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21.
For a model of diallelic loci with arbitrary epistasis, Barton and Turelli [2004. Effects of genetic drift on variance components under a general model of epistasis. Evolution 58, 2111-2132] gave results for variances among and within replicate lines obtained by inbreeding without selection. Here, we discuss the relation between their population genetic methods and classical quantitative genetic arguments. In particular, we consider the case of no dominance using classical identity by descent arguments, which generalizes their results from two alleles to multiple alleles. To clarify the connections between the alternative methods, we obtain the same results using an intermediate method, which explicitly identifies the statistical effects of sets of loci. We also discuss the effects of population bottlenecks on covariances among relatives.  相似文献   
22.
Measurement of net ecosystem exchange was made using the eddy covariance method above three forests along a north-south climatic gradient in Sweden: Flakaliden in the north, Knottåsen in central and Asa in south Sweden. Data were obtained for 2 years at Flakaliden and Knottåsen and for one year at Asa. The net fluxes (Nep) were separated into their main components, total ecosystem respiration (Rt) and gross primary productivity (Pg). The maximum half-hourly net uptake during the heart of the growing season was highest in the southernmost site with ?0.787 mg COm?2 s?1 followed by Knottåsen with ?0.631 mg COm?2 s?1 and Flakaliden with ?0.429 mg COm?2 s?1. The maximum respiration rates during the summer were highest in Knottåsen with 0.245 mg COm?2 s?1 while it was similar at the two other sites with 0.183 mg COm?2 s?1. The annual Nep ranged between uptake of ?304 g C m?2 year?1 (Asa) and emission of 84 g C m?2 year?1 (Knottåsen). The annual Rt and Pg ranged between 793 to 1253 g C m?2 year?1 and ?875 to ?1317 g C m?2 year?1, respectively. Biomass increment measurements in the footprint area of the towers in combination with the measured net ecosystem productivity were used to estimate the changes in soil carbon and it was found that the soils were losing on average 96–125 g C m?2 year?1. The most plausible explanation for these losses was that the studied years were much warmer than normal causing larger respiratory losses. The comparison of net primary productivity and Pg showed that ca 60% of Pg was utilized for autotrophic respiration.  相似文献   
23.
Based on theories of mire development and responses to a changing climate, the current role of mires as a net carbon sink has been questioned. A rigorous evaluation of the current net C-exchange in mires requires measurements of all relevant fluxes. Estimates of annual total carbon budgets in mires are still very limited. Here, we present a full carbon budget over 2 years for a boreal minerogenic oligotrophic mire in northern Sweden (64°11′N, 19°33′E). Data on the following fluxes were collected: land–atmosphere CO2 exchange (continuous Eddy covariance measurements) and CH4 exchange (static chambers during the snow free period); TOC (total organic carbon) in precipitation; loss of TOC, dissolved inorganic carbon (DIC) and CH4 through stream water runoff (continuous discharge measurements and regular C-concentration measurements). The mire constituted a net sink of 27±3.4 (±SD) g C m−2 yr−1 during 2004 and 20±3.4 g C m−2 yr−1 during 2005. This could be partitioned into an annual surface–atmosphere CO2 net uptake of 55±1.9 g C m−2 yr−1 during 2004 and 48±1.6 g C m−2 yr−1 during 2005. The annual NEE was further separated into a net uptake season, with an uptake of 92 g C m−2 yr−1 during 2004 and 86 g C m−2 yr−1 during 2005, and a net loss season with a loss of 37 g C m−2 yr−1 during 2004 and 38 g C m−2 yr−1 during 2005. Of the annual net CO2-C uptake, 37% and 31% was lost through runoff (with runoff TOC>DIC≫CH4) and 16% and 29% through methane emission during 2004 and 2005, respectively. This mire is still a significant C-sink, with carbon accumulation rates comparable to the long-term Holocene C-accumulation, and higher than the C-accumulation during the late Holocene in the region.  相似文献   
24.
A roving tower concept was used to compare a semi-arid grassland site in Inner Mongolia (China), which was fenced in 1979 and ungrazed thereafter (UG79) with differently grazed semi-arid steppe ecosystems. The study was conducted during three consecutive years characterised by contrasting precipitation. The different grazing intensities included continuously and moderately grazed (CG), winter grazed (WG), and heavily grazed (HG). Here, we compare the energy fluxes and surface parameters that characterise the differently managed plots. The main focus is on sensible heat flux (H), available energy (AE), surface temperature (T ( s )), and surface albedo (alpha). Systematic errors were excluded by a side-to-side intercomparison of the instruments, and systematic climatic differences were minimised by the close distance between the fixed and the roving eddy covariance tower. Statistically, AE and T ( s ) were always significantly different between two simultaneously measured grazing intensities. Whereas AE was higher at UG79 in all years (mean difference of about 19Wm(-2)), T ( s ) was typically lower at UG79 (mean differences of 0.4 degrees C to about 2 degrees C). The exception was the end of the vegetation period in 2004 when T ( s ) was 0.6 degrees C higher at UG79 compared to CG. At UG79 alpha was typically significantly lower, and H was typically significantly higher. Consequently, latent heat fluxes (both as energy balance residual and directly measured) do not differ much between the different grazing intensities. It is concluded, that (1) the roving tower concept is able to detect differences due to grazing, (2) differences between the sites can be attributed to real surface differences, and (3) differences due to grazing intensities are small compared to interannual differences in surface fluxes.  相似文献   
25.
A study was conducted to understand the potential of Landsat-8 in the estimation of gross primary production (GPP) and to quantify the productivity of maize crop cultivated under hyper-arid conditions of Saudi Arabia. The GPP of maize crop was estimated by using the Vegetation Photosynthesis Model (VPM) utilizing remote sensing data from Landsat-8 reflectance (GPPVPM) as well as the meteorological data provided by Eddy Covariance (EC) system (GPPEC), for the period from August to November 2015. Results revealed that the cumulative GPPEC for the entire growth period of maize crop was 1871 g C m−2. However, the cumulative GPP determined as a function of the enhanced vegetation index – EVI (GPPEVI) was 1979 g C m−2, and that determined as a function of the normalized difference vegetation index – NDVI (GPPNDVI) was 1754 g C m−2. These results indicated that the GPPEVI was significantly higher than the GPPEC (R2 = 0.96, P = 0.0241 and RMSE = 12.6%). While, the GPPNDVI was significantly lower than the GPPEC (R2 = 0.93, P = 0.0384 and RMSE = 19.7%). However, the recorded relative error between the GPPEC and both the GPPEVI and the GPPNDVI was −6.22% and 5.76%, respectively. These results demonstrated the potential of the landsat-8 driven VPM model for the estimation of GPP, which is relevant to the productivity and carbon fluxes.  相似文献   
26.
Rank-based regression for analysis of repeated measures   总被引:1,自引:0,他引:1  
Wang  You-Gan; Zhu  Min 《Biometrika》2006,93(2):459-464
  相似文献   
27.
We combined Eddy‐covariance measurements with a linear perturbation analysis to isolate the relative contribution of physical and biological drivers on evapotranspiration (ET) in three ecosystems representing two end‐members and an intermediate stage of a successional gradient in the southeastern US (SE). The study ecosystems, an abandoned agricultural field [old field (OF)], an early successional planted pine forest (PP), and a late‐successional hardwood forest (HW), exhibited differential sensitivity to the wide range of climatic and hydrologic conditions encountered over the 4‐year measurement period, which included mild and severe droughts and an ice storm. ET and modeled transpiration differed by as much as 190 and 270 mm yr?1, respectively, between years for a given ecosystem. Soil water supply, rather than atmospheric demand, was the principal external driver of interannual ET differences. ET at OF was sensitive to climatic variability, and results showed that decreased leaf area index (L) under mild and severe drought conditions reduced growing season (GS) ET (ETGS) by ca. 80 mm compared with a year with normal precipitation. Under wet conditions, higher intrinsic stomatal conductance (gs) increased ETGS by 50 mm. ET at PP was generally larger than the other ecosystems and was highly sensitive to climate; a 50 mm decrease in ETGS due to the loss of L from an ice storm equaled the increase in ET from high precipitation during a wet year. In contrast, ET at HW was relatively insensitive to climatic variability. Results suggest that recent management trends toward increasing the land‐cover area of PP‐type ecosystems in the SE may increase the sensitivity of ET to climatic variability.  相似文献   
28.
3×3完全双列杂交F1不同阶段生长特点的分析   总被引:1,自引:0,他引:1  
为了了解鲤杂交F1不同组合、不同阶段生长性状的变化情况,研究以建鲤、黄河鲤和黑龙江野鲤3个鲤品种双列杂交F1为试验材料,通过组合、组合内性别间、性别、不同时期体重、体增重以及协方差分量的分析,来确定完全双列杂交F1生长性状的变化特点,以及在此过程中起重要作用的影响因素。结果表明:不同时期各个组合体重不同,不同时期组合内性别间体重差异不同;不同时期不同性别间体重差异不同;不同协方差分量,同一组合PIT标记17个月时的体重的最小二乘估计值不同,同一个协方差分量,9个组合中极值估计值出现的组合也不同;除PIT标记17个月后的体厚作为协方差分量外,性别之间体重没有差异,其余分量均是雌鱼体重显著高于雄鱼体重。这些说明选取合适的协方差分量对组合的选择和育种的结果有重要影响。  相似文献   
29.
华北平原冬小麦农田蒸散量   总被引:5,自引:3,他引:2  
以华北平原冬小麦农田为研究对象,采用涡度相关技术和热红外遥感技术,研究了不同环境条件下土壤含水量与农田蒸散量及作物冠层温度的关系.结果表明,冬小麦在农田郁闭(LAI≥3)、晴天和土壤相对含水量低于田间持水量65%的情况下,蒸发比值日变化正午前后出现相对较低且平稳的变化趋势.在晴天情况下,农田潜热通量与作物冠层温度日变化和季节变化均呈极显著的非线性相关关系,而冠气温差、农田相对蒸散量则与0~100 cm土层的土壤相对含水量密切相关.以13:30~14:00的平均冠层温度值Tc、日最高气温Ta max和日净辐射总量Rnd为统计数据,确立了冬小麦农田日蒸散量ETd (mm)估算简化模式参数.  相似文献   
30.
Summary At present, genetic evaluation in livestock using best linear unbiased prediction (BLUP) assumes autosomal inheritance. There is evidence, however, of X-chromosomal inheritance for some traits of economic importance. BLUP can accommodate models that include X-chromosomal in addition to autosomal inheritance. To obtain BLUP with autosomal and X-chromosomal additive inheritance for a population in which allelic frequency is equal in the sexes, and that is in gametic equilibrium, we write y i = xi + ai + si + ei, where y i is the phenotypic value for individual i, xi, is a vector of constants relating y i to fixed effects, is a vector of fixed effects, a i is the additive genetic effect for autosomal loci, S i is the additive genetic effect for X-chromosomal loci, and e i is random error. The covariance matrix of a i's is A A 2 , where A is the matrix of twice the co-ancestries between relatives for autosomal loci, and A 2 is the variance of additive genetic effects for autosomal loci. The covariance matrix of s i's is S F 2 , where S is a matrix of functions of co-ancestries between relatives for X-chromosomal loci and F 2 is the variance of additive genetic effects for X-chromosomal loci for noninbred females. Given the covariance matrices of random effects a i, si, and e i, BLUPs of autosomal and of X-chromosomal additive effects can be obtained using mixed model equations. Recursive rules to construct S and an efficient algorithm to compute its inverse are given.Dedicated to the memory of Dr. C. R. Henderson, whose encouraging comments stimulated the research in this paper. Supported in part by the Illinois Agricultural Experiment Station, Hatch Project 35-0367, Estimation of Genetic Parameters.  相似文献   
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