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41.
I. G. Burns 《Plant and Soil》1992,142(2):221-233
A method is described for determining the way in which growth rate varies with plant nutrient concentration using a simple nutrient interruption technique incorporating only 2 treatments. The method involves measuring the changes in growth and nutrient composition of otherwise well-nourished plants after the supply of one particular nutrient has been withheld. Critical concentrations are estimated from the relationship between the growth rate (expressed as a fraction of that for control plants of the same size which remained well-nourished throughout) and the concentration of the growth-limiting nutrient in the plants as deficiency developed. Trials of the method using young lettuce plants showed that shoot growth rate was directly proportional to total N (nitrate plus organic N) concentration, and linearly or near-linearly related to K and P concentration over a wide range; the corresponding relationship for nitrate was strongly curvi-linear. Critical concentrations (corresponding to a 10% reduction in growth rate) determined from these results were similar to critical values calculated from models derived from field data, but were generally higher than published estimates of critical concentration (based on reductions in shoot weight) for plants of a similar size. Reasons for these discrepancies are discussed. Nitrate, phosphate or potassium concentrations in sap from individual leaf petioles were highly sensitive to changes in shoot growth rate as deficiency developed, with the slope of the relationships varying with leaf position, due to differences both in their initial concentration and in the rates at which they were utilized in individual leaves. Each nutrient was always depleted more quickly in younger leaves than in older ones, providing earlier evidence of deficiency for diagnostic purposes. Although the plants were capable of accumulating nitrate, phosphate and potassium well in excess of that needed for optimum dry matter production during periods of adequate supply, the rate of mobilization of these reserves was insufficient to prevent reductions in growth rate as the plants became deficient. This brings into question the validity of the conventional concept that luxury consumption provides a store of nutrients which are freely available for use in times of shortage. The implications of these results for the use of plant analysis for assessing plant nutrient status are discussed.  相似文献   
42.
Adult reproductive performance is linked to the period of feeding done by the final instar larva after attainment of a larval critical weight (LCW). The highest weight attained by a final instar larva is referred to as the larval maximum weight (LMW) and is the onset of the pre-pupal period. The relationships between LCW, pupal weight (PW) and adult weight (AW) are described as functions of the LMW. In the leafroller Cnephasia jactatana (Walker) (Lepidoptera: Tortricidae) LCW was dependent on larval size and was approximately 75% of the mean LMW. LCW was about 29 mg and 36 mg for male and female larvae of 1.18 mm and 1.20 mm head-capsule width, respectively. Over three successive generations of laboratory rearing, PW was approximately 30% and 25% lower than the LMW for males and females, respectively. AW was consistently about 50% and 40% lower than the PW for males and females, respectively. The decrease in weight from LMW to PW was named as the constant DP and found to be 0.3 for males and 0.25 for females. The total decrease from LMW to AW was the constant DA and was 0.6 for males and 0.5 for females. The duration of the latent feeding period was positively correlated to PW and AW. LCW may be used to derive quality indices that describe and predict pupal and adult performance.
Résumé Les performances reproductives sont liées à la période d'alimentation du dernier stade larvaire après l'obtention d'un poids critique (LCW). Le poids maximal atteint au dernier stade larvaire est défini comme le poids larvaire maximal (LMW), il correspond au début de la période prénymphale. Les relations entre poids de la chrysalide (PW) et poids de l'audulte AW) sont présentées comme des fonctions de LMW). Chez Cnephasia jactatana Walker (Lep. Tortricidae), LCW dépend de la taille de la chenille et correspond à environ 75% de la valeur moyenne de LMW. LCW est respectivement de 29 mg et 36 mg pour les chenilles mâles et femelles dont les capsules céphaliques ont 1,18 et 1,20 mm. Pour 3 générations successives, PW est environ 30% et 25% inférieur à LMW des mâles et des femelles. La régression du poids de LMW à PW est désignée comme la constante DP et vaut 0,3 pour les mâles et 0,25 pour les femelles. La régression de LMW à AW est désignée comme la régression DM et vaut 0,6 pour les mâles et 0,5 pour les femelles. La durée de la période d'alimentation latente est liée positivement à PW et AW. LCW peut être utilisé comme indice dérivé décrivant et prédisant les potentialités nymphales et imaginales.
  相似文献   
43.

1. 1.|Critical thermal maxima (CTMax) and minima (CTMin) were measured to evalute thermal hardening in Rana catesbeiana.

2. 2.|Tadpoles show heat hardening and CTMax acclimation, and both responses are influenced by developmental stage.

3. 3.|The first evidence of cold hardening in vertebrates is reported here.

4. 4.|Heat hardening significantly reduces cold tolerance, but there is otherwise no evidence of a cross-hardening effect.

Author Keywords: Thermal acclimation; thermal hardening; hardening; heat hardening; cold hardening; critical thermal maxima; critical thermal minima; developmental stage; metamorphosis; tadpoles; Rana catesbeiana  相似文献   

44.
K. S. Chung 《Hydrobiologia》1981,78(2):177-181
The acclimation rates of temperature changes in Cyprinodon dearborni, collected from Laguna Los Patos, Cumana, Venezuela, were determined by the critical thermal maximum method. At an increase in temperature (from 24 to 31°C) fish started to gain acclimation level after 3 hours and took 3 days to fully get up to a higher level of resistance to heat death; however, at a decrease in temperature (from 3 t to 24°C) fish began to lose its acclimation level after 12 days and required 39 days to reach a lower level of resistance to thermal death.  相似文献   
45.
46.
The molting process and body growth in Rhodnius prolixus (Hemiptera: Reduviidae) (Ståhl, 1859) are significantly influenced by the availability and quality of food. Based on the body weight of each stage, the present study provides estimates of a potential critical weight threshold required for molt initiation in R. prolixus. In addition, a new measure given by the area under the weight curve is proposed, which encapsulates both body weight and time. It is shown that this measure is consistent with the data, and allows the estimation of a pre‐refractory period (i.e. the time interval between the moment at which the critical weight threshold is reached and the moment when no further meals are accepted). The present analysis estimates the critical weight threshold as 1.6, 5.3, 12.9, 42.0 and 97.0 mg for stages 1–5, respectively, whereas the values of the area under the curve threshold as 5, 16, 31.2, 159.7 and 329.9 mg days for stages 1–5, respectively. The results of the present study confirm the existence of a weight‐dependent mechanism for the initiation of molting in R. prolixus.  相似文献   
47.
48.
Plasmalogenase has been assayed by conversion of the fatty aldehydes, released by hydrolysis of the vinyl ether bond of plasmalogens, to long-chain alcohols by horse liver alcohol dehydrogenase. The reaction was followed spectrophotometrically by measuring the oxidation of NADH. The assay is sufficiently sensitive to enable plasmalogenase activity to be determined in isolated oligodendroglia and derived membranes and in brain microsomal membranes using 50-250 micrograms protein.  相似文献   
49.
Open‐circuit voltages of lead‐halide perovskite solar cells are improving rapidly and are approaching the thermodynamic limit. Since many different perovskite compositions with different bandgap energies are actively being investigated, it is not straightforward to compare the open‐circuit voltages between these devices as long as a consistent method of referencing is missing. For the purpose of comparing open‐circuit voltages and identifying outstanding values, it is imperative to use a unique, generally accepted way of calculating the thermodynamic limit, which is currently not the case. Here a meta‐analysis of methods to determine the bandgap and a radiative limit for open‐circuit voltage is presented. The differences between the methods are analyzed and an easily applicable approach based on the solar cell quantum efficiency as a general reference is proposed.  相似文献   
50.
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