LITERATURE REVIEW Genus Loerzingia Airy
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Thysanoptera, Phlaeothripinae)
Zootaxa 4759 (3): 421–426 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2020 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4759.3.8 http://zoobank.org/urn:lsid:zoobank.org:pub:F725F128-FCF3-4182-8E88-ECC01F881515 Two new monobasic thrips genera for a gall-inducing species and its kleptoparasite (Thysanoptera, Phlaeothripinae) LAURENCE A. MOUND & ALICE WELLS Australian National Insect Collection CSIRO, PO Box 1700, Canberra, ACT 2601 [email protected] Abstract Drypetothrips korykis gen. et sp.n. is described as inducing leaf-margin galls on a small tree in Australia, Drypetes deplanchei [Putranjivaceae]. This thrips is similar in appearance to the smaller species of the genus Kladothrips that induce galls on Acacia species. The galls are invaded by a phytophagous kleptoparasitic thrips, Pharothrips hynnis gen. et sp.n., females of which have a forked plough-like structure protruding ventrally on the frons that is unique amongst Thysanoptera. Key words: autapomorphy, systematic relationships, leaf-margin galls, Australia Introduction The small tree, Drypetes deplanchei [Putranjivaceae], is widespread across northern Australia as far south as New- castle on the east coast. This tree is sometimes referred to as native holly, because the leaf margins can be sharply dentate, but these margins may also be almost smooth, and a species of thrips has been found inducing rolled margin galls on both leaf forms (Fig. 1). These galls and their thrips have been found at sites near Taree in coastal New South Wales, and also at Mt. Nebo near Brisbane in south-eastern Queensland. -
CGGJ Vansteenis
BIBLIOGRAPHY : ALGAE 3957 X. Bibliography C.G.G.J. van Steenis (continued from page 3864) The entries have been split into five categories: a) Algae — b) Fungi & Lichens — c) Bryophytes — d) Pteridophytes — e) Spermatophytes 8 General subjects. — Books have been marked with an asterisk. a) Algae: ABDUS M & Ulva a SALAM, A. Y.S.A.KHAN, patengansis, new species from Bang- ladesh. Phykos 19 (1980) 129-131, 4 fig. ADEY ,w. H., R.A.TOWNSEND & w„T„ BOYKINS, The crustose coralline algae (Rho- dophyta: Corallinaceae) of the Hawaiian Islands. Smithson„Contr„ Marine Sci. no 15 (1982) 1-74, 47 fig. 10 new) 29 new); to subfamilies and genera (1 and spp. (several key genera; keys to species„ BANDO,T„, S.WATANABE & T„NAKANO, Desmids from soil of paddyfields collect- ed in Java and Sumatra. Tukar-Menukar 1 (1982) 7-23, 4 fig. 85 species listed and annotated; no novelties. *CHRISTIANSON,I.G., M.N.CLAYTON & B.M.ALLENDER (eds.), B.FUHRER (photogr.), Seaweeds of Australia. A.H.& A.W.Reed Pty Ltd., Sydney (1981) 112 pp., 186 col.pl. Magnificent atlas; text only with the phyla; ample captions; some seagrasses included. CORDERO Jr,P.A„ Studies on Philippine marine red algae. Nat.Mus.Philip., Manila (1981) 258 pp., 28 pi., 1 map, 265 fig. Thesis (Kyoto); keys and descriptions of 259 spp„, half of them new to the Philippines; 1 new species. A preliminary study of the ethnobotany of Philippine edible sea- weeds, especially from Ilocos Norte and Cagayan Provinces. Acta Manillana A 21 (31) (1982) 54-79. Chemical analysis; scientific and local names; indication of uses and storage. -
The Plant Press
Department of Botany & the U.S. National Herbarium The Plant Press New Series - Vol. 17 - No. 1 January-March 2014 Botany Profile Research Scientist Spills the Beans By Gary A. Krupnick magine starting a new job by going population genetics to phylogenetics and rial of Psoraleeae and soybean (Glycine away on a three-month field excur- systematics. max). In 2007, Egan became a postdoc- sion to the remote forests of China, n 2001 she began her graduate years toral research associate in Doyle’s lab, I studying the phylogenetic systematics Japan, and Thailand after only two weeks at Brigham Young University, initially on the job, before having a chance to set- working on a doctoral thesis in cancer of subtribe Glycininae (Leguminosae). tle into your new office and unpack your I Egan’s research has determined that research. Her preliminary studies utilized boxes. Continue imagining that while phylogenetics as a means of bioprospect- tribe Psoraleeae is nested within subtribe you are away on your Asian expedition, ing, looking at the chemopreventive ability Glycininae, and is a potential progenitor you find out that your employer, the U.S. and phenolic content of the mint family, genome of the polyploid soybean. federal government, has shut down for 16 Lamiaceae. Unsatisfied with the direc- During her postdoctoral research, days, forcing you into “furlough in place” tion of her thesis, Egan switched to Keith Egan began collaborating with several status (non-duty and non-pay). Such is Crandall’s invertebrate biology laboratory, scientists studying soybean genome evo- the life of Ashley N. Egan, the Depart- with the understanding that Egan would lution. -
COMMELINACEAE 鸭跖草科 Ya Zhi Cao Ke Hong Deyuan (洪德元)1; Robert A
Flora of China 24: 19–39. 2000. COMMELINACEAE 鸭跖草科 ya zhi cao ke Hong Deyuan (洪德元)1; Robert A. DeFilipps2 Herbs annual or perennial, sometimes woody at base. Stems with prominent nodes and internodes. Leaves alternate, distichous or spirally arranged, sessile or petiolate; leaf sheath prominent, open or closed; leaf blade simple, entire. Inflorescence usually of cin- cinni in panicles or solitary, sometimes shortened into heads, sometimes sessile with flowers fascicled, sometimes axillary and pene- trating enveloping leaf sheath, rarely flowers solitary and terminal or axillary. Flowers bisexual, rarely unisexual, actinomorphic or zygomorphic. Sepals 3, free or connate only at base, often boat-shaped or carinate, sometimes galeate at apex. Petals (2 or)3, free, sometimes connate and tubular at middle and free at 2 ends (Cyanotis), sometimes clawed. Stamens 6, free, all or only 2 or 3 fertile; filaments glabrous or torulose villous; anthers parallel or slightly divergent, longitudinally dehiscent, rarely dehiscent by apical pores; staminodes 1–3; antherodes 4-lobed and butterflylike, 3-sect, 2-lobed and dumbbell-shaped, or entire. Ovary 3-loculed, or reduced to 2-loculed; ovules 1 to several per locule, orthotropous. Fruit a loculicidal, 2- or 3-valved capsule, rarely baccate and indehiscent. Seeds few, large; endosperm copious; hilum orbicular or linear. About 40 genera and 650 species: mainly in tropical regions, fewer species in subtropical and temperate regions; 15 genera (two introduced) and 59 species (12 endemic, three introduced) in China. Hong Deyuan. 1997. Commelinaceae. In: Wu Kuo-fang, ed., Fl. Reipubl. Popularis Sin. 13(3): 69–133. 1a. Inflorescence penetrating leaf sheath, sessile, capitate; fertile stamens 6. -
(RET) Trees from Kerala Part of Western Ghats
KFRI Research Report No. 526 ISSN 0970-8103 Population evaluation and development of propagation protocol for three Rare, Endangered and Threatened (RET) trees from Kerala part of Western Ghats By Somen C.K. Jose P.A. Sujanapal P. Sreekumar V.B. Kerala Forest Research Institute, Peechi, Thrissur, Kerala (An Institution under Kerala State Council for Science Technology and Environment, Sasthra Bhavan, Thiruvananthapuram) K F R I KFRI Research Report No. 526 ISSN: 0970-8103 Population evaluation and development of propagation protocol for three Rare, Endangered and Threatened trees from Kerala part of Western Ghats (Final Report of project KFRI 611/11) by Somen, C.K Jose, P.A. Sujanapal, P. Sreekumar, V.B. Kerala Forest Research Institute, Peechi, Thrissur, Kerala. (Research Institution under Kerala State Council for Science Technology and Environment, Sasthra K F R I Bhavan, Thiruvananthapuram) June 2017 Project Particulars 1. Title of the project : Population evaluation and development of propagation protocol for three rare endangered and threatened (RET) trees from Kerala part of Western Ghats 2.Department/ organization : Kerala Forest Research Institute, implementing the project Peechi. 3. Principal Investigator Dr. C.K. Somen Tree Physiology Department Kerala Forest Research Institute 4. Co – investigators Dr. P. A. Jose Dr. P. Sujanapal Dr. V. B. Sreekumar Kerala Forest Research Institute, Peechi, Thrissur. 5. Project Fellow R.R. Rajesh 5. Name of the funding agency Plan Grant of the Kerala Forest Research Institute, Peechi. i Contents Page No. Acknowledgements iii Abstract v 1.0 Introduction 1 1.1 Objectives 3 2.0 Methodology 2.1 Selection of sites and study area 4 2.2 Species description 4 2.3 Survey, selection of plots and sampling 8 2.4 Biodiversity indices 12 2.5. -
Epiphyte Diversity and Fragmented Forests
Selbyana 23(1): 121-130. 2002 EPIPHYTEDIVERSITY IN PRIMARYAND FRAGMENTEDFORESTS OF CAMEROON,CENTRAL AFRICA: A PRELIMINARYSURVEY BERNARD-ALOYSNKONGMENECK University of Yaounde 1, Department of Plant Biology, l? 0. Box 812, Yaounde, Cameroon, West Africa MARGARETD. LOWMAN*AND JOHNT. ATWOOD The Marie Selby Botanical Gardens, 81 1 S. Palm Avenue, Sarasota, Florida, 34236 USA. E-mail: [email protected]; [email protected] ABSTRACT.In this study our objectives were to compare the diversity of epiphytes in undisturbed and fragmented forests, to identify the most abundant host tree species. and to collect specimens for the Uni- versity of Yaounde. To protect epiphytes in villages where these plants are often perceived as parasites (especially of fruit trees), the senior author organized conservation classes for local villagers who partici- pated in data collection at each site. Preliminary results showed that epiphytic flora was rich in disturbed forests of Cameroon and that preservation of forest fragments may benefit epiphyte conservation. The most abundant host tree species differ in both intact and disturbed habitats at each site. Human disturbance, despite reducing epiphyte population sizes, serves as a catalyst for promoting change (and perhaps a short- term increase) in diversity by increasing habitat diversity. Key words: Africa, biodiversity, Cameroon, epiphyte, forest, orchid, tropics INTRODUCTION natural and disturbed forest tracts within the three tropical forests. Epiphytes are components of tropical rain for- N~~~ large and conspicuous epiphytes, ests. Much information on their relative diver- collect voucher specimens for herbaria in E~- sity and abundance exists for major equatorial . rope, ~f~i~~,and ~~~~i~~ the first set forests in Mexico (Williams-Linera et al. -
Impatiens Siangensis (Balsaminaceae), a New Species from Arunachal Pradesh, India
Phytotaxa 192 (2): 117–120 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Correspondence ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.192.2.5 Impatiens siangensis (Balsaminaceae), a new species from Arunachal Pradesh, India RAJIB GOGOI* & SOURAVJYOTI BORAH Botanical Survey of India, Arunachal Pradesh Regional Centre, Senki View, Itanagar-791111, India.*E. mail: [email protected] Abstract Impatiens siangensis Gogoi, a new species, is described and illustrated from Arunachal Pradesh, India. The new species dif- fers from I. marianae Hooker by the absence of white blotches on the upper leaf surface, flowers only partially purple, bracts ovate, glabrous, lateral sepals glabrous, dorsal petal glabrous, navicular, lower sepal with straight purple streaks and spur almost straight. The new species differs from I. porrecta Wallich in having stems, leaves, and floral parts glabrous, stems branched, flowers partially purple, lower sepal navicular with straight purple streaks and spur almost straight. Key words: Balsaminaceae, new taxa, taxonomy, Siang valley Introduction Impatiens Linnaeus (1753: 937) is the largest genus in the Balsaminaceae, with more than 900 species distributed worldwide except in Latin America (Chen et al. 2008). Most of the species occur in Africa and Asia. The centre of origin has been suspected in south China (Yuan et al. 2004, Janssenset al. 2007, Chen et al. 2008, Mabberley 2008), although Bhaskar (2012) noted that the most primitive species of Impatiens, with lowest chromosome numbers and the largest sized chromosomes, are recorded from the Western Ghats and thus argued that the centre of origin lies in the Western Ghats, South India. -
Vascular Plant Composition and Diversity of a Coastal Hill Forest in Perak, Malaysia
www.ccsenet.org/jas Journal of Agricultural Science Vol. 3, No. 3; September 2011 Vascular Plant Composition and Diversity of a Coastal Hill Forest in Perak, Malaysia S. Ghollasimood (Corresponding author), I. Faridah Hanum, M. Nazre, Abd Kudus Kamziah & A.G. Awang Noor Faculty of Forestry, Universiti Putra Malaysia 43400, Serdang, Selangor, Malaysia Tel: 98-915-756-2704 E-mail: [email protected] Received: September 7, 2010 Accepted: September 20, 2010 doi:10.5539/jas.v3n3p111 Abstract Vascular plant species and diversity of a coastal hill forest in Sungai Pinang Permanent Forest Reserve in Pulau Pangkor at Perak were studied based on the data from five one hectare plots. All vascular plants were enumerated and identified. Importance value index (IVI) was computed to characterize the floristic composition. To capture different aspects of species diversity, we considered five different indices. The mean stem density was 7585 stems per ha. In total 36797 vascular plants representing 348 species belong to 227 genera in 89 families were identified within 5-ha of a coastal hill forest that is comprises 4.2% species, 10.7% genera and 34.7% families of the total taxa found in Peninsular Malaysia. Based on IVI, Agrostistachys longifolia (IVI 1245), Eugeissona tristis (IVI 890), Calophyllum wallichianum (IVI 807), followed by Taenitis blechnoides (IVI 784) were the most dominant species. The most speciose rich families were Rubiaceae having 27 species, followed by Dipterocarpaceae (21 species), Euphorbiaceae (20 species) and Palmae (14 species). According to growth forms, 57% of all species were trees, 13% shrubs, 10% herbs, 9% lianas, 4% palms, 3.5% climbers and 3% ferns. -
Habitats 0-Year
Table S1: The total number of recorded species per habitat (in brackets) and the number of shared species across habitats. 0-year- 3-year- 5-year- Restored Habitats Reference old old old combined 0-year-old (36 spp.) - 25 spp. 24 spp. - 25 spp. 3-year-old (40 spp.) 25 spp. - 28 spp. - 30 spp. 5-year-old (44 spp.) 24 spp. 28 spp. - - 40 spp. Restored combined (59 - - - - 49 spp. spp.) Reference (70 spp.) 25 spp. 30 spp. 40 spp. 49 spp. - Table S2: Checklist of plant species found in the restored and reference habitats. Species Family Upland area Lowland area 0-year- 3-year- 5-year- 0-year- 3-year- 5-year- old old old Reference old old old Reference habitat habitat habitat habiat habitat habitat habitat habitat Harpephyllum caffrum Bernh. Anacardiaceae X X X X X X X - Protorhus longifolia (Bernh.) Engl. Anacardiaceae - X X X - - - X Sclerocrya birrea (A.Rich.) Hochst. subsp. caffra (Sond.) Kokwaro Anacardiaceae - - - - - - - - Searsia chirindensis (Baker f.) Moffett Anacardiaceae - - X X - X X X Searsia dentata (Thunb.) F.A.Barkley Anacardiaceae - - - - - - - - Searsia lucida (L.) F.A.Barkley Anacardiaceae X - - - - X - - Searsia pentheri (Zahlbr.) Moffett Anacardiaceae - - X - - - - X Searsia rehmanniana (Engl.) Moffet Anacardiaceae X - - X - X X - Annona senegalensi Pers. Annonaceae - - - - - - - - Rauvolfia caffra Sond. Apocynaceae X X - X - - - X Tabernaemontana ventricosa Hochst. ex A.DC. Apocynaceae X X - X - - - X Cussonia spicata Thunb. Araliaceae - - - - - - - - Cussonia zuluensis Strey Araliaceae - - - X - - X - Phoenix reclinata Jacq. Arecaceae X X - - - - X X Aloe ferox Mill. Asphodelaceae - - X - - - X - Brachylaena discolor DC. Asteraceae X X X - - X - - Kigelia africana (Lam.) Benth. -
Woody and Herbaceous Plants Native to Haiti for Use in Miami-Dade Landscapes1
Woody and Herbaceous Plants Native to Haiti For use in Miami-Dade Landscapes1 Haiti occupies the western one third of the island of Hispaniola with the Dominican Republic the remainder. Of all the islands within the Caribbean basin Hispaniola possesses the most varied flora after that of Cuba. The plants contained in this review have been recorded as native to Haiti, though some may now have been extirpated due in large part to severe deforestation. Less than 1.5% of the country’s original tree-cover remains. Haiti’s future is critically tied to re- forestation; loss of tree cover has been so profound that exotic fast growing trees, rather than native species, are being used to halt soil erosion and lessen the risk of mudslides. For more information concerning Haiti’s ecological plight consult references at the end of this document. For present purposes all of the trees listed below are native to Haiti, which is why non-natives such as mango (the most widely planted tree) and other important trees such as citrus, kassod tree (Senna siamea) and lead tree (Leucanea leucocephala) are not included. The latter two trees are among the fast growing species used for re-forestation. The Smithsonian National Museum of Natural History’s Flora of the West Indies was an invaluable tool in assessing the range of plants native to Haiti. Not surprisingly many of the listed trees and shrubs 1 John McLaughlin Ph.D. U.F./Miami-Dade County Extension Office, Homestead, FL 33030 Page | 1 are found in other parts of the Caribbean with some also native to South Florida. -
Fl. China 11: 218–221. 2008. 17. DRYPETES Vahl, Eclogae Amer. 3
Fl. China 11: 218–221. 2008. 17. DRYPETES Vahl, Eclogae Amer. 3: 49. 1810. 核果木属 he guo mu shu Li Bingtao (李秉滔 Li Ping-tao); Michael G. Gilbert Cyclostemon Blume. Trees or shrubs, dioecious; indumentum of simple hairs, often absent. Leaves alternate; stipules 2; petioles short; leaf blade simple, base often asymmetrical, margin entire or serrate, venation pinnate. Inflorescences axillary, sometimes grouped into glomerules, racemes, or panicles. Male flowers pedicellate or sessile; sepals 4–6, distinct, usually unequal, imbricate; petals absent; stamens 1–25, 1 to several whorls surrounding disk or outer ones inserted at margin or sinus of disk, inner ones inserted on disk; filaments free; anthers bilocular, usually introrse, rarely extrorse, longitudinally dehiscent; disk flattened or concave, margin shallowly or deeply fid; rudimentary ovary very small or absent. Female flowers solitary, axillary, sometimes on older branches; sepals as in male; petals absent; disk annular; ovary 1- or 2(or 3)-loculed; ovules 2 per locule; style short, stigmatiform; stigmas 1 or 2(or 3), usually dilated, peltate or reniform. Fruit a drupe, subglobose or ovoid, 1- or 2(or 3)-celled, seeds 1 per locule; exocarp leathery or nearly so; mesocarp fleshy or woody; endocarp woody, papery, or crustaceous. Seeds without caruncle; endosperm fleshy; cotyledons larger and flattened. About 200 species: tropical and subtropical Africa, America, and Asia; 12 species (two endemic) in China. The timber from several species is valued. Key to fruiting material 1a. Ovary and drupe 1-locular. 2a. Fruits glabrous. 3a. Branchlets and petioles puberulent when young; lateral veins 6–8 pairs; stipules linear, persistent; stamens ca. -
Phytogeography of African Commelinaceae
Bothalia 14, 3 & 4: 553-557 (1983) Phytogeography of African Commelinaceae R. B. FADEN* ABSTRACT Africa (including Madagascar) has nearly twice as many species of Commelinaceae as any other continent (approximately 270 species, or about 40% of the total in the family). Of the 17 genera which are native, seven (Anthericopsis, Coleotrype, Palisota, Polyspatha, Pseudoparis, Stanfieldiella and Triceratella) are endemic, the highest percentage generic endemism of any continent. Within Africa gcneric diversity is slightly higher in western than in eastern tropical floras. Species richness, however, is greatest in eastern Africa, mainly due to a high diversity of species of Commelina and Aneilema. Africa shares more genera with Asia (nine) than with any other continent. Only one African genus, Buforrestia, is neither endemic nor shared with Asia. Its western African/northeastern South American distribution is unique in the family. Besides Buforrestia, only five other genera of Commelinaceae (out of a total of 50 in the family), occur in both the Old and New Worlds. These genera. Aneilema, Commelina, Floscopa, Murdannia and Pollia are all very widespread in the Old World, occurring in Australia and Asia in addition to Africa (both continental and Madagascar). Madagascar is relatively poor in species (31). but these include the endemic Madagascan genus Pseudoparis, the sole African species of Rhopalephora, and the largest number of species of the Afro-Malagasy endemic genus Coleotrype. The high rate of generic endemism of Commelinaceae in Africa probably indicates that Africa was one of the ancient centres of diversity for the family. The high species diversity is more likely due to relatively recent radiations by genera pre-adapted to survival in non-forest habitats.