2019 January February Caleyi 2.Cdr
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Actes Du 15E Colloque Sur Les Orchidées De La Société Française D’Orchidophilie
Cah. Soc. Fr. Orch., n° 7 (2010) – Actes 15e colloque de la Société Française d’Orchidophilie, Montpellier Actes du 15e colloque sur les Orchidées de la Société Française d’Orchidophilie du 30 mai au 1er juin 2009 Montpellier, Le Corum Comité d’organisation : Daniel Prat, Francis Dabonneville, Philippe Feldmann, Michel Nicole, Aline Raynal-Roques, Marc-Andre Selosse, Bertrand Schatz Coordinateurs des Actes Daniel Prat & Bertrand Schatz Affiche du Colloque : Conception : Francis Dabonneville Photographies de Francis Dabonneville & Bertrand Schatz Cahiers de la Société Française d’Orchidophilie, N° 7, Actes du 15e Colloque sur les orchidées de la Société Française d’Orchidophilie. ISSN 0750-0386 © SFO, Paris, 2010 Certificat d’inscription à la commission paritaire N° 55828 ISBN 978-2-905734-17-4 Actes du 15e colloque sur les Orchidées de la Société Française d’Orchidophilie, D. Prat et B. Schatz, Coordinateurs, SFO, Paris, 2010, 236 p. Société Française d’Orchidophilie 17 Quai de la Seine, 75019 Paris Cah. Soc. Fr. Orch., n° 7 (2010) – Actes 15e colloque de la Société Française d’Orchidophilie, Montpellier Préface Ce 15e colloque marque le 40e anniversaire de notre société, celle-ci ayant vu le jour en 1969. Notre dernier colloque se tenait il y a 10 ans à Paris en 1999, 10 ans c’est long, 10 ans c’est très loin. Il fallait que la SFO renoue avec cette traditionnelle organisation de colloques, manifestation qui a contribué à lui accorder la place prépondérante qu’elle occupe au sein des orchidophiles français et de la communauté scientifique. C’est chose faite aujourd’hui. Nombreux sont les thèmes qui font l’objet de communications par des intervenants dont les compétences dans le domaine de l’orchidologie ne sont plus à prouver. -
Australian Orchidaceae: Genera and Species (12/1/2004)
AUSTRALIAN ORCHID NAME INDEX (21/1/2008) by Mark A. Clements Centre for Plant Biodiversity Research/Australian National Herbarium GPO Box 1600 Canberra ACT 2601 Australia Corresponding author: [email protected] INTRODUCTION The Australian Orchid Name Index (AONI) provides the currently accepted scientific names, together with their synonyms, of all Australian orchids including those in external territories. The appropriate scientific name for each orchid taxon is based on data published in the scientific or historical literature, and/or from study of the relevant type specimens or illustrations and study of taxa as herbarium specimens, in the field or in the living state. Structure of the index: Genera and species are listed alphabetically. Accepted names for taxa are in bold, followed by the author(s), place and date of publication, details of the type(s), including where it is held and assessment of its status. The institution(s) where type specimen(s) are housed are recorded using the international codes for Herbaria (Appendix 1) as listed in Holmgren et al’s Index Herbariorum (1981) continuously updated, see [http://sciweb.nybg.org/science2/IndexHerbariorum.asp]. Citation of authors follows Brummit & Powell (1992) Authors of Plant Names; for book abbreviations, the standard is Taxonomic Literature, 2nd edn. (Stafleu & Cowan 1976-88; supplements, 1992-2000); and periodicals are abbreviated according to B-P- H/S (Bridson, 1992) [http://www.ipni.org/index.html]. Synonyms are provided with relevant information on place of publication and details of the type(s). They are indented and listed in chronological order under the accepted taxon name. Synonyms are also cross-referenced under genus. -
Species List
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
AUSTRALIAN ORCHID NAME INDEX (27/4/2006) by Mark A. Clements
AUSTRALIAN ORCHID NAME INDEX (27/4/2006) by Mark A. Clements and David L. Jones Centre for Plant Biodiversity Research/Australian National Herbarium GPO Box 1600 Canberra ACT 2601 Australia Corresponding author: [email protected] INTRODUCTION The Australian Orchid Name Index (AONI) provides the currently accepted scientific names, together with their synonyms, of all Australian orchids including those in external territories. The appropriate scientific name for each orchid taxon is based on data published in the scientific or historical literature, and/or from study of the relevant type specimens or illustrations and study of taxa as herbarium specimens, in the field or in the living state. Structure of the index: Genera and species are listed alphabetically. Accepted names for taxa are in bold, followed by the author(s), place and date of publication, details of the type(s), including where it is held and assessment of its status. The institution(s) where type specimen(s) are housed are recorded using the international codes for Herbaria (Appendix 1) as listed in Holmgren et al’s Index Herbariorum (1981) continuously updated, see [http://sciweb.nybg.org/science2/IndexHerbariorum.asp]. Citation of authors follows Brummit & Powell (1992) Authors of Plant Names; for book abbreviations, the standard is Taxonomic Literature, 2nd edn. (Stafleu & Cowan 1976-88; supplements, 1992-2000); and periodicals are abbreviated according to B-P-H/S (Bridson, 1992) [http://www.ipni.org/index.html]. Synonyms are provided with relevant information on place of publication and details of the type(s). They are indented and listed in chronological order under the accepted taxon name. -
Ecological and Genetic Evidence for Cryptic Ecotypes in a Rare Sexually Deceptive Orchid, Drakaea Elastica
Erschienen in: Botanical Journal of the Linnean Society ; 177 (2015), 1. - S. 124-140 https://dx.doi.org/10.1111/boj.12230 Ecological and genetic evidence for cryptic ecotypes in a rare sexually deceptive orchid, Drakaea elastica MYLES H. M. MENZ1,2,3*, RYAN D. PHILLIPS1,2,4, JANET M. ANTHONY1,2, BJÖRN BOHMAN4,5,6, KINGSLEY W. DIXON1,2 and ROD PEAKALL4 1Kings Park and Botanic Garden, West Perth, WA 6005, Australia 2School of Plant Biology, The University of Western Australia, Crawley, WA 6009, Australia 3Institute of Ecology and Evolution, University of Bern, Baltzerstrasse 6, 3012 Bern, Switzerland 4Evolution, Ecology and Genetics, Research School of Biology, The Australian National University, Canberra, ACT 0200, Australia 5Research School of Chemistry, The Australian National University, Canberra, ACT 0200, Australia 6School of Chemistry and Biochemistry, The University of Western Australia, Crawley, WA 6009, Australia Species with specialized ecological interactions present significant conservation challenges. In plants that attract pollinators with pollinator-specific chemical signals, geographical variation in pollinator species may indicate the presence of cryptic plant taxa. We investigated this phenomenon in the rare sexually deceptive orchid Drakaea elastica using a molecular phylogenetic analysis to resolve pollinator species boundaries, pollinator choice experiments and a population genetic study of the orchid. Pollinator choice experiments demonstrated the existence of two ecotypes within D. elastica, each attracting their own related but phylogenetically distinct pollinator species. Despite the presence of ecotypes, population genetic differentiation was low across populations at six microsatellite loci (FST = 0.026). However, Bayesian STRUCTURE analysis revealed two genetic clusters, broadly congruent with the ecotype distributions. -
Checklist of the Orchids of Australia Including Its Island Territories
Checklist of the Orchids of Australia Including its Island Territories Gary N. Backhouse Robert J. Bates Andrew P. Brown Lachlan M. Copeland Second Edition Contents Introduction ........................................................................................ page 1 Australia orchid genera ...................................................................... page 4 Australia species ................................................................................. page 7 Non-native (exotic or weed) species ................................................ page 57 Australia hybrids ............................................................................... page 58 Australian Capital Territory species .................................................. page 69 Australian Capital Territory hybrids .................................................. page 72 New South Wales species ................................................................. page 73 New South Wales hybrids ................................................................. page 86 Northern Territory species ............................................................... page 88 Queensland species .......................................................................... page 89 Queensland hybrids .......................................................................... page 99 South Australia species ................................................................... page 100 South Australia hybrids .................................................................. -
Adaptive Radiation by Intra-Specific Competition for Mnesic Pollinators Michel Baguette, Joris Bertrand, Virginie Marie Stevens, Bertrand Schatz
Why are there so many bee-orchid species? Adaptive radiation by intra-specific competition for mnesic pollinators Michel Baguette, Joris Bertrand, Virginie Marie Stevens, Bertrand Schatz To cite this version: Michel Baguette, Joris Bertrand, Virginie Marie Stevens, Bertrand Schatz. Why are there so many bee-orchid species? Adaptive radiation by intra-specific competition for mnesic pollinators. Biological Reviews, Wiley, 2020, 95 (6), pp.1630-1663. 10.1111/brv.12633. hal-02995675 HAL Id: hal-02995675 https://hal.archives-ouvertes.fr/hal-02995675 Submitted on 27 Apr 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Why are there so many bee-orchid species? Adaptive radiation by intra-specific competition for mnesic pollinators Michel Baguette1,2,*, Joris A. M. Bertrand3, Virginie M. Stevens2, and Bertrand Schatz4 1Institut Systématique, Evolution, Biodiversité (ISYEB), UMR 7205 Museum National d’Histoire Naturelle, CNRS, Sorbonne Université, EPHE, Université des Antilles, F-75005 Paris, France 2Centre National de la Recherche Scientifique and Université Paul Sabatier Toulouse III, SETE Station d’Ecologie Théorique et Expérimentale, UMR 5321, F-09200 Moulis, France 3LGDP (Laboratoire Génome et Développement des Plantes) UMR5096, Université de Perpignan Via Domitia -CNRS, F-66860 Perpignan, France 4CEFE (Centre d'Ecologie Fonctionnelle et Evolutive) UMR 5175, CNRS – Université de Montpellier – Université Paul Valéry – EPHE, 1919 Route de Mende, 34293 Montpellier, France *Author for correspondence at address 1 (E-mail: [email protected]; Tel.:+ 33 6 26 03 38 11). -
Cf. Eria Dacrydium. Syn. E. Biflora. Dactyl-: Used in Combwds., Ref. Daktylos: Digit
dacrydium: ref. dakrydion: a little tear (: tear-drop). cf. Eria dacrydium. syn. E. biflora. dactyl-: used in combwds., ref. daktylos: digit. Mostly taken as: finger, but can also be: toe. For any organ or part alluded to resemble a finger; having, or like a finger. dactyla: digit; finger. cf. Lepanthes dactyla. x Dactyleucorchis: Soó 1966. Noted the name was taken from Dactylorhiza and Leucorchis, as it seemed to have qualities of both. syn. x Pseudorhiza P.F.Hunt. dactylifera: finger + bearing. cf. Eulophia dactylifera. dactyliferum: finger + see -fer: bearing. Alluding to the labellum callus. cf. Oncidium dactyliferum. dactylina: digit; finger + like. cf. Lepanthes dactylina. dactylinum: digit; finger + like. cf. Cryptocentrum peruvianum ssp.dactylinum. Dactylis: see dactyl-: digit; finger, or toe. eg. Dactylis glomerata. x Dactylitella: P.F.Hunt & Summerh.1965. Noted the name was taken from the parents, reported to be a cross of Nigritella x Dactylorhiza. syn. x Dactylodenia. x Dactylocamptis: P.F.Hunt & Summerh.1965. Noted the name is taken from the parents, the result of Anacamptis x Dactylorhiza. ex Switzerland, cf. x Dactylocamptis weberi (M.Schulze) Soó 1966. Noted as monotypic. dactyloceras: finger + horn. cf. Podangis dactyloceras. Dactyloceras: Garay & H.R.Sweet 1968: finger + horn. syn. x Orchidactylorhiza. dactyloclinium: finger + small bed. cf. Epidendrum dactyloclinium. x Dactylodenia: Garay & H.R.Sweet 1966. Noted the name is taken from the parents as it’s a cross of Dactylorhiza x Gymnadenia. eg. x Dactylodenia varia. Listed as ex westn. Europe and Great Britain. dactylodes: digit; finger + resembling. cf. Dendrobium dactylodes. Dactyloglossum: P.F.Hunt & Summerh.1965. Noted the name is taken from the parents as it was thought to be a cross of Coeloglossum x Dactylorhiza. -
Rotating Arrays of Orchid Flowers: a Simple and Effective Method for Studying Pollination in Food Deceptive Plants
diversity Communication Rotating Arrays of Orchid Flowers: A Simple and Effective Method for Studying Pollination in Food Deceptive Plants Daniela Scaccabarozzi 1,2,3,* , Andrea Galimberti 4 , Kingsley W. Dixon 1 and Salvatore Cozzolino 2 1 School of Molecular and Life Sciences, Curtin University, Bentley, WA 6102, Australia; [email protected] 2 Department of Biology, University of Naples Federico II, 80126 Naples, Italy; [email protected] 3 Department of Biodiversity and Attractions, Conservation Kings Park Science, Perth, WA 6005, Australia 4 Dipartimento di Biotecnologie e Bioscienze, Università degli Studi di Milano-Bicocca, 20126 Milano, Italy; [email protected] * Correspondence: [email protected] Received: 27 May 2020; Accepted: 19 July 2020; Published: 22 July 2020 Abstract: Floral deception has been observed in several genera in angiosperms, but is most common in the Orchidaceae. Pollination mechanisms in food deceptive plants are often difficult to assess, as visitation frequency by insects requires numerous hours of field observations to ascertain. Here, for the first time, we describe in detail and validate a simple and effective method that extends previous approaches to increase the effectiveness of pollination studies of food deceptive orchids. We used an orchid of southwest Australia, Diuris brumalis (Orchidaceae), that visually mimics model plants belonging to the genus Daviesia (Faboideae). Arrays of orchid flowers were placed and moved systematically in proximity to model plants, resulting in rapid attraction of the pollinators of D. brumalis. We compared pollinaria removal (as an indicator of pollination success) in naturally growing orchids with pollinaria removal in arrays of orchid flowers in the same sites. -
Pyrazines Attract Catocheilus Thynnine Wasps
Insects 2014, 5, 474-487; doi:10.3390/insects5020474 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Article Pyrazines Attract Catocheilus Thynnine Wasps Bjorn Bohman 1,2,3,* and Rod Peakall 2,3 1 Research School of Chemistry, The Australian National University, Canberra ACT 0200, Australia 2 Research School of Biology, The Australian National University, Canberra ACT 0200, Australia; E-Mail: [email protected] 3 School of Chemistry and Biochemistry, The University of Western Australia, Crawley WA 6009, Australia * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +61-2-61253158. Received: 28 March 2014; in revised form: 10 June 2014 / Accepted: 16 June 2014 / Published: 19 June 2014 Abstract: Five previously identified semiochemicals from the sexually deceptive Western Australian hammer orchid Drakaea livida, all showing electrophysiological activity in gas chromatography–electroantennogram detection (EAD) studies, were tested in field bioassays as attractants for a Catocheilus thynnine wasp. Two of these compounds, (3,5,6-trimethylpyrazin-2-yl)methyl 3-methylbutanoate and 2-(3-methylbutyl)-3,5,6- trimethylpyrazine, were attractive to male wasps. Additionally, the semiochemical 3-(3-methylbutyl)-2,5-dimethylpyrazine, a close analogue to 2-(3-methylbutyl)-3,5,6- trimethylpyrazine, identified in five other species of thynnine wasps, was equally active. The three remaining compounds from D. livida, which were EAD-active against Catocheilus, did not attract the insects in field trials. It is interesting that two structurally similar compounds induce similar behaviours in field experiments, yet only one of these compounds is present in the orchid flower. -
Conservation of a Critically Endangered Orchid Drakaea Elastica Lindl
Conservation of a critically endangered orchid Drakaea elastica Lindl. in the context of nutritional requirements and saprophytic competency of the mycorrhizal fungus and its propagation Siti Nurfadilah This thesis is presented for the degree of Master The University of Western Australia School of Plant Biology 2010 ABSTRACT Drakaea elastica is a critically endangered orchid species that is a habitat specialist of nutrient deficient sandy soil and is dependent on a slow growing mycorrhizal fungus for its nutrient supply in its entire life cycle. In the conservation of this species, understanding the biology and ecology of the mycorrhizal fungus, especially the critical aspects determining the growth and the survival of the mycorrhizal fungus, is essential. The aim of this research is to investigate nutritional requirements, factors limiting the growth and survival, and saprophytic competency of the slow growing mycorrhizal fungus of Drakaea elastica in terms of its capacity to utilize a variety of nutrient sources (C, N, and P) relative to other sympatric faster growing orchid mycorrhizal fungi. The assessment of the capacity of Drakaea elastica mycorrhizal fungus in axenic liquid media containing single nutrient sources showed that it utilised a variety of C, N, and P sources for its growth. A wide range of C sources that Drakaea elastica mycorrhizal fungus required for its growth encompassed glucose and mannose (monosaccharide), cellobiose (disaccharide), cellulose, pectin, starch, and xylan (polysaccharides). The mycorrhizal fungus did not grow on the other C substrates, galactose, rhamnose, arabinose (monosaccharide) and tannic acid (polysaccharides). Ammonium, a variety of amino acids (aspartic acid, glutamic acid, glutamine, asparagine, alanine, arginine, and glycine), and protein BSA are essential N sources required for the growth of Drakaea elastica mycorrhizal fungus. -
Biodiversity Summary: Swan, Western Australia
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations.