Acid-volatile sulfide and simultaneously extracted metals in surface sediments of the southwestern coastal Laizhou Bay, Bohai Sea: Concentrations, spatial distributions and the indication of heavy metal pollution status

Surface sediments were collected from the coastal waters of southwestern Laizhou Bay and the rivers it connects with during summer and autumn 2012. The acid-volatile sulfide (AVS) and simultaneously extracted metals (SEM) were measured to assess the sediment quality. The results showed that not all sediments with [SEM]-[AVS] > 0 were capable of causing toxicity because the organic carbon is also an important metal-binding phase in sediments. Suppose the sediments had not been disturbed and the criteria of US Environmental Protection Agency had been followed, heavy metals in this area had no adverse biological effects in both seasons except for few riverine samples. The major ingredient of SEM was Zn, whereas the contribution of Cd - the most toxic metal studied - to SEM was 0 were capable of causing toxicity because the organic carbon is also an important metal-binding phase in sediments. Suppose the sediments had not been disturbed and the criteria of US Environmental Protection Agency had been followed, heavy metals in this area had no adverse biological effects in both seasons except for few riverine samples. The major ingredient of SEM was Zn, whereas the contribution of Cd - the most toxic metal studied - to SEM was <1%. The distributions of AVS and SEM in riverine sediments were more easily affected by anthropogenic activity compared with those in marine sediments. (C) 2013 Elsevier Ltd. All rights reserved

Colloidal toxic trace metals in urban riverine and estuarine waters of Yantai City, southern coast of North Yellow Sea

The environmental characteristics of colloidal toxic trace metals Cd, Cu and Pb in riverine and estuarine waters collected from two urban rivers of Yantai City in eastern China, the Guangdang and Xin'an Rivers, were investigated using a modified centrifugal ultrafiltration (CUF) method in conjunction with acid extraction and inductively coupled plasma mass spectrometry. The target metals in dissolved pool were divided into four CUF fractions, i.e. <1 kDa, 1-3 kDa, 3-10 kDa and 10 kDa-0.2 mu m, and the results showed that colloidal Cd, Cu and Pb were dominated by 1-10 kDa (1-3 and 3-10 kDa), 1-3 kDa and 10 kDa-0.2 lm fractions, respectively. The coagulation/flocculation of low-molecular-weight (1-10 kDa) colloidal Cd and Cu in the estuaries was obvious and strong, while the enrichment of dissolved Pb in the 10 kDa-0.2 lm fraction may be mainly related to its biogeochemical interactions with Fe-oxides, which is easy to occur in macromolecular colloids. In addition, the actual molecular weight cutoffs (MWCOs) of the three used CUF units with nominal MWCOs of 1, 3 and 10 kDa were determined to be 4.9, 8.5 and 33.9 kDa, respectively, indicating that membrane calibration is essential for explaining the actual fraction of dissolved trace metals and verifying the integrity of ultrafiltration membrane. Overall, the results in this study provide a further understanding of the heterogeneity in biogeochemical features, migration and fate of toxic trace metals in aquatic ecosystems, especially that of the river-sea mixing zone. (C) 2019 Elsevier B.V. All rights reserved

Papel de la bahía de Jiaozhou como una fuente/depósito de CO2 durante un ciclo estacional

The seasonal evolution of dissolved inorganic carbon (DIC) and CO2 air-sea fluxes in the Jiaozhou Bay was investigated by means of a data set from four cruises covering a seasonal cycle during 2003 and 2004. The results revealed that DIC had no obvious seasonal variation, with an average concentration of 2035 µmol kg-1 C in surface water. However, the sea surface partial pressure of CO2 changed with the season. pCO2 was 695 µatm in July and 317 µatm in February. Using the gas exchange coefficient calculated with Wanninkhof’s model, it was concluded that the Jiaozhou Bay was a source of atmospheric CO2 in spring, summer, and autumn, whereas it was a sink in winter. The Jiaozhou Bay released 2.60 x 1011 mmol C to the atmosphere in spring, 6.18 x 1011 mmol C in summer, and 3.01 x 1011 mmol C in autumn, whereas it absorbed 5.32 x 1010 mmol C from the atmosphere in winter. A total of 1.13 x 1012 mmol C was released to the atmosphere over one year. The behaviour as a carbon source/sink obviously varied in the different regions of the Jiaozhou Bay. In February, the inner bay was a carbon sink, while the bay mouth and the outer bay were carbon sources. In June and July, the inner and outer bay were carbon sources, but the strength was different, increasing from the inner to the outer bay. In November, the inner bay was a carbon source, but the bay mouth was a carbon sink. The outer bay was a weaker CO2 source. These changes are controlled by many factors, the most important being temperature and phytoplankton. Water temperature in particular was the main factor controlling the carbon dioxide system and the behaviour of the Jiaozhou Bay as a carbon source/sink. The Jiaozhou Bay is a carbon dioxide source when the water temperature is higher than 6.6°C. Otherwise, it is a carbon sink. Phytoplankton is another controlling factor that may play an important role in behaviour as a carbon source or sink in regions where the source or sink nature is weaker.La evolución estacional del carbono inorgánico disuelto (DIC) y el intercambio de flujos de CO2 aire-mar en la bahía de Jiaozhou han sido investigados a partir de datos obtenidos en 4 campañas oceanográficas que cubren un ciclo estacional entre 2003 y 2004. Los resultados muestran que el DIC no presenta una clara variación estacional con una concentración promedio de 2035 μmol kg-1 C en el agua de superficie. No obstante la presión parcial de CO2 en el agua superficial cambiaba con la estación. La PCO2 era de 695 μatm en Julio y 317 μatm en febrero. Utilizando el coeficiente de intercambio de gases calculado con el modelo de Wanninkhof concluíamos que la bahía de Jiaozhou era una fuente de CO2 a la atmósfera en primavera, verano y otoño, mientras que era un depósito de CO2 en invierno. La bahía proporcionaba 2.60 × 1011 mmol C a la atmósfera en primavera, 6.18 × 1011 mmol C en verano, y 3.01 × 1011 mmol C in otoño, mientras absorbia 5.32 × 1010 mmol C desde la atmósfera en invierno. Un total de 1.13 × 1012 mmol C eran liberados a la atmósfera durante un año. El comportamiento como fuente/depósito de carbono, obviamente era diferente en las distintas regiones de la bahía de Jiaozhou. En Febrero, la parte interior de la bahía era un depósito para el carbono, mientras que la desembocadura y la parte exterior actuaba como fuente de carbono. En Junio y Julio, las partes interna y externa de la bahía eran fuentes de carbono, pero la intensidad era diferente, incrementando desde la parte interior a la exterior de la bahía. En Noviembre, la parte interior de la bahía era fuente de carbono, pero la desembocadura de la bahía se comportaba como depósito de carbono. El exterior de la bahía era una fuente poco importante de CO2. Estos cambios están controlados por muchos factores, siendo los mas importantes la temperatura y el fitoplancton. Especialmente, la temperatura del agua era el factor principal en el control del dióxido de carbono en el sistema y del comportamiento de la bahía de Jiaozhou como fuente/depósito de carbono. La bahía de Jiaozhou es una fuente de dióxido de carbono cuando la temperatura del agua es mas alta que 6.6ºC. Si no es así es un depósito de carbono. El fitoplancton es el otro factor de control que puede jugar un papel importante en el comportamiento como fuente o depósito de carbono en regiones donde el carácter de fuente o depósito es debil.

The influence of summer hypoxia on sedimentary phosphorus biogeochemistry in a coastal scallop farming area, North Yellow Sea

In situ field investigations coupled with laboratory incubations were employed to explore the surface sedimentary phosphorus (P) cycle in a mariculture area adjacent to the Yangma Island suffering from summer hypoxia in the North Yellow Sea. Five forms of P were fractionated, namely exchangeable P (Ex-P), iron-bound P (Fe-P), authigenic apatite (Ca-P), detrital P (De-P) and organic P (OP). Total P (TP) varied from 13.42 to 23.88 mu mol g(-1) with the main form of inorganic P (IP). The benthic phosphate (DIP) fluxes were calculated based on incubation experiments. The results show that the sediment was an important source of P in summer with similar to 39% of the bioavailable P (Bio-P) recycled back into the water column. However, the sediment acted a sink of P in autumn. The benthic DIP fluxes were mainly controlled by the remobilizing of Fe-P, Ex-P and OP under contrasting redox conditions. In August (hypoxia season), similar to 0.92 mu mol g(-1) of Fe-P and similar to 0.52 mu mol g(-1) of OP could be transformed to DIP and released into water, while similar to 0.36 mu mol g(-1) of DIP was adsorbed to clay minerals. In November (non-hypoxia season), however, similar to 0.54 mu mol g(-1) of OP was converted into DIP, while similar to 0.55 mu mol g(-1) and similar to 0.28 mu mol g(-1) of DIP was adsorbed to clay minerals and bind to iron oxides. Furthermore, scallop farming activities also affected the P mobilization through biological deposition and reduced hydrodynamic conditions. The burial fluxes of P varied from 11.67 to 20.78 mu mol cm(-2) yr(-1) and its burial efficiency was 84.7-100%, which was consistent with that in most of the marginal seas worldwide. This study reveals that hypoxia and scallop farming activities can significantly promote sedimentary P mobility, thereby causing high benthic DIP flux in coastal waters. (C) 2020 Elsevier B.V. All rights reserved

Concentration and fractionation of trace metals in surface sediments of intertidal Bohai Bay, China

Surface sediments from intertidal Bohai Bay were sampled for the geochemical and environmental assessment of six trace metals (Cd, Cr, Cu, Ni, Pb and Zn). Results indicate that sediment grain size plays an important role in controlling the distribution and fractionation of them. Metal concentrations in clayey silt sediments are all clearly higher than in sand and silty sand ones. Cd and Pb in clayey silt sediments are more mobile than in sand and silty sand ones. Two sediment quality guidelines and two geochemical normalization methods (index of geoaccumulation and enrichment factor) were used to judge the potential risk and accumulation of metals. According to the mean probable effects level quotient, the combination of studied metals may have a 21% probability of being toxic. The sediments with high fraction of clay and silt have been contaminated by trace metals to various degrees, among which Cr contributes the most to contamination. (C) 2012 Published by Elsevier Ltd.Surface sediments from intertidal Bohai Bay were sampled for the geochemical and environmental assessment of six trace metals (Cd, Cr, Cu, Ni, Pb and Zn). Results indicate that sediment grain size plays an important role in controlling the distribution and fractionation of them. Metal concentrations in clayey silt sediments are all clearly higher than in sand and silty sand ones. Cd and Pb in clayey silt sediments are more mobile than in sand and silty sand ones. Two sediment quality guidelines and two geochemical normalization methods (index of geoaccumulation and enrichment factor) were used to judge the potential risk and accumulation of metals. According to the mean probable effects level quotient, the combination of studied metals may have a 21% probability of being toxic. The sediments with high fraction of clay and silt have been contaminated by trace metals to various degrees, among which Cr contributes the most to contamination. (C) 2012 Published by Elsevier Ltd