Sister chromatid exchanges in first-trimester chorionic villi after in vivo and in vitro exposure to diagnostic ultrasound

A study was done to evaluate the effects of diagnostic ultrasound on sister chromatid exchange (SCE) in first-trimester chorionic villi under controlled technical conditions. Chromosome analysis was performed by the direct method using spontaneous mitoses from the cytotrophoblast layer, and SCE visualization was accomplished by a 72 h treatment with 5-bromodeoxyuridine (BrdU) at a concentration of 10μg/ml. The slides were stained with ac ridine orange. Immediately before first-trimester chorionic villus sampling, a group of ten pregnant women was exposed to diagnostic ultrasound for 20min (in vivo exposure). This group of patients was compared with a control group who were not exposed. A mean value of SCE/cell frequency of 4·2 ± 0·2 was found in the exposed pregnancies, while a value of 3·7 ± 0·2 was observed in the control group. After in vitro exposure of chorionic villi obtained from elective abortions, the frequency of SCE/cell did not differ significantly among samples with different exposures (1,2, and 3 h) and controls. The positive control (mitomycin C) yielded a significant increase in SCE frequency.     

Pelagic crinoids (Roveacrinida, Crinoidea) discovered in the Neogene of Poland

Until recently, it has been assumed that pelagic crinoids, the roveacrinids (Roveacrinida, Crinoidea), became extinct during the Cretaceous-Paleogene boundary event. Recent finds of well-preserved roveacrinidal remains (brachials and radials) in the Danian (Early Paleogene) of Poland showed that they survived into the earliest Cenozoic. This group was thus characterized as a "dead clade walking". Here, we present fossil evidence that these pelagic crinoids survived in Poland until at least the Middle Miocene (Badenian, ca. 14?Myr ago)-more than 50?Myr after their supposed extinction. These Miocene roveacrinids constitute the first documented evidence of Roveacrinida in strata of Neogene age, thus prolonging the stratigraphic range of pelagic crinoids. This find characterizes the order as a "Lazarus taxon" rather than a "dead clade walking" group.     

The hunter becomes the hunted: when cleptobiotic insects are captured by their target ants

Here we show that trying to rob prey (cleptobiosis) from a highly specialized predatory ant species is risky. To capture prey, Allomerus decemarticulatus workers build gallery-shaped traps on the stems of their associated myrmecophyte, Hirtella physophora. We wondered whether the frequent presence of immobilized prey on the trap attracted flying cleptoparasites. Nine social wasp species nest in the H. physophora foliage; of the six species studied, only Angiopolybia pallens rob prey from Allomerus colonies. For those H. physophora not sheltering wasps, we noted cleptobiosis by stingless bees (Trigona), social wasps (A. pallens and five Agelaia species), assassin bugs (Reduviidae), and flies. A relationship between the size of the robbers and their rate of capture by ambushing Allomerus workers was established for social wasps; small wasps were easily captured, while the largest never were. Reduviids, which are slow to extract their rostrum from prey, were always captured, while Trigona and flies often escaped. The balance sheet for the ants was positive vis-à-vis the reduviids and four out of the six social wasp species. For the latter, wasps began by cutting up parts of the prey’s abdomen and were captured (or abandoned the prey) before the entire abdomen was retrieved so that the total weight of the captured wasps exceeded that of the prey abdomens. For A. pallens, we show that the number of individuals captured during attempts at cleptobiosis increases with the size of the Allomerus’ prey.     

A methodological proposal for the evaluation of farmer’s adaptation to climate variability, mainly due to drought in watersheds in Central America

The current study shows the process and the results of a methodology proposed to contribute with the issue of how to evaluate the adaptation to climate variability and future climate change. The proposed methodology consists of a standard to evaluate farmer’s adaptation to climate variability, mainly due to drought in watersheds in Central America; and was created with contributions from experts and professionals around this region. The phases for this process were: (1) literature review about the topic, (2) development of a preliminary standard, (3) expert interviews for the evaluation of this preliminary standard, (4) construction of a standard to evaluate the issue of adaptation to climate variability emphasizing drought through contributions from experts and their preliminary evaluations, (5) applicability test of this standard for the evaluation of climate variability under real conditions and (6) application of this standard through a case study in the Aguas Calientes river sub-watershed in Nicaragua, which permanently undergoes drought problems and climate variability. This standard has five main principles that go from the general, considering regional and national policies and institutionalism, to the specifics at the level of watersheds. In addition to those principles, the standard contains ten criteria, 26 indicators and 51 verifiers distributed among the main five principles. In the process for testing this standard in the Aguas Calientes river watershed in Nicaragua, the score for the general applicability to this standard was middle-level (score of 3 in a scale of 1 to 5), although, for the main principles of this standard, the score was four (high).     

The presence of females modulates the expression of a carotenoid-based sexual signal

Several environmental factors have been shown to shape the pattern of investment of carotenoids into the expression of sexual signals. Surprisingly, the impact of the social environment has been neglected. If a carotenoid-based sexual trait is used by females to choose a mate or by males to assess the quality of potential competitors for mates, males, in the presence of females, should upregulate expression of the trait. We tested this hypothesis in male zebra finches that were housed either with females or in a male-only social environment. Additionally, to investigate whether the social modulation of the expression of a sexual trait depends on the physiological need of carotenoids, we challenged half of the males with Escherichia coli lipopolysaccharide (LPS). We found that the social environment modulated the expression of bill color, with males kept in the presence of females harboring a redder bill at the end of the 3 weeks that the experiment lasted. Males injected with LPS showed duller bill color regardless of the presence of females, and social interactions with females result in upregulated bill color similarly for phosphate-buffered saline (PBS) and LPS males. Thus, social environment and immune activation had an additive effect on the expression of bill color. The effect of social environment on plasma carotenoids was less clear. Indeed, a first replicate of the entire experiment showed that both immune challenge and social context affected bill color, with a negative effect of immune challenge and a positive effect of the presence of females on circulating carotenoids. However, a second replicate of the experiment showed only a negative effect of the immune challenge. These results, therefore, suggest that the social environment can affect the expression of carotenoid-based sexual traits under both benign and carotenoid-demanding conditions. Whatever the signaling function of bill color (female mate choice or male–male competition for mates), the observed flexibility may be adaptive because the expression of the signal can be modulated depending on the expected rewards or costs associated with the presence or absence of females. Nevertheless, the mechanisms underlying such an effect are still unknown.