ALBERT

Description: The sedimentation regime off Northwest Africa is shaped by: (1) structur~al factors. which result in generallv low relief on land. shelf widths between 40 and more than 120 km. and av-erage sfope inclinations between 10 30' and 30; (2) land climates. which contral the delivery of terrigenous particles to the margin: (3) water movements including boundary currents and upwelling; and (4) the post- Pleistocene sea level rise. This chapter combines published and new results arising from research into the sedimentation processes off Northwest Africa. and emphasizes particularly the activities of the Kiel marine geological group during the past few years. Reviews of cruise activities and results were given in Closs et al. (1969) (Meteor cruise 8. 1967. off Morocco) . Seibold (1972) (Meteor cmise 25 . 1971. off Sahara to Central Senegal). Seibold and Hinz (1976) (Meteor cmise 39,1975 . and Valdivia cruise 10. 1975, from Morocco to South Senegal), and Waiden et al. (1974) (Meteor cmise 30, 1973, off Sierra Leone). Some of these cmises were used for pre- or post-site surveys for the Deep-Sea Drilling Project, or to add undisturbed Quaternary cores to the Glomar Challenger cores (leg 41, ] 975; Lancelot, et al .• 1978); leg 47 A, Arthur er al .• 1979; Lutze et al., 1979). We have concentrated our geological investigations on a number of standard profiles from the shelf to the upper continental rise as given in Figure 1. The manuscript was finished May 1979.

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: El género Plagiochila (hepatica) esta representada en las Islas Galapagos por ocho (8) especies diferentes: P. bursata (Desv.) Lindenbg., P. galapagona Inoue, P gradsteinii Inoue, P. guilleminiana Mont., P. inouei Grolle, P. scabrifolia Inoue, P. spinifera Ångstr. y P. subplana Lindenbg. El endemismo en este género es más alto que en otros géneros de las hepaticas, con cinco (5) especies que comienzan a conocerse solamente de los Galapagos ( P. galapagona, gradsteinii, scabrifolia, inouei, y spinifera). Las otras tres (3) son comunes y ampliamente distribuidas a lo largo de la America tropical. La mayoría de las especies estan restringidas a las zonas altas-húmedas de vegetación de las Islas Galapagos (matorrales de Zanthoxylum, Miconia y pampa) excepto P. guilleminiana muy común, la cual puede presentarse en la zona seca de transición de bosque. La más amplia variación de Plagiochila ha sido vista en Isabela (Cerro Azul), San Cristobal y Santa Cruz.

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: Nanocyperion communities (s.l.) are considered here as “warp-and-woof” communities; the Nanocyperion components are described separately as synusiae. On the Netherlands Frisian Islands, four main synusiae have been recognized. Raunkiaer life form spectra show few differences between the communities. Life strategy spectra of the Nanocyperion synusiae, based on systems for phanerogams (modified after Bakker 1966) and bryophytes, yield the clearest patterns. A comparison of the ecology of the communities and an interpretation of the spectra in terms of avoidance of stress or competition suggest that inundations and standing crop of the communities are the main factors determining the distribution of the synusiae. Winter inundations overrule the influence of differences in productivity level, which becomes prominent in drier situations.

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: 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: 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: The Colombian representatives of the lichen family Parmeliaceae with linear lobes and marginal cilia have been revised. A key is given and morphology, chemistry and distribution are treated of 12 species in three genera: Cetrariastrum Sipm. gen. nov, with C. andense (Kärnef.) Sipm. comb. nov., C. dubitans Sipm. spec. nov. and C. equadoriense (Sant.) Sipm. comb. nov., Everniastrum with E. catawbiense (Degel.) Hale, E. cirrhatum (Fr.) Hale, E. columbiense (Zahlbr.) Hale, E. fragile Sipm. spec. nov., E. planum Sipm. spec. nov., E. sorocheilum (Vain.) Hale and E. vexans (Zahlbr.) Hale, and Parmelina cleefii Sipm. spec. nov. and P. swinscowii (Hale) Hale.

Description: Nineteen species of Stereocaulon are treated from the northern Andes, mainly from Colombia. Descriptions and keys are given, with notes on the north-Andean distribution and ecology. Seven species are new for the Colombian flora, viz. St. atlanticum, St. claviceps, St. corticatulum (chem. strain with atranorin and perlatolic acid), St. delisei, St. microcarpum, St. pachycephalum and St. pomiferum. St. crambidiocephalum is reported for the first time from Costa Rica, as is St. didymicum from Venezuela, and St. delisei is reported for the first time from the New World (Colombia and Costa Rica). St. cornutum Müll. Arg. is reduced to synonymy under St. pityrizans Nyl.

Description: Gradstein et al. (1982) propose to conserve four generic names of Lejeuneaceae: Lopholejeunea (Spruce) Schiffn., Acrolejeunea (Spruce) Schiffn., Trachylejeunea (Spruce) Schiffn. and Taxilejeunea (Spruce) Schiffn., each of which was introduced as a subgeneric name in Lejeunea by Spruce (1884), and subsequently raised to generic rank by Schiffner in his treatment of the Hepaticae in Engler-Prantl (preprint 1893) [see proposals to conserve 675-678 see p. 746]. Although Spruce (l.c.) used for his Lejeunea species a binary nomenclature by combining subgeneric names with specific epithets, it is clear (e.g. text, index) that the binomina are meant as Lejeunea combinations and they are considered as such by most authors (see Gradstein et al. for further details). Before 1893, however, the Sprucean subgeneric names were used in various papers by F. Stephani in a “seeming” generic rank; indeed Stephani now and then referred to them as “genus.” A chronological survey of a number of relevant papers by Stephani, mainly those published in Hedwigia, was given by Bonner et al. (1961), in conjunction with a brief discussion of the subject of this paper. These authors were the first to realize that on the basis of Art. 42 ICBN some generic names in Lejeuneaceae, e.g. Taxilejeunea and Trachylejeunea, can be considered as validly published by Stephani in Hedwigia 28, 1889. Later on Grolle (1979) demonstrated valid publication of monotypic new Lejeuneaceae genera by Stephani in the Bot. Gaz. 15, 1890, e.g. Lopho-Lejeunea and Acro-Lejeunea. For an evaluation of the status of Lopho- Lejeunea Steph., Acro-Lejeunea Steph., Trachylejeunea Steph. and Taxilejeunea Steph., one might consider these names against the background of the entire context of Stephani’s work on Lejeuneaceae until 1893. As the survey of Stephani’s papers in Bonner et al. is rather incomplete, and as there are several points of divergence in opinion, a new analysis of Stephani’s relevant papers (before Sep 1893) is presented below.

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: 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: During 1981 the Botanical Survey of India had again collections made. We list them in the same manner as on pages 3559-3560. In Andaman & Nicobar Is.: Great Nicobar, 300 specimens. In Andhra Pradesh: Anantagiri, Endrika Hills, Ganganaju-medugula, Paderu, 1590. In Arunachal Pradesh: Ganganagar, Hapoli, Naharlagan, Namdapha Biosphere Reserve of Tirap Distr., Tamer Road, Tiruli of Subansiri Distr., Ziro, 1054. In West Bengal: areas of Jalpaiguri, Bankura and Midnapur Districts, places of Bangaon, Tantulia and Basirhat of 24-Parganas Districts, Jaldapara Reserve, Totopara, &c., 2240. In Gujrat: Lalpur and vicinity, 1090. In Karnataka: vicinity of S. Karnataka River-Mulla Periyar and catchment areas, 500. In Kerala: Alleppey, Anathode, Cannanore, Devicolam, Kakki, Kasargod, Kokharjam, Munnar Peermade, Muzhiyar, Pachakanam, Pamba Dam areas, Peruvanzuzhi, Ponnambala Medu, Sabarigiri, 4150. In Madhya Pradesh; areas of Panna Distr., 800. In Maharashtra: Bhimsankar, Janar, Purandar, 985. In Meghalaya: Cherrapunjee, Nongapoh, Sunnapahar of Khasi Hills, Jowai, Jorain of Saintea Hills, Tura of Garo Hills Distr., 3500. In Nagaland: areas of Mekokchung, Tuensang, Wokha, Zunbebato Districts, 500. In Rajasthan: Jaisalmer and areas of Barmer Distr., 1000. In Sikkim: Burtuk Busty, Chakung, Changu, Chuten, Enchy Monastery, below Honuman Top, Jorethang, Lower Bustak, Ranipal, Reumtek, Sang Ratepani, Sinchey, Singtham East, Soren, Suntale forests, Tadong, 4800. In Tamil-Nadu: Kannayakumari, Sethur Hills, Srivilliputhur R.F., 2090. In Uttar Pradesh: Agra-Khal, Ballaieri, Chamoli Chakrata, Dudhwa Nat. Park, Govana, Khan-Khaliadha, Mussoorie, Pam Vali-Kantha, Panwali, Parbagi, Rajkhark, Saharshradhara, 2500.

Description: Because of their fleshy nature, thin leaves and membranous sepals and petals, Impatiens tend to make particularly poor herbarium specimens. If dried while still attached to the leafy part of the plant the flowers generally become badly crumpled and brittle. In such a state their more important characters become unrecognisable, and it is rarely possible to restore them to any useful degree. The leaves may also become badly crushed especially if they are not pressed absolutely flat. The collectors’ time may thus be completely wasted.

Description: Dr. M.M.J. van Balgooy and his companions on the Celebes Expedition, Dr. E. Hennipman, Mr. G.J. de Joncheere and Dr. E.F. de Vogel left Leiden on 5 April 1979, visited the SING and BO-Herbaria on the way. In Celebes visit was paid to Hasanudin University at Ujung Pandang (olim Makassar), in Bali to the Botanical Garden at Bedugul. In the course of August they returned to Holland. See also Exploration. The Botanical Survey of India kindly sent the following list of changes: D.K. Banerjee: to the Industrial Section of the Indian Museum at Calcutta; N. Bhargava: to the Northern Circle, Dehra Dun; U.C. Bhattacharyya: Deputy Director, Northern Circle, Dehra Dun; B.N. Chakraborty: Assistant curator, Industrial Section, Indian Museum, Calcutta; U. Chatterjee: Botanist, Eastern Circle, Shillong; Mrs. Dr. S.J. Das: Botanist, Eastern Circle, Shillong; P.K. Hajra: to HQ, Howrah; B. Krishna: to HQ, Howrah; Ram Lall: Botanist, Central Circle, Allahabad; C.L. Malhotra: to Northern Circle, Dehra Dun; P.C. Pant: to Northern Circle, Dehra Dun; B.B. Pramanick: Botanist, CAL-Herbarium, Howrah; M.K.V. Rao: to Andaman Circle, Port Blair; Dr. G.P. Roy: to Central Circle, Allahabad; B.D. Sharma: Deputy Director, Western Circle, Poona; Dr. R.C. Srivastava: Systematic Botanist, Eastern Circle, Shillong; C.R. Tarafder: Botanist, CAL-Herbarium, Howrah. Proficiat to all!

Description: The entries have been split into five categories: a) Algae — b) Fungi & Lichens — c) Bryophytes — d) Pteridophytes — e) Spermatophytes & General subjects. — Books have been marked with an asterisk. The SEM-observation of plant material normally requires dehydrated, dry specimens coated with carbon or metal. Unfortunately, the standard drying methods (including the critical-point-drying-technique) often cause shrinking and deformation of the specimen surface; therefore, SEMstudies on plant ontogeny are rather difficult, material- and time-consuming. Experiments using deep-frozen specimens have been carried out in England and in the USA, but have proved not satisfying.

Description: Loss of species is the key issue of conservation. Contrary to misuse of land which is visible to anybody with eyes to see, the issue of extinction is sly, treacherous, and open to clear perception only for experts. It touches on quality, and reaches far out in time: hard things to grasp for non-biologists. Thus an extra responsibility devolves on those who are in a position to know and to speak. The value of the genetic resource base has been set forth in e.g. the book by O.H. Frankel & E. Bennett, Genetic resources in plants (1970), and in the BIOTROP symposium edited by J.T. Williams e.a., South East Asian plant genetic resources (1975); Myers adds many striking facts: half the prescriptions in the U.S.A. contain a drug of natural origin. The cardiac drug reserpine, from Rauvolfia, costs $ 1.25 per gram to synthesize, $ 0.75 from natural sources. The anti-polio vaccin was developed in experiments in chimpanzees. The Amerindians in Amazonia know 750 medicinal plant species. Now the possibility of massive destruction of tropical forests — where most species are located — casts some frightening shadows on the future. The question how to cope with the threat appears to be connected with human ethics and the international order. Consequently, most publications on the subject suffer from a partial lack of maturity: don’t look to Myers for ethics, nor to the Routleys for biology. It seems therefore advisable that on the part of all disciplines a common fund of knowledge and insight be built up. In my efforts, great stimulation was received from correspondence with Dr. Willem Meijer (Botany, University of Kentucky, Lexington, Ky. 40506, U.S.A.), who in his disinterested manner never fails to come up with things true and shocking.

Description: Apocynaceae wanted — pickled. Mary E. Fallen, Systematische Botanik, Zollikerstrasse 107, CH-8008 Zürich, Switzerland, who has done considerable morphological work on development of the reproductive organs in Apocynaceae, has been frustrated in her many efforts to obtain suitable material of Lepinia and Lepiniopsis. Ample information on both can be found in Pacific Plant Areas 3, Blumea Suppl. 5 (1966) 112-113, with map and description. The very oddly shaped fruit of Lepinia (W. Pacific) has been depicted in Blumea 11 (1962) 302, Van Steenis’s paper on the Land Bridge Theory. The one of Lepiniopsis (E. Malesia) seems to be buoyant. Also material of Anechites (Central America) is needed; it may be closely related to Condylocarpon. Any stages of flowers can be used, from tiny green buds at initiation up through anthesis, as well as fruiting stages. They should be pickled in FAA. Expenses of handling and postage will gladly be refunded. Vials with the liquid can be provided. Thanks on her behalf!

Description: Several aspects of the sexuality in Mucorales are discussed. It is stated that neither heterothallism nor homothallism are absolute conditions and that a continuum exists between zygospores and azygospores. Mating type switching as known in ascomycetous yeasts would explain several up to now inexplicable phenomena.

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: 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: Twelve species are recognized of which five (P. womersleyi, P. brassii, P. hooglandii, P. schoddei. and P. clemensae) are described as new. Nine species are reduced to synonymy (P. warburgii, P. puberula, P. myriantha, P. paniculata, P. parvifolia, P. acuminata, P. habbamensis, P. pulchra and P. dallmannensis). All twelve species occur in New Guinea, only one (P. arfakiana) extending westwards into Sulawesi. P. incana, P. gracilis and P. hypargyrea may also occur in Queensland in addition to the three species already described from Australia.

Description: Two gynoecial primordia are initiated as discrete units but soon get interconnected by the occurrence of interprimordial growth between them. A rim of meristematic tissue thus produced gives rise to the ovary wall by zonal growth. The residual floral apex grows parallel to the gynoecial primordia in the form of a septum. The two placental ridges arise from the inner lateral walls of the ovary, grow into the ovarian cavity, and ultimately fuse with the axial septum. The anterio- posterior region of the ovary wall also grows into the ovarian cavity to form a false septum which divides each locule into two. The Labiatae show a placentation which is neither true axile nor true parietal but an intermediate condition between the two, as the septum grows like in a typical axile placentation and the placentae like in typical parietal placentation. The gynobase in Labiatae is considered to be carpellary in nature.

Description: Two new genera and nineteen new species of Dicotyledons from Papua New Guinea collected and described by A. Gilli (1980) have been examined by specialists. These families are Begoniaceae, Cruciferae, Elaeocarpaceae, Euphorbiaceae, Hypericaceae, Leguminosae, Rosaceae, Rubiaceae, Saxifragaceae, and Sterculiaceae. Both new genera are reduced: Melachone to Amaracarpus (Rub.), Disaster to Commersonia (Sterc.). Supposed new generic records to Malesia proved erroneous: a new Thelygonum belongs to Nertera (Rub.), and a Trochiscus to Nasturtium (Cruc.); the Viburnum from Papua is a Psychotria (Rub.). All species are reduced to those already known. It is advocated as undesirable to describe novelties from odd tropical plant collections.

Description: In the present work details are given in the first place for the Malesian Olacaceae, representing the basis of my forthcoming treatment of the family in ‘Flora Malesiana’, in which full descriptions of the Malesian genera and species will be given. As the Olacaceae of Malesia are connected with those of South and Southeast Asia on the one, and those of Australia and the Pacific on the other side, it has been necessary to study the respective materials too. A part of the Malesian genera is represented also in Africa inch Madagascar, and even in Central and South America; the appertaining species have been studied but are not mentioned in this paper. A critical elaboration of the family for Africa and America is urgently needed, but will, as far as can be seen, be of no influence of the delimitation and scientific names of the Asiatic-Malesian Olacaceae.

Description: The genus Badusa is transferred from the Cinchoneae to the Condamineae subtribe Portlandiinae: it is closely related to Morierina. A new species B. palawanensis is described from Palawan, and a new subspecies from Biak, B. corymbifera ssp. biakensis.

Description: The Australian genus Wilkiea is recorded for Papua New Guinea. One species, W. foremanii, is described from the Wharton Range.

Description: Sericolea is a genus endemic to New Guinea. The relevant literature is surveyed. Descriptions are given of all species and keys provided to the 15 species and all infraspecific taxa accepted. Two species are described as new: S. coodei and S. microphylla. A new subspecies of S. brassii A. C. Sm. is recognized: ssp. carrii. S. arfakensis Gibbs, S. gracilis (Laut.) Schltr., and S. novoguineensis Gibbs reduced by Coode in a recent paper are reinstated and S. glabra Schltr.. also reduced by Coode, is recognized as a variety of S. micans Schltr. Three new varieties are distinguished in S. gaultheria (F. v. M.) Schltr. and one in S. novoguineensis Gibbs.

Description: Being occupied with studies on the Convolvulaceae of Netherlands India I met with a remarkable specimen in the Buitenzorg Herbarium, collected by Dr. O. POSTHUMUS during the expedition in Djambi (Sumatra) in the year 1925. At first sight this plant seemed to be a Merremia. A closer examination, however, soon showed some important differences with that genus, especially in respect to the corolla, which has a long, narrow and rather fleshy tube and a limb with 5 short, reflexed (or patent?) lobes. Each lobe is deeply bifid, so that the limb appears 10-lobed. The middle part of the lobes is fleshy just as the tube; it corresponds with a midpetaline field of the corolla of most genera of Convolvulaceae, the lateral parts of the lobes (lobules) are much thinner, membranaceous and nerved. They represent the interpetaline fields of the Convolvulaceous corolla. In general there is a resemblance with the essential corolla construction of many species of Erycibe, where the lobes are also bifid and possess a thick middle part and two membranaceous lobules. The lobules in the new genus are not fully equal in size, those on the right of each lobe, as seen from the inside of the corolla being always slightly larger. The corolla is fully glabrous or bears some papillae at the base of the filaments. The pistil has a two-celled ovary, each cell with 2 ovules and bears a long, filiform style with two globular, papillose stigmas, exactly as in Merremia. I suppose this plant to be closely related to that genus, but as the corolla with its fleshy tube and remarkable lobes is so different from all other species, it is impossible to incorporate it in Merremia without important alteration of the generic limits. I, therefore, propose to establish a new genus, under the name of Decalobanthus (derived from dexa, ten, λoβoς, lobe and άνζος, flower).

Description: Being engaged during several years with a revision of the grasses preserved in the Rijks-Herbarium at the University of Leyden, my attention was called to the group of the Stipeae, and especially to the very difficult genus of Aristida. After an exhaustive study of the literature, I thought it desirable to have a monograph of this genus, containing extensive keys for the determination of all the species hitherto known, and I resolved to prepare such a work. It has been my good fortune that I had at my disposal not only the valuable collections of the Rijks-Herbarium, but that by the courtesy of the directors of the great herbaria in Europe and in America, I could study many thousands of specimens, among them authentic specimens and types. So several years elapsed before the revision was finished. Before I am going to publish my work, it seemed desirable to prepare a preliminary paper on the subject, dealing with the literature studied and the results of the critical examination of the types, moreover the new species found in herbaria are included in this paper. To find easily the original description and the type specimen, I give in alphabetical order all the species and varieties hitherto described, no matter if they are accepted in my monograph as valid or not.

Description: This publication presents a catalogue of the taxa of the neotropical family Loricariidae, the mailed catfishes, including about 600 described species and 70 genera. An attempt is made to assign each species to its proper genus and to arrange the genera into an approximate phylogenetic order. Numerous new combina tions have become necessary. A new tribe, consisting of two new subtribes, and three new genera are herein established. Notes on type-material, recorded in the literature subsequent to an original description, are added. Literature references aim to include all publications containing original descriptions and proposals of new names.

Description: The present study deals with the taxonomy of a family of the brown algal order Sphacelariales in Europe. The taxonomy of this order is much influenced by the works of Sauvageau as published between 1900 and 1914. A short survey of the work on Spacelariales by him and his phycological predecessors is given in the introduction. The order Sphacelariales is described and its nomenclatural history is given. Other paragraphs deal with distribution, morphology and the used descriptive terminology, ecology, variability and culture studies, reproduction and life-history, systematic position and classification. In the notes on morphology the history of the descriptive terminology is incorporated, as well as discussions on the correct use of this terminology. Most technical terms are also included in the glossary, located near the end of this book. In the sections on ‘Form range and cultures’ and on ‘Reproduction and life-history’ the methods used for unialgal cultures and methods for chromosome counts are discussed. Also a review of life-histories in Sphacelariales is incorporated, as well as a discussion on the criteria used for the distinction of taxa and the delimination of the order. A key to the families concludes the treatment of the order. The family Sphacelariaceae, which is the largest and most cosmopolitan family of the order, is treated in a similar way. The two genera in this family, the monotypic genus Sphacella and the complex genus Sphacelaria, which contains four subgenera, seven sections and 16 species in Europe, are also treated in comparable paragraphs. Keys to the taxa and to ecological growth-forms (ecads) are given. In the paragraph on relationship of genera, subgenera, sections and species, several approaches for the construction of a classification are mentioned. The phyletic-cladistic approach, based upon methods developed by Hennig (1950), is discussed in detail. One conclusion is that the genus Choristocarpus cannot be considered to belong to a monophyletic group together with the Sphacelariaceae. Further it can be concluded that the Sphacelariaceae all belong to one group with a monophyletic origin. The monotypic genera Battersia, Disphacella and Chaetopteris have to be included into the genus Sphacelaria. Sphacella, however, is maintained as a monotypic genus. For nomenclatural reasons Sphacelaria reticulata (formerly Disphacella reticulata) must be chosen as type-species of the genus Sphacelaria. The descriptions of family, genera and sections are usually short, but the descriptions of the species are comprehensive and contain a formal description and a list of dimensions. The paragraphs on distribution start with summaries of coastal regions where the species occur. Each summary is followed by an extract of the list of collections and relevant references. Distribution maps are added. Full lists of collections and references for all species are published separately. Important taxonomic conclusions occur in Sphacelaria reticulata (was Disphacella reticulata (Lyngb.) Sauv.), in S. radicans (ecad libera found in the Baltic), in S. nana (= S. britannica Sauv.) which include S. saxatilis and which is different from S. rigidula (= S. furcigera Kütz.), in S. plumigera (unattached growthform = ecad pinnata, found in the Baltic), in S. mirabilis (was Battersia mirabilis Reinke ex Batt.), in S. fusca (different from S. rigidula), in S. cirrosa (includes S. bipinnata (Kütz.) Sauv. and S. hystrix Suhr ex Reinke which are incorporated amongst the five different ecads of the species) and in S. sympodiocarpa (which cannot be incorporated into one of the described subgenera). Most details of morphology are depicted.

Description: In der obersenonen Mastrichter Tuffkreide finden sich kleine Zähne, die durch ihre glatten Kauflächen und die Furchen an den Seiten des oberen Teiles an Kauplatten von Myliobatis erinneren, einen Rochentypus, der ein an durophage Lebensweise angepasstes Gebiss hat. Niemals findet man aber die für diese Familie so typische langgestreckte Form der Zahnplatten; die Zahnoberfläche hat immer rhombische Form. Dames hat eine ausführliche Beschreibung von diesen Zähnen gegeben, die er für Reste eines Cestracion-artigen Namen Rhombodus Binkhorsti Haies hielt, dem er den gab. Ich möchte hier nur noch einige kurze Bemerkungen hinzufügen. Die Abbildungen (fig. 1) zeigen den typischen rhombenförmigen Umriss der Kaufläche (d). Die durch eine in der Richtung der kurzen Diagonale verlaufende, tiefe Rinne in zwei Hälften geteilte Wurzel hat ebenfalls die Gestalt eines Rhombus (fig. 1, b, e). An der Grenze von Krone und Wurzel findet sich an der einen Seite eine Rinne, an der anderen Seite eine vorspringende Leiste (fig. 1 c). Zusammen mit den verticalen Furchen, mit denen die Seiten versehen sind, hat diese Leiste zur Verbindung der Zähne untereinander zu einem Mahlpflaster gedient. Neben dieser regelmässigen Form, die besonders den grösseren Zähnen eigen ist, fanden sich aber Exemplare, die eine Abweichung zeigen, indem nämlich entweder zwei Seiten eines spitzen Winkels des Rhomboïds länger sind wie die beiden anderen, oder das Rhomboïd unsymmetrisch zusammengepresst ist. Es scheint mir, dass dies nicht eine zufällige Variation ist, sondern dass wir gerade durch diese Eigentümlichkeit etwas mehr über die ganze Zusammenstellung des Gebisses erfahren können. Wie ich unten noch näher auseinandersetzen werden, muss man nämlich Rhombodus zu den durophagen Stachelrochen stellen. Bei diesen findet man sehr oft gerade die grössten Zähne in der Mitte des Kiefers. Wenn man nun die Zahl der Zahnreihen, wie es gewöhnlich bei den grosszähnigen Rochen der Fall ist Rhombodus-Unterkiefers zu 7 bis 9 annimmt, so könnte man das Gebiss eines auf eine Weise rekonstruieren, wie es fig. 3 A zeigt, (wobei die verschiedenen obengenannten Formen vorkommen). Es wäre wohl ein grosser Zufall wenn man noch einige Zähne im ursprünglichen Verband finden würde. Wenn einmal die knorpeligen Kiefer aufgelöst sind, bieten die Seitenfurchen nicht genug Festigkeit und fallen die einzelnen Zähne auseinander.

Description: Da die Originale der von Göppert aus dem Tertiär von Java beschriebenen Arten Piperites Hasskarlianus und Junghuhnites javanicus nicht mehr vorhanden sind, die vorliegenden Beschreibungen für eine Bestimmung aber nicht ausreichen, so sind sie aus der fossilen Flora Javas zu streichen. Das gilt auch von Miquelites elegans, dessen schlechte Erhaltung eine sichere Bestimmung unmöglich macht. Bredaea moroides dagegen ist ebenso wie Naucleoxylon spectabile Crié sowie ein bisher unbeschriebenes Kieselholz von Java eine Dipterocarpacee. Die Stücke werden beschrieben als Dipterocarpoxylon moroides, D. spectabile und D. Göpperti n. sp. Die Frage, ob es möglich ist, diese wie andere fossile Dipterocarpoxyla bestimmten rezenten Dipterocarpaceengattungen zuzuweisen, soll später erörtert werden. Frankfurt a/M. Geologisch-Paläontologisches Institut der Universität.

Description: This compilation of stratigraphic and structural data accompanying the (re)issue of the 1:50000 sheets completes the project initiated by Prof. L.U. de Sitter in 1950. The total area mapped comprises about 400 km² in a strip more than 150 km from east to west. This part of the Hercynian tectogene is characterized by a very consistent sequence of Palaeozoic shelf sediments only interrupted by syn- to late-orogenetic flysch-molasse development. Neither of these sequences lend themselves to a simple geosynclinal model. Only the suprastructures of the orogene are exposed here; essentially decollement thrusting and folding. Fold and thrust vergences vary through 180° giving the centripetal pattern of the well-known Knee of Asturias. Very minor amounts of igneous rock have been mapped although activity in some form has been registered throughout most of the systems represented. The degree of metamorphism is so slight to have been negligible for the mapping.

Description: Laboratory-reared larvae of the spider crab, H. araneus L., were studied with regard to their fresh weight (FW), dry weight (DW), carbon (C), nitrogen (N), hydrogen (H), and energy content (J; estimated from C). FW remains fairly constant in each larval stage, regardless of feeding or starving conditions. This is due to regular changes in water content as opposed to those in organic constituents. There is a considerable gain (by a factor of 2 to 3) within each of these two instars. In the magalopa also a high amount of C, N, H, and energy is accumulated, but most of this gain is lost again during the last third of its stage duration. In all larval stages, weight-specific energy (J/mg DW) follows rather a cyclic pattern with decreases before and after molts, and increases during intermolt periods. It shows a decreasing trend during larval development. During starvation, biomass declines in an exponential pattern. Larvae of all stages die, when ca. 40 to 60% of their living substance and energy is lost.

Description: Parasitological investigations on herring gulls (Larus argentatus) and greater black-backed gulls (L. marinus) from Heligoland showed a high occurrence and abundance of the nematode species Cosmocephalus obvelatus, Paracuaria tridentate, Tetrameres fissispina and Capillaria contorta. The species specific distribution of the nematodes in distinct areas of oesophageal and stomach compartments, the morphological adaptations to their environment, as with the change of host tissue caused by heavy infestations, are the theme of the present article. The pathogenity is discussed. (German)

Description: Filtration rate (F) and ingestion rate (I) were measured in the rotifer B. plicatilis feeding on the flagellate Dunaliella spec. and on yeast cells (Saccharomyces cerevisiae ). 60-min experiments in rotating bottles servedas a standard for testing methodological effects on levels of F and I. A lack of rotation reduced F values by 40%, and a rise in temperature from 18 degree to 23.5 degree C increased them by 42%. Ingestion rates increased significantly up to a particle (yeast) concentration of ca. 600-800 cells/µl; then they remained constant, whereas filtration rates decreased beyond this threshold. Elemental analyses ofrotifers and their food suggest that B. plicatilis can ingest up to 0.6 mJ or ca. 14% of its own body carbon within 15 min. The long term average was estimated as 3.4 m/ind or ca. 75% of body carbon/d.

Description: Seasonal variations of size-frequency distribution, sex ratio, and percentage of egg-carrying females andjuveniles in a population of J. falcata inhabiting jetties at Helgoland Harbour are described. Reproductionoccurs all the year round, but 2 maxima and thus, 2 main generations per year can be observed: a weaker onein winter, and a more pronounced one in late spring/early summer. Biochemical composition and energycontents of J. falcata show only in part a seasonal cycle. There is an inverse relationship between the proteinand lipid fractions, whereas the former is negatively, the latter positively correlated with the amount ofsuspended food in the water. Protein, carbohydrates, lipid and the weight-specific energy equivalent show adecreasing trend with increasing size of the amphipods, while chitin significantly reveals an opposite trend.

Description: This publication deals with some agaves which were collected by me participating as biologist in a geological excursion under Prof. Dr. L. M. R. Rutten and Mrs. Dr. C. J. Rutten-Pekelharing, in the beginning of 1930, to the West Indies. From 14 April to 4 May we camped in the western part of Curaçao, from 10 May to 10 June Bonaire was visited and from 16 June to 9 July we passed through Aruba. In preference to the collection of a large number of different forms of Agave, an intensive investigation of the forms found on a few localities was made. I hoped thereby to acquire some information about the variability, and insight into the problem of the concept of species, not to be obtained by the study of herbarium material. — Other material was collected during an excursion to the mainland, following an invitation by the „Caribbean Petroleum Company”.

Description: Acrodiclidium Nees, Laur. Disp. Progr. (1833), p. 13; id., Syst. Laur. (1836), p. 266; Endl., Gen. (1837), p. 319, n. 2042; id., Ench. (1841), p. 197; Dietrich, Synops. Pl. II (1840), p. 1332; Spach, Hist. nat. Véget., Phaner. X (1841), p. 471; Steudel. Nomencl. ed. 2 (1841), p. 21; Meissn., Gen. I (1836—43), p. 326, II, p. 238; Reichb., Nom., p. 71, n. 2668; Orbigny, Diet. univ. VII (1846), p. 259; Lindl., Veg. Kgd. (1846), p. 537; Griseb., Fl. Brit. W. I. isl. I (1860), p 280; Meissn. in D.C., Prodr. XV, 1 (1864), p. 84; id. in Fl. Bras. V, 2 (1866), p. 172; Benth. in Benth. et Hook., Gen. III (1880), p. 154; Baillon, Hist. II (1870), p. 474;. Pfeiffer, Nomencl. (1873), p. 35; Durand, Index Gen. (1888), p. 349, n. 6190; Mez in Jahrb. Bot. Gart. Berl. V (1889), p. 81; Pax in Engl.-Prantl, Pfl. fam. III, 2 (1889), p. 123; Dalla Torre et Harms, Gen. (1900—07), p. 178, n. 2819; Britton and Wilson, Porto Rico and Virg. isl. (1924), p. 316; Lemée, Dict. I (1929), p. 50; Benoist in Arch. Bot. V (1931), p. 65; Kosterm. in Pulle, Fl. Surin. II (1936), p. 315; — Licaria Aubl., Guia. I (1775), p. 313; Nees, Syst., p. 344; Endl., Gen, p. 320; id., Ench., p. 197; Spach., l.c.; Steudel, l.c., p. 41; Meissn., Gen. II, p. 238; Lindl., l.c.; Meissn. in D.C., l.c., p. 259; Benth., l.c., p. 150; Baillon, l.c., p. 452; Pfeiffer, l.c., p. 107; Durand, l.c., p. 489; Mez, l.c., p. 220;. dalla Torre, l.c., p. 177 et 585; Lemée, l.c., IV, p. 85; Benoist l.c., p. 274; Kosterm. in Meded. Bot. Mus. Utrecht 25 (1936), p. 34; id. in Pulle, l.c., p. 323; — Evonymodaphne Nees, Syst., p. 244 et 263; Lindl., Syst. ed 2 (1836), p. 442; Endl., Gen. p. 319;. id., Ench., p. 197; Dietrich, l.c., p. 1332; Spach, l.c.; Steudel, l.c., p. 621; Meissn., Gen. I, p. 326; id. II, p. 238; Rchb., l.c.; Lindl., l.c., p. 537; Meissn. in D.C., l.c., p. III; id. in Fl. Bras., p. 203; Benth., l.c., p. 158; Baillon, l.c., p. 437; Pfeiffer, l.c., p. 1322; Durand, l.c., p. 349; Mez, l.c., p. 82; dalla Torre, l.c., p. 177; — Triplomeia Rafin., Fl. Tellur. (1838), p. 134; dalla Torre, l.c., p. 178; Mez, l.c. Type species: Acrodiclidium brasiliense Nees.

Description: Daltonia fenestrellata Griffin was collected by A. M. Cleef in the Andes of Colombia in 1973. It is characterized by the cuspidate, incurved or recurved leaf tips, the elongated juxtacostal cells and the apically scabrous seta. It seems most closely allied to D. gomezii Crosby of Costa Rica.

Description: In the spring of 1966, the junior author (H. Inoue) made a bryophyte collecting trip to Ceylon (now Sri Lanka) with the support of the Japan Society for the Promotion of Science. The collections have served as a basis for reviews of individual liverwort genera or families occurring in Ceylon, e.g. Frullania (Hattori, 1979) and Plagiochila (Inoue, 1979). The present paper deals with the species of Lejeuneaceae subfamily Ptychanthoideae, which comprises the more robust members of this large tropical family. In his catalogue of the liverworts of Ceylon, Abeywickrama (1959) recorded 18 species of Ptychanthoideae, belonging to the genera Archilejeunea (1 sp.), Brachiolejemea (1 sp.), Lopholejeunea (2 sp.), Mastigolejemea (2 sp.), Ptychanthus (4 spp.), Ptychocoleus (5 spp.), Spruceanthus (1 sp.), Thysananthus (1 sp.), and Trocholejeunea (1 sp.). Unfortunately, his catalogue does not provide precise information on specimens or literature on which individual species records for Ceylon were based. Most of the species listed by Abeywickrama had been treated by Verdoorn (1934) in his monograph of Asiatic Ptychanthoideae. Some are now considered synonyms, however, whereas in other cases some doubts may be cast about the correctness of the identification. Since we have not been able to locate all specimens on which previous Ceylon records of Ptychanthoideae were based, the present review should be considered preliminary.

Description: In plots B1, 2, and 4 in 1978 only a single species once covered over 12.5% of the surface: Leontodon hispidus. A few species covered sometimes about 5-10%, like Briza media, Triselum flavescens, Lotus corniculatus, Leontodon hispidus, and Knautia arvensis. In the course of the study the occasional dominance of certain species disappeared (Table 2). Most species covered less than 5%, but the number of individuals often fluctuated strongly from one species to another. In plots B3 and B5 a much stronger dominance could be observed than in the non-fertilized plots (Fig. 5). In 1978 the grasses Festuca rubra and Dactylis glomerata covered from 10—40% of the surface, the coverage of other species, particularly forbs, amounting to less than 1%, e.g., Ononis repens, Plantago lanceolata, Ranunculus acris, and Chrysanthemum leucanthemum. A few constantly present forbs, initially covering about 25%, like Centaurea pratensis and Lathyrus pratensis in plot B5 did not keep up this high coverage. This also holds for forbs that established themselves in the fertilized plots after a few years and attained a rather high coverage, like Heracleum sphondylium in plot B3.

Description: The well-known and widespread lichen species Cladonia furcata (Huds.) Schrad. is usually very constant in its chemistry: fumarprotocetraric acid is its main secondary metabolite, sometimes accompanied by atranorin. Recently a new chemical strain, characterised by the presence of psoromic acid instead of fumarprotocetraric acid or atranorin, was found in Portugal by the first two authors during phytosociological investigations of heath vegetations. The plants are preserved in the herbarium of the Institute of Systematic Botany, University of Utrecht (U), leg. Barendregt & v.d. Dries nr. 1-2 (U). Morphologically the plants with psoromic acid represent the slender form of C. furcata. which is the predominant form in lowland western Europe (fig. 1). The podetia are c. 3 cm long and up to 0.8 mm wide, branching regularly but not very densily dichotomously, and olivaceous green to brownish in colour. Their habit varies from creeping and loosely tufted to erect and densily tufted. Squamules are present only occasionally, on the lower parts of the podetia, and are roundish with a crenulated margin, up to c. 1.2 mm wide.

Description: The rice weeds project. In 1976, a joint project was set up under the aegis of the Netherlands University Foundation For International Cooperation (NUFFIC, Box 90734, The Hague), by the universities of Utrecht and Amsterdam and the Royal Tropical Institute (KIT) on the Dutch side, and BIOTROP (Box 17, Bogor) on the Indonesian side. Coordinators are Professor R. van der Veen and Mr. P.J. van Rijn. Its objective is the study of weeds and their ecology in the rice fields of Indonesia. A sharp distinction between dry and wet rice fields cannot be made for this kind of work: the dikes in the wet rice areas often carry dry rice weeds, and where locally fields are irrigated but part of the time, the weed flora assumes a mixed or successional character. More workable is the distinction between permanent rice fields on the one hand, and those under shifting cultivation regimes on the other; the latter have been excluded from the study.

Description: BABU, C.R., Herbaceous Flora of Dehra Dun, 721 p., 1 map (1977, Publ. & Information Directorate, New Delhi). 8°. Rs. 144, $ 50.00, £ 22.00. A useful local Flora which will be very handy for schools, colleges, foresters, agriculturists and laymen as well. It is a very full flora, with a key to the families, and within the families keys to the genera and species respectively. Emphasis is on the species, which all carry a description; there are no generic descriptions, only a brief indication of the size of the genus and its occurrence in India.

Description: This book is designed as a practical guide for the identification of fossil and extant woods with the aid of a marginally perforated card key, based on the ones devised by Clarke and perfected in the well-known Hardwood and Softwood keys published by the Princes Risborough Laboratory in 1961 and 1948 (1966) respectively. Using the cards originally prepared for Metcalfe and Chalk’s Anatomy of the Dicotyledons, the Princes Risborough cards, and numerous additions to these sets, the authors have gained considerable experience with this time-honoured identification method. A microfiche of these cards can be purchased separately from the Botanical Museum of Harvard University. Besides general chapters and appendices on for instance wood structure and variability, and how to prepare wood for microscopic examination and how to use the key cards, the main body of the book consists of a richly illustrated catalogue of diagnostic characters to be used in wood identification. It is in this section that the book shows most of its weaknesses. This is because of numerous mistakes in the choice of illustrations or misleading legends to the latter. For instance: fig. 3c (p. 24) is said to show abrupt latewood in Larix laricina, but the earlywood-latewood transition zone is not included in the photomicrograph; on p. 68 the vessels of Nyssa are said to be predominantly in multiples of four or more but the photograph illustrates vessel pairs alternating with fibres (i.e., vessel multiples in a distinct radial pattern; the latter feature is illustrated on p. 69 with examples showing no sign of such a pattern at all!); the tangential vessel arrangement of fig. 4b, p. 70 is in fact oblique; Myrica is incorrectly credited with ephedroid perforations on p. 73; Sphenostemon pictured with the most beautiful example of scalariform intervessel pits is said to show spiral thickenings instead (p. 74); long and slender pit canals are mistaken for plasmodesmata on p. 83; essentially similar fibre-tracheids in Eucryphia are classified as belonging to two fibre types (p. 87); fibres of Sleumerodendron are mistaken for vascular tracheids and crystals in the Dicotyledons are illustrated with an example from Gnetum (p. 124). The quality of many of the photomicrographs leaves much to be desired.

Description: Acanthaceae. At C, Dr. Bertel Hansen took an interest in the family, and began by going through the many papers by C.E.B. Bremekamp. Annonaceae. Mr. Paul Kessler, Botanik, Universität, Box 3049, Kaiserslautern, W. Germany, has undertaken work on Orophea.

Description: Caudex erect, short-creeping or long-creeping, rarely scandent; vascular structure in all cases a radially symmetrical dictyostele; scales usually thin, not peltate, in almost all cases bearing both marginal and superficial Unicellular hairs which are either acicular or glandular. Vascular strands at base of stipe 2, linear in section (rarely with an additional pair of small ones), uniting upwards to a U-shape; a linear aerophore with stomata continuous along each side of stipe and rachis. Fronds usually pinnate with crenate or lobed pinnae, in a few cases simple or bipinnate, never with basiscopically enlarged basal pinnae; apical lamina usually triangular and lobed, grading into upper pinnae, in some cases pinna-like; lower pinnae in many cases gradually much reduced or with abrupt transition to a series of small rudiments; a small aerophore, sometimes swollen or elongate, present at the base of each pinna; a translucent membrane present in the base of each sinus between adjacent pinna-lobes; venation in each pinna consisting a costa bearing costules, each costule bearing pinnately-arranged veins in a pinna-lobe; veins free in deeply lobed pinnae, or basal veins in adjacent lobes anastomosing to form an excurrent vein, which may be joined by other veins, terminating at the base of a sinus-membrane, successive veins Passing to the sides of the sinus-membrane where this is elongate. Indument: scales always present at base of stipe, gradually smaller upwards, uunute (often consisting of a single row of cells) on the distal parts of fronds, often nearly all caducous; adaxial surface of rachis and costae a'ways bearing antrorsely curved acicular unicellular hairs, in a few cases a'so septate acicular hairs; abaxial surface of rachis and costae usually bearing a different indument consisting of more slender unicellular acicular and/or glandular hairs or sessile glands of various forms (forked hairs in Ampelopteris only); surface of lamina between veins either quite glabrous or more often with a distinctive complement of hairs and glands different adaxially and abaxially. Sori borne on abaxial surface of veins, orbicular or sometimes elongate, indusiate or not; indusia reniform, glabrous or bearing hairs and/or glands, in some cases very small, athyrioid in some species of Coryphopteris; sporangia sometimes bearing glands or short acicular hairs (setae) near annulus, often with a hair of distinctive form on the sporangium-stalk; spores in almost all cases monolete, with perispore of varied form, in Trigonospora trilete. Gametophyte in all cases symmetrical-cordate, with unicellular chlorophyllous hairs on all parts, these hairs with ± swollen rounded tips which become wax-encrusted; in most cases, usually as a late development, unicellular acicular hairs, comparable with those on the sporophyte, may occur; other types of hair may be distinctive of some genera. Distribution. Throughout the tropics, especially in wetter areas; species few in temperate regions (5 in Europe), almost 1000 in all. The majority are terrestrial ferns of forest, but a few (especially in Christella few and Macrothelypteris) occur in open places only, and a (Cyclosorus, Thelypteris) in open swamps; some are adapted to grow on rocks by streams; very few are scandent; a few are casually epiphytic.

Description: Cladobotryum penicillatum sp. nov. was isolated from Alnus twigs in New Forest, Hampshire, U. K., in 1971, and from Sebacina effusa in the Houtribbos Forest, O.- Flevoland Polder, Netherlands, in 1980. The species has conidia intermediate in dimension between C. varium and C. mycophilum, and it differs from both species by having rather slow-growing colonies and long conidiophores with apical penicillate branching. Conidiogenesis is basipetal and retrogressive.

Description: In this second report on types of entolomatoid fungi in the Velenovský Herbarium at Prague* (PRC and PRM) seven of Velenovský’s new species in Entoloma, two in Eccilia and one described in Clitocybe are treated. For each taxon microscopical characters are given, followed by a consize discussion on its status.

Description: An introduction is given to the taxonomy of Entoloma subgenus Leptonia, followed by a revision of its section Leptonia. Eleven species are recognized, fully described and illustrated, of which three are new, viz.: Entoloma carbonicola, E. tjallingiorum and E. allochroum.

Description: Unter allen Flechten unterscheidet sieh die nur aus Norwegen bekannte Gattung Moriola dadurch, dass ihr Lager aus Goniocysten besteht, das sind kugel- oder länglichrunde oder unregelmässig gestaltete braune Behälter mit netzartiger Oberfläche, von denen braune, zylindrische oder schwach torulöse Hyphen entspringen und bis zur nächsten, manchmal weit entfernten Goniocyste hinkriechen. Auf diesem Wege, auch wenn sie zu mehreren nebeneinander herlaufen, vereinigen sie sich nie zu einer strauch-, oder blatt-, nicht einmal zu einer krustenformigen Lagermasse. Diese besteht ausschliesslich aus zerstreuten Goniocysten und den sie verbindenden Hyphen, die bei Moriola pseudomyces (Fig. 1—4) meist über morschem Holz, bei Moriola sanguifica über fremdem Algenlager ausgebreitet sind. Die braune Panzerkruste der Goniocysten entsteht dadurch, dass die dünnen zylindrischen Hyphenzellen unter Beibehaltung ihrer Dicke (2 µ), stark in die Breite wachsen und die Gestalt von Kugelsektoren annehmen. Sie werden meistens nicht viel über 2 µ dick, können aber bis 4 µ dick werden, wenn sich die Aussenwand höckerartig verdickt. Näheres hierüber in meiner Osloer Arbeit¹) und in den Berichten der Deutschen Botanischen Gesellschaft 2). Die Früchte einer von Herrn P. GROENHART an mich übersandten Flechte (Fig. 5—7) sind von ihm in 3000 m Höhe auf Java gesammelt worden und entwickeln ihre sporenreichen Perithezien auf einem etwa 1 cm mächtigen, lockeren Lagermasse von fast rein schwarzer Färbung. Diese rührt von Holzkohle her, die in grösseren oder ganz kleinen Bruchstücken, selten in Form angekohlter Zweige zwischen und unter den Goniocysten liegen. Die in den Goniocysten der tieferen Schichten enthaltenen Gonidien sind alle abgestorben und sehen jetzt braun aus. Nur in den Goniocysten der obersten Schicht sind die Gonidien noch jugendfrisch, sehen hellgrün aus und heben sieh deutlich von der dunkelbraunen, 4 µ dicken Kruste ab: eine einfache d.h. einkammerige Goniocyste mit 21.8 µ. Durchmesser, so dass auf den Innenraum fast 14 µ Durchmesser kamen; in ihr hatten drei Gonidien Platz. Bei einer anderen, zusammengesetzten Goniocyste hatte sich an diametral gegenüberliegenden Punkten der Goniocyste je eine Gonidie angesetzt und war von der braunen Kruste auch noch umwachsen worden, so dass die beiden kleinen Endkammern je eine Gonidie enthielten, die Mittelkammer deren drei. Es kommen aber auch noch grössere zusammengesetzte Goniocysten vor, deren Mittelkammer 5 und mehr Gonidien enthält.

Description: C. G. G. J. VAN STEENIS, Maleische Vegetatieschetsen — Toelichting bij de plantengeografisohe kaart van Nederlandsch Oost-Indië (Sketches of Malaysian vegetations — Comments to the phytogeographical map of Netherlands East India) — Reprinted from the „Tijdschrift van het Koninklijk Nederlandsch Aardrijkskundig Genootschap”, Ser. II, Vol. 52, Jan.-March-May 1935, 112 pp. (repagination [Pages in the original: 25—67, 171—203, 363—398] with 46 photographs, 36 of which in the reprint only, and a phytogeographical map. The reprint preceded by a short preface, a (too) short index and a dedication to FRANZ JUNGHUHN „as a memory to his arrival in Java, one hundred years ago”. It is a great pleasure to me indeed to announce here, more particularly on behalf of those readers who are not familiar with the Dutch language, this excellent work on the phytogeography of Malaysia, published in the Journal of the Royal Netherlands Geographical Society and therefore, moreover, likely less accessible to many botanists abroad. The author has, though only about 6 years engaged in botanical work in the tropics, gathered a remarkably thorough knowledge of the rich flora of this region, no doubt one of the most interesting ones, from a biogeographic standpoint, on earth. As the phytogeography of these parts has mostly, since JUNGHUHN’S „Java” (1854), been only dealt with in scattered papers, VAN STEENIS has in the publication under reference, as well as in some others that preceded it ¹), done a pioneer work in his attempt to give a comprehensive and more or less complete survey of the current problems. Our gratitude and admiration is not in the least diminished by the fact that this work shows certain traces of cursoriness and disequilibriousness, as well as a certain want of continuity and well-ponderedness. These features are mostly inherent to all pioneer work and the author himself states in the preface, that this work is meant as a provisional publication; this is in accordance with the title, which, by the way, could have been more adequately chosen, e. g.: Materials to Malaysian Phytogeography („Maleische” is, in my opinion, in Dutch a less felicitous word). Indeed, this paper contains a great many informations and stimulating ideas, and moreover, an almost complete bibliography, also of many papers in Dutch. It may be supposed indeed that there is, at present, hardly any other botanist available who is more capable than VAN STEENIS to continue this work and to prepare, some time, a complete „Phytogeography of Malaysia”, to which we are looking forward with great interest.

Description: Besides the Umbelliferae of the Netherlands Indies proper, also those of the Malay Peninsula and the non-Dutch parts of Borneo and New Guinea have been taken up in this revision. The materials examined belong to the following Herbaria: (B) = the Herbarium of the Botanic Garden, Buitenzorg. (BD) = the Herbarium of the Botanical Museum, Berlin—Dahlem. (BM) = the Herbarium of the British Museum of Natural History, London. (E) = the Herbarium of the Botanic Garden, Edinburgh. (G) = the Herbarium of the University, Groningen. (K) — the Herbarium of the Botanic Gardens, Kew. (L) = the National Herbarium (Rijksherbarium), Leiden. (NY) = the Herbarium of the Botanic Garden, New York. (Pa) = the Herbarium of the Java Sugar Experiment Station, Pasoeroean. (S) = the Herbarium of the Botanic Gardens, Singapore. (Sa) = the Herbarium of the Sarawak Museum, Kuching. (U) = the Herbarium of the University, Utrecht. Most of the herbarium materials were sent to Groningen to be examined there. Moreover I had the opportunity to work a few weeks in the Kew Herbarium and in that of the British Museum of Natural History in London.

Description: The article contains a discussion regarding the different identity of the specimens J. F. Duthie 3858 in the Kew (K), and the Calcutta (CAL) and Poona (BSI) herbaria. The specimens at CAL and BSI represent a new species of Arenaria, which is described here.

Description: The genera Microlaena R. Br., Petriella Zotov, and Tetrarrhena R. Br. are included in Ehrharta Thunb. (Gramineae-Ehrharteae), which necessitates four new combinations in the latter. In Malesia Ehrharta is represented by two taxa originally included in Microlaena: E. diplax F. v. Muel. var. giulianettii (Stapf) L. P. M. Willemse (M. giulianettii Stapf) and E. stipoides Labill. var. stipoides [M. stipoides (Labill.) R. Br. var. stipoides]. Descriptions of and notes on these taxa are given.

Description: Attention is drawn to the unusual distribution of flowers and inflorescences in a number of species, and to certain peculiarities of branching and phyllotaxy. The latter are explained by a heterophylly which so far has escaped notice, involving the formation and early disappearance of a pair of minute intercalary cataphylls. A similar branching pattern and flower distribution is evident in Helicanthes.