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: Some fifty years after the Snellius I expedition (1929-1930) a Dutch-Indonesian joint expedition is carried out (1984-1985) in the Eastern Indonesian archpelago. Based on two months (September -October 1984) of research at nine different reef localities, a first report will be presented on the general morphology, composition and condition of recent and fossil reefs of these areas. The research areas that will be discussed are the following: Ambon: In the bay of Ambon fringing and patch reefs heavily damaged by silting up, caused by soi1. erosion on the island. North East Ambon an elevated reef from the old Pleistocene. Lucipara islands: Exposed very isolated atoll with some sand cays. Tukang Besi islands: Atoll reefs of Kaledupa. Binongko reef terraces; fossil cliffs modelled from massive Pleistocene reef limestone by coastal abrasion during tectonic uplift of the island; extensive reef terrace dating from the last interglacial; living reef not at the moment constructive. Sumba: East Sumba fringing reefs with influence of land and population. Young Pleistocene reef near Melolo, older terraces higher up. Komodo: Various fringing and patch reefs bordering the east side of the National Park of Komodo. Current swept reefs in the strait of Linta. Gililawa Laut and Tinandja lo~r Miocene reefs. Sumbawa: Fringing reefs in Telok Moti Toi and Sanggar bay near Tambora volcano (erupted in 1815). Coral growth in Bima bay. Pleistocene reef north east of Bima. Taka Bone Rate: Large pseudo atoll with small sand cay reefs (e.g. Tinandja) exposed reefs, coral banks and lagoons. Salayer: fringing reefs at west coast around islands Guang and Sahuluan. Pliocene reefs on both islands; Bahuluan with volcanic core. Sulawesi: Coral reef complex on the shallow shelf off South West Sulawesi, with three rows of reefs, most emerging as sand cay reefs. Because of young Holocene reg~ession in front of Ujung Pandang. Influence of sedimentation and population. Apart from these investigations during the Snellius II expedition, a long term project has been carried out since 1979 in the last area mentioned. A continuation of reef research is planned there, in close cooperation with UnHas (University of Ujung Pandang). The presentation of results will be accompanied by maps and photographs.

Description: In this precursory paper to the forthcoming Flora Neotropica monograph of Rollinia 12 new species are described. One new combination is made, and there is a note on the correct author citation for Rollinia dolabripetala. Mr. E. J. van Marle, a former student at the University of Utrecht, contributed the description of one of the new species.

Description: There exist three different kinds of leaf arrangement in neotropical species of Rinorea. 1. an alternate leaf arrangement consisting of only laminar leaves; 2. an alternate leaf arrangement consisting of laminar leaves in the apical part of the branchlets and scale-like ones subpersistent in the basal part; 3. an apparently opposite leaf arrangement consisting of laminar leaves together with a pair of inconspicuous and soon deciduous scale-like leaves at the base of the inflorescences. In this article hypotheses have been constructed how one kind of leaf arrangement can be derived from the other, how these three different kinds of leaf arrangements can be correlated with the arrangements of the inflorescences and those of the branchlets, and finally how an apparently opposite leaf arrangement also can be correlated with a so called Fagerlind tree model.

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 problems of reconstructing historical relationships for areas of endemism from distributional data for groups of taxa and the cladistic relationships among the members of those groups can be solved by applying the two principles of parsimony and mutual inclusion or exclusion (compatibility) of components. Components can be extracted from a data matrix by means of transcription into partial monothetic sets. The data matrix thus derived represents the distribution over areas for the monophyletic groups in one or more cladograms. It is derived from two different matrices by boolean multiplication. The first matrix gives the binary representation of distributions of taxa over areas of endemism; the second describes the cladogram for the same taxa, in terms of character states converted into binary form by additive binary coding. The derived data matrix can be used in historical biogeography to represent the given phyletic data ( Assumption 0 here newly defined), and can be amended to reflect Assumptions 1 or 2 to accomodate the problems of wide-spread taxa and missing areas. Areacladograms are determined from the derived matrix by searching for the largest sets of mutually compatible components. Area-cladograms are evaluated in terms of support (vicariance) and contradiction (ad hoc interpretations such as dispersal and extinction). Area-cladograms that best fit the data matrix regarding the balance between support and contradiction are selected as the best possible recontructions of relationships among the areas of endemism. The procedure is illustrated by the example of the poeciliid fish genera Heterandria and Xiphophorus, and several other standard examples.

Description: Aublet based Tontelea and its only named species, T. scandens, on material he collected in French Guiana, illustrated as pl. 10 in the original publication. Aublet’s specimens are incorporated in the herbarium of J. J. Rousseau (now located in the Paris Herbarium in herbier Denaiffe) and also in the Herbarium of the British Museum. The sheet in herbier Denaiffe was identified by Lanjouw and Uittien (1940) as the original for Aublet’s pl. 10, which shows a flowering twig, analysis of a flower, and a detached leaf much larger than the leaves on the twig. From a photograph of this sheet it appears that the inflorescence is reproduced only in fragmentary form in the drawing. In the latter the inflorescence is represented as a rather short, few-branched, flowering twig, whereas in the specimen the inflorescence is strictly dichotomously branched many times with occasional supernumerary branches in the leaf axils. The sheet also has four detached leaves.

Description: There comes a time in the history of nearly every genus when it becomes almost immoral to add new species without first having surveyed the genus as a whole. Dendrophthora has reached this state. From the time of its first recognition as a separate entity to the present, new species have been described, often on very tenuous grounds, and usually without an indication of infrageneric relationships, until today we are faced with a staggering mass of specific epithets in complete chaos. The genus has not been comprehensively studied for more than half a century, and no balanced attempt has as yet been made to establish natural divisions within. Having become interested in the morphology of this and the related genus Phoradendron (KUIJT, 1959), I was naturally led on to some taxonomic considerations. My stay in Europe in 1958-1959 enabled me to visit the major European herbaria, and the notes and sketches accumulated there soon pointed the way to the present work.

Description: This catalogue provides an annotated listing of the liverworts and hornworts from the Guianas (Guyana, Surinam, French Guiana), based on the literature and on new data that have become available in the framework of the “Flora of the Guianas” project. In total 375 species in 93 genera are recorded, including more than 100 species and 28 genera new to the Guianas. A list of synonyms (including 30 new ones), a systematic arrangement of the genera and families, and an index to the collectors are also given.

Description: This paper follows upon an earlier paper in the series “Studies in Annonaceae” (Maas et al. 1986). Twelve new species are described, viz. 2 in Duguetia, 1 in Ephedranthus, 5 in Guatteria, 2 in Hornschuchia, 1 in Tetrameranthus, and 1 in Unonopsis. A new combination is made in Enicosanthellum. Some amendments and additions to the revision of Tetrameranthus (Westra 1985), including an updated key, are given. Monocarpia euneura Miq. appears to have priority over M. marginalis (R. Scheffer) James Sincl. Additional collections have been made of the rare species Bocagea longepedunculata Martius, Xylopia crinita R.E. Fries, and Xylopia excellens R.E. Fries. Attention is drawn to several recent collections from Bahia, Brazil, which are perhaps referable to Unonopsis stipitata Diels. H. León, Popayán, and D. Sánchez S., Medellín, contributed to three of the new species.

Description: 1. The chromosome numbers of 10 species of the genus Viola in the Netherlands were determined. 2. Viola riviniana has various chromosome numbers: 2n = 35, 40, 45, 46, 47 (most often 2n = 40). 3. It was not possible to find a correlation between the external morphology and the various chromosome numbers in V. riviniana. 4. Despite the variability of V. riviniana it proved impossible to divide the Dutch material into subspecies. 5. Some differential characters of V. riviniana and V. reichenbachiana are described. 6. V. canina is not variable in cytological respect in the Netherlands. 7. V. calaminaria is not related to V. lutea but to the V. tricolor complex.

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: A. DE CANDOLLE’s (1830) treatment of the genus Campanula lists 137 species. Many new species were described since, so that the total number of species should be estimated to be at least twice that number. A new monograph of the genus is, therefore, highly desirable (CLIFFORD CROOK, 1951). Any classification into subgenera and sections, based on herbarium studies, is bound to meet considerable difficulties on account of the great uniformity among many floral characters of the various species. Cytological information may prove very valuable in order to arrive at a modern classification of the species within the genus.

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: 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: Haesselia roraimensis gen. et spec. nov. (Cephaloziaceae) from the foot of Mt. Roraima (Guyana) is described and figured. The new genus has been assigned to the subfamily Trabacelluloideae together with Fuscocephaloziopsis Fulf. and Trabacellula Fulf., two other neotropical genera of Cephaloziaceae with convex leaves.

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: Chemical analysis of representatives of about thirty genera of Lejeuneaceae has shown that the terpenoid and flavonoid content of the Lejeuneaceae is basically comparable to that of other Hepaticae and quite diversified. Among the terpenoids detected, some are common throughout the family (elemenenes, germacrenes), others are distributed more restrictedly and are indicative of evolutionary relationships among genera, e.g. borneols (Nipponolejeunea), pinguisanines (Acrolejeunea complex), striatenes (Ptychanthoideae, Omphalanthus complex), calamenanes ( Lopholejeunea) and labdanes (Ptychanthus, Tuzibeanthus). Flavonoids are present in smaller amounts than terpenoids and comprise some compounds unique to bryophytes (lutonarin, kaempferol-3-methylether). The genus Omphalanthus stands out by its total inability to biosynthesize flavonoids. At the species level the chemical constitution may vary considerably and in some species evidence for the existence of chemical races was detected.

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: A revision has been made of the hepatic genus Brachiolejeunea (Spruce) Schiffn. (family Lejeuneaceae, subfamily Ptychanthoideae). Within this genus two subgenera were recognised: subg. Brachiolejeunea and subg. Plicolejeunea Schust. (n order to distinguish taxonomic entities within these subgenera and to evaluate their affinities, the morphology and anatomy of the gametophyte and the sporophyte have been studied. Data on cytology and sporeling development, obtained from living and cultured specimens, were added. Sporophyte characters have been studied with light microscopy (LM) and scanning electron microscopy (SEM). Besides a considerable reduction in the number of accepted species, the main result of this study is that the traditional delimitation of Brachiolejeunea cannot be maintained. The two subgenera appear to be different in many characters, several of them new, and are accordingly elevated to generic level. The genus Brachiolejeunea (4 species) now comprises only the former subgenus of that name; the generic name Frullanoides Raddi is reinstated for the subg. Plicolejeunea (7 species and 1 subspecies). For both genera the morphology and anatomy are described, the previously neglected sporophyte generation being treated in particular detail. In each of the genera a different type of sporophyte is present; a “fenestrate-type” in Frullanoides, a “nodular-type” in Brachiolejeunea. From a of the distribution patterns it appears that both genera probably originated in the western part of Gondwanaland. Brachiolejeunea is confined to that area and may presently be characterized as a Neotropical-montane element. One species of Frullanoides is pantropical, the others are neotropical. The species of Brachiolejeunea are predominantly epiphytes of mountain forests and have a rather narrow drought tolerance; the species of Frullanoides generally occur in a greater variety of habitats and have a wider drought tolerance. A consideration of generic relationships shows that the affinities of genera are very different. For both genera identification keys are provided, each species and subspecies is illustrated and for each taxon the following information is provided: synonymy with relevant literature and typification, a description, geographical distribution with distribution map, and notes on ecology, differentiation and variation. The second part of this study contains a short review of the genus Blepharolejeunea S. Arnell, which has been emended to accommodate several diverging species of Brachiolejeunea and Dicranolejeunea. Blepharolejeunea is related to both genera and is characterized as a Neotropical-montane element. In the third part of this study the sporophyte generation in the subfam. Ptychanthoideae is analysed with Scanning Electron Microscopy. Fenestratetype and nodular-type sporophytes are described and the different affinities of these types are discussed. The new tribe Brachiolejeuneae van Slageren & Berendsen is created to accommodate the genera of Ptychanthoideae with nodular-type sporophytes.

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.