S3307对盆栽一串红的矮化效应

一串红喷施S3307后,植株高度降低,株型紧凑,节间缩短,叶色变浓,花序整齐,花色鲜艳.以20 mg*L- 1 S3307喷1次的矮化效果为最佳.     

Evaluation of two approaches to genotyping major histocompatibility complex class I in a passerine-CE-SSCP and 454 pyrosequencing

Genes of the highly dynamic major histocompatibility complex (MHC) are directly linked to individual fitness and are of high interest in evolutionary ecology and conservation genetics. Gene duplication and positive selection usually lead to high levels of polymorphism in the MHC region, making genotyping of MHC a challenging task. Here, we compare the performance of two methods for MHC class I genotyping in a passerine with highly duplicated MHC class I genes: capillary electrophoresis-single-strand conformation polymorphism (CE-SSCP) analysis and 454 GS FLX Titanium pyrosequencing. According to our findings, the number of MHC variants (called alleles for simplicity) detected by CE-SSCP is significantly lower than detected by 454. To resolve discrepancies between the two methods, we cloned and Sanger sequenced a MHC class I amplicon for an individual with high number of alleles. We found a perfect congruence between cloning/Sanger sequencing results and 454. Thus, in case of multi-locus amplification, CE-SSCP considerably underestimates individual MHC diversity. However, numbers of alleles detected by both methods are significantly correlated, although the correlation is weak (r = 0.32). Thus, in systems with highly duplicated MHC, 454 provides more reliable information on individual diversity than CE-SSCP.     

Pupal RNA interference methods for analyzing adult development in stag beetles

Holometabolous insects dramatically change their morphology via molt, both from larva to pupa and from pupa to adult. In nonmodel insects, RNA interference (RNAi) is a strong tool for analyzing gene function during postembryonic development. In many cases, larval RNAi is effective for analyzing genes involved in morphogenesis via metamorphosis. However, RNAi of genes involved in development sometimes results in lethality before animals metamorphose to pupae and/or adults, making it impossible to analyze their function during the pupal period. In this study, we establish a pupal RNAi system in the stag beetle Dorcus rectus. We selected the genes white and scarlet for RNAi knockdown to investigate appropriate injection timing and position. Both genes are known to be involved in eye pigmentation. By using these candidate genes, we demonstrate the potential of pupal RNAi in this experimental system. This method will be useful for analyzing pupal-specific morphogenesis including fine-shaping of the enlarged male mandible in this species.     

Staining of proteins on SDS polyacrylamide gels and on nitrocellulose membranes by Alta, a colour used as a cosmetic

We describe here the use of Alta, a pre-existing scarlet-red stain of cosmetic use, for staining proteins on sodium dodecyl sulfate (SDS) polyacrylamide gels, as well as for a single step staining of gels and nitrocellulose membranes during Western blot analysis. This stain, which is composed of 0.8% Crocein scarlet (brilliant crocein) and 0.2% Rhodamine B, is inexpensive, easy to use and nearly as sensitive as Coomassie Brilliant Blue (CBB) R-250. The gels can be stained in 10% Alta (2 h) and can be destained effectively only with 7% acetic acid as opposed to the conventional destainer (methanol/acetic acid/water) required for CBB-stained gels. In an alternative procedure, the proteins can be stained on the gel while electrophoresis by simply using 5% Alta in the top tank buffer and the stain can be viewed under UV-transilluminator. This procedure can also be used for Western blot analysis, as a single step procedure for staining of proteins on the gel as well as on the nitrocellulose membrane, as the stain is retained on the membrane after protein transfer. Thus, this staining procedure allows monitoring of proteins after each step in the Western blot, thereby eliminating the need to run separate gels for staining and Western blot analysis, and also the need for Ponceau Red S staining of the nitrocellulose membrane during Western blot analysis.     

Isolation and biochemical analysis of a temperature-sensitive scarlet eye color mutant of Drosophila melanogaster

Six new EMS-induced scarlet mutants were selected. Four of these were partially pigmented, with xanthommatin levels ranging from 12% to 45% of normal. In one (st ^754ts), pigment production was temperature sensitive; the level of xanthommatin changed from less than 10% of normal at 29 C to more than 70% at 18 C. In all of the new mutants tested, the level of early pupal 3-hydroxykynurenine was as low as low as that in st ¹. Thus reduced larval accumulation of this metabolite also appears to be a characteristic feature of scarlet mutants. Temperature-pulse and temperature-shift experiments were carried out with st ^754ts to determine the temperature-sensitive period for the scarlet gene during development. The major sensitive period commenced prior to the onset of pigmentation and was over before adult emergence. Thus the initiation of xanthommatin synthesis is not brought about by the activation of the scarlet gene. In similar experiments carried out with a temperature-sensitive white mutant (w ^bl), a similar temperature-sensitive period was obtained.This work was supported by Grant D2 75/15248 from the Australian Research Grants Committee and also by Grant GB 27599 from The National Science Foundation to Professor M. M. Green.     

Management for oak regeneration: Short-term effects on the bird community and suitability of shelterwood harvests for canopy songbirds

Interest in regenerating oaks (Quercus spp.) has promoted use of partial harvesting techniques that create an open forest structure. From 2007 to 2009, we studied songbirds in mixed-oak forests in southeastern Ohio, comparing shelterwoods recently harvested to 50% stocking and closed-canopy mature second-growth. We surveyed birds using distance-based methods (56 line transects in 18 stands at 4 forests). We intensively investigated suitability of shelterwoods for canopy-nesting species by examining habitat preferences, as measured by settlement patterns, age distributions, and site fidelity; we also examined nesting success. Several midstory and ground-nesting species were 26–73% less abundant in shelterwood than unharvested stands, whereas shrub-nesting species increased >100% several years post-harvesting. Canopy-nesting species were 31–98% more abundant in shelterwoods, but cerulean warbler (Setophaga cerulea) responses varied by forest. Patterns of settlement and site fidelity were generally similar among stands. Proportions of young males were actually greater for several species in shelterwood than unharvested stands, which may have been a consequence of young birds colonizing newly created (or improved) habitat. Even in our predominantly forested study system, nesting success (>700 nests) was low, ranging from 15% to 19% for yellow-throated vireos (Vireo flavifrons) and cerulean warblers, to 27–36% for scarlet tanagers, blue-gray gnatcatchers (Polioptila caerulea) and eastern wood-pewees (Contopus virens). However, nest survival did not differ between shelterwood and unharvested stands, possibly because numbers of avian predators did not change with harvesting. Despite increased numbers of brown-headed cowbirds (Molothrus ater) in shelterwoods, only 2% of canopy nests in which young could be identified were parasitized. Although these results suggest shelterwood harvests containing abundant overstory trees can provide short-term breeding habitat for canopy songbirds, long-term responses of birds to partial harvesting may differ from those documented here depending on different management options employed. Management for oak regeneration will typically remove all overstory trees later in the cutting cycle, initially resulting in loss of nesting substrates and hence breeding habitat for canopy songbirds. © 2011 The Wildlife Society.