Hydrothermal Mineralizing Processes and Associated Sedimentation in the Santorini Hydrothermal Embayments

Abstract

Seven sediment cores from the Palaea and Nea Kameni hydrothermal embayments (PK and NK) on Santorini have been studied by using sediment smear slides, X-ray diffraction, and radiocarbon techniques to determine their lithology, mineralogy, and age, respectively. The cores have been analyzed chemically for a suite of elements, including selective chemical leaching, to determine the partition of elements between coexisting phases. Lithologically and chemically, the sediments from the two embayments are very different. Sediments from PK are oxidized in the upper parts of the cores and reduced at depth; they comprise mainly hydrothermal pyritiferous diatomaceous ooze with minor Fe oxyhydroxide, volcanic debris, gypsum, and siderite. Sediments from NK are oxidized throughout and comprise predominantly amorphous iron oxyhydroxides and goethite; they are thought to have formed by direct precipitation from solution. In PK, biogenic, detrital seawater evaporate, and hydrothermal sediment phases have been identified but only the detrital inputs can be correlated between cores. Mn shows a pronounced enrichment towards the outer part of the embayment because of its dispersion down the embayment and precipitation in the more-oxidizing sediments towards the open sea. In NK, the sediments contain detrital, seawater evaporate, and hydrothermally precipitated and scavenged phases. The presence of substantial amounts of organic matter in the PK sediments but not in the NK sediments is probably the main reason why geochemical processes in the two embayments are different.

Age dates obtained from the cores by using the ¹⁴C technique indicate that sedimentation in the PK embayment commenced at ～ 50 AD, whereas in the NK embayment it commenced at ～ 1900 AD, which is consistent with the known history of Santorini. Based on these dates, calculated metal accumulation rates in both embayments are higher than in any other dated hydrothermal metalliferous sediments with the exception of those in the Atlantis II Deep of the Red Sea. Sediment ponding in the embayments is the principal cause of these results.     

Trace metal composition of and accumulation rates of sediments in the Upper Gulf of Thailand

Sediment cores and grab samples were collected in the Upper Gulf of Thailand to determine sedimentation rates and to determine if metal concentrations reflect anthropogenic inputs.Accumulation rates of sediments in the Upper Gulf measured using the ²¹⁰Pb method, appear to vary from ca. 4 to 11 mm yr^?1. Sediment budgets suggest that little of the sediment delivered to the Upper Gulf by the major rivers is ultimately transported to the Lower Gulf. Metal concentrations in Upper Gulf sediments appear to be dominantly controlled by natural inputs.     

Hydrothermal Mineralizing Processes and Associated Sedimentation in the Santorini Hydrothermal Embayments

Seven sediment cores from the Palaea and Nea Kameni hydrothermal embayments (PK and NK) on Santorini have been studied by using sediment smear slides, X-ray diffraction, and radiocarbon techniques to determine their lithology, mineralogy, and age, respectively. The cores have been analyzed chemically for a suite of elements, including selective chemical leaching, to determine the partition of elements between coexisting phases. Lithologically and chemically, the sediments from the two embayments are very different. Sediments from PK are oxidized in the upper parts of the cores and reduced at depth; they comprise mainly hydrothermal pyritiferous diatomaceous ooze with minor Fe oxyhydroxide, volcanic debris, gypsum, and siderite. Sediments from NK are oxidized throughout and comprise predominantly amorphous iron oxyhydroxides and goethite; they are thought to have formed by direct precipitation from solution. In PK, biogenic, detrital seawater evaporate, and hydrothermal sediment phases have been identified but only the detrital inputs can be correlated between cores. Mn shows a pronounced enrichment towards the outer part of the embayment because of its dispersion down the embayment and precipitation in the more-oxidizing sediments towards the open sea. In NK, the sediments contain detrital, seawater evaporate, and hydrothermally precipitated and scavenged phases. The presence of substantial amounts of organic matter in the PK sediments but not in the NK sediments is probably the main reason why geochemical processes in the two embayments are different. Age dates obtained from the cores by using the 14 C technique indicate that sedimentation in the PK embayment commenced at approximately 50 AD, whereas in the NK embayment it commenced at approximately 1900 AD, which is consistent with the known history of Santorini. Based on these dates, calculated metal accumulation rates in both embayments are higher than in any other dated hydrothermal metalliferous sediments with the exception of those in the Atlantis II Deep of the Red Sea. Sediment ponding in the embayments is the principal cause of these results.     

High rates of hydrothermal activity at the west rift of the Easter Microplate deduced from metalliferous sediment composition

Based on the mineralogy and composition of sediment cores from three locations along the East Pacific Rise, sediments from 12°58’ N are shown to contain about 34% metalliferous sediment (on a carbonate‐ and salt‐free basis) whereas those from 23°50’ S and 27°24’ S each contain about 73% metalliferous sediment. The latter two cores are situated near the West Rift of the Easter Microplate. The metalliferous contents of the sediments at 23°50’ S and 27°24’ S are among the highest recorded on the East Pacific Rise. The distribution of elements with depth in these cores indicates that the hydrothermal activity has lasted more than 100,000 years. These data suggest that the West Rift of the Easter Microplate is a highly prospective site for submarine hydrothermal minerals. This is in accord with the high rate of ocean spreading (15–16 cm/yr) and the complex processes of plate extension and rotation there.     

Regional geochemistry of sediments from the Hellenic volcanic arc in regard to submarine hydrothermal activity

Some 600 surface sediment samples from the Hellenic Volcanic Arc region have been analyzed by bulk and HCl selective leach geochemical techniques. Geostatisti‐cal analysis, followed by further selective leaches on a number of samples, has been used in order to identify any regional hydrothermal influence on the sediments and/or any local hydrothermal metal enrichments. The two main sediment components affecting the geochemical variability in the region are biogenic carbonate and volcaniclastic/terrigenous detritus. Proximity to islands appears to be the primary factor controlling the variability in these components. Sediments from deeper water, to the south of the Hellenic Volcanic Arc and in the Anydros Basin, exhibit some elevated levels of Mn, Co, and Cu, probably of hydrogenous origin. No widespread hydrothermal influence to the sediments in the region is recognized, although this could in part be due to the high sedimentation rates in the region. Localized hydrothermal inputs to sediments are, however, recognized proximal to Santorini, in particular within the northern part of the central caldera. These are predominantly of Fe and associated adsorbed/coprecipitated elements along with some Mn enrichment. Several samples proximal to Milos, just off the coast in the northern part of the central Milos embayment, also show enrichments of commonly hydrothermally associated elements, including Mn, Cu, Zn, and Pb. Data suggest that these enrichments could, in part, be due to weathering of “on‐land”; mineralization as well as hydrothermal inputs.     

The effects of semi-lunar spring and neap tidal change on nitrification, denitrification and N2O vertical distribution in the intertidal sediments of the Yangtze estuary, China

To explore the influences of semi-lunar spring and neap tidal changes on nitrogen cycling in intertidal sediments, a comparative study among waterlogged, desiccated and reflooded systems was carried out in August 2005 and February 2006 by analyzing nitrification, denitrification and N₂O depth profiles in the intertidal flats of the Yangtze estuary. Laboratory experiments showed that alternating emersion and inundation resulted in the significant changes in nitrification and denitrification rates in the intertidal sediment systems. Due to the desiccation-related effects, lowest nitrification and denitrification rates were observed in the desiccated sediment cores. Highest nitrification and denitrification rates were however detected in the waterlogged and reflooded systems, respectively. It is hypothesized that the highest nitrification rates in the waterlogged sediments were mainly attributed to higher nitrifier numbers and NH₄⁺ being more available, whereas the availability of NO₃⁻ might dominate denitrification in the reflooded sediments. In addition, the highest N₂O concentrations were detected in the reflooded sediment cores, and the lowest found in the dried sediment cores. It was also shown that N₂O in the intertidal sediments was mainly from nitrification under the desiccated condition. In contrast, N₂O in the intertidal sediments was produced mainly via denitrification under the waterlogged and reflooded conditions. It is therefore concluded that the semi-lunar tidal cycle has a significant influence on nitrification, denitrification and N₂O production in the intertidal sediment systems.     

大西洋洋中脊海底表层热液沉积物的铅同位素组成及其地质意义

新测得 TAG热液区中 6件海底表层热液沉积物样品的铅同位素组成 ,其变化范围不大 ,具有均一性的特征。在 Pb- Pb图解上 ,热液沉积物的铅同位素数据大多落在 MARB的铅同位素组成范围内 ,与大西洋沉积物和 Fe- Mn结核相比明显具较少的放射成因铅 ,反映其上部洋壳岩石为该区热液沉积物的形成提供了铅。对比研究表明 ,因不同地质 -构造环境中的海底热液区为热液沉积物形成提供物源的情况不同 ,是导致有沉积物覆盖洋中脊中热液沉积物的铅同位素组成与无沉积物覆盖洋中脊不同的主要原因。海底扩张中心的扩张速率与热液沉积物的铅同位素组成有一定的对应关系 ,但其并不是热液沉积物铅同位素组成的唯一控制因素     

Apports de nutriments et développement phytoplanctonique en baie de Seine

As part of the Programme National d'Océanographie Côtière, the nutrient dynamics of the Bay of Seine were studied between 1992 and 1994 in order to complement work on ecological modelling. Firstly, the River Seine's nutrient fluxes were established: 80 000–130 000 t a⁻¹ of dissolved inorganic nitrogen, 6 400–8 4001 a⁻¹ of dissolved phosphorus and 20 000–77 000 t a⁻¹ of dissolved silicium. Estuarine processes were taken into account. Consequences of nutrient loading for the bay were then evaluated at the pelagic level (nutrient and chlorophyll enrichments) and the benthic level (distribution of various phosphorus fractions in superficial sediments). The large continental inputs always induce concentration gradients in the water from the mouth of the river to the northwest of the bay. The northward spreading of fine particulate matter controls the distribution of adsorbed phosphate and iron-aluminium bound phosphate in sediments. In contrast, calcium bound phosphate, the main fraction in sediments, is not affected by river inputs. Organic phosphorus in sediments is related to phytoplankton blooms, with increasing concentrations during productive periods; afterwards the fast recycling prevents sedimentary accumulation. The nutrient depletions observed beyond the turbid plume during spring 1992 enabled the calculation of nutrient uptake rates, and the comparison of these rates with phytoplankton biomass (chlorophyll a + phaeopigments). Ratios of nutrient consumption to pigment concentration were estimated at 1 μmol μg⁻¹ for nitrogen, 0.05 for phosphorus and 0.5 for silicate. These values, as N/P and Si/N uptake ratios (respectively 17.5 and 0.4), were similar to usual values.     

Natural background and anthropogenic inputs of polycyclic aromatic hydrocarbons (PAH) in sediments of South-Western Barents Sea

Polycyclic aromatic hydrocarbons (PAH) were measured in sediment cores from 13 locations in South-Western Barents Sea as part of a detailed study of the Norwegian seabed under the MAREANO program. The generally low PAH levels found, an average around 200 ng g⁻¹ dry weight for sum PAH, indicate low inputs of petroleum hydrocarbons to the marine environment in the area. Differences in PAH composition and various PAH ratios indicate a natural, mostly petrogenic origin of PAH in sediments from the open sea locations, while the fjord locations show higher pyrogenic PAH contents with an increase towards upper sediment layers, indicating low inputs from human activities. Petrogenic PAH levels increase in deeper sediments at open sea locations, also when normalised to total organic carbon (TOC) contents, suggesting natural leakages of oil-related hydrocarbons in the area.     

Accumulation of Phosphorus and Heavy Metals in the Peel-Harvey Estuary in Western Australia: Results of a Preliminary Study

Concentrations of P and of heavy metals (Zn, Cd, Pb, Cu) were determined in sediment cores from the Peel-Harvey Estuary in Western Australia. Two cores were extracted, each representing one of the two basins of the estuary. Sediments were dated by surplus²¹⁰Pb, by¹³⁷Cs and by changes in the Fe/S ratio. Increasing exports of P from the mainly agricultural catchments have resulted in more than a doubling of both total P and acid extractable inorganic P in sediments of the estuary. Accumulation of P in the estuary is less than expected for complete retention of inputs of P from the major tributaries. Historical data show that since 1950 average concentrations of dissolved inorganic P have approximately doubled in the Peel Inlet and increased by times seven in the Harvey Estuary. Increases in concentrations in surface sediments of acid extractable Zn, Cd, Pb and Cu are noticeable in the Peel Inlet, and of Zn and Cd in the Harvey Estuary. The greatest increase, relative to background, is shown by Zn. Concentrations of extractable Zn and Cd in surface sediments are similar to those estimated from average concentrations in the water column for equilibrium adsorption to organic matter in sediments. Extractable Pb is greater than estimated for equilibrium adsorption to sediments. Extractable Cu is of the order of what can be expected for equilibrium adsorption to sediments in the Peel Inlet, but is less than expected in the Harvey Estuary.     

Sediment-water exchange of Mn,Fe, Ni and Zn in Galveston Bay,Texas

In-situ benthic flux studies were conducted at three stations in Upper Galveston Bay twice during March 1996 to directly measure release rates of dissolved Mn, Fe, Ni and Zn from the sediments. Results showed reproducible increases with time in both replicate light and light–dark benthic chambers, resulting in average fluxes of −1200±780, −17±12, −1.6±0.6 and −2.4±0.79 μmol m⁻² day⁻¹ for Mn, Fe, Ni and Zn, respectively. Sediment cores collected during 1994–1996 showed that surficial pore water concentrations were elevated compared to overlying water column concentrations, suggesting diffusive release from the sediments. Diffusive flux estimates of Mn and Zn agreed in direction with chamber fluxes measured on the same date, but only accounted for 5–38% of the measured flux. Diffusive fluxes of Fe agreed with measured fluxes at the near Trinity River station but overestimated actual release in the mid and outer Trinity Bay regions, possibly due to inaccurate determination of the Fe pore water gradients or rapid oxidation processes in the overlying water at these stations.In general, measured fluxes of Mn and Ni were higher in the mid Trinity Bay region and suggested a mechanism for the elevated trace metal concentrations previously reported for this region of Galveston Bay. However, the fluxes of Fe were highest in close proximity to the Trinity River, supporting the elevated Fe concentrations measured in this region during this and other studies, and decreased towards middle and outer Trinity Bay. Trace metal turnover times were between 0.1 and 1.2 days for Mn, between 1.3 and 4.6 days for Fe, and between 27 and 100 days for Ni and 12–20 days Zn, and were considerably shorter than the average Trinity Bay water residence time (1.5 years) for this period. Comparing area averaged benthic inputs to Trinity River inputs shows the sediments to be a significant source of trace metals to Galveston Bay. However, while benthic inputs of trace metals were measured, water column concentrations remained low despite rapid turnover times for Mn and Fe, suggesting removal of these metals from the water column after release from the sediments.     

Sediment accumulation rates along the inner eastern Brazilian continental shelf

Box cores were collected close to river mouths along the eastern Brazilian shelf at water depths of 10–30 m. One core was taken from more than 1000 m depth at the shelf slope. ²¹⁰Pb and ²²⁶Ra activities were measured to establish sediment accumulation rates. Seven of the 10 cores exhibited an exponential decrease with depth of excess ²¹⁰Pb activities. The sediments from the sheltered Sudeste Channel off Caravelas revealed the highest sediment accumulation rate of 0.81 cm yr⁻¹. The sediments at the shelf slope seaward of the Rio Doce revealed the lowest accumulation rate of 0.13 cm yr⁻¹. Sediment accumulation rates increased towards the Caravelas Bank. Current patterns and the morphology of the seabed favor sediment deposition in this area.     

Influence of the hydrothermal vents on the distribution of benthic foraminifera from the Guaymas Basin,Mexico

The distribution and composition of four benthic foraminifera assemblages from the Guaymas Basin are depicted through Q- and R-mode Factor Analysis. One of these assemblages is distributed near hydrothermal vents,* another developed away from the influence of the vents, and the other two assemblages are found in the subbottom sediments.Biostratigraphic analysis of five cores collected within the hydrothermal region suggest that the foraminiferal remains have been affected by aselective dissolution process. Only small species, such asBulimina spinosa andBolivina sp 2, have been preserved in the subbottom sediments which have been influenced by the hydrothermal activity.     

西南印度洋中脊表层沉积物中存在热液组分的地球化学证据

Hydrothermal materials in deep-sea sediments provide a robust tracer to the localized hydrothermal activity at mid-ocean ridges. Major, trace and rare earth element(REE) data for surface sediments collected from the ultraslow spreading Southwest Indian Ridge are presented to examine the existence of hydrothermal component.Biogenic carbonate oozes dominate all the sediment samples, with CaO content varying from 85.5% to 89.9% on a volatile-free basis. The leaching residue of bulk sediments by ~5% HCl is compositionally comparable to the Upper Continental Crust(UCC) in SiO_2, Al_2O_3, CaO, MgO, alkali elements(Rb, Cs) and high field strength elements(Nb, Ta, Zr, Hf, Ti). These detritus-hosted elements are inferred to be prominently derived from the Australian continent by means of eolian dust, while the contribution of local volcaniclastics is insignificant. In addition, the residual fraction shows a clear enrichment in Fe, Mn, and Ba compared with the UCC. Combining the positive Eu anomaly of residual fraction which is opposed to the UCC but the characteristic of hydrothermal fluids and associated precipitates occurred at mid-ocean ridges, the incorporation of localized hydrothermal component can be constrained. REE mixing calculations indicate that more than half REE within the residual fraction(~55%–60%) are derived from a hydrothermal component, which is inferred to be resulted from a diffuse fluid mineralization. The low-temperature diffuse flow may be widely distributed along the slow-ultraslow spreading ridges where crustal faults and fissures abound, and probably have a great mineralization potential.     

Bacterial iron oxide reduction in a terrigenous sediment-impacted tropical shallow marine carbonate system, north Jamaica

Discovery Bay, a carbonate-dominated embayment in north Jamaica, has been subject to inputs for 40 years of iron-rich bauxite sediment associated with the local mining and transport of processed bauxite. As such, this site is an ideal natural laboratory to study the records and impacts of iron oxide inputs upon geochemical, diagenetic, and microbial processes in tropical carbonate sediments.Total Fe contents in sites in the bay not receiving bauxite inputs are negligible and porewater Ca²⁺, SO₄²⁻ and Cl⁻ indicate that bacterial sulphate reduction is an important process. In contrast, surface sediments receiving bauxite inputs contain significant total Fe, from 44 μmol/g in shallow (5 m water depth) sites to 110 μmol/g in deeper (20 m water depth) sites. Up-core increases in total Fe record increased temporal inputs into the bay. Within these Fe-rich sediments porewater data shows the presence of Fe^II released by bacterial Fe^III reduction. There is no direct evidence for significant bacterial sulphate reduction in these sediments. Iron oxides within all bauxite-impacted sediments display a high potential reducibility, from 40% to 80% of the total Fe present as dithionite-extractable Fe^III. Experimental analysis of the potential susceptibility to, and rates of, bacterial Fe^III reduction, utilising Discovery Bay sediment and Shewanella putrefaciens CN32 (a known Fe^III-reducer) has confirmed the high bacterial reducibility of iron oxides within the sediment. Up to 75% of initial dithionite-extractable Fe^III in the sediments was reduced over 15 days.The presence of iron oxides within the Discovery Bay shallow marine carbonate systems has markedly altered the chemical diagenetic processes taking place, with a shift from apparent dominance of bacterial sulphate reduction at non-impacted (Fe-poor) sites, to highly significant bacterial Fe^III reduction in Fe-rich bauxite-impacted sediments. Given the perceived global increases in terrigenoclastic sediment inputs into tropical carbonate systems as a result of land-use and climate changes, coupled with the documented role that iron oxide reduction plays in nutrient and contaminant cycling in sediment systems, more research into the perturbation of early diagenesis by iron oxide inputs is required.     

Accumulation of sediments,trace metals (Pb,Cu) and total hydrocarbons in Narragansett Bay,Rhode Island

The accumulation of sediments, trace metals and hydrocarbons has been estimated from the analysis of the sediment from six coring sites in Narragansett Bay. Radionuclides (²³⁴Th_xs, ²¹⁰Pb_xs, ^239,240Pu) with known input functions and trace metals (Cu, Pb) were used. We estimate that 6·9 × 10⁴ tons of sediments, 51–90 tons of Pb, 72–100 tons of Cu and 400–1000 tons of total hydrocarbons accumulate annually under present conditions in the bay. This represents 64–117% (Pb), 89–123% (Cu) and 23–58% (hydrocarbons), respectively, of present day inputs to the bay. Furthermore, close to 100% of the particle-reactive radionuclides ²¹⁰Pb and ^239,240Pu accumulate in the bay. Present day inputs to the bay were calculated independently as 77–80 tons Pb and 81 tons of Cu. Sewage effluents were the dominant source of Cu, whereas atmospheric deposition and urban runoff were most important for Pb. Dredging activities by the U.S. Army Corps of Engineers between 1946 and 1971 removed more sediments from the bay than would have accumulated during the same time in the undredged areas of the bay. Copper smelting and coal mining on the shores of the upper bay during 1866–1880 left an imprint in the sediments which is still evident. Model derived accumulation rates of Pb, Cu and coal during that time were 3–4 times present-day inputs.     

Meiobenthic Organisms as Indicators of Mixing Processes in the Baltic Surface Sediments*

Abstract. Two sediment cores were collected in the southern Baltic Sea and sliced into 1.0cm-thick layers. Sediments of each layer were analysed for activities of ²¹⁰Pb, ¹³⁷Cs, ¹³⁴Cs and for the density of meiobenthic organisms (meiofauna). Zones with the rapid mixing occur in the uppermost layers (0–3 cm) of the cores based on ^I34Cs profiles. The extent and density of meiofauna confirmed the rapid mixing and revealed layers with slow mixing (4–8 cm). Sedimentation rates were derived from ²¹⁰Pb profiles below the mixing zones (1.21 and 1.72 mm a-^I) and were confumed by ¹³⁷Cs distribution. Of twenty-one major meiofauna taxa commonly found in the Baltic sediments, three were present in the cores.     

ALVIN investigation of an active propagating rift system,Galapagos 95.5° W

ALVIN investigations have defined the fine-scale structural and volcanic patterns produced by active rift and spreading center propagation and failure near 95.5° W on the Galapagos spreading center. Behind the initial lithospheric rifting, which is propagating nearly due west at about 50 km m.y.^–1, a triangular block of preexisting lithosphere is being stretched and fractured, with some recent volcanism along curving fissures. A well-organized seafloor spreading center, an extensively faulted and fissured volcanic ridge, develops ~ 10 km (~ 200,000 years) behind the tectonic rift tip. Regional variations in the chemical compositions of the youngest lavas collected during this program contrast with those encompassing the entire 3 m.y. of propagation history for this region. A maximum in degree of magmatic differentiation occurs about 9 km behind the propagating rift tip, in a region of diffuse rifting. The propagating spreading center shows a gentle gradient in magmatic differentiation culminating at the SW-curving spreading center tip. Except for the doomed rift, which is in a constructional phase, tectonic activity also dominates over volcanic activity along the failing spreading system. In contrast to the propagating rift, failing rift lavas show a highly restricted range of compositions consistent with derivation from a declining upwelling zone accompanying rift failure. The lithosphere transferred from the Cocos to the Nazca plate by this propagator is extensively faulted and characterized by ubiquitous talus in one of the most tectonically disrupted areas of seafloor known. The pseudofault scarps, where the preexisting lithosphere was rifted apart, appear to include both normal and propagator lavas and are thus more lithologically complex than previously thought. Biological communities, probably vestimentiferan tubeworms, occur near the top of the outer pseudofault scarp, although no hydrothermal venting was observed.     

Sedimentation rates and heavy metal pollution of sediments in the Seto Inland Sea

Sedimentation rates in ten sediment cores from Hiroshima Bay in the Seto Inland Sea of Japan were determined with the |2210|0Pb technique, and heavy metals were analyzed. The sedimentation rates vary from 0.18 to 0.33 g cm|2-2|0 yr|2-1|0. The highest sedimentation rates were observed in the northern part of the bay at the mouth of Ota River, while lower sedimentation rates not more than 0.20 g cm⁻² yr⁻¹ were observed at stations close to narrow water-ways, or where water depth was shallow. The contents of copper and zinc in the sediment cores began to increase around 1930 as a result of increased human activity, and have remained almost unchanged since 1970 possibly because of regulation of pollutant discharge. The natural background values of copper and zinc in the sediment of this bay range from 16 to 27 mgkg⁻¹ and 70 to 105 mg kg⁻¹, respectively. The total amounts of anthropogenic copper and zinc deposited in the sediments since about 1930 are estimated to be 0.5–2.7 ton km⁻² and 2.2–14.5 ton km⁻², respectively. At the present-day, the anthropogenic loads of copper and zinc to the sediments of the whole bay are 26 ton yr⁻¹ and 183 ton yr⁻¹, and these values constitute 39% and 48% of the total sedimentary loads at the present-day, respectively.     

Depositional history of organic contaminants on the Palos Verdes Shelf, California

During more than 60 years, sedimentation on the Palos Verdes Shelf has been dominated by time-varying inputs of municipal wastewater from the Los Angeles County Sanitation Districts (LACSD) and debris from the Portuguese Bend Landslide (PBL). The present study examines the depositional history of wastewater-derived organic contaminants at a site approximately 6–8 km downcurrent from the outfall system. Sediments at this location are impacted by contributions from both sources, but the relative influence of the sources has changed over time. Two classes of hydrophobic organic contaminants (chlorinated hydrocarbons, long-chain alkylbenzenes) were determined in sediment cores collected in 1981 and 1992. Using molecular stratigraphy, we determined average sedimentation rates (cm/year) and mass accumulation rates (g cm⁻² year⁻¹) for the following periods: 1955–1965, 1965–1971, 1971–1981 and 1981–1992. The results show that sedimentation and mass accumulation rates increased from 1955 to 1971 and decreased from 1971 to 1981. These trends are consistent with historical information on the emission of suspended solids from the outfall system, indicating that the discharge of wastes dominated sedimentation at the site during this period. In the 1980s and early 1990s, however, mass accumulation rates increased in spite of continually decreasing emissions of wastewater solids. Several lines of evidence indicate that this increase was due to mobilization of debris from the PBL during and after unusually strong winter storms in the 1980s. As a result, heavily contaminated sediments deposited during the years of greatest waste emissions (i.e. 1950–1970) have been buried to greater sub-bottom depths, thereby reducing their availability for mobilization to the overlying water column. These results highlight the dynamic nature of sedimentation in contaminated coastal ecosystems and its importance to the long-term fate and effects of toxic substances.