Freshwater Invertebrates
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Cladocera: Anomopoda: Daphniidae) from the Lower Cretaceous of Australia
Palaeontologia Electronica palaeo-electronica.org Ephippia belonging to Ceriodaphnia Dana, 1853 (Cladocera: Anomopoda: Daphniidae) from the Lower Cretaceous of Australia Thomas A. Hegna and Alexey A. Kotov ABSTRACT The first fossil ephippia (cladoceran exuvia containing resting eggs) belonging to the extant genus Ceriodaphnia (Anomopoda: Daphniidae) are reported from the Lower Cretaceous (Aptian) freshwater Koonwarra Fossil Bed (Strzelecki Group), South Gippsland, Victoria, Australia. They represent only the second record of (pre-Quater- nary) fossil cladoceran ephippia from Australia (Ceriodaphnia and Simocephalus, both being from Koonwarra). The occurrence of both of these genera is roughly coincident with the first occurrence of these genera elsewhere (i.e., Mongolia). This suggests that the early radiation of daphniid anomopods predates the breakup of Pangaea. In addi- tion, some putative cladoceran body fossils from the same locality are reviewed; though they are consistent with the size and shape of cladocerans, they possess no cladoceran-specific synapomorphies. They are thus regarded as indeterminate diplostracans. Thomas A. Hegna. Department of Geology, Western Illinois University, Macomb, IL 61455, USA. ta- [email protected] Alexey A. Kotov. A.N. Severtsov Institute of Ecology and Evolution, Leninsky Prospect 33, Moscow 119071, Russia and Kazan Federal University, Kremlevskaya Str.18, Kazan 420000, Russia. alexey-a- [email protected] Keywords: Crustacea; Branchiopoda; Cladocera; Anomopoda; Daphniidae; Cretaceous. Submission: 28 March 2016 Acceptance: 22 September 2016 INTRODUCTION tions that the sparse known fossil record does not correlate with a meager past diversity. The rarity of Water fleas (Crustacea: Cladocera) are small, the cladoceran fossils is probably an artifact, a soft-bodied branchiopod crustaceans and are a result of insufficient efforts to find them in known diverse and ubiquitous component of inland and new palaeontological collections (Kotov, aquatic communities (Dumont and Negrea, 2002). -
Swede's Forest SNA Bioblitz Results
Swede Forest SNA Bioblitz Findings Species found at the June 17, 2017 bioblitz. Bacteria: Birds: • Apical chlorosis of Canada thistle aka PST – • Ring-necked Pheasant (Phasianus colchicus) (Pseudomonas syringae pv. tagetis) • Pied-billed Grebe (Podilymbus podiceps) Fungi and Lichens: • American White Pelican (Pelecanus erythrorhynchos) • Crown Rust (Puccinia coronata) • Green Heron (Butorides virescens) Amphibians: • Killdeer (Charadrius vociferus) • Mourning Dove (Zenaida macroura) • Northern Leopard Frog (Rana pipiens) • Turkey Vulture (Cathartes aura) • Eastern Gray Treefrog (Hyla versicolor) • Bald Eagle (Haliaeetus leucocephalus) • Belted Kingfisher (Megaceryle alcyon) Reptiles: • Eastern Kingbird (Tyrannus tyrannus) • Red-sided Garter Snake (Thamnophis sirtalis • Great Crested Flycatcher (Myiarchus crinitus) parietalis) • Eastern Wood-Pewee (Contopus virens) • Plains Garter Snake (Thamnophis radix) • Brown-headed Cowbird (Molothrus ater) • Redbelly Snake (Storeria occipitomaculata) • Red-winged Blackbird (Agelaius phoeniceus) • Five-lined Skink (Plestiodon fasciatus) • Orchard Oriole (Icterus spurius) • Western Painted Turtle (Chrysemys picta belli) • Baltimore Oriole (Icterus galbula) • Common Grackle (Quiscalus quiscula) Mammals: • American Goldfinch (Spinus tristis) • Eastern Cottontail (Sylvilagus floridanus) • Lark Sparrow (Chondestes grammacus)— • Whitetail Deer (Odocoileus virginianus) confirmed nesting • White-footed Mouse (Peromyscus leucopus) • Chipping Sparrow (Spizella passerina) • Coyote (Canis latrans) scat • Clay-colored -
Dragonflies (Odonata) of the Northwest Territories Status Ranking And
DRAGONFLIES (ODONATA) OF THE NORTHWEST TERRITORIES STATUS RANKING AND PRELIMINARY ATLAS PAUL M. CATLING University of Ottawa 2003 TABLE OF CONTENTS Abstract ....................................................................3 Acknowledgements ...........................................................3 Methods ....................................................................3 The database .................................................................4 History .....................................................................5 Rejected taxa ................................................................5 Possible additions ............................................................5 Additional field inventory ......................................................7 Collection an Inventory of dragonflies .............................................8 Literature Cited .............................................................10 Appendix Table 1 - checklist ...................................................13 Appendix Table 2 - Atlas and ranking notes .......................................15 2 ABSTRACT: occurrences was provided by Dr. Rex Thirty-five species of Odonata are given Kenner, Dr. Donna Giberson, Dr. Nick status ranks in the Northwest Territories Donnelly and Dr. Robert Cannings (some based on number of occurrences and details provided below). General distributional area within the territory. Nine information on contacts and locations of species are ranked as S2, may be at risk, collections provided by Dr. Cannings -
List of Animal Species with Ranks October 2017
Washington Natural Heritage Program List of Animal Species with Ranks October 2017 The following list of animals known from Washington is complete for resident and transient vertebrates and several groups of invertebrates, including odonates, branchipods, tiger beetles, butterflies, gastropods, freshwater bivalves and bumble bees. Some species from other groups are included, especially where there are conservation concerns. Among these are the Palouse giant earthworm, a few moths and some of our mayflies and grasshoppers. Currently 857 vertebrate and 1,100 invertebrate taxa are included. Conservation status, in the form of range-wide, national and state ranks are assigned to each taxon. Information on species range and distribution, number of individuals, population trends and threats is collected into a ranking form, analyzed, and used to assign ranks. Ranks are updated periodically, as new information is collected. We welcome new information for any species on our list. Common Name Scientific Name Class Global Rank State Rank State Status Federal Status Northwestern Salamander Ambystoma gracile Amphibia G5 S5 Long-toed Salamander Ambystoma macrodactylum Amphibia G5 S5 Tiger Salamander Ambystoma tigrinum Amphibia G5 S3 Ensatina Ensatina eschscholtzii Amphibia G5 S5 Dunn's Salamander Plethodon dunni Amphibia G4 S3 C Larch Mountain Salamander Plethodon larselli Amphibia G3 S3 S Van Dyke's Salamander Plethodon vandykei Amphibia G3 S3 C Western Red-backed Salamander Plethodon vehiculum Amphibia G5 S5 Rough-skinned Newt Taricha granulosa -
Hull Fouling Is a Risk Factor for Intercontinental Species Exchange in Aquatic Ecosystems
Aquatic Invasions (2007) Volume 2, Issue 2: 121-131 Open Access doi: http://dx.doi.org/10.3391/ai.2007.2.2.7 © 2007 The Author(s). Journal compilation © 2007 REABIC Research Article Hull fouling is a risk factor for intercontinental species exchange in aquatic ecosystems John M. Drake1,2* and David M. Lodge1,2 1Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556 USA 2Environmental National Center for Ecological Analysis and Synthesis, 735 State Street, Suite 300, Santa Barbara, CA 93101 USA *Corresponding author Current address: Institute of Ecology, University of Georgia, Athens, GA 30602 USA E-mail: [email protected] (JMD) Received: 13 March 2007 / Accepted: 25 May 2007 Abstract Anthropogenic biological invasions are a leading threat to aquatic biodiversity in marine, estuarine, and freshwater ecosystems worldwide. Ballast water discharged from transoceanic ships is commonly believed to be the dominant pathway for species introduction and is therefore increasingly subject to domestic and international regulation. However, compared to species introductions from ballast, translocation by biofouling of ships’ exposed surfaces has been poorly quantified. We report translocation of species by a transoceanic bulk carrier intercepted in the North American Great Lakes in fall 2001. We collected 944 individuals of at least 74 distinct freshwater and marine taxa. Eight of 29 taxa identified to species have never been observed in the Great Lakes. Employing five different statistical techniques, we estimated that the biofouling community of this ship comprised from 100 to 200 species. These findings adjust upward by an order of magnitude the number of species collected from a single ship. -
Biodiversity and Trophic Ecology of Hydrothermal Vent Fauna Associated with Tubeworm Assemblages on the Juan De Fuca Ridge
Biogeosciences, 15, 2629–2647, 2018 https://doi.org/10.5194/bg-15-2629-2018 © Author(s) 2018. This work is distributed under the Creative Commons Attribution 4.0 License. Biodiversity and trophic ecology of hydrothermal vent fauna associated with tubeworm assemblages on the Juan de Fuca Ridge Yann Lelièvre1,2, Jozée Sarrazin1, Julien Marticorena1, Gauthier Schaal3, Thomas Day1, Pierre Legendre2, Stéphane Hourdez4,5, and Marjolaine Matabos1 1Ifremer, Centre de Bretagne, REM/EEP, Laboratoire Environnement Profond, 29280 Plouzané, France 2Département de sciences biologiques, Université de Montréal, C.P. 6128, succursale Centre-ville, Montréal, Québec, H3C 3J7, Canada 3Laboratoire des Sciences de l’Environnement Marin (LEMAR), UMR 6539 9 CNRS/UBO/IRD/Ifremer, BP 70, 29280, Plouzané, France 4Sorbonne Université, UMR7144, Station Biologique de Roscoff, 29680 Roscoff, France 5CNRS, UMR7144, Station Biologique de Roscoff, 29680 Roscoff, France Correspondence: Yann Lelièvre ([email protected]) Received: 3 October 2017 – Discussion started: 12 October 2017 Revised: 29 March 2018 – Accepted: 7 April 2018 – Published: 4 May 2018 Abstract. Hydrothermal vent sites along the Juan de Fuca community structuring. Vent food webs did not appear to be Ridge in the north-east Pacific host dense populations of organised through predator–prey relationships. For example, Ridgeia piscesae tubeworms that promote habitat hetero- although trophic structure complexity increased with ecolog- geneity and local diversity. A detailed description of the ical successional stages, showing a higher number of preda- biodiversity and community structure is needed to help un- tors in the last stages, the food web structure itself did not derstand the ecological processes that underlie the distribu- change across assemblages. -
Casleguard Cave 2005
Castleguard Cave 2005 First ascent of the 200-foot aven Text by Marek Vokáˇc Photos by Christian Rushfeldt, Bjørn Myrvold, Jørn Halvorsen, Marek Vokáˇc First edition October 27, 2006 Copyright notice: Overall copyright © 2006 Marek Vokáˇc. Photographers retain their copy- right © to individual images as specified in photo credits/captions. Permission is generally granted for individual, non-commercial use of this report, provided due credit is given. Parks Canada is additionally granted permission for other non-commercial use and distribution. Author contact: Marek Vokáˇc Thorleifs Allé 5c 0489 Oslo Norway email: [email protected] Telephone: +47 934 92 857 Cover photo: Marek Vokáˇcclimbing the aven, by Christian Rushfeldt (CC05-064) Dedicated to all whose generous support made this trip possible, and a success: my wife and children; the team; their families; and our colleagues and employers Introduction Castleguard Cave lies in the heart of the Rocky Mountains, close to the Saskatchewan Glacier. To get to the cave from Calgary, one drives the beautiful Icefields Parkway, past Lake Louise and Banff, preferably staying at the Saksatchewan Crossing hotel. Getting to the cave entrance is a full-day ski trip. The cave itself was known early in the 1900’s, and was visited by tourists with horses and mules. The biggest attraction were the sudden floods coming out of the entrance, where the dry opening would change into a roaring river in a few seconds. Modern cave exploration started in 1967, during the summer. The explorers were caught by a sudden rise in the water and trapped inside the first drop. After 18 hours the water level dropped enough for them to get out; soon after that, the waters rose again and ran for weeks. -
Natural Resource Inventory Smith-Sargent
NATURAL RESOURCE INVENTORY of the SMITH-SARGENT ROAD PROPERTY Holderness, NH FINAL REPORT [Smith-Sargent Property Upper Marsh as seen from south boundary] Compiled by: Dr. Rick Van de Poll Ecosystem Management Consultants 30 N. Sandwich Rd. Center Sandwich, NH 03227 603-284-6851 [email protected] Submitted to: Holderness Conservation Commission June 30, 2016 i SUMMARY Between October 2015 and June 2016 a comprehensive natural resources inventory (NRI) was completed by Ecosystem Management Consultants (EMC) of Sandwich, NH on the 8.5-acre town conservation land at the corner of Sargent Road and Smith Road in Holderness, NH. Managed by the Holderness Conservation Commission (HCC), this parcel was obtained largely for the complex wetland system that occupies more than 65% of the parcel. The purpose of the NRI was to inform the town about the qualities of the natural resources on the lot, as well as to determine whether or not the site would be suitable for limited environmental education for the general public. Three site visits were conducted at the Sargent-Smith Road Property for the purpose of gathering NRI data. A fourth visit was also made on November 15, 2015 for the purpose of educating the HCC and other town officials about the extent and functional value of the wetlands on the parcel. The first field visit in October provided an initial review of the location of the parcel, the boundary of the wetland, and the plant and animal resources present. A second site visit in January was held for the purpose of tracking mammals during good snow cover. -
Growth Mechanisms of Speleothems in Castleguard Cave, Columbia Icefields, Alberta, Canada
Arctic and Alpine Research ISSN: 0004-0851 (Print) 2325-5153 (Online) Journal homepage: https://www.tandfonline.com/loi/uaar19 Growth Mechanisms of Speleothems in Castleguard Cave, Columbia Icefields, Alberta, Canada T. C. Atkinson To cite this article: T. C. Atkinson (1983) Growth Mechanisms of Speleothems in Castleguard Cave, Columbia Icefields, Alberta, Canada, Arctic and Alpine Research, 15:4, 523-536 To link to this article: https://doi.org/10.1080/00040851.1983.12004379 Copyright 1983 Regents of the University of Colorado Published online: 01 Jun 2018. Submit your article to this journal Article views: 64 View related articles Citing articles: 4 View citing articles Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=uaar20 Arctic and Alpine Research, Vol. 15, No.4, 1983, pp. 523-536 GROWTH MECHANISMS OF SPELEOTHEMS IN CASTLEGUARD CAVE, COLUMBIA ICEFIELDS, ALBERTA, CANADA* T. C. ATKINSON School ofEnvironmental Sciences, University ofEast Anglia, Norwich NR4 7TJ, England, U.K. ABSTRACT In spite of its location beneath high alpine terrain and active glaciers, Castleguard Cave contains many actively growing calcite'speleothems. Four hypotheses as to their growth mechanism were tested against field data on water chemistry, temperatures, CO 2 content of cave air, and evaporation rates. The hypotheses were (1) that a biogenic source of high PC02 is unlikely, so calcite deposition by CO 2 degassing would require a nonbiogenic source; (2) warming of water after entering the cave, or in passage through the rocks above it might cause calcite supersaturation; (3) calcite might be deposited because of evaporation of seep age; and (4) waters dissolving several Ca-bearing minerals might precipitate calcite as the least soluble by the common-ion effect. -
Ecography ECOG-02578 Pinkert, S., Brandl, R
Ecography ECOG-02578 Pinkert, S., Brandl, R. and Zeuss, D. 2016. Colour lightness of dragonfly assemblages across North America and Europe. – Ecography doi: 10.1111/ecog.02578 Supplementary material Appendix 1 Figures A1–A12, Table A1 and A2 1 Figure A1. Scatterplots between female and male colour lightness of 44 North American (Needham et al. 2000) and 19 European (Askew 1988) dragonfly species. Note that colour lightness of females and males is highly correlated. 2 Figure A2. Correlation of the average colour lightness of European dragonfly species illustrated in both Askew (1988) and Dijkstra and Lewington (2006). Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Note that the extracted colour values of dorsal dragonfly drawings from both sources are highly correlated. 3 Figure A3. Frequency distribution of the average colour lightness of 152 North American and 74 European dragonfly species. Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Rugs at the abscissa indicate the value of each species. Note that colour values are from different sources (North America: Needham et al. 2000, Europe: Askew 1988), and hence absolute values are not directly comparable. 4 Figure A4. Scatterplots of single ordinary least-squares regressions between average colour lightness of 8,127 North American dragonfly assemblages and mean temperature of the warmest quarter. Red dots represent assemblages that were excluded from the analysis because they contained less than five species. Note that those assemblages that were excluded scatter more than those with more than five species (c.f. the coefficients of determination) due to the inherent effect of very low sampling sizes. -
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1 Mobilising molluscan models and genomes in biology 2 Angus Davison1 and Maurine Neiman2 3 1. School of Life Sciences, University Park, University of Nottingham, NG7 2RD, UK 4 2. Department of Biology, University of Iowa, Iowa City, IA, USA and Department of Gender, 5 Women's, and Sexuality Studies, University of Iowa, Iowa, City, IA, USA 6 Abstract 7 Molluscs are amongst the most ancient, diverse, and important of all animal taxa. Even so, 8 no individual mollusc species has emerged as a broadly applied model system in biology. 9 We here make the case that both perceptual and methodological barriers have played a role 10 in the relative neglect of molluscs as research organisms. We then summarize the current 11 application and potential of molluscs and their genomes to address important questions in 12 animal biology, and the state of the field when it comes to the availability of resources such 13 as genome assemblies, cell lines, and other key elements necessary to mobilising the 14 development of molluscan model systems. We conclude by contending that a cohesive 15 research community that works together to elevate multiple molluscan systems to ‘model’ 16 status will create new opportunities in addressing basic and applied biological problems, 17 including general features of animal evolution. 18 Introduction 19 Molluscs are globally important as sources of food, calcium and pearls, and as vectors of 20 human disease. From an evolutionary perspective, molluscs are notable for their remarkable 21 diversity: originating over 500 million years ago, there are over 70,000 extant mollusc 22 species [1], with molluscs present in virtually every ecosystem. -
Reanalysis and Revision of the Complete Mitochondrial Genome of Artemia Urmiana Günther, 1899 (Crustacea: Anostraca)
diversity Article Reanalysis and Revision of the Complete Mitochondrial Genome of Artemia urmiana Günther, 1899 (Crustacea: Anostraca) Alireza Asem 1,2,† , Amin Eimanifar 3,†, Weidong Li 4,*, Chun-Yang Shen 5, Farnaz Mahmoudi Shikhsarmast 1,6, Ya-Ting Dan 7, Hao Lu 1,2, Yang Zhou 8, You Chen 1,9, Pei-Zheng Wang 1,9,* and Michael Wink 10 1 Key Laboratory of Utilization and Protection of Tropical Marine Living Resources, Hainan Tropical Ocean University, Sanya 572000, China; [email protected] (A.A.); [email protected] (F.M.S.); [email protected] (H.L.); [email protected] (Y.C.) 2 College of Fisheries and Life Sciences, Hainan Tropical Ocean University, Sanya 572000, China 3 Independent Senior Scientist, Industrial District, Easton, MD 21601, USA; [email protected] 4 College of Ecology and Environment, Hainan Tropical Ocean University, Haikou 570000, China 5 Department of Biology, Chengde Medical University, Chengde 067000, China; [email protected] 6 College of Marine Science and Technology, Hainan Tropical Ocean University, Sanya 572000, China 7 College of Marine Science, Shanghai Ocean University, Shanghai 200000, China; [email protected] 8 Institute of Deep Sea Science and Engineering, Chinese Academy of Science, Sanya 572000, China; [email protected] 9 College of Ecology and Environment, Hainan Tropical Ocean University, Sanya 572000, China 10 Institute of Pharmacy and Molecular Biotechnology (IPMB), Heidelberg University, Im Neuenheimer Feld 364, 69120 Heidelberg, Germany; [email protected] * Correspondence: [email protected] (W.L.); [email protected] (P.-Z.W.) † Equal contribution as first author. Abstract: In the previously published mitochondrial genome sequence of Artemia urmiana (NC_021382 [JQ975176]), the taxonomic status of the examined Artemia had not been determined, due to partheno- Citation: Asem, A.; Eimanifar, A.; Li, W.; Shen, C.-Y.; Shikhsarmast, F.M.; genetic populations coexisting with A.