Molecular insight into the population structure of common and spotted dolphins inhabiting the pelagic waters of the Northeast Atlantic

Several cetacean species exhibit fine-scale population structure despite their high dispersal capacities and the apparent continuity of the marine environment. In dolphins, most studies have focused on coastal areas and continental margins, and they revealed differentiated populations within relatively small geographic areas, sometimes in conjunction with a specialisation for different habitats (ecotypes). We analysed the population genetic structure of short-beaked common dolphins (Delphinus delphis) and Atlantic spotted dolphins (Stenella frontalis) in the Azores and Madeira, the two most isolated archipelagos of the North Atlantic. The archipelago of the Azores is divided into three groups of islands and stands 900 km away from Madeira. It is not known whether individuals migrate between groups of islands and archipelagos, nor whether distinct ecotypes are present. These questions were investigated by genetic analyses of 343 biopsy samples collected on free-ranging dolphins. The analyses consisted in sequencing part of the mitochondrial hyper-variable region, screening up to 14 microsatellite loci, and molecular sexing. Results did not unravel any population structure at the scale of the study area. Lack of differentiation matches expectations for spotted dolphins, which are transient in both archipelagos, but not for common dolphins, which are present year-round in the Azores and potentially resident. Absence of genetic structure over hundreds and even thousands of kilometres implies the existence of gene flow over much larger distances than usually documented in small delphinids, which could be achieved through individual movements. This finding indicates that population structure in oceanic habitat differs from that observed in coastal habitat.     

Analysis of time-scaling properties in forest-fire sequence observed in Italy

The investigation of the temporal fluctuations in forest fires is an important topic in the context of environmental sciences. Time-scaling scale-invariant methodologies have been used to characterize the temporal properties of forest-fire sequences detected in the Italian territory. Our findings reveal that the fire sequences can be considered as fractal processes with a high degree of time-clusterization of the events. The time-clustering phenomenon is clearly visible from timescales of order of days. Furthermore the fire sequences observed with decreasing latitude tend to be more time-clusterized.     

Bio-based Films and Coatings: Sustainable Polysaccharide Packaging Alternatives for the Food Industry

Journal of Polymers and the Environment - Polymers used as raw materials for synthetic packaging, i.e., those obtained from petroleum-derived sources, are resistant to degradation. Because of this,...     

Spatial distribution of trace elements in surface sediments of Hooghly (Ganges) river estuary in West Bengal,India

The spatial distribution of trace elements in surface sediments of the Hooghly estuary was studied over the monsoons in 2014–2017. As, Cd, Ni, Pb and U were two- to sixteen-fold the crust means with increasing levels toward the estuary, with Ni peak during the post-monsoon. Pearson’s correlation matrix, cluster analysis, enrichment factors and pollution index revealed the anthropic source and association of trace elements with Fe, Mn and Al and of Pb with U. Geoaccumulation index revealed for Ni an extremely contaminated situation at the estuary water during monsoon and for Cd a heavily contaminated situation at freshwater location. The potential contamination index was >6; thus, sediments were very severely contaminated by As, Cd and Ni with worst situation for As and Cd at fresh and brackish water and during post-monsoon. The overall ecological risk was severe, 300≤RI<600 at all sites and seasons, especially after the monsoon, at fluvial and brackish locations.

     

Synthesis and application of graphene oxide as a nanoadsorbent to remove Cd (II) and Pb (II) from water: adsorption equilibrium,kinetics, and regeneration

Environmental Science and Pollution Research - In this work, graphene oxide (GO) was synthesized by the modified Hummers method. The nanomaterial was characterized by FTIR and Raman spectroscopy,...     

Evaluation of boron removal from water by hydrotalcite-like compounds

Layered double hydroxides (LDHs) or hydrotalcite (HT)-like compounds with different kinds of metal ions (Mg-Al and Mg-Fe) in the brucite-like sheets were prepared and their adsorption properties were studied in the boron removal from aqueous solution under laboratory conditions. The hydrotalcites were synthesized by the coprecipitation method and were characterized by chemical analyses, X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR) and specific surface area measurements (BET). The affinity of these materials with a mixture of B(OH)(3) and B(OH)(4)(-) was studied as a function of contact time, initial pH of the solutions, HT quantity and B concentration (adsorption isotherms). It was found that 120 min is enough time for the equilibrium state to be reached in boron adsorption. Boron removal was independent of the initial pH of the solutions because of the high buffering capacity of the LDHs. On the other hand, the adsorption capacity increases with increasing the adsorbent quantity. The adsorption isotherms, described by the Langmuir model, are of L-type, suggesting that B(OH)(4)(-) is adsorbed preferentially on HT-like materials. Besides, Mg-Al hydrotalcites showed higher adsorption capacity than Mg-Fe. We proposed that in Mg-Al hydrotalcites, the boron removal occurs by both adsorption on external surface and ion exchange, whereas for Mg-Fe it occurs only by surface adsorption. After treatment of a solution containing 5.2 mgBl(-1) with Mg-Al hydrotalcites the final boron concentration reached the recommended limit by WHO for drinking water (0.5 mgl(-1)).     

Resilience thinking applied to fisheries management: perspectives for the mullet fishery in Southern-Southeastern Brazil

The mullet fishery system encompasses a complex arrange of ecological and socioeconomic factors interacting in multiple scales on the Southern-Southeastern Brazilian coast. Similarly, to other fisheries in developing countries, overfishing and poor governance have been threatening the resilience of the mullet fishery. In this paper, we explore aspects related to fisheries management from the perspective of the concept of resilience. The industrial and artisanal fishery sectors represent the different stakeholders. The main issues of concern are related to failures in the fisheries management to properly address equity in resource access and resource use sustainability among stakeholders. Asymmetry in technology and political and economic power affect food security and income generation especially for subsistence and small-scale fishing. Despite changes in rules-in-use, overfishing and conflicts between resource users are still relevant. Fishery dynamics and resource availability are greatly affected locally by forces such as pollution, urbanization, non-selective fishing, and regionally, by the El Niño Southern Oscillation (ENSO), and industrial (purse-seine) fishery. Considering the influence of ENSO on this fishery, a time span of at least 7 years to investigate this system could provide better answers to improve the management. Effective resilient fisheries should rely on three aspects. First, there should be a flexible fish allocation system based on ecosystem variability. Secondly, fish allocation should prioritize food security and poverty alleviation. Thirdly, a monitoring system should be implemented that takes into consideration ecosystem, fisheries and human dimensions to support a flexible and adaptive fisheries management, with resilient fisheries as an ultimate goal.     

Adsorption behavior of alpha -cypermethrin on cork and activated carbon

Studies were undertaken to determine the adsorption behavior of alpha -cypermethrin [R)-alpha -cyano-3-phenoxybenzyl(1S)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate, and (S)-alpha-cyano-3-phenoxybenzyl (1R)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate] in solutions on granules of cork and activated carbon (GAC). The adsorption studies were carried out using a batch equilibrium technique. A gas chromatograph with an electron capture detector (GC-ECD) was used to analyze alpha -cypermethrin after solid phase extraction with C18 disks. Physical properties including real density, pore volume, surface area and pore diameter of cork were evaluated by mercury porosimetry. Characterization of cork particles showed variations thereby indicating the highly heterogeneous structure of the material. The average surface area of cork particles was lower than that of GAC. Kinetics adsorption studies allowed the determination of the equilibrium time - 24 hours for both cork (1-2 mm and 3-4 mm) and GAC. For the studied alpha -cypermethrin concentration range, GAC revealed to be a better sorbent. However, adsorption parameters for equilibrium concentrations, obtained through the Langmuir and Freundlich models, showed that granulated cork 1-2 mm have the maximum amount of adsorbed alpha-cypermethrin (q(m)) (303 microg/g); followed by GAC (186 microg/g) and cork 3-4 mm (136 microg/g). The standard deviation (SD) values, demonstrate that Freundlich model better describes the alpha -cypermethrin adsorption phenomena on GAC, while alpha -cypermethrin adsorption on cork (1-2 mm and 3-4 mm) is better described by the Langmuir. In view of the adsorption results obtained in this study it appears that granulated cork may be a better and a cheaper alternative to GAC for removing alpha -cypermethrin from water.