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IntroductionCobalt is the most important critical element in ferromanganese crusts. Co concentration in the Fe-Mn crusts is one of the key parameters for determination of the Co resource. Thus, it is essential to clarify the controls on the variations of Co concentration of ferromanganese crusts.MethodsTo clarify the controls on Co concentration of hydrogenetic nonphosphatized ferromanganese crusts, an equation was deduced based on Fick’s First Law: Co(%)=Mn02(%)·Dsw·cswδ·zGR·Ssp, and eight potential controls were gleaned from this equation, including dilution, diffusivity of Co ions in seawater (Dsw), temperature which controls the Dsw, Co ion concentration in seawater (Csw), the diffusion distance of Co ions near the interface of seawater and Fe-Mn crusts (δ), thickness of one molecular layer (z), growth rate (GR), and specific surface area of Fe-Mn crusts (Ssp). To constrain the value of Co ion diffusion gradients (Csw¯/δ) and consequently verify the proposed equation, we determined the Co concentrations, growth rates, and specific surface area of the outermost layer of Fe-Mn crusts, and calculated diffusivity of Co2+.ResultsThe Csw¯/δ for the Fe-Mn crusts from Caiwei seamount (Magellan seamounts) was determined to be 295-496 pM/mm, which are reasonable for the Co ion concentrations and seawater mixing in the deep ocean.DiscussionAccording to the equation established in this study, the trend of decreasing Co concentrations in Fe-Mn crusts with increasing water depth is controlled mainly by dilution and to a lesser extent by seawater Co ion concentration, temperature of seawater, and consequently the diffusivity of Co ions in seawater.

Abstract The polar oceans play a vital role in regulating atmospheric CO2 concentrations (pCO2) during the Pleistocene glacial cycles. However, despite being the largest modern reservoir of respired carbon, the impact of the subarctic Pacific remains poorly understood due to limited records. Here, we present high-resolution, 230Th-normalized export productivity records from the subarctic northwestern Pacific covering the last five glacial cycles. Our records display pronounced, glacial-interglacial cyclicity superimposed with precessional-driven variability, with warm interglacial climate and high boreal summer insolation providing favorable conditions to sustain upwelling of nutrient-rich subsurface waters and hence increased export productivity. Our transient model simulations consistently show that ice sheets and to a lesser degree, precession are the main drivers that control the strength and latitudinal position of the westerlies. Enhanced upwelling of nutrient/carbon-rich water caused by the intensification and poleward migration of the northern westerlies during warmer climate intervals would have led to the release of previously sequestered CO2 from the subarctic Pacific to the atmosphere. Our results also highlight the significant role of the subarctic Pacific in modulating pCO2 changes during the Pleistocene climate cycles, especially on precession timescale ( ~ 20 kyr).

Thirteen Short sediment cores (30-50 cm) were collected from Bohai Sea, Yellow Sea and Changjiang Estuary in China, and the early diagenesis of several redox sensitive metals (Fe, Mn, Mo, U and V, referring to as RSMs) in sediment were studied. The recycling process of Mo and Mn was closely correlated with each other, generating benthic fluxes diffusing upward from sediment to overlying water column, and the flux rates are related to the organic carbon oxidation rates. The recycling of U and V were more tightly coupled with Fe oxides, generating benthic fluxes going downward into the sediment in most cores. Significant authigenic accumulation of U, in contrary to little to no accumulation of Mo and V, were found in the study region, even in Changjiang Estuary where hypoxic condition was often found during summer. Benthic diffusive fluxes were compared with authigenic mass accumulate rates (MAR), which indicated that, besides the benthic diffusion process, there are other processes controlling the authigenic accumulation of the RSMs. The close relationships between authigenic accumulation of RSMs with OCburial and OCburial with Sburial, indicating the authigenic accumulation of RSMs is a consequence of redox environment in shelf sediment, which directly influencing the organic carbon degradation process. Compared with other continental margin, moderate enrichment of U was found in China continental sediment. The authigenic U accumulation in BS and NYS sediments accounted for 20 - 68% of the Yellow River input, whilst in SYS sediments accounted for ~ 64% of the Yellow River and Changjiang River input, which acting as important U sinks that cannot be ignored.

AbstractThe mineralogical and geochemical compositions of the sediments deposited by rivers have been used extensively to evaluate past chemical weathering and the physical erosion history of drainage basins at different time scales. However, the role of sediment sorting in the mineralogical and geochemical compositions of river sediment needs to be better constrained because it could significantly modify proxies used to evaluate weathering intensity in the past. In this study, major and trace element concentrations and mineralogical compositions were determined on seven different grain-size fractions of riverbed samples taken from the Pahang and Kelantan Rivers in the Malay Peninsula. The main aims are to assess chemical weathering and the fractionation of alkali elements during sediment transportation under tropical climate conditions. Fine sediments (from

Abstract In this study, sediments were collected from two different sites in the deep-sea hydrothermal region of the South Atlantic Ocean. Two microbial enrichment cultures (H7S and H11S), which were enriched from the sediments collected at two sample sites, could effectively degrade petroleum hydrocarbons. The bacterial diversity was analyzed by high-throughput sequencing method. The petroleum degradation ability were evaluated by gas chromatography–mass spectrometry and gravimetric analysis. We found that the dominant oil-degrading bacteria of enrichment cultures from the deep-sea hydrothermal area belonged to the genera Pseudomonas, Nitratireductor, Acinetobacter, and Brevundimonas. After a 14-day degradation experiment, the enrichment culture H11S, which was obtained near a hydrothermal vent, exhibited a higher degradation efficiency for alkanes (95%) and polycyclic aromatic hydrocarbons (88%) than the enrichment culture H7S. Interestingly, pristane and phytane as biomarkers were degraded up to 90% and 91% respectively by the enrichment culture H11S, and six culturable oil-degrading bacterial strains were isolated. Acinetobacter junii strain H11S-25, Nitratireductor sp. strain H11S-31 and Pseudomonas sp. strain H11S-28 were used at a density ratio of 95:4:1 to construct high-efficiency oil-degrading consortium H. After a three-day biodegradation experiment, consortium H showed high degradation efficiencies of 74.2% and 65.7% for total alkanes and PAHs, respectively. The degradation efficiency of biomarkers such as pristane and high-molecular-weight polycyclic aromatic hydrocarbons (such as CHR) reached 84.5% and 80.48%, respectively. The findings of this study indicate that the microorganisms in the deep-sea hydrothermal area are potential resources for degrading petroleum hydrocarbons. Consortium H, which was artificially constructed, showed a highly efficient oil-degrading capacity and has significant application prospects in oil pollution bioremediation.

AbstractThe Sea of Japan (JS), a unique marginal sea without any large river influxes in the western Pacific, provides ample information about the evolution of sea level, East Asian monsoons (EAM), sea ice activity, and ocean currents in geological time. However, insufficient investigation in the western JS limits our knowledge of East Asian climate change. This study utilizes major and trace elements and Pb isotopes of fine siliciclastic components (

AbstractThe continental margin is one of the major depocenters for terrigenous sediments in the world ocean. Complex interactions between land and sea control the sedimentary processes along the continental margin. The Okinawa Trough (OT) receives huge amounts of terrigenous materials transported by rivers from the adjacent landmass, while the Kuroshio Current (KC) and the North Pacific Intermediate Water jointly play major roles in oceanic climate and regional deposition patterns of terrigenous sediments. Various studies have investigated the changes in terrigenous sediment provenance in the central OT only since the last glacial. Still, few studies focus on more long-term variations in terrigenous deposition over the last few glacial-interglacial cycles. Here, we report a new high-resolution sediment geochemistry record of a well-dated core MD01-2404 taken from the central OT covering a timespan of 92 kyr. Our results show dynamic glacial-interglacial changes in sediment compositions and terrigenous deposition patterns. Bulk sediments in MD01-2404 comprise relatively high biogenic components during interglacials, while higher terrigenous fractions during the last deglacial and glacial periods. We suggest that the provenance of terrigenous sediments is mainly derived from Taiwanese rivers, Yangtze River, and Yellow River with hydrothermal inputs. During the time interval of 37 to 46 kyr, a new finding of “Negative Ce Anomaly Event” in the central OT firstly reported here is attributed to a combination of suboxic conditions in deep and pore waters and the addition of depleted Ce-bearing sediments. Temporal changes of deposition patterns in the central OT are attributed to complex interactions among dynamic glacial-interglacial changes in eustatic sea level, the East Asian summer monsoon, and the KC.

Abstract Lithogenic grain-size, geochemical elements of core sediments from the central Bay of Bengal (BoB) were analyzed to identify sediment provenance and explore the regional “source-sink” processes since 25 ka. Based on the geochemical compositions of core BoB-88, relative contributions of three end-member sources (Himalayan, Myanmar, Indian Peninsula) were calculated and support the general understanding that Himalayan sources were dominant since the last glacial period, which could reach 70% on average in our study. However, sediments from the Indian Peninsula and Myanmar also contributed nonnegligible materials to the central BoB since 25 ka, especially the former shows an obvious increase since 7.5 ka, which was neglected in the previous studies. To trace the sedimentary processes of different provenance terrigenous materials and reveal their response to climate changes, four typical stages with obvious provenance percent variation, including the Last Glacial Maximum period (LGM), Heinrich 1 (H1), Early Holocene Climate Optimum (EHCO), and mid-late Holocene period, were highlighted and discussed. Sea-level change played a dominant role in the glacial-interglacial scale by controlling the transition of deposition center between the shelf/subaquatic delta and the Bengal Fan, especially for sediment from the Himalayan source, exerting influence on contributions from different provenance end-members between the Holocene and the last glacial period. The opposite directions of the southwest and northeast monsoon current in the BoB have a significant influence on the transfer of the Indian Peninsula and Myanmar materials to the studied core, which led to an increase of up to 11% than the average of the Indian Peninsula and a decrease of up to 9% than the average of the Myanmar source during the Holocene. The balance between sea level (limited transport to the deep sea) and ISM (improved erosion production and output to the BoB) during the mid-late Holocene period maintained the stability of Himalayan source percent. Due to the control of the ISM variations, the Himalayan source showed a decrease of up to 20% and 21% than average during the LGM and H1 period, respectively, and an increase of up to 14% than average during the EHCO. The Myanmar source exhibited fluctuations around the average value during the LGM period, but an obvious increase of up to 21% during the H1 period and a decrease up to 8% during the EHCO, while the Indian Peninsula source percent showed little variations during the LGM and H1, but a decrease of up to 6% during the EHCO. Obvious 1/4 processional and millennial periodic changes (5.0 kyr and 1.1 kyr) of contribution proportions from three end-members provide additional evidences for the climate control on the regional source-sink processes and proved the controlled mechanisms of the orbital parameters and possible influence from the solar activity on millennial scales.

Early diagenesis processes and the geochemistry of redox-sensitive elements (RSEs) in four sediment cores in an active hydrothermal field in the southern Okinawa Trough (OT) was investigated. Dissolved Fe, Mn, ΣHS–, and several other RSEs (Mo, U, and V) in pore water were measured. We also studied metal distribution in sediments using sequential extraction methods. Very high dissolved Fe concentrations (∼140 μmol L–1) but insignificant dissolved Mn were observed in surficial pore waters in the station adjacent to the hydrothermal vent, where highly reactive Fe, Mo, U in the sediments were also measured. Such an atypical diagenetic sequence found in those cores could be driven by the overwhelmingly high reactive Fe fraction (mostly Fe oxides) delivered from the vents. Consequently, significant upward benthic fluxes of Fe and Mo were estimated for the studied stations. In addition, we performed a principal component analysis (PCA), together with relative ratios of carbonate-related elements (Sr, Ca, Mg), to identify particles’ origins in the hydrothermal field; two endmembers being the hydrothermal source and hydrogenous processes. This comprehensive study on a unique set of samples collected by advanced technology provided valuable data to demonstrate distinctive geochemical features that occur in hydrothermal sediments.

Investigating the composition and distribution of pelagic marine sediments is fundamental in the field of marine sedimentology. The spatial distributions of surface sediment are unclear due to limited investigation along the Emperor Seamount Chain of the North Pacific. In this study, a suite of sedimentological and geochemical proxies were analyzed, including the sediment grain size, organic carbon, CaCO3, major and rare earth elements of 50 surface sediment samples from the Emperor Seamount Chain, spanning from ∼33°N to ∼52°N. On the basis of sedimentary components, we divide them into three Zones (I, II, and III) spatially with distinct features. Sediments in Zone I (∼33°N–44°N) and Zone III (49.8°N–53°N) are dominated by clayey silt, and mainly consist of sand and silty sand in Zone II. The mean grain size of the sortable silt shows that the hydrodynamic condition in the study area is significantly stronger than that of the abyssal plain, especially at the water depth of 1,000–2,500 m. The CaCO3 contents in sediments above 4,000 m range from 20 to 84% but decrease sharply to less than 1.5% below 4,000 m, confirming that the water depth of 4,000 m is the carbonate compensation depth of the study area. Strong positive correlations between Al2O3 and Fe2O3, TiO2, MgO, and K2O (R > 0.9) in the bulk sediments indicate pronounced contributions of terrigenous materials from surrounding continent mass to the study area. Furthermore, the eolian dust makes contributions to the composition of bulk sediments as confirmed by rare earth elements. There is no significant correlation between grain size and major and minor elements, which indicates that the sedimentary grain size does not exert important effects on terrigenous components. There is significant negative δCe and positive δEu anomalies at all stations. The negative Ce anomaly mainly exists in carbonate-rich sediments, inheriting the signal of seawater. The positive Eu anomaly indicates widespread volcanism contributions to the study area from active volcanic islands arcs around the North Pacific. The relative contributions of terrestrial, volcanic, and biogenic materials vary with latitude and water depth in the study area.

The Sea of Japan (JS) is a unique marginal sea in the western North Pacific that is characterized by four shallow straits. It can provide information about the paleoenvironment, for instance indicating variations in the East Asian Monsoon, Tsushima Warm Current, sea ice coverage, and Westerly Jet. Compared with other marginal seas in the western North Pacific, the JS is currently the only marginal sea without influx from large rivers. It is, therefore, of interest to determine the source of terrigenous sediments over time, particularly in the western JS, which has been less investigated in previous reports. In this study, a suite of multi-proxies including Sr and Nd isotopes and minor elements were measured for fine fractions (

Coastal sediments not only contain a majority of trace metals, but they also act as a source of dissolved metal ions to the overlying water column. Distinguishing the level of trace metal enrichment from the natural input in sediments is therefore important to determine the distribution and sources of land-derived detritus and pollutants in the coastal region. This study investigates fine (2) for As, Cd, and Pb, suggesting that the sediments were likely enriched by these elements. A comparative study of trace metals concentrations and EF with other coastal regions of China, however, revealed that the study area is in a pristine environmental condition compared to other coastal regions of eastern China. Factor analysis identified three dominant sedimentological and geochemical associations, accounting for ∼70% of total variance, recognize terrigenous input, heavy mineral role and anthropogenic input in controlling the distribution of most elements in the study area.