Paleoclimatic implications of late quaternary lacustrine sediments in Western Nubia, Sudan

Owing to the hypercontinental location of Western Nubia, secular fluctuations of climate have been filtered and wet phases can be considered as representative of conditions throughout the southeastern Sahara. The study area is crossed by the 20-mm isohyet; between 9300 and about 4000 yr B.P., however, there were widespread lake and swamp environments with freshwater molluscs, ostracods, and diatoms, and a species-rich savanna mammal fauna. The center of the West Nubian Basin (approx. 18°N), an area of about 20,000 km², was occupied by a semiaquatic landscape which was situated at the same latitude as Paleolake Chad. From extensive lake carbonates up to about 4 m thick, a long-term rise of the groudwater table is inferred. Environments developed that now exist at about latitude 13°N. Radiocarbon dates from lake sediment sequences cluster between 30,000 and 21,000 yr B.P., indicating a Pleistocene wet phase. A gap in radiocarbon dates between 21,000 and 11,000 yr B.P. signals a phase of hyperaridity, similar to the present hyperarid phase, with eolian deflation and deposits of sand being the dominant forms of erosion and accumulation.     

Calcium isotope evidence for suppression of carbonate dissolution in carbonate-bearing organic-rich sediments

Pore fluid calcium isotope, calcium concentration and strontium concentration data are used to measure the rates of diagenetic dissolution and precipitation of calcite in deep-sea sediments containing abundant clay and organic material. This type of study of deep-sea sediment diagenesis provides unique information about the ultra-slow chemical reactions that occur in natural marine sediments that affect global geochemical cycles and the preservation of paleo-environmental information in carbonate fossils. For this study, calcium isotope ratios (δ^44/40Ca) of pore fluid calcium from Ocean Drilling Program (ODP) Sites 984 (North Atlantic) and 1082 (off the coast of West Africa) were measured to augment available pore fluid measurements of calcium and strontium concentration. Both study sites have high sedimentation rates and support quantitative sulfate reduction, methanogenesis and anaerobic methane oxidation. The pattern of change of δ^44/40Ca of pore fluid calcium versus depth at Sites 984 and 1082 differs markedly from that of previously studied deep-sea Sites like 590B and 807, which are composed of nearly pure carbonate sediment. In the 984 and 1082 pore fluids, δ^44/40Ca remains elevated near seawater values deep in the sediments, rather than shifting rapidly toward the δ^44/40Ca of carbonate solids. This observation indicates that the rate of calcite dissolution is far lower than at previously studied carbonate-rich sites. The data are fit using a numerical model, as well as more approximate analytical models, to estimate the rates of carbonate dissolution and precipitation and the relationship of these rates to the abundance of clay and organic material. Our models give mutually consistent results and indicate that calcite dissolution rates at Sites 984 and 1082 are roughly two orders of magnitude lower than at previously studied carbonate-rich sites, and the rate correlates with the abundance of clay. Our calculated rates are conservative for these sites (the actual rates could be significantly slower) because other processes that impact the calcium isotope composition of sedimentary pore fluid have not been included. The results provide direct geochemical evidence for the anecdotal observation that the best-preserved carbonate fossils are often found in clay or organic-rich sedimentary horizons. The results also suggest that the presence of clay minerals has a strong passivating effect on the surfaces of biogenic carbonate minerals, slowing dissolution dramatically even in relation to the already-slow rates typical of carbonate-rich sediments.     

Geochemistry of deep-sea sediments in two cores retrieved at the mouth of the Coatzacoalcos River delta,western Gulf of Mexico,Mexico

Coastal margins, especially the river-influenced coastal areas, are considered as active interfaces between the continental and oceanic environments, which have huge dispersal of detrital materials and heavy metal input. It is well determined that the fine-grained sediments are important reservoir for the accumulation of heavy metals. In this study, we analyzed the radiocarbon age, texture, organic matter, carbonate content, and geochemical compositions of two sediment cores (GM42 and GM44) retrieved in front of the Coatzacoalcos River mouth basin, southwestern Gulf of Mexico (～864 and 845 m water depth, respectively). Our objective was to infer the sedimentation rate, intensity of weathering, provenance, and influence of anthropogenic activities on heavy metal contamination in sediments. The radiocarbon-age measurements of mixed planktonic foraminifera for core GM44 reveals an age of 21,289 ± 136 cal. years B.P., which fall within the Late Glacial Maximum (LGM; 21000 ± 2000 years B.P). The calculated sedimentation rate for core GM42 (~0.013 cm/year) is lower than in core GM44 (0.022 cm/year), which is probably due to the variations in detrital sediment input and/or seafloor topography. The weathering indices such as chemical index of alteration (CIA), chemical index of weathering (CIW), and plagioclase index of alteration (PIA) suggested that the source area experienced low to moderate intensity of chemical weathering under warm to humid climatic conditions. The SiO₂/Al₂O₃, Al₂O₃/Na₂O, and K₂O/Al₂O₃ ratio values indicated moderate to high compositional maturity. The major and trace element concentrations suggested that the sediments were likely derived from intermediate source rocks. The heavy metal contents indicated that the sediments were not contaminated by the industrial waste disposals supplied by the Coatzacoalcos River. The redox proxy sensitive elements such as V, Cr, Cu, and Zn indicated an oxic depositional environment for the deep-sea sediment cores. The application of discrimination diagrams for the geochemistry data revealed a passive margin setting for the sediment cores. The compositional variations observed at the upper sections (<30 cm) between the two sediment cores revealed that the type of detrital sediments supplied by the Coatzacoalcos River to the deep sea area is not uniform, which is also revealed by the variation in sedimentation rate.     

A method for quantitative evaluation of carbonate dissolution in deep-sea sediments and its application to paleoceanographic reconstruction

A method is proposed by which the degree of attrition of the tests of certain foraminifera species, such as Globorotalia menardii and Globorotalia tumida, is used to “scale” the amount of CaCO₃ that has been dissolved from sediment. The scale is calibrated experimentally in the laboratory. The method has been applied to three calcareous cores from the Pacific and the Indian Oceans. It is shown that the original CaCO₃ contents in these cores were high (82–95%) and relatively uniform compared to the present down-core values. About 65 to 85% of the originally deposited CaCO₃ has been dissolved, corresponding to dissolution rates on the order of 0.1-0.3 moles/cm²/yr. These results indicate that appreciable solution could have occurred on sea floor rich in calcareous sediments and that the variation in CaCO₃ content in a core may have resulted largely from dissolution. The difference in the degree of solution between glacial and interglacial sediments in these cores is not so distinct, with ? 10% less intense dissolution during glacial times on the average. However, the dissolution minimum occurring around the late Wisconsin glaciation (10,000–20,000 yr B.P.) previously noted in several cores elsewhere is confirmed. At that time, near the site of core M70 PC-20 in the southwest Pacific, the $\text{CO}{}_3{}^{\mathrm{2?}}$ concentration of the bottom water is estimated to have been approximately 5% higher than the present value, and the calcite lysocline was about 300 m deeper. To evaluate possible variations in CaCO₃ deposition rate across the glacial-interglacial transitions requires precise age control, which the present study lacks.     

Calcium carbonate dissolution in deep sea sediments: reconciling microelectrode, pore water and benthic flux chamber results

We report the benthic fluxes of O₂, titration alkalinity (TA), Ca²⁺, NO₃⁻, PO₄³⁻, and Si(OH)₄ from in situ benthic flux chamber incubations on the Ceara Rise and Cape Verde Plateau and compare them to previously published results. We find within analytical uncertainty that the TA flux is twice the calcium flux, suggesting that dissolution/precipitation of CaCO₃ is the principal mechanism controlling benthic TA and Ca²⁺ fluxes. At sites where the sediments contain significant (>35%) CaCO₃ and the overlying waters are supersaturated with respect to CaCO₃, the ratios of the total dissolution rate to the remineralization rate are significantly less than at all other study sites. We propose that these observations can be explained by precipitation of fresh CaCO₃ at the supersaturated sediment surface followed by redissolution deeper in the sediments because of metabolically-produced CO₂. A numerical simulation is presented to demonstrate the feasibility of this explanation. In addition, surface exchange reactions in high-CaCO₃ sediments coupled with high rates of particle mixing may also impact rates of metabolic dissolution and depress chamber-derived estimates of carbonate alkalinity and calcium benthic fluxes. These results suggest that at supersaturated, high CaCO₃ locations, previous models of sediment diagenesis may have overestimated the impact of metabolic dissolution on the preservation of CaCO₃ deposited on the sea floor.     

Geochemistry of late quaternary sediments from Tecocomulco lake, central Mexico: Implication to chemical weathering and provenance

This paper presents the first detailed multi-element geochemical data from the late Quaternary sediments of the Tecocomulco lake basin (central Mexico) and rocks exposed in the basin catchments to understand the extents of chemical weathering and provenance of the siliciclastic fractions. Ternary diagrams of A-CN-K, A-C-N and A-CNK-FM and elemental ratios suggest that most of the lacustrine sediments were derived from mafic volcanic deposits comprising the Chichicuatla and the Apan-Peñon andesites and the Apan-Tezontepec basaltic-andesites. The felsic tephra layers have chemical compositions comparable to the Acoculco volcanic sequences. The calculated indices of chemical weathering such as chemical index of alteration (CIA), plagioclase index of alteration (PIA) and chemical index of weathering (CIW) indicate low to extreme chemical weathering for the lacustrine sediments and low chemical weathering for tephra layers. The varying degree of chemical weathering in lacustrine sediments is related to the fluctuating average annual precipitation during the late Quaternary. However, the low weathering of tephra layers are due to their higher rate of deposition. The dacite-rhyolitic tephra layers of ca. 31,000 ¹⁴C yr BP are relatively more weathered compared to the unweathered rhyolitic tephra of ca. 50,000 ¹⁴C yr BP. This could be due to the rapid deposition of ca. 200 cm of tephra layers during the ca. 50,000 ¹⁴C yr BP volcanic eruption that might have prevented the interaction between tephra layers and weathering agents.     

The distribution of dibenzothiophenes in Gulf of Mexico sediments

Sediment extracts from 81 piston cores taken in water depths between 70 and 1200 m on the Gulf of Mexico continental shelf and slope were analyzed for dibenzothiophenes by capillary gas chromatography with flame photometric detection (FPD). The major aromatic sulfur compounds detected were dibenzothiophene; methyl, ethyl and propyl dibenzothiophenes; two unidentified sulfur compounds; and a series of benzothiophenes. In general, benzothiophenes (BTs) were detected at only trace levels though this may be due to loss during the analysis. Dibenzothiophenes (DBTs) concentrations ranged from <1 to 1725 ng/g, with an average of 139 ng/g. Vertical distributions generally showed significant increases in DBTs concentrations with depth. DBTs distributions in sediment extracts were similar to oils produced in the northern Gulf of Mexico. Variations from this composition may be due to microbial degradation in the near subsurface. The vertical and molecular distribution of DBTs suggests that the source of DBTs in the Gulf of Mexico sediments studied is upward migrating petroleum. Two unidentified compounds are speculated to be derivatives of DBTs, caused by indigenous microbial activity. This study suggests that DBTs may be useful for detecting seepage from deeper, more mature, source rocks and/or reservoired petroleum.     

Contaminants in sediments from the central Gulf of Mexico

Surface sediment samples at 89 locations and 300-cm cores from 43 sites in the Mississippi Sound were examined for evidence of pollutant impact upon this coastal environment. Chemical variables determined were total organic carbon, Kjeldahl nitrogen, phenols, and hydrocarbons. Values of these pollutant indicators were about the same or lower in Gulf of Mexico samples compared to Missippi Sound sediments and considerably lower than those from rivers and bays emptying into the sound, indicating limited impact from sites of pollutant sources into the sound. Concentrations of sedimentary pollutants peaked in the Pascagoula River where levels of total organic carbon (TOC), Kjeldahl nitrogen (TKN), phenols, and hydrocarbons exceeded sound values by one to three orders of magnitude. Analysis of cores shows pollutant intrusion to sediment strata predating industrial development. The level of pollution varies from site to site but fortunately is only serious at localized sites within the sound.     

10Be meltwater signal in Orca basin sediments,Gulf of Mexico

An increase in the cosmogenic beryllium-10 content of the Orca basin sediments due to the flooding of the Gulf of Mexico (GM) by meltwaters during the late Wisconsin interglacial is reported. A strong negative correlation (γ =-0.99) betweenδ ¹⁸ O (in the range o f-1.5‰ to +0.5‰) and¹⁰Be/Al ratio is seen. During intense flooding reflected by a decrease in δ¹⁸O by ∼ 2‰, this correlation may not hold as some of the sediments with low¹⁰Be/Al ratio and deposited on the shelf and slope regions of the GM during the earlier glacial period would also be washed into the basin. The deposited sediment would then be a mixture with a¹⁰Be/Al ratio lower than expected from the correlation     

On the relationship between silica and carbonate diagenesis in deep-sea sediments

Silica diagenesis and carbonate diagenesis are interrelated. This is confirmed by observations of DSDP Sites 462, 463, 465, 466, and 577. Carbonate sediments containing chert (1) tend to be more indurated and display more advanced diagenetic alterations, regardless of sub-bottom depth; and (2) microfossil components are more strongly affected (overgrown and/or dissolved), while the amount of micritic particles and larger, euhedral calcite crystals is greater. In addition, mass physical properties, porosity in particular, vary more widely in sediment sections containing chert. Furthermore, in the studied similarly composed sediments recrystallization of biogenic opal is indicated by a significant reduction of the specific surface area, reaching a minimum value when quartz is formed.One possible mechanism involved is the production of «surplus« dissolved carbonate created by the replacement of carbonate material by silica during the process of chert formation and silicification. The «extra« carbonate is then available for precipitation as overgrowths and cement outside the chert nodules and silicified zones. Hence silica diagenesis, if it occurs early enough in the sediment, bears some influence on carbonate diagenesis. It is therefore suggested that silica diagenesis be added to the list of factors included in the «diagenetic potential« equation ofSchlanger &Douglas (1974).

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Zusammenfassung Die Diagenese von biogenem Silikat und Karbonat steht in engem Zusammenhang, wie Beobachtungen an Sedimenten der DSDP Sites 462, 463, 465, 466 und 577 zeigen. Karbonatische Sedimente, die biogenes SiO₂ enthalten, zeichnen sich aus durch (1) größere Verfestigung und stärkere diagenetische Veränderungen — unabhängig von der Tiefe im Sediment, (2) mehr Lösung und Überwuchs an Mikrofossil-Komponenten, (3) höheren Anteil mikritischer Partikel wie auch größerer idiomorpher Kalzitkristalle, (4) stärkere Variation der sedimentphysikalischen Eigenschaften, speziell der Porosität und damit zusammenhängender Parameter.Die Umkristallisation des biogenen SiO₂ führt in ähnlich Zusammengesetzen Sedimenten zu einer drastischen Abnahme der spezifischen Oberfläche. Minimalwerte werden erreicht, wenn sich Quarz bildet.Diagenetisch wichtig ist die Produktion von zusätzlichem Karbonat durch die Silizifizierung von Karbonatschalen. Dieses »Überschuß«-Karbonat wird dann als Überwuchs, Zement oder außen an den »Hornstein«-Aggregaten gefällt. Demzufolge beeinflußt die Diagenese von biogenem SiO₂ auch die Karbonatdiagenese. Daher ist es sinnvoll, die Diagenese von biogenem SiO₂ mit zu den Faktoren zu rechnen, die das »diagenetische Potential« — wie esSchlanger &Douglas (1974) definierten — ausmachen.

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Résumé L'étude de sédiments provenant des sites DSDP 462, 463, 465, 466 et 577 montre qu'il existe une relation entre la diagenèse de la silice et celle du carbonate biogéniques. Les sédiments carbonatés qui renferment de la silice biogémque présentent: 1) une induration plus marquée et des modifications diagénétiques plus poussées — et ce indépendamment de la profondeur sous la surface du fond; 2) une dissolution et/ou un accroissement plus développés des micro-fossiles; 3) une plus grande teneur en particules micritiques et une plus grande taille des calcites idiomorphes; 4) un éventail plus large de leurs propriétés physiques, particulièrement de la porosité et des paramètres qui en dépendent.La cristallisation de l'opale biogénique, dans des sédiments de compositions semblables, se traduit par une réduction drastique de la surface spécifique, qui atteint une valeur minimale lorsque du quartz est formé.Un rôle diagénétique important est joué par l'excès de carbonate dissous engendré par la silicification de coquilles carbonatées; cet excès de carbonate est dès lors disponible pour la précipitation des auréoles d'accroissement et du ciment hors des nodules de chert et des zones silicifiées. Il s'ensuit que la diagenèse du SiO₂ biogénique influence la diagenèse du carbonate. Il conviendrait dès lors d'ajouter la diagenèse de la silice à la liste des facteurs qui interviennent dans l'équation du «potentiel diagénétique» deSchlanger etDouglas (1974).

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462, 463, 465, 466 577, . , , : 1) , ; 2) ; 3) , 4) , . SiO₂ . . . »« , , « ». , .. «, 1974 Schlanger & Douglas.

     

Mineralogy,geochemistry, and radiocarbon ages of deep sea sediments from the Gulf of Mexico,Mexico

The mineralogy, geochemistry, and radiocarbon ages of two sediment cores (GMX1 and GMX2) collected from the deep sea area of the Southwestern Gulf of Mexico (∼876–1752 m water depth) were studied to infer the sedimentation rate, provenance, heavy metal contamination, and depositional environment. The sediments are dominated by silt and clay fractions. The mineralogy determined by X-Ray diffractometry for the sediment cores reveals that montmorillonite and muscovite are the dominant clay minerals. The sections between 100 and 210 cm of the sediment cores GMX1 and GMX2, respectively, are characterized by the G. menardii group and G. Inflata planktonic foraminiferal species, which represent the Holocene and Pleistocene, respectively. The radiocarbon-age measurements of mixed planktonic foraminifera varied from ∼268 to 45,738 cal. years B.P and ∼104 to 25,705 cal. years B.P, for the sediment cores GMX1 and GMX2, respectively. The variation in age between the two sediment cores is due to a change in sediment accumulation rate, which was lowest at the location GMX1 (0.006 cm/yr) and highest at the location GMX2 (0.017 cm/yr).The chemical index of alteration (CIA), chemical index of weathering (CIW), and index of chemical maturity (ICV) values indicated a moderate intensity of weathering in the source area. The total rare earth element concentrations (∑REE) in the cores GMX1 and GMX2 vary from ∼94 to 171 and ∼78 to 151, respectively. The North American Shale Composite (NASC) normalized REE patterns showed flat low REE (LREE), heavy REE (HREE) depletion with low negative to positive Eu anomalies, which suggested that the sediments were likely derived from intermediate source rocks.The enrichment factor of heavy metals indicated that the Cd and Zn concentrations in the sediment cores were impacted by an anthropogenic source. The redox-proxy trace element ratios such as V/Cr, Ni/Co, Cu/Zn, (Cu + Mo)/Zn, and Ce/Ce* indicated that the sediments were deposited under an oxic depositional environment. The similarity in major element concentrations, REE content, and the NASC normalised REE patterns between the cores GMX1 and GMX2 revealed that the provenance of sediments remained relatively uniform or constant during deposition for ∼4.5 Ma. The major and trace element based multidimensional discrimination diagrams showed a rift setting for the core sediments, which is consistent with the geology of the Gulf of Mexico.     

Coastal morphology and late quaternary history,Cayman Islands,West Indies

Instrumental surveys of coastal profiles in the Cayman Islands, western Caribbean, reveal the presence of a horizontal erosional bench at +1.9 m on Grand Cayman and a deep horizontal notch at +6.4 m on Cayman Brac, but no raised erosional features on Little Cayman. Each island is surrounded by a horizontal constructional raised reef, usually below +2 m, here dated by U-series methods as 124,000 ± 8000 yr old, and hence broadly contemporary with other western Atlantic raised reefs of similar elevations. The different raised erosional features indicate independent vertical tectonic movement of the three islands, predating the formation of the raised reef. The accordance and horizontality of the raised reef indicates stability of the islands since the last interglacial times. An erosional notch at present sea level has formed since the sea reached its present level less than 2100 B.P., and algal benches on exposed coasts are also in equilibrium with present conditions.     

Climate and ocean variability during the middle and late Holocene recorded in laminated sediments from Alfonso Basin, Gulf of California, Mexico

A laminated sequence (core BAP96-CP 24°38.12′N, 110°33.24′W; 390 m depth) from the Alfonso Basin in Bay of La Paz, southern Gulf of California, contains a record of paleoceanographic and paleoclimatic changes of the past 7900 yr. Radiolarian assemblages and magnetic susceptibility are used as proxies of oceanographic and climatic variability. The records provide a regional scenario of the middle and late Holocene, suggesting two major climatic regimes and several millennial-scale events. Conditions relatively warmer and drier than today occurred from 7700 to 2500 cal yr BP, promoting the intensification of evaporation processes and the prevalence of the Gulf of California water in the Basin. These conditions correlate with strong droughts in the middle Holocene of North America and with minimal incursion of tropical waters into the Gulf of California. Proxies indicate a warm scenario and the dominance of the Equatorial Surface Water in the Alfonso Basin from 2400 to 700 cal yr BP, suggesting the intensification of ENSO cycles. A climatic signal between 1038 and 963 cal yr BP may be correlated with global signal of the “Medieval Warm Period.” Several cooling events are recognized at 5730, 3360, 2700, 1280 and 820 cal yr BP and are associated with intensification of northwest winds leading to upwellings and enhanced productivity in the Basin.     

A geochemical study of some lithified carbonate sediments from the deep-sea

Unconsolidated oozes, partially lithified oozes, recrystallized limestones, dolostones and crystalline aragonite are some of the varieties of carbonate sediment that have been found in the deep-sea; chemical and isotopic analyses of these varieties are presented here. The consolidated oozes and recrystallized limestones are low-Mg calcites and are often associated with basement rock (generally serpentinized peridotite or basalt) detritus. Lithification is suggested to arise from changes in the carbonate-equilibria system of the interstitial waters resulting from chemical degradation of the igneous rocks. When compared to unconsolidated oozes, lithification is seen to be accompanied by loss of Sr and a slight increase in B, Ba, Co, Cr, Ni and Y in most instances. The tuffaceous limestones are also low-Mg calcites, but are characterized by low Sr and relatively high B, Ba, Co, Cr, Cu, Ni, V, Y and Zn concentrations compared to the oozes. Three dolostones are described of very different isotopic and chemical composition, possibly indicating three different pathways of dolomitization. One with much depleted ¹³C and high Ba concentrations is probably derived from waters containing carbon from a fractionated organic source. Another is not greatly different from the consolidated limestones in minor and trace element composition and may be derived from them. The third variety is characterized by low concentrations of Sr, B, Ba, Cu and Y and relatively high concentrations of Pb: Crystalline aragonite is commonly found in many areas associated with serpentinized peridotite. This aragonite is characterized by relatively high concentrations of Sr and Ni; petrographic and isotopic analyses indicate precipitation from cold, carbonate-rich solutions percolating through the peridotite.     

Land-derived organic matter in surface sediments from the Gulf of Mexico

Lignin oxidation products and ¹³C/¹²C ratios were compared as indicators of land-derived organic matter in surface sediments from the western Gulf of Mexico. Whole sediments were reacted with cupric oxide to yield phenolic oxidation products that indicated the types and relative amounts of the lignins that were present.Measurements of lignin concentration and carbon isotope abundances both indicated a sharp offshore decrease of land-derived organic matter in most areas of the western Gulf. This decrease results primarily from mixing of terrestrial and marine organic matter. The terrestrially derived material in these sediments has a lignin content similar to that of grasses and tree leaves. Flowering plants contribute most of the sedimented lignin compounds. These lignins apparently occur in the form of well-mixed plant fragments that are transported to sea by rivers and deposited primarily on the inner continental shelf.     

Organic carbon isotope ratios of recent sediments from coastal lagoons of the Gulf of Mexico,Mexico

The stable carbon isotope composition sedimentary organic carbon was determined in the sediments of seven coastal lagoons of the Gulf of Mexico, Mexico. For most of the lagoons the δ¹³C values for sediments ranged from ?20.1 to ?23.9%. Anomalously low values, ?26.8 to 29.3%. were determined in sediments of two of the studied lagoons, probably due to the presence of organic carbon from anthropogenic sources, naturally absent in these environments. The δ¹³C values determined in the tissues of oysters collected at the same time in the different lagoons were very similar to those recorded in the sediments.     

Normalization of metal concentrations in estuarine sediments from the Gulf of Mexico

Metal concentrations were examined in sediments from 497 sites within the estuaries of the Gulf of Mexico by the United States Environmental Protection Agency's Environmental Monitoring and Assessment Program (EMAP). Data were normalized for extant concentrations of aluminum to isolate natural factors from anthropogenic ones. The normalization was based on the hypothesis that metal concentrations vary consistently with the concentration of aluminum, unless metals are of anthropogenic origin. Strong linear correlations (>75% variation explained) were observed between Al and Cr, Cu, Pb, Ni, and Zn. Moderate correlations (50–75% variation explained) were observed between Al and As or Ag. Weak but significant correlations (30–40% variation explained) were observed between Al and Hg or Cd. Based on these results, the spatial extent of contamination was examined. About 39% of sites with contamination by at least one metal occurred near population centers, industrial discharge sites, or military bases. The remainder of the observed contamination represented a dispersed pattern, including the lower Mississippi River (7%) and numerous agricultural watersheds (54%), suggesting that the contamination might be from nonpoint sources.     

Concentrations of elements and metals in sediments of the southeastern Gulf of Mexico

. This paper deals with the extent of contamination in sediments of the southeast Gulf of Mexico. The concentration of elements (SiO2, Al2O3, Fe2O3, Na2O, MgO, CaO, and K2O) and heavy metals (Cu, Cd, Zn, Co, Pb, Ag, Cr, Ni, V, and Ba) were determined. The elemental composition of sediments is influenced by the Grijalva–Usumacinta–Terminos System at the east and the Tabasco lagoon system (El Carmen–La Machona) at the west coast of the study area. Concentrations of Ni, V, and Ba were anomalously high at some sites. Oil production activities in the vicinity of the sites may be responsible for the high values. Correlations of metal concentrations to elemental composition were performed. No significant relationships between metals and elements were found for most metals (p>0.05), suggesting that metals are not significantly associated with naturally occurring aluminosilicates, iron hydroxide, and calcium carbonate minerals of sediments. Other sources such as organic matter may be contributing to the total concentration of metals. The comparison of metal content in sediments of the southeast Gulf of Mexico with metals of the other areas of the Gulf of Mexico suggests that it is relatively contaminated with Cd, Pb, and Ni. The probable causes of contamination are briefly discussed.     

Abandoned shorelines and the late quaternary history of lake George,New South Wales

A study of the geomorphology, surficial sediments, and soils of the Lake George Basin, in particular those at its northwestern end, led to the recognition of a set of abandoned shoreline features lying at a range of altitudes up to 37 m above lake bottom. The altitudes and soils were used to establish a relative age sequence of abandoned shorelines which was related to an absolute time‐scale by radiocarbon dating.     

Conceptual hydrochemical model of late Pleistocene aquifers at the Samario–Sitio Grande petroleum reservoir,Gulf of Mexico,Mexico

Carbon-14 concentrations between 0.83 and 11.79 pmC of formation water from the Activo Samaria–Sitio Grande petroleum reservoir in SE-Mexico, extracted from 3500 to 4500 m.b.s.l., indicate a common infiltration event of surface water during the late Pleistocene period. Mixing of two components – meteoric water and seawater, previously evaporated at the surface – explain the widespread mineralization (TDI = 15–257 g/L) of Na–Cl and Na–Ca–Cl type reservoir water. Statistical discrimination by clustering and a heterogeneous chemical–isotopic fluid composition indicate the existence of 4 different water types as part of local aquifer systems, which are separated by normal and thrust faults. Tectonic horst and graben structures show an ambiguous, individual hydraulic behaviour – as permeable conduits and/or as impermeable barriers, causing the local limitation of aquifer extent. The recent increase of water production in petroleum wells is not related to the injection of surface water, but the long-term extraction of oil reserves is modifying the original position and flow direction of the reservoir aquifers. The rise of the initial groundwater level reflects the final stage of an exhausted petroleum reservoir with coning effects of underlying aquifer systems. The flexible change towards superior production intervals could represent a feasible technique to avoid the abrupt closure of invaded production wells.