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151.
Stanislas Talaga Frédéric Petitclerc Jean-François Carrias Olivier Dézerald Céline Leroy Régis Céréghino Alain Dejean 《Landscape Ecology》2017,32(9):1805-1818
Context
Many aquatic communities are linked by the aerial dispersal of multiple, interacting species and are thus structured by processes occurring in both the aquatic and terrestrial compartments of the ecosystem.Objectives
To evaluate the environmental factors shaping the aquatic macroinvertebrate communities associated with tank bromeliads in an urban landscape.Methods
Thirty-two bromeliads were georeferenced to assess the spatial distribution of the aquatic meta-habitat in one city. The relative influence of the aquatic and terrestrial habitats on the structure of macroinvertebrate communities was analyzed at four spatial scales (radius = 10, 30, 50, and 70 m) using redundancy analyses.Results
We sorted 18,352 aquatic macroinvertebrates into 29 taxa. Water volume and the amount of organic matter explained a significant part of the taxa variance, regardless of spatial scale. The remaining variance was explained by the meta-habitat size (i.e., the water volume for all of the bromeliads within a given surface area), the distance to the nearest building at small scales, and the surface area of buildings plus ground cover at larger scales. At small scales, the meta-habitat size influenced the two most frequent mosquito species in opposite ways, suggesting spatial competition and coexistence. Greater vegetation cover favored the presence of a top predator.Conclusions
The size of the meta-habitat and urban landscape characteristics influence the structure of aquatic communities in tank bromeliads, including mosquito larval abundance. Modifications to this landscape will affect both the terrestrial and aquatic compartments of the urban ecosystem, offering prospects for mosquito management during urban planning.152.
John B. Graham Joan I. Nassauer William S. Currie Herbert Ssegane M. Cristina Negri 《Landscape Ecology》2017,32(5):1023-1037
Context
Wild bee populations are currently under threat, which has led to recent efforts to increase pollinator habitat in North America. Simultaneously, U.S. federal energy policies are beginning to encourage perennial bioenergy cropping (PBC) systems, which have the potential to support native bees.Objectives
Our objective was to explore the potentially interactive effects of crop composition, total PBC area, and PBC patches in different landscape configurations.Methods
Using a spatially-explicit modeling approach, the Lonsdorf model, we simulated the impacts of three perennial bioenergy crops (PBC: willow, switchgrass, and prairie), three scenarios with different total PBC area (11.7, 23.5 and 28.8% of agricultural land converted to PBC) and two types of landscape configurations (PBC in clustered landscape patterns that represent realistic future configurations or in dispersed neutral landscape models) on a nest abundance index in an Illinois landscape.Results
Our modeling results suggest that crop composition and PBC area are particularly important for bee nest abundance, whereas landscape configuration is associated with bee nest abundance at the local scale but less so at the regional scale.Conclusions
Strategies to enhance wild bee habitat should therefore emphasize the crop composition and amount of PBC.153.
Helena Tukiainen Janne Alahuhta Richard Field Terhi Ala-Hulkko Raino Lampinen Jan Hjort 《Landscape Ecology》2017,32(5):1049-1063
Context
‘Conserving Nature’s stage’ has been advanced as an important conservation principle because of known links between biodiversity and abiotic environmental diversity, especially in sensitive high-latitude environments and at the landscape scale. However these links have not been examined across gradients of human impact on the landscape.Objectives
To (1) analyze the relationships between land-use intensity and both landscape-scale biodiversity and geodiversity, and (2) assess the contributions of geodiversity, climate and spatial variables to explaining vascular plant species richness in landscapes of low, moderate and high human impact.Methods
We used generalized additive models (GAMs) to analyze relationships between land-use intensity and both geodiversity (geological, geomorphological and hydrological richness) and plant species richness in 6191 1-km2 grid squares across Finland. We used linear regression-based variation partitioning (VP) to assess contributions of climate, geodiversity and spatial variable groups to accounting for spatial variation in species richness.Results
In GAMs, geodiversity correlated negatively, and plant species richness positively, with land-use intensity. Both relationships were non-linear. In VP, geodiversity best accounted for species richness in areas of moderate to high human impact. These overall contributions were mainly due to variation explained jointly with climate, which dominated the models. Independent geodiversity contributions were highest in pristine environments, but low throughout.Conclusions
Human action increases biodiversity but may reduce geodiversity, at landscape scale in high-latitude environments. Better understanding of the connections between biodiversity and abiotic environment along changing land-use gradients is essential in developing sustainable measures to conserve biodiversity under global change.154.
Krystina D. Mossop Nicholas P. Moran David G. Chapple Bob B. M. Wong 《Landscape Ecology》2017,32(5):1065-1078
Context
Dispersal has important fitness consequences for individuals, populations, and species. Despite growing theoretical insights into the evolution of dispersal, its behavioral underpinnings remain empirically understudied, limiting our understanding of the extent and impact of responses to landscape-level heterogeneity of environments, and increasing the risk of inferring species-level responses from biased population sampling.Objectives
We asked if predictable ecological variation among naturally fragmented arid waterbodies is correlated with disparate dispersal responses of populations of the desert goby Chlamydogobius eremius, which naturally inhabits two habitat “types” (permanent springs, ephemeral rivers), and different levels of hydrological connectivity (high and low) that potentially convey different costs and benefits of dispersal.Methods
To test for possible behavioral divergence between such populations, we experimentally compared the movement behaviors (correlates of emigration and exploration) of wild-caught fish. We used two biologically relevant spatial scales to test movement relevant to different stages of the dispersal process.Results
Behavior differed at both spatial scales, suggesting that alternative dispersal strategies enable desert gobies to exploit diverse habitat patches. However, while emigration was best predicted by the connectivity (flood risk) of fish habitats, exploration was linked to their habitat type (spring versus river).Conclusions
Our findings demonstrate that despite a complex picture of ecological variation, key landscape factors have an overarching effect on among-population variation in dispersal traits. Implications include the maintenance of within-species variation, potentially divergent evolutionary trajectories of naturally or anthropogenically isolated populations, and the direction of future experimental studies on the ecology and evolution of dispersal behavior.155.
156.
Context
Spatial heterogeneity has myriad influences on ecosystem processes, ecosystem services, and thus the sustainability of urban areas. It acts as a medium for urban design, planning, and management to determine how processes affecting sustainability can operate and interact. Therefore, how spatial heterogeneity is conceptualized and measured in cities is crucial for enhancing sustainability.Objectives
We show that the two most commonly used, but contrasting paradigms of urban ecology, ecology IN versus ecology OF the city, determine how spatial heterogeneity is thought of and used in different ways. We identify the key implications of these theoretical contrasts for the practice and assessment of sustainability in urban areas.Methods
We review and compare the different ways in which ecology IN versus ecology OF the city affect how to conceptualize, model and map urban spatial heterogeneity. We present a new framework to guide the comparison of spatial heterogeneity under the two paradigms.Results and conclusion
The integrative nature of this new framework becomes apparent under the ecology OF the city paradigm, because it recognizes the hybrid social and bioecological nature of heterogeneity in urban ecosystems. The hybrid approach to patchiness resonates with the three pillars of sustainability—environment, society, and economy. We exemplify how the more comprehensive and integrated framework of spatial heterogeneity under the ecology OF the city paradigm (1) supports more effective measurement and integration of the three components of sustainability, (2) improves management of heterogeneous urban ecosystems, and (3) satisfies calls for improved ecological tools to support urban ecosystem design.157.
Context
Regime shifts are well known for driving penetrating ecological change, yet we do not recognise the consequences of these shifts much beyond species diversity and productivity. Sound represents a multidimensional space that carries decision-making information needed for some dispersing species to locate resources and evaluate their quantity and quality.Objectives
Here we assessed the effect of regime shifts on marine soundscapes, which we propose has the potential function of strengthening the positive or negative feedbacks that mediate ecosystem shifts.Methods
We tested whether biologically relevant cues are altered by regime shifts in kelp forests and seagrass systems and how specific such shifted soundscapes are to the type of driver; i.e. local pollution (eutrophication) vs. global change (ocean acidification).Results
Here, we not only provide the first evidence for regime-shifted soundscapes, but also reveal that the modified cues of shifted ecosystems are similar regardless of spatial scale and type of environmental driver. Importantly, biological sounds can act as functional cues for orientation by dispersing larvae, and observed shifts in soundscape loudness may alter this function.Conclusions
These results open the question as to whether shifted soundscapes provide a functional role in mediating the positive or negative feedbacks that govern the arrival of species associated with driving change or stasis in ecosystem state.158.
Context
The assessment of land-use impacts on biodiversity is one of the central themes of landscape ecology and conservation biology. However, due to the complexity of biodiversity, it is impossible to obtain complete information about the diversity of all species even for small areas, necessitating the selection of individual species or assemblages thereof as species surrogate. In parts of the world where taxonomic expertise is lacking, species identification has hindered progress in biodiversity conservation, and the only practical, relatively-accurate option, is the use of taxonomic minimalism.Objective
We carried out a rapid biodiversity assessment based on three surrogates—land-use (driver-surrogate), terrestrial arthropods (species-surrogate) and morphospecies (taxonomic-surrogate)—to determine the impacts of land-use on biodiversity of the Western Region (Ghana), an area covering ~4 % of the West African biodiversity hotspot.Method
We used diversity profiles to visualize the distribution of a total of 8848 arthropod individuals over seven land-use types which define the complete heterogeneity of the landscape.Results
Here, we present both sample and asymptotic diversity profiles of arthropod morphospecies for each land-use type and the potential of each land-use type for conserving arthropods.Conclusions
We conclude that (1) the morphospecies approach is useful for detecting differences in species diversity of land-use types; (2) the concept of asymptotic diversity may not be necessary for land-use based biodiversity comparison; and (3) maximum diversity profiles are useful for determining the land-use conservation values in cases where pristine areas are not available.159.
Pablo M. Vergara Luis O. Meneses Audrey A. Grez Madelaine S. Quiroz Gerardo E. Soto Christian G. Pérez-Hernández Paola A. Diaz Ingo J. Hahn Andrés Fierro 《Landscape Ecology》2017,32(2):279-293
Context
Interactions between landscape-scale processes and fine-grained habitat heterogeneity are usually invoked to explain species occupancy in fragmented landscapes. In variegated landscapes, however, organisms face continuous variation in micro-habitat features, which makes necessary to consider ecologically meaningful estimates of habitat quality at different spatial scales.Objectives
We evaluated the spatial scales at which forest cover and tree quality make the greatest contribution to the occupancy of the long-horned beetle Microplophorus magellanicus (Coleoptera: Cerambycidae) in a variegated forest landscape.Methods
We used averaged data of tree quality (as derived from remote sensing estimates of the decay stage of single trees) and spatially independent pheromone-baited traps to model the occurrence probability as a function of multiple cross-scale combinations between forest cover and tree quality (with scales ranging between 50 and 400 m).Results
Model support and performance increased monotonically with the increasing scale at which tree quality was measured. Forest cover was not significant, and did not exhibit scale-specific effects on the occurrence probability of M. magellanicus. The interactive effect between tree quality and forest cover was stronger than the independent (additive) effects of tree quality and particularly forest cover. Significant interactions included tree quality measured at spatial scales ≥200 m, but cross-scale interactions occurred only in four of the seven best-supported models.Conclusions
M. magellanicus respond to the high-quality trees available in the landscape rather than to the amount of forest per se. Conservation of viable metapopulations of M. magellanicus should consider the quality of trees at spatial scales >200 m.160.