scholarly journals Uniparental ancestry markers in Chilean populations

2016 ◽  
Vol 39 (4) ◽  
pp. 573-579 ◽  
Author(s):  
Camilla Dutra Vieira-Machado ◽  
Maluah Tostes ◽  
Gabrielle Alves ◽  
Julio Nazer ◽  
Liliana Martinez ◽  
...  
Keyword(s):  
2019 ◽  
Vol 139 (4) ◽  
pp. 340-344 ◽  
Author(s):  
Marcos V. Goycoolea ◽  
Mario Castro ◽  
Marcelo Galvez ◽  
Carlos Montoya ◽  
Jorge Fuentes ◽  
...  

Zootaxa ◽  
2011 ◽  
Vol 2880 (1) ◽  
pp. 20 ◽  
Author(s):  
HELEN DÍAZ-PÁEZ ◽  
MARCELA A. VIDAL ◽  
JUAN C. ORTIZ ◽  
CARMEN A. ÚBEDA ◽  
NÉSTOR G. BASSO

The frog genus Atelognathus is currently represented by nine species distributed in Argentinean and Chilean Patagonia. It is mainly distributed in Argentina, and there are only three species in Chile (A. ceii, A. grandisonae and A. jeinimenensis). Regarding the morphological relationships among Atelognathus species, Meriggio et al. (2004) suggest that A. jeinimenensis is more related to A. salai than other species. A. salai was described from Laguna Los Gendarmes (Argentina), 90 km air line from the type locality of A. jeinimenensis. This paper presents a morphological analysis and a study of population genetics using mtDNA nucleotide data from Argentinean and Chilean localities to assess the genetic distance between A. salai and A. jenimenensis. We obtained 477 bp-long d-loop sequences from 51 Atelognathus specimens collected in four localities. According to our results, the morphological differences between A. salai and A. jeinimenensis populations are limited to size, and there are no distinctive characteristics that would separate two species, in addition to which a simple geographic pattern of genetic diversity suggests a single species of Atelognathus. Also, the populations from Chile (Cerro Castillo, RN Lago Jeinimeni and Chile Chico) and Argentina (Laguna de Los Gendarmes) have low levels of genetic divergence that may be consistent with glaciations during the Late Pleistocene. We propose Atelognathus jeinimenensis as a junior synonym of A. salai and that the Chilean populations should be assigned to A. salai.


2005 ◽  
Vol 95 (4) ◽  
pp. 289-298 ◽  
Author(s):  
L.M. Winder ◽  
C.B. Phillips ◽  
C. Lenney-Williams ◽  
R.P. Cane ◽  
K. Paterson ◽  
...  

AbstractEight South American geographical populations of the parasitoidMicroctonus hyperodaeLoan were collected in South America (Argentina, Brazil, Chile and Uruguay) and released in New Zealand for biological control of the weevilListronotus bonariensis(Kuschel), a pest of pasture grasses and cereals. DNA sequencing (16S, COI, 28S, ITS1, β-tubulin), RAPD, AFLP, microsatellite, SSCP and RFLP analyses were used to seek markers for discriminating between the South American populations. All of the South American populations were more homogeneous than expected. However, variation in microsatellites and 16S gene sequences corroborated morphological, allozyme and other phenotypic evidence of trans-Andes variation between the populations. The Chilean populations were the most genetically variable, while the variation present on the eastern side of the Andes mountains was a subset of that observed in Chile.


Zootaxa ◽  
2011 ◽  
Vol 3135 (1) ◽  
pp. 55
Author(s):  
PABLO TETA ◽  
ULYSES F. J. PARDIÑAS ◽  
GUILLERMO D’ELÍA

Central Chilean populations of the mouse Loxodontomys Osgood were traditionally (e.g., Pine et al., 1979) included as part of the single species recognized in the genus, L. micropus (Waterhouse). Later, Spotorno et al. (1998) considered that they belong to an up to then undescribed species for which they coined the name L. pikumche. This taxon, with type locality in “... Cajón del Río Maipo, sector Cruz de Piedra (34º 10’ S 69º 58’ W, 2.450 msnm), a 55 km S de la Central Hidroeléctrica de Las Melosas... en la Cordillera de la Región Metropolitana” is characterized by a 2n = 32 (NF = 34) and some subtle morphological differences with L. micropus (that, in turn, has a 2n = 34, NF = 36; Spotorno et al., 1998; Teta et al., 2009). More recently, Novillo et al. (2009) reported the first record of L. pikumche in the Argentinean province of Mendoza and added some putative morphological differences with L. micropus to those previously listed by Spotorno et al. (1998). As discussed by Cañon et al. (2010), the morphological characters  documented as differences by Novillo et al. (2009) have some degree of variation within populations of L. micropus s.s. (e.g., zygomatic plate morphology, lateral profile of nasals, development of posterior palate process; see Hershkovitz, 1962; Steppan, 1995) or were based on misinterpretation of some features (e.g., both specimens studied by Novillo et al. [2009] has posteriorly divergent toothrows, and not only that of micropus). Indeed, the distinction of L. pikumche was recently put in interdict by Cañon et al. (2010) on the base of molecular and morphological evidence. These authors remarked that several putative diagnostic characters (e.g., molar root numbers, incisor orientation, shape of upper incisor dentine fissure) vary within and among populations of L. micropus s.s. Further, Cañon et al. (2010) suggested that L. pikumche may be a junior synomyn of L. m. alsus (Thomas, 1919).


1975 ◽  
Vol 123 (3) ◽  
pp. 185-198 ◽  
Author(s):  
D. Fr�as L. ◽  
R. Godoy ◽  
P. Iturra ◽  
S. Koref-Santib��ez ◽  
J. Navarro ◽  
...  

1978 ◽  
Vol 5 (6) ◽  
pp. 533-538 ◽  
Author(s):  
Carlos Y. Valenzuela ◽  
Francisco Rothhammer ◽  
Ranajit Chakraborty

2016 ◽  
Vol 82 (1-2) ◽  
pp. 16-20
Author(s):  
Mónica Acuña ◽  
Eric Pinto ◽  
Paulina Olivares ◽  
Carolina Ríos

Behaviour ◽  
1997 ◽  
Vol 134 (1-2) ◽  
pp. 105-125 ◽  
Author(s):  
Patricia Campos ◽  
Marisol Bustamante ◽  
José Luis Cancino ◽  
Raltl Godoy-Herrera

AbstractThe patterns of movement and foraging were investigated in larvae of the Chilean sympatric species D. melanogaster and D. simulans. Frequencies of 'rover', 'sitter' and 'digger' larvae, as well as locomotion and the angle size of turning were recorded in nutritive and non-nutritive environments. In these environments the sibling species differ in frequencies of 'rover', 'sitter' and 'digger' larval phenotypes. There are also differences in these frequencies between the populations of each species and across larval age. As development proceeds, the larvae of D. melanogaster and D. simulans become more diverse in their behaviours. Depending on larval age, strain and species, larval locomotion may be: i) similar in the presence and in the absence of food (D. simulans), ii) lower in yeast suspension than on agar (D. melanogaster), iii) higher in the presence of food than on agar (D. simulans). The angle size of larval turning also shows variability which depends on larval age, strain and species. Statistical significance of the correlation between locomotion and turning, and the regression of turning on locomotion in larvae of D. melanogaster and D. simulans depends on larval age, strain, species and the environment in which the larvae grow.


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