Seasonal variations in the speciation of dissolved iodine in the Chesapeake Bay

The speciation of dissolved iodine and the distributions of the iodine species in the deep Chesapeake Bay underwent seasonal variations in response to changes in the prevailing redox condition. In the deep water, the ratios of iodate to iodide and iodate to inorganic iodine decreased progressively from the Winter through the Summer as the deep water became more poorly oxygenated before they rebounded in the Fall when the deep water became re-oxygenated again. The composition of the surface water followed the same trend. However, in this case, the higher biological activities in the Spring and the Summer could also have enhanced the biologically mediated reduction of iodate to iodide by phytoplankton and contributed to the lower ratios found during those seasons. Superimposed on this redox cycle was a cycle of input and removal of dissolved iodine probably as a result of the interactions between the water column and the underlying sediments. Iodine was added to the Bay during the Summer when the deep water was more reducing and removed from the Bay in the Fall when the deep water became re-oxygenated. A third cycle was the inter-conversion between inorganic iodine and ‘dissolved organic iodine’, or ‘‘DOI’’. The conversion of inorganic iodine to ‘DOI’ was more prevalent in the Spring. As a result of these biogeochemical reactions in the Bay, during exchanges between the Bay and the North Atlantic, iodate-rich and ‘DOI’-poor water was imported into the Bay while iodide- and ‘DOI’-rich water was exported to the Atlantic. The export of iodide from these geochemically reactive systems along the land margins contributes to the enrichment of iodide in the surface open oceans.     

The distribution of brachyuran crustacean megalopae in the waters of the York river, lower Chesapeake Bay and adjacent shelf: Implications for recruitment

Vertical and horizontal distributions are described for megalopae of 11 brachyuran taxa common to the lower Chesapeake Bay and adjacent shelf. Three distribution patterns are apparent from horizontal distribution.

1. (1) More than 75% of the megalopae of estuarine adults, such as Hexapanopeus angustifrons, Neopanope sayi, Panopeus herbstii, Rhithropanopeus harrisii and Pinnotheres ostreum, are retained in estuarine waters.

2. (2) The megalopae of three estuarine taxa, Callinectes sapidus, Uca spp. and Pinnixa sp., are most abundant on the shelf.

3. (3) More than 90% of the megalopae of the shelf species, Portunus sp., Cancer irroratus and Libinia spp. remained in shelf waters.

Vertical distributions indicate the megalopae of a majority of estuarine crabs are epibenthic when waters are stratified. Exceptions include the megalopae of both Rhithropanopeus which are found slightly shallower in well mixed waters and Callinectes sapidus which are generally most abundant in the neuston. The megalopae of two shelf species, Portunus sp. and Cancer irroratus, reach highest densities in surface waters, while those of Libinia spp. are common in the epibenthos.Megalopal distributions analyzed with respect to water column stratification show megalopae never reached highest densities within the layer of the pycnocline. The megalopae of five species show significant shifts in vertical distributions between stratified and homogeneous water columns.     

Total selenium and selenium (IV) in the James River estuary and southern Chesapeake Bay

The concentrations of total selenium (Se) and Se (IV) were determined in the surface waters of 30 stations located in the James River and southern Chesapeake Bay. The concentrations of total Se and Se (IV) ranged from 0·28 to 1·91 nM and from 0·07 to 1·36 nM, respectively, between salinities of 31·78 and 0·06‰. The concentration of Se (VI), calculated as the difference between the concentrations of total Se and Se (IV), ranged from 0·08 to 0·67 nM. While total Se seemed to be conservative in this study area at salinities above 0·36‰, Se (IV) might have been removed during estuarine mixing. The removal of Se (IV) occurred primarily at salinities below 4‰ possibly via the oxidation of Se (IV) to Se (VI).     

长江口及杭州湾邻近海域夏季表层海水中的溶解无机碳

根据2004年8月在长江口、杭州湾附近海域获得的调查资料对表层水中Ph值、总碱度和溶解无机碳的分布特征及其与环境参数的关系进行了研究,并由此得到了溶解无机碳的组成情况.结果表明,HCO3-、CO23-;和CO2(T)占溶解无机碳浓度百分比分别为80.33%～97.75%、0.61%～19.42%和0.25%～2.34%,平均值分别为(93.28±3.68)%、(5.58±4.03)%和(1.14±0.43)%.水文、浮游植物等对各参数的分布具有重要影响,但对不同参数的影响程度不同.     

The composition of phytoplankton within the Chesapeake Bay plume and adjacent waters off the Virginia coast,U.S.A.

Phytoplankton composition differences were used to identify and plot the extent of the Chesapeake Bay plume over the continental shelf. Distinct but different phytoplankton assemblages were noted within the plume for March, June and October 1980. The major constituents in the plume were Skeletonema costatum, a variety of other diatoms and an unidentified ultraplankton component assumed to consist of several cyanophycean and chlorophycean species. The shelf plankton outside of the plume was mainly characterized by the coccolithophores and other phytoplankters that formed different seasonal assemblages than what was within the plume. Patchiness and fluctuations in the shape, size and extent of the plume were noted. A total of 235 species is given, with their presence within the plume and at shelf stations indicated.     

Methylmercury production in sediments of Chesapeake Bay and the mid-Atlantic continental margin

Methylmercury (MeHg) concentration and production rates were studied in bottom sediments along the mainstem of Chesapeake Bay and on the adjoining continental shelf and slope. Our objectives were to 1) observe spatial and temporal changes in total mercury (HgT) and MeHg concentrations in the mid-Atlantic coastal region, 2) investigate biogeochemical factors that affect MeHg production, and 3) examine the potential of these sediments as sources of MeHg to coastal and open waters. Estuarine, shelf and slope sediments contained on average 0.5 to 1.5% Hg as MeHg (% MeHg), which increased significantly with salinity across our study site, with weak seasonal trends. Methylation rate constants (k_meth), estimated using enriched stable mercury isotope spikes to intact cores, showed a similar, but weaker, salinity trend, but strong seasonality, and was highly correlated with % MeHg. Together, these patterns suggest that some fraction of MeHg is preserved thru seasons, as found by others [Orihel, D.M., Paterson, M.J., Blanchfield, P.J., Bodaly, R.A., Gilmour, C.C., Hintelmann, H., 2008. Temporal changes in the distribution, methylation, and bioaccumulation of newly deposited mercury in an aquatic ecosystem. Environmental Pollution 154, 77] Similar to other ecosystems, methylation was most favored in sediment depth horizons where sulfate was available, but sulfide concentrations were low (between 0.1 and 10 μM). MeHg production was maximal at the sediment surface in the organic sediments of the upper and mid Bay where oxygen penetration was small, but was found at increasingly deeper depths, and across a wider vertical range, as salinity increased, where oxygen penetration was deeper. Vertical trends in MeHg production mirrored the deeper, vertically expanded redox boundary layers in these offshore sediments. The organic content of the sediments had a strong impact on the sediment:water partitioning of Hg, and therefore, on methylation rates. However, the HgT distribution coefficient (K_D) normalized to organic matter varied by more than an order of magnitude across the study area, suggesting an important role of organic matter quality in Hg sequestration. We hypothesize that the lower sulfur content organic matter of shelf and slope sediments has a lower binding capacity for Hg resulting in higher MeHg production, relative to sediments in the estuary. Substantially higher MeHg concentrations in pore water relative to the water column indicate all sites are sources of MeHg to the water column throughout the seasons studied. Calculated diffusional fluxes for MeHg averaged  1 pmol m^− 2 day^− 1. It is likely that the total MeHg flux in sediments of the lower Bay and continental margin are significantly higher than their estimated diffusive fluxes due to enhanced MeHg mobilization by biological and/or physical processes. Our flux estimates across the full salinity gradient of Chesapeake Bay and its adjacent slope and shelf strongly suggest that the flux from coastal sediments is of the same order as other sources and contributes substantially to the coastal MeHg budget.     

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.     

Dissolved Iodate and Total Iodine During an Extreme Hypoxic Event in the Southern Benguela System

Dissolved iodate and total iodine were studied in St Helena Bay, South Africa, during a period of acute hypoxia, following upwelling off Cape Columbine. Despite the generally high concentrations of chlorophyll α (10–30 mg m⁻³) total iodine concentration was essentially constant in the main part of the Bay, and similar to that found elsewhere in the oceans. Occasional, lower concentrations of total iodine (0·28 to 0·42 μM) were found with exceptionally high chlorophyll α concentrations (500 mg m⁻³) in shallow waters. In contrast, iodate was found to be reduced to iodide at both the surface and the bottom of the Bay. The implications of these changes are discussed, given that the surface waters reflect sustained eutrophication while the bottom waters are hypoxic as a result of the organic-rich sediment from the waters above.     

Grain size composition and transport of sedimentary organic carbon in the Changjiang River (Yangtze River) Estuary and Hangzhou Bay and their adjacent waters

Surface sediments from the Changjiang River(Yangtze River) Estuary,Hangzhou Bay,and their adjacent waters were analyzed for their grain size distribution,organic carbon(OC) concentration,and stable carbon isotope composition(δ13C).Based on this analysis,about 36 surface sediment samples were selected from various environments and separated into sand(0.250 mm,0.125–0.250 mm,0.063–0.125 mm) and silt(0.025–0.063 mm)fractions by wet-sieving fractionation methods,and further into silt-(0.004–0.025 mm) and clay-sized(0.004mm) fractions by centrifugal fractionation.Sediments of six grain size categories were analyzed for their OC andδ13C contents to explore the grain size composition and transport paths of sedimentary OC in the study area.From fine to coarse fractions,the OC content was 1.18%,0.51%,0.46%,0.42%,0.99%,and 0.48%,respectively,while theδ13C was –21.64‰,–22.03‰,–22.52‰,–22.46‰,–22.36‰,and –22.28‰,respectively.In each size category,the OC contribution was 42.96%,26.06%,9.82%,5.75%,7.09%,and 8.33%,respectively.The OC content in clay and fine silt fractions(0.025 mm) was about 69.02%.High OC concentrations were mainly found in offshore modern sediments in the northeast of the Changjiang River Estuary,in modern sediments in the lower estuary of the Changjiang River and Hangzhou Bay,and in Cyclonic Eddy modern sediments to the southwest of the Cheju Island.Integrating the distribution of terrestrial OC content of each grain size category with the δ13C of the bulk sediment indicated that the terrestrial organic material in the Changjiang River Estuary was transported seaward and dispersed to the Cyclonic Eddy modern sediments to the southwest of the Cheju Island via two pathways:one was a result of the Changjiang River Diluted Water(CDW) northeastward extending branch driven by the North Jiangsu Coastal Current and the Yellow Sea Coastal Current,while the other one was the result of the CDW southward extending branch driven by the Taiwan Warm Current.     

Sea-bed Mixing and Particle Residence Times in Biologically and Physically Dominated Estuarine Systems: a Comparison of Lower Chesapeake Bay and the York River Subestuary

Biologically dominated lower Chesapeake Bay and the physically dominated York River subestuary are contrasted in terms of the dynamics of sediment mixing, strata formation and sea-bed particle residence times. Two lower bay sites were examined; both are located within the bay stem plains and are characterized by muddy sand and an abundance of large, deep-dwelling organisms. X-radiographs indicate extensive biological reworking of sediments, with no long-term preservation of physical stratification.²¹⁰Pb profiles reveal low sediment accumulation rates at both lower bay sites (<0·1 cm year⁻¹), but significant differences in biological mixing depths (25vs40 cm) and biodiffusivity (>80vs6–30 cm²year⁻¹). In contrast, the York River site, located within a partially-filled palaeochannel, is predominantly mud with a depauperate benthic community dominated by small, short-lived, shallow-dwelling organisms. Although²¹⁰Pb accumulation rates at the York River site (<0·2 cm year⁻¹) are similar to those measured in the lower bay, there is little bioturbation. In addition, transient bed forms at the York River site form laterally persistent, linear ridges and furrows sub-parallel to the channel, spaced 10–20 m apart. These observations, coupled with evidence of episodic erosion and deposition from radioisotope and porosity profiles, and X-radiographs, suggest that the upper 60–120 cm of the sea-bed are dominated by physical mixing. Deep mixing and low accumulation rates result in long residence times of particles in the mixed upper portion of the sea-bed (10²year) at both locations, despite different mixing controls [i.e. biological (diffusive)vsphysical (advective)].     

胶州湾沉积物中有机质的来源与组成及其对百年尺度环境变化的指示

The Jiaozhou Bay is characterized by heavy eutrophication that is associated with intensive anthropogenic activities. Four core sediments from the Jiaozhou Bay are analyzed using bulk technologies, including sedimentary total organic carbon(TOC), total nitrogen(TN), the stable carbon(δ~(13)C) and nitrogen(δ~(15) N) isotopic composition to obtain the comprehensive understanding of the source and composition of sedimentary organic matter and further shed light on the environmental changes of the Jiaozhou Bay on a centennial time scale.Results suggest that the TOC and TN concentrations increase in the upper core, having indicated a probable eutrophication process since the 1920 s in the inner bay and the 2000 s in the bay mouth. The TOC and TN concentrations outside the bay have also changed since 1916 owing to the variation of terrigenous input.Considering TOC/TN ratio, δ~(13) C and δ~(15) N, it can be concluded there is a mixture of terrigenous and marine organic matter sources in the study area. A simple two end-member(terrigenous and marine) mixing model usingδ~(13) C indicats that 45%–79% of TOC in the Jiaozhou Bay is from the marine source. The environmental changes of the Jiaozhou Bay are recorded by geochemical proxies, which are influenced by the intensive anthropogenic activities(e.g., extensive use of fertilizers, and discharge of sewage) and climate changes(e.g., rainfall).