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101.
Carrie J. Ewing Constance E. Hausman John Pogacnik Jason Slot Pierluigi Bonello 《Forest Pathology》2019,49(2)
Beech leaf disease (BLD) is a currently undiagnosed and seemingly lethal disease that was discovered in 2012 on American beech trees (Fagus grandifolia) in north‐east Ohio in the United States. Since its discovery, BLD has spread rapidly and can now be found in forests in 10 counties in Ohio, eight counties in Pennsylvania and five counties in Ontario, Canada. The initial symptoms of the disease appear as a dark green, interveinal banding pattern on the lower canopy foliage. These initial symptoms typically occur in the shrub or sampling layer of a beech stand. The later symptoms result in solidly darkened leaves that are shrunken and crinkled. The symptoms appear to progress through the buds as the affected buds are eventually aborted and no new leaves are produced. We fear this disease has the potential to drastically alter the Eastern deciduous forests of the United States on its own and through potential compounding disease effects. In addition, BLD poses a threat to global forests as symptoms of the disease were detected on European (F. sylvatica) and Oriental (F. orientalis) beech species in nurseries in north‐eastern Ohio. Due to its rapid spread and variability in environmental conditions where it has been detected, it seems unlikely that BLD is an abiotic disorder. Thus, intense efforts are underway to determine the causal agent of BLD. Relevant stakeholders are advised to be alert for BLD symptoms in beech forests in the Northern Hemisphere, and substantial resources should be invested in understanding this emerging forest disease. 相似文献
102.
Spring-flushing, over-wintered buds of Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) produce new buds that may follow various developmental pathways. These include second flushing in early summer or dormancy before flushing during the following spring. Second flushing usually entails an initial release of apical dominance as some of the current-season upper lateral buds grow out. Four hypotheses concerning control of current bud outgrowth in spring-flushing shoots were tested: (1) apically derived auxin in the terminal spring-flushing shoot suppresses lateral bud outgrowth (second flushing); (2) cytokinin (0.5 mM benzyladenine) spray treatments given midway through the spring flush period induce bud formation; (3) similar cytokinin spray treatments induce the outgrowth of existing current lateral buds; and (4) defoliation of the terminal spring-flushing shoot promotes second flushing. Hypothesis 1 was supported by data demonstrating that decapitation-released apical dominance was completely restored by treatment with exogenous auxin (22.5 or 45 mM naphthalene acetic acid) (Thimann-Skoog test). Hypothesis 2 was marginally supported by a small, but significant increase in bud number; and Hypothesis 3 was strongly supported by a large increase in the number of outgrowing buds following cytokinin applications. Defoliation produced similar results to cytokinin application. We conclude that auxin and cytokinin play important repressive and promotive roles, respectively, in the control of second flushing in the terminal spring-flushing Douglas-fir shoot. 相似文献
103.
Crude methanol and water extracts of 36 plants, employed in the treatment of diseases of probable bacterial etiology by the Venda people, were screened for antibacterial activity. Combretum molle, Peltophorum africanum, Piper capense, Terminalia sericea and Zanthoxylum davyi were the most active and presented MIC values < or =1.00 mg/ml. 相似文献
104.
Forest responses to climate change in the northwestern United States: Ecophysiological foundations for adaptive management 总被引:1,自引:0,他引:1
Daniel J. Chmura Paul D. Anderson Glenn T. Howe Constance A. Harrington Jessica E. Halofsky David L. Peterson David C. Shaw J. Brad St.Clair 《Forest Ecology and Management》2011,261(7):1121-1142
Climate change resulting from increased concentrations of atmospheric carbon dioxide ([CO2]) is expected to result in warmer temperatures and changed precipitation regimes during this century. In the northwestern U.S., these changes will likely decrease snowpack, cause earlier snowmelt, increase summer evapotranspiration, and increase the frequency and severity of droughts. Elevated [CO2] and warmer temperatures may have positive effects on growth and productivity where there is adequate moisture or growth is currently limited by cold. However, the effects of climate change are generally expected to reduce growth and survival, predispose forests to disturbance by wildfire, insects, and disease; and ultimately change forest structure and composition at the landscape scale. Substantial warming will likely decrease winter chilling resulting in delayed bud burst, and adversely affect flowering and seed germination for some species. The extent of these effects will depend on the magnitude of climate change, the abilities of individual trees to acclimate, and for tree populations to adapt in situ, or to migrate to suitable habitats. These coping mechanisms may be insufficient to maintain optimal fitness of tree populations to rapidly changing climate. Physiological responses to climatic stresses are relatively well-understood at the organ or whole-plant scale but not at the stand or landscape scale. In particular, the interactive effects of multiple stressors is not well known. Genetic and silvicultural approaches to increase adaptive capacities and to decrease climate-related vulnerabilities of forests can be based on ecophysiological knowledge. Effective approaches to climate adaptation will likely include assisted migration of species and populations, and density management. Use of these approaches to increase forest resistance and resilience at the landscape scale requires a better understanding of species adaptations, within-species genetic variation, and the mitigating effects of silvicultural treatments. 相似文献
105.
Constance I. Millar 《New Forests》1987,1(3):231-238
Presented here are results of rooting studies using hedges established from juvenile seedlings of blue and green foliaged bishop pine (Pinus muricata D. Don) from Mendocino and Sonoma Counties, California. Rootability, averaged over all clones and all setting dates, was 88%. The average time for 50% of the cuttings to root was 6 months. In general, cuttings began to root rapidly in late winter/early spring. The time of year when cuttings were set determined how soon they began a phase of rapid rooting, with cuttings set in winter and early spring beginning faster than other setting dates. The period of rapid rooting lasted 2–3 months until mid/late summer, beyond which time, rooting was slow. Population and family differences in rooting were not significant; differences in rooting among clones, however, were large and significant. Analyses of clones in two experiments indicated that rooting was heritable. 相似文献
106.
107.
Douglas H. Constance 《Agriculture and Human Values》2009,26(1-2):3-14
The critical studies in the Sociology of Agriculture can be generally divided into four questions: Agrarian, Environmental, Food, and Emancipatory. While the four questions overlap and all address social justice concerns, there is a chronological sequence to the studies. In this presidential address presented at the joint meetings of the Agriculture, Food, and Human Values Society and the Association for the Study of Food in Society held in June 2008 in New Orleans, LA, I provide an overview of the four questions and call for researchers and activists in agrifood studies to engage as public social scientists to bring about a more just and equitable agrifood system. 相似文献
108.
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110.
Constance L 《Science (New York, N.Y.)》1983,222(4628):1113-1114