A Late Jurassic fossil assemblage in Gondwana: Biostratigraphy and correlations of the Tacuarembó Formation, Parana Basin, Uruguay

The Tacuarembó Formation has yielded a fossil assemblage that includes the best known body fossils, consisting of isolated scales, teeth, spines, and molds of bones, recovered from thin and patchy bonebeds, from the Botucatu Desert, Parana Basin, South America. The remains are preserved in the sandstones widespread around the city of Tacuarembó. We propose a new formalized nomenclature for the Tacuarembó Formation, naming its “Lower” and “Upper” members as the Batoví (new name) and Rivera (new rank) members, respectively. An assemblage zone is defined for the Batoví Member (fluviolacustrine and aeolian deposits). In this unit, the freshwater hybodontid shark Priohybodus arambourgi D’Erasmo is well represented. This species was previously recorded in Late Jurassic–Early Cretaceous units of the Sahara and the southern Arabian Peninsula. Globally considered, the fossil assemblage of this member (P. arambourgi, dipnoan fishes, Ceratosaurus-like theropods, and conchostracans) is indicative of a Kimmeridgian–Tithonian age, which in combination with the stratigraphic relationships of the Tacuarembó Formation with the overlying basalts of the Arapey Formation (132 My average absolute age) implies that the latter was deposited during the Kimmeridgian–Hauterivian interval.     

Steady flows driven by sources of random strength in heterogeneous aquifers with application to partially penetrating wells

Average steady source flow in heterogeneous porous formations is modelled by regarding the hydraulic conductivity K(x) as a stationary random space function (RSF). As a consequence, the flow variables become RSFs as well, and we are interested into calculating their moments. This problem has been intensively studied in the case of a Neumann type boundary condition at the source. However, there are many applications (such as well-type flows) for which the required boundary condition is that of Dirichlet. In order to fulfill such a requirement the strength of the source must be proportional to K(x), and therefore the source itself results a RSF. To solve flows driven by sources whose strength is spatially variable, we have used a perturbation procedure similar to that developed by Indelman and Abramovich (Water Resour Res 30:3385–3393, 1994) to analyze flows generated by sources of deterministic strength. Due to the linearity of the mathematical problem, we have focused on the explicit derivation of the mean head distribution G _d (x) generated by a unit pulse. Such a distribution represents the fundamental solution to the average flow equations, and it is termed as mean Green function. The function G _d (x) is derived here at the second order of approximation in the variance σ² of the fluctuation (where K _A is the mean value of K(x)), for arbitrary correlation function ρ(x), and any dimensionality d of the flow domain. We represent G _d (x) as product between the homogeneous Green function G _d ⁽⁰⁾(x) valid in a domain with constant K _A , and a distortion term Ψ _d (x) = 1 + σ²ψ _d (x) which modifies G _d ⁽⁰⁾(x) to account for the medium heterogeneity. In the case of isotropic formations ψ _d (x) is expressed via one quadrature. This quadrature can be analytically calculated after adopting specific (e.g.. exponential and Gaussian) shape for ρ(x). These general results are subsequently used to investigate flow toward a partially-penetrating well in a semi-infinite domain. Indeed, we construct a σ²-order approximation to the mean as well as variance of the head by replacing the well with a singular segment. It is shown how the well-length combined with the medium heterogeneity affects the head distribution. We have introduced the concept of equivalent conductivity K ^eq(r,z). The main result is the relationship where the characteristic function ψ^(w)(r,z) adjusts the homogeneous conductivity K _A to account for the impact of the heterogeneity. In this way, a procedure can be developed to identify the aquifer hydraulic properties by means of field-scale head measurements. Finally, in the case of a fully penetrating well we have expressed the equivalent conductivity in analytical form, and we have shown that (being the effective conductivity for mean uniform flow), in agreement with the numerical simulations of Firmani et al. (Water Resour Res 42:W03422, 2006).     

O,p'-DDT induction of vitellogenesis and its inhibition by tamoxifen in Nile tilapia (Oreochromis niloticus)

In order to investigate the mechanism by which o,p'-DDT disrupts endocrine functioning of Nile tilapia in vivo, the estrogenicity of o,p'-DDT was investigated in conjunction with 17beta-estradiol (E2) and tamoxifen. Mature, male tilapia were treated intraperitoneally with o,p'-DDT (60 mg/kg, one dose) or E2 (5 mg/kg, four doses) in the presence or absence of tamoxifen (5 mg/kg, six doses) for 12 days and then plasma vitellogenin (Vtg) (measured as alkaline-labile phosphorous), E2, and testosterone (T) were measured. Vtg levels were increased dramatically by E2 (1,744 +/- 171 microg/ml) and moderately by o,p'-DDT (82 +/- 15 microg/ml) compared with controls (23 +/- 3.5 microg/ml). Tamoxifen alone had no effect on Vtg production, but inhibited both E2 and o,p'-DDT stimulated vitellogenesis. T levels were reduced with E2 administration (1,688 +/- 383 pg/ml) and declined further with the combined treatment of E2 and tamoxifen (281 +/- 70 pg/ml), compared with controls (6,558 +/- 1,438 pg/ml). Tamoxifen or o,p'-DDT alone did not affect T levels, but their combined treatment did (2,069 +/- 647 pg/ml). The results of this study suggest that o,p'-DDT is weakly estrogenic in male tilapia, and that this activity may be mediated through the estrogen receptor.     

An aromatase inhibitor and tamoxifen decrease plasma levels of o,p-DDT and its metabolites in Nile tilapia (Oreochromis niloticus)

The objective of this study was to determine if tamoxifen or an aromatase inhibitor (4-hydroxyandrostenedione; 4-OHA) affected plasma concentrations of o,p^′-DDT and its metabolites, o,p^′-DDD and o,p^′-DDE, in mature tilapia. Male and female tilapia were injected 6 times intraperitoneally with o,p^′-DDT (40 mg/kg) alone or in combination with 4-OHA (2 mg/kg) over a 12 day period. An additional group of male fish was injected with tamoxifen (5 mg/kg) plus o,p^′-DDT. At the end of the treatment period, plasma samples were extracted and analyzed by GC/ECD. Females injected only with o,p^′-DDT had significantly higher levels of o,p^′-DDT compared with males. Interestingly, females and males treated concomitantly with o,p^′-DDT and 4-OHA or tamoxifen had significantly lower concentrations of plasma o,p^′-DDT (about 50%) compared with fish treated with only o,p^′-DDT. These initial results suggest that an interaction between endocrine-active compounds occurs in vivo in tilapia and may involve alterations in metabolism of o,p^′-DDT.     

Characterization of cholinesterase activity from different tissues of Nile tilapia (Oreochromis niloticus)

Cholinesterases (ChE) from brain, muscle and liver in Nile tilapia (Oreochromis niloticus) were characterized using three substrates: acetylthiocholine iodide, propionylthiocholine iodide, and butyrylthiocholine iodide. Eserine was used as a total ChE inhibitor; BW284c51 and iso-OMPA were used as selective inhibitors for acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), respectively. The results indicate that AChE is the enzyme present in brain, whereas in both liver and muscle, the presence of atypical ChEs are suggested. These findings indicate that characterization of ChE is necessary prior to use in monitoring programs.     

Effects of Pleistocene environmental changes on the distribution and community structure of the mammalian fauna of Mexico

Biological communities in Mexico experienced profound changes in species composition and structure as a consequence of the environmental fluctuations during the Pleistocene. Based on the recent and fossil Mexican mammal checklists, we determine the distribution, composition, diversity, and community structure of late Pleistocene mammalian faunas, and analyze extinction patterns and response of individual species to environmental changes. We conclude that (1) differential extinctions occurred at family, genus, and species level, with a major impact on species heavier than 100 kg, including the extinction all proboscideans and several ruminants; (2) Pleistocene mammal communities in Mexico were more diverse than recent ones; and (3) the current assemblages of species are relatively young. Furthermore, Pleistocene relicts support the presence of biogeographic corridors; important refugia existed as well as centers of speciation in isolated regions. We identified seven corridors: eastern USA–Sierra Madre Oriental corridor, Rocky Mountains–Sierra Madre Occidental corridor, Central United States–Northern Mexico corridor, Transvolcanic Belt–Sierra Madre del Sur corridor, western USA–Baja California corridor, Tamaulipas–Central America gulf lowlands corridor, and Sonora–Central America Pacific lowlands corridor. Our study suggests that present mammalian assemblages are very different than the ones in the late Pleistocene.     

Geologic evolution of the Donguinyó-Huichapan caldera complex,central Mexican Volcanic Belt,Mexico

The Donguinyó-Huichapan caldera complex is located 110 km to the NNW of Mexico City, in the central sector of the Mexican Volcanic Belt. It is a 10 km in diameter complex apparently with two overlapping calderas, each one related to an ignimbrite sequence that contrasts in composition, mineralogy, welding, distribution, and physical aspect. The geologic evolution of this complex includes the following phases, 1) A first caldera formed at 5.0 ± 0.3 Ma, with the eruption of several discrete pulses of andesitic to trachydacitic pyroclastic flows that produced a series of densely welded ignimbrites; 2) At 4.6 ± 0.3 Ma, several small shield volcanoes and cinder cones built the rim of this caldera and erupted basaltic-andesite and andesitic lava flows; 3) At 4.2 ± 0.2 Ma, a second caldera was formed associated to the eruption of the Huichapan Tuff, which is a rhyolitic pyroclastic sequence consisting of minor unwelded ignimbrites, pumice fall and surge deposits, and a voluminous welded ignimbrite; 4) Also yielding an age of 4.2 ± 0.2 Ma, several trachydacitic lava domes were extruded along the new ring fracture and formed the rim of the Huichapan caldera, as well as five intra-caldera domes of dacitic and trachydacitic composition. Peripheral volcanism includes a large 2.5 ± 0.1 Ma shield volcano that was emplaced on the Huichapan caldera rim.The two calderas that form the Donguinyó-Huichapan complex have contrasting differences in volcanic styles that were apparently due to their differences in composition. Products erupted by the Donguinyó caldera are basaltic-andesite to trachydacitic in composition, whereas Huichapan caldera products are all high-silica rhyolites.