Oxidation of small aromatic compounds in rainwater by UV/H2O2: Optimization by response surface methodology.

The presence of aromatic compounds in rainwater is a matter of concern, mainly when the use of rainwater in buildings is intended. The present work aimed to assess the oxidation of a mixture of small aromatic compounds (benzoic, 3,5-dihydroxybenzoic and syringic acids) in rainwater by the UV/H2O2 process, and the possibility of its optimization by the response surface methodology. The extent of oxidation was assessed by ultraviolet-visible and molecular fluorescence spectroscopies. During the oxidation of the mixture new chromophoric compounds were formed at an initial stage, but they were then degraded at a later stage. The increase of the H2O2 concentration, resulted in a higher extent of oxidation, while the initial pH value showed no influence in the oxidation of the mixture. The optimization of the oxidation was performed using the uniform design with the factors: initial H2O2 concentration, initial pH, and reaction time. The response surface model found, through the best subsets regression, described the extent of oxidation as function of the following variables: initial H2O2 concentration and reaction time, interaction between them, and also their respective quadratic forms. The optimal conditions, the lowest H2O2 concentration (3.1 mM) for a selected maximum reaction time (4 h), were applied to rainwater samples spiked with the mixture of contaminants and resulted in an extent of oxidation higher than 99.5%, validating the application of the model to real samples. Therefore, the UV/H2O2 process coupled to its optimization via response surface methodology may be an alternative for rainwater treatment in buildings.

Sources of carbohydrates on bulk deposition in South-Western of Europe.

Scarce information is available concerning the presence of carbohydrates in rainwater. The existence of carbohydrates in bulk deposition at the town of Estarreja (Portugal), at industrial (I) and background (BG) locals, in winter and spring seasons 2016, was assessed. Seventeen carbohydrates and related compounds were identified: monosaccharides (ribose, arabinose, xylose, glucose, galactose, fructose), disaccharides (sucrose, trehalose, maltose, cellobiose), polyols (arabinitol, xylitol, myo-inositol, mannitol, glucitol, maltitol), and the anhydromonosaccharide levoglucosan. Higher content of carbohydrates was observed in spring (BG: 670 nM; I: 249 nM) than in winter (BG: 168 nM; I: 195 nM), and fructose was the carbohydrate with the highest contribution in both seasons (spring: 32%/44% (I/BG); winter: 24% (at both sites)). Fructose, myo-inositol, glucose and sucrose showed higher volume-weighted averages (VWA) concentrations in spring than in winter, possibly due to biogenic emissions typical of spring, such as pollen, and fungal spores for myo-inositol. Fructose may have derived from isomerization of glucose in biomass burning, namely in winter. Levoglucosan and galactose presented higher VWA concentration in winter than in spring, suggesting a seasonal effect related with the biomass combustion. The carbohydrates VWA concentrations were similar for samples associated with maritime and terrestrial air masses, indicating that local sources were their main contributors. Source assessment of carbohydrates by factor analysis suggested: biogenic sources for the arabinitol, myo-inositol, glucose, fructose and sucrose; soil dust for the trehalose; and anthropogenic sources from biomass burning for the galactose, arabinose and levoglucosan. The bulk deposition showed to be fundamental on removing carbohydrates from the atmosphere.

Using integrative taxonomy to establish the status of Alpheus peasei (Armstrong, 1940) (Decapoda: Alpheidae) as a single species throughout its distribution.

The distribution of the western Atlantic snapping shrimp Alpheus peasei (Armstrong, 1940) has a large gap (approx. 12° of latitude) between Tobago and the northeast of Brazil (State of Ceará). Here we analyzed specimens of A. peasei from its entire distribution range and type-locality (Bermuda), to test the hypothesis that they belong to a single species. The morphological analysis included the usual taxonomic characters as well as additional ones (such as mouthparts). The molecular analysis was based on the mitochondrial genes Cytochrome Oxidase I and 16S rRNA. The results of both analyses were congruent and indicated that A. peasei is a single species throughout its known distribution. As such, they indicated a connectivity between Northwestern and Southwestern Atlantic populations of A. peasei. The gap in distribution may be explained by scarce samplings in the North Brazil Shelf province and/or by passive larval dispersal. Our results also extend the known distribution of A. peasei in the northwestern Atlantic (Barbados, Belize and Costa Rica), and add a new record from the Brazilian coast (Pernambuco).

White bean (Phaseolus vulgaris L.) as a sorbent for the removal of zinc from rainwater.

The present work aimed to assess the sorption capacity of the common white bean (Phaseolus vulgaris L.) to remove Zn(II) from rainwater, rendering it suitable for use in buildings, and the efficiency of the process was evaluated for two initial Zn(II) concentrations, representing high (100 µg L-1) and very high (500 µg L-1) levels of Zn(II) in rainwater. The effects of the amount of beans (1, 5 and 10 beans per 50 mL), as well as the initial pH values of the zinc solution [acid (4), neutral (5.6) and basic (7) for atmospheric waters] were also assessed. The removal of Zn from water was affected by the change in pH values. When 5 and 10 beans were used, after 4 h and 2 h of contact time, respectively, the accumulated Zn(II) on the beans was released back into the solution, and this release occurred first for the highest tested pH value. The sorption rate of Zn(II) from the solution increased with the increasing amount of beans, but for 5 and 10 beans this only took place up to 4 h and 2 h, respectively. Furthermore, the removal percentages of Zn(II) increased with the increase of the initial concentrations of the metal in water. Kinetic studies revealed that a pseudo-first-order model provided the best fitting for the experimentally obtained values. Fourier transform infrared spectroscopy coupled with attenuated total reflectance (FTIR-ATR) analyses of the bean shells and cores indicated that contact with a Zn(II) solution did not cause notable alterations to the chemical structures of these bean components. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX) analyses suggested that the process of sorption occurred at the surface of the beans (shells). The results obtained in this study also suggest that the matrix of rainwater samples did not interfere with the removal of metal, and that the process of the removal of Zn(II) by the white beans can be applied to real samples. On the whole, results indicate that for the removal of Zn(II) from rainwater, 1 bean up to 6 h, or 5 and 10 beans up to 2 h can be used per 50 mL for the removal of up to 60% of Zn(II) present in water, thus constituting a viable solution for the effective reduction of this metal in rainwater.

Oxidation of benzoic acid from biomass burning in atmospheric waters.

This work evaluates the degradation of benzoic acid, a tracer from biomass burning, by different oxidation agents (Fe (III); H2O2; sunlight; and combinations of the previous ones) in model solutions and in real atmospheric waters. The extent of reactions was assessed by Ultraviolet-Visible and molecular fluorescence spectroscopies. The oxidation of benzoic acid occurred with the chemical oxidants Fe (III), H2O2, Fe (III) and H2O2 simultaneously in the presence of sunlight, and with Fe (III) and H2O2 simultaneously in the absence of light. The decrease of the pH value from neutral to acid for atmospheric waters generally increased the extent of oxidation. Sunlight was an important oxidation agent, and its combination with chemical oxidants increased the oxidation rate of benzoic acid, possibly due to the photogeneration of hydroxyl radicals. The results also suggested the occurrence of direct and indirect photolysis of benzoic acid in atmospheric waters. Moreover, the oxidation of benzoic acid produced new and more complex chromophoric compounds, which were then degraded. In addition, the nocturnal period is not sufficient for the full degradation of benzoic acid and of the intermediates formed by Fenton-like oxidation. The diurnal period may be enough for their full degradation through photo-Fenton-like oxidation, but this depends on the composition of the atmospheric waters, namely of the chromophoric content. Thus, this study highlights that benzoic acid from biomass burning, and its derivatives, may persist in atmospheric waters for periods of longer than one day, becoming available for other reactions, and may also affect the terrestrial and aquatic ecosystems through the wet depositions.

Degradation of polyethylene microplastics in seawater: Insights into the environmental degradation of polymers.

Microplastic contamination of aquatic environments has become an increasingly alarming problem. These, defined as particles <5 mm, are mostly formed due to the cracking and embrittlement of larger plastic particles. Recent reports show that the increasing presence of microplastics in the environment could have significant deleterious consequences over the health of marine organisms, but also across the food chain. Herein, we have studied the effects of artificial seawater on polyethylene (PE)-based beads by exposing them up to eight weeks to saltwater in stirred batch reactors in the dark and examined the structural and morphological changes these endured. Electron microscopy observations showed that artificial seawater induces severe microcracking of the pellets' surfaces. Additionally, Fourier transform infrared spectroscopy (FTIR) analyses evidenced the formation of oxidized groups whenever these particles were exposed to water and an increase in organic matter content of the waters in which the pellets were kept was evidenced by Raman spectroscopy. There were also noticeable consequences in the thermal stability of the polyethylene pellets, as determined by thermogravimetric studies (TGA). Furthermore, the parallel exposure of polyethylene pellets to UV radiation yielded less pronounced effects, thus underscoring its lower preponderance in the degradation of this material. These results highlight the importance of determining the mechanisms of degradation of microplastics in marine settings and what the implications may be for the environment. Overall, the herein presented results show that a relatively short period of time of accelerated exposure can yield quantifiable chemical and physical impacts on the structural and morphological characteristics of PE pellets.

Going Beyond Academic Integrity Might Broaden our Understanding of Plagiarism in Science Education: A Perspective from a Study in Brazil.

Fostering innovation and creativity is a priority in the science and education policy agenda of most countries, which have advocated that innovative minds and processes will boost scientific and economic growth. While our knowledge society has embraced this view, fostering creativity is among the major challenges faced by educators and policymakers. For example, plagiarism, which may be considered a form of imitation and repetition, is a global concern at schools and universities. However, most discussions focus on academic integrity, which, we believe, leaves some gaps in the approach to the problem. As part of an ongoing project on plagiarism, science and education policy, we show results from a survey sent to 143 high-school science teachers at one of the most highly regarded federal schools in Brazil. Among respondents (n=42), about 50% admit that students plagiarize in assignments. Additionally, many of these educators suggest that the way biology, chemistry and physics are taught at school stimulates more repetition than creativity. Our findings are consistent with the need for a broader perspective on plagiarism and with initiatives to stimulate creativity and critical thinking among students. Although we offer a perspective from Brazil, it may illuminate current discussions on plagiarism, particularly in emerging countries.

Going Beyond Academic Integrity Might Broaden our Understanding of Plagiarism in Science Education: A Perspective from a Study in Brazil

ABSTRACT Fostering innovation and creativity is a priority in the science and education policy agenda of most countries, which have advocated that innovative minds and processes will boost scientific and economic growth. While our knowledge society has embraced this view, fostering creativity is among the major challenges faced by educators and policymakers. For example, plagiarism, which may be considered a form of imitation and repetition, is a global concern at schools and universities. However, most discussions focus on academic integrity, which, we believe, leaves some gaps in the approach to the problem. As part of an ongoing project on plagiarism, science and education policy, we show results from a survey sent to 143 high-school science teachers at one of the most highly regarded federal schools in Brazil. Among respondents (n=42), about 50% admit that students plagiarize in assignments. Additionally, many of these educators suggest that the way biology, chemistry and physics are taught at school stimulates more repetition than creativity. Our findings are consistent with the need for a broader perspective on plagiarism and with initiatives to stimulate creativity and critical thinking among students. Although we offer a perspective from Brazil, it may illuminate current discussions on plagiarism, particularly in emerging countries.

Stability of different influenza subtypes: How can high hydrostatic pressure be a useful tool for vaccine development?

BACKGROUND: Avian influenza A viruses can cross naturally into mammals and cause severe diseases, as observed for H5N1. The high lethality of human infections causes major concerns about the real risk of a possible pandemic of severe diseases to which human susceptibility may be high and universal. High hydrostatic pressure (HHP) is a valuable tool for studies regarding the folding of proteins and the assembly of macromolecular structures such as viruses; furthermore, HHP has already been demonstrated to promote viral inactivation. METHODS: Here, we investigated the structural stability of avian and human influenza viruses using spectroscopic and light-scattering techniques. We found that both particles have similar structural stabilities and that HHP promotes structural changes. RESULTS: HHP induced slight structural changes to both human and avian influenza viruses, and these changes were largely reversible when the pressure returned to its initial level. The spectroscopic data showed that H3N2 was more pressure-sensitive than H3N8. Structural changes did not predict changes in protein function, as H3N2 fusion activity was not affected, while H3N8 fusion activity drastically decreased. The fusion activity of H1N1 was also strongly affected by HHP. In all cases, HHP caused inactivation of the different influenza viruses. CONCLUSIONS: HHP may be a useful tool for vaccine development, as it induces minor and reversible structural changes that may be associated with partial preservation of viral biological activities and may potentiate their immunogenic response while abolishing their infectivity. We also confirmed that, although pressure does not promote drastic changes in viral particle structure, it can distinctly affect viral fusion activity.

Biodegradation of polyethylene microplastics by the marine fungus Zalerion maritimum.

Plastic yearly production has surpassed the 300milliontons mark and recycling has all but failed in constituting a viable solution for the disposal of plastic waste. As these materials continue to accumulate in the environment, namely, in rivers and oceans, in the form of macro-, meso-, micro- and nanoplastics, it becomes of the utmost urgency to find new ways to curtail this environmental threat. Multiple efforts have been made to identify and isolate microorganisms capable of utilizing synthetic polymers and recent results point towards the viability of a solution for this problem based on the biodegradation of plastics resorting to selected microbial strains. Herein, the response of the fungus Zalerion maritimum to different times of exposition to polyethylene (PE) pellets, in a minimum growth medium, was evaluated, based on the quantified mass differences in both the fungus and the microplastic pellets used. Additionally, molecular changes were assessed through attenuated total reflectance Fourier transform Infrared Spectroscopy (FTIR-ATR) and Nuclear Magnetic Resonance (NMR). Results showed that, under the tested conditions, Z. maritimum is capable of utilizing PE, resulting in the decrease, in both mass and size, of the pellets. These results indicate that this naturally occurring fungus may actively contribute to the biodegradation of microplastics, requiring minimum nutrients.

Development of an electrochemical biosensor for alkylphenol detection.

In this work, electrochemical biosensors based on field effect transistors (FET) with single-walled carbon nanotubes (SWCNT) were constructed as disposable analytical devices to detect alkylphenols through immunoreaction using 4-nonylphenol (NP) as model analyte, and validated by comparison with enzyme-linked immunosorbent assay (ELISA). The calibration curve displays a working range with five concentrations between 5 and 500µgL(-1), and for each concentration, five biosensors were analysed for reproducibility estimation and two analytical measurements were performed for each biosensor for repeatability estimation. The accuracy of the biosensors was validated by analyzing NP contents in ten spiked artificial seawater samples and comparing these results to those obtained with the traditional ELISA methodology. Excellent analytical performance was obtained with reproducibility of 0.56±0.08%, repeatability of 0.5±0.2%, limit of detection for NP as low as 5µgL(-1), and average recovery between 97.8% and 104.6%. This work demonstrates that simple biosensors can be used to detect hazardous priority substances in seawater samples, even at low concentrations.

Composites based on PET and red mud residues as catalyst for organic removal from water.

In this study, we obtained a composite based on carbon/iron oxide from red mud and PET (poly(ethylene terephthalate)) wastes by mechanical mixture (10, 15 and 20wt.% of PET powder/red mud) followed by a controlled thermal treatment at 400°C under air. XRD analyses revealed that the α-Fe2O3 is the main phase formed from red mud. TPR analyses showed that the iron oxide present in the composites undergoes reduction at lower temperature to form Fe(2+) species present in Fe3O4, indicating that the iron oxide in the composite can exhibit greater reactivity in the catalytic processes compared to the original red mud. In fact, catalytic tests showed that the composites presented higher capacity to remove methylene blue dye (MB), presenting about 90% of removal after 24h of reaction. The MB removal was also monitored by mass spectrometer with ionization via electrospray (ESI-MS), which demonstrated the occurrence of the oxidation process, showing the formation of MB oxidation products. The stability of the composites was confirmed after four reuse cycles. The results seem to indicate that PET carbon deposited over the iron oxide from red mud promotes adsorption of the contaminant allowing its contact with the iron atoms and their consequent reaction.

Fenton-like oxidation of small aromatic acids from biomass burning in atmospheric water and in the absence of light: Identification of intermediates and reaction pathways.

A previous work showed that the night period is important for the occurrence of Fenton-like oxidation of small aromatic acids from biomass burning in atmospheric waters, which originate new chromophoric compounds apparently more complex than the precursors, although the chemical transformations involved in the process are still unknown. In this work were identified by gas chromatography-mass spectrometry (GC-MS) and by electrospray mass spectrometry (ESI-MS) the organic intermediate compounds formed during the Fenton-like oxidation of three aromatic acids from biomass burning (benzoic, 4-hydroxybenzoic and 3,5-dihydroxybenzoic acids), the same compounds evaluated in the previous study, in water and in the absence of light, which in turns allows to disclose the chemical reaction pathways involved. The oxidation intermediate compounds found for benzoic acid were 2-hydroxybenzoic, 3-hydroxybenzoic, 4-hydroxybenzoic, 2,3-dihydroxybenzoic, 2,5-dihydroxybenzoic, 2,6-dihydroxybenzoic and 3,4-dihydroxybenzoic acids. The oxidation intermediates for 4-hydroxybenzoic acid were 3,4-hydroxybenzoic acid and hydroquinone, while for 3,5-dihydroxybenzoic acid were 2,4,6-trihydroxybenzoic and 3,4,5-trihydroxybenzoic acids, and tetrahydroxybenzene. The results suggested that the hydroxylation of the three small aromatic acids is the main step of Fenton-like oxidation in atmospheric waters during the night, and that the occurrence of decarboxylation is also an important step during the oxidation of the 4-dihydroxybenzoic and 3,5-dihydroxybenzoic acids. In addition, it is important to highlight that the compounds produced are also small aromatic compounds with potential adverse effects on the environment, besides becoming available for further chemical reactions in atmospheric waters.

Vanillic and syringic acids from biomass burning: Behaviour during Fenton-like oxidation in atmospheric aqueous phase and in the absence of light.

Biomass combustion is a threat to the environment since it emits to the atmosphere organic compounds, which may react and originate others more aggressive. This work studied the behaviours of vanillic and syringic acids, small aromatic tracers of biomass burning, during Fenton-like oxidation in aqueous phase and absence of light. For both compounds, the extent of oxidation increased with pH decrease from neutral to acid in atmospheric waters, but for vanillic acid the neutral pH was not able of promoting the oxidation. With the oxidation of both acids were formed chromophoric compounds, and the formation rate increased with the degree of electron-donator substituents in benzene ring. The initial and produced compounds were not totally degraded up to 24h of reaction at pH 4.5, suggesting that the night period may be not sufficient for their full degradation in atmospheric waters. The major compounds formed were the 3,4-dihydroxybenzoic acid for vanillic acid, and the 1,4-dihydroxy-2,6-dimethoxybenzene for syringic acid. These findings suggest the occurrence of an ipso attack by the hydroxyl radical preferential to the methoxy and carboxyl groups of vanillic and syringic acids, respectively. It is important to highlight that for both aromatic acids the main compounds produced are also small aromatic compounds.

Label-free disposable immunosensor for detection of atrazine.

This work reports the construction of a fast, disposable, and label-free immunosensor for the determination of atrazine. The immunosensor is based on a field effect transistor (FET) where a network of single-walled carbon nanotubes (SWCNTs) acts as the conductor channel, constituting carbon nanotubes field effect transistors (CNTFETs). Anti-atrazine antibodies were adsorbed onto the SWCNTs and subsequently the SWCNTs were protected with Tween 20 to prevent the non-specific binding of bacteria or proteins. The principle of the immunoreaction consists in the direct adsorption of atrazine specific antibodies (anti-atrazine) to SWCNTs networks. After exposed to increasing concentrations of atrazine, the CNTFETs could be used as useful label-free platforms to detect atrazine. Under the optimal conditions, a limit of detection as low as 0.001 ng mL(-1) was obtained, which is lower than that of other methods for the atrazine detection, and in a working range between 0.001 and 10 ng mL(-1). The average recoveries obtained for real water samples spiked with atrazine varied from 87.3% to 108.0%. The results show that the constructed sensors display a high sensitivity and could be useful tools for detecting pesticides like atrazine at low concentrations. They could be also applied to the determination of atrazine in environmental aqueous samples, such as seawater and riverine water.

Pressure-Inactivated Virus: A Promising Alternative for Vaccine Production.

In recent years, many applications in diverse scientific fields with various purposes have examined pressure as a thermodynamic parameter. Pressure studies on viruses have direct biotechnological applications. Currently, most studies that involve viral inactivation by HHP are found in the area of food engineering and focus on the inactivation of foodborne viruses. Nevertheless, studies of viral inactivation for other purposes have also been conducted. HHP has been shown to be efficient in the inactivation of many viruses of clinical importance and the use of HHP approach has been proposed for the development of animal and human vaccines. Several studies have demonstrated that pressure can result in virus inactivation while preserving immunogenic properties. Viruses contain several components that can be susceptible to the effects of pressure. HHP has been a valuable tool for assessing viral structure function relationships because the viral structure is highly dependent on protein-protein interactions. In the case of small icosahedral viruses, incremental increases in pressure produce a progressive decrease in the folding structure when moving from assembled capsids to ribonucleoprotein intermediates (in RNA viruses), free dissociated units (dimers and/or monomers) and denatured monomers. High pressure inactivates enveloped viruses by trapping their particles in a fusion-like intermediate state. The fusogenic state, which is characterized by a smaller viral volume, is the final conformation promoted by HHP, in contrast with the metastable native state, which is characterized by a larger volume. The combined effects of high pressure with other factors, such as low or subzero temperature, pH and agents in sub-denaturing conditions (urea), have been a formidable tool in the assessment of the component's structure, as well as pathogen inactivation. HHP is a technology for the production of inactivated vaccines that are free of chemicals, safe and capable of inducing strong humoral and cellular immune responses. Here we present a current overview about the pressure-induced viral inactivation and the production of inactivated viral vaccines.

Fenton-like oxidation of small aromatic acids from biomass burning in water and in the absence of light: implications for atmospheric chemistry.

The oxidation of organic compounds from biomass burning in the troposphere is worthy of concern due to the uncertainty of chemical transformations that occur during the reactions and to the possibility of such compounds producing others more aggressive to the environment in general. In this work was studied the oxidation of relevant atmospheric organic compounds resulting from biomass burning, three small aromatic acids with similar molecular structures (benzoic, 4-hydroxybenzoic and 3,5-dihydroxybenzoic acids), in aqueous phase and in the absence of light. The oxidation process used was the Fenton-like reaction and it was evaluated by ultraviolet-visible and molecular fluorescence spectroscopies. The extent of oxidation of the acids depended on the pH of the solution, and the rate of reaction increased as the pH decreased from neutral (5) to acid (4) in atmospheric waters. Even in the absence of light, Fenton-like oxidation of the three acids originated new chromophoric compounds, which tended to be more complex than the reactants. However, after the formation of new compounds they were totally oxidized for 3,5-dihydroxybenzoic acid and only partially degraded for benzoic and 4-hydroxybenzoic acids, at least after 48 h of reaction at pH 4.5. Furthermore, the night period may be sufficient for a full degradation of the 3,5-dihydroxybenzoic acid and of their oxidation products in atmospheric waters. Thus, the results obtained in this study highlight that organic compounds from biomass burning with similar molecular structures may have different behavior regarding to their reactivity and persistence in atmospheric waters, even without light.

Dissolved organic and inorganic matter in bulk deposition of a coastal urban area: an integrated approach.

Bulk deposition can remove atmospheric organic and inorganic pollutants that may be associated with gaseous, liquid or particulate phases. To the best of our knowledge, few studies have been carried out, which simultaneously analyse the presence of organic and inorganic fractions in rainwater. In the present work, the complementarity of organic and inorganic data was assessed, through crossing data of some organic [DOC (dissolved organic carbon), absorbance at 250 nm (UV250nm), integrated fluorescence] and inorganic [H(+), NH4(+), NO3(-), non sea salt sulphate (NSS-SO4(2-))] parameters measured in bulk deposition in the coastal urban area of Aveiro. The organic and inorganic parameters analysed were positively correlated (p<0.001) except for H(+), which suggests that a constant fraction of chromophoric dissolved organic matter (CDOM) came from anthropogenic sources. Furthermore, the inverse correlations observed for the organic and inorganic parameters with the precipitation amount suggest that organic and inorganic fractions were incorporated into the rainwater partially by below-cloud scavenging of airborne particulate matter. This is in accordance with the high values of DOC and NO3(-) found in samples associated with marine air masses, which were linked in part to the contribution of local emissions from vehicular traffic. DOC of bulk deposition was the predominant constituent when compared with the constituents H(+), NH4(+), NO3(-) and NSS-SO4(2-), and consequently bulk deposition flux was also highest for DOC, highlighting the importance of DOC and of anthropogenic ions being simultaneously removed from the atmosphere by bulk deposition. However, it was verified that the contribution of anthropogenic sources to the DOC of bulk deposition may be different for distinct urban areas. Thus, it is recommended that organic and inorganic fractions of bulk deposition are studied together.

Potamalpheops tyrymembe sp. n.: the first southwestern Atlantic species of the shrimp genus Potamalpheops Powell, 1979 (Caridea: Alpheidae).

A new species of the alpheid shrimp genus Potamalpheops Powell, 1979, P. tyrymembe sp. n., is described based on several specimens collected from burrows of the ucidid crab Ucides cordatus (Linnaeus, 1763) and other, unknown burrowing decapods, on a mangrove flat between the Baiano and Serra rivers, Povoado de Tremembé, Maraú, state of Bahia, Brazil (14º08'51.9"S, 39º05'04.4"W). The new species belongs to the P. monodi (Sollaud, 1932) species group, based on the presence of two pairs of spiniform setae on the distal margin of the telson and non-enlarged male chelipeds. It is characterized by a short rostrum and absence of setae on the pterygostomial angle of the carapace.