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51.
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Fusarium wilt caused by Fusarium oxysporum Schlechtend.: Fr f. sp. ciceris (Padwick) Matuo & Sato is a devastating disease of chickpea. The current study was conducted to determine the inheritance of the gene(s) for resistance to race 4 of fusarium wilt and to identify linked RAPD markers using an early wilting line, JG-62, as a susceptible parent. Genetic analysis was performed on the F1s, F2s and F3 families from the cross of JG-62 × Surutato-77. The F3 families were inoculated with a spore suspension of the race 4 wilt pathogen and the results were used to infer the genotypes of the parent F2 plants. Results indicated that two independent genes controlled resistance to race 4. Linkage analysis of candidate RAPD marker, CS-27700, and the inferred F2 phenotypic data showed that this marker locus is linked to one of the resistance genes. Allelism indicated that the two resistance sources, Surutato-77 and WR-315, shared common alleles for resistance and the two susceptible genotypes, C-104 and JG-62, carried alleles for susceptibility. The PCR-based marker, CS-27700, was previously reported to be linked to the gene for resistance to race 1 in a different population which suggested that the genes for resistance to races 1 and 4 are in close proximity in the Cicer genome. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   
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Lignin is considered to be a crucial component controlling litter decomposition but its role in the production of dissolved organic matter (DOM) from litter is not well understood. Our main objective therefore was to examine the amounts and properties of DOM produced in decomposing litter, with special emphasis on the role of lignin degradation. We exposed litter of five different tree species (Sycamore maple, Mountain ash, European beech, Norway spruce, Scots pine) in litterbags at the soil surface of two neighbouring sites to degradation under field conditions. Litterbags were sampled eight times during 27 months of exposure in the field. We determined mass loss and characterized the lignin fraction by two different methods (van Soest procedure, acid‐detergent lignin: ADL, CuO oxidation). Litter was irrigated in the laboratory and leachates were analysed for dissolved organic carbon (DOC) and characterized by UV and fluorescence spectroscopy. Litter decomposition followed a two‐stage model characterized by initially rapid and then decreasing degradation with time. In the initial phase of litter decomposition, leached amounts of DOM decreased with time and no effects of lignin degradation were found. The contents of ADL in the litter residues and CuO oxidation products suggest larger degradation and oxidation of lignin in beech, spruce and pine litter than in maple and ash litter. The production of DOM from litter with larger lignin degradation increased in the second phase of decomposition, when mass loss exceeded 10–20%. In contrast, DOM produced from litter showing weak lignin degradation (maple, ash) did not increase further in the second phase of decomposition. In the leachates of litter with large lignin degradation (beech, spruce, pine), UV absorbance and fluorescence spectroscopy indicated a larger increase in the contribution of lignin‐derived compounds to DOM with increasing mass loss than for litter species with relatively stable lignin. We conclude that degradation of lignin is an important control on DOM production during the second phase of litter decomposition.  相似文献   
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The potential for sulfate retention is an important soil feature for buffering of atmospheric acid deposition. We studied the effects of increasing additions of different neutral salts and acids on mobilization and retention of SO4 2- in acid forest soils. Soils containing up to 11 mmol SO4 2- kg-1 were equilibrated with H2O, NaCl, MgCl2, and HCl. Release of SO4 2- was highest with H2O and NaCl additions and lowest when HCl was used. Increasing the ionic strength of the added solutions caused decreasing SO4 2- concentrations in equilibrium solution. Decreasing pH in equilibrium solution was found to be the reason for the decrease in release. Even when the pH was < 4, the SO4 2- release decreased. We assume that this finding resulted from the fact that in the soils studied the SO4 2- sorption was controlled by the high contents of Fe oxides/hydroxides. Experiments with Na2SO4, MgSO4, and H2SO4 demonstrated that the B horizons already containing high amounts of SO4 2- were still able to retain SO4 2-. Sulfate retention increased in the order Na2SO4 < MgSO4 < H2SO4, which corresponds to increasing H+ availability. The higher SO4 2- retention along with MgSO4 compared to Na2SO4 may be caused by higher potential of Mg to mobilize soil acidity compared to Na.  相似文献   
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The protective impact of aggregation on microbial degradation through separation has been described frequently, especially for biotically formed aggregates. However, to date little information exists on the effects of organic‐matter (OM) quantity and OM quality on physical protection, i.e., reduced degradability by microorganisms caused by physical factors. In the present paper, we hypothesize that soil wettability, which is significantly influenced by OM, may act as a key factor for OM stabilization as it controls the microbial accessibility for water, nutrients, and oxygen in three‐phase systems like soil. Based on this hypothesis, the first objective is to evaluate new findings on the organization of organo‐mineral complexes at the nanoscale as one of the processes creating water‐repellent coatings on mineral surfaces. The second objective is to quantify the degree of alteration of coated surfaces with regard to water repellence. We introduce a recently developed trial that combines FTIR spectra with contact‐angle data as the link between chemical composition of OM and the physical wetting behavior of soil particles. In addition to characterizing the wetting properties of OM coatings, we discuss the implications of water‐repellent surfaces for different physical protection mechanisms of OM. For typical minerals, the OM loading on mineral surfaces is patchy, whereas OM forms nanoscaled micro‐aggregates together with metal oxides and hydroxides and with layered clay minerals. Such small aggregates may efficiently stabilize OM against microbial decomposition. However, despite the patchy structure of OM coating, we observed a relation between the chemical composition of OM and wettability. A higher hydrophobicity of the OM appears to stabilize the organic C in soil, either caused by a specific reduced biodegradability of OM or indirectly caused by increased aggregate stability. In partly saturated nonaggregated soil, the specific distribution of the pore water appears to further affect the mineralization of OM as a function of wettability. We conclude that the wettability of OM, quantified by the contact angle, links the chemical structure of OM with a bundle of physical soil properties and that reduced wettability results in the stabilization of OM in soils.  相似文献   
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Collembola and microbial biomass C were investigated in a field experiment with controlled agricultural traffic and crop rotation over a period of 27 months. The wheel-induced compactive efforts were applied according to management practices within the crop rotation of sugar beet, winter wheat, and winter barley. Increasing wheel traffic produced increasing soil compaction, mainly due to a reduction in surface soil porosity. Increasing soil compaction was accompanied by a decrease in microbial biomass C and the density of collembola. The influence of soil compaction on microbial biomass C was smaller than that of the standing crop. However, for collembola, especially euedaphic species, a reduction in pore space appeared to be of more importance than the effects of a standing crop. Within the crop rotation, microbial biomass C and the density of collembola increased in the order sugar beet, winter wheat, and winter barley.  相似文献   
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