ALBERT

Description: From a bryological point of view Greenland is not well known in detail. Unlike Siberia or Arctic America, it is not known through a few large collections, but through multitudes of mostly relatively small gatherings. In this arctic island that is almost 2000 miles long and extends from below 60° N.lat. to nearly 84° N.lat., travel and logistics are difficult. Consequently no over-all study of the whole island has been made, although many collections have been achieved through casual or intensive studies of small areas. Like the other contributions to the knowledge of the bryoflora of Greenland this paper will only deal with a rather limited area; the Angmagssalik district on the East coast of Greenland, ranging from 65° N.lat. to 67°20' N.lat. In 1887 Lange and Jensen published the first and until now the only comprehensive review of specimens and publications on the Musci of Greenland. In their paper the first moss collection from the Angmagssalik area was reported, made in 1884-1885 in the course of ethnographical studies by Gustav Holm (Sphagnum girgensohnii and Polytrichum juniperinum), the first European to visit this part of East Greenland.

Description: Contrary to Europe, with only one Caltha species, North America has at least three species of this genus. These are the polymorphic C. palustris L., also widely distributed in Europe, the floating aquatic C. natans Pall, and the polymorphic C. leptosepala-biflora group. Two previous papers (Smit 1967, 1968) dealt with taxonomic aspects of C. palustris, that in North America were not essentially different from those of European material.

Description: The chromosome numbers of 16 species of Angiosperms, collected in Cameroun and the Ivory Coast, were determined. The numbers given for 14 species are new, in the remaining species the results of other authors could be confirmed.

Description: As an introduction to a number of researches of his own the author wishes to give the following data: „Veen” has two meanings in Dutch: 1. in a petrographic sense (peat) Von Büllow’s definition was accepted: „Torf” ist zu deflnieren als ein meist dunkles, kohlenstoffreiches und ± saures Gemenge unvollständig spezifisch-zersetzter Pflanzenteile, das erdgeschichtlich jüngste Glied der Verwantschaftsreihe der Kohlen, dessen Bildung noch heute andauert.” 2. in a plant-sociological-geographic sense (bog) the following definition has been suggested: a bog is a plot, the surface of which consists of a layer of peat, either covered or not with vegetation, with which that layer is genetically connected. The classification of bogs according to their position with regard to the water-level of the surroundings (Staring) and that of the geological chart were rejected on account of their ambiguous character. The classification suggested by Van Baren according to the environment in which the bogs have been formed, was likewise thought insufficient. Preference was given to the classification according to the plants which gave rise to the peat (eutrophic, mesotrophic and oligotrophic bogs) and according to the origin of the water needed for peat formation (topogenous, ombrogenous and soligenous bogs). The conditions of peat-formation are of a botanical (presence of a vegetation and micro-organisms), climatologic (presence of a certain temperature and moisture) and geological nature (presence of a basin, valley or dead river-branch, certain level of ground water, a possible impervious layer). With reference to a number of authors (Picardt; Van Lier; Grisebach, Venema and Staring; Weber) the alteration in conception as to peatformation from the 17th via the 18th and 19th to the 20th century has been given. The word „Peel” cannot be derived from „palus”. Nothing is certain about its origin. It may mean the low land, bog or marsh. The bogs of the Peel lie on the Brabant-Limburg border-plateau (fig. 2). Lorié and Pannekoek van Rheden have shown that the peatformation of the Peel is likely to have occurred in channels, which have been formed by the Meuse, in co-operation with wind and rain (fig. 4). The bogs were therefore in the first instance topogenous formations, which afterwards developed into ombrogenous bogs. For his own research the author collected peat in three ways: 1. by cutting lumps of peat from open profiles; 2. by boring with a simple peat-bore (photograph 1); 3. by boring with the Utrecht peat-bore, an improvement on Dachnowski’s (fig. 5). To assist in the pollen-analytic examination the samples were treated according to Erdtman’s method. The latter has the following advantages compared with the usual treatment with a 10% KOH-solution: 1. the surface-structures of the pollen-grains are more distinct and as a result the grains themselves can be recognized better; 2. the pollen is more concentrated, so that in spite of the method taking up much time, a saving of time is possible. How the method is applied may be found in the chapter concerned (p. 38 and following). For the stratigraphic examination the samples were broken apart in a glass-bowl of water and viewed with a binocular microscope. Dry sandy samples were broken in water, when seeds and other vegetative parts came floating to the top; next they were put with a brush on thick blotting paper and studied through the binocular microscope. The designations for the sediments and species of peat have been derived from Fægri & Gams. For Scheuchzeria peat a new designation has been added. A plea was made for replacing the word pollen-analysis by „palynology”. A survey of the observations and examinations up to abt. 1935 closes the introduction (see the diagrams of Weber, Erdtman and Duyfjes in the figs. 6, 7, 8 and 9). The author’s own research refers to the Southern and Astense Peel, as in the remaining grounds of the geological chart indicated I 4v (= raised bog) no samples could be taken owing to the digging off having progressed too far. 10 profiles were examined. The situation of the bore-sites has been given in the geological chart of the grounds (fig. 3). The result of the examination (figs. 10—27) and the discussion on it may be summerized as follows: Zoning of pollen-diagrams The sub-zoning of the late- and post-glacial periods according to Blytt & Sernander has proved useful as a zoning of pollen-diagrams, provided atlantic and sub-boreal are joined. It is desirable to replace Blytt & Sernander’s terminology by a different one, because the authors gave a climatologic connotation to their names of periods. The limit between pleistocene and holocene was drawn between preboreal and boreal as Florschütz did. As phases of the holocene the following names were suggested: young post-glacial = sub-atlantic mid post-glacial = sub-boreal and atlantic old post-glacial = boreal. Neither in the Peel nor elsewhere in Holland have Allerød-deposits been found. They are not likely to be found either, as on account of the long distance from the land-ice-margin the flora will have been hardly or not at all influenced by the Allerød interstadial period. For Holland therefore the zoning of the late-glacial according to Firbas (1935) may be considered sufficient. The names of the periods do not bear a climatologic connotation as those of the post-glacial phases do. For the sake of a unity the following names have been suggested: young late-glacial = pre-boreal mid late-glacial = sub-arctic period old late-glacial = arctic period. Forest-history In a table (p. 98), in which likewise the Peel diagrams of Weber, Erdtman and Duyfjes have been inserted, the examined profiles have been arranged from North to South. From each profile it has been stated whether it originated in a certain period (+) or not (—). The sub-arctic phase was characterized by forests of Betula and Pinus and was followed by the pre-boreal phase, in which Corylus and Alnus occurred. Also from the other Dutch diagrams (see list on p. 99) it appeared that in the Netherlands the Alnus pollen occurs with an equal frequency before, during and after that of the Quercetum mixtum. The old post-glacial zone of the diagrams shows a peak in the Pinusline. In contrast with the from Mid-Europe there is not always a maximum in the Corylus-curve after the Pinus-peak. In other Dutch diagrams this phenomenon is likewise found. Only in 28% of all Dutch profiles with a boreal zone does a hazel-maximum succeed a Pinus one. They often co-incide (16%), while in the remaining cases no hazelpeak has been established. There is no fixed order of sequence in the occurrence of the components of the Quercetum mixtum, either in the Peel or elsewhere in Holland. The mid post-glacial is the phase of culmination of warmth-loving forest elements: Alnus pollen shows the highest percentage in this zone. Quercus pollen also occurs in great quantities, while Ulmus and Tilia take up an important place up to the „Grenzhorizont”. The absolute and empiric Fagus pollen limits are found at different heights in the mid post-glacial zone of the diagrams, the rational limit lies somewhere near the „Grenzhorizont”. In the young post-glacial phase the Fagus pollen attains fairly high percentages (up to 30%). The maxima in the East and South-east of the Netherlands are between 20% and 38%; they decrease towards the coast and increase towards the South-east (Hautes Fagnes, Belgium) and East (Germany). It seems incorrect to class the Netherlands almost entirely among the oak-alderterritory poor in beeches, as Firbas did. An attempt has been made to fit the Peel-diagrams into Overbeck & Schneider’s zonation system. For the territory for which it has been made there are already difficulties (p. 104), for use in the Peel and other Dutch diagrams there are even more objections (p. 68, 104). Godwin’s zonation system appeared to be a little less forced, but not quite useful on account of too many details. From his horizons that of Ulmus proved useless for the continent. Neither for the Peel nor for the Netherlands and its surrounding territory can a detailed zonation system be designed. It has proved difficult to proceed any farther than Rudolph’s „Grundsukzession”: birch, pine-hazel-mixed oak-forest-beech, in which the alder generally joins the mixed oak-forest and the hornbeam the beech. Before drawing far-reaching conclusions from the course of the curves (as has been done by some authors) more palynological researches are needed in accordance with the actuality principle, known from geology. Pollen-grains from warmth-loving trees in seemingly sub-arctic spectra In profile 4 (Deurnse Peel II) pollen-grains of Abies, Alnus, Picea, Tilia, Ulmus and Corylus were found in the „late-glacial” zone (figs. 14, 15). Investigations were made as to which of the following possibilities would be the cause of their appearance: 1. in taking and preparing the samples pollution occurred; 2. pollen-transport over long distances has taken place; 3. the pollen-grains found have got secondarily into the deposit; 4. warmth-loving trees have occurred in favourable circumstances in the late-glacial phase or 5. in an interstadial period or in an interglacial phase. The said pollen-grains probably hail from a Würm interstadial or interglacial phase. Interglacial peat On the site of the bore-point 7 it was possible to collect samples from the layers under the peat. The upper 40 cm of the diagram Griendtsveen IX (fig. 27) of this profile proved a repetition of the lower 40 cm of the Griendtsveen I profile (fig. 18). The diagram shows that pollen of Carpinus, Picea and Abies occurs showing the deposit to be of interglacial age. The pollen-curves, however, pass unnoticed from an interglacial into a post-glacial portion. The limit is likely to be found between the two, about 30 cm below the mowing field. There is therefore a great stratigraphic hiatus. Pollen-analytically it could not be decided from which interglacial period the profile hails; on account of its situation on the middle terrace, it was deemed likely that it was an Eem sea deposit. The examined profile probably corresponds to Jessen & Milthers’ zone g; showing it to have been formed at the end of the Eem sea period. The Meuse therefore cannot have flowed through this part of the Astense Peel after the mid Eemean phase. Stratigraphy This is difficult to summarize. Compare various profiles. Individual mention may be made here of: 1. peat on a podsol layer; this was found in two places (Deurnse Peel I Kraaienhut and Griendtsveen VIII). Peat-formation may be thought to have occurred in the following way: heather started growing on drift-sand giving rise to a podsol layer. As the latter is impervious the vegetation surface became marshy. The heath was replaced by a Caricetum from which peat arose. Gradually more Eriophorum occurred, from which almost pure vaginatum peat arose. The bog-surface grew moister and moister, Sphagnum cuspidatum and Scheuchzeria could grow on it and formed a „Vorlaufstorf”. Only then could non-extremehydrophile Sphagna join in peat-formation. 2. the occurrence of Scheuchzeria-peat after the „Grenzhorizont” period. This species of peat, which is often found at the basis of the old Sphagnum-peat as a mesotrophic transition vegetation, has for the Netherlands only been found in the young post-glacial phase in the Peel (Deurnse Peel I Kraaienhut, Griendtsveen V and VIII and Nederweerd). At present the plant is very rare. The severe decline of this plant was also observed elsewhere. Probably it is caused by the gradual drying up or reclaiming of the raised bogs. Of the present station of Scheuchzeria near Ommen a short description has been given (p. 59 and photographs 2, 3, 4). 3. the „Grenzhorizont”. Where the young Sphagnum-peat has not been dug for the preparation of moss-litter, the Peel bogs show a clear „Grenzhorizont” (photograph 8). The conceptions about its origin have been discussed. The distinct separation between the old and the young Sphagnum-peat was not considered sufficiently explained. Though on the whole the „Grenzhorizont” is synchronous in the North-west European profiles, the point of transition from old to young Sphagnumpeat was fairly unstable and easily changeable as to time. Generally the date of the „Grenzhorizont” is fixed at about 500 A.D., though there are differences in opinion. There is a lack of archeological correlation which renders a correct dating impossible. Interference of man in the Peel Three ways of interference were stated: 1. peat has been dug off for the greater part in the territory of the Peel: young Sphagnum-peat for the preparation of moss-litter, old Sphagnum-peat for fuel. The trees which appeared when the bog was dug up in the „Veenderij der Maatschappij Griendtsveen” are sometimes in so good a condition, that they are used for building sheds. The 1 st, 2nd and 4th beam in the foreground of the shed in photo 5 has been sawn from a 30 m long subfossil pine. 2. in a native peat-digging it was possible to collect recent young Sphagnum-peat. 40 to 50 years ago the peasants living there had dug peat in holes, which were afterwards left to themselves. Sphagnum started growing again and the holes were filled in again. The diagram (fig. Griendtsveen VII) represents the surrounding heath with scattered pines and birches, sown by the wind, and a pine-plantation close by. 3. in the profiles Nieuwe Peel, Griendtsveen VI and VII it has been fixed by the indications given by Firbas, that only in the surface layers of the bog has corn-pollen occurred. So in these parts cultivation of cereals will be of recent date. This also appeared from the history of the reclamation of the said territory.

Description: The chromosome number of 157 species of Angiospermae occurring in the Netherlands is dealt with.

Description: Name: Wahlenbergia marginata (Thunb.) DC. Monogr. Camp. (1830) 143. Family: Campanulaceae.

Description: Alangium LAMK.—M. M. J. van Balgooy, Pac. Plant Areas 2: map 72. Complete; Old World, also incl. Indo-Malesia, E. Australia, Pacific (Solomons, New Caledonia, New Hebrides, Fiji); delineated except in Africa and Madagascar, localities indicated only in the Pacific, species density; monograph.

Description: The Upper Hunter palynological assemblage described includes 54 species, assigned to 29 genera. Seven genera (Scabratisporites, Guttatisporites, Lapposisporites, Pseudogravisporites, Paralundbladispora, Taeniaepollenites and Tubantiapollenites) and 39 species are new; three generic descriptions are emended (Apiculatasporites, Colpectopollis and Angustisulcites) and three new combinations are proposed. Bisaccate pollen grains average 84 %; within this group no Upper Permian elements could be demonstrated. The assemblage is compared with other European Lower and Middle Triassic assemblages; there are no close similarities to assemblages outside Europe.

Description: In a previous palynological study in Cocoid palms the present authors (Punt and Wessels Boer, 1966) were able to demonstrate a rather strong but not absolute correlation between the pollen types and the staminate flower types within the genus Attalea in the broad sense. The existence of partly apparently primitive, partly very advanced flower types within the otherwise close related group of Geonomoid palms made it worthwhile to investigate the same feature in this group. The Geonomoid palms are usually considered to comprise 7-9 genera of monoecious Arecoid palms which share a large number of characteristics (Burret, 1930; Moore, 1966). The group is very obviously a most natural one. The generic distinctions are mainly based on the flower morphology, notably on differences found in the androeceum and pistil.

Description: The chromosome numbers of 31 species of Angiospermae collected in S. Brazil were determined. Of these species 5 were studied before, the other numbers are new, 11 are first counts for genera and one even for a family. Some notes on the cytology and morphology are added.

Description: In this preliminary investigation attention was paid to pollen morphology of West-European species of the Rosaceae. Some new terms were used like fastigium, endocingulus etc. The terminology of Iversen and Troels-Smith has been followed in addition to improvements by Erdtman. A key is given to the types and subtypes for the use of pollen analytical investigators. Sanguisorba officinalis appeared to be always 3-colporate and not 6-colporate.

Description: A palynological assemblage obtained from marly limestones of the Dutch Lower Muschelkalk is discussed. A qualitative analysis has disclosed its great resemblance to Upper Bunter (Röt) assemblages ; however, differences in quantitative composition were demonstrated. Utilizing palynological data new information can be added to the knowledge of the European Middle Triassic flora.

Description: The water economy, the mineral content of the soil, and human influence are the principal ecological factors governing the variation of the heath vegetation of a limited region. Sloping of the surface is also an important factor. In hilly country it is of a twofold nature: on the one hand the difference between high and low altitudes, based on the water economy, on the other hand differences in (micro-) climate. If the hills are higher, this results in greater climatic differences. In extremely oceanic and in boreal regions a rise in altitude of 100 m is sufficient for creating a noticeable decrease in temperature and an increase in precipitation, aerial moisture, and wind force. This results in the occurrence on the hills of heath communities that have their main distribution more to the North. The same observation was made by Gimingham (1961). On Slieve League on the Donegal coast (Ireland) Salix herbacea and Lycopodium selago occur in the heath at an altitude of 600 m, near Tongue on the Scottish north coast Dryas octopetala, Saxifraga oppositifolia, Alchemilla alpina and Thalictrum alpinum at an altitude of 60 m. West of Apeldoorn in the Netherlands are found extensive stretches of heath with abundant Vaccinium myrtillus and V. vitis-idaea at an elevation of 60-80 m, even on south-facing slopes. This is an area with high precipitation due to ascending air west of the hill ridge of the Eastern-Veluwe. Here the Vacciniums, elsewhere requiring the protection of the forest, can tolerate the habitat of the open heath (Stoutjesdijk, 1959; De Smidt, 1966). Higher elevation combined with north-facing slopes creates extreme conditions e.g. on Roc Trévézel (300—360 m) in Brittany, with Vaccinium myrtillus, Melampyrum pratense, Hymenophyllum wilsonii and Rhytidiadelphus loreus. These species are virtually lacking in the surrounding plains where the heath consists of such South Atlantic species as Erica cinerea, E. ciliaris, Ulex gallii, Lobelia urens, Lithospermum prostratum and Symethis planifolia.

Description: Frutex epiphyticus, ramis quadrangularibus, angulis lenticellatis. Folia ramorum fertilium petiolis 2-5 mm longis, 1.5-2 mm latis; lamina chartacea vel subcoriacea, oblanceolato-oblonga vel interdum elliptico-oblonga, 9-14 cm longa, 3-4.5 cm lata, ápice acuminata, acumen 1-2 cm longum, basi attenuata, costa subtus prominente, nervis lateralibus supra et subtus prominentibus vel prominulis, glandulis hypophyllis aliquot patelliformibus vel foveolatis, parvis, 3-5 in folii parte inferiore oblique seriatis, aliis minutis, punctiformibus, nigricantibus, aequaliter dispersis. Flores in racemis umbelliformibus (20-) 30-45-floris; rhachis ad circa 1 cm longa; nectaria clavato-cucullata, stipitata, stipes 5-8 mm longus, cucullus 1-1.5 cm longus, circa 4-5 mm diametro, ore late-rotundata, margine plerumque recurvo, apiculata; pedicelli 5-7 cm longi, lenticellati; bracteolae sepaloideae, circa 1 mm longae, 2-3 mm latae; sepala suborbicularia vel reniformia, circa 2-3 mm longa, circa 4-5 mm lata, margine glandulosa; corolla oblongo-subconoidea, circa 1 cm longa, circa 4-5 mm diametro; stamina 18-33, filamentis applanatis, liberis, inaequalibus, in alabastro 4-6 mm longis, antheris linearibus, 3-5 mm longis, circa 1 mm latis, basi subsagittatis; ovarium circa 2-3 mm diametro, 6-11-loculare. Fructus globosus, circa 9 mm diametro, stylo persistenti ornatus. Typus : Costa Rica, vicinity of Vara Blanca, North slope of Central Cordillera, between Poás and Barba Volcanoes, alt. 1700 m, April 1938, Skutch 3762 (holotype US; isotypes GH, MO, NY, S). Paratypes; Costa Rica: Heredia: Cerro de las Caricias, North of San Isidro. Standley & Valerio 52202, 52248,52375 (US); Panama:Chiriquí: Boquetedistrict, Bajo Chorro, Davidson 398 (GH, US).

Description: Although algology deals with a large group of plants, widespread and of a great morphological diversity, the history of this branch of botany is fairly young. Linnaeus (1753) listed in his Species Plantarum under the heading “Cryptogamia—Algae” only five genera of plants which are still accepted as algae at the present time. Under the same heading he also described a number of liverworts, lichens and sponges and a few other things.

Description: Joseph Gaertner (1732-1791) was the first to develop a carpological taxonomy in his book De fructibus et seminibus plantarum (1788-1791). The scope and background of this work are discussed; its history is sketched on the basis of the Banks correspondence at the British Museum; the main sources of material are listed. A brief outline of Gaertner’s life is given, also mainly based on letters from him and his contemporaries to Joseph Banks.

Description: Previously, the chromosome numbers of some species of Loganiaceae were dealt with (Gadella, 1961, 1962, 1963). The chromosome numbers of 7 species are reported in this paper, of which 4 species, all belonging to the genus Strychnos, had not been investigated cytologically before. The materials, kindly supplied to me by Dr. A. J. M. Leeuwenberg and by Ir. F. Breteler, were collected in the form of seed-samples in the Ivory Coast and in Cameroun. The plants of 2 species originate from botanical gardens. Living material of all species (except for Strychnos lernata Gilg. ex Lwb.) is grown in the botanical garden of Wageningen (WAG). The determination of the chromosome numbers was based on the study of roottipmitoses. Roottips of the plants were fixed in Karpechenko, embedded in paraffin, sectioned at 15 micron and stained according to Heidenhain’s haematoxylin method. The results may be summarized as follows: 1. Nuxia floribunda Benth.: 2n = 38 Origin of the material: S. Africa, obtained from the University of Stellenbosch. Seeds probably collected in the wild. Herbarium material of the mother-plant: J. J. Bos, no. 310 (WAG). Herbarium material of seedling: A. J. M. Leeuwenberg no. 3665 (WAG). References: Gadella (1963): 2n = 38. 2. Strychnos dinklagei Gilg.: 2n = 44 Origin of the material: Ivory Coast, Forêt d’Abouabou, between Abidjan and Grand Bassam. Herbarium material of the mother-plant: R. A. A. Oldeman no. 845 (WAG). Herbarium material of the seedling: A. J. M. Leeuwenberg no. 3561 (WAG). References: Gadella (1963); 2n = 44. 3. Strychnos innocua Del. subsp. innocua: 2n = 44 Origin of the material: Ivory Coast, 16 km S. of Ferkéssédougou. Herbarium material of the mother-plant: A. J. M. Leeuwenberg no. 4435 (ABI, WAG). 4. Strychnos millepunctata Leeuwenberg: 2n= 441) Origin of the material: Ivory Coast, Forêt d’Abouabou, between Abidjan and Grand Bassam. Herbarium material of the mother-plant: J. J. F. E. de Wilde & A. J. M. Leeuwenberg no. 3447 (ABI, WAG). 5. Strychnos samba Duvign.: 2n = 44 Origin of the material: Cameroun, 4 km S. of Nguélémendouka. Herbarium material of the mother-plant: F. J. Breteler no. 2051 (WAG). 6. Strychnos spinosa Lam.: 2n = 44 Origin of the material: obtained from the botanical garden of Groningen, the Netherlands, origin unknown. Herbarium material of cutting: A. J. M. Leeuwenberg no. 3564 (WAG). References: Mangenot and Mangenot (1958): 2n = 44. Miège (1960): 2n = 44. Gadella (1962): 2n = 44. 7. Strychnos ternata Gilg. ex Leeuwenberg: 2n = 44 1) Origin of the material: Cameroun, 27 km from Bertoua on road to Bétaré Oya. Herbarium material of the mother-plant: F. J. Breteler no. 2196 (WAG). Herbarium material of the seedling: F. J. Breteler no. 2994 (WAG). Twenty-one species of the genus Strychnos have been studied up to the present. The following chromosome numbers have been counted: 2n = 24 (3 species, counted by Mohrbutter, 1936); 2n = 44 (16 species); 2n = 88 (2 species). From these data the conclusion may be drawn that the more common basic number of the genus Strychnos is X = 11 or 1 = 22.

Description: A suitable subtitle for this paper would have been “The rise and fall of a family”. What is usually called the Cyphellaceae is an instructive example of a situation not uncommonly encountered in the current systematics of mycology: a family retained in a traditional sense by some mycologists and considered by them as good a family as any, while others are convinced that it is nothing but a handy bin from which part of the contents has already been taken out and disposed of by scattering it over various groups, but which is still needed for keeping what remains. We do not yet know what to do with this considerable remainder, mainly because the published accounts are inadequate and the species have not yet been scrutinized anew in the light of present-day taxonomic requirements. In order to understand the basic idea of the Cyphellaceae the type species may be briefly introduced. The fact that Cyphella digitalis was originally described as Peziza digitalis is telling, and one could not do better than characterize it as a ‘discomycete’ with basidia, viz. a cup-shaped fruit-body with the hymenium lining the smooth inside or ‘disk’. If one were pressed to form an opinion about its taxonomic position from a dried, not annotated collection and without the aid of the microscope, one would even now, very likely, dispose of it as a discomycete. However, there is little doubt that in nature the cup is directed downward at least when mature, in contradistinction to the average discomycete in which the hymenium containing the asci is directed upward. This difference is a reflection of the two modes of violent spore discharge inherent in the hymenomycetous basidium and ascus; it has been explained through Buller’s well-known researches. The cups in the various species are not always typically cup-shaped; in a number they are more or less tubular or else more flattened and even disk-like.

Description: La systématique scientifique, qui classe tous les êtres vivants, actuels et fossiles, d’après leurs affinités naturelles ou présumées telles, doit pouvoir donner à chaque taxon un nom stable, permettant de le désigner avec son rang taxonomique et de l’identifier facilement. La nomenclature botanique n’échappe pas à cette exigence et depuis que C. Linné généralisa, en 1753, la nomenclature binominale, le besoin s’est fait sentir de compléter et de préciser, sur le plan international, les principes et les règles établis par l’illustre botaniste suédois.

Description: From the general discussion of the effect of mass selection on the genotypic array of the next generation we have seen that under certain conditions mass selection can lead to homozygosity, but does not do so necessarily. Outcrossing, mutations and disadvantages of certain genotypes may prevent reaching equilibrium condition with complete homozygosity even in the simplest case of one locus with two alleles. It depends on the magnitude of these factors and the degree of heterozygosity of the variety how close to genetic uniformity we ultimately can come. The advancing of one generation has only a small effect, which becomes less as the frequency of one of the genotypes becomes less. Mass selection can reduce segregation in a variety, but only in ideal situations and only in small steps. Obviously the most effective way to promote genetic uniformity is to begin with non-segregating material obtained through careful inbreeding and within-family selection. Then, if this is available, mass selection is hardly necessary and seed collection should be done so as to prevent a return to a heterozygous condition. When only segregating populations are available, some changes can be expected if the selection intensity is low, but they will not be great and may not be noticed until after several generations. Returning to the original question of the stability of the tobacco variety, the conclusion can be drawn that when large numbers of plants from a field are selected as seedplants the changes in the next generation as a whole will be small, regardless of the selection procedure used. When 10-30 % of all plants are allowed to produce seed we cannot expect important changes. Also, when the environmental variations are as great as in shade tobacco, the possibilities of selecting against certain genotypes for a number of characteristics simultaneously becomes virtually impossible. Concerning whether or not mass selection can lead to improvements in the variety, it was explained that the selection intensity and the heritability of a character determine the selection response. Perhaps this response can be predicted in the case of one character, but it becomes difficult, if not impossible, to forecast the results when many characters are involved at the same time. Reference was also made to a selection index which has been effective in livestock breeding. Even if an index could be determined for shade tobacco, its use is not necessarily effective, as Kempthorne (1957) pointed out. The genotype-environment interaction makes questionable the choice of certain fields over others. Without experiments, such questions cannot be answered. It is likely that mass selection with low selection pressure changes a variety very little. Again, in a field where up to 30 % of the plants are selected for seed, the pressure cannot be very great and we should not expect great changes. Only when a few plants are carefully selected for certain characters should progress become noticeable, as is the experience of single plant selection in plant breeding. We conclude that mass selection for seed and plant breeding to improve a variety should not be confused with each other. Each has its own aims and methods, which are not interchangeable. Where uncertainty exists about seed, progeny tests usually are made to compare a seed with the parent seed. Bolsunov (1959) has described a number of such procedures for tobacco, though the more elaborate of them appear impractical.

Description: Eén van de grote giften van A. A. Pulle, Lanjouw’s voorganger als Hoogleraar in de Bijzondere Plantkunde en de Plantengeographie te Utrecht, was zijn goede keus van medewerkers. Hij kon die keus maken dank zij een andere gift, die van leermeester. Pulle’s stimulerende activiteit als hoogleraar luidde de wedergeboorte in van de Nederlandse plantensystematiek door een stroom van leerlingen waarvan er velen ook nu nog een belangrijke rol spelen in de botanische wereld. Vele van Pulle’s leerlingen uit de eerste tijd moesten Utrecht verlaten omdat er in de twintiger jaren nu eenmaal nog geen sprake was van een redelijk gesalariëerde wetenschappelijke staf. Eén leerling echter werd zo gefascineerd door de vele mogelijkheden die het Utrechtse instituut bood, dat hij bleef, niettegenstaande de soms zeer ongunstige economische en organisatorische omstandigheden. Deze leerling, Lanjouw, toonde reeds toen de taaie volhardendheid die zijn medewerkers en leerlingen in later jaren zo goed leerden kennen en waarderen. Reeds van de eerste jaren van zijn assistentschap aan stonden Lanjouw de idealen voor ogen die hij in de loop van zijn lange loopbaan van assistent tot directeur voor het grootste gedeelte zou weten te realiseren. Deze loopbaan begon toen hij op 1 januari 1926 benoemd werd tot assistent bij de Bijzondere Plantkunde. In het jaar waarin we het feit herdenken dat het veertig jaar geleden is dat Lanjouw verbonden werd aan het Botanisch Museum valt ook de honderdenvijftigste verjaardag van het herbarium. Plantensystematiek is te Utrecht in meerdere of mindere mate beoefend van de stichting van de Universiteit af. Op 30 oktober 1816 echter werd het eerste herbarium voor de Universiteit verworven. In 1966 herdenken we dus eigenlijk twee jubilea. De periode van werkelijk actief systematisch onderzoek is echter veel korter geweest: de korte jaren van Miquel’s werkzaamheid (1859-1871) en de periode die in 1906 begon met de aanstelling van Pulle tot Lector in de plantensystematiek. Pulle gaf, voor het eerst na Miquel, en mede dank zij de stimulerende invloed van Went, een nieuwe stoot aan het plantensystematisch onderzoek in Nederland en wel vooral aan het onderzoek van de tropische flora’s. Een reeks van leerlingen wijdde zich onder zijn leiding aan de studie van de flora’s van Suriname en Nederlands Indië. Het is voldoende hierbij de namen van van Sloten, Lam, van Steenis, en Uittien te noemen om deze ontwikkeling te illustreren. Lanjouw koos voor zijn proefschrift de Surinaamse Euphorbiaceae en het was uit dit werk dat de „Flora of Suriname” voortkwam. Zonder ook maar iets tekort te doen aan de rol van Pulle kan gezegd worden dat van het begin van zijn loopbaan af Lanjouw actief heeft medegewerkt aan de opbouw van het Botanisch Museum en dat hij bij de ontwikkeling van de zo belangrijke „Flora of Suriname” een doorslaggevende rol heeft gespeeld. Zijn dissertatie „The Euphorbiaceae of Suriname” vormde, ten dele, tegelijk de eerste aflevering van de Flora.

Description: The somewhat peculiar genus Vahlia Thunb. (1782) was formerly regarded as an anomalous member of the Saxifragaceae, but in 1959 it was segregated as the monotypic family Vahliaceae by Dandy (in Hutchinson, Fam. Fl. Pl. ed. 2, 1: 461). The genus includes about three species, all of them highly variable in stature, flower size, and indumentum; this has resulted in the description of more than twenty “species”, whose names now appear in synonymy. This note, however, is chiefly concerned with the generic name, since it appears that Vahlia Thunb. is not correct under the Code and must be replaced by Bistella Adans. (1763). In the synonymy under the new combinations, all the relevant names so far traced are included, but it may well be that an experimental approach to the problem of specific and infraspecific limits and the taxonomic value of the characters hitherto relied upon for differentiation would result in considerable changes. Bistella Adans. (1763) was cited in the form “ Bistella Lippi 243 – Ascyroides Lippi” and the name than fell into abeyance until it was resuscitated by Delile in 1826. He described plants collected by Cailliaud, and identified a number of them with those of Lippi. In particular, he identified Lippi 243 (and 244) with the Cailliaud plant which he named “ Bistella geminiflora Delil. (Descript, des plantes découv. par M. Cailliaud, pl. II. fig. 4). – Ascyroides Lippi (Manusc. nos. 243 et 244).” It must be emphasized that the taxonomic identification of “ Bistella Del.” with Vahlia Thunb. has never been questioned, but the identity of Adanson’s Bistella with Bistella geminiflora Del. has been overlooked; this species, as represented by Lippi’s plant, is the type of the generic name Bistella Adans.

Description: A survey is given of the types of the sclereids and the sclereid patterns occurring in the leaves of the Marcgraviaceae. Eight main categories of sclereids are distinguished on the base of the morphology of the sclereids. A comparison is made with the foliar sclereids found in some other families. The systematic value and the function of the sclereids are briefly discussed. Some new combinations of names are published.

Description: Among the endemic and sometimes localized genera of the Cruciferae occurring in South America, Mathewsia stands apart as an element of the distinctive desert flora of southwestern Peru and western Chile. As far as present records show, the genus is confined to a relatively narrow strip wholly west of the main Cordillera, not far from the Pacific Ocean. Some species are confined to washes or small arroyos known as quebrades. Others occur as part of the lomas vegetation of western Peru. Populations of the same species occupying different quebradas often differ from each other to a limited degree and in many instances probably little or no gene exchange occurs between them. The intervening dry areas, separating one quebrada from another, are completely unsuited to the growth of Mathewsia and form a natural barrier to the spread of any given population. Thus, with habitats only spottily available, the evolutionary divergence that has resulted in localized species of Mathewsia is readily understandable. One of the real difficulties in studying a group of species inhabiting areas that have been infrequently visited by botanists, is the paucity of available material. Furthermore, unlike some species of Cremolobus (Khanna and Rollins, 1965), the numbers of individuals in a given locality appear to be few and scattered. In some instances, only a single specimen of a given species has been found for study in all of the herbaria consulted. Under these circumstances, the bare essentials of the species are all that can be given and nothing can be said about their variation or distribution. The purpose of this paper is to present, as a first approximation, a taxonomic treatment of Mathewsia that will provide a sound basis for further research on the genus.

Description: Eight species of the genus Sanguisorba L. were studied. Two distinct types could be recognized, viz., the Sanguisorba minor and the Sanguisorba officinalis type. Sanguisorba filiformis (Hooker fil.) Handell-Mazzetti appeared to be a transition between these two types.

Description: Studies in the Moraceae showed that Acanthinophyllum should be regarded as congeneric with Clarisia, and that Clarisia spruceana and Aliteria sagoti are conspecific with Clarisia ilicifolia. Some characters of the inflorescences and seeds and the position of Clarisia and its relationships with Trophis and Sorocea are discussed.

Description: The pollenflora of the browncoal mined in the quarry “Maria Theresia”, Herzogenrath, Western Germany has been investigated. Samples were taken along a section of 12.50 meters at intervals of 50 centimeters. Identifications were made on the basis of form-genera and form-species; this working method gives a broad information on pollen types, but does not relate the fossil pollen types primarily to recent plant taxa. Pollen types which are considered to belong to Betulaceae/Myricaceae make up the biggest part of the pollen assemblages. The construction of a “Composite diagram” for Betulaceae/Myricaceae proved to be useful and might give a better idea on paleoecologic conditions. The stratigraphic position of the browncoal examined is thought to be Lower “Hauptflöz”, possibly Morken or Frimmersdorf Horizont.

Description: Nooit zal ik die Donderdagmorgen 10 Augustus 1944 vergeten, toen ik op het laboratorium hoorde dat in de krant — wie las dat vod nog in die tijd — stond dat UITTIEN gefusilleerd was. Het drong eerst niet goed tot mij door. Het kon niet waar zijn. De krant werd gehaald. Ja, daar stond zijn naam in een lange lijst van lotgenoten en het verschrikkelijke, het onherroepelijke, begon langzaam tot mij door te dringen. Koud en gevoelloos stond daar het bericht, van een leugenachtige argumentatie voorzien, dat men ook UITTIEN, die zachtmoedige, gevoelige, intelligente man, had vermoord. Woorden waren hiervoor op dat moment niet te vinden. Ik had alleen behoefte zijn oudste zuster, waaraan hij zeer gehecht was, op te zoeken. Door de slechte treinverbindingen kon ik eerst de volgende dag naar Brummen. Daar trof ik een diep verslagen kring van familie en vrienden van UITTIEN. Wij konden het ons nog zo moeilijk realiseren dat wij hem niet weer zouden zien. Eerst nu wij hem voor goed verloren hadden beseften wij in volle omvang hoe groot wel de plaats was die hij in ons aller leven innam. Van nature had UITTIEN weinig belangstelling voor politiek. Hij vond dat hij daar niets van wist en er dus ook niet aan mee behoefde te doen. Hij had dan ook de gewoonte zijn stembiljet blanco, ja zelfs zonder het open te vouwen, weer meteen in de bus te laten glijden, zeer tot ongenoegen van de partij-mannen die bij een dergelijke gelegenheid op het stembureau plegen te zitten. Wel was hij met hart en ziel het Koninklijk Huis toegedaan. Later heeft hij zijn blanco stemmerij opgegeven, daar het hem duidelijk was dat hij op die manier ongewild toch wel eens de door hem toen reeds verafschuwde N.S.B. zou kunnen steunen. De gang van zaken in Duitsland opende hem de ogen en reeds voor de oorlog liet hij zijn antinazi instelling duidelijk blijken. Zo zond hij na de overval van de Duitsers op Tsjecho-Slowakije een paar overdrukjes aan een botanicus in dat land met op het adres: .... Tsjecho-Slovakia, temporarily occupied by Germany. Dit had tot zijn intens genoegen een geheel onverwacht gevolg, n.1. een stroom van overdrukjes van allerlei Tsjechische botanici waarvan hij nog nooit gehoord had. Na de overval op ons land, het bombardement van Rotterdam, dat diepe indruk op hem maakte, en de daarop volgende bezetting, was UITTIEN dan ook een felle tegenstander van Duitsers en N.S.B.ers. Hij uitte dat waar hij kon in woord en daad. Op de Middelbare Koloniale Landbouwschool te Deventer waar hij leraar was, leidde dat tot wrijvingen met een N.S.B.-collega, die alles aan zijn Duitse meesters rapporteerde. Op 31 Aug. 1941, de verjaardag van H.M. de Koningin, kwam het tot een ernstige, maar niet onvermakelijke botsing met de Deventer zwarthemden, vanwege het feit dat hij binnenshuis met een oranjedas rondliep. Zijn huis aan de Dahliastraat werd door de N.S.B.ers belegerd, hetgeen een grote volksoploop en kloppartij tot gevolg had. Korte tijd daarna werd hij wegens dit feit en zijn „tartende” houding tegen de N.S.B.-collega ontslagen. Daar het departement een gunstige wachtgeldregeling maakte was dit geheel tot zijn genoegen. Sindsdien toch kon UITTIEN zich met nog meer energie wijden aan de taak, die hij zich ten bate van de oorlogvoering gesteld had, nl. het bijhouden van een uitvoerig dagboek en het verspreiden van door de radio opgevangen nieuwsberichten en van illegaal uitgegeven geschriften. Het is buitengewoon jammer dat dit dagboek in de laatste oorlogsmaanden door brand verloren is gegaan. Zijn folkloristische neigingen kwamen hem bij het samenstellen van dit dagboek goed van pas. Dagelijks tekende hij alles aan wat hij hoorde. Elk nieuwtje, elk gerucht, elke anecdote, met nauwkeurige opgave van plaats, tijd enz. Hoewel dus alles door elkaar kwam te staan, nl. alleen in de volgorde zoals hij de berichten kreeg, was het toch een verhaal dat men met spanning zat te lezen. Dat kwam natuurlijk ook vooral door de originele wijze waarop hij het gehoorde op schrift stelde. Zijn dagboek zou ongetwijfeld voor de geschiedschrijving van deze jaren van belang zijn geweest. Hoe ver zijn medewerking aan de illegale bladen zich uitstrekte, kan ik niet zeggen, daar hij dat begrijpelijk ook voor zijn familie en naaste vrienden verborgen hield. Wellicht heeft hij wel eens iets in deze bladen geschreven, maar zijn voornaamste medewerking was zeker de verspreiding. Op 29 Januari 1944 werd hij, op grond van verdenking van medewerking aan de verspreiding van „Trouw”, gearresteerd en naar het concentratiekamp Vught overgebracht. Voor zover wij wisten was er echter geen enkel positief bewijs tegen hem. Dat was dan ook waarschijnlijk de reden dat hij zelf dacht vrij te komen. De weinige brieven die hij uit zijn gevangenschap mocht schrijven waren merendeels opgewekt en getuigden van zijn onvergankelijke gevoel voor humor. Helaas werden zijn optimistische gedachten, geuit in zijn laatste brief, niet tot werkelijkheid. Hij schreef daarin dat hij nu wel spoedig dacht thuis te komen. In plaats daarvan werd echter zijn groep plotseling voor een standgerecht gebracht, en niet voor een gewone militaire rechtbank waarop zij recht hadden. De zaken gingen voor de Duitsers in die dagen slecht. De Amerikanen en Engelsen waren in het Westen doorgebroken. Vermoedelijk is er uit Berlijn een bericht gekomen, dat maar weer eens een voorbeeld moest worden gesteld om de schrik erin te houden. Zo werden deze mensen zonder dat iemand iets van de gang van zaken afwist ter dood veroordeeld en gefusilleerd. Weer was op een misdadige wijze met verkrachting van elk begrip van humaniteit en rechtsgevoel, aan 23 landgenoten het leven ontnomen, rouw en verbeten woede achterlatend.

Description: In Sweden Erlandsson (1942) showed that the species Parnassia palustris L. has two chromosome numbers, 2n = 18 and 2n = 36. Rozanova (1940) found the same numbers in plants collected in the U.S.S.R. Some morphological differences could be demonstrated in the Swedish material (Erlandsson, 1942). This was confirmed by Löve and Löve (1944) and, therefore, these authors (1950) distinguish 2 species: the diploid Parnassia palustris L. em. Löve and the tetraploid Parnassia obtusiflora Rupr. em. Löve, also separated by sterility barriers and by their geographical distribution. In the Netherlands a tetraploid population was found by Gadella and Kliphuis (1963). As the tetraploid population occurs in an area situated far south of the circumpolar distribution area of the tetraploid plants, it seemed worthwhile to determine the chromosome numbers of other plants of Parnassia palustris L. growing in the Netherlands.

Description: Protium aracouchini (Aubl.) March. var. angustifolium Swart n. var. Folia 1- usque ad 5-juga; interjugum basale petiolo plerumque longius sed interjugis aliis brevius; petioluli breves; foliola oblongolanceolata 7.5-10 cm longa, 2-2.75 cm lata, apicem versus distincte angustata, apice gradatim in acumen lineare sexies usque ad nonies longius quam latius acuminato; nervi sec. utrinque usque ad 20. Holotypus: Lindeman 4504 (U, 078268B).

Description: Les systèmes radiculaires des espèces des prés salés du Juncion maritimi ont été étudiés. Nous avons distingué six types morphologiques principaux d’enracinement. Les particularités des différents types et espèces ont été décrites et dessinées. La répartition des différents types d’enracinement dans le Junco-Triglochinetum et le Caricetum divisae a été interprétée écologiquement. Les racines de nombreuses espèces du Juncion maritimi sont pourvues de lacunes aérifères. C’est une adaptation au niveau élevé de la nappe phréatique. La résistance mécanique du sol a également une influence sur le système radiculaire. La concurrence des systèmes radiculaires a été discutée. On a essayé de différencier les groupements végétaux par leurs types d’enracinement. Je tiens à remercier M. J. Braun-Blanquet, directeur de la Station Internationale de Géobotanique Méditerranéenne et Alpine à Montpellier, de son aide et de l’intérêt stimulant qu’il a porté à mon travail, et M. J.-M. Betsch de son conseil. Les subventions de la Koninklijke Nederlandse Akademie van Wetenschappen (Montpellier fonds) et du Utrechts Universiteitsfonds m’ont facilité le séjour à la Station et rendu possible ces recherches.

Description: In February and early March, 1961, the senior author spent three weeks on a small savanna in the approximate centre of Suriname, South of Tafelberg, (map 1). He was accompanied by Mr. W. H. A. Hekking. The time was spent in exploring the flora of the savanna and the adjacent forest. As a detailed study of the vegetation of the savannas of northern Suriname was then in progress, several extensive papers being in preparation (Heyligers, 1963; Van Donselaar, 1965; Van Donselaar-Ten Bokkel Huinink, 1966), it was felt that a more thorough inventory of the vegetation and the flora of the savanna might be rewarding. When a general impression of the plant-cover of the area had been obtained, eight representative sample-plots were selected, their vegetation was analyzed and described after the method of the French-Swiss school of phytosociology, and pits were dug in the soil down to bedrock, samples being taken in every distinctive-looking layer. This work was carried out jointly by the senior author and W. H. A. Hekking; part of the floristic exploration was also done by or with Dr. R. M. Tryon, Harvard Herbarium, Cambridge, Mass. The results are here presented. It was felt that in order to integrate them with those obtained elsewhere in Suriname, the collaboration of a specialist familiar with the Suriname savannas in general was required. This was the junior author’s task, who, after his prolonged work on the savannas of northern Suriname, later expanded his work to those of the southern part of the country. The preliminary results of the last-named study are in the press; more detailed field work is in progress as this paper goes to the press.

Description: The pollen assemblages of a core in the coniferhardwood formation in northwestern Minnesota are compared with the floristics of the recent vegetation in the region. Percentage levels of the main tree components have been compared first with those from recent surface samples taken at the same short distance from various types of upland forests and second with the regional values of the pollen rain in this area (McAndrews 1966). To that end all the data were recalculated on the basis of special pollen sums. The regional diagram of Stevens Pond shows basically the same assemblage zones as established by McAndrews but without the late-glacial Picea-Populus assemblage zone. The pollen in the following Pinus-Pteridium assemblage zone has been interpreted as derived from a pine forest. During the midpostglacial expansion of the prairie eastwards the regional vegetation must have been a Quercus savanna, locally with prairie. Corylus reaches relatively high percentages in this zone. Among the prairie elements especially the occurrence of Lilium philadelphicum may be noted. In the next zone the pollen diagram shows a rise of the curves of mesic elements. In spite of this the comparison with recent surface samples indicates a xerophytic Quercus forest rather than a mesophytic deciduous forest. In the following Pinus assemblage zone pine was present along the margin of Stevens Pond and is therefore overrepresented in the diagram. In the uppermost zone the pollen curves show the effect of logging of the forest about 1900. Pollen of cultivated and introduced plants appear in this zone. Many local pollen types were found, on account of local overrepresentation. This made it possible to compare the local Stevens Pond sequence with the composition of recent lowland vegetation types. The pollen sequence was similar to a large extent to the recent pattern of lake filling, starting with a eutrophic vegetation of Typha latifolia and Salix in the prairie period and leading to a Larix forest and then to a mesotrophic Picea mariana forest, the present edaphic climax on peaty soils. There is a delay, however, in the introduction of acidophilous species, the Larix forest being without Sphagnum and Ericaceae. This is explained by assuming an influence of the vegetation of the surrounding slopes upon the local vegetation. About 1900 the bog forest was destroyed by logging operations and replaced by the present Typha latifolia mat.

Description: Arbor 8 m alta, altitudine pectoris 20 cm diam.; ramuli teretes, glabri. Folia coriacea, glabra, plana, late elliptica vel late obovata, apice obtusa, rotundata vel subacuminata, basi attenuata et in petiolum decurrentia, 9-12 cm longa, 5-7½ cm lata, statu sicco supra viridia, leviter nitida, infra olivacea, opaca, marginibus subrevolutis, integris; costa et nervi primarii utraque facie prominentes, nervi primarii infimi tenues, inconspicui, spatio brevi margine paralleli, ii paris secundi costae paralleli et valde proximi supra basin folii, tum divergentes sub angulo 30°, plus minusve recti inter costam et marginem et 1-1½ cm a margine remoti, nervis primariis paris tertii coniuncta in parte tertia superiore laminae; nervi primarii tenuiores singuli vel plures primariis maioribus intercalati; venae secundariae leves, paucae, ad marginem et apicem laminae arcuatim coniunctae, rete supra occulto, infra minime claro; petiolus 1-2 cm longus, 2 mm crassus. Inflorescentiae axillares, 10-14 cm longae; rhachis glabra; flores geminati; pedicellus communis perbrevis, pedicellus communis cum individuali 4-4½ mm longus, glaber; bracteae minimae, triangulares mox deciduae; alabastra cylindrica, apice clavata, lutea, 8-9 mm longa; lobi perianthii glabri, crassi, apice leviter excavati, 8-9 mm longi, 1 mm lati, anthesi recurvati, pallide flavo virides; filamenta brevissima, lata, parte superiore loborum perianthii affixa; antherae 2.6 mm longae; ovarium brevissime et adpresse fusco-pilosum, 2 mm altum, sensim in stylum protractum; stylus apice leviter clavatus, stigmate terminali; glandulae disci quaternae liberae, crassae, subglobosae, 0.4 mm altae et latae. Fructus ignotus.

Description: Some of the basic concepts common to plant taxonomy, palaeobotany and palynology are discussed such as “taxon”, “taxonomic categories”, “genus and species concepts”, as well as “organ and form genera”. The development of the specifically palaeobotanical and palynological concepts of organ and form genera is briefly treated in the light of the shaping of palaeobotanical thought and methods since Adolphe Brongniart. The need for a single category of an artificial nature (i.e., form genus) is acknowledged; the need for a second category of such nature (i.e., organ genus) is questioned. The general guide lines for good palynological practice given by Faegri et al. (1950) are recommended for future use and are reprinted as an appendix to this paper.

Description: Three genera of the Proteaceae belonging to the tribe Grevilleeae occur in the Guianas and Brazil: Roupala, Panopsis, and Euplassa. The microscopical wood structure of one of these genera, Euplassa, has not been described before. Anatomically it proves to be nearly identical with Panopsis which it also resembles in general properties. Roupala differs in several respects. Within the genera differences are not fundamental and chiefly a matter of numbers and dimensions. A key to the genera is given. The relation of these three genera with the two other members of the tribe in South America, Orites and Gevuina, is discussed.

Description: *Burkill, I.H.: Chapters on the history of botany in India, 1965, xi + 245 pp., 4 portr., 2 maps. Manager of Publications, Government of India Press, Delhi 8. Sh. 12/6, or $ 1.98. It was not necessary to mention that Burkill began compiling this book at the age of 81 to finish it at 93, for, although the last two chapters are miscellaneous in contents, it could as well have been written by a man thirty years younger. Everybody will regret that the book ends at the time Burkill’s own contributions to Indian botany began, notably about 1900. As for the period covered, and that is from the earliest beginnings, the book is a rich store of information. It was published in chanters in the Journal of the Bombay Natural History Society 4 and has now, after considerable revision by the author, been brought out by the Botanical Survey of India, preceded by an Introduction by Father H. Santapau, the Director, who therein put Burkill’s considerable merits for Indian botany on record.

Description: Roxburgh, W., Plants of Coromandel, etc. Add (to Fl.Mal. I, 4, 1954, p. CLXXI): cf. D. Wood, Not. R.Bot.Gard.Edinb. 29 (1969) 211-212.

Description: The following families are already revised and will be included in Flora Malesiana vol. 4, part 1 which is made ready for the press: Aceraceae, Actinidiaceae s.str., Alangiaceae, Ancistrocladaceae Aponogetonaceae, Burmanniaceae, Geratophyllaceae, Cochlospermaceae, Hydrocaryaceae, Juncaginaceae, Moringaceae, Myoporaceae, Nyssaceae, Philydraceae, Plumbaginaceae, Podostemonaceae Sarcospermaceae, Sphenocleaceae, Stackhkousiaceae, Styracaceae, Trigoniaceae, Zygophyllaceae.

Description: The Arnold Arboretum of Harvard University, Jamaica Plain, Mass. The Gray Herbarium of Harvard University, Cambridge, Mass. U.S. National Herbarium, Smithonian Institution, Washington, DC. New York Botanical Gardens, Bronx Park, Fordham Br.P.O., N.Y. Bot. Gardens, Ann. Arbor, Mich. University of California, Department of Botany, Berkeley, Cal. Field museum of natural History, Department of Botany, Chicago, Ill. Great Britain. Royal Botanic Gardens, Kew-Surrey (except types) British Museum, Natural History, Bot. Department, Cromwell Road, London SW & Botany School, Cambridge.

Description: Mr C.T. White is to be congratulated on being presented with, the Mueller Memorial Medal awarded by the Adelaide Meeting of the Australian and New Zealand Association for the Advancement of Science, Aug. 1946. This award is in recognition of his work on the systematic botany of Queensland. Dr Ir J.Ph. Pfeiffer, Director of Research, B.P.M.-lab., Amsterdam, died Nov. 18, 1947, at Amsterdam, 58 years old. He was formerly wood-technologist, and collected plants in Simaloer Island, NW Sumatra.

Description: The affinity of the Malesian genus Lophopyxis has a checkered history, a survey of which was given by L.B. Holthuis & H.J. Lam, in Blumea 5 (1942) 205-208, fig. 7. It has been referred to Flacourtiaceae, Icacinaceae, Euphorbiaceae, Olacaceae, and Saxifragaceae. Hitherto no attention was paid to the similarity with Gouania in the Rhamnaceae, which it resembles in toothed leaves, presence of stipules, panicled spike-like inflorescences, and the occurrence of tendrils in these.

Description: Dr. B.O. van Zanten, Groningen, will soon finish the revision of Malesian species of Racopilum and Powellia (Racopilaceae). Mr. J.H. Hilbrands has in 1968/69 worked on the species of the genus Papillaria of Malesia and adjacent countries (at Groningen, under supervision of Dr. van Zanten).

Description: Bignoniaceae. Dr van Steenis is wording on a revision of the Malaysian Bignoniaceae for Flor. Mal.. Burmanniaceae. Dr F.P. Jonker, Herbarium, & Museum voor Systematische Botanie, Lange Nieuwstraat 106, Utrecht, Holland, is preparing a new revision of the Burmanniaceae for Fl. Mal.

Description: Taxonomists working with material collected by the Sarawak Forest Department have often been hard put to decide how to quote numbers. Is the departmental series number preceeded by a letter S, or an F, or would it be best to quote only the collector and the number? I have tried to unravel the history of the Sarawak Forest Department herbarium number series in order to provide a guide to unequivocal citation. This has not been easy, as all collecting books previous to 1951 have disappeared, apparently during the second world war; many of the herbarium collections are now missing at Kuching and Kepong, where most were distributed, for the same reasons, though there seem also to have been large gaps in the series where numbers were never used. What has eventually been brought to light has been a masterpiece of confusion only vied with in complexity by its Sarawakian forbear, the remarkable numbering, or rather lettering, system of Haviland (explained in Kew Bull. 1907, 197— 198).

Description: These small structures in nerve axils at the underside of leaves have given food to various theories and have been nonetheless in phytographic and taxonomic neglect almost from the beginning. That was in 1887, when the Swede A.N. Lundstroem published an extensive paper, in which he explained domatia as structures intended to accommodate mites – hence the word acarodomatia – which latter would in turn benefit the plant by cleansing the leaves from fungus spores. Lundstroem arrived at this hypothesis on the strength of ideas current in that time, about the existence of symbiotic relations between ants and plants; it was in the heydays of teleology. A closer investigation left little of the illusions about mutual benefit between ants and plants, but such critical interest was never focused on the supposed relation between mites and plants. Recently I could grow a few domatia-bearing species under acari-free conditions; the plants with their domatia did as well as in the open. Yet it is hard to prove that Lundstroem was wrong, but a combination of the experiment, the wellknown fact that domatia are inhabited by acari as often as not, and the origin of the hypothesis make if very unlikely that mites will creep into domatia for other reasons than a natural preference for shelter in small holes. All other (physiological) explanations are unconvincing, too, and so for the time being an explanation is lacking – provided that such an explanation would be necessary.

Description: Index Kewensis. Suppl. 10. (1936-1940). Clarendon Press, Oxford, £4/4. (1947). Check List of British vascular plants (Journ. Ecol. 33 (1946) 308-347). Nomenclature accepted by the Brit. Ecol. Soc. to uniformize the binary names used for British plants.

Description: Index to the Enumeration of the Orchidaceae of Sumatra, by J.J. Smith. At the Rijksherbarium there was a handwritten copy compiled by the late Dr. J.J. Smith of his important enumeration of Sumatran Orchids, published in Fedde, Repertorium 32 (1933) 130-386, which was obviously for reasons of economy not printed. The author left a note to the Librarian of the Rijksherbarium saying that it is indispensable for consulting this work, as many orchid names were here reduced to synonymy for the first time. This is now available for orchidologists and libraries in stencilled form in the same format as the Enumeration, with the Library of the Rijksherbarium, Schelpenkade 6, Leyden, Holland.

Description: Dr. P. S. Ashton of Kuching went on leave at the end of September 1965, to return mid-1966. In Europe he hopes to consult some Herbaria for type materials of Dipterocarpaceae. Mr. M. M. J. van Balgooy of the Rijksherbarium travelled in New Guinea, Australia, Lord Howe Island, and Java, from 30 March to 14 August 1965.

Description: Field work on the Ceylon Flora. Trimen’s ”Handbook” on the flora of Ceylon, published between 1893-1900, is one of the finest floras ever written of a tropical area. It is a five volume descriptive work that served very adequately for many years. It is now not only out-of-date, but completely unobtainable. The Smithsonian Institution, in cooperation with the University of Ceylon and the Royal Botanic Gardens, Peradeniya, is initiating a project to bring up to date and republish the Trimen ”Handbook” by providing an opportunity for field work in Ceylon.

Description: Bakhuizen van den Brink, Jr, R.C.: Een bijdrage tot de kennis van de Melastomataceae van den Maleischen Archipel in het bijzonder van die van Nederlandsch-Indië. Thesis. Gouda 1943, VIII 31 pp. (in Dutch). Extract from the general and critical parts of the extensive study; no latin descriptions.

Description: In 1969 Indonesian botany suffered a severe loss by the untimely death of Dr. B. Prijanto, at the end of April. He was the head of the Forest Exploration Division, Forest Research Institute, Bogor. He belonged to that still very small, but admirable circle of young able Indonesian botanists built up in the early sixties, largely through the efforts of Dr. Kostermans. Dr. Prijanto studied palynology for one year at Stockholm, after which he proceeded to Edinburgh where he received a thorough training under Dr. Burtt, working largely on the systematics of Scrophulariaceae, in connection with problems in Gesneriaceae. He was a very nice and energetic man, full of plans for the future exploration of Indonesian forests. Our sympathy goes to his young wife, whom he had married only a few months before. He was a victim of an unfortunate car accident in SW. Celebes. The accident occurred when he was hunting for Eucalyptus with two Australian foresters, who both met an untimely death as well, one of them being Mr. E. Larsen, of Canberra. Another thing that lamed botanical activity at Bogor was the serious trouble which Dr. Kostermans ran into with the police by whom he was detained. We hope that he will soon be cleared and that this will be a mere incident which will not affect his energy nor his enthusiasm for Indonesian botany. Unfortunately, through this mishap, he was unable to lead the Seminars on botany in August, neither could he accompany the British Museum Botanical Expedition to Central Celebes led by Dr. Jermy. These tasks were taken over by Dr. Rifai. Dr. Kostermans was also unable to attend the opening of the partly finished new Herbarium building in October, towards the planning of which he had contributed so much.

Description: *Allen, B. Molesworth: Malayan Fruits. An introduction to the cultivated species (with Thai and Tamil names). 1967, 245 pp., 73 fig., 10 photo., 1 tab. 8°. Donald Moore Press Ltd. Singapore. M$ 7.50. A popular guide in a handy well illustrated and wellprinted cheap hook of the most common edible fruits. By the ”quick guide” on the table one can orient himself on the identity; also within the genera there is a key to the species or varieties. Each species is fully described and for the layman a glossary of botanic terms is added, for the housewife a list of recipes.

Description: Mr R.E. Holttum, Director of the Botanic Gardens, Singapore, who was on leave in England from July to mid-November, reported that Mr C.X. Furtado has returned to Singapore and is working on the genus Calamus as part of his revision of the Palmae of the Malay Peninsula. Mr Holttum ’aims at getting a revised Flora of the Malay Peninsula written, of which he himself will be responsible for most of the Monocotyledones except Aroids and Palms. Mr M.R. Henderson is working on some families of Dicotyledones. This Flora must be fuller than Ridley’s, and with sufficient introductory matter and illustrations to make it intelligible to the ordinary resident who is prepared to take soms interest in local plants’. Mr Holttum will retire in 1950; he will then devote his time to revise Flora Malesiana, series II, Pteridophyta. Mr Holttum spent a fortnight in Holland, in October, and discussed the contributions to Flora Malesiana which can be prepared at Singapore on the basis of mutual cooperation. Dr A.J.G.H. Kostermans has been appointed Forest Botanist in the Forest Experiment Station, Buitenzorg, Java. He has resumed his studies on the Malaysian Lauraceae.

Description: Flora of Java. Dr C.A. Backer has been working towards the composition of a Dutch-written Flora of Java since about 1903, at first in Java, and onwards of 1931 in Holland. When the war started it was thought safer to mimeograph the MS. as far as it was finished, in order to save the writers’ labours against the chance of complete destruction by bombing or other causes. Prof. Dr H.J. Lam managed to get a number of subscribers and funds for a mimeograph edition. This constitures the ”Nooduitgave” (emergency edition) in which up till now 120 families have appeared in 7 folio volumes. The edition was limited to ca 25 copies. It is the intention to edit 2 volumes more, and then stop it. Circumstances necessitate the printed edition to be written in English to which the author has now consented, and which he will manage himself, Prof. Lam also succeeded in getting a number of temporary cooperators who have assisted Dr Backer in revising some families, viz. Dr A.D.J. Meeuse, A.G.L. Adelbert, and R.C. Bakhuizen van den Brink Jr, whilst the specialists Dr J. Wasscher, Dr S.J. van Ooststroom and Miss Dr G.J.H. Amshoff and the late Prof. Dr B.H. Danser made contributions. She revisions are now nearing completion. Only very few families, mostly sympetalous, are not yet finished. The flora will include the Pteridophytes (more than 500 in Java) and through the consent of Mrs Smith also the Orchidaceae (ca 700!); the latter will be revised on the basis of the MS. revision left by the late Dr J.J. Smith. In the emergency edition practically all synonyms have been omitted for brevity’s sake. It is to be hoped that they will be re-inserted in the scientific edition now aimed at. Endless labours have been spent in identifying the species described under various names, and to a certain extent these synonyms have shaped the specific delimitations and argumentate the present conceptions. They can be omitted in a concise popular flora, but not in the work now prepared. It has taken a long way to reach the present state to account for the flora of Java, but we are sure that the work will certainly be the most valuable contribution towards the flora of Java ever made, as its author possesses an unsurpassed field knowledge combined with a very critical taxonomical point of view.

Description: We are glad to be able to add to the list of herbaria which have agreed to send on loan herbarium specimens to collaborators of the Flora Malesiana: Herbarium of the Forestry Department, Sandakan, British North Borneo. Mr H.G. Keith, Conservator of Forests is in charge. Herbarium of the Forestry Department, Lae, Territory of New Guinea. Mr J.S. Womersley, Forest Botanist, is in charge (see p. 61).

Description: Dr C.A. Backer is now preparing the MS. on the Orchidaceae for the Flora of Java on the basis of a MS. by the late Dr J.J. Smith. Mr J. Monachino has finished his revision of the genus Alstonia (Apoc.); it is expected to be published early in 1949 in ”Pacific Science”, Hawaii.

Description: It is a great pleasure to announce that the technical difficulties delaying the printing of Flora Malesiana have now been overcome. The first part of volume 4 is in the press and, in all probability, will appear towards the end of this year. Sample sheets of volumes 1, 2, and 3 will be added to the initial instalment of volume 4. Owing to a generous grant by the Netherlands Indies Government of this first issue of the 4th vol. 2500 copies will be printed and distributed to all individual botanists and institutions which are believed to have an interest in the Flora, in order to enable them to form an idea of the scope, execution, and costs of subscription of the work. Those receiving this Bulletin will also receive the initial part. It is expected that volume 1 – which will be issued as one whole – will be in print at the end of this year.

Description: Ashton, P.S.: A Manual of the Dipterocarp Trees of Brunei State and of Sarawak. Supplement. Borneo Literature Bureau, Rock Road, Kuching, Sarawak (Printed by Cathay Press, Hong Kong). 1968. viii + 129 pp., 15 fig., 20 pl. (photogr.), large 8°, clothbound. M$ 18.00 + postage M$ 1.30; bank charges of M$ 1.75 are required on foreign cheques. This ’Supplement’ records all Dipterocarpaceae from Sarawak, to the huge number of 247, 12 of which are yet undescribed by being insufficiently known. In the large Brunei Manual, published by the Oxford University Press (1964), 153 of these species had already been fully described; besides in that book very full evidence was given in many other aspects. This information is not repeated here. The Supplement provides keys (one botanical and one field key in all cases) to genera and all 247 species quoting all Sarawak collections, and providing for a full botanical description of all species not recorded in the Brunei book. It is therefore to be used together with the latter. A great asset as a precursor to the Malesian dipterocarps. The work is excellently printed on good paper.—v.St.

Description: Prom Dr Y. TSIANG, now residing at the Bot. Institute, Sun Yatsen Univ., 30 Fat-Ching Road, Canton, China, we received a set of three volumes published during World War II, all prepared by G. Masumune. They are the following: Enumeratio Phanerogamarum Bornearum. 739 pp. (1942) 1) An attempt to give a revised edition of MERRILL’s Enumeration of 1921. The Introduction and notes under the species are in Japanese characters. The number of genera recorded is 1310, the number of species 7201. Pamilies are arranged in a systematic sequence; an index to family and genus names concludes the volume. In some cases, new combinations are made, e.g. by reduction of Rigiolepis to Vaccinium (Eric.), further in Hanguana, Porterandia, & c. The work has been done rather uncritical: e.g. Styrax agrestis and St. serrulatus are both entered, though ithas been shown that the Bornean record of the latter is wrong and must be replaced by the former species. Peliosanthes albida is both mentioned under Liliacease and Haemodoraceae; Aletris foliolosa is mentioned in Aletris, but A. rigida is entered in Meta-aletris though the two are difficult to distinguish. Nomenclature is not up to date (see Chloranthus, Trema, & c.). A large number of important publications on the Flora of Borneo pubished posterior to 1921 are neglected. The author has apparently far underrated the difficulties in composing a cyclopedia. The latin-written text is full of errors.

Description: ( (Report in the ”Gardens’ Bulletin, Singapore”, vol. XI, pt 4, 1947). Prior to the Japanese attack on Malaya, most of the senior staff of the Gardens were seconded for other duties under the Department of Food Control and Information, for at least part of the time. The result was that botanical work was reduced, and considerable arrears of unnamed and undistributed specimens accumulated. The Gardens were maintained as usual, with the addition of demonstration plots of vegetables.

Description: The practice of citing collections made in institutional series by the letters of that series instead of by the collector’s name (e.g. FB 23435 instead of Aquilar & Valderrama FB 23435) led, with the publication of so many Identification Lists, to the dishing out of an alphabet soup that many a botanist or curator of collections may find hard to digest. In itself, the system of collecting in long institutional series is an excellent one, permitting great economy in space when collections are to be cited. The oldest series seems to be the KB-one, dating from about 1870, established by Scheffer, followed early in this century by the BS and FB series, established by Merrill. A good number-stamp may have contributed much to the success and consistency with which the series were maintained for a long time. In other institutes, there has been created what Dr. Ashton characterized as ”a masterpiece of confusion”, the unravelling of which, as can be seen from his paper on ”The numbering of Sarawak Forest Department collections” in this Bulleton on pp. 1432-1435 (1966), requires a good deal of research. The purpose of this paper is only to give a list of abbreviations in use between Thailand and the Solomons, for the guidance of those who compile, and those who use Identification lists. These Lists, products of the work for the Flora Malesiana, serve as documentation as well as being of use for the identification of Malesian duplicates not seen by a taxonomist himself. When compiling and using such a list, three questions are to be considered.

Description: Brizicky, G.K. (1901-1968) Research Botanist, Harvard Herbarium, died of a heart attack, June 15, 1968.

Description: In 1826 REINWARDT published in ”Sylloge Plantarum” &c, vol. 2, pp. 1-15 under the title ”Nova plantarum indicarum genera” an article containing descriptions of some Malaysian genera of phanerogams. Amongst them is described on pag 1: Angiopetalum punctatum Reinw. n.g.n.sp. from Java. Though assigned to the Myrsinaceae by DALIA TORRE & HARMS this genus has hitherto remained obscure, and has not even been mentioned by MIQUEL. However, there is a name Allopetalum punctatum REINW. mentioned by SCHEFFER (De Myrsin. 1967, 93) as a MS. name in the synonymy of Ardisia pumila BL., also mentioned by MEZ (Pfl. Reich 9 (1902) 171) for that plant, which is now commonly known as Labisia pumila (BL.) B. & H. The type specimens of Allopetalum punctatum REINW. at Leyden (sheets 908.133.- 614 and 903.255 – 190) are undoubtedly the type specimens of Angiopetalum punctatum REINW. The name under which this species was published differs from that found in REINWARDT’s handwriting hut this is of small significance. Many name-changes occur in the materials assembled by KUHL & VAN HASSELT, ZIPPEL, REINWAKDT (and BLUME) whose herbaria were left in BLUME’s care. On the type sheet of Orescia montana REINW. in the same paper of REINWARDT’s I found on the labels the following MS. names: Lysimachia montana BL., Phaemeria montana, Rumeria montana and Lysimachia cuspidata BL, an embarrassing choice from which only the last one has been validly published. In the case of Angiopetalum, REINWARDT who had probably the herbarium not at his disposal copied the name from MS. notes, the herbarium being with BLUME either in Java or at Brussels. Later he hardly paid any attention to phytography or nomenclature.

Description: As was pointed out in the first instalment, the management of Flora Malesiana acknowledge collaborating and co-operating institutions; for this purpose a distinction was made between collaborators and co-operators. The former take an active part in the composition of the work (by revising certain families or large groups), the latter give assistance through the loan of specimens, information about collections, biblographical assistance etc.

Description: Since the last Bulletin was published we have to regret the loss of one of the last of the Mohikans of the Treub period of ’s-Lands Plantentuin (Kebun Raya Indonesia) at Buitenzorg (Bogor), namely of Dr. Charles Bernard, born 1876 in Geneva, who died at Amsterdam, 29th July 1967, aged 90. He studied at Geneva, finished his education by getting his degree in 1894, after which he remained for six years assistant to Prof. Dr. R. Chodat under whom he prepared a doctor’s thesis in 1901 (published 1903) on the embryology of some parasitic plants which led him to consider Lathraea as a scrophulariaceous genus.

Description: Small trees, mostly deciduous, bark gummy, wood soft, roots thickened, pungent; trunk often inflated. Leaves spread, imperfectly 2—4-imparipinnate; tissue with myrosin cells; pinnae opposite, provided with stipitate glands at the base of the petiolules and pinnae. Leaflets small, opposite, entire, all articulated. Stipules represented by blunt knobs. Flowers bisexual, zygomorphic, white (or yellow streaked red), in axillary panicles. Calyx tube short, as a hypanthium; lobes 5 imbricate, spreading or reflexed, separately dropping. Petals 5 free, anterior one largest and erect, others reflexed, posterior smallest. Disk lining the calyx tube, with a short free margin bearing the androecium. Perfect stamens 5 epipetalous; anthers dorsifixed, 1-celled, oblong, when lengthwise opened broader. Staminodes 5, subulate, with or without rudimentary anthers. Ovary superior, shortly stalked, 1-celled with 3 parietal placentas. Style filiform, stigma small. Ovules ~, in 2 series on each placenta. Capsule linear, beaked, 3—6-angled; valves thick, spongy, on the inside with pitted cavities in 1 row along the median line. Seeds 3-winged (or exalate), body roundish large. Embryo exalbuminous, straight, containing oil. Distr. Ca 10 spp., confined to the semi-arid countries of Somaliland, Madagascar, SW. Africa, NE. Africa, Asia Minor, 2 spp. in India.

Description: Small trees, shrubs or twining woody plants, rarely herbs; branches terete. Glands present in various parts. Indumentum consisting of simple hairs, or in Viburnum sometimes lepidote; glandular hairs mostly present. Stems often pithy. Leaves decussate, simple or deeply divided (Sambucus), sometimes provided with pitted or cup-shaped glands exuding resin. Stipules absent or very small. Flowers ♀, actinomorphic or zygomorphic, mostly cymosely arranged, 4—5-merous; outer flowers in an inflorescence sometimes differing from the normal ones, rarely ( Sambucus p.p.) some fls aborted into extra-floral nectaries. Calyx adnate to the ovary, (4—)5-fid or -toothed, mostly constricted below the limb; sepals often enlarged in fruit. Corolla epigynous, gamopetalous, sometimes 2-lipped, lobes mostly imbricate in bud. Stamens inserted on the corolla tube, alternating with the lobes, extrorse or introrse. Anthers free, 2-celled, dorsifixed, versatile, cells parallel, opening lengthwise, mostly introrse; filaments sometimes reflexed or curved in bud. Ovary inferior, 1-(2-)3-5(-8)-celled, in fruit cells sometimes partly abortive. Style terminal, often slender with one knoblike stigma, or 3 short partly connate styles. Ovules 1(-~), pendulous or axile. Fruit a drupe or berry, rarely a capsule. Seeds often only one per fruit, often with bony testa. Endosperm copious, sometimes ruminate; embryo straight, often small and linear, axial, cotyledons oval or oblong. Distr. Ca 10-14 genera, mainly distributed on the N. hemisphere, in the tropics mostly confined to the mountains, on the S. hemisphere only Viburnum and Sambucus, an endemic genus in New Zealand, two monotypic endemic genera in New Caledonia, in Australia only Sambucus in the eastern part.

Description: Annual or perennial herbs or shrubs, often fleshy, glabrous, papillate or hairy. Leaves opposite or alternate, exstipulate, sometimes seemingly wanting, stalked or sessile, entire, dentate-serrate-lobed or irregularly gashed. Flowers solitary, 2—3-nate or glomerate, usually sessile, either axillary or in terminal or axillary dense or interrupted spikes or panicles, ♀ or unisexual, monochlamydous, rarely achlamydous, small; bracts present or absent, usually small, rarely leafy. Perianth herbaceous or sometimes scarious, rarely (in ♀) absent, 3—5-partite with (in bud) imbricate segments, or sometimes almost entirely gamophyllous and then shortly lacerate-dentate or unilaterally cleft, persistent, after anthesis accrescent or not. Stamens often the same number as tepals and opposite to them, sometimes fewer, usually inserted on or near base of perianth; filaments free or shortly connate; anthers dorsifixed or inserted in a basal cleft, 2-celled (4-locellate); cells bursting longitudinally. Ovary free or at the base adnate to the perianth, 1-celled; ovule 1, basal, sessile and erect or suspended from a funicle; styles or stigmas 2-5, linear. Utricle either enclosed by the perianth or not, indehiscent or rarely operculate; seed erect, oblique or horizontal, usually compressed; endosperm mostly present, peripheral, surrounding the embryo; embryo annular or spirally twisted. Distr. Species numerous, inhabitants of the temperate and tropical zones of both hemispheres.

Description: Delicate, annual or perennial herbs, aquatic and then either entirely submersed, or floating in the upper part, or, in humid localities, not rarely terrestrial and creeping, with slender stems. Leaves opposite, at the summits of floating stems often spuriously rosulate, exstipulate, small, linear, elliptic, oblong or spathulate, entire, herbaceous, in the Mal. sp. triplenerved. Flowers minute, unisexual, axillary, solitary or rarely one ♂ and one ♀ flower from the same axil, often with 2 caducous, transversal, opposite, tender concave bracts. Calyx and corolla absent, ♂: Stamen 1; filament thin, anther 2-celled, cells bursting lengthwise, the slits becoming confluent at the top. ♀: Ovary sessile or subsessile, 4-lobed, 4-celled. Ovule solitary in each cell, pendulous from the top of the cavity. Styles 2, free, often long, papillose. Fruit 4-lobed, with longitudinally margined or winged lobes. Testa membranous; endosperm fleshy; embryo terete, straight. Distr. Only genus in the family, worldwide distributed, not yet known from S. Africa and in various regions scarce, in Malaysia apparently very rare, the only record proving its being indigenous is from the New Guinean highlands. Because of their small size terrestrial forms are easily overlooked.

Description: In volume 53 of the Arquivos do Museu Nacional (pp. 1-54, 15 fig., 6 tables) there is an interesting ecological account on the vegetation of the famous Itatiaia Range by Mr. F. Segadas-Vianna and Leda Dau (co-author on climatology). The advantage of these two papers (vegetation and climate) is that they provide pertinent data and a fair description.

Description: Trees (or shrubs), often deciduous, producing gum and an orange juice. Leaves spread, palmatilobed, often with domatia in the axils of the main ribs; stipules caducous. Flowers actinomorphic, bisexual, showy, mostly golden-yellow, paniculate or racemose. Sepals 5 imbricate. Petals 5, imbricate or contorted, emarginate. Stamens ~, with free filaments, equal or subequal; anthers 2-celled, linear, basifixed, opening by introrse, short, often confluent pore-like slits. Ovary 1-celled with laminal placentas projecting into the cell, or perfectly or imperfectly 3-celled, the upper portion remaining 1-celled; ovules ~, style simple, stigma punctiform. Capsule 3—5-valved, valves of the endocarp separating from and alternating with those of the pericarp. Seeds covered by woolly hairs, mostly cochleate-reniform; endosperm copious, rich in oil; embryo large, conforming to the shape of the seed; cotyledons broad. Distr. Ca 15 spp., mostly in trop. and subtropical America, some in trop. Africa and SE. Asia, 3 species in N. Australia, rare in Malaysia; G. gillivrayi is possibly the only native Malaysian species. LAM assumed the genus to belong to the ‘antarctic’ type(Blumea 1 (1935) 135), but it is manifestly peri-tropical.

Description: My visit to and trips in Taiwan, in 1966, brought me into close contact with the wonderfully rich and varied flora of this large island which is fairly easily accessible if one speaks Chinese or is accompanied by Chinese companions, as was my privilege. As is well known the woody flora of Taiwan is tolerably well known, by the excellent work of Kanehira (1936), followed by the modern works of Prof. Tang-shui Liu (2 vols, 1960-1962) and Prof. Li (1963).

Description: Evergreen, glabrous trees or shrubs, without resin-tubes. Leaves spread, simple, entire, more or less crowded towards the ends of the shoots, shining, exstipulate; midrib sulcate; shoots with perular terminal buds. Branches often in pseudowhorls. Inflorescences terminal, sometimes lateral, generally not exceeding the leaves. Flowers on the ultimate axis in fascicles of 3, towards the end solitary, pedicellate, bracteate. Calyx deeply 5-lobed, fleshy, persistent, petaloid, lobes inequal, concave, imbricate, 2 outermost smallest. Petals 5, thinner than the sepals, inserted at the margin of the disk-like receptacle. Stamens 5, attached to the base of the petals; filaments flattened or terete, slightly thickened towards the base; anthers dorsifixed, dehiscing lengthwise, intrors. Staminodes petaloid, dentate in the upper half, top mostly pointed, alternating with the petals. Disk glands 5, ovoid to ellipsoid, epistaminodial. Ovary ovoid, originally 2-celled, one cell soon abortive. Styles 1-2; stigma punctiform. Ovule 1, pendulous, anatropous. Fruit drupaceous, or a nut, with fibrous endocarp. Testa membranous; cotyledons planoconvex; albumen absent. Distr. Four spp., one each in New Zealand and adjacent islands, N. Caledonia, the New Hebrides, and N. Queensland & E. Malaysia.

Description: Mostly perennial, paludose, grass-like herbs with fibrous roots; stembase very rarely thickened, often profusely producing shoots. Leaves basal, distichous on each shoot, ensiform, linear or filiform, sometimes twisted; sheaths with a membranous margin (in Mal. spp.) producing mucilage (?always), with or without a short ligule; limb glabrous or with numerous, small hard papillae, sometimes with a stout nerve in either margin. Flowers ♀♂, in terminal, few- to many-flowered heads, 3-merous, yellow to white, ephemeral, each in the axil of a conspicuous bract; bracts conchate, imbricate, spirally arranged, lower ones sterile; one to few flowers simultaneously in anthesis. Peduncles scape-like, terete to compressed, sometimes winged or ribbed, glabrous or with numerous hard papillae, at the base with some sheaths provided with a short limb. Bracts entire, ciliate, fimbriate or lacerate, with one complete main nerve and some complete or incomplete longitudinal secondary (descending) nerves, in the apical part mostly with a small minutely-papillose field. Calyx zygomorphic; lateral sepals navicular, with entire, dentate or ciliate crest, wings membranous, entire, glabrous or ciliate; median sepal membranous, spathelliform or cap-shaped, enveloping the corolla, mostly obovate, 1-3(-5)-nerved, pushed out by the corolla in anthesis(?always). Corolla actinomorphic, ephemeral; petals with an orbicular to obovate limb and a long, narrow claw, free, cohering mutually or by the staminodes. Stamens mostly 3 fertile epipetalous inserted on the petals and 3 alternating staminodes, staminodes rarely absent, or all stamens fertile; filaments short; anthers basifix, dehiscing lengthwise extrorsely. Ovary superior, sessile to stipitate (in Australian spp. sometimes with 3 hard swellings at the top), 1- or 3-celled, or incompletely 3-celled. Placentas parietal, central, or basal, with ~ ovules; styles filiform, apex 3-fid, stigmas mostly capitate. Fruit shape similar to that of the ovary but larger, loculicidally 3-valved. Seeds ellipsoid to obovoid, often ribbed, with a long funicle. Distr. Xyridaceae are confined to the tropics throughout the world including the southern parts of North America; east of Malaysia and Australia hitherto only recorded from the Patau group (Korror) and New Caledonia.

Description: The Flora Malesiana is not preceded by a general key enabling one to identify any unknown native or wild plant to the family or genus to which it belongs. This is certainly a serious lack and presents a formidable handicap to inexperienced taxonomists in rapid naming current collections. However, there are several forcing arguments for omitting—at present—such an attempt which in itself would present no facile task, and could be accomplished only by a taxonomist thoroughly acquainted with the Malaysian flora. One could of course use some world key as a basis and cut out the entries leading to genera or families not represented in the Malaysian flora, but this procedure would be unsatisfactory, specially as these world keys make little use of vegetative characters; the latter appear to me very important specially in the earlier forks of the keys.

Description: Annual or perennial, unarmed or spinous, bitter herbs or undershrubs, often glandular-hairy. Stem terete, farctate, with a peripheral whorl of air-vessels. Leaves spread, simple, entire, exstipulate. Flowers ♀, actinomorphic, solitary, opposite or between the leaves, or by stunting of the leaves, more or less arranged in a racemiform or paniculiform inflorescence, distinctly pedicelled, lilac blue. Calyx persistent, 5-partite to near the base, segments lanceolate, imbricate in bud, after anthesis not or hardly accrescent. Corolla gamopetalous, deeply 5-partite; limb rotate; segments imbricate in bud, oval, obtuse. Stamens 5, free, inserted in the throat of the corolla, alternating with the segments; filaments filiform from a broadened base, glabrous or papillate; anthers 2-celled, bifid at the base and apex, opening lengthwise. Disk absent. Ovary superior, 2- (rarely 3-, very rarely more-) celled; placentas adnate to the dissepiment, spongy, entire or in cross-section bifid; styles 2 (rarely 3 or more), free; stigmas capitate-clavate. Ovules ~. Capsule globose or ellipsoid, loculicid, or both loculicid and septicid, 2(rarely more)-valved, or bursting irregularly. Seeds ~, very small, longitudinally ribbed; endosperm small, straight. Distr. Species ± 20, in the tropics of both hemispheres; in Malaysia 2, of which one indigenous, the other introduced and naturalized in Java.

Description: Rhizomes (rarely spiny) producing annual, mostly twining shoots, in Malaysia twining either to the right (fig. 4c) or the left (fig. 4a). Stems consisting of a main stem and sterile branches, both bearing leafless flowering axes. Leaves petiolate, generally cordate, simple and entire or palmately lobed, or palmately compound, except in the latter triplinerved; apex generally glandular, developed before the blade (forerunner tip); blade usually glandular on the lower side chiefly towards the base. Flowers hermaphrodite or dioecious, ♀ with staminodes, ♂ without even a rudimentary ovary, actinomorphic, 3-merous, mostly inconspicuous and greenish, ♂ often massed together and scented. Tepals in two whorls of 3. Stamens in 2 whorls of 3, the inner sometimes sterile; anthers usually introrse. Torus an urceolate, perianthoid chamber in Stenomeris, a saucer or cup in many spp. of Dioscorea, fleshy in Dioscorea § Enantiophyllum, in some spp. enlarged into a cone making the stamens appear to be connate. Style 1 with 3 bifid stigmas. Ovary 3-locular, inferior, sometimes separated from the perianth by a constriction. Ovules 2 in each cell or ~ (in Stenomeris), anatropous. Fruit a capsule, but it breaks up rather than dehisces in Trichopus. Seeds winged or wingless (in Trichopus); endosperm horny, embryo in a marginal pocket. Distr. Ca 9 genera and about 600 spp. (Dioscorea large, the other genera small or monotypic). Pantropic with considerable extensions into temperate regions. The Stenomerideae and Trichopodeae are restricted to the warm humid regions where Nepenthes grows and their geologic history must have been that of Nepenthes: they may be regarded as the survivors of the hermaphrodite ancestry of the Dioscoreeae.

Description: Herbs or shrubs, sometimes parasitic, usually with twining stems, occasionally prostrate or creeping, or erect, very rarely trees, often with milky juice. Leaves mostly spirally arranged, in parasitic species absent or nearly so, usually petioled; petiole sometimes with extra-floral nectaries. Stipules absent, pseudostipules (leaves of axillary shoot) rarely present. Inflorescences mostly cymose, one- to many-flowered, with mostly opposite or subopposite bracts at the base of the cymes or under the solitary flowers; rarely racemose. Flowers generally hermaphrodite, actinomorphic, rarely slightly zygomorphic, usually 5-merous, rarely 4-merous, various in size and colour, often showy. Sepals usually free, imbricate, with quincuncial aestivation, often persistent, sometimes accrescent in fruit. Corolla sympetalous, of various shapes, often funnel-shaped or campanulate, more rarely rotate, salver-shaped or urceolate; the limb nearly entire or more or less deeply lobed, often contorted-plicate in bud, or valvate or induplicate-valvate. Stamens isomerous, alternating with the corolla-lobes, adnate to the corolla, with usually slender, often filiform filaments and introrse or laterally and longitudinally dehiscing anthers. Pollen smooth or spinulose. Disk mostly present, annular or cupular. Ovary superior, mostly of 2 carpels, 2- or 1-celled, sometimes 4-celled by development of accessory partitions, rarely of 3 carpels and 3-celled; ovules 2 in each carpel, sessile, erect, anatropous. Style 1, often filiform, simple or forked, or 2 free styles, rarely very short or absent. Stigma entire or 2-lobed, rarely 3-lobed, or stigmas 2-4, of various shape, globular or ellipsoid to filiform, sometimes applanate, rarely peltate, kidney-shaped, conical or funnel-shaped. Fruit a capsule dehiscing by valves or circumscissile or irregularly dehiscing, rarely a berry or nut-like. Seeds as many as ovules or fewer; endosperm cartilaginous; cotyledons generally folded, sometimes obscure or absent. Distr. Ca 55 genera, with ca 1650 spp., widely distributed in the tropical, subtropical and temperate regions of both hemispheres; the greater part of the species in the tropics and subtropics of America and Asia. The larger genera Cuscuta (ca 165 spp.), Convolvulus (ca 250 spp.) and Ipomoea (ca 500 spp.) nearly throughout the range of the family but Convolvulus more in the temperate parts and Ipomoea more in the tropics and subtropics. Other large genera as Evolvulus (ca 100 spp.) and Jacquemontia (ca 120 spp.) nearly confined to America. Argyreia (ca 90 spp.) confined to tropical Asia. Malaysia, and a single sp. in Australia, and Merremia (ca 80 spp.) circumtropical. Several monotypic or small genera in E. Africa, Madagascar, and Australia.

Description: It is not without some pride and much satisfaction that the present volume, fourth planned in the series, second in sequence of publication, is brought to a successful end. Satisfaction I feel through the fact that the scheme and aim of this work is not only understood by the scientific-botanical world, but has also been accepted in the administrative world: Notwithstanding the long term scope of the work, the High Government of the Republic of Indonesia, having realized the essential value of basic scientific work in the natural sciences for the welfare of the future generations of its young nation, has been instrumental in authorizing the Director of Kebun Raya Indonesia (Botanic Gardens of Indonesia, Bogor) to create a Flora Malesiana Foundation. Sponsored by the Indonesian Government, this Foundation knits together the work and interest of the Herbarium Bogoriense of Kebun Raya Indonesia and the Netherlands Rijksherbarium at Leyden, the direction of which have officially agreed to a long-range close co-operation.

Description: Halophobous, aquatic or palustrial perennial herbs, rooting in the mud or freefloating. Stem erect or floating, solid, with numerous air-chambers as are the petioles. Leaves rosulate or alternate, or solitary at the top of the stem, emersed, floating or submerged, broad or narrow, curvinerved (when emersed); petioles sheathing at the base. Flowers ♀, ephemerous, mostly in racemiform, spiciform, subumbelliform or paniculiform inflorescences which are subtended by 1-2 spathelike or tubular leaf-sheaths, rarely solitary or pairwise in the leaf-axils. Bracts minute or absent. Flowers often simultaneously or centrifugally expanding. Perianth choriphyllous or gamophyllous, 6-merous, actinomorphic or zygomorphic, blue or lilac, rarely yellow, after anthesis marcescent and tightly including the ovary or the fruit. Stamens 6 or 3, rarely 1, on the base, in the tube or in the throat of the perianth, often unequal; filaments free; anthers 2-celled, cells bursting lengthwise, rarely opening by pores. Ovary superior, sessile, 3-celled, with axile placentas or 1-celled with 3 parietal or with 1 apical placenta. Ovules numerous or 1 and then pendulous from the apex of the cell. Style 1; stigma entire or minutely 3-lobed. Fruit a 3-valved capsule or indehiscent. Seed(s) longitudinally ribbed. Embryo central, terete, straight, hardly shorter than the copious, mealy endosperm. Distr. About 8 small genera and ± 25 species, 6 genera confined to the New World, one in Madagascar, one widely distributed in the Old World; in Malaysia one native genus, one introduced and abundantly naturalized, and one occasionally cultivated as an ornamental.

Description: Erect tall annual, usually branched. Leaves simple, with 2 free stipules, in the lower part of the stem opposite, in the higher part spirally arranged, long-petioled, palmate, 3—11-foliolate. Flowers (♂) (♀) or mostly (♂♀). Male flowers in short, dense cymes, which are united into lax, foliate, terminal panicles, very shortly pedicelled. Tepals 5, free, oblong, membranous, imbricate. Stamens 5, epitepalous; filaments erect and short in bud, linear, with a narrowed apex; anthers comparatively large, basifixed, 2-celled, cells opening longitudinally, rudimentary ovary absent. Female flowers solitary in the axil of a small, primary, membranous, entire bract closely enveloping the ovary, each enveloped by a spathaceous, conspicuous, acuminate, secondary bract. Perianth absent. Ovary sessile, 1-celled; style central; stigmas 2, sessile, long, filiform, caducous. Ovule solitary, pendulous. Achene closely enveloped by the much enlarged, secondary bract, broadly oval, with a concave rimmed base, much compressed, faintly keeled on the lateral margins; pericarp smooth, hard, crustaceous, easily splitting into two halves; albumen unilateral, scanty, fleshy; embryo large, horseshoe-shaped; cotyledons large; radicle long. Distr. Monotypic, native of Central Asia, cultivated in tropical Asia, naturalized in N. America.

Description: Small trees or erect shrubs. Leaves spirally arranged, simple, petioled, entire, palmatinerved, densely red-dotted. Stipules small, very caducous. Flowers in terminal corymbs or panicles, actinomorphic, ♀, rather large. Pedicel with 5-6 apical glands. Sepals 4-5, free, imbricate in bud, falling off as soon as the flower expands. Petals 4-7, free, imbricate in bud. Stamens numerous, inserted on an annular hypogynous disk; filaments thin, free; anthers horseshoe-shaped, passing over the top of the filament and with both ends closely applied to i , 2-celled; cells opening in the middle (on the top of the filament) by short slits which unite into a spuriously apical pore. Ovary superior, usually bristly, 1-celled, with 2 opposite parietal slightly intruding placentas. Style 1, sinuous, rather thick; stigma 2-dentate. Ovules very numerous. Capsule compressed contrary to the placentas, usually softly prickly, rarely smooth, loculicidally bivalved; endocarp membranous, separating from the valves. Seeds numerous, obovoid, angular; testa fleshy, very densely studded with small, round, red, sessile glands; albumen well-developed, not oil-containing; embryo rather large. Distr. Monotypic, native and cultivated in tropical America; cultivated in many other tropical countries.

Description: Annual (?)laticiferous herbs, with the habit of Phytolacca. Stem erect, somewhat succulent. Leaves spirally arranged, simple, entire, exstipulate. Inflorescences terminal, densely spicate, acropetal. Flowers subtended by a bract and two bracteoles, bisexual, actinomorphic. Calyx tube adnate to the ovary; segments 5, united below, imbricate, connivent, persistent. Corolla campanulate-urceolate, perigynous; lobes 5, imbricate. Stamens 5, epipetalous, alternating with the corolla lobes; filaments short; anthers rounded, 2-locular, dehiscing longitudinally. Ovary semi-inferior, 2-locular; style short, stigma capitate; ovules attached to large spongy stipitate axile placentas. Capsule cuneate-obconic, 2-locular, membranous, circumscissile; seeds ~, minute, oblong, rugose-costate, albumen very scanty or none (?); embryo axile, straight, subterete. Distr. Mono-generic, almost pantropical.

Description: Submerged, rootless, monoecious freshwater plants. Leaves verticillate, 2-4 times forked, segments linear dentate. Flowers actinomorphic, solitary, axillary, unisexual. Perianth valvate, segments 9-12, persistent, narrow. ♂: stamens 8-24; anthers nearly sessile rather broad, connective pointed, the 2 cells mostly crowned by a minute bristle; ovary rudiment absent. ♀: ovary superior, sessile, 1-celled with 1 ovule; style persistent, subulate, sulcate towards the apex; stamen rudiments absent. Fruit oblong, compressed, warty, not dehiscent, near the base with 2 straight or curved soft spines, or unarmed. Distr. Ca 2 spp., both ubiquitous.

Description: Annual or perennial, saprophytic or autotrophic herbs; the saprophytic species often colourless. Leaves usually spread or alternate, entire, simple, without stipules; non-saprophytic species with a radical rosette of linear leaves; stem leaves often reduced to small scales; sometimes the basal part of the stem provided with many decurrent, grass-like leaves. Flowers ♀♂, usually actinomorphic, solitary or in capitate or cymose inflorescences. Perianth corolline; limb consisting of 2 whorls; tube sometimes 3-winged. Anthers 3, subsessile in the perianth throat and dehiscing laterally with horizontal slits,or 6, hanging down in the perianth tube and dehiscing with longitudinal slits. Connective large, often appendiculate. Style filiform or shortly cylindrical or conical. Stigmas 3, sometimes connate. Ovary inferior, 1-celled with parietal placentation, or 3-celled with axile placentation. Ovules ~, anatropous, with 2 integuments; funicles often rather long. Fruit usually capsular, sometimes fleshy, crowned by the persistent perianth tube and the style, or by a thickened persistent basal ring of the perianth tube, dehiscing irregularly or with transverse slits at the top. Seeds ~, small, subglobose to linear, sometimes with loose, reticulate testa, with endosperm. Distr. About 125 species, widely distributed in the tropics of both hemispheres, also in subtropical America, Chicago area, Moçambique, Southern China, Japan, Southern Australia, New Zealand and Tasmania. As many species are rare, it is possible that only a part of their area is known. Most of them are found in moist regions. Among the autotrophic Malaysian Burmanniaceae there are 3 rather common species which are widely spread, viz Burmannia coelestis, B. disticha and B. longifolia. The latter two are absent from Java and the Lesser Sunda Islands, the former occurs in Java proper only in its western part. Of the saprophytic Malaysian species only 3 have been often collected, viz Burmannia championii, B. lutescens, and Gymnosiphon affinis.

Description: Trees, shrubs or lianas, rarely subherbaceous. Glands (in Mal. spp.) often present on the leaf-bases or petioles, and in lower marginal crenations. Indumentum of simple hairs, glandular hairs or multicellular hairs secreting calcium oxalate and forming scales, or present beneath the cuticle making the surface of the leaf minutely verruculose and sometimes pellucid-punctate. Leaves opposite, verticillate, spiral, or alternate, petioled (rarely sessile), exstipulate, simple, almost always entire. Flowers ♀♂ ♀♂ or ♀♂ and ♂ in the same inflorescences, usually protogynous, usually actinomorphic, rarely slightly zygomorphic, in axillary or extra-axillary elongated or subcapitate spikes or racemes or in terminal and sometimes axillary panicles. Receptacle (calyx-tube) usually in two distinct parts, the lower receptacle surrounding and adnate to the inferior ovary and the upper receptacle produced beyond to form a short or long tube terminating in the calyx-lobes, the latter sometimes poorly developed. Calyx-lobes 4 or 5 (rarely 6-8) or almost absent, sometimes accrescent ( Calycopteris). Petals 4 or 5 or absent, conspicuous or sometimes very small, inserted near the mouth of the upper receptacle. Stamens usually twice as many as the petals, borne inside the upper receptacle usually in two series, exserted or included; anthers dorsifixed, usually versatile (or rarely adnate to the filaments). Disk intrastaminal, usually present, hairy or glabrous. Style usually free (attached for part of its length to the upper receptacle in Quisqualis). Ovary inferior (semi-inferior in the West-African genus Strephonema), unilocular, with usually 2 (sometimes 2-6) pendulous, anatropous ovules of which only 1 usually developes. Fruit (botanically a pseudocarp) very variable in size and shape, fleshy or dry, usually indehiscent, often variously winged or ridged, 1-seeded. Albumen absent. Distr. 18 genera with c. 450 spp. in the tropics and subtropics: 2 are circumtropical ( Combretum and Terminalia), and are much the largest genera, 1 is confined to North Australia and Queensland (Macropteranthes), 2 confined to tropical Asia ( Finetia and Calycopteris) , 3 occur in Asia and Africa (Anogeissus, Lumnitzera, and Quisqualis), 1 is confined to Madagascar (Calopyxis), 3 are confined to tropical Africa (Guiera, Pteleopsis and Strephonema), 2 occur in tropical Africa and tropical America (Conocarpus and Laguncularia) and the remaining four ( Buchenavia, Bucida, Ramatuela and Thiloa) are confined to tropical and subtropical America.

Description: For various reasons the space occupied by pre-Linnean Malaysian phytography in this concise history seems too large and out of proportion in comparison to the survey of post-Linnean work. Modern plant description, though based on, and derived from, ancient beginnings and traditions, maintains but slender contacts with plant sciences earlier than the 18th century and it might claim to be allotted by far the larger space on account of its superior results, its greatly increased efficiency, its Consciousness of limitations and capabilities, its output, and its clearness of purpose. There exists, however, during the last decade, an increasing interest in the nearly forgotten botany of centuries long past, not only because of a certain taste for the quaint and attractive flavour of scientific efforts from minds so remote from our own, but also on account of a growing insight into the hidden springs of modern thought and method, which flow deeply, emerge unexpectedly, and appear to rise from distant roots. There is also, in connexion with this, the absorbing spectacle of discovery and of growth i.e. the development of a field of human culture that has bound devoted and excellent personalities in its service from the first glimmerings of our civilization.

Description: Scandent shrubs (often erect in youth), without resin; branches sympodial with a series of circinate woody hooks in one plane. Leaves spread, simple, entire, often rosette-crowded, cuneiform, penninervous, reticulate-veined, glabrous, both surfaces minutely pitted, each pit with a peltate small hair secreting a waxlike substance; petiole articulated, scar on the twigs often saddle-shaped; stipules absent. Flowers ♀♂, actinomorphic small. Inflor. few or several times dichotomous or spike-like, often provided with said hooks and single reduced bract-like leaves, branches often recurved. Pedicels articulated. Bracts with a glandular-thickened base, margin fimbriate-membranous. Calyx tube short, at length adnate to the base of the ovary; lobes 5 inequal imbricate, enlarged and wing-like in fruit. Petals 5, united at the base, slightly contorted in bud. Stamens mostly 10, rarely 5, the episepalous slightly longer. Filaments with broadened base; anthers basifixed, ± introrse to ± latrorse, 2-celled, opening lengthwise. Ovary for the greater part inferior, consisting of 3 carpels, 1-celled, protruding into a nippleshaped elongation bearing 3 articulated erect styles with a punctiform or horseshoe-shaped stigmatic apex; nipple enlarging in fruit. Ovule 1, basal, ascending, with 2 integuments. Nut not dehiscent, crowned by the enlarged calyx. Seed roundish with testa intruding between the cerebral-like folds of the endosperm. Exocarp leathery. Embryo straight, erect, obliquely placed; cotyledons diverging; hypocotyl rather thick. Distr. Disjunct, ca 3 spp. in trop. W. Africa, and 9 in SE. Asia, from the Deccan to Burma, Indochina, Hainan, S. China, the Malay Peninsula, Borneo and Sumatra (cf. fig. 2).

Description: Floating aquatic herbs with dimorphic leaves, submerged ones opposite pinnatifid rootlike, apical ones in a rosette, rhomboid, dentate, with spongy often inflated petiole, arranged in leaf-mosaic; stipules 4-8, minute. Flowers bisexual, small, solitary, axillary, short-pedicelled, 4-merous, white or lilac. Petals imbricate. Disk present. Ovary half-inferior with 1 style and 2-4 persistent sepals turning often to thorns or horns. Fruit mostly 1-celled, 1-seeded, shell bone-hard; thorns after withering often set with barbs at the apex. Seed often producing 2-5 free germ-stalks. Distr. Several species in the Old World, but not known from Australia.