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21.
Dissolved inorganic carbon (DIC) is the most important carbon component in karst aquatic system where fluid is highly transmissive, but has rarely been examined in the subtropical karst critical zone (K-CZ). In this study, concentrations of dissolved solutes and isotopic compositions of DIC (δ13CDIC) at 11 sites of a 73.4 km2 karstic catchment in Southwestern China were analysed monthly in order to uncover the spatiotemporal variations of both DIC and its dominant sources, and to identify relevant controlling factors. Both DIC concentrations and δ13CDIC were highly variable, ranging from 2.52 to 5.85 mmol l−1 and from −15.7 to −4.5‰, respectively. DIC in underground water (UGW) was higher in concentration and more depleted in 13C compared to surface water (SFS). DIC concentrations showed an inconsistent seasonal trend with other solutes, with higher values in the wet season at some sites. δ13CDIC values were lower in the wet season than in the dry season. The results of mixing model IsoSource revealed spatiotemporal patterns of DIC sources. During the dry season, carbonate weathering was the primary contributor to DIC in UGW (excluding in the middle reaches). However, during the wet season, soil CO2 was the dominant source of DIC in both UGW and SFS, and it was higher than in the dry season. Overall, there are significant spatiotemporal disparities and highly transmissive characteristics of both DIC and its sources in the K-CZ, which are controlled by multiple factors. This study also highlights that rainfall may play a crucial role in accelerating carbon dynamics in the K-CZ. High-frequency sampling campaigns in high-flow periods and deep analyses are needed in future work to elucidate the related processes and mechanisms. © 2019 John Wiley & Sons, Ltd. 相似文献
22.
Application of a Bayesian model to infer the contribution of coalbed natural gas produced water to the Powder River,Wyoming and Montana 下载免费PDF全文
The Powder River Basin (PRB) of Wyoming and Montana contains significant coal and coal bed natural gas (CBNG) resources. CBNG extraction requires the production of large volumes of water, much of which is discharged into existing drainages. Compared to surface waters, the CBNG produced water is high in sodium relative to calcium and magnesium, elevating the sodium adsorption ratio (SAR). To mitigate the possible impact this produced water may have on the quality of surface water used for irrigation, the State of Montana passed water anti‐degradation legislation, which could affect CBNG production in Wyoming. In this study, we sought to determine the proportion of CBNG produced water discharged to tributaries that reaches the Powder River by implementing a four end‐member mixing model within a Bayesian statistical framework. The model accounts for the 87Sr/86Sr, δ13CDIC, [Sr] and [DIC] of CBNG produced water and surface water interacting with the three primary lithologies exposed in the PRB. The model estimates the relative contribution of the end members to the river water, while incorporating uncertainty associated with measurement and process error. Model results confirm that both of the tributaries associated with high CBNG activity are mostly composed of CBNG produced water (70–100%). The model indicates that up to 50% of the Powder River is composed of CBNG produced water downstream from the CBNG tributaries, decreasing with distance by dilution from non‐CBNG impacted tributaries from the point sources to ~10–20% at the Montana border. This amount of CBNG produced water does not significantly affect the SAR or electrical conductivity of the Powder River in Montana. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
23.
Jennifer Vandenhecke Matthieu Waeles Jean-Yves Cabon Cédric Garnier Ricardo D. Riso 《Estuarine, Coastal and Shelf Science》2010
Over this one-year study, the variations of inorganic As species were examined monthly along the salinity gradient of the Penzé estuary (NW France) in relation with different biogeochemical parameters. In most cases, dissolved As exhibited a non-conservative behaviour which resulted from the competition between two major processes. In the upstream section of the estuary, a strong input of both total inorganic As and As(III) occurred. Then, the removal of the same species, under precipitation of iron oxides/oxyhydroxides, was observed in the low-salinity range (S < 10). Using our experimental data, the fluxes of the various As species were estimated for the first time in estuarine waters. Inputs from the river were mainly constituted of particulate As (∼70%). Conversely, dissolved species were predominant in the net fluxes (∼65%) and As(III) accounted for ∼15% of the dissolved net flux. 相似文献
24.
Yu Xia Zhou Weijian Wang Yunqiang Cheng Peng Hou Yaoyao Xiong Xiaohu Du Hua Yang Ling Wang Ya 《地理学报(英文版)》2020,30(6):921-934
The vertical distribution and exchange mechanisms of soil organic and inorganic carbon(SOC, SIC) play an important role in assessing carbon(C) cycling and budgets. However, the impact of land use through time for deep soil C(below 100 cm) is not well known. To investigate deep C storage under different land uses and evaluate how it changes with time, we collected soil samples to a depth of 500 cm in a soil profile in the Gutun watershed on the Chinese Loess Plateau(CLP); and determined SOC, SIC, and bulk density. The magnitude of SOC stocks in the 0–500 cm depth range fell into the following ranking: shrubland(17.2 kg m~(-2)) grassland(16.3 kg m~(-2)) forestland(15.2 kg m~(-2)) cropland(14.1 kg m~(-2)) gully land(6.4 kg m~(-2)). The ranking for SIC stocks were: grassland(104.1 kg m~(-2)) forestland(96.2 kg m~(-2)) shrubland(90.6 kg m~(-2)) cropland(82.4 kg m~(-2)) gully land(50.3 kg m~(-2)). Respective SOC and SIC stocks were at least 1.6-and 2.1-fold higher within the 100–500 cm depth range, as compared to the 0–100 cm depth range. Overall SOC and SIC stocks decreased significantly from the 5 th to the 15 th year of cultivation in croplands, and generally increased up to the 70 th year. Both SOC and SIC stocks showed a turning point at 15 years cultivation, which should be considered when evaluating soil C sequestration. Estimates of C stocks greatly depends on soil sampling depth, and understanding the influences of land use and time will improve soil productivity and conservation in regions with deep soils. 相似文献
25.
矿物在油气形成过程中的作用 总被引:4,自引:0,他引:4
模拟实验结果表明,矿物组成对煤岩样品的模拟实验结果具有很大的影响,不同的矿物以及同一种矿物在不同的有机质热演化阶段,对有机质形成石油和天然气的过程均具有非常明显的影响:高岭土矿物在高温热演化阶段对有机质形成气态烃的过程具有一定的催化能力;碳酸钙(CaCO3)在中—低热演化阶段能抑制气态物质的形成,而在较高的热演化阶段则对煤生成气态物质的过程具有一定的催化作用;四氧化三铁(Fe3O4)在主要的模拟实验阶段对煤生成气态物质的过程均具有一定的催化作用;硫化亚铁(FeS)在低温热演化阶段对天然气的形成具有一定的抑制作用,而在高温热演化阶段则对天然气的形成具有较明显的催化作用;元素硫(S)在不同的热演化阶段对天然气的形成过程均具有非常明显的催化作用。矿物介质不仅对气态产物的产率有比较明显的影响,而且对液态产物的产率也有较明显的影响。模拟实验结果表明:高岭土和四氧化三铁(Fe3O4)在中、低温模拟实验阶段对“氯仿沥青A”的形成具有较明显的催化作用;硫化亚铁(FeS)在整个模拟实验的全过程中对“氯仿沥青A”的形成均具有明显的催化作用;碳酸钙(CaCO3)矿物对“氯仿沥青A”的形成具有明显的抑制作用;元素硫(S)对“氯仿沥青A”的形成具有非常明显的催化作用。 相似文献
26.
一种用磷酸钙法高效转染HEK 293T细胞方法的建立 总被引:1,自引:0,他引:1
利用磷酸钙转染法将lacZ-pShuttle质粒导入HEK 293T细胞中,实验证明,pH值、DNA纯度、转染后培养时间和甘油休克时间是影响转染效率的重要因素.转染后培养6h进行甘油休克效果最佳,比培养0h直接进行休克转染效率升高584.4%;甘油休克时间为4.5min时转染效果最佳,比不用甘油休克转染效率升高130.8%.通过对影响转染的几个条件进行优化,建立了1种可以高效转染HEK 293T细胞的方法,且简便易行. 相似文献
27.
沉积物对磷酸盐的吸附与释放 总被引:3,自引:0,他引:3
本实验研究黄河口水文站沉积物对黄河水磷的吸附释放过程和东海111号站位沉积物对海水磷的吸附释放过程。并摸拟黄河沉积物在海水中磷的吸附释放过程。结果表明:底沉积物对磷的吸附相当迅速,无论是河泥还是海泥在24h内均能达到吸附平衡。吸附量与沉积物的量和水中原有磷的浓度有关,在不同的pH条件下,沉积物对磷的吸附是有显著差别的 相似文献
28.
1993/1994年南极夏季对中国南极长城湾及附近海区表层海水四种营养盐浓度及其分布状况作了调查。结果表明,NH4-N、NO3-N、NO2-N及PO4-P的大致浓度分别是2.13、7.07、0.74和1.12μg·dm-3。一般来说,湾内高于湾外氮盐于12月份常出现高值。四种形态的无机盐类之最高、最低浓度出现的时间和站位不尽一致。∑N/P递减次序大致是12月,2月,1月。水温变化与NH4-N、PO4-P浓度和∑N/P的变化常较一致,而与NO2-N则常不一,一些站位上营养盐浓度偏低可能与浮游植物摄取有关。结果显示了调研海区的浅水内湾特征。浮游植物所需营养充分。该湾仍维持正常状态。 相似文献
29.
30.
Helen C. Bostock Bruce W. HaywardHelen L. Neil Kim I. CurrieGavin B. Dunbar 《Deep Sea Research Part I: Oceanographic Research Papers》2011,58(1):72-85
We have compiled carbonate chemistry and sedimentary CaCO3% data for the deep-waters (>1500 m water depth) of the southwest (SW) Pacific region. The complex topography in the SW Pacific influences the deep-water circulation and affects the carbonate ion concentration ([CO32−]), and the associated calcite saturation horizon (CSH, where ??calcite=1). The Tasman Basin and the southeast (SE) New Zealand region have the deepest CSH at ∼3100 m, primarily influenced by middle and lower Circumpolar Deep Waters (m or lCPDW), while to the northeast of New Zealand the CSH is ∼2800 m, due to the corrosive influence of the old North Pacific deep waters (NPDW) on the upper CPDW (uCPDW). The carbonate compensation depth (CCD; defined by a sedimentary CaCO3 content of <20%), also varies between the basins in the SW Pacific. The CCD is ∼4600 m to the SE New Zealand, but only ∼4000 m to the NE New Zealand. The CaCO3 content of the sediment, however, can be influenced by a number of different factors other than dissolution; therefore, we suggest using the water chemistry to estimate the CCD. The depth difference between the CSH and CCD (??ZCSH−CCD), however, varies considerably in this region and globally. The global ??ZCSH−CCD appears to expand with increase in age of the deep-water, resulting from a shoaling of the CSH. In contrast the depth of the chemical lysocline (??calcite=0.8) is less variable globally and is relatively similar, or close, to the CCD determined from the sedimentary CaCO3%. Geochemical definitions of the CCD, however, cannot be used to determine changes in the paleo-CCD. For the given range of factors that influence the sedimentary CaCO3%, an independent dissolution proxy, such as the foraminifera fragmentation % (>40%=foraminiferal lysocline) is required to define a depth where significant CaCO3 dissolution has occurred back through time. The current foraminiferal lysocline for the SW Pacific region ranges from 3100-3500 m, which is predictably just slightly deeper than the CSH. This compilation of sediment and water chemistry data provides a CaCO3 dataset for the present SW Pacific for comparison with glacial/interglacial CaCO3 variations in deep-water sediment cores, and to monitor future changes in [CO32−] and dissolution of sedimentary CaCO3 resulting from increasing anthropogenic CO2. 相似文献