Seagrasses from the Philippines
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Karyomorphometric Analysis of Somatic Chromosomes of Selected
Aquatic Botany 133 (2016) 45–49 Contents lists available at ScienceDirect Aquatic Botany jou rnal homepage: www.elsevier.com/locate/aquabot Short communication Karyomorphometric analysis of somatic chromosomes of selected seagrasses of families Hydrocharitaceae and Cymodoceaceae ∗ K. Vanitha, Pon. Subhashini, T. Thangaradjou Centre of Advanced Study in Marine Biology, Faculty of Marine Sciences, Annamalai University, Parangipettai 608 502, Cuddloare, India a r t i c l e i n f o a b s t r a c t Article history: Chromosome numbers of eleven seagrass species were determined. The highest chromosome number Received 22 July 2015 was recorded in Halodule spp. (2n = 44) and the lowest chromosome number was observed in Cymodocea Received in revised form 15 May 2016 rotundata (2n = 14). Chromosome numbers were identical or closely related among different species in Accepted 17 May 2016 the same genus. Karyomorphology was mapped for nine species (Halodule pinifolia, Halodule uninervis, Available online 24 May 2016 Halodule wrightii, Syringodium isoetifolium, Enhalus acoroides, Halophila beccarii, Halophila ovalis (subsp. ovalis and ramamurthiana) Halophila ovata and Thalassia hemprichii). Length of the chromosomes of these Keywords: species varied from 7.81 to 336.63 m while the fundamental arm number ranged between 36 and 85. Marine angiosperms Cytogenetics The results confirm the karyotypic variation among the studied species, indicating that this characteristic Karyomorphology can be used to confirm taxonomic identity of species which are morphologically very similar (eg. Halodule Karyotypic formula spp.). All tested species were diploid, except for Cymodocea rotundata. Indian ocean © 2016 Elsevier B.V. All rights reserved. 1. Introduction bers indicates inconsistency for the same species, however such information would add knowledge on the evolution of the genera Seagrasses represents the paraphyletic group of marine and family in the world. -
"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Global Seagrass Distribution and Diversity: a Bioregional Model ⁎ F
Journal of Experimental Marine Biology and Ecology 350 (2007) 3–20 www.elsevier.com/locate/jembe Global seagrass distribution and diversity: A bioregional model ⁎ F. Short a, , T. Carruthers b, W. Dennison b, M. Waycott c a Department of Natural Resources, University of New Hampshire, Jackson Estuarine Laboratory, Durham, NH 03824, USA b Integration and Application Network, University of Maryland Center for Environmental Science, Cambridge, MD 21613, USA c School of Marine and Tropical Biology, James Cook University, Townsville, 4811 Queensland, Australia Received 1 February 2007; received in revised form 31 May 2007; accepted 4 June 2007 Abstract Seagrasses, marine flowering plants, are widely distributed along temperate and tropical coastlines of the world. Seagrasses have key ecological roles in coastal ecosystems and can form extensive meadows supporting high biodiversity. The global species diversity of seagrasses is low (b60 species), but species can have ranges that extend for thousands of kilometers of coastline. Seagrass bioregions are defined here, based on species assemblages, species distributional ranges, and tropical and temperate influences. Six global bioregions are presented: four temperate and two tropical. The temperate bioregions include the Temperate North Atlantic, the Temperate North Pacific, the Mediterranean, and the Temperate Southern Oceans. The Temperate North Atlantic has low seagrass diversity, the major species being Zostera marina, typically occurring in estuaries and lagoons. The Temperate North Pacific has high seagrass diversity with Zostera spp. in estuaries and lagoons as well as Phyllospadix spp. in the surf zone. The Mediterranean region has clear water with vast meadows of moderate diversity of both temperate and tropical seagrasses, dominated by deep-growing Posidonia oceanica. -
Reassessment of Seagrass Species in the Marshall Islands1
Micronesica 2016-04: 1–10 Reassessment of Seagrass Species in the Marshall Islands 1 ROY T. TSUDA Department of Natural Sciences, Bishop Museum, 1525 Bernice Street, Honolulu, HI 96817, USA [email protected] NADIERA SUKHRAJ U.S. Fish and Wildlife Service, Pacific Islands Fish and Wildlife Office, 300 Ala Moana Blvd., Honolulu, HI 96850, USA [email protected] Abstract—Recent collections of specimens of Halophila gaudichaudii J. Kuo, previously identified as Halophila minor (Zollinger) den Hartog, from Kwajalein Atoll in September 2016 and the archiving of the specimens at BISH validate the previous observation of this seagrass genus in the Marshall Islands. Previously, no voucher specimen was available for examination. Molecular analyses of the Kwajalein Halophila specimens may demonstrate conspecificity with Halophila nipponica J. Kuo with H. gaudichaudii relegated as a synonym. Herbarium specimens of Cymodocea rotundata Ehrenberg and Hemprich ex Ascherson from Majuro Atoll were found at BISH and may represent the only specimens from the Marshall Islands archived in a herbarium. Cymodocea rotundata, however, has been documented in past literature and archived via digital photos in its natural habitat in Majuro. The previous validation of Thalassia hemprichii (Ehrenberg) Ascherson with specimens, and the recent validation of Halophila gaudichaudii and Cymodocea rotundata with specimens reaffirm the low coral atolls and islands of the Marshall Islands as the eastern limit for the three species in the Pacific Ocean. Introduction In a review of the seagrasses in Micronesia, Tsuda et al. (1977) reported nine species of seagrasses in Micronesia with new records of Thalassodendron ciliatum (Forsskål) den Hartog from Palau, and Syringodium isoetifolium (Ascherson) Dandy and Cymodocea serrulata (R. -
Karyotype Variations in Seagrass (Halodule Wrightii Ascherson¬タヤ
Aquatic Botany 136 (2017) 52–55 Contents lists available at ScienceDirect Aquatic Botany journal homepage: www.elsevier.com/locate/aquabot Short communication Karyotype variations in seagrass (Halodule wrightii Ascherson—Cymodoceaceae) a b,∗ a Silmar Luiz da Silva , Karine Matos Magalhães , Reginaldo de Carvalho a Graduate Program in Botany—PPGB and Cytogenetic Plant Laboratory of the Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, CEP: 52171-900, Recife, Pernambuco, Brazil b Aquatic Ecosystems Laboratory of the Federal Rural University of Pernambuco, Rua Dom Manoel de Medeiros, s/n, Dois Irmãos, CEP: 52171-900, Recife, Pernambuco, Brazil a r t i c l e i n f o a b s t r a c t Article history: Karyotype variations in plants are common, but the results of cytological studies of some seagrasses Received 26 June 2015 remain unclear. The nature of the variation is not clearly understood, and the basic chromosomal num- Received in revised form 5 August 2016 ber has still not been established for the majority of the species. Here, we describe karyotype variations in Accepted 15 September 2016 the seagrass Halodule wrightii, and we suggest potentially causative mechanisms involving cytomixis and Available online 16 September 2016 B chromosomes. We prepared slides using the squashing technique followed by conventional Giemsa and C-banding, and silver nitrate and a CMA/DAPI staining. Based on intraspecific analysis, the diploid chromo- Keywords: some number of H. wrightii exhibited a variation from 2n = 24 to 2n = 39; 2n = 38 was the most frequent. In Cytomixis Seagrass general, we characterized the karyotype as an asymmetrical, semi-reticulated interphase nucleus with a chromosomally uniform condensation pattern. -
The Sea-Grasses of Brazil Ligulate, Linear, Leaf-Tip
Acta Bot. Need. October 512-516 21(5), 1972, p. The sea-grasses of Brazil C. den Hartog Rijksherbarium, Leiden There is still hardly anything known aboutthe occurrence of sea-grasses in South America. The number of records is extremely small. Therefore, one wonders whether these plants are extremely rare or absent along long stretches of coast, whether it is that have been overlooked or just they by botanists. It seems that the latterapplies to the coast of Brazil, from where up to nowonly two collections had been recorded (Setchell 1934; den Hartog 1970). Thanks to the active, gratefully acknowledged co-operation of Dr. Liliane Forneris (Universidade de Sao Paulo) I received a number of sea-grasses from several places along the Brazilian coast. I am also indebted to Dr. Emilia Santos (Museu Nacional, Rio de Janeiro) and Dr. Graziela M. Barroso (Jardim Botanico, Rio de Janeiro) for and sending me a specimen a photograph, respectively, of Halophila decipiens. Further, I am grateful to Dr. V. J. H. de Jilovice de Sternberg (Com- panhia ‘Algimar’, Rio de Janeiro) for his co-operation in obtaining material. At present there are 5 species now known from Brazil. KEY TO THE SEA-GRASSES OF BRAZIL 1. Leaves with 3 Tannin cells ligulate, linear, nerves. present. 2. Leaf-tip bicuspidate; leaves Va-l mm wide 1. Halodule wrightii obtuse with 2. Leaf-tip or emarginate, very faintly developed lateral teeth, or without such teeth; leaves wider than 1 mm. 3. Leaf-tip emarginate 2. Halodule emarginata 3. Leaf-tip obtuse 3. Halodule lilianeae 1. -
Flowering and Seed Production in the Subtropical Seagrass, Halodule Wrightii (Shoal Grass)
University of Texas Rio Grande Valley ScholarWorks @ UTRGV Biology Faculty Publications and Presentations College of Sciences 5-2016 Flowering and seed production in the subtropical seagrass, Halodule wrightii (shoal grass) Joseph L. Kowalski The University of Texas Rio Grande Valley Hudson R. DeYoe The University of Texas Rio Grande Valley Follow this and additional works at: https://scholarworks.utrgv.edu/bio_fac Part of the Biology Commons Recommended Citation Kowalski, Joseph L. and DeYoe, Hudson R.. "Flowering and seed production in the subtropical seagrass, Halodule wrightii (shoal grass)" Botanica Marina, vol. 59, no. 2-3, 2016, pp. 193-199. https://doi.org/ 10.1515/bot-2015-0099 This Article is brought to you for free and open access by the College of Sciences at ScholarWorks @ UTRGV. It has been accepted for inclusion in Biology Faculty Publications and Presentations by an authorized administrator of ScholarWorks @ UTRGV. For more information, please contact [email protected], [email protected]. DE GRUYTER Botanica Marina 2016; 59(2-3): 193–199 Short communication Joseph L. Kowalski* and Hudson R. DeYoe Flowering and seed production in the subtropical seagrass, Halodule wrightii (shoal grass) DOI 10.1515/bot-2015-0099 and Kowalski 2014). Halodule wrightii Ascherson (shoal Received 26 November, 2015; accepted 14 April, 2016; online first 25 grass) did not experience overall decline and remains an May, 2016 abundant and ecologically important seagrass that often grows in disturbed sediments (Pulich 1982). Reproduc- Abstract: Reproductive structures of the seagrass, tive structures of H. wrightii have been found from Brazil, Halodule wrightii Ascherson (shoal grass) are cryptic several localities along the Gulf of Mexico and Caribbean and ephemeral, but were found on several occasions at Sea and the east coast of North America (Table 1). -
Halodule in Bermuda
THE SEAGRASS HALODULE IN BERMUDA J.M. Bilewitch1, K.A. Coates1, S.A. Manuel1, J.W. Fourqurean2, W.J. Kenworthy3 1DEPT OF CONSERVATION SERVICES, BDA; 2FLORIDA INTERNATIONAL UNIV, MIAMI, USA; 3NOAA, BEAUFORT, NC USA Introduction Results Comprehensive benthic surveys done between 2006 and 2009 show that Halodule in The seagrass Halodule bermudensis den Hartog 1964 was described as an endemic Bermuda is a widespread, shallow-water organism found both inshore and at offshore Bermudian species. (See type location in Fig. 4) reef-associated sites (Figs 4 & 5). When sediment conditions and light levels are adequate for supporting seagrass beds, the density of Halodule in the beds is probably controlled by nutrient availability. Species Halodule sp Common name shoal grass Maximum 12.5 m depth Light 25-65% requirement (median 50%) Prevalence common (11.1%) flowers in May- Reproduction July; female only Fig. 1. Leaf tips (above) and original specimen (right) Fig. 4. Present distribution of Halodule in of H. bermudensis. Scale for tips = 1 mm. Bermuda; sample locations for genetic and leaf tip material ↓; and type location for H. Fig. 5. Ecology of Halodule in Bermuda. However, specimens of Halodule collected in Bermuda are more frequently referred to bermudensis Halodule wrightii Ascherson. The taxonomic question of “what is H. wrightii?” is complicated by such things as the presence of two very distinct forms of Halodule on the herbarium All leaf tips examined had a distinct mid-projection and two small lateral teeth; blade width sheets of the type material. Den Hartog (1964), among others, recognized that the original about 1 to 1.4 mm (Figs 6 & 7). -
Of Abu Dhabi Emirate, United Arab Emirates MARINE and COASTAL ENVIRONMENTS of ABU DHABI EMIRATE, UNITED ARAB EMIRATES
of Abu Dhabi Emirate, United Arab Emirates MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . II of Abu Dhabi Emirate, United Arab Emirates Page . III MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . IV MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES H. H. Sheikh Khalifa bin Zayed Al Nahyan President of the United Arab Emirates Page . V MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . VI MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES H. H. Sheikh Mohammed bin Zayed Al Nahyan Crown Prince of Abu Dhabi, Deputy Supreme Commander of the UAE Armed Forces Page . VII MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES Page . VIII MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES H. H. Sheikh Hamdan bin Zayed Al Nahyan Deputy Prime Minister Page . IX MARINE AND COASTAL ENVIRONMENTS OF ABU DHABI EMIRATE, UNITED ARAB EMIRATES s\*?*c*i]j6.%;M"%&9+~)#"$*&ENL`\&]j6. =';78G=%1?%&'12= !"##$" 9<8*TPEg-782#,On%O)6=]KL %&'( )*+,-. 2#,On#X%3G=FON&$4#*.%&9+~)#"$*&XNL %?)#$*&E, &]1TL%&9+%?)':5=&4O`(.#`g-78 %!/ اﻷوراق اﻟﻘﻄﺎﻋﻴﺔ fJT=V-=>?#Fk9+*#$'&= /%*?%=*<(/8>OhT7.F 012(.%34#56.%-78&9+:;(<=>=?%@8'-/ABC $L#01i%;1&&!580.9,q@EN(c D)=EF%3G&H#I7='J=:KL)'MD*7.%&'-(8=';78G=NO D)$8P#"%;QI8ABCRI7S;<#D*T(8%.I7)=U%#$#VW'.X JG&Bls`ItuefJ%27=PE%u%;QI8)aEFD)$8%7iI=H*L YZZ[\&F]17^)#G=%;/;!N_-LNL`%3;%87VW'.X NL]17~Is%1=fq-L4"#%;M"~)#"G=,|2OJ*c*TLNLV(ItuG= )aE0@##`%;Kb&9+*c*T(`d_-8efJG=g-78012 -
Background Document for Cymodocea Meadows
Background Document for Cymodocea meadows Biodiversity Series 2010 OSPAR Convention Convention OSPAR The Convention for the Protection of the La Convention pour la protection du milieu Marine Environment of the North-East Atlantic marin de l'Atlantique du Nord-Est, dite (the “OSPAR Convention”) was opened for Convention OSPAR, a été ouverte à la signature at the Ministerial Meeting of the signature à la réunion ministérielle des former Oslo and Paris Commissions in Paris anciennes Commissions d'Oslo et de Paris, on 22 September 1992. The Convention à Paris le 22 septembre 1992. La Convention entered into force on 25 March 1998. It has est entrée en vigueur le 25 mars 1998. been ratified by Belgium, Denmark, Finland, La Convention a été ratifiée par l'Allemagne, France, Germany, Iceland, Ireland, la Belgique, le Danemark, la Finlande, Luxembourg, Netherlands, Norway, Portugal, la France, l’Irlande, l’Islande, le Luxembourg, Sweden, Switzerland and the United Kingdom la Norvège, les Pays-Bas, le Portugal, and approved by the European Community le Royaume-Uni de Grande Bretagne and Spain. et d’Irlande du Nord, la Suède et la Suisse et approuvée par la Communauté européenne et l’Espagne. Acknowledgement This document has been prepared by Beatriz Ayala for WWF as lead party. Photo acknowledgement Cover page: © Alexandra H Cunha, LIFE-BIOMARES 2 Contents Background Document for Cymodocea meadows .............................................................................4 Executive Summary ...........................................................................................................................4 -
Kimberley Marine Biota. Historical Data: Marine Plants
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 84 045–067 (2014) DOI: 10.18195/issn.0313-122x.84.2014.045-067 SUPPLEMENT Kimberley marine biota. Historical data: marine plants John M. Huisman1,2* and Alison Sampey3 1 Western Australian Herbarium, Science Division, Department of Parks and Wildlife, Locked Bag 104, Bentley DC, Western Australian 6983, Australia. 2 School of Veterinary and Life Sciences, Murdoch University, Murdoch, Western Australian 6150, Australia. 3 Department of Aquatic Zoology, Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australian 6986, Australia. * Email: [email protected] ABSTRACT – Here, we document 308 species of marine flora from the Kimberley region of Western Australia based on collections held in the Western Australian Herbarium and on reports on marine biodiversity surveys to the region. Included are 12 species of seagrasses, 18 species of mangrove and 278 species of marine algae. Seagrasses and mangroves in the region have been comparatively well surveyed and their taxonomy is stable, so it is unlikely that further species will be recorded. However, the marine algae have been collected and documented only more recently and it is estimated that further surveys will increase the number of recorded species to over 400. The bulk of the marine flora comprised widespread Indo-West Pacific species, but there were also many endemic species with more endemics reported from the inshore areas than the offshore atolls. This number also will increase with the description of new species from the region. Collecting across the region has been highly variable due to the remote location, logistical difficulties and resource limitations. -
Rare Plants of Louisiana
Rare Plants of Louisiana Agalinis filicaulis - purple false-foxglove Figwort Family (Scrophulariaceae) Rarity Rank: S2/G3G4 Range: AL, FL, LA, MS Recognition: Photo by John Hays • Short annual, 10 to 50 cm tall, with stems finely wiry, spindly • Stems simple to few-branched • Leaves opposite, scale-like, about 1mm long, barely perceptible to the unaided eye • Flowers few in number, mostly born singly or in pairs from the highest node of a branchlet • Pedicels filiform, 5 to 10 mm long, subtending bracts minute • Calyx 2 mm long, lobes short-deltoid, with broad shallow sinuses between lobes • Corolla lavender-pink, without lines or spots within, 10 to 13 mm long, exterior glabrous • Capsule globe-like, nearly half exerted from calyx Flowering Time: September to November Light Requirement: Full sun to partial shade Wetland Indicator Status: FAC – similar likelihood of occurring in both wetlands and non-wetlands Habitat: Wet longleaf pine flatwoods savannahs and hillside seepage bogs. Threats: • Conversion of habitat to pine plantations (bedding, dense tree spacing, etc.) • Residential and commercial development • Fire exclusion, allowing invasion of habitat by woody species • Hydrologic alteration directly (e.g. ditching) and indirectly (fire suppression allowing higher tree density and more large-diameter trees) Beneficial Management Practices: • Thinning (during very dry periods), targeting off-site species such as loblolly and slash pines for removal • Prescribed burning, establishing a regime consisting of mostly growing season (May-June) burns Rare Plants of Louisiana LA River Basins: Pearl, Pontchartrain, Mermentau, Calcasieu, Sabine Side view of flower. Photo by John Hays References: Godfrey, R. K. and J. W. Wooten.