土壤碳循环研究进展及干旱区土壤碳循环研究展望   总被引：5，自引：1，他引：4  

许文强  陈曦  罗格平  蔺卿 《干旱区地理》2011,(4)

土壤碳库动态及其驱动机制是陆地生态系统碳循环与全球变化研究的热点问题之一。随着各国对《京都议定书》的重视,农业土壤碳库变化及其源汇效应研究不断加强,但以往研究土壤碳循环主要是针对有机碳,较少考虑无机碳的作用和地位,干旱区土壤无机碳储量巨大,其在区域碳循环过程中的贡献日益显著,这使得干旱区土壤碳循环研究必须同时考虑土壤有机碳和无机碳的行为。国内外关于农业土壤有机碳动态的研究主要围绕农业土壤有机碳储量、固碳潜力等问题展开,研究区多为湿润、半湿润地区;国际上对农业土壤无机碳动态的研究主要集中在干旱区土地管理措施对土壤发生性碳酸盐碳的形成与转化方面,研究方法以稳定同位素技术为主,但目前关于中国干旱区农业土壤无机碳动态的研究还较为薄弱。因此,应加强干旱区绿洲土壤碳循环研究,深入分析干旱区绿洲土壤碳的源/汇效应;探讨土壤无机碳动态变化的机理。  相似文献   

Mixing of magmatic CO₂ into volcano groundwater flow at Aso volcano assessed combining carbon and water stable isotopes     

Makoto Yamada  Shinji Ohsawa  Kohei Kazahaya  Masaya Yasuhara  Hiroshi Takahashi  Kazuhiro Amita  Hideo Mawatari  Shin Yoshikawa 《Journal of Geochemical Exploration》2011

To understand deep groundwater flow systems and their interaction with CO₂ emanated from magma at depth in a volcanic edifice, deep groundwater samples were collected from hot spring wells in the Aso volcanic area for hydrogen, oxygen and carbon isotope analyses and measurements of the stable carbon isotope ratios and concentrations of dissolved inorganic carbon (DIC). Relations between the stable carbon isotope ratio (δ¹³C_DIC) and DIC concentrations of the sampled waters show that magma-derived CO₂ mixed into the deep groundwater. Furthermore, groundwaters of deeper areas, except samples from fumarolic areas, show higher δ¹³C_DIC values. The waters' stable hydrogen and oxygen isotope ratios (δD and δ¹⁸O) reflect the meteoric-water origin of that region's deep groundwater. A negative correlation was found between the altitude of the well bottom and the altitude of groundwater recharge as calculated using the equation of the recharge-water line and δD value. This applies especially in the Aso-dani area, where deeper groundwater correlates with higher recharge. Groundwater recharged at high altitude has higher δ¹³C_DIC of than groundwater recharged at low altitude, strongly suggesting that magmatic CO₂ is present to a much greater degree in deeper groundwater. These results indicate that magmatic CO₂ mixes into deeper groundwater flowing nearer the magma conduit or chamber.  相似文献   

胶磷矿晶体结构研究   总被引：1，自引：0，他引：1  

黄小芬  张覃 《矿物学报》2011,31(3):566-570

详细叙述了磷灰石的晶体结构,并采用多种方法对磷灰石结构中配位多面体各元素间的化学键力进行计算,分析了磷灰石的表面特性。针对贵州典型磷矿区具有代表性的胶磷矿试样,其主要由微晶磷灰石组成,采用x射线衍射分析了胶磷矿试样的物相组成、结晶度、晶胞参数以及磷灰石晶粒大小。在扫描电子显微镜下,2种胶磷矿多呈集合体形态,两种胶磷矿中磷酸盐矿物主要为氟磷灰石。  相似文献   

春季水华对南黄海总溶解态无机砷生物地球化学行为的影响   总被引：1，自引：0，他引：1  

孙友旭  任景玲  刘素美  刘诚刚 《海洋学报》2015,37(4):16-27

利用氢化物发生-原子荧光光谱法(HG-AFS)对2007年3月30日至4月23日南黄海海域总溶解态无机砷(TDIAs,[TDIAs]=[As5+]+[As3+])的含量进行了测定,其中针对水华中心区域(BM1站)进行了25h的连续观测,以探讨春季水华对有毒类金属元素砷的生物地球化学行为的影响。结果表明,TDIAs的浓度范围为7.9~22.3nmol/L,平均值为(17.8±1.9)nmol/L。TDIAs在南黄海的分布主要表现为由近岸向外海逐渐升高的趋势,最大值出现在南部海域底层海水中。近岸海域表、底层TDIAs的含量相当,而中、南部海域由于存在明显的密度跃层,表、底层TDIAs的浓度具有显著性差异。2007年3月31日至4月1日研究区域西南部受到沙尘天气和降雨的影响,表层海水中TDIAs的含量显著升高。研究区域中、南部海域在观测期间暴发了典型的黄海春季水华,通过大面观测和对重点区域的连续观测可以发现,水华期间TDIAs的分布和磷酸盐类似,与Chl a呈现出较好的负相关关系(r=0.51,P0.05,n=39)。经初步计算,浮游植物水华对10m以上表层水体中TDIAs的清除量约为2.4nmol/L,占表层保有量的15%左右。通过箱式模型计算得出黄海TDIAs的停留时间约为(18.2±8.5)a,远远低于大洋。通过对该海域砷、磷摩尔比值的计算可以发现,南黄海砷、磷摩尔比值约为大洋中的20倍左右,这可能会引起浮游生物对砷酸盐的大量吸收和转化,从而带来潜在的生态危机,需要引起足够的重视。  相似文献   

中国东海济舟岛南部春季水华的影响要素研究     

FU Dongyang  HUANG Zhaojun  ZHANG Yuanzhi  PAN Delu  DING Youzhu  LIU Dazhao  ZHANG Ying  MAO Zhihu  CHEN Jianfang 《海洋学报(英文版)》2015,34(3):51-58

A soil circulation occurs in the south of Cheju Island in the spring. Nutrients and its influence on chlorophyll a(Chl a) around the circulations were studied from April 9 to May 6, 2007. Spring bloom with elevated concentrations of Chl a was observed during the investigation. High concentrations of phosphate, nitrate and silicate at 0.6, 12, and 8 mmol/m3, respectively, were detected. A low water temperature prevented the growth of phytoplankton. Chl a concentrations in the study area might be strongly associated with the high silicate concentration.  相似文献   

酸雨对桂林枯水期岩溶地下水δ13C_DIC及碳汇效应的影响   总被引：1，自引：0，他引：1       下载免费PDF全文

黄奇波  覃小群  刘朋雨  唐萍萍 《地球科学》2015,40(7):1237-1247

定量评价硫酸对岩溶碳汇效应的影响有助于提高岩石风化碳汇通量估算精度, 对当前全球气候变化研究意义重大.选取受酸雨影响的桂林岩溶区为研究对象, 在枯水期对研究区14个岩溶大泉和15条地下河水化学成分和碳同位素进行了测试分析, 结果表明: 岩溶大泉和地下河中阳离子以Mg2+和Ca2+为主, 阴离子以HCO₃-为主, 分别占阳离子和阴离子组成的90%以上, SO₄2-含量较低, 其含量范围为0.004~0.213mmol/L; 所占阴离子组成比例为0.12%~6.11%;δ13C_DIC、[Ca2++Mg2+]/[HCO₃-]更偏向于碳酸溶解端元, 离硫酸溶解端元距离远, 证实硫酸参与碳酸盐岩的溶解对地下水无机碳(dissolved inorganic carbon, 简称DIC)及δ13C_DIC的影响有限; 与Sr2+/Ca2+值一样, δ13C_DIC主要受径流条件控制, 其大小可以反映地下水径流条件的强弱.利用化学计量关系计算出由硫酸溶蚀碳酸盐岩的平均比例为22.64%, 产生的DIC(HCO₃-_H2SO4)占总DIC的平均比例为13.04%, 碳酸产生的DIC(HCO₃-_H2CO3)占地下水总DIC的比例为86.96%, 其中来源于土壤大气中的HCO₃-比例为43.48%.因此, 扣除硫酸对地下水中DIC的贡献后, 岩溶碳汇效应将减少13.04%.   相似文献   

脑动脉粥样硬化斑块中钙化物矿物学特征研究     

李源  王长秋  孟繁露  李艳  鲁安怀  杨重庆  于启  李康 《岩石矿物学杂志》2015,34(6):963-970

脑动脉钙化与脑动脉系统病变有密切联系。本文从矿物学角度出发,使用偏光显微镜(POM),扫描电子显微镜(SEM)、透射电子显微镜(TEM)、显微红外光谱(micro-FTIR)、同步辐射微区X射线衍射(μ-SRXRD)以及同步辐射微区X射线荧光光谱(μ-SRXRF)对脑动脉粥样硬化斑块中的钙化样品进行了研究。结果表明,钙化主要有球状和块状两种集合体形态,球状钙化具有同心环状或同心放射状构造,直径约0.3~5μm;块状钙化中可见球状钙化被杂乱分布的柱状纳米晶体包裹。钙化主要矿物相为B型碳羟磷灰石(B-CHA),并含Na、Mg、Zn、Fe和Sr等元素,与主动脉钙化中的矿物组成类似。钙化在其形成初期呈分散的小球状,后期大量球体逐渐被CHA纳米晶体充填胶结形成了致密的块状钙化。  相似文献   

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

Huang Sijing  Li Xiaoning  Wu Wenhui  Zhang Meng  Hu Zuowei  Liu Sibing  Huang Keke  Zhong Yijiang 《地球科学进展》2015,30(11):1185-1197

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.  相似文献   

Dissolved inorganic carbon evolution in neutral discharge from mine tailings piles          下载免费PDF全文

Hendratta N. Ali  Eliot A. Atekwana 《水文研究》2016,30(13):2079-2091

We measured the concentrations of dissolved inorganic carbon (DIC) and major ions and the stable carbon isotope ratios of DIC (δ¹³C_DIC) in two creeks discharging from carbonate‐rich sulphide‐containing mine tailings piles. Our aim was to assess downstream carbon evolution of the tailings discharge as it interacted with the atmosphere. The discharge had pH of 6.5–8.1 and was saturated with respect to carbonates. Over the reach of one creek, the DIC concentrations decreased by 1.1 mmol C/l and δ¹³C_DIC increased by ~4.0‰ 200 m from the seep source. The decrease in the DIC concentrations was concomitant with decreases in the partial pressure of CO_2(aq) because of the loss of excess CO_2(aq) from the discharge. The corresponding enrichment in the δ¹³C_DIC is because of kinetic isotope fractionation accompanying the loss of CO_2(g). Over the reach of the other creek, there was no significant decrease in the DIC concentrations or notable changes in the δ¹³C_DIC. The insignificant change in the DIC concentrations and the δ¹³C_DIC is because the first water sample was collected 160 m away from the discharge seep, not accessible during this research. In this case, most of the excess CO_2(aq) was lost before our first sampling station. Our results indicate that neutral discharges from tailings piles quickly lose excess CO_2(aq) to the atmosphere and the DIC becomes enrich in ¹³C. We suggest that a significant amount of carbon cycling in neutral discharges from tailings piles occur close to the locations where the discharge seeps to the surface. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

A long‐term study of stable isotopes as tracers of processes governing water flow and quality in a lowland river basin: the upper Thames,UK          下载免费PDF全文

W. George Darling  Michael J. Bowes 《水文研究》2016,30(13):2178-2195

A long‐term study of O, H and C stable isotopes has been undertaken on river waters across the 7000‐km² upper Thames lowland river basin in the southern UK. During the period, flow conditions ranged from drought to flood. A 10‐year monthly record (2003–2012) of the main River Thames showed a maximum variation of 3‰ (δ¹⁸O) and 20‰ (δ²H), although interannual average values varied little around a mean of –6.5‰ (δ¹⁸O) and –44‰ (δ²H). A δ²H/δ¹⁸O slope of 5.3 suggested a degree of evaporative enrichment, consistent with derivation from local rainfall with a weighted mean of –7.2‰ (δ¹⁸O) and –48‰ (δ²H) for the period. A tendency towards isotopic depletion of the river with increasing flow rate was noted, but at very high flows (>100 m³/s), a reversion to the mean was interpreted as the displacement of bank storage by rising groundwater levels (corroborated by measurements of specific electrical conductivity). A shorter quarterly study (October 2011–April 2013) of isotope variations in 15 tributaries with varying geology revealed different responses to evaporation, with a well‐correlated inverse relationship between Δ¹⁸O and baseflow index for most of the rivers. A comparison with aquifer waters in the basin showed that even at low flow, rivers rarely consist solely of isotopically unmodified groundwater. Long‐term monitoring (2003–2007) of carbon stable isotopes in dissolved inorganic carbon (DIC) in the Thames revealed a complex interplay between respiration, photosynthesis and evasion, but with a mean interannual δ¹³C‐DIC value of –14.8 ± 0.5‰, exchange with atmospheric carbon could be ruled out. Quarterly monitoring of the tributaries (October 2011–April 2013) indicated that in addition to the aforementioned factors, river flow variations and catchment characteristics were likely to affect δ¹³C‐DIC. Comparison with basin groundwaters of different alkalinity and δ¹³C‐DIC values showed that the origin of river baseflow is usually obscured. The findings show that long‐term monitoring of environmental tracers can help to improve the understanding of how lowland river catchments function. Copyright © NERC 2015. Hydrological Processes © 2015 John Wiley & Sons, Ltd.  相似文献