南海北部表层颗粒有机碳的季节和年际变化遥感分析

海洋颗粒有机碳（POC）是海洋固碳的一个关键参数。为了研究南海北部陆架及海盆表层POC浓度的时空分布特征以及变化趋势,本文利用2009-2011年4个季节的实测数据,对NASA发布的MODIS/AQUA卫星月平均POC遥感产品,进行了验证和校正;并利用校正后的遥感数据分析了2003-2014年POC的时空分布特征和变化趋势。发现POC遥感产品与南海北部实测数据具有较好的线性关系（R2=0.72）,但存在系统性偏高,需利用实测数据对遥感数据进行区域性校正。分析校正后的遥感数据发现,南海北部陆架POC浓度较高,平均为（33.34±8.02）mg/m3;吕宋海峡西南海域浓度较低,平均为（29.25±6.20）mg/m3;中央海盆区浓度最低,平均为（27.02±4.84）mg/m3。春夏季POC浓度较低,最低值一般出现在5月,冬季（12月至翌年1月）POC浓度达到最高。利用2003-2014年的长时间序列遥感叶绿素（Chl a）和海表温度（SST）、混合层深度（MLD）模式数据,以及实测数据对南海北部POC浓度的影响机制进行了分析。发现POC与Chl a在秋冬呈现较好的相关关系（R2=0.51）,但在春夏季较离散,表明秋冬季生物作用对POC影响较大。2003-2014年期间,POC与Chl a、MLD及SST存在明显的年际变化,但并没有显著的上升或下降趋势。     

Large 14C age offsets between the fine fraction and coexisting planktonic foraminifera in shallow Caribbean sediments

Absolute chronologies in paleoceanographic records are often constructed using the ¹⁴C dating of coarse fraction foraminifera (>150 μm). However, due to processes such as changes in sediment sources or abundances, sedimentation rates, bioturbation, reworking, the adsorption of modern carbon, etc., several studies conducted in different environmental settings have shown time-lags between records obtained from various granulometric fractions. In this study, we examined temporal phasing between the coarse foraminifera and fine fractions by studying changes in the abundances of δ¹⁸O, the ¹⁴C ages of the planktonic foraminifera Globigerinoides ruber (G. ruber, 250–350 μm), and the sediment fine fraction (<63 μm) over the last 45 ka in a core obtained from the northern Caribbean Sea. All of the records were found to be in phase during part of the Holocene (at least for the last ≈6 ka). As determined from δ¹⁸O records and ¹⁴C ages, the fine fraction was younger than G. ruber during the Last Deglaciation (of 1.89 ka). The coupling between bioturbation and changes in the fine fraction, and G. ruber abundances, as tested using a numerical model of the bioturbation record within a mixed-layer depth of 8 cm, was sufficient to explain the results. ¹⁴C age discrepancies increased from 5.64 to 8.5 ka during Marine Isotopic Stages (MIS) 2 and 3, respectively. These chronological discrepancies could not be explained by only one process and seemed to result from the interplay between mechanisms: size-differentiated bioturbation (for 1.5 to 2.5 ka), the adsorption of modern atmospheric CO₂ (for 3.04 to 5.92 ka), and variations in sedimentological processes that influenced the fine carbonate fraction. However, even if variations in the mineralogical composition of the fine carbonate fraction were identified using scanning-electron microscopy observations, X-ray diffraction measurements, and geochemical analyses (the mol % MgCO₃ of magnesian calcite and the Sr/Ca ratio of the bulk fine fraction), they can not account for the observed age differences. The results presented for core MD03-2628 extend beyond this case study because they illustrate the need for a detailed characterization of the various size fractions prior to paleoclimate signal interpretations, especially for chronological studies.     

Evaluating carbon storage on subalpine lake deltas

Mountainous regions are important contributors to the terrestrial organic carbon (OC) sink that affect global climate through the regulation of carbon‐based greenhouse gases. However, mountain OC dynamics are poorly quantified. We quantified OC storage in subalpine lake deltas in the Washington Central Cascades and Colorado Front Range with the objectives of determining the magnitude of transient carbon storage and understanding the differences in storage between the two ranges. We used field, laboratory, and GIS techniques to determine the magnitude of and controls on the subalpine lake delta OC pool in 26 subalpine lake deltas. Soil moisture, soil texture, mean basin slope, and delta valley confinement are significantly correlated with soil carbon on deltas. Average soil OC concentration on subalpine lake deltas ranges from 3 to 41%, and stocks range from 140 to 1256 Mg C/ha. Surprisingly, the carbon content of subalpine lake deltas is not significantly different between the two regions, despite stark contrasts in their climate, vegetation, and total ecosystem carbon stocks. We present a conceptual model that invokes geomorphic and biogeochemical processes to suggest that carbon is more likely to reach subalpine lake deltas from the upstream basin in the Colorado Front Range compared with the Washington Central Cascades, thus accounting for the similarity in OC storage between the two regions despite differences in total ecosystem carbon stocks and climate. This points to a complex interaction among carbon production, transport, and stability in each region, and supports the idea that geomorphic and biogeochemical processes determine the magnitude of transient OC storage more strongly than primary productivity or climate. Copyright © 2017 John Wiley & Sons, Ltd.     

The Paleoceanography during the Time with High δ13C of Phanerozoic marine carbonates

Carbon isotopic composition of marine carbonates is a record for various important geological events in the process of earth development and evolution. The carbonates of Carboniferous, Permian and Triassic, as the transition from Paleozoic to Mesozoic-Cenozoic have very high ¹³C value. Taking this as the main point, and combined with the oxygen, strontium isotopic composition in carbonates, distribution of carbonate basin area through geologic time, the correlation of carbon isotopic composition of marine carbonates to sea level change, organic carbon burial flux, exchange of CO₂ content in atmosphere and ocean, and long cycle evolution of the earth ecosystems were approached. The results are shown as follows: ①The interval of ¹³C >3‰ during Phanerozoic was concentrated in Carboniferous, Permian and the beginning of Triassic, but the beginning of Triassic was characterized by higher frequency and larger fluctuations in ¹³C value during a short time, whereas the Carboniferous-Permian presented a continuously stable high ¹³C value, indicating a larger amount of organic carbon accumulation in this time interval. Relatively high ¹⁸O values during this time was also observed, showing a long time of glaciations and cold climate, which suggest a connection among rapid organic carbon burial, cold climate, as well as pCO₂ and pO₂ states of atmosphere. ②The over consumption of atmosphere CO₂ by green plants during the time with high ¹³C of seawater forced CO₂ being transferred from ocean to atmosphere for the balance, but the decrease in the seawater amount and water column pressure caused by the global cooling could weaken dissolution capacity of CO₂ in seawater and carbon storage of marine carbonates, and also reduce the carbonate sedimentary rate and decrease the carbonate basin area globally from Devonian to Carboniferous and Permian. During the middle-late Permian carbonate was widely replaced by siliceous sediments even though in shallow carbonate platform, which resulted in the decrease of marine invertebrates, suggesting the Permian chert event should be global. ③The Phanerozoic ⁸⁷Sr/⁸⁶Sr trend of seawater showed a sharp fall in Permian and drop to a minimum at the end of the Permian, indicting input of strontium from the submarine hydrothermal systems (mantle flux). Such process should accompany with a supplement of CO₂ from deep earth to atmosphere and ocean system, but the process associated with widespread volcanism and rises of earth’s surface temperature pricked up the mass extinction during the time of end Permian. ④Cold climate and increase of continental icecap volume, the amalgamation of northern Africa and Laurentia continentals were the main reasons responsible for the sea level drop, but the water consumption result from the significantly increased accumulation of organic carbon should also be one of the reasons for the sea level drop on the order of tens of meters. ⑤The mass extinction at the end Permian was an inevitable event in the process of earth system adjustment. It was difficult for marine invertebrates to survive because of the continuously rapid burial of organic carbon, and of the decrease of sea water amount and its dissolution ability to CO₂. At last, at the end of Paleozoic, the supplement of CO₂ to atmosphere and ocean by widely magma activities resulted in a high temperature of earth surface and intensified mass extinction.     

Anthropogenic influences on hydrocarbon contents of sediments deposited in eastern Lake Ontario since 1800

 The amounts and types of extractable hydrocarbon components in sediment cores from the Rochester Basin of eastern Lake Ontario provide a record of environmental changes that have accompanied the settlement and population growth of the surrounding land areas. Sediments deposited prior to the mid-1800s contain low concentrations of hydrocarbons that are dominated by land-plant wax components. Concentrations begin to rise in the late 1800s as erosion of soil and nutrients from watershed areas accelerated. This pattern continues into modern times. Episodes of enhanced aquatic productivity are sometimes recorded in twentieth-century sediments by the dominance of algal hydrocarbons, but land-plant components typically predominate. Petroleum residues begin to appear in sediments deposited in the late 1800's but remain minor constituents of the hydrocarbon contents of modern sediments in the Rochester Basin. Received: 21 March 1995 · Accepted: 11 August 1995     

Nature of the Ore-Forming Fluid at the Quaternary Noya Gold Deposit in Kyushu,Japan

We discuss the nature of the ore-forming hydrothermal fluid in the Noya gold-bearing calcite-quartz-adularia veins of central Kyushu, Japan on the basis of oxygen, carbon, and strontium isotope ratios, and aqueous speciation calculations for the present-day geothermal fluid. The isotopic values of the Noya ore-forming fluid were estimated to be −6.5‰ for δ¹³C and −7.5‰ for δ¹⁸O. The oxygen isotopic equilibrium temperatures for vein calcite are more than 180°C at the bottom of the Noya mineralization zone, and decrease with increasing elevation. As the temperature decreased, the dominant carbon species in the fluid changed from H₂CO₃ to HCO₃^- at about 120°C. The equilibrium temperatures for vein quartz are consistent with the calcite calculations. The carbon and oxygen isotope trends of the Noya vein calcite and the isotope ratios of strontium suggest that the fluids that precipitated the Noya veins were controlled by an andesite-dominated geology. Chondrite-normalized REE patterns for the white-colored veins from wells 51-WT-1 and 51-WT-2 displayed a light REE-rich pattern with positive Eu anomalies, suggesting the existence of a reducing environment for the fluid. The pyrite-rich gray-colored veins and a silicified rock from well 51-WT-2 showed higher REE concentrations than did the white veins. Altered host andesitic rocks have similar REE patterns to that of the silicified rock, and have higher REE contents than the others in the drill cores. Aqueous speciation calculations showed that the fluid in the hydrothermal reservoir is currently in muscovite stability. The fluid at the ore-mineralization stage may have contained more potassium or have had a higher pH, so that adularia precipitated with calcite and quartz, as well as gold. Fluid boiling at depth in the system produced the gold-bearing calcite-quartz-adularia veins.     

Model simulations of carbon sequestration in the northwest Pacific by patch fertilization

Iron fertilization of nutrient-rich surface waters of the ocean is one possible way to help slow the rising levels of atmospheric CO₂ by sequestering it in the oceans via biological carbon export. Here, I use an ocean general circulation model to simulate a patch of nutrient depletion in the subpolar northwest Pacific under various scenarios. Model results confirm that surface fertilization is an inefficient way to sequester carbon from the atmosphere (Gnanadesikan et al., 2003), since only about 20% of the exported carbon comes initially from the atmosphere. Fertilization reduces future production and thus CO₂ uptake by utilizing nutrients that would otherwise be available later. Effectively, this can be considered as leakage when compared to a control run. This “effective” leakage and the actual leakage of sequestered CO₂ cause a significant, rapid decrease in carbon retention (only 30–45% retained after 10 years and less than 20% after 50 years). This contrasts markedly with the almost 100% retention efficiency for the same duration using the same model, when carbon is disposed directly into the northwest Pacific (Matsumoto and Mignone, 2005). As a consequence, the economic effectiveness of patch fertilization is poor in two limiting cases of the future price path of carbon. Sequestered carbon in patch fertilization is lost to the atmosphere at increasingly remote places as time passes, which would make monitoring exceedingly difficult. If all organic carbon from one-time fertilization reached the ocean bottom and remineralized there, acidification would be about −0.05 pH unit with O₂ depletion about −20 μmol kg⁻¹. These anomalies are probably too small to seriously threaten deep sea biota, but they are underestimated in the model because of its large grid size. The results from this study offer little to advocate purposeful surface fertilization as a serious means to address the anthropogenic carbon problem.     

红树林海岸的沉积物输运和碳沉降特征

Mangroves play an important role in sequestering carbon and trapping sediments. However, the effectiveness of such functions is unclear due to the restriction of knowledge on the sedimentation process across the vegetation boundaries. To detect the effects of mangrove forests on sediment transportation and organic carbon sequestration, the granulometric and organic carbon characteristics of mangrove sediments were investigated from three vegetation zones of four typical mangrove habitats on the Leizhou Peninsula coast. Based on our results, sediment transport was often "environmentally sensitive" to the vegetation friction. A transition of the sediment transport mode from the mudflat zone to the interior/fringe zone was often detected from the cumulative frequency curve. The vegetation cover also assists the trapping of material, resulting in a significantly higher concentration of organic carbon in the interior surface sediments. However, the graphic parameters of core sediments reflected a highly temporal variability due to the sedimentation process at different locations. The sediment texture ranges widely from sand to mud, although the sedimentary environments are restricted within the same energy level along the fluvial-marine transition zone. Based on the PCA results, the large variation was mainly attributed to either the mean grain size features or the organic carbon features. A high correlation between the depth and δ13C value also indicated an increasing storage of mangrove-derived organic carbon with time.