Elva Escobar Briones

Sediment community metabolism associated with continental shelf hypoxia, Northern Gulf of Mexico

Net fluxes of respiratory metabolites (O2, dissolved inorganic carbon (DIC), NH4+, NO3−, and NO2−) across the sediment-water interface were measured using in-situ benthic incubation chambers in the area of intermittent seasonal hypoxia associated with the Mississippi River plume. Sulfate reduction was measured in sediments incubated with trace levels of35S-labeled sulfate. Heterotrophic remineralization, measured as nutrient regeneration, sediment community oxygen consumption (SOC), sulfate reduction, or DIC production, varied positively as a function of temperature. SOC was inversely related to oxygen concentration of the bottom water. The DIC fluxes were more than 2 times higher than SOC alone, under hypoxic conditions, suggesting that oxygen uptake alone cannot be used to estimate total community remineralization under conditions of low oxygen concentration in the water column. A carbon budget is constructed that compares sources, stocks, transformations, and sinks of carbon in the top meter of sediment. A comparison of remineralization processes within the sediments implicates sulfate reduction as most important, followed by aerobic respiration and denitrification. Bacteria accounted for more than 90% of the total community biomass, compared to the metazoan invertebrates, due presumably to hypoxic stress.

Ammonium excretion by benthic invertebrates and sediment-water nitrogen flux in the Gulf of Mexico near the Mississippi River outflow

Benthic macroinvertebrate biomass and ammonium excretion rates were measured at four stations in the Gulf of Mexico near the Mississippi River mouth. Calculated areal excretion rates were then compared to sediment-water nitrogen fluxes measured in benthic bottom lander chambers at similar stations to estimate the potential importance of macroinvertebrate excretion to sediment nitrogen mineralization. Excretion rates for individual crustaceans (amphipods and decapods) was 2–21 nmoles NH4+ (mg dry weight)−1 h−1. The mean excretion rates for the polychaetes, Paraprionaspio pinnata [6–12 nmoles NH4+ (mg dry weight)−1h−1] and Magelona sp. [27–53 nmoles NH4+ (mg dry weight)−1h−1], were comparable or higher than previous measurements for similar size benthic or pelagic invertebrates incubated at the same temperature (22±1°C). Although the relatively high rates of excretion by these selective feeders may have been partially caused by experimental handling effects (e.g., removal from sediment substrates), they probably reflected the availability of nitrogen-rich food supplies in the Mississippi River plume. When the measured weight-specific rates were extrapolated to total areal biomass, areal macroinvertebrate excretion estimates ranged from 7 μmole NH4+ m−2h−1 at a 40-m deep station near the river mouth to 18 μmole NH4+ m−2h−1 at a shallower (28-m deep) station further from the river mouth. The net flux of ammonium and nitrate from the sediments to the water measured in bottom lander chambers in the same region were 15–53 μmole NH4+ m−2h−1 and −25–21 μmole NO3− m−2h−1. These results suggest that excretion of NH4+ by macroinvertebrates could be a potentially important component of benthic nitrogen regeneration in the Mississippi River plume-Gulf shelf region.

Sediment community biomass and respiration in the Northeast water polynya, Greenland: a numerical simulation of benthic lander and spade core data

Sediment community metabolism (oxygen demand) was measured in the Northeast Water (NEW) polynya off Greenland employing two methods: in situ benthic chambers deployed with a benthic (GOMEX) lander and shipboard laboratory Batch Micro-Incubation Chambers (BMICs) utilizing ‘cores’ recovered from USNEL box cores. The mean benthic respiration rate measured with the lander was 0.057 mM O2 m−2 h−1 (n = 5); whereas the mean measured with the BMICs was 0.11 mM O2 m−2 h−1 (n = 21; p < 0.01 that the means were the same). In terms of carbon fluxes (14 and 27 mg C m−2 d−1), these respiration rates represent ca. 5–15% of the average net primary production measured in the euphotic zone in 1992. The biomass of the bacteria, meiofauna and macrofauna were measured at each location to quantify the relationship between total community respiration and total community biomass (mean 1.42 g C m−2). Average carbon residence time in the biota, calculated by dividing the biomass by the respiration, was on the order of 50–100 days, which is comparable to relatively oligotrophic continental margins at temperate latitudes. The biomass and respiration data for the aerobic heterotrophic bacteria, the infaunal invertebrates (meiofauna and macrofauna), and the epifaunal megabenthos (two species of brittle stars) are summarized in a ‘steady-state’ solution of a sediment food chain model, in terms of carbon. This carbon budget illustrates the relative importance of the sediment-dwelling invertebrates in the benthic subsystem, compared to the bacteria and the epibenthos, during the summer open-water period in mud-lined troughs at depths of about 300 m. The input needed to drive heterotrophic respiratory processes was within the range of the input of organic matter recorded in moored, time-sequencing sediment traps. A time-dependent numerical simulation of the model was run to investigate the potential responses of the three size groups of benthos to abrupt seasonal pulses of particulate organic matter. The model suggests that there is a time lag in the increase in bottom community biomass and respiration following the POC pulse, and provides hypothetical estimates for the potential carbon storage in the summer (open water), followed by catabolic losses during each ensuing winter (ice covered). This sequence of storage and respiration may contribute to the process of seasonal CO2 ‘rectification’ (sensu Yager et al., 1995) in some Arctic ecosystems.

Carbon stable isotopes ratios of pelagic and littoral communities in Alchichica crater-lake, Mexico

Carbon stable isotope ratios were determined in dominant biotic components of pelagic and littoral systems in Alchichica crater-lake. Results showed that carbon signatures were significantly different between both systems. The pelagic environment was more depleted (−26.15 to −15.14 per mille) than the littoral zone (−21.03 to −17.91 per mille). The potential source end-point in the simplified pelagic community was established to be diatomaceous phytoplankton; its predicted value was −21.7 per mille. There is a clear evidence that Nodularia does not sustain the pelagic food chain. In contrast, the highly diverse littoral community was sustained by epiphytes. No allochthonous sources seemed to influence this food web. 13C enrichment was observed along the components of both systems with fractionations of 0.8 to 1.4 per mille. The contribution of the seagrass Ruppia maritima is probably associated with the detritus pathway. Carbon source partitioning between both systems was not recorded. The δ13C in Alchichica crater-lake was more enriched than in other saline lakes and could be attributed to different salinity and CO2 concentrations among lakes.