Damages observed in locations of Oaxaca due to the Tehuantepec Mw8.2 earthquake,Mexico

On September 7, 2017, at 23:49 h (local time), a Mw8.2 intermediate-depth normal-fault earthquake occurred in the Gulf of Tehuantepec, 133 km away from Pijijiapan, Chiapas, and about 700 km away from Mexico City. This event caused 95 fatalities and severe damage to different types of structures located close to the epicenter. The main objective of this work is to present observed damages caused in the state of Oaxaca by this earthquake, which were mainly concentrated in self-built houses and historical and ancient buildings. The locations visited by the reconnaissance team of the Institute of Engineering from UNAM in Oaxaca included Salina Cruz, Tehuantepec, Ixtaltepec, Juchitán, Huatulco and La Ventosa.

     

Organic and organometallic compounds in estuarine sediments from the Gulf of Mexico (1993–1994)

Sediment samples from 281 estuarine sites in the Gulf of Mexico were collected in 1993–1994 and analyzed for several classes of organic and organometallic compounds as part of the Environmental Monitoring and Assessment Program of the United States Environmental Protection Agency. Polynuclear aromatic hydrocarbons (PAHs) were the contaminant class found most frequently and in the highest concentrations; the sum of 24 congeners (ΣPAHs) ranged from <5 ng g^?1 to 15.500 ng g^?1 (dry wt basis). A low percentage of samples (3.9%) exceeded 2000 ng g^?1 ΣPAHs, and only six samples (2.1%) exceeded 4000 ng g^?1, a level above which adverse biological effects may be expected to occur. Less than 4% of sediments exceeded 20 ng g^?1 for the sum of 20 polychlorinated biphenyls (ΣPCBs) and only four samples (1.4%) exceeded 20 ng g^?1 for the sum of several organochlorine pesticides (ΣOCPs). A sample from Freeport Harbor, Texas, contained 4230 ng g^?1 ΣPAHs, 322 ng g^?1 ΣPCBs, and 49.6 ng g^?1 ΣOCPs. Tributyltin exceeded 100 ng g^?1 in only four samples, all of which were from stations in Corpus Christi Bay or Galveston Bay in Texas. The detection of a suite of organophosphate pesticides was very rare and did not exceed 15 ng g^?1. Sediments from the tidally influenced section of the Mississippi River in Louisiana contained low to moderate levels of all classes of organic compounds. The most contaminated sites were in urban estuaries (e.g., Corpus Christi, Galveston, and Pensacola (Florida bays), underscoring the need to concentrate future monitoring and assessment efforts at the regional and local level.     

Oil seepage and carbonate formation: A case study from the southern Gulf of Mexico

Oil seeps from the southern Gulf of Mexico can be regarded as natural laboratories where the effect of crude oil seepage on chemosynthesis‐based communities and carbonate precipitation can be studied. During R/V Meteor cruise 114 the seep sites UNAM (Universidad Nacional Autónoma de México) Ridge, Mictlan Knoll and Tsanyao Yang Knoll (Bay of Campeche, southern Gulf of Mexico) were investigated and sampled for authigenic carbonate deposits containing large amounts of liquid oil and solid asphalt. The δ¹³C values of individual carbonate phases including: (i) microcrystalline matrix aragonite and calcite; (ii) grey, cryptocrystalline to microcrystalline aragonite; and (iii) clear, fibrous aragonite cement, are between ?30‰ and ?20‰, agreeing with oil as the primary carbon source. Raman spectra reveal that residual heavy oils from all sites are immature and most likely originate from the same reservoir. Geochemical batch modelling using the software code PHREEQC demonstrates how sulphate‐driven oxidation of oil‐derived low‐molecular to high‐molecular weight hydrocarbons affects carbonate saturation state, and shows that the oxidation state of carbon in hydrocarbon compounds and oxidation rates of hydrocarbons control carbonate saturation and precipitation at oil seeps. Phase‐specific trace and rare earth element contents of microcrystalline aragonite and calcite, grey cryptocrystalline aragonite and clear aragonite were determined, revealing enrichment in light rare earth elements for grey aragonite. By comparing trace element patterns of carbonates with those of associated oils, it becomes apparent that liquid hydrocarbons constitute an additional source of trace metals to sedimentary pore waters. This work not only demonstrates that the microbial degradation of oil at seeps may result in the precipitation of carbonate minerals, it also elucidates that trace metal inventories of seep carbonates archive diagnostic elemental patterns, which can be assigned to the presence of heavy hydrocarbons in interstitial pore waters.     

Aquatic hydrocarbon distributions in the Seine estuary: Biogenic polyaromatics and n-alkanes

Dissolved and particulate hydrocarbons of biogenic origin were investigated for the first time in surface waters along the Seine River and its estuary. They comprise n-alkanes (n-ALKs) and diagenetic polycyclic aromatic hydrocarbons (PAHs). Samples were collected in three different sections of the estuary: the riverine zone, the mixing zone, and the marine zone. At the river mouth, two mooring stations were used for the collection of samples over tidal cycles. Total particulate n-ALK concentrations ranged from 31 ng 1^?1 to 2,918 ng 1^?1, or 5 μg g^?1 dry ng 1^?1, or 2 μg g^?1 of SM. Concentrations varied with the SM load and could be related to sedimentation and estuarine mixing. The sources of the n-ALKs were different in each zone of the estuary. The dissolved n-ALKs displayed lower concentrations than the particulate phase, varying from 136 ng 1^?1 to 344 ng 1^?1, while biogenic dissolved PAHs were almost absent.     

Derivation of the Chortis and Chiapas blocks from the western Gulf of Mexico in the latest Cretaceous–Cenozoic: the Pirate model

Currently, two basic models describe the genesis of the Caribbean Plate: (i) a Pacific model that derives the Caribbean Plate off southern Mexico and (ii) an in situ model. The Pacific model requires the 1100–1400 km sinistral displacement recorded across the Cayman Trough to pass through the Gulf of Tehuantepec into the Middle America Trench, but no evidence of such a connection exists. The in situ model is inconsistent with the 1100–1400 km displacement across the Cayman Trough. A way through this impasse is indicated by the northwestward curvature of active oblique reverse to sinistral transcurrent faulting in southeast Mexico. Extending this potential solution back to ca. 80 Ma forms the basis of the new Pirate model, in which the Caribbean Plate and the Chortis and Chiapas blocks are derived from the northwest by anticlockwise rotation during the latest Cretaceous and Cenozoic. Following passage of the Chortis Block, the northern and southern parts of the Yucatan block collided along the intra-Yucatan suture, producing the 11–9 Ma Chiapas fold-and-thrust belt. The Pirate model accounts for the N-trending segment of the Laramide Sierra Madre Oriental–Zongolica foldbelts by anticlockwise drag, Palaeogene palaeocanyons, the second, 66–40 Ma phase of rifting in the western Gulf of Mexico, and post-10 Ma extension in the Chortis Block (Chortis–Sula rift province). Impingement of the East Pacific Rise on the Middle America Trench led to modification of the Pirate model involving subduction erosion of the ～200 km-wide, Eocene–Oligocene forearc at ca. 25 Ma, opening of the Gulf of California at ca. 6 Ma, and birth and ESE movement of the Southern Mexico block (<5 Ma) followed by its fragmentation. The Pirate mechanism indicates that the North American Plate is relatively weak and so tears and rotates into the trailing edge of the Caribbean Plate.     

The distribution, sources and toxicity risks of polycyclic aromatic hydrocarbons and n-alkanes in riverine and estuarine core sediments from the Daliao River watershed

The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g^?1OC^?1 and 6.60 to 366.20 μg g^?1OC^?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQ_BaP) and dioxins (TEQ_TCDD) furnished a consistent assessment of the PAHs in the sediment cores.     

Hydrocarbons in Mississippi Fan and intraslope basin sediments

Aliphatic and aromatic hydrocarbons in sediments of the middle and lower Mississippi Fan and two intraslope basins in the Gulf of Mexico are derived from terrestrial organic matter and thermogenic, mature hydrocarbons. The terrestrial hydrocarbon component consists primarily of terrigenous, plant biowaxes (n-alkanes with 21 to 33 carbons). The occurrence of thermogenic hydrocarbons in immature near-surface sediments, their molecular distributions and concentration variations with depth suggest that the majority of these mature hydrocarbons have migrated from a source much deeper in the sediment column. A portion of the thermogenic hydrocarbons may be derived from recycled material and includes phenanthrene, methyl phenanthrenes, chrysene and benzopyrenes. The migrated, thermogenic hydrocarbons include normal and isoprenoid alkanes with less than 21 carbons, naphthalene, methyl naphthalenes, ethyl naphthalenes and other aromatics of similar volatility (i.e., biphenyl, acenaphthene and fluorene). Triterpane, sterane and aromatized sterane distributions suggest that the thermogenic hydrocarbons at both sites have a common source and are overprinted with immature sediment hydrocarbons. The biomarker distributions and carbon isotopic compositions of the thermogenic hydrocarbons are atypical for petroleum produced in the Gulf of Mexico. Molecular distributions of the hydrocarbons are constant, regardless of the present depth of occurrence, suggesting that they have migrated in a separate phase. The upward migration of hydrocarbons from deeper sources is a wide-spread phenomenon in the Gulf of Mexico with several documented cases of massive seepage (visible oil) as well as the more diffuse permeation of Pleistocene sediments of the Mississippi Fan and two intraslopes reported here.     

Oil exploration in the Southern Gulf of Mexico and the Chicxulub impact

Discovery of the Chicxulub multi-ring impact crater came as a result of oil exploration surveys in the southern Gulf of Mexico. Subsequent studies on the Chicxulub impact and the Cretaceous/Palaeogene (K/Pg) boundary have revealed links between the impact and hydrocarbons, with implications for the K/Pg global environmental and climatic effects, as well as for oil exploration in the Gulf.     

The Los Chocoyos Ash, guatemala: A major stratigraphic marker in middle America and in three ocean basins

The Los Chocoyos Ash, having erupted from vents near the Lake Atitlán caldera, Guatemala, is perhaps the largest Quaternary silicic pyroclastic unit in Central America. It consists of an underlying H-tephra member and an overlying ash-flow member. One-hundred-and-five samples of ash from the Guatemalan Highlands and deep-sea cores in the equatorial Pacific and Gulf of Mexico were analyzed by neutron activation and/or electron microprobe. Glass shard chemistry, determined by microprobe, is useful for distinguishing several very widespread, distinct, deep-sea ash layers, but needs support from trace-element data when applied on land to distinguish between many individual eruptions from the same province. Data from this study support the correlation of the Worzel ‘D’ layer and the Los Chocoyos Ash proposed by Hahn et al. (1979) and Bowles et al. (1973). Chemical data from this study are used to correlate the Y-8 ash layer of the Gulf of Mexico with the Los Chocoyos Ash. The recognition of the Los Chocoyos Ash in the Gulf of Mexico and equatorial Pacific increases the known areal extent of the unit to more than 6 × 10⁶ km² and allows an age of 84,000 yr B.P. to be assigned to the formation on the basis of oxygen-isotope stratigraphy, biostratigraphy, and Pa-Th-isotope data. Trace-element data obtained from seven other ash layers in the Gulf of Mexico and the equatorial Pacific, when combined with new land-based data, should allow further correlation and dating of ash units in Central America.     

Meteorological analysis of the tornado in Ciudad Acuña,Coahuila State,Mexico, on May 25, 2015

Extreme meteorological conditions favor the development of severe storms and tornadoes that may have largely impacts on the population despite its relatively short life. Tornadic severe storms have been documented around the World. In Mexico (MEX), the study of the occurrence of tornadoes and severe storms is relatively new. In this research, we have selected an event of severe tornadic storm in Ciudad Acuña, Mexico. The storm was driven by a frontal system moving southward from USA converging with a warmer moist air flux from the Gulf of Mexico. The tornado strikes on the Northeast of Mexico, in Coahuila State, on May 25, 2015. Imagery of infrared channel from GOES 13 satellite and the presence of a hook echo in radar data of May 25, 2015, indicate a supercell structure. The maximum values of radial velocity were about ?20 and 15 m s^?1. In this study, the WRF model was used in order to simulate the mesoscale meteorological conditions of the tornado. Model simulations capture atmospheric features observed in Doppler radar. The simulated storm-relative helicity values were between 400 and 500 m² s^?2. The simulated convective available potential energy values were of 3000 J kg^?1. These values were higher than values for convective storms, located over the region of Ciudad Acuña in Mexico and Del Rio in USA. The supercell was a result of high humidity and temperature gradients, conditioned by frontal activity and moisture flux intensifications from the Gulf of Mexico.

     

Some observations on the stable carbon isotope composition of dissolved and particulate organic carbon in the marine environment

δ¹³C_PDB compositions for 39 samples of dissolved organic carbon (DOC) from the Gulf of Mexico-Caribbean Sea-Atlantic Ocean system, the South Pacific and Ross Sea are reported. Deep water values are similar with a mean of ?21.8%. attesting to the homogeneity of the oceanic DOC pool. In Antarctic waters, a 5%. difference between DOC and particulate organic carbon (POC), with POC having values similar to modern plankton (δ¹³C_PDB approx ?27%.) supports the idea of the transient nature of POC as compared to DOC.Total, lipid, acid hydrolyzed, amino acid and residue fractions of POC are about 5, 3, 7, 5 and 3%. respectively, more negative in 2000 m water as compared to surface water samples from the Gulf of Mexico.     

Soot in Cretaceous-Paleogene boundary clays worldwide: is it really derived from fossil fuel beds close to Chicxulub?

High soot contents have been reported in Cretaceous-Paleogene boundary (KPB) clays worldwide. One of the interpretations suggests this material comes from combustion of fossil fuels such as crude oil, coal or oil shales near the Chicxulub impact site. Combustion was triggered by the KPB impactor. In this Note, I show that the estimated mass of crude oil (or fossil hydrocarbons in general) burned (ca. 10¹⁷?C10¹⁹ g), based on the average amount of soot (0.0022?C0.012 g cm^?2) or elemental carbon (0.011 g cm^?2) found at the marine KPB sites, contradicts the fossil hydrocarbons hypothesis.     

A chemical survey of the Mississippi estuary

A “snap shot” survey of the Mississippi estuary was made during a period of low river discharge, when the estuarine mixing zone was within the deltaic channels. Concentrations of H⁺, Ca²⁺, inorganic phosphorus and inorganic carbon suggest that the waters of the river and the low salinity (<5‰) portion of the estuary are near saturation with respect to calcite and sedimentary calcium phosphate. An input of oxidized nitrogen species and N₂O was observed in the estuary between 0 and 4‰ salinity. The concentrations of dissolved NH₄ ⁺ and O₂, over most of the estuary, appeared to be influenced by decomposition of terrestrial organic matter in bottom sediments. The estuarine bottom also appears to be a source of CH₄ which has been suggested to originate from petroleum shipping and refining operations. Estuarine mixing with offshore Gulf waters was the dominant influence on distributions of dissolved species over most of the estuary (i.e., from salinities >5‰). The phytoplankton abundance (measured as chlorophylla) increased as the depth of the mixed layer decreased in a manner consistent with that expected for a light-limited ecosystem. Fluxes of NO₃ ^?+NO₂ ^? and soluble inorganic phosphorus to the Gulf of Mexico were estimated to be 3.4±0.2×10³ g N s^?1 and 1.9±0.2 g P s^?1 respectively, at the time of this study.     

Impacts of Hypoxia on Zooplankton Spatial Distributions in the Northern Gulf of Mexico

The northern Gulf of Mexico (NGOMEX) was surveyed to examine the broad-scale spatial patterns and inter-relationships between hypoxia (<2?mg?L^?1 dissolved oxygen) and zooplankton biovolume. We used an undulating towed body equipped with sensors for conductivity, temperature, depth, oxygen, fluorescence, and an optical plankton counter to sample water column structure, oxygen, and zooplankton at high spatial resolution (1?m??vertical; 0.25?C1?km??horizontal). We contrast the distribution of zooplankton during summer surveys with different freshwater input, stratification, and horizontal and vertical extent of bottom-water hypoxia. Bottom-water hypoxia did not appear to influence the total amount of zooplankton biomass present in the water column or the areal integration of zooplankton standing stock in the NGOMEX region surveyed. However, where there were hypoxic bottom waters, zooplankton shifted their vertical distribution to the upper water column during the day where they normally would reside in deeper and darker waters. When bottom waters were normoxic (>2?mg?L^?1 dissolved oxygen), the daytime median depth of the water column zooplankton was on average 7?m deeper than the median depth of zooplankton in water columns with hypoxic bottom waters. A reduction in larger zooplankton when there were hypoxic bottom waters suggests that if zooplankton cannot migrate to deeper, darker water under hypoxic conditions, they may be more susceptible to size-selective predation by visual predators. Thus, habitat compression in the northern Gulf of Mexico due to hypoxic bottom water may have implications for trophic transfer by increasing the contact between predators and prey.     

Tephrochronology of the western Gulf of Mexico for the last 185,000 years

Tephra in 31 piston cores from the western Gulf of Mexico and 7 piston cores from the equatorial Pacific were analyzed by electron microprobe. Six ash layers in the western Gulf of Mexico were easily distinguished by TiO₂, FeO, and CaO contents and correlated by geochemistry in order to determine the distribution pattern for each ash layer. Correlation by geochemistry is an easier, more accurate method than biostratigraphic correlation; some of the tephras were miscorrelated by biostratigraphy. The six tephras were dated by geochemical identification in a piston core with oxygen-isotope stratigraphy and the ages are Y5 (30,000 yr B.P.), Y6 (65,000 yr B.P.), Y8 (84,000 yr B.P.), X2 (110,000 yr B.P.), W1 (136,000 yr B.P.), and W2 (185,000 yr B.P.). Data from this study corroborated correlations of the Y8 tephra in the western Gulf of Mexico with the D layer in the eastern equatorial Pacific Ocean. None of the other five layers in the Gulf of Mexico, however, were found in the Pacific Ocean. The limited distribution of the Y5, Y6, X2, and W2 ash layers close to Mexico indicates possible sources in Mexico. Tephra from the late Pleistocene La Primavera pumice in Mexico, however, does not correlate with the marine tephra.     

Tidal river sediments in the Washington,D.C. area. II. Distribution and sources of organic contaminants

Concentration of aliphatic, aromatic, and chlorinated hydrocarbons were determined from 33 surface-sediment samples taken from the Tidal Basin, Washington Ship Channel, and the Anacostia and Potomac rivers in Washington, D.C. In conjunction with these samples, selected storm sewers and outfalls also were sampled to help elucidate general sources of contamination to the area. All of the sediments contained detectable concentrations of aliphatic and aromatic hydrocarbons, DDT (total dichlorodiphenyltrichloroethane), DDE (dichlorodiphenyldichloroethene), DDD (dichlorodiphenyldichloroethane), PCBs (total polychlorinated biphenyls) and total chlordanes (oxy-, α-, and γ-chlordane and cis + trans-nonachlor). Sediment concentrations of most contaminants were highest in the Anacostia River just downstream of the Washington Navy Yard, except for total chlordane, which appeared to have upstream sources in addition to storm and combined sewer runoff. This area has the highest number of storm and combined sewer outfalls in the river. Potomac River stations had lower concentrations than other stations. Total hydrocarbons (THC), normalized to the fine-grain fraction (clay + silt, < 63 μm), ranged from 120 μg g^?1 to, 1,900 μg g^?1 fine-grain sediment. The hydrocarbons were dominated by the unresolved complex mixture (UCM), with total polycyclic aromatic hydrocarbons (PAHs) concentrations ranging from 4 μg g^?1 to 33 μg g^?1 fine-grain sediment. Alkyl-substituted compounds (e.g., C1 to C4 methyl groups) of naphthalene, fluorene, phenanthrere + anthracene, and chrysene series dominated the polycyclic aromatic hydrocarbons (PAHs). Polycyclic aromatic hydrocarbons, saturated hydrocarbons, and the unresolved complex mixture (UCM) distributions reflect mixtures of combustion products (i.e., pyrogenic sources) and direct discharges of petroleum products. Total PCB concentrations ranged from 0.075 μg g^?1 to 2.6 μg g^?1 fine-grain sediment, with highest concentrations in the Anacostia River. Four to six C1-substituted biphenyls were the most-prevalent PCBs. Variability in the PCB distribution was observed in different sampling areas, reflecting, differing proportion of Arochlor inputs and degradation. The concentration of all contaminants was generally higher in sediments closer to known sewer outfalls, with concentrations of total hydrocarbon, PAHs, and PCBs as high as 6,900 μg g^?1, 620 μg g^?1, and 20 μg g^?1 fine-grain sediment, respectively. Highest PCB concentrations were found in two outfalls that drain into the Tidal Basin. Concentrations of organic contaminants from sewers draining to the Washington Ship Channel and Anacostia River had higher concentrations than sediments of the mid-channel or river. Sources of PCBs appear to be related to specific outfalls, while hydrocarbon inputs, especially PAHs, are diffuse, and may be related to street runoff. Whereas most point-source contaninant inputs have been regulated, the importance of nonpoint source inputs must be assessed for their potential addition of contaminants to aquatic ecosystems. This study indicates that in large urban areas, nonpoint sources deliver substantial amounts of contaminants to ecosystems through storm and combined sewer systems, and control of these inputs must be addressed.     

Nutrient transport in a riverine-influenced,tidal freshwater bayou in Louisiana

Transport of ammonium (NH₄ ⁺), nitrate + nitrite (NO₃ ^?), total Kjeldahl nitrogen (TKN), soluble reactive phosphate (SRP), and total suspended solids (TSS) was measured in a freshwater tidal bayou located in a marsh system near the mouth of the Atchafalaya River in Louisiana. Sampling was conducted six times over one year and was timed to assess effects of seasonal variation in river flow and mean sea level of the Gulf of Mexico on material fluxes. Net fluxes of all materials were large and ebb directed in all seasons except fall, when net transport was 2 to 3 orders-of-magnitude smaller than in any other season. These results demonstrate that riverine forcing was the primary influence on materials transport in all seasons except fall when tidal forcing was most important. The range of net fluxes (g s^?1) for each nutrient was as follows (a negative sign indicates a net export toward the Gulf): NO₃ ^?, ?0.006 to ?6.69; TKN, 0.09 to ?10.41; NH₄ ⁺, ?0.02 to ?1.36; SRP, ?0.001 to ?0.53; TSS, ?2 to ?81. Analysis of nutrient concentrations indicated the marsh/aquatic system removed NO₃ ^?, SRP, and TSS from the water column from late spring through early fall and released NH₄ ⁺ and TKN in summer. The results of this study show that net materials export per unit cross section channel area increased as riverine influence increased.     

Small Spatial Scale Variation in Fish Assemblage Structure in the Vicinity of the Northwestern Gulf of Mexico Hypoxic Zone

Seasonal hypoxia [dissolved oxygen (DO)?≤?2 mg?l^?1] occurs over large regions of the northwestern Gulf of Mexico continental shelf during the summer months (June–August) as a result of nutrient enrichment from the Mississippi–Atchafalaya River system. We characterized the community structure of mobile fishes and invertebrates (i.e., nekton) in and around the hypoxic zone using 3 years of bottom trawl and hydrographic data. Species richness and total abundance were lowest in anoxic waters (DO?≤?1 mg?l^?1) and increased at intermediate DO levels (2–4 mg?l^?1). Species were primarily structured as a benthic assemblage dominated by Atlantic croaker (Micropogonias undulatus) and sand and silver seatrout (Cynoscion spp.), and a pelagic assemblage dominated by Atlantic bumper (Chloroscombrus chrysurus). Of the environmental variables examined, bottom DO and distance to the edge of the hypoxic zone were most strongly correlated with assemblage structure, while temperature and depth were important in some years. Hypoxia altered the spatial distribution of both assemblages, but these effects were more severe for the benthic assemblage than for the pelagic assemblage. Brown shrimp, the primary target of the commercial shrimp trawl fishery during the summer, occurred in both assemblages, but was more abundant within the benthic assemblage. Given the similarity of the demersal nekton community described here to that taken as bycatch in the shrimp fishery, our results suggest that hypoxia-induced changes in spatial dynamics have the potential to influence harvest and bycatch interactions in and around the Gulf hypoxic zone.     

Distribution of polycyclic aromatic hydrocarbons in recent sediments of Sundarban mangrove wetland of India and Bangladesh: a comparative approach

The present work is the first attempt to compare the data of a comprehensive study of the origin and distribution of 16 priority pollutant polycyclic aromatic hydrocarbons (PAHs) in surface sediments (<63 μm) from 18 sampling stations, 9 from Sundarban of Bangladesh and 9 from Indian counterpart. Σ19PAHs concentration in sediments showed wide variations from 208.3 to 12,993.1 ng g^?1 dry weight in Indian Sundarban, whereas 208.4 to 4,687.9 ng g^?1 in the case of Bangladesh. Fluoranthene, pyrene, benzo(b)fluoranthene, benzo(a)pyrene and dibenzo(a,h)anthracene were predominant species for both the countries. The PAH diagnostic ratios indicated that the PAHs in sediments from both the countries were of mixed source of hydrocarbons of both petrogenic and pyrolytic origin. According to the numerical effect-based sediment quality guidelines, the levels of PAHs in the Sundarban wetland of Bangladesh and India should not exert adverse biological effects. The TEQ values calculated for samples from the Bangladesh and Indian Sundarban varied from 13.68 to 1,014.75 and 1.31 to 2,451 ng g^?1 d.w. with an average of 221.02 and 358.63 ng g^?1, respectively. The overall contamination status of PAH was higher in India than Bangladesh.     

The effect of long-term soil irrigation by wastewater on organic matter, polycyclic aromatic hydrocarbons, and heavy metals evolution: case study of Zaouit Sousse (Tunisia)

Irrigation by treated wastewater (TWW) can pollute the soil by different organic and inorganic compounds. The pollution level can depend on the irrigation period, soil nature, and wastewater characteristics. Since 1989, the Zaouit Sousse area (central Tunisian) has been irrigated by treated wastewater. The irrigation period and the mineralogy of soil composition change from one locality to another in Zaouit Sousse area. In this work, we are interested in organic compounds, polycyclic aromatic hydrocarbons (PAHs), and heavy metals (HMs) evolution. One control soil (S1) and four irrigated areas soil (S2, S3, S4, and S5) were chosen. The soil samples differ by the irrigation period and soil characteristics. Total PAHs content in control soil was 66.2 ng?g^?1 and in irrigated areas were between 46.23 and 129.51 ng?g^?1. The PAHs content in irrigated soil, except S5 which has been irrigated with wastewater for 20 years and contains the highest clay fraction percent, decreased with the irrigation period (from 0 to 20 years). The microbial degradation may decrease the PAHs concentrations in the soil thanks to bacterium brought by TWW and the important soil permeability. Concentration of heavy metals ranged from 24 to 1,320 μg?L^?1. The HMs (Cu, Cr, Zn, Fe, Ni, Pb, and Cd) contents decreased with the irrigation period (from 10 to 20 years). So, following the PAHs aerobic bio-degradation, this organic compound discharges their absorbed heavy metals which leached to deeper levels. The Cr, Cu, Al, Zn, and Cd mobility depend on the clay yield too. However, the PAHs and Pb mobility are also related to humic substance quantities. Cr and Cu have affinities both to clay and humic substance quantities.