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151.
Fracture toughness of horns and a reinterpretation of the horning behaviour of bovids 总被引:1,自引:0,他引:1
The keratinous horns of bovids are used in intraspecific combat to gain access to females in oestrus. Horn sheath keratin is a composite material consisting of stiff protein fibres and a pliant protein matrix. Unlike antlers, horns are permanent structures which are likely to accumulate damage during fighting. Therefore, horn sheath keratin should be resistant to fracture (tough) and insensitive to surface defects (scratches and cracks) which may weaken horns by acting as stress concentrators.
The effect of water on the toughness and notch-sensitivity of horn sheath keratin was investigated in three-point bending and tensile tests. Several measures of toughness were made on dry (0% water content), fresh (20%) and wet (40%) horn keratin, including total work of fracture, Gurney & Hunt work of fracture, critical strain energy release rate and critical stress intensity factor.
The mean total work of fracture of fresh horn is about 40 kJ/m2 which is relatively much greater than most biological and synthetic materials. Most of the work of fracture is due to plastic yielding of the matrix (50–75%); the rest is due to crack-tip specific fracture mechanisms such as fibre pull-out and Cook Gordon crack-stopping. Dehydration reduces the total work of fracture of horn keratin by preventing the yielding of the matrix.
The strength of fresh and wet horn is insensitive to notches, but dry horn is very notch-sensitive. Therefore, bovids must avoid dehydration of their horns due to the desiccating effect of the environment. The 'horning' behaviour of bovids may be a maintenance activity which ensures that the horn sheath is adequately hydrated to remain tough and notch-insensitive. 相似文献
The effect of water on the toughness and notch-sensitivity of horn sheath keratin was investigated in three-point bending and tensile tests. Several measures of toughness were made on dry (0% water content), fresh (20%) and wet (40%) horn keratin, including total work of fracture, Gurney & Hunt work of fracture, critical strain energy release rate and critical stress intensity factor.
The mean total work of fracture of fresh horn is about 40 kJ/m
The strength of fresh and wet horn is insensitive to notches, but dry horn is very notch-sensitive. Therefore, bovids must avoid dehydration of their horns due to the desiccating effect of the environment. The 'horning' behaviour of bovids may be a maintenance activity which ensures that the horn sheath is adequately hydrated to remain tough and notch-insensitive. 相似文献
152.
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154.
广西北部罗汉果根结线虫病研究 总被引:7,自引:0,他引:7
罗汉果根结线虫是罗汉果的一个重要病害。在室内盆栽接种条件下,该线虫年发生6代。本文叙述了线虫的生物学及其寄主植物。防治试验结果表明。穴施灭克磷等是有效的。土壤翻晒也能消灭大部分土中线虫,病薯用热处理也有很好的效果。 相似文献
155.
本文比较了中药灵香草Lysimachia foenum-graecum Hance及其混淆品种垂花香草Lysimaehia nutantiflora Chen et C.M.Hu的植物形态、药材性状以及茎、叶组织显微特征。指出垂花香草无灵香草特有的芳香。也无药用记载。应仔细区别,不宜混用。 相似文献
156.
9-β-
-Arabinofuranosyl-2-fluoroadenine (F-ara-A) and 9-β-
-arabinofuranosyladenine (ara-A) are purine nucleoside analogues which are incorporated into nucleic acids. This study demonstrates the mutagenic properties of F-ara-A and ara-A and provides evidence for mechanisms by which the arabinosyl nucleosides induce mutation. At the drug dosages that evoked exponential cell killing, F-ara-A and ara-A caused a significant increase in the number of 6-thioguanine-resistant mutants in Chinese hamster ovary cells. Southern analyses showed that 15 of 16 drug-induced mutants had lost all or part of the HPRT gene, whereas no loss of the gene was found in 4 spontaneous mutants. We conclude that both F-ara-A and ara-A induced mutation predominantly by causing deletion of genetic method. The remarkable frequency of gene deletion among these drug-induced mutations is discussed with respect to possible mechanisms of action of arabinosyl nucleosides in mutational studies. 相似文献
157.
Maintenance of low cl concentrations in mesophyll cells of leaf blades of barley seedlings exposed to salt stress 下载免费PDF全文
The concentrations of vacuolar Na+ and Cl− in the epidermal and mesophyll cells of the leaf blade and sheath of Hordeum vulgare seedlings (cv California Mariout and Clipper) were measured by means of quantitative electron probe x-ray microanalysis. A preferential accumulation of Cl− in vacuoles of epidermal cells in both blade and sheath and a low level in mesophyll cells of the blade were evident in plants grown in full strength Johnson solution. The concentration of Cl− in the mesophyll cells of the blade remained at a low level after exposure to 50 or 100 millimolar NaCl for 1 day or to 50 millimolar for 4 days, while at the same time the concentration of Cl− in the epidermis and mesophyll of the sheath showed a dramatic increase. Clipper generally contained more Cl− in the mesophyll cells of the blade than California Mariout. A greater accumulation of Na+ in the mesophyll of the sheath relative to that of the blade was only apparent after treatment with 100 millimolar NaCl for 1 day or 50 millimolar for 4 days. These results confirm the suggestion that sheath tissue is capable of accumulating excess Cl− (and to a lesser extent Na+) and suggest that the site of regulation of Cl− concentration in the barley leaf is located in the mesophyll cells of the blade. 相似文献
158.
Lysophosphatidate acyltransferase activities in the microsomes from palm endosperm, maize scutellum, and rapeseed cotyledon of maturing seeds 总被引:8,自引:5,他引:3
Lysophosphatidate (LPA) acyltransferase (EC 2.3.1.51) in the microsomes from palm endosperm (Syagrus cocoides Martius), maize scutellum (Zea mays L.), and rapeseed cotyledon (Brassica napus L.) of maturing seeds were studied for their specificities toward the acyl moiety of the substrates lysophosphatidate and acyl coenzyme A (CoA). The LPA acceptor greatly influenced the acyl CoA specificity of the enzyme and vice versa. With 1-oleoyl-lysophosphatidate (LPA-18:1), the palm enzyme was equally active on oleoyl CoA and lauroyl CoA, whereas the maize and rapeseed enzymes were more active on oleoyl CoA than on lauroyl CoA. With 1-lauroyl-lysophosphatidate (LPA-12), which generated less activity than LPA-18:1, the palm enzyme was three times more active on lauroyl CoA than on oleoyl CoA. LPA-12 was an inactive substrate for the maize and rapeseed enzymes. The selectivity of the enzymes was also studied using a mixture of LPA-18:1 and LPA-12, as well as lauroyl CoA and oleoyl CoA. Under this selectivity condition and compared to the specificity condition, the enzymes from all the three seeds exerted stronger preference for oleoyl moiety in either the LPA or acyl CoA, and again, only the palm enzyme could act on LPA-12. Similar studies, although in lesser detail, showed that the enzymes from soybean and castor bean were similar to the maize and rapeseed enzymes in having little activity on substrates containing lauroyl moiety. The results demonstrate the importance of the acyl group in the sn-1 position of LPA in determining the acyl preference in the sn-2 position in phosphatidate synthesis. The palm enzyme appears to be the only one capable of synthesizing phosphatidates containing high amounts of lauric moieties. 相似文献
159.
Comparative biochemical and immunological studies of the glycine betaine synthesis pathway in diverse families of dicotyledons 总被引:10,自引:0,他引:10
Elizabeth A. Weretilnyk Sebastian Bednarek Kent F. McCue David Rhodes Andrew D. Hanson 《Planta》1989,178(3):342-352
Members of the Chenopodiaceae can accumulate high levels (>100 mol·(g DW)-1) of glycine betaine (betaine) in leaves when salinized. Chenopodiaceae synthesize betaine by a two-step oxidation of choline (cholinebetaine aldehyde betaine), with the second step catalyzed by betaine aldehyde dehydrogenase (BADH, EC 1.2.1.8). High betaine levels have also been reported in leaves of species from several distantly-related families of dicotyledons, raising the question of whether the same betaine-synthesis pathway is used in all cases.Fast atom bombardment mass spectrometry showed that betaine levels of >100 mol·(g DW)-1 are present in Lycium ferocissimum Miers (Solanaceae), Helianthus annuus L. (Asteraceae), Convolvulus arvensis L. (Convolvulaceae), and Amaranthus caudatus L. (Amaranthaceae), that salinization promotes betaine accumulation in these plants, and that they can convert supplied choline to betaine aldehyde and betaine. Nicotiana tabacum L. and Lycopersicon lycopersicum (L.) Karst. ex Farw. (Solanaceae), Lactuca sativa L. (Asteraceae) and Ipomoea purpurea L. (Convolvulaceae) also contained betaine, but at a low level (0.1–0.5 mol·(g DW)-1. Betaine aldehyde dehydrogenase activity assays, immunotitration and immunoblotting demonstrated that the betaine-accumulating species have a BADH enzyme recognized by antibodies raised against BADH from Spinacia oleracea L. (Chenopodiaceae), and that the Mr of the BADH monomer is in all cases close to 63 000. These data indicate that the cholinebetaine aldehydebetaine pathway may have evolved by vertical descent from an early angiosperm ancestor, and might be widespread (albeit not always strongly expressed) among flowering plants. Consistent with these suggestions, Magnolia x soulangiana was found to have a low level of betaine, and to express a protein of Mr 63 000 which cross-reacted with antibodies to BADH from Spinacia oleracea.Abbreviations BADH
Betaine aldehyde dehydrogenase
- DCIMS
desorption chemical ionization mass spectrometry
- FABMS
fast atom bombardment mass spectrometry
- Mr
relative molecular mass
- PAGE
polyacrylamide gel electrophoresis
- SDS
sodium dodecyl sulfate
- TLC
thin-layer chromatography 相似文献
160.
Andrew A. Lackner Morten Schidt Gary C. Armitage Peter F. Moore Robert J. Munn Preston A. Marx Murray B. Gardner Linda J. Lowenstine 《Journal of medical primatology》1989,18(3-4):195-207
Simian acquired immune deficiency syndrome (SAIDS) caused by the type D retrovirus SRV-1 results in opportunistic infections and a spectrum of oral lesions similar to those seen in humans with AIDS. To better understand the pathogenesis of these oral lesions we have retrospectively examined the oral mucosa from ten rhesus monkeys that died with SAIDS and prospectively examined the oral mucosa of ten additional animals inoculated with SRV-1 to determine at what time, and in what cells SRV-1 infection of the oral mucosa occurs. Using single and double label immunohistologic techniques, and electron microscopy we detected SRV-1 in clusters of oral epithelial cells and rare Langerhans cells as early as 1 month postinoculation. 相似文献