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1.
Beech (Fagus sylvatica L.) seedlings were cultivated from seeds sown in pots or directly in the ground in outdoor chambers that were transparent to solar radiation, and provided either ambient air or CO(2)-enriched air (ambient + 350 &mgr;mol mol(-1)). The rooting volume was high in all experiments. In the short-term experiment, potted plants were assigned to a factorial CO(2) x nutrient treatment (optimal nutrient supply and severe nutrient shortage) for 1 year. In the long-term experiment, plants were grown directly in the ground and received an optimal supply of water and nutrients in both CO(2) treatments for 3 years. Nutrient stress caused carboxylation capacity (V(m)) to decrease in the potted seedlings exposed to CO(2)-enriched air during their first growing season. In the long-term experiment with optimal nutrient supply, CO(2)-enriched air did not affect V(m), but caused an upward acclimation of maximum electron transport rate (J(m)). Consequently, there was a 14% increase in the J(m)/V(m) ratio, indicating nitrogen reallocation to maintain an equilibrium between RuBP consumption and RuBP regeneration. Both V(m) and J(m) decreased during the growing season in both CO(2) treatments. Although upward acclimation of J(m) was no longer apparent at the end of the third growing season, plants in CO(2)-enriched air maintained a higher J(m)/V(m) ratio than plants in ambient air, indicating that photosynthetic acclimation always occurred. Second flush leaves appeared during each growing season. When expressed on the basis of foliar nitrogen concentration, their photosynthetic characteristics (V(m) and J(m)) were enhanced compared with other leaves. Because the number of second flush leaves was also increased in the elevated CO(2) treatment, this response should be taken into account when modeling the effects of elevated CO(2) concentration on canopy photosynthesis. Stomatal conductance decreased in response to atmospheric CO(2) enrichment; however, the stomatal response to irradiance followed a single relationship based on two stomatal conductance models.  相似文献   
2.
European Journal of Forest Research - Studies on wood basic density (BD) vertical variations become essential to predict more accurately the within-stem distributions of biomass and wood quality in...  相似文献   
3.
African elephants can affect the quality of the habitat of other species by breaking or uprooting trees and shrubs in savannas. Their effect on vegetation has been widely studied but less is known about the effects of such vegetation changes on other animals. We studied how changes in the vegetation caused by elephants influence the selection of microhabitats by five African herbivore species (giraffe, kudu, steenbok, impala, and zebra) in Hwange National Park, Zimbabwe. There was no clear significant effect of overall elephant-induced vegetation changes on microhabitat selection except for the small species (steenbok and impala) that used vegetation modified by elephants preferentially. This is consistent with a medium-term browsing facilitation hypothesis. More subtle possible effects were detected for larger browsers (giraffe and kudu). They selected areas with broken and uprooted plants and avoided coppiced areas. All of the browsers selected sites characterized by plants uprooted and broken by elephants, which were associated with a higher visibility, and ultimately a better probability of detecting an approaching predator, suggesting that perceived predation risk plays an important role in microhabitat selection. These results illustrate how elephants can initiate indirect effects that influence microhabitat selection by other herbivores. Understanding the indirect effects of elephants through changes in food availability and predation risk thus needs further investigation. The results of this study do not provide support for the hypothesis that elephant-induced changes in the structure of habitats have caused the declines in the populations of the other herbivores in the study area.  相似文献   
4.
Following seed treatment of wheat (Triticum aestivum L.) with 14C-labelled triticonazole at a dose of 1·8 g kg-1 seed, the uptake of radioactivity by shoots and roots was investigated from the two- to three-leaf stage up to the beginning of the booting phase, 80 days after sowing. Triticonazole equivalents taken up by wheat plants reached 5·7% and 14·6% of the applied dose in the shoots and the roots, respectively. Between the two- to three-leaf stage and the beginning of the booting phase, the concentration of triticonazole equivalents in the shoots decreased from 2·5 to 0·15 μg g-1 fresh weight. This was attributed to uptake of triticonazole by roots not keeping pace with shoot growth and increased retention in the roots of triticonazole taken up. The main factor limiting the uptake of triticonazole by the roots may be the rapid growth of the uptake-active apical root parts out of the dressing zone which had formed in the soil. Distribution of triticonazole equivalents taken up by the main shoot showed a decreasing concentration gradient from the oldest to the youngest leaf. An increase in the seed treatment dose was investigated as a way to increase the concentration of triticonazole in the shoots, but its influence remained limited. © 1998 SCI  相似文献   
5.
The uptake of 14C-labelled triticonazole by wheat caryopses during imbibition was investigated. The uptake from an aqueous solution appeared to be driven by mass flow rather than by accumulation in seed lipids. During treatment with a liquid seed-dressing preparation of triticonazole, c. 1 μg triticonazole per caryopsis (2·4% of applied triticonazole) entered the seed. During germination in soil, another c. 1 μg triticonazole per caryopsis entered the seed in 24 h. In killed seeds, no penetration was observed between 24 h and 72 h after the beginning of imbibition. After seed treatment and imbibition in soil, triticonazole appeared to be located in the seed coats and embryo, but not in endosperm; experiments suggested that the testa acted as a barrier. Under our conditions, the pathway from seed coats to shoots was not an important route for triticonazole uptake by the shoots. © 1997 SCI.  相似文献   
6.
Variation in movement between individuals can have important ecological effects on populations and ecosystems, yet the factors driving differences in movement and their consequences remain poorly understood. Here, individual variability in the movements of juvenile (age 0 +  and 1 +  year) pike Esox lucius was assessed using passive integrated transponder (PIT) telemetry in off‐channel nursery areas over a 26‐ month period. Differences in the movement patterns of individuals were tested against their body sizes, ages, growth rates and trophic positions using data collected through a combination of catch‐and‐release sampling and stable isotope analyses. Results revealed that variation in movement between individuals was affected by age, with 1 +  individuals moving more than individuals of age 0 + , but not length. Individuals whose TP was low on their initial capture event moved significantly less than those with a higher initial TP. Individuals that moved more grew faster and achieved a higher final TP. These results suggest that higher activity (i.e., increased movement) increases resource acquisition that enhances growth rates, which could ultimately maximise individual performances.  相似文献   
7.
During the summer of 2010, 31 species including fish, echinoderms, gastropods, crustaceans, cephalopods and sponges were sampled in the Bay of Villefranche on the French Mediterranean coast and screened for the presence of PLTX-group toxins using the haemolytic assay. Liquid chromatography tandem mass spectrometry (LC-MS/MS) was used for confirmatory purposes and to determine the toxin profile. The mean toxin concentration in the whole flesh of all sampled marine organisms, determined using the lower- (LB) and upper-bound (UB) approach was 4.3 and 5.1 µg·kg−1, respectively, with less than 1% of the results exceeding the European Food Safety Authority (EFSA) threshold of 30 µg·kg−1 and the highest values being reported for sea urchins (107.6 and 108.0 µg·kg−1). Toxins accumulated almost exclusively in the digestive tube of the tested species, with the exception of octopus, in which there were detectable toxin amounts in the remaining tissues (RT). The mean toxin concentration in the RT of the sampled organisms (fishes, echinoderms and cephalopods) was 0.7 and 1.7 µg·kg−1 (LB and UB, respectively), with a maximum value of 19.9 µg·kg−1 for octopus RT. The herbivorous and omnivorous organisms were the most contaminated species, indicating that diet influences the contamination process, and the LC-MS/MS revealed that ovatoxin-a was the only toxin detected.  相似文献   
8.
9.

Background

Protein N-glycosylation is initiated within the endoplasmic reticulum through the synthesis of a lipid-linked oligosaccharides (LLO) precursor. This precursor is then transferred en bloc on neo-synthesized proteins through the action of the oligosaccharyltransferase giving birth to glycoproteins. The N-linked glycans bore by the glycoproteins are then processed into oligomannosides prior to the exit of the glycoproteins from the endoplasmic reticulum and its entrance into the Golgi apparatus. In this compartment, the N-linked glycans are further maturated in complex type N-glycans. This process has been well studied in a lot of eukaryotes including higher plants. In contrast, little information regarding the LLO precursor and synthesis of N-linked glycans is available in microalgae.

Methods

In this report, a user-friendly extraction method combining microsomal enrichment and solvent extractions followed by purification steps is described. This strategy is aiming to extract LLO precursor from microalgae. Then, the oligosaccharide moiety released from the extracted LLO were analyzed by multistage tandem mass spectrometry in two models of microalgae namely the green microalgae, Chlamydomonas reinhardtii and the diatom, Phaeodactylum tricornutum.

Results

The validity of the developed method was confirmed by the analysis of the oligosaccharide structures released from the LLO of two xylosyltransferase mutants of C. reinhardtii confirming that this green microalga synthesizes a linear Glc3Man5GlcNAc2 identical to the one of the wild-type cells. In contrast, the analysis of the oligosaccharide released from the LLO of the diatom P. tricornutum demonstrated for the first time a Glc2Man9GlcNAc2 structure.

Conclusion

The method described in this article allows the fast, non-radioactive and reliable multistage tandem mass spectrometry characterization of oligosaccharides released from LLO of microalgae including the ones belonging to the Phaeodactylaceae and Chlorophyceae classes, respectively. The method is fully adaptable for extracting and characterizing the LLO oligosaccharide moiety from microalgae belonging to other phyla.
  相似文献   
10.
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