Analysis of the genotoxic potential of low concentrations of Malathion on the Allium cepa cells and rat hepatoma tissue culture

Based on the concentration of Malathion used in the field, we evaluated the genotoxic potential of low concentrations of this insecticide on meristematic and F₁ cells of Allium cepa and on rat hepatoma tissue culture (HTC cells). In the A. cepa, chromosomal aberrations (CAs), micronuclei (MN), and mitotic index (MI) were evaluated by exposing the cells at 1.5, 0.75, 0.37, and 0.18 mg/mL of Malathion for 24 and 48 hr of exposure and 48 hr of recovery time. The results showed that all concentrations were genotoxic to A. cepa cells. However, the analysis of the MI has showed non-relevant effects. Chromosomal bridges were the CA more frequently induced, indicating the clastogenic action of Malathion. After the recovery period, the higher concentrations continued to induce genotoxic effects, unlike the observed for the lowest concentrations tested. In HTC cells, the genotoxicity of Malathion was evaluated by the MN test and the comet assay by exposing the cells at 0.09, 0.009, and 0.0009 mg/5 mL culture medium, for 24 hr of exposure. In the comet assay, all the concentrations induced genotoxicity in the HTC cells. In the MN test, no significant induction of MN was observed. The genotoxicity induced by the low concentrations of Malathion presented in this work highlights the importance of studying the effects of low concentrations of this pesticide and demonstrates the efficiency of these two test systems for the detection of genetic damage promoted by Malathion.     

水环境:巴西大西洋流域盆地的人为压力和生态系统变化

发展中国家中正面临经济发展挑战的那些人口密集的流域盆地和海岸带地区可能会在各种问题上受到中度或严重的环境影响.这些由巴西东北部至南部流向大西洋海岸的汇水盆地包括广阔的气候带和多种生态系统.盆地边界以内分布着大西洋雨林、大范围的半干旱热带旱生林(caatinga)、广阔的树木及灌木林地(cerrado)、巴西6670km 海岸线的一大部分及其海洋生态系统.在过去的几十年中,这些自然资源上的人类活动不断发展.海滨化已给沿海生境及生物群落造成了沉重的负担.caatinga和cerrado中的大部分原生植被遭到了破坏,仅存留了7%的大西洋原始雨林.河口、海湾和沿海泻湖也遭到了无法恢复的破坏.土地使用、筑坝和分水等活动已成为造成生境丧失和水生生态系统改变的主要原因.尽管巴西东北部地区的干旱和东南部及南部地区的富庶和工业化之间形成明显反差,但给上述两种地区的生境和生物群落造成的影响是同样严重的.阻止环境恶化的努力没有见到效果.为此建议,应该实行将重点集中在水生生态系统完整性的一些更加综合性的环境政策,而不是把重点单独地集中在自然资源上.     

Prenatal analysis of the insulin receptor gene in a family with leprechaunism

Leprechaunism is an autosomal recessive disease characterized by intrauterine and postnatal growth restriction, loss of glucose homeostasis, and severe insulin resistance. This disease is caused by a failure of function of the insulin receptor and is lethal early in life. Here we report the prenatal diagnosis of leprechaunism in one consanguineous family, Atl-1, in which two homozygous-affected siblings died with leprechaunism. The mutation in their insulin receptor impaired insulin binding and altered receptor signalling. Prenatal diagnosis could not be accomplished using insulin binding to cultured amniocytes, but was possible using mutational analysis of the insulin receptor gene in DNA from amniotic cells.     

The impact of the 12 May 2008 Wenchuan earthquake on industrial facilities

This study describes the results of a field trip to the area affected by the 12 May, 2008, Wenchuan earthquake to analyse its impact on industrial facilities. The damage severity correlates well with the age of the plant, with older facilities having suffered more extensive and severe damage than those built more recently according to the latest design codes. The main cause of worker death and injury was the collapse of warehouses, office and manufacturing buildings. This concerned mostly concrete structures with insufficient confinement or poor reinforcement. The falling debris resulted in equipment damage and loss, as well as pipe severing and crushing. Pipes were also severed or bent when connected tanks were displaced or buildings collapsed. Numerous hazardous-materials releases occurred with spills being the dominant accident scenario. In some sites soil–liquefaction induced damage was evident, highlighting the need to consider potential site effects when selecting the location for a facility. The impact of the Wenchuan earthquake on chemical facilities confirms the findings from other earthquakes in terms of typical Natech damage and failure modes, as well as of hazardous-materials release potential and mechanisms.     

Environmental Subsidiarity as a Guiding Principle for Forestry Governance: Application to Payment for Ecosystem Services and REDD+ Architecture

This article describes and proposes the “environmental subsidiarity principle” as a guiding ethical value in forestry governance. Different trends in environmental management such as local participation, decentralization or global governance have emerged in the last two decades at the global, national and local level. This article suggests that the conscious or unconscious application of subsidiarity has been the ruling principle that has allocated the level at which tasks have been assigned to different agents. Based on this hypothesis this paper describes the principle of subsidiarity and its application to environmental policies within forest governance and proposes the “environmental subsidiarity” principle as a critical conceptual tool for sustainable resource management. The paper explains as an example how “environmental subsidiarity” is the key principle that can link payment for ecosystem services (PES) with environmental public policies and applies this principle with all its political consequences to reducing emissions from deforestation and forest degradation, and enhancing forest carbon stocks in developing countries (REDD+) architecture. It concludes by showing how the adoption of “environmental subsidiarity” as a ethical principle could help to maximize benefits to all stakeholders involved in PES schemes such as REDD+.     

First trimester diagnosis of β-thalassaemia in a twin pregnancy

This paper reports the results of first trimester prenatal diagnosis in a twin pregnancy at risk for homozygous β°−thalassaemia (β°−39 mutant). Trophoblast samples from both twins were obtained at 10 weeks gestation with a forceps guided by ultrasound. Trophoblast DNA analysis, carried out with the oligonucleotide technique, revealed that one fetus was homozygous and the other heterozygous for the β−39 mutant. This diagnosis was confirmed at 17 weeks gestation by amniocyte DNA analysis. DNA polymorphism analysis within the α-globin gene provided useful genetic markers for twin differentiation.     

Prenatal diagnosis of dyssegmental dwarfism

Fetal ultrasound evaluations at 18 weeks gestation on two consecutive pregnancies of a woman who previously gave birth to a stillborn female affected with dyssegmental dwarfism, resulted in accurate diagnoses of unaffected and affected fetuses. Marked disorganization of vertebral bodies and associated encephalocele found in two affected cases in this family are consistent with the original observation of this new syndrome as two major aspects which differentiate it from other forms of lethal dwarfism.