Chemistry, temperature, and faunal distributions at diffuse-flow hydrothermal vents : comparison of two geologically distinct ridge systems

Author Posting. © The Oceanography Society, 2012. This article is posted here by permission of The Oceanography Society for personal use, not for redistribution. The definitive version was published in Oceanography 25, no. 1 (2012): 234–245, doi:10.5670/oceanog.2012.22.Diffuse-flow, low-temperature areas near hydrothermal vents support life via chemosynthesis: hydrogen sulfide (and other reduced chemical compounds) emanating from the subsurface is oxidized with bottom-water oxygen through bacterial mediation to fix carbon dioxide and produce biomass. This article reviews the in situ diffuse-flow chemistry (mainly H2S and O2) and temperature data collected in 2006 and 2009 along the Eastern Lau Spreading Center (ELSC), and from 2004 to 2008 at 9°N along the East Pacific Rise (9 N EPR), predominantly around macrofauna that contain endosymbionts at these two hydrothermal vent regions. More than 48,000 and 20,000 distinct chemical and temperature data points were collected with a multi-analyte electrochemical analyzer in the diffuse-flow waters at 9 N EPR and the ELSC, respectively. Despite their different geological settings and different macrofauna (two different species of snails and mussels at the ELSC versus two different species of tubeworms and mussels at 9 N EPR), there are similarities in the temperature and chemistry data, as well as in the distributions of organisms. The pattern of water chemistry preferred by the provannid snails (Alviniconcha spp., Ifremeria nautilei) and Bathymodiolus brevior at the ELSC is similar to the water chemistry pattern found for the siboglinid tubeworms (Tevnia jerichonana, Riftia pachyptila) and the Bathymodiolus thermophilus mussels at 9 N EPR. The eruptions at 9 N EPR in 2005 and 2006 resulted in increased H2S concentrations, increased H2S/T ratios, and an initial change in the dominant tubeworm species from Riftia pachyptila to Tevnia jerichonana after the eruption created new vent habitats. In 2005, two sites at 9 N EPR showed major increases in the H2S/T ratio from 2004, which suggested a probable eruption in this basalt-dominated system. At the ELSC, there was a decrease in the H2S/T ratio from northern to southern sites, which reflects the change in geological setting from basalt to andesite and the shallower water depths at the southern sites.This work was supported by NSF grants OCE-0240896, OCE-073243 (ELSC), OCE-0308398 (OTIC), OCE-0326434, and OCE-0937324 (EPR) to GWL; ESI-0087679, OCE-9529819, and OCE-0327353 to RAL; OCE-0327261, OCE-0328117, OCE-0451983 to TMS; and OCE 0240985 and OCE 0732333 to CRF

Functions of height and width dimensions in the intertidal mussel, Mytilus californianus

Author Posting. © National Shellfisheries Association, 2008. This article is posted here by permission of National Shellfisheries Association for personal use, not for redistribution. The definitive version was published in Journal of Shellfish Research 27 (2008): 385-392, doi:10.2983/0730-8000(2008)27[385:FOHAWD]2.0.CO;2.A mussel's shell records its history of growth. We investigated variability in the size and shape of mussel shells of Mytilus californianus Conrad (1837) to test the hypothesis that the mussel shell provides information on the contemporary condition of the mussel. Two factors were associated with shape: an epithelial discoloration and the Sr/Ca in the shell nacre. Sr/Ca data distinguished the mussel populations as did a discriminate analysis that included the trace metal ratios; Sr/Ca, Mg/Ca, Mn/Ca, Ag/Ca, Cd/Ca, Ba/Ca, and Pb/Ca. Size varied independently of shape and was not associated with the two factors. However, a null model that describes the morphological variability in height and width suggests that mussel size also plays a central role in partitioning phenotypic variability. These analyses of contemporary factors coupled with analyses of morphological variability holds promise for addressing the functional roles of mussel height and width and what proportion of phenotypic variability can be attributed to environmental factors

Speciation of manganese in Chesapeake Bay waters by voltammetric methods

The Mn(II) to Mn(O) reduction wave (peak) at a mercury electrode was investigated for its analytical usefulness in anoxic Chesapeake Bay waters which contain significant quantities of dissolved and particulate organic matter. The Mn(II) to Mn(O) reduction is characteristic for all Mn(II), MN(III) and MN(IV) complexes and thus represents total dissolved Mn. It does not provide information on only the Mn(II) oxidation state as suggested previously. Inorganic Mn(II) and organic Mn(III) complexes were studied by sampled d.c. polarography, differential pulse polarography, cyclic voltammetry and square wave voltammetry. All methods show that the Mn(II) to Mn(O) reduction is quasi-reversible in sea water. Square wave voltammetry was used for analytical work on field samples. Both Mn(II) and Mn(III) give similar current versus concentration slopes for the Mn(II) to Mn(O) peak when added to Chesapeake Bay samples. The minimum detection limit is near 200 to 300 nM. Comparison of organic free and organic rich laboratory and field samples shows that Ep shifts to more negative potentials for the organic rich samples. Thus, a major finding of this voltammetric study is that manganese can be complexed by organic ligands in marine systems with zones characterized by high organic matter decomposition and low O2 concentrations. Organic complexation of dissolved Mn may have important consequences for Mn chemistry in marine systems characterized by an oxic / anoxic interface

Short-Term and Interannual Variability of Redox-Sensitive Chemical Parameters in Hypoxic/Anoxic Bottom Waters of the Chesapeake Bay

A combination of CTD casts, discrete bottle sampling and in situ voltammetric microelectrode profiling was used to examine changing redox conditions in the water column at a single station south of the Bay Bridge in the upper Chesapeake Bay in late July/ early August, 2002–2005. Short-term (2–4 h) fluctuations in the oxic/suboxic/anoxic interface were documented using in situ voltammetric solid-state electrodes. Profiles of dissolved oxygen and sulfide revealed tidally-driven vertical fluctuations of several meters in the depth and thickness of the suboxic zone. Bottom water concentrations of sulfide, Mn2+ and Fe2+ also varied over the tidal cycle by approximately an order of magnitude. These data indicate that redox species concentrations at this site varied more due to physical processes than biogeochemical processes. Based on analysis of ADCP data, tidal currents at this station were strongly polarized, with the principal axis of tidal currents aligned with the mainstem channel. Together with the chemical data, the ADCP analysis suggests tidal flushing of anoxic bottom waters with suboxic water from north of the site. The present study is thus unique because while most previous studies have focused on processes across relatively stable redox interfaces, our data clearly demonstrate the influence of rapidly changing physical mixing processes on water column redox chemistry. Also noted during the study were interannual differences in maximum bottom water concentrations of sulfide, Mn2+ and Fe2+. In 2003, for example, heavy spring rains resulted in severe hypoxia/anoxia in June and early July. While reported storm-induced mixing in late July/early August 2003 partially alleviated the low-oxygen conditions, bottom water concentrations of sulfide, Mn2+ and Fe2+ were still much higher than in the previous year. The latter implies that the response time of the microbial community inhabiting the suboxic/anoxic bottom waters to changing redox conditions is slow compared to the time scale of episodic mixing events. Bottom water concentrations of the redox-sensitive chemical species should thus be useful as a tracer to infer prior hypoxic/ anoxic conditions not apparent from ambient oxygen levels at the time of sampling

Variations in sediment production of dissolved iron across a continental margin not dominated by major upwelling or riverine inputs

Despite the undeniable effect of iron on shaping patterns of ocean productivity, the relative importance of the different sources of this limiting nutrient to the ocean is still under debate. Although global estimates indicate that the benthic input of iron to the oceans is significant, most studies have investigated continental margins exposed to either upwelling or large riverine inputs, environments that are not representative of the majority of the oceans. Additionally, the number of studies that report dissolved iron concentrations in continental slope sediments is limited, despite the fact that these regions between the shelf edge and the continental rise make up >5% of the sedimentary surface area of the global ocean. The sedimentary flux of iron has traditionally been considered negligible due to the rapid oxidation of Fe²⁺ in oxic waters and poor solubility of the Fe(III) product. The recent realization that ferric iron may be stabilized in solution by organic ligands during oxidation near the sediment-water interface suggests that a significant fraction of the dissolved iron pool may be present under the form organic-Fe(III) complexes that could eventually reach the overlying waters. In this study, the speciation and biogeochemical importance of iron was determined in intact sediment cores along a transect across the entire continental margin near Cape Lookout, North Carolina, a region not dominated by upwelling or riverine inputs that is representative of most passive continental margins. Rates of diffusive oxygen uptake (DOU) and maximum diffusive fluxes of both dissolved Fe²⁺ and organic-Fe(III) complexes decreased from the coastal zone to the continental shelf, remained low on the shelf and the upper continental slope, but rebounded to reach a maximum in mid-slope sediments where concentrations of Fe(III) oxides were the highest along the transect. In turn, DOU decreased and dissolved iron was below detection in lower-slope sediments, indicating that mid-slope sediments represent depocenters where Fe(III) oxides and organic matter may accumulate. Pore water sulfate and sulfide concentrations as well as separate sediment incubations confirmed that sulfate reduction does not greatly influence the cycling of iron in these sediments. The production of dissolved organic-Fe(III) in these continental margin sediments is likely regulated by a combination of aerobic oxidation in the presence of natural organic ligands near the sediment-water interface, dissimilatory iron reduction, or chemical oxidation of Fe(II) complexed to natural organic ligands. Fluxes of Fe²⁺ and organic-Fe(III) complexes across the sediment-water interface were not observed. However, diffusive fluxes of Fe²⁺ and organic-Fe(III) complexes into the oxic zone of these sediments (<1 cm from the sediment-water interface) and production of dissolved Fe(III) in sediment slurry incubations suggest that complexation of Fe(III) in these sediments may contribute to the stabilization and potential transport of dissolved iron into oxygenated deep ocean waters. Extrapolation to the global ocean suggests that mid-slope depocenters contribute considerably to the iron inventory of the ocean, thus warranting the need for measurement of benthic iron fluxes and dissolved iron speciation in these environments

Chemistry, Temperature, and Faunal Distributions at Diffuse-Flow Hydrothermal Vents: Comparison of Two Geologically Distinct Ridge Systems

Diffuse-flow, low-temperature areas near hydrothermal vents support life via chemosynthesis: hydrogen sulfide (and other reduced chemical compounds) emanating from the subsurface is oxidized with bottom-water oxygen through bacterial mediation to fix carbon dioxide and produce biomass. This article reviews the in situ diffuse-flow chemistry (mainly H2S and O2) and temperature data collected in 2006 and 2009 along the Eastern Lau Spreading Center (ELSC), and from 2004 to 2008 at 9°N along the East Pacific Rise (9 N EPR), predominantly around macrofauna that contain endosymbionts at these two hydrothermal vent regions. More than 48,000 and 20,000 distinct chemical and temperature data points were collected with a multi-analyte electrochemical analyzer in the diffuse-flow waters at 9 N EPR and the ELSC, respectively. Despite their different geological settings and different macrofauna (two different species of snails and mussels at the ELSC versus two different species of tubeworms and mussels at 9 N EPR), there are similarities in the temperature and chemistry data, as well as in the distributions of organisms. The pattern of water chemistry preferred by the provannid snails (Alviniconcha spp., Ifremeria nautilei) and Bathymodiolus brevior at the ELSC is similar to the water chemistry pattern found for the siboglinid tubeworms (Tevnia jerichonana, Riftia pachyptila) and the Bathymodiolus thermophilus mussels at 9 N EPR. The eruptions at 9 N EPR in 2005 and 2006 resulted in increased H2S concentrations, increased H2S/T ratios, and an initial change in the dominant tubeworm species from Riftia pachyptila to Tevnia jerichonana after the eruption created new vent habitats. In 2005, two sites at 9 N EPR showed major increases in the H2S/T ratio from 2004, which suggested a probable eruption in this basalt-dominated system. At the ELSC, there was a decrease in the H2S/T ratio from northern to southern sites, which reflects the change in geological setting from basalt to andesite and the shallower water depths at the southern sites