ALBERT

Description: https://www.researchgate.net/publication/230891291_The_Orbital_Theory_of_Pleistocene_Climate_Support_frim_a_Revised_Chronology_of_the_Marine_d18O_Record

Description: Summary Holocene sediments of the North Lagoon, Bermuda, were studied with shallow seismic reflection profiles (200 km CSP-survey, UNIBOOM-system) and vibration coring (40 sediment cores, pneumatic vibration corer, Meischner et al., 1981). Seismic Stratigraphy Four seismic sequences are distinguishable by seismic stratigraphy. All seismic sequences correspond to depositional sequences built up during high sea levels in interglacial times. The seismic sequences are separated by unconformities which are often strongly reflective and correspond to emersion planes during glacial phases. The upper sequence (sequence 4) is related to Holocene sediments. The pre-Holocene bedrock is divided into three different seismic sequences (Kuhn et al., 1981): Sequence 1: oldest Pleistocene sequence (pre-Sangamon sea-level highstands), upper boundary with levelled relief (lower boundary not discernible), composed of strongly cemented carbonate sediments, forms the bedrock below Three Hill Shoals Sequence 2: Sangamon (125 ky sea-level highstand), distinct surface morphology, forms the bedrock of a large area below Holocene sediments, Holocene reefs grew up on elevations of the sequence 2 surface, the Holocene reef rim was developed on an elevated rim of sequence 2 Sequence 3: youngest Pleistocene sequence (Sangamon, 105 and 85 ky sealevel highstands lower than recent), deposited mainly in depressions of the bedrock deeper than -15 m below recent Mean Sea Level, levelling the older relief, peat sedimentation in places The distribution of recent reef areas and lagoonal basins is strongly controlled by pre-Holocene topography and geology of the bedrock. During the Holocene approx. 1050 x 106 m3 of carbonate sediments were deposited in the North Lagoon (290 km2) and approx. 1350 x 106 m3 in the reef rim area (170 km2). Sedimentology There are no larger oscillations of the Holocene sea level identifiable in the sedimentological record. The pre-Holocene topography was gradually drowned during the Holocene sea-level rise. At first, the depositional depressions were separated and landlocked. Fresh water peat marshes, fresh water ponds, marine ponds and bays were formed. With rising sea level, the land barriers were more and more eroded, drowned and lost their influence on the back-barrier sedimentation area. Autochthonous and allochthonous peat, lime gyttja and carbonate mud are a typical transgressive back-barrier sediment sequence. After destruction of the barrier, the depositional milieu changed from restricted marine to normal marine, open lagoonal. Sea-grass sediments and nearly mud-free carbonate sand were deposited in shallow water in an exposed environment. Hydrodynamic energy decreases with increasing water depth in the lagoonal basin. A more densely growing reef rim and intralagoonal reef growth added to the protection of the deeper lagoonal floors. Fine-grained sediments were deposited in this environment. They are distributed over a large area of the North Lagoon and form the top of the transgressive lagoonal sediment sequence. Holocene reefs mainly developed on rises of the pre-Holocene surface. In the early Holocene, solid reef build-ups were able to keep up with the rapid rise of sea level. Sand pockets in the reefs were left behind and filled up mainly in the later Holocene. The percentage of fine-grained sediments, produced and resuspended in the reef rim and deposited in the near lagoonal back-reef zone, increased during the Holocene. Two models of Holocene sedimentation in a depression and on an elevation of the pre-Holocene surface illustrate the dependence of vertical facies gradation on pre-Holocene topography. Trends of the mostly polymodal grain-size distributions of the Holocene sediments are a coarsening-upward in the back-barrier and a fining-upward in the lagoonal sediment sequences. Change in the composition of the molluscan fauna in the Holocene sediments (particle size 〉 2000 µm) is an Indication for fades changes. Gastropods are abundant in the basal backbarrier sediments. Bivalves are rare and their diversity 1s low. Sea-grass sediments contain Codakia orbicularis and Astraea phoebia shells. In the sheltered lagoonal environment shell fragments 〉 2000 µm become rare, common species are Gouldia cerina, Pitar fulminata and Finella sp. (approx. 1000 µm). Fine-grained reef-rim derived sediments differ from lagoonal sediments by a higher percentage of Homotrema rubrum fragments and Alcyonaria spicules.

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

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

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

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

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

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

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

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

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

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

Description: ANDERSON, J.A.R., A checklist of the trees of Sarawak, 364 pp. (1983, Dewan Bahasa dan Pustaka Cawangan Sarawak, for Forest Department, Kuching, Sarawak). Cloth Mal$ 15.00. When Dr. Anderson retired from the Forest Department in 1973 he left the manuscript of this checklist for publication. Unfortunately publication was delayed for 10 years. It contains data on over 2500 arboreous plant species. The text consists mainly of two parts: the first is a list of vernacular names with their scientific equivalents, the second is a list of plant names alphabetically arranged by family. Each species is concisely annotated with its vernacular name(s), maximum diameter, ecology, frequency, soils, etc. Species names have been coded: the first two figures are for the family, the next two for the genus and the last two for the species. A list is given of the trees of the peat-swamp forests of which Anderson was a great expert. A small draw-back is that the literature of the last ten years has not been included. Nevertheless this is a most helpful book. — C.G.G.J. van Steenis.

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

Description: Small evergreen trees, shrubs or lianas; two genera ( Cansjera and Opilia) are known to be root-parasites. Leaves distichous, simple, usually extremely variable in form and size, entire, exstipulate, pinnately veined; dried leaves mostly finely tubercled by cystoliths located in the mesophyll. Inflorescences axillary or cauliflorous, panicle-like, racemose, umbellate (in Africa) or spicate; bracts narrowly ovate or scale-like, in Opilia peltate, often early caducous. Flowers small, (3—) 4—5) (—6)-merous, mainly bisexual, sometimes unisexual and plants then dioecious ( Gjellerupia, Melientha, and Agonandra) or gynodioecious (Champereia). Perianth with valvate, free or sometimes partly united tepals (in ♀ flowers of Gjellerupia wanting). Stamens as many as and opposite to the tepals (in ♀ flowers only small staminodes); anthers introrse, 2-celled, longitudinally dehiscent. Disk intrastaminal, lobed (lobes alternating with the stamens), annular, or cupular. Ovary superior, 1-celled; style short or none, stigma entire or shallowly lobed. Ovule 1, pendulous from the apex of a central placenta, anatropous, unitegmic and tenuinucellar. Fruit drupaceous, pericarp rather thin, mesocarp ± fleshy-juicy, endocarp woody or crustaceous. Seed large, conform to the drupe, without testa; hilum basal, often in a funnel-shaped cavity. Embryo terete, embedded in rich, oily endosperm, nearly as long as the seed or shorter, with 3—4 linear cotyledons, radicle often very short. Distribution. There are 9 genera with about 30 spp., widespread in the tropics. Rhopalopilia is restricted to Africa and Madagascar, Agonandra to South and Central America. In Malesia: 7 genera, 5 of these only known from the eastern Old World (1 endemic: Gjellerupia in New Guinea); Opilia and Urobotrya occur also in tropical Africa.

Description: Monoecious, medium-sized to very large trees (rarely shrubby in very exposed situations). Either four independent cotyledons or two fused pairs (which may be retained in the seed after germination). The growing point of foliage shoots quite distinct between the two genera, being just a few highly reduced leaves in Araucaria and a highly organized bud formed of overlapping scales in Agathis. The leaves vary from scales or needles to broad leathery forms with many parallel veins sometimes on the same plant at different stages of growth. Pollen produced in cylindrical cones from one to as much as twenty cm long with numerous pedunculate spirally placed microsporophylls each with several to many pendent elongated pollen sacs attached to the lower side of an enlarged shieldlike apex which also projects apically more or less overlapping the adjacent microsporophylls. Pollen cones solitary, terminal or lateral, on branches separate from those bearing seed cones, subtended by a cluster of more or less modified leaves in the form of scales, deciduous when mature. Pollen globular, without ‘wings’. Seeds produced in large, well-formed cones which disintegrate when mature, dispensing the seeds in most cases with the help of wing-like structures; the seed cone terminal on a robust shoot or peduncle with more or less modified leaves that change in a brief transition zone at the base of the cone into cone bracts, formed of numerous spirally-placed bract complexes, usually maturing in the second year. Individual seed cone bract leathery or woody and fused with the fertile scale which bears one large inverted seed on its upper surface. Distribution. The 40 species in two genera are well represented in Malesia (13 spp.) and extend eastward and southward into Fiji, New Caledonia (18 spp.), Australia, and New Zealand, with 2 spp. also in the cooler parts of South America, giving the family a distinct Antarctic relationship. Only one species of Araucaria (in South America) occurs completely outside of the tropics, while the majority of the species in the family belong in the lowland tropics and others grow in the tropical highlands.

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

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

Description: Many botanists must have wondered why as yet no volume of Flora Malesiana was dedicated to the outstanding botanist Carl Ludwig Blume, undisputed pioneer in planning the compilation of a ‘Flora Malesiana’. The writing of this Dedication would have been greatly facilitated if a full biography of BLUME had been existent, but none is available; there is not even a bibliography of his works. Only recently, in 1979, two biographical attempts were made, by J. MACLEAN and by A. DEN OUDEN, but only for the period 1820-1832; together with other biographical and obituary notes they are here assembled in Appendix B. I have also compiled a bibliography: Appendix A.²

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

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

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

Description: Erect or straggling herbs, shrubs or trees, sometimes monoecious or dioecious, the herbs sometimes rhizomatous; branches sometimes jointed at the nodes, sometimes without vessels ( Sarcandra). Leaves simple, decussate or sometimes whorled in fours, serrate, crenate or dentate, the teeth often thickened at the apex, penninerved, usually petiolate; petioles more or less connected at the base at least by a transverse line or connate into a distinct sheath; in Ascarina often alternating with leafless internodes which have the petiolar sheath; stipules minute to fairly conspicuous, subulate, borne on the petiole bases or sheath, occasionally pectinate. Flowers much reduced, without perianth, fully unisexual or essentially bisexual with the reduced anther-bearing organ adnate to the side of the ovary; arranged in spicate, paniculate, or capitate axillary or terminal inflorescences. — Male flowers bracteate or not, apparently consisting of 1—5 stamens, or in Hedyosmum consisting of numerous anthers in a cone-like structure; if 3 then the whole forming a fused 3-lobed organ sometimes enveloping the female flower by its edges, the central anther with 2 or aborted loculi and the laterals with single loculi, simply lobed or with connectives slightly to considerably produced so that the whole organ is 3-fingered; if with only 2 anther locelli then these on either side of a thickened filament plus connective. — Female flowers naked or enclosed by a cupular bract, the perianth adnate to the ovary, often minutely or shortly dentate at the apex and the ovary thus inferior; ovary 1-locular; stigma sessile or style short; truncate, 2-lipped, depressed or subcapitate (or horseshoe-shaped in one species), rarely linear or clavate. Ovule solitary, orthotropous, pendulous, bitegmic and crassinucellate. Drupes fleshy, small, ovoid or globose, sometimes more or less 3-sided in Hedyosmum, free or united into a mass by the bracts; endocarp hardened and crustaceous. Seeds subglobose, exarillate, with copious fleshy or oily endosperm and minute embryo, the cotyledons divaricate or scarcely formed. Distribution. Four genera with about 80 species. Since VESTER’S (1940) small-scale map the family (Ascarina) has been found in Madagascar. It is mainly tropical but Ascarina extends south to North Island of New Zealand (fig. 6) and Chloranthus and Sarcandra extend north to Japan, China, Korea and the eastern U.S.S.R. (Ussuri).

Description: Trees or shrubs (or rarely suffrutices outside Malesia). Leaves simple, alternate, often coriaceous, glabrous or with an indumentum on undersurface, margin entire; petioles often with 2 lateral glands. Stipules 2, minute and caducous to large and persistent, usually linear-lanceolate. Inflorescence racemose, paniculate or cymose; flowers bracteate and usually bibracteolate; bracts and bracteoles small and caducous or larger and enclosing flower or groups of flowers and persistent. Flowers actinomorphic to zygomorphic, hermaphrodite or rarely polygamous, markedly perigynous. Receptacle campanulate to cylindrical or rarely flattened cupuliforum, often gibbous at base; calyx lobes 5, imbricate, often unequal, erect or reflexed. Petals 5 (absent in some Neotropical species), inserted on margin of disk, commonly unequal, imbricate, deciduous, rarely clawed. Stamens indefinite, 2—60 (to 300 in Neotropics), inserted on margin of the disk, in a complete circle or unilateral, all fertile or some without anthers and often reduced to small tooth-like staminodes; filaments filiform, free or ligulately connate, short and included to long and far exserted; anthers small, 2-locular, longitudinally dehiscent, glabrous or rarely pubescent. Ovary basically of three carpels but usually with only one developed, the other two aborted or vestigial, variously attached to (the base, middle or mouth of) receptacle, usually sessile or with short gynophore, pubescent or villous; ovary unilocular with two ovules or bilocular with one ovule in each locule. Ovules erect, with micropyle at base (epitropous). Style filiform, basally attached; stigma 3-lobed or truncate. Fruit a fleshy or dry drupe of varied size, interior often densely hairy; endocarp much varied, thick or thin, fibrous or bony, often with a special mechanism for seedling escape. Seed erect, exalbuminous, the testa membraneous; cotyledons amygdaloid, plano-convex, fleshy, sometimes ruminate. Germination hypogeal with the first leaves opposite or alternate or epigeal with opposite first leaves. An extensive review of the generic limits of the family has been published: G.T. PRANCE & F. WHITE, The genera of Chrysobalanaceae: a study in practical and theoretical taxonomy and its relevance to evolutionary biology, Phil. Trans. Roy. Soc. London 320 (1988) 1—184. This contains full details of taxonomic history, morphology, anatomy, pollen, ecology and distribution of the family. A condensed version of these subjects is given here. Details of the Neotropical members of the family are given in: G.T. PRANCE, Chrysobalanaceae, Flora Neotropica 9 (1972) 1—410. The African members of the family were treated in: F. WHITE, The taxonomy, ecology and chorology of African Chrysobalanaceae (excluding Acioa), Bull. Jard. Bot. Nat. Belg. 46 (1976) 265—350.

Description: Perennial herbs, more commonly woody at the base, undershrubs or shrubs, erect, scrambling or scandent, sometimes high lianas. Rhizome not rarely tuberous. Branches often slightly swollen and jointed at nodes. Hairs simple, uni- or multicellular, short ones often with a hooked apex. Leaves simple, spiral or alternate, petioled (without an abscission zone), exstipulate; midrib usually prominent beneath, elevated or flat above; nervation commonly palmate, or pinnate, nerves often obliquely extending towards the margin. Flowers bisexual, actinomorphic or zygomorphic, solitary, fasciculate, or in axillary or cauligerous, racemose, paniculate or cymose inflorescences, usually only one or two flowers open at a time; bracts present and often persistent; pedicel often hardly distinct from the ovary. Calyx petaloid, gamosepalous, 3- (or 6-) lobed or 1-lipped; lobes valvate or induplicate. Petals (in Mal.) absent. Disk (?) 0, rarely present (e.g. a few Thottea spp.). Stamens 6 (4 or 5 in some extra-Mal. Aristolochia spp.) or 6—c. 36 (—46), in 1 whorl or in 2 (3 or 4) whorls (Thottea); filaments free or slightly mutually united at the base, and/or almost completely adnate to the style column to form a gynostemium; anthers free (Thottea) or dorsally united with the style column (Aristolochia), each consisting of 2 thecae with 4 pollen sacs, extrorse, rarely introrse (extra-Mal. spp.), dehiscing longitudinally. Ovary inferior (rarely half-inferior in extra-Mal. genera), 4—6-carpellate, 4—6-celled, syncarpous (or ± apocarpous in extra-Mal. Saruma); placentae parietal (distinct when young, then intruding and connivent axially, thus often seemingly axile); ovules usually many, anatropous, in 1 or 2 vertical rows in each locule of the ovary, horizontal or pendulous; style-column 3—many-lobed, sometimes some of the lobes redivided; stigmas or stigmatic tissue apical, lateral, or on the surface of style lobes. Fruits capsular or siliquiform (follicular or cocci in extra- Mal. genera), 4—6-celled; dehiscing apically towards the base (basipetal, e.g. Thottea) or basally towards the apex (acropetal, e.g. most Aristolochia); septicidal, rarely septifragal (some extra-Mai. Aristolochia) or bursting irregularly (extra-Mal. Asarum); rarely indehiscent (W. African Pararistolochia). Seeds many in each locule (1-seeded in extra-Mal. Euglypha), often coated with remains of placental tissue (membranous when dry), horizontal or pendulous, variously shaped; ovate, deltoid or triangular, flat, convex-concave, or longitudinally curved, or oblong (and triangular in cross-section), rugose, finely verrucose, or smooth, immarginate (Thottea; Aristolochia, p.p.) or winged (Aristolochia, p.p.); albumen fleshy, copious; embryo minute, cotyledons two, distinct. Distribution. There are 7 genera, Aristolochia worldwide, Asarum over the northern hemisphere, Thottea in continental Southeast Asia and Malesia, Pararistolochia in tropical Africa, and 3 monotypic genera, viz. Saruma in China, Holostylis and Euglypha in South America. As to number of species, Aristolochia is by far the largest with some 300 spp., largely concentrated in the New World, especially in Central and South America, in Malesia with 28 spp.; Asarum (incl Hexastylis and Heterotropa) with possibly some 70 spp. in northern temperate regions, Thottea with 26 spp., of which 22 in Malesia, and Pararistolochia with 12 spp. in West Africa.

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

Description: Type material of Tulasnella cystidiophora Höhn. & Litsch. has been studied. The species is characterized by often moniliform gloeocystidia and clamp-less hyphae (at least in the subhymenium).

Description: A new species, Alstonia undulifolia Kochummen & Wong, is described from the Malay Peninsula. Two sections of the genus occur in the Malay Peninsula, Alstonia sect. Monuraspermum Mon. and Alstonia sect. Alstonia, the latter being the correct name for what was previously known as sect. Pala (Adr. Juss.) Benth. Various characteristics, including growth architecture, are examined for their usefulness in distinguishing these two sections of the genus. In comparing A. angustiloba Miq. and A. pneumatophora Berger, both of which have not been properly differentiated by characteristics of the reproductive organs, A. pneumatophora var. petiolata Mon. is reduced to synonymy under A. angustiloba. A key to the seven species of Alstonia native to the Malay Peninsula is provided.

Description: Revision of the Malesian species of the genus Steganthera, which centres in New Guinea; precursor to treatment in Flora Malesiana. There are 16 species accepted; 5 are described as new, 12 names are reduced, 3 are excluded and 9 are imperfectly known.

Description: In a recent thesis B.S. Fey (Zürich) has developed a new theory about the origin of the cupule in Fagaceae. He has concluded that the appendages (spines, lamellae, etc.) on the outside of the cupule are regularly arranged and that they reflect a condensation (concrescence) of a dichasial flower system, so that cupule and fruit(s) form together the representation of one ancestral inflorescence; the cupular appendages would then largely represent the bracts of the ancestral inflorescence. This stands in contrast with former opinions, in which the cupule was interpreted as of separate vegetative origin from the nut(s) which was (were) the remain (s) of the inflorescence.

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

Description: Recent studies in Sabah and Sarawak have demonstrated the presence of an undescribed species of Podocarpus.

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

Description: Pholidota kinabaluensis is transferred to the new monotypic genus Entomophobia. Coelogyne phaiostele, C. ridleyana, and Pholidota triloba are identical and transferred to the new genus Geesinkorchis, that also comprises the new species G. alaticallosa. The monotypic genus Sigmatochilus is reduced to Chelonistele, in which C. dentifera and C. lurida var. grandiflora are described as new. Chelonistele crassifolia is regarded as a variety of C. sulphurea.

Description: The genera Hunteria and Lepiniopsis of the family Apocynaceae are in Malesia represented by one species each. Distribution and ecology are cited in full.

Description: Five new species of Rafflesia (Rafflesiaceae) are described, while attention is drawn to a sixth, possibly also new one. A key to all recognized species is given.

Description: The morphology and leaf anatomy of Myxopyrum is described and a key to the species is given. Of the 15 species previously described four species and two subspecies are recognised: M. nervosum Bl. (synonyms M. horsfieldii, M. zippelii) with one subspecies coriaceum (Bl.) Kiew (synonym M. ellipticum), M. ovatum Hill (synonyms M. macrolobum, M. cordatum, M. philippinensis), M. pierrei Gagnep. (synonym M. hainanense) and M. smilacifolium Bl. (synonym M. serrulatum) with one subspecies confertum (Kerr) Kiew. Myxopyrum enerve Steen. is Chionanthus enerve (Steen.) Kiew. Descriptions for the extra-Malesian species, M. smilacifolium, is given.

Description: In subgenus Malachobatus twenty Malesian species are recognized, one of them ( Rubus moluccanus L.) with four varieties. Synonymy, descriptions, habitat notes, etc. are given. New names: R. moluccanus L. var. discolor (Bl.) Kalkm. and var. angulosus Kalkm. A key is given to the Malesian species.

Description: In Southeast Asia (excluding India) 44 taxa are recognized, 39 species, of which four are newly described ( I. kerrii, I. luzoniensis, I. emmae, and one unnamed species A, which will be treated by Nguyen Van Thuan, Paris), four subspecies, one of which is new (I. sootepensis subsp. acutifolia) and three are new combinations ( (I. suffruticosa subsp. guatemalensis, I. trifoliata subsp. unifoliata, I. trita subsp. scabra) ), and one variety which is a new combination I. spicata var. siamensis). A key, descriptions and full synonymy are given as well as 4 distribution maps and 5 figures.

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

Description: Species of the genera Tylos Latreille and Ligia Fabricus from the New World are recorded and knowledge of their distribution and systematics is summarized. Tylos marcuzzii Soika is redescribed with new illustrations. Ligia callani Collinge is reduced to a synonym of L. platycephala Van Name. New distribution records in the Caribbean and other regions are given for species of the two genera.

Description: Dr. Ernst Frederik Jacobi, who was a member of the Editorial Board of this journal for exactly 20 years, reached the age of 65 on September 11, 1973 and retired. Dr. Jacobi was appointed Director of the Amsterdam Zoo (officially: of the Royal Zoological Society “Natura Artis Magistra”) on April 1, 1953, in succession to Dr. A. L. J. Sunier. The function of Director of the Zoo automatically means also the membership of the Editorial Board of “Bijdragen tot de Dierkunde”. This periodical was published by the Royal Zoological Society until vol. 28 of 1949 (the last volume edited by Dr. Jacobi’s predecessor), but owing to the difficult financial situation of the Society, its publication was interrupted from 1949 to 1959, when vol. 29 appeared. From this volume onward, the “Bijdragen” appeared at regular periods, first once a year, later twice a year; also, the periodical was no longer published by the Royal Zoological Society solely, but by a committee (called so beautifully the “Board of Supervisors on the Management of the Artis Library”, the Artis Library being the library of the Society, though since 1938 chiefly managed by the University of Amsterdam).

Description: Five halacarid species, found in the mesopsammal of Caribbean Islands, are described, viz. Halacarellus tropicalis n. sp., Copidognathus grandiosus n. sp., Agaue arubaensis n. sp., Scaptognathus ornatus n. sp., and Limnohalacarus cultellatus Viets, 1940. H. tropicalis is the first member of the genus Halacarellus reported from tropical beaches.

Description: Seven springs in the Middle Atlas and five in the Rif have been studied. These show a great diversity of crenal habitats: water temperature ranges from 8.7° to 21°C, and the flow from 1 l/s to 1,800 l/s. Based on hydrologic and thermic characteristics, a spring typology is provided. The invertebrate community consists of 60 species, among which 4, found in the Rif, are new to science: Protonemura sp. (Plecoptera), Obuchovia sp. (Diptera, Simuliidae), Rhyacophila fonticola n. sp., and Philopotamus ketama n. sp. (Trichoptera). The new Trichoptera are both described. Two rare endemic species (the planarian Acromyadenium maroccanum and the coleopteran Elmis atlantis) have been found in a cold-water spring in the Middle Atlas; two black-fly species ( Cnetha carthusiensis and Simulium lamachei), new to North Africa, have been collected in a cold-water spring in the Rif. The cold-water spring community shows a high rate of endemism. Seven endemic cold-stenothermous species constitute a most characteristic crenon fauna in northern Morocco. The fauna of warmer springs (18° ≤ temp. ≤ 21°C) contains potamophilous and thermophilous species, a few of them belonging to the Ethiopian fauna. A comparative study of spring and rhithric communities of Morocco shows that, in the Middle Atlas and the Rif, cold-water springs became refugia for cold-stenothermous, west-palaearctic species; in the past, these species occupied a larger territory which has been reduced after recent climatic and hydrologic changes.

Description: Rates of food uptake were measured for individually reared larvae of the spider crab Hyas araneus L. feeding on freshly hatched Artemia nauplii at constant 12 degree C. Feeding rates (FR) of crab larvae were given as number of nauplii and amounts of dry weight, carbon, nitrogen, hydrogen, and energy (estimated from C) consumed per day. In both zoeal stages FR increased during postmoult and intermoult, remained high during early and intermediate premoult, and decreased again during late premoult. No clear pattern was found in the course of daily FR of the megalopa. Gross growth efficiencies (K sub(1)) showed a dramatic decrease from postmoult to early premoult (〉 60 to 〈 20%) in both zoeal stages. Daily consumption expressed as % body weight also decreased significantly in these instars. Average daily FR were highest in the zoea II, lowest in the megalopa, and intermediate in the zoea I. Since development of the megalopa took the longest time, the total amount of food consumed by this instar was equal to consumption in both zoeal stages combined.

Description: Duration of development in the larval and early juvenile stages H. coarctatus was studied in relation to temperature, and compared at extreme (18 and 6 °C) than at intermediate (9 to 15 °C) temperatures. The results were used to estimate the duration of development from hatching to the third crab stage in the field. Settling and metamorphosis was predicted to occur mainly during June. Biomass increased exponentially during larval development. Juvenile growth was also exponential and was maximum at 9 degree C, and minimum at 18 and 6 °C.

Description: Statistically significant differences were found in development duration of Hyas araneus L. larvae hatching on different days from the same egg batch. Larvae from different females show a decreasing trend in development time the later they hatch during the season. This trend was found in all larval instars; it was particularly apparent in the megalopa. Development durations in the 2 zoeal stages are positively correlated with each other, i.e. individuals developing slower than the average in the first larval instar tend to delay moulting also in the second instar. There are negative correlations between larval development time in all stages and the size of juvenile crabs, i.e. weak individuals tend to develop more slowly and to become smaller juveniles than the average. These larvae show lower accumulation rates of biomass already during the first zoeal stage. Larval development rates (at 12 °C) were not clearly affected by the temperature prevailing during previous embryonic development, but embryos incubated at higher temperatures tended to become smaller crabs.

Description: Exuvial losses in relation to late premoult matter and energy, and in relation to growth achieved during each instar, were studied in laboratory-reared larvae and early juveniles of the decapod H. araneus (L.). Changes of composition during development were measured in the complete body and in the exuvia from hatching through the second crab stage. Rates of exuvial loss increased during development in all parameters measured. They were generally highest in inorganic carbon and lowest in N. six to 7% of late premolte energy was lost by moulting zoeae, i.e. 9 to 13% of the energy produced during these stages. The megalopa lost 13%, and juveniles 19 to 20% of their LPRM energy ( similar to 29 to 41% of growth). During complete larval development of H. araneus a total of 18% of produced energy was lost at ecdysis. The same amount had been reported in the literature for larval development of 3 other decapod species.

Description: The influence of continuous and differential transitory starvation on the moult cycle and morphogenesis of H. araneus L. larvae was studied in laboratory experiments. Larvae starved from hatching (zoea I) or from moulting to later instars (zoea II, megalopa) develop, independently of food supply, to Stage C (intermoult). Postmoult Stages (A and B) and parts of intermoult are completed by utilizing internal body reserves under such conditions but cuticle formation is terminated at an advanced but incomplete stage within intermoult. In the zoea-II instar there is morphogenesis in appendages (pereiopod and pleopod buds) during continuous starvation. This supports the hypothesis that moult cycle and morphogenesis may be partly independent processes which are normally synchronized.