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PLOS ONE  2013 

Meiofauna Metabolism in Suboxic Sediments: Currently Overestimated

DOI: 10.1371/journal.pone.0059289

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Abstract:

Oxygen is recognized as a structuring factor of metazoan communities in marine sediments. The importance of oxygen as a controlling factor on meiofauna (32 μm-1 mm in size) respiration rates is however less clear. Typically, respiration rates are measured under oxic conditions, after which these rates are used in food web studies to quantify the role of meiofauna in sediment carbon turnover. Sediment oxygen concentration ([O2]) is generally far from saturated, implying that (1) current estimates of the role of meiofauna in carbon cycling may be biased and (2) meiofaunal organisms need strategies to survive in oxygen-stressed environments. Two main survival strategies are often hypothesized: 1) frequent migration to oxic layers and 2) morphological adaptation. To evaluate these hypotheses, we (1) used a model of oxygen turnover in the meiofauna body as a function of ambient [O2], and (2) performed respiration measurements at a range of [O2] conditions. The oxygen turnover model predicts a tight coupling between ambient [O2] and meiofauna body [O2] with oxygen within the body being consumed in seconds. This fast turnover favors long and slender organisms in sediments with low ambient [O2] but even then frequent migration between suboxic and oxic layers is for most organisms not a viable strategy to alleviate oxygen limitation. Respiration rates of all measured meiofauna organisms slowed down in response to decreasing ambient [O2], with Nematoda displaying the highest metabolic sensitivity for declining [O2] followed by Foraminifera and juvenile Gastropoda. Ostracoda showed a behavioral stress response when ambient [O2] reached a critical level. Reduced respiration at low ambient [O2] implies that meiofauna in natural, i.e. suboxic, sediments must have a lower metabolism than inferred from earlier respiration rates conducted under oxic conditions. The implications of these findings are discussed for the contribution of meiofauna to carbon cycling in marine sediments.

References

[1]  Glud RN (2008) Oxygen dynamics of marine sediments. Marine Biology Research 4: 243–289.
[2]  Franco M, Vanaverbeke J, Van Oevelen D, Soetaert K, Costa MJ, et al. (2010) Respiration partitioning in contrasting subtidal sediments: seasonality and response to a spring phytoplankton deposition. Marine Ecology 31: 276–290.
[3]  Braeckman U, Provoost P, Moens T, Middelburg JJ, Soetaert K, et al. (2011) Biological vs. physical mixing effects on benthic food web dynamics. PLoS One 6: e18078.
[4]  Moodley L, Middelburg JJ, Boschker HT, Duineveld GC, Pel R, et al. (2002) Bacteria and Foraminifera: key players in a short-term deep-sea benthic response to phytodetritus. Marine Ecology-Progress Series 236: 23–29.
[5]  Wenzh?fer F, Glud RN (2002) Benthic carbon mineralization in the Atlantic: a synthesis based on in situ data from the last decade. Deep Sea Research Part I: Oceanographic Research Papers 49: 1255–1279.
[6]  Huettel M, R?y H, Precht E, Ehrenhauss S (2003) Hydrodynamical impact on biogeochemical processes in aquatic sediments. Hydrobiologia 494: 231–236.
[7]  Aller R (1988) Benthic fauna and biogeochemical processes in marine sediments: the role of burrow structures. In: Nitrogen Cycling in Coastal Marine Environments. Chichester: John Wiley & Sons Ltd. 301–338.
[8]  Nicol J (1967) The Biology of Marine Animals, 2.ed. London: Sir Isaac Pigman & Sons Ltd. 1967. 699 pp. Internationale Revue der gesamten Hydrobiologie und Hydrographie 53.
[9]  Reise K (1985) Macrofauna promotes meiofauna. Tidal flat ecology. An experimental approach to species Interactions 54: 119–145.
[10]  Reise K, Ax P (1979) A meiofaunal “thiobios” limited to the anaerobic sulfide system of marine sand does not exist. Marine Biology 54: 225–237.
[11]  Hendelberg M, Jensen P (1993) Vertical distribution of the nematode fauna in a coastal sediment influenced by seasonal hypoxia in the bottom water. Ophelia 37: 83–94.
[12]  Wetzel MA, Fleeger JW, Powers SP (2001) Effects of hypoxia and anoxia on meiofauna: a review with new data from the Gulf of Mexico. Coastal and Estuarine Studies 58: 165–184.
[13]  Steyaert M, Moodley L, Vanaverbeke J, Vandewiele S, Vincx M, et al. (2005) Laboratory experiments on the infaunal activity of intertidal nematodes. Hydrobiologia 540: 217–223.
[14]  Soetaert K, Muthumbi A, Heip C (2002) Size and shape of ocean margin nematodes: morphological diversity and depth-related patterns. Marine Ecology-Progress Series 242: 179–193.
[15]  Powell E (1989) Oxygen, sulfide and diffusion: why thiobiotic meiofauna must be sulfide-insensitive first-order respirers. Journal of Marine Research 47: 887–932.
[16]  Soetaert K, Herman PMJ (2009) A practical guide to ecological modelling: using R as a simulation platform. Springer Verlag.
[17]  Higgins RP, Thiel H (1988) Introduction to the study of meiofauna. Smithsonian Institution Press, London.
[18]  Gerlach SA (1971) On the importance of marine meiofauna for benthos communities. Oecologia 6: 176–190.
[19]  Wieser W, Ott J, Schiemer F, Gnaiger E (1974) An ecophysiological study of some meiofauna species inhabiting a sandy beach at Bermuda. Marine Biology 26: 235–248.
[20]  Wieser W, Schiemer F (1977) The ecophysiology of some marine nematodes from Bermuda: seasonal aspects. Journal of Experimental Marine Biology and Ecology 26: 97–106.
[21]  Warwick RM (1981) The influence of temperature and salinity on energy partitioning in the marine nematode Diplolaimelloides bruciei. Oecologia 51: 318–325.
[22]  Mahaut M, Sibuet M, Shirayama Y (1995) Weight-dependent respiration rates in deep-sea organisms. Deep-Sea Research Part I-Oceanographic Research Papers 42: 1575–1582.
[23]  Moens T, Vincx M (2000) Temperature, salinity and food thresholds in two brackish-water bacterivorous nematode species: assessing niches from food absorption and respiration experiments. Journal of experimental marine biology and ecology 243: 137–154.
[24]  Wieser W, Kanwisher J (1961) Ecological and physiological studies on marine nematodes from a small salt marsh near Woods Hole, Massachusetts. Limnology and Oceanography : 262–270.
[25]  Ott J, Schiemer F (1973) Respiration and anaerobiosis of free living nematodes from marine and limnic sediments. Netherlands Journal of Sea Research 7: 233–243.
[26]  Calow P, Woolhead A (1977) The relation between ratio, reproductive effort and age-specific mortality in the evolution of life history strategies: some observations on freshwater triclads. Journal of Animal Ecology 46: 765–782.
[27]  Atkinson HJ (1975) The functional significance of the haemoglobin in a marine nematode, Enoplus brevis (Bastian). The Journal of experimental biology 62: 1–9.
[28]  Cullen DJ (1973) Bioturbation of superficial marine sediments by interstitial meiobenthos. Nature 242: 323–324.
[29]  Moens T, Herman PMJ, Verbeeck L, Steyaert M, Vincx M (2000) Predation rates and prey selectivity in two predacious estuarine nematodes. Marine Ecology-Progress Series 205: 185–193.
[30]  Moodley L, Steyaert M, Epping E, Middelburg JJ, Vincx M, et al. (2008) Biomass-specific respiration rates of benthic meiofauna: Demonstrating a novel oxygen micro-respiration system. Journal of Experimental Marine Biology and Ecology 357: 41–47.
[31]  Moodley L, Hess C (1992) Tolerance of infaunal benthic foraminifera for low and high oxygen concentrations. The Biological Bulletin 183: 94–98.
[32]  Goldstein ST, Watkins GT, Kuhn RM (1995) Microhabitats of salt marsh foraminifera: St. Catherines island, Georgia, USA. Marine Micropaleontology 26: 17–29.
[33]  Goldstein ST, Harben EB (1993) Taphofacies implications of infaunal foraminiferal assemblages in a Georgia salt marsh, Sapelo Island. Micropaleontology : 53–62.
[34]  Fenchel T (1975) Factors determining the distribution patterns of mud snails (Hydrobiidae). Oecologia 20: 1–17.
[35]  Newell R (1979) Biology of intertidal animals. Marine Ecological Surveys, Ltd., Faversham.
[36]  Soetaert K, Vincx M, Wittoeck J, Tulkens M, Van Gansbeke D (1994) Spatial patterns of Westerschelde meiobenthos. Estuarine, Coastal and Shelf Science 39: 367–388.
[37]  Steyaert M, Herman PMJ, Moens T, Widdows J, Vincx M (2001) Tidal migration of nematodes on an estuarine tidal flat (the Molenplaat, Schelde Estuary, SW Netherlands). Marine Ecology-Progress Series 224: 299–304.
[38]  Steyaert M (2003) Spatial and temporal scales of nematode communities in the North Sea and Westerschelde. PhD Thesis Ghent University, Ghent, Belgium : 114 pp.
[39]  Modig H, ólafsson E (1998) Responses of Baltic benthic invertebrates to hypoxic events. Journal of Experimental Marine Biology and Ecology 229: 133–148.
[40]  Steyaert M, Moodley L, Nadong T, Moens T, Soetaert K, et al. (2007) Responses of intertidal nematodes to short-term anoxic events. Journal of Experimental Marine Biology and Ecology 345: 175–184.
[41]  Frenzel P, Boomer I (2005) The use of ostracods from marginal marine, brackish waters as bioindicators of modern and Quaternary environmental change. Palaeogeography, Palaeoclimatology, Palaeoecology 225: 68–92.
[42]  Jahn A, Gamenick I, Theede H (1996) Physiological adaptations of Cyprideis torosa (Crustacea, Ostracoda) to hydrogen sulphide. Marine ecology progress series. Oldendorf 142: 215–223.
[43]  Herman PMJ, Vranken G, Heip C (1984) Problems in meiofauna energy-flow studies. Hydrobiologia 118: 21–28.
[44]  Franco MA, Soetaert K, Costa MJ, Vincx M, Vanaverbeke J (2008) Uptake of phytodetritus by meiobenthos using C-13 labelled diatoms and Phaeocystis in two contrasting sediments from the North Sea. Journal of Experimental Marine Biology And Ecology 362: 1–8.
[45]  Guilini K, Van Oevelen DD, Soetaert K, Middelburg JJ, Vanreusel A (2010) Nutritional importance of benthic bacteria for deep-sea nematodes from the Arctic ice margin: results of an isotope tracer experiment. Limnology and Oceanography 55: 1977–1989.
[46]  Ingels J, Van den Driessche P, De Mesel I, Vanhove S, Moens T, et al. (2010) Preferred use of bacteria over phytoplankton by deep-sea nematodes in polar regions. Marine Ecology-Progress Series 406: 121–133.
[47]  Pasotti F, De Troch M, Raes M, Vanreusel A (2012) Feeding ecology of shallow water meiofauna: insights from a stable isotope tracer experiment in Potter Cove, King George Island, Antarctica. Polar Biology : 1–12.
[48]  Pozzato L, Van Oevelen D, Moodley L, Soetaert K, Middelburg J (subm.) Carbon processing at the deep-sea floor of the Arabian Sea Oxygen Minimum Zone: a tracer approach. Journal of Sea Research.
[49]  Andrassy I (1956) The determination of volume and weight of nematodes. Acta Zoologica Hungarica : 1–15.
[50]  Wieser W (1960) Benthic studies in Buzzards Bay. II. The meiofauna. Limnology and Oceanography : 121–137.
[51]  De Bovée F (1987) Biomasse et équivalents énergétiques des nématodes libres marins = Biomass and energetic equivalent on the free-living marine nematodes. Cahiers de biologie marine 28: 367–372.
[52]  De Bovee F, Labat JP (1993) A Simulation Model of a Deep Meiobenthic Compartment: A Preliminary Approach. Marine Ecology 14: 159–173.
[53]  Moens T, Vincx M (1997) Observations on the feeding ecology of estuarine nematodes. Journal of the Marine Biological Association of the UK 77: 211–227.
[54]  Moens T, Van Gansbeke D, Vincx M (1999) Linking estuarine nematodes to their suspected food. A case study from the Westerschelde Estuary (south-west Netherlands). Journal of the Marine Biological Association of the UK 79: 1017–1027.
[55]  Moens T, Verbeeck L, Vincx M (1999) Feeding biology of a predatory and a facultatively predatory nematode (Enoploides longispiculosus and Adoncholaimus fuscus). Marine Biology 134: 585–593.
[56]  Moodley L, Chen G, Heip C, Vincx M (2000) Vertical distribution of meiofauna in sediments from contrasting sites in the Adriatic Sea: clues to the role of abiotic versus biotic control. Ophelia 53: 203–212.
[57]  Soetaert K, Petzoldt T (2009) FME: A Flexible Modelling Environment for inverse modelling, sensitivity, identifiability, monte carlo analysis. R package version 1. CRAN website. Available: http://cran.r-project.org/web/packages/F?ME/index.html. Accessed 2013 Mar 1.
[58]  Epping E, Van der Zee C, Soetaert K, Helder W (2002) On the oxidation and burial of organic carbon in sediments of the Iberian margin and Nazaré Canyon (NE Atlantic). Progress in Oceanography 52: 399–431.

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