Elmer's Island Management Plan
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Benthic Invertebrate Community Monitoring and Indicator Development for Barnegat Bay-Little Egg Harbor Estuary
July 15, 2013 Final Report Project SR12-002: Benthic Invertebrate Community Monitoring and Indicator Development for Barnegat Bay-Little Egg Harbor Estuary Gary L. Taghon, Rutgers University, Project Manager [email protected] Judith P. Grassle, Rutgers University, Co-Manager [email protected] Charlotte M. Fuller, Rutgers University, Co-Manager [email protected] Rosemarie F. Petrecca, Rutgers University, Co-Manager and Quality Assurance Officer [email protected] Patricia Ramey, Senckenberg Research Institute and Natural History Museum, Frankfurt Germany, Co-Manager [email protected] Thomas Belton, NJDEP Project Manager and NJDEP Research Coordinator [email protected] Marc Ferko, NJDEP Quality Assurance Officer [email protected] Bob Schuster, NJDEP Bureau of Marine Water Monitoring [email protected] Introduction The Barnegat Bay ecosystem is potentially under stress from human impacts, which have increased over the past several decades. Benthic macroinvertebrates are commonly included in studies to monitor the effects of human and natural stresses on marine and estuarine ecosystems. There are several reasons for this. Macroinvertebrates (here defined as animals retained on a 0.5-mm mesh sieve) are abundant in most coastal and estuarine sediments, typically on the order of 103 to 104 per meter squared. Benthic communities are typically composed of many taxa from different phyla, and quantitative measures of community diversity (e.g., Rosenberg et al. 2004) and the relative abundance of animals with different feeding behaviors (e.g., Weisberg et al. 1997, Pelletier et al. 2010), can be used to evaluate ecosystem health. Because most benthic invertebrates are sedentary as adults, they function as integrators, over periods of months to years, of the properties of their environment. -
Jacksonville, Florida 1998 Odmds Benthic Community Assessment
JACKSONVILLE, FLORIDA 1998 ODMDS BENTHIC COMMUNITY ASSESSMENT Submitted to U.S. Environmental Protection Agency, Region 4 61 Forsyth St. Atlanta, Georgia 30303 Prepared by Barry A. Vittor & Associates, Inc. 8060 Cottage Hill Rd. Mobile, Alabama 36695 (334) 633-6100 November 1999 TABLE OF CONTENTS LIST OF TABLES ………………………………………….……………………………3 LIST OF FIGURES ……………………..………………………………………………..4 1.0 INTRODUCTION ………..…………………………………………………………..5 2.0 METHODS ………..…………………………………………………………………..5 2.1 Sample Collection And Handling ………………………………………………5 2.2 Macroinfaunal Sample Analysis ……………………………………………….6 3.0 DATA ANALYSIS METHODS ……..………………………………………………6 3.1 Assemblage Analyses ..…………………………………………………………6 3.2 Faunal Similarities ……………………………………………………….…….8 4.0 HABITAT CHARACTERISTICS ……………………………………………….…8 5.0 BENTHIC COMMUNITY CHARACTERIZATION ……………………………..9 5.1 Faunal Composition, Abundance, And Community Structure …………………9 5.2 Numerical Classification Analysis …………………………………………….10 5.3 Taxa Assemblages …………………………………………………………….11 6.0 1995 vs 1998 COMPARISONS ……………………………………………………..11 7.0 SUMMARY ………………………………………………………………………….13 8.0 LITERATURE CITED ……………………………………………………………..16 2 LIST OF TABLES Table 1. Station locations for the Jacksonville, Florida ODMDS, June 1998. Table 2. Sediment data for the Jacksonville, Florida ODMDS, June 1998. Table 3. Summary of abundance of major taxonomic groups for the Jacksonville, Florida ODMDS, June 1998. Table 4. Abundance and distribution of major taxonomic groups at each station for the Jacksonville, Florida ODMDS, June 1998. Table 5. Abundance and distribution of taxa for the Jacksonville, Florida ODMDS, June 1998. Table 6. Percent abundance of dominant taxa (> 5% of the total assemblage) for the Jacksonville, Florida ODMDS, June 1998. Table 7. Summary of assemblage parameters for the Jacksonville, Florida ODMDS stations, June 1998. Table 8. Analysis of variance table for density differences between stations for the Jacksonville, Florida ODMDS stations, June 1998. -
Tube Epifaum of the Polychaete Phyllopchaetopterus Socialis
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Repository Open Access to Scientific Information from Embrapa Estuarine, Coastal and Shelf Science (1995) 41, 91–100 Tube epifauna of the Polychaete Phyllochaetopterus socialis Claparède Rosebel Cunha Nalessoa, Luíz Francisco L. Duarteb, Ivo Pierozzi Jrc and Eloisa Fiorim Enumod aDepartamento de Zoologia, CCB, Universidade Federal de Pernambuco, 50670-901, Recife, PE, Brazil, bDepartamento de Zoologia, Instituto Biologia, C.P. 6109, Universidade Estadual de Campinas, 13.081-970, Campinas, SP, Brazil, cEmbrapa, NMA, Av. Dr. Julio Soares de Arruda, 803 CEP 13.085, Campinas, SP, Brazil and dProtebras, Rua Turmalina, 79 CEP 13.088, Campinas, SP, Brazil Received 8 October 1992 and in revised form 22 June 1994 Keywords: Polychaeta; tubes; faunal association; epifauna; São Sebastião Channel; Brazil Animals greater than 1 mm, found among tangled tubes of Phyllochaetopterus socialis (Chaetopteridae) from Araçá Beach, São Sebastião district, Brazil, were studied for 1 year, with four samples in each of four seasons. They comprised 10 338 individuals in 1722·7 g dry weight of polychaete tubes, with Echino- dermata, Polychaeta (not identified to species) and Crustacea as the dominant taxa. The Shannon–Wiener diversity index did not vary seasonally, only two species (a holothurian and a pycnogonid) showing seasonal variation. Ophiactis savignyi was the dominant species, providing 45·5% of individuals. Three other ophiuroids, the holothurian Synaptula hidriformis, the crustaceans Leptochelia savignyi, Megalobrachium soriatum and Synalpheus fritzmuelleri, the sipunculan Themiste alutacea and the bivalve Hiatella arctica were all abundant, but most of the 68 species recorded occurred sparsely. -
<I>Diopatra Cuprea</I>
BULLETIN OF MARINE SCIENCE, 40(1): 11-21, 1987 ROLE OF DIOPATRA CUPREA BOSC (POLYCHAETA: ONUPHIDAE) TUBES IN STRUCTURING A SUBTROPICAL INFAUNAL COMMUNITY Suzanne M. Ban and Walter G. Nelson ABSTRACT An a priori hypothesis predicted that in the vicinity of aggregated Diopatra cuprea tubes an enhanced infaunal density and species richness would be found, resulting from a biological refuge effect of the tubes. To test this hypothesis, cores were taken over a 5-month period in both vegetated, Halodule wrighti! Aschers. beds, and unvegetated areas of a site in the Indian River lagoon, Florida. An inner, 0.01 m2, frame was placed to enclose densities of 0, I, or 4 D. cuprea tubes, while an outer concentric, 0.02 m2, frame was placed so that it enclosed the smaller frame, plus a surrounding area lacking in D. cuprea tubes. The presence of D. cuprea tubes was found to have no consistent significant effect on the abundance and number of infaunal species found in either the vegetated or unvegetated areas. Laboratory experiments employing a benthic predator, Callinectes, were carried out in order to determine whether D. cuprea tubes andlor H. wrightii rhizome mats actually constitute a barrier to predation. Significantly higher survivorship of the bivalve Mulinia lateralis Say, used as prey, was found in laboratory treatments containing 10 tubes per 0.01 m2 versus treatments containing 4 or a tubes per 0.01 m2. Highest survivorship of bivalves was found in treatments containing a H. wrightii rhizome mat; tubes placed within the mat did not enhance clam survivorship. The discrepancy between the findings of this study, and previous studies on the refuge effect of D. -
Foraging and Mobility in Three Species of Aciculata (Annelida: Polychaeta)
FORAGING AND MOBILITY IN THREE SPECIES OF ACICULATA (ANNELIDA: POLYCHAETA) PARDO, E. V. and AMARAL, A. C. Z. Departamento de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, C. P. 6109, CEP 13083-970, Campinas, São Paulo, Brazil Correspondence to: Erica Veronica Pardo, Departamento de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, C. P. 6109, CEP 13083-970, Campinas, São Paulo, Brazil, e-mail: [email protected] Received February 3, 2005 – Accepted August 22, 2005 – Distributed November 1, 2006 (With 1 figure) ABSTRACT Aspects of feeding, such as food capture and ingestion, as well as mobility of the polychaetes Eurythoe complanata, Marphysa formosa and Diopatra aciculata, from São Sebastião Channel (São Sebastião, state of São Paulo) were observed in laboratory conditions. Eurythoe complanata, a carnivorous species, fed exclusively on pieces of fish with the aid of strong muscular retractable lips, and detected the presence of food by chemical stimuli. Diopatra aciculata, an omnivorous species, captured and ingested different kinds of food with the aid of its jaws, generating a flow of water through its tube by which it detects the presence of food and oxygenates its gills. Marphysa formosa also used its jaws to bite and lacerate food. These species showed greater or lesser degrees of intolerance to light. Keywords: foraging, mobility, Aciculata, Polychaeta, Annelida. RESUMO Forrageamento e mobilidade em Polychaeta Alguns aspectos da atividade alimentar, tais como a captura e ingestão de alimento, bem como a mobilidade dos poliquetas Eurythoe complanata, Marphysa formosa e Diopatra aciculata, procedentes do Canal de São Sebastião (São Sebastião, SP), foram observados em laboratório. -
Benthic Habitats of the Delaware
BENTHICHABITATSOF THEDELAWAREBAY BenthicHabitatsoftheDelawareBay BenthicHabitatsofDelawareBay MarkG.Anderson,JosephA.M.Smith,andBartholomewD.Wilson INTRODUCTION ThissectiondescribesandmapsthemajorphysicalhabitatsoftheDelawareBayseafloor.Weused informationonbenthicorganisms,theirdistributionandtheirrelationshipstophysicalfeatures,to delimitadistinctsetofenvironmentsrepresentingthevarietyofbenthichabitatsintheBay.As individualspeciesareadaptedtovariationsindepth,sedimentsize,seabedtopographyandsalinity,we examinedthesefactorsinrelationshiptotheorganismcompositionandclassifiedthemintobasictypes toillustratethediversityofconditionsexistingontheseafloor.Wehopethatthisbenthichabitatmapof theDelawareBay,basedonpreviouslycollecteddata,willprovideabetterunderstandingofthe abundanceanddistributionofseafloorhabitattypes. Benthicorganismsarethosethatinhabittheseafloor;fromtheGreekwordbenthos,meaning“depths ofthesea.”Basedonajustasmallsample(246samples),theseafloorhabitatsoftheDelawareBay containover300speciesin8phylaincluding: 106speciesofarthropods(crabs,lobsters,shrimp,barnacles) 75speciesofmollusks(clams,scallops,squid,limpets,seaslugs,snails) 130speciesofannelids(seaworms) 8speciesofechinoderms(seastars,seaurchins,seacucumbers,sanddollars) 5speciesofcnidarians(corals,anemones,jellyfish) 4speciesofchordates(seasquirts) 1speciesofporiferans(sponges) 6speciesofnemerteans(ribbonworms) Thedistributionsandlifehistoriesofbenthicorganismsaretiedtotheirphysicalenvironment.Filter feederstendtodominateonshallowsandybottomswhiledepositfeeders,maydominateinfine -
Tube-Forming Polychaetes Enhance Invertebrate Diversity and Abundance in Sandy Sediments of Mozambique, Africa
African Journal of Marine Science 2011, 33(2): 327–332 Copyright © NISC (Pty) Ltd Printed in South Africa — All rights reserved AFRICAN JOURNAL OF MARINE SCIENCE ISSN 1814–232X EISSN 1814–2338 doi: 10.2989/1814232X.2011.600433 Short Communication Tube-forming polychaetes enhance invertebrate diversity and abundance in sandy sediments of Mozambique, Africa MS Thomsen1,2*, MF Muth3 and KJ McGlathery3 1 Marine Department, National Environmental Research Institute, University of Aarhus, PO Box 4000, Roskilde, Denmark 2 School of Plant Biology, University of Western Australia, Crawley 6009 WA, Australia 3 Department of Environmental Sciences, University of Virginia, 291 McCormick Rd, Clark Hall, Charlottesville, VA 22904, USA * Corresponding author, e-mail: [email protected] Manuscript received March 2011; accepted May 2011 In marine soft-bottom systems, polychaetes can increase habitat complexity by constructing rigid tubes (e.g. several onuphid species) that contrast with surrounding topographically flat sediments. These structures can provide predation refuges and increase larval settlement and thereby increase the richness and abundance of fauna. We collected invertebrate samples from an intertidal flat with low onuphid tube density (2.7 m–2) in Mozambique and document that more organisms (70 times higher mollusc abundances) and more species (15 times more mollusc species) were found associated with solitary tubes of an onuphid polychaete compared with surrounding sand habitats. These results are in agreement with tube versus sand comparisons from soft-bottom systems in the North Atlantic where polychaete tube densities are often much higher. Keywords: habitat formation, onuphid polychaete, species richness, western Indian Ocean Introduction Species that form or modify habitat, often referred to as (Thomsen et al. -
Initial Survey of Plum Island's Marine Habitats
Initial Survey of Plum Island’s Marine Habitats New York Natural Heritage Program Initial Survey of Plum Island’s Marine Habitats Emily S. Runnells Matthew D. Schlesinger Gregory J. Edinger New York Natural Heritage Program and Steven C. Resler Dan Marelli InnerSpace Scientific Diving A report to Save the Sound April 2020 Please cite this report as follows: New York Natural Heritage Program and InnerSpace Scientific Diving. 2020. Initial survey of Plum Island’s marine habitats. Report to Save the Sound. Available from New York Natural Heritage Program, Albany, NY. Available at www.nynhp.org/plumisland. Cover photos (left to right, top to bottom): Bryozoans and sponges; lion’s mane jellyfish; flat-clawed hermit crab; diver recording information from inside quadrat; bryozoans, sponges and northern star corals. All photos herein by the authors. Contents Introduction ........................................................................................................................................................ 1 Methods ............................................................................................................................................................... 1 Results .................................................................................................................................................................. 6 Discussion and Next Steps ............................................................................................................................... 9 Acknowledgments........................................................................................................................................... -
Some Intertidal and Shallow Water Polychaetes of the Caribbean Coast of Costa Rica
Some intertidal and shallow water polychaetes of the Caribbean coast of Costa Rica Harlan K. Dean1, 2 1. Department of Biology, University of Massachusetts- Boston, Boston, Massachusetts 02125-3393, USA; [email protected] 2. Department of Invertebrates, Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, Massachusetts 02138, USA Received 09-VII-2016. Corrected 06-IX-2016. Accepted 07-X-2016. Abstract: The polychaete fauna of the Caribbean coast of Costa Rica has been inadequately characterized with only nine species previously reported. Collections of polychaetes from intertidal coralline rocks and several shal- low sub-tidal sites on the Caribbean coast of Costa Rica have been examined and 68 species were identified. Of these, 66 are new records for Costa Rica. Rev. Biol. Trop. 65 (1): 127-152. Epub 2017 March 01. Key words: Annelida, Polychaeta, Caribbean Sea, Costa Rica, marine biodiversity, intertidal. The Caribbean coast of Costa Rica is species from the rocky intertidal of Cahuita. shorter (212 km) when compared with its Nonetheless, the occurrence of only nine known Pacific Coast (1 254 km) (Cortés & Wehrt- species of polychaetes indicates that this taxon mann, 2009). Much of the Caribbean coast is has been largely neglected in this region. sandy beaches with some rocky areas and coral In this paper materials collected during reefs in the Southern portion. Sea-grass beds several trips to the Caribbean coast of Costa also occur in the lagoons of the coral reefs and Rica funded by Centro de Investigación en consist mainly of Thalassia testidunum with Ciencias del Mar y Limnología (CIMAR), some Syringodium filiformis interspersed (Cor- University of Costa Rica (UCR), were ana- tés & Wehrtmann, 2009). -
Florida Keys Species List
FKNMS Species List A B C D E F G H I J K L M N O P Q R S T 1 Marine and Terrestrial Species of the Florida Keys 2 Phylum Subphylum Class Subclass Order Suborder Infraorder Superfamily Family Scientific Name Common Name Notes 3 1 Porifera (Sponges) Demospongia Dictyoceratida Spongiidae Euryspongia rosea species from G.P. Schmahl, BNP survey 4 2 Fasciospongia cerebriformis species from G.P. Schmahl, BNP survey 5 3 Hippospongia gossypina Velvet sponge 6 4 Hippospongia lachne Sheepswool sponge 7 5 Oligoceras violacea Tortugas survey, Wheaton list 8 6 Spongia barbara Yellow sponge 9 7 Spongia graminea Glove sponge 10 8 Spongia obscura Grass sponge 11 9 Spongia sterea Wire sponge 12 10 Irciniidae Ircinia campana Vase sponge 13 11 Ircinia felix Stinker sponge 14 12 Ircinia cf. Ramosa species from G.P. Schmahl, BNP survey 15 13 Ircinia strobilina Black-ball sponge 16 14 Smenospongia aurea species from G.P. Schmahl, BNP survey, Tortugas survey, Wheaton list 17 15 Thorecta horridus recorded from Keys by Wiedenmayer 18 16 Dendroceratida Dysideidae Dysidea etheria species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 19 17 Dysidea fragilis species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 20 18 Dysidea janiae species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 21 19 Dysidea variabilis species from G.P. Schmahl, BNP survey 22 20 Verongida Druinellidae Pseudoceratina crassa Branching tube sponge 23 21 Aplysinidae Aplysina archeri species from G.P. Schmahl, BNP survey 24 22 Aplysina cauliformis Row pore rope sponge 25 23 Aplysina fistularis Yellow tube sponge 26 24 Aplysina lacunosa 27 25 Verongula rigida Pitted sponge 28 26 Darwinellidae Aplysilla sulfurea species from G.P. -
Table S32. Distribution of Coarse Sediments and Macroinfauna on the Mississippi
Table S32. Distribution of coarse sediments and macroinfauna on the Mississippi- Alabama continental shelf during winter and summer along three transects. C = western transect near Chandeleur Islands; M = middle transect south of Mobile Bay; D = eastern transect near DeSoto Canyon. (From Harper 1991; Darnell 1991a, b.) Sand and Gravel (%) Depth Winter Summer (m) C M D Avg. C M D Avg. 20 52.4 83.8 75.8 70.7 59.1 94.7 94.9 82.9 50 37.7 90.4 93.1 73.7 23.4 91.0 91.3 68.6 100 4.5 60.5 62.6 42.5 10.8 57.9 77.1 48.6 200 0.3 4.8 4.6 3.2 0.5 5.8 7.4 4.6 Avg. 23.7 59.9 59.0 47.5 23.5 62.4 67.7 51.2 Total invertebrates (no./m²) 20 1,642 1,601 1,111 1,451 505 1,683 1,822 1,337 50 316 750 832 633 311 1,701 922 978 100 291 415 871 526 326 404 967 566 200 946 183 182 457 152 402 185 246 Avg. 794 737 749 762 324 1,048 974 782 Polychaetes (no./m²) 20 1,180 1,090 486 912 293 854 823 657 50 178 305 490 324 233 732 594 520 100 193 259 601 351 243 262 630 378 200 915 116 89 373 80 305 93 159 Avg. 617 443 417 492 212 538 535 428 Mollusks (no./m²) 20 123 127 174 141 89 527 407 341 50 46 214 115 125 11 653 73 246 100 32 80 23 45 20 63 38 40 200 14 7 10 10 26 27 9 21 Avg. -
1 Northwest Florida Species List
NORTHWEST FLORIDA SPECIES LIST This list, which contains shells found in the onshore and offshore waters of the Florida Panhandle, was prepared by the members of the Gulf Coast Shell Club. The list is arranged alphabetically by family. The numbers to the left of the shell name refer to the corresponding species as found in American Seashells, Second Edition by Dr R. Tucker Abbott. An asterisk indicates that a name change to the family, species, genus, (or all) has occurred since publication. Shells annotated with a superscript 1 indicate form names that may or may not be valid but are useful for identification. Shells annotated with a superscript 2 are shells from the 1994 Keeler and Robertson survey of the Apalachicola Marine Estuary and immediate offshore areas and represent species not currently held by GCSC members but that are deemed native to our area. Common name for the shell and its normal adult size range columns are included. There are 635 shells (including forms) on this list as of the latest update in March, 2013. Our thanks go to Dr. Harry Lee of the Jacksonville Shell Club for his assistance in this compilation. A caution: Any list of this type is subject to frequent name changes as the science involved progresses. GASTROPODA Family/Genus/Species Common Name Size (mm) ACTEONIDAE 3888 Acteon candens Rehder, 1939 Rehder’s Baby Bubble 5-10 3887 Acteon (Rictaxis) punctostriatus (C B Adams, 1840)* Pitted Baby Bubble 3-8 APLYSIIDAE (Nudibranch) Aplysia fasciata Poiret, 1789 Mottled Sea Hare 50 4166 Aplysia dactylomela Rang, 1828 Spotted Sea Hare 100-125 ARCHITECTICIDAE 0938 Architectonica nobilis Roding, 1798 Common Sundial 20-64 0943 Psilaxis krebsii (Morch, 1875) Beaded Sundial 7-13 BUCCINIDAE 2425 Antillophos candeanus (d’Orbigny, 1842)* Beaded Phos 12-30 2398 Engina cf.