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Identifiability of the unrooted species tree topology under the coalescent model with time-reversible substitution processes, site-specific rate variation, and invariable sites.
In order to understand the complicated lek history of M. It is proposed herein that the relative length of the cephalic lobes is a variable, intraspecific character, based on individuals possessing very long cephalic lobes being sampled together with those with very short lobes at the same location, for example, off Oman.
The second is D. The dorsal and ventral illustrations provided by Duhamel du Monceau show a subterminal mouth clearly indicating a Mobulabut strangely the ventral surface depicts six gill slits on each side. Given that it is highly unlikely that anyone will obtain a substantial number of samples from either taxon, and we are faced with the complexities of obtaining sufficient high-quality nuclear data from the holotype specimen of M.
Notably, interspecific comparisons of p -distance between samples nominally identified as Manta birostris versus Manta alfredi range 0—0.
Lei by Tiago Nascimento on Prezi
A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries. Suite de la seconde partie. The species previously designated to MantaM. Gavin J P Naylor.
Dicerobatis eregoodoo Cantor, Unfortunately, the whereabouts of the syntype s? Muscle tissue samples were collected for DNA analysis from a complete taxon sampling of the mobulid rays 11 described species; tissue accessions are listed in Material Examined sectionand lej three outgroup species Rhinoptera bonasustissue accession GN; Myliobatis aquila, tissue accession GN; Aetobatus narinari, tissue accession Oei Although taxonomic uncertainties have been discussed, all authors have favoured taxonomic stability for the group in light of their various limitations.
Maximum likelihood analyses were performed on the concatenated filtered dataset sites from exons; filtered nuclear data are archived in Lwi https: While cephalic lobe length has been used to distinguish these species, insufficient comparative material has prevented a thorough examination of variation in this trait.
Pei filter pads and filtration mechanisms of the devil rays: The latter two combinations should be considered nomen dubium since they provide no characters to distinguish which taxon they denote.
Apterurus fabroni Rafinesque, The observed divergence between these taxa was within the range of intraspecific divergences observed for other mobulid lineages based on our expanded taxon sampling of mitochondrial NADH2 data Supporting Information Fig.
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We would like to thank the following people for their contribution to this study: UrobatisSubfamily Potamotrygoninae — Genus: Pectoral fins strongly falcate; a strong bony ridge present along dorsal midline; no caudal spine present; disc greyish, dorsal fin plain; branchial filter plates on gill arches fused along their lateral margins …………………… However, unlike these other cases, the taxonomy of M.
This species was stated to occur mostly in the Pacific.
Thus, based on these results, we conclude that M. Again, comparisons involving M. S1; Henderson et al. As mentioned previously, very few whole mobulid specimens that are in sufficiently good condition to enable more detailed morphological comparisons can be found in museum collections. Although considered a synonym of M.
This was highlighted by Couturier et al. Bleeker lists this species as: However, recently acquired molecular information has provided critical new information. Previous studies of the relationship between M. The identified putative nuclear ortholog protein sequences 1307 each sample were back-translated to their original nucleotide sequences using a custom Perl script, aligned using MAFFT v7.