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161.
Jeong CK Lee HY Kim SB Choi SJ Kim JH Kim K Han SS Lee HS 《Pest management science》2001,57(5):427-431
To investigate the hepatic metabolism of the new insecticide flupyrazofos [O,O-diethyl O-(1-phenyl-3-trifluoromethylpyrazol-5-yl) phosphorothioate], isolated rat liver was perfused with flupyrazofos under single-pass conditions. In outflow perfusate and bile, 1-phenyl-3-trifluoromethyl-5-hydroxyprazole (PTMHP), PTMHP-sulfate and PTMHP-glucuronide conjugates were identified as the metabolites of flupyrazofos. However, O,O-diethyl O-(1-phenyl-3-trifluoromethylpyrazol-5-yl) phosphate (flupyrazofos oxon) was not detected. A HPLC method with UV detection was used to investigate the hepatic disposition of flupyrazofos and its metabolite PTMHP. The concentrations of flupyrazofos, PTMHP and PTMHP conjugates in outflow perfusate reached steady-state levels within 20 min after commencing perfusion of 7.3 microM flupyrazofos. At steady state, the mean extraction ratio of flupyrazofos was 0.93 (+/- 0.01) and clearance was 26.1 (+/- 0.2) ml min-1 which nearly approached perfusate flow rate (28 ml min-1). PTMHP accounted for 55.7 (+/- 5.8)% of eliminated flupyrazofos and was recovered as unchanged PTMHP, PTMHP-sulfate and PTMHP-glucuronide in the bile as well as the outflow perfusate. 相似文献
162.
近年来,从华东地区患腹泻仔猪中分离到一些表达K88菌毛的大肠杆菌,这些菌株只与K88a因子单抗反应,而不与b、c、d因子单抗反应。通过K88常规血清交叉吸收试验、SDS-PAGE、Western印迹,表明这些菌株不仅与K88ac参考菌株C83907制备的c因子血清反应,而且与以分离株SEC586制备且经K88ab、K88ac、K88ad参考菌株吸收后的血清也反应。对分离株SEC586、SEC464的K88主要亚单位结构基因faeG的克隆、测序,发现该基因由846对核苷酸组成,编码菌毛主要亚单位的262个氨基酸及21个氨基酸的信号肽,比国外报道的K88ac FaeG亚单位(263个氨基酸)少了1个氨基酸,比K88ab、K88ad(265个氨基酸)少了3个氨基酸。SEC586、SEC464菌株的FaeG亚单位氨基酸序列的同源性为97.7%,它们与K88ac的同源性为94.7%和96.2%;与K88ab的同源性为90.1%和91.2%;与K88ad的同源性为87.0%和88,6%。结果表明,新分离的K88ac大肠杆菌黏附素主要亚单位已发生了部分变异。 相似文献
163.
164.
Recent research shows that land use history is an important determinant of current ecosystem function. In the United States,
characterization of land use change following European settlement requires reconstruction of the original property mosaic.
However, this task is difficult in unsystematically surveyed areas east of the Appalachian Mountains. The Gwynns Falls watershed
(Baltimore, MD) was originally surveyed in the 1600-1700s under a system of warrants and patents (commonly known as ‘metes
and bounds’). A method for the reconstruction and mapping of warrant and patent properties is presented and used to map the
original property mosaic in the Gwynns Falls watershed. Using the mapped mosaic, the persistence of properties and property
lines in the current Gwynns Falls landscape is considered. The results of this research indicate that as in agricultural areas,
the original property lines in the Gwynns Falls watershed are persistent. At the same time, the results suggest that the property
mosaic in heavily urbanized/suburbanized areas is generally ‘reset.’ Further, trends in surveying technique, parcel size,
and settlement patterns cause property line density and property shape complexity to increase in the less urbanized upper
watershed. The persistence of original patterns may be damping expression of heterogeneity gradients in this urban landscape.
This spatial pattern of complexity in the original mosaic is directly opposite of hypothesized patterns of landscape heterogeneity
arising from urbanization. The technique reported here and the resulting observations are important for landscape pattern
studies in areas settled under unsystematic survey systems, especially the heavily urbanized areas of the eastern United States.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
165.
166.
本文依据小沙子湖湖积剖面的年代学、沉积学、地球化学与矿物学分析,探讨了湖积剖面的建造与库木库里沙漠发育的关系,认为,在该湖积剖面建造中,沙漠尚未出现,库木库里沙漠的形成在距今6000年前以后。 相似文献
167.
博斯腾湖生态环境的演变 总被引:5,自引:3,他引:5
本文叙述了近30年来博斯腾湖水位、容积、水质、芦苇资源、渔业资源、水生生物等的变化,并对博斯腾湖未来的环境演变作了预测。 相似文献
168.
Infection of groundnut leaves with the early leaf spot pathogen Cercospora arachidicola leads to a marked increase in extracellular 1,3-β-glucanase activity, limited to the infected tissue. Three isoforms of low molecular weight and extreme pI values, typical of pathogenesis-related proteins, were induced. These β-glucanases, when acting together, were capable of degrading the pathogen cell wall in vitro. Glucanases from homogenates of infected leaf tissue were partially purified by ion-exchange chromatography to give enzymes with molecular weights of 35, 32 and 20 kDa and pI values of 3·8, 3·6 and > 9, respectively. They were electrophoretically identical to the β-glucanases found in the intercellular washing fluid. Treatment of groundnut plants with 200 μM mercuric chloride induced the accumulation of identical extracellular β-glucanases. During the course of the infection an increase in peroxidase activity was also observed, but chitinase activity remained more or less constant. 相似文献
169.
C. Caprari C. Bergmann Q. Migheli G. Salvi P. Albersheim A. Darvill F. Cervone G. De Lorenzo 《Physiological and Molecular Plant Pathology》1993,43(6)
Extracellular endopolygalacturonase, purified from the pathogenic fungus Fusarium moniliforme, consists of four molecular forms (38, 41·5, 45, and 48·5 kDa, respectively. Three forms (38, 41·5, and 45 kDa) were purified to homogencity by FPLC on a Mono S column followed by electroelution after SDS-PAGE. The N-terminal amino acid sequences of each of the three forms, and of a mixture containing all four forms were shown to be identical to that predicted from the nucleotide sequence of the endopolygalacturonase gene previously cloned from F. moniliforme. Enzymatic deglycosylation experiments revealed the presence of N-linked, high mannose oligosaccharide side-chains on all four forms of endo polygalacturonase. Hydrogen fluoride catalysed chemical deglycosylation of the polygalacturonase mixture yielded a single polypeptide with an apparent molecular mass of 36·2 kDa. Southern blot analysis, carried out at high stringency with an endopolygalacturonase-specific probe on genomic DNA digested with three different restriction enzymes, showed a single hybridizing restriction fragment in all three digests. A single 2·0 Mb chromosome hybridized with the endo polygalacturonase-specific probe, as shown by Southern blot analysis of F. moniliforme chromosomes separated by CHEF electrophoresis. Northern blot analysis revealed only one mRNA species 1350 nt encoding endo polygalacturonase. These data indicate that a single gene encodes the endopolygalacturonases of F. moniliforme. 相似文献
170.
OBJECTIVE: To quantify stripping in traditional dipping operations and to revise dipping methods, based on prediction of stripping so that a more stable concentration of pesticide in the dipwash is achieved. DESIGN AND METHODS: Plunge and shower dips were operated sequentially according to traditional and revised dipping instructions. Dips were operated by continuous and intermittent replenishment. Samples of mixed dipwash were collected periodically and assayed for pesticide (diazinon) concentration. RESULTS: Diagrammatic representations of pesticide concentration versus number of sheep dipped indicated traditional dipping leads to wide variations in the concentration of pesticide in dipwash during dipping. Intermittent replenishment led to a 'saw-tooth' pattern in the pesticide concentration. Traditional continuous replenishment (using the starting concentration of pesticide) indicated both the rate and extent of stripping was higher in shower dipping. If sufficient sheep were dipped, equilibrium was reached between the rate of pesticide replenishment and removal. An alternative method of dip operation by continuous replenishment, using a low starting concentration of pesticide and a replenishment concentration high enough to offset the pesticide loss through stripping resulted in a more stable concentration of pesticide in the dip. CONCLUSION: Revision of dipping instructions can lead to exposure of sheep to stable concentrations of stripping pesticide during dipping. 相似文献