The false limpet Siphonaria gigas, a simultaneous hermaphrodite, lives in pairs in rock fissures on the Pacific coast of Panama

The pulmonate limpet Siphonaria gigas, a simultaneous hermaphrodite, lives in the mid- to upper-intertidal zone on rocky shores in the tropical Eastern Pacific. Samples along five transects taken in June–July, 2004, on Culebra Point (8º54′N to 79º31′W), Republic of Panama, showed that 71 % of the population occurred in fissures, a significant preference for this habitat. Of 200 adults in 27 fissures, 150 lived side by side in pairs with their shells touching or nearly so, a significant deviation from the number of pairs expected given a random arrangement. Pair frequency did not increase with limpet density suggesting pairing was not an incidental consequence of crowding. Pair living was unknown in the genus Siphonaria, and is very uncommon among simultaneous hermaphrodites. Reproductive synchrony and restrictions on movement due to predation and environmental stress may limit opportunities for encountering and mating with multiple partners favoring pair living in S. gigas.     

Side effects of the herbicide triasulfuron on collembola under laboratory conditions

Triasulfuron, a member of the sulfonylureas class of herbicides, was tested under laboratory conditions on the collembolan Onychiurus pseudogranulosus. Pure triasulfuron and commercial formulations at different rates (starting from a dose about 5 times the recommended agricultural rate) were tested separately on one-week old juveniles and adults reared in the laboratory. The persistence of the herbicide at the end of the trials lasting 30 and 60 days was verified by HPLC analysis. Laboratory tests indicated that only the rates exceeding 500 times the soil concentration expected soon after field application of the herbicide directly affected the tested species.     

Maltooligosaccharides in the northwestern Adriatic Sea

The aim of this study was to monitor for the first time the oligosaccharide pattern in the northwestern Adriatic Sea. Oligosaccharides are components of the low-molecular-weight fraction of dissolved organic matter (DOM). They perform an important ecological function in the microbial loop prompting substrates for bacterial degradation. In particular, our investigation focused on maltooligosaccharides (glucose α 1–4 linked). The analyses were carried out using a dialysis-charcoal column sorption pre-concentration method, followed by liquid chromatography-tandem mass spectrometry analyses with a triple quadrupole mass spectrometer operating in multiple reaction monitoring mode. During the study period, the concentration of maltooligosaccharides with a low degree of polymerisation (ranging from maltose to maltotetraose) was higher than other maltooligosaccharides (maltopentaose and maltoeptaose) and all together they reached their highest concentration in June. This concentration was temporally shifted from a long period of diatom bloom (from January to April). Furthermore, the annual maltooligosaccharide trend was monitored together with several chemical, physical and biological parameters to investigate their potential role on the maltooligosaccharide accumulation. Our results suggested that the maltooligosaccharide accumulation could be related to the water column stratification.     

Forecasting the consequences of accidental releases of radionuclides in the atmosphere from ensemble dispersion modelling.

The RTMOD system is presented as a tool for the intercomparison of long-range dispersion models as well as a system for support of decision making. RTMOD is an internet-based procedure that collects the results of more than 20 models used around the world to predict the transport and deposition of radioactive releases in the atmosphere. It allows the real-time acquisition of model results and their intercomparison. Taking advantage of the availability of several model results, the system can also be used as a tool to support decision making in case of emergency. The new concept of ensemble dispersion modelling is introduced which is the basis for the decision-making application of RTMOD. New statistical parameters are presented that allow gathering the results of several models to produce a single dispersion forecast. The devised parameters are presented and tested on the results of RTMOD exercises.     

Solving mercury (Hg) speciation in soil samples by synchrotron X-ray microspectroscopic techniques

Direct mercury (Hg) speciation was assessed for soil samples with a Hg concentration ranging from 7 up to 240 mg kg⁻¹. Hg chemical forms were identified and quantified by sequential extractions and bulk- and micro-analytical techniques exploiting synchrotron generated X-rays. In particular, microspectroscopic techniques such as μ-XRF, μ-XRD and μ-XANES were necessary to solve bulk Hg speciation, in both soil fractions <2 mm and <2 μm. The main Hg-species found in the soil samples were metacinnabar (β-HgS), cinnabar (α-HgS), corderoite (Hg₃S₂Cl₂), and an amorphous phase containing Hg bound to chlorine and sulfur. The amount of metacinnabar and amorphous phases increased in the fraction <2 μm. No interaction among Hg-species and soil components was observed. All the observed Hg-species originated from the slow weathering of an inert Hg-containing waste material (K106, U.S. EPA) dumped in the area several years ago, which is changing into a relatively more dangerous source of pollution.     

Solid-phase extraction for multi-residue analysis of pesticides in honey

A fast and simple multi-residue method for the analysis of 15 organophosphorus (OP), 17 organochlorine (OC), 8 pyrethroids (PYR), 12 N-methyl-carbamate (NMC) pesticide residues and bromopropylate in honey is presented. Ready-to-use EXtrelutNT 20 column, eluted with dichloromethane, was used to extract the pesticide residues from the aqueous-acetone honey sample, obtaining a clean extract directly analyzable. Determination was carried out by gas chromatography (GC) coupled with flame photometric detector (FPD) for OP compounds and by GC coupled with mass spectrometry detector (MSD) for OC and PYR pesticides and bromopropylate. The NMC pesticides were analysed by liquid chromatography-double derivatization coupled with spectrofluorimetric detector (LC/DD/Fl). This method allows the determination of the 53 pesticide residues at low concentrations (0.0005-0.074 mg/kg) and can be used to assess the compliance with the Maximum Residues Levels (MRLs) set by the European Union. The performance of the method was evaluated and specificity, linearity, recovery, repeatability, reproducibility, limit of quantification (LOQ) and limit of detection (LOD) were determined. A good linearity (r(2)≥ 0.99) was found in the range 0.0005-0.074 mg/kg for the majority of the compounds studied. Most of the pesticides had recoveries in the range 70-103 % and values of relative standard deviation (RSD) < 20 for repeatability and reproducibility, showing good accuracy and precision of the method. Aldicarb partially degraded in aldicarb sulphoxide during the analytical procedure, giving anomalous values. The LOQ for all pesticides investigated was from 0.0005 to 0.025 mg/kg while the LOD ranged from 0.0002 to 0.008 mg/kg.     

Determination of acidic herbicides in cereals by QuEChERS extraction and LC/MS/MS

A simple and rapid method has been studied for the determination of acidic herbicides (2,4-D, Dichlorprop, Dichlorprop-p, Fluazifop, Fluroxypyr, MCPA, Mecoprop and Mecoprop-p) on cereals (rye). The method involves an alkaline hydrolysis with sodium hydroxide in order to release covalently bound compounds, prior to QuEChERS extraction, followed by neutralization and analysis via liquid chromatography-double mass spectrometry LC/MS/MS. The performance of the method either with or without alkaline hydrolysis was studied in terms of recovery rates and limit of quantification (LOQ). In either case, recoveries were determined at four spiking levels (0.02 mg/kg, 0.05 mg/kg, 0.1 mg/kg and 0.5 mg/kg) with 5 replicates for each level. Mean recoveries ranged from 90 to 120 %, whereas relative standard deviations (RSD %) proved to be less than 20 %. Quantitative analysis was carried out by the internal standard (Nicarbazin) and the LC/MS/MS analysis was performed in electrospray ionisation (ESI) negative mode using a Zorbax XCB Eclipse column. The developed method was applied to the analysis of several cereals commercially available like as rye flour, oat meal, oat flakes and dehusked oat. Residue levels were found below the limit of quantification (LOQ) of the method. The method has been tested in EU Proficiency Tests for cereals with good results.     

Meteorological and pedological influence on the PCBs distribution in mountain soils

Polychlorinated biphenyls (PCBs) are a threat to environmental and human health due to their persistence and toxicological effects. In this paper, we analyse some meteorological and organic-matter-related effects on their distribution in the soils of an Alpine environment that is not subject to direct contamination. We collected samples and measured the contamination of 12 selected congeners from three soil layers (O, A1 and A2) and from North-, plain- and South-facing slopes on six different dates spanning the entire snowless portion of the year. We recorded the hourly air and soil temperatures, humidity and rainfall in the study period. We found evidence that PCBs contamination in soils varies significantly, depending on sampling date, layer and aspect. The observed seasonal trend shows an early summer peak and a rapid decrease during June. The layer effect demonstrates higher dry-weight-based concentrations in the O layer, whereas the differences are much smaller for SOM-based concentrations. Different factors caused significantly higher concentrations in northern soils, with a N/S enrichment factor ranging from 1.8 to 1.5 during the season. The southern site has significantly more rapid early-summer re-volatilisation kinetics (half-time of 16 d for South, 25 d for North).     

Occurrence of Fipronil in residential house dust in the presence and absence of pets: a hint for a comprehensive toxicological assessment

The presence of the insecticide Fipronil and its main products of toxicological relevance, namely Sulfone and Desulfinyl, was assessed in 161 residential house dust samples in the absence (N?=?101) and presence (N?=?60) of cats and dogs in Italy. High-resolution mass spectrometry analysis revealed a significant difference (p?<?0.001) in the dust contamination in the presence of pets (median: 467 vs. 24?ng/g dry weight), even if the highest value was found in the absence of pets (82,069 vs. 67,799?ng/g dry weight). Fipronil intake estimates from dust in toddlers, computed according to US-EPA and EU-ECHA guidelines, ranged from 333 to 556 and from 20 to 34?ng/kg per day for acute and chronic scenario, respectively. Dust seemed not able itself to lead to Fipronil overexposure with respect to acute and chronic toxicity health-based guidance values. Kittens were potentially overexposed to Fipronil under both acute (26,076?ng/kg per day) and chronic (1,633?ng/kg per day) scenarios. The mild symptomatology associated with acute intoxication could possibly determine case underreporting within pharmacosurveillance schemes. Its administration was estimated in 7.3–9.7 tons per year. Such a range suggests its prudent use under strict veterinary control to prevent pest resistance and ecotoxicological outcomes.     

Poly(lactic acid)/Cellulose Composites Obtained from Modified Cotton Fibers by Successive Acid Hydrolysis

This work is focused on the hydrolysis of cotton fibers from waste textiles to obtain micro and nanofibers to be used as reinforcements in polymer composites. To promote their compatibility with polymeric matrix, hydrolyzed cotton fibers were surface modified with various silane compounds. Thus, these fibers were mixed with commercial poly(lactic acid) (PLA) at 5% w/w loading by melt compounding. Acid treatments caused a decrease of the crystallinity index whereas the thermal stability was significantly improved, especially for cellulose fibers hydrolyzed in two steps. Morphological analysis revealed a reduction of the fibers diameter and a decrease of their length as a consequence of the hydrolysis. NMR analysis confirmed the silanization of the fibers by reaction with the silane agent. Tensile tests revealed that silanization treatments were able to increase the composite Young’s modulus and the stress at break with respect to the neat matrix, indicating that silanization improved the polymer/fiber compatibility interfacial adhesion. The overall results demonstrated that applying suitable surface modification strategies, waste cotton textiles can be effectively recycled as fillers in polymer based composites.