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161.
Total arsenic (As) and its compounds were determined in liver, kidney, muscle, and stomach contents of green turtles (Chelonia mydas). Total As concentrations in the muscle were higher than those in the kidney and liver. Arsenobetaine (AB) was the predominant compound in all the three tissues and its levels were positively correlated with total As concentrations. This indicates that AB greatly contributes to As accumulation in green turtles. Higher concentrations of remaining As in the sample after extraction were detected in the liver, implying that lipid-soluble or protein bound As compounds accumulate in the liver of green turtles. Total As levels in tissues showed significant negative correlations with standard carapace length. The size-dependence of As accumulation in green turtles may be related to their feeding habit, shifting from carnivore to herbivore at different growth stages. Concentrations of AB and dimethylarsinic acid (DMA) were low in the stomach contents but high in the tissues, implying bioaccumulation of these arsenicals in green turtles.  相似文献   
162.
Heavy oil contamination is one of the most important environmental issues. Toxicities of polycyclic aromatic hydrocarbons (PAHs), including immune toxicities, are well characterized, however, the immune toxic effects of heavy oil, as a complex mixture of PAHs, have not been investigated. In the present study, we selected Japanese flounder (Paralichthys olivaceus) as a model organism, and observed alteration of immune function by the exposure to heavy oil. To analyze the expression profiles of immune system-related genes, we selected 309 cDNAs from our flounder EST library, and spotted them on a glass slide. Using this cDNA array, alteration of gene expression profiles was analyzed in the kidneys of flounders exposed to heavy oil. Six Japanese flounders (mean body weight: 197 g) were acclimated to laboratory conditions at 19–20 °C. Three fish were exposed to heavy oil C (bunker C) at a concentration of 3.8 g/L for 3 days, and the others were kept in seawater without heavy oil and used as the control. After the exposure period, the fish were transferred into control seawater and maintained for 4 days, and then they were dissected and their kidneys were removed. Total RNA was extracted from the kidney samples to use in gene expression analyses. The microarray detected alteration of immune system-related genes in the kidneys of heavy oil-exposed flounders, including down-regulation of immunoglobulin light chain, CD45, major histocompatibility complex class II antigens and macrophage colony-stimulating factor precursor, and up-regulation of interleukin-8 and lysozyme. These results suggest that pathogen resistance may be weakened in heavy oil-exposed fish, causing a subsequent bacterial infection, and then proinflammatory genes may be induced as a defensive response against the infection. Additionally, we found candidate genes for use as biomarkers of heavy oil exposure, such as N-myc downstream regulated gene 1 and heat shock cognate 71 kDa proteins.  相似文献   
163.
Four seal species (Phoca caspica, Phoca sibirica, Phoca hispida and Phoca largha) and one whale (Orcinus orca) from Russia and Japan were examined to determine the body distribution, bioaccumulation and contamination status of tris(4-chlorophenyl) methane (TCPMe) and tris(4-chlorophenyl) methanol (TCPMOH). Lipid normalized concentrations of TCPMe and TCPMOH were comparable in various organs and tissues, implying that their body distribution is followed to the lipid-dependent accumulation, similar to that for other organochlorines. The highest body burden of these compounds was found in the blubber. Bioaccumulation potential of TCPMe and TCPMOH was high and comparable to PCBs and DDTs. Relatively higher concentrations of TCPMe and TCPMOH were observed in Caspian seal than in other seal species examined. TCPMOH concentration in killer whale was the highest of the marine mammals examined. Another peak detected had similar mass spectrum to TCPMOH, however, at a different retention time, suggesting the presence of an isomer of TCPMOH.  相似文献   
164.
An array of five bottom-tethered moorings with 19 PARFLUX time-series sediment trap at three depths (1 and 2 km below the surface, and 0.7 km above the sea-floor) was deployed in the western Pacific sector of the Southern Ocean, along 170°W. The five stations were selected to sample settling particles in the main hydrological zones of the Southern Ocean. The sampling period spanned 425 days (November 28, 1996–January 23, 1998) and was divided into 13 or 21 synchronized time intervals. A total of 174 sequential samples were recovered and analyzed to estimate fluxes of total mass (TMF), organic carbon, carbonate, biogenic silica, and lithogenic particles. The fluxes of biogenic material were higher than anticipated, challenging the notion that the Southern Ocean is a low-productivity region. Organic carbon fluxes at 1 km depth within the Polar Frontal Zone and the Antarctic Zone were relatively uniform (1.7–2.3 g m−2 yr−1), and about twice the estimated ocean-wide average (ca. 1 g m−2 yr−1). Carbonate fluxes were also high and uniform between the Subantarctic Front and ca. 64°S (11–13 g m−2 yr−1). A large fraction of the carbonate flux in the Antarctic Zone was due to the presence of pteropod shells. Coccoliths were found only to the north of the Polar Front, and calcium carbonate became the dominant phase in the Subantarctic Zone. In contrast, carbonate particles were nearly absent near 64°S. Latitudinal variations in biogenic silica fluxes were substantial. The large opal flux (57 g m−2 yr−1) measured in the Antarctic Zone suggests that opal productivity in this region has been previously underestimated and helps to explain the high sedimentary opal accumulation often found south of the Polar Front. Unlike biogenic material, fluxes of lithogenic particles were among the lowest measured in the open-ocean (0.12–0.05 g m−2 yr−1), reflecting a very low dust input.  相似文献   
165.
Blubber and liver samples were obtained for analysis of wide ranges of contaminants from killer whales (Orcinus orca) which were locked away in drifting sea ice on the coast of Rausu, the Shiretoko Peninsula in Eastern Hokkaido, Japan in February 2005. Among the organohalogen compounds analyzed, DDTs were the predominant contaminants with concentrations ranging from 28 to 220 microg/g on a lipid-weight basis followed by PCBs and other organochlorine pesticides. PBDEs levels were two or three orders of magnitude lower than those of PCBs and DDTs. 2,3,7,8-Tetrachlorodibenzo-p-dioxin toxic equivalents (TEQs) derived by WHO mammal-TEF in killer whales were in the range of 110-440 pgTEQ/g. Mono-ortho coplanar PCBs contributed to 75-98% of total TEQs, indicating coplanar PCBs are significant contaminants for risk assessment in this species. The fact that hepatic residue levels of butyltins (from 13 to 770 ng/g wet weight) were much higher than those of phenyltins may be reflecting extensive use of tributyltin as antifouling paint.  相似文献   
166.
167.
Series of α, β, ω and (ω-1) hydroxy fatty acids (FAOHs) were determined in several freshwater and brackish water lacustrine sediments in Japan. Analytical procedure used was digestion of the solvent-extracted sediment with HF/HCl followed by solvent and saponification extraction of the residue. Abundances of α/β and ω-FAOH determined by this procedure were 2–3 times higher than those obtained by single alkaline saponification and of the same order with those provided by HCl hydrolysis. Major portion of α/β-FAOH was obtained by solvent extraction of the acid-treated sediments, while subsequent alkaline saponification was needed for the majority of ω-FAOH to be recovered. Thus determined FAOHs comprised 33–61% (Av. = 42%) of the “bound” acid constituents in the lacustrine surface sediments. The α/β and ω-FAOH composition was principally the same among the samples examined, except for relative proportions of the iso to anteiso C15 and C17 ß(α)-FAOH, which showed significant variations in the ranges of 0.30–1.1 and 0.46–1.5, respectively. In the holomictic lakes, the ratios together with the same ratios of the “bound” branched monocarboxylic acids tended to decrease with increasing water depth of the lakes, suggesting that the ratios may indicate an extent of the early diagenetic alteration of the bacteria-derived lipids either in water column or in surface sediment.  相似文献   
168.
A granular material consists of an assemblage of particles with contacts newly formed or disappeared, changing the micromechanical structures during macroscopic deformation. These structures are idealized through a strain space multiple mechanism model as a twofold structure consisting of a multitude of virtual two‐dimensional mechanisms, each of which consists of a multitude of virtual simple shear mechanisms of one‐dimensional nature. In particular, a second‐order fabric tensor describes direct macroscopic stress–strain relationship, and a fourth‐order fabric tensor describes incremental relationship. In this framework of modeling, the mechanism of interlocking defined as the energy less component of macroscopic strain provides an appropriate bridge between micromechanical and macroscopic dilative component of dilatancy. Another bridge for contractive component of dilatancy is provided through an obvious hypothesis on micromechanical counterparts being associated with virtual simple shear strain. It is also postulated that the dilatancy along the stress path beyond a line slightly above the phase transformation line is only due to the mechanism of interlocking and increment in dilatancy due to this interlocking eventually vanishing for a large shear strain. These classic postulates form the basis for formulating the dilatancy in the strain space multiple mechanism model. The performance of the proposed model is demonstrated through simulation of undrained behavior of sand under monotonic and cyclic loading. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   
169.
Boninites are widely distributed along the western margin of the Pacific Plate extruded during the incipient stage of the subduction zone development in the early Paleogene period. This paper discusses the genetic relationships of boninite and antecedent protoarc basalt magmas and demonstrates their recycled ancient slab origin based on the T–P conditions and Pb–Hf–Nd–Os isotopic modeling. Primitive melt inclusions in chrome spinel from Ogasawara and Guam islands show severely depleted high‐SiO2, MgO (high‐silica) and less depleted low‐SiO2, MgO (low‐silica and ultralow‐silica) boninitic compositions. The genetic conditions of 1 346 °C at 0.58 GPa and 1 292 °C at 0.69 GPa for the low‐ and ultralow‐silica boninite magmas lie on adiabatic melting paths of depleted mid‐ocean ridge basalt mantle with a potential temperature of 1 430 °C in Ogasawara and of 1 370 °C in Guam, respectively. This is consistent with the model that the low‐ and ultralow‐silica boninites were produced by remelting of the residue of the protoarc basalt during the forearc spreading immediately following the subduction initiation. In contrast, the genetic conditions of 1 428 °C and 0.96 GPa for the high‐silica boninite magma is reconciled with the ascent of more depleted harzburgitic source which pre‐existed below the Izu–Ogasawara–Mariana forearc region before the subduction started. Mixing calculations based on the Pb–Nd–Hf isotopic data for the Mariana protoarc basalt and boninites support the above remelting model for the (ultra)low‐silica boninite and the discrete harzburgite source for the high‐silica boninite. Yb–Os isotopic modeling of the high‐Si boninite source indicates 18–30 wt% melting of the primitive upper mantle at 1.5–1.7 Ga, whereas the source mantle of the protoarc basalt, the residue of which became the source of the (ultra)low‐Si boninite, experienced only 3.5–4.0 wt% melt depletion at 3.6–3.1 Ga, much earlier than the average depleted mid‐ocean ridge basalt mantle with similar degrees of melt depletion at 2.6–2.2 Ga.  相似文献   
170.
In order to understand organotin accumulation in marine mammals, the present study determined the concentrations of butyltins (BTs) in various tissues and organs and described their distribution patterns relative to sex, age and geographical factors. Both cetaceans and pinnipeds showed higher BTs concentrations in the liver amongst various tissues and organs. In addition, noticeably high concentrations were found in the hair of pinnipeds, indicating possible excretion of BTs through shedding. BTs composition in mammals and their prey organisms suggested that pinnipeds have a stronger capacity to degrade BTs as compared to cetaceans. No age trends of BTs concentrations were observed in pinnipeds, while cetaceans showed increasing levels in immature growth stages. Comparing butyltin concentrations in various marine mammals, cetaceans retained higher butyltin concentrations than pinnipeds. These specific accumulation patterns found in marine mammals are probably attributable to the lower breakdown capacity of BTs in cetaceans and the significant excretion of BTs through shedding in pinnipeds. Unlike organochlorines, comparable residue levels of butyltins were found in male and female marine mammals. Such a trend suggests that butyltins are less transferable through gestation and lactation from mother to fetus/pup. On a global perspective, residue levels were found to be prominent in the coastal waters of developed nations. The present contamination by BTs may pose a considerable toxic threat to some coastal species of cetaceans. A relatively high percentage of BTs in total tin was found in the liver of cetaceans. This finding suggests that the hepatic tin in cetaceans exists predominantly in organic forms such as butyltin compounds, implying further that tin residues in marine mammals mostly reflects input from anthropogenic sources.  相似文献   
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