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DENNSTAEDTIACEAE 1. MONACHOSORUM Kunze, Bot. Zeitung (Berlin) 6: 119. 1848
This PDF version does not have an ISBN or ISSN and is not therefore effectively published (Melbourne Code, Art. 29.1). The printed version, however, was effectively published on 6 June 2013. Yan, Y. H., X. P. Qi, W. B. Liao, F. W. Xing, M. Y. Ding, F. G. Wang, X. C. Zhang, Z. H. Wu, S. Serizawa, J. Prado, A. M. Funston, M. G. Gilbert & H. P. Nooteboom. 2013. Dennstaedtiaceae. Pp. 147–168 in Z. Y. Wu, P. H. Raven & D. Y. Hong, eds., Flora of China, Vol. 2–3 (Pteridophytes). Beijing: Science Press; St. Louis: Missouri Botanical Garden Press. DENNSTAEDTIACEAE 碗蕨科 wan jue ke Yan Yuehong (严岳鸿)1, Qi Xinping (齐新萍)2, Liao Wenbo (廖文波)3, Xing Fuwu (邢福武)4, Ding Mingyan (丁明艳)3, Wang Faguo (王发国)4, Zhang Xianchun (张宪春)5, Wu Zhaohong (吴兆洪 Wu Shiew-hung)4; Shunshuke Serizawa6, Jefferson Prado7, A. Michele Funston8, Michael G. Gilbert9, Hans P. Nooteboom10 Plants terrestrial, sometimes climbing. Rhizome usually long creeping, solenostelic, siphonostelic, or polystelic, usually covered with multicellular hairs, less often with few-celled, cylindrical, glandular hairs or multicellular bristles, scales absent. Fronds medium-sized to large, sometimes indeterminate, monomorphic; stipes not articulate to rhizome, usually hairy, rarely glabrous; lamina 1–4-pinnately compound, thinly herbaceous to leathery, hairy or glabrous, without scales; rachis grooved adaxially, some- times with buds (Monachosorum); pinnae opposite or alternate; veins usually free, pinnate or forked, not reaching margin, reticulate without included veinlets in Histiopteris. Sori marginal or intramarginal, linear or orbicular, terminal on a veinlet or on a vascular commissure joining apices of veins; indusia linear or bowl-shaped, sometimes double with outer false indusium formed from thin reflexed lamina margin and inconspicuous inner true indusium; paraphyses present or not. -
Electrophorus Electricus ERSS
Electric Eel (Electrophorus electricus) Ecological Risk Screening Summary U.S. Fish and Wildlife Service, August 2011 Revised, July 2018 Web Version, 8/21/2018 Photo: Brian Gratwicke. Licensed under CC BY-NC 3.0. Available: http://eol.org/pages/206595/overview. (July 2018). 1 Native Range and Status in the United States Native Range From Eschmeyer et al. (2018): “Distribution: Amazon and Orinoco River basins and other areas in northern Brazil: Brazil, Ecuador, Colombia, Bolivia, French Guiana, Guyana, Peru, Suriname and Venezuela.” Status in the United States This species has not been reported as introduced or established in the United States. This species is in trade in the United States. From AquaScapeOnline (2018): “Electric Eel 24” (2 feet) (Electrophorus electricus) […] Our Price: $300.00” 1 The State of Arizona has listed Electrophorus electricus as restricted live wildlife. Restricted live wildlife “means wildlife that cannot be imported, exported, or possessed without a special license or lawful exemption” (Arizona Secretary of State 2006a,b). The Florida Fish and Wildlife Conservation Commission has listed the electric eel Electrophorus electricus as a prohibited species. Prohibited nonnative species, "are considered to be dangerous to the ecology and/or the health and welfare of the people of Florida. These species are not allowed to be personally possessed or used for commercial activities” (FFWCC 2018). The State of Hawaii Plant Industry Division (2006) includes Electrophorus electricus on its list of prohibited animals. From -
Laws of Malaysia
LAWS OF MALAYSIA ONLINE VERSION OF UPDATED TEXT OF REPRINT Act 716 WILDLIFE CONSERVATION ACT 2010 As at 1 December 2014 2 WILDLIFE CONSERVATION ACT 2010 Date of Royal Assent … … 21 October 2010 Date of publication in the Gazette … … … 4 November 2010 Latest amendment made by P.U.(A)108/2014 which came into operation on ... ... ... ... … … … … 18 April 2014 3 LAWS OF MALAYSIA Act 716 WILDLIFE CONSERVATION ACT 2010 ARRANGEMENT OF SECTIONS PART I PRELIMINARY Section 1. Short title and commencement 2. Application 3. Interpretation PART II APPOINTMENT OF OFFICERS, ETC. 4. Appointment of officers, etc. 5. Delegation of powers 6. Power of Minister to give directions 7. Power of the Director General to issue orders 8. Carrying and use of arms PART III LICENSING PROVISIONS Chapter 1 Requirement for licence, etc. 9. Requirement for licence 4 Laws of Malaysia ACT 716 Section 10. Requirement for permit 11. Requirement for special permit Chapter 2 Application for licence, etc. 12. Application for licence, etc. 13. Additional information or document 14. Grant of licence, etc. 15. Power to impose additional conditions and to vary or revoke conditions 16. Validity of licence, etc. 17. Carrying or displaying licence, etc. 18. Change of particulars 19. Loss of licence, etc. 20. Replacement of licence, etc. 21. Assignment of licence, etc. 22. Return of licence, etc., upon expiry 23. Suspension or revocation of licence, etc. 24. Licence, etc., to be void 25. Appeals Chapter 3 Miscellaneous 26. Hunting by means of shooting 27. No licence during close season 28. Prerequisites to operate zoo, etc. 29. Prohibition of possessing, etc., snares 30. -
Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi
Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 (http://www.accessscience.com/) Article by: Boschung, Herbert Department of Biological Sciences, University of Alabama, Tuscaloosa, Alabama. Gardiner, Brian Linnean Society of London, Burlington House, Piccadilly, London, United Kingdom. Publication year: 2014 DOI: http://dx.doi.org/10.1036/1097-8542.680400 (http://dx.doi.org/10.1036/1097-8542.680400) Content Morphology Euteleostei Bibliography Phylogeny Classification Additional Readings Clupeomorpha and Ostariophysi The most recent group of actinopterygians (rayfin fishes), first appearing in the Upper Triassic (Fig. 1). About 26,840 species are contained within the Teleostei, accounting for more than half of all living vertebrates and over 96% of all living fishes. Teleosts comprise 517 families, of which 69 are extinct, leaving 448 extant families; of these, about 43% have no fossil record. See also: Actinopterygii (/content/actinopterygii/009100); Osteichthyes (/content/osteichthyes/478500) Fig. 1 Cladogram showing the relationships of the extant teleosts with the other extant actinopterygians. (J. S. Nelson, Fishes of the World, 4th ed., Wiley, New York, 2006) 1 of 9 10/7/2015 1:07 PM Teleostei - AccessScience from McGraw-Hill Education http://www.accessscience.com/content/teleostei/680400 Morphology Much of the evidence for teleost monophyly (evolving from a common ancestral form) and relationships comes from the caudal skeleton and concomitant acquisition of a homocercal tail (upper and lower lobes of the caudal fin are symmetrical). This type of tail primitively results from an ontogenetic fusion of centra (bodies of vertebrae) and the possession of paired bracing bones located bilaterally along the dorsal region of the caudal skeleton, derived ontogenetically from the neural arches (uroneurals) of the ural (tail) centra. -
May 2014. Orchid Specialist Group Newsletter
ORCHID CONSERVATION NEWS The Newsletter of the Orchid Specialist Group of the IUCN Species Survival Commission Issue 1 May 2014 The Value of Long Term Studies Editorial Endangered Hawaiian endemic, Peristylus holochila, initiates anthesis in vitro and ex vitro Long term agricultural field experiments at Lawrence W. Zettler Rothamstead, England, are notable because when they Shanna E. David began in 1843, the founders could not possibly have predicted what might be discovered over the following Orchid Recovery Program, Department of Biology 160 years. The conservation value of long term studies Illinois College, 1101 West College Avenue of orchids was discussed in 1990 by the late Carl Olof Jacksonville, IL 62650 USA Tamm, Uppsala, Sweden, when he presented his observations of individual plant behaviour at the ([email protected]) International Orchid Symposium. His conclusion after some 40 years of observation was simple: long term Only three orchid species are native to the Hawaiian observations are essential to conservation and that archipelago: Anoectochilus sandvicensis (Hawaiian individual plant tracking of selected orchid taxa was Jeweled Orchid, ke kino o kanaloa), Liparis hawaiensis recommended. (Hawaii Widelip Orchid, awapuhiakanaloa) and Peristylus (Platanthera) holochila (Hawaiian Bog Two papers have recently been published that Orchid, puahala a kane). Of these three, by far the rarest demonstrate the conservation potential of decades-long is P. holochila (Fig. 1) consisting of 33 known plants studies. Joyce and Allan Reddoch summarized what scattered amongst three islands as of 2011 (Kauai, has been learned from some four decades of monitoring Maui, Molokai). 22 species in Gatineau Park, QC, Canada (Reddoch & Reddoch, 2014). -
ECOLOGY of NORTH AMERICAN FRESHWATER FISHES
ECOLOGY of NORTH AMERICAN FRESHWATER FISHES Tables STEPHEN T. ROSS University of California Press Berkeley Los Angeles London © 2013 by The Regents of the University of California ISBN 978-0-520-24945-5 uucp-ross-book-color.indbcp-ross-book-color.indb 1 44/5/13/5/13 88:34:34 AAMM uucp-ross-book-color.indbcp-ross-book-color.indb 2 44/5/13/5/13 88:34:34 AAMM TABLE 1.1 Families Composing 95% of North American Freshwater Fish Species Ranked by the Number of Native Species Number Cumulative Family of species percent Cyprinidae 297 28 Percidae 186 45 Catostomidae 71 51 Poeciliidae 69 58 Ictaluridae 46 62 Goodeidae 45 66 Atherinopsidae 39 70 Salmonidae 38 74 Cyprinodontidae 35 77 Fundulidae 34 80 Centrarchidae 31 83 Cottidae 30 86 Petromyzontidae 21 88 Cichlidae 16 89 Clupeidae 10 90 Eleotridae 10 91 Acipenseridae 8 92 Osmeridae 6 92 Elassomatidae 6 93 Gobiidae 6 93 Amblyopsidae 6 94 Pimelodidae 6 94 Gasterosteidae 5 95 source: Compiled primarily from Mayden (1992), Nelson et al. (2004), and Miller and Norris (2005). uucp-ross-book-color.indbcp-ross-book-color.indb 3 44/5/13/5/13 88:34:34 AAMM TABLE 3.1 Biogeographic Relationships of Species from a Sample of Fishes from the Ouachita River, Arkansas, at the Confl uence with the Little Missouri River (Ross, pers. observ.) Origin/ Pre- Pleistocene Taxa distribution Source Highland Stoneroller, Campostoma spadiceum 2 Mayden 1987a; Blum et al. 2008; Cashner et al. 2010 Blacktail Shiner, Cyprinella venusta 3 Mayden 1987a Steelcolor Shiner, Cyprinella whipplei 1 Mayden 1987a Redfi n Shiner, Lythrurus umbratilis 4 Mayden 1987a Bigeye Shiner, Notropis boops 1 Wiley and Mayden 1985; Mayden 1987a Bullhead Minnow, Pimephales vigilax 4 Mayden 1987a Mountain Madtom, Noturus eleutherus 2a Mayden 1985, 1987a Creole Darter, Etheostoma collettei 2a Mayden 1985 Orangebelly Darter, Etheostoma radiosum 2a Page 1983; Mayden 1985, 1987a Speckled Darter, Etheostoma stigmaeum 3 Page 1983; Simon 1997 Redspot Darter, Etheostoma artesiae 3 Mayden 1985; Piller et al. -
INTRODUCTION the Orchid Flora of Thailand Is Rather Well Known
THAI FOR. BULL. (BOT.) 43: 24–29. 2015. A new species of the genus Peristylus (Orchidaceae) from southern Thailand HUBERT KURZWEIL1 & PETCH TRIPETCH2 ABSTRACT. A new species of the genus Peristylus Blume is described from Phangnga Province in Peninsular Thailand. On account of its small size, slender habit, lip shape and spur shape the species is very distinct from any other species found in Thailand and neighbouring countries. A morphological description, short notes on the distribution, ecology, phenology and conservation as well as illustrations of the species are provided. KEY WORDS: Orchidaceae, Peristylus, new species, Thailand. INTRODUCTION entire lip. The spur is normally shorter than the ovary and can be cylindric or globular. Differences The Orchid Flora of Thailand is rather well from the related genus Habenaria Willd. are the known compared with some of the surrounding convex and often cushion-like stigmas which are countries, but discoveries of new distribution adnate to the lip base. records or entirely new species continue to be made, indicating that our knowledge of the Thai orchids is far from complete. The Thai species of the genus Peristylus minimus Kurzweil & Tripetch, sp. nov. Peristylus Blume have recently benefi tted from Differs from other species in the region in its taxonomic studies (Seidenfaden, 1977; Kurzweil, small plant size and slender habit, the shallowly 2010, 2011). During fl oristic inventory work plants three-lobed lip and the clavate and deeply bifi d belonging to this genus were found in Phangnga spur. Type: Thailand, Phangnga Province, Sa Nang Province in Peninsular Thailand which differ strikingly Manora Forest Park, on limestone rock, 490 m, 15 from all other species known in mainland SE Asia. -
Celestial Pearl Danio", a New Genus and Species of Colourful Minute Cyprinid Fish from Myanmar (Pisces: Cypriniformes)
THE RAFFLES BULLETIN OF ZOOLOGY 2007 55(1): 131-140 Date of Publication: 28 Feb.2007 © National University of Singapore THE "CELESTIAL PEARL DANIO", A NEW GENUS AND SPECIES OF COLOURFUL MINUTE CYPRINID FISH FROM MYANMAR (PISCES: CYPRINIFORMES) Tyson R. Roberts Research Associate, Smithsonian Tropical Research Institute Email: [email protected] ABSTRACT. - Celestichthys margaritatus, a new genus and species of Danioinae, is described from a rapidly developing locality in the Salween basin about 70-80 km northeast of Inle Lake in northern Myanmar. Males and females are strikingly colouful. It is apparently most closely related to two danioins endemic to Inle, Microrasbora rubescens and "Microrasbora" erythromicron. The latter species may be congeneric with the new species. The new genus is identified as a danioin by specializations on its lower jaw and its numerous anal fin rays. The colouration, while highly distinctive, seems also to be characteristically danioin. The danioin notch (Roberts, 1986; Fang, 2003) is reduced or absent, but the danioin mandibular flap and bony knob (defined herein) are present. The anal fin has iiiSVz-lOV: rays. In addition to its distinctive body spots and barred fins the new fish is distinguished from other species of danioins by the following combination of characters: snout and mouth extremely short; premaxillary with an elongate and very slender ascending process; mandible foreshortened; body deep, with rounded dorsal and anal fins; modal vertebral count 15+16=31; caudal fin moderately rather than deeply forked; principal caudal fin rays 9/8; scales vertically ovoid; and pharyngeal teeth conical, in three rows KEY WORDS. - Hopong; principal caudal fin rays; danioin mandibular notch, knob, and pad; captive breeding. -
Nervilia Cumberlegei (Orchidaceae), a Newly Recorded Orchid from Myanmar
Bull. Natl. Mus. Nat. Sci., Ser. B, 47(1), pp. 41–44, February 22, 2021 Nervilia cumberlegei (Orchidaceae), a Newly Recorded Orchid from Myanmar Myo Min Latt1,2, Byung Bae Park1 and Nobuyuki Tanaka3,* 1 Department of Environment and Forest Resources, College of Agriculture and Life Science, Chungnam National University, Republic of Korea 2 Department of Environmental Economic, Policy and Management, University of Forestry and Environmental Sciences, Yezin, Myanmar 3 Department of Botany, National Museum of Nature and Science, 4–1–1 Amakubo, Tsukuba, Ibaraki 305–0005, Japan *E-mail: [email protected] (Received 6 November 2020; accepted 23 December 2020) Abstract Nervilia cumberlegei (Orchidaceae) is recorded in Myanmar for the first time. A description, locality information and photographs are provided. Thus far N. cumberlegei is known only from Taiwan and Thailand. This discovery in Myanmar represents the western edge of the species distribution. Key words: Burma, section Linervia, Tanintharyi, taxonomy, terrestrial orchid. (Pridgeon et al., 2005; Tang et al., 2018) and Introduction flowers followed by a vegetative stem bearing a Nervilia Comm. ex Gaudich. is commonly single photosynthetic leaf (Niissalo et al., 2020). known as ‘shield orchid’. Most species grow in Nervilia plants have antioxidant and antibacterial forested habitats and are shade-demanders (Gale properties (Ruthisha et al., 2018) and are used as et al., 2018). The genus Nervilia is most diverse traditional medicine. Medicinal orchids are con- in tropical Asia, although it is widely distributed siderably threatened by anthropogenic impacts in the Old World tropics, from Australasia and such as habitat destruction, and illegal collection the South-west Pacific Islands to sub-Saharan for commercial and subsistence uses (Pant et al., Africa (Pettersson, 1991; Gale et al., 2015, 2002; Pant, 2013). -
The AQUATIC DESIGN CENTRE
The AQUATIC DESIGN CENTRE ltd 26 Zennor Road Trade Park, Balham, SW12 0PS Ph: 020 7580 6764 [email protected] PLEASE CALL TO CHECK AVAILABILITY ON DAY Complete Freshwater Livestock (2019) Livebearers Common Name In Stock Y/N Limia melanogaster Y Poecilia latipinna Dalmatian Molly Y Poecilia latipinna Silver Lyre Tail Molly Y Poecilia reticulata Male Guppy Asst Colours Y Poecilia reticulata Red Cap, Cobra, Elephant Ear Guppy Y Poecilia reticulata Female Guppy Y Poecilia sphenops Molly: Black, Canary, Silver, Marble. y Poecilia velifera Sailfin Molly Y Poecilia wingei Endler's Guppy Y Xiphophorus hellerii Swordtail: Pineapple,Red, Green, Black, Lyre Y Xiphophorus hellerii Kohaku Swordtail, Koi, HiFin Xiphophorus maculatus Platy: wagtail,blue,red, sunset, variatus Y Tetras Common Name Aphyocarax paraguayemsis White Tip Tetra Aphyocharax anisitsi Bloodfin Tetra Y Arnoldichthys spilopterus Red Eye Tetra Y Axelrodia riesei Ruby Tetra Bathyaethiops greeni Red Back Congo Tetra Y Boehlkea fredcochui Blue King Tetra Copella meinkeni Spotted Splashing Tetra Crenuchus spilurus Sailfin Characin y Gymnocorymbus ternetzi Black Widow Tetra Y Hasemania nana Silver Tipped Tetra y Hemigrammus erythrozonus Glowlight Tetra y Hemigrammus ocelifer Beacon Tetra y Hemigrammus pulcher Pretty Tetra y Hemigrammus rhodostomus Diamond Back Rummy Nose y Hemigrammus rhodostomus Rummy nose Tetra y Hemigrammus rubrostriatus Hemigrammus vorderwimkieri Platinum Tetra y Hyphessobrycon amandae Ember Tetra y Hyphessobrycon amapaensis Amapa Tetra Y Hyphessobrycon bentosi -
Investigations Into the Presence of Nidoviruses in Pythons Silvia Blahak1, Maria Jenckel2,3, Dirk Höper2, Martin Beer2, Bernd Hoffmann2 and Kore Schlottau2*
Blahak et al. Virology Journal (2020) 17:6 https://doi.org/10.1186/s12985-020-1279-5 RESEARCH Open Access Investigations into the presence of nidoviruses in pythons Silvia Blahak1, Maria Jenckel2,3, Dirk Höper2, Martin Beer2, Bernd Hoffmann2 and Kore Schlottau2* Abstract Background: Pneumonia and stomatitis represent severe and often fatal diseases in different captive snakes. Apart from bacterial infections, paramyxo-, adeno-, reo- and arenaviruses cause these diseases. In 2014, new viruses emerged as the cause of pneumonia in pythons. In a few publications, nidoviruses have been reported in association with pneumonia in ball pythons and a tiger python. The viruses were found using new sequencing methods from the organ tissue of dead animals. Methods: Severe pneumonia and stomatitis resulted in a high mortality rate in a captive breeding collection of green tree pythons. Unbiased deep sequencing lead to the detection of nidoviral sequences. A developed RT-qPCR was used to confirm the metagenome results and to determine the importance of this virus. A total of 1554 different boid snakes, including animals suffering from respiratory diseases as well as healthy controls, were screened for nidoviruses. Furthermore, in addition to two full-length sequences, partial sequences were generated from different snake species. Results: The assembled full-length snake nidovirus genomes share only an overall genome sequence identity of less than 66.9% to other published snake nidoviruses and new partial sequences vary between 99.89 and 79.4%. Highest viral loads were detected in lung samples. The snake nidovirus was not only present in diseased animals, but also in snakes showing no typical clinical signs. -
Orchid Historical Biogeography, Diversification, Antarctica and The
Journal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Orchid historical biogeography, ARTICLE diversification, Antarctica and the paradox of orchid dispersal Thomas J. Givnish1*, Daniel Spalink1, Mercedes Ames1, Stephanie P. Lyon1, Steven J. Hunter1, Alejandro Zuluaga1,2, Alfonso Doucette1, Giovanny Giraldo Caro1, James McDaniel1, Mark A. Clements3, Mary T. K. Arroyo4, Lorena Endara5, Ricardo Kriebel1, Norris H. Williams5 and Kenneth M. Cameron1 1Department of Botany, University of ABSTRACT Wisconsin-Madison, Madison, WI 53706, Aim Orchidaceae is the most species-rich angiosperm family and has one of USA, 2Departamento de Biologıa, the broadest distributions. Until now, the lack of a well-resolved phylogeny has Universidad del Valle, Cali, Colombia, 3Centre for Australian National Biodiversity prevented analyses of orchid historical biogeography. In this study, we use such Research, Canberra, ACT 2601, Australia, a phylogeny to estimate the geographical spread of orchids, evaluate the impor- 4Institute of Ecology and Biodiversity, tance of different regions in their diversification and assess the role of long-dis- Facultad de Ciencias, Universidad de Chile, tance dispersal (LDD) in generating orchid diversity. 5 Santiago, Chile, Department of Biology, Location Global. University of Florida, Gainesville, FL 32611, USA Methods Analyses use a phylogeny including species representing all five orchid subfamilies and almost all tribes and subtribes, calibrated against 17 angiosperm fossils. We estimated historical biogeography and assessed the