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81.
Availability of Phosphate Reserves in Arable Soils - Long Term Field Experiments for Assessing Soil P Reserves and Critical Soil Test Values - The objective of this work is to quantify the plant availability of soil P reserves accumulated by former fertilizer applications, the possibility of utilizing them by arable field crops and to determine critical soil test values. For this purpose several long term field experiments with large plots without replicates were initiated in 1977 on luvisols from loess (pH 6.8 – 7.4) in Lower Saxony with a sugar beet - winter wheat - winter barley/winter wheat crop rotation. Annual P applications were 0, 45, 90, 135 and 180 kg P2O5/ha as triple phosphate. Application of other fertilizers and plot management were according to farmer's practice. Despite of high yield levels phosphate response of plants was only 2 % at its maximum in the average of all crops in 15 years. This was confirmed by small plot experiments with four replicates placed into the large plots after 9 years, when soil P levels had been differentiated under the influence of plant P removal and P application. Herewith in agreement, shoot P concentration was found within the range generally regarded sufficient. It is therefore concluded that plant P demand has been fully satisfied by soil P reserves. Soil P test values, monitored by the P(H2O) method of Sissingh, decreased markedly in 15 years, when no P was applied, they remained approximately constant when P application was equal to P removal and they increased when P addition was higher than P removal. Plants on a site with 4 mg P(H2O)/L initially had severe P deficiency. Maximum yield was obtained when the soil P level was raised to 11 mg P(H2O)/L. It is concluded that P reserves, which are often high in German arable soils, can be utilized by field crops and thus be lowered to about 10 mg P(H2O)/L by reducing or omitting P dressings. For practical purposes it is suggested to restrict P application, if necessary at all, to the sugar beet crop in the rotation because they often respond more than small grain.  相似文献   
82.
Arsenic speciation in farmed Hungarian freshwater fish   总被引:2,自引:0,他引:2  
Arsenic speciation analysis was carried out on freshwater farmed fish collected from an area with elevated groundwater arsenic concentrations in Hungary as well as from outside of the area (control samples). The arsenic species were determined by high-performance liquid chromatography-inductively coupled plasma mass spectrometry on methanol extracts of the muscle tissue from the fish. Catfish (Claries gariepinus) were raised in geothermal water where the average total arsenic concentrations were 167 (contaminated sites) and 15.1 ng As mL(-1) (control); they were all fed an artificial diet containing 2880 microg As kg(-1) total arsenic, mostly present as arsenobetaine. In the catfish, the accumulated total arsenic (2510-4720 microg As kg(-1)) was found mostly in the form of arsenobetaine suggesting that uptake of arsenic was dominated by their diet. Carp (Cyprinus carpio) were cultured in surface lakes with no significant arsenic pollution and had total arsenic concentrations ranging from 62 to 363 microg As kg(-1). The arsenic species found in the carp extracts differed markedly from those in the catfish in that no arsenobetaine was detected. Most samples of carp from the investigated sites contained low concentrations of As(III) (arsenite), As(V) (arsenate), MA (methylarsonate), and DMA (dimethylarsinate), and no other compounds were detected. The four individuals from the control site, however, all contained appreciable levels of oxo-arsenosugar-glycerol and oxo-arsenosugar-phosphate. Indeed, the oxo-arsenosugar-phosphate dominated the speciation pattern for these carp contributing about 75% of the sum of species. The contrast between these two freshwater aquaculture species regarding total arsenic and arsenic species has relevant toxicological aspects in terms of food safety.  相似文献   
83.
Wheat cultivars differ widely in manganese (Mn) efficiency. To investigate the reasons for different Mn efficiencies, a pot experiment with soil, a solution‐culture experiment, and model calculations were carried out. The pot experiment was conducted with wheat (Triticum aestivum L. cvs. PBW 373, PBW 154, PBW 343, PBW 138, and Triticum durum L. cvs. PBW 34 and PDW 233) grown in a screen house in India. The soil was a loamy sand with pH 8.1, DTPA‐extractable Mn 1.62 mg (kg soil)–1, and initial soil solution Mn concentration (CLi) of 0.19 μM. When fertilized with 50 mg Mn (kg soil)–1, CLi increased to 0.32 μM. At CLi 0.19 μM, wheat cv. PBW 373 produced 74% of its maximum shoot dry weight (SDW) with 64% of its maximum root length (RL), while cv. PDW 233 produced only 25% of its maximum SDW with 11% of its maximum RL. The other wheat cultivars were between these extremes. Manganese deficiency caused a reduction in shoot growth, but more strongly reduced root growth. The low Mn efficiency of T. durum cv. PDW 233 was related to a strong depression of its root growth. Manganese influx was similar for all cultivars. In solution culture below 1 μM Mn, under controlled climate‐chamber conditions, Mn influx was linearly related to Mn concentration. Both the efficient cv. PBW 343 and the inefficient cv. PDW 233 had a similar influx. Uptake kinetic parameters from the solution experiment together with soil and plant parameters from the pot experiment were used in a mechanistic nutrient‐uptake model. Calculated values of Mn influx for wheat grown in soil were 55% to 74% of measured values. A sensitivity analysis showed that increasing CLi or the slope of the uptake isotherm by about 30% would be enough to reach the observed influx. The results of this research indicate that an increase of Mn solubility by microbial or chemical mobilization would increase Mn uptake. But on the other hand, no chemical mobilization would be required to increase Mn uptake if the plant improved its uptake kinetics. Low Mn efficiency of some wheat cultivars was related to their reduced root growth at low soil Mn supply.  相似文献   
84.
Longitudinal studies evaluating the evolution of clinical, haematological, biochemical findings in young dogs exposed for the first time to multiple vector-borne pathogens have not been reported. With the objective of assessing the evolution of clinical, haematological and biochemical findings, these parameters were serially monitored in naturally infected dogs throughout a 1-year follow-up period. Young dogs, infected by vector-borne pathogens based on cytology or polymerase chain reaction, were examined clinically and blood samples were obtained at seven different follow-up time points. Dogs were randomized to group A (17 dogs treated with a spot-on formulation of imidacloprid 10% and permethrin 50%) or to group B (17 dogs untreated). In addition, 10 4-month-old beagles were enrolled in each group and used as sentinel dogs. At baseline, Anaplasma platys was the most frequently detected pathogen, followed by Babesia vogeli, Bartonella spp., Ehrlichia canis and Hepatozoon canis. Co-infections with A. platys and B. vogeli, followed by E. canis and B. vogeli, A. platys and H. canis and A. platys and Bartonella spp. were also diagnosed. In dogs from group B, abnormal clinical signs were recorded at different time points throughout the study. No abnormal clinical signs were recorded in group A dogs. Thrombocytopenia was the most frequent haematological alteration recorded in A. platys-infected dogs, B. vogeli-infected dogs and in dogs co-infected with A. platys and B. vogeli or A. platys and Bartonella spp. Lymphocytosis was frequently detected among dogs infected with B. vogeli or co-infected with A. platys and B. vogeli. Beagles were often infected with a single pathogen rather than with multiple canine vector-borne pathogens. There was a significant association (p<0.01) between tick infestation and A. platys or B. vogeli, as single infections, and A. platys and B. vogeli or A. platys and Bartonella spp. co-infections. This study emphasizes the clinical difficulties associated with assigning a specific clinical sign or haematological abnormality to a particular canine vector-borne disease.  相似文献   
85.
Serological diagnosis of acute and chronic Q fever in humans relies on detection of antibodies to phase I (PhI) and II (PhII) antigens of Coxiella (C.) burnetii. Although phase-specific antigens are available, they are not yet used in ruminants as they are in humans. This study focuses on phase-specific serology as a tool for analysis of the dynamics of infection in cattle. As a prerequisite, sero-prevalence in Bavarian cattle (1) and sero-prevalences for age-groups (2) were determined by ELISA (CHEKIT Q-Fever; mix of PhI/PhII-antigen). Subsequently, phase-specific antigens were coated onto ELISA plates individually and tests were simultaneously applied in an endemically infected herd with about 90 dairy cows and 250 calves/heifers in April 2005, March 2006 and retrospectively in May and October 2004. From April 2005 onward, placentas were analysed for C. burnetii by PCR (3). (1) Sero- and herd prevalences based on 21,051 sera from 603 Bavarian dairy farms collected in 2003 were 14.8% ± 0.48% and 72.3% ± 3.6%, respectively. (2) Analysis of 3965 animals from 105 farms for which age was reported revealed a base level of sero-prevalence of less than 5% in 1-2 years old animals, it increased to 15% in 2-3 years old and reached a plateau (25-30%) in cows four years and older. (3) In May 2004 and April 2005 a peak of PhI(-)/PhII(+)-prevalence in primiparous cows (2.0-3.5 years) was observed; but not in October 2004 and March 2006. The PhI(-)/PhII(+)-pattern in primiparous cows changed to negative (one-third), PhI(+)/PhII(+) (1/3) or persisted (1/3). In contrast, sero-conversion was rare in multiparous cows (>3.5 years). If the PhI(-)/PhII(+) pattern was detected, it was due to an infection in preceding years. This pattern persisted (2/3) or changed to negative (1/3); a change to PhI(+)/PhII(+) did not occur. PhI(-)/PhII(+) in heifers (1-2 years) always changed to negative. Detection of PhII-antibodies was significantly associated with PCR-positive placentas. Remarkably, 45% of sera with the PhI(-)/PhII(+) pattern were negative for the CHEKIT Q-Fever ELISA, thus this test missed an important group of infected animals.  相似文献   
86.
The formation of furan upon sterilization of a lipid-containing starch gel was investigated in the presence of various antioxidants, namely, α-tocopherol, β-carotene, and ascorbic acid, with and without proteins. Results indicated that α-tocopherol did not significantly influence furan formation from oxidized lipids. β-Carotene, suggested previously to be a furan precursor itself, did influence the generation of furan in a concentration-dependent manner, although to a limited extent. Surprisingly, the presence of lipids seemed to limit the furan generation from β-carotene. Interestingly, the addition of ascorbic acid to the emulsions containing soybean or sunflower oils considerably enhanced the formation of furan from these oils. This was also the case when fresh oils were applied, shown previously to be nearly unable to generate furan. This observation can be explained by an intensified ascorbic acid degradation stimulated by the presence of lipids.  相似文献   
87.
The origin of Saturn's narrow G ring has been unclear. We show that it contains a bright arc located 167,495.6 +/- 1.3 km from Saturn's center. This longitudinally localized material is trapped in a 7:6 corotation eccentricity resonance with the satellite Mimas. The cameras aboard the Cassini spacecraft mainly observe small (1 to 10 micrometers) dust grains in this region, but a sharp decrease in the flux of energetic electrons measured near this arc requires that it also contain larger (centimeter- to meter-sized) bodies whose total mass is equivalent to that of a approximately 100-meter-wide ice-rich moonlet. Collisions into these bodies may generate dust, which subsequently drifts outward to populate the rest of the G ring. Thus, the entire G ring could be derived from an arc of debris held in a resonance with Mimas.  相似文献   
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Applications of polyphosphate‐based fertilizers have been reported to have a positive impact on crop yields as compared to orthophosphate sources. Since plants take up P mainly as orthophosphate, hydrolysis rates of polyphosphates into orthophosphates will determine their fertilizer ability. Laboratory and soil incubation experiments were performed to evaluate hydrolysis rates of pyrophosphate (PP), tripolyphosphate (TP), and trimetaphosphate (TMP) in water as well as in two soils having different P‐fixing capacities. P availability was characterized by measuring the orthophosphate (ortho‐P) and polyphosphate (poly‐P) concentration in soil solution as well as the calcium‐acetate‐lactate (CAL)‐extractable amounts of both forms. In water, PP was completely hydrolyzed within 15 d, whereas TMP was hydrolyzed only to about 30% after 90 d. In the two soils, polyphosphates hydrolyzed during the incubation period increasing ortho‐P concentration in soil solution as well as in CAL extract. At the end of the incubation, no significant differences in ortho‐P concentration in soil solution and CAL extract were found in the sandy soil, whereas in the silty‐loam soil, polyphosphate applications resulted in higher soil‐solution ortho‐P concentration. Although polyphosphate hydrolysis is mainly affected by the soil‐specific enzymatic activity, it seems that polyphosphates and/or hydrolysis products are preferentially adsorbed/precipitated compared to ortho‐P in the silty loam, thereby influencing the P availability from polyphosphate sources.  相似文献   
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