Rate of Filtering of Fecal Pellets by Acartia Omorii (Copepoda; Calanoida)

Total Page:16

File Type:pdf, Size:1020Kb

Rate of Filtering of Fecal Pellets by Acartia Omorii (Copepoda; Calanoida) Journal of the Oceanographical Society of Japan Vol.42, pp.487 to 489, 1987 Short Note Rate of Filtering of Fecal Pellets by Acartia omorii (Copepoda; Calanoida) Tenshi Ayukait Abstract: Adult females of Acartia omorii were allowed to feed on fecal pellets voided by its juveniles (copepodite stages I and II) in a mixture with the diatom Thalassiosira decipiens. The rate of filtering of pellets by adult females was 50.3•}11.5ml indiv-1d-1, being twice as high as the rate of filtering of T. decipiens. Suspended particulate organic matter in sea- The details of the rearing method have been water is composed mainly of non-living particles described elsewhere by Ayukai (1986). All such as so-called organic detritus and organic experiments were carried out at 17•Ž in the aggregates (ref. Nishizawa, 1966, 1969). The darkness using 100-ml bottles as experimental concentration of living phytoplankton, in turn, vessels. is generally no more than the level for herbivo- The rate of defecation by juvenile A. omorii rous calanoid copepods to meet the basic food was preliminarily determined. A single juvenile requirements (Mullin and Brooks, 1976). The was placed into bottles containing T. decipiens utilization of non-living particles by copepods at different concentrations between 200-1,400 has been a matter of interest (Poulet, 1976; cells These bottles were set onto a grazing Heinle et al., 1977; Roman, 1984). wheel rotated at 0.25 rpm. After 14 hr incuba- Fecal pellets are one typical form of organic tion, 1ml of borax-neutralized formalin was detritus. PaffenhOfer and Strickland (1970) were added to the bottles. Each bottle was allowed first to document "coprophagy" by copepods, to stand and the supernatant was withdrawn PaffenhOfer and Knowles (1979) reported that with a siphon. Residual water was transferred two species of copepods consumed naupliar fecal to a counting chamber and the size and number pellets as fast as they did phytoplankton the of pellets were measured under an inverted volume of which was similar to that of the microscope. pellets. The defecation rate of juvenile A. omorii was In the present study, adult females of Acartia plotted against the initial concentration of T. omorii (Ueda, 1986) were allowed to feed on decipiens because no significant change in the fecal pellets voided by its juveniles (copepodite concentration was observed (Fig. 1). The stages I and II) in a mixture with the diatom critical concentration for saturation of the de- Thalassiosira decipiens (13.4 pm ESD,=equiva- fecation rate was about 1,000 cells ml-1 of T. lent spherical diameter; 1270 ƒÊm3V,=volume). decipiens. The pellets observed above the critical The importance of fecal pellets as a food source concentration had an equivalent spherical dia- was evaluated by asking whether or not adult meter of 25.3 ƒÊm and a volume of 1.62•~104ƒÊm3. female A. omorii selectively fed on pellets rather During 14 hr incubation, about 20% of pellets than the diatom. were partially broken. The partial disintegra- Juvenile and adult female A. omorii used were tion of pellets little affected the determination reared from eggs on cultured phytoplankton . of the defecation rate, but was liable to be a * Received 20 June 1986; in revised form 7 No - Source of error in examining the utilization of vember 1986; accepted 28 November 1986. pellets. Since the continuous stirring of water † Faculty of Agriculture, Tohoku University, with a grazing wheel might result in an in- Sendai, 980, Japan. creased percentage of broken pellets, water in 488 Ayukai Table 1. Average concentration, filtering rate and ingestion rate of adult female Acartia omorii feeding on fecal pellets voided by its juveniles (copepodite stages I and II) in a mix- ture with the diatom Thalassiosira decipiens. Data are the mean•} the 95% confidence limits. Fig. 1. Relationship between the concentration the average. As shown in Fig. 1, the defeca- of the diatom Thalassiosira decipiens and the defecation rate of juvenile Acartia omorii tion rate of juvenile A. omorii became saturated (copepodite stages I and II). The curve is above 1,000 cells ml-1 of T. decipiens. The drawn freehand. defecation rate of juvenile A. omorii, therefore, is assumed to be constant throughout 20 hr in- the bottles was periodically stirred in the follow- cubation. ing experiment. As a result, the percentage of The rates of filtering and ingestion by adult broken pellets in the control bottles was reduced female A. omorii on cells and pellets are sum- to half. marized in Table 1. Injured juveniles were The rates of filtering and ingestion by adult found in 2 out of 35 experimental bottles, and female A. omorii on cells and pellets were de- results from these bottles were discarded. In termined. First, ten juveniles were placed into addition, the final concentration of T. decipiens each of 45 bottles and allowed to feed on T. in 4 out of the remaining 33 bottles was higher decipiens at the initial concentration of 1,360 than the average concentration in the control cells Water in these bottles was stirred bottles, and their results were also excluded every 2 hr. After 12 hr incubation, 1ml of borax- from the calculation of the filtering rate. neutralized formalin was added to five bottles The filtering rate of adult female A. omorii for counts of cells and pellets. on pellets was 50.3•}11.5ml indiv-1d-1, being Second, a single female was pipetted into each twice as high as that on T. decipiens of small of 35 bottles. These bottles together with five size (Table 1). This result agrees with a well control bottles were further incubated for 8 hr. known trend that copepods selectively ingest The bottle used was 8cm in height and juvenile large particles over small ones (e. g. Frost, 1972). fecal pellets had theoretical sinking rates of 15- and suggests that adult female A. omorii in 20cm hr-1, which were calculated according to nature prefer to utilize large sinking pellets Stokes' equation modified by Komar et al.(1981). rather than small phytoplankton. Thus water in the bottles was stirred every Cowey and Corner (1966) reported that amino 20min in order to suspend pellets. acid composition of fecal pellets voided by the Juvenile fecal pellets were easily distinguished copepod Calanus finmarchicus resembled that of from those of females by their size. The numbers its algal diet. Paffenhofer and Knowles (1979) of T. decipiens and intact pellets were counted successfully reared the copepod Calanus helgol- under an inverted microscope. The rates of andicus from copepodite stage III to adult stage, ingestion and filtering by adult female A. omorii offering fecal pellets as the sole diet. Although on cells and pellets were calculated from the more studies on the nutritive value of pellets difference between initial and final concentrations, are required, the active utilization of pellets according to Frost's equations (1972). seems important for copepods to survive in After 20 hr incubation, the concentration of food-limited environments. T. decipiens was reduced to 980 cells ml-1 on Rate of filtering of fecal pellets by Acartia omorii 489 Acknowledgement natural copepod and euphausiid fecal pellets. I wish to express my sincere thanks to Pro- Limnol. Oceanogr., 26, 172-180. fessor S. Nishizawa, Tohoku University, for Mullin, M. M. and E. R. Brooks (1976): Some con- continuing guidance and encouragement through sequences of distributional heterogeneity of phyto- out the present study. plankton and zooplankton. Limnol. Oceanogr., 21, 784-796. Nishizawa, S.(1966): Suspended material in the sea. References Inf. Bull. Planktl. Japan, 13, 1-33. Ayukai, T.(1986): Feeding elasticity of a planktonic Nishizawa, S.(1969): Suspended material in the sea. marine copepod Acaria clausi (Copepoda: Cala- 2. Reevaluation of the hypothesis. Bull. Plankton noida). Ph. D. thesis, Tohoku University, Japan, Soc. Japan, 16, 1-42. 121 pp. PaffenhOfer, G. -A. and J. D. H. Strickland (1970): A Cowey, C. B. and E. D. S. Corner (1966): The amino- note on the feeding of Calanus helgolandicus on acid composition of certain unicellular algae, and detritus. Mar. Biol., 5, 97-99. of the faecal pellets produced by Calanus fin- PaffenhOfer, G.-A. and S. C. Knowles (1979): Ecologi- marchicus when feeding on them. p.225-231. In: cal implications of fecal pellet size, production Some Contemporary Studies in Marine Science, and consumption by copepods. J. Mar. Res., 37, ed. by H. Barnes, George Allen and Unwin Ltd. 35-49. London. Poulet, S. A.(1976): Feeding of Pseudocalanus minu- Frost, B. W.(1972): Effects of size and concentration tus on living and non-living particles. Mar. Biol., of food particles on the feeding behavior of the 34, 117-125. marine planktonic copepod Calanus pacificus. Roman, M. R.(1984): Utilization of detritus by the Limnol. Oceanogr., 17, 805-815. copepod, Acartia tonsa. Limnol. Oceanogr., 29, Heinle, D. R., R. P. Harris, J. F. Ustach, and D. A. 949-959. Flemer (1977): Detritus as food for estuarine Ueda, H.(1986): Taxonomic reexamination and copepods. Mar. Biol., 40, 341-353. geographical distribution of copepods known as Komar, P. D., A. P. Morse, L. F. Small and S. W. Acartia clausi in Japanese coastal waters. J. Fowler (1981): An analysis of sinking rates of Oceanogr. Soc. Japan, 42, 134-138. Aoartia omorii (Copepoda: Calanoida) の 糞 粒 に 対 す る 濾 水 速 度 鮎 貝 天 志* 要 旨:室 内 実 験 系 に お い て,榛 脚 類 の 一 種Acartia して 与 え,雌 成 体 の 両者 に 対 す る摂 食 に つ い て 調 べ た. omoriiの 雌 成 体 に,そ の 幼 体(copepodite stages I-II) 雌 成 体 の 糞 粒 に 対 す る炉 水 速 度 は50.3±11.5 ml indiv-1 の 糞 粒 及 び 硅 藻 の 一 種Thalassiosira decipiensを 混 合 d-1で,T.decipiensに 対 す る濾 水 速度 の 約2倍 に 相 当 *東 北 大 学 農 学 部 〒980仙 台 市 堤 通 雨 宮 町1-1 す る高 い 値 で あ った..
Recommended publications
  • Acartiidae Sars, G.O. 1903
    Acartiidae Sars G.O, 1903 Genuario Belmonte Leaflet No. 194 I February 2021 ICES IDENTIFICATION LEAFLETS FOR PLANKTON FICHES D’IDENTIFICATION DU ZOOPLANCTON Revised version of Leaflet No. 181 ICES INTERNATIONAL COUNCIL FOR THE EXPLORATION OF THE SEA CIEM CONSEIL INTERNATIONAL POUR L’EXPLORATION DE LA MER International Council for the Exploration of the Sea Conseil International pour l’Exploration de la Mer H. C. Andersens Boulevard 44–46 DK-1553 Copenhagen V Denmark Telephone (+45) 33 38 67 00 Telefax (+45) 33 93 42 15 www.ices.dk [email protected] Series editor: Antonina dos Santos and Lidia Yebra Prepared under the auspices of the ICES Working Group on Zooplankton Ecology (WGZE) This leaflet has undergone a formal external peer-review process Recommended format for purpose of citation: Belmonte, G. 2021. Acartiidae Sars G.O, 1903. ICES Identification Leaflets for Plankton No. 194. 29 pp. http://doi.org/10.17895/ices.pub.7680 ISBN number: 978-87-7482-555-5 ISSN number: 2707-675X Cover Image: Inês M. Dias and Lígia F. de Sousa for ICES ID Plankton Leaflets This document has been produced under the auspices of an ICES Expert Group. The contents therein do not necessarily represent the view of the Council. © 2021 International Council for the Exploration of the Sea. This work is licensed under the Creative Commons Attribution 4.0 International License (CC BY 4.0). For citation of datasets or conditions for use of data to be included in other databases, please refer to ICES data policy. |ii ICES Identification Leaflets for Plankton No.
    [Show full text]
  • Seasonal Succession of Four Acartia Copepods (Copepoda, Calanoida) in Okkirai Bay, Sanriku, Northern Japan
    Plankton Benthos Res 7(4): 188–194, 2012 Plankton & Benthos Research © The Plankton Society of Japan Seasonal succession of four Acartia copepods (Copepoda, Calanoida) in Okkirai Bay, Sanriku, northern Japan YUICHIRO YAMADA*, ATSUSHI KOBIYAMA & TAKEHIKO OGATA School of Marine Biosciences, Kitasato University, 1–15–1 Kitasato, Minami-ku, Sagamihara 252–0329, Japan Received 17 April 2012; Accepted 4 September 2012 Abstract: Seasonal changes in abundance of four neritic Acartia species (A. hudsonica, A. omorii, A. longiremis and A. steueri), including identifiable copepodid stages, were investigated in the inner reaches of Okkirai Bay, Sanriku, northern Japan, to elucidate their seasonal succession patterns. Samples were collected monthly at intervals from Au- gust 2007 to July 2009 by vertical hauls of a NORPAC net of 100 μm mesh aperture. For identification of morphologi- cally allied A. omorii and A. hudsonica, the dimensional differences between them were statistically analyzed for the stages of C4 to C6. The dominant species were A. longiremis in the colder season and A. steueri in the warmer sea- son. A. longiremis and A. omorii appeared from early spring (February or March) to summer with numerical peaks in April. These April peaks were considered to result from immigration from outside the bay with intrusions of Oyashio Current water. A. steueri increased during the summer with a peak in September, then decreased until December or January, and disappeared for two or three months from April, when they were probably only present as diapausing eggs. A. hudsonica occurred from early spring to mid-summer as in A. omorii but with higher abundances in summer than in spring, though the seasonal abundances varied somewhat between years.
    [Show full text]
  • The Copepod Acartia Tonsa Dana in a Microtidal Mediterranean Lagoon: History of a Successful Invasion
    water Article The Copepod Acartia tonsa Dana in a Microtidal Mediterranean Lagoon: History of a Successful Invasion Elisa Camatti *, Marco Pansera and Alessandro Bergamasco Consiglio Nazionale delle Ricerche, Istituto di Scienze Marine (CNR ISMAR), Arsenale Tesa 104, Castello 2737/F, 30122 Venezia, Italy; [email protected] (M.P.); [email protected] (A.B.) * Correspondence: [email protected]; Tel.: +39-041-2407-978 Received: 13 May 2019; Accepted: 5 June 2019; Published: 8 June 2019 Abstract: The Lagoon of Venicehas been recognized as a hot spot for the introduction of nonindigenous species. Several anthropogenic factors as well as environmental stressors concurred to make this ecosystem ideal for invasion. Given the zooplankton ecological relevance related to the role in the marine trophic network, changes in the community have implications for environmental management and ecosystem services. This work aims to depict the relevant steps of the history of invasion of the copepod Acartia tonsa in the Venice lagoon, providing a recent picture of its distribution, mainly compared to congeneric residents. In this work, four datasets of mesozooplankton were examined. The four datasets covered a period from 1975 to 2017 and were used to investigate temporal trends as well as the changes in coexistence patterns among the Acartia species before and after A. tonsa settlement. Spatial distribution of A. tonsa was found to be significantly associated with temperature, phytoplankton, particulate organic carbon (POC), chlorophyll a, and counter gradient of salinity, confirming that A. tonsa is an opportunistic tolerant species. As for previously dominant species, Paracartia latisetosa almost disappeared, and Acartia margalefi was not completely excluded.
    [Show full text]
  • Physiological Responses of the Copepods Acartia Tonsa and Eurytemora Carolleeae to Changes in the Nitrogen:Phosphorus Quality of Their Food
    Nitrogen Article Physiological Responses of the Copepods Acartia tonsa and Eurytemora carolleeae to Changes in the Nitrogen:Phosphorus Quality of Their Food Katherine M. Bentley, James J. Pierson and Patricia M. Glibert * Horn Point Laboratory, University of Maryland Center for Environmental Science, P.O. Box 775, Cambridge, MD 21613, USA; [email protected] (K.M.B.); [email protected] (J.J.P.) * Correspondence: [email protected] Abstract: Two contrasting estuarine copepods, Acartia tonsa and Eurytemora carolleeae, the former a broadcast spawner and the latter a brood spawner, were fed a constant carbon-based diatom diet, but which had a variable N:P content, and the elemental composition (C, N, P) of tissue and eggs, as well as changes in the rates of grazing, excretion, egg production and viability were measured. To achieve the varied diet, the diatom Thalassiosira pseudonana was grown in continuous culture at a constant growth rate with varying P supply. Both copepods altered their chemical composition in response to the varied prey, but to different degrees. Grazing (clearance) rates increased for A. tonsa but not for + E. carolleeae as prey N:P increased. Variable NH4 excretion rates were observed between copepod 3− species, while excretion of PO4 declined as prey N:P increased. Egg production by E. carolleeae was highest when eating high N:P prey, while that of A. tonsa showed the opposite pattern. Egg viability by A. tonsa was always greater than that of E. carolleeae. These results suggest that anthropogenically changing nutrient loads may affect the nutritional quality of food for copepods, in turn affecting their elemental stoichiometry and their reproductive success, having implications for food webs.
    [Show full text]
  • Feeding Interactions Between Planktonic Copepods and Red-Tide Flagellates from Japanese Coastal Waters
    MARINE ECOLOGY PROGRESS SERIES Vol. 59: 97-107, 1990 Published January 11 Mar. Ecol. Prog. Ser. 1 Feeding interactions between planktonic copepods and red-tide flagellates from Japanese coastal waters Shin-ichi Uye, Kazuhiro Takamatsu Faculty of Applied Biological Science, Hiroshima University, Saijo-cho, Higashi-Hiroshima 724, Japan ABSTRACT. Feeding interactions between inshore marine copepods Pseudodiapto~nusmarinus and Acartia ornonl, and 15 red-tide flagellates were studied by examining egesbon rate, mortality and egg production rate of the copepods offered a suspension of each phytoplankton species. Among several species of poor quality as food, Olisthodiscus luteus (Raphidophyceae) was nearly completely rejected by P. mannus, and Gymnodinium nagasakiense (Dinophyceae), Heterosigma akashiwo (Raphidophy- ceae, Nagasak~University strain), Chattonella marina (Raphidophyceae) and Fibrocapsa japonica (Raphidophyceae) were almost entirely rejected by A. omorii. Since these flagellates are of preferred cell size and have no hard undigestible cell walls, the rejective feeding by copepods was suspected to be chemically mediated. Effects of chemical stimuli from 0. luteus (to P. marinus) and G. nagasakiense (to A. omorii) were examined in detail by conducting comparative feeding experiments in a suspension of Heterocapsa triquetra (Dinophyceae), a normally edible species. Addition of filtrate from the cell- homogenate of exponentially growing 0. luteus or G. nagasakiense to the suspension reduced copepod filtering rate on H. triquetra, indicating deterrent chemical compounds are intracellularly present. These compounds were ephemeral, being deactivated within 12 h at 20°C. Chemically-mediated rejection by copepods is an important factor in the development of monospecific red tides. INTRODUCTION of copepods: they captured, handled (probably tasted) and ingested (or rejected) particles according to their A considerable amount of data has been compiled on quality.
    [Show full text]
  • Effects of Temperature and Phytoplankton Community
    www.nature.com/scientificreports OPEN Efects of temperature and phytoplankton community composition on subitaneous and resting egg production rates of Acartia omorii in Tokyo Bay Ayumi Tsunashima1, Hiroshi Itoh2 & Toshiya Katano 1* To clarify the efects of temperature and phytoplankton community composition on Acartia omorii (Copepoda: Calanoida) egg production, its abundance and egg production rates were investigated from 2016 to 2018 in Tokyo Bay, Japan. Abundance was high from March to May (> 3.0 × ­104 individuals m−3) and low or undetected from late June to December (≤ 0.4 × ­104 individuals m−3). In 2018, most eggs were subitaneous until April; diapause eggs appeared in May when the water temperature −1 −1 exceeded 20 °C. The weight-specifc egg production rate (SEPR, Cegg Cfemale ­day ) had two peaks. In the frst peak in January, > 90% of eggs were subitaneous; in contrast, in the second peak in May, 60% of eggs were unhatched, including diapause eggs. The frst peak of subitaneous eggs may contribute to planktonic population development from March to May. In contrast the second peak of diapause eggs probably enhances their recurrence in the next winter. Multiple regression analysis revealed that subitaneous SEPR showed a negative response, whereas diapause SEPR showed a positive response to temperature. Subitaneous SEPR positively correlated with the proportion of small diatoms in phytoplankton carbon biomass, whereas unhatched SEPR positively correlated with the proportion of inedible preys in large diatoms and dinofagellates. Edible diatoms may induce subitaneous egg production, whereas low-food availability may induce diapause egg production. These results suggest that phytoplankton composition and water temperature have strong impacts on the dynamics of A.
    [Show full text]
  • Feeding of Copepods on Natural Suspended Particles in Tokyo Bay*
    Journal of the Oceanographical Society of Japan Vol.44, pp.217 to 227, 1988 Feeding of Copepods on Natural Suspended Particles in Tokyo Bay* Atsushi Tsudat and Takahisa Nemotot Abstract: Community grazing rates of copepods were estimated from data taken during three cruises in Tokyo Bay, based on bottle incubations and a temporal variation of gut fluorescence. Special attention was paid to the feeding selectivity in the estimations. Differential grazing was observed in the copepod communities: Acartia omorii, abundant in February, selectively fed on the particles of dominant size classes, while Oithona davisae, dominant throughout the year, and Centropages abdominalis selected large particles (>20ƒÊm). The maximum filtering rates on certain size classes were several times the average. In addition, a 34-hr investi- gation of the gut fluorescence of copepods revealed nocturnal feeding in Paracalanus spp., Pseudodiaptomus marinus and Oithona davisae. Copepod communities collected with a net (95-ƒÊm mesh opening) were esti- mated to graze, in February 3.0%, in August 3.1-4.5% and in November 4.2-11.9 % of the standing crops of phytoplankton or suspended particlesper day. 1. Introduction O.aruensis(Nishida,1985),is the most domi- Inner Tokyo Bay is a temperate, semi-closed nant species throughout the year, especially bay connected with the offshore waters by Uraga between July and September, while a calanoid. Strait. Eutrophication in the bay began in the copepod Acartia omorii, formerly identified as 1960's and increased until the early 1970's to A. clausi (Ueda, 1986) is abundant from Feb- the level sustained at present (Unoki and Kishi- ruary to June (Anakubo, 1982).
    [Show full text]
  • Effect of Pyridine Triphenyl Borane (KH101) on the Reproduction Of
    IIFET 2004 Japan Proceedings EFFECT OF PYRIDINE TRIPHENYL BORANE(KH101) ON THE REPRODUCTION OF CALANOID COPEPOD, ACARTIA AMORII BRADFORD °∗ 1 Md. Khaled Hossain, •∗ 2 Takashi Ishimaru and °∗ 3 Seiichi Takeda ° Department of Marine Science and Technology • Department of Ocean Sciences ∗ Tokyo University of Marine Science and Technology Konan 4-5-7, Minato-ku, Tokyo 108-8477, Japan, 1 [email protected], 2 [email protected], 3 [email protected] ABSTRACT Currently documented that pyridine triphenyl borane (KH101) is possible to use as an alternative of tributyltin based antifouling biocide in coastal and marine environment. But its impact on marine life especially on smaller zooplankton is so far unknown. The present study was conducted to determine the effect of KH101 on adult survival, egg production and egg hatch of a calanoid copepod, Acartia omorii under bath administration. Survival was observed every 24h for 10 days. Each 10 individuals of adult female were incubated at different concentrations of KH101 (0.001, 0.01, 0.1, 1, 10 and 100µg/L) with food (Isochrysis sp.+Tetraselmis sp., ratio 1:1). Egg production was examined through the incubation of single gravid female with above conditions but only at 0.001, 0.01, 0.1 and 1µg/L of KH101 concentrations. Egg hatching success was determined for each 60 eggs at different concentrations of KH101, which were obtained from pre-exposed female at the same concentration. LC50s were obtained in 0.1, 1, 10 and 100µg/L concentrations of KH101 after 168, 96, 48 and 24h, respectively. Significant (P<0.05) decrease in egg production and egg hatching success were obtained at 1µg/L level.
    [Show full text]
  • 40 (5) 2019 Special Issue
    Journal Home page : www.jeb.co.in « E-mail : [email protected] Special Issue TM Journal of Environmental Biology TM p-ISSN: 0254-8704 e-ISSN: 2394-0379 JEB CODEN: JEBIDP DOI : http://doi.org/10.22438/jeb/40/5(SI)/SI-19 White Smoke Plagiarism Detector Just write. Effect of temperature on egg development time and productivity of Acartia steueri and population variations of family Acartiidae in Dadaepo Beach, Busan, Korea Paper received: 30.10.2018 Revised received: 06.03.2019 Accepted: 16.03.2019 Abstract Authors Info 1 1 1 Aim: This research aimed to study the effect of temperature on egg production rate, egg development time, Y.J. Jo , W. Park *, B. W. Lee , 2 3 hatching success rate and egg size of Acartia steueri and seasonal variation of species composition of family C. G. Kang and Y.E. Kim Acartiidae. 1 Department of Marine Biology, Pukyong National University, Methodology: Population variations of Acartiidae were investigated based on weekly collected samples Busan, 48513, Korea from Dadaepo beach, Busan, Korea. Live copepods were reared in laboratory at five temperature regimes 2 (10, 14, 18, 22 and 26℃) to estimate temperature effects on the egg development time and productivity of A. School of Earth Sciences and steueri. Environmental Engineering, GIST, Gwangju, 61005, Korea Results: Total five acartiid species were found in the study area: Acartia omorii, A. steueri, A. pacifica, A. 3 Department of Marine erythraea, and A. sinjiensis. A. steueri and A. omorii were dominated in colder months from January to April, Biotechnology, Soonchunhyang while A. pacifica, A.
    [Show full text]
  • Emergence Patterns of Small Subtidal Arthropods in Relation to Day/Night
    Journal of Oceanography, Vol. 56, pp. 295 to 310, 2000 Emergence Patterns of Small Subtidal Arthropods in Relation to Day/Night, Tidal, and Surface/Bottom Factors: Investigations in the Boreal Sea, Japan (Akkeshi, Hokkaido) MASAYUKI SAIGUSA*, KAZUSHI OISHI, AKIHIRO IKUMOTO, HIROSHI IWASAKI and MICHIHIRO TERAJIMA Department of Biology, Faculty of Science, Okayama University, Tsushima 2-1-1, Okayama 700-8530, Japan (Received 20 January 1999; in revised form 24 September 1999; accepted 8 October 1999) The emergence of small arthropods was studied in the boreal sea, Japan (Akkeshi, Keywords: Hokkaido). In the shallow subtidal zone, two impeller pumps were set in the surface ⋅ Daily (=diel) and bottom waters. The pumps ran continuously for 25 days (22 August–16 Septem- rhythm, ⋅ ber, 1998), and invertebrates were sampled using a nylon net (300 to 500 µm in mesh day/night, ⋅ size). The small arthropods collected with the net belonged to 16 orders comprising dispersal, ⋅ emergence pattern, about 60 taxa. In the dominant 23 taxa, a two-way ANOVA was applied to determine ⋅ Hokkaido whether there was any significant difference in abundance between day and night (Akkeshi), and between surface and bottom. While emergence of 15 taxa (65%) was significantly ⋅ small arthropods, different with regard to the day/night factor, that of the other 8 taxa (35%) was not. ⋅ surface/bottom, As to the difference between the two depths, the distribution of 15 taxa (65%) was ⋅ swimming activity. significantly different. Furthermore, in 25 taxa for which over 100 specimens were collected in each of the two depths of water, emergence patterns were examined with regard to the synchrony with day/night and tidal cycles.
    [Show full text]
  • Zooplankton Invasions: a Brief Review, Plus Two Case Studies from the Northeast Pacific Ocean
    Hydrobiologia 480: 87–110, 2002. 87 C.E. Lee, S. Strom & J. Yen (eds), Progress in Zooplankton Biology: Ecology, Systematics, and Behavior. © 2002 Kluwer Academic Publishers. Printed in the Netherlands. Zooplankton invasions: a brief review, plus two case studies from the northeast Pacific Ocean Stephen M. Bollens1,2, Jeffery R. Cordell3, Sean Avent1 & Rian Hooff1 1Romberg Tiburon Center for Environmental Studies and Department of Biology, San Francisco State University, 3152 Paradise Drive, Tiburon, CA 94920, U.S.A. 2Moss Landing Marine Laboratories, California State University, 8272 Moss Landing Road, Moss Landing, CA 95039, U.S.A. 3School of Aquatic and Fishery Sciences, University of Washington, Seattle, WA 98195, U.S.A. Tel: 415-338-3512. Fax: 415-435-7121. E-mail: [email protected] Key words: zooplankton, invasion, ecology, non-indigenous, copepods, estuaries Abstract Invasions of aquatic habitats by non-indigenous species (NIS), including zooplankton, are occurring at an alarming rate and are causing global concern. Although hundreds of such invasions have now been documented, surprisingly little is known about the basic biology and ecology of these invaders in their new habitats. Here we provide an overview of the published literature on NIS zooplankton, separated by life history (holoplankton vs. meroplankton), habitat (marine, estuarine, freshwater), and biological level of organization or topic (e.g. distribution and range extension, physiology, behavior, feeding, community impacts, ecosystem dynamics, etc). Amongst the many findings generated by our literature search, perhaps the most striking is the paucity of studies on community and ecosystem level impacts of NIS zooplankton, especially in marine and estuarine systems. We also present some results from two ongoing studies of invasive zooplankton in the northeast Pacific Ocean – Pseudodiaptomus inopinus in Washington and Oregon coastal estuaries, and Tortanus dextrilobatus in San Francisco Bay.
    [Show full text]
  • PHYLUM ARTHROPODA: Subphylum Crustacea: Class Maxillipoda
    MARINE ZOOPLANKTON OF SOUTHERN BRITAIN Part 2: Arachnida, Pycnogonida, Cladocera, Facetotecta, Cirripedia and Copepoda David V.P. Conway Edited by Anthony W.G. John Marine Biological Association Occasional Publications0 No 26 1 MARINE ZOOPLANKTON OF SOUTHERN BRITAIN Part 2: Arachnida, Pycnogonida, Cladocera, Facetotecta, Cirripedia and Copepoda David V.P. Conway Marine Biological Association, Plymouth, UK Edited by Anthony W.G. John Marine Biological Association of the United Kingdom Occasional Publications No 26 Front cover from top, left to right: Two types of facetotectan nauplii and a cyprid stage from Plymouth (Image: R. Kirby); Larval turbot (Scophthalmus maximus) faeces containing skeletons of the copepod Pseudocalanus elongatus, their undigested eggs and lipid droplets; The cladoceran Podon intermedius; Zooplankton identification course in MBA Resource Centre; Nauplius stage of parasitic barnacle, Peltogaster paguri. 2 Citation Conway, D.V.P. (2012). Marine zooplankton of southern Britain. Part 2: Arachnida, Pycnogonida, Cladocera, Facetotecta, Cirripedia and Copepoda (ed. A.W.G. John). Occasional Publications. Marine Biological Association of the United Kingdom, No 26 Plymouth, United Kingdom 163 pp. Electronic copies This guide is available for free download, from the National Marine Biological Library website - http://www.mba.ac.uk/NMBL/ from the “Download Occasional Publications of the MBA” section. © 2012 by the Marine Biological Association of the United Kingdom. No part of this publication should be reproduced in any form without consulting the author. ISSN 02602784 This publication has been prepared as accurately as possible, but suggestions or corrections that could be included in any revisions would be gratefully received. [email protected] 3 Preface The range of zooplankton species included in this series of three guides is based on those that have been recorded in the Plymouth Marine Fauna (PMF; Marine Biological Association.
    [Show full text]