Methods for identifying species by using short orthologous DNA sequences, known as ''DNA barcodes,'' have been proposed and initiated to facilitate biodiversity studies, identify juveniles, associate sexes, and enhance forensic analyses. The cytochrome c oxidase 1 sequence, which has been found to be widely applicable in animal barcoding, is not appropriate for most species of plants because of a much slower rate of cytochrome c oxidase 1 gene evolution in higher plants than in animals. We therefore propose the nuclear internal transcribed spacer region and the plastid trnH-psbA intergenic spacer as potentially usable DNA regions for applying barcoding to flowering plants. The internal transcribed spacer is the most commonly sequenced locus used in plant phylogenetic investigations at the species level and shows high levels of interspecific divergence. The trnH-psbA spacer, although short (Ϸ450-bp), is the most variable plastid region in angiosperms and is easily amplified across a broad range of land plants.Comparison of the total plastid genomes of tobacco and deadly nightshade enhanced with trials on widely divergent angiosperm taxa, including closely related species in seven plant families and a group of species sampled from a local flora encompassing 50 plant families (for a total of 99 species, 80 genera, and 53 families), suggest that the sequences in this pair of loci have the potential to discriminate among the largest number of plant species for barcoding purposes.angiosperm ͉ internal transcribed spacer ͉ Plummers Island ͉ species identification ͉ trnH-psbA

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Rapid cycles of gene duplication and loss appear to have been going on in the region coding for the a chain of adult hemoglobin. This is inferred from restriction endonuclease analysis of the a gene region in five species of apes, whose common ancestor lived about 10 million years ago. Because all five species resemble humans in having duplicate a genes, the duplicate state of this region is probably at least as old as the common ancestor of all these species. However, the a polypeptides within these species are about 10 times more alike than is expected for 10 million years of divergent evolution.

We have found that human and ape ribosomal genes undergo concerted evolution involving genetic exchanges among nucleolus organizers on nonhomologous chromosomes. This conclusion is based upon restriction enzyme analysis of the ribosomal gene families in man and five ape species. Certain structural features were found to differ among (but not within) species even though the ribosomal genes have a multichromosomal distribution. Genetic exchanges among nucleolus organizer regions may be related to the well-known phenomenon of acrocentric chromosome associations observed in man and apes. Length variation in a region of the nontranscribed spacer was found in both chimpanzee species we examined. The nature of this length variation was found to be identical to that previously described in man. The origin of the length variation and its polymorphism within these three species might be explained by unequal alignment and unequal crossing-over among the ribosomal genes. An especially surprising finding was a nucleotide sequence polymorphism present in each individual human and ape we examined. Some ribosomal genes of each individual have a HindIl site in the 28S gene about 800 base pairs from the EcoRI site in this gene. The remaining 28S genes lack this HindII site. The presence of this polymorphism within individuals of every species we examined suggests that it has been maintained by natural selection.

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Understanding the relationships within the Caryophyllaceae has been difficult, in part because of arbitrarily and poorly defined genera and difficulty in determining phylogenetically useful morphological characters. This study represents the most complete phylogenetic analysis of the family to date, with particular focus on the genera and relationships within the large subfamily Alsinoideae, using molecular characters to examine the monophyly of taxa and the validity of the current taxonomy as well as to resolve the obscure origins of divergent taxa such as the endemic Hawaiian Schiedea. Maximum parsimony and maximum likelihood analyses of three chloroplast gene regions (matK, trnL-F, and rps16) from 81 newly sampled and 65 GenBank specimens reveal that several tribes and genera, especially within the Alsinoideae, are not monophyletic. Large genera such as Arenaria and Minuartia are polyphyletic, as are several smaller genera. The phylogenies reveal that the closest relatives to Schiedea are a pair of widespread, largely Arctic taxa, Honckenya peploides and Wilhelmsia physodes. More importantly, the three traditional subfamilies (Alsinoideae, Caryophylloideae, and Paronychioideae) are not reflective of natural groups; we propose abandoning this classification in favor of a new system that recognizes major lineages of the molecular phylogeny at the tribal level. A new tribe, Eremogoneae Rabeler & W.L. Wagner, is described here.