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971.
Masotti V Juteau F Bessière JM Viano J 《Journal of agricultural and food chemistry》2003,51(24):7115-7121
The volatile components of the aerial parts of Artemisia molinieri, an endemic wormwood of southern France, were analyzed by GC and GC-MS. Among the 69 compounds identified, major components were ascaridole (19-76%), alpha-terpinene (traces-36%), p-cymene (1-17%), 1,8-cineole (0.3-8%), and germacrene D (0.6-15%). Quantitative variations have been characterized following the season, the phenological cycle, and the aging of the plants. Bioassays have been performed on a sample of essential oil, which has shown a strong inhibition of the growth of both tested yeasts (Candida albicans and Saccharomyces cerevisiae var. chevalieri) and minor activity on both tested Gram-negative bacteria (Escherichia coli and Enterococcus hirae). The oils have shown interesting antioxidant activities on the basis of alpha-tocopherol as reference compound, up to 400-1200%. 相似文献
972.
Reactions of anthocyanins and tannins in model solutions 总被引:1,自引:0,他引:1
Salas E Fulcrand H Meudec E Cheynier V 《Journal of agricultural and food chemistry》2003,51(27):7951-7961
The reaction between procyanidin dimer Ec-EcG (B2 3'-O-gallate) and malvidin 3-O-glucoside (Mv3glc) was studied in a model solution system at two different pH values, 2.0 and 3.8. Disappearance of both species was much faster at pH 3.8 than at pH 2.0. That of Mv3glc was increased in the presence of Ec-EcG, whereas that of Ec-EcG was the same in the presence or absence of the anthocyanin. Values of absorbance at 520 nm measured at pH 2.0 were correlated with the amount of residual Mv3glc. Those measured at pH 3.8 hardly changed during the incubation, but absorbance values at 420 and 620 nm as well as resistance to sulfite bleaching were much increased, confirming that Mv3glc was converted to other pigments. Anthocyanin-flavanol adducts were observed at both pH values, but their structures were different. At pH 2.0, cleavage of the procyanidin linkage followed by nucleophilic addition of flavanol or anthocyanin moieties led to (Ec)(n)-EcG and (Ec)(n)-Mv3glc, respectively. At pH 3.8, nucleophilic addition of Ec-EcG onto the anthocyanin yielded Mv3glc-(Ec-EcG). 相似文献
973.
974.
Tolerance to zinc (Zn) deficiency was examined for three wheat (Triticum aestivum L.) and three barley (Hordeum vulgare L.) varieties grown in chelator‐buffered nutrient solution. Four indices were chosen to characterize tolerance to Zn deficiency: (1) relative shoot weight at low compared to high Zn supply (“Zn efficiency index”), (2) relative shoot to root ratio at low compared to high Zn supply, (3) total shoot uptake of Zn under deficient conditions, and (4) shoot dry weight under deficient conditions. Barley and wheat exhibited different tolerance to Zn deficiency, with barley being consistently more tolerant than wheat as assessed by all four indices. The tolerance to Zn deficiency in the barley varieties was in the order Thule=Tyra>Kinnan, and that of wheat in the order Bastian=Avle>Vinjett. The less tolerant varieties of both species accumulated more P in the shoots than the more tolerant varieties. For all varieties, the concentrations of Mn, Fe, Cu, and P in shoot tissue were negatively correlated with Zn supply. This antagonism was more pronounced for Mn and P than for Cu and Fe. Accumulation of Cu in barley roots was extremely high under Zn‐deficient conditions, an effect not so clearly indicated in wheat. 相似文献
975.
EL-Habib Dakir María-Luisa Ruiz Pedro García Marcelino Pérez de la Vega 《Genetic Resources and Crop Evolution》2002,49(6):619-631
The genetic variation existing in a set of barley (Hordeum vulgare L.) landrace samples recently collected in Morocco was estimated. Two kinds of genetic markers, seed storage proteins (hordeins) and random amplified polymorphic DNA (RAPD), were used. Only six out of 31 landraces were subjected to RAPD analysis. Both kinds of markers, RAPD and storage proteins, yielded similar results, showing that the level of variation observed in Moroccan barley was high: all landraces showed variability; 808 different storage protein patterns (multilocus associations) were observed among 1897 individuals (2.32 seeds per association, on average) with an average of 43 multilocus associations per accession. In general, genetic variation within accessions was higher than between accessions. The 100 polymorphic RAPD bands generated by 21 effective primers were able to generate enough patterns to differentiate between uniform cultivars and even between individuals in variable accessions. One of the aims of this work was to compare the effectiveness of RAPD versus storage protein techniques in assessing the variability of genetic resource collections. On average hordeins were more polymorphic than RAPDs: they showed more alternatives per band on gels and a higher percentage of polymorphic bands, although RAPDs supply a higher number of bands. Although RAPD is an easy and standard technique, storage protein analysis is technically easier, cheaper and needs less sophisticated equipment. Thus, when resources are a limiting factor and considering the cost of consumables and work time, seed storage proteins must be the technique of choice for a first estimation of genetic variation in plant genetic resource collections. 相似文献
976.
Carlos?Wildt Oriol?Gibert José?Luis?CortinaEmail author Giuliana?Coscera 《Journal of Soils and Sediments》2004,4(3):184-191
Goal, Scope and Background The remediation of heavy-metalcontaminated soils and sediments is of significant value to industrial areas around the world.
The spread of such pollutants can result in a potential risk of entering the groundwater system and being transported to potential
receptors. Leaching techniques can be an effective treatment option for the metal removal from soils and sediments. This approach
consists of washing or leaching the contaminated soil with an appropriate reagent and the subsequent treatment of the leaching
in an above-ground installation (on-site treatment) where metals can be removed and concentrated into a smaller volume. Among
the heavy metals, chromium is a commonly identified soil contaminant, particularly in sites with intensive economic activities
including agriculture, industrial, mining and mineral,processing.
Objective The objective of this work was the evaluation and development of a leaching process for the remediation of soils and sediments
polluted with chromium at laboratory scale. Chromium soil pollution was generated after the breakdown of a channel containing
chromium wastes from a tannery plant. The pollution extension has been estimated to be on the order of thousands of tonnes
of soil to be treated, with chromium contents ranging from 500 to 17,000 mg kg-1 soil.
Methods The whole process investigated in this study integrates three stages; a) chromium leaching from a sediment using a diluted
sulphuric acid solution, b) treatment of the leaching effluents with a magnesium oxide/limestone mixture for the precipitation
of chromium hydroxide after acidity neutralisation, and c) polishing step to remove the eventual remaining chromium by adsorption
onto natural zeolite. The amount of contaminated sediment treated ranged from 0.5 to 2 kg with chromium contents of between
2000 and 17,000 mg kg-1.
Results and Discussion The paper describes results on the performance of the process and the optimisation of steps including influence of acid sulphuric
concentration, chromium removal efficiency as well as alkaline reactive mixture proportions. Effluents from the leaching cells
showed a significant decay on the chromium concentration with the increase of leaching runs and a high content of acidity
(pH values close to 0.5). The treatment of these effluents in a second cell containing magnesium oxide/ limestone mixtures
resulted in a high efficiency in neutralisation of acidity (pH values around 7) and chromium removal (concentrations below
5 mg 1-1). The passage through a third compartment containing zeolite as an adsorbent decreased the chromium concentration below 0.5
mg 1-1,
Conclusions From the results obtained on the chromium leaching and immobilisation with magnesium oxide/limestone mixture at a laboratory
scale, it could be pointed out that: (a) diluted sulphuric acid solutions (3%) demonstrated a high efficiency on chromium
removal from sandy polluted soils on the kilogram scale, (b) mixtures of magnesium oxide/limestone demonstrated a high capacity
to neutralise the residual high acidity present on the effluents and to remove chromium by precipitation and (c) between the
limestone and caustic magnesia mixtures, those containing more than 60% of caustic magnesia provide the higher efficiency.
Recommendation and Outlook Future work would be directed to the evaluation of the integrated process of leaching and chromium precipitation on column
at a scale of 100 to 1000 kg. 相似文献
977.
Jiménez A Rodríguez R Fernández-Caro I Guillén R Fernández-Bolaños J Heredia A 《Journal of agricultural and food chemistry》2001,49(1):409-415
Olive fruits at three stages of ripening (green, cherry, and black) have been studied. After cell wall isolation, the compositions of the cell wall and that of the phosphate-soluble polysaccharides were determined. In cell walls, decreases in arabinose, xylose, glucose, and uronic acid levels were observed, together with a slight increase in mannose on ripening. At the beginning of ripening, fragments of pectic polymers were the major constituents of the phosphate-soluble fraction, with the hemicellulosic ones increasing toward the end of the process. The molecular weight of the fragments solubilized was approximately 6 kDa. After cell wall fractionation, the pectic polysaccharides soluble in imidazole and sodium carbonate were also studied. In both fractions, between the green and cherry stages of ripening, a significant loss of homogalacturonans took place. Between the cherry and black stages of ripening, rhamnogalacturonan side chains were also released in addition to homogalacturonans. In any of the pectic fractions, changes in apparent molecular weight were quantified. 相似文献
978.
Senocq D Dupont D Rolet-Répécaud O Faurie F Levieux D 《Journal of agricultural and food chemistry》2001,49(3):1571-1577
To investigate plasmin activity in cheese, we produced antibodies to bovine beta-casein with controlled specificity, suitable as markers of the integrity of the major bonds involved in its initial breakdown. Sixteen rabbits were immunized with synthetic substitutes for six plasmin-sensitive peptides. Antisera raised to the peptides (f20-39), (f40-56), (f94-113), (f184-202), and (f193-209) recognized beta-casein in ACP-ELISA, Western-blot, and biosensor assays. Casein in vitro hydrolysis by plasmin or chymosin reduced the detection of these determinants in ACP-ELISA, in agreement with the enzymatic sensitivity of bonds included within the binding sites, or in their neighborhood. Antiserum to (f20-39) in particular allowed the specific detection of plasmin cleavage at the bond generating gamma1-CN. Antisera to C-terminus preferentially detected the cleavage by chymosin. Immunoassays using these antibodies would allow in situ monitoring of significant proteolysis events without bias originated in the secondary degradation of the released peptides. 相似文献
979.
The oxidation process of 13 edible oil samples with different proportions of oleic, linoleic, and linolenic acyl groups has been studied using Fourier transform infrared spectroscopy. The oxidation experiments were carried out by heating the samples in a convection oven at 70 degrees C. Duplicate spectra were recorded from a film of pure oil between two disks of KBr for each sample every day during the course of the oxidation, and frequency data of each band of the spectrum were collected automatically. Changes in the values of the frequency of most of the bands of the spectra were observed. The shiftings of the frequency value of specific bands allowed one to distinguish between the different stages of the oxidation process and to establish the oxidation degree of each oil sample. This methodology could be useful to evaluate the oxidative stability of edible oils in a simple, fast, and accurate way. 相似文献
980.
Joaquin Gutiérrez Hugo Travieso M. Aurora Pubillones 《Water, air, and soil pollution》1993,68(3-4):315-323
A method has been developed that uses a mixed solution of NaOH, NaCl and cysteine to digest fish. Inorganic Hg and MgHg were determined by cold vapor atomic absorption (CVAAS) using a selective reduction step with SnCl2 and SnCL2-solutions. Ethyl alcohol was satisfactorily used to prevent excessive foaming. Two optimum digestion procedures were established: (1) using a dry block heater at 90 °C for 1 hr and (2) overnight digestion at 25 to 30 °C. Differences between both were not significant (95%) in the range of 30 to 500 ng g?1 Hg (II) and MeHg in fish. Reduction of the Hg signal due to matrix effects in different fish species was evaluated (95 to 60%). Oily fish, shrimp and lobsters gave the highest reduction. Internal calibration by addition of Hg standards are strongly recommended when exact determinations are needed. The detection limit obtained was near 10 ng g?1. Signals were linear in the concentration range studied (30 to 500 ng g?1). Accuracy of analyses was in the order of 5% or better, with a relative standard deviation of 5%. The method could be applied to other environmental matrices: hair, urine and blood, with some modifications. 相似文献