A comparison of microplastic contamination in freshwater fish from natural and farmed sources

Contamination of aquatic systems mainly by urbanization and poor sanitation, deficient or lack of wastewater treatments, dumping of solid residues, and run off has led to the presence of particles, including manmade polymers, in tissues of many marine and freshwater species. In this study, the prevalence of microplastics (MPs) in freshwater fish from farmed and natural sources was investigated. Oreochromis niloticus from aquaculture farms in the Huila region in Colombia, and two local species (Prochilodus magdalenae and Pimelodus grosskopfii), naturally present in surface waters were sampled. Of the particles identified, fragments were the predominant type in the three tissue types (stomach, gill, and flesh) derived from farmed and natural fishes. MicroFT-IR spectroscopy was conducted on 208 randomly selected samples, with 22% of particles identified as MPs based on spectra with a match rate ≥ 70%. A total of 53% of identified particles corresponded to cellophane/cellulose, the most abundant particle found in all fish. Not all fish contained MPs: 44% of Oreochromis farmed fish contained MPs, while 75% of natural source fish contained MPs in any of its tissues. Overall, polyethylene terephthalate (PET), polyester (PES), and polyethylene (PE) were the prevalent MPs found in the freshwater fish. A broader variety of polymer types was observed in farmed fish. The edible flesh part of fish presented the lower prevalence of MPs compared to gill and stomach (gut), with gut displaying a higher frequency and diversity of MPs. This preliminary study suggests that the incidence and type of MPs varies in farmed verses natural fish sources as well as across different tissue types, with significantly less detected within the edible flesh tissues compared with stomach and gill tissues.

     

Enhanced biological nitrogen and phosphorus removal from sewage driven by fermented glycerol: comparative assessment between sequencing batch- and continuously fed-structured fixed bed reactor

Environmental Science and Pollution Research - The nutrient biological removal from sewage, especially from anaerobic reactor effluents, still represents a major challenge in conventional sewage...     

Bias in protected‐area location and its effects on long‐term aspirations of biodiversity conventions

To contribute to the aspirations of recent international biodiversity conventions, protected areas (PAs) must be strategically located and not simply established on economically marginal lands as they have in the past. With refined international commitments under the Convention on Biological Diversity to target protected areas in places of “importance to biodiversity,” perhaps they may now be. We analyzed location biases in PAs globally over historic (pre‐2004) and recent periods. Specifically, we examined whether the location of protected areas are more closely associated with high concentrations of threatened vertebrate species or with areas of low agricultural opportunity costs. We found that both old and new protected areas did not target places with high concentrations of threatened vertebrate species. Instead, they appeared to be established in locations that minimize conflict with agriculturally suitable lands. This entrenchment of past trends has substantial implications for the contributions these protected areas are making to international commitments to conserve biodiversity. If protected‐area growth from 2004 to 2014 had strategically targeted unrepresented threatened vertebrates, >30 times more species (3086 or 2553 potential vs. 85 actual new species represented) would have been protected for the same area or the same cost as the actual expansion. With the land available for conservation declining, nations must urgently focus new protection on places that provide for the conservation outcomes outlined in international treaties.     

Comparative sensitivity of a tropical mysid Metamysidopsis insularis and the temperate species Americamysis bahia to six toxicants

The sensitivity of the tropical mysid, Metamysidopsis insularis relative to that of the sub-tropical North American mysid, Americamysis bahia was determined by comparing their acute toxicity to six toxicants. The 96 h LC50 values for M. insularis ranged from 0.03 mg L^?1 (cadmium (Cd) chloride) to 466 mg L^?1 (potassium chloride (KCL) whereas those for A. bahia ranged from 0.1 mg L^?1 for Cd chloride to 501 mg L^?1 for KCl. The interspecies correlation indicated that the mean acute toxicities for M. insularis showed a high positive correlation with A. bahia (r ² = 1.0). Data suggest there were no significant differences between acute toxic responses of the two species to these toxicants. The results suggest that though M. insularis and A. bahia occur in different climatic zones, the difference in relative sensitivities of the two species due to temperature preferenda may be negligible. Consequently, M. insularis may be considered suitable tropical test species for use in toxicity testing in Trinidad and Tobago.     

Induction of mercury‐binding peptide in whole cells and anucleated cells of Acetabularia calyculus

The present study reports the isolation and partial purification of a mercury‐binding polypeptide in whole and anucleated cells of Acetabularia calyculus. Sephadex G‐75 Gel filtration showed that cells exposed to Hg exhibit a major peak of protein(s) concomitant with both, a major peak of Hg (revealed by atomic absorption spectroscopy), and the major peak of mercury‐thiolate complex (based on a high 254 nm absorbance) accompanied by high content of SH groups. SDS‐Page electrophoresis showed that this peak contains one major polypeptide of apparent molecular weight 27.000 dalton. These results are in agreement with our previous finding of unusually high bioconcentration factor of Hg in Acetabularia related to the induction of a polypeptide in both, whole and anucleated cells of Acetabularia, in presence of Hg.     

Formation and degradation of triademinol after the use of triadimefon in a wheat monoculture]

During two vegetation periods, the behaviour of the triadimefon metabolite, triadimenol, in different plant parts of winter wheat and in soil was investigated. The fungicide Bayleton DF (triadimefon + captafol) was applied at the beginning of earing. Different ratios of triadimenol-A/-B were found in individual plant parts. Triadimenol-A predominated in the two uppermost leaves, and triadimenol-B in the roots and in the soil. No residues of triadimenol were found in grain at harvest time (detection limit 0.01 mg/kg).     

Fate of polydimethylsilicone in biosolids-amended field plots

This research examined the fate of polydimethylsilicones (PDMS) in agricultural test plots amended with municipal biosolids. This 4 yr field study involved addition of 0, 15, and 100 Mg ha(-1) of municipal biosolids, which contained ambient concentrations of PDMS (1272 mg kg(-1) biosolids), to corn and soybean test plots. Soil samples collected at intermittent time intervals were analyzed for soil water, soil organic C, extractable PDMS and PDMS hydrolysis products. Above normal precipitation during the field study maintained soil water levels in excess of 100 g kg(-1) for most of the testing period of 1994-1998. Under these conditions half-lives for PDMS (based on field dissipation data) ranged from 876 to 1443 d. When biosolids amended soil samples were brought into the laboratory and subjected to more rapid drying, >80% of the PDMS was transformed to lower molecular weight hydrolysis products within 20 d. No difference in relative PDMS transformation rates were evident for soils that received PDMS in the form of a biosolids amendment or directly dosed to the soil (in the absence of biosolids) indicating little if any effect of direct PDMS-biosolids interactions on PDMS transformation rates. These results support that the overriding factor controlling the fate of PDMS in field soils is the soil moisture content.     

Initial results of environmental monitoring in the Texas Rio Grande Valley

Previous studies have suggested that a segment of human disease may be attributable to environmental exposures. These may include exposure to chemicals released from a broad range of natural and man-made sources. The purpose of this study was to develop the sampling methodology and prepare a preliminary database on the presence of various organic chemicals in environmental media in two South Texas counties bordered by the Rio Grande River. A third county, located approximately 150 miles north of the Rio Grande River, was also sampled. The South Texas counties were the focus of study due to an increased incidence of anencephalic births in recent years. The environmental media that was sampled included surface water and sediment from the Rio Grande River and irrigation canals, as well as soil from adjacent cropland and pastures. Samples were collected using United States Geological Survey (USGS) quadrangle maps (7.5'; 1:24,000 scale) to identify the area of interest. At least one sampling location was established in each quadrangle. A pond sampler was used for the collection of surface water samples, while soil was collected with a stainless steel trowel. Sediment samples were collected directly in a glass jar. Solid samples were extracted in a soxhlet extractor using methylene chloride. Organic chemicals were concentrated from water samples on a Sep-Pak cartridge and the organics eluted with methanol/acetonitrile. Extracts were analyzed using GC-MS. All of the surface water samples contained aliphatic hydrocarbons and plasticizers, while soil samples contained aliphatics, plasticizers, pesticides, and industrial estrogens. Specific chemicals detected in environmental samples included atrazine and benzene dicarboxylic acid. Contaminant levels in sediments were generally higher than were detected in other media. The results demonstrate the broad variability of contaminant types and concentrations in environmental samples. Although this study presents only a very preliminary characterization of a large area of South Texas, the data indicate a number of pesticides and xenobiotic estrogens that were identified in environmental samples. Additional data providing more details of spatial and temporal distribution of contaminants as well as wildlife studies are needed.     

Organic matter characteristics and nutrient content in eroded soils

Twenty-one severely eroded soils of SE Spain (Torriorthent xeric soils) were studied. These soils form a fragile system characterized by soils with a low density of plant cover (<5%), are loamy and occur in a semiarid climate. The soils formerly were used for agricultural purposes but were abandoned at least 15 years ago. These eroded soils had a low total organic carbon content, and their humic substances, humic acid carbon, and carbohydrates were lower compared with soils that had never been cultivated (natural soils). The variables in which the effects of erosion were particularly noted were those related with the active organic matter (respiration and water-soluble organic matter). Those eroded soils with higher salt content showed lower organic matter and carbohydrate contents. Only total nitrogen was correlated with the carbon fractions in the eroded soils.     

Changes in carbon fractions during composting and maturation of organic wastes

Seven mixtures from four organic residues—an aerobic sewage sludge, a city refuse, a peat residue, and a grape debris—were composted, and the changes undergone by their different carbon fractions during their composting and maturation were studied. In most cases a decrease in carbon fractions during the composting and maturation processes was observed. The extractable carbon, however, increased during maturation. Organic matter mineralization was greater in the composts with city refuse than in those with sewage sludge. The samples with peat residue showed the lowest decreases in carbon fractions. During maturation, an increase of humiclike fraction was observed, which was reflected by a decrease in the soluble carbon-precipitated carbon ratio at pH 2. Water-soluble carbon was the carbon fraction most easily degradable by microorganisms, and its amount correlated significantly with composting time in all the samples.