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101.
The objectives of this study were to investigate the seasonality, abundance, sources and bioreactivity of organic matter in the water column of the western Arctic Ocean. The concentrations of particulate and dissolved amino acids and amino sugars, as well as bulk properties of particulate and dissolved organic matter (DOM), were measured in shelf, slope and basin waters collected during the spring and summer of 2002. Particulate organic matter concentrations in shelf waters increased by a factor of 10 between spring and summer. Dissolved organic carbon (DOC) and nitrogen (DON) concentrations exhibited only minor seasonal variations, whereas dissolved amino acid concentrations doubled between spring and summer, and dissolved amino sugars increased by 31% in shelf waters of the Chukchi and Beaufort Seas. Concentrations of DOC did not exhibit a significant seasonal change in surface waters of the Canada Basin, but dissolved amino acid concentrations increased by 45% between spring and summer. No significant seasonal differences were detected in the concentration or composition of DOM in waters below 100 m in depth. Concentrations of particulate and dissolved amino acids and amino sugars were strongly correlated with chlorophyll-a, indicating a plankton source of freshly produced organic matter. The amino acid and amino sugar compositions of freshly produced DOM indicated that a large portion of this material is bioavailable. While freshly produced DOM was found to be relatively bioreactive, preformed DOM in the Arctic appears to be less bioreactive but similar in degradation state to average DOM in the Atlantic and Pacific. These data demonstrate substantial summer production of POM and DOM on the Chukchi and Beaufort shelves that is available for utilization in shelf waters and export to the Canada Basin.  相似文献   
102.
Shelf break systems are highly dynamic environments. However little is known about the influence that benthic interactions and water mass mixing may have on vertical distributions of iron in these systems. Dissolved Fe (< 0.4 μm) concentrations were measured in samples from nine vertical profiles across the upper slope (150–2950 m water depth) at the Atlantic Ocean–Celtic Sea shelf break. Dissolved iron concentrations varied between less than 0.2 and 5.4 nM, and the resulting detailed section showed evidence of a range of processes influencing the Fe distributions. The near sea floor data were interpreted in terms of release and removal processes. The concentrations of dissolved Fe present in near seabed waters were consistent with release of Fe from in situ remineralisation of particulate organic matter at two upper slope stations, and possibly release from pore water upon resuspension on shelf. Lateral transport of dissolved iron was evident from elevated Fe concentrations in an intermediate nepheloid layer and its advection along isopycnals. Surface waters at the shelf break also showed evidence of vertical mixing of deeper iron-rich waters. These waters contained macronutrients that sustained primary productivity in these otherwise nutrient-depleted surface waters. The data also suggest some degree of stabilisation of relatively high concentrations of iron, presumably through ligand association or as colloids. This study supports the view that lateral export of dissolved iron to the interior of the ocean from shelf and coastal zones and may have important implications for the global budget of oceanic iron.  相似文献   
103.
Large volume water samples were taken at Porte du Scex and Bouveret at the mouth of the Upper Rhone River as it enters Lake Geneva. Samples were taken every two weeks during 1982 up until August 1983. Water samples were analyzed for total phosphorus (TP), and soluble reactive phosphorus (SRP) and were centrifuged in the field using a continuous flow centrifuge to recover the suspended solids following sieving at 63 µm. The < 63 µm solids were analyzed for total particulate phosphorus (TPP), organic phosphorus (OP), apatite phosphorus (AP) and non apatite inorganic phosphorus (NAIP). The > 63 µm were similarly analyzed and the weight of total solids in both size fractions recorded. Results were compared throughout the period of record to the hydrograph situated at Porte de Scex. The annual cycle of the Rhone can be divided into a low turbidity, low flow winter period (SED 1) and high flow, high turbidity summer season designated (SED 2). Turbidity is well related to discharge. The > 63 µm sediment is mobilized at 200 m3 s–1 and thereafter increases in concert with, though at a faster rate than, the < 63 µm fraction. The coarse fraction contains significant quantities of phosphorus and in 1982 accounted for 26% of the TPP loading. OP and NAIP are higher in SED 1 than in SED 2 though AP remains constant throughout the year. OP is believed to be driven primarily from point sources whereas NAIP, in addition to point sources, has secondary sources in spring and summer due to sheet erosion from the agricultural soils of the valley. Loadings of phosphorus were calculated by four methods which showed internal consistency though they were higher than previous estimates. Bioavailable phosphorus (BAP) was estimated to account for some 20% of the total phosphorus loading of some 1500 tonnes; BAP is here taken to be the sum of SRP and NAIP and is that portion of the phosphorus load believed to be available to generate phytoplankton growth.  相似文献   
104.
Ambient particulate sulfate measurements have been intermittently performed at a rural site in Israel over a period of more than two years. Concurrent measurements of ambient pollutants (SO2, NO–NOx, and O3), as well as meteorological data, were also carried out. The daily data included four particulate sulfate samples representing four successive 6 h accumulating periods. The measured concentrations of sulfate ions ranged from a low 2 g m-3 observed during the winter season to a high of >50 g m-3 obtained during the summer. Little correlation was obtained between the sulfate concentration and either O3 or SO2, although sulfate and O3 showed a similar diurnal and annual trend. Based on the data distribution and on a photochemical model, it was concluded that a large part of the particulate sulfate observed at the eastern coast of the Mediterranean Sea must be related to long-range transport from distant sources.  相似文献   
105.
106.
《国际泥沙研究》2020,35(5):444-454
Turbidity is used as a surrogate for suspended sediment concentration (SSC), and as a regulatory tool for indicating land use disturbance and environmental protection. Turbidity relates linearly to suspended material, however, can show non-linear responses to particulate organic matter (POM), concomitant with changes in particle size distribution (PSD). In the paper the influence of ultra-fine particulate matter (UFPM) on specific turbidity and its association with POM in suspended sediment are shown for alpine rivers in the Southern Alps of New Zealand. The approach was two-fold: a field-based investigation of the relations between SSC, POM, and turbidity sampled during event flow; and experimental work on hydrodynamic particle size effects on SSC, POM, PSD, and turbidity. Specific turbidity changes over event flow and are sensitive to increasing proportional amounts of sand, UFPM, and POM in suspension. Furthermore, the UFPM is the size fraction (<6 μm) where POM increases. The implications of the current study are that the slopes of turbidity-SSC relations are undesirable in locations that may be dominated by cyclic release of POM or distinct pulses of fine-grained material. At locations where the turbidity-SSC slopes approximate 2, the POM proportion is usually <10% of the total suspended load. However, when turbidity-SSC slopes are <1 this is likely caused by high amounts of side-scatter from UFPM concomitant with higher proportions of POM. Thus, the use of turbidity as a proxy for determining SSC may have serious consequences for the measurement of representative suspended sediment data, particularly in locations where POM may be a significant contributor to overall suspended load.  相似文献   
107.
The present work aimed at studying the origin of particulate organic matter in Guanabara Bay and in some rivers of the Guanabara basin by using elemental composition, isotopic ratios (δ13C and δ15N) and molecular markers (sterols) in samples collected in two periods (winter and summer). Elemental and isotopic compositions were determined by dry combustion and mass spectrometry, respectively, while sterols were investigated by GC–FID and GC–MS. Higher sterol concentrations were present in the north-western part of the bay in winter (5.10–23.5 μg L–1). The high abundance of algal sterols (26–57% of total sterols), the elemental composition (C/N=6–8) and the isotopic signatures (δ13C=−21.3‰ to −15.1‰ and δ15N=+7.3‰ to +11.1‰) suggested the predominance of autochthonous organic matter, as expected for an eutrophic bay, although seasonal variation in phytoplankton activity was observed. Coprostanol concentration (fecal sterol) was at least one order of magnitude higher in the particulate material from fluvial samples (4.65–55.98 μg L–1) than in the bay waters (<0.33 μg L–1). This could be ascribed to a combination of factors including efficient particle removal to sediments in the estuarine transition zone, dilution with bay water and bacterial degradation during particle transport in the water column.  相似文献   
108.
Variations in phosphorus (P) speciation were compared for two types of pilot scale wetlands: a blast furnace slag‐based constructed wetland (SCW), and a gravel‐based constructed wetland (GCW). Synthetic secondary effluent was used as the influent of the wetlands, which contained 1.1 mg/L P with more than 95% present as soluble reactive P (SRP). However, dissolved organic phosphorus (DOP) and particulate phosphorus (PP) emerged in the water along both wetlands. The levels of these three P species varied between the two wetlands. The GCW was more efficient than SCW at removing SRP, but showed a different trend. SRP decreased continually in the SCW, while it increased at the end of the GCW due to biological release. DOP was constant in SCW and GCW, and the mean value was 0.023 and 0.020 mg/L, respectively. The mean values of PP in the GCW ranged between 0.093 and 0.216 mg/L; much higher than the 0.05 ± 0.01 mg/L measured in the SCW. Sequential extractions showed that iron bound PP (Fe‐PP), aluminum bound PP (Al‐PP), organic PP (Org‐PP) and occluded PP (Oc‐PP) were the major components of PP at most locations of the GCW. Fe‐PP decreased from 0.53 to 0.14 mg/L in the upper layer, with DO steady at about 0.15 mg/L at the bottom. Oc‐PP increased at each layer. Al‐PP and Org‐PP were steady in the first 140 cm of the GCW, but decreased sharply at the end. Considering the variation of SRP, DOP and PP fractionations, it can be seen that PP exchanged intensively with SRP in the GCW, and might act as an intermediate in the P removal process. Part of the SRP was first transformed into PP, and then absorbed by substrates or deposited in the wetlands. P removal was mainly via Ca precipitation in the SCW, but involved multiple mechanisms in the GCW, such as precipitation, adsorption and biological interactions. The multiple P removal mechanisms might be the reason for the low proportion of SRP, and the better P removal efficiency observed in the GCW.  相似文献   
109.
The Odra river flood of 1997 was a rare hydrological as well as an interesting sedimentological event. At Hohenwutzen (Lower Odra River) we observed the suspended particulate matter transport and the temporal development of water and solidsπ pollution with heavy metals and As. While the suspended particulate matter concentration decreased the trace element concentrations increased during the flood by fractionation of particles and solution processes. Because of a successive flooding of differently contaminated sedimentary sources and polluted regions the contents of heavy metals developed irregularly. Their median particulate concentrations did not exceed the values of older samples taken under mean discharge conditions between 1989 and 1995. The dissolved amounts correspond to those of the Elbe river in 1990. During the flood the dissolved share of all analyzed total element contents increased. The total loads increased 4fold (Cr) to 17fold (Cd).  相似文献   
110.
In order to recognize lateral and seasonal variations in composition of suspended particulate matter (SPM) in the Odra Estuary, samples were taken at four sites in the period July 1996 - July 1997 monthly if possible. The contents of the elements Si, Ti, Al, Fe, Mn, Mg, Ca, Na, K, P, C, S as well as Ba, Cr, Sr, V, Zn, Cu, Zr, and of the minerals illite, chlorite, smectite, kaolinite and others have been determined. The decreasing influence of the river Odra towards the open sea could be realized with the help of the contents of the minerals quartz, smectite, and of the elements Ba, Cr, K, P, Si and other. 60% of the seasonal and lateral variations can be explained by changing contents of total carbon (TC), total organic carbon (TOC), Al, Fe, Si, Ti, P, Mn, and Ba. They are mainly caused by differences in the production of organic matter, resuspension, riverine input, and redox-sensitive processes.  相似文献   
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