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An acid inhibitor, probably abscisic acid (ABA) in low concentrations was found to be present in bean seeds. The evidence is based on data from paper electrophoresis, chromatography, UV absorption and growth inhibition in the Lemna bioassay, sensitive down to a concentration of 10-11M ABA or 0.02–0.03 ng/flask. The inhibitor level as measured by this bioassay decreases considerably with increasing soaking time. Acid ether-soluble inhibitors could even be detected in the soaking water from the soaked seeds.  相似文献   
224.
Summary

Chemical communication is an ancient yet still immensely important part of reproduction. Amongst all invertebrates, the most sophisticated “chemical languages” are used by social insects. Here the sex- and caste-specific pheromonal messages consist of multicomponent mixtures. In the neotropical stingless bee Scaptotrigona postica, an inhabitant of dense tropical rain forests, the cephalic volatiles of a queen transmit information on her reproductive status to males. A distinct ontogenetic pattern of the queen pheromone composition allows drones to discriminate receptive virgins which are then chased during the short nuptial flight through the forest understorey. By means of gas chromatographic/mass spectroscopic analyses, the numerous volatile compounds found in pentane extracts of individual bee heads could be identified. Qualitative as well as quantitative changes of these volatiles in the course of imaginal development could be determined, and bioassays with synthetic compounds were undertaken in order to decode the chemical signals used during the short encounter of a young queen and her mate.  相似文献   
225.
Trials were carried out with benomyl and dodemorph in 1970, 1971 and 1972, with triarimol in 1971 and with MBC in 1972. In 1970 and 1971 there were some indications that dodemorph was a more effective eradicant but the differences between materials generally appeared less important than the timing of the spray application. An attempt in 1972 to obtain better control by applying sprays in relation to predictions of mildew growth, based on temperature and humidity, was only partially successful. No significant effects of mildew on leaf area or number of flowers could be demonstrated. High levels (25 and 50%) of mildew were associated with small leaves but this may reflect only the abundance of such leaves at periods generally favourable for mildew. The rate of increase of mildew appeared to be directly related to rate of host growth. The significance of this is discussed.  相似文献   
226.
The ability of Sphaerotheca mors-uvae to perennate as cleistocarps, and as mycelium in buds was examined during the winters of 1965-6, 1966-7 and 1967-8 in relation to its two principal hosts, gooseberry and black currant. Cleistocarps on black currant leaves were examined from August 1965 to April 1966 and from July 1966 to March 1967. In 1965 cleistocarps were first observed on the leaves on 5 August; in 1966 on 11 July. These continued to develop through August and September and by October approximately 70% contained well-defined ascospores. The ascospore content remained generally at this level until February 1966 and November 1966; then the numbers of cleistocarps with ascospores fell and by April 1966 and March 1967 few such cleistocarps remained. From 21 March 1966 and 15 February 1967, but not otherwise, discharge of ascospores from the overwintered cleistocarps was readily obtained in laboratory tests. The viability and infectivity of the ascospores was demonstrated by allowing them to discharge on to leaf discs of black currant in the laboratory and also on to leaf discs and plants in the field. Sporulating colonies of S. mors-uvae developed within 8 days. Cleistocarps from shoots of black currant were examined from 4 August 1966 to 9 March 1967, and from 27 July 1967 to 1 January 1968. They developed in a similar manner to those on black currant leaves and by September in both 1966 and 1967 over 60% contained ascospores. This level was not maintained; the number of cleistocarps with ascospores fell gradually and by 8 December 1966 and 1 January 1968 few remained. Only in one laboratory test (21 November 1967) were ascospores discharged from a sample of these cleistocarps. Cleistocarps from shoots of gooseberry were examined from July 1966 to March 1967, and from August 1967 to January 1968. The pattern of ascospore development and subsequent decline in number of cleistocarps with ascospores was similar to that observed for black currant shoots. No discharge of ascospores could be demonstrated in laboratory tests. Evidence that S. mors-uvae perennates in buds of gooseberry was obtained by dissecting buds and by inducing buds on surface-sterilized shoots to burst under conditions which precluded chance infection. Field observations also suggested that bud infection occurred on gooseberry. Similar experiments failed to demonstrate the fungus in buds of black currant, and there was no indication of bud infection of this host in the field.  相似文献   
227.
ABSTRACT Dose-response curves are presented for the diuretic activity in aqueous extracts of brain, retrocerebral complex, and ventral nerve cord ganglia from Acheta domesticus . Diuretic activity is highest in extracts of brain and corpora cardiaca. In comparison with such extracts, those of the suboesophageal ganglia and thoracic ganglia I-III produce truncated responses, whilst abdominal ganglia 1–4 show evidence of an inhibition of the diuretic response at high doses. ED50 values, obtained from Hill plots, are similar for extracts of brain, corpora cardiaca, corpora allata, and abdominal ganglia, but are 3–4 times higher for extracts of suboesophageal and thoracic ganglia.
Separation of aqueous extracts of corpora cardiaca by reversed-phase HPLC yields a number of fractions which stimulate fluid secretion in isolated tubules. Diuretic activity in these fractions is destroyed by treatment with Pronase E, and on this basis is identified as peptidic. In general, diuretic activity is found in the same RP-HPLC fractions prepared from aqueous extracts of brain, suboesophageal ganglia, thoracic ganglia I-III, and abdominal ganglia 1–4.  相似文献   
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