Regional geochemistry of trace elements in Chesapeake Bay sediments

The concentrations of Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb in 177 surface sediment samples from throughout Chesapeake Bay are reported. Analyses were made of both unfractionated samples and the <63 μm fractions. Analytical uncertainty, always less than ±10%, controlled reproducibility in analyses of the <63 μm fractions, but sampling variance controlled reproducibility in the unfractionated samples, especially when coarse-grained sediments were being analyzed. Sediments in the northernmost part of the bay are enriched relative to average continental crust in all elements except Cr. This reflects the composition of dissolved and suspended material being delivered to that region by the Susquehanna River. The enriched sediments appear not to be transported south of Baltimore in significant quantily. Zinc, cadmium, and lead are enriched relative to average crust throughout the bay and in most other estuaries in the eastern United States.     

Clay mineral distributions and source discrimination of upper Quaternary sediments,lower Chesapeake Bay,Virginia

Discriminant function analysis of clay mineral data from five cores of upper Quaternary sediment indicates that marine inputs are a significant source of fine-grained sediment near Thimble Shoal Channel, a major natural channel in lower Chesapeake Bay. Illite, of predominantly marine origin, is found to be enriched in clay fractions of three cores adjacent to the channel, relative to two cores near the mouth of the James River estuary. Thimble Shoal Channel is a significant repository and conduit for fine-grained sediment from the shelf. This result is analogous to previous results showing that the shelf is the dominant source of fine sand in the lower bay. Sediment in Thimble Shoal Channel reflects a shelf source even at the landward end, an area which was previously thought to be dominated by deposition from the James River.     

Isotope and trace element geochemistry of sediments from the Barbados Ridge-Demerara Plain region,Atlantic Ocean

Twenty-four piston core sediment samples and 13 sediments and 3 basalts from DSDP Leg 78 Site 543 were analyzed for Sr, Nd and Pb isotopic compositions. The results show sediment with highly radiogenic Pb${}^{206}\text{Pb}{}^{204}\text{Pb}$ up to 19.8) and rather radiogenic Sr and unradiogenic Nd has been deposited in the region since the Cretaceous. The source of this sediment is probably the Archean Guiana Highland, which is drained by the Orinoco River. Pb and Sr isotopic compositions and sediment thickness decrease and${}^{143}\text{Nd}{}^{144}\text{Nd}$ increases northward due to a decrease in turbiditic component. This decrease is partly due to the damming action of basement ridges. Rare earth concentrations in the sediments are somewhat low, due to the abundance of detrital and biogenic components in the sediment and rapid sedimentation rates. Both positive and negative Ce anomalies occur in the surface sediments, but only positive Ce anomalies occur in the Site 543 sediments. It is unlikely that sediment subducted to the source region of Lesser Antilles arc magmas could be the cause of negative Ce anomalies in those magmas.Isotopic compositions of Site 543 basalts show some effect of contamination by seawater-basalt reaction products and sediments. Beyond this, however, they are typical of “normal” depleted MORB.     

The trace element geochemistry of Corsican ophiolites

Ultramafic rocks, gabbros, plagiogranites, dolerites and basaltic dikes and pillows lavas of the ophiolite slices of eastern Corsica have been metamorphosed in both oceanic and orogenic environments. The trace element content of the metabasaltic rocks which exhibit a tholeiitic differentiation trend towards a ferrobasaltic composition, is similar to that of oceanic basalts. The cumulate sequence is interpreted to have been formed by fractional crystallization from an olivine-tholeiite magma. The troctolites representing cumulates derived from melts representing liquid fractions in the range F=1-0.85, gabbros from melts with F=0.85-0.45, and ferrogabbros and plagiogranites from melts with F<0.45. An oceanic environment with moderate spreading rates and magmatic processes similar to present-day normal oceanic ridge segments is considered the more probable original setting of the Corsican ophiolites.Financial support by C.N.R. (Italy) and A.T.P. Géodynamique de la Méditerranée Occidentale C.N.R.S. (France)     

Isotope and trace element geochemistry of Colorado Plateau volcanics

Basalts from the San Francisco Peaks and North Rim of Grand Canyon, nephelinites from the Hopi Buttes and Navajo minettes (Colorado Plateau) have been analyzed for trace element contents and Sr, Nd, Pb isotope compositions. The ages increase eastward from the Quaternary (basalt) to 5 Ma (nephelinite) and 30 Ma (minette) as does the depth of melt generation inferred from xenolith mineralogy and major element geochemistry.

The three rock types present an enrichment of incompatible elements (although minettes present negative concentration spikes for Nb, Zr, Ti, Ba, Sr) relative to other magma types. The chondrite-normalized Ce/Yb ratio changes from 8–22 (basalt) to 25–30 (nephelinite) and 33–60 (minette) and reflects small degrees of partial melting of a mantle source with a garnet/clinopyroxene ratio increasing with depth. The negative Eu anomaly present in minette, the low Sr/Nd and high Pb/Ce suggest the presence of a recycled continental crust component in their mantle source.

The ⁸⁷Sr/⁸⁶Sr ratio varies from 0.7032-0.7045 (basalt and nephelinite) to 0.7052-0.7071 (minette), while ε_Nd is remarkably more constant at +0.8 to +3.7 (nephelinite) and −2.6 to +2.2 (basalt and minette). Good linear correlations are observed in both ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb vs. ²⁰⁶Pb/²⁰⁴Pb diagrams with basalt being the least and nephelinite the most radiogenic and indicate a 2.3 ±0.1 Ga age and a Th/U of 3.4.

Three lithospheric source components are indicated: a) an OIB-type depleted mantle source, b) an end-member with unradiogenic Sr, Nd and Pb for basalt and nephelinite and c) a recycled crustal component for minette.     

The geochemistry of redox sensitive trace metals in sediments

We analyzed the redox sensitive elements V, Mo, U, Re and Cd in surface sediments from the Northwest African margin, the U.S. Northwest margin and the Arabian Sea to determine their response under a range of redox conditions. Where oxygen penetrates 1 cm or less into the sediments, Mo and V diffuse to the overlying water as Mn is reduced and remobilized. Authigenic enrichments of U, Re and Cd are evident under these redox conditions. With the onset of sulfate reduction, all of the metals accumulate authigenically with Re being by far the most enriched. General trends in authigenic metal accumulation are described by calculating authigenic fluxes for the 3 main redox regimes: oxic, reducing where oxygen penetrates ≤1 cm, and anoxic conditions. Using a simple diagenesis model and global estimates of organic carbon rain rate and bottom water oxygen concentrations, we calculate the area of sediments below 1000 m water depth in which oxygen penetration is ≤1 cm to be 4% of the ocean floor. We conclude that sediments where oxygen penetrates ≤1 cm release Mn, V and Mo to seawater at rates of 140%–260%, 60%–150% and 5%–10% of their respective riverine fluxes, using the authigenic metal concentrations and accumulation rates from this work and other literature. These sediments are sinks for Re, Cd and U, with burial fluxes of 70%–140%, 30%–80% and 20%–40%, respectively, of their dissolved riverine inputs. We modeled the sensitivity of the response of seawater Re, Cd and V concentrations to changes in the area of reducing sediments where oxygen penetrates ≤1 cm. Our analysis suggests a negligible change in seawater Re concentration, whereas seawater concentrations of Cd and V could have decreased and increased, respectively, by 5%–10% over 20 kyr if the area of reducing sediments increased by a factor of 2 and by 10%–20% if the area increased by a factor of 3. The concentration variations for a factor of 2 increase in the area of reducing sediments are at about the level of uncertainty of Cd/Ca and V/Ca ratios observed in foraminifera shells over the last 40 kyr. This implies that the area of reducing sediments in the ocean deeper than 1000 m (4%) has not been greater than twice the present value in the recent past.     

Lignin geochemistry of sediments from the Narragansett Bay Estuary

Cupric oxide oxidation has been employed to characterize the lignin geochemistry of Narragansett Bay sediments. Lignin concentrations throughout the estuary are low when expressed on a carbon-normalized basis, but can be characterized as enriched when expressed on a mass-normalized basis. This implies substantial dilution of the sedimentary lignin by inputs of lignin-poor carbon. Lignin concentrations do not correlate with the ¹³C isotopic composition of the sedimentary organic matter. These results are consistent with a sediment lignin component consisting of varying amounts of vascular plant debris and lignin-depleted organic matter, the latter originating from both marine (planktonic) and terrestrial (uncharacterized) sources. Compositional plots of lignin-derived phenols show that sediments in the upper estuary are influenced to a greater extent by gymnosperm lignin sources than those in the mid-and lower estuary. Given the extent to which the upper estuary is affected by pollution sources, inputs from anthropogenic discharges are the most likely cause of these compositional differences. However, an evaluation of processed paper products as an “anthropogenic” lignin source indicates that the lignin content of these materials is insufficient to account for the levels found in the sediments. Subsurface lignin compositions at an upper estuary site reveal that lignin originating from the inferred anthropogenic sources disappears at a depth shallower than that which would be expected based on the distribution of other trace organic pollutants (hydrocarbons and several synthetic organic compounds). We speculate that differences in either the depositional history or the degree of preservation of these two compound classes are responsible for the observed trends.     

Major and trace element geochemistry of superficial sediments and suspended particulate matter of shallow saline lakes in Eastern Austria

General geochemical parameters of water, superficial sediments, and suspended particulate matter (SPM) were determined from small shallow saline lakes (soda ponds) as well as from lake Neusiedlersee in eastern Austria. Additionally, instrumental neutron activation analysis (INAA) was used to determine the distribution of major, rare earth and other trace elements in superficial sediments and SPM. Chemical results show remarkable differences in salinity and ionic strength between the investigated ponds. Anthropogenic effects, such as drawdown of ground water level and a loss of lake water due to drainage, are clearly reflected in obtained chemical and geological data. Due to a strong dependence of the complexation and scavenging behavior of the rare earth elements (REE) on ionic strength, a significant difference between REE concentrations in soda ponds with different anthropogenic impact was found. The content and composition of authigenic evaporitic minerals in superficial sediments and SPM clearly differ with a fluctuating water level and salt concentration. Furthermore, we determined the distribution of major and trace elements in superficial sediments of a nearby fluvial system. Our results show a clear correlation between REE superficial sediment concentrations in anthropogenically degraded soda ponds and fluvial system. Therefore, we assume that REE concentrations of sediments and SPM are suitable for the study of geochemical changes of inland saline lakes due to anthropogenic impacts on water balance.     

The effect of bridge piles on stratification in lower Chesapeake Bay

Tidally-forced flow beneath the existing trestle of the Chesapeake Bay Bridge-Tunnel causes significant distortion of the ambient density field in the immediate vicinity of the trestle due to flow over the scour zone around the pilings. Effects are minimal a short distance away from the trestle. Contrary to previous studies, stratification was not appreciably stronger during neap as compared to spring tide periods at the time of these observations, but a tendency toward such a state was detected. Estimates of piling-induced destratification based on direct observations of temperature, salinity, and currents near the pilings indicate that piling effects are substantially less than naturally occurring destratification due to bottom and wind stresses.     

Petrology and trace element geochemistry of the Papuan Ultramafic Belt

New petrologic and geochemical data are presented for a suite of rocks from the Papuan Ultramafic Belt (PUB), Papua New Guinea. Tectonite harzburgites at the base of the ophiolite have extremely refractory, uniform mineralogy, and are exceptionally depleted in lithophile elements. These features are consistent with the proposed origin of these rocks as depleted upper mantle, residual after extraction of a basaltic melt. The tectonite peridotites are overlain by a thick sequence of layered ultramafic and mafic cumulates containing olivine, orthopyroxene, clinopyroxene and plagioclase as the major cumulus phases. Early cumulates are characterized by magnesian olivine Mg₉₀, orthopyroxene Mg₉₀ and calcic plagioclase An₈₆, and exhibit cryptic variation towards more iron-rich and sodic compositions. Abundances of incompatible elements in the cumulates are extremely low which, together with the nature of the cumulus phases, points to a magnesian olivine-poor tholeiite or magnesian quartz tholeiite parent magma(s) strongly depleted in incompatible elements. Highly fractionated iron-rich products of this parent magma type are represented by the LREE-depleted lavas in the overlying basalt sequence which, although resembling the most depleted mid-ocean ridge basalts (MORB) in terms of their low abundances of incompatible elements, have higher abundances of transition metals and lower abundances of Ti, HREE and other high valence cations compared to common MORB of similar Mg/(Mg+Fe) ratio.Eocene tonalites intruding the PUB are genetically unrelated to the ophiolites, and appear to be related to the Ti-poor high-Mg andesites of Cape Vogel and similar andesites and dacites at the northern end of the PUB. These rocks are considered to represent the early stages of island-arc magmatism associated with a northeastward-dipping subduction zone in the early Eocene immediately prior to emplacement of the PUB.     

黄河、长江与韩国Keum、Yeongsan江沉积物常量元素地球化学特征

运用同样的样品采集和测试方法比较分析了我国的长江和黄河以及韩国的Keum和Yeongsan江的常量元素地球化学特征。韩国河流沉积物中Ca及碳酸盐含量显著低于长江和黄河,而其他元素含量则在二者之间;黄河沉积物以总无机碳(TIC)、Na和Ca含量高为特征,而长江沉积物则显著富集Ti和P。Keum和Yeongsan江沉积物中P、Ca、Fe和Mg在酸溶相中比例可达30％～66％,而K、Al和Ti则富集在残渣相中。韩国河流沉积物极低的Ca含量同流域缺乏碳酸盐源岩密切相关,其沉积物主要由侏罗一晚白垩纪的花岗岩经过中等程度的化学风化而成。虽然Ca在中韩河流沉积物之间含量差异显著,但必须谨慎运用全钙含量来识别海区物源。而沉积物中非碳酸盐态钙(Ca^*)及相应的K／Ca^*和Al／Ca^*比更适合用来示踪黄河及Keum和Yeongsan江沉积物;Ti则可以用来区分长江与其他河流沉积物。     

赣中古塘地区锡石LA-ICP-MS U-Pb年代学及微量元素地球化学特征

江西中部相山矿田及其周边铀多金属成矿作用复杂。近些年,在其南部古塘地区地表新发现了一处锡石矿化带,赋存于加里东期花岗岩中。通过对该矿点锡石开展原位LA-ICP-MS U-Pb定年和微量元素分析,获得其²⁰⁷Pb/²⁰⁶Pb-²³⁸U/²⁰⁶Pb谐和年龄为150.44±2.78 Ma、下交点年龄为150.64±2.78 Ma,两者相近,可以代表该锡石矿的成矿年龄,与矿化带周边的燕山期山心单元花岗岩成岩年龄（152.4±1.1 Ma）相近。微量元素中,高场强元素Ti、Nb、Ta富集明显。与Sn容易发生类质同象的Mn、Nb、Hf、Ta等4种元素彼此正相关性明显,Fe和Mo呈正相关关系,却与Nb、Mn、Hf、Ta均呈现负相关性。在W-Fe图解中,处于花岗岩岩浆热液型锡矿床的右侧,说明研究区成矿物质应该主要来自岩浆热液,而且成矿温度较高。古塘地区锡石矿与山心单元花岗岩虽然具有相近的成矿、成岩年龄,但由于后者具有极高的氧逸度,不利于Sn元素的富集,而与Mo成矿有关;与山心单元花岗岩中可见辉钼矿矿囊而未发现锡矿化的地质现象保持一致。

     

Vertical distribution of infauna in sediments of a subestuary of central Chesapeake Bay

The vertical distribution of infauna was quantified in eight strata from 0–35 cm in sand and mud sediments of a lower mesohaline subestuary of Chesapeake Bay. Large numbers of small polychaetes, amphipods, and clams occurred in the upper 5 cm of both sediment types, whereas large clams (Macoma balthica in mud andMya arenaria in sand) extended down to 30 cm and comprised most of the biomass in their respective sediment types. There was extensive overlap of the species inhabiting both sediment types. Vertical stratification within and among species apparently reflected constraints on burrowing depth related to body size rather than resource partitioning among competitors. The maximal sediment penetration of 35 cm, which was exhibited byHeteromastus filiformis, was considerably less than the maximal penetration for deep burrowing species in some marine infaunal communities. Several species which burrowed deeper than 5 cm exhibited significant temporal shifts in their vertical distribution.     

Pb-Sr-He isotope and trace element geochemistry of the Cape Verde Archipelago

New lead, strontium and helium isotopic data, together with trace element concentrations, have been determined for basalts from the Cape Verde archipelago (Central Atlantic). Isotopic and chemical variations are observed at the scale of the archipelago and lead to the definition of two distinct groupings, in keeping with earlier studies. The Northern Islands (Santo Antão, São Vicente, São Nicolau and Sal) present Pb isotopic compositions below the Northern Hemisphere Reference Line (NHRL) (cf. Hart, 1984), unradiogenic Sr and relatively primitive ⁴He/³He ratios. In contrast, the Southern Islands (Fogo and Santiago) display Pb isotopes above the NHRL, moderately radiogenic Sr and MORB-like helium signatures. We propose that the dichotomy between the Northern and Southern Islands results from the presence of three isotopically distinct components in the source of the Cape Verde basalts: (1) recycled ∼1.6-Ga oceanic crust (high ²⁰⁶Pb/²⁰⁴Pb, low ⁸⁷Sr/⁸⁶Sr and high ⁴He/³He); (2) lower mantle material (high ³He); and (3) subcontinental lithosphere (low ²⁰⁶Pb/²⁰⁴Pb, high ⁸⁷Sr/⁸⁶Sr and moderately radiogenic ⁴He/³He ratios). The signature of the Northern Islands reflects mixing between recycled oceanic crust and lower mantle, to which small proportions of entrained depleted material from the local upper mantle are added. Basalts from the Southern Islands, however, require the addition of an enriched component thought to be subcontinental lithospheric material instead of depleted mantle. The subcontinental lithosphere may stem from delamination and subsequent incorporation into the Cape Verde plume, or may be remnant from delamination just before the opening of the Central Atlantic. Basalts from São Nicolau reflect the interaction with an additional component, which is identified as oceanic crustal material.     

Rare earth element geochemistry of oceanic ferromanganese nodules and associated sediments

Analyses have been made of REE contents of a well-characterized suite of deep-sea (> 4000 m.) principally todorokite-bearing ferromanganese nodules and associated sediments from the Pacific Ocean. REE in nodules and their sediments are closely related: nodules with the largest positive Ce anomalies are found on sediments with the smallest negative Ce anomalies; in contrast, nodules with the highest contents of other rare earths (3 + REE) are found on sediments with the lowest 3 + REE contents and vice versa. ${}^{143}\text{Nd}{}^{144}\text{Nd}$ ratios in the nodules (～0.51244) point to an original seawater source but an identical ratio for sediments in combination with the REE patterns suggests that diagenetic reactions may transfer elements into the nodules. Analysis of biogenic phases shows that the direct contribution of plankton and carbonate and siliceous skeletal materials to REE contents of nodules and sediments is negligible. Inter-element relationships and leaching tests suggest that REE contents are controlled by a P-rich phase with a REE pattern similar to that for biogenous apatite and an Fe-rich phase with a pattern the mirror image of that for sea water. It is proposed that 3 + REE concentrations are controlled by the surface chemistry of these phases during diagenetic reactions which vary with sediment accumulation rate. Processes which favour the enrichment of transition metals in equatorial Pacific nodules favour the depletion of 3 + REE in nodules and enrichment of 3 + REE in associated sediments. In contrast, Ce appears to be added both to nodules and sediments directly from seawater and is not involved in diagenetic reactions.     

Predators of juvenile blue crabs outside of refuge habitats in lower Chesapeake Bay

Blue crabsCallinectes sapidus in lower Chesapeake Bay are subject to high rates of predation during the late summer of their first year of growth as they migrate out of vegetated nursery habitats. Predators, potentially contributing to this pattern, were identified in video-recorded field observations of tethered juvenile crabs (20–25 mm carapace width). Predators were also tested in large laboratory tanks containing similarly-sized untethered crabs as prey. Seven different predators attacked tethered crabs in the field. Only two predators, larger blue crabs and northern puffers,Sphoeroides maculatus, consistently succeeded in preying on crabs in both field and laboratory settings. These results confirm the importance of cannibalism on juvenile blue crabs and identify puffers as a potentially overlooked source of predation pressure.     

Mineralogy,major and trace element geochemistry of riverbed sediments in the headwaters of the Yangtze,Tongtian River and Jinsha River

We collected riverbed sediments of the headwaters of the Yangtze River (Chumaer River, Tuotuo River, Gaerqu River and Buqu River), Tongtian River and Jinsha River (HTJR) flowing on the eastern Tibetan Plateau and analyzed their mineralogical features, major and trace element contents. The results show: (i) very poor correlations of Na₂O, K₂O, CaO, Ba, and Sr to SiO₂, LREE to Th, HREE to Hf, and Ta/La to Ti, and characteristics of Eu anomaly (the ratios of (Eu/Eu^*)_N range from 0.60 to 0.83 with an average value of 0.71) all indicate that the Jinsha River sediments have not undergone much mineralogical sorting; (ii) illite and chlorite are predominant clay minerals, and quartz, calcite, dolomite, albite, and K-feldspar are prevailing non-clay minerals. The characteristics of mineral assemblage indicate relatively weak chemical weathering degree in these river basins; (iii) very high contents of Fe₂O₃, MgO, TiO₂, Sc, V, Cr, Co, and Ni at Panzhihua mainly result from the huge-sized V–Ti magnetite deposits occurred in layered gabbroic intrusion; and (iv) the chemical alteration index (CIA) in the HTJR ranges from 46.5 to 69.2 and with an average value of 60.5 which indicates relatively weak weathering degree.     

Vulnerability of Hampton Roads,Virginia to Storm-Surge Flooding and Sea-Level Rise

Sea-level rise will increase the area covered by hurricane storm surges in coastal zones. This research assesses how patterns of vulnerability to storm-surge flooding could change in Hampton Roads, Virginia as a result of sea-level rise. Physical exposure to storm-surge flooding is mapped for all categories of hurricane, both for present sea level and for future sea-level rise. The locations of vulnerable sub-populations are determined through an analysis and mapping of socioeconomic characteristics commonly associated with vulnerability to environmental hazards and are compared to the flood-risk exposure zones. Scenarios are also developed that address uncertainties regarding future population growth and distribution. The results show that hurricane storm surge presents a significant hazard to Hampton Roads today, especially to the most vulnerable inhabitants of the region. In addition, future sea-level rise, population growth, and poorly planned development will increase the risk of storm-surge flooding, especially for vulnerable people, thus suggesting that planning should steer development away from low-lying coastal and near-coastal zones.     

Experimental geochemistry of Pu and Sm and the thermodynamics of trace element partitioning

The partitioning of Pu and Sm between diopside/liquid and whitlockite/liquid has been investigated experimentally to evaluate the geochemical coherence of Pu and the light REEs. ${}^{\mathrm{Pu}}\text{D}{}^{\mathrm{Sm}}\text{D}$ is 2̃ for both diopsidic pyroxene and whitlockite. This small amount of fractionation would be decreased further if Pu were compared to Ce or Nd. Our experimental results thus validate the suggestion that Pu behaves as a LREE during igneous processes in reducing environments.Our data and the data of Ray et al. (1983) indicate that temperature rather than melt composition is the most important control on elemental partitioning. This is true even though we demonstrate that additions of only 1–2 wt.% of P₂O₅ to the diopside-anorthite-albite system change ^PuD_cpx by a factor of two. Our data suggest that P₂O₅ in aluminosilicate melts serves as a complexing agent for the actinides and lanthanides.     

Effects of low dissolved oxygen events on the macrobenthos of the lower Chesapeake Bay

The effects of low dissolved oxygen or hypoxia (<2 mg l^?1) on macrobenthic infaunal community structure and composition in the lower Chesapeake Bay and its major tributaries, the Rappahannock, York, and James rivers are reported. Macrobenthic communities at hypoxia-affected stations were characterized by lower species diversity, lower biomass, a lower proportion of deep-dwelling biomass (deeper than 5 cm in the sediment), and changes in community composition. Higher dominance in density and biomass of opportunistic species (e.g., euryhaline annelids) and lower dominance of equilibrium species (e.g., long-lived bivalves and maldanid polychaetes) were observed at hypoxia-affected stations. Hypoxia-affected macrobenthic communities were found in the polyhaline deep western channel of the bay mainstem north of the Rappahannock River and in the mesohaline region of the lower Rappahannock River. No hypoxic effects on the infaunal macrobenthos were found in the York River, James River, or other deep-water channels of the lower Chesapeake Bay.