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1.
An accurate method for the determination of the volume of wood samples was developed which involves soaking in mineral turpentine. The effect of this soaking procedure on the dry mass of the samples was determined and found to be negligible.  相似文献   
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Past land‐use changes, intensive cropping with large proportions of root crops, and preferred use of mineral fertilizer have been made responsible for proceeding losses of soil organic C (SOC) in the plough layer. We hypothesized that in intensive agriculturally managed regions changes in SOC stocks would be detectable within a decade. To test this hypothesis, we tracked the temporal development of the concentrations and stocks of SOC in 268 arable sites, sampled by horizon down to 60 cm in the Cologne‐Bonn region, W Germany, in 2005 and in 2013. We then related these changes to soil management data and humus balances obtained from farmers' surveys. As we expected that changes in SOC concentrations might at least in part be minor, we fractionated soils from 38 representative sites according to particle size in order to obtain C pools of different stability. We found that SOC concentrations had increased significantly in the topsoil (from 9.4 g kg?1 in 2005 to 9.8 g kg?1 in 2013), but had decreased significantly in the subsoil (from 4.1 g kg?1 in 2005 to 3.5 g kg?­1 in 2013). Intriguingly, these changes were due to changes in mineral‐bound SOC rather than to changes in sand‐sized organic matter pools. As bulk density decreased, the overall SOC stocks in the upper 60 cm exhibited a SOC loss of nearly 0.6 t C (ha · y)?1 after correction by the equivalent soil mass method. This loss was most pronounced for sandy soils [?0.73 t SOC (ha · y)?1], and less pronounced for loamy soils [?0.64 t SOC (ha · y)?1]; silty soils revealed the smallest reduction in SOC [?0.3 t SOC (ha · y)?1]. Losses of SOC occurred even with the overall humus balances having increased positively from about 20 kg C (ha · y)?1 (2003–2005) to about 133 kg C (ha · y)?1 (2005–2013) due to an improved organic fertilization and intercropping. We conclude that current management may fail to raise overall SOC stocks. In our study area SOC stocks even continued to decline, despite humus conservation practice, likely because past land use conversions (before 2005) still affect SOC dynamics.  相似文献   
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Journal of Plant Diseases and Protection - Crop sequence patterns are considered as those schemes farmers apply within a single field to succeed crops over time, regardless of whether the same crop...  相似文献   
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Journal of Plant Diseases and Protection - Weed species within arable farming systems act as a source of food and provide habitat for various taxa at higher trophic levels. Using field experiments...  相似文献   
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Heartwater is a tick borne disease that affects ruminants and wild animals in Africa south of the Sahara. It is caused by Ehrlichia ruminantium and transmitted by the tick Amblyomma hebraeum. The protocols currently used to detect heartwater take several days to complete. Here, we describe the development of a pCS20 quantitative real-time PCR TaqMan probe assay to detect E. ruminantium in livestock blood and ticks from the field. The assay is based on the conserved pCS20 gene region of E. ruminantium that contains two overlapping genes, rnc and ctaG [Collins, N.E., Liebenberg, J., De Villiers, E.P., Brayton, K.A., Louw, E., Pretorius, A., Faber, F.E., Van Heerden, H., Josemans, A., Van Kleef, M., Steyn, H.C., Van Strijp, M.F., Zweygarth, E., Jongejan, F., Maillard, J.C., Berthier, D., Botha, M., Joubert, F., Corton, C.H., Thomson, N.R., Allsopp, M.T., Allsopp, B.A., 2005. The genome of the heartwater agent Ehrlichia ruminantium contains multiple tandem repeats of actively variable copy number. PNAS 102, 838-843]. The pCS20 quantitative real-time PCR TaqMan probe was compared to the currently used pCS20 PCR and PCR/(32)P-probe test with regards to sensitivity, specificity and the ability to detect DNA in field samples and in blood from experimentally infected sheep. This investigation showed that the pCS20 quantitative real-time PCR TaqMan probe was the most sensitive assay detecting seven copies of DNA/mul of cell culture. All three assays, however, cross react with Ehrlichia canis and Ehrlichia chaffeensis. The pCS20 real-time PCR detected significantly more positive field samples. Both the PCR and pCS20 real-time PCR could only detect E. ruminantium parasites in the blood of experimentally infected sheep during the febrile reaction. The PCR/(32)P-probe assay, however, detected the parasite DNA 1 day before and during the febrile reaction. Thus, because this new quantitative pCS20 real-time PCR TaqMan probe assay was the most sensitive and can be performed within 2h it is an effective assay for epidemiological surveillance and monitoring of infected animals.  相似文献   
8.
Glyphosate is the most widely used herbicidal active ingredient in the world. In Germany, the distributed amounts have been doubled during the last ten years. There is public concern and criticism on this extensive use and use limitations are claimed. However, also loss of efficacy as reported from countries with high use intensity of glyphosate reduces long term use of these herbicides. Recently, scientific studies aimed to quantify the economic benefits of glyphosate to estimate the costs of losing or banning this herbicide. In this text, possibilities of reductions of glyphosate use in arable farming are discussed to obtain a necessary extent. It is pointed out, that those uses are preferential, that enable minimum soil cultivation that minimize soil erosion. Post-harvest applications have the potential for use reductions, due to replacement techniques such as soil cultivation that are available. Pre-harvest applications, which are targeted for crop maturation only, should not be used as a routine. It is suggested to seek for best management practices of glyphosate use.  相似文献   
9.
Serological visualization of interleukin 2   总被引:5,自引:0,他引:5  
Interleukin 2, a lymphokine that acts as a second signal of cellular immune response by way of its action as a T-cell growth factor, was morphologically identified by immunoperoxidase staining. With the use of a monoclonal antibody to interleukin 2 and several complex-forming antisera, the lymphokine was readily distinguished in cytocentrifuge preparations of peripheral blood leukocytes stimulated with a T-cell mitogen. When preparations of cloned interleukin 2 producer and responder cells were stained by the same procedures, discrete patterns of both responder and producer cell phenotypes were revealed. Interleukin 2 producer T cells exhibited a characteristic intense, ringlike cytoplasmic staining, whereas the responder cells (as exemplified by interleukin 2-dependent cell lines) exhibited a less intensive, spotlike membrane staining. In addition, intense membrane localization of interleukin 2, reminiscent of potential capping phenomena, could be observed in stained preparations of cloned responder cells.  相似文献   
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