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101.
The ongoing climatic changes potentially affect plant growth and the functioning of temperature‐limited high‐altitude and high‐latitude ecosystems; the rate and magnitude of these biotic changes are, however, uncertain. The aim of this study was to reconstruct stand structure and growth forms of Larix sibirica (Ledeb.) in undisturbed forest–tundra ecotones of the remote Polar Urals on a centennial time scale. Comparisons of the current ecotone with historic photographs from the 1960s clearly document that forests have significantly expanded since then. Similarly, the analysis of forest age structure based on more than 300 trees sampled along three altitudinal gradients reaching from forests in the valleys to the tundra indicate that more than 70% of the currently upright‐growing trees are <80 years old. Because thousands of more than 500‐year‐old subfossil trees occur in the same area but tree remnants of the 15–19th century are lacking almost entirely, we conclude that the forest has been expanding upwards into the formerly tree‐free tundra during the last century by about 20–60 m in altitude. This upward shift of forests was accompanied by significant changes in tree growth forms: while 36% of the few trees that are more than 100 years old were multi‐stem tree clusters, 90% of the trees emerging after 1950 were single‐stemmed. Tree‐ring analysis of horizontal and vertical stems of multi‐stemmed larch trees showed that these trees had been growing in a creeping form since the 15th century. In the early 20th century, they started to grow upright with 5–20 stems per tree individual. The incipient vertical growth led to an abrupt tripling in radial growth and thus, in biomass production. Based on above‐ and belowground biomass measurements of 33 trees that were dug out and the mapping of tree height and diameter, we estimated that forest expansion led to a biomass increase by 40–75 t ha?1 and a carbon accumulation of approximately 20–40 g C m?2 yr?1 during the last century. The forest expansion and change in growth forms coincided with significant summer warming by 0.9 °C and a doubling of winter precipitation during the 20th century. In summary, our results indicate that the ongoing climatic changes are already leaving a fingerprint on the appearance, structure, and productivity of the treeline ecotone in the Polar Urals.  相似文献   
102.
Laccases are blue-copper enzymes, which oxidize phenolic substrates and thereby reduce molecular oxygen. They are widespread within fungi and are involved in lignin degradation or secondary metabolism such as pigment biosynthesis. Many fungi contain several laccases, not all of whose functions are known. In Aspergillus nidulans one, yA, is expressed during asexual development and converts a yellow precursor to the green pigment. We identified a second laccase gene, which encodes a 66.3-kDa protein 37.6% identical to laccase I of A. nidulans. The protein harbors an N-terminal secretion signal, and three characteristic copper-binding centers. The enzyme localizes at the growing hyphal tip. The gene was therefore named tilA (=tip laccase). Deletion or overexpression of the gene had no discernible phenotype under laboratory conditions.  相似文献   
103.
对罗氏沼虾卵子极体排出时间和第一次卵裂时间进行了观察,并在此基础上,采用热休克和细胞松弛素 B(C,B)两种诱导方法成功诱导出了罗氏沼虾四倍体。石蜡切片显示,当罗氏沼虾卵子完全成熟时,第一极体已经 排出。第二极体排出的时间约在受精后55min。经过雌性原核和雄性原核的联会,第一次卵裂的时间约在受精后 210-230min。设计了多种处理条件,其中热休克诱导罗氏沼虾四倍体的最好条件是:受精后210min,用40℃水温处 理胚胎1.5min,在这种条件下,最高可以得到35.86%的四倍体率;而C.B诱导罗氏沼虾四倍体的最好条件是:受精 后230min,用1.0mg/L的C.B处理胚胎10min,此时最高四倍体诱导率达33.78%。  相似文献   
104.
The frequency of black bear (Ursus americanus) sightings, vehicle collisions, and nuisance incidents in the coastal region of South Carolina has increased over the past 4 decades. To develop the statewide Black Bear Management and Conservation Strategy, the South Carolina Department of Natural Resources needed reliable information for the coastal population. Because no such data were available, we initiated a study to determine population density and genetic structure of black bears. We selected 2 study areas that were representative of the major habitat types in the study region: Lewis Ocean Bay consisted primarily of Carolina Bays and pocosin habitats, whereas Carvers Bay was representative of extensive pine plantations commonly found in the region. We established hair snares on both study areas to obtain DNA from hair samples during 8 weekly sampling periods in 2008 and again in 2009. We used genotypes to obtain capture histories of sampled bears. We estimated density using spatially explicit capture–recapture (SECR) models and used information-theoretic procedures to fit parameters for capture heterogeneity and behavioral responses and to test if density and model parameters varied by year. Model-averaged density was 0.046 bears/km2 (SE = 0.011) for Carvers Bay and 0.339 bears/km2 (SE = 0.056) for Lewis Ocean Bay. Next, we sampled habitat covariates for all locations in the SECR sampling grid to derive spatially explicit estimates of density based on habitat characteristics. Addition of habitat covariates had substantial support, and accounted for differences in density between Carvers Bay and Lewis Ocean Bay; black bear density showed a negative association with the area of pine forests (4.5-km2 scale) and a marginal, positive association with the area of pocosin habitat (0.3-km2 scale). Bear density was not associated with pine forest at a smaller scale (0.3-km2), nor with major road density or an index of largest patch size. Predicted bear densities were low throughout the coastal region and only a few larger areas had high predicted densities, most of which were centered on public lands (e.g., Francis Marion National Forest, Lewis Ocean Bay). We sampled a third bear population in the Green Swamp area of North Carolina for genetic structure analyses and found no evidence of historic fragmentation among the 3 sampled populations. Neither did we find evidence of more recent barriers to gene exchange; with the exception of 1 recent migrant, Bayesian population assignment techniques identified only a single population cluster that incorporated all 3 sampled areas. Bears in the region may best be managed as 1 population. If the goal is to maintain or increase bear densities, demographic connectivity of high-density areas within the low-density landscape matrix is a key consideration and managers would need to mitigate potential impacts of planned highway expansions and anticipated development. Because the distribution of black bears in coastal South Carolina is not fully known, the regional map of potential black bear density can be used to identify focal areas for management and sites that should be surveyed for occupancy or where more intensive studies are needed. © 2012 The Wildlife Society.  相似文献   
105.
The black bear Ursus americanus is an endangered species in Mexico. Its historical distribution has decreased by approximately 80% although its current distribution is not known with precision; it is only reported to be present in the mountains of Northern Mexico. This study proposes two ensemble models: Mexicós black bear (a) potential distribution compared with Natural Protected Areas (NPAs); and, (b) persistence areas for 2024. The current distribution variables are coniferous forest, elevation and dry forest. Suitable habitat for black bear (354,047 km2, 18.07% of the country) was found mainly in the north of the Sonoran biogeographical zone, along the Sierra Madre Occidental, the center and south of the Sierra Madre Oriental and some northern regions of the Altiplano Norte. Comparing these areas with NPAs documented that only 12.41% of potential distribution coincided with current suitable habitat. There are unprotected areas in Sierra Madre Occidental center and central and southern of Sierra Madre Oriental. The model for 2024 indicates a reduction of suitable habitat of 64.5%, mainly in the northern Sonoran zone and the center Sierra Madre Occidental. On the other hand, areas that will persist (125,673 km2) are located along the two main mountain ranges of Mexico. Identification of these sites will allow strengthening of long-term conservation strategies.  相似文献   
106.
107.
We developed 29 forensic quality tetranucleotide microsatellite loci for the identification of individual black bear (Ursus americanus). Allele number averaged 5.35 and ranged from 3 to 11. The eight markers selected for forensic use permit the identification and exclusion of individual bear with a probability of identity of approximately 8.1 × 10−8 (approximately one per 12 million).  相似文献   
108.
Data improving the characterization of the marine Euplotes species, E. petzi Wilbert and Song, 2008, were obtained from morphological, ecological and genetic analyses of Antarctic and Arctic wild-type strains. This species is identified by a minute (mean size, 46 μm × 32 μm) and ellipsoidal cell body which is dorsally decorated with an argyrome of the double-patella type, five dorsal kineties (of which the median one contains 8–10 dikinetids), five sharp-edged longitudinal ridges, and a right anterior spur. Ventrally, it bears 10 fronto-ventral, five transverse, two caudal and two marginal cirri, 30–35 adoral membranelles, and three inconspicuous ridges. Euplotes petzi grows well at 4 °C on green algae, does not produce cysts, undergoes mating under the genetic control of a multiple mating-type system, constitutively secretes water-borne pheromones, and behaves as a psychrophilic microorganism unable to survive at >15 °C. While the α-tubulin gene sequence determination did not provide useful information on the E. petzi molecular phylogeny, the small subunit rRNA (SSU rRNA) gene sequence determination provided solid evidence that E. petzi clusters with E. sinicus Jiang et al., 2010a, into a clade which represents the deepest branch at the base of the Euplotes phylogentic tree.  相似文献   
109.
P. Apostolakos  B. Galatis 《Protoplasma》1985,128(2-3):120-135
Summary The preprophase-prophase initial aperture (IA) cells ofMarchantia paleacea undergo a particular sequence of protoplasmic changes, which reflects the establishment of an unusual premitotic polarization. The marking feature of preprophase-prophase thallus cells is the shape of the nucleus which becomes spindle-shaped. This phenomenon accompanies the organization of an extranuclear microtubule (MT) sheath, nucleated and/or organized by distinct polar MT organizing centres (MTOCs).The interphase MTs disappear after activation of polar MTOCs. In preprophase IA cells incomplete preprophase MT bands (PMBs) are organized. They consist of PMB portions which traverse only small portions of the cell cortex at the level of the future cytokinesis and do not form a complete ring. In the same cells other MT bundles, independent of the incomplete PMBs terminate in the cortical cytoplasm abutting on the lower part of the intercellular spaces (ISs) or the surface cavities (SCs). Almost complete or complete PMBs are organized in IA cells in which the plane of PMB formation coincides with that passing through ISs of the same growth.The observations suggest that in preprophase-prophase IA cells ofMarchantia paleacea cortical MTOCs function in regions distant from each other: One region is the PMB cortical cytoplasm, probably that covering the wall edges, and the other is the one adjacent to the lower part of the wall facing the IS(s) or that underlying the SCs. The competition between the cortical MTOCs as well as between them and the polar ones may be responsible for the organization of incomplete PMBs.  相似文献   
110.
Operon structure of flagellar genes in Salmonella typhimurium   总被引:7,自引:0,他引:7  
Summary In Salmonella typhimurium, more than 40 genes have been shown to be involved in flagellar formation and function and almost all of them have been assigned to three regions of the chromosome, termed region I, region II, and region III. In the present study, a large number of transposon-insertion mutants in these flagellar genes were isolated using Tn10 and Mud1. The flaV gene was found to be a strong hot spot for Tn10 insertion. Complementation analysis of the polarity effects exerted by the transposon-insertion mutants defined 13 different flagellar operons; 3 in region I, 4 in region II, and 6 in region III. These results are compared with the reported arrangement of the corresponding genes in Escherichia coli.  相似文献   
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