Partitioning of benthic community respiration in the Arctic (northwestern Barents Sea)

For marine benthos communities, the assessment of a respiration budget encompassing the entire size range from microbes to mobile megafauna has seldom been attempted. An interdisciplinary field study in high Arctic waters (northwestern Barents Sea) in June/July 1991 provided the opportunity to concurrently est~rnate the oxygen uptake of the different benthic community fractions by a variety of approaches at water depths of 80 to 1010 m. The bulk respiration of micro-, meioand small macrobenthos was assessed by sediment community oxygen consumption (SCOC) rates measured by shipboard sediment-water incubations of virtually undisturbed cores. The oxygen uptake of community portions not sampled adequately by corers (megabenthic inand epifauna, including fish) was estimated by applying individual metabolic rates to density or biomass figures derived from seabed images, box corer samples or trawl catches. The respiration estimates of the various community fractions were subsequently compiled in synoptic models of the total benthic community oxygen consumption (BCOC) and its partitioning. In the study area, 2 benthic habitat types were distinguished, differing substantially in depth, sediment texture and, thus, benthic respiration pattern: (1) shallow shelf banks (<200 m) where the seabed is composed of coarse sediments and stones, and (2) deeper trenches or slopes (>200 m) characterized by fine sediments. On the banks, the patchiness of epibenthic brittle stars, which locally occurred in very high densities (up to 700 ind. m-'), controlled the benthic community respiration. On average, the megafauna was estimated to contribute about 25% to the median BCOC of about 90 pm01 0, m-' h-' (equivalent to an organic carbon mineralizat~on rate of 21 mg C m-? d-'). In the shelf trenches and on the slope, however, smaller endobenthic organisms predominated. SCOC, according to our estimates of meioand macrofaunal respiration, was dominated by the oxygen uptake of microorganisms and accounted for about 85% of the median BCOC of about 140 ~lmol 0, m-' h-' (35 mg C n r 2 d-l). Our results suggest that current models of benthic community respiration should be amended, particularly for Arctic shelf b~otopes where abundant megafauna may represent an important pathway of the benth~c energy flow.

[1]  Kenneth L. Smith Metabolism of two dominant epibenthic echinoderms measured at bathyal depths in the Santa Catalina Basin , 1983 .

[2]  A. Dye A study of benthic oxygen consumption on exposed sandy beaches , 1981 .

[3]  K. Smith,et al.  Organic carbon mineralization in the Santa Catalina Basin: benthic boundary layer metabolism , 1987 .

[4]  S. Gerlach,et al.  Size spectra of benthic biomass and metabolism , 1985 .

[5]  J. Grant,et al.  Size partitioning of microbial and meiobenthic biomass and respiration on Brown's Bank, south-west Nova Scotia , 1987 .

[6]  G. Graf Benthic-pelagic coupling: a benthic view , 1992 .

[7]  L. Peck,et al.  Two methods for the assessment of the oxygen content of small volumes of seawater , 1990 .

[8]  A. Clarke Life in cold water: the physiological ecology of polar marine ectotherms , 1983 .

[9]  H. Asmus Field measurements on respiration and secondary production of a benthic community in the northern Wadden Sea , 1982 .

[10]  S. Gerlach,et al.  Abundance, biomass, size-distribution and bioturbation potential of deep-sea macrozoobenthos on the Vøring plateau (1200-1500 m, Norwegian Sea) , 1991 .

[11]  R. Warwick,et al.  Ecological and metabolic studies on free-living nematodes from an estuarine mud-flat , 1979 .

[12]  P. F. Scholander,et al.  Climatic Adaptation in Arctic and Tropical Poikilotherms , 1953, Physiological Zoology.

[13]  G. Lopez,et al.  Bacterial abundance in relation to surface area and organic content of marine sediments , 1985 .

[14]  M. Aschan,et al.  Latitudinal gradients in the structure of macrobenthic communities: a comparison of Arctic, temperate and tropical sites , 1993 .

[15]  P. Schwinghamer,et al.  Partitioning of production and respiration among size groups of organisms in an intertidal benthic community , 1986 .

[16]  C. Mcroy,et al.  Pelagic-benthic coupling on the shelf of the northern Bering and Chukchi Seas. Ill Benthic food supply and carbon cycling , 1989 .

[17]  K. Smith Oxygen demands of San Diego Trough sediments: an in situ study1 , 1974 .

[18]  K. SmithJr. Benthic community respiration in the N.W. Atlantic Ocean: in situ measurements from 40 to 5200 m , 1978 .

[19]  G. Winberg,et al.  Rate of Metabolism and Food Requirements of Fishes , 1962 .

[20]  T. Blackburn,et al.  Arctic sediments (Svalbard): consumption and microdistribution of oxygen , 1994 .

[21]  G. Gust,et al.  Impact of bioroughness on interfacia solute exchange in permeable sediments , 1992 .

[22]  G. Hempel On the biology of polar seas, particulary the Southern Ocean , 1985 .

[23]  D. Connelly,et al.  A multiple corer for taking virtually undisturbed samples from shelf, bathyal and abyssal sediments , 1984 .

[24]  J. Barry,et al.  The influence of oceanographic processes on pelagic-benthic coupling in polar regions: A benthic perspective , 1991 .

[25]  Craig W. Emerson,et al.  Benthic oxygen consumption on continental shelves off eastern Canada , 1991 .

[26]  J. Grebmeier,et al.  Pelagic benthic coupling on the shelf of the northern Bering and Chukchi Seas-II. Benthic community structure , 1989 .