ALBERT

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

Description: 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: Twelve species of terricolous microlichens from the Angmagssalik District, Southeast Greenland, are reported: Caloplaca friesii, C. livida, Lecanora boligera, Lecidea oligotropha and Leciophysma arctophila, which are new to the lichen flora of Greenland, Rinodina conradi, which is new to the eastcoast, and Baeomyces roseus, B. rufus, Buellia geophila, B. punctata, Caloplaca tornoensis and Mycoblastus tornoensis, new to Southeast Greenland. In a discussion of the greenlandic distribution, unpublished records from the herbarium of Copenhagen (C) are incorporated. Notes on the habitats are given and the pertinent phytosociological units indicated. Some morphological and anatomical characters are commented upon briefly.

Description: The 16 recognized species of Sorocea are listed with their synonyms and distribution. Two new taxa are described: S. steinbachii C.C. Berg and S. hirtella Mildbread ssp. oligotricha Akkermans & Berg. Three new combinations are made: S. muriculata Miquel ssp. uaupensis (Baillon) C.C. Berg, S. trophoides W. Burger ssp. rhodorachis (Cuatrecasas) C.C. Berg, and S. sprucei (Baillon) Macbride ssp. saxicola (Hassler) C.C. Berg. A key to the species is presented.

Description: The genus Praravinia was created by KORTHALS (in TEMMINCK, Verhand. Nat. Gesch. Ned. Overz. Bezitt., Bot., p. 189, tab. 41, 1839-1842) for a plant which he had collected in the south-eastern part of Borneo. He described it as similar in habit and doubtless nearly related to Urophyllum WALL. His diagnosis of the genus, however, does not substantiate this point of view, for it contains two statements which seem to exclude the possibility of a near affinity: the aestivation of the corolla lobes is described as imbricate, whereas in Urophyllum and its allies it is always valvate, and the number of corolla lobes is said to be half as large as that of the stamens, a condition unknown not only in Urophyllum but in the whole family. As in the description of the species the aestivation is correctly set down as valvate, the first statement need not trouble us: the word “imbricate” in the generic diagnosis is obviously a slip of the pen. The other statement, however, is repeated in the description of the species, but it strikes one as anomalous that immediately afterwards the 8—12 stamens are said to alternate with the corolla lobes, as this of course would be impossible when the latter were but half as numerous as the first. The discrepancy between the number of the corolla lobes and of the stamens led MIQUEL in his “Flora Indiae Batavae II, p. 225 (1857)” to consider Praravinia as a quite singular genus, rather out of place in the family Rubiaceae: it reminded him, he says, of the Samydeae (Flacourtiaceae). When he wrote this, he knew the genus merely from the description given by KORTHALS, but afterwards he found an opportunity to study the latter’s material. In his “De quibusdam Rubiaceis, Apocyneis et Asclepiadeis” (Ann. Mus. Bot. Lugd.-Bat. IV, p. 136, 1869) he proposes, as a result of this investigation, to exclude the genus from the Rubiaceae, and to raise it to family rank. The new family, for which he introduces the name Metrocladeaceae, should be regarded, however, as nearly related to the Rubiaceae. The description of the genus given by MIQUEL is much more detailed than the original one, but it unfortunately repeats its principal errors: the corolla is described as 4- to 6-merous, and its aestivation as imbricate. The male flower dissected by him is preserved in the Utrecht Herbarium; it is a fairly young bud, opened by a longitudinal slit. The corolla lobes had apparently been separated by a slight pressure, but I at once got the impression that it had been insufficient to effect a complete separation, and that the lobes were still cohering in pairs. I have boiled the flower therefore once more, and by exercising in my turn a slight pressure I succeeded in setting all the lobes free. Since then I have seen mature flowers of this and other species in which the isomery of corolla and androecium was unmistakable. MIQUEL’s speculations on the taxonomic position of the genus were based therefore on a false supposition, and need no further consideration; the analysis carried out below will show that KORTHALS was quite right when he placed Praravinia in the neighbourhood of Urophyllum.

Description: Protium Pullei Swart n.sp. Arbor circ. 12 m alta. Ramuli robusti 4 mm diam. teretes glabri fusci lenticellis oblongis ferrugineis muniti. Folia trifoliolata 17 (16—21) cm longa glabra, petiolis robustis semiteretibus 4.5 cm longis basi incrassatis demum transverse rimosis, petiolulis semiteretibus robustis utrinque subincrassatis 1 cm longis sed terminalibus 2.25 cm longis, foliolis oblongo-ellipticis II (7.5—13) cm longis 5 (3.75—5.5) cm latis, apice abruptius acuminatis, acumine sublineari 8 (5—10) mm longo 2.5 (2—3) mm lato, basi cuneata, margine integro, coriaceis utrinque nitidis laevibus supra glaucescentis infra viridis, nervis secundariis utrinque II, nervis prim. et sec. utrinque prominentibus. Inflorescendae axillares breves pauce ramosae pauciflorae circ. 1 cm longae. Ramuli teretes striati cum pedicellis teretibus flore aequilongis bracteis bracteolisque triangularibus obtusis densiuscule puberulis. Flores 5-meri glabri. Calyx cupuliformis lobis oblongo-triangularibus acutis tubo aequilongis. Petala valvata oblongo-triangularia acuto apiculo inflexo carnosa. Stamina 10. Discus 10-lobis glaber. Pistillum glabrum, ovario late ovoideo stigmate 5-lobo coronato. Type: Maguire 24784 in herb. NY, 17 Sept. 1944, Suriname, Tafelberg, mixed transition high-low bush, 5 km S.W. of Savanna I.

Description: Neohattoria Kamim. is a monotypic genus of the Jubulaceae (= Frullaniaceae) with a single species, N. herzogii (Hatt.) Kamim., known from central to northern Japan and the southern part of the Kurile Islands. The present genus was segregated from Frullania by Kamimura (1961; sub. nom. Hattoria Kamim. nom. illeg., non Schust., 1961) on the basis of the branching type, the shape of the first leaf and underleaf on branch, the total lack of secondary pigmentation, the uniform cell structure of the stem in cross section, and the strongly toothed leaf lobes. The generic concept of Neohattoria was greatly expanded by Schuster (1970), who included eight species and classified them into two subgenera, subgen. Neohattoria (with a single species) and subgen. Microfrullania Schust. (with seven species); however, Hattori et al. (1972) transferred all species of subgen. Microfrullania to a newly segregated genus Schusterella Hatt. et al., thus retaining the monotypic status of Neohattoria. As already described and illustrated by Hattori (1955), Kamimura (1961), Mizutani (1961), Ladyzhenskaja (1963), Schuster (1970), and Hattori et al. (1972), Neohattoria herzogii is closely related to species of both Jubula and Frullania. Regarding the taxonomic desposition of Neohattoria, Mizutani (1961) and Mizutani & Hattori (1969) placed it with Jubula in a subfamily Jubuloideae of Lejeuneaceae and Hattori et al. placed it in Jubulaceae (s. lat.). But, Kamimura (1961), Schuster (1970, 1979), and Guercke (1978) placed it more close to Frullania, e.g. in a subfamily Frullanioideae of Jubulaceae (s. lat.); more recently, Asakawa et al. (1979b), admitting three distinct families, Jubulaceae, Frullaniaceae, and Lejeuneaceae, placed Neohattoria and Jubula in the Jubulaceae (s. str.) but Frullania and Schusterella in the Frullaniaceae.

Description: Of the family Oenotheraceae the genus Jussieua is the only one occurring in Suriname. The peculiar Oocarpon torulosum (Arn.) Urb., which has been recorded from Amazonian Peru, Brazil, British and French Guiana, Cuba and Santo Domingo, has up till now not been collected in the colony, but on account of its presence in the neighbouring countries it is there also to be expected. As for the name of the only Suriname genus, it was spelled by LINNAEUS in Genera Plantarum, ed. I (1737), p. 126, Jussieua but afterwards in his Flora Zeylanica (1747), p. 75, changed in Jussiaea.

Description: Zeer geachte Toehoorderessen en Toehoorders, Bij het beginnen van een wetenschappelijk onderzoek zal meestal degene die zich daaraan gezet heeft, allereerst het antwoord dienen te vinden op enkele fundamentele vragen. Zijn deze primaire vragen beantwoord, dan is de weg gebaand voor verder onderzoek en voor algemene theoretische beschouwingen. Deze fundamentele vragen zijn echter niet voor elke onderzoeker en ook niet voor elk onderzoek in een zelfde tak van wetenschap steeds gelijk. Dit hangt af van vele factoren, zoals: uiteindelijk doel van de studie, aard van het materiaal, geaardheid vooral van de onderzoeker, enz. Vandaag wil ik met U behandelen de hoofdvragen, die zich bij mij, voor de aan mij toevertrouwde onderdelen van de botanie steeds op de voorgrond plaatsen en de wijze waarop ik die beantwoorden pleeg te interpreteren voor het verdere onderzoek. Hierdoor zal ik tevens de gelegenheid hebben, om aan te stippen in welke richting wij op het gebied van de bijzondere plantkunde en de plantengeografie nog onderzoekingen kunnen verrichten, die ons inzicht in het geheel aanmerkelijk kunnen verruimen. Voor ik met mijn eigenlijke onderwerp begin, moet ik toch iets zeggen over wat „bijzondere plantkunde” is. Ik zal er niet te veel over uitweiden, daar, zoals Koningsberger en Reinders in het voorwoord van het eerste deel van het Leerboek der Algemeene Plantkunde terecht opmerken, de scheiding tussen „algemene” en „bijzondere” plantkunde uiteraard onscherp is. Volgens de letter van de gebruikelijke terminologie zou eigenlijk alles wat niet „algemeen” is thuis horen onder de bijzondere plantkunde. Zover wil ik niet gaan, want dat zou mijn taak wel heel omvangrijk maken en afgezien van het feit dat het buiten mijn kunnen zou komen te vallen, denk ik ook dat mijn collega voor de algemene plantkunde ernstige bezwaren zou maken indien ik datgene van de plantenphysiologie dat zeker niet algemeen is te noemen, voor mijzelf zou gaan opeisen. Ik wil daarom beginnen de physiologie, hoe bijzonder deze hier en daar ook moge zijn, maar onmiddellijk in zijn geheel bij de algemene plantkunde te plaatsen. Voor de rest zou ik mijn bovengenoemde definitie, dus „bijzonder” is alles wat niet „algemeen” is, in grote trekken willen volgen, met dien verstande dat ik mij natuurlijk wil houden aan de veelal gebruikelijke taakverdeling, zodat b.v. de „algemene” morphologie en anatomie van de Angiospermen, die in feite in het plantenrijk als geheel, „bijzonder” is, bij de „algemene plantkunde” wordt ondergebracht. De speciale en vergelijkende morphologie van deze groep reken ik echter zeer zeker tot de mij toegewezen tak van wetenschap. Ook de afgrenzing met de genetica is niet scherp. Indien men elk onderzoek waarbij niet uitsluitend op het phaenotype maar ook op het genotype gelet wordt, tot de genetica wil rekenen, dan zal de betrekkelijk jonge experimentele plantensystematiek of biosystematiek geen deel kunnen uitmaken van de bijzondere plantkunde. De genetici zullen het mij wel niet euvel duiden, dat ik ook deze tak van onderzoek laat staan bij de bijzondere plantkunde, waaruit zij is voortgekomen en waarvoor zij van zoveel betekenis is.

Description: Xylopia surinamensis R. E. Fr. n. sp. — Ramuli novelli dense aureo-ferrugineo-sericei, vetustiores plus minus glabrescentes et cortice densissime lenticellifero punctato vestiti; internodia 0,5—1 cm longa. Foliorum petiolus sericeo-tomentosus, 5—7 mm longus; lamina rigida, anguste lanceolata, basi rotundato-truncata, apicem versus sensim longeque attenuata, summo apice obtusa, supra ab initio glaberrima sed densissime verruculoso-punctata, subtus dense argenteosericea, 8—11 cm longa et 2—2,5 cm lata; costa supra valde impressa glaberrima, subtus prominens teres; nervi secundarii cum venulis vix conspicui. Flores in inflorescentiis densis nonnulli; bracteae numerosae, late ovatae, 1,5—2 mm longae. Sepala fere omnino coalita, calycem cupuliformem semiglobosum argenteo-sericeum 2—3 mm altum et 5—6 mm latum formantia. Petala exteriora linearia obtusa, extus argenteo-sericea, circ. 13 mm longa et 2 mm lata, prope basin subito dilatata; interiora linearia, acuta, quadrangulari-prismatica, utrinque cinereo-puberula, 12 mm longa et 1—1,2 mm crassa. Staminum filamenta 0,2 mm longa; antherae circ. 1 mm longae, locellatae, connectivi discus glaber; stamina exteriora plus minus sterilia. Pistilla numerosa (fere 30); ovaria dense sericea, circ. 1 mm longa, styli 1 mm et stigmata 1 mm longa. (Fructus ignotus). Suriname: Boschreserve, Sectio O (florifera Junio 1944. — Wood Herbarium Surinam No. 139). Typus speciei in Herb. Utrecht).

Description: The name Pleiocarpidia was coined by K. SCHUMANN (ENGLER und PRANTL, Natürliche Pflanzenfamilien, Nachträge I, p. 314, 1897) for a genus described in 1873 by HOOKER f. (BENTHAM et HOOKER, Genera Plantarum II (1), p. 71) as Aulacodiscus: HOOKER’S genus had to be rebaptized, because the name Aulacodiscus had been used already in 1844 by EHRENBERG for a genus belonging to the Diatomeae. A proposal made by O. KUNTZE(POST et KUNTZE, Lexicon, 1904) to change the spelling of the name introduced by SCHUMANN in Pliocarpidia can not be accepted, as there is no rule prescribing the transcription of the Greek diphthong in the manner advocated by the proposer. The plant on which HOOKER’S genus was founded, a small tree not uncommon in the Malay Peninsula, had been described already several years before by WIGHT (Calc. Journ. Nat. Hist. VII, p. 144, 1847) under the name Axanthes enneandra. The specific epithet points to the presence of nine stamens in the flower, but this is exceptional: in the flowers investigated by me the ordinary number proved to be seven. The genus Axanthes Bl., to which the species had been referred by WIGHT, was reduced shortly afterwards by BENTHAM and HOOKER f. (Niger Flora,p. 396,1849) and independently by KORTHALS (Ned. Kruidk. Arch. II, 2, p. 194,1851) to Urophyllum Wall. Later HOOKER made an exception for Axanthes enneandra Wight. The flowers of this plant were described by him as 8- to 16-merous, and on account of this character and of the presence of a “peltate stigma” he referred it to a new genus. Afterwards a second species from the same region was described by KING and GAMBLE under the name Aulacodiscus Maingayi, but this proved identical with the first (cf. RIDLEY, Flora of the Malay Peninsula II, p. 64, 1923). A really new species, however, was found in Mindanao: it was described by Merrill as Pleiocarpidia lanaensis.

Description: Among the Acanthaceae grown in the glasshouses of the University Botanic Garden, Utrecht, a plant labelled Aphelandra velutina drew my attention, first, because it obviously belonged to an entirely different genus, and secondly, because a description under this name could nowhere be found. The coincidence of these two grounds for bewilderment might be explained by assuming that Aphelandra was merely a perversion, probably caused by the inadvertency of a transcriber, of the true generic name. This sounded plausible enough, but the name itself could not be found, for all attempts to refer the plant to one of the existing genera failed. It looked as if the plant might have been described somewhere, but for the time being there was no indication at all as to the whereabouts of this description. A clue to the origin of the name was obtained some time afterwards when I found in the Utrecht herbarium a specimen belonging to the same species which was labelled Eranthemum velutinum: the specific epithet, therefore, was the same, but the generic name was different and, as I will show presently, nearer to the mark. The specimen, which dated from 1922, had been collected by the roadside in the Buitenzorg suburb Kotta Paris, and had apparently been named by an official of the Buitenzorg Botanic Gardens. It is, however, certainly no native Javanese plant, for the flora of Java, and particularly that of Buitenzorg, is well known, and a rather conspicuous plant like this one could not have escaped the attention: it was obviously a runaway from one of the neighbouring gardens.

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

Description: The species Polypodium banaense C.Chr. is transferred to Crypsinus. The recognition of a genus Phymatopteris Pic. Ser. (= Phymatopsis J.Sm.) separate from Crypsinus is discussed.

Description: The six species of Curtia, including a hitherto undescribed species published here, as well as the monotypic genus Hockinia can be distinguished from each other by the seed coat structure. The anticlinal walls and the cuticle provide the most useful information. Curtia tenuifolia appears to be a complex species, but subsp. tenella can be readily separated from this complex by the seed coat structure. Heterostyly has been found in C. tenuifolia subsp. tenuifolia, C. obtusifolia, and Hockinia montana, but differences in seed coat structure can not be correlated with long-, short-, and equal-styled flowers. The differences in seed coat structure, the length of the seeds, and the number of cells per seed plead for maintaining Hockinia (closely related to Curtia) as a distinct genus. One new species of Curtia is described and a new combination is made.

Description: SETTEN, A. K. van & KOEK-NOORMAN, J.: Studies in Annonaceae. VI. A leafanatomical survey of genera of Annonaceae in the Neotropics. — Bot. Jahrb. Syst. 108: 17—50. 1986. — ISSN 0006-8152. Within the scope of the multidisciplinary research project on systematics of Annonaceae, a survey of the leafanatomical features and their distribution in the neotropical Annonaceae is presented. The studied specimens form a rather homogeneous group, as may appear from the family description given here. A detailed study of the leafanatomical features reveals, that differences are mainly found in the indument, the position and contents of the idioblasts, the structure of the primary vein, the type of crystals in the epidermal cells, and the type of sclereids. Based on character states, phenetic similarities and differences are discussed and compared with the classifications of FRIES (1959) and WALKER (1971).

Description: One new species of Dorstenia from Brazil is described: D. carautae C.C. Berg, and four new combinations are made: D. cayapia Vellozo subsp. asaroides (Hooker) C.C. Berg, D. cayapia Vellozo subsp. paraguariensis (Hassler) C.C. Berg, D. cayapia Vellozo subsp. vitifolia (Gardner) C.C. Berg, and D. ramosa (Desvaux) Carauta, Valente & Sucre subsp. dolichocaula (Pilger) C.C. Berg. A list of and a key to the 22 Dorstenia species distinguished in south-eastern tropical America are presented, together with synonymy and distributional data.

Description: Dames en Heren, In een universitair blad kwam onlangs de mededeling voor, dat aan een hoogleraar, die zich in dezelfde moeilijkheid bevindt als ik, nl. dat hij in de loop van deze cursus 70 jaar is geworden, een afscheidscollege zou worden aangeboden. Ik vond dat een sympathiek plan. Als men met college geven, ondanks de daaraan verbonden bezwaren, de 70-jarige leeftijd heeft gehaald, is het werkelijk geen overbodige weelde dat een ander de taak voor deze laatste keer van hem overneemt.

Description: It is the fate of most historic personalities that in the course of time their work sinks almost completely into oblivion, and that the few lingering reminiscences of their achievements are transmitted to later generations in the form of second- or third-hand quotations, usually mixed with more or less anecdotic episodes from their life. It must be admitted that LINNÉ occupies in this respect a comparatively favourable position, for most educated people will remember that they heard in their school days of at least three things which are credited to him, in the first place that he produced a classification of the plant kingdom which is based on the number of stamens and carpels, the so-called sexual system, in the second place that he was the first who consistently applied the binomial nomenclature, i.e. the custom to designate an organism by a combination of two names, viz. a generic and a specific one, and thirdly that he was the originator of the pronouncement “Species to numeramus quot diversae formae in principio sunt creatae” (We count so many species as in the beginning different forms were created). Other achievements of LINNÉ may have been of greater importance, but it are these three things for which he is most generally remembered. The pronouncement quoted above, which means that the groups of individuals which form the species are descended from ancestors that owed their origin to an act of creation, derives its historic importance from the part it played in the debates on the theory of evolution. As it implies that the species are constant, it became the watchword of the antagonists. It is, however, rather strange that this pronouncement has so often been quoted, for it is found in LINNÉ’s earlier works only, and was in the later ones replaced by another statement that flatly denies the constancy of the species.

Description: Recently a multidisciplinary investigation program on the systematics of Annonaceae was started at Utrecht with special emphasis on the Neotropics. This project will be carried out largely within the framework of the UNESCO-project Flora Neotronica. The first goal is to provide a modern classification of the family as a whole, the second is the publication of a series of monographs for Flora Neotropica. The project has been planned and started in close consultation with leading botanists on the Neotropical flora. The Annonaceae are a family of pantropical distribution with between 2000 and 2500 species in ca. 130 genera as presently understood. In the Neotropics the family is represented by ca. 750 species and 35 genera. It is a family of trees, shrubs, and lianas. Its place is within the order of the Magnoliales and its supposedly closest relative is the family of the Myristicaceae. The Annonaceae, although generally considered primitive in many features, nevertheless offer a number of specialized features as well This makes it a promising object using various kinds of comparative morphological, karyological, and anatomical data. Besides, many species are of medicinal or commercial value, such as various species of Annona and Rollinia, the fruits of which are commonly eaten in most countries of Central America and South America; the Soursop (Annona muricata) is widely cultivated throughout the tropics.

Description: Erismadelphus Mildbr. is remarkable because it is the only African genus of the Vochysiaceae, a family represented in tropical America by no less than 5 genera and 180 species. Erismadelphus was discovered in 1913 by Prof. J. MILDBREAD and has hitherto been represented by only one species: E. exsul Mildbr. Recent examination of the African collections has, however, revealed the existence of two other taxa. Unfortunately the type of E. exsul (Mildbraed s.n. from Elon, French Cameroons) was destroyed at Berlin during the 1939-45 war and no duplicates or cotypes are known to exist. In response to an enquiry Prof. MILDBREAD, to whom we are very grateful, informed one of us that in his view Corbisier 1362 from Eala in Belgian Congo was identical with his original type. Prof. MILDBRAED and KEAY have, in fact, together examined Corbisier 1362 in the Herbarium of the Jardin Botanique de l’Etat at Bruxelles through the courtesy of Prof. ROBYNS. Duplicates of Corbisier 1362 are at Kew and Paris, they agree in every respect with MILDBRAED’s original description and figure and we therefore propose that this specimen be adopted as the neotype (lectotype).

Description: A new species of Asterophorum, A. mennegae, is described from the Sipaliwini Savanne (Suriname). The position of Asterophorum within the family is briefly reviewed, and a key to the 2 species is given.

Description: The originally monotypic eastern Malaysian genus Schiffneriolejeunea Verdoorn 1933 has now become a widespread, pantropical group of about fifteen species by the inclusion of species from the genus Ptychocoleus Trev. nom. illeg. Six species are known from Asia, three of which constitute the sect. Saccatae (Verdoorn) Gradst. & Terken comb. nov. These are the widespread Schiffneriolejeunea tumida (Nees) Gradst., the eastern Malaysian S. cumingiana (Mont.) Gradst. and S. nymannii (Steph.) Gradst. & Terken comb. nov. Schiffneriolejeunea tumida is a rather polymorphic species in which two not sharply defined varieties may be distinguished: S. tumida var. tumida with more or less involuted leaf margins, and S. tumida var. haskarliana (Gott.) Gradst. & Terken comb. nov. with plane margins.

Description: JEAN BAPTISTE CHRISTOPHE FUSÉE AUBLET est né à Salon (Provence) le 4 nov. 1720 et mort à Paris le 6 mai 1778. Dès son enfance il se passionna pour l’étude des plantes. Il alla étudier la botanique à Montpellier. De Montpellier il se rendit à Lyon, où il fit la connaissance de CHRISTOPHE DE JUSSIEU et il s’engagea dans le service des hôpitaux de l’armée commandée par l’infant DON PHILIPPE. Dégoûté bientôt de la vie des camps, il prit son congé, et vint à Paris. Là il se logea dans la maison du chimiste VANEL, suivait les cours de chimie de ROUELLE, visitait les environs de Paris en naturaliste et consultait BERNARD DE JUSSIEU comme une bibliothèque, pour nous servir de son expression. Ensuite il s’engagea au service de l’état et fut chargé d’établir à l’île-de-France (Mauritius) une pharmacie centrale et un jardin de botanique. Il s’embarqua en décembre 1752 et arriva vers la fin du mois d’août suivant. Il y fit un séjour de neuf ans, pendant lequel il envoya maintes fois des collections de plantes, de minéraux et d’animaux à la patrie. A peine de retour en France, il reçut l’ordre de s’embarquer à Bordeaux pour la Guyane. Il mit à la voile le 20 mai 1762, et mouilla l’ancre le 23 juillet à l’île de Cayenne. Le 24 sept. 1764 AUBLET prit un moment la direction de l’établissement colonial du môle Saint-Nicolas à Saint Domingue; et au commencement de l’année suivante il revint en France. C’est à Paris qu’il profita des conseils de BERNARD DE JUSSIEU pour mettre en ordre ses collections de plantes et pour rédiger l’important ouvrage, qui a pour titre: Histoire des plantes de la Guiane françoise, Londres et Paris, 1775, 4 vol. in 4°, dont deux de planches. Ces notices biographiques ont été empruntées à la Nouvelle Biographie Universelle, vol. III, Paris, 1852 et à l’introduction précédant son livre et écrite par AUBLET lui-même.

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

Description: The subject of this study are soil samples taken in the “Makkumer Waard”, a wide expanse of low-lying land, which follows the Frisian coast. Stratigraphical and palynological investigations showed that in the beginning of the Atlanticum the area lay below the level of the sea, but that gradually the influence of the sea decreased and peat formation became possible. From the transition from marine deposits to Sphagnum peat (— 4,55 m to — 3,50 m) we must conclude that there has been a temporary standstill in the transgression, or even a regression, in the middle of the Atlanticum. Towards the end of the Atlantic period a sudden marine transgression followed, which deposited a layer of sand and clay on the Sphagnum peat (— 3,50 m to — 3,30 m). Shortly before the beginning of the Subboreal (which probably sets in at — 3,10 m) an important regression began and an Eriophorum peat was formed directly on the clay (—3,30 m to —3.00 m). It is probable that the peat formation went on in the Subatlanticum, but the younger Sphagnum peat is no longer present, for a third marine transgression, which lead to the formation of the “Zuiderzee”, washed away the peat and deposited the younger sea sand. The data obtained from the Makkum profile proved to agree very well with the results of other investigators who worked in the area round the North-sea.

Description: What KIAERSK wrote in 1893 in the preface of his “Enumeratio Myrtacearum Brasiliensium” is still largely valid. It is often most difficult to define a species belonging to this family, not only because, in the absence of ripe seeds, the genus is not easily ascertainable, but also because of the strong variability shown by the vegetative characters. Thanks to the examination of the rich Guiana material preserved in the herbaria of Genève, Kew, Leiden, New York, Paris and Utrecht, I have usually been able to delimit the species in a satisfactory way; their allocation to a definite genus, however, is often a difficult problem. During the preliminary stage of this investigation, which was interrupted by the war, it was of great advantage to me that I could study the Guiana specimens of the Leiden herbarium. In order to avoid misinterpretations, I have tried to base my conclusions as far as possible on an examination of either the types themselves or of duplicates of the latter. Several of these types, especially those that form part of the earlier collections of Guiana plants, e.g. of the collection Aublet, and of the collections Desfontaines (herb. Florence) and De Candolle (Genève) had never before been reexamined, and BERG, the last monographer of the South American Myrtaceae (in Linnaea XXVII (1855—56), XXIX (1858) and XXX (1861) has either neglected these species or given an, often incorrect, interpretation based on the description alone. For this reason the second part of this paper will be devoted to a short survey of these earlier types. My best thanks are due to the directors of all herbaria mentioned. Moreover, I have to thank the “Van Eedenfonds”, whose financial aid enabled me to pay a visit to Kew and to the British Museum.

Description: Whilst studying the material of the genus Securidaca for the “Flora of Suriname”, I found it in most cases extremely difficult or even impossible to identify the species. The original descriptions are, as a rule, very short, and they have been based for a good deal on incomplete material: mature fruits, for instance, are often missing. Hence it is not surprising that on quite a number of species the opinions of taxonomists disagree. Accordingly on the one hand we may find in the various collections the most different species lumped together under the same name, while on the other hand one and the same species may appear under several names. A study of the type specimens therefore, was obviously very desirable. I am indebted to the “VAN EEDEN FONDS” for enabling me to visit the Herbarium in Paris, where I could clear up some misunderstandings with regard to the Suriname species. This study includes all the Suriname specimens preserved in the Herbaria of Utrecht, Leiden, Kew, Brussels, Geneva and Berlin, together with the material collected outside Suriname and available in the Utrecht and Paris collections, and the British Guiana plants of the Kew Herbarium. To get an impression of the genus as a whole, several species not occurring in Suriname have been studied, but a thorough investigation was made of the Suriname ones only. The results of this investigation will be given below.

Description: In my first paper (1951) a part of the tribe Eupodostemeae was revised, viz. the genera Apinagia, Marathrum, Rhyncholacis, Lophogyne, Monostylis, Jenmaniella, Wettsteiniola and Macarenia. The second part deals with the subfamily Tristichoideae, which comprises the genera Tristicha and Weddellina, and the tribe Mourereae of the subfamily Podostemoideae, which consists of the genera Mourera, Lonchostephus, and Tulasneantha.

Description: Among the material collected by LANJOUW and LINDEMAN during the Suriname Expedition 1948—’49 a specimen of Mabea taquari Aubl. was found whose flowers showed some interesting deviations from the normal structure. In the “Flora of Suriname” vol. II, part 1 (1932), p. 78 LANJOUW states that the female flower of the genus Mabea Aubl. is apetalous and provided with a 5- or 6- partite calyx. In a re-investigation of the specimens preserved in the Utrecht Herbarium this could as a rule be confirmed.

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

Description: A phytosociological survey based on methods of the Zürich-Montpellier School was carried out in the páramo vegetation of the Cordillera Oriental, Colombia. The study area covers about 10,000 and comprises the páramo between the Nevado de Sumapaz (3°55'N, 4250 m), the Sierra Nevada del Cocuy (6°25'N, 5493 m) and the Páramo del Almorzadero (7°N, 4375 m). The páramo vegetation was studied along various altitudinal transects from the upper forest line (3000-3500 m) up to the lower limit of the snowcap (4800 m). A general description of the study area includes data on geology, geomorphology, soils, climate, flora, phytogeography, morphological characters of the vegetation, fauna and landuse. The evolution and Quaternary history of páramo vegetation and climate is reviewed, incorporating the first data from the Lateglacial and Holocene of the Páramo de Sumapaz. The general altitudinal zonation of the páramo vegetation was studied and is presented for both the dry and the humid side of the Cordillera. The zonal and azonal plant communities are described including their physiognomy, composition and syntaxonomy, habitat and distribution. Eighty five syntaxa from the rank of variant to that of the class are newly described, 17 of which are provisional. The vegetation is not ranked syntaxonomically yet, but described on the basis of preliminary tables. A number of azonal communities, part of them of lesser extent, are described in a similar way. The páramo vegetation is primarily determined by the tropical diurnal high mountain climate. The diversity of the páramo vegetation is related to temperature (altitudinal gradient) and to humidity (dry and wet climate). The presence of zonal bunchgrass páramo, bamboo-bunchgrass páramo or bamboo páramo mainly depends on the complex interrelation between these factors. Finally a synthesis is provided on ecology, morphology and phytogeography of the páramo vegetation of the study area.

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

Description: The wood and leaf anatomy of representatives of the 9 genera of the Opiliaceae are described in detail. It is possible to separate the genera on the base of both wood- and leaf anatomical characters. Herein the presence of cystoliths of varying shape and size is important. Some comments on the taxonomy and possible phylogeny of the familiy are given.

Description: Isoëtes Palmeri with a distribution in the High Andes from the Páramo of Venezuela to the Páramo of Ecuador is described as a new taxon, and dedicated to the then American specialist of the genus, Thomas Chalkley Palmer (1860-1934). The new species belongs to the tropical-Andeanaustral-antarctic section Laeves, described as new here as well. The publication of the new species had to be anticipated to the projected monographic treatment of the South-American representatives of the genus Isoëtes, as A.M. Cleef, Utrecht intends to base a new association, the Isoëtetum Palmeri on this new taxon, observed and collected by him at many instances within the Colombian Páramo between 1971 and 1980 in the context of the preparation of his doctoral thesis now under way.

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

Description: In his introductory statements to 'The Symposium on the Phylogeny and Classification of the Filicopsida' which was held in London, 1972, HOLTTUM, when dealing with 'dubious groups of relationships which would particularly repay investigation', mentioned the Polypodiaceae first (HOLTTUM, 1973: 6). Talking about Polypodiaceae the present authors deal with the Polypodiaceae sensu stricto only, thus excluding the Cheiropleuriaceae, Dipteridaceae, Grammitidaceae, and also the Loxogrammaceae, taxa which were formerly (or are still) included in the Polypodiaceae sensu lato. As delineated in this way, this almost exclusively pantropical family consists of about 600 species and an indefinite number of genera.

Description: The new species Coussapoa manuënsis C.C. Berg is described.

Description: Until recently relatively little attention has been paid to the study of chromosomes in liverworts. The first substantial contributions were made by Heitz (1927, 1928) and Lorbeer (1934). In the second half of this century chromosome studies on liverworts were mainly carried out in Europe (e.g. Fritsch 1972; Newton 1977, 1979) and Japan (e.g. Tatuno 1959; Segawa 1965a, b, c; Inoue 1968). Inoue (in Koponen 1979) reports that until now 28% of all bryophyte species in Japan have been investigated as to their chromosome complement. A comprehensive, but rather outdated, survey of chromosome numbers in Hepaticae and Anthocerotae was given by Berrie (1960). Work on a new, updated survey is now underway (Fritsch, in prep.). In the present article results are presented of a cytotaxonomic investigation of European species of the genera Aneura and Riccardia (Aneuraceae). Most specimens were gathered in the Netherlands, but some chromosome counts based on French and German plants are also included.

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

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

Description: IUCN, says the paper Categories, Objectives and Criteria for Protected Areas, ”is dedicated to the wise use of the Earth’s natural resources and to the maintenance of the Planet’s natural diversity.” What to think of the sequence? Use first, maintain second? And this comes from the International Union for the Conservation of Nature and Natural Resources? ”The World National Parks Congress, taking place in Bali, Indonesia, October 11-22, 1982, will provide case studies from around the world to illustrate how the various categories of protected areas are meeting the needs of countries of all economic, social, cultural, and political backgrounds,” writes J.A. McNeely, the secretary of the Commission on National Parks and Protected Areas, in a special issue of the Swedish journal Ambio (11: 237. 1982). ”No longer just playgrounds for vacationers and means for conserving natural heritage, protected areas have become an inseparable part of the modern human ecosystem.”

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

Description: Dr J. Hutchinson retired after 44 years of service in the Royal Botanic Gardens at Kew (May 31, 1948), as Keeper of the Museum. He will devote his time mainly to the writing of some general handbooks especially his Genera Plantarum. He was succeeded by F.N. Howes, D. Sc. Mr H.K. Airy Shaw was appointed Principal Scientific Officer, Royal Botanic Gardens, Kew, on Dec. 31st, 1948.

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

Description: Mrs. Delia D. Adefuin, Museum Research Assistant, Manila, is pursuing her M.S. in Botany degree. She is currently the Secretary of the Fern Society of the Philippines. She is working on the Fern Flora of Metro Manila and is preparing the manuscript of a pictorial encyclopedia which will include descriptions of species and horticultural recommendations. Miss Barbro Axelius (S) collected and studied Xanthophytum and Lerchea (Rubiaceae) in Sarawak, Kalimantan and Sumatra, August 1982- February 1983.

Description: Tropical Botany in Aberdeen University. This was started by Professor J.W.H. Trail, who held the chair from 1877 to 1919, and travelled in the Amazon Valley (1873-75) mainly collecting cryptogams and studying palms. He was succeeded by Prof. W.G. Craib (1920-33) who was never in the tropics but devoted his work to the Flora of Siam, based on the collections of A.F.G. Kerr, and assisted by Miss E.C. Barnett. After a considerable lag, tropical botany was revived by the energetic efforts of Dr. P. Ashton as lecturer in systematics and ecology of the eastern tropics, establishing ties with Malayan colleges in teaching and research. This is at present perpetuated by two lecturers, Dr. K. Jong and Dr. M.D. Swaine, the latter’s experience lying largely in the tropics of West Africa. In addition Dr. N.M. Pritchard, Dr. J.B. Kenworthy and Dr. G. Hadley have been on secondment to the University of Malaya, while Dr. I. Alexander made research visits to India, Ghana and Peru. Over the years the Department has provided undergraduate and research training to innumerable students from many different tropical countries, some of which attained responsible posts, e.g. Prof. E. Soepadmo. Important courses in tropical biology are given, not available elsewhere in the U.K. (started 1973). The benefits for Aberdeen students is important: amongst others they led to expeditions to various parts of the tropics, recently to Sabah and to the Ivory Coast. Royal Society Tropical Rain Forest Collaborative Research Programme. Arising out of a feasibility study by Dr. T.C. Whitmore and P.F. Cockburn, the theme ’Recovery of tropical rain forest after disturbance’ was adopted as the initial basis of the programme. Possible territories for the research include Sabah and the Philippines. Detailed plans for a 5-year project are being prepared in consultation with colleagues in Southeast Asia.

Description: Some news was received on the revegetation of Krakatau, and the small new cone, Anak Krakatau (Krakatau Jr) as visited by a party in August 1951. Krakatau. The camp was made in the SE.corner of the island. In several places the old substratum has been traced, and in the basal layer of the ash covers, which attain sometimes 30 m thickness, remains are found of former woody share vegetation. Bases of tree trunks have partly been buried in their upright position. Some of these are charred, and have apparently been burned during the eruption; others are not charred, or have been charred only very superficially.

Description: A growing interest in the Flora Malesiana was a chief characteristic of 1950. The number of free subscriptions increased to over 320 and the total of subscriptions, therefore, to over 620 as the Government of Indonesia receives 300 copies for official purposes. The first volume of series I, the Cyclopaedia of Botanical Exploration in Malaysia, which contains the main bibliographical and biographical data of all collectors in Malaysia, accompanied when advisable by an itinerary and information concerning the collections, has now been printed. It is expected that the volume will appear before the end of the year thus bringing Mrs.M.J. van Steenis-Kruseman’s patient and devoted work during more than 12 years to a conclusion.

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

Description: Alphen de Veer, E.J. van: Een teratologisch novum (Chron. Naturae 105, 1949, 150-152, 3 fig.). Peculiar polyconal monstruosity of Pinus merkusii. Anonymous: Lijst van boomsoorten verzameld in de Afd. Kapoeas-Barito, Z. Borneo. Ditto, in de Afd. Bandjermasin, Hoeloe Soengel, Z.O. Borneo. Ditto, in de Afd. Samarinda, O. Borneo. Rapport v.h. Bosbouwproefstation Buitenzorg no. 2, 3 & 5, 76, 61 & 48 pp. March, April 1949. Mimeograph. Lists of tree species collected, arranged both by native names and Latin names; of each species the number of specimens and durability class is added.

Description: It is with the utmost regret that we announce the sudden and quite unexpected death of Dr. Marius Jacobs, editor of this Bulletin. See the obituary on page 3869. He was co-editor of the Flora Malesiana Bulletin for nr. 17 (1962) to nr. 22 (1968) and took full responsibility onwards of nr. 27 (1974). He showed great ability in enlarging its scope and we have many letters in our archives expressing appreciation and admiration for the lively and informative style in which he edited the Bulletin. I had to take over the editorial work for this number at short notice, but I was greatly helped by a number of Rijksherbarium colleagues, which help is gratefully acknowledged. In this way the delay has been kept to a minimum. It is, however, possible that some news items etc. have not been printed and that information submitted to Dr. Jacobs has not been entered due to this sudden change of editorship. I offer my apologies if this has happened and hope that (if still relevant) the news will again be forwarded to the new editor, Dr. J.F. Veldkamp, Rijksherbarium, who will take over starting next number.

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

Description: Centenary of the Kew Herbarium and Library. If we are well informed the centenary of the Herbarium” and Library of the famous Royal Botanic Gardens, Kew, occurs in 1953 and will be informally celebrated by an Exhibition in the Herbarium on the 8th and 9th of May, 1953, which will, we assume, be attended by many of the countless friends of this Mekka of Botany and in honour of the unsurpassed service which it renders to botanists all over the world. Indonesian timbers. A sample proof sheet was received of a book to be issued by the Indonesian Forest Research Station at Bogor. This will comprise a botanical treatment of about 400 of the most important timbers of Indonesia. Each species is to occupy 4 pages, viz a full page drawing, and one page for the text in 3 languages: Indonesian, Dutch, and English. Each description consists of the name and synonyms, preferent vernacular name, other vernacular names, geographical distribution, habitat circumscription, habit description, technical-botanical description, and notes. No mention is made of the anatomical characters of the wood; these will be published in a separate book which is prepared simultaneously. The book will probably be finished in 1956.

Description: Dr R.C. Bakhuizen van den Brink Jr, Leyden, made a provisional revision of the genus Ophiorrhiza (Rubiaceae). Onwards of 1953 he will be working on the completion of Backer’s Flora of Java. Dr M.J. Baumann-Bodenheim who made a big collection of plants in New Caledonia during the past two years has been temporarily appointed at the Bot. Garden Zürich for the working out of this collection.

Description: It is advised to address all mail with destination Royal Botanic Gardens, Buitenzorg, in future as ’Royal Botanic Gardens, Bogor (Buitenzorg)’ The present number, Flora Malesiana Bulletin No. 6, concluded the 1st volume. The second volume of the Flora Malesiana Bulletin begins with no. 7.

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: The Botanical Survey of India continued to make collections during 1982, with the following results: Andaman & Nicobar Is.: Shola Bag, Mt Harriet, Jirkathang, Poona Nallah, Saddle peak, Diglipur, Rutland I. & Little I., 2875 specimens. Arunachal Pradesh: Various areas of Kameng Distr., Subansiri Distr., 9750 specimens. Assam: Garampani, 60 specimens. West Bengal: Darjeeling, Jalpaiguri, Hollong, Jaldapara, Chilapata, Salkumar, Daidaighat, Barasat, 2665 specimens. Bihar: Madhuban, Nimiaghat, Paresnath Hills, 315 specimens. Dehra Dun: Chakrata, Missoori, 325 specimens. Gujrat: Catchment and submergence areas of Sipu Reservoir Project, 1505 specimens. Kerala: Trichur, Idduki, Silent Valley, Valra Reserve Forest, Cannanore, Trivandrum, 3770 specimens. Madhya Pradesh: Kanha National Park, Chhodarpur Distr., 1190 specimens. Maharashtra: Areas of Jalgaon Distr. and Buldhana Distr., 4390 specimens. Manipur: Cherrapunjee, Mawphlong, Sorharim, areas of West Khasi Hills Districts, 2000 specimens. Rajasthan: Bharatpur, Desert National Park, 1605 specimens. Sikkim: Rangpo, Singtham, Bumbing, Manuring, Duga, Pandam, Takchi, Meli, areas of Gangtok, Chungtham, Lachi, Thanga, Panthang, 2590 specimens. Uttar Pradesh: Gori & Kali Valley, Chittoragarh Distr., 500 specimens.

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: 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: The ultrastructure of the spore walls of Beenakia dacostae (Beenakiaceae, Gomphales) has been studied. Spore walls are mainly composed of a distinct episporium and a thick, dark, ornamented ectosporium. The general structure is identical with that of other members of the Gomphales, such as Gomphus and Ramaria

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

Description: During an ecological study of fungi of the tidal mudflats in Kuwait, a Sporothrix species has been recorded twice, in 1977 and 1980. It differs from other species of the genus (de Hoog, 1974, 1978) in several characters and is here described as a new species. A comparison with similar species of the genus is added.

Description: In Madroño (1936) Herre has lamented the disappearance of lichen species through the disastrous interference of man. Unavoidably, the advance of civilised modern life is linked with destruction of the vegetation. This applies all the more as the endangered area is more densely populated and it certainly applies most alarmingly to the lichen flora of the Netherlands. Here, every way-side tree felled is an irreparable loss to the epiphytic lichen communities, every acre of heath burnt or turned into arable land is a blow to our stock of terrestrial lichen species, whereas the use of dry fertilisers and the spraying of orchards are very effective in killing any lichen in the neighbourhood that otherwise might have survived. A comparison of the material preserved in the older collections with what can be found nowadays, clearly shows what has gone lost. It is sad to think that an ever increasing number of species are on their way to total extermination. However, from a thorough investigation of the epiphytic communities of cryptogams latterly started by Mr J. J. Barkman, it becomes apparent that at least to some extent the losses may be compensated by the discovery of species hitherto overlooked or not recognised. It is on such and other finds that I intend to report from time to time.

Description: In einem jüngst erschienenen Aufsatz schreibt Du Rietz (1941 S. 6): ”Pylaiella rupincola (Aresch.) Kylin ist mit Conferva litoralis L. identisch. Kein Grund liegt vor anzunehman‘, dass Linné die auf Ascophyllum an der schwedischen Westküste wachsende Pylaiella litoralis sensu Kylin gekannt und in seine Conferva litoralis miteinbezogen hat. Der Name Pylaiella litoralis (L.) Kjellm. muss deshalb für P. rupincola (Aresch.) Kylin beibehalten werden. Für P. litoralis sensu Kylin schlägt Verf. den neuen Namen Pylaiella Kylinii vor.“ Bei meinen Untersuchungen über Pylaiella litoralis (1933 und 1937) war ich zu der Auffassung gekommen, dass diese Art in sich zwei verschiedene Arten enthielt. Für die eine behielt ich den Namen P. litoralis (L.) Kjellm., die andere nannte ich P. rupincola (Aresch.) Kylin 1937 S. 5, und dies zwar aus historischen Gründen. In der Literatur hatte man nämlich die im allgemeinen auf den gröberen Fucaceen epiphytisch wachsende Pylaiella als die Hauptform betrachtet, die im allgemeinen auf Felsen wachsende rupincola dagegen als eine Nebenform. Und um nun die Nomenklatur, in der Weise wie sie sich historisch entwickelt hatte, so wenig als irgend möglich zu verändern, bezeichnete ich die Hauptform als P. litoralis (L.) Kjellm., die Nebenform dagegen als B. rupincola (Aresch.). Kylin. Du Rietz behauptet jetzt, dass ich die Nomenklaturgesetzte übertreten habe. Ehe ich indessen diese Frage des näheren auseinandersetze, werde ich P. litoralis und P. rupincola kurz besprechen.

Description: Anne Antoinette van Bosse, fille de M. Jacob van Bosse et de Mme Jaqueline Jeanne née Reynvaan, naquit à Amsterdam le 27 mars 1852. Très jeune encore elle perdit sa mère; sa soeur, son ainée de 10 ans, prit sa place aussi bien qu’elle put. Outre cette soeur elle avait trois frères. Selon l’usage de cette époque les familles aisées n’envoyaient pas leurs filles à l’école, ainsi Anna van Bosse reçut à la maison son instruction par une institutrice de nationalité suisse. La botanique et la zoologie furent d’emblée ses branches préférées; les fréquentes visites au jardin zoologique ”Artis“ y contribuèrent pour une grande part. l’Observation des animaux exotiques lui procurait un grand plaisir et jusqu’à présent elle porte un grand intêret à ”Artis“.

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: Summarizing, it appears that Eucommia has the greatest number of characters in common with the Urticales. This is shown by the similarity of the inflorescences as well as by the unisexual flowers and the dioecy. In both groups the pistil consists of 2 connate carpels and the ovary is usually 1-celled by abortion, while the stigmata are generally papillate. Further general points of relation with the Urticales are the originally spiral phyllotaxis, which becomes later on pseudo-distichous, simple vessel perforations, libriform with bordered pits, unicellular hairs and the occurrence of calciumcarbonate and silica as well as of latex elements. Yet, it seems difficult to indicate any particular family in the Urticales to which Eucommia should be most related. While the fruit recalls Ulmus and the latex elements Urtica and Cannabis, the spirally thickened vessel walls remind us of some Morus species. In addition, Eucommia is isolated by the facts that in the Urticales the perianth is never entirely wanting, that there is only one ovule in the cell of the ovary, that stipules are very frequent, that calciumoxalate is characteristic (it is wanting in Eucommia) and that the superficial suberization is subepidermal in the Urticales and epidermal in Eucommia. After the Urticales the Euphorbiaceae-Hippomaneae seem to be the nearest of kin, on account of a number of anatomical and morphological characters. However, the Euphorbiaceae usually possess a 3-celled ovary, a 2-celled one occasionally occurs in the Hippomaneae. Next follow the Hamamelidaceae which have, however, two fertile carpels but of which Distylium and Altingia show a reduction in the perianth and the latter moreover a similar leaf shape.

Description: Among the collections of Knema acquired by the Rijksherbarium since the publication of my new account of the genus Knema, in Blumea 25, 1979: 321 — 478, a few specimens caused problems with the identification, and at closer examination these yielded facts of interest which are published here. Some specimens represented stages not yet known, for instance fruits, or male flowers, while other specimens meant a significant range extension of the species. Two new species and one new subspecies are described. For easy reference, the sequence and numbers of the species presently treated correspond with the numbers as used in the account of 1979. The new species bear the number of the species after which they appear in the general key of 1979, with the addition ‘-bis’.

Description: The early development (ontogeny) of the carpels of 20 species belonging to 8 apocarpous families was investigated with the scanning electron microscope. The results indicate that on the floral apex a circular or a convex meristem develops into an obliquely ascidiate primordium by unequal growth of its periphery. By further unequal growth it develops into a young carpel. The terminal mouth of a cup becomes the lateral cleft of a carpel. The different forms of the young carpels in different species are defined by the varying degree of development of the adaxial region of the initial meristem and/or its margin on the side of the floral apex. This hypothesis is theoretically evaluated.

Description: A revision of the species, comprised in the section Eu-Protium of the genus Protium from the region from Asia to Australia incl., might., in view of the elaborate publications by H. J. Lam (The Burseraceae of the Malay Archipelago and Peninsula etc., Bull. Jard. bot. Buitenzorg, S. 3, 12, 1932, p. 318—324) and J. J. Swart (A Monograph of the genus Protium and some allied genera, Rec. Trav. bot. néerl., 39, 1942, p. 211—146), seem superfluous. However, an examination of the Clemens material from New-Guinea of 1939 and of the type material of the thusfar mysterious Bursera tonkinensis Guill. justified the publication of some notes thereon. To these some remarks concerning observations on other species have been added. I am much indebted to the directors of the following herbaria for the loan of material: the herbarium of the Botanisches Museum, Berlin; the herbarium of the Arnold Arboretum, Jamaica Plain, Mass. (A); the herbarium of the Royal Botanic Gardens, Kew; the herbarium of the Museum d’Histoire Naturelle, Paris; the herbarium of the Botanical Institute, Wroclaw (BRSL); the “Rijksherbarium”, Leiden (L).

Description: The island of Enggano is the most southern of a series of islands situated parallel to the Western coast of Sumatra. In 1936 the island was visited by Dr. W. J. LüTJEHARMS, who stayed there from the end of May to the beginning of July collecting materials for the Herbaria at Buitenzorg and Leiden. During this excursion he also collected some zoocecidia, which were sent to me for classification by the Director of the Rijksherbarium, Leiden. The collection consists of 16 galls on various plants; many of them were already known as occurring in other parts of the Malay Archipelago; others are new, these are marked with an asterisk. A collection of 16 galls is actually to small to give insight into the wealth of galls of this tropical island; so far, however, nothing was known about the galls of the island, and since it is unlikely that the place will before long again be examined as to its galls, I deemed it worthwile to describe this small collection.

Description: In Malesia the genus Tephrosia is represented by 20 species, native or introduced and naturalized, including 6 subspecies and 5 varieties; 4 species are restricted to Malesia. Two of these species are newly described: T. barbatala and T. elliptica; the former includes one new variety (var. glabra). Two new subspecies and one new variety are distinguished: T. filipes subsp. longifolia, T. purpurea subsp. barbigera, and T. maculata var. elongata. Two taxa are given a new status: T. maculata var. appressepilosa and T. pumila subsp. aldabrensis. Four species, T. dichotoma, T. repentina, T. coarctata, and Kiesera sumatrana are for the first time sunk into synonymy. A key to the taxa, synonymy, and full descriptions with plates and distribution maps are given.