Baseline Survey of Zooplankton of Barnegat Bay
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Copepod Distribution and Production in a Mid-Atlantic Ridge Archipelago
Anais da Academia Brasileira de Ciências (2014) 86(4): 1719-1733 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 http://dx.doi.org/10.1590/0001-3765201420130395 www.scielo.br/aabc Copepod distribution and production in a Mid-Atlantic Ridge archipelago PEDRO A.M.C. MELO1, MAURO DE MELO JÚNIOR2, SILVIO J. DE MACÊDO1, MOACYR ARAUJO1 and SIGRID NEUMANN-LEITÃO1 1Universidade Federal de Pernambuco, Departamento de Oceanografia, Av. Arquitetura, s/n, Cidade Universitária, 50670-901 Recife, PE, Brasil 2Universidade Federal Rural de Pernambuco, Unidade Acadêmica de Serra Talhada, Fazenda Saco, s/n, Zona Rural, 56903-970 Serra Talhada, PE, Brasil Manuscript received on October 3, 2013; accepted for publication on March 11, 2014 ABSTRACT The Saint Peter and Saint Paul Archipelago (SPSPA) are located close to the Equator in the Atlantic Ocean. The aim of this study was to assess the spatial variations in the copepod community abundance, and the biomass and production patterns of the three most abundant calanoid species in the SPSPA. Plankton samples were collected with a 300 µm mesh size net along four transects (north, east, south and west of the SPSPA), with four stations plotted in each transect. All transects exhibited a tendency toward a decrease in copepod density with increasing distance from the SPSPA, statistically proved in the North. Density varied from 3.33 to 182.18 ind.m-3, and differences were also found between the first perimeter (first circular distance band) and the others. The total biomass varied from 15.25 to 524.50 10-3 mg C m-3 and production from 1.19 to 22.04 10-3 mg C m-3d-1. -
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MARINE ECOLOGY PROGRESS SERIES Vol. 166: 301-306, 1998 Published May 28 Mar Ecol Prog Ser l NOTE Diel vertical movement by mesograzers on seaweeds Cary N. Rogers*, Jane E. Williamson, David G. Carson, Peter D. Steinberg School of Biological Science. University of New South Wales. Sydney 2052. Australia ABSTRACT- Diel vertical movement is well documented for nutrients across trophic levels in such systems (Kitting many zooplankton. The ecology of small benthic herbivores et al. 1984, Longhurst & Harrison 1989). which use seaweeds as food and habitat, known as 'meso- Arguably, the dominant model to explain die1 verti- grazers', is similar in some regards to zooplankton, and we hypothesised that mesograzers might also exhlbit diel pat- cal movement by zooplankton is avoidance of visually terns of movement on host algae. We studied 3 non-swim- feeding predators in surface waters during the day ming species of mesograzer, the sea hare Aplysia parvula, the (Zaret & Suffern 1976, Stich & Lampert 1981, Bollens & sea urchin Holopneustes purpurascens, and the prosobranch Frost 1989).This model is supported by studies of both mollusc Phasianotrochus eximius. All exhibited diel move- & ment on host algae. This behaviour occurred on different host demersal and pelagic zooplankton (Robertson algae, despite variation in algal morphology and other char- Howard 1978, Alldredge & King 1985, Ohman 1990, acters. Possible factors causing diel movement by mesograz- Osgood & Frost 1994), although the impact of preda- ers include predation, nutritional gain, avoidance of photo- tion on zooplankton vanes with nntogenetic stage, damage, micro-environmental vanation near host algae, and food availability, and predator evasion or defence reproductive strategies. -
Zooplankton Community Response to Seasonal Hypoxia: a Test of Three Hypotheses
diversity Article Zooplankton Community Response to Seasonal Hypoxia: A Test of Three Hypotheses Julie E. Keister *, Amanda K. Winans and BethElLee Herrmann School of Oceanography, University of Washington, Box 357940, Seattle, WA 98195, USA; [email protected] (A.K.W.); [email protected] (B.H.) * Correspondence: [email protected] Received: 7 November 2019; Accepted: 28 December 2019; Published: 1 January 2020 Abstract: Several hypotheses of how zooplankton communities respond to coastal hypoxia have been put forward in the literature over the past few decades. We explored three of those that are focused on how zooplankton composition or biomass is affected by seasonal hypoxia using data collected over two summers in Hood Canal, a seasonally-hypoxic sub-basin of Puget Sound, Washington. We conducted hydrographic profiles and zooplankton net tows at four stations, from a region in the south that annually experiences moderate hypoxia to a region in the north where oxygen remains above hypoxic levels. The specific hypotheses tested were that low oxygen leads to: (1) increased dominance of gelatinous relative to crustacean zooplankton, (2) increased dominance of cyclopoid copepods relative to calanoid copepods, and (3) overall decreased zooplankton abundance and biomass at hypoxic sites compared to where oxygen levels are high. Additionally, we examined whether the temporal stability of community structure was decreased by hypoxia. We found evidence of a shift toward more gelatinous zooplankton and lower total zooplankton abundance and biomass at hypoxic sites, but no clear increase in the dominance of cyclopoid relative to calanoid copepods. We also found the lowest variance in community structure at the most hypoxic site, in contrast to our prediction. -
Observing Copepods Through a Genomic Lens James E Bron1*, Dagmar Frisch2, Erica Goetze3, Stewart C Johnson4, Carol Eunmi Lee5 and Grace a Wyngaard6
Bron et al. Frontiers in Zoology 2011, 8:22 http://www.frontiersinzoology.com/content/8/1/22 DEBATE Open Access Observing copepods through a genomic lens James E Bron1*, Dagmar Frisch2, Erica Goetze3, Stewart C Johnson4, Carol Eunmi Lee5 and Grace A Wyngaard6 Abstract Background: Copepods outnumber every other multicellular animal group. They are critical components of the world’s freshwater and marine ecosystems, sensitive indicators of local and global climate change, key ecosystem service providers, parasites and predators of economically important aquatic animals and potential vectors of waterborne disease. Copepods sustain the world fisheries that nourish and support human populations. Although genomic tools have transformed many areas of biological and biomedical research, their power to elucidate aspects of the biology, behavior and ecology of copepods has only recently begun to be exploited. Discussion: The extraordinary biological and ecological diversity of the subclass Copepoda provides both unique advantages for addressing key problems in aquatic systems and formidable challenges for developing a focused genomics strategy. This article provides an overview of genomic studies of copepods and discusses strategies for using genomics tools to address key questions at levels extending from individuals to ecosystems. Genomics can, for instance, help to decipher patterns of genome evolution such as those that occur during transitions from free living to symbiotic and parasitic lifestyles and can assist in the identification of genetic mechanisms and accompanying physiological changes associated with adaptation to new or physiologically challenging environments. The adaptive significance of the diversity in genome size and unique mechanisms of genome reorganization during development could similarly be explored. -
AGUIDE to Frle DEVELOPMENTAL STAGES of COMMON COASTAL
A GUIDE TO frlE DEVELOPMENTAL STAGES OF COMMON COASTAL, GeORGES BANK AND GULF OF MAINE COPEPODS BY Janet A. Murphy and Rosalind E. Cohen National Marine Fisheries Service Northeast Fisheries Center Woods Hole Laboratory Woods Hole, MA 02543 Laboratory Reference No. 78-53 Table of Contents List of Plates i,,;i,i;i Introduction '. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 1 Acarti a cl aus; .. 2 Aca rtia ton sa .. 3 Aca rtia danae .. 4 Acartia long; rem; s co e"" 5 Aetidi us artllatus .. 6 A1teutha depr-e-s-s-a· .. 7 Calanu5 finmarchicus .............•............................ 8 Calanus helgolandicus ~ 9 Calanus hyperboreus 10 Calanus tenuicornis .......................•................... 11 Cal oca 1anus pavo .....................•....•....•.............. 12 Candaci a armata Ii II .. .. .. .. .. .. .. .. .. .. 13 Centropages bradyi............................................ 14 Centropages hama tus .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. .. 15 ~ Centropages typi cus " .. " 0 16 Clausocalanus arcuicornis ..............................•..•... 17 Clytemnestra rostra~ta ................................•.•........ 18 Corycaeus speciosus........................................... 19 Eucalanus elongatu5 20 Euchaeta mar; na " . 21 Euchaeta norveg; ca III co .. 22 Euchirel1a rostrata . 23 Eurytemora ameri cana .......................................•.. 24 Eurytemora herdmani , . 25 Eurytemora hi rundoi des . 26 Halithalestris croni ..................•...................... -
Australian Marine Zooplankton-Calanoid Copepods Part 2
Phylum Arthropoda Order Calanoida Candacia truncata Family Candaciidae Dana, 1849 Size ♂ Male: 1.87 – 2.11 mm scale: mm A1 P5 Male • Geniculate right A1 has a series of stout proximal segments followed by a thin section, then a broad club 1.0 section, beyond club section, segment 16 has a finger-like protrusion which is difficult to observe clearly; fused segments 17 and 18 are characteristically curved • Last prosome somite symmetrical with sharp points • P5 left segment 4 with 3 setae; right P5 not chelate and segment 3 urosome terminates in long plumose setae • Urosome and caudal rami symmetrical with no projections Ecology • Specialised predator, grasping prey with large and robust maxillae • Larvaceans are major prey item Source Boxshall & Halsey (2004) Bradford-Grieve (1999) Chen and Zhang (1965) Conway (2003) Tanaka (1935) ; Chen & Zhang (1965) Greenwood (1978) Razouls et al. (2010) preserved specimen Tanaka (1935) (Full reference available at http://www.imas.utas.edu.au/zooplankton/references ) Compiled: C. H. Davies & A. S. Slotwinski 2012 Images: AusCPR Verified: K. M. Swadling 2013 Phylum Arthropoda Centropages australiensis Order Calanoida Fairbridge, 1944 Family Centropagidae Synonyms None ♀ exopod 2 spine-like scale: mm process Size Female: 1.43 mm 1.0 Genus notes • Small to medium size • Cephalosome and pedigerous somite 1 are fused (fusion lines visible on sides) • Single naupliar eye P5 • Lateral corners of posterior prosome often end in asymmetrical points • Characteristic undulating edge on last prosomal somite between -
Bioprospecting Marine Plankton Heni Abida, Sandrine Ruchaud, Laurent Rios, Anne Humeau, Ian Probert, Colomban De Vargas, Stéphane Bach, Chris Bowler
Bioprospecting Marine Plankton Heni Abida, Sandrine Ruchaud, Laurent Rios, Anne Humeau, Ian Probert, Colomban de Vargas, Stéphane Bach, Chris Bowler To cite this version: Heni Abida, Sandrine Ruchaud, Laurent Rios, Anne Humeau, Ian Probert, et al.. Bioprospecting Marine Plankton. Marine drugs, MDPI, 2013, 11 (11), pp.4594-4611. 10.3390/md11114594. hal- 01258229 HAL Id: hal-01258229 https://hal.archives-ouvertes.fr/hal-01258229 Submitted on 27 Jan 2016 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. Distributed under a Creative Commons Attribution| 4.0 International License Mar. Drugs 2013, 11, 4594-4611; doi:10.3390/md11114594 OPEN ACCESS marine drugs ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Review Bioprospecting Marine Plankton Heni Abida 1, Sandrine Ruchaud 2, Laurent Rios 3, Anne Humeau 4, Ian Probert 5, Colomban De Vargas 6, Stéphane Bach 2,* and Chris Bowler 1,* 1 Environmental and Evolutionary Genomics Section, Institut de Biologie de l’Ecole Normale Supérieure (IBENS), Centre National de la Recherche Scientifique (CNRS) UMR8197 INSERM -
Zooplankton Migration Patterns at Scotton Landing: Behavioral Adaptations Written by Lauren Zodl, University of Delaware
Zooplankton Migration Patterns at Scotton Landing: Behavioral Adaptations written by Lauren Zodl, University of Delaware Summary: Zooplankton have evolved specific migration patterns that increase their chances of survival. These migrations patterns are behavioral adaptations and they are unique to each species of zooplankton in the Delaware Bay. Students will determine how zooplankton from the St. Jones River migrate and how these adaptations increase their chances of survival. Students will also explore Simpson’s diversity index. Activity Use: This activity can be used as a part of any unit on biology, evolution, adaptations, ecology, diversity, and more. Target Grade Level: High School Standards Addressed: LS1.A: Structure and Function LS1.B: Growth and Development of Organisms LS1.C: Organization for Matter and Energy Flow in Organism LS1.D: Information Processing LS2.A: Interdependent Relationships in Ecosystems LS2.B: Cycles of Matter and Energy Transfer in Ecosystems LS2.C: Ecosystem Dynamics, Functioning, and Resilience LS2.D: Interactions and Group Behavior Lesson Time: Two 45 minute periods Essential Question: How do the behavioral adaptations of zooplankton, specifically their migration patterns, increase their chances of survival? SMART Objectives: After completing this activity, students will be able to: 1. Name two zooplankton species in the Delaware Bay. 2. Describe two different migration patterns that zooplankton use. 3. Explain how behavioral adaptations of zooplankton increase their chances of survival. 4. Describe and interpret data from a diversity index. Vocabulary/Key Terms: Behavioral Adaptation, Diel Vertical Migration, Tidal Migration, Acartia tonsa, Rhithropanopeus harrisii, Estuary, Holoplankton, Meroplankton, Diversity This work is supported by a grant from the Delaware National Estuarine Research Reserve. -
Holoplankton, Meroplankton, and Meiofauna Associated with Marine Snow
MARINE ECOLOGY PROGRESS SERIES Vol. 156: 75-86, 1997 Published September 25 Mar Ecol Prog Ser Holoplankton, meroplankton, and meiofauna associated with marine snow Alan L. Shanks1#*,Keith Walters2 'Oregon Institute of Marine Biology, University of Oregon, PO Box 5389, Charleston, Oregon 97420, USA '~epartmentof Biology, PO Box 60, Middle Tennessee State University, Murfreesboro, Tennessee 37132, USA ;\BSTRACT. The associations of holoplankton, meroplankton and me~ofaunawith marine snow, as well CIS thelr behavior upon encountering marine snow, were investigated using SCUBA in the field and a vertical flume in the laboratory. Field san~pleswere collected in the Atlantic Ocean off Charleston, South Carolina, USA. (3 dates) and in the Pacific Ocean at 2 locations in the San Juan Islands, Wash- ington, USA (7 dates). Aggregates were present and abundant on all days (range 1 to 63 aggregates I-') but constituted a small percentage of the water column by volume (avg 0.078%). Holoplanktonic adult caldnoid and cyclopoid copepods, larvaceans, and copepod nauplii were found on aggregates. On average cl "/o of the calanoid and cyclopoid copepods sampled were on aggregates, indicating a weak dasociation with marine snow. In contrast, on average 2.6'%) of the larvaceans and 4.8% of the copepod nauplii sampled resided on aggregates, where they were, respectively, 33 to 62 times more concen- trated on marine snow compared to the surrounding water. Percentages of harpacticoid copepods, nematodes, and foraminiferans on aggregates were 12.4, 69.9 and 47.2% respectively, and all were significantly concentrated on aggregates. Cyprids, bryozoan cyphonautes, and Iarval echinoderms were either weakly assoc~atedwith or not found on aggregates. -
Western Pacific Zooplankton Community Along Latitudinal and Equatorial Transects in Autumn 2017 (Northern Hemisphere)
diversity Article Western Pacific Zooplankton Community along Latitudinal and Equatorial Transects in Autumn 2017 (Northern Hemisphere) Yi Long 1, Md Abu Noman 2, Dawei Chen 1, Shihao Wang 1,3, Hao Yu 1,3, Hongtao Chen 4, Min Wang 5 and Jun Sun 1,2,* 1 Research Centre for Indian Ocean Ecosystem, Tianjin University of Science and Technology, Tianjin 300457, China; [email protected] (Y.L.); [email protected] (D.C.); [email protected] (S.W.); [email protected] (H.Y.) 2 College of Marine Science and Technology, China University of Geosciences (Wuhan), Wuhan 430074, China; [email protected] 3 Institute of Marine Science and Technology, Shandong University, Qingdao 266200, China 4 Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao 266100, China; [email protected] 5 College of Marine Life Science, Ocean University of China, Qingdao 266003, China; [email protected] * Correspondence: [email protected] Abstract: During the autumn of 2017, a study was conducted to assess the zooplankton community composition in three sections (two latitudinal, going from Japan to the equator, and one longitudinal on the equator) of the Western Pacific Ocean. A total of 384 species of zooplankton adults and 21 groups of zooplankton larvae were identified, with copepods being the predominant taxon. The common dominant species across the three sections were Acrocalanus gibber, Canthocalanus pauper, Oithona similis, Paracalanus aculeatus, and Oncaea venusta. Zooplankton abundance was the highest in the equator section, with a mean abundance of 258.94 ± 52.57 ind./m3. Comparatively, Citation: Long, Y.; Noman, M.A.; a low abundance was recovered from the Subtropical Countercurrent (STCC) region, while the Chen, D.; Wang, S.; Yu, H.; Chen, H.; highest abundance holding stations were located in the eastern equatorial and North Equatorial Wang, M.; Sun, J. -
The “Metacopepod” Project: Designing an Integrated DNA Metabarcoding and Image Analysis Approach to Study and Monitor Biodiversity of Zooplanktonic Copepods
The “MetaCopepod” project: Designing an integrated DNA metabarcoding and image analysis approach to study and monitor biodiversity of zooplanktonic copepods. PanagiotisPanagiotis KasapidisKasapidis HellenicHellenic CentreCentre forfor MarineMarine ResearchResearch (HCMR),(HCMR), InstituteInstitute ofof MarineMarine Biology,Biology, BiotechnologyBiotechnology andand AquacultureAquaculture P.O.Box 2214, 71003 Heraklion Crete, Greece 1 The “MetaCopepod” project Aim: to develop a novel methodology, based on the combination of DNA metabarcoding and image analysis, to assess and monitor the diversity of marine zooplanktonic copepods (and cladocera), in the Mediterranean and the Black Sea, in a high-throughput, cost- effective, accurate and quantitative way. Coordinator: Dr. Panagiotis Kasapidis, Hellenic Centre for Marine Research (HCMR), GREECE Study area: Mediterranean and the Black Sea Duration: Feb. 2014 – Oct. 2015 Budget: 180,000 euros Funding: European Social Fund (ESF) and National Funds through the National Strategic Reference Framework (NSRF) 2007-2013, Operational Programme "Education and Life-Long Learning", Action "ARISTEIA II", Greek Ministry of Education and Religious Affairs, General Secretary of Research and Technology. 2 Studying zooplankton diversity: limitations of traditional approaches ● Quite laborious (sorting, identification under stereoscope) → bottleneck in sample processing. ● Requires local taxonomic expertise ● Difficult to identify immature stages ● Misidentifications ● Cryptic species 3 Image analysis + Pros -
A Guide to Marine Plankton
"Knowledge of the oceans is more than a matter of curiosity. Our very survival may hinge upon it.“ - John F. Kennedy - Quick Plankton Guide Conscinodiscus Chaetoceros Chaetoceros Ditylum Navicula Cylindrotheca Stephanopyxis Thalassionema dinoflagellate dinoflagellate dinoflagellate Licmorpha Protoperidinium Ceratium Ceratium ciliates radiolarian foramniferan jelly medusa jelly medusa ctenophore ctenophore Oweniidae larva Quick Plankton Guide polychaete larvae arrow worm snail veliger pteropod bivalve veliger cladoceran copepod nauplius copepod cumacean krill barnacle nauplius barnacle cyprid shrimp crab zoea crab megalop urchin larva sea star larva tunicate larva fish egg fish larva Diatoms Taxonomy Size Kingdom: Protista 5-60 µm Phylum: Bacillariophyta chains can be longer Diatoms are single-celled algae, usually golden-brown or yellow-green. Diatoms typically dominate the phytoplankton community in temperate regions. They are important producers, forming the base of ocean food chains. Diatoms are probably the single most important food source in the ocean. Energy source Sun - Diatoms are photosynthesizers. Predators Zooplankton. Life span A few days to a few weeks. Viewing tips To see phytoplankton well, you typically need 100X magnification or greater. It is easy to flood plankton with too much light, so reduce light and illuminate the slide from below. Interesting facts Diatoms produce oxygen through the process of photosynthesis and, along with the other phytoplankton, are responsible for 50-85% of the Earth’s oxygen. Diatoms use oil and many spines to help stay afloat in the ocean. Some also form chains to increase their ability to float. Floating near the surface is important because diatoms need the sun to produce energy, and the sunlight only penetrates to approx.