青藏高原东部长江流域盆地陆地化学风化研究

长江河水主要离子由流域盆地碳酸盐岩的风化所控制,沱沱河和楚玛尔河受蒸发盐岩影响较为明显;河水溶质载荷Si,Si/TZ *,Si/(Na* K)等指标表明,长江流域盆地地表硅酸盐岩风化还是浅表层次的;金沙江地表化学剥蚀速率为1.74×103mol/yr.km2,雅砻江为1.69×103mol/yr.km2,大渡河为1.57×103mol/yr.km2,岷江为1.88×103mol/yr.km2,长江河源区楚玛尔河为2.32×103mol/yr.km2,沱沱河为1.37×103mol/yr.km2,流域地表化学剥蚀速率可与世界上其它造山带的河流进行对比。     

Late Quaternary denudation of the Alps,valley and lake fillings and modern river loads

Erosional denudation of the Alps and their role as sediment source underwent major changes throughout the Quaternary, by repeated glaciation and deglaciation. The sediment fluxes of 16 major Alpine drainage basins were quantified by determining the sediment volumes which have been trapped in valleys and lake basins. These became sedimentologically closed after the last glacier retreat around 17 000 cal. BP. The sediment volumes distributed over their provenance areas yield mean mechanical denudation rates between 250 to 1060 mm ka^–1. In contrast, modern denudation rates, derived from river loads and delta surveys, range from 30 to 360 mm ka^–1. Relief, such as mean elevation and slope, turned out to be the primary control of both modern and Late Glacial mechanical denudation. Rock types seem to be responsible for some scatter of the data, but their role is masked by other factors. Modern denudation rates increase with higher proportions of bare rocks and glaciated area, but decrease with forest cover. An area-weighted extrapolation of the studied drainage basins to the entire Alps on the basis of major morphotectonic zones yields a mean denudation rate of 620 mm ka^–1 over the last 17 000 years. This rate clearly exceeds the modern rate of 125 mm ka^–1. Lake sediments and palaeoclimatic reconstructions confirm that the sediment yield of the Alps reached a maximum during deglaciation when large masses of unconsolidated materials were available, vegetation was scarse, and transport capacities were high. During the early Holocene sediment yield declined to a minimum before some climate deterioration and human activities again accelerated erosional processes. Assuming a denudation rate in the early Holocene half of the modern one, the Late Glacial denudation rates must have been in the order of 1100 to 2900 mm ka^–1. Consequently, denudation rates during a glacial/interglacial cycle probably varied by a factor of 14, which lies well within the range of other studies in central Europe, Scandinavia and North America. From large scale sediment budgets of perialpine sedimentary basins the overall denudation rate of the Alps during the Quaternary has been c. 400 mm ka^–1, i.e. about one third lower than the estimate for the last 17000 years. This can be well explained by the outstanding role which deglaciation played in the time span studied here.     

Effects of quarry mining and of other environmental impacts in the mountainous Chicam-Toctina drainage basin (Córdoba, Argentina)

 The environmental conditions prevailing in the Chicam-Toctina drainage system (approx. 138 km² in Córdoba, Argentina) are considered representative of a number of catchments in Argentina's Sierras Pampeanas Range. Two groups of ions reflect the sources of dissolved species in the catchment: a) a group (Cl^–, SO^2– ₄, and Na⁺) which recognizes natural and anthropogenic sources, and which exhibits significant correlations with N^– ₃ and NO^– ₂, and b) another group of components (Ca²⁺, Mg²⁺, and HCO^– ₃) which is clearly controlled by carbonate rocks and their waste rock products. In the headwaters, stockpiled marble quarry mining wastes provide a more open system to CO₂ gaseous exchange than the outcropping rocks, thus promoting the increase of carbonate dissolution (up to 4.88 g km^–2 s^–1 during the rainy season). This specific yield was 20% higher than the amount estimated for an area with fewer extended mining activities. The dissolved load delivered by the upper reaches is subjected in the lower drainage area to various processes, mainly controlled by the presence of the city of Alta Gracia (approx. 40,000 inhabitants). In the dry season, due to nutrient inputs supplied by the city, photosynthetic activity plays a major role controlling stream pH. Hence, the high values of calcite saturation indexes and the increase of CaCO₃ concentration in bed sediments can be explained by calcite precipitation. Such a process could be accompanied by the coprecipitation on calcium carbonate of low solubility heavy metal carbonates. Received : 17 January 1997 · Accepted : 31 March 1997     

Major ion chemistry of the Ganga source waters: Weathering in the high altitude Himalaya

A systematic study of the major ion chemistry of the Ganga source waters—the Bhagirathi, Alaknanda and their tributaries—has been carried out to assess the chemical weathering processes in the high altitude Himalaya. Among major ions, Ca, Mg, HCO₃ and SO₄ are the most abundant in these river waters. These results suggest that weathering of carbonate rocks by carbonic and sulphuric acids dominates in these drainage basins. On an average, silicate weathering can contribute up to ∼ 30% of the total cations. The concentration of total dissolved salts in the Bhagirathi and the Alaknanda is 104 and 115mg/l, respectively. The chemical denudation rate in the drainage basins of the Bhagirathi and the Alaknanda is, respectively, 110 and 137 tons/km²/yr, significantly higher than that derived for the entire Ganga basin, indicating intense chemical erosion of the Himalaya.     

The impact of diamond extraction on natural denudation rates in the Diamantina Plateau (Minas Gerais,Brazil)

The ¹⁰Be method was used to investigate the effect of mining activities on the natural denudation rates in alluvial sediments from catchments of the Southern Espinhaço Range (SER) in Minas Gerais State (Brazil). In this region, which is predominantly composed of quartzites, the ¹⁰Be concentrations were measured in alluvial sediments from catchments in a preserved natural area of the Serra do Cipó National Park and on the Diamantina Plateau, which was subjected to diamond extraction from beginnings of XVIII century until the end of the XX. Two types of drainage were identified in the Diamantina Plateau area: (i) reworked drainage (alluvial sediments reworked by panning) and (ii) overloaded drainage (alluvial sediments originating from panning processes on saprolites located upstream). The mean denudation value for the natural drainages (∼4.4 m.My-1) is similar to that of the reworked drainages (∼4.3 m.My-1) However, the denudation rates obtained for eleven samples from three sites in overloaded basins range from ∼6.4 m My-1 to ∼22.8 m My-1 and are thus higher than those determined for the reworked and natural basins. These results show that despite the alluvium deposits have been intensely reworked by panning, the values of denudation rates were not changed, they are similar to denudation rates from the natural drainages. However, the natural rates are lower than those affected by panning processes on saprolites.     

Chemical weathering of carbonates and silicates in the Han River basin,South Korea

A detailed investigation of the fluvial geochemistry of the Han River system allows to estimate the rates of chemical weathering and the consumption of CO₂. The Han River drains approximately 26,000 km² and is the largest river system in South Korea in terms of both water discharge and total river length. It consists of two major tributaries: the North Han River (NHR) and the South Han River (SHR). Distinct differences in basin lithology (silicate vs. carbonate) between the NHR and SHR provide a good natural laboratory in which to examine weathering processes and the influence of basin geology on water quality. The concentrations of major elements and the Sr isotopic compositions were obtained from 58 samples collected in both summer and winter along the Han River system in both 2000 and 2006. The concentrations of dissolved loads differed considerably between the NHR and SHR; compared with the SHR, the NHR had much lower total dissolved solids (TDS), Sr, and major ion concentrations but a higher Si concentration and ⁸⁷Sr/⁸⁶Sr ratio. A forward model showed that the dissolved loads in the NHR came primarily from silicate weathering (55 ± 11%), with a relatively small portion from carbonates (30 ± 14%), whereas the main contribution to the dissolved loads in the SHR was carbonate weathering (82 ± 3%), with only 11 ± 4% from silicates. These results are consistent with the different lithologies of the two drainage basins: silicate rocks in the NHR versus carbonate rocks in the SHR. Sulfuric acid derived from sulfide dissolution in coal-containing sedimentary strata has played an important role in carbonate weathering in the SHR basin, unlike in the NHR basin. The silicate weathering rate (SWR) was similar between the NHR and SHR basins, but the rate of CO₂ consumption in the SHR basin was lower than in the NHR basin due to an important role of sulfuric acid derived from pyrite oxidation.     

Metallogeny of the Shilu Fe–Co–Cu deposit,Hainan Island,South China: Constraints from fluid inclusions and stable isotopes

The Shilu deposit is a world-class Fe–Co–Cu orebody located in the Changjiang area of the western part of Hainan Island, South China. The distribution of Fe, Co, and Cu orebodies is controlled by strata of the No. 6 Formation in the Shilu Group and the Beiyi synclinorium. Based on a petrological study of the host rocks and their alteration assemblages, and textural and structural features of the ores, four mineralization stages have been identified: (1) the sedimentary ore-forming period; (2) the metamorphic ore-forming period; (3) the hydrothermal mineralization comprising the skarn and quartz–sulfide stage; and (4) the supergene period. The fluid inclusions in sedimentary quartz and/or chert indicate low temperatures (ca. 160 °C) and low salinities from 0.7 to 3.1 wt.% NaCl_eq, which corresponds to densities of 0.77 to 0.93 g/cm³. CO₂-bearing or carbonic inclusions have been interpreted to result from regional metamorphism. Homogenization temperatures of fluid inclusions for the skarn stage have a wide range from 148 °C to 497 °C and the salinities of the fluid inclusions range from 1.2 to 22.3 wt.% NaCl_eq, which corresponds to densities from 0.56 to 0.94 g/cm³. Fluid inclusions of the quartz–sulfide stage yield homogenization temperatures of 151–356 °C and salinities from 0.9 to 8.1 wt.% NaCl_eq, which equates to fluid densities from 0.63 to 0.96 g/cm³.Sulfur isotopic compositions indicate that sulfur of the sedimentary anhydrite and Co-bearing pyrite, and the quartz–sulfide stage, was derived from seawater sulfate and thermochemical sulfate reduction of dissolved anhydrite at temperatures of 200 °C and 300 °C, respectively. H and O isotopic compositions of the skarn and quartz–sulfide stage demonstrate that the ore-forming fluids were largely derived from magmatic water, with minor inputs from metamorphic or meteoric water. The Shilu iron ore deposit has an exhalative sedimentary origin, but has been overprinted by regional deformation and metamorphism. The Shilu Co–Cu deposit has a hydrothermal origin and is temporally and genetically associated with Indosinian granitoid rocks.     

Linking source and sink: Evaluating the balance between onshore erosion and offshore sediment accumulation since Gondwana break-up, South Africa

The geomorphic origin and evolution of the tectonically unique interior highland of southern Africa, the Kalahari Plateau, and its flanking low-lying coastal planes, remain largely unresolved because of a lack of regional quantitative analyses of its uplift and erosion history. Here we focus on the southern Cape, South Africa and link onshore denudation, based on new apatite fission track thermochronology results, to offshore sediment accumulation, using abundant well data and a seismic reflection profile. We attempt to relate source and sink in order to resolve some first order issues concerning timing of the exhumation and development of the topographic features of southern Africa. The volume of sediment accumulated off South Africa's south coast is calculated using 173 wells and a seismic reflection profile. A total, uncompacted, sediment volume of 268,500 km³ accumulated off South Africa's south coasts since  136 Ma, in the Outeniqua and Southern Outeniqua Basins. Accumulation volumes and rates were highest in the early Cretaceous (48,800 × 10⁴ km³ at  8150 km³/Ma from  136 to 130 Ma, and 57,500 × 10⁴ km³ at 5750 km³/Ma from  130 to 120 Ma) and mid–late Cretaceous (83,700 × 10⁴ km³ at 3200 km³/Ma from  93 to 67 Ma). Volumes and accumulation rates were lowest for the early–mid-Cretaceous (47,400 × 10⁴ km³ at 1750 km³/Ma from  120 to 93 Ma) and the Cenozoic (31,200 × 10⁴ km³ at 450 km³/Ma from  67 to 0 Ma). Although our analysis shows that the accumulated volume of offshore sediments does not match the calculated volume of onshore erosion, as quantified through apatite fission track thermochronology (e.g. Tinker, J.H., de Wit, M.J., Brown, R., 2008. Mesozoic exhumation of the 439 southern Cape, South Africa, quantified using apatite fission track thermochronology. Tectonophysics, doi: 10.1016/j.tecto.2007.10.009), the timing of increased sediment accumulation closely matches the timing of increased onshore denudation. This suggests that the greatest volumes of material were transported from source to sink during two distinct Cretaceous episodes, and that the processes driving onshore denudation decreased by an order of magnitude during the Cenozoic.     

Modelling of stream run-off and sediment output for erosion hazard assessment in Lesser Himalaya: need for sustainable land use plan using remote sensing and GIS: a case study

Assessment and inventory on soil erosion hazard are essential for the formulation of successful hazard mitigation plans and sustainable development. The objective of this study was to assess and map soil erosion hazard in Lesser Himalaya with a case study. The Dabka watershed constitutes a part of the Kosi Basin in the Lesser Himalaya, India, in district Nainital has been selected for the case illustration. The average rate of erosion hazard is 0.68 mm/year or 224 tons/km²/year. Anthropogenic and geo-environmental factors have together significantly accelerated the rate of erosion. This reconnaissance study estimates the erosion rate over the period of 3 years (2006–2008) as 1.21 mm/year (398 tons/km²/year) in the barren land having geological background of diamictite, siltstone and shale rocks, 0.92 mm/year (302 tons/km²/year) in the agricultural land with lithology of diamictite, slates, siltstone, limestone rocks, while in the forest land, it varies between 0.20 mm/year (66 tons/km²/year) under dense forest land having the geology of quartzwacke and quartrenite rocks and 0.40 mm/year (132 tons/km²/year) under open forest/shrubs land having geological setup of shale, dolomite and gypsum rocks. Compared to the intensity of erosion in the least disturbed dense forest, the erosion rate is about 5–6 times higher in the most disturbed agricultural land and barren land, respectively. The erosion hazard zones delineated following scalogram modelling approach. Integrated scalogram modelling approach resulted in severe classes of soil erosion hazard in the study area with numerical values of Erosion Hazard Index (EHI) ranging between 01 (very low hazard) and 5 (very high hazard).     

Geological and environmental implications in the reclamation of limestone quarries in Sierra de Callosa (Alicante,Spain)

Sierra de Callosa have an area of 8 km² and a maximum altitude of 566 masl. Geologically, it is found to be primarily comprised of carbonated rocks. Mine spoils coming from limestone quarries extraction are often used in the working reclamation process. These materials could be actually employed profitably once conveniently amended with organic matter. A study on the temporary evolution of nutrients and several physical–chemical parameters in a mineral waste amended with municipal solid waste (MSW) compost has been carried out. The effect of incorporating such waste to mine spoils in an arid gravel quarry has been studied, quantifying the temporal evolution of nutrients and several physical–chemical parameters in the mixture. Three plots have been prepared with mine spoils proceeding from a limestone quarry located in the south of the province of Alicante (municipality of Redován). These plots have been amended with 3 kg/m² of MSW compost. Texture, pH, electrical conductivity, oxidizable organic matter, N-Kjeldahl, available P, Na, K, Ca, Mg, Fe, Mn, Cu and Zn were analysed. The results reflected the contribution of nutrients to the substrate after the MSW addition. The variability of the information indicated the heterogeneity of the MSW composition, as well as the difficulty of obtaining a homogeneous MSW mixture–mineral waste.     

Hydrochemistry of the Amur River: Weathering in a Northern Temperate Basin

We report the dissolved major element, organic carbon, and δ¹³C_DOC, δ¹³C_POC, δD, δ¹⁸O, and ⁸⁷Sr/⁸⁶Sr composition of 19 summer samples from the Amur River. The Amur transported 2.6 Tg C/year of total organic carbon to the Sea of Okhotsk. The physical weathering rate (PWR) based on suspended particulate material was 13 (1.4–14) tons/(km² year), and the chemical weathering rate based on total dissolved solids was 7 (4.3–46) tons/(km² year). We further quantified the sources of the dissolved cations using an inverse model: rain accounted for 2 (0.6–5)%, evaporite 3 (0.7–7)%, carbonate 51 (29–74)%, and silicate 45 (25–64)%. The silicate weathering rate (SWR) in the Amur basin was 23 (15–98) × 10³ mol/(km² year) or 0.67 (0.40–2.81) tons/(km² year), comparable to those of the Siberian rivers and the Mackenzie at higher latitudes. The SWR of the Amur was negatively correlated with elevation and relief, and positively correlated with runoff.     

Natural and anthropogenic budgets of a small watershed in the massif central (France): Chemical and strontium isotopic characterization of water and sediments

A small watershed (160 km²) located in the Massif Central (France) has been chemically, isotopically and hydrologically studied through its dissolved load, bed sediments and soils. This watershed is underlain by basaltic bedrock and associated soils in which the vegetation is dominated mainly by meadows.Dissolved concentrations of major ions (Cl, SO₄, NO₃, HCO₃, Ca, Na, Mg, K, Al and Si), trace elements (Rb and Sr) and strontium isotopes have been determined for two different hydrologic periods on the main stream of the Allanche river and its tributaries.The major objectives of this study were to characterize the chemical and isotopic signatures of each reservoir occurring in the watershed. Changes in chemical and isotopic signatures are interpreted in terms of fluctuations of the different components inputs: rainwater, weathering products, anthropogenic addition.Water quality may be influenced by natural inputs (rainwater, weathering processes) and anthropogenic additions (fertilizers, road salts, etc.). Precipitation serves as a major vehicle for dissolved chemical species in addition to the hydrosystem and, in order to constrain rain inputs, a systematic study of rainwaters is carried out over a one year period using an automatic collector. Corrections of rainwater addition using chloride as an atmospheric input reference were computed for selected elements and the Sr/Sr ratio. After such corrections, the geochemical budget of the watershed was determined and the role of anthropogenic additions evaluated through the relationship between strontium isotopes and major and trace element ratios. Thus, 10% of Ca and Na originate in rainwater input, 40 to 80% in fertilizer additions and 15 to 50% in rock weatheringThe cationic denudation rates for this watershed are around 0.3 g s^–1 km² during low water discharge and 0.6 g s^–1 km² in high water stage. This led to a chemical denudation rate of 5.3 mm/1000 years.For solid matter, the normalization of chemical species relative to parent rocks shows the depletion or enrichment in soils and sediments. The use of K and Ca as mobile reference illustrates the weathering state of soils and sediments relative to parent rocks. This weathering state for bed sediments range from 15 to 45% for the K normalization and from 2 to 50% for the Ca normalization. For the soils, the weathering state ranges from 15 to 57% for the K normalization and from 17 to 90% for the Ca normalization.     

Geochemistry of organic-rich river waters in Amazonia: Insights on weathering processes of intertropical cratonic terrain

In this study, eight organic-rich rivers that flow through the Brazilian craton in the southwestern Amazon rainforest are investigated. This investigation is the first of its type in this area and focuses on the effects of lithology, long-term weathering, thick soils, forest cover and hydrological period on the dissolved load compositions in rivers draining cratonic terrain. The major dissolved ion concentrations, alkalinity (TAlk), SiO₂, trace element concentrations, and Sr isotope contents in the water were determined between April 2009 and January 2010. In addition, the isotopic values of oxygen and hydrogen were determined between 2011 and 2013. Overall, the river water is highly dilute and dominated by the major dissolved elements TAlk, SiO₂ and K⁺ and the major dissolved trace elements Al, Fe, Ba, Mn, P, Zn and Sr, which exhibit large temporal and spatial variability and are closely correlated with the silicatic bedrock and hydrology. Additionally, rainwater and recycled water vapor and the size of the basin contribute to the geochemistry of the waters. The total weathering flux estimated from our results is 2–4 t km⁻².yr⁻¹, which is one of the lowest fluxes in the world. The CO₂ consumption rate is approximately 21–61 10³ mol km⁻² yr⁻¹, which is higher than expected given the stability of the felsic to basic igneous and metamorphic to siliciclastic basement rocks and the thick tropical soil cover. Thus, weathering of the cratonic terrain under intertropical humid conditions is still an important consumer of CO₂.     

A geological model of London and the Thames Valley,southeast England

Many geological survey organisations have started delivering digital geological models as part of their role. This article describes the British Geological Survey (BGS) model for London and the Thames Valley in southeast England. The model covers 4800 km² and extends to several hundred metres depth. It includes extensive spreads of Quaternary river terraces and alluvium of the Thames drainage system resting on faulted and folded Palaeogene and Cretaceous bedrock strata. The model extends to the base of the Jurassic sedimentary rocks.     

Karstification in Miocene gypsum: an example from Sivas, Turkey

In this study, karstification developed in the Miocene gypsum which covers a large area around Sivas, Turkey, the relation between regional tectonics and karstification, and hydrogeological features have been investigated. The karstic features in the gypsum have developed conforming to the fault zones and the general strikes of gypsum beds. In the study area, numerous dolines (sinkholes) and ponors (swallow holes) of different sizes are observed. Most of these karstic features are in the different-sized longitudinal depressions (troughs) which conform to the tectonic structures. These karstic features occur NE-SW along bedding planes and about NW-SE and NE-SW along fault zones. At the intersections, high-capacity (yield) karst springs (Göydün and Seyfe springs) are observed. The Göydün and Seyfe springs issue from the karstified gypsum aquifer, with an average discharge of 1.10 m³/s and 0.25 m³/s, respectively. In addition, there are some low-yield (a few l/s) springs in the same drainage area. The surface drainage area of the springs is 64 km², and the precipitation in this area cannot provide the total groundwater discharging from Göydün and Seyfe springs. Water budget calculations indicate that more than 70% of the water discharged by these two springs is provided from the adjacent basins. The Göydün and Seyfe springs are rich in dissolved solids and average electrical conductivities (EC) are about 13?000 μS/cm. The major cations in the waters are Ca and Na; major anions are SO₄ and Cl, and the waters are brackish. Because of these properties, especially in summer and autumn, the springs cause extreme salinization in K?z?l?rmak river.     

Sediment supply from the Betic-Rif orogen to basins through Neogene

We present a quantification of total and partial (divided by time slices) sedimentary volumes in the Neogene basins of the Betic-Rif orogen. These basins include the Alboran Sea, the intramontane basins, the Guadalquivir and Rharb foreland basins and the Atlantic Margin of the Gibraltar Arc. The total volume of Neogene sediments deposited in these basins is ~ 209,000 km³ and is equally distributed between the internal (Alboran Basin and intramontane basins) and the external basins (foreland basins and Atlantic Margin). The largest volumes are recorded by the Alboran Basin (89,600 km³) and the Atlantic Margin (81,600 km³). The Guadalquivir and Rharb basins amount 14,000 km³ and 14,550 km³, respectively whereas the intramontane basins record 9235 km³. Calculated mean sediment accumulation rates for the early-middle Miocene show an outstanding asymmetry between the Alboran basin (0.24 mm/yr) and the foreland basins (0.06-0.07 mm/yr) and the Atlantic Margin (0.03 mm/yr). During the late Miocene, sedimentation rates range between 0.17 and 0.18 mm/yr recorded in the Alboran Basin and 0.04 mm/yr in the intramontane basins. In the Pliocene-Quaternary, the highest sedimentation rates are recorded in the Atlantic Margin reaching 0.22 mm/yr. Sedimentary contribution shows similar values for the inner and outer basins with a generalized increase from late Miocene to present (from 3500 to 6500 km³/My). Interestingly, the Alboran Basin records the maximum sedimentary contribution during the late Miocene (5500 km³/My), whereas the Atlantic Margin does during the Pliocene-Quaternary (6600 km³/My). The spatial and time variability of the sediment supply from the Betic-Rif orogen to basins is closely related to the morphotectonic evolution of the region. The high sedimentation rates obtained in the Alboran Basin during the early-middle Miocene are related to active extensional tectonics, which produced narrow and deep basins in its western domain. The highest sedimentary contribution in this basin, as well as in the foreland and intramontane basins, is recorded during the late Miocene due to the uplift of wide areas of the Betics and Rif chains. The analysis of the sedimentary supply also evidences strong relationships with the post-Tortonian crustal thickening and coeval topographic amplification that occurred in the central Betics and Rif with the concomitant evolution of the drainage network showing the fluvial capture of some internal basins by rivers draining to the Atlantic Ocean (the ancestral Guadalquivir).     

Analysis of the Chesapeake Bay Hypoxia Regime Shift: Insights from Two Simple Mechanistic Models

Recent studies of Chesapeake Bay hypoxia suggest higher susceptibility to hypoxia in years after the 1980s. We used two simple mechanistic models and Bayesian estimation of their parameters and prediction uncertainty to explore the nature of this regime shift. Model estimates show increasing nutrient conversion efficiency since the 1980s, with lower DO concentrations and large hypoxic volumes as a result. In earlier work, we suggested a 35% reduction from the average 1980–1990 total nitrogen load would restore the Bay to hypoxic volumes of the 1950s–1970s. With Bayesian inference, our model indicates that, if the physical and biogeochemical processes prior to the 1980s resume, the 35% reduction would result in hypoxic volume averaging 2.7 km³ in a typical year, below the average hypoxic volume of 1950s–1970s. However, if the post-1980 processes persist the 35% reduction would result in much higher hypoxic volume averaging 6.0 km³. Load reductions recommended in the 2003 agreement will likely meet dissolved oxygen attainment goals if the Bay functions as it did prior to the 1980s; however, it may not reach those goals if current processes prevail.     

西昌盆地白果湾组致密砂岩油气形成关键指标评价与有利区优选

综合钻井、大量实测剖面、样品测试分析和区域地质资料,对西昌盆地白果湾组烃源岩生烃强度、镜质体反射率、砂岩储层物性等关键指标进行了系统评价.西昌盆地上三叠统白果湾组主要油气储层类型为中-粗砂岩,有利层段主要发育在白果湾组一段、三段和四段,砂岩具有中孔低渗、区域分布广、厚度大等特征,ZD-1井揭示砂岩含油气性好.西昌盆地白...     

Solute generation and CO2 consumption during silicate weathering under subtropical,humid climate,northern Okinawa Island,Japan

The chemical characteristics of freshwaters draining the silicate rocks in the northern part of Okinawa Island were studied to understand solute generation processes, and to determine rates of chemical weathering and CO₂ consumption. It was observed that the water chemistry is highly influenced by marine aerosols, contributing more than 60% of total solute. Significant positive correlations observed for chloride versus dissolved silica and chloride versus bicarbonate suggest a strong influence of evapotranspiration on the seasonality of solute concentration. It was also found that chemical weathering has been highly advanced in which the dominant kaolinite minerals are being gibbsitized. Carbonic acid was found to be the major chemical weathering agent, releasing greater than 80% of weathering-derived dissolved cations and silica while the remaining portion was attributed to weathering by sulfuric acid generated via oxidation of pyrite contained in the rocks. The flux of basic cations, weathering-derived silica and CO₂ consumption were relatively high due to favourable climatic condition, topography and high rate of mechanical erosion. Silicate weathering rates for basic cations were estimated to be 6.7–9.7 ton km^− 2 y^− 1. Carbon dioxide consumed by silicate weathering was 334–471 kmol km^− 2 y^− 1 which was slightly higher than that consumed by carbonate weathering. In general, divalent cations (Mg and Ca) and bicarbonate alkalinity derived from carbonate dissolution were higher than those from silicate weathering. As a consequence, the evolution of chemical species in the freshwaters of northern area of Okinawa Island to a large extent could be explained by mixing of two components, characterized by waters with Na⁺ and Cl⁻ as predominant species and waters enriched with Ca²⁺ and HCO₃⁻.