Seedling vigour is an important characteristic in relation to crop growth and yield. Traits such as photosynthetic capacity and chlorophyll content contribute significantly to seedling establishment at the early growth stage in various crop species, including rice. A diverse panel of 227 rice varieties from several countries was evaluated to determine chlorophyll contents at multiple time points during the seedling stage using a soil–plant analysis development (SPAD) meter, a non‐destructive portable device. Using new statistical approaches, several chromosomal regions associated with variations in chlorophyll content in the third leaf at 13, 16 and 19 days after imbibition were detected. A single nucleotide polymorphism (SNP) cluster on the end of chromosome 11 was significantly associated with the onset of leaf senescence. This region was enriched with genes related to cell death and the stress response. We have identified rice germplasm showing delayed‐senescence phenotypes, these could be suitable donors and genetic resources for breeding, and the use of significant SNP markers associated with these traits could enhance the efficiency of their selection in breeding programmes. 相似文献
We present an overview of a research platform that provides essential germplasm, genotypic and phenotypic data and analytical tools for dissecting phenotype–genotype associations in rice. These resources include a diversity panel of 400 Oryza sativa and 100 Oryza rufipogon accessions that have been purified by single seed descent, a custom-designed Affymetrix array consisting of 44,100 SNPs, an Illumina GoldenGate assay consisting of 1,536 SNPs, and a suite of low-resolution 384-SNP assays for the Illumina BeadXpress Reader that are designed for applications in breeding, genetics and germplasm management. Our long-term goal is to empower basic research discoveries in rice by linking sequence diversity with physiological, morphological, and agronomic variation. This research platform will also help increase breeding efficiency by providing a database of diversity information that will enable researchers to identify useful DNA polymorphisms in genes and germplasm of interest and convert that information into cost-effective tools for applied plant improvement. 相似文献
The protein requirements for optimal growth and health of juvenile New Zealand black‐footed abalone (Haliotis iris) under different water temperatures were investigated. Six diets with different crude protein amounts (0, 10, 20, 30, 40 and 45%) and two temperature regimes (13–21 and 8–16 °C) were used to culture juvenile abalone over a 4‐month period. Growth (shell lengths and animal weights) and health (survival, activity and mucous production) parameters were recorded for animals within all protein and temperature combinations. Proximate analyses and amino acid profiles were also performed on the diets, soft bodies (including gonad), and shells to evaluate the overall nutrient contents (diet and animal) and requirements (animal). The results indicate that the protein requirements for juvenile H. iris are higher when the environmental temperatures are low. Thus, increasing the dietary protein level results in better growth [i.e. increase in soft body (including gonad) crude protein and mean protein gain] and health (i.e. more goblet cells and thicker epithelial layers). Results from amino acid profiles in abalone soft bodies (including gonad) and shells show that these parameters did not change considerably with different dietary protein levels, but temperature did affect the concentration of several amino acids in both soft bodies (including gonad) and shells. 相似文献
Microalgal biofilms with different amino acid profiles were investigated for their ability to induce abalone, Haliotis iris, attachment, metamorphosis, shell stage, and survival. Twenty microalgal strains, isolated from rocky shores and sandy estuaries, were grown in the laboratory to produce young and matured monospecific biofilms. Abalone larvae were exposed to the different biofilm treatments and controls (no biofilms) for 7 (attachment and metamorphosis) and 14 (shell stage and survival) d. The larvae performed significantly better in biofilms compared with controls across microalgal strains, but attachment, metamorphosis, shell stage, and survival were generally less than about 50, 35, 25, and 25%, respectively. Some microalgal strains belonging to the same species but collected from different sites had different effects on the larvae, likely due to variations in biochemical composition and activity among strains. Although no clear relationship was found between the microalgal amino acid profiles and larval processes, percentage biofilm cover and total amino acids were positively correlated with some of these processes. In addition, abalone performed significantly better when exposed to mature compared with young biofilms. These results may be due to the greater amounts of microalgal cells and their extracellular polymers within older biofilms, which may cue larvae toward more nutritionally favorable environments. 相似文献
Physical properties which included shell stiffness, egg weight, width and length, shell weight and thickness, percentage shell, shell weight per unit area, shape index and roundness were studied in relation to maximum force and energy absorbed at failure in 2733 eggs produced by sixty SCWL pullets. Pooled‐egg, bird‐average and individual‐bird bases were used for correlation and regression analyses.
All physical properties in combination accounted for 61.9 and 88.2 per cent of the variation in force and 19.6 and 59.5 per cent of energy absorbed at failure in pooled‐egg and bird‐average analyses respectively. The non‐destructive measurements of shell stiffness, egg size and shape gave R2 values of 60.5 and 86.9 per cent with force and 16.2 and 55.0 per cent with energy in corresponding analyses.
Shell stiffness proved to be the most important predictor of force at failure. Analyses in which variation of shell stiffness was explained by other physical properties supported the conclusion based on theories of elasticity applied to shell structures that shell stiffness was largely an indirect measurement of egg shell quantity together with lesser effects of egg size and shape.
Bird‐to‐bird variation in relations between physical properties and shell strength was evident from individual bird analyses. Coefficients of determination from force at failure regressed on shell stiffness had a mean value of 0.455 with a standard deviation of 0.178 (n = 60). 相似文献
Indole-3-carbinol (I3C), a potential anticancer substance, can be found in cruciferous (cabbage family) vegetables, mainly cauliflower and Chinese cabbage. However, the bioactivity of I3C on the apoptotic effects of murine leukemia WEHI-3 cells and promotion of immune responses in leukemia mice model are unclear. In this study, we investigated the effect of I3C on cell-cycle arrest and apoptosis in vitro and immunomodulation in vivo. I3C decreased the viable WEHI-3 cells and caused morphological changes in a concentration- and time-dependent manner. I3C also led to G0/G1 phase arrest, decreased the levels of cyclin A, cyclin D, and CDK2, and increased the level of p21(WAF1/CIP1). Flow cytometric analyses further proved that I3C promoted ROS and intracellular Ca(2+) production and decreased the levels of ΔΨ(m) in WEHI-3 cells. Cells after exposure to I3C for 24 h showed DNA fragmentation and chromatin condensation. Comet assay also indicated that I3C induced DNA damage in examined cells. I3C increased the levels of cytochrome c, FADD, GADD153, GRP78, and caspase-12 as well as induced activities of caspase-3, -8, and -9. Moreover, I3C attenuated NF-κB DNA binding activity in I3C-treated WEHI-3 cells as shown by EMSA and Western blotting analyses. In the in vivo study, we examined the effects of I3C on WEHI-3 leukemia mice. Results showed that I3C increased the level of T cells and decreased the level of macrophages. I3C also reduced the weights of liver and spleen, and it promoted phagocytosis by macrophages as compared to the nontreated leukemia mice group. On the basis of our results, I3C affects murine leukemia WEHI-3 cells both in vitro and in vivo. 相似文献