some thought should be given to the following considerations. In the first place there is again a growing custom with several to incorporate so much (often unnecessary or unwanted) detail in descriptions to obscure the important and really distinctive characters. Everybody can understand that, whereas a herbarium botanist may often be very glad to have 30 specimens collected during 150 years, which is a fraction of a fraction of the millions of specimens of the sum of the populations growing in nature during that period, it is a vainless attempt to encompass on the basis of three dozen specimens the complete polymorphism in great detail. If one wants to make such elaborate descriptions, one should split them into a diagnostic description followed by additional measurements and characters of secondary value. This is a compulsory courtesy against those who will consult such elaborate descriptions. With more collections coming in it is clear that there will be always minor deviations from the additional descriptive part, but more rarely in the diagnostic part; in the latter case one is becoming alert.

Description: In chapter VII of his book ”Wanderings in the Great Forests of Borneo” Beccari records his ascent of Mount Poi (Poe, Pueh) in south-western Sarawak, and subsequently Poi has been cited as the type locality for a number of species described from his material. The purpose of this note is to put on record the fact that although Beccari ascended the Poi range, he did not climb Gunong Poi, as that name is used on modern maps, but a more south-easterly peak in the range, Gunong Berumput (Gunong Rumput). In August 1962 I collected on Gunong Beruraput with my colleague P.J.B. Woods: the choice of this peak rather than Gunong Poi itself was made on the advice of Mr B.E. Smythies, Conservator of Forests, who said he thought we should find it more interesting. On returning home I re-read Beccari’s book and realized immediately that we had virtually followed in his footsteps.

Description: Professor and Mrs Ernst Abbe spent May-August 1964 in Sarawak, making intensive collections of developing inflorescences of Fagaceae for morphological studies. Mr N. G. Bisset of Kuala Lumpur visited Sabah and Sarawak from April to July 1964. On several trips he collected resin samples of Dipterocarpaceae, and leaf and bark samples of Euphorbiaceae, Rubiaceae, Simaroubaceae, Gnetum, Gleichenia, Apocynaceae, Strychnos, Icacinaceae, and others, all for phytochemical investigation.

Description: History of Indian Botany. It is with great pleasure that Mr I.H. Burkill wrote us that the third and final instalment of his History of Indian Botany was ready for fair copying, Xmas 1959. The Bombay Natural History Society contemplates reprinting the three chapters in one booklet. Pacific Plant Areas (see p. 645). The text and maps of the first instalment are finished now.

Description: Previous to the 4th UNESCO Expedition, Dr H. Sleumer of the Rijksherbarium made three trips together with Mr Tem Smitinand, first to Doi Chiengdao and Doi Suthep in the North (Aug. 15-21, 1963), then to the Khao Yai National Park in Central Siam (Aug. 28-29), then to Pha Nok Khao and Phu Krading South of Loie in NE. Siam (Sept. 8-11). The 4th UNESCO Training Expedition was conducted by Mr Tem Smitinand of the Royal Forest Department, Bangkok, and Dr H. Sleumer of the Rijksherbarium, the latter serving as only instructor. The 10 participants, from Vietnam (1), the Philippines (1), Malaya (2), Singapore (1), Indonesia (2) and Thailand (3) started from a base camp 44 km from the highway from Suratthani to Takuapa in the Peninsula on Sept. 19, 1963. They investigated the flora of 7 limestone hills in the region: Khao Phra Rahu, Khao Lek, Khao Wong, Khao Ne Dang, Khao Pak Chawng, Khao Lang Tao, Khao Dai Kuad, ranging in altitude from 180 to 500 m. Each of these hills had a few peculiar species which were not found on the other hills, although in general the flora, especially in the lower slopes, was the same; 156 herbarium numbers with duplicates were here collected.

Description: Archer, Mildred: Natural History drawings in the India Office Library. London. H.M. Stat. Office 1962. ix + 116 pp., 25 pl. Clothbound Sh. 27/6. This is a catalogue of the c. 5000 drawings still extant in the India Office Library of which only a few hundreds are of plants, the rest representing animals. There is an extensive introduction in which the activities of the persons involved in their donation are explained, which gives the book an interesting biographical and historical aspect. A beautifully executed work showing wide knowledge of its author. -- v. St. Fleming, Charles A.: New Zealand Biogeography. Tuatara 10, 1962, 53-108, 15 fig.

Description: The Natural History of Rennell Island, British Solomon Islands. Scientific Result of the Danish Rennell Expedition, 1951, and the British Museum (Natural History) Expedition, 1959. Vol. 5 (Botany and Geology), ed. by Torben Wolff. Danish Science Press, Copenhagen, 1960, 7-152 pp., many figs and photogr. This volume was issued in 5 instalments. The first (1957) contains a paper by N. Foged: Diatoms from Rennell Island. The second (1958) contains papers by E.B. Bartram: Musci, by T. Wolff: Vascular Plants from Rennell and Bellona Islands (a list of 31 spp. identified by F.R. Fosberg, and a few names of seeds), and by J.C. Grover: The Geology of Rennell and Bellona. The third instalment (1960) contains papers by T. Levring: A List of Marine Algae from Rennell Island, and by Lise Hansen: Some Macromycetes from Rennell and Alcester Islands. For the botanist may also be of interest T. Wolff’s general introduction in vol. 1 of the series (1955) 9-31. Proceedings of the Symposium on Humid Tropics Tjiawi (Indonesia) December 1958. Publication of Unesco Science Cooperation Office for Southeast Asia. Printed at New Delhi, no date; received March 1961; xv + 312 pp., map of Brunei, vegetation maps, photogr. Biographical notes of authors; discussions. Sponsored by the Council for Sciences in Indonesia and Unesco; Chairman Prof. Kusnoto Setyodiwiryo.

Description: For the pollination of their flowers, plants of the genus Ficus are absolutely dependent upon the activity of small insects, the ”fig wasps” (Hymenoptera Chalcidoidea, family Agaonidae). Consequently, no account of Ficus can be exhaustive without considering the entomological data. On the other hand, the fig wasps can only develop in the gall flowers of the fig receptacle. Consequently again, in the evaluation of the data on fig wasps, great stress should be laid on the botanical evidence. These statements may serve as ample justification for the appearance of an entomologists’ notes in this botanical bulletin. Since 1960 I am working through a large collection of Indo-malayan and Papuan fig wasps, mainly consisting of the collection made by Dr. J. van der Vecht at Bogor, and material sent by Dr. E.J.H. Corner from various parts of Malaya, Indonesia, Papua, and Melanesia. As the study of the fig wasps is still in its analytical stage, progress is slow, but the results are promising.

Description: Alston, A.H.G. J.A. Crabbe, A.H.G. Alston (1902-1958). A bibliography of his writings, with a short introduction and a list of new taxa and nomenclatural changes published by him. J. Soc. Biol. Nat. Hist. 3 (1960) 383-404.

Description: Balan Menon, P.K.: Taxonomic value of wood anatomy seen through Malayan woods. The Malayan Forester 24 (1961) 290- 301. Mr Menon, who is a wood technologist at the Forest Research Institute, Kepong, Malaya, presented this paper at the Hawaii Congress. In it, he gives a series of classifications of Malayan woods on the basis of anatomical features which can be seen by a hand-lens, he distinguishes 18 classes, notably woods with: ring-porous structure, exclusively solitary pores, multiple vessel-perforation, vestured (vessel) pits, scalariform intervessel pits, ripple marks, broad rays, uniseriate rays, septate fibres, distinctly bordered fibre pits, tanniferous tribes, latex tribes, horizontal canals, vertical canals, included phloem, mucilage or oil cells, silica inclusion, raphides.

Description: From the ”Procèes-Verbaux des Séances de l’Académie tenues depuis la fondation de l’Institut jusqu’au mois d’août 1835. Publ. conf. à une décision de l’Académie par M.M. les secrétaires perpétuels. Tomes 1-10, 1910-1922”, several publication dates of the parts of French works could be stated with more certainty. It is a pity, however, that no information whatsoever is given on the contents of the publications (i.c. fascicles). Bélanger, Ch. P., Voyage aux Indes-Orientales, etc. 1825-29. Botanique I. Phanérogames-Botanique II. Cryptogamie.

Description: Endlicher, S.: Genera plantarum. 1836-40. Index. -----: Ibid. Suppl. 1842. Index. Index nominum genericorum. Card index I.A.P.T. In course of preparation.

Description: Mr C. Jeffrey of the Kew herbarium, who works on Cucurbitaceae, has been to the Seychelles for botanical collecting and exploration, his letter of Jan. 20, 1962 is interesting enough to quote the following passage from: ”You may be interested in a few impressions of the Seychelles flora, discounting introduced naturalized species, which now I fear cover most of the islands, I gain the impression that here we have a number of long-isolated and endemic species (perhaps some may prove subspecies?) of mixed African, Mascarene, and SE. Asian affinities, and mostly confined to higher ground on the larger islands, together with a number of indigenous non-endemic species which formed most of the original lowland vegetation, but some of which also occur in the higher parts, which are mostly (but not all) otherwise SE. Asian to Malaysian in distribution (the others are mostly Afro-Mascarene) or palaeotropical.

Description: Trees, shrubs, herbs, or armed climbers; roots not rarely tuberous. Indument consisting of simple hairs. Leaves simple, exstipulate, opposite or rarely in whorls or pseudowhorls, sometimes unequal in one pair. Inflorescence cymose, often thyrsoid, corymbose or umbellate terminal or axillary, sometimes cauliflorous. Bracts and bracteoles present, sometimes very small, not rarely early caducous. Flowers actinomorphic, bisexual or unisexual by reduction; pedicelled, with 1-3 bracteoles sometimes coloured, or sustained by an involucre. Perianth tubular, campanulate, funnel-shaped, or urceolate, sometimes articulated with the pedicel; the basal part persistent, enclosing the receptacle, tubular, club- or funnel-shaped, often accrescent; the apical, mostly circumscissile caducous part plicate or valvate in bud, with (4—)5—10 lobes, green or coloured. Stamens 1-40, rarely more, in 1-2 whorls, connate at the base, free from the perianth; anthers 2-locular, latrorse, basifixed. Ovary (sub)sessile, superior, 1-celled, with one erect, anatropous ovule. Style terminal, stigma capitate or fimbriate- to shortly lobed. Basal persistent part of the perianth accrescent in fruit and enveloping the fruit, the whole being known as anthocarp; anthocarp indehiscent, smooth, or with viscid ribs and glands, sometimes the glands accrescent into prickles; pericarp thin. Seed 1; embryo straight or folded; endosperm mealy or reduced to a gelatinous rest. Distribution. About 26 genera with 300 spp. in the New World, particularly in South America, with poor representations of mostly widespread (native or introduced) species in the warm parts of the Old World. Although the family is predominantly tropical, its area reaches to 38° SL in New Zealand and to 45° SL in Argentina. In Malesia there are 19 spp. in 4 genera, of which only Pisonia is undoubtedly native.

Description: Trees, shrubs, woody climbers, or herbs. Hairs simple, stellate, or glandularcapitate; colleters often present in the axils of the leaves, stipules, and sepals (among Mal. genera absent in Buddleja only). Leaves nearly always opposite, entire or nearly so, penninerved, rarely 3-7-plinerved (Strychnos) or curvinerved (Mitrasacme); ; stipules interpetiolar (in many genera reduced to a stipular line) in some genera moreover intrapetiolar. Flowers in cymose to thyrsiform (rarely racemose or spicate) inflorescences or solitary, 5-(rarely 4-, in Anthocleista up to 16-)merous, nearly always bisexual, actinomorphic (in some genera slightly zygomorphic). Disk sometimes present (not in Mal. spp.). Sepals united or free. Corolla gamopetalous, very rare with a corona. Stamens isomerous in Mal. spp. in 2 extra-Mal. genera less), alternating, inserted on the corolla tube (with one exception in Buddleja), , included or exserted; anthers basifixed or sometimes slightly (in the Spigelieae), , slightly to deeply bifid at base, lengthwise dehiscent. Ovary superior (in Polypremum, Cynoctonum, and Mitrasacme p.p. semi-inferior), (1-)2(-4)-celled, placentas axile (parietal if 1-celled), often peltate; ovules l-~ per cell, amphitropous or anatropous; style usually one. Fruit always superior, capsular, baccate, or drupaceous. Seeds 1-~, with copious endosperm; embryo minute straight, cotyledons small. Distribution. About 28 genera with some 600 spp., almost confined to the tropics of both eastern and Western hemispheres, a few genera extending to the warm-temperate regions, mainly towards the south. In Malaysia 11 genera with 80 spp.

Description: Families and higher taxa have been entered under their name. Names of families which have been revised in volumes 4, 5, and 6 have been entered and are printed in bold type, so that as far as this is concerned this index is complete for all preceding volumes as well.

Description: Trees or shrubs, very rarely herbs or fleshy saprophytes. Leaves spiral, sometimes opposite or pseudowhorled, simple, entire, crenate or serrate, mostly evergreen and ± coriaceous (Malesia), exstipulate (stipule-like perulae of axillary buds occur in Diplycosia and Vaccinium p.p.). Flowers bisexual (rarely functionally unisexual; or the plant dioecious in extra-Mal.), characteristically regular, (4-)5 (rarely 6-7)-merous. Inflorescences terminal or axillary, entirely covered by perulae in bud, mostly in racemes, these sometimes arranged to panicles or condensed to umbels, or reduced to few-flowered fascicles, or even to a solitary flower. Sepals (reduced in Monotropastrum and Wirtgenia) very rarely free, generally connate below to a calyx tube, the latter free or ± adnate to the ovary, persistent, whether or not accrescent in fruit, lobes imbricate or open in bud. Corolla campanulate to funnel-shaped, urceolate or cylindric, sometimes slightly zygomorphous, caducous, lobed to various degree, lobes imbricate (sometimes ± contorted), rarely valvate in bud. Stamens usually 10 (rarely 5, 8, or up to 20), obdiplostemonous, rarely haplostemonous, inserted at the outer margin of the disk between its lobes, or slightly attached to the base of the corolla; filaments free (Malesia); anthers dorsifixed to almost basifixed, the 2 cells (thecae) not rarely extending into free or connate tubules, these muticous or sometimes (bi)aristate distally by the prolonged back-wall, opening by terminal or introrse, very rarely extrorse pores or slits, not rarely with projecting dorsal appendages or spurs; pollen in tetrads, simple in Monotropoideae. Gynoecium syncarpous, 5- or pseudo-10-, rarely 2-4- or 6-7-celled. Disk hypogynous or epigynous, often fleshy and nectariferous, entire or mostly 5-10-lobed. Ovary 1, superior, half-inferior or inferior, generally with as many cells as carpels; placentation central, with 1 or 2 lamellas per cell, each bearing mostly numerous, rarely 1, anatropous or obliquely amphitropous, 1-tegumented ovulus. Style 1; stigma obtuse, capitate or peltate, whether or not 5-7-lobed. Fruit a 5(-7)-valved, septicidal or (sometimes lately or irregularly) loculicidal capsule, which may be ± included by the accrescent, ± fleshy calyx, or a rather dry to fleshy berry (Malesia). Seeds usually numerous, small, whether or not winged or tailed at one or both ends; testa thin, often reticulate; embryo cylindric, small, with copious endosperm. Distribution. About 125 genera with approximately 3500 spp., predominantly woody, all over the world.

Description: This smallish family, containing five genera¹, is almost confined to the northern hemisphere in both the Old and New World, overstepping the equator only in Ecuador and Peru in S. America and in Malaysia, where it is found southward to Java and New Guinea. Among the genera Huertea is confined to Peru and the West Indies (Cuba, Haiti). Tapiscia and Euscaphis are East Asian. Staphylea is widely distributed in the subtropical and temperate zone on the northern hemisphere. Turpinia is subtropical and tropical, it is the only genus represented in Malaysia. It is remarkable that the distributional areas of the latter two genera seem to exclude one another save for a slight overlapping in SE. Asia.

Description: The completion of the sixth volume of this Flora gives me the privilege to dedicate this to the memory of ELMER DREW MERRILL, a man who has achieved more for the knowledge of the Malesian flora than any other individual botanist. It is neither my intention to give nor is it the proper place for a full biography of this most distinguished American scientist, as it would for the greater part be duplication of his own ‘Autobiographical’ (1953), the scholarly essay by ROBBINS (1958), and the vivid life sketch by SCHULTES (1957), which together give the story of his life, his ambitions, his personality, his immense drive, his multiple interests, his capacity for establishing botanical periodicals as well as successfully filling the posts of Dean of a Faculty of Agriculture, director of the Bureau of Science at Manila, director of the New York Botanical Gardens, and administrator of Botanical Collections of Harvard University.

Description: Within the Helobieae there has been a great deal of controversial opinion about the evaluation of the genera belonging to the Potamogetonaceae, among which Najas finds by almost unanimous opinion its closest relatives. Generally Najas has been accepted to represent a separate monotypic family on account of the basal ovule and the structure of the anther (with a thin, tight, 2-lipped envelope and apically escaping pollen). The closest allied genus among Potamogetonaceae seems to be Zannichellia, which is by HUTCHINSON (1934) accepted as a separate family, Zannichelliaceae, put together with Najadaceae in his order Najadales. Within the Helobieae some authors accept the structure of Najadaceae as primitive, notably CAMPBELL (1897) and RENDLE (1930), but others find it a derived, advanced state within the order, cf. HUTCHINSON (1934) and LAWRENCE (1951).

Description: Annual or perennial herbs, erect, ascending or prostrate, less than 1½ m high. Leaves spirally arranged or alternate (often various in one plant), or opposite, often in a basal rosette, exstipular, simple, sometimes lobed, penninerved. Inflorescences racemose, terminal (sometimes axillary) racemes or umbels, or flowers in whorls, or solitary axillary. Bracts small or leafy. No bracteoles. Flowers bisexual, actinomorphic (rarely zygomorphic), isomerous, in Mal. always 5-merous, often dimorphous in sexual organs. Calyx dentate or cleft, persistent, sometimes leafy, rarely coloured ( Glaux). Corolla connate, shallowly to deeply cleft (free in Pelletiera), in bud often quincuncial or contorted, variously coloured (absent in Glaux). Stamens inserted on the corolla, epipetalous, rarely alternating With staminodes or their vestiges; anthers dorsifixed or versatile, sometimes basifixed; cells opening with apical pores or latrorse, filaments free or connate. Disk absent. Ovary superior (in Samolus semi-inferior), 1-celled with ~ ovules on a free central placenta; style simple. Capsule mostly 5-valved (valves epi- or alternisepalous) or 10-valved, sometimes irregularly bursting, or circumsciss. Seeds mostly ~, often angular, small; embryo straight, endosperm present; integuments 2. Distribution. Genera 21 with approximately 900 spp., all over the world, but mainly developed in the temperate and cold regions of the northern hemisphere; in the tropics mostly on the mountains. The largest genera, Primula (incl. Androsace) with c. 500 spp. and Lysimachia with c. 150 spp. are almost confined to the northern hemisphere and centre in the Sino-Himalayan region. In Malaysia and Melanesia Primula extends across the equator and finds its southernmost stations in the Old World. Lysimachia and Anagallis have a worldwide area. It is remarkable that the almost cosmopolitan species Samolus valerandi L., which occurs in the surrounding continents of Asia and Australia and is widely distributed in the Pacific (New Caledonia, Loyalty Is., Norfolk I., Chatham, Auckland Is., Kermadec, New Zealand, and Easter I.), has never been found in Malaysia.

Description: Description de Psilocybe callosa (Fr. per Fr.) Quél., espèce oubliée et mal connue, et de deux espèces nouvelles.

Description: Ample collections preserved at Uppsala under the name Hydnum versipelle and two exsiccata of Sarcodon laevigatus were examined and compared with the original descriptions. The material of Hydnum versipelle is shown to be heterogeneous, comprising three collections belonging to Sarcodon amarescens, and ten collections of a species which has the main characters of Sarcodon laevigatus. The few differences observed are attributed to differences of a chemical nature, and Hydnum versipelle is formally reduced to the synonymy of Sarcodon laevigatus.

Description: Mycoleptodonoides Nikol. is compared with other genera, Hydnum aitchisonii Berk, is redescribed, and for it the new combination Mycoleptodonoides aitchisonii (Berk.) Maas G. is proposed.

Description: J. J. Smith was born June 29th, 1867, at Antwerp, where his father was the director of the Netherlands’ Railway Post Office. In 1872 the family moved to Utrecht and in 1875 to Amsterdam. Smith spent his school days in the capital. His leisure hours were occupied by growing and sketching plants and tending such animals as mice and keeping an aquarium and a terrarium. His 10th birthday was celebrated by the establishment of a private herbarium, the first plant inserted being Bellis perennis. His years at secondary school were greatly influenced by the then teacher of Natural History, Dr J. C. Costerus, who advised Smith to look for a position in horticulture. Horticultural schools being not yet ”en vogue“, Smith got his education in this field at the Horticulturist’s Messrs Groenewegen & Co., Amsterdam. In these years the Orchids began to impress him and Smith spent his few free hours in making pictures of flowering species. The connection with Dr Costerus was continued. Together they looked after their herbaria and later on started to study teratologica, found in the Groenewegen gardens and greenhouses, a field in which both would publish several valuable papers later on. After having been working for his firm for 3½ years, Smith went to Kew where he stayed one year and afterwards to Brussels for completing his horticultural knowledge and skill. At Brussels he was working one year in the famous Orchid nursery of Messrs Linden, and then another year at the ”Jardin Botanique“.

Description: Pendant une tournée du chalutier ”De Lanessan“ de l’Institut Océanographique de Nhatrang (Annam) vers le récif Tizard¹) en avril 1936, une collection d’algues marines a été constituée, provenant des îlots Itu-Aba, Sand Caye et Nam Yit. La situation de ces îlots est environ 10° de latitude Nord et 114° de longitude Est. Qu’il me soit permis de remercier M. R. Serène de l’Institut Océanographique de l’Indochine à Cauda par Nhatrang, qui m’a confié l’étude de cette collection.

Description: In continuation of a previous publication by Lam, in which meiomery and pleiomery in male flowers of Canarium decumanum were described, the same phenomenon is now discussed concerning the fruits of C. Mehenbethene (176 of one single tree) and C. commune (1126 fruits mixed from more than one tree). An investigation of the material gave the following results: 1. C. commune and C. Mehenbethene are closely related; the latter may prove to be a polyploid of the former. Their areas are partly overlapping, but C. commune has its centre in the Moluccas, C. Mehenbethene in New Guinea and W. Polynesia. 2. A tendency to reduce the number of ovules and carpels in the ovary is assumed. By means of a statistical method (”phase index“) the position of either species in the phases of this regression is indicated. 3. From this, it is concluded that C. Mehenbethene represents a more advanced phase than C. commune and that therefore an eastward migration must be accepted. This agrees with other facts stated earlier, both in the Burseraceae and in other plant families of western origin. 4. In Canarium commune pleiomery is found in 2.3% of the fruits, meiomery in 0.45%, which agrees fairly well with the figures found earlier for the corolla and the androeceum of the male flowers of C. decumanum (0.9% and 0.3% respectively). 5. The desirability is expressed to investigate the following points: a. the ontogeny and the fertilization of ovaries and ovules in Canarium. b. cytological relations between related trees in the tropics, especially as far as they may supply indications towards migration tracks (cf. the work of Hagerup on Vaccinium [Hereditas 18, 1933]). c. the ”phase index“ of a number of related Canarium species. d. the exact distribution of some of the phases mentioned along those migration tracks which are both geologically and biogeographically supported (e.g. Sunda centre—Philippines, Philippines—Moluccas—New Guinea, New Guinea—Moluccas—Central Celebes, Malay Peninsula—Sumatra—Java, etc.).

Description: Im Jahre 1907 wurde ich als Botaniker der Gouvernements China-Plantagen in Tjinjiroean bei Pengalengan, West-Java, angestellt, wo ich bis 1916 arbeitete. Tjinjiroean liegt etwa 1566 m über dem Meere und hat ein sehr feuchtes Klima. Es war sehr interessant nachzugehen, welche aus der Ebene von Java und aus Europa eingeführten Pflanzen dort wachsen würden. Was würde der Einfluss des Klimas, der Meereshöhe, der Temperatur, u.s.w. auf die Pflanzen sein? In Tjinjiroean fand ich sogleich viele eingeführte Pflanzen, welche dort üppig wuchsen. In den Chinaplantagen fand ich Georginen und Tropaeolum majus L. verwildert; in meinem Garten blühte Richardia africana Kunth reichlich, bildete Früchte, welche wieder zahlreiche Pflanzen lieferten. Nur einige interessante Pflanzen werde ich hier weiter erwähnen.

Description: Een man, die zich nimmer op den voorgrond stelde en wiens naam toch in de geheele botanische wereld bekend is, moet wel heel wat in die wereld hebben gepresteerd. Zoo’n man is Dr J. J. Smith, die op 29 Juni 1937 zijn 70sten verjaardag viert. Zeventig jaar te worden is op zichzelf beschouwd geen verdienste, maar het geeft vrienden en vereerders zulk een mooie gelegenheid den jubilaris eens te toonen, hoe zeer men zijn werk waardeert!

Description: Het lijkt mij niet mogelijk een juisten indruk te krijgen van de beteekenis van J. J. Smith’s phytographisch werk voor den huidigen kweeker, zonder de belangrijkste phasen in de geschiedenis der Orchidophilie in Europa kort te schetsen, die aan dit werk zijn voorafgegaan. Deze geschiedenis heeft zich practisch geheel in Engeland afgespeeld. Dit machtige rijk, in zijn gouden eeuw onbetwist heerscher ter zee, had ter behartiging van zijne overzeesche belangen de beschikking over een kolossale handelsvloot. De bemanningen der schepen voerden van heinde en verre allerlei rariteiten mede, ook levende planten en dieren. Op deze wijze kwamen in de laatste helft der achttiende eeuw de eerste exotische Orchideeën binnen uit gebieden, die niet al te ver van Engeland af lagen: Jamaica, de Bahama-eilanden, Trinidad.

Description: Het is mij een bijzonder voorrecht, om uit het leven van Dr Smith eenige bijzonderheden te mogen vertellen, waarvan enkele wellicht minder algemeen bekend zijn. Deels heb ik de gegevens geput uit datgene wat van zijn levensloop bekend is, deels stammen ze uit mijn persoonlijk contact met Dr Smith, en de gelegenheid van dit jubileum lijkt mij bij uitstek geschikt om dezen te bescheiden werker in het licht te plaatsen waarin hij behoort te staan. In de beginjaren van mijn loopbaan als Hortulanus van ’s Lands Plantentuin was Dr Smith voor mij de groote vraagbaak, was hij de man die met zijn groote liefde voor en zijn uitgebreide kennis van den Plantentuin mij als het ware heeft ingewerkt en opgeleid.

Description: Some collections which I received recently, contain interesting addenda to former studies of the paleotropical Frullaniaceae (cf. especially “De Frullaniaceis VII”, Ann. Bryol. Suppl. Vol. I, 1930) and Lejeuneaceae Holostipae (esp. “De Frullaniaceis XVII”, Ann. Bryol. Suppl. Vol. IV, 1934).

Description: Durch die extremen Existenzbedingungen, welche die Mangroven als: Formation bestimmen, sollte man glauben, dass die ökologischen Probleme, die sich in dieser Hinsicht zeigen, leicht gelöst werden könnten, um so mehr, weil diese Pflanzengenossenschaft relativ arm an Arten ist. Dass dies jedoch nicht der Fall ist, möge hier im Hinblick auf die Verbreitung der Lumnitzera-Arten im Malaiischen Archipel mit einigen Beispielen gezeigt werden. Im Jahre 1924 habe ich kurz auf die Verbreitung von 3 Lumnitzera- Arten im genannten Gebiet hingewiesen ¹). Meine Absicht war, speziell auf die unerklärliche Erscheinung aufmerksam zu machen, dass L. littorea (Jack) Voigt das Küstengebiet rund um die Java See, im Gegensatz zu L. racemosa Willd., vermeidet, obwohl beide Arten nicht nur in, sondern auch ausserhalb des Malaiischen Archipels vorkommen, ja selbst zusammen in ziemlicher Nähe angetroffen werden. Bevor wir diese Erscheinung noch einmal näher betrachten, möchte ich an der Hand von beigefügter Karte (Fig. 1) das gesamte Verbreitungsgebiet nachgehen. Dieses Gebiet liegt nahezu vollkommen innerhalb der Wendekreise der alten Welt ²): Die Mangroven, wozu Lumnitzera gehört, finden als selbständige Waldoder Gebüschformation ihre natürliche Begrenzung ungefähr auf den gleichen Breiten. Nur L. racemosa überschreitet grade an 2 Stellen die- Wendekreise: An der Ostküste von Afrika streckt sie sich südlich vom Steinbrockkreis bis in die Mangroven bei Durban aus, während sie nördlich vom Wendekreis des Krebses noch in dem Riu Kiu (Lu Tschu) Archipel, nördlich von Formosa vorkommt.

Description: De publicatie van dit deel is mogelijk gemaakt door den geldelijken steun van vele van Smith’s vrienden, wier handteekeningen zijn vereenigd in een album, dat hem is aangeboden tezamen met dit Jubileum-Supplement van „Blumea” en de speciale aflevering van het „Bulletin du Jardin botanique de Buitenzorg”. Het oude Menangkabausche echte gouddraadweefsel uit Kota Gadang, dat heeft gediend voor de banden van het album en van de voor Dr Smith bestemde exemplaren van „Blumea” en het „Bulletin”, dankt het Comité ad hoc aan Dr E. R. Jacobson te Bandoeng.

Description: ROXBURGH described in his Flora in the year 1820 a very curious annual grass and placed it in the genus Eleusine as E. verticillata ROXB.. This grass has spikelets which agree in many characters with those of the genus Eleusine, especially as to the rugose grain with a caducous pericarp, but differing from Eleusine in the up to 20-flowered spikelets and in the lemmas with a three-cuspidate summit. The many-flowered spikelets give the plant more the habit of an Eragrostis and under this genus a specimen was mentioned by WALLICH in his Catalogue. There are in the characters of the spikelets many other differences with the genus Eleusine and with Eragrostis. KUNTH and STEUDEL, indeed placed the plant under Leptochloa and there are still other opinions about this plant. An advancement in this matter was the opinion of LINDLEY, who published in the year 1836 a new genus Acrachne WIGHT et ARN., in the second edition of his ”Natural System of Botany“, p. 381, based upon ROXBURGH’s Eleusine verticillata, The name Acrachne was already given by WIGHT et ARNOTT as Acrachne eleusinoides, a nomen in WIGHT, Cat. no. 1760. This name was placed by STEUDEL in the year 1854 under E. verticillata ROXB., a name also accepted by NEES. The name Acrachne, although based upon a species which was validly published, was, however, not described by LINDLEY and the combination A. verticillata was not made by LINDLEY. At that time the genus Acrachne was therefore not valid.

Description: This extensive collection, famous among algologists both of the Old and the New World, forms part of the collections of the National Herbarium (Rijksherbarium) Leiden since 1934. About fifty years ago it was started by Mrs. Dr. A. A. WEBER-VAN BOSSE (1852—hodie), an enthusiastic pupil of HUGO DE VRIES. The colonies of Nostoc, living in the ditches round about the Dutch village of Doom, evoked her admiration, which was the primary cause of an intense study in the freshwater as well as in the marine Algae. In the harbour of Den Helder North Sea Algae were collected; by collecting Algae on trips to the French Atlantic Coasts and several times to Norway (1883—1885) and further on a South African journey (1894—1895) the herbarium grew, as it did by the Malaysian specimens collected in Java, Celebes, etc. (1888—1889). During this Malaysian tour Mrs. WEBER worked in Tjibodas, where she described the new genus Phytophysa. In Sumatra (West Coast, Lake of Manindjau) she discovered in collaboration with her husband, MAX WEBER, a new case of symbiosis between Algae and Sponges.

Description: Spiranthes sinensis (Pers.) Ames, also known under the synonym S. australis (R. Br.) Lindl., is a terrestrial orchid widely spread in Asia, which is rather well known in Western Europe, because it has repeatedly been found growing spontaneously in pots in orchidhouses. In Blumea 6(2): 361 (1950) the plant described as Ophrys lancea Thunb. ex Sw. was considered to be identical with the first and it was thought that the recombination Spiranthes lancea (Thunb. ex Sw.) B. B. S. was necessary. The reasons given for this transfer were: (1) the short diagnosis of Ophrys lancea given by Winberg in Florula Javanica, p. 8 (1825); (2) the original diagnosis of O. lancea in Swartz’s well-known dissertation on the classification of orchids in Kongl. Vet. Akad. Handl. Stockh. 21: 223 (1800); (3) the presence of the apparent holotype in the Thunberg herbarium (Uppsala).

Description: Thanks to the kind cooperation of Dr. ROBERT PILGER, Director of the Botanical Gardens and Museums at Berlin-Dahlem, I have recently had the privilege of studying and photographing a unique specimen belonging to that institution, which bears the words „Schizostachyum Blumii nobis”, in the hand of NEES, the author of the species. Although there are no data on the sheet to indicate its source, or the date of the determination, this presumably represents NEES’S type³) of this species (which is the type species of the genus). At any rate, the available evidence 4) points to that conclusion, and the specimen agrees in all respects with NEES’ description of the genus and of the type species (NEES, 1829, pp. 534—5). Since the original characterizations are so brief and, since those parts referring to the spikelets are so difficult to interpret, I present here a full description 5) of the rather fragmentary type specimen.

Description: This is the second contribution to a series of papers dealing with the Convolvulaceae of Malaysia (Malay Peninsula and Archipelago, Philippine Islands and New Guinea). The genera worked out here belong to the tribe Convolvuleae; they are numbered VIII—XV. Genus VII, Erycibe, belonging to the Erycibeae shall be treated afterwards in a special monograph. With regard to the geographic arrangement of the specimens mentioned, some alterations had to be introduced due to the new limitation of the residencies in the island of Java. The names and limits of these residencies are now brought into line with the data of the ”Atlas van Tropisch Nederland“ ²).

Description: In Blumea, Vol. II, 1937, pp. 239 to 277, appeared an article bearing the above title. It is a description of an excursion to the Salajar Islands, situated south of Celebes; lists of the plants found in the islands are appended. Prof. Dr C. E. B. BREMEKAMP wrote to me that in the Leiden Herbarium a small collection of plants, collected by me in the Salajar Islands, and long ago lent to the late Dr TH. VALETON, have been found. This collection contained, apart from the Rubiaceae, the special subject of Dr VALETON, some representatives of other plant families. Prof. BREMEKAMP sent me a list of names of these plants, for which I tender him my cordial thanks. Besides he communicated to me that a few plants are mentioned under wrong names in the original publication. They are: nr. 86 of Djampea is not Ophiorrhiza neglecta BL., but O. parviflora REINW. Besides the number mentioned, 1573, two other specimens of this plant were collected in the same island, nr. 1618 and nr. 1633, both at an altitude of 200 m.

Description: § 1. Das Ziel der Untersuchung war den Bau des Blütenstandes und der Blüten von Arceuthobium Dacrydii RIDLEY zu ermitteln und festzustellen, ob diese Pflanze wirklich ein Arceuthobium ist oder, wie eine oberflächliche Untersuchung des Blütenstandes es vermuten liess, eine Korthalsella; und falls letzteres sich wirklich als richtig herausstellen sollte, weiter festzustellen, wie der Bau des Andrözeums dieser Art ist, welches für Arten dieser Gattung von VAN TIEGHEM, HAYATA und LECOMTE in verschiedener Weise beschrieben wird. § 2. Material und Methode. Das Material zu dieser Untersuchung stammte von Pflanzen, welche 1931 von Zweigen von Podocarpus imbricata BLUME im Walde des Naturreservates Tjibodas auf dem Gunung Gedé in Westjava gesammelt wurden, und zwar teilweise von F. W. WENT oder C. G. G. J. VAN STEENIS s.n. (vgl. Bull. Jard. Bot. Buitenz., ser. 3, 11, p. 456) und teilweise von W. M. DOCTERS VAN LEEUWEN (NO. 14166). Die letzteren wurden freundlichst vom Sammler aus seinen Privatsammlungen zur Verfügung gestellt. Die spezifische Identität mit dem ursprünglichen Arceuthobium Dacrydii wurde durch erneute Vergleichung mit dessen Typus, der sich im Besitze des Botanischen Gartens zu Singapore befindet und nochmals gütigst von der Direktion dieses Institutes für unsern Zweck zugesandt wurde, festgestellt.

Description: Referring to the identification of BRASS 5219 from Papua as a representative of the Verbenaceous Faradaya chrysoclada K. SCHUM. by E. BEER and H. J. LAM (Blumea 2, 1936, 225), Dr C. G. G. J. VAN STEENIS, the monographer of the Malaysian Bignoniaceae drew our attention to the possibility that this identification might be incorrect. It was suggested that the specimen and also all specimens hitherto known as Faradaya chrysoclada might be Bignoniaceous and might belong to Deplanchea tetraphylla (R. BR.) V. STEENIS, as all other Faradayas known are lianas, whereas F. chrysoclada was reported to possess the tree habit, as the Deplancheas. We therefore asked on loan the materials of both species from the Herbarea at Berlin (B) and Kew (K), that from Berlin including the type specimen of Faradaya chrysoclada. Our thanks are due to the directors of the Herbaria of Berlin and Kew for kindly lending us the material desired.

Description: The present investigation arose from a discussion between Dr van Steenis and Mr C. T. White in July 1950 concerning a plant from North Queensland, collected by Mr L. J. Brass. The specimen was pre-identified as an Aristotelia but also showed similarity with the Papuan genus Sericolea. The need was felt to investigate the distinction between the two genera. Mr White was very keen to investigate the problem himself but this was unfortunately prevented by his untimely death, only two weeks after this discussion. The problem has rested ever since, until in 1963 I had to verify the distinction between the two genera for my work on the Pacific flora, a work executed under a grant from the Netherlands Organisation for the Advancement of Pure Research (Z.W.O.).

Description: Mr F. H. Hildebrand, who is going gradually through the tree species from New Guinea, pointed my attention to this species, the type of which is in the Rijksherbarium at Leyden (in fruiting state). It was collected by Zippelius who rightly recognized its alliance; he added a MS description and gave it the MS name Epicharis lasiocarpa. Miquel subsequently described it in the genus Dysoxylum, but the curved fern-like leaftip and other characters leave no doubt about its belonging to Chisocheton. There are at Leyden two further collections of it from New Guinea, both made by Teysmann, HB 6058 and 6060.

Description: The Salajar Islands strew the Flores Sea between Celebes and Flores. The group consists of no less than 73 smaller and larger islands. The principal islands are: Salajar or Tanadoang, Djampea, Kalao, Kalaotoa, and Bonerate. A number of smaller islands form together the group of the so-called Tiger Islands, and to the south of them arc the very small, low Pasitaloe Islands. The Salajar group is situated between Long. 119°50’ E. and 121°30’ E. and between Lat. 5°36’ S. and 7°25’ S. See the map on p. 240. In May 1913, I was enabled to visit this territory, thanks to a financial allowance of the „Maatschappij ter bevordering van het Natuurkundig Onderzoek der Nederlandsche Kolonien” (Society for the Promotion of the Scientific Investigation of the Netherlands Colonies), for short: „Treub Society”, and also of the „Provinciaal Utrechtsch Genootschap voor Kunsten en Wetenschappen” (Utrecht Provincial Society for Arts and Sciences). The publication of the present paper was enabled by financial support of the „Leidsch Universiteitsfonds” (Leiden University Fund). I beg to tender my best thanks for all this valuable support here.

Description: This is the first contribution to a series of papers dealing with the Convolvulaceae of Malaysia (Malay Peninsula and Archipelago, Philippines and New Guinea). As far as possible the contributions will be published in accordance with the systematical arrangement of the genera. For a survey on this arrangement I refer to HAULIER'S fundamental work on this matter published in 1893 in the 16th volume of ENOLER'S Botanische Jahrbücher, entitled: ”Versuch einer natürlichen Gliederung der Convolvulaceen auf morphologischer und anatomischer Grundlage“. After all genera will have been published, a determination key will be added, based on the genera of the area under consideration, in which I hope to take especially account of the characters of the Malaysian species. Meanwhile the key published by HAULIER in the above mentioned paper can be provisionally used. On account of the structure of the pollen grains the Convolvulaceae as a whole can be subdivided, as has been proposed by HAULIER, into two groups, viz. the Psiloconiae with smooth pollen grains and the Echinoconiae with spinose ones. The former of these groups contains seven tribes, viz. 1. Cuscuteae, 2. Wilsonieae (not in Malaysia), 3. Dichondreae, 4. Dicranostyleae, 5. Poraneae, 6. Erycibeae and 7. Convolvuleae. Of the six genera worked out here, Cuscuta belongs to the Cuscuteae, Dichondra to the Dichondreae, Evolvulus, Bonamia and Neuropeltis to the Dicranostyleae and Porana to the Poraneae. For the limitation and description of the tribes see HALLIER l.c. and in ENGLER’S Botanische Jahrbücher, Vol. XVIII, 1894, p. 92, under Prevostea.

Description: G. abbreviata J.J.S. in Fedde, Rep. 35, 1934, 292; Sleum., Reinwardtia 4, 1957, 172. SUMATRA. Tapanuli, Tele, S. of Sidikalang, Alston 14878. Westcoast, G. Singgalang, 1900 m, Meijer 5919.

Description: The publication of the supplement 1 of the well known and essential reference work of “A Bibliography of Eastern Asiatic Botany” is very welcome. It is a continuation of the original work, which closed with 1936, and extends through 1958. It covers the botanical literature on eastern Asia, as indicated by the title, which comprises China, Japan, Korea, Ryukyu, Mongolia and Soviet eastern Asia, as well as the major published papers appertaining to adjacent areas. It has been prepared on essentially the same pattern as the original volume while the subject index has been treated perhaps in a more thorough manner. The volume contains over 11,000 extensively and carefully annotated entries occupying 414 pages. The work is in English but the titles, papers and author names in oriental characters are fully cited, which is an improvement as compared with the original volume. It includes now the original Chinese, Japanese and Korean titles and author names as published in oriental characters as well as translations or transliterations of them. In addition, the supplement fortunately covers the extensive Russian literature, nearly 1600 entries, on Soviet eastern Asia. All Russian titles are transliterated into Roman letters and are also translated. All these improvements make this bibliography more complete than the original volume and extend its usefulness.

Description: Years ago I intensively studied the grasses of the tribe of the Maydeae. The results of my investigations were published in an article ”A contribution to the knowledge of the Indian Maydeae“, issued in the ”Mededeelingen van ’s Rijks Herbarium“ no. 67 (1931). In this paper the grasses of this tribe from the Old World were treated and especially the various genera were characterized according to their caryopses. The curious form and the place of the hilum of the caryopsis were accepted as characters of high importance to distinguish and to establish the various genera, and it was especially the genus Polytoca, which was more sharply defined by the place of the hilum, the lower margins of the grain enclosing a cavity at the bottom of which is found the hilum. In the genus Chionachne such a cavity is not present and the hilum is found at the back of the grain. I accepted 4 species of the genus Chionachne. One of them, viz. Ch. Koenigii (SPRENGEL) THWAITES, is rather widely distributed from British India and Ceylon to Tonkin and from Celebes to Queensland. Ch. biaurita HACKEL is endemic in the Philippines and Ch. semiteres (BENTH.) HENR. was only observed in the Deccan Peninsula and Burma. The fourth species was mentioned by me from Queensland as being Chionachne Sclerachne BAILEY. The type of BAILEY was not represented in the Kew Herbarium and I saw only a fragment from a plant collected by F. v. MUELLER, which I accepted as being BAILEY’s species. DOMIN mentioned from Queensland only Polytoca cyathopoda (F. v. M.) BAILEY and not having seen DOMIN’s plant I had only to accept that the identification was correct. Recently Mr. HUBBARD from the Kew Herbarium could examine DOMIN’s plant and found that it belonged to the genus Chionachne.

Description: The flowering specimens of Glyptopetalum are very difficult to separate from those of Euonymus except by examining the number of ovules in each cell of the ovary. The ovules are mostly 2, rarely 3—12, per cell in Euonymus and there is only one in Glyptopetalum. However, the genus Glyptopetalum can be easily distinguished from Euonymus, or recognized, by the characteristic persistent columella of the fruit and the branched raphe of the seed (cf. also Fl. Mai. 1, 5, 1963, 256 and fig. 711). In preparing the Celastraceae for the Flora Malesiana, two additional extra-Malaysian species of Glyptopetalum have been found: a new one from Thailand and a new combination for the flora of China. The range of distribution of this genus is now extending to southwestern China.

Description: Within the genus Vaccinium L. this revision of its Malaysian species — which comprises more than half of the total number of species of the genus — is the last in a series of modern treatments made for North America by W. H. Camp, for the Pacific area by C. Skottsberg, and for tropical America and tropical Asia by the present author. The work formerly done in Malaysian Vaccinium has been limited to islands, as that by J. J. Smith and Schlechter for a part of New Guinea, by Copeland f. for the Philippines, and by Amshoff for Java, with the shortcomings necessarily connected with such too local work. The sections proposed for the Malaysian species in my general system in 1941 have been found still useful and are kept here except a nomenclatural change in one section and the expansion in species due to the large amount of indetermined material collected in Celebes and especially in New Guinea.