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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 -
Biogeography of the Monocotyledon Astelioid Clade (Asparagales): a History of Long-Distance Dispersal and Diversification with Emerging Habitats
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2021 Biogeography of the monocotyledon astelioid clade (Asparagales): A history of long-distance dispersal and diversification with emerging habitats Birch, Joanne L ; Kocyan, Alexander Abstract: The astelioid families (Asteliaceae, Blandfordiaceae, Boryaceae, Hypoxidaceae, and Lanari- aceae) have centers of diversity in Australasia and temperate Africa, with secondary centers of diversity in Afromontane Africa, Asia, and Pacific Islands. The global distribution of these families makes this an excellent lineage to test if current distribution patterns are the result of vicariance or long-distance dispersal and to evaluate the roles of tertiary climatic and geological drivers in lineage diversification. Sequence data were generated from five chloroplast regions (petL-psbE, rbcL, rps16-trnK, trnL-trnLF, trnS-trnSG) for 104 ingroup species sampled across global diversity. The astelioid phylogeny was inferred using maximum parsimony, maximum likelihood, and Bayesian inference methods. Divergence dates were estimated with a relaxed clock applied in BEAST. Ancestral ranges were reconstructed in ’BioGeoBEARS’ applying the corrected Akaike information criterion to test for the best-fit biogeographic model. Diver- sification rates were estimated in Bayesian Analysis of Macroevolutionary Mixtures [BAMM]. Astelioid relationships were inferred as Boryaceae(Blandfordiaceae(Asteliaceae(Hypoxidaceae plus Lanariaceae))). The crown astelioid node was dated to the Late Cretaceous (75.2 million years; 95% highest posterior densities interval 61.0-90.0 million years) with an inferred Eastern Gondwanan origin. However, aste- lioid speciation events have not been shaped by Gondwanan vicariance. Rather long-distance dispersal since the Eocene is inferred to account for current distributions. -
(Asparagaceae) by Female Cecidomyiidi Flies: Larvae of Pollinator Feed on Fertile Pollen in Anthers of Anthetic Bisexual Flowers 1
American Journal of Botany 101 ( 9 ): 1519 – 1531 , 2014 . P OLLINATION OF VIETNAMESE A SPIDISTRA XUANSONENSIS (ASPARAGACEAE) BY FEMALE CECIDOMYIIDI FLIES: LARVAE OF POLLINATOR FEED ON FERTILE POLLEN IN ANTHERS OF 1 ANTHETIC BISEXUAL FLOWERS N IKOLAY A . V ISLOBOKOV 2,3,8 , T ATIANA V. G ALINSKAYA 4 , G ALINA V. D EGTJAREVA 5 , C ARMEN M . V ALIEJO-ROMAN 6 , T AHIR H. SAMIGULLIN 6 , A NDREY N. KUZNETSOV 3,7 , AND D MITRY D. SOKOLOFF 2 2 Department of Higher Plants, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia; 3 Joint Russian-Vietnamese Tropical Scientifi c and Technological Center, CauGiay, Hanoi, Vietnam; 4 Department of Entomology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia; 5 Botanical Garden, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia; 6 A.N. Belozersky Institute of Physico-Chemical Biology, M.V. Lomonosov Moscow State University, Moscow 119234, Russia; and 7 A.N. Severtsov Institute of Ecology and Evolution of Russian Academy of Sciences, Moscow 119071, Russia • Premise of the study: Aspidistra is a species-rich, herbaceous monocot genus of tropical Southeast Asia. Most species are re- cently discovered and apparently endangered, though virtually nothing is known about their biology. Species of the genus are primarily distinguished using fl ower morphology, which is enormously diverse. However, the pollination process has not been directly observed in the center of diversity of the genus (N Vietnam and S China). Indirect and partly direct data on the only widely cultivated species of the genus (A. elatior ) placed it among angiosperms with the most unusual pollination biology, though these data are highly controversial, suggesting pollen transfer by mollusks, crustaceans, fl ies, or possibly tiny soil in- vertebrates such as collembolans. -
Evolutionary History of the Monocot Flower1
618 Annals of the Missouri Botanical Garden EVOLUTIONARY HISTORY OF Margarita V. Remizowa, 2 Dmitry D. Sokoloff, 2 and Hydatellaceae. Indeed, detailed descriptions of TRIMEROUS -PENTACYCLIC FLOWERS the waterlily female gametophyte, which closely 1 and P. J. Rudall 3 THE MONOCOT FLOWER resembles that of Hydatellaceae (Friedman, 2008; The typical monocot groundplan consists of six Rudall et al., 2008), were published relatively tepals in two alternating whorls (generally not recently (Winter & Shamrov, 1991a, b; Williams & differentiated into petals and sepals), six stamens in two alternating whorls, and three carpels (i.e., ABSTRACT Friedman, 2002; Friedman & Williams, 2003), and an earlier report of monocot-type sieve element trimerous-pentacyclic flowers). Sectorial differentia- This paper reviews monocot flower structure and gynoecium development and evaluates these data to clarify the plastids in Hydatellaceae is not supported in a new tion in monocot flowers was discussed in detail by evolutionary history of the monocot flower. Despite some congruence between molecular and morphological data regarding the investigation (Tratt et al., 2009). Endress (1995), who noted that this arrangement is delimitation and phylogenetic relationships of monocots, there is currently no universally accepted view on the morphology of more readily achievable in trimerous than in pentam- the ancestral monocot flower, reflecting a high degree of parallelism in monocot floral evolution. We focus on two character However, despite some congruence between molec- suites that encompass the key features of monocot flowers: (1) the typical monocot groundplan of trimerous-pentacyclic ular and morphological data on the delimitation and erous flowers because the sectors are broader. In flowers, and (2) a character suite related to carpel fusion, including postgenital fusion between carpels and the presence of phylogenetic relationships of monocots, their floral many monocots, tepals and stamens inserted on the septal nectaries. -
ASBS Newsletter 124
No.No. 124 124 SeptemberSeptember 20052005 PPrice:rice: $5.00$5.00 Australian Systematic Botany Society Newsletter 124 (September 2005) AUSTRALIAN SYSTEMATIC BOTANY SOCIETY INCORPORATED Council President Vice President John Clarkson Darren Crayn Centre for Tropical Agriculture Royal Botanic Gardens Sydney PO Box 1054 Mrs Macquaries Road MAREEBA, Queensland 4880 SYDNEY NSW 2000 tel: (07) 4048 4745 tel: (02) 9231 8111 email: [email protected] email: [email protected] Secretary Treasurer Brendan Lepschi Anna Monro Centre for Plant Biodiversity Research Centre for Plant Biodiversity Research Australian National Herbarium Australian National Herbarium GPO Box 1600 GPO Box 1600 CANBERRA ACT 2601 CANBERRA ACT 2601 tel: (02) 6246 5167 tel: (02) 6246 5472 email: [email protected] email: [email protected] Councillor Councillor Kirsten Cowley Marco Duretto Centre for Plant Biodiversity Research Tasmanian Herbarium Australian National Herbarium Private Bag 4 GPO Box 1600, CANBERRA ACT 2601 HOBART, Tasmania 7001 tel: (02) 6246 5024 tel.: (03) 6226 1806 email: [email protected] email: [email protected] Other Constitutional Bodies Public Officer Hansjörg Eichler Research Committee Kirsten Cowley Barbara Briggs Centre for Plant Biodiversity Research Rod Henderson Australian National Herbarium Betsy Jackes (Contact details above) Tom May Chris Quinn Chair: Vice President (ex officio) Affiliate Society Papua New Guinea Botanical Society ASBS Web site www.anbg.gov.au/asbs Webmaster: Murray Fagg Centre for Plant Biodiversity Research Australian National Herbarium Email: [email protected] Loose-leaf inclusions with this issue • Notice of Annual General Meeting for 2006 and proposed changes to ASBS constitution Publication dates of previous issue Austral.Syst.Bot.Soc.Nsltr 123 (June 2005 issue) Hardcopy: 15th July 2005; ASBS Web site: 18th July 2005 Australian Systematic Botany Society Newsletter 124 (September 2005) ASBS Inc. -
1998 WWF South East Queensland Rainforest Recovery Conference Proceedings
Rainforest Recovery for the New Millennium Proceedings of the World Wide Fund For Nature 1998 South-East Queensland Rainforest Recovery Conference Rainforest Recovery for the New Millennium Proceedings of the WWF (World Wide Fund For Nature) Australia 1998 South-East Queensland Rainforest Recovery Conference, held at the Tanyalla Conference Centre, Tannum Sands via Gladstone, Queensland, from August 31 to September 4, 1998. Edited by Bruce Boyes, Conference Chairperson and Project Coordinator, WWF South-East Queensland Rainforest Recovery Project. Published by WWF (World Wide Fund For Nature) Australia, GPO Box 528, Sydney, NSW, 2001. © WWF (World Wide Fund For Nature) Australia, Sydney, NSW, 1999. © (authored contributions): Bruce Boyes, Cr. George Creed, Cr. Peter Corones, Jamie Pittock, W.J.F. McDonald, P.A.R. Young, M.A. Watson, Karin Hall, Bruce Tinworth, Steve Fox, Max Roberts, Trudy Townson, Maureen Schmitt. Arnold Rieck, Barrie Craig, Alex Rankin, R. John Hunter, Siobhan Bland, Michael Gregory, Glenda Pickersgill, Graham McDonald, John M. Clarke, Adrian C. Borsboom, Michael Cunningham, Harry B. Hines, D.P.A. Sands, S.E. Scott, Peter O’Reilly (Jnr), Geoffrey C. Smith, Nadya Lees, John Palmer, Don Lynch, Ernie Rider, Dennis Martin, Frank Bowman, Nicholas Cox, Stephen Martin, Alistair Melzer, Joy Brushe, Wayne Houston, Kylie Freebody, Sue Vise, Geoff Edwards, Ian & Cathy Herbert, Carl Binning, Leo Ryan, Nancy Cramond. ISBN 1-875941-12-6 Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without written permission from WWF, GPO Box 528, Sydney, NSW, 2001 or, in the case of authored contributions, from the stated author or authors. -
Approved Conservation Advice for Neoastelia Spectabilis
This Conservation Advice was approved by the Minister / Delegate of the Minister on: 1/10/2008 Approved Conservation Advice (s266B of the Environment Protection and Biodiversity Conservation Act 1999) Approved Conservation Advice for Neoastelia spectabilis This Conservation Advice has been developed based on the best available information at the time this Conservation Advice was approved; this includes existing plans, records or management prescriptions for this species. Description Neoastelia spectabilis, Family Asteliaceae, also known as Silver Sword Lily, is a tufted herb. Leaves are linear with drooping ends, 60–165 cm long and 2.5–6 cm wide, with green and smooth upper surfaces, and silver-white lower surfaces. Flowers are white and clustered onto numerous branches off a central stem 25–70 cm long. Fruit are pale green berries, 10–15 mm in diameter, with small black seeds (Williams, 1987; Harden, 1993; DECC, 2005a). Conservation Status Neoastelia spectabilis is listed as vulnerable. This species is eligible for listing as vulnerable under the Environment Protection and Biodiversity Conservation Act 1999 (Cwlth) (EPBC Act) as, prior to the commencement of the EPBC Act, it was listed as vulnerable under Schedule 1 of the Endangered Species Protection Act 1992 (Cwlth). N. spectabilis is also listed as vulnerable under the Threatened Species Conservation Act 1995 (NSW). Distribution and Habitat Neoastelia spectabilis is known from small populations within the New England National Park and Bellinger River State Forest, on the eastern edge of the New England Tablelands, NSW. Population numbers are unknown. Neoastelia spectabilis occurs in Nothofagus moorei forest at altitudes of 900–1150 m, either in rock crevices on steep slopes adjacent to waterfalls, or in seepage areas on steep rocky slopes (Williams, 1987; Harden, 1993; DECC, 2005a). -
Forests of East Australia: the 35Th Biodiversity Hotspot
Chapter 16 Forests of East Australia: The 35th Biodiversity Hotspot Kristen J. Williams, Andrew Ford, Dan F. Rosauer, Naamal De Silva, Russell Mittermeier, Caroline Bruce, Frank W. Larsen, and Chris Margules Abstract The newly identified “Forests of East Australia” Global High Bio- diversity Hotspot corresponds with two World Wildlife Fund (WWF) Ecoregions: the Eastern Australian Temperate Forests and Queensland’s Tropical Rain forests. The region contains more than 1,500 endemic vascular plants, meeting the criterion for global biodiversity significance, and more than 70% of natural areas have been cleared or degraded, meeting the criterion for a hotspot. The hotspot, although covering a large latitudinal range (15.5–35.6 South), has a predominantly summer rainfall pattern with increasing rainfall seasonality northwards into tropical areas of north Queensland. It covers large tracts of elevated tablelands and drier inland slopes, particularly in New South Wales, where it extends inland beyond the New England Tablelands and the Great Dividing Range. Varied soils result in a mosaic pattern of vegetation. Sclerophyllous communities dominated by Australia’s iconic plant, the gum-tree (Eucalyptus species), are the most prevalent vegetation type. Significant areas of rain forest exist throughout the region, much of which has persisted continuously since Gondwanan times, providing a rich living record of evolution over more than 100 million years. The human population of the hotspot as of 2006 was over nine million, with a population density of 36 people per square kilometer, mainly concentrated along the coast. About 18% of the land area is under some form of formal protection for its natural values. -
Evolution and Expression Patterns of TCP Genes in Asparagales
ORIGINAL RESEARCH published: 17 January 2017 doi: 10.3389/fpls.2017.00009 Evolution and Expression Patterns of TCP Genes in Asparagales Yesenia Madrigal 1, Juan F. Alzate 2 and Natalia Pabón-Mora 1* 1 Facultad de Ciencias Exactas y Naturales, Instituto de Biología, Universidad de Antioquia, Medellín, Colombia, 2 Centro Nacional de Secuenciación Genómica, Sede de Investigación Universitaria, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia CYCLOIDEA-like genes are involved in the symmetry gene network, limiting cell proliferation in the dorsal regions of bilateral flowers in core eudicots. CYC-like and closely related TCP genes (acronym for TEOSINTE BRANCHED1, CYCLOIDEA, and PROLIFERATION CELL FACTOR) have been poorly studied in Asparagales, the largest order of monocots that includes both bilateral flowers in Orchidaceae (ca. 25.000 spp) and radially symmetrical flowers in Hypoxidaceae (ca. 200 spp). With the aim of assessing TCP gene evolution in the Asparagales, we isolated TCP-like genes from publicly available databases and our own transcriptomes of Cattleya trianae (Orchidaceae) and Hypoxis decumbens (Hypoxidaceae). Our matrix contains 452 sequences representing the three major clades of TCP genes. Besides the previously identified CYC specific core eudicot duplications, our ML phylogenetic analyses recovered an early CIN-like duplication predating all angiosperms, two CIN-like Asparagales-specific duplications and a duplication prior to the diversification of Orchidoideae and Epidendroideae. Edited by: In addition, we provide evidence of at least three duplications of PCF-like genes in José M. Romero, University of Seville, Spain Asparagales. While CIN-like and PCF-like genes have multiplied in Asparagales, likely Reviewed by: enhancing the genetic network for cell proliferation, CYC-like genes remain as single, Jill Christine Preston, shorter copies with low expression. -
Fleshy Fruits in Liliflorous Monocots Finn N
Aliso: A Journal of Systematic and Evolutionary Botany Volume 22 | Issue 1 Article 11 2006 Fleshy Fruits in Liliflorous Monocots Finn N. Rasmussen University of Copenhagen Signe Frederikson University of Copenhagen Bo Johansen University of Copenhagen Lise Bolt Jørgenson University of Copenhagen Gitte Peterson University of Copenhagen; Natural History Musem of Denmark Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Rasmussen, Finn N.; Frederikson, Signe; Johansen, Bo; Jørgenson, Lise Bolt; and Peterson, Gitte (2006) "Fleshy Fruits in Liliflorous Monocots," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 22: Iss. 1, Article 11. Available at: http://scholarship.claremont.edu/aliso/vol22/iss1/11 Aliso 22, pp. 135-147 © 2006, Rancho Santa Ana Botanic Garden FLESHY FRUITS IN LILIIFLOROUS MONOCOTS FINN N. RASMUSSEN, 1 SIGNE FREDERIKSEN, Bo JOHANSEN, LISE BOLT J0RGENSEN, GITTE PETERSEN,2 AND OLE SEBERG2 Biological Institute, University of Copenhagen, Gothersgade 140, DK-1 /23 Copenhagen K, Denmark 1Corresponding author ([email protected]) ABSTRACT Fleshy fruits occur in several monocot orders and families, and it is generally assumed that they have been derived from capsular fruits many times during the evolution of monocot lineages. Huber hypothesized in 1969 that most capsules in Asparagales are derived secondarily from berries and that this transformation was correlated with the evolution of phytomelan-coated seeds, a pivotal character in his circumscription of Asparagales as part of reclassifying Liliaceae s.l. Dahlgren and co-workers suggested several parallel derivations and "reversals" in this character, e.g., the transformation se quence trifollicular fruits __.. -
World Heritage and Associative Natural Values of the Central Eastern Rainforest Reserves of Australia
WORLD HERITAGE AND ASSOCIATIVE NATURAL VALUES OF THE CENTRAL EASTERN RAINFOREST RESERVES OF AUSTRALIA R. John Hunter NSW National Parks and Wildlife Service Originally published June 2003 Revised December 2004 i By channels of coolness the echoes are calling And down the dim gorge I hear the creek falling It lives in the mountains where mosses and sedges Touch with their beauty the bank and the ledges Through breaks in the cedar and sycamore bowers Struggles the light that is sweet to the flowers; And softer than slumber and sweeter than singing, The notes of the bell-birds are running and ringing. ‘Bellbirds’ by Henry Kendall ii EXECUTIVE SUMMARY This report reviews the World Heritage values of the Central Eastern Rainforest Reserves of Australia (CERRA) World Heritage Area. The assessment of World Heritage values is based on the criteria for World Heritage listing. CERRA was inscribed on the World Heritage list as a site with outstanding universal significance in terms of its natural heritage. The property satisfied three of the four possible criteria for the listing of a natural property. The criteria for World Heritage listing have changed since the listing of CERRA, but this has little effect on this review because the changes generally amount to a re-arrangement of themes within the criteria for which the property is listed. This review identifies attributes, which demonstrate the values under each criterion. Threats to these attributes are identified and the condition of integrity is assessed. World Heritage values Criterion (i): ‘be outstanding examples representing major stages of Earth’s history, including the record of life, significant on-going geological processes in the development of landforms, or significant geomorphic or physiographic features.’ Values related to this criterion and key attributes supporting these values are as follows. -
The Victorian Naturalist
The Victorian Naturalist Volume 112(1)1995 February Conservation of Invertebrates Published by The Field Naturalists Club of Victoria since 1884 Notice of the Annual General Meeting The Annual General Meeting of the Field Naturalists Club of Victoria will be held at the Herbarium, Birdwood Avenue, South Yarra, 8 pm, Monday, 10 April 1995. Agenda 1. Confirmation of the minutes of the previous Annual General Meeting held 11 April 1994. 2. Receipt and adoption of Annual Report for the year ended 3 1 December 1 994. Receipt and adoption of Financial Statements and associated reports. Election of Members of Council. Election of Office Bearers. Appointment of Auditors (remuneration to be determined by Council). Any other business of which proper notice has been given in accordance with the Articles of Association. 8. President's Address. Election of Councillors and Office Bearers All members of Council and Office Bearers retire annually but arc eligible for re-election. Nominations by two financial members of the Club are required for the following positions: Council President 2 Vice-Presidents Secretary Treasurer Six other members Office Bearers Assistant Treasurer Excursion Secretary Editor (The Victorian Naturalist) Sales Officer (Books) Editor (The Newsletter) Sales Officer (The Victorian Naturalist) Librarian Activities Co-ordinator Conservation Coordinator Publicity Officer membCrS are Ufged t0 ensure its fimn^hP k °W"S viability by 6 P nS Wit h ° Pers ns Wi,lin£ and abIc to contribute to vftie unoSr nT° , g rUl W°rk of lhc Club Arrange a nomination yourself ' for S^^SSor encourage some otherT appropriate member to be nominated Nominations should be in the hands of the Secretary before the Annual General Nomination Forms are available from the Secretary, Geol, Paterson, 5716436.