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51.
52.
Temperate forest soils store large amounts of organic matter and are considered as net sinks for atmospheric carbon dioxide. Information about the sink strength and the turnover time of soil organic carbon (SOC) is required to assess the potential response of soils to climate change. Here we report on stocks, turnover times (TT) and accumulation of SOC in bulk soil and density fractions from genetic horizons of a Podzol in the Fichtelgebirge, Germany. Stocks of SOC, total nitrogen and exchangeable cations determined in nine quantitative soil pits strongly varied with stone content and thickness of horizons in both the organic layer and the mineral soil. On the basis of radiocarbon signatures, mean turnover times of 4, 9 and 133 years, respectively, were calculated for Oi, Oe and Oa horizons from three soil pits, using a non-steady-state model. The Oa horizons accumulated 4–8 g C m−2 year−1 whereas the Oi and Oe horizons were close to steady-state during the past decade. Free particulate organic matter (FPOM) was the most abundant fraction in the Oa and EA horizons with TT of 70–480 years. In the B horizons, mineral associated organic matter (MAOM) dominated with over 40% of total SOC and had TT of 390–2170 years. In contrast to other horizons, MAOM in the Bsh and Bs horizon had generally faster TT than occluded particulate organic matter (OPOM), possibly because of sorption of dissolved organic carbon by iron and aluminium oxides/hydroxides. Our results suggest that organic horizons with relatively short turnover times could be particularly vulnerable to changes in climate or other disturbances. 相似文献
53.
Freezing and thawing may substantially influence the rates of C and N cycling in soils, and soil frost was proposed to induce NO losses with seepage from forest ecosystems. Here, we test the hypothesis that freezing and thawing triggers N and dissolved organic matter (DOM) release from a forest soil after thawing and that low freezing temperatures enhance the effect. Undisturbed soil columns were taken from a soil at a Norway spruce site either comprising only O horizons or O horizons + mineral soil horizons. The columns were subjected to three cycles of freezing and thawing at temperatures of –3°C, –8°C, and –13°C. The control columns were kept at constant +5°C. Following the frost events, the columns were irrigated for 20 d at a rate of 4 mm d–1. Percolates were analyzed for total N, mineral N, and dissolved organic carbon (DOC). The total amount of mineral N extracted from the O horizons in the control amounted to 8.6 g N m–2 during the experimental period of 170 d. Frost reduced the amount of mineral N leached from the soil columns with –8°C and –13°C being most effective. In these treatments, only 3.1 and 4.0 g N m–2 were extracted from the O horizons. Net nitrification was more negatively affected than net ammonification. Severe soil frost increased the release of DOC from the O horizons, but the effect was only observed in the first freeze–thaw cycle. We found no evidence for lysis of microorganisms after soil frost. Our experiment did not confirm the hypothesis that soil frost increases N mineralization after thawing. The total amount of additionally released DOC was rather low in relation to the expected annual fluxes. 相似文献
54.
Drying and rewetting (D/W) of soils often resulted in the release of soluble phosphorus (P) and nitrogen (N), thereby changing the availability of both nutrients. Most experiments on D/W have been conducted with disturbed mineral soil samples and with rewetting of the soil samples by abrupt change in the water potential. Here, we studied the effect of D/W on the leaching of P and N from undisturbed forest floors of a European beech and a Norway spruce site under near field conditions of desiccation and rewetting. We hypothesized that even under realistic rewetting of undisturbed forest floors, the leaching of P and N is increased after D/W and that the effects are less pronounced for spruce than for beech because of the larger hydrophobicity of the spruce forest floor. Undisturbed forest floor columns were subjected to desiccation at 20°C until a matrix potential of –100 MPa (pF 6.0) was reached, while controls were kept at moist conditions. Columns were irrigated by 22 mm day?1 from day 1–3 and by 10 mm day?1 from day 4–14 given in automated short pulses. Leachates from the soil columns were analyzed for orthophosphate, total P, NH4, NO3, and total N. In the spruce forest floor the concentrations of total P in leachates and the leachate fluxes were strongly increased after D/W. The increase of solute P was less for beech than for spruce coinciding with less actual rewetting of the beech forest floor. Leaching of total N from the spruce forest floor was not affected by D/W, however, concentrations and leaching of NH4 increased, while leaching of NO3 decreased. For beech the leaching of total N and NH4 increased after D/W, while NO3 leaching decreased. The results indicate that also under realistic conditions, D/W of forest floors increases solute P and leads to changes in the ratio of NH4/NO3 in solution, thereby altering the availability of the nutrients. 相似文献
55.
Mai-Van?Dinh Alexander?GuhrEmail authorView authors OrcID profile Alfons?R.?Weig Egbert?Matzner 《Biology and Fertility of Soils》2018,54(6):761-768
Drying and rewetting (D/W) of soils often leads to a pulse of total dissolved phosphorus (TDP) by lysis of sensitive microorganisms. The relevance of D/W on the P cycle in ecosystems depends on the duration of the TDP release. In forest soils, the forest floor represents a hotspot of microbial activity and is often prone to D/W. Here, we investigated the dynamics of TDP, the microbial P pool (Pmic), and the composition of microbial communities after D/W. Samples were taken from Oi and Oe layers of a European beech and a Norway spruce site and desiccated up to ??100 MPa (pF 6) at 20 °C, while controls were kept moist. TDP and Pmic were measured 0, 1, 3, 7, and 14 days after rewetting and the composition of microbial communities was analyzed by automated ribosomal intergenic spacer analysis after 14 days. After D/W, the largest TDP net release (D/W-control) was from Oe layers with 40–50 mg P kg?1 and inorganic P as the dominant fraction. The TDP concentrations decreased strongly in Oi layers within 1 (beech) to 4 (spruce) days, while remaining stable in Oe layers. The TDP dynamics were linked to the decrease and recovery of Pmic after D/W. Pmic dynamics differed between layers and stand types, suggesting the influence of microbial communities with different D/W sensitivities. The composition of microbial communities varied strongly among sites and layers, while D/W only affected the composition of bacterial and fungal communities in the spruce Oe layer. D/W of forest floors increases the plant available P and affects the P cycle in forest ecosystems. 相似文献
56.
57.
Mercury (Hg) and methylmercury (CH3Hg+) are global pollutants, but little information is available on their distribution and mobility in soils and catchments of Central Europe. The objective of this study was to investigate the pools and mobility of Hg and CH3Hg+ in different forest soils. Upland and wetland forest soils, soil solutions and runoff were sampled. In upland soils the highest contents of total-Hg were found in the Oh layer of the forest floor (>400 ng g-1) and the storage of non geogenic total-Hg (calculated for 60 cm depth) was about 120 mg/m2. The storage of total-Hg was one order of magnitude lower in wetland soils as compared to the upland soils. By far the largest proportion of total-Hg in soils was bound in immobile fractions. The depth gradients of CH3Hg+ did not correspond to those of total-Hg and the highest contents of CH3Hg+ in upland soils were observed in the litter layer of the forest floor and in the Bsv horizon. The CH3Hg+ content of the wetland soils was generally much higher in comparison with upland soils. CH3Hg+ in solution was found in the forest floor percolates of upland soils and in wetland soils, but not in soil solutions from mineral soil horizons. Gaseous losses of Hg as well as methylation of Hg are likely in wetland soils. The latter might be highly relevant for CH3Hg+ levels in runoff. 相似文献
58.
The forest floor represents the major source of dissolved organic carbon (DOC) and nitrogen (DON) in forest soils. The release mechanisms of DOC and DON from forest floors and their environmental controls as well as the dynamics of concentrations and fluxes are still poorly understood. We investigated the effect of drying and rewetting on the release of DOC and DON from a Norway spruce forest floor. Undisturbed soil columns of 17 cm diameter and 15—20 cm height were taken with 7 replicates from the forest floor of a mature Norway spruce (Picea abies [L.] Karst.) site and established at 10°C in the laboratory. Columns were exposed to different periods of drying (3, 5, 10, 20 days). Each drying period was followed by a rewetting for 5 days at an irrigation rate of 10 mm d—1 with a natural throughfall solution. The percolates from the forest floor were collected daily and analyzed for DOC, total N, NH4, NO3, pH, electrical conductivity and major ions. Drying for 10 and 20 days decreased the water content of the Oi horizon from 280% dry weight to about 30%. The water content of the Oe and the Oa horizon only changed from about 300% to 200%. The fluxes of DOC from the forest floor were moderately effected by drying and rewetting with an increase after 3 and 5 days of drying, but a decrease after 10 and 20 days. On the contrary, the drying for 10 and 20 days resulted in a drastic increase of the DON fluxes and a subsequent decrease of the DOC/DON ratios in the forest floor percolates from about 50 to 3.3. These results suggest that the mechanisms for DOC release in forest floors differ from those for DON and that drying and rewetting cause temporal variations in the DOC/DON ratios in forest floor percolates. 相似文献
59.
Marie‐France Dignac Ingrid Kgel‐Knabner Kerstin Michel Egbert Matzner Heike Knicker 《植物养料与土壤学杂志》2002,165(3):281-289
Due to high nitrogen deposition in central Europe, the C : N ratio of litter and the forest floor has narrowed in the past. This may cause changes in the chemical composition of the soil organic matter. Here we investigate the composition of organic matter in Oh and A horizons of 15 Norway spruce soils with a wide range of C : N ratios. Samples are analyzed with solid‐state 13C nuclear magnetic resonance (NMR) spectroscopy, along with chemolytic analyses of lignin, polysaccharides, and amino acid‐N. The data are investigated for functional relationships between C, N contents and C : N ratios by structural analysis. With increasing N content, the concentration of lignin decreases in the Oh horizons, but increases in the A horizons. A negative effect of N on lignin degradation is observed in the mineral soil, but not in the humus layer. In the A horizons non‐phenolic aromatic C compounds accumulate, especially at low N values. At high N levels, N is preferentially incorporated into the amino acid fraction and only to a smaller extent into the non‐hydrolyzable N fraction. High total N concentrations are associated with a higher relative contribution of organic matter of microbial origin. 相似文献
60.
Organotin compounds (OTC) are deposited from the atmosphere into terrestrial ecosystems and can accumulate in soils. We studied the adsorption and desorption of methyltin and butyltin compounds in organic and mineral soils in batch experiments. The adsorption and desorption isotherms for all species and soils were linear over the concentration range of 10–100 ng Sn ml?1. The strength of OTC adsorption correlated well with the carbon content and cation exchange capacity of the soil and was in the order mono‐ > di‐ > tri‐substituted OTCs and butyltin > methyltin compounds. The OTC adsorption coefficients were much larger in organic soils (Kd > 104) than in mineral soils. The adsorption and desorption showed a pronounced hysteresis. Trimethyltin adsorption was partly reversible in all soils (desorption 2–12% of the adsorbed amounts). Dimethyltin, tributyltin and dibutyltin exhibited reversible adsorption only in mineral soils (desorption 4–33% of the adsorbed amounts). Mono‐substituted OTCs adsorbed almost irreversibly in all soils (desorption < 1% of adsorbed amounts). Trimethyltin was more mobile and more bioavailable in soils than other OTCs. It might therefore be leached from soils and accumulate in aquatic ecosystems. The other OTCs are scarcely mobile and are strongly retained in soils. 相似文献