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Distribution, population dynamics and growth rates of Thysanopoda acutifrons, Thysanoessa inermis and Nematobrachion boöpis in the Irminger Sea, North Atlantic

Published online by Cambridge University Press:  29 October 2012

R.A. Saunders*
Affiliation:
British Antarctic Survey, High Cross, Madingley Road, Cambridge, CB3 0ET, UK Scottish Oceans Institute, University of St Andrews, East Sands, St Andrews, KY16 8LB, UK
J. Rasmussen
Affiliation:
Marine Scotland, PO Box 101, 375 Victoria Road, Aberdeen, AB11 9DB, UK
G.A. Tarling
Affiliation:
British Antarctic Survey, High Cross, Madingley Road, Cambridge, CB3 0ET, UK
A.S. Brierley
Affiliation:
Scottish Oceans Institute, University of St Andrews, East Sands, St Andrews, KY16 8LB, UK
*
Correspondence should be addressed to: R.A. Saunders, British Antarctic Survey, High Cross, Madingley Road, Cambridge, CB3 0ET, UK email: [email protected]

Abstract

Euphausiids are an important component of the northern North Atlantic ecosystem and several species are found in the Irminger Sea. However, data on euphausiids in this region are few, particularly for Thysanopoda acutifrons, Thysanoessa inermis and Nematobranchion boöpis. In this paper, we present the first data since the 1930s on the seasonal distribution and population dynamics of these species from net haul data collected in the Irminger Sea during winter, spring and summer 2001–2002. Thysanoessa inermis was the most numerically abundant (0.63–26.62 ind. 1000 m−3) of the three species in the region and comprised a biomass of 3.92–41.74 mg 1000 m−3. The species was largely found in the upper regions of the water column (0–400 m) and was distributed in the more on-shelf/shelf-break regions around East Greenland and Iceland. Growth rates were around 0.03 mm d−1for T. inermis and there was some evidence that either the timing of spawning was delayed, or larval development was prolonged in the region. Thysanopoda acutifrons was predominantly distributed below 400 m in more oceanic regions and had a low abundance (1.23–1.64 ind. 1000 m−3) throughout the Irminger Sea. However, the species comprised a relatively high proportion of biomass (19.39–31.33 mg 1000 m−3) due to its large body size. Our data showed that the species had low rates of growth (0.04 mm d−1) and development throughout the year, and that the reproductive season occurred during the overwintering period (November/December) once individuals had reached two years of age. Nematobranchion boöpis mainly occurred below 400 m at low abundance (0.06–0.18 ind.1000 m−3) levels throughout the region. The species was largely found where Atlantic waters prevailed in the Irminger Current and its growth rates were variable (0.02–0.06 mm d−1). Nematobranchion boöpis was a year-round spawner and the species had fairly rapid rates of post-larval development, with the newly spawned 0-group reaching sexual maturity within the first 6 months. Data presented in this paper provide useful baselines for understanding the possible impacts of long-term, broad-scale environmental change on the ecology of euphausiid communities in the Irminger Sea.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2012 

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References

REFERENCES

Aitchison, J. (1955) On the distribution of a positive random variable having a discrete probability mass at the origin. Journal of the American Statistical Association 50, 901908.Google Scholar
Astthorsson, O.S. and Gislason, A. (1997) Biology of euphausiids in the subarctic waters of Iceland. Marine Biology 129, 319330.CrossRefGoogle Scholar
Astthorsson, O.S. and Pálsson, O.K. (1987) Predation on euphausiids by cod, Gadus morhua, in winter in Icelandic waters. Marine Biology 96, 327334.CrossRefGoogle Scholar
Bamstedt, U. and Karlson, K. (1998) Euphausiid predation on copepods in coastal waters of the Northeast Atlantic. Marine Ecology Progress Series 172, 149168.CrossRefGoogle Scholar
Barange, M. (1990) Vertical migration and habitat partitioning of 6 euphausiid species in the North Benguela upwelling system. Journal of Plankton Research 12, 12231237.CrossRefGoogle Scholar
Beaugrand, G. (2003) Long-term changes in copepod abundance and diversity in the north-east Atlantic in relation to fluctuations in the hydroclimatic environment. Fisheries Oceanography 12, 270283.CrossRefGoogle Scholar
Boysen, E. and Buchholz, F. (1984) Meganyctiphanes norvegica in the Kattegat. Studies on the annual development of a pelagic population. Marine Biology 79, 195207.CrossRefGoogle Scholar
Dalpadado, P. and Skjoldal, H.R. (1996) Abundance, maturity and growth of the krill species Thysanoessa inermis and T. longicaudata in the Barents Sea. Marine Ecology Progress Series 144, 175183.CrossRefGoogle Scholar
de la Mare, W. (1994) Estimating krill recruitment and its variability. CCAMLR Science 1, 5569.Google Scholar
Dickson, B., Yashayaev, I., Meincke, J., Turrell, B., Dye, S. and Holfort, J. (2002) Rapid refreshening of the deep North Atlantic Ocean over the past four decades. Nature 416, 832837.CrossRefGoogle Scholar
Einarsson, H. (1945) Euphausiacea. I. Northern Atlantic species. Dana Report 27, 1185.Google Scholar
Falk-Petersen, S., Hagen, W., Kattner, G., Clarke, A. and Sargent, J. (2000) Lipids, trophic relationships, and biodiversity in Arctic and Antarctic krill. Canadian Journal of Fisheries and Aquatic Sciences 57 (Supplement 3), 178191.CrossRefGoogle Scholar
Falk-Petersen, S. and Hopkins, C.C.E. (1981) Ecological investigations on the zooplankton community of Balsfjorden, northern Norway: population dynamics of the euphausiids Thysanoessa inermis (Krøyer), Thysanoessa raschii (M. Sars) and Meganyctiphanes norvegica (M. Sars) in 1976 and 1977. Journal of Plankton Research 3, 177192.CrossRefGoogle Scholar
Gonzalez, C., Bruno, I. and Paz, X. (2000) Food and feeding of deep-sea redfish (Sebastes mentella Travin) in the North Atlantic. NAFO Scientific Council Studies 33, 89101.Google Scholar
Greene, C.H., Pershing, A.J., Conversi, A., Planque, B., Hannah, C., Sameoto, D., Head, E., Smith, P.C., Reid, P.C., Jossi, J., Mountain, D., Benfield, M.C., Wiebe, P.H. and Durbin, E. (2003) Trans-Atlantic responses of Calanus finmarchicus populations to basin-scale forcing associated with the North Atlantic Oscillation. Progress in Oceanography 58, 301312.CrossRefGoogle Scholar
Heath, M.R., Rasmussen, J., Ahmed, Y., Allen, J., Anderson, C.I.H., Brierley, A.S., Brown, L., Bunker, A., Cook, K., Davidson, R., Fielding, S., Gurney, W.S.C., Harris, R., Hay, S., Henson, S., Hirst, A.G., Holliday, N.P., Ingvarsdottir, A., Irigoien, X., Lindeque, P., Mayor, D.J., Montagnes, D., Moffat, C., Pollard, R., Richards, S., Saunders, R.A., Sidey, J., Smerdon, G., Speirs, D., Walsham, P., Waniek, J., Webster, L., Wilson, D., NERC Marine Productivity Programme (Funder) and The Scottish Executive Environment and Rural Affairs Department (Funder) (2008) Spatial demography of Calanus finmarchicus in the Irminger Sea. Progress in Oceanography 76, 3988.CrossRefGoogle Scholar
Hind, A., Gurney, W.S.C., Heath, M. and Bryant, A.D. (2000) Overwintering strategies in Calanus finmarchicus. Marine Ecology Progress Series 193, 95107.CrossRefGoogle Scholar
Hirst, A.G., Roff, J.C. and Lampitt, R.S. (2003) A synthesis of growth rates in marine epipelagic invertebrate zooplankton. Advances in Marine Biology 44, 1142.CrossRefGoogle ScholarPubMed
Holliday, N.P., Waniek, J., Davidson, R., Wilson, D., Brown, L., Sanders, R., Pollard, R.T. and Allen, J.T. (2006) Large-scale physical controls on phytoplankton growth, part 1: hydrographic zones, mixing and stratification. Journal of Marine Systems 59, 201218.CrossRefGoogle Scholar
Jörgensen, G. and Matthews, J.B.L. (1975) Ecological studies on the deep water pelagic community of Korsfjorden, western Norway. Population dynamics of six species of euphausiid in 1968 and 1969. Sarsia 59, 6784.CrossRefGoogle Scholar
Kinsey, S.T. and Hopkins, T.L. (1994) Trophic stratergies of euphausiids in a low-latitude ecosystem. Marine Biology 118, 651661.CrossRefGoogle Scholar
Kulka, D.W. and Corey, S. (1978) The life history of Thysanoessa inermis in the Bay of Fundy. Canadian Journal of Zoology 56, 492506.CrossRefGoogle Scholar
Lavender, K.L., Davis, R.E. and Owens, W.B. (2000) Mid-depth recirculation observed in the interior Labrador and Irminger Seas by direct velocity measurements. Nature 407, 6669.CrossRefGoogle ScholarPubMed
Lindley, J.A. (1977) Continuous plankton records: the distribution of the Euphausiacea (Crustacea: Malacostraca) in the North Atlantic and the North Sea, 1966–1967. Journal of Biogeography 4, 121133.CrossRefGoogle Scholar
Lindley, J.A. (1978) Population dynamics and production of euphausiids. I. Thysanoessa longicaudata in the North Atlantic. Marine Biology 46, 121130.CrossRefGoogle Scholar
Lindley, J.A. (1980) Population dynamics and production of euphausiids. II. Thysanossa inermis and T. raschi in the North Sea and American coastal waters. Marine Biology 59, 225233.CrossRefGoogle Scholar
Makarov, R.R. and Denys, C.J. (1981) Stages of sexual maturity of Euphausia superba. BIOMASS Handbook 11, 113.Google Scholar
Mauchline, J. (1960) The biology of the euphausiid crustacean, Meganyctiphanes norvegica Sars. Proceedings of the Royal Society of Edinburgh. Series B 67, 141179.Google Scholar
Mauchline, J. (1980a) The biology of Euphausiids. Advances in Marine Biology 18, 373623.Google Scholar
Mauchline, J. (1980b) Measurement of body length of Euphausia superba Dana. BIOMASS Handbook 4, 19.Google Scholar
Mauchline, J. (1985) Growth and production of Euphausicea (Crustacea) in the Rockall Trough. Marine Biology 90, 1926.CrossRefGoogle Scholar
Mauchline, J. and Fisher, L.R. (1969) The biology of Euphausiids. Advances in Marine Biology 7, 1454.Google Scholar
Methot, R.D. (1986) A frame trawl for sampling juvenile fish. CalCOFI Report 27, 267278.Google Scholar
Noji, T.T. (1991) The influence of macrozooplankton on vertical particulate flux. Sarsia 76, 19.CrossRefGoogle Scholar
Pearcy, W.G., Hopkins, C.C.E., Grönvik, S. and Evans, R.A. (1979) Feeding habits of cod, capelin, and herring in Balsfjorden, northern Norway, July–August 1978: the importance of euphausiids. Sarsia 64, 269277.CrossRefGoogle Scholar
Peck, L.S., Webb, K.E. and Bailey, D.M. (2004) Extreme sensitivity of biological function to temperature in Antarctic marine species. Functional Ecology 18, 625630.CrossRefGoogle Scholar
Pinchuk, A.I. and Hopcroft, R.R. (2007) Seasonal variations in the growth rates of euphausiids (Thysanoessa inermis, T. spinifera, and Euphausia pacifica) from the northern Gulf of Alaska. Marine Biology 151, 257269.CrossRefGoogle Scholar
Quetin, L.B., Ross, R.M., Frazer, T.K., Amsler, M.O., Wyatt-Evens, C. and Oakes, S.A. (2003) Growth of larval krill, Euphausia superba, in fall and winter west of the Antarctic Peninsula. Marine Biology 143, 833843.CrossRefGoogle Scholar
Richardson, A.J. and Schoeman, D.S. (2004) Climate impact on plankton ecosystems in the north east Atlantic. Science 305, 16091612.CrossRefGoogle Scholar
Ross, R.M. and Quetin, L.B. (1989) Energetic cost to development to the 1st feeding stage of Euphausia superba Dana and the effects of delays in food availability. Journal of Experimental Marine Biology and Ecology 133, 103127.CrossRefGoogle Scholar
Ross, R.M., Quetin, L.B., Baker, K.S., Vernet, M. and Smith, R.C. (2000) Growth limitation in young Euphausia superba under field conditions. Limnology and Oceanography 45, 3143.CrossRefGoogle Scholar
Ross, R.M., Quetin, L.B. and Kirsch, E. (1988) Effect of temperature on development times and survival of early larval stages of Euphausia superba Dana. Journal of Experimental Marine Biology and Ecology 121, 5571.CrossRefGoogle Scholar
Sanders, R., Brown, L., Henson, S.A. and Lucas, M. (2005) New production in the Irminger Basin during 2002. Journal of Marine Systems 55, 291310.CrossRefGoogle Scholar
Saunders, R.A., Ingvarsdottir, A., Rasmussen, J., Hay, S.J. and Brierley, A.S. (2007) Regional variation in distribution pattern, population structure and growth rates of Meganyctiphanes norvegica and Thysanoessa longicaudata in the Irminger Sea, North Atlantic. Progress in Oceanography 72, 313342.CrossRefGoogle Scholar
Siegel, V. (2000a) Krill (Euphausiacea) demography and variabilty in abundance and distribution. Canadian Journal of Fisheries and Aquatic Sciences 57 (Supplement 3), 151167.CrossRefGoogle Scholar
Siegel, V. (2000b) Krill (Euphausiacea) life history and aspects of population dynamics. Canadian Journal of Fisheries and Aquatic Sciences 57 (Supplement 3), 130150.CrossRefGoogle Scholar
Tarling, G.A. (2010) Population dynamics of Northern krill (Meganyctiphanes norvegica Sars). Advances in Marine Biology 57, 5990.CrossRefGoogle ScholarPubMed
Tattersall, W.M. (1911) Schizopodous Crustacea from the north-east Atlantic slope. Second supplement. Fisheries, Ireland, Scientific Investigation, 1910, pp. 177.Google Scholar
Tesch, F.W. (1971) Age and growth. In Ricker, W.E. (ed.) A manual on methods for the assessment of secondary production in fresh waters. Volume 17. IBP Handbook. Oxford & Edinburgh: Blackwell Scientific Publications, pp. 98130.Google Scholar
Thomasson, M.A., Johnson, M.L., Stromberg, J.O. and Gaten, E. (2003) Swimming capacity and pleopod beat rate as a function of sex, size and moult stage in Northern krill Meganyctiphanes norvegica. Marine Ecology Progress Series 250, 205213.CrossRefGoogle Scholar
Vikingsson, G.A. (1997) Feeding of fin Whales (Balaenoptera physalus) off Iceland—diurnal and seasonal variation and possible rates. Journal of Northwest Atlantic Fisheries Science 22, 7789.CrossRefGoogle Scholar