Accumulation rate and heavy metal pollution in Osaka Bay sediments

The accumulation rates of sediment cores in Osaka Bay have been determined by using²¹⁰Pb dating technique. In the upper 10 cm²¹⁰Pb_ex contents show a constant value with depth. The accumulation rates below the homogeneous layer of sediments ranging from 0.12 to 0.61cm y^–1 (0.067–0.34 g cm^–2 y^–1) were obtained. The higher contents of Zn, Cu, Pb and Cr were observed in the upper 10 to 30 cm of sediments. Assuming that the increment of heavy metal content in sediments is due to anthropogenic origin, the amount of anthropogenic input of heavy metals into sediments were estimated to be 1,300–2,700g cm^–2 for Zn, 150 – 480 for Cu, 360 – 410 for Pb and 320 – 480 for Cr. The increment appears to start about 100 years ago. In surfical sediments most of heavy metal contents exceeded the background content, and then most part of Osaka Bay is polluted by heavy metals.     

渤海湾表层沉积物元素地球化学分布特征与影响因素

对取自渤海湾的307个表层沉积物进行了元素测试和粒度分析。渤海湾表层沉积物的常微量元素呈现4种组合:富集于粗粒沉积区的SiO_2、Na_2O亲碎屑元素组合;富集于细粒沉积区的以Al_2O_3和重金属元素为代表的亲黏土元素组合;与缺氧环境有关的MnO、V、TOC元素组合和与河流输入有关的陆源CaO、TiO_2元素组合。粒度粗细主导了渤海湾元素含量分布的整体格局;海域河流物源供应不同较大影响了渤海湾南部(富Na_2O、CaO和SiO_2)和北部(富Ba和P_2O_5)在元素含量上的差异;高流速潮流对海底的冲刷再分配导致曹妃甸南侧Sr、Ca元素的条带状富集异常;有机质在细粒沉积区的富集导致缺氧环境的形成和K_2O、Mn、V、自生黄铁矿的海洋自生化学沉积;人类活动导致以Pb为代表的重金属污染在河流入海口、港口及沿岸海域的元素分布异常;曹妃甸沙坝内侧的泻湖(海洋钙质生物沉积)与沙坝外侧水下岸坡(陆源碎屑沉积)的截然不同的物源,导致了独特地貌沉积环境下元素分布的局部差异。     

Rare earth elements and Opal/CaCO<Subscript>3</Subscript> ratio of sinking particles observed with a time-series sediment trap at the mouth of Tokyo Bay

A time-series sediment trap was deployed from December 1994 to February 2002 at the mouth of Tokyo Bay (35°03′ N, 139°40′ E; water depth, 850 m). Sinking particles were obtained with a time interval of one week at a depth of approximately 100 m above the sea floor. Observed total mass fluxes varied from 3.3 to 226.7 g/m²/day with an average of 28.0 g/m²/day. Concentrations of rare earth elements, Al, Ca and Si in particulate materials were measured. The combustible fraction at 450°C is assumed to be equivalent to the organic matter content. Contents of biogenic materials, namely organic matter, opal and calcium carbonate, were about 30% and the content of lithogenic material was about 70%. Using La/Yb ratios of particles from the sediment trap and Tama-gawa River and surface sediment of Tokyo Bay, it was estimated that about 50% of the lithogenic particles collected in the sediment trap at the mouth of Tokyo Bay originated from resuspended surface sediment in Tokyo Bay. An increasing trend of Opal/CaCO₃ ratio in the sinking particles was found in the spring season. It is suggested that the relative increase of diatoms is due to the decreasing dissolved inorganic nitrogen input into Tokyo Bay.     

Heavy metals and accumulation rates of sediments in Osaka Bay,the Seto Inland Sea,Japan

The metal load into sediments and the change in the sedimentary environment of Osaka Bay in the Seto Inland Sea have been studied through geochemical analysis of core sediments, using both Pb-210 dating and a selective chemical leaching technique. Analytical results from a 6-m core of sediment show that copper and zinc pollution started in the late 1800's and the present enrichment ratios of copper and zinc, relative to background levels (20 mg kg^–1 for Cu and 94 mg kg^–1 for Zn), are 2.8 and 4.1, respectively. The present anthropogenic copper and zinc loads into Osaka Bay sediments, are 47 and 368 ton yr^–1, while natural copper and zinc loads are 40 and 186 ton yr^–1, respectively. Osaka Bay sediment at the present day is considered to be seriously polluted by zinc, now. The vertical profiles of copper and zinc in four successively separated fractions (10% acetic acid soluble fraction: F-HAC, 0.1M hydrochloric acid-soluble fraction: F-HCl, hydrogen peroxide-soluble fraction: F-H₂O₂ and hydrofluoric acid-soluble fraction: F-HF) from the core sediments indicate that enrichments of copper and zinc in the upper layer of the sediment are dependent on increases in the metal contents of the F-HAC, F-HCl and F-H₂O₂ fractions. Copper in F-HAC, and zinc in F-HAC and F-HCl, seem to be of anthropogenic origin.Results of sequential studies of the whole Seto Inland Sea can be summarized as follows: At the present time, the sedimentary loads of copper and zinc over the whole Seto Inland Sea area are 630 and 3,500 ton yr^–1, respectively, while the natural and anthropogenic loads are 320 and 310 ton yr^–1 for copper and 1,800 and 1,700 ton yr^–1 for zinc, respectively.     

Silver in Tokyo Bay estuarine waters and Japanese rivers

Dissolved and particulate concentrations of silver in Tokyo Bay estuarine waters and Japanese rivers were determined in this study. The dissolved silver concentrations in the surface water of Tokyo Bay range from 5.9 to 15.1 pmol kg⁻¹, which is comparable to those in the surface water of the Japan Sea, but two or three times higher than those in the surface water of the open ocean. However, elevated concentrations of dissolved silver are not found in Tokyo Bay compared with those in other highly urbanized estuaries, such as San Francisco Bay (20∼243 pmol kg⁻¹). In the Tokyo Bay estuary, silver typically exhibits non-conservative mixing behavior, which is a common feature in the other estuaries reported previously. Dissolved silver concentrations decrease with salinity from the rivers to the mouth of Tokyo Bay. Silver is efficiently scavenged by suspended particulates, as evidenced by the high conditional distribution coefficients for silver throughout the estuary (log K_d > 5.0 ± 0.6). The silver fluxes into Tokyo Bay via inflowing rivers and atmospheric deposition were estimated as 83 kg y⁻¹ and 15 kg y⁻¹, respectively. A simple budget calculation shows that the silver supplied from rivers and atmosphere must be rapidly scavenged within the Tokyo Bay estuary.     

渤海湾北部和西部海域表层沉积物中无机碳形态研究

采用氯化钠(NaC1)、氨水(NH3·H2O)、氢氧化钠(NaOH)、盐酸羟胺(NH2OH·HC1)溶液对渤海湾北部和西部海域表层沉积物中无机碳进行了连续浸取,并将无机碳分为5种赋存形态:交换态(NaCl相)、弱碱结合态(NH3·H2O相)、强碱结合态(NaOH相)、弱酸结合态(NH2OH·HCl相)和残渣态.同时,结...     

Temporal variation in mass fluxes and the major components of sinking particles in Sagami Bay, off Japan

Sinking particles were collected using time-series sediment traps deployed at 350 and 20 mab at Site SB (34° 58.5’N, 139° 20.9’E, 1544 m depth) near the center of Sagami Bay, off Japan with high time resolutions of 5-8 days (March 1997 to August 1998) and 3-4.5 days (March 1998 to August 1998), respectively. The major components (CaCO₃, OM, opal, and clay) of these sinking particles and surface bottom sediments were determined using a stepwise leaching method combined with gravimetry. Average total mass fluxes were 1480, 5560 and 3068 mg/m²/year at 350 mab, at 20 mab, and in the surface sediments, respectively, indicating an enhanced collection of sinking particles at 20 mab. Clay was the dominant component and biogenic components (opal+OM+CaCO₃) were dominated mainly by opal and secondly by OM. On average, opal and CaCO₃ contents decreased gradually as clay content increased with increasing depth from 350 mab-20 mab and in the surface sediments, indicating dissolution of opal and CaCO₃ through sinking, rebound, resuspension or sedimentation processes. Thirteen total mass flux peaks at 17--40-day intervals were observed at 350 mab during the period from March 1997 to August 1998 except for winter, while eight peaks were observed at 20 mab for the period from March 1998 to August 1998. Two types of total mass peaks can be distinguished: one with a clear increase in biogenic flux (opal+OM+CaCO₃) and little or no increase in clay flux and termed a bloom type (B-type), and the other with a clear increase in clay flux, little increase in biogenic flux and termed a resuspension type (R-type). Some R-type peaks, but not all, coincided with total mass flux peaks observed at the mouth of Tokyo Bay and suggested the possibility of the effect of particulate materials transported from Tokyo Bay to site SB. The enormously large peak observed at 20 mab in late May 1998 and that at 350 mab in early June 1998 were considered to be due to some physical perturbations from an earthquake swarm near site SB during the period from April to June 1998. The 17--40-day periodicity was associated clearly with the change in biogenic flux dominated by opal flux and is thought to reflect the periodicity of biological productivity dominated by diatoms in the euphotic zone of Sagami Bay.     

Distribution of major and trace elements in surface sediments of Hangzhou Bay in China

The Inductively Coupled Plasma Optical Emission Spectrometer was used to analyze sediment samples collected from the Hangzhou Bay to determine major and trace elemental concentrations. Based on these concentrations, the study area can be classified into three geochemical provinces. Province I covers the northern Hangzhou Bay area and contains high concentrations of Al₂ O₃ , Fe₂ O₃ , MgO, Na₂ O, K₂ O, MnO, Cr, Cu, Ni, Pb, V, Co and Zn. Province III is located in the western Hangzhou Bay, near the Qiantang River mouth, and contains high concentrations of SiO₂ , Na₂ O, P₂ O₅ , TiO₂ , Cr, Sr, Zr. Province II is located in the middle and eastern Hangzhou Bay, with the medium concentrations of major and trace elements. The results also demonstrate that the grain size is the dominating factor controlling the spatial variations of elemental concentrations, and the Changjiang River （Yangtze River） and Qiantang River sediments play an important role in the distribution of these elements. Anthropogenic impact on heavy metal concentrations （especially Cr, Sr and Zr） can be detected in the surface sediments near the Qiantang River mouth.     

Precipitation of authigenic uranium in suboxic continental margin sediments from the Okinawa Trough

Concentrations of U and Th isotopes in Okinawa Trough and East China Sea sediment cores were determined by isotope dilution inductively coupled plasma-mass spectrometry (ID-ICP-MS) to investigate the behavior of redox sensitive uranium in suboxic hemipelagic sediments and determine their significance in oceanic uranium balance. ²³⁸U concentrations and ²³⁸U/²³²Th activity ratios in the East China Sea sediments showed no remarkable variation with depth. However, ²³⁸U and ²³⁸U/²³²Th ratios in the Okinawa Trough sediments were low in the surface oxidizing layer but increased where the suboxic condition was encountered. The distribution profiles of ²³⁰Th and ²³²Th concentrations were relatively constant with depth in both the Okinawa Trough and East China Sea sediment cores. These results suggested that there has been post-depositional precipitation of authigenic uranium within the suboxic Okinawa Trough sediment column. The post-depositional precipitation rates of authigenic uranium were estimated to be 47 ± 5 to >62 ± 8 ng cm⁻² yr⁻¹; these rates were comparable to those previously reported for several anoxic sediments. A mechanism controlling precipitation of uranium may be the downward diffusion of uranium U(VI), reduction to U(IV) and finally precipitation onto the solid phase. The accumulation rate of uranium for the Okinawa Trough sediments was approximately eight times higher than the world average rate reported for suboxic sediments. This removal of uranium in the oceanic budget increases the importance of the suboxic sediment sink.     

Vertical profiles of nitrous oxide and dissolved oxygen in marine sediments

The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N₂O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N₂O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO₃⁻) and nitrite (NO₂⁻) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N₂O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N₂O, NO₃⁻ and NO₂⁻ were lower than in the overlying water. In most East China Sea sediments, both N₂O and NO₃⁻ decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N₂O and NO₃⁻ consumption by denitrification at anoxic microsites. N₂O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N₂O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N₂O and NO₃⁻ in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m⁻² h⁻¹ in Koaziro Bay in the spring, −29 to −21 nmolN m⁻² h⁻¹ in the summer, −46 to 37 nmolN m⁻² h⁻¹ in the East China Sea, 0.17 to 0.23 nmolN m⁻² h⁻¹ in the equatorial Pacific, and <±0.2 nmolN m⁻² h⁻¹ in the subtropical North Pacific, respectively.     

Deep penetrating benthic oxygen profiles measured in situ by oxygen optodes

For the first time in situ, deep penetrating O₂ profiles were measured in abyssal sediments in the western South Atlantic. Construction of deep penetrating O₂ optodes and adaptation to a benthic profiling lander are described. The opto-chemical oxygen sensors allow measurements to a depth of 55 cm in marine sediments. A vertical resolution of 0.5 cm was used to determine the O₂ dynamics in those oligotrophic deep sea sediments; the oxygen concentration across the sediment water interface was measured with a resolution of 100 μm. Oxygen penetration depth (OPD), diffusive oxygen uptake (DOU) and oxygen consumption rates were determined at four stations north of the Amazon fan and one at the Mid-Atlantic Ridge. Diffusive oxygen uptake rates ranged from 0.1 to 0.9 mmol m⁻² d⁻¹; the oxygen penetration depth ranged from 8 to 26 cm. Carbon consumption rates calculated from the diffusive oxygen uptake rates were in the range of 0.3–3.0 g C m⁻² a⁻¹. Comparison between in situ and laboratory DOU and OPD measurements confirmed previous findings that core recovery and warming have strong effects on the oxygen dynamics in deep sea sediments. Laboratory measurements yielded a decrease of 50–75% in OPD and consequently an increase in DOU by 1.5 and 18-times. Deep penetrating oxygen optodes provide a new tool to accurately determine oxygen dynamics (and thereby calculate carbon mineralization rates) in oligotrophic sediments. However, oxygen optodes as used in this study do not resolve the diffusive boundary layer (DBL). The data show that deep penetrating O₂ optodes in combination with high-resolution O₂ microelectrodes give a complete picture of the oxygen dynamics, including the DBL, in deep sea sediments.     

Pb and Cs in sediments from Sagami Bay, Japan: sedimentation rates and inventories

Profiles of the radioisotopes ²¹⁰Pb and ¹³⁷Cs were determined in 15 sediment cores collected from Sagami Bay, Japan. The activities of ²¹⁰Pb_ex (unsupported) in core top sediments increased with water depth from 25 dpm g⁻¹ on the upper continental slope off the mouth of Tokyo Bay to an average of 283 dpm g⁻¹ at the deep-sea station SB. The high ²¹⁰Pb trapping efficiency of settling particles expected from the results of the sediment trap experiment near the SB site suggests that effective ²¹⁰Pb enrichment in surface sediments may occur during resuspension and lateral transportation of particles via the benthic nepheloid layer on the continental slope. In several cores, ¹³⁷Cs profiles showed an increase, a distinct peak, and then a decrease to an undetectable level downcore. These profiles can be compared with the temporal change of bomb-produced ¹³⁷Cs fallout.The mean sedimentation rates estimated by the ²¹⁰Pb_ex inventory method, rather than using ²¹⁰Pb_ex profiles, ranged from 0.06 g cm⁻² y⁻¹ to 0.14 g cm⁻² y⁻¹. The average value of the rates in SB cores was calculated to be 0.11 g cm⁻² y⁻¹, which was similar to that calculated under the assumption that the age of the ¹³⁷Cs peak corresponds to its maximum fallout year in 1963.Although ¹³⁷Cs inventories represented one tenth of the anthropogenic fallout of ¹³⁷Cs until 1997, they correlated with the increase in ²¹⁰Pb_ex inventory. This suggests that the scavenging of refractory ¹³⁷Cs as well as ²¹⁰Pb by settling particles in the water column can lead to the formation of a time marker layer even in deep-sea sediment core, such as at the SB site.     

Transport processes deduced from geochemistry and the void ratio of surface core samples, deep sea Sagami Bay, central Japan

Sagami Bay is a deep-water foreland basin with an average sedimentary rate of approximately 0.1 g/cm²/year. It is an appropriate area to study for better understanding of sedimentary processes in a setting with a high sedimentation rate. Seven multiple core samples, 30-50 cm thick, were obtained from Sagami Bay. Four of the core samples were taken from the Tokyo submarine fan system (Tokyo canyon floor, Tokyo fan valley and its levee, the distal fan margin). Two samples were obtained from the Sakawa fan delta and the adjacent topographic high. The remaining one was from an escarpment of the Sagami submarine fault. Variations in chemical composition can be recognized at every coring site. They show two different sediment sources: the sediments of the Tokyo submarine fan system and those from Sakawa fan delta. Further, there are differences in chemical composition between canyon floor and levees even within the Tokyo submarine fan system. The results suggest that the sedimentary process is strongly controlled not by vertical particle settling but by a hyperpycnal flow process. The proxies obtained from the core samples do not reflect conditions in the water column immediately overlying the sea floor. Rather, they are controlled by conditions on the adjacent continental shelf or/and shallow basins, which are the areas of primary accumulation.     

In situ evaluation of nearshore marine and fresh pore water transport into Flamengo Bay,Brazil

Transport between pore waters and overlying surface waters of Flamengo Bay near Ubatuba, Brazil, was quantified using natural and artificial geochemical tracers, ²²²Rn, Cl⁻, and SF₆, collected from multi-level piezometers installed along a transect perpendicular to the shore. Eight sampling ports positioned along the length of the piezometers allowed sampling of pore waters at discrete depth intervals from 10 to 230 cmbsf (centimeters below seafloor). Small volume samples were collected from the piezometers using a peristaltic pump to obtain pore water depth profiles. Pore water ²²²Rn is deficient in shallow sediments, allowing application of a diffusion-corrected ²²²Rn exchange rate. This model estimates the magnitude of pore water exchange rates to be about 130–419 cm/day. An SF₆-saturated fluorescein dye tracer was gently pumped into deep pore waters and exchange rates estimated from this method range from 29 to 185 cm/day. While absolute rates are higher using ²²²Rn than SF₆, rates are of similar magnitudes and the trends with distance from shore are the same – flow is greatest 6 m from shore and decreases by more than 50% further offshore. A Cl⁻ mass balance indicates the greatest fraction of fresh SGD occurs along an apparent preferential flow path in sediments within 5–7 m of the shoreline (87%). Recirculating bay waters through sediments dominate pore water advection at 10 m offshore where only 4% of the flow can be attributed to a freshwater source. Both fresh and marine sources combine to make up submarine groundwater discharge to coastal water bodies. The magnitude of fresh aquifer discharge is often a spatially variable and minor component of the total discharge.     

Air-sea exchange of mercury in Tokyo Bay

In Tokyo Bay the concentrations of dissolved gaseous mercury (DGM) in the surface seawater and total gaseous mercury (TGM) over the sea were measured during December 2003, October 2004 and January 2005. Based on these data, the evasional fluxes of mercury from the sea surface were estimated using a gas exchange model. In addition, an automatic wet and dry deposition sampler was used to measure the wet and dry depositional fluxes of mercury from December 2003 to November 2004 at three locations in and near Tokyo Bay. The results indicate that the average DGM and TGM levels of seven locations are 52 ± 26 ng m⁻³ and 1.9 ± 0.6 ng m⁻³, respectively, which shows that the surface seawater in Tokyo Bay is supersaturated with gaseous mercury, leading to an average mercury evasional flux of 140 ± 120 ng m⁻²d⁻¹. On the other hand, the annual average wet and dry depositional fluxes of mercury at three locations were 19 ± 3 μg m⁻²yr⁻¹ and 20 ± 9 μg m⁻²yr⁻¹, respectively. These depositional fluxes correspond to the daily average total depositional flux of 110 ± 20 ng m⁻²d⁻¹. Thus, it is suggested that in Tokyo Bay, the evasional fluxes of mercury are comparable to the depositional fluxes.     

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.     

Partitioning of heavy metals into mineral and organic fractions in a sediment core sample from Osaka Bay

Partitioning of copper, zinc, iron and manganese into oxide, sulfide, organic and silicate fractions has been determined with a selective chemical leaching technique on sediment samples from a core collected in Osaka Bay. The samples have been dated by the²¹⁰Pb method. Most of the copper and zinc in the polluted surface sediment layer are contained in both oxide and sulfide fractions. This suggests that the transformation of oxides and hydroxides to sulfides under anoxic conditions within the sediment is significant for the fixation of copper and zinc discharged through human activities into the sediment. Manganese is apparently enriched in oxide and hydroxide fractions of the surface layer due to the post-depositional migration of manganese within the sediment. The copper, zinc and manganese contents of the 30 % H₂O₂ soluble fraction (mostly organic fraction) decrease with depth in the sediment core, and correlate significantly with the organic carbon content. The heavy metal (Cu, Zn, Fe and Mn) contents of the silicate fraction, without exchangeable sites, are almost constant with depth.     

Sedimentary record of redox-sensitive elements (U, Mn, Mo) in a transitory anoxic basin (the Thau lagoon, France)

In order to further document the relation between redox conditions and the sedimentary record of Mn, U and Mo in a transitory anoxic water basin, their distribution has been studied along two profiles in the Thau lagoon (France). Sediments and pore-water have been sampled at two contrasting sites located, respectively, in the shellfish-farming area and in the centre of the lagoon. In the shellfish-farming area, the particulate organic carbon (POC) data indicate a more rapid organic matter mineralisation compared to the centre of the lagoon. This results in a sharper redox gradient characterized by the appearance of H₂S in pore-water a few millimetres below the sediment–water interface. In the centre of the lagoon, H₂S appears at a depth of 35 cm.In both cores, sedimentary Mn is relatively depleted through out the whole sedimentary column and varies with the proportion of clay minerals. After an initial release into solution at the sediment–water interface in relation to Mn-oxide reductive dissolution, authigenic U is immobilized when sulphides appear. Despite the occurrence of anoxic conditions at the sediment–water interface at the site influenced by shellfish farming, the burial of U is reduced by bioturbation, which raises reducing sediments to the surface. In the centre of the lagoon, Mo profiles reflect continuous diffusion into pore water and immobilization at 15 cm probably in anoxic microenvironments. At shellfish farms, dissolved Mo undergoes removal with sulphides but contrary to U, sedimentary Mo does not appear to be strongly affected by bioturbation. The profile indicates an increase in the frequency of anoxia crises during the second half of the 20th century.     

Microbial biogeochemistry and bioturbation in the sediments of Great Bay, New Hampshire

The influence of bioturbation on certain aspects of the biogeochemistry of sulfur and iron was examined in shallow-water sediments of Great Bay Estuary, New Hampshire. A bioturbated (JEL) and non-bioturbated (SQUAM) site were compared. Annual sulfate reduction measured with ³⁵S, was 4·5 times more rapid at JEL. A significant portion of this difference was attributed to rapid rates which occurred throughout the upper 12 cm of sediment at JEL due to infaunal reworking activities. Sulfate reduction decreased rapidly with depth at SQUAM. FeS in the upper 2 cm at JEL increased in concentration from 3 to 45 μmol ml⁻¹ from early May to late July while only increasing from 3 to 8 μmol ml⁻¹ at SQUAM. Infaunal irrigation and reworking activities caused rapid and continous subsurface cycling of iron and sulfur at JEL. This maintained dissolved iron concentrations at 160–170 μM throughout the summer despite rapid sulfide production. Therefore, dissolved sulfide never accumulated in JEL pore waters. Although dissolved organic carbon (DOC) was generated during sulfate reduction, bioturbation during summer caused a net removal of DOC from JEL pore waters. Sulfate reduction rates, decomposition stoichiometry and nutrient concentrations were used to calculate turnover times of nutrients in pore waters. Nutrient turnover varied temporally and increased three-to five-fold during bioturbation. A secondary maximum in the abundance of recoverable sulfate-reducing bacteria occurred at 10 cm in JEL sediments only during periods of active bioturbation, demonstrating the influence of macrofaunal activities on bacterial distributions.     

A carbon budget in Tokyo Bay

Organic carbon flux from eutrophicated Tokyo Bay to the Pacific Ocean is estimated as 260 ton C day^–1 based on the horizontal gradient of COD and the dispersion coefficient at the bay mouth. Also, carbon flux from the air or from the open ocean to Tokyo Bay is estimated as 156 ton C day^–1. If we suppose that five percent of the coastal seas in the world might be eutrophicated as Tokyo Bay and the organic carbon flux from the shelf to the open ocean in other coastal seas might be one third of that in Tokyo Bay, 1.12 G tons year^–1 would be transported from the eutrophicated coastal seas to the open ocean and such carbon flux may account for the missing sink in the global carbon budget.