BackgroundDNA barcoding as a tool for species identification has been successful in animals and other organisms, including certain groups of plants. The exploration of this new tool for species identification, particularly in tree species, is very scanty from biodiversity-rich countries like India. rbcL and matK are standard barcode loci while ITS, and trnH-psbA are considered as supplementary loci for plants.Methodology and Principal FindingsPlant barcode loci, namely, rbcL, matK, ITS, trnH-psbA, and the recently proposed ITS2, were tested for their efficacy as barcode loci using 300 accessions of tropical tree species. We tested these loci for PCR, sequencing success, and species discrimination ability using three methods. rbcL was the best locus as far as PCR and sequencing success rate were concerned, but not for the species discrimination ability of tropical tree species. ITS and trnH-psbA were the second best loci in PCR and sequencing success, respectively. The species discrimination ability of ITS ranged from 24.4 percent to 74.3 percent and that of trnH-psbA was 25.6 percent to 67.7 percent, depending upon the data set and the method used. matK provided the least PCR success, followed by ITS2 (59. 0%). Species resolution by ITS2 and rbcL ranged from 9.0 percent to 48.7 percent and 13.2 percent to 43.6 percent, respectively. Further, we observed that the NCBI nucleotide database is poorly represented by the sequences of barcode loci studied here for tree species.ConclusionAlthough a conservative approach of a success rate of 60–70 percent by both ITS and trnH-psbA may not be considered as highly successful but would certainly help in large-scale biodiversity inventorization, particularly for tropical tree species, considering the standard success rate of plant DNA barcode program reported so far. The recommended matK and rbcL primers combination may not work in tropical tree species as barcode markers.
Floodwater was characterized through ®eld surveys over three years in rainfed lowland and deepwater rice areas of Eastern India. Measurements focused on dissolved O 2 and CO 2 , pH and irradiance during¯ash¯oods in rice ®elds. Over locations and time, dissolved O 2 concentrations ranged from zero to 0.28 mol m 73 (0±1.1 times air-saturated water at 30 8C) while dissolved CO 2 ranged from 0.28 to 1.96 mol m 73 (31±217 times air-saturated water). Floodwater pH varied from 6.6 to 9.7. Irradiance decreased with depth in the water pro®le to an extent depending on turbidity. Turbidity varied greatly over locations and time. The signi®cance of these measurements in assessing rice submergence tolerance is discussed.
In this study Tyagi et al. determined the genetic diversity and population structure of the model plant, Arabidopsis thaliana. These populations inhabit west Himalaya, an undersampled region. Using 19 genomic SSR and 11 chloroplast markers they determined that these populations are highly structured and genetically distinct from the rest of the world populations. They also observed that the populations were structured at the altitudinal level. Additionally their molecular clock analysis showed that these populations are not recent introductions and have inhabited the Himalayan region for about 130,000 years.
Low productivity of pilosae type lentils grown in South Asia is attributed to narrow genetic base of the released cultivars which results in susceptibility to biotic and abiotic stresses. For enhancement of productivity and production, broadening of genetic base is essentially required. The genetic base of released cultivars can be broadened by using diverse types including bold seeded and early maturing lentils from Mediterranean region and related wild species. Genetic diversity in eighty six accessions of three species of genus Lens was assessed based on twelve genomic and thirty one EST-SSR markers. The evaluated set of genotypes included diverse lentil varieties and advanced breeding lines from Indian programme, two early maturing ICARDA lines and five related wild subspecies/species endemic to the Mediterranean region. Genomic SSRs exhibited higher polymorphism in comparison to EST SSRs. GLLC 598 produced 5 alleles with highest gene diversity value of 0.80. Among the studied subspecies/species 43 SSRs detected maximum number of alleles in L. orientalis. Based on Nei’s genetic distance cultivated lentil L. culinaris subsp. culinaris was found to be close to its wild progenitor L. culinaris subsp. orientalis. The Prichard’s structure of 86 genotypes distinguished different subspecies/species. Higher variability was recorded among individuals within population than among populations.
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