ALBERT

Description: The three species Galium silvaticum L., Galium aristatum L. and Galium schultesii Vest show differences in morphology, cytology and geographical distribution. These differences are described and discussed. Crossing experiments between the three species were without results. No hybrid could be obtained. Galium silvaticum, Galium aristatum and Galium schultesii must be considered as separate species.

Description: Although a large number of Tortricoid species and several genera from the Indo-Malayan region have been described by earlier authors (Walker, Snellen, Walsingham, Meyrick, and a few others), no survey of the present group has ever been made. Edward Meyrick, the author of most of the new names, has never attempted a synopsis of the Olethreutinae. He made surveys of the Australian and New Zealand Tortricoidea (1911), but the results are too superficial for our modern standards. During a long sojourn, working and collecting in Java, I became greatly fascinated by that fauna. Having completed a number of preliminary studies of the subfamily Tortricinae (1939 et seq.), I turned next to the South Asiatic, especially Javanese, Olethreutinae. After a long delay due to World War II, their revision has been initiated by the study of the two then least known and most confused genera, Bactra Stephens and Lobesia Guenée (Diakonoff, 1950 et seq.).

Description: Some rain and savanna forests of western Suriname (Corantijn R., Winana Creek; Upper Marataka R.; Upper Nickerie R;) were studied and their composition was compared with that of forests of other parts of Suriname and Guyana. The savanna forests of western Suriname proved to be much related to Guyanan ( Walabaand Dakama-) savanna forests as described by Davis & Richards (1934) and Fanshawe (1952). On the other hand, there was less relationship as regards rain forests of western Suriname when compared with ones of Guyana and other parts of Suriname, except for the Demerara greenheart forest of the Upper Marataka R., which was closely related to the Demerara greenheart forests of Guyana as described by Davis & Richards (1934). In addition an upland rain forest was studied near Blanche Marie falls, Upper Nickerie R., which proved to be very much like that of the Stofbroekoe Mts., eastern Suriname, as described by Schils (1960). Species/area curves for some rain and savanna forests are given. The geographical distribution of some common western Surinam tree species was studied; of the seventeen species studied one was endemic for Suriname. An annotated list of all species of trees and palms occurring in the explored areas is provided.

Description: Three sections with a total number of four species of the genus Phyllanthus have been examined. The pollen grains show a strong resemblance to each other and also the taxonomic arguments to differentiate between the three sections proved to be rather weak. Because of both palynological and taxonomic reasons the sections Ceramanthus Baillon, Cluytiopsis Mueller Arg. and Anisolobium Mueller Arg. have been united into one section; viz. section Ceramanthus Baillon s.l.

Description: Dicranella riparia (H. Lindb.) Mårt. & Nyh. is reported for the first time from Greenland, where it was found on a fluvioglacial delta in the Angmagssalik District in plant communities belonging to the association Calamagrosto-Ditrichetum (all. Calamagrostion neglectae). This is the sixth locality known, and the first outside Fennoscandia.

Description: The samples of the genus Calypogeia in the dutch institutional herbaria and private collections, those of C. arguta excluded, have been re-identified, according to the revision of the Swiss Calypogeias by Bischler (1957); distribution maps are given for all the taxa. More exact circumscriptions are given of several differentiating characters which were already established by previous authors. In C. fissa and C. sphagnicola the areolation of the leaves appeared to be a new differentiating character: in C. fissa the cells in the middle of the leaf show a great variation in length, whereas in C. sphagnicola the cell size is uniform. These differences are shown in histograms. C. muelleriana appeared to be restricted to the diluvial parts of the country, whereas C. fissa is common on both alluvium and diluvium; c. neesiana, C. sphagnicola and C. trichomanis are very rare, so that no clear geographical distribution can be given.

Description: This study deals with the taxa of the section Rubus of the genus Rubus L., so far as they are found in the Guelders district within the flora of the Netherlands. It concerns fifty species and some subspecies and varieties, mainly of the subsections Fruticosi Wimm. et Grab. and Discolores P. J. Müller. The similarity with the bramble-flora of northern Germany is obvious. A number of species, that occur in the latter region are absent however. Species of Central-European hills and mountains are as good as limited to the southern border of the Veluwe, which is mostly considered to belong to the Subcentreuropean district. South-European, often calciphilous species are absent. The nomenclature in the genus Rubus is very confused. There is an abundance of homonyms and synonyms. The number of misidentifications is rather large, meaning that a great deal of the literature is unreliable. The descriptions with many authors are absolutely insufficient, and type-specimens are often with difficulty or not at all to be traced. The difficulties arise from the fact that many taxa are not clearly separated. Some of them are well distinguishable, others are related by transitions. From a geographical point of view there is much difference as well. Some species have as their area almost the whole of Europe, others are limited to a very restricted area. In addition there is a difference in chromosome numbers (from diploids (2n = 14) to hexaploids (2n = 42). Most taxa are tetraploid. The abundance of forms within the section Rubus arises from a partly apomictic, partly amphimictic propagation. To set up some order in all those differences, the author has made the following distinctions: morphologically there are the different ranks of species and infraspecific taxa. Geographically distinctions have been made by means of a code of the capitals A to D inclusive: A indicates the taxa with the largest area, D the local taxa. Cytologically a code of Roman numerals has been given: I for diploids, II for polyploids. Beside the introductory theoretical part a short description of all taxa of the section above the specific rank has been given. All species and infraspecific taxa of this section, that are found to occur in the Guelders district have been described in detail, with mention of the type-specimen. Pictures have been added of the newly described taxa, and of some others as well. Maps of the distribution in the Netherlands of all the taxa have been inserted.

Description: This paper is an addendum to the author’s (1971) paper. At the time that the latter paper was finished, there were difficulties in taking photographs of the newly described male fructifications. Subsequently those difficulties have been solved, and the present paper contains the photographs of the male fructifications of the type specimens of Hastystrobus muirii v. Kon., Masculostrobus harrisii v. Kon., and Pityanthus scalbiensis v. Kon., and the photographs of the male fructifications, as described in the above-mentioned paper, of Ginkgo huttoni (Heer) Sternberg and Brachyphyllum crucis Kendall. All specimens are preserved in the Division of Palaeobotany and Palynology, Botanical Museum and Herbarium, State University, Utrecht, The Netherlands. Most of the photographs were taken with the specimens illuminated obliquely in air, but some were taken with the specimens flooded with oil. This procedure is generally applied when the specimen requires enhancement of contrast, so that details are more evident than if the specimen was photographed dry.

Description: Since the completion of Radlkofer’s monumental work on the Sapindaceae in Engler’s series “Das Pflanzenreich” 50 years have now elapsed, almost 40 since its publication. It is still the basis of virtually all taxonomic studies in the family. Some of the gerontogean genera have since been the subject of revisional work (Leenhouts 1969, 1971), but for the neogean representatives there are only some regional treatments (e.g. Rambo 1952; Barkley 1957; Reitz 1962; Soukup 1969), apart from descriptions of new taxa scattered through the literature. When studying the taxa native to Suriname in connection with the preparation of a supplement to the family treatment published previously in the “Flora of Suriname” (Uittien 1937) it soon became apparent to me that the genus Talisia was particularly incompletely known when Uittien published his account of the family, actually not much more than an extract from Radlkofer’s work. The number of species known or to be expected from Suriname proved to have doubled; this is not due to inadequateness of Uittien’s work but to much more extensive collecting. Two of the species met with since could not be identified with any species dealt with by Radlkofer or described after his time: these are described as new below. In order to establish that they were truly undescribed the descriptions and, where possible, types and/or other authentic specimens of all species described after Radlkofer were checked. A list of these follows; it may serve as a kind of bibliographic supplement to Radlkofer’s monograph. The two species marked with an asterisk have been posthumously listed in the supplement to his work.

Description: Dicranella staphylina Whitehouse, a species recently described from Great Britain, is now recorded from Belgium, Denmark and The Netherlands. A new combination, Anisothecium staphylinum (Whitehouse) Sipman, Rubers & Riemann, is proposed. A study of the costal anatomy revealed that A. staphylinum in this respect most resembles A. rufescens.

Description: The author studied the morphology of Blackstonia perfoliata s.l. and compared its variability with that of the other representatives of the genus. She also carried out ecological studies of “Blackstonia perfoliata ssp. serotina” on the Dutch island Voorne and compared her results with those in the literature relating to B. perfoliata in some adjacent regions, notably the Upper Rhine area. On morphological and ecological grounds B. perfoliata ssp. perfoliata and ssp. serotina are to be regarded as two distinct species, B. perfoliata and B. acuminata.

Description: In a forthcoming publication (Kramer, in prep.) floristic and taxonomic data of the pteridophyte flora of Suriname will be assembled, with keys and notes on their local distribution and ecological preference. The present paper deals with the geographical distribution of Suriname pteridophytes beyond the boundaries of Suriname (Fig. 2), a subject that lies beyond the scope of a local fern Flora. In the past, some (but relatively not very many) authors of fern Floras included a paragraph on the distribution of the taxa (Posthumus, 1928; Christensen, 1932; Backer & Posthumus, 1939). In some other fern Floras some space is devoted to ecology, but very little to geography (Holttum, 1954). In still others, considerations of a general kind on ecology and geography are altogether lacking (Vareschi, 1969). Lyell (1870), in his rather little-known book on the distribution of ferns, tried to bring together all the data known at his time; his work is now, of course, almost exclusively of historical significance.

Description: The pollen analyse of a raised-bog on the High Vosges crest shows the vegetation regional development since 3200 years. A prehistoric civilization, the Gallo-roman period, the great migrations and the Carolingian period are reflected in the pollen diagram by N.A.P. minima and maxima. A discussion on curves fluctuations of the main A.P. follows.

Description: Cytological investigations within Galium palustre L. showed the occurrence of three cytotypes, a diploid with 2n=24 chromosomes, a tetraploid with 2n=48 and an octoploid with 2n=96. Comparative morphological investigations, together with transplantation and crossing experiments confirmed the complexity of the species. The cytotypes are here considered to be subspecies of Galium palustre L.

Description: The wood descriptions of Juniperus communis L. ssp. communis are compared with those of earlier authors. The average and maximum tracheid lengths and the ray height distribution frequencies offer a means of separating the wood of the erect J. communis L. ssp. communis from that of the subspecies nana Syme with an entirely different habit.

Description: Caudalejeunea grolleana Gradst. spec. nov. from Madagascar is referred to this genus with some doubt because of the absence of gemmiparous branches. Ptychocoleus cristilobus (Steph.) Steph. from S. E. Asia has gemmiparous branches and therefore is a true Caudalejeunea: C. cristiloba (Steph.) comb. nov. This species is remarkable by its complicated ciliate leaflobule and by its polystratose rhizoid-disc. Two subspecies are distinguished: ssp. cristiloba from Burma, Andaman Is., Thailand, and Singapore, and ssp. samoana (Steph.) comb. nov. (Caudalejeunea samoana Steph.) from Samoa. Both C. grolleana and C. cristiloba have a 4-5-carinate perianth, which shows that the trigonous perianth present in most species of Caudalejeunea is not a stable character of this genus.

Description: Dalbergia and Machaerium are two distinct genera. The former genus Ecastophyllum is a distinct entity in the genus Dalbergia. The former genus Drepanocarpus differs from Machaerium only in certain pod characters and is considered as congeneric with it.

Description: Cytologioal investigations within Galium boreale L. showed the occurrence of tetraploids (2n=44) as well as hexaploids (2n=66) in Europe. Comparative morphological studies failed to demonstrate any differences in characters between the two cytotypes. Crosses between the tetraploid and hexaploid were unsuccessful, due to the occurrence of a strong and effective barrier between the two levels of ploidy. From a taxonomical point of view the two cytotypes are considered as to belong to the same taxon.

Description: The chromosome numbers of 67 species of Dutch Angiosperms were determined. Notes on 11 species are added.

Description: With the appearance in 1889 of Engler’s treatment of the Urticales in “Die natürlichen Pflanzenfamilien” there came a pause in the interesting development of the classification of this group, which was defined, albeit somewhat vaguely, by A.L. de Jussieu in 1789 in his “Genera Plantarum” as the order Urticeae. Since the 1830’s, many, including Gaudichaud, Trécul, Miquel, Bureau, Eichler, Baillon, and Bentham, have contributed to the establishment of the Engler system which until recently has been generally accepted. An important moment in this history was the appearance of Trécul’s treatment of the then most problematical group, the “family” Artocarpeae. Trécul (1847) considered the “families” which at that time were distinguished within the “class” Urticineae, viz Moreae, Urticeae, Ulmeae, Celtideae, and Cannabineae, as being very closely related to the Artocarpeae. Along with the Conocephaleae, split off from the Artocarpeae, we find these “families” as tribes of the “class” Urticaceae in the “Genera Plantarum” of Bentham and Hooker (1880) and as subfamilies or families in Engler: the subfamilies Moroideae, Artocarpoideae, Conocephaloideae, and Cannaboideae in the family Moraceae, the subfamilies Ulmoideae and Celtoideae in the family Ulmaceae, and finally the family Urticaceae. Since the end of the last century and until recently no revisions of any large groups of Moraceae and Urticaceae had appeared. But with the development of monographic taxonomic research the system has come out of its static situation, as can be seen from the study by Corner (1962). He proposed a new delimitation of the Moraceae and Urticaceae and another subdivision of the Moraceae sensu stricto.

Description: Controversy over the taxonomic relationship of the Taxineae with the Coniferineae has created a new interest in the field of wood anatomy. This has been reflected by the flurry of investigations being conducted in families such as the Podocarpaceae. The systematic position of Amentotaxus is somewhat uncertain (see Keng, 1969). While many authors place Amentotaxus in the Taxaceae, this genus has also been referred to the Cephalotaxaceae or even considered to represent a separate family, the Amentotaxaceae. When Kudo and Yamamoto (1931) described this last family, it was considered to be represented by only a single species, Amentotaxus argotaenia (Hance) Pilger. In his revision of Amentotaxus Li (1952) recognized four species. However, the description and publication of three new species of Amentotaxus based on leaf morphology would appear to have been overly optimistic and has not gone unchallenged. Hu (1964) recognized only three of the species, since she thought that Amentotaxus cathayensis Li could not be usefully upheld as distinct. Moreover, Chuang and Hu (1963) considered that Amentotaxus formosana Li was better referred to Amentotaxus argotaenia (Hance) Pilger. The divergence of opinion has increased the need to investigate any anatomical features that may be of taxonomic importance. In connection with this work it was thought an examination of the wood anatomy would be worthwhile, even though taxonomic evaluation at the subgeneric level is not often successful in this field. A comparative study of the wood anatomy within the genus Amentotaxus is considerably limited by the lack of availability of suitable material; most locations of Amentotaxus are in China. The scanty and now somewhat rare wood specimens were collected before 1935, with the exception of some from Taiwan.

Description: This paper is a preliminary account of investigations on species of Campylopus, mainly from the high Andes of Colombia and from adjacent regions. The studies are based on herbarium specimens, field studies and cultural experiments. The genus Campylopus was founded by Bridel (1819) on the basis of a curved seta only and included, therefore, species of Grimmia and other genera. Later he modified his earlier circumscription (Bridel 1826) so that the genus then contained (except for one uncertain species) only species of Campylopus as known today. A subdivision of the genus was made by Limpricht (1886) based on the structure of the costa as seen in cross section: Pseudocampylopus Costa without stereids, ventral layer of large cells, other cells containing chlorophyll with moderately thickened walls. Campylopus Costa with dorsal stereid groups. Palinocraspis Costa with dorsal and ventral groups of stereids.

Description: A key is offered to the wood of 35 out of 38 Inga species known from Suriname and the other Guianas. The wood structure indicates that the sections Leptinga, Diadema, Bourgonia and Euinga sensu Bentham are taxonomically sound. Section Pseudinga is unnatural and should be subdivided. The author is in favour of keeping the sections Leptinga and Diadema apart.

Description: Peculiar slit-like apertures in the walls of the fibre tracheids of Dicranostyles mildbraediana described in a previous paper, were recognized by the co-author as the result of a ‘soft-rot’ fungal attack. Consequently these structures are not a characteristic feature of this species.

Description: A small set of bryophytes collected on the islands of Malta and Gozo in April-May, 1968, and April, 1969, by K. U. Kramer and L. Y. Th. Westra (Utrecht) was handed to the author for identification. The results are presented here as a supplement to a paper on the vascular plants of the Maltese islands (Kramer et al. 1972). The collections are deposited in the herbarium of the State University of Utrecht. In the past few years many new data have been published on the bryophytes of the Mediterranean islands, cf. Sunding (1967,1971), Koppe (1965), Lübenau & Lübenau (1970), Düll (1967), Gradstein (1971), and Townsend (1965). The liverwort flora of the Mediterranean coasts is being studied thoroughly by Jovet-Ast & Bischler (cf. 1968). Yet the bryophyte flora of the Maltese islands received very little attention in the literature. A brief survey of the main data follows here.

Description: The chromosome numbers of 85 species of flowering plants from the Canary Islands were determined; 5 of the counts turned out to be new. Notes on some species are given. Numbers deviating from previous counts proved to occur in Polycarpaea divaricata (Pit.) Poir. and Koeleria phleoides (Vill.) Pers. 49 counts are new for the Canary Islands and are listed in table 2.

Description: The present paper, the fifth¹) in this series, is a continuation of the documented list of chromosome numbers of Angiospermae occurring in the Netherlands. In this paper 49 species and two hybrids are listed. Some species show variation in chromosome number, as was concluded after comparison of our results with those of other authors [cf. the lists published by Löve and Löve (1961); Cave et al. (1956-1964); Ornduff (1967, 1968, 1969); Solbrig and Gadella (1970); Moore (1970)]. Some notes on 14 species and two hybrids are given.

Description: The circular which was enclosed in Bulletin 24 has received full attention of our readers and a large number of cards were received. The large majority favours the continuation of our annotated bibliography as it is, not cutting off references on the Australian and Pacific floras, and not discarding the references on the Cryptogams. A review of Mr. Ferguson’s Index is given on p. 1912. October 21, 1970, Foundation Flora Malesiana existed twenty years. This anniversary was marked by a small festivity in the Rijksherbarium. Although curtailed financially since January 1958, it has kept its promise to promote all studies encompassing progress of the botany and plant geography of the Malesian subcontinent. It is gratifying that with the distinct tendency of the rehabilitation of the economical and political situation in Indonesia during the last few years, science in general, and biology in particular, are getting a new impetus. Amongst others through international agreement and co-operation, two master organisations have been set up, SEAMEC and BIOTROP, the latter being the centre of biological studies and education allotted to Bogor. It is clear that this focus will be a great stimulant and will sponsor biological activity. It was particularly pleasant to learn from Professor Sarwono and Dr. Didin, chairman and secretary of LIPI respectively, that this general scientific rehabilitation scheme included assistance towards the Flora Malesiana Foundation. Although the scientific elaboration of Flora Malesiana has been transferred as a major work project to the Rijksherbarium, a necessity since 1958, there are various desiderata left, amongst others contributions from Indonesian systematists. Unfortunately, the net result of Dr. Kostermans’s efforts to have promising Indonesian students thoroughly trained and prepared to share the tremendous task still before us, is meagre. Two of them, Dr. Soegeng and Dr. Didin, are occupied with very responsible and very necessary but largely administrative tasks, Dr. Prijanto died unexpectedly, and Dr. Soepadmo spends his time largely on educational matters. Clearly something must be done and we trust that in the near future creative work by Indonesian systematists can be resumed. We shall, I sincerely hope, overcome, and the future carries certainly very promising features for a more intense co-operation. And disinterested loyal co-operation is the very basis of ensuring achievement. It is with immense satisfaction that I see this perspective of a bright future ahead.

Description: Dr. W. Meijer, who is Dutch-born, worked in Indonesia from 1951 to 1958, first at Bogor, then at Pajakumbuh, Sumatra, and was Forest Botanist in Sabah for several years, revisited Indonesia with a National Science Foundation travel grant under an NSF-AID (Agency for International Development) program for Scientists and Engineers in Economic Development. The University of Kentucky Research Foundation covered part of the travel costs in Indonesia together with the Regional Center for Tropical Biology (BIOTROP) in Bogor, and Weyerhaeuser Timber Co., which is now also financing the printing at U.K. of a guide on trees in Indonesia which should be an excellent tool for better training of foresters in Dendrology (tree knowledge). The Japanese Sumitomo Timber Company also acted as liaison for Dr. Meijer during his visit to East Kalimantan. Dr. Meijer has written a fully documented final report which he hopes to submit to the Indonesian government through its Academy of Science. Parts of the report will be published in the Indonesian Forestry Journal and in International Nature Conservation Journals. He hopes for continuing support from the University, its Office for International Affairs, and the U.K. Research Foundation to get this report published. Officials in the World Bank in Washington D.C. and the Smithsonian Institution have also expressed great interest in the results of Dr. Meijer’s recent mission to Indonesia. The editor is glad to print this preliminary report:

Description: Dr. J.A.R. Anderson, who retired from the Sarawak Forest Service, and now lives at 15 Church Hill, Edinburgh EH10 4BG, will continue his interest in Malesian botany and ecology as a consultant forester and ecologist. The MS. of a project on which he had been working for several years is now in the final stage. This is a ”Check List of the Trees of Sarawak”; the scientific names will be coded and alphabetically arranged by families, genera and species, together with a moderately comprehensive list of vernacular names. This should be of value to the Forest Department in Sarawak. Miss P. Aston, senior botanist at the Melbourne Herbarium, is Australian liaison officer at Kew where she will remain until mid-1974. She is specialized in aquatic plants of Australia on which subject she wrote a most informative book (1973) which will be duly reviewed in this journal.

Description: The entries have been split into five categories: a) Algae – b) Fungi & lichenes – c) Bryophytes – d) Pteridophytes – e) Spermatophytes & General subjects. — Books have been marked with an asterisk.

Description: Harold St. John has (in Le Naturaliste Canadien 98, 1971, 571-580) given an evaluation of J.R. & G. Forster plants described in their Characteres generum which is newly dated to have been issued March 1, 1776. We feel induced to correct some inaccuracies. Gingidium montanum (l.c. 574, no. 21) — later transferred to Ligusticum as L. gingidium by Forster f., Prod. (1736) 22; DC., Prod. 4 (1830) 159, as an illegitimate homotypic synonym — is unnecessarily named as a new (superfluous) combination Angelica forsteriana St. John. Hooker f., Handb. New Zeal.Fl. (1867) 97, had this (according to the present Code, art. 72) correctly named Angelica gingidium, as because of the earlier Angelica montana Brot. (1804) he could not use the epithet montanum. For the rest Dawson (New Zeal.J.Bot. 5, 1967, 90) has reinstated the generic name Gingidium. He has still more recently changed the name Gingidium Forst., non Hill (1756), into Gingidia as Hill’s herbal has been said to be declared nomenclaturally valid.

Description: History. In order to understand its present function, a short historical account is necessary. Bibliotheca Bogoriensis is the oldest science library in Indonesia, established in 1842 at the proposal of J.K. Hasskarl, assistant hortulanus of the ’s-Lands Plantentuin in Buitenzorg, West Java (now called Kebun Raya Indonesia Bogor). The very first 25 books were bought from Dr. Jacques Pierot, a botanist who was sent by the Dutch Government to China. Ever since many visiting botanists left or sold their book collection, the reason why Bibliotheca avails of fine old antiquarian books in the field of botany. Among the library’s treasures are the reprint collection belonging to Melchior Treub with his own hand-written catalogue, as well as his correspondence, and all his awards received from many countries and scientific societies in the world.

Description: In mid-1971 Dr. K. Iwatsuki made a four-weeks’ collecting trip in Thailand, 10 Sept.- 10 Oct. From Oct. 1971 till mid-January 1972 a joint Leyden exploring expedition was made by Mr. C.P. van Beusekom and Mr. R. Geesink to various parts of Thailand.

Description: I must apologize that this Bulletin appears late. Material had been assembled for it and I had anticipated to compose this number about Christmas 1971. But on my birthday, 31 Oct. 1971, it was announced as a complete surprise that the firm of Brill was authorised to publish a book on the Javanese Mountain Flora of which the core is 57 hand-coloured plates on which 456 different species are depicted. The fieldwork was done, and drawings were composed in 1939-1941. After the war no publisher could be found; a precursor with 4 plates appeared in Endeavour (21, 1962, 183-193). The condition attached to this allowance was that I should promise stante pede to deliver the text by end December 1971 or at least as soon as possible, because the promotors of the plan intended to present me with the printed book on the occasion of my retiring from office, 1 Sept. 1972. So the rather peculiar situation arose that I had to make my own present. With my already tight time schedule for my last year of office I hesitatingly agreed. The available text was, however, very incomplete, having been written in the war prison camp, thirty years ago. Moreover it was at that time intended to be very popular for a pocket size atlas, as Schröter’s ’Pflanzenführer fur Alpenwanderer’ which had stood model for the purpose. With the generous life-size plates and folio format book now envisaged to edit, this text had to be completely rewritten in much enlarged scope and all captions carefully checked with the present literature and with the herbarium. Though the plates are explained by the captions, the general text also needed illustration and so figures had to be made or selected and photographs sorted. I had to give this project absolute priority. Notwithstanding the most liberal assistance rendered to me by my senior staff members, to whom I could entrust several time-consuming official duties, the composition of the text was real slave labour for seven days a week until late for five months. The captions were delivered end January, the general text May 22nd. The colour plates are printed and come out magnificently, practically as good as the original water-colour drawings, and the captions are by now in page proof, so that I hope the work will indeed be printed early September and available in October. Publication of Flora Malesiana proceeds well. In April 1971 the third instalment of the Fern volume appeared (Lindsaea-group by Dr. Kramer) and the text for a fourth instalment by Prof. Holttum & Drs. Hennipman is almost finished in MS. The final instalment of vol. 6 is in press and will appear presumably in September. Of vol. 7 the first instalment containing revisions of 12 families appeared in Jan. 1972. The second instalment of vol. 7 is in print (Fagaceae, Passifloraceae) and will appear in autumn. There is the prospect of publishing in the rather near future three very large families: Moraceae, Cyperaceae and Dipterocarpaceae. From the third chapter of this Bulletin it can be observed that progress with revisional work is satisfactory, though speed of publication still falls short of my expectation.

Description: Families and higher taxa have been entered under their name. Names of families which have been revised in volumes 4, 5, 6, and 7 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: In the past century Cornaceae were mostly delimited in a wide sense and they represented a fairly heterogeneous assemblage. HARMS (Ber. Deut. Bot. Ges. 15, 1897, 28 and in E. & P. Nat. Pfl. Fam. 3, 8, 1898, 255) distinguished 7 subfamilies. Of these Garryoideae were later mostly recognized as a separate family Garryaceae, as Alangioideae Alangiaceae, Nyssoideae and Davidioideae together as Nyssaceae, leaving Cornaceae with the remaining three subfamilies Cornoideae, Curtisioideae (monotypic, South Africa) and Mastixioideae (monotypic, Indo-Malesian tropics). Cf. WANGERIN, Pfl. Reich Heft 414 (1910) 18. In recent years, however, the other genera (6) of the Cornoideae, besides Cornus, have also been recognized as monotypic families, with the exception of Corokia which was transferred to Saxifragaceae-Escallonioideae. Notably TAKHTAJAN (Proiskh. Prokruitosem. Rast.: 89, non vidi) is in favour of these monotypic families. In his ‘Flowering Plants’ (ed. C. JEFFREY; 1969: 227) he accepted 7 segregate families besides Cornaceae sens. str. (omitting mention of two Madagascan genera, one of which he had formerly also raised to family rank, according to SHAW, 1973). These 7 families he arranged, together with Araliaceae and Umbelliferae, in the order Cornales, a phylogenetic construction of affinity not much different from earlier conceptions. The general impression is thus that the distinction of the segregate families is largely an inflation in rank.

Description: Monoecious trees or rarely shrubs, in Mai. evergreen, sometimes buttressed or with stilt-roots; growth mode flushwise, with perular buds. Hairs simple or stellate or fasciculate, rarely with resiniferous colleters, or scales on pits on the underside of the leaf. Leaves simple, spirally arranged, rarely in whorls of 3 or distichous, sometimes crowded near the top of each flush, penninerved, in Mal. entire or rarely crenate or sinuate. Stipules present, caducous or rarely rather long persistent, rarely interpetiolar or peltately attached. Inflorescence a cyme or a simple or branched spike, bracteate, ♂, ♀, androgynous (with the ♀ flowers borne on the lower part) or mixed. Flowers unisexual or functionally so. — ♂ Flowers: solitary or in dichasial clusters of 2-30 along the rachis, sessile or pedicelled; perianth campanulate or tubular, 6(-9)-lobed, or irregularly incised; stamens (4-)6-12(-90), filaments filiform, long exserted, free or rarely connate at the base; anthers linear to reniform, dorsi- or basifixed, lengthwise dehiscent; pistillode absent or present, densely hairy. — ♀ Flowers: sessile, solitary or in dichasial clusters of 2-15, surrounded by a cupule; ovary inferior, 2-6(-9)-celled, usually hairy; ovules anatropous, 2 per cell, apical and collateral; perianth usually regularly 6-lobed, sometimes poorly developed; staminodes 6-12, or absent; styles as many as ovary cells, terete, rather short, conical or tongue-shaped; stigmas capitate, punctiform, or covering the inner surface of the styles. Cupules solitary or in dichasial clusters, often woody, rarely reduced or absent, from saucer- or cup-shaped to enclosing the fruit, indehiscent or splitting into 2-8 or more ± equal segments, rarely consisting of 2 free segments, variously muricate, spiny, squamose, or with concentric or spiral lamellae, very rarely almost smooth. Fruit an indehiscent nut (achene), 1-3-celled, sometimes falsely multiseptate, rounded or sharply 2-3-angular. Seed one, exalbuminous; embryo-large; cotyledons large, flat-convex, plicate or ruminate; germination epigeal or hypogeal. Recent distribution. Seven genera with possibly c. 700 spp., the majority on the northern hemisphere. In the Old World the distribution extends southwards from 62°N in Scandinavia southheastwards to Kashmir and then northeastwards to the Sea of Okhotsk at c. 55°N. In Africa, Fagaceae are confined to the northern rim in the western Mediterranean region. In Asia Fagaceae are absent from the dry parts of the Middle East, from the Deccan Peninsula and Ceylon, from the desert and colder parts of China, from Manchuria, and from the extreme northern parts of Japan. In America, the distribution extends from Canada and the United States southwards to Central America, as far south as a few scattered localities in Columbia, in South America. On the southern hemisphere, Fageceae are present in Malesia, in the scarce wet parts of East Australia, in Tasmania, New Caledonia, and in New Zealand (otherwise absent from Pacific islands); in South America they occur from Fuegia and Staten I. northwards to Argentina and on the western slopes of the Andes in Chile up to 33°S. Fig. 1.

Description: Asher’s Guide to botanical periodicals is a 3-weekly printed announcement of articles published in more than five thousand selected periodicals, in the field of: anatomy bibliography botanical history cytology dendrology ecology economic botany evolution floristics horticulture hydrobiology limnology medical mycology microbiology morphology palaeobotany palynology personalia pharmaceutical botany phytochemistry phytogenetics phytogeography plant physiology plant taxonomy toxicology Symposium and Congress Proceedings also to be included in the journal. An author index and plant name index taken from the titles of the articles will be added annually.

Description: Dr. J.A.R. Anderson, Kuching, was on leave in spring 1971; he would return in the middle of the year for a final short tour. Dr. Anderson’s merits for the development of Botany in Sarawak are extremely large; it is a great pity to see such most experienced personalities leave the scene. We are thankful for his important endeavours and wish him a happy retirement. Prof. Dr. C.D.K. Cook, Zürich, is preparing a manual for the identification of aquatic plants.

Description: Mostly climbing herbs or lianas with axillary tendrils, rarely erect herbs, shrubs or small trees, glabrous or hairy, in Mal. not spiny. Branching usually by a supraaxillary serial bud. Leaves (mostly) spirally arranged, simple or compound, pinninerved or palminerved, entire or lobed; petiole or blade-base often with 1-many glands, and often glands on margin and lower surface of the blade. Stipules present. Inflorescences essentially axillary, cymose, sessile or peduncled, 1-many-flowered, ending in (a) tendril (s) or not. Bracts and bracteoles mostly small. Flowers often stiped, articulate to the pedicel, actinomorphic, bisexual or functionally unisexual (either with staminodes or a vestigial ovary, and then plants mostly dioecious) or polygamous. Perianth mostly 2-seriate, mostly persistent, the segments free or partially connate (Adenia p.p.), inserted on the rim of the saucer- or cup-shaped or tubiform hypanthium. Sepals (4—)5( 6), imbricate. Petals (4-)5(-6), mostly imbricate. Corona inserted on the hypanthium, mostly a complicated structure, composed either of filaments, hairs, or appendages, or membranous, annular, or composed of scales (disk), or in addition with ‘septa’ (Adenia p.p.), rarely corona absent (Adenia p.p.). Stamens 4-10, inserted mostly at the base of the hypanthium, or on an androgynophore (mostly hypogynous), (mostly) opposite the sepals; filaments free or partially connate into a tube; anthers 2-celled, longitudinally dehiscent, sometimes apiculate. Ovary superior, subsessile or on a gynophore or androgynophore, 1-celled, 3(-5)-carpellate; placentas 3(-5), parietal; ovules many, anatropous; integuments 2; styles 1 or 3 (-5), very short to distinct, sometimes partially connate; stigmas ± globose, or capitate, or papillate, or much divided. Fruit a loculicidally 3(-5)-valved capsule, or berry-like. Seeds mostly numerous, mostly compressed, often beaked, enveloped by a (membranous or juicy) aril; funicles often distinct; testa crustaceous (coriaceous), mostly striate, reticulate or pitted; endosperm (copious) horny; embryo straight; cotyledons foliaceous. Cf. HARMS in E. & P. Nat. Pfl. Fam. ed. 2, 21 (1925) 470-507. Distribution. About 10 genera and 500 spp., almost entirely confined to the tropics: in America c. 350 spp. (mainly Passiflora, a few species in Dilkea, Mitostemma, Tetrastylis), in Africa (incl. Madagascar) c. 110 spp. (mainly Adenia c. 80 spp., Tryphostemma c. 20 spp., Deidamia, incl. Efulensia, Crossostemma, c. 6 spp., incl. Schlechterina, 2 spp.), in Asia and Australia c. 40 spp. (Passiflora c. 20 spp., Adenia 14 spp., Hollrungia 1 sp., Tetrapathaea 1 sp. in New Zealand).

Description: Herbs, sometimes with scaly rhizomes, bulbs, bulbils or stolons, or woody perennials, shrubs, lianas or trees. Leaves penninerved, digitately or pinnately trifoliolate, imparipinnate or paripinnate, basal, alternate, subopposite or apically tufted. Stipules sometimes present. Petioles with basal joint, petiolules articulated. Inflorescences basal, axillary or pseudoterminal, cymose to pseudumbellate, rarely racemose, 1-many-flowered, bracteate and bracteolate. Flowers ♂♀, very rarely also ♂ specimens (Dapania), actinomorphic, 5-merous, hetero-tri-, -di-, or homostylous, sometimes cleistogamous. Pedicels articulate. Sepals imbricate, free or connate at base, sometimes with apical calli (Oxalis), persistent. Petals contort, quincuncial or cochlear, free but usually cohesive above the base (‘pseudosympetal’), clawed (sometimes minutely so), glabrous or inside sometimes with minute papillae or pilose. Filaments 10, obdiplostemonous, connate at base into an annulus, persistent, the epipetalous (shorter) sometimes with a basal gland near the insertion of the petals, or sometimes with 2 scales or dark lines on the annulus (Dapania), rarely without anthers; the episepalous (longer) with a dorsal tooth (Oxalis) ) or hunchbacked; anthers dorsifixed, versatile, 2-celled, dehiscing extrorsely by longitudinal slits. No disk. Ovary 5-celled, superior; styles 5, terminal, persistent, free, in LF¹ and MF erect, in SF patent to recurved, rarely reduced (♂ flowers); ovules 1-2-several per cell in 1-2 rows, epi- and anatropous, pendulous, superposed, bitegmic. Fruit capsular, loculicid, 5-celled, dry, rarely fleshy and indehiscent. Seeds usually with an aril; endosperm copious, fleshy, rarely absent; embryo straight. Distribution. 6(7?) genera with c. 850 spp. Of the Malesian representatives Oxalis, the largest genus, is most numerous in S. America and S. Africa and Biophytum in S. America and Madagascar; Dapania has 2 spp. in Malesia and 1 in Madagascar; Sarcotheca (11 spp.) is endemic in Malesia, while Averrhoa (2 spp.) assumedly also originated here; it is now cultivated pantropically.

Description: Trees or shrubs, evergreen (Mal. spp.); leaf-scars large. Leaves crowded towards the end of the shoots, spiral, simple, exstipulate, serrate with glandular teeth, often with an apical gland, more rarely entire; nerves a little decurrent along the midrib, both midrib and nerves ± impressed above, ± prominent beneath. Indumentum of branchlets, leaves and inflorescences consisting of simple, and/or long, fascicled and ± patent, and/or minor, ± depressed stellate hairs. Flowers bisexual, regular, 5(-6)-merous. Inflorescences sometimes simple solitary terminal racemes, but mostly consisting of a terminal raceme and several lower approximate racemes, each of the latter from the axil of a ± reduced or caducous leaf, thus forming together a panicle-, fascicle- or umbel-like inflorescence; bracts mostly caducous during anthesis, rarely subpersistent. Calyx lobes 5 (-6), persistent, quincuncially imbricate, united at the base only. Petals 5 (-6), generally free, sometimes cohering to some degree, alternate with the calyx lobes, rather early caducous, generally sweet-scented. Stamens 10(—12) in 2 whorls of 5(-6), the outer whorl opposite the petals, the inner one opposite the calyx lobes; filaments adnate to the corolla at the extreme base; anthers dorsifixed, overturned outwards in bud, erect in anthesis, introrse, upper part of cells ± divergent, opening with apical, slitlike pores; pollen grains single, tricolporate, psilate. Ovary superior, 3-celled, with axile placentation; ovules ∞, small, anatropous; style simple, mostly shortly, very rarely hardly divided into three apical lobes, sometimes more deeply so and trifid, each lobe stigmatic at the top. Fruit a 3-valved, loculicidal capsule, the septae of which become loose from the persistent central axis, subtended or ± enclosed at maturity by the persistent calyx. Seeds ∞, small, subovoid to irregularly angular or subtrigonous, with a foveolate-reticulate testa (all Mal. spp.). Endosperm fleshy. Embryo cylindrical. Distribution. A small, monogeneric family in the Ericales, of (sub)tropical Asiatic-Malesian, and temperate and tropical American distribution, and with 1 sp. in Macaronesia (Madeira, and formerly in Teneriffe).

Description: The entries have been split into five categories: a) Algae — b) Fungi & Lichenes — c) Bryophytes — d) Pteridophytes — e) Spermatophytes & General subjects. — Books have been marked with an asterisk.

Description: Shrubs, small trees, or lianas, in Malesia evergreen, or herbs. Stipules present. Leaves in Malesia spirally arranged, sometimes distichous, simple, the margin often shallowly incised; generally stalked. Inflorescences axillary variously modified bundles, or racemes, or panicles, sometimes terminal, or flowers solitary in the leaf axils; bracts small; pedicels often articulated, whether in the lower or in the upper part; bracteoles, if present, small and in the lower part of the pedicel. Flowers bisexual or rarely dioecious, actinomorphic or zygomorphic, particularly in the corolla; the parts often persistent in fruit. Sepals 5, the median one adaxial (posterior), free or occasionally for a small portion connate, often ciliate. Petals 5, free, generally sessile, the median one abaxial (anterior), often longer and differently shaped, the base then mostly with a sac or spur. Androecium often cylindrical, stamens 5, episepalous; filaments often more or less connate into a tube, in the Malesian genera with zygomorphic flowers, those near the odd petal with a recurved fleshy appendage; anthers introrse, in Malesia nearly always the connective at the top produced into an approximately triangular membranous appendage converging with the others, cells sometimes with a small appendage at the top. Gynoecium superior, sessile, ovary small, subglobose, one-locular, with generally 3 carpels, the median one adaxial, each carpel with a parietal placenta in the middle bearing 1-many anatropous ovules; style straight or, in the zygomorphic flowers S-shaped with the stigma curved towards the odd petal and club-shaped with variations. Fruit in Malesia capsular, the carpels thickened to boat-shaped leathery or woody valves (in the latter eventually the endocarp separated from the pericarp) which spread and often compress upon dehiscence. Seeds 1-many, sessile, one to a few mm in size, often with distinct raphe, sometimes with funicular outgrowths; rich in endosperm; embryo straight. Distribution. A pantropical family; only Viola is cold-loving. Hybanthus extends into the subtropics‘ so does Melicytus (Pacific Plant Areas n. 103, Blumea Suppl. 5, 1966) in Polynesia and New Zealand. Hymenanthera (congeneric with the former? l.c. n. 104) is temperate in SE. Australia and New Zealand. Number of genera 16, 8 of them American; the largest are Viola, currently credited with c. 400 spp., Rinorea with c. 200, Hybanthus with perhaps 70, and there are about 50 more in the other genera altogether. Total number of species c. 720, in Malesia 31, two of these introduced.

Description: Cyclopaedia p. xxiii-xxix add: F. de Lahaie, see C. A. G. RICHE. C. A. G. Riche and F. de Lahaie, naturalists of the voyage in ‘La Recherche’ and ‘L’Espdrance’ in search of La Pdrouse, 1791-1794, collected in Mauritius and Reunion. Part of the plants have erroneously been labelled ‘Java’.

Description: Trees, or whether or not climbing shrubs, or lianas. Leaves spirally arranged, rarely opposite, simple, entire or lobed (in Mal. never crenate or serrate), pennior palmatinerved, exstipulate. Inflorescences mostly axillary, sometimes terminal, rarely extra-axillary, or from old wood, in spikes or spike-like racemes, or often in cymes, both spikes and cymes not rarely collected to panicles or heads, very rarely reduced to few-flowered fascicles or to a solitary flower. Flowers bi- or unisexual, in the latter case at least functionally so, i.e. the plants dioecious, actinomorphic, (4-)5(-6)-, by reduction rarely in part 3-merous, cyclic (with sepals or calyx lobes and petals) or rarely spiral (with petals only in Pyrenacantha, or without petals in the ♀ flowers of Platea and some spp. of Iodes and Gomphandra). Pedicels, if any, articulated with the calyx. Sepals 4-6, free or mostly connate below to various degree to a 4-6-lobed calyx, the lobes imbricate or valvate, generally persistent. Petals 4-6, free or connate below to various degree, sometimes to a tube, the lobes valvate, very rarely subimbricate, tip inflexed, mostly caducous, sometimes persistent. Stamens as many as sepals or petals, episepalous, inserted basally or sometimes in the upper part of the tube; filaments subulate, fleshy, often flattened, or filiform, not rarely with clavate subglandular elongate hairs distally; anthers 2-celled, cells often diverging below, basifixed, latrorse or introrse, in Polyporandra dismissing the pollen from numerous operculate pores. Disk whether or not present, either annular or cup-like, free or adnate to the ovary, or a unilateral fleshy scale. Ovary free, 1-celled (in Pseudobotrys, Gonocaryum and Citronella 2-celled with an empty tube-like unilateral cell) (in Mai.); ovules 2 (rarely 1 abortive), apical, pendent, anatropous, apotropous, unitegmic; style 1 or none; stigma punctiform, subcapitate or peltate, entire or slightly 2-5-lobed or -crenate, often depressed to one side. Drupe ellipsoid to globose, often laterally compressed and almond-like; exocarp generally thin-fleshy; endocarp thin-crustaceous to thick-woody, sometimes spongious or fibrous, often veined or ribbed lengthwise or reticulate-lacunose outside, smooth or with tubercles or blunt aculei inside, the seed pitted then. Seed 1, exarillate, generally with abundant endosperm, which rarely is ruminate; embryo straight; cotyledons whether or not foliaceous. Distribution. About 56 genera with c. 300 spp., all woody, predominantly in the tropics, rapidly decreasing in number towards the subtropics; 5 genera with part of their species in the temperate zones of Africa, Asia, Australia and S. America.

Description: Trees, shrubs, lianas, very rarely herbaceous (extra-Mal.); twigs often lenticellate and nodes with gland fields; spines very rare (extra-Mal.). Stipules absent. Leaves simple or mostly compound (digitate or impari-1-4-pinnate), (in Mal.) decussate, rarely in whorls of 3-4, often provided with glands underneath, in the New World often provided with terminal tendrils, rarely scattered or in pseudo-whorls (extra- Mal.); domatia sometimes present (fig. 8b, 23h). Inflorescences bracteate, cymose, but not rarely thyrses contracted to racemiform or racemose inflorescences, or even reduced to solitary flowers (extra-Mal.), terminal, axillary or from the old wood. Pedicels mostly with 1-2 bracteoles. Flowers usually very showy, rather large, bisexual, articulate with the pedicel or not. Calyx connate, closed in bud and later (not rarely irregularly) splitting into lobes, or cupular, or spathaceous, or lobed from the beginning and with equal or unequal, valvate lobes, developing earlier than the corolla, often glandular outside and inside with water and slime producing glands and hydathodes, persistent or circumscissile caducous along an abscission line. Corolla sympetalous, campanulate, tubular, funnel- or salver-shaped, mostly zygomorphic, lobes equal or unequal, valvate or imbricate in bud, tube often with a narrow cylindrical (constricted) lower part (basal tube) and a widened upper part (upper tube). Stamens 5 almost equal, or mostly 4 didynamous, the 5th sterile, rudimentary, adnate to the corolla tube, mostly inserted at the rim of the basal tube and not rarely (glandular) hairy at the insertion, more rarely inserted higher up. Anthers basifixed, 2-celled, rarely one cell barren or 1-celled, introrse, dehiscing lengthwise, usually the anthers connivent in pairs; anther cells often free and divergent, connective not rarely produced. Disk intrastaminal, mostly annular, rarely absent. Ovary superior, 2-celled, rarely 1- or 4-celled (extra-Mal.); style filiform, stigma usually 2-lipped, sensitive. Ovules (in Mal.) in each cell on the septum in two or more rows of 3-~, mostly on 2 placentas. Capsule 2-valved, either loculicid with the septum perpendicular to the valves — sometimes provided with an additional transverse false septum — or septicid with the septum parallel with the valves, or (extra-Mal.) an indehiscent, 1-celled, soft or hard-shelled, pulpy berry. Seeds in each cell attached to the dissepiment in one or more rows, inserted transverse to axis of fruit, anatropous, mostly on both sides with hyaline wings; embryo exalbuminous, the cotyledons mostly notched, sometimes on both sides. Germination always epigeal. Distribution. About 120 genera and some 650 spp., mainly in the tropics and subtropics, roughly between 40° N and 30-35° S, very few in the warm-temperate zone; in Malesia: 14 native genera of which 2 are endemic, viz Hieris in Penang and Lamiodendron in Papuasia. Among the remaining 12 one occurs through the Old World (Dolichandrone), 7 are shared with continental SE. Asia (two of which extend also to Africa and Madagascar: Fernandoa, Stereospermum) and 4 with Australia and Melanesia; the latter occur in Malesia only in the east except Deplanchea which ranges westward to Sumatra.

Description: Perennial waterplants with a tuberous, elongate or cylindrical and often branched rootstock or rhizome which produces a tuft of leaves and the inflorescences. Leaves submerged and/or floating (very seldom emerged), with a mostly distinct midrib and one or more pairs of parallel main nerves, connected by numerous cross-veins. Inflorescence long-peduncled, emerging above the water surface, in bud enveloped by a caducous or rarely persistent spathe, composed of 1 (in Mal.) or 2-11 spikes. Flowers (in Mal.) bisexual, spirally arranged, turned towards all directions. Tepals 2, mostly persistent, rarely caducous. Stamens 6, in 2 whorls. Ovaries 3(-4-5), free, sessile, narrowed into the style with a stigmatic ridge on the inner side; ovules 2-8 per carpel. Fruits with a mostly distinct, lateral or terminal, often curved beak. Seeds without endosperm; testa mostly a single envelope, sometimes, however, split into two envelopes, the inner one, brown and closely fitting the embryo, the outer loose, transparent and reticulately veined; embryo with the plumule fitting in a groove or not, or without plumule (the embryos of all species with a double testa seem to have no plumule). Distr. About 40 spp. described, from Africa (Ethiopia to the Cape), Madagascar, India & Ceylon, through SE. Asia (to c. 30° NL) and Malesia to SW., N. and E. Australia (to 34° SL), centering in Africa and Madagascar.

Description: Trees, shrubs or perennial or annual herbs. Leaves simple, opposite and decussate (Mal. spp.), entire (Mal. spp.), sessile to shortly petioled, often with ± translucent and sometimes black or red glandular dots and/or lines. Stipules 0. Inflorescences terminal and sometimes axillary, very rarely axillary only, cymose to thyrsoid or rarely racemose, bracteate at least initially, 1-~-flowered. Flowers bisexual, actinomorphic, homostylous or heterodistylous. Sepals 5 (Mal. spp.), free or ± united, imbricate, entire or with margin variously divided and often glandular, lamina glandular like the leaves, usually with greater proportion of glands linear rather than punctiform, persistent (Mal. spp.). Petals 5 (Mal. spp.), free, imbricate (contorted), alternisepalous, entire or with margin variously divided and often glandular, lamina usually glandular like the leaves, sometimes with nectariferous basal appendage, glabrous (Mal. spp.), caducous or persistent. Stamen fascicles 5 (Mal. spp.), epipetalous, free or variously united, each with 1-~ stamens; filaments variously united or sometimes apparently free, the free part usually slender; anthers 2-thecal, dorsifixed, often with gland terminating connective. Staminodial fascicles 3 or 0 (Mal. spp.), when present alternating with stamen fascicles. Ovary 1, superior, 5—3-celled or 1-celled with 5-2 parietal placentas; styles 5-3 (2), free or ± united, ± slender; stigma punctiform to capitate; ovules ~-2 on each placenta (Mal. spp.), anatropous, horizontal or ascending. Fruit capsular (Mal. spp.), dehiscing septicidally or loculicidally. Seeds ~-1 on each placenta, sometimes winged or carinate; embryo cylindric, straight or curved, with cotyledons longer to shorter than hypocotyl; endosperm absent. Distribution. There are 7 genera with c. 550 spp., cosmopolitan except for Arctic regions and most of Polynesia, but only Hypericum and Triadenum occur outside the tropics and immediately adjacent areas. Of the three tribes, the Vismieae (3 genera) occur in Africa (including Madagascar) and America, the Cratoxyleae (3 genera) in Madagascar, Indo-Malesia, E. Asia and NE. America, and the Hypericeae (Hypericum) throughout most of the range of the family except for most lowland tropical areas. In Malesia only two genera are present: Cratoxylum BL. and Hypericum L.

Description: In this paper the new species Myxarium crystallinum is described and its relationships with Tremella grilletii and Sebacina sphaerospora discussed. The two latter species are transferred to the genus Myxarium Wallr. An account of a third British gathering of Tremiscus helvelloides is given, together with a detailed review of its world-wide distribution, since it is one of the species included in the European Mapping Scheme for fungi.

Description: Annual or perennial, often grass-like herbs, only the monotypic African genus Microdracoides tree-like; the perennial spp. with short- or long-creeping, mostly sympodial rhizome not rarely emitting stolons. Stems solid, exceptionally hollow, sometimes septate, often trigonous, more rarely 2-sided or terete, or 4-, 5-, or multangular, usually nodeless below the inflorescence. Leaves often 3- ranked, more rarely distichous or polystichous, basal and/or cauline, usually sheathing at the base, the sheaths closed (in Mal.), very rarely open, the blades as a rule sessile, linear (grass-like) or setaceous, rarely lanceolate and petioled, rarely much reduced or even absent; sheath and blade whether or not separated by a rim of short hairs or by a membranous ligule almost completely fused to the upper surface of the blade. Flowers simple, inconspicuous, each subtended by a bract (glume), arranged in small spiciform units (spikelets), in subfam. Caricoideae strictly unisexual, in subfam. Cyperoideae tribe Hypolytreae composed of monandrous lateral ‘flowers’ and a terminal ovary, in tribe Cypereae reduced to bisexual synanthia, a few of which may be functionally male or female by abortion of the other sex. Spikelets often (always?) cymose (‘pseudo-spikelets’), (1-) few- to many-flowered. Inflorescence paniculate, anthelate, capitate, or spicate, with few to many spikelets, rarely reduced to a single spikelet, often subtended by 1-several leafy involucral bracts, Perianth consisting of bristles, hairs, or scales, but often absent. Stamens often 3, not rarely reduced to 2 or 1, very rarely more than 3 to numerous; filaments ligulate, free, only in a few Carex spp. connate, sometimes strongly elongating after anthesis; anthers basifixed, introrse, opening lengthwise by a slit. Ovary solitary, superior, usually 2- or 3-carpellate, unilocular; style not rarely thickened at the base, the thickened part whether or not articulated with the ovary; stigmas 2 or 3 (rarely more), only in a few spp. style unbranched; ovule solitary, erect from the base of the ovary, anatropous. Fruit indehiscent, a nut (often termed achene), sessile, or seated on a disk, free, or surrounded by a modified prophyll (perigynium, utricle). Seed erect, with thin testa not adhering to the pericarp; embryo small, at least partly surrounded by abundant mealy or fleshy endosperm. Dist ribution. About 70-80 genera with probably some 4000 spp., throughout the world.

Description: In the former century Byblis was mostly included in the Droseraceae, for example by BENTHAM & HOOKER. f. (Gen. P1. 1, 1859, 220); even ENGLER had it in that position in 1912 (Syllabus ed. 7, 329). PLANCHON had in 1848 (Ann. Sc. Nat. III, 9, 1848, 80, 90) already pointed to affinity with Cheiranthera of the Pittosporaceae; HALLIER f. merged Byblis and Roridula with Tremandraceae, curiously referring this to an Ochnaceous assemblage (Abh. Gebiete Naturw. Hamburg 18, 1903, 53). About the same time LANG argued (Flora 88, 1901, 179) that on morphological and anatomical grounds Byblis cannot belong to Droseraceae, but should be referred to Lentibulariaceae. DIELS (Pfl. R. Heft 26, 1907, 51) and DOMIN (Act. Bot. Bohem. 1, 1922, 1) definitely concluded to the alliance with Pittosporaceae, and so did HUTCHINSON (1926, 1959) and SCHULTZE-MENZ (Syllabus 1964): resemblance with Drosera is superficial, sympetaly unimportant. HALLIER f. and HUTCHINSON include the S. African genus Roridula also in the family Byblidaceae, but others regard this as an allied family.

Description: Newly discovered mycorrhizal relationships of boletes (with Nothofagus, Shorea, Quercus humboldtii, Alnus jorullenses, Eucalyptus, and Leptospermum) are discussed. Type studies on Fistulinella, Boletus granulatus var. capricollensis, Boletogaster, and Gastroboletus are reported. The following new combinations are proposed: subsections Pictini and Spectabiles in sect. Solidipes of Suillus; Suillus ochraceoroseus; Chalciporus piperatus, C. rubinus, C. rubinellus, and the new section Eximia of Leccinum, with L. eximium (Peck) Sing. The interpretation of Porphyrellus pseudoscaber on the basis of topotypical material is indicated.

Description: The ascomycete Anixiopsis peruviana Cain is transferred to a new genus Xanthothecium v. Arx & Samson. The name Leucothecium emdenii v. Arx & Samson, gen. nov., spec. nov. is proposed for a soil-borne fungus with light coloured, smooth cleistothecia, catenulate asci, lenticular ascospores and an arthroconidial state. The relationships of both genera are discussed.

Description: A general consideration is given on various aspects of the taxonomy of Operculate Discomycetes. The thesis is advanced that the genus, rather than the species, may represent the basic evolutionary unit. More detailed considerations are devoted to a few topics, for instance to the systematic position of the genera Cyttaria and Medeolaria.

Description: De in Nederland waargenomen soorten van Taraxacum uit de sectie Spectabilia Dahlst. zijn: T. anglicum Dahlst., T. euryphyllum (Dahlst.) Christ., T. hygrophilum v. S., T. johannis-jansenii v. S. en T. nordstedii Dahlst. Op de kaartjes is hun verspreiding weergegeven, in hoofdzaak berustend op gegevens van na 1950 (fig. 1, a—d). Zou men de oudere gegevens daaruit weglaten, zo zou het beeld dat de kaartjes bieden niet noemenswaard worden beïnvloed. Bij de steeds verder schrijdende cultuurmaatregelen worden deze, op natuurlijke standplaatsen groeiende soorten ernstig bedreigd. Volledigheidshalve zij vermeld dat nog twee nieuwe soorten uit deze sectie te zijner tijd in de Acta Botanica Neerlandica zullen worden gepubliceerd: T. duvigneaudii v. S. (Gouda-Waddinxveen) en T. zevenbergend v. S. (Hijzen bij Moergestel en Houtakker bij Tilburg).

Description: In 1960 I made a preliminary analysis of the floristic distribution of the native Phanerogam genera of the Pacific islands, which amounted to 1511 genera in all. The aims of the present work have been to record these more accurately and more critically in detail, especially with regard to native versus introduced, to complete the survey with new records from new explorations made during the interval, and to evaluate new taxonomic literature on Pacific genera. The present list amounts to a total of 1666 genera, as far as known in July 1969, listed in an Appendix. The floristic relationships of the Pacific islands and the surrounding continental areas are established and a hierarchical subdivision of the flora of the Pacific islands based on demarcations in it is made. Furthermore a nomenclatural stabilization of the names and ranks of the subdivisions is attempted. Chapter IV, 3. An attempt was also made to find factual data on the correlation between distribution and means of dispersal. Chapter IV, 4. Secondary aims were to review earlier attemps towards a subdivision of the Pacific flora (Chapter II), two other secondary purposes to see whether traces of the historic plant-geography of the Pacific flora are still reflected in the present flora (Chapter V), and finally to compare geographic subdivisions and other data from non-Phanerogam taxa, mostly animals, with floristics. Chapter VI. Chapter III is devoted to an explanation and a discussion of the methods employed. Arguments are given why only Phanerogams have been considered and why only native genera have been used for computing results. Chapter III, 1—2. Arguments are given for employing the genus as a working unit. It is shown that the genus is much less susceptible to variability in taxonomic concepts than either the species or the family. Besides it is comparatively easy to establish the distribution of a genus fairly reasonably from literature. Chapter III, 3. Chapter III, 4 is devoted to a discussion on the sources of information on which this work is based, comprising i.a. literature, herbarium collections and personal information. Many errors are contained in the first two of these and it cannot be avoided that some mistakes have not been detected. Also, the island groups have been investigated with a varying degree of intensity. The island groups in the Pacific are taken as geographic units of which there are 36. The surrounding land masses are divided into 12 main areas. Chapter III, 5. Of each genus occurring in any of the 36 Pacific unit areas the full distribution is traced. See Appendix. From a comparative study of generic ranges, it has appeared that they exhibit a restricted number of recognizable patterns, 17 of which have been distinguished. These I have called distribution types in this work. Chapter III, 6. The choice of geographic unit areas introduces a certain element of arbitrariness. Each island group can then be characterized by its set of distribution types: the distribution types spectra. It is also possible to calculate floristic relationships or resemblance between the island groups, for which a number of methods are discussed and evaluated. It appears that basically all methods lead to more or less similar conclusions. Chapter III, 9. As a test for the validity of the conclusions based on the distribution of all genera, similar calculations were performed on 345 revised or otherwise well-known taxa. Although the percentages of the distribution types are slightly different the general conclusions are corroborated. Chapter III, 7. In addition, an attempt has been made to find whether there is a correlation between the distribution and the means of dispersal of these revised or otherwise well-known taxa. Chapter III, 8. One of the most important results of this work is the census of Pacific genera. See Appendix. By using the method of distribution types spectra, demarcation knots and other methods it has been possible to find demarcations and to define phytochores. The main demarcation is that between the New and Old World floras. A hierarchy is set up of subdivisions which is illustrated in fig. 35 and tabulated in table 6. It appears that a strong demarcation exists between the islands on the American side of the Pacific (Galapagos, Juan Fernandez, etc.) and the western islands. Hawaii and SE. Polynesia form the easternmost frontier of the OldWorld flora. This conclusion was reached almost unanimously by all phytogeographers, one of the earliest being Engler after whom I have proposed to name this demarcation: Engler’s line. In the W. Pacific Bonin in the north and New Zealand and adjacent islands in the south show a sharp demarcation from the rest, Bonin forming part of the E. Asiatic region, and New Zealand forming a distinct subregion of the Australian. New Caledonia cannot be satisfactorily placed. It shows relations with New Guinea, Queensland and the Pacific in about equal measure. Besides it abounds in endemics, some of which are highly peculiar in various aspects. The remaining part of the Pacific shows an essentially Malesian character, decreasing in strength from west to east. The New Hebrides with Fiji, Samoa and Tonga form a subprovince as does SE. Polynesia, Hawaii is considered a separate province of the Malesian subregion. Unlike the islands west of Engler’s line the American Pacific islands show very little mutual floristic alliance, but they all have a characteristic American flora. Comparisons with subdivisions and demarcations of other groups of organisms show that often, but not always, the same barriers are respected by unrelated groups. My data give certain indications about the past but no attempt has been made to correlate the conclusions with contemporary geological theories. The regularity of distribution patterns, the close floristic alliance among the islands west of Engler’s line independent of their distance from each other, combined with the fact that dispersal spectra show no clear correlation between distribution and ‘dispersibility’, suggests an old relictual character of the flora rather than a young one built up by random long-distance dispersal. This applies especially to the W. Carolines, the Melanesian islands, Lord Howe I. and New Zealand, i.e. islands more or less within the Andesite line, which are much richer and contain many poor dispersers. For Hawaii also a better accessibility in the past seems indicated. The regular decrease in the number of taxa in proportion to their distance from source areas is discussed. An attempt is made to explain the phenomenon. A tentative conclusion is reached that impoverishment and other phenomena attributed to oceanic islands are not restricted to these. A large scale comparative study of continental and island floras is needed.

Description: In January 1971 Dr. Simon Jan van Ooststroom, senior botanist of the Rijksherbarium, retired on reaching the age of 65, having been on the staff since November 1934. Though this event will to a certain extent change, but not interrupt, his work, it is nevertheless worth commemorating, as he has so many contacts at home and abroad, all of whom have profited from his wide knowledge which he shared freely. He was born in Rotterdam in 1906, where he received his primary and part of his secondary education. He completed the latter in Schiedam and entered the University of Utrecht in 1924. He became the assistant of Prof. Dr. A. Pulle in January 1927. By chance he became interested in the genus Evolvulus and this led him to compose an excellent world monograph of this genus for which he was awarded his doctor’s degree in 1934 and which furthermore caused a life-long interest in the bindweed family, on which he became a most reliable authority, especially for the Indo-Australian region. Many papers emanated from these studies, culminating in his treatment (assisted by Dr. R. D. Hoogland) of the family in Flora Malesiana (1953).

Description: Merrill (Philip. J. Sc. 2, 1907, Bot. 284) based Mearnsia on specimens collected from Mount Halcon in the Phillipines and dedicated the genus to Major Mearns who accompanied him on the expedition. Merrill described the flowers of the sole species (M. halconensis) as 4-merous with 8 stamens and 2 carpels and the capsule as dehiscing by ‘a single slit at the apex only and inside the persistent calyx tube’.

Description: A peculiar structural detail, occurring during the development of ovules, seems to have passed almost unnoticed till the present day. It concerns the distal rim of either the outer or the inner integument, which appears to be slightly lobed in the ovules of several unrelated plants. In a recent note (1970) I called attention to this feature. It is known from Juglans and Platycaria (Warming, 1878; Leroy, 1955; Boesewinkel and Bouman, 1967), where the single integument is two-lobed. Warming mentioned two more cases, namely Lagarosiphon and Symplocarpus; however, I cannot confirm his observations from dried material. I noticed it myself in Scyphostegia horneensis, in Caloncoba welwitschii, and in Sterculia alexandri. In these three species the lobes occur at the rim of the outer integument. To these can now be added Hernandia peltata. However, in that species the lobes occur at the rim of the inner integument.

Description: The new scheme of classification presented in this paper is based on the examination of all species in the family Thelypteridaceae which I have been able to trace in the Old World. I have gradually compiled a list of about 700 names (basionyms) and have examined type or other authentic material of all but a small proportion; and in the course of study of specimens in many herbaria I have noted about another 50 species which appear to be undescribed. I have attempted to re-describe all the previously-named species, noting characters not mentioned in existing descriptions, especially the detailed distribution of hairs and glands, including those on the body and stalk of sporangia, and characters of spores. It is probable that there remain some published names, not yet detected by me, which refer to species of the family, but I think there are not many. I have also made a study of all generic and infrageneric names which are typifiable by species of Thelypteridaceae, and in doubtful cases I have tried to clarify and fix the typification. As already reported in the second paper of this series (Blumea 18: 195—215), I have had the help of Dr. U. Sen and Miss N. Mittra in examining anatomical and other microscopic characters of some type species, and hope to present further information of this kind later.

Description: Until now three species of apetalous Hamamelidoideae have been reported from Taiwan (Li, 1963): Distylium gracile Nakai, Distylium racemosum Sieb. & Zucc., and Sycopsis formosana (Kanehira) Kanehira & Hatusima (close to or identical with S. sinensis Oliver). A list of the specimens of the Herbarium of the National Taiwan University, Taipei (TAI), kindly sent by Prof. Ch. E. DeVol (Oct. 3, 1970), contains the same three species.

Description: On 29 July 1974 dr. J. H. Kern died at the age of 70. At the occasion of his official retirement from the Rijksherbarium staff (January 1969) Van Steenis and Van Ooststroom gave due recognition to his achievements in tropical botany and to his share in the progress of the knowledge of the Dutch flora. There is no need to repeat here what was written at that time (Blumea 17, 1969, 1—3 and Gorteria 4, 1968, 69—72). After his retirement he was appointed honorary collaborator of the Rijksherbarium and at first he continued his work more or less as usual. However, his health soon became worse and his deteriorating eyesight prevented him from working with the microscope. Consequently, he could not finish the revision of Carex and Uncinia for Flora Malesiana, the only genera which still were missing from his manuscript. It was decided that the family would be published without these genera; the unfinished manuscript will be left to another botanist to be put into final shape. Together with professor Van Steenis he made the manuscript ready for the press, but only some days after a first copy had been received from the printers, Jan Kern suddenly died.

Description: After the completion of my revision of Lepisanthes (Blumea 17, 1969, p. 33—91) I paid a visit to the herbaria at London (BM) and Kew (K). This led to a few alterations and additions, the main of which are the following.

Description: As explained in Takhtajan’s preface this book is not a mere translation of his ‘The origin of Angiospermous plants’ (1961, in Russian), but an entirely new book. I find this true and not true. Comparing it with the Origin (1958 translation of the 1954 Russian version) the essence of the new book was there given in a nutshell. In size, chapter subjects, argumentation, and bibliographic documentation, the work is very much extended and it makes very interesting reading indeed. The sequence of the chapters is logical, almost always leading to distinct synthesis. Properly it is a critical commented survey of many opinions — Takhtajan being clearly in complete command of the huge literature on the subject — but from which the author follows his own line of choice and judgement, accepting or rejecting with brief but clear comments. The whole argumentation is admirably concise and rouses admiration for covering this vast subject, comprising taxonomy, plant distribution, morphology, palynology, genetics, population dynamics, flower biology, anatomy, paleozoology, etc. Major questions are embodied in subsequent paragraphs: polyphyletism is rejected; ancestors must be sought among heterosporous ferns or fern-like plants followed by pteridosperms and certain gymnosperms, although direct ancestors cannot be indicated; the basal flower type of angiosperms was bisexual. Takhtajan attaches great importance to occurrence of plants in small populations, especially in mountain plants, facilitating chance variations and genetic drift, rapid spread of mutant genes, which is important for evolution. This entails that missing links are almost never fossilized. Micro-evolution is equalized with macro-evolution. Neoteny (on which Takhtajan devoted a former work) can lead to despecialisation through which phenotypic simplification the complexity of the genome remains intact; it may provide for a maximum phenotypic effect by a minimal genotypic change. Primitive wood structure of early Winteraceous angiosperms is understandable by neotenic origin. Evolution of angiosperms was not only rapid, but also discontinuous as a result of neoteny. Developing in the mountains ‘in many ..... small ..... populations ..... the earliest angiosperms found themselves under conditions most favourable to evolutionary radiation. And if we bear in mind that their evolution was closely tied to the evolution of insects and was based on the complex and peculiar mechanism of mutual selection, then the extraordinary speed of their initial differentiation becomes even more readily understandable.’ Protection of the ovules arose as a selection against damage by ‘early pollinating insects’; this made simplification of their structure possible which led to smaller ovules (loss of thickened integuments, sclerotesta, etc.) and enabled the angiosperms to observe the greatest economy of material in construction of the ovules and ♀ gametophyte, and it also made possible the perfection of the process of pollination. ‘The acquisition of the stigma was undoubtedly a very great event in the evolutionary history of seedplants.’ ‘The primitive insects searched for pollen (beetles), nectar searching ones were a further perfection; this again led to a very great advance in cross-pollination; and as a corollary to a greatly increased rate of evolution, which still continues.’ ‘Isolation of a population is well known to be a prelude to the formation of a new species.’ The question of the hypothetical reconstruction of the first flowering plants is approached by the ‘hypothetico-deductive method’. Knowing the basic evolutionary pathways of angiosperms and the main lines of specialisation of their organs and tissues, we may by extrapolation extend these lines mentally into the past to the lowest possible level of specialisation’, but somewhat further on he writes ‘This reconstruction of the ancestors of the living angiosperms depends on the truth of the assumption that they combined in one plant all the most archaic characters that are now found distributed among the living fossils.’ I have italicized in the citations two words that are in contradiction; furthermore I would like to point out that whereas each plant we know possesses both primitive and derived characters, we cannot make an exception for an ancestral plant; one which would contain all the archaic characters must logically be an idealized fiction.

Description: Since Hornemann (Fl. Dan. 9, 1816, p. 3, pl. 1501) published the name Zostera marina var. angustifolia together with a very poor drawing and the extremely short diagnosis ‘foliis subenerviis’ several interpretations of the identity of this taxon have been given. Some authors regarded it as a separate species closely related to Z. marina L., e.g. Reichenbach (1c. Fl. Germ. 7,1845, p. 3, as Z. angustifolia), and Tutin (J. Bot. 74, 1936, p. 227—230, as Z. hornemanniana). Others thought that it was a hybrid between Z. marina and Z. noltii Hornem., e.g. Ascherson (in Boissier, Fl. Orient. 5, 1882, p. 25), Prahl (Krit. Fl. Schlesw.- Holst. 2, 1890, p. 211), and Rouy (Fl. Fr. 13, 1912, p. 290, as Z. hornemanni). Recently I myself expressed the opinion that Hornemann’s variety was merely a brackish-water form of Z. noltit (Den Hartog, Sea-grasses of the world, 1970, p. 68). Thanks to the kindness of Mr. A. Hansen I was able to study two sheets of original material of Hornemann’s taxon and as a result all the above-mentioned interpretations can be ruled out. One of the two sheets is marked ‘cotypus’ and is labelled ‘Zostera marina angustifolia, e sinu Othiniensi, Hornemann’, the labelling in the characteristic handwriting of Prof. J. W. Hornemann himself. The specimens mounted on this sheet are all extremely narrow-leaved Z. marina. The specimens on the other sheet are very similar, and were collected from the same place; the labelling, however, is in the handwriting of N. Hofmann Bang, who was a close friend of Hornemann and owned the manor Hofmannsgave near the type locality.

Description: Rumphius (Herb. Amboin. 3, 1743, 19, t. 7) was the first to use the name Metrosideros, but of the 6 species he listed only the first, M. vera, belongs to the Myrtaceae. The same species is assumed to be the basis of Nani Adanson (Adanson, Families des Plantes 2, 1763, 88). Adanson did not list any species, but the assumption is based on the description and the fact that Rumphius had given the vernacular name of his Metrosideros vera as ‘Nani tree’.

Description: In April 1969 I paid a visit to Ceylon for a week, allowing me to study for the first time the collections of the Department of Agriculture, Peradeniya (PDA), including Thwaites type specimens. My stay was made possible through the Smithsonian Flora of Ceylon Project. The study of Thwaites’ type material revealed some new facts affecting the synonymy of Ochna jabotapita L. and O. obtusata DC. It had previously come to my attention that materials distributed as O. moonii Thw. under number C.P. 1224 belonged to either O. obtusata (BM, BO) or O. lanceolata Spreng. (K, P) (see also the note on page 26 of my revision). I subsequently found that all three species of Ochna in Ceylon were represented on the sheet in PDA, obviously bearing Thwaites’ holotype. From this and accompanying sheets it is clear that the material belonging to O. jabotapita should in fact be designated as the holotype of Thwaites’ species. Consequently, the whole paragraph under O. moonii on page 30 of my revision should be transferred from the synonymy of O. obtusata to that of O. jabotapita. The phrase ‘excl. syn. O. quarrosa L. sensu Moon = O. jabotapita L. ’should be deleted. The type should be referred to as C.P. 1224 p.p. (PDA p.p. holo).

Description: A comparison of the structure of the flowers of various genera of the tribe Passifloraceae-Passifloreae supported the view of staminodial origin of the disk. The East African genus Schlechterina is kept separate from the West African genus Crossostemma. The genus Efulensia from Equatorial Africa is recognized beside the Madagascan genus Deidamia. Revised key to the genera of the Passifloreae, together with short descriptions.

Description: A massive, expensive book, principally an atlas of small botanical drawings (line drawings, c. 10 by 6 cm, two to a page), each provided with the Latin and vernacular name, a concise 2—4 line descriptive note, and the use of the plant. A similar text is added in Japanese. Most pictures are reproduced at ½ nat. size. Species are arranged alphabetically within the families which are in turn arranged according to the Englerian system. Only Gymnosperms and Angiosperms are included. Prof. Corner is responsible for checking the names and the brief descriptive notes. The pictures were drawn by Prof. Watanabe during World War II for the Japanese Military Administration at the Singapore Botanic Gardens. Two volumes of these drawings were already published in small octavo in 1945 at Singapore, one on Medicinal Plants, the second on Edible Plants. A selection of some 200 plates was also later published by Prof. H. B. Gilliland in his ‘Common Malayan Plants’ in 1958 (University of Malaya Press, Singapore). The present work embraces all pictures made by Prof. Watanabe, many unpublished before, with addition of a number not made at Singapore, amongst them several of rare parasitic and saprophytic species from Borneo and Celebes, Pandanus from New Guinea, and other interesting odds, even from Japan, the Bonins, etc.

Description: The pollen morphology of all 7 species of the genus Crossonephelis was studied and found to be rather uniform, supporting Leenhouts’ circumscription of the genus. Minor inter- and intraspecific differences are present. Within Lepisantheae a close resemblance exists with the pollen of some species of Placodiscus, while the pollen of Lepisanthes is less similar and specialized in a different direction.

Description: The pollen morphology of 18 out of 22 species of the genus Lepisanthes, as recently revised, was studied. General pollen morphology is rather uniform, but taxonomically significant differences exist in shape, relative length of ektoapertures, endoaperture development, and in the sculpture of the tectum. Detailed descriptions are presented and special attention is given to intraspecific variability. 10 Pollen types are recognized, most of which are linked by transitions. Morphological trends are established and the extent to which they indicate natural relationships is evaluated. In subgenera Lepisanthes and Erioglossum a less evolved but more variable pollen morphology is present, while in subgenera Otophora and Aphania derived pollen types occur, which agrees well with macromorphological evidence. Subgenus Erioglossum appears pollenmorphologically closely related to subgenus Lepisanthes. Subgenus Aphania can, both macro- and pollenmorphologically, be derived from subgenus Otophora. Within Lepisanthes tetraphylla close parallels exist between macromorphological and palynological interpretations of natural affinities between the numerous races. Lepisanthes fruticosa, in contrast, shows on both counts rather wide and continuous intraspecific variability. Also in Lepisanthes senegalensis continuous pollenmorphological variability is present, but here a clinal pattern can be detected. In general, geographically isolated or endemic forms in Lepisanthes show a tendency to develop deviating pollen types.

Description: This work is the first of its kind in so far that it gives an account of the chemotaxonomy of a large family of plants and its implications on the taxonomy of that family. The ideas for this book were derived from a symposium, to which all the 19 authors contributed, ‘The Comparative Biochemistry of the Leguminosae’, which was held at the John Innes Institute, Hertfordshire. The first chapter, by V. H. Heywood, gives a ‘Systematic Purview’ of the family. Chapter 2—14 provide a description of the known distribution of both low molecular weight and macromolecular constituents. In several chapters the methods used are also extensively discussed. Often the information of the various chapters has been obtained by workers belonging to other disciplines than taxonomy, and little attention has been given to taxonomic methods. Several of the chapters lack a summary and a discussion of the taxonomic implications.

Description: Only two species of Gastonia occur in Malesia, but each has a complex taxonomie history. The species which became known first, G. papuana Miq., is evidently an uncommon plant of coastal and lowland forest, but with a very wide range. It has been collected only once, or at most a few times, from each of many islands of the Malayan Archipelago and once from the mainland of the Peninsula. Most of these collections were made in the nineteenth or early twentieth centuries. Only in western New Guinea has this species been collected in more recent times within our area. The distribution of this species shows several disjunctions, the most striking being that between West Irian and its only known locality in the extreme east of the Solomon Islands. It is interesting that this gap corresponds with the distributional range of the second species, G. spectabilis (Harms) Philipson, which overlaps that of G. papuana only in the west of New Guinea (fig. 1). The widely dispersed range of G. papuana has resulted in its being described as several distinct species from different parts of its range. It was first named in 1863, when three names appeared in two genera. Miquel (1863) applied the names Tetraplasandra paucidens and Gastonia papuana to this species, and Teysmann and Binnendijk (1863) described it as Tetraplasandra eupteronoides. I am grateful to Professor van Steenis for information on the sequence of publication of these names. Miquel’s publication was issued on 2 July 1863 (Stafleu, 1967). A report in volume 27 of the ‘Natuurkundig Tijdschrift voor Nederlandsch Indië’ states that volume 25 was issued in six instalments, the first of which appeared in 1862. The five remaining parts appeared in 1863. Professor van Steenis has examined the publication and concludes that page 416, on which the name T. eupteronoides appeared, belongs to the final instalment, and must therefore have been issued late in 1863, and in any event later than July. For this reason, Miquel’s names take precedence over that of Teysmann & Binnendijk. Of Miquel’s two names, I have chosen to use that which he placed in Gastonia. In this way the need for a new combination is avoided. As can be seen from its synonymy this species was described from other islands by subsequent authors.

Description: In the Cyclopaedia of Malaysian Collectors and Collections, Mrs. M. J. van Steenis-Kruseman (Flora Malesiana I, I, 1950, 248a, 527b) stated that plants of Herb. Houttuyn, which Houttuyn had acquired from various collectors, were subsequently incorporated in other herbaria, that of Burman in particular. Merrill had questioned this in his work on Houttuyn (J. Arn. Arb. 19, 1938, 291—375, reviewed in Fl. Mal. Bull. no. 17, 1962, 906), as he could not locate a single sheet of Houttuyn’s collection. He only mentioned (l.c.p. 310) that in the Copenhagen Herbarium, in Herb. Vahl, there would be a fragmentary specimen of Myristica fragrans on the back of which was noted ‘ded. Houttuyn’. We could not find this photographed in the IDC microcards of Herb. Vahl.

Description: A subdivision of the pollen types encountered in Lecythidaceae is proposed. The presence of a demarcation line between an original colpate and a derived syncolpate pollen type is confirmed. The significance of pollen characters for taxonomic subdivision is evaluated and it is concluded that the subdivision proposed by Niedenzu in 1892 agrees best with the pollen evidence. Pollen morphology does not yet provide any clear indications of wider affinities of the family, except in a negative sense.

Description: In the herbarium in Kiel the holotype of Sphacelaria paniculata was located. Australian material, known under the names Halopteris hordeacea (Harvey) Sauv., H. spicigera (Aresch.) Moore or H. gracilescens (J. Ag.) Womersl. has as correct name Halopteris paniculata (Suhr) P. v. R. comb. nov.

Description: This book is an exploration into the field of Plant Morphology. It deals with the placentation of the ovules in ten families of Centrospermae — including the Cactaceae — and in the Primulaceae. The core is formed by a very close observation and a complete documentation of the histogenesis of the ovary wall, the septs, and the placentae in four Caryophyllaceous species. Furthermore, the result is compared with similar known and newly discovered features in other species and in the other families. It appears that the ovary is composed of a cup of sterile phyllomes which surrounds a central body. This central part is built up by two alternating sets of five axial placentae bearing the ovules. The septs grow from the cup inwards and fuse with the placentae and their ovules. The pattern of the vascular bundles is in full accordance with the histogenetic results. Variations on this theme occur in the other species and families, the ultimate stage in reduction being an ovary with a solitary terminal ovule. However, the Primulaceae do not fit in this scheme; they cannot be considered as Centrospermae.

Description: In continuation of a former study on the ‘Elevation Effect’ in the Swiss mountain flora (Backhuys, 1968), the distribution of six Taraxacum species in Switzerland was examined in detail. This was enabled by the preceding monographic study by J. L. van Soest (1969). The interesting point was to compare species of one genus with a common dispersal mechanism. Data on the vertical distribution are provided in table I and diagrams 1—6. It was found that all six species show an elevation effect which varies from 200—750 m. In five species this range is as narrow as 500—750 m. See table II. It is concluded that in spite of the very obvious dispersal mechanism (parachute-achenes) the species are apparently not capable to colonise ‘mountain islands’ the summit altitude of which is situated between the lowest known locality and the lowest mountain island on which the species concerned is found. These data support the view that the elevation effect is a plant-geographical rule of universal validity for mountain plants.

Description: Though the embryo provides one of the main generic characters of Haplolobus, up till now nothing was known about its germination or seedling (blastogeny). That is why the first author, when revising the genus Haplolobus (Leenhouts, 1972) contacted Mr. J. S. Womersley, Chief Division of Botany, Department of Forests, at Lae, Papua and New Guinea, and asked him for either viable seeds, or seedlings. We are very obliged to him and to the Department of Forests for providing us with both, including herbarium and spirit material of seedlings and a herbarium specimen of the parent tree. The latter was collected under nr. NGF 49210 (Henty) at Markham Point near Lae, and could be identified as Haplolobus floribundus H. J. Lam ssp. floribundus group A. The seedlings were collected 8 weeks after being sown in the Lae Botanic Garden; they were preserved under nr. NGF 49275. It is a pity that the seeds sown in the Botanic Garden at Leiden did not germinate.

Description: A historical survey of the family is followed by a discussion of the systematic position, the affinities within the family, the morphology, anatomy, phytochemical characters, flower biology, geographical distribution, dispersal, and growth. A key to the species is given. Each taxon has been described and provided with its full synonymy. All specimens have been cited except in those cases where more than 5 collections were made in one partial area (country, province, district, or small island). A complete identification list will be issued separately. In this revision of Taccaceae 1 genus and 10 species are accepted; 8 species are restricted to Indo-Malesia (SE. Asia to the Solomons), 1 to tropical South America, and 1 species occurs from the tropical west coast of Africa eastwards to Easter Island in the eastern Pacific. Two new species have been described, one from Borneo and one from the Solomons and New Guinea, and one new combination has been proposed. The genus Schizocapsa and a large number of specific names have been reduced. The species synonymy is considerable and comprises not less than 49 specific epithets. This situation is due to the fact that some widely distributed species have proved to be very variable. The material which I had at my disposal was considerably larger than previous workers, especially Limpricht, had in hand. As a result of this rich material numerous locally described species could no longer be maintained.

Description: Trifolium repens has been introduced purposely or casually in the mountains of Luzon and East Java; it has now also turned up in New Guinea. EAST NEW GUINEA. Morobe Dist., Wau Subdist., Edie Creek, bank over gold workings, growing in profusion, NGF 12152 A. N. Millar, 14 Aug. 1968.

Description: Dispela ripot i toktok long wok bilong Dr C. Kalkman na Mr W. Vink, bilong Rijksherbarium long Leiden, Holland, wantaim Mr A. N. Gillison na Mr D. G. Frodin bilong Division bilong wok long Botany, long Lae. Oli bin mekim dispela wok long yar 1966 long ol dispela pies klostu long Tari: mauden Ambua, mauden Ne, mauden Kerewa na wanpela pies istap namel oli kolim Ibiwara. Oli bungim ol plaua, ol lip bilong diwai na ol diwai; olgeta samting em oli bungim wantaim inap long 1,975. Bihain, bai oli salim ol dispela samting igo long ol masta long university or bigpela skul we oli wokim wanpela buk oli kolim Flora. Dispela ripot bai toksave long ol kain diwai i stap long bus na ol kain plaua antap long mauden. Ripot ia i pinisim lukluk long plaua, long lain oli kolim Ericaceae i stap long ol dispela ples na antap long mauden Giluwe, mauden Kubor na mauden Wilhelm. Mipela i laik tok tenkyu long ol pipal bilong Tigibi na Benaria em oli bin wok wantaim mipela.

Description: Taxonomic revision, precursory to the treatment of the Rosaceae in Flora Malesiana. Generic limits in tribus Sorbeae are discussed, Stranvaesia is included in Photinia (5 spp. in Malesia), Micromeles (1 sp. in Malesia) is treated as generically different from Sorbus. Apart from these, there are in Malesia representatives of Eriobotrya and Rhaphiolepis (both 1 sp.), and some more species are cultivated and occasionally naturalized. No new species are described. New combinations: Photinia serratifolia (basionym Crataegus serratifolia Desf., replacing illegitimate Photinia serrulata Lindl.), Photinia nussia (basionym Pyrus nussia D. Don, transferred from Stranvaesia), Rhaphiolepis philippinensis (basionym Eriobotrya philippinensis Vidal), Micromeles corymbifera (basionym Vaccinium? corymbiferum Miq., known as Sorbus granulosa (Bertol.) Rehd. or Pyrus granulosa Bertol.).

Description: A key is given to 7 species, 6 of which occur in Malesia. Of each the basionyms and a restricted synonymy are given, besides notes on their distribution. Rotala diversifolia Koehne, hitherto only known from Thailand, appears to occur in several localities in Malesia. A new combination, R. catholica (Cham. & Schlechtend.) B. van Leeuwen, is proposed for the American R. dentifera (A. Gray) Koehne, introduced in Luzon.

Description: The species at present known as Metrosideros elegans was the basis for Ballardia Montr., Mem. Acad. Lyon 10 (1860) 204. The later described species of the M. elegans group were placed in Metrosideros Banks ex Gaertn., Fruct. I (1788) 170, t. 34, and Beauvisage (1901) finally sank Ballardia in Metrosideros when he combined B. elegans Montr., Mem. Acad. Lyon 10 (1860) 205, with M. laurifolia var. minor Br. et Gris, Bull. Bot. Soc. Fr. 12 (1865) 300 under the binomial Metrosideros elegans. The group has remained in Metrosideros since that time. So far as is known the group is restricted to New Caledonia. The species may occur at quite low elevations, but are most common between about 300 and 1,500 metres altitude in forest or shrubland.

Description: It has been suspected for some time that Tetrameles nudiflora occurs in the Cape York Peninsula region of Queensland. The late Mr. L. S. Smith (Queensland Herbarium) referred some sterile specimens to this species, but, as far as is known, he never saw fertile material from Queensland. Mr. G. C. Stocker (Forestry and Timber Bureau, Atherton) collected good fruiting material of this species in the McIlwraith Ra. (13°50' S, 143°20' E) in November 1971 (Stocker 820). This appeared to be the first collection of fertile material. However, subsequent discussion with Mr. J. G. Tracey and Dr. L. J. Webb (Rain Forest Ecology Section, Commonwealth Scientific and Industrial Research Organisation) revealed that they had collected flowering material from large leafless trees in October 1968 at Claudie River (12°43' S, 143°17' E) and in October 1969 at McIlwraith Range and Rocky River ( Webb & Tracey 8230A, 9293A, and 9746A). Inspection of the Webb and Tracey specimens revealed that they were in fact Tetrameles nudiflora. Field evidence suggests that two of the suites of specimens, i.e. Webb & Tracey 9293A and Stocker 820, were from the same tree on the western slopes of McIlwraith Range. The specimens all agree with the description of Tetrameles nudiflora by van Steenis (Fl. Mal. I, 4, 1953, 385).

Description: From 1970 up to 1973 plankton sampling was executed as part of the “Cooperative Investigations in the Caribbean and Adjacent Rerions” (Cicar-project). For the stationlist one is referred to Van der Spoel & Koperdraat (1974). During the cruises 21-23, 27-29, 31-35 and 37-38 a 3 PK Stork/ Pelger vacuum pump was used for sampling. The samples examined in this study are all pump samples. The plankton collected from 4500 litre filtered water was settled during 24 hours. The volumina were divided into six classes: 0-0.5 ml; 0.5-2 ml; 2-5 ml; 5-10 ml; 10-25 ml and 25 ml. The colour of the samples was distinguished as green, red, white and brown. Slides made from subsamples showed that the red colour of the preserved samples stands for a high percentage (up to 93%) of zooplankton; green means that the sample consists mainly (78-94%) of diatoms with large volume, like Coscinodiscus species. The white colour is an indication of small diatoms and other phytoplankton, while the brown coloured samples contain more detritus (average 22.5%) than other samples. The results of the volume and colour measurements are presented in figure 2-12. These maps show in the coastal waters of the Guyana’s a high primary production. This production is in March (Fig. 4) as well in April (Fig. 5) high at a certain distance from the coast. Near the coast and further seaward near the continental slope the production is far lower. This also becomes clear in figure 13 up to 20, in which the ratio of sand, detritus, phyto- and zooplankton is given. Hulbert a.o. (1969) and Cadée (pers.comm.) found in those months near the coast a small strip with a high primary production. The high production is caused by the upwelling of nutrientrich water at the continental slope, because the Amazon outflow contains hardly phosphates and nitrates (Ryther a.o., 1969). This upwelling also explains the high quantity of sand found in the samples before the continental shelf (Fig. 13 and 17). It appears that the diatoms which are dominant in the samples (Fig. 21) -taken in a short period and rather close- belong to different groups. This could be an indication for different watermasses in which the circumstances are optimal for the different diatoms. It was not possible to discover a relation between the different phytoplankton populations and the physical and chemical data (Fig. 22). It is therefore improbable that the different phytoplankton populations are caused by different watermasses. They form rather different stages in the succession of one bloom. The diversity of the phytoplankton (Tabel 1 and 2) is very low. Although this is normal during the bloom, the main reason for this low diversity must be found in the hydrographical situation; in regions with upwelling the diversity drops (Margalef, 1967). In figure 23 the diatoms and dinoflagellates are divided into littoral, neritic and oceanic species. The coastal samples contain a lot of littoral species, in the region with a high primary production mainly neritic species are found and beyond the continental shelf the population is typical oceanic. On this ground the supposition that in this region different watermasses don’t mix is untenable. The suggestion of Ryther a.o. (1967) that the outflow of the Amazon mixes fast with the Guyana current seems to be right. The variation in average length of two Coscinodiscus species in relation to hydrographical circumstances neither gave further information about different watermasses (Fig. 24 and 25). Noteworthy is the relation that seems to exist between the length of both species and the salinity and Si-content of the sample. Coscinodiscus asteromphalus Ehr, has greater cells at a high salinity and smaller cells with increasing Si-content. With Coscinodiscus concinnus Schm. the relation is more clear, but just the reverse. About the situation in the eastern Caribbean hardly any information can be offered. The sampling method was too incomplete. In October primary production is found in the Gulf of Maracaïbo. The quantity of settled material in these regions is considerably lower than off the coast of the Guyanas. During the whole year blue algae and dinoflagellates are dominant (Fig.37). Only in the sample of 18 June Chaetoceros was dominant. This indicates the oceanic character of the region. A total impression of the samples shows a production period in January and in August-October.

Description: The present bibliography on pelagic Tunicates has been compiled over a period of 4 years, mainly by the first author. It is meant, not as an official publication, but as a working aid for students of pelagic Tunicates. It comprises about 1300-1400 different titles of books and articles. For obvious reasons the mere listing of all those titles in alphabetical order would be impractical for specialized demands. Splitting this list in as many subheadings as possible in a way like the Zoological Record would be ideal. However, many articles and books are difficult to place under one heading; the same titles would have to be mentioned under a number of different headings. With as many headings as possible this would mean a multiplication of the 1300-1400 titles to an impractical amount. Moreover, at present only part (60%) of the titles mentioned below have been checked and abstracted by the authors; for specialized subheading all articles and books need to be studied. It was decided to meet both ends and an unspecialized subdivision was made into six headings: Copelata, Salpidae, Doliolidae, Pyrosomidae, General Zooplankton and General Tunicates. The important articles or books concerning more than one of the systematic groups have been listed under more than one heading. For instance: “Thompson, H. Pelagic Tunicates of Australia” can be found under Copelata as well as under Salpidae, Doliolidae or Pyrosomidae. General zooplankton papers or books, in which pelagic Tunicates are not a major subject, are not listed under several headings, but are compiled under “General Zooplankton”. General articles or books on various subjects of the Tunicata as a whole are listed under “General Tunicates”.

Description: The mites listed in the present paper have been collected by the junior author and Drs. N. J. J. KOK during a stay in Surinam from 6.VII—1.XI.1971 with financial aid of the Netherlands Foundation for the Advancement of Tropical Research (WOTRO). The collection enlarges our knowledge on parasites of nasal cavities of hosts from Surinam (FAIN & LUKOSCHUS, 1971).

Description: The present paper deals with some gomphids from South America. Besides descriptions of a number of new species additional notes on several Selysian and other, little-known species, elucidated with illustrations of important details, are offered in order to obtain a better insight into the characteristics of these dragonflies. Lectotypes are selected and confusions in respect to the generic or specific status of some species are unraveled. Of nearly all the gomphids from Surinam the larval stages are described or discussed. The identity of several larvae is ascertained by the actual rearing of some individuals. The discovery of two new Agriogomphine species resulted in a classification of the members of the Agriogomphus complex into two genera only instead of four. Undoubtedly of greater importance is the attempt to acquire a satisfactory division of the large genus Gomphoides sensu Selysi 1854. In doing so, the erection of a new genus was necessary. The material from Surinam here recorded has been assembled in the first instance by the author himself during a period of ten years of odonatological research carried out in that country (1955—1965), but a comprehensive and very valuable part is from Dr. D. C. GEIJSKES. I would like to express here my thanks for his consent to describe his gomphid material. This privilege enabled me to clear up several intriguing problems on the regional gomphid fauna.

Description: Se trata de las espécies del grupo nebulosus del género Gelastocoris. Según el autór este grupo contiene una espécie con dos subespécies. Gelastocoris nebulosus nebulosus (Guérin) con sinónimas G. flavus (Guérin), G. apureensis Melin, G. monrosi De Cario, G. paraguayensis De Carlo y G. vianai De Carlo, tiene una distribución de la Venezuela y las Guayanas hasta el Paraguay y el NE de la Argentina. Gelastocoris nebulosus quadrimaculatus (Guérin), con sinónimas G. bergi De Carlo y G. bolivianus De Carlo, tiene una distribución andina, de Perú hasta el Chile (Santiago) y el NO de la Argentina.