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  • Articles  (126,898)
  • Data  (11)
  • 1945-1949  (126,909)
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  • 101
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    In:  Flora Malesiana Bulletin (0071-5778) vol.3 (1948) nr.1 p.58
    Publication Date: 2015-06-05
    Description: It is a pleasure to announce the appearance of ”The Gardens’ Bulletin, Singapore” in continuance of the widely appreciated ”The Gardens’ Bulletin, Straits Settlements”. The latter periodical was discontinued after volume XI, part 3, published Aug. 30, 1941 had appeared. Vol. XI, part 4, issued Sept. 30th, 1947 contains a concise history of the Singapore Botanic Gardens during the period 1941-1946. We are obliged for permission to reprint that important communication in this Bulletin. The Gardens regret the loss of Mr J.C. Nauen, an officer of outstanding ability in charge of the Waterfall Gardens, Penang. He was taken prisoner by the Japanese and died on the Siam-Burma railroad, Oct. 1943. Messrs Holttum and Henderson prepared some important contributions on Filicales, Orchidaceae, Cyperaceae, Gramineae, and on Eugenia respectively.
    Repository Name: National Museum of Natural History, Netherlands
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  • 102
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    In:  Flora Malesiana Bulletin (0071-5778) vol.5 (1949) nr.1 p.123
    Publication Date: 2015-06-05
    Description: The first instalment of ”Flora Malesiana” was published in the last days of December 1948. The issue was 2500 copies, of which 1500 have been distributed. It contains a notice on 4 unnumbered pages (the first the provisional title page) which explains the scheme for the whole of the Flora while a brief outline is given of the contents of volumes 1-4 of the first series.
    Repository Name: National Museum of Natural History, Netherlands
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  • 103
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    In:  Flora Malesiana Bulletin (0071-5778) vol.2 (1947) nr.1 p.51
    Publication Date: 2015-06-05
    Description: Mr O.H. Selling, Vice-curator of Collections, Naturhistoriska Riksmuseum, Palaeobotaniska Avdelningen, is working on a revision of the genus Schizaea. Dr G. Kükenthal works towards the end of his monograph of the Cyperaceae-Rhynchosporoideae.
    Repository Name: National Museum of Natural History, Netherlands
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  • 104
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    In:  Flora Malesiana Bulletin (0071-5778) vol.3 (1948) nr.1 p.55
    Publication Date: 2015-06-05
    Description: From various sources the editor of this Bulletin has received ample information on the proceedings of botanical research and publication relating to the Malaysian flora. He will be grateful for any notes and references on work in progress. He specially asks co-operation in the completion of the ”Iconotheca” of Malaysian plant collectors and phytographers, of which he invites directors and librarians to take part. It is astonishing that he did not succeed in acquiring any picture of some very Important botanists and collectors, such as Th. Horsfield. William Jack, H. Kunstler, C. Boden Kloss. A.D.E. Elmer, H.O. Forbes, Ch. Gaadichaud, J.D. Haviland, James Motley, L.Th. Leschenault, E.W. Hullett, etc. etc. (cf. page 46). Through the care of Dr. Fr. Verdoorn a limited number of binders were made and distributed to libraries and co-operators to keep the several numbers of this Bulletin, until they are ready to be bound. The editor expects they will be found useful.
    Repository Name: National Museum of Natural History, Netherlands
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  • 105
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.113
    Publication Date: 2015-04-20
    Description: Annual or perennial herbs, never woody shrubs (in Malaysia). Stems often furrowed and with soft pith. Leaves alternate along the stems, often also in rosettes; petiole usually with a sheath, sometimes with stipules at the base; lamina usually much divided, sometimes entire. Flowers polygamous, in simple or compound umbels, sometimes in heads, terminal or leaf-opposed, beneath with or without involucres and involucels. Calyx teeth 5, often obsolete. Petals 5, alternate with the calyx teeth, equal or outer ones of the inflorescence enlarged, entire or more or less divided, often with inflexed tips, inserted below the epigynous disk. Stamens alternate with the petals, similarly inserted. Disk 2-lobed, free from the styles or confluent with their thickened base, forming a stylopodium. Ovary inferior; styles 2. Fruits with 2 one-seeded mericarps, connected by a narrow or broad junction (commissure) in fruit separating, leaving sometimes a persistent axis ( carpophore) either entire or splitting into 2 halves; mericarps with 5 longitudinal ribs, 1 dorsal rib at the back of the mericarp, 2 lateral ribs at the commissure; 2 intermediate ribs between the dorsal and the lateral ones; sometimes with secondary ribs between the primary ones, these without fascicular bundles; often vittae in the ridges between the ribs or under the secondary ribs, and in the commissure, seldom under the primary ribs. Distr. Numerous genera and species, all over the world. The representatives native in Malaysia belong geographically to five types. (1) Ubiquitous genera ( Hydrocotyle, Centella, Oenanthe); one species, Hydrocotyle vulgaris, shows a remarkable disjunction, occurring in Europe & N. Africa and also in New Guinea, Australia and the Marshall Islands. (2) Western elements are Sanicula (wide-spread in the N. hemisphere but absent from New Guinea and Australia), Heracleum and Pimpinella; though some spp. are endemic their close relatives are found in SE. Asia. (3) A distinctly N. element is the Japano-Formosan Peucedanum japonicum in the islands N. of Luzon. (4) A distinct Australian element is Trachymene which centers in Australia and occurs also in New Caledonia and Fiji; this genus shows a relatively rich secondary centre in East Malaysia; another Australian alliance is found in ubiquitous Eryngium of which the only native Malaysian species hitherto known is allied to Australian spp. (5) A distinct Subantarcticdistributed genus is Oreomyrrhis which centers in New Guinea by 4 spp.; one of these occurs from Kinabalu to Australia, New Zealand to Andine South America as far as Mexico; a marked instance of the ancient alpine-Papuan South Pacific plant refuge (v. ST.).
    Repository Name: National Museum of Natural History, Netherlands
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  • 106
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.265
    Publication Date: 2015-04-20
    Description: Shrubs, trees, or prostrate plants. Leaves spread, rarely opposite, entire or toothed, exstipulate. Flowers ♀, zygomorphic, rarely almost actinomorphic, small, axillary, solitary or usually in clusters of 2,3 or more. Calyx and corolla 5-lobed. Stamens 4, rarely 5, in pairs of unequal length, inserted on the corolla-tube and alternate with the lobes. Anther-cells opening lengthwise, confluent at the apex, usually forming a single reniform cell after dehiscence. Ovary superior, not lobed, 2—10-celled with 1 ovule in each cell, rarely 2-celled with 2 ovules per cell. Style simple entire or obscurely notched at the apex. Drupe 2—10-celled. Distr. Ca 35 spp., largely in Australia, 1 species in E. Asia, further in the Pacific, Rodriguez Isl. and Mauritius.
    Repository Name: National Museum of Natural History, Netherlands
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  • 107
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.5
    Publication Date: 2015-04-20
    Description: After the appearance of RUMPHIUS’S Herbarium Amboinense, the result of lifelong research into the botanical treasures of the Malaysian Archipelago, the first comprehensive work on the flora of these islands was begun by C. L. BLUME, the second Director of the Botanic Gardens at Buitenzorg. His Bijdragen lot de Flora van Nederlandsch Indie (Contributions to the Flora of the Netherlands Indies) consisted of numerous brief botanical diagnoses mostly, however, of Javan species. Shortly after followed his Flora Javae and later Rumphia. None of these books represent a ‘flora’; neither completeness was aimed at nor keys were given. The first design for a flora of the whole of Malaysia seems to have been drafted by the Swiss botanists H. ZOLLINGER and his teacher, A. MORITZI.¹ I have not succeeded in tracing any further results of their plans.
    Repository Name: National Museum of Natural History, Netherlands
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  • 108
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.517
    Publication Date: 2015-04-20
    Description: Perennial ± succulent herbs, often somewhat woody and procumbent and rooting at the base, often clothed with branched multicellular hairs; habit sometimes recalling certain Gesneriaceae (Cyrtandra, etc.). Leaves alternate, simple, mostly ± asymmetrical, sinuate-denticulate or subentire, ± fleshy, petiolate, exstipulate. Inflorescences axillary, cymose, often scorpioid, acropetal, solitary or 2-3 together in each axil. Bracts usually rather large and membranous. Flowers hermaphrodite (rarely unisexual), actinomorphic (calyx excepted), shortly pedicelled or sessile. Calyx-tube campanulate or linear-cylindric, adnate to the ovary by means of 5 longitudinal septa formed by the continuation of the filaments, leaving 5 deep nectariferous pits below the petals; lobes 5, imbricate, mostly membranous, persistent, unequal (2 larger and 3 smaller), coloured (mostly whitish). Corolla inserted at the apex of the calyx-tube, variously gamopetalous or less frequently choripetalous, ± campanulate, mostly fleshy or cartilagineous, occasionally delicate in texture, persistent, segments or petals 5 (rarely 4), valvate (sometimes induplicate), often reflexed at the apex. Stamens 5, alternipetalous, shortly adnate to the corolla (when gamopetalous); filaments persistent; anthers ovate, oblong or linear, introrse, basifixed, dehiscing by slits. Ovary inferior, 2-locular; placentas axile, bifid, multi-ovulate; style short, thick, simple; stigma massive, oblongcylindric, often strongly 5-ribbed. Ovules very minute, very numerous, pendulous, anatropous, with 1 integument. Fruit baccate, indehiscent. Seeds minute, ovoid; testa reticulate, brown; embryo minute; albumen copious. Distr. One genus. From Lower Burma, Indo-China and Kwangtung, throughout Malaysia to Central New Guinea-Java and the Lesser Sunda Islands excepted. Fig. 1.
    Repository Name: National Museum of Natural History, Netherlands
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  • 109
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.529
    Publication Date: 2015-04-20
    Description: The family consists of 5 genera, if Donatia FORST., of which the systematic position is not at all certain, is included. Four genera are confined to Australia, Tasmania, New Zealand and the Magellan region of South America. Stylidium is almost entirely Australian, but a few spp. occur in Malaysia, Ceylon, and continental SE. Asia.
    Repository Name: National Museum of Natural History, Netherlands
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  • 110
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.65
    Publication Date: 2015-04-20
    Description: Mostly annual, rather small, of peculiar habit, often moss-like, gregarious, confined to swift running water in streams and cascades. Tissues with silicium. Roots often thallose, flat, stem sometimes absent. Leaves mostly alternate, sometimes scattered, decussate or distichous, base often provided with a sheath, and sometimes stipulelike appendages, often dentate or divided. Flowers terminal, often in cymose inflor., mostly ♀♂, actinomorphic to zygomorphic. Perianth of 3-5 free or subconnate tepals, if reduced to two small, ovate or linear appendages, the bud is enveloped by an originally closed thin ‘spathella’. Stamens hypogyn, 1-~, often 2 unilateral, frequently monadelphic. Anthers mostly introrse, 2—4-locular, splitting lengthwise. Pollen grains single, or in twos or fours. Ovary superior, ovate to elliptic, mostly 2-, rarely 3-locular with thickened central placenta and thin septa. Ovules ~; styles as many as carpels, free, rarely 1. Capsule septicid (often) ribbed; seeds ~, minute, exalbuminous, epidermis mucilaginous. Distr. Principally confined to the tropics throughout the world, not yet recorded from the Pacific islands and the greater part of Australia, northward as far as S. Japan, in Malaysia apparently very rare. The locality closest to Malaysia is isthmian Siam where Dr A. KEITH found Podostemon ?algaeformis BTH. in the nineties.
    Repository Name: National Museum of Natural History, Netherlands
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  • 111
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.57
    Publication Date: 2015-04-20
    Description: Glabrous, annual or perennial herbs. Leaves distichous, radical, entire, linear, with a sheath. Inflorescence terminal, spicate or racemose. Flowers bisexual, actinomorphic, small, inconspicuous, mostly green. Perianth segments 6, conchiform. Stamens 6 (or partly reduced), epi-tepalous. Anthers sessile, extrorse, cells 2. Carpels 6, or less by abortion, free or united, or partly free; ovule 1 per cell, basal, erect; style mostly absent. Pericarp dry. Seed exalbuminous, embryo straight. Distr. Cosmopolitan, the majority of the ca 15 spp. known from the S. hemisphere. The Malaysian species is the only one of subg. Cycnogeton (ENDL.) BUCH., distinct by entirely free carpels.
    Repository Name: National Museum of Natural History, Netherlands
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  • 112
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.245
    Publication Date: 2015-04-20
    Description: Erect, ascending, climbing or floating perennials, often robust, stoloniferous or not. Leaves spirally arranged or bifarious, subsessile or distinctly stalked, ovatelanceolate or oblong-lanceolate-linear, with or without a spirally coiled, tendril-like apex; their sheaths embracing the stem, either closed all round or more or less deeply split on the anterior side. Blade closely longitudinally nerved or subpenninerved; nerves connected by numerous short, often oblique transverse veinlets. Flowers arranged in terminal, sessile or peduncled panicles, sessile, actinomorphic, ♀ or unisexual, rather small. Perianth hypogynous, calycine or corolline. Tepals 6, 2-seriately imbricate, free or shortly connate, persistent. Stamens in ♀ and ♂ 6, free; anthers basifixed, 2-celled; cells bursting by an introrse longitudinal slit. Ovary in ♀ and ♀ superior, sessile, 3-celled; cells with a solitary ovule in the inner angle; stigmas 3 or one deeply 3-lobed stigma, sessile. Fruit drupaceous, indehiscent. Seeds or kernels 1-3; albumen copious; embryo small. Distr. Genera 3, in the tropics of the Old World, all of them in Malaysia.
    Repository Name: National Museum of Natural History, Netherlands
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  • 113
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.37
    Publication Date: 2015-04-20
    Description: Trailing shrubs or lianas without special organs for climbing, branches rarely flexuose; stem with wide vessels, raphides in the flowering parts; bark often with short linear lengthwise lenticels. Growth in flushes from terminal and axillary buds. Indumentum of stellate or simple hairs. Stipules minute, obsolete, or absent. Leaves simple, scattered, petiolate, serrate or callous-dentate, penninervous, midrib sulcate, veins in cross-bars, veinlets reticulate. Inflor. lateral, often on a common peduncle forked at the apex, cymose, often pseudo-umbellate; bracts 2, at the apex of the peduncle. Flowers mostly white, dioecious (or polygamous), 5(-4)- merous. Sepals distinctly imbricate (rarely valvate), free or subconnate at the base, persistent. Stamens (10-) ~, in ♀ fls with short filaments and small sterile anthers; filaments thin, anthers versatile, base divaricate, attached in the middle, reflexed in bud, dehiscing lengthwise. Disc absent. Ovary free, superior, tomentose (or glabrous), (5-) ~-celled; ovules attached on the central axis. Styles free, (5-) ~, persistent, elongating after flowering in ♀, ±clavate, spreading, in ♂ ovary small, with minute styles. Berry glabrous (or hairy), often spotted by lenticels, oblong. Seeds ~, small, biconvex, oblong, immersed in pulp; testa cartilagineous, reticulate-pitted, dark when dry; albumen copious; integuments 1; embryo cylindrical straight, cotyledons short. Distr. Ca 30 spp. from W. Malaysia & Himalaya to Sachalin, Japan and Formosa, centering in China and Japan.
    Repository Name: National Museum of Natural History, Netherlands
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  • 114
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.210
    Publication Date: 2015-04-20
    Description: Perennial or annual herbs, tufted or with an erect or creeping rhizome. Stems mostly leafy only at the base but sometimes also in the higher parts. Leaves spirally arranged, cylindric to flat and grass-like, mostly linear or filiform, sheathing at the base or entirely reduced to a sheath; sheaths open or closed, sometimes ciliate at the top. Flowers mostly proterogynous and anemophilous, solitary or in anthelas, panicles, corymbs or heads, usually small, actinomorphic, ♀ or (♂) (♀).Tepals 6, free, in two whorls, rarely only 3, glumaceous or coriaceous, rarely white. Stamens 3-6, when 3 opposite the outer tepals; filaments thin; anthers basifixed, introrse; cells opening longitudinally; pollen in tetrads. Ovary superior, 1-celled or divided by 3 septa into 3 cells; style short to long; stigmas 3, papillose; ovules 3, inserted at the base of the ovary or numerous and biseriate on 3 parietal placentas. Fruit a dry, 1- or 3-celled capsule, loculicidally 3-valved. Seeds sometimes tailed; embryo in the middle or at the base of the endosperm, small. Distr. Genera 8, with 250-300 species, especially in the temperate and cold regions of both hemispheres; in the tropics restricted to the mountainous districts.
    Repository Name: National Museum of Natural History, Netherlands
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  • 115
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.226
    Publication Date: 2015-04-20
    Description: Shrubs or small trees, usually spiny. Leaves opposite, alternate or fascicled, exstipulate, simple, entire, penninerved, small. Flowers terminal and subterminal, sessile or nearly so, rather large, ♀, actinomorphic. Calyx thickly coriaceous, coloured, gamophyllous; tube campanulate-urceolate, adnate to the ovary and produced above it, inside with an annular thickening; segments 5-9, valvate in bud, ovate-triangular, acute, persistent. Petals the same number as calyx-lobes and alternating with them, imbricate and strongly crumpled in bud, obovate, deciduous. Stamens very numerous, inserted on the annular thickening of the calyx, deciduous; filaments incurved in bud, filiform, free; anthers dorsifixed, 2-celled; cells bursting longitudinally. Ovary entirely inferior or free at the top; cells several in 2-3 superposed rows, exceptionally 1-seriate; ovules numerous; those of the lower cells axile, of the upper parietal; style 1, robust, with a thickened base; stigma capitate. Berry large, subglobose, crowned by the unaltered calyx-segments, thick-walled, finally bursting irregularly, entirely filled up by the seeds. Seeds very numerous; outer layer of testa thick, fleshy-juicy; inner layer horny; endosperm none; cotyledons convolute. Distr. Two spp. viz P. protopunica BALF. f. confined to Socotra, and P. granatum L., a plant of very ancient cultivation in S. Europe, N. Africa, the Orient, tropical Asia, Malaysia, and China. Also introduced in the New World.
    Repository Name: National Museum of Natural History, Netherlands
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  • 116
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.11
    Publication Date: 2015-04-20
    Description: Perennial lactiferous freshwater herbs, rhizome short tuberous with fibrous roots. Leaves radical, submerged or floating, base sheathing, oblong to linear, entire or crisped, often long-petiolate; nerves lengthwise parallel, connected by numerous oblique transverse veins. Spike emerging from the water, simple or 2-8-forked, without bracts, subtended by a mostly caducous basal sheath (spathe). Flowers bisexual (rarely by abortion unisexual), small, spicate-scapose, white, rose, purple, yellow or yellowish-green. Perianth segments 2 (1-3, or absent), equal or unequal, usually persistent. Stamens in 2 rows, 6 (or more), free, hypogynous, persistent; filament filiform; anthers extrorse, small, 2-celled. Pollen subglobose or ellipsoid. Gynaecium superior, apocarpous; carpels 3-6, sessile, each with a simple style. Ovules 1-8 (or more), anatropous. Mature carpels inflated, opening along the back. Seeds without endosperm; outer testa often loose; embryo straight, elongate. Distr. About 40 spp. described, Africa, Madagascar, Ceylon, SE. Asia, through Malaysia (very rare) to N. Australia, centering in Africa and Madagascar.
    Repository Name: National Museum of Natural History, Netherlands
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  • 117
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.107
    Publication Date: 2015-04-20
    Description: Herbs or undershrubs. Leaves simple. Stipules absent. Flowers bisexual, actinomorphic, often in unilateral inflorescences, or subumbellate. Bracts often sheathing, dry and membranous. Bracteoles 2. Calyx tubular, gamosepalous, often conspicuously ribbed, folded, the membranous folds often hyaline, lobes 5, often scarious. Petals free, but mostly connate at the base, contorted. Disk 0. Stamens 5, epipetalous, and connate with their base. Anthers 2-celled, opening lengthwise. Ovary superior, mostly sessile, often angled, 1-celled with 1 ovule pendulous from a basal funicle; styles 5, free or variously connate; stigma subcapitate. Capsule membranous, mostly included, circumscissile near the thin base, rarely valvate from the base upwards. Seed 1, with or without endosperm, cylindric. Distr. Throughout the world, ca 10 genera.
    Repository Name: National Museum of Natural History, Netherlands
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  • 118
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.290
    Publication Date: 2015-04-20
    Description: Erect, perennial herbs; rootstock horizontal; stem-base (?always) provided with 2 elongated, spindle-shaped, subterranean tubers. Leaves decussate, dentate to pinnatifid, exstipulate, mostly crowded into a basal pseudo-rosette, cauline ones distant, gradually reduced; base decurrent into the petiole; petioles clasping the stem. Panicle terminal, bracteate, branches decussate, forked, cymose, outermost in triads; rachis and branches distinct from the stem by the presence of capitate-glandular hairs. Flowers ♀, articulated on a short pedicel, 5-merous, subactinomorphic. Base of the pedicel sustained by 2 narrow, ciliate, 1-nerved bracts ending in a thickened (?glandular), blunt nerve-tip. Ovary surrounded by 4 conspicuously capitate-glandular, persistent bracts connate at their extreme base and cuspidulate (in fruit hooked) at their apex ( outer epicalyx) and a tubular, 8-ribbed, utricle-shaped, persistent inner epicalyx with a slight constriction at its apex below a minute, crenulate or toothed limb. Calyx minute, epigynous, 5-lobed. Corolla epigynous, gamophyllous, white, pink or red, caducous; tube funnel-shaped; lobes 5, equal, rounded, erect, imbricate in bud. Stamens 4, equal, alternating with the lobes; filaments free towards the apex of the tube; anthers intrors, dorsifixed. Style 1, terete, stigma capitate. Ovary 1-celled, narrow. Ovule 1, pendulous from the apex of the cell to halfway the ovary. Fruit 1-seeded, thin-walled, surrounded by the inner epicalyx, and this in turn by the hardened, 4-lobed, capitate-glandular outer epicalyx, the tips of which are hooked; fruit with epicalyces breaking off from the top of the pedicel as a diaspore. Seed oblong, subterete, acutish towards both ends, smooth but for two faint, longitudinal ridges; albumen plentiful; embryo scarcely shorter than the seed. Distr. Two spp., from the Sikkim-Himalaya, S. China and Formosa, to E. Malaysia.
    Repository Name: National Museum of Natural History, Netherlands
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  • 119
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.49
    Publication Date: 2015-04-20
    Description: Evergreen trees or shrubs. Leaves simple, spirally arranged, sometimes pseudoalternate, margin entire or toothed, mostly with stellate or lepidote indumentum. Stipules O. Flowers bisexual, actinomorphic, axillary or terminal. Calyx tubular more or less adnate to the ovary; lobes if present valvate. Corolla rarely of free petals, mostly united in a basal tube, 4-7, valvate or imbricate. Stamens equal and alternate, or double the number of the petals, mostly adnate to the tube. Disk absent; anthers 2-celled, introrse, splitting lengthwise. Ovary superior, rarely semiinferior, 3—5-celled. Style 1; stigma punctiform to 3—5-lobed. Ovules l-~ in each cell, axile. Fruit capsular (rarely drupaceous) 1—~-seeded, dehiscent or not, pericarp often thick and woody or corky, with a persistent calyx. Seeds with copious endosperm and straight or slightly curved embryo. Distr. Ca 12 genera mostly in the N. hemisphere, absent in Australia and the Central Pacific, richly developed in E. Asia. No Styracacea has yet been found in the Philippines proper, Central & East Java, and the Lesser Sunda Isl.. Sumatra is the richest centre in Malaysia.
    Repository Name: National Museum of Natural History, Netherlands
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  • 120
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.253
    Publication Date: 2015-04-20
    Description: Perennial herbs, with a short, often strong-smelling rootstock. Lowest leaves in a basal rosette, higher ones decussate, simple, odd-pinnate or deeply pinnatifid, exstipulate but those of one pair often connected by a raised line, radical ones often long-petioled. Flowers small, ♀ or unisexual, bracteate, sessile, cymose; cymes united into an often large, terminal panicle or corymb. Bracts small, opposite, persistent, oblong or linear, on the ultimate branchlets of the inflorescence only one bract of each pair flowerbearing. Calyx small, persistent; limb during anthesis short, inrolled, deeply divided into 10 or more segments, these in fruit unrolling, much accrescent, finally widely patent, plumose, pappuslike. Corolla gamopetalous, caducous after anthesis, small; tube funnel-shaped, much widened above the very short, narrow basal part, unequalsided; lobes 5, patent, oblong, imbricate in bud. Stamens 3, inserted about halfway down on the corolla-tube, alternating with the lobes, exserted or not; filaments thin; anthers small, versatile, 2-celled, ovalsuborbicular, or sub-biglobose, cells opening lengthwise. Ovary inferior, 3- celled, only one cell perfect, 1-ovuled, the two others barren or imperfect; ovule pendulous. Style thin, filiform, shortly 3-lobed or subentire, glabrous, exserted or not. Fruit small, dry, indehiscent, 1-seeded, ovate-oblong, much compressed, with 3 dorsal, 1 ventral, and 2 marginal ribs, 1-celled, the two barren or imperfect cells either enlarged or reduced to narrow ridges. Seed pendulous; albumen absent or scanty. Distr. Very many spp. centering in Andine Chile, the others nearly all on the N. hemisphere, scarce in the mountainous districts of the tropics, absent from Australia, in Malaysia only known from Central Sumatra and Java.
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  • 121
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    In:  Blumea. Supplement (0373-4293) vol.3 (1946) nr.1 p.71
    Publication Date: 2015-03-06
    Description: In the following account the author of the present paper has endeavoured to compile all available information regarding this interesting member of the Gramineae-Zoysieae. As the genus under consideration has in many cases been incorrectly described, it appeared highly desirable to amend the faults and inaccuracies committed by both the original author of the genus and various subsequent taxonomists. The results of these investigations are being put forward in the following pages.
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  • 122
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    In:  Blumea. Supplement (0373-4293) vol.3 (1946) nr.1 p.56
    Publication Date: 2015-03-06
    Description: In this paper two grasses from New Guinea are described as new species. One of these is proposed as the type of a new genus, the other is referred to a hitherto supposed monotypic genus which is suggested as the type of a new tribe. Ancistragrostis S. T. Blake; genus novum, e tribu Agrostidearum, affine Deyeuxiae Beauv., sed glumis atque lemmate induratis, lemmate quam glumis conspicue longiore ejus arista robusta uncinata distinguendum.
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  • 123
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    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.6 (1947) nr.1 p.310
    Publication Date: 2015-03-06
    Description: The “Notes on the Flora of Java” I and II published in Bull. Jard. hot. Buitenz., Sér. III, Vol. XVI², 107—110 (1939) and in Blumea V, No. 3, 490—525 (1945). Next to these the present paper has two other precursors published under different titles but serving entirely the same purpose, which exists in the publishing of all the observations (including new species and nomenclatorial changes) made during the preparation of a Flora of Java under the direction of Dr C. A. Backer (see introduction to Notes II).
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  • 124
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    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.5 (1945) nr.3 p.554
    Publication Date: 2015-03-06
    Description: The following notes are mainly based upon a small but interesting collection of plants, made in 1937—1939 by Mr C. Monod de Froideville, Civil Service Officer in the Netherlands Indies, during his extensive trips in the southern and central parts of the island of Celebes. His hobby was the study of Leguminosae and about half of his collection consists of representatives of that natural order. For several reasons, however, they have been left out of the present paper, for one thing since Mr Monod is intending to deal with them later on himself, a task, which circumstances unfortunately prevent him from accomplishing at present; and secondly since they promise geographically less important results than most other families, many of them being anthropochorous. However, beside Leguminosae, Mr Monod collected a good many other plants and though some of his material was necessarily scanty on account of the fact that the proper purpose of his trips lay outside purely botanical observations, it contains enough remarkable specimens, especially from the practically unknown interior of Central Celebes (Mt. Mamboeliling), to justify a record of them. Mr Monod has proved to be a keen observer and a thorough amateur botanist and geologist. Several of the specimens had been provisorily checked by Dr C. G. G. J. van Steenis, Buitenzorg, which was a great help in their final identification. Regarding this, it was my good fortune to win the help of several specialists in identifying specimens belonging to families falling within the scope of their special study. Thus I am indebted to the following investigators for their kind collaboration: Miss Dr G. J. H. Amshoff (Utrecht): Urticaceae. Dr R. C. Bakhuizen van den Brink (Leiden) : Melastomataceae. Dr C. E. B. Bremekamp (Bilthoven) : Acanthaceae, Rubiaceae. Dr J. Th. Henrard (Leiden) : Graminead. Dr F. P. Jonker (Utrecht) : Burmanniaceae. Miss Dr J. Th. Koster (Leiden) : Compositae. Dr S. J. van Ooststroom (Leiden)': Convolvulaceae, Violaceae. Dr J. J. Smith (Oegstgeest) : Orchidaceae. Dr H. Uittien † (Deventer) : Cyperaceae.
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  • 125
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    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.6 (1947) nr.1 p.274
    Publication Date: 2015-03-06
    Description: When studying the marine species of the genus Cladophora in the Netherlands, I had the disposal of the material of the National Herbarium at Leiden, the herbaria of the Universities of Amsterdam, Groningen and Utrecht and those of the “Zoölogisch Station” at Den Helder and the “Koninklijke Nederlandse Botanische Vereniging” at Leiden. It is a pleasure to me to express my best thanks to the directors of the Institutes mentioned above, for putting the material at my disposal, and to Miss Dr J. Th. Koster, who gave me much valuable help. Especially the material of the National Herbarium at Leiden was very interesting to me, since it contains the herbaria of Kützing, Hauck, and very many reliable exsiccata, so it was possible to compare some Dutch species with the original specimens.
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  • 126
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    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.5 (1945) nr.3 p.692
    Publication Date: 2015-03-06
    Description: Planta parva. Caules erecti, tenues, basi tantum ramosi, basi radicantes, c. 23 cm longi, inferne vaginati, superne 3—4-foliati. Folia erecto-patentia, lanceolata, acuminata, acutissima, basi acuta, nervis 5 majoribus sicco subtus et etiam supra prominentibus pluribusque tenuibus, sicco membranacea, ad c. 8—12 cm longa, 1.85—2.2 cm lata, ultimum multo angustius; vagina elongata, tubulosa, prominenter nervosa. Inflorescentia terminalis, erecta, simplex, densissime multiflora, quaquaversa, pedunculo c. 3 cm longo, inferne vagina folii ultimi incluso, superne vaginula lineari c. 3 cm longa donato, rachide c. 1.2 cm longa. Bracteae valde approximatae, patentissimae vel subpatentissimae, e basi triangula longe subulato-lineari-acuminatae, 5-nerviae, ad c. 0.7 cm longae, basi dilatata fere 0.3 cm longa 0.25 cm lata, superiores minores. Flores patentes, non resupinati, c. 0.75 cm longi, sepalis petalisque divergentibus. Sepalum dorsale cum ovario angulum obtusum faciens, incurvulum, oblongum, apicem versus angustatum, obtusum, concavum, parte inferiore dorso parce patentissime puberulum, 3-nervium, c. 0.65 cm longum, 0.225 cm latum. Sepala lateralia marginibus anticis c. 1/3 longitudinis connata atque rotundato-saccata, divergentia, 2/5 partibus superioribus recurvula, oblique oblonga, subsigmoidea, apice angustata, acutiuscula, valde concava, dorso nonnullis pilis brevibus inspersa, 3-nervia, costa media dorso incrassata, c. 0.64 cm longa, 0.2 cm lata. Petala oblique elliptica, subfalcatula, obtiuscula, canaliculato-concava, 3-nervia, costa media dorso valde incrassata inter sepala prominente et pilis raris inspersa, c. 0.6 cm longa, 0.25 cm lata. Labellum cum ovario angulum obtusum faeiens, gynostemio parallelum, valde concavum, 2/5 partibus superioribus valde recurvum, apice incurvulum, subtus alte sulcatum, intus valde 3-costatum, costa intermedia in 1/3 supra basin terminante, costis exterioribus intramarginalibus in bene 2/3 supra basin arcuato-incurvis et terminantibus, inexplanatum c. 0.475 cm longum, explanatum ambitu quinquangulari-ovatum, infra medium utrinque leviter obtusangule dilatatum, apice in laminam triangulam obtusam crenulatam contractum, 3-nervium, totum fere 0.6 cm longum, fere 0.4 cm latum, lamina 0.15 cm longa, 0.175 cm lata. Gynostemium cum ovario angulum obtusum faciens, rectum, apicem versus paulum incrassatum, dorso convexum, c. 0.375 cm longum, clinandrio concavo, subquadrangulo cum costa longitudinali. Anthera conspicua, cucullata, cordata, acuta, lobulis basilaribus brevissimis rotundatis, connectivo convexo-costiformi, fere 0.25 cm longa. Pollinia 2, clavata, sulcata, cum stipite longo lineari et glandula parva oblonga fere 0.3 cm longa. Rostellum porrectum, e basi lata acuminatum, acute bidentatum. Stigma margine inferiore semirotundatum productumque. Ovarium 6-sulcatum, pilis raris brevibus inspersum, c. 0.45 cm longum. Soemba: In the eastern part, Maoemaroe, in forest. (Iboet n. 425, 7 May 1925; “flowers white”).
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  • 127
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    In:  Studies on the Fauna of Curaçao and other Caribbean Islands (0166-5189) vol.3 (1948) nr.1 p.1
    Publication Date: 2014-10-27
    Description: The material on which the present paper is based was collected in fresh- and brackish-water habitats on the islands of the Leeward Group, West Indies, in 1936 and 1937. For completeness sake specimens from brackish water and from some isolated salt-water habitats — already studied by the author (K. STEPHENSEN, 1933a and 1933b) — were included. It seems highly probable that the greater part of the species treated below are also represented in the litoral fauna of the open sea. The occurrence of the species on the various islands may be summarized as follows (see also Table 1.)
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  • 128
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    In:  Studies on the Fauna of Curaçao and other Caribbean Islands (0166-5189) vol.3 (1948) nr.1 p.78
    Publication Date: 2014-10-27
    Description: The smaller islands of the Caribbean Sea support relatively few species of ants. Even in the largest island in the West Indies, Cuba, there were in 1934 only about 90 forms (species, subspecies and „varieties”) known and this number has not been greatly increased since. During the 1930’s there were recorded in the entire West Indies some 450 forms and at the present time the number can hardly much exceed 500. By way of comparison, the most recent enumeration of ants of the United States (1947) shows 742 kinds. The larger proportion of these West Indian ants occur on such islands as Hispaniola which offer varied and stable habitats. The small islands have relatively few species and these are in the large part common tropicopolitan forms which tend to drive out the endemic species. Few endemic species appear to remain in the Lesser Antilles, for example. Although dr HUMMELINCK told me he was not trying to gather representative material — especially on the islands of Curaçao, Aruba and Bonaire, in which collecting has been done in 1930 by dr H. J. MACGILLAVRY and the late dr L. W. J. VERMUNT — the present collection is of particular interest since it was made on many small islands whose ant fauna was hitherto completely unknown. A few records from the adjacent mainland and some other localities are also included (see Table 7). The value of the Caribbean records is enhanced by the fact that ant populations on small islands may tend to vary from time to time or to be replaced by populations of other species, not to speak of the possibility of speciation itself taking place in geographically isolated places. They also record the presence of specific cosmopolitan „vagrants” on specific islands and some of these ants are still spreading.
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  • 129
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    In:  Flora Malesiana Bulletin (0071-5778) vol.5 (1949) nr.1 p.124
    Publication Date: 2015-06-05
    Description: Father G. Peekel died Febr. 19, 1949, in the Bismarck Arch. He is known as a plant collector since 1908 when he was stationed in the Bismarck Archipelago. In this Bulletin (p. 44) the rescue of his MS. Flora of the Bismarcks was announced. Many of his specimens formed the subject of contributions to Malaysian phytography (cf. ”Beiträge zur Flora Papuasiens” in Engler’s Bot. Jahrb. since 1912, and ”Plantae Peekelianae” by L. DIELS). Peekeliodendron SLEUMER, and numerous plant species commemorate his name. Prof. Dr R. Kanehira died at Tokyo on November 27th, 1948. During the Japanese occupation of Java he was Head of the Herbarium and of the Library (”Bibliotheca”) at Buitenzorg. See also under ”Miscellaneous”.
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  • 130
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    In:  Flora Malesiana Bulletin (0071-5778) vol.5 (1949) nr.1 p.128
    Publication Date: 2015-06-05
    Description: Prospects for an Indonesian Agar-agar Industry. – An Indonesian agar-agar industry seems possible. Seaweeds containing a sufficient percentage of agar-agar to make them eligible for industrial purposes, are found in suitable quantities in Indonesian waters. Dr J. S. Zaneveld, the recently arrived algologist of the Buitenzorg Herbarium (cf. p. 85), is at present at Batavia occupied in collecting scientific and practical data in view of a future industrial development of these natural resources. Dr Ch.J. Bernard, is Chairman of the new established Union Internationale pour la Protection de la Nature residing at Brussels, Rue Montoyer, 42. We are sure that the fast disappearing autochthonous fauna and vegetation of Indonesia will receive all possible attention.
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  • 131
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    In:  Flora Malesiana Bulletin (0071-5778) vol.5 (1949) nr.1 p.126
    Publication Date: 2015-06-05
    Description: Dr C.A. Backer finished the MS on the Amaranthaceae for the Flora Malesiana; he started work on the Chenopodiaceae, Aizoaceae and other families. Mr R.D. Hoogland, Leyden, finished the revision of Malaysian Tetracera, Acrotrema, Didesmandra and Hibbertia. He will soon start to work on Wormia and Dillenia.
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  • 132
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    In:  Flora Malesiana Bulletin (0071-5778) vol.2 (1947) nr.1 p.52
    Publication Date: 2015-06-05
    Description: Blake, S.T.: The Cyperaceae collected in New Guinea by L.J. Brass II (Journ. Arn. Arbor. 28 (1947) 207-229, 1 fig. 2 pl.). Deals with the genera Hypolytrum, Thoracostachyum, Paramapania, Mapania, Lepironia, Cyperus, Eleocharis, Bulbostylis, Fuirena, Lipocarpha. Two new species of Cyperus, 1 of Mapania and 1 of Paramapania are described. Bremekamp, C.E.B.: A monograph of the genus Acranthera Arn. ex Meisn. (Rub.) (Journ. Arnold Arb. 28 (1947) 261-308). The genus is known from Ceylon and SE Asia to W Malaysia. It is subdivided into 9 subgenera; 35 spp. are recognized of which 14 are new to science. Psilobium Jack and Gonyanera Korth. are reduced.
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  • 133
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    In:  Flora Malesiana Bulletin (0071-5778) vol.4 (1948) nr.1 p.84
    Publication Date: 2015-06-05
    Description: H.M. The Queen of the Netherlands has made Dr E.D. Merrill, Arnold Professor of Botany at Harvard University, an Officer in the Order of Oranje and Nassau, with which honour we congratulate both Dr Merrill and Malaysian botany. Dr A.C. Smith of the Arnold Arboretum has been appointed ass. curator of the U.S. National Herbarium, Smithsonian Institution, Washington, DC.
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  • 134
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    In:  Flora Malesiana Bulletin (0071-5778) vol.3 (1948) nr.1 p.69
    Publication Date: 2015-04-20
    Description: Blume, C.L. Museum Botanicum. 2 volumes. The dates given by BLUME for each separate part of volume 1 (1849-1851) seem always to have been considered to be correct. However, those of the 2nd volume are partly wrong: the preface is dated 1852, and may have been printed at that time, but the book was then not distributed. Each part consists of 16 pages.
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  • 135
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    In:  Flora Malesiana Bulletin (0071-5778) vol.3 (1948) nr.1 p.57
    Publication Date: 2015-06-05
    Description: Dr H.C.D. de Wit started a revision of Malaysian Bauhinia, this being part of his work on the Caesalpiniaceae of Malaysia; he is working in the Eijksherbarium, Leyden, Holland. Mr R.A. Blakelock, is revising the genus Evonymus at the Roy. Bot. Gardens, Kew-Surrey.
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  • 136
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    In:  Flora Malesiana Bulletin (0071-5778) vol.4 (1948) nr.1 p.94
    Publication Date: 2015-04-20
    Description: As noted in Dr L.G.M. Baas Becking’s Postscript to Mr van Bemmel’s article in Chronica Naturae Vol. 104, part 4, the new systematics has not been entirely neglected by botanists. I would like to put a further botanical vieuwpoint on this subject. Firstly, I suggest that there is no sharp distinction between the old systematics and the new; secondly, I would emphasize that systematics of the primary descriptive type are an essential basis for the new systematics, and that we are still a long way from completeness in our primary systematic study of Malaysian plants. Systematics of the primary descriptive type need not be out of touch with modern scientific thought. The field botanist in the tropics cannot regard the subject of his study as dead material. But his first job is to classify his material so that others may have an intelligible guide to it. And he cannot classify it without some recognized code of procedure and of nomenclature. It is true that in the past the choice of the correct name for a taxonomic group has too often occupied ”the central position of systematic work”. But to a botanist with a modern scientific outlook, the search for the correct name is merely the last step in a study, a step necessary in order to correlate his work with what has gone before.
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  • 137
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    In:  Flora Malesiana Bulletin (0071-5778) vol.3 (1948) nr.1 p.72
    Publication Date: 2015-06-05
    Description: Though the list of nomina generica conservanda must be kept as small as possible, both the spirit of the rules and wish of all taxonomists is to aim at stabilizing nomenclature. In general the number of new combinations necessary through the digging up of an old name or the discovery of the identity of a mis-identified plant will be decisive. If the number of new combinations towards the one or the other side are nearly equal, the generic name which has been in current use will generally be favoured. If no new combinations are necessary, the current use only will be regarded as the reasonable decision.
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  • 138
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    In:  Flora Malesiana Bulletin (0071-5778) vol.3 (1948) nr.1 p.75
    Publication Date: 2015-06-05
    Description: Aide, F., A. Gaoili & R.J. Cochico: Jatropha curcas L. (tuba) as a source of natural dye. (Philip. J. Sc. 77 (1947) 55-60). Anonymus: Bosbouw op Ceram. (Forestry in Ceram Island, Moluccas). (Econ. Weekblad v. Ned. Ind. 1947, no. 14).
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  • 139
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    In:  Flora Malesiana Bulletin (0071-5778) vol.4 (1948) nr.1 p.99
    Publication Date: 2015-06-05
    Description: In the past half century much efforts have been made to establish the exact publication dates of several important books, serials, and other issues. An admirable attempt towards assembling these data is the ”Journal of the Society for the Bibliography of Natural History” of which 13 parts have appeared (1936-43). A disadvantage of this journal to the botanist is that it has many pages devoted to zoological publications. Besides, it is exceedingly expensive. Many data are found in the Journal of Botany, the Kew Bulletin and the Journal of the Arnold Arboretum mainly composed by Barnhart, Britten, Fernald, Jackson, Marshall, Merrill, Kuntze, Sherborn, Sprague, Stearn, Wiltshear, Woodward.
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  • 140
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    In:  Flora Malesiana Bulletin (0071-5778) vol.5 (1949) nr.1 p.135
    Publication Date: 2015-04-20
    Description: One of the causes of instability in botanical nomenclature is found in that our predecessors did not verify the nomenclatural bearing of an unknown number of (often very rare) works. In PENNANT’s 4-volume ”Outlines of the Globe” (1800), a standard geographical work at its time (1) a chapter was found recently devoted to a ”Flora Indica”. The compiler had unintentionally made some name changes which remained unrecorded in scientific botany. Not long ago ROTHMALER unearthed many such works (2). It must be realized that, quite probably, many other works will be detected necessitating future unexpected and undesirable name changes. Our proposal is to exclude, onwards of 1951, for botanical nomenclature, all works which, up till that date, have not been used for purposes of priority. In other words, to declare these to be ”nomenclaturally extinct”.
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  • 141
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.591
    Publication Date: 2015-04-20
    Description: It seemed useful to correct some errors which have crept into the text of volume 4 as well as to add some additional data which came to our knowledge and are worth recording. Valuable help in general was rendered by Dr R. C. BAKHUIZEN VAN DEN BRINK Jr, for additions to the Burmanniaceae by Dr F. P. JONKER, for Chenopodiaceae by Dr C. A. BACKER, for Viburnum by Mr J. H. KERN, for Xyris by Dr P. VAN ROYEN, and for a grass by Dr P. JANSEN. Printing errors have only been corrected if they may give rise to confusion. The page numbers a and b denote respectively the left and right column.
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  • 142
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.203
    Publication Date: 2015-04-20
    Description: Annual herbs. Leaves stipulate, opposite or verticillate, simple. Flowers axillary, solitary, glomerate or fascicled, actinomorphic, ♀, small or minute; sepals 2-5, free or shortly connate, imbricate in bud, pellucid or with pellucid margins, 1-nerved or nerveless, persistent. Petals the same number as sepals, not or slightly surpassing them, imbricate in bud, free, membranous, persistent. Disk absent. Stamens as many as petals (and alternating with them) or more, but not more than twice their number, persistent; anthers dorsifixed, small, 2-celled; cells bursting longitudinally. Ovary superior, 2—5-celled, isomerous (except in Bergia trimera); cells ~-ovuled. Ovules in the inner angles of the cells. Styles equal in number to the cells, free, short, persistent. Capsule small, septicidally dehiscent. Seeds many, minute, oblong, straight or curved, in transverse section terete; embryo straight or curved; cotyledons short; no endosperm. Distr. Genera 2, in the temperate and tropical zones of both hemispheres, both of them in Malaysia.
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  • 143
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.216
    Publication Date: 2015-04-20
    Description: Annual or perennial herbs, often strongly smelling, frequently clothed with glandular or mucigenous hairs (the latter consisting of a very shortly stalked 4-lobed knob becoming slimy when wetted). Leaves opposite or the upper spirally arranged, exstipulate, petioled, simple or the lower 3-partite or palmately 3-foliolate. Flowers ♀, either solitary in leaf-axils (often between 2 glands), or in terminal racemes, nodding, zygomorphic. Calyx deeply 5-partite. Corolla much exceeding the calyx, gamopetalous, mostly very oblique; tube widened upwards; lobes 5, in bud imbricate, the anterior one much the largest. Stamens inserted near base of corolla, included, either 2 (anterior ones) perfect with 3 staminodes or 4 perfect, didynamous, with or without 1 posticous staminode; anthers free or cohering in pairs. 2-celled; connective often gland-tipped; cells parallel or widely diverging, opening lengthwise. Disk hypogynous, fleshy. Ovary superior, either 1-celled with 2 opposite parietal deeply intruded, T-shaped placentas touching in the middle and consequently spuriously 4-celled, or 2—4-celled and then the cells often halved by a parietal radial spurious dissepiment. Ovule either 1 in each compartment, or numerous and superposed. Style long; stigma 2—4-lamellate. Drupe or capsule; cells 1- of more-seeded. No endosperm; cotyledons flat. Distr. About 60 spp. belonging to 3 genera ( Martyniaceae proper) in the tropics and subtropics of America and to ± 15 in the Old World which, the Australian Josephinia excepted, are confined to or centering in Africa; many genera are monotypic. Some spp. are now ubiquitous weeds having escaped from cultivation. Of the genera treated here only Josephinia is native to Malaysia.
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  • 144
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    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.224
    Publication Date: 2015-04-20
    Description: Much-branched, erect or rambling shrubs, armed with axillary spines. Leaves opposite, often with rudimentary stipules, simple, quite entire. Flowers in axillary or terminal racemes or panicles, or in axillary fascicles, unisexual (monoecious or dioecious) or sometimes partly bisexual, actinomorphic, 4-merous. Calyx campanulate, 4-lobed or 2—4-partite. Petals 4, free, imbricate in bud, oblong or lanceolate. Disk absent. ♂: Stamens 4, alternating with the petals, longer than the corolla, in ♀ reduced to staminodes; filaments slender, free or connate at the base; anthers oval, cells 2, back to back, opening longitudinally; no rudimentary ovary. ♀: Staminodes 4, not exceeding the corolla, anthers barren. Ovary superior, globose, 2-celled or imperfectly 4-celled; ovules 4, erect from the base; style short or almost absent; stigma subsessile, large, deeply bifid. ♀ like ♀, but with 4 perfect stamens. Berry globose; with a thin endocarp. Seeds 1-3, erect, flat, orbicular, exalbuminous; cotyledons cordate, thick; testa coriaceous. Distr. Few spp. in tropical and subtropical Africa and tropical Asia, one extending into West Malaysia.
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  • 145
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    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.233
    Publication Date: 2015-04-20
    Description: Aquatic often rather large perennial herbs with creeping, subterranean stolons. Stem simple or branched, leafy at the base, stiff or flaccid, erect or floating, bearing a terminal spike or panicle. Leaves long, linear from a sheathing base. Flowers (♂♀), crowded in separate globose clusters; lower clusters ♀, in or above the axil of a leafy bract, stalked or sessile; higher clusters ♂, bractless or with a small bract. ♂: Perianth actinomorphic, choriphyllous. Tepals 3(-6), spathulate. Stamens 3(-6); filaments free or connate at the base; anthers basifixed, oblong; pollen globose. ♀: Tepals as in ♂ but larger. Ovary 1, exceptionally 2, sessile with a narrow base, unilocular; ovule 1, pendulous; style 1, usually simple, rarely forked; stigma unilateral, short. Fruits densely crowded, sessile with a narrow base, crowned by the style, indehiscent; exocarp spongy, endocarp hard; testa thin; embryo in the middle of the mealy endosperm. Distr. Temperate and colder regions of the N. hemisphere, crossing the tropics in Malaysia over the mountains towards Australia and New Zealand. About 15 species have been distinguished, in Malaysia only one sp. occurs.
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  • 146
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    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.382
    Publication Date: 2015-04-20
    Description: Dioecious trees (or tall herbs), often lepidote or hairy. Leaves large, simple, entire or dentate, spirally arranged, palminerved (or compound), often asymmetric. Stipules 0. Flowers actinomorphic, valvate, unisexual, rarely polygamous, in elongate, bracteate, caducous spikes or panicles.—♂ Flowers: sepals 4-9, free and very unequal or connate in a lobed tube, isomerous, in ♂ Tetrameles with a few occasionally additional lobules. Petals free, isomerous or 0. Stamens isomerous and episepalous, filaments often long; anthers basifix, intrors or latrors, incurved in bud. Rudimentary ovary present or 0.—♀ Flowers: sepals connate above the ovary or free. Petals and rudimentary stamens 0. Styles isomerous, opposite the calyx lobes, mostly inserted on the margin of the calyx, (2-fid, filiform), club-shaped, or with a capitate stigma. Ovary inferior, 1-celled, with 3-8 parietal, alternisepalous placentas. Ovules ~. Capsule opening at the apex with slits or splitting laterally; pericarp membranous. Seeds ~, very small, ovate or spindleshaped; testa punctate or scrobiculate, outer sheet loosely covering the embryo. Albumen 0. Embryo straight, cylindric. Distr. Three genera with 4 spp., Datisca (herbaceous) with one sp. in Asia and one in W. Central America, Tetrameles and Octomeles both with one Indomalaysian sp..
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  • 147
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    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.141
    Publication Date: 2015-04-20
    Description: Trees, shrubs, lianas or perennial herbs. Leaves spirally arranged, opposite in one species only (Madagascar). Blade simple or, rarely, (only in Acrotrema) to threefold pinnatisect. Stipules absent, but in Acrotrema and a number of species of Dillenia petiole with stipule-like, often wholly or partly caducous wings. Inflorescence cymose or racemose, sometimes reduced to a single flower, terminal or axillary. Flowers ♀♂, actinomorphic to (mainly in the androecium) zygomorphic, hypogynous, mostly yellow or white. Sepals (3-) 4-5 (-20), imbricate, persistent in fruit. Petals (2-) 3-5 (-7), caducous usually within half a day after opening of the flower, imbricate in bud, all equal, apex rounded or emarginate. Stamens ~-3, often partly staminodial, free or partly coherent by their filaments, centrifugal. Anthercells basifix, oblong to linear, opening with an apical pore or a longitudinal slit. Carpels 1-±20, free or connate along the central axis only, with free styles. Ovules ~-1, anatropous, apotropous, on an axile placenta. Fruit dehiscent or indehiscent, in the latter case permanently enclosed by the sepals. Seeds arillate or with a rudimentary aril, with abundant endosperm and a minute, straight embryo. Distr. Ca 10 genera, of which one circumtropical (Tetracera), 3 confined to tropical S. America, one in the Old World tropics from Madagascar to the Fiji Islands (Dillenia), one endemic in Ceylon (Schumacheria), one in S. India, Ceylon, and the Malay Peninsula (Acrotrema, fig. 5), one endemic in Borneo (Didesmandra), one endemic in Australia ( (Pachynema), and one on the southern hemisphere from Madagascar to the Fiji Islands, mainly in Australia (Hibbertia, fig. 3). Many species are relatively limited in distribution, none is distributed throughout Malaysia.
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  • 148
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    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.242
    Publication Date: 2015-04-20
    Description: Perennial, palustrial or aquatic herbs with a creeping rhizome; stems erect, solid, submerged at the base. Leaves biseriate, partly radical or subradical, partly cauline, lower congested, higher remote, elongate-linear, rather thick and spongy, bluntmargined; their sheathing bases excreting slime on their inner side. Flowers very numerous, very closely packed in 2 or less often 3, superposed, contiguous or more or less remote terete unisexual spikes; upper spike male; the 1-2 lower ♀; all spikes at the base with a foliaceous bract which falls off long before anthesis; the ♀ spikes here and there between the flowers often with a similar bract. ♂ Flowers consisting of 3 flat hairs together surrounding 2-5 stamens; anthers basifixed, linear, 2-celled; connective shortly produced; cells back to back, bursting longitudinally; pollengrains free or cohering in tetrads. Rachis of ♀ spathe closely studded with patent cylindrical thickish excrescences; between these excrescences and on their basal part beset with flowers containing a fertile ovary; higher part of the excrescences bearing rudimentary ovaries. ♀ Flowers with or without a very narrow bracteole; bracteole with a more or less broadened, often dentate-acuminate apex either entirely hidden by the flowers or their apex visible externally. Ovary borne by a long very thin stalk (gynophore) which bears long hairs on its base, fusiform, 1- celled; style distinct thin; stigma broadened, unilateral, linear or spathulate. Fruit small, fusiform, or elongate-ovoid, falling off together with its stalk from the pilose axis of the spike, finally bursting by a longitudinal slit; seed pendulous, striate; endosperm mealy; embryo narrow, straight, nearly as long as the seed. Distr. Throughout the world between the arctic circle and lat. 35 S, comprising ± 7 spp., in Malaysia only one very variable species.
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  • 149
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    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.35
    Publication Date: 2015-04-20
    Description: Annual, or perennial herbs with a rhizome. Leaves scattered, entire. Stipules 0 or very small. Racemes terminal. Flowers bisexual, regular, 5-merous, in groups in the axils of bracts. Sepals usually more or less connate, rarely free. Corolla perigynous or almost hypogynous, petals long-clawed, rarely entirely free, usually free at the base, connate in the upper portion of the claws, lobes imbricate spreading. Stamens 5, inserted on the margin of the calyx tube, free, usually unequal (2 shortest), included in the corolla tube. Ovary (2-)3(-5) celled, lobed, each cell with 1 erect ovule. Style with (2-)3(-5) stigmatic lobes, partly sunk in the ovary. Fruit with (2-)3(-5) one-seeded cocci and a columella. Distr. Ca 19 spp. in Australia, 4 in Tasmania, 1 in New Zealand and 1 in Malaysia, Australia and Micronesia (Palau, Jap).
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  • 150
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    Unknown
    In:  Flora Malesiana - Series 1, Spermatophyta (0374-7778) vol.4 (1948) nr.1 p.601
    Publication Date: 2015-04-20
    Description: Suprageneric epiphels have been entered under the family name to which they belong preceded by the indication of their rank (tribes, e.g.). Supraspecific epithets have been entered under the generic name to which they belong preceded by the indication of their rank (sections, series).
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  • 151
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    In:  Blumea. Supplement (0373-4293) vol.3 (1946) nr.1 p.83
    Publication Date: 2015-03-06
    Description: Peculiarities in leaf anatomy support the opinion that the name Triodia R. Br. should be confined to the Australian species. The leaves of species of Plectrachne Henr. are quite different from those of Triraphis mollis, though formerly included in this genus, but are remarkably similar to those of Triodia.
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  • 152
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    In:  Blumea. Supplement (0373-4293) vol.3 (1946) nr.1 p.4
    Publication Date: 2015-03-06
    Description: On October 16th 1946 Dr J. Th. Henrard will have reached the pensionable age of sixty five years. In accordance with the legal prescriptions he is due to take leave officially as keeper of the ”Rijksherbarium“. The present director, Prof. Dr H. J. Lam, invited me to write a short biography of Dr Henrard on this occasion. Having been Henrard’s eldest colleague till 1934 at the institution, I accepted willingly. Jan Theodoor Henrard was born October 16th, 1881 at Maastricht, where his father, J. B. Henrard, was director of the Weight and Measures Office. There is a legend in the family that the Henrards originated from the Vendée (in France) as descendants of a Huguenot-refugee. Owing to this duties J. B. Henrard was often transferred with his family from one locality to the other; his children got their education in different towns of the country. Jan visited the elementary school at Maastricht. The secundary school he followed at Zwolle and Leeuwarden respectively. At Zwolle he made the acquaintance of two well-known Dutch florists, Lako, a teacher at the secundary school and Carmiggelt, an official at his fathers office. From them Jan gathered already an extensive knowledge of the Dutch flora. His final high school certificate he got at Sneek on August 10th, 1901 (Diploma H. B. S.).
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  • 153
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    Unknown
    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.6 (1947) nr.1 p.282
    Publication Date: 2015-03-06
    Description: Some time ago I proposed elsewhere (1) a new system of the Cormophyta. Since the periodical, whose hospitality was my privilege, may not reach many taxonomists who still may be expected to be interested in the proposal, I deem it justified to briefly review the results at which I arrived in the present journal; and this will give me an opportunity to explain one or two points of a nomenclatural nature which, it seems to me, were perhaps somewhat insufficiently elucidated in the paper quoted. As a matter of course, for details as well as for the full argumentation of my views I have to refer to that publication.
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  • 154
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    Unknown
    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.5 (1945) nr.3 p.709
    Publication Date: 2015-03-06
    Description: Neuwiedia (sect. Euneuwiedia) Griffithii Rehb.f. Xenia Orch. II (1874), 215; Rolfe in Journ. Linn. Soc. XXV (1890), 235, 241, t. XLVIII, fig. 2—9; in Orch. Rev. II (1894), 276; IV (1896), 329; Hook. f. Fl. Br. Ind. VI (1890), 176; in Bot. Mag. CXXI (1895), t. 7425; Krzl. Orch. I (1897), 4; Pfitz. in Pflanzenr. IV. 50 (1903), 5; Ridl. in Journ. Linn. Soc. XXXII (1896), 416; Mat. Fl. Mal. Penins. I (1907), 231; Fl. Mal. Penins. IV (1924), 296. Planta in genere parva. Caulis erectus, rigidus, teres, dilute viridis, c. 14 cm longus, 0.63 cm diam., c. 10-folius. Folia erecto-patentia, recurva, lanceolata, sensim longe et acutissime acuminata, basi acuta sensim in petioluin contracta, plicaita, nervis c. 7 subtus prominentibus, nervis tenuioribus alternantibus, papyracea, utrinque nitidule viridia, c. 18.5— 22 cm longa, 4—5 cm lata, summa minora; petiolus latus, canaliculatus, 3-costatus, cum vagina tubulosa antice basi excepta rumpente c. 5.5—6.5 cm longus. Inflorescentia erecta, foliis multo brevior, subdense multiflora, cylindrica, pedunculo hirtello, atroviridi, c. 4 cm longo, nonnullis vaginulis in bracteas vergentibus donato, rachide angulato-cylindrica, patentissime hirtella, atroviridi, c. 6.5 cm longa. Bracteae patentes, incurvulae, e basi ovata sensim longe subulato-acuminatae, anguste obtusae, basi rachidem semiamplectentes, praesertim basi concavae, dorso et margine hirtellae, 3-nerviae, virides, ad c. 1.4 cm longae, superiores minores. Flores quaquaversi, parvuli, patentes, nutantes, sepalis dorso patentissime superne patenter strigillosis petalisque conniventibus, concavis, tenuibus, albis, pallide flavescenti-apiculatis. Sepalum dorsale ellipticum, apiculo tereti strigilloso, valde concavum, totum c. 0.83 cm longum, apiculo 0.05 cm, 0.4 cm latum. Sepala lateralia oblique ovato-elliptiea, apice cucullatoobtusa cum apiculo recto tereti-subulato strigilloso 0.08 cm longo, concava, costa media dorso convexo-incrassata, tota c. 0.87 cm longa, 0.375 cm lata. Petala late elliptico-obovata, obtusa, apice vix cucullata, basi margine antico vix unguiculato-contraeta, concava, costa media dorso valde incrassata strigosaque apice in apiculum brevem producta in praefloratione inter sepala prominente, c. 0.8 cm longa, 0.525 cm lata. Labellum a gynostemio subrectangule patens et recurvulum, supra basin obtusangule incurvum, stigma paululum superans, valde concavum, explanatum cuneato-angulato-obovatum, apice cucullato-obtusissimum, ungue cuneato excepto leviter crispulum et erosulum, basi intus valde convexoincrassatum, costa media dorso valde prominente et strigosa apice in apiculum incurvulum teretem hirtellum producta, fere 0.8 cm longum, mucrone 0.05 cm longo, 0.6 cm latum. Gynostemium totum c. 0.62 cm, usque ad apicem antherarum 0.4 cm longum. Stamina 3, glabra, inferne cum stylo in columnam rotundato-trigonam supra subtusque 2-sulcatum, c. 0.13 cm longam connata, superne divergentia, filamenti dorsalis pars libera a dorso compressa, oblonga, vix flavescenti-alba, c. 0.1 cm longa; filainentorum lateralium pars libera dorsali similis, 0.13 cm longa; antherae conniventes, fere basifixae, introrsae, praesertim dorsalis valde incurvae, cordatae, apicem versus paululum angustatae, late obtusae, lobis basilaribus obtusis, dorso valde convexae cum sulco levi longitudinali, crassae, vix flaveseenti-albae, dorsalis fere c. 2 cm longa, 0.14 cm lata, laterales bene 0.2 cm longae, 0.175 cm latae. Stylus undatus, teres, leviter clavatus, apice (stigmate) obtusus et papillosus, albus, basi dilute. sulphureus, totus c. 0.6 cm, parte libera 0.525 cm longus. Ovarium pedieellatum curvulum, rotundato-trigonum, patentissime strigillosum, pedicello apicem versus incrassato, pallide viridi, c. 0.33 cm longo, ovario trigono-ellipsoideo, viridi, c. 0.4 cm longo, fere 0.3 cm diam., apice in rostrum apice obliquum pallide viride dorso c. 0.275 cm longum contractum.
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  • 155
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    Unknown
    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.6 (1947) nr.1 p.266
    Publication Date: 2015-03-06
    Description: After a paper had been published i.a. on the species of Stevia of the collection mentioned in the heading¹) another Stevia from the same collection came into the author’s hands. It proved to be new. The American genus Stevia has been treated in local revisions by B. L. Robinson (in Gray Herb. Harvard Univ. V, 90, 1930, 36—159; 96, 1931, 28—49; 100, 1932, 20—69). Its floral characters are fairly uniform, but the pappus shows a great diversity. The 5 achenes in a head do not mature at the same time. The genus Stevia seems to have its greatest development in Bolivia, where it is represented by 44 species. The next representation is in Peru with 24 and in Argentina with 23 species. Section Eustevia, Robinson.
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  • 156
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    Unknown
    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.5 (1945) nr.3 p.700
    Publication Date: 2015-03-06
    Description: In Blumea V (1943), 316, I published a list of the Orchidaceae collected by Dr van Steenis in Atjeh. In this list a certain number of specimens were purposely omitted, on account of the fact that flowers had been preserved in alcohol, which material, however, was apparently not extant in Leiden. Under these conditions I have worked up the herbarium so far as possible from the dried specimens only. Peristylus goodyeroides (D. Don) Lndl. Gen. et Sp. Orch. (1835), 299; etc.
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  • 157
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    Unknown
    In:  Blumea - Biodiversity, Evolution and Biogeography of Plants (0006-5196) vol.5 (1945) nr.3 p.689
    Publication Date: 2015-03-06
    Description: 1a. Parasitic plants with filiform, twining stems, leafless or with minute pale scales. Flowers small, in clusters or short racemes; corolla mostly with 5 episepalous fimbriate scales inside ( Cuscuteae Hall, f.) 1. Cuscuta b. Non-parasitic plants with green leaves 2 2a. Pollen spinulose ( Echinoconiae Hall.f.) 18 b. Pollen not spinulose ( Psiloconiae Hall.f.) 3
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  • 158
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    In:  Studies on the Fauna of Curaçao and other Caribbean Islands (0166-5189) vol.3 (1948) nr.1 p.29
    Publication Date: 2014-10-27
    Description: Whilst visiting the Leeward Group, in 1936—1937, I couldn’t help being fascinated by the striking occurrence of representatives of the arachnid order Chelonethida on every island of this arid region which invited me to an investigation of its soil fauna. This first publication of a serial on a group in which so much taxonomical work has still to be done, may be considered as the inevitable aftereffect of these first-sight impressions. My grateful thanks to JOSEPH C. CHAMBERLIN (Forest Grove, Oregon) and C. CLAYTON HOFF (Fort Collins, Colorado) for their interest in my work and to WILLIS J. GERTSCH and E. BROWNING for letting me have the loa.n of some material deposited in The American Museum of Natural History and the British Museum (Natural History).
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  • 159
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    In:  Studies on the Fauna of Curaçao and other Caribbean Islands (0166-5189) vol.3 (1948) nr.1 p.21
    Publication Date: 2014-10-27
    Description: This small paper consists only of an enumeration of the specimens collected by Dr. HUMMELINCK in 1936 and 1937, together with the records of land and fresh water decapods from the articles by RATHBUN (1936) and SCHMITT (1936) on the collections made in 1930. Identifications of many of the brachyuran crabs were made by the late Dr. MARY J. RATHBUN (U.S. National Museum). The senior author is responsible for the identifications of the remainder of the crabs, as well as of the anomurans, while the junior author has determined the caridean species. The material has been deposited in the U.S. National Museum, 'with the exception of the specimens of Coenobita, most of the Gecarcinus, and some of Macrobrachium faustinum, Cardisoma and Uca, which have been presented to the Rijksmuseum van Natuurlijke Historie at Leiden.
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  • 160
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    In:  Leidse Geologische Mededelingen (0075-8639) vol.14 (1949) nr.2 p.1
    Publication Date: 2014-10-27
    Description: In the Bergamasc Alps we have observed one major unconformity between the Basement rock and the overlying Permian. The total absence of any recognisable Palaeozoic sedimentary rocks accentuates this unconformity, and moreover this enormous hiatus makes the dating of any Palaeozoic event impossible. However, by comparison with the Central Alps and Kärnten, we learned that the Asturian orogenitic phase precedes the deposition of the first volcanic sediments. In analogy with the Aar and Gotthard masses we presumed the intrusion of the less metamorphic ortho rocks of the Basement, the granodiorite and the gneiss chiaro, to be of Upper Carboniferous age. The close resemblance of the chemical composition and differentiation of the Permian volcanic rocks and the Upper Carboniferous intrusive rocks induces us to assemble this period of magmatic activity into one period of Permo-Carboniferous age. In long NE—SW striking anticlinal zones these intrusives have penetrated into the old paraschists, causing some contact metamorphism. In the Lugano region where the volcanoes are better preserved and the differentiation of the lavas is more complete, we have seen 1) that the last feature of magmatic activity had been the pressing out of the granophyr, an acid igneous rock, in a very large dome-like structure. The chemical composition of this granophyr is so much like that of the gneiss chiaro or the granites of the Val Rossiga that there can be little doubt that they all belong to the same magmatic source. Also, the intrusive rocks of the Err-Bernina, Lower East-Alpine thrustsheets and their Permian porphyries have a similar chemical composition and must be closely related to our intrusive and volcanic rocks. Hence the whole region of what Later became the Alpine geosyncline was in Permo-Carboniferous time the scene of extensive intrusion and extrusion of igneous rocks. In Permian time the topographical surface was above sea level in the Lugano region where erosion was active and the volcanoes were formed in a mountainous country, but it was mostly covered by shallow water further east. In the later stages of this period considerable tangential forces shaped long anticlines, pressed out the granophyr magma to the surface and formed the very deep central Permian trough and the Camonica uplift of the Bergamasc Alps (see Plate XLIII). Other structural features are indicated, but only these two latter structures, the Camonica uplift and the Permian trough, are clearly visible, and they may be the result of faulting instead of folding. The shape of the Permian trough with its steep flanks and flat bottom would indicate perhaps a fault trough rather than a syncline. This trough is flanked in the NW by the Averara ridge, which, however, is a more pronounced uplift in the Middle Triassic than in the Permian. Whether the Brinzio-Maroggio anticline of the Lugano district, along which the volcanoes are arranged, must also be regarded as a Permo-Carboniferous structure can not he ascertained. Both the Lower Permian (Collio) and the Upper Permian (Verrucano) increase in thickness in eastern direction (compare fig. 16 and 17). In the Lugano region the Verrucano is only preserved in the small outcrops of the San Martino conglomerate at both sides of the Lugano lake. East of the Como lake it has a thickness of less than 50 m, but increases gradually to sonic 800 m in the eastern Bergamasc Alps. The Collio has a similar development of its thickness but is in the west a pure volcanic formation and is first observed round the Valsassina core as a sedimentary rock, further west only irregular patches of volcanic rocks have been deposited. In the East Alpine thrustsheets the Verrucano is generally present but not in great thicknesses, except in the Campo sheet. The Permian in the Lower East Alpine sheets (Bernina sheet) consists of porphyries only. The western limit of the Permian is again observed in the Helvetian thrustsheets, where the most western Axen sheet does not contain any Permian, whilst the more eastern Glarner and Mürtschen sheets contain thick Verrucano masses. The same wedging out of the Permian towards the west is observed along the Tavetscher zone between the Gotthard and Aar massives. The Triassic of the Lombardic Alps is its most interesting and best developped formation. The Werfenian of Lugano consists of a simple coarse sandstone, and the upper dolomitic member is encountered for the first time in the Valsassina. Through the whole Bergamasc Alps the Werfenian is rather sandy but becomes more and more shaly and calcareous towards the east, apparently we pass from a purely continental region in the west to a marine facies in the east. The same tendency was found in the Upper Permian where the Bellerophon horizon of South Tirol sets in above the Verrucano from the Brenta group eastwards. The development of the Middle Triassic as Anisian and Ladinian in distinct facies, in the Bergamasc Alps increasing in thickness in eastern direction, connects with the development of these stages on the Mt. Giorgio, where the Salvatore dolomite is already split in two by the Bituminous Horizon on the boundary between the two stages. The Middle Triassic from Lugano, with its Salvatore dolomite where Anisian and Ladinian can hardly he distinguished, slowly develops in the Bergamasc facies of Ladinian Esino dolomite-limestone and Anisian Gracilisschists and Trinodosus horizon. We have seen that the northerly facies of the Ladinian contains mostly Buchensteiner and Wengener, in the southerly facies the Esino occupies the whole Ladinian. Over the Averara ridge both stages are much thinner and incomplete, and the Anisian increases in thickness towards the Val Camonica, whereas the Ladinian decreases. Here we find also the distinct Wengener splinter shale basin. On the westerly border of the Camonica ridge many facies changes take place. FABER (lit. 21) pointed out that the wedging out of the Collio, the facies change from cavernous dolomite to Elto dolomite of the Upper Werfenian, and the rapid transition from Wengener shales to Esino dolomite all occur on approximately the same line, the one above the other. In Southern Tirol the Middle Triassic has much the same development, the total thickness depending mostly on the presence of thick reef limestone (dolomite), e.g. the Schlern dolomite or Marmolata limestone. One pecularity is, however, very striking in the region between the Pale San Martino and the Adamello and that is the disappearance of the Raibler as a distinct lithological horizon. The merging of Carnian and Ladinian dolomites sets in in the Val Camonica, in the Brenta group only occasionally some Upper Raibler mals are observed and the Raibler appears again north of the Pale San Martino. At the same time the Lower Ladinian facies of Buchensteiner and Wengener is also absent. Elsewhere the Raibler, although very variable, has very much the same shallow water facies, with occasional tuffogenous intercalations. Is is much thinner in the Lugano region. The Upper Triassic and Rhaetic are very different in the regions of Tirol, Bergamasc Alps and Lugano. In the east the two formations are developped as one dolomitic mass, the Dachstein dolomite; in the Bergamasc Alps we find a thick Norian Hauptdolomite and a complete series of well developped Rhaetic series, whereas in the Lugano region the Rhaetic is either absent or represented by the Upper member, the Conchodon dolomite. At the same time the Liassic rests here uncomformably on the Rhaetic or Norian with the typical transgressive Hierlatz facies. The Liassic siliciferous limestones are very much the same from west to east, somewhat thicker in the west, specially in the large complex from the Mt. Generoso to the Como Lake. The comparison of the three regions, Lugano, Bergamasc Alps and South Tirol has been summarized in a tabel. The boundaries between these geographical units are not constant though. The boundary between Tirol and Bergamasc Alps lies during the Norian-Rhetic in the Brenta group and in the Carnian-Ladinian and in the Permian west of Val Camonica. The Collio reappears even in a thick complex east of the Camonica ridge in the Val Trompia. The boundary between the Lugano region and the Bergamasc Alps is even less fixed, it lies somewhere between the Generoso and the Alta Brianza Lecco region, but can not be determined much further as the Liassic limestones cover all the older formations between these two points. The Averara ridge, altough very pronounced in the Permian, Lower and Middle Triassic is not a facies boundary, at both sides the facies is very similar. It has always been known that the Lombardic Trias facies is very much alike that of the East Alpine thrustsheets. Both in the Helvetian and in the Pennine zones of the Alpine sedimentation basin the Triassic is very poorly developped, and can in no way be compared to that of the Southern and Eastern Alps. When we consider the conformity between the Lombardic and eastern Alps facies somewhat closer, we observe a great similarity between the Lugano region and the Lower East Alpine unit. Both have porphyries in the Permian and no Verrucano, in both the boundary between Ladinian and Anisian is very vague. The whole Triassic in the Err-Bernina sheets is much reduced as compared to the Triassic of Campo- and Silvretta thrustsheets. The Rhetic is much completer in the Err-Bernina than in the Lugano region, but both are again characterized by thick siliciferous Lias limestones, which is transgressive with a Hierlatz limestone facies on the Rhetic and Norian in both tectonical units. The Middle East-Alpine thrustsheet, the Camposheet and its accessory units, is characterized in the Münster valley by a thick Verrucano series of some 600 m. with pebbles of quartzporphyry and granite. Porphyry sheets are lacking in this serie. The Triassic of the Camposheet as a whole is much thicker than that of the Lower East-Alpine sheets, but the Anisian is not very thick yet, much less than in the Upper East-Alpine sheets, and the Werfenian is hardly represented. Lugano Bergamasc Alps South Tirol Liassic Siliciferous limestone 100—1000 m. Transgressive Hierlatz facies Siliciferous limestone 500—1000 m. Limestone 300—400 m. Rhetic. Absent, or only Upper member Conchodon dolomite Complete from Alta Brianza to Brenta group 550—800 m. Daehstein dolomite ;' 1000 1400 m Norian Hauptdolomite 250 m. 1200 m. Hauptdolomite Carnian Series of shales, marl, dolomite 100—350 m. Thick series of shales, marl, dolom. and sandstones 250—700 m. Western facies Eastern facies Schlern dolomite porphyries, tufs etc. from Pale S. Martino 150 m shale Sst. dolomite Northern facies Southern facies Northern facies Southern facies Marmolata St. Cassian limestone Wengener Esino limestone Wengener sst. and sh. Buchensteiner chert, limestone 600—1200 Esino dolomite, limestone Wengener, splinter shale facies Ladinian Salvatore dolomite 300—600 m Salvatore dot. Bituminous horizon Mendola dolomite Buchensteiner or Beitzi sch. Anisian Trinodosus hor. 50—150 m. Gracilis Schists from W—E 150—450 m., Nodulous limest. Mendola dolomite Gracilis schists marls, dolom. """"Werfenian 50 m. sandstone Cavernous dolomite 200—450 m. shale, marl, sst. Servino Campiler sch. 250 m. Gastropod, list. Seiser sch. 80 m. Permian absent or porphyries, tufs etc. basal congl. Verrucano from WE 50—800 m. Collio, porph. vole. sst. tufs etc. central Collio shale basin 0—2000 m. Basal conglomerate Bellerophon hor. 0—250 m. Ciavflpnn Sst 100 9.CV\ m (Vermomnn} Bozener porphyries Basal conglomerate (Collio) The Ladinian is present as Wettersteindolomite (250—600m) without the typical Partnach facies of the Upper East-Alpine thrustsheets. The Raibler is some 400 m thick, dolomites, shales, shaly limestones, rauhwacke and gypsum, porphyrites etc. The Norian is very thick, 500—2000m, and developed as typical Hauptdolomite, whereas the Rhetic is present in the facies of the Kössener schists, black and reddish shaly limestones and shales, which can be compared to the Lombardic facies of the Scisti neri. The agreement with our western Bergamasc Alps is striking. Exeptionally thick Norian, Esinodolomite, thin Anisian, and thick Verrucano are the characteristics of the region between the Valsassina and the Val Seriana. The Werfenian is much completer in Lombardia, and the Collio of the central trough is absent in the Camposheet but in general the similarity is not less striking than that of the Err-Bernina sheet with the Lugano-Grigna region. The Averara ridge although not the boundary between the two facies, can possibly be correlated with the geoanticlinal ridge between the Lower and Upper East-Alpine sheets. The Upper East-Alpine thrustsheets, (Lechtal, Silvretta) show a great similarity with the eastern Bergamasc Triassic. The Werfenian has an Upper Rauhwacke member, the Anisian shows the nodulous limestone (Reiflinger Knollenkalk), the Gracilis limestone, the brachiopod limestone etc. in exactly the same facies. The Ladinian is not identical to such a degree as the lower members of the Triassic, but the Arlberg Limestone and dolomite can be very well compared to the Esino limestone and the Partnachschichten to the Wengener shales (splinter-shales!). The Carnian again is very similar, rauhwacke, marls, gypsum, shales and sandstones, black limestones are present in both units. In the Lechtal sheet the Norian Dachstein limestone and the Rhetic Dachstein corraline limestone are only separated by the „Kössenerschichten”, corraline limestone and shales of the Lower Rhetic. The Norian is reduced in comparison with that of the Camposheet. The Carnian of the Ducan region is exeptionally thick, some 900 m, with an upper 300 m of Upper-Carnian dolomites 1). Such development of the southerly part of the Upper East Alpine thrustsheet can already be regarded as a transition to the Camonica facies where nearly the whole 700m thick Raibler is developped as dolomites. Striking as the agreement of the development of the sedimentary sequence in Lombardia and in the east Alpine thrustsheets may be, great differences can also be noted. First of all the Permian of the Bergamasc Alps with its central Permian trough with 1500—2000 m of Lower Permian Carona shales and volcanic rocks can not be found back in the Eastern Alpine thrustsheets. In the second place the typical development of the Lower Ladinian in Buchensteiner and Wengener facies is restricted to the Southern Alps and Tirol. Finally the „Flecken mergel”, (mottled marls), and Allgäuschiefer of the Liassic of the eastern Alpine facies are not represented in Lombardia. On the other hand the abyssal facies of Upper Liassic, Dogger and Malm in Radiolarite and Aptici limestone and marl is present in both stratigraphical units. That great differences exist between two regions, which in their original position in the geosyncline are widely separated although in the same basin, is quite logical. Lombardia is the southwesterly extension of a large basin, of which the East-Alpine thrustsheets occupy the centre and the north easterly end. Moreover the basin must have widened out considerably in NE direction. That the troughs and ridges opened fan-like in this direction from Lombardia follows from the fact that the E—W distance from L. Maggiore to the Val Camonica is less than the combined breadth of the East Alpine thrustsheets. Moreover we must not forget that even in the small width of the Bergamasc Alps already considerable facies change from North to South could be demonstrated, both in the Ladinian and in the Anisian. The main differences are found, as mentioned above, in the Permian and in the Lower Liassic, particularly in the Middle and Upper East-Alpine sheets. The development of the Permian in the Bergamasc Alps is due to late Variscian movements which apparently are not parallel to the Alpine geosyncline, and therefore need not continue in similar facies in the direction of the Alpine geosyncline. The Liassic Allgäuschiefer of the East-Alpine facies can be regarded as a transition between the penninic Bündnerschiefer facies and the Lombardic silieiferous limestone facies. The Cretaceous of the East Alpine basins can in no way be compared to the Lombardic Majolica and Scaglia. This is due to the fact that in Upper Cretaceous time the Alpine orogeny attacked this northern part of the Alpine geosyncline, whereas Lombardia remained mostly undisturbed. The dividing line between the southern and eastern Alps originated with the folding of the East-Alpine sheets, and became accentuated when the Pennine sheets were folded in the Oligocene, and became still more pronounced when the uplift of the central folded system occurred in the post Oligocene Insubric phase. In the tectonical part we have shown that the youngest Tertiary tectonical direction is purely W—E. The Orobic thrustfault and its accessories cut off obliquely the older ENE—WSW structures as for instance the Orobic anticline. This latter direction is mainly pronounced in the anticlinal structures, e.g. the Brinzio-Marroggio anticline, the Orobic anticline, the Cabianca-Trabuchello anticline, and the Cedegolo anticline, but also in some faults as the Clusone and Bondione faults. The great thrustmovements, the Grigna thrustsheets, the thrusting against the Valtorta and the Valcanale faults, further the Timogno and Ardesio thrusts, and the eastern thrusts of the Pzo Camino and the Palline Borno-Lozzio masses is all bound to the E—W strike or the N—S compression. The Insubric line, the boundary between the Southern Alps and the Central Alps, i.e. the division line between Pennine root zone and the Orobic zone, has also a W—E strike from the Lago Maggiore to Dinaro. Therefore also this major tectonical line probably originated only in a later period of the folding process. This conclusion is in complete accordance with the views of the general conception of the Alpine orogeny, which places the origin of the Insubric line in the post Oligocene, older Insubric phase. In this phase the roots of the Pennine thrustsheets were tilted in a vertical position. The Insubric phase, the tilting of the root zones is naturally a time of uplift, the Central Alps rose above their fore- and hinterland. This is also the origin of the several fault steps we could discern in the Bergamasc Alps. In the Younger Insubric phase (Pliocene) when the final compression took place, all the Bergamasc thrustsheets were formed, they were sheared of their substratum from a higher step and pushed over the lower step. The N—S faulting has a intermediate position, it is younger than the old anticlinal folding and older than the final thrust, and is probably connected with the older Insubric phase when the uplifting of the steps occurred. The stratigraphic comparison has made it clear that the southern, the central and the eastern Alpine basins were portions of one geosyncline, separated from another probably by ridges, geanticlines, but still forming together one continuous unit. This connection was ruptured by the first severe Upper-Cretaceous Alpine orogenesis, the origin of the east-Alpine thrustsheets. At that moment an oblique line cut a southern minor portion from the rest. This rupture line later became the Insubric line. By its present position we can still follow its course in the original basin, because the southern Alps are only little changed in aspect compared to the more central parts. West of the Lago Maggiore it followed the ridge dividing the southern basins from the central Pennine ones, then, north of this lake it curves round to an E—W strike thus cutting obliquely through the basin structures. It retains this diagonal coarse untill it had crossed or just reached the very important Camonica geanticline, it then swung back to its original direction parallel to this ridge along the so called Judicaria line. Finally it resumes its E—W strike as the Pusteria line and limites southern Tirol to the North, separating this region from the East Alpine thrustsheets. This early boundary line is not quite identical with the Insubric line, because the latter cuts occasionally with a very sharp angle through the root zones of the Pennine thrustsheets, but the two lines are sufficiently alike to identifie them for our purpose. The remarkable wavy course of the Pusteria-Insubric line is thus due to the fact that the N—S compressional direction necessitated an E—W strike but the existing inhomogenities of the region indicated a NE—SW strike, between those two influences the result alternated. The ENE—WSW anticlinal structures being older than the original Insubric line, belong therefore to a prae-Cretaceous or Cretaceous phase, a phase which also accounts for the totally different facies of the Cretaceous in East-Alpine and Lombardic sedimentary-basins. If this is true some erosion on the crests of the Cretaceous structures may have taken place before the much later, probably Pliocene, finial compression took place. RASSMUS 1) has thoroughly treated the Cretaceous folding phase of the Lombardic Alps. The Scaglia of the foothills, in which unfortunately no fossils of stratigraphic value have been found, belongs probably to the Cenomanian-Turonian and is a typical regressive facies with which the Alpine sedimentary cycle closes. In the thick Santonian gravels, which were deposited in the Po plain, the material is derived from Liassic and Jurassic rocks, but also of Triassic rocks and even of Permian porphyrites. This conglomerate can he regarded as a equivalent of the Gosau Schists of the northern Alps. The folding phase preceding the erosion can be put therefore in one of the subhercynic phases of Stille. Undoubtedly the final thrusting has therefore been preceded by erosion, and we may presume that some of the thrusting has the character of „reliefüberschietrangen” as advocated by AMPFERER 2). In general, however, our thrustsheets are of too small dimensions to allow the determination of the characteristics of this particular way of thrusting. This phenomenon may to a certain extent account for the fact that the Grigna thrustsheets pass over the faulted and folded underground with plane thrustplanes without being affected in the least by these structures. I can not find much evidence in favour of such theory, though, because most of the structural features of the underground are of equally recent datum as the thrusting movement, or only very slightly older. The Valtorta fault for instance is certainly older than the thrusting, both because the thrustplanes pass over the fault and because the Norian and Raibler of the southern limb have been pressed against it. But it is not as old as the Orobic anticline, although it is fairly parallel to this structure, because it certainly belongs to the phase of uplifting of the central Alps, the older Insubric phase, and therefore not to the Cretaceous phase of folding. Still, even between the Older and Younger Insubric phases some erosion may have taken place, that is between the Miocene and the Lower Pliocene, and the height differences along this fault may have been removed to some extent. The same is true for the Clusone fault in connection with the Presolana sheet and the Pilo fault in connection with the Lozio overthrust. Let us summarize the results of our deductions in a short tabel. Extensive denudation removing all palaeozoic sedimentary rocks. Asturian folding followed by extensive intrusion of acid magmas in long stretched NE—SW zones. Permian. Erosion continues in the west. Magmatic intrusion is followed by widespread volcanic action. In the east deposition of large subaquatic volcanic sediments. Saalic compression, origin of central Permian Collio trough, Camonica uplift and extrusion of granophyr, Erosion in the western region continues, in the east deposition of Verrucano conglomerates. Triassic. Continuous sedimentation in the south-east Alpine basin of Triassic rocks. Older Kimmeric phase uplift of the Arzo anticline followed by erosion and transgressive Hierlatz facies in the Lugano-Lower East Alpine region. In the Lugano region the movement started already in the Rhaetic. Sedimentation of Liassic and of abyssal Dogger and Malm and bathyal Lower Cretaceous. Austrian or Subhercynic folding („Juvavische phase” of R. Staub) origin of long ENE—WSW anticlines. Only the first beginnings of the strong Cretaceous orogenesis of the East-Alpine sheets has effected Lombardia, later in this phase the eastern Alps were cut off along a diagonal line partly following the anticlinal ridges and were severely compressed in thrustsheets. The major Pennine (Oligocene) phase of the folding of the Pennine sheets and further compression of the east Alpine sheets did not reach the southern alps. Insubric phases, lste phase. The central Alps were raised to considerable height, the roots were tilted in vertical position and the ,,steps"""" of the Lombardic Alps were formed. Origin of BNE—WSW faults (Valtorta, Clusone, Valcanale faults). N—S striking fault systems (Val Vedra fault trough, Manina fault troughs). Intrusion of Adamello tonalite. 2nd. phase. N"""" to S compression, the lower limbs of the ENB—WSW faults were pressed against the fault, origin of Timogno and Ardesio thrusts. Origin of Tertiary dikes. 3rd. phase. Possibly some erosion. Strong N to S compression. Origin of Orobic thrust and accessory thrusts, (Jrigna thrustsheets, Arera thrust, Palline-Borno and Lozzio oventhrusts and the Presolana and ('amino thrustsheets. Often renewed activity along existing faults (Clusone fault). The age of these Insubric phases can be judged by the fact that the Miocene inolasse has been folded, and that (the horizontal Pliocene has been deposited in fjords eroded in a strongly dissected landscape.
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    In:  Leidse Geologische Mededelingen (0075-8639) vol.14 (1949) nr.2 p.258
    Publication Date: 2014-10-27
    Description: Pollen analytical and geological investigations of the Lower and Middle Pleistocene in the Northern Netherlands. The Pleistocene deposits in the northern part of the Netherlands, form through their extreme thickness up to more than 300 m, a promising object for study from the stratigraphical point of view. The boulder clay of the penultimate glaciation lies in the province of Drente at or near the surface, but in northerly and westerly directions it dips away beneath Upper Pleistocene and Holocene deposits. The Pleistocene deposits below this boulder clay form the subject of the present paper. In the first chapter the existing opinions regarding the stratigraphy are briefly reviewed. Van Cappelle (1888, 1891, 1892a, 1892b) and Lorié (1887a, 1893, 1899) described several borings already in the last century. They found the boulder clay in general to be underlain by a fine grained sand below which a coarse sand occurred, containing many Scandinavian erratics. Both, Lorié and Van Cappelle considered the coarse sands as having been deposited under the simultaneous influence of southern rivers and northern fluvio-glacial streams. Therefore it was assumed that a Scandinavian ice-front was at that time not too far distant. Van Cappelle believed that this ice-front belonged to an older glaciation than that from which the boulder clay originated, since he found in the fine sediments some rare plant remains which indicated a temperate climate. Lorié, however, took the ice-front to be a mere oscillation of the same glaciation which deposited the boulder clay. Later geologists agreed with Lorié (Tesch, 1934, 1937, 1947; Steenhuis, 1939), basing their opinion on a correlation with the central part of the Netherlands, where a coarse zone occurs above the Nede clay representing the Mindel-Riss Interglacial (Florschütz and Jonker, 1942). It is at present generally accepted that these coarse gravel containing sands form one continuous horizon which was deposited during the first cold stage of the Riss glaciation, whereas the boulder clay represents the second cold stage. Hardly anything is known about deeper horizons in the northern Netherlands. According to Tesch and Steenhuis Mindel-Riss Interglacial deposits are lacking; the Mindel Glacial stage is perhaps represented by an other zone of coarse deposits overlying again a series of fine grained sediments. The base of the Pleistocene is formed by marine beds which, in the opinion of Tesch (1934, 1937), comprise in part, the Günz Glacial stage, since the molluscan fauna of the middle part bears a distinctly arctic character. Since the stratigraphy was based on lithological criteria alone it seemed desirable to investigate whether it could be confirmed on palaeontological grounds. For this purpose pollen analysis proved to be the most suitable method, since the sequence of sediments under review is accessible only in borings, which seldom yield macroscopic fossils. In chapter II some technical aspects of the pollen analytical research are discussed. The material available consisted of samples of some rare peat beds, of samples of often thick clay beds and of lumps of clay and peat, which are found sometimes in sand samples. Such lumps probably originate from very thin peat beds, which were not differentiated in the sample as separate layers. This is proved by the similarity between the spectra of these lumps and the spectra of thin beds found in situ in nearby borings (table II and III, p. 272). In general very sandy samples were not analysed. unless they were very humic and nearly sandy peat in appearance (table IV, p. 273). The samples investigated proved to be rich enough in pollen to furnish reliable counts. A number of absolute pollen frequencies of different materials are given in table I (p. 271). All the samples were prepared after the technique introduced by Erdtman (1943). Some spectra indicated pollen of tertiary genera, which became extinct in western Europe at the beginning of the Pleistocene period. These pollens are clearly derived from tertiary deposits, but the same may be the case with other pollen of less diagnostic character. The question thus arises to which extent the pollen content of the strata under study has been derived from older series. The correction technique developed by Iversen (1936), who subtracted the clearly secondary pollen he found in a boulder clay from the spectrum he obtained in the complex overlying it, could not be applied in our case, where the sediments studied unfortunately underly the boulder clay. It might be feasible to correct contaminated spectra by comparing them with pure spectra from nearly the same depth, so that possible climatic differences can be disregarded. Contaminated spectra were found in several thick clay complexes. In these cases intercalations of peat beds which could have yielded uncontaminated material for comparison do not occur. Therefore the amount of contamination could not be estimated and all spectra given are uncorrected. However, we have indicated in the diagrams the amount of typical tertiary pollen (T) and of Hystrix (H), expressed in percentages of the tree pollen. However, four arguments indicate that the amount of reworked pollen in general not great: 1. the low frequency of Hystrix, which proved to be a measure of the impurity in Iversen’s material; 2. the absolute pollen frequencies of the impure spectra as compared with the pure ones; 3. the very small pollen content of the boulder clay; 4. the similarity of pure and impure spectra in corresponding zones of different diagrams. The depth given for each spectrum in the diagrams corresponds with the average depth of top and bottom of the sample (in metres below N. A. P. = high water at Amsterdam). In chapter III the results of the pollen analysis are discussed, whereas in chapter IV a stratigraphical interpretation is attempted after comparing the diagrams. The number of Lower and Middle Pleistocene pollen diagrams from western Europe is still very limited. The most important diagrams are those from Quakenbrück (Wildvang, 1935; Jonas, 1937a) and Ummendorf (Selle, 1941), both from western Germany. The diagrams from Starup and Harreskov, published in the classical paper by Jessen and Milthers (1928), have not been used since it is quite uncertain whether the penultimate interglacial referred to by the authors can be correlated with the Mindel-Riss or the Riss-Warthe Interglacial. Of the borings investigated (for localities compare map, fig 1) Bantega yielded by far the best diagram. This boring has specially been carried out for this purpose and yielded a complete sequence of undisturbed cores. The diagram is found to be in close agreement with those of Quakenbrück and Ummendorf: during the hardwood phase the mixed oak forest reached its maximum at an early date (20.65—20.85m); only afterwards Carpinus and Abies appeared and Picea had a distinct (double) maximum after the climatic optimum of the hardwood phase (18.54 and 17.94 m). There can be no doubt as to the Mindel-Riss Interglacial age of this diagram. The same interglacial epoch can, based on a smaller number of spectra still clearly be recognized in some other diagrams viz. Bergumerheide (41.60—65.0 m), Sneek (24.0—46.0 m), Spannenburg (20.40—88.0 m), Lemsterland (15.58— 54.47 m) and Gasselte (27.80—62.65 m). Furthermore Bergumerheide (7.00 m) and Spannenburg (9.30 m) show a temperate spectrum close below the boulder clay, representing probably the Riss I/II Interstadial stage. Three deeper borings again show beneath the Mindel-Riss Interglacial a number of spectra with a temperate character. In a few of these pollen of Pterocarya occur (Spannenburg, 211.90 to and deeper; Lemsterland 153,40 m). Pterocarya has long been known from the Tegelen clay, but the age of this famous locality has not yet been determined with certainly. Tesch (1934, 1937) and Florschütz (1939) hold the view that it represents the Günz-Mindel Interglacial, but at present some authors consider the Tegelen clay as belonging to the Günz I/II Interstadial. Our palaeontological knowledge of the Lower Pleistocene is still too incomplete to solve the problem. We do not know whether some so-called tertiary relics (for inst. Tsuga, Pterocarya) which occur in the Tegelen clay, range upward into the first interglacial or not. In this respect we may remark that the diagrams from Spannenburg and Lemsterland possess no indications of cold spectra which could he interpreted as Günz II Glacial stage. An equivalent of the Tegelen clay has probably been found at Bergumerheide. Florschütz (1938) mentioned Azolla tegeliensis (155—157 m) which he suggested as a characteristic species of the zone of Tegelen. At Spannenburg another species (A. filiculoides) which is characteristic for the Nede clay (Mindel-Riss Interglacial) has been found between 25 and 40 m. A boring near Dordrecht however, yielded both species from the same bed. Bergumerheide shows between the horizon with A. tegeliensis and the Mindel-Riss Interglacial deposits a third zone with spectra of a temperate climate and without tertiary relics (88.0—125.25 m). This strongly suggests that the zone of Tegelen belongs to the Günz I/II Interstadial and that the abovementioned horizon at Bergumerheide represents the Günz-Mindel Interglacial. Perhaps the spectra between 187.15 and 197.90 m of Spannenburg belong to the same horizon. An entirely different picture is shown by the diagrams of Assen and Winschoten. Pinus predominates throughout the diagrams, but nearly all spectra are contaminated with tertiary pollen and with Hiystrix. As we do not know to which degree the percentages of certain genera are overrated, the diagrams are less valuable. The diagram of Assen is particularly monotonous. Winschoten shows rather high Alnus percentages in the lower part. The same has been observed in a thin peat bed of the boring Zuidbroek (93.17—93.27 m, table V, p. 291), which possesses 2% Tsuga pollen. Since in this case we have no reason to believe that the sample is contaminated, it must be assumed that the entire pollen content is autochthonous and therefore the spectrum probably represents the (Günz I/II Interstadial. The same horizon can perhaps be recognized in the nearby boring at Winschoten. The same picture as at Assen and Winschoten is shown by the diagram of Drouwen and the lower part of Sneek. We shall see later that geological considerations are of assistance in interpreting these profiles. In chapter V further consideration is given to the Middle Pleistocene marine horizon and a new conclusion has been reached regarding the age of this deposit which has a hearing upon the general understanding of the glacial stratigraphy of the northern Netherlands. In two borings the Middle Pleistocene sediments are partly developed in marine facies (Bergumerheide 46.00—62.00 m; Sneek 31.00—42.00 m). The marine deposits lie above a coarse fluviatile series which is generally held to be of early Riss Glacial age. The pollen diagrams prove the marine sediments to be deposited between the mixed oak forest phase and the Picea phase, i. e. in the second half, of the Mindel-Riss Interglacial. The underlying coarse deposits must therefore have been laid down during the first half of the same interglacial. A Mindel-Riss Interglacial transgression is known from England as well as from Germany. In East Anglia the Corton Sands (Baden-Powell and Reid Moir, 1942; Zeuner, 1945) and in N. W. Germany the sediments of the Holstein-See (Grahle, 1938) were deposited during this transgression. The molluscan fauna (Tesch, 1939) proves to be somewhat colder in character than the landflora which is understandable since the sea transgressed from the north and consequently introduced northern species. On the other hand free immigration from the south was possible by land. Reid (1890) has already pointed out that different conclusions may be reached regarding climatic conditions from a comparison of marine and terrestrial organisms. Furthermore several rivers are known to have had their main aggradation phases during interglacial times when the rising sea level decreased their transporting capacity and thus were forced to deposit their load. As Zeuner (1945) stated we have to distinguish between thallassostatic terraces in the lower and climatic terraces in the middle courses. All classic studies of river terraces have been made of climatic terraces with glacial aggradation and interglacial valley formation. The lower courses of two west European rivers have been studied from the eustatic point of view: the Somme (Commont, 1910; De Lamothe, 1918; Breuil and Koslowski, 1931/32) and the Thames (King and Oakley, 1936) and the results are briefly reviewed. It seems that the same conditions which obtained in the lower Somme and the lower Thames were present in the northern part of the Netherlands: the principal factors affecting the behaviour of the rivers were oscillations of the sealevel during glacial and interglacial times, although terraces in the morphological sense did not develop owing to the gradual subsidence of the North Sea basin. Since all relevant deposits are entirely covered by younger sediments we do not yet know where in this country the transition occurs from the type of sedimentation typical for the lower course of the rivers under predominant marine influence to the climatic terraces of their middle course. Three marine transgressions are known to have occurred in the Netherlands Pleistocene: 1° the Eemian, of Riss-Würm Interglacial age which has long been generally recognized; 2° the Middle Pleistocene transgression, the Mindel-Riss Interglacial age of which has now been proved by the pollen diagrams; and 3° the Lower Pleistocene transgression (Icenian), the exact age of which is still unknown. Therefore the question arises whether this oldest transgression might be connected with the first interglacial. This point is discussed in chapter VI. Tesch (1934, 1937) argued that the middle part of the marine Lower Pleistocene represents the Günz Glacial stage on the ground that its molluscan fauna is distinctly arctic in character. Unfortunately the oldest marine deposits occur in only one of the borings investigated (Lemsterland). A few spectra immediately above this horizon show a temperate character. Though the horizon from which the spectra are derived may possibly be separated from the marine deposits by a stratigraphical hiatus, we must consider the possibility that the marine Lower Pleistocene horizon has not been deposited under such cold conditions as would appear from the conclusions of Tesch. The lowermost spectrum shows a small amount of Pterocarya pollen, suggesting, in accordance with our present state of knowledge, a Günz I/II Interstadial age rather than a Günz-Mindel interglacial age. However, if Pterocarya would still prove to have occurred in Günz-Mindel Interglacial time, the marine Lower Pleistocene could be ascribed to a Günz-Mindel Interglacial age. Incidentally, during this epoch, a high sea-level has been observed all over the world. The map (fig. 2) shows the location of all borings of more than 150 m deep, whereas some other important borings have been added in the southern part of the area. The following is an explanation of the figures shown on the map with each boring: if two figures are given the first means the depth to the top of the marine Lower Pleistocene in metres, whilst the second, in brackets, indicates the lowest level reached without penetrating this marine horizon. One figure in brackets indicates the greatest depth reached. In this case no marine Lower Pleistocene or older formations have been met with. A figure preceded by T means that the Tertiary has been reached at this depth without encountering marine Lower Pleistocene. The map shows that the Lower Pleistocene in a marine facies is restricted to the western part of the area. Since the base of the marine beds has nowhere been reached we do not know whether it is transgressive, as it is in the southern Netherlands. Comparing the figures of Zwartsluis, Vollenhove and Lemsterland with that of Spannenburg, there is a striking difference which suggests that the marine horizon has disappeared by erosion in the sub-soil of Spannenburg. The profile of Spannenburg gives no evidence of the relative age of the sediments present as compared with the marine deposits elswhere. It follows from the above that the Pleistocene of the area under investigation is not composed of a number of continuous horizons laid down one upon the other. Up to now it was assumed that coarse sediments represented cold or glacial periods, whereas finer deposits corresponded with wanner and intraglacial phases. However comparing the results of the Spannenburg and Lemsterland borings in this light, we are struck by the fact that the deposits of the Mindel Glacial phase at Lemsterland are composed of coarse grained sediments, whilst the equivalent interval at Spannenburg is fine grained. Both show, however, spectra indicating a cold climate. Furthermore at Bergumerheide a continuous coarse section is formed which shows a diagram containing successively warm, cold and again warm spectra, which correspond with the Günz-Mindel Interglacial, Mindel Glacial and Mindel-Riss Interglacial respectively. This demonstrates that grain size alone is not indicative of the climatic conditions prevailing during sedimentation. A number of borings have been investigated from a sedimentary penological viewpoint by Edelman (1933) and by Böhmers (1937). From a stratigraphical viewpoint, the B-Scheemda group is most interesting. It is characterized by high percentages of para-metamorphic minerals, the amount of which decreases from east to west. Edelman therefore looked for their origin in an easterly direction. Later he suggested that this group might have been deposited during the Mindel glaciation, when the courses of German rivers were deflected through the northern Netherlands by the icefront (Edelman, 1939). In the boring at Urk the most conspicuous B-Scheemda influence occurs between 66 and 99 m; in the Kippenburg boring between 66 and 92 m, whilst the nearest wells of Lemsterland and Spannenburg show spectra with a cold character at corresponding depths. In the Suameer boring the B-Scheemda influence is, according to Böhmers, most distinctly developed between 163 and 175 m. However, his mineralogical table (Böhmers, 1937, p. 62) shows the presence of two more horizons with rather high percentages of para-metamorphic minerals, viz. between 122 and 142 m and between 70 and 80 m. The lowest interval could not be investigated for its pollen content. The 122—142 m interval is unfortunately barren of pollen but the underlying and overlying beds contain a temperate flora. The uppermost zone (70—80 m) is apparently equivalent to the Mindel Glacial interval as established at nearby Bergumerheide. Thus it is obvious that the B-Scheemda group or a mineral aggregate comparatively rich in parametamorphic minerals fluctuated at different times and that these fluctuations might correspond to periodic deflections of the Germanic rivers into the northern part of the Netherlands. A discussion of the considerable clay deposits, which puzzled Lorié already half a century ago, is given in chapter VII. These deposits are known from a limited number of localities. In general all fine grained sediments between the boulder clay and the upper coarse horizon have been considered to form one unit, comprising the Riss I/II Interstadial as well as the early fluvioglacial deposits. The pollen diagrams strongly indicate that this cannot be the case. The clay deposits of Bantega and the upper clay of Spannenburg are undoubtedly of Mindel-Riss Interglacial age. Assen and Winschoten, however, represent another, probably glacial type, also by their content of reworked pollen. Of further localities known to have very thick clay beds Dronrijp is the most interesting. Here the clay is clearly deposited in a valley cut in the marine Mindel-Riss Interglacial series and therefore is apparently younger. As the boulder clay shows hardly any depression above the clay, the valley must have been filled up before the Riss ice reached the region (pl. XLVI). All localities with clay deposits thicker than 70 m, including occasionally fine sand beds, have been shown in black on the map (fig. 3). The two figures given indicate the top and bottom of the clay horizon, unless the second figure is in brackets, which means that at that depth the base has not been reached. Their distribution suggests that the localities belong to two valleys, one running from east to west and a second one from southeast to northwest. The thick clay deposits in the lower half of the Sneek boring correspond, from a pollen analytical point of view, to the clay deposits of Assen and Winschoten, which are of a post Mindel-Riss Interglacial age. The clay of Sneek however, is covered by the marine Mindel-Riss Interglacial beds and must therefore be older. This suggests that the thick clay beds of other localities might also have been deposited in two phases, although separating interglacial beds are lacking in most of the profiles. The clay itself is an unpromising medium for pollen analysis, but better results may be obtained from the border regions where intercalations of sands with peat might occur. The profiles (fig. 4) show a gradual thinning out of the coarse deposits in the direction of Assen. The profile at Drouwen, in the vicinity of Gasselte, yielded spectra with a cold character and with reworked pollen above (see plate XLV) as well as below (refer table, p. 290) the coarse horizon. Strong evidence therefore exists that thick clay beds were deposited twice in valleys of glacial age during the Lower and Middle Pleistocene. The older of the two deposits apparently correspond with the „Lauenburger Ton” from northwestern Germany (Schucht, 1912). Apart from the above discussed valley systems of Sneek and Dronrijp a still younger valley system is known to exist. It developed after the above mentioned two valley systems had been filled up and it still existed at the time the Riss ice arrived because we find a mantle of boulder clay deposited in the bottom as well as on the flanks of these valleys. Such valleys have been recognized below the present Overijselse Vecht and the Ems rivers. Essentially we have recognized three periods during which valleys were formed in Middle Pleistocene times. The first (Sneek) is pre Mindel-Riss Interglacial and therefore probably of Mindel Glacial age. The second (Dronrijp) and the third (Vecht-Ems) both occur between the Mindel-Riss Interglacial and the arrival of the Riss ice and therefore probably correspond with the two cold stages of the Riss Glacial. From this scheme it might be concluded that the Riss ice reached the Netherlands during the Riss II stage. Chapter VIII summarizes in Dutch the sequence of events during the Lower and Middle Pleistocene and we refer to table (p. 333) for a chronological representation of most of the above described events.
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    In:  Bijdragen tot de Dierkunde (0067-8546) vol.28 (1949) nr.1 p.32
    Publication Date: 2014-11-07
    Description: For certain reasons I wished to train a young chimpanzee to choose from two similar boxes the one characterised by the ticking of a metronome inside it. My subject was a young male chimpanzee (Pan leucoprymnus Lesson), approximately three years old, Tommy by name. He was a good-natured chap, quite tame, and already for some years in captivity. When we knew each other a little better, he would welcome me every morning with a hearty “uhuh”, as soon as he heard my steps, and after the experiments of the day we would take leave by shaking hands as old friends. Tommy was rather lazy and not so playful as most young chimpanzees, but this quality made working with him easier and more regular. With a few exceptions it did not give much trouble to make 50—60 trials with him each day.
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    In:  Bijdragen tot de Dierkunde (0067-8546) vol.28 (1949) nr.1 p.315
    Publication Date: 2014-11-07
    Description: The distribution of fresh-water fishes like that of other groups, has been widely utilized by zoogeographers, but with widely divergent acumen and success. At one extreme are those non-ichthyologists who have uncritically utilized for evidence certain groups whose distribution happens to support whatever theory they may be espousing. At the other extreme is the work of careful ichthyologists like DE BEAUFORT (1913) and REGAN (1922) whose thorough knowledge of the groups with which they are working demands the most careful consideration of their conclusions. However, no zoogeographer who utilizes the evidence of diverse groups can be familiar at first hand with all of them, and the difficulty facing such workers is that of seeking out the really dependable evidence in those groups he does not know well. Aside from the difficulty of selecting dependable authorities or systematic works, the zoogeographer desiring to use the evidence of fresh-water fishes has another troublesome matter to contend with. This is the differing tolerance of salt-water exhibited by different groups of fresh-water fishes. As one example, and one which has frequently troubled zoogeographers, we may mention the Galaxiidae, fresh-water fishes of Southern South America, Africa, Australia, and New Zealand, whose distribution has been held by some to be evidence for continental drift or southern intercontinental land-bridges. Ichthyologists now know that these fishes are, as a group, salt-tolerant and possibly either anadromous or catadromous, and that they are not really strong evidence for continental connections simply because it seems possible that they may cross ocean barriers.
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  • 164
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    In:  Bijdragen tot de Dierkunde (0067-8546) vol.28 (1949) nr.1 p.57
    Publication Date: 2014-11-07
    Description: In all snakes, the Boidae and Xenopeltidae excepted, only the right lung is well developed, while the left lung is rudimentary or absent (BUTLER, 1895). The right lung consists of an anterior alveolar part that is strongly vascularized, and of a posterior smooth-walled air-sac that is anangious. Between these two parts a transitional zone may be present, in which the wall of the lung shows a faint reticulate pattern, and which receives some very fine branches from the pulmonary vessels. In a number of snakes, among which the Viperidae, the situation becomes more complicated. In these snakes the membrane that connects the dorsal ends of the incomplete tracheal cartilages has become greatly expanded, and this dorsal wall has developed an alveolar structure. COPE (1894, p. 218) very aptly has named this the tracheal lung. When the tracheal lung has very strongly developed, it sometimes merges gradually into the right lung. In species with a rudimentary left lung, its opening into the trachea may be considered to mark the end of the trachea, and consequently also the beginning of the right lung. In other species a slight change in the structure of the alveoles may mark the boundary, but in a number of species it becomes a more or less arbitrary procedure to draw a boundary between the tracheal lung and the right lung. For the purpose of the present note it suffices, however, to consider as right lung that part of the respiratory tract that lies posterior to the middle of the heart. The development of the tracheal lung, and the relative size of the alveolar part of the right lung and of the air-sac vary according to genera and species.
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  • 165
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    In:  Bijdragen tot de Dierkunde (0067-8546) vol.28 (1949) nr.1 p.530
    Publication Date: 2014-11-07
    Description: Tijdens het directoraat van Prof. Dr. J. E. W. IHLE is mij op het Zoölogisch Laboratorium steeds vrijheid gelaten om bij de studenten belangstelling te wekken voor hydrobiologisch onderzoek. Hoewel de Hoogleraar IHLE dit onderdeel der biologie zelf niet beoefende, verleende hij hiervoor met grote bereidwilligheid alle materiële steun, waartoe de bescheiden middelen van het laboratorium hem in staat stelden. Wij beschikken thans dan ook over een kern van literatuur op hydrobiologisch gebied, waartoe niet weinig heeft bijgedragen de aankoop van de gehele separatencollectie van wijlen Dr. H. C. REDEKE, waarvoor de steun van de Vereeniging „Het Natuur- en Geneeskundig Congres” werd verkregen. Onder auspiciën van het Zoölogisch Laboratorium werden in de jaren 1940 en 1941 cursussen georganiseerd op het gebied der hydrobiologie, waaraan respectievelijk 35 en 43 studenten deelnamen. Op deze cursussen werden door de volgende sprekers het woord gevoerd. In September 1940 door Dr. H. C REDEKE over Watertypen in Nederland, door Dr. B. HAVINGA over de Fauna van het IJselmeer, door Mej. A. P. C. DE VOS over Leeftijden van vissen en de biologie van de snoekbaars, door Dr. J. HEIMANS over Desmidiaceën, door Dr. G. BARENDRECHT over Waterinsecten, door Dr. C. O. van REGTEREN ALTENA over Mollusken, door Ir. K. W. H. LEEFLANG over het Waterleidingbedrijf, door den Heer A. VAN DER WERFF over Diatomeën, door Dr. Ir. T. Y. KINGMA BOLTJES over de biologische zelfreiniging van het water, door Mevr. N. L. WIBAUT-ISEBREE MOENS over zoutgehalten in Noord-Holland, door Prof. Dr. N. H. SWELLENGREBEL over Malariamuggen en door Mej. Dr. A. G. VORSTMAN over de Cyclus van het plankton gedurende een jaar aan de hand van het plankton in het Kinselmeer.
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  • 166
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    In:  Bijdragen tot de Dierkunde (0067-8546) vol.28 (1949) nr.1 p.164
    Publication Date: 2014-11-07
    Description: Before the outbreak of the war with Japan the author had the intention to publish an extensive account on the occurrence of an aestuarine fishfauna in and in front of the large aestuarines and river-mouths so often found in India, Burma, Malaya, Thailand and Indo China and in the Greater Sunda Islands, Sumatra and Borneo, the rivers of the latter two islands being the special field of investigation. However as a consequence of the war all, thus far, unpublished notes and the greater part of the collections were lost as is the case with a most interesting sample of an aestuarine fishfauna from South New Guinea, where biologically the same conditions exist as in Sumatran and Bornean rivermouths. This last collection remained partly unpacked when war broke out and its still unassorted part disappeared. Only about 20 % of the total was found back in a more or less good condition.
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    Publication Date: 2015-10-23
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    Zeitschrift für Gletscherkunde und Glazialgeologie
    In:  EPIC3Innsbruck, Zeitschrift für Gletscherkunde und Glazialgeologie
    Publication Date: 2019-07-17
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    Svenska Hydr.-Biol. Kommissionens
    In:  EPIC3Göteborg, Svenska Hydr.-Biol. Kommissionens
    Publication Date: 2017-04-25
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 15(1/2), pp. 18-20, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 15(1/2), pp. 5-9, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 15(1/2), pp. 25-27, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 15(1/2), pp. 9-11, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 16(1/2), pp. 69, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 16(1/2), pp. 84, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 17(1/2), pp. 154-163, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 17(1/2), pp. 176, ISSN: 0032-2490
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    Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research
    In:  EPIC3Polarforschung, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research & German Society of Polar Research, 17(1/2), pp. 179, ISSN: 0032-2490
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