Geology topics

A. VanGeen

Publications and source records attributed to A. VanGeen.

At least 19 recordsLinked to original sources

USGS2014

Detecting well casing leaks in Bangladesh using a salt spiking method

We apply fluid-replacement logging in arsenic-contaminated regions of Bangladesh using a low-cost, down-well fluid conductivity logging tool to detect leaks in the cased section of wells. The fluid-conductivity tool is designed for the developing world: it is lightweight and easily transportable, operable by one person, and can be built for minimal cost. The fluid-replacement test identifies leaking casing by comparison of fluid conductivity logs collected before and after spiking the wellbore with a sodium chloride tracer. Here, we present results of fluid-replacement logging tests from both leaking and non-leaking casing from wells in Araihazar and Munshiganj, Bangladesh, and demonstrate that the low-cost tool produces measurements comparable to those obtained with a standard geophysical logging tool. Finally, we suggest well testing procedures and approaches for preventing casing leaks in Bangladesh and other developing countries.

Ground Water↗

USGS2006

Sediment Cd and Mo accumulation in the oxygen-minimum zone off western Baja California linked to global climate over the past 52 kyr

Concentrations of organic carbon (orgC), cadmium (Cd), and molybdenum (Mo) were measured in two sediment cores raised from depths of 430 and 700 m within the oxygen-minimum zone (OMZ) off southern Baja California at a temporal resolution of e10.5 kyr over the past 52 kyr. These records are supplemented with diffuse spectral reflectance (DSR) measurements obtained on board ship soon after collection at a resolution of e10.05 kyr. In the core from 700 m depth, a component extracted from the DSR data and the three geochemical proxies generally vary in concert with each other and over a wide range (4-22% orgC; 1-40 mg/kg Cd; 5-120 mg/kg Mo). Intervals of increased orgC, Cd, and Mo accumulation generally correspond to warm periods recorded in the oxygen-isotopic composition of Greenland ice, with the exception of the Bolling/Allerod which is only weakly expressed off Baja California. Concentrations of the biogenic proxies are higher in the core from 430 m depth, but erratic sediment accumulation before 15 ka precludes dating of the older intervals that are laminated and contain elevated orgC, Cd, and Mo concentrations. The new data provide further evidence of an intimate teleconnection between global climate and the intensity of the OMZ and/or productivity along the western margin of North America. On the basis of a comparison with Cd and Mo records collected elsewhere in the region, we conclude that productivity may actually have varied off southern Baja California by no more than a factor of 2 over the past 52 kyr. Copyright 2006 by the American Geophysical Union.

Paleoceanography↗

USGS2004

Mg/Ca, Sr/Ca, and stable isotopes in modern and Holocene Protothaca staminea shells from a northern California coastal upwelling region

This study explores the potential of intertidal Protothaca staminea shells as high-resolution geochemical archives of environmental change in a coastal upwelling region. Mg/Ca and Sr/Ca ratios were analyzed by excimer laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS) at sub-weekly temporal resolution in shells growing ???1 mm per month. Growth patterns of a modern P. staminea shell from Humboldt Bay, California, collected in December 1999 made it possible to infer a lifespan from 1993 to 1998. Growth hiatuses in the shell may have excluded records of extreme events. Mg/Ca ratios appeared to be partly controlled by water temperature; the correlation coefficient between temperature and Mg/Ca was r = 0.71 in one of four growth increments. Significant year-to-year differences in the sensitivity of Mg/Ca to temperature in P. staminea could not be explained, however. Sr/Ca ratios appeared to be more closely related to shell growth rate. Oxygen isotopes, measured at 2-week temporal resolution in the same shell, did not show a clear relation to local temperature in summer, possibly because temperatures were higher and less variable at the King Salmon mudflat, where the shell was collected, than in the main channel of Humboldt Bay, where water properties were monitored. Negative shell ??13C values (<-0.5???) marked spring and summer coastal upwelling events. The Mg contents of P. staminea midden shells dated to ???3 ka and ???9 ka were significantly lower than in the modern shell. This may have resulted from degradation of a Mg-rich shell organic matrix and precluded quantitative interpretation of the older high-resolution records. Elevated ??13C values in the ???3 ka shell suggested that the individual grew in highly productive or stratified environment, such as a shallow coastal embayment or lagoon. Copyright ?? 2004 Elsevier Ltd.

Geochimica et Cosmochimica Acta↗

USGS2004

Enhanced marine productivity off western North America during warm climate intervals of the past 52 k.y

Studies of the Santa Barbara Basin off the coast of California have linked changes in its bottom-water oxygen content to millennial-scale climate changes as recorded by the oxygen isotope composition of Greenland ice. Through the use of detailed records from a sediment core collected off the Magdalena Margin of Baja California, Mexico, we demonstrate that this teleconnection predominantly arose from changes in marine productivity, rather than changes in ventilation of the North Pacific, as was originally proposed. One possible interpretation is that the modern balance of El Nin??o-La Nin??a conditions that favors a shallow nutricline and high productivity today and during warm climate intervals of the past 52 k.y. was altered toward more frequent, deep nutricline, low productivity, El Nin??o-like conditions during cool climate intervals. ?? 2004 Geological Society of America.

Geology↗

USGS2003

Metal uptake by phytoplankton during a bloom in South San Francisco Bay: Implications for metal cycling in estuaries

The 1994 spring phytoplankton bloom in South San Francisco Bay caused substantial reductions in concentrations of dissolved Cd, Ni, and Zn, but not Cu. We estimate that the equivalent of ~60% of the total annual input of Cd, Ni, and Zn from local waste‐water treatment plants is cycled through the phytoplankton in South Bay. The results suggest that processes that affect phytoplankton bloom frequency or intensity in estuaries (e.g. nutrient enrichment) may also affect metal trapping. The bloom was characterized by hydrographic surveys conducted at weekly intervals for 9 weeks. Metal samples were collected from the water column on three occasions, timed to bracket the period when the bloom was predicted. Factors that might confound observations of biological influences, such as freshwater inputs, were relatively constant during the study. Before the bloom, concentrations of dissolved Cd were 0.81 ± 0.02 nmol kg −1 , Zn concentrations were 19.8 ± 1.5 nmol kg −1 , Ni were 42 ± 1.4 nmol kg −1 , and Cu were 37 ± 1.4 nmol kg −1 . These values are elevated relative to riverine and coastal end‐members, reflecting inputs from wastewater and(or) sediments. At the height of the bloom, dissolved Zn, Cd, and Ni were reduced to 19, 50, and 75% of their prebloom concentrations, respectively. Dissolved Cu concentrations increased 20%. The mass of Cd taken up by phytoplankton was similar to the mass of Cd removed from solution if particle settling was considered, and Cd concentrations estimated in phytoplankton were higher than concentrations in suspended particulate material (SPM). Particulate concentrations of Zn and Ni during the bloom appeared to be dominated by the influence of changes in resuspension of Zn and Ni‐rich sediments.

California↗

USGS2003

On the preservation of laminated sediments along the western margin of North America

Piston, gravity, and multicores as well as hydrographic data were collected along the Pacific margin of Baja California to reconstruct past variations in the intensity of the oxygen-minimum zone (OMZ). Gravity cores collected from within the OMZ north of 24??N did not contain laminated surface sediments even though bottom water oxygen (BWO) concentrations were close to 5 ??mol/kg. However, many of the cores collected south of 24??N did contain millimeter- to centimeter-scale, brown to black laminations in Holocene and older sediments but not in sediments deposited during the Last Glacial Maximum. In addition to the dark laminations, Holocene sediments in Soledad Basin, silled at 290 m, also contain white coccolith laminae that probably represent individual blooms. Two open margin cores from 430 and 700 m depth that were selected for detailed radiocarbon dating show distinct transitions from bioturbated glacial sediment to laminated Holocene sediment occurring at 12.9 and 11.5 ka, respectively. The transition is delayed and more gradual (11.3-10.0 ka) in another dated core from Soledad Basin. The observations indicate that bottom-water oxygen concentrations dropped below a threshold for the preservation of laminations at different times or that a synchronous hydrographic change left an asynchronous sedimentary imprint due to local factors. With the caveat that laminated sections should therefore not be correlated without independent age control, the pattern of older sequences of laminations along the North American western margin reported by this and previous studies suggests that multiple patterns of regional productivity and ventilation prevailed over the past 60 kyr. Copyright 2003 by the American Geophysical Union.

Paleoceanography↗

USGS2000

Authigenic molybdenum formation in marine sediments: A link to pore water sulfide in the Santa Barbara Basin

Pore water and sediment Mo concentrations were measured in a suite of multicores collected at four sites along the northeastern flank of the Santa Barbara Basin to examine the connection between authigenic Mo formation and pore water sulfide concentration. Only at the deepest site (580 m), where pore water sulfide concentrations rise to >0.1 μM right below the sediment water interface, was there active authigenic Mo formation. At shallower sites (550, 430, and 340 m), where pore water sulfide concentrations were consistently <0.05 μM, Mo precipitation was not occurring at the time of sampling. A sulfide concentration of ∼0.1 μM appears to be a threshold for the onset of Mo-Fe-S co-precipitation. A second threshold sulfide concentration of ∼100 μM is required for Mo precipitation without Fe, possibly as Mo-S or as particle-bound Mo.

Geochimica et Cosmochimica Acta↗

USGS1999

Dissolved sulfide distributions in the water column and sediment pore waters of the Santa Barbara Basin

Dissolved sulfide concentrations in the water column and in sediment pore waters were measured by square-wave voltammetry (nanomolar detection limit) during three cruises to the Santa Barbara Basin in February 1995, November–December 1995, and April 1997. In the water column, sulfide concentrations measured outside the basin averaged 3 ± 1 nM ( n = 28) in the 0 to 600 m depth range. Inside the basin, dissolved sulfides increased to reach values of up to 15 nM at depths >400 m. A suite of box cores and multicores collected at four sites along the northeastern flank of the basin showed considerable range in surficial (<0.5 cm) pore-water sulfide concentrations: <0.008, 0.01, 0.02, to as much as 0.4 μM at the 340, 430, 550, and 590 m sites, respectively. At a core depth of 10 cm, however, pore–water sulfides exhibited an even wider range: 0.005, 0.05, 0.1, and 100 μM at the same sites, respectively. The sulfide flux into the deep basin, estimated from water-column profiles during three cruises, suggests a fairly consistent input of 100–300 nmole m −2 h −1 . In contrast, sulfide fluxes estimated from pore-water sulfide gradients at the sediment water interface were much more variable (−4 to 13,000 nmole m −2 h −1 ). Dissolved silicate profiles show clear indications of irrigation at shallow sites (340 and 430 m) in comparison to deeper basin sites (550 and 590 m) with low (<10 μM) bottom-water dissolved-oxygen concentrations. Pore-water profiles indicate ammonia generation at all sites, but particularly at the deep-basin 590 m site with concentrations increasing with sediment depth to >400 μM at 10 cm. Decreases in water-column nitrate below the sill depth indicate nitrate consumption (−55 to −137 μmole m −2 h −1 ) similar to nearby Santa Monica Basin. Peaks in pore-water iron concentrations were generally observed between 2 and 5 cm depth with shallowest peaks at the 590 m site. These observations, including observations of the benthic microfauna, suggest that the extent to which the sulfide flux, sustained by elevated pore-water concentrations, reaches the water column may be modulated by the abundance of sulfide-oxidizing bacteria in addition to iron redox and precipitation reactions.

Geochimica et Cosmochimica Acta↗

USGS1999

Constraints on the sedimentation history of San Francisco Bay from 14C and 10Be

Industrialization and urbanization around San Francisco Bay as well as mining and agriculture in the watersheds of the Sacramento and San Joaquin rivers have profoundly modified sedimentation patterns throughout the estuary. We provide some constraints on the onset of these erosional disturbances with 10Be data for three sediment cores: two from Richardson Bay, a small embayment near the mouth of San Francisco Bay, and one from San Pablo Bay, mid-way between the river delta and the mouth. Comparison of pre-disturbance sediment accumulation determined from three 14C-dated mollusk shells in one Richardson Bay core with more recent conditions determined from the distribution of 210Pb and 234Th [Fuller, C.C., van Geen, A., Baskaran, M, Anima, R.J., 1999. Sediment chronology in San Francisco Bay, California, defined by 210Pb, 234Th, 239,240Pu.] shows that the accumulation rate increased by an order of magnitude at this particular site. All three cores from San Francisco Bay show subsurface maxima in 10Be concentrations ranging in magnitude from 170 to 520 x 106 atoms/g. The transient nature of the increased 10Be input suggests that deforestation and agricultural develop- ment caused basin-wide erosion of surface soils enriched in 10Be. probably before the turn of the century.

California↗

USGS1999

A record of estuarine water contamination from the Cd content of foraminiferal tests in San Francisco Bay, California

A five-year dissolved Cd time series from San Francisco Bay and adjacent coastal water shows that the composition of surface water towards the mouth of the estuary is determined largely by the effect of coastal upwelling. Cd concentrations inside and outside the estuary (0.2-1.0 nmol/kg) increase as Cd-rich deep water is advected to the surface near the coast during spring and summer. On average, the mean Cd concentrations inside San Francisco Bay (0.54 nmol/kg) during 1991-1995 was significantly higher than outside (0.35 nmol/kg), however. Surface samples collected throughout San Francisco Bay confirm an internal Cd source unrelated to river discharge. The Cd content of the test of a benthic foraminifer (Elphidiella hannai) in a dated sediment core from San Francisco Bay was measured to determine if the water column Cd enrichments in San Francisco Bay could be related to the rapid development of the watershed. The method is based on the observation that the Cd/Ca ratio of carefully cleaned tests of foraminifera is, determined by the dissolved Cd content of overlying water at the time of test formation. Pre-industrial foraminiferal Cd/Ca ratios in the sediment core average 274 ?? 15 nmol/mol (n = 19) nmol/mol. Foraminiferal Cd/Ca ratios increased to 386 ?? 33 nmol/mol (n = 19) over the past several decades indicating a 40% increase in the mean Cd content of surface water in Central San Francisco Bay. We suggest that, in addition to Cd discharges into the estuary, indirect consequences of agricultural development in the Central Valley of California could have contributed to this increase. This new method to reconstruct estuarine contamination is not affected by some of the processes that complicate the interpretation of changes in bulk sediment metal concentrations.

Marine Chemistry↗

USGS1999

Sedimentary record of anthropogenic and biogenic polycyclic aromatic hydrocarbons in San Francisco Bay, California

Dated sediment cores collected from Richardson and San Pablo Bays in San Francisco Bay were used to reconstruct a history of polycyclic aromatic hydrocarbon (PAH) contamination. The sedimentary record of PAHs in Richardson Bay shows that anthropogenic inputs have increased since the turn of the century, presumably as a result of increasing urbanization and industrialization around the Bay Area. Concentrations range from about 0.04-6.3 ??g g-1. The dominant origin of the PAHs contributing to this modern contamination is from combustion processes. Depth profiles in San Pablo Bay indicate higher concentrations of PAHs since the 1950s than during the late 1800s, also presumably resulting from an increase in urbanization and industrialization. Total PAHs in San Pablo Bay range from about 0.04-1.3 ??g g-1. The ratios of methylphenanthrenes/phenanthrene and (methylfluoranthenes + methylpyrenes)/fluoranthene were sensitive indicators of anthropogenic influences in the estuary. Variations in the ratio of 1,7-dimethylphenanthrene/2,6-dimethylphenanthrene indicate a gradual replacement of wood by fossil-fuel as the main combustion source of PAHs in. San Francisco Bay sediments. The profile of perylene may be an indicator of eroding peat from marshlands.

California↗

USGS1999

A record of hydrocarbon input to San Francisco Bay as traced by biomarker profiles in surface sediment and sediment cores

San Francisco Bay is one of the world's largest urbanized estuarine systems. Its water and sediment receive organic input from a wide variety of sources; much of this organic material is anthropogenically derived. To document the spatial and historical record of the organic contaminant input, surficial sediment from 17 sites throughout San Francisco Bay and sediment cores from two locations Richardson Bay and San Pablo Bay were analyzed for biomarker constituents. Biomarkers, that is, 'molecular fossils', primarily hopanes, steranes, and n-alkanes, provide information on anthropogenic contamination, especially that related to petrogenic sources, as well as on recent input of biogenic material. The biomarker parameters from the surficial sediment and the upper horizons of the cores show a dominance of anthropogenic input, whereas the biomarker profiles at the lower horizons of the cores indicate primarily biogenic input. In the Richardson Bay core the gradual upcore transition from lower maturity background organics to a dominance of anthropogenic contamination occurred about 70-100 years ago and corresponds to the industrial development of the San Francisco Bay area. In San Pablo Bay, the transition was very abrupt, reflecting the complex depositional history of the area. This sharp transition, perhaps indicating a depositional hiatus or erosional period, dated at pre-1952, is clearly visible. Below, the hiatus the biomarker parameters are immature; above, they are mature and show an anthropogenic overlay. Higher concentrations of terrigenous n-alkanes in the upper horizons in this core are indicative of an increase in terrigenous organic matter input in San Pablo Bay, possibly a result of water diversion projects and changes in the fresh water flow into the Bay from the Delta. Alternatively, it could reflect a dilution of organic material in the lower core sections with hydraulic mining debris.

California↗

USGS1999

Historical trends of metals in the sediments of San Francisco Bay, California

Concentrations of Ag, Al, Cr, Cu, Fe, Hg, Mn, Ni, Pb, V and Zn were determined in six sediment cores from San Francisco Bay (SFB) and one sediment core in Tomales Bay (TB), a reference estuary. SFB cores were collected from between the head of the estuary and its mouth (Grizzly Bay, GB; San Pablo Bay, SP; Central Bay, CB; Richardson Bay, RB, respectively) and ranged in length from 150 to 250 cm. Concentrations of Cr, V and Ni are greater than mean crustal content in SFB and TB sediments, and greater than found in many other coastal sediments. However, erosion of ultramafic rock formations in the watershed appears to be the predominant source. Baseline concentrations of other metals were determined from horizons deposited before sediments were influenced by human activities and by comparing concentrations to those in TB. Baseline concentrations of Cu co-varied with Al in the SFB sediments and ranged from 23.7±1.2 μg/g to 41.4±2.4 μg/g. Baseline concentrations of other metals were less variable: Ag, 0.09±0.02 μg/g; Pb, 5.2±0.7 μg/g; Hg, 0.06±0.01 μg/g; Zn, 78±7 μg/g. The earliest anthropogenic influence on metal concentrations appeared as Hg contamination (0.3–0.4 μg/g) in sediments deposited at SP between 1850 and 1880, apparently associated with debris from hydraulic gold mining. Maximum concentrations of Hg within the cores were 20 times baseline. Greater inventories of Hg at SP and GB than at RB verified the importance of mining in the watershed as a source. Enrichment of Ag, Pb, Cu and Zn first appeared after 1910 in the RB core, later than is observed in Europe or eastern North America. Maximum concentrations of Ag and Pb were 5–10 times baseline and Cu and Zn concentrations were less than three times baseline. Large inventories of Pb to the sediments in the GB and SP cores appeared to be the result of the proximity to a large Pb smelter. Inventories of Pb at RB are similar to those typical of atmospheric inputs, although influence from the Pb smelter is also suspected. Concentrations of Hg and Pb have decreased since the 1970s (to 0.30 μg/g and 25 μg/g, respectively) and were similar among all cores in 1990. Early Ag contamination was perhaps a byproduct of the Pb smelting process, but a modern source of Ag is also indicated, especially at RB and CB.

California↗

USGS1999

Chlorinated hydrocarbon pesticides and polychlorinated biphenyls in sediment cores from San Francisco Bay

Sediment cores of known chronology from Richardson and San Pablo Bays in San Francisco Bay, CA, were analyzed for a suite of chlorinated hydrocarbon pesticides and polychlorinated biphenyls to reconstruct a historic record of inputs. Total DDTs (DDT = 2,4'- and 4,4'-dichlorodiphenyltrichloroethane and the metabolites, 2,4'- and 4,4'-DDE, -DDD) range in concentration from 4-21 ng/g and constitute a major fraction (> 84%) of the total pesticides in the top 70 cm of Richardson Bay sediment. A subsurface maximum corresponds to a peak deposition date of 1969-1974. The first measurable DDT levels are found in sediment deposited in the late 1930's. The higher DDT inventory in the San Pablo relative to the Richardson Bay core probably reflects the greater proximity of San Pablo Bay to agricultural activities in the watershed of the Sacramento and San Joaquin rivers. Total polychlorinated biphenyls (PCBs) occur at comparable levels in the two Bays (< 1-34 ng/g). PCBs are first detected in sediment deposited during the 1930's in Richardson Bay, about a decade earlier than the onset of detectable levels of DDTs. PCB inventories in San Pablo Bay are about a factor of four higher in the last four decades than in Richardson Bay, suggesting a distribution of inputs not as strongly weighed towards the upper reaches of the estuary as DDTs. The shallower subsurface maximum in PCBs compared to DDT in the San Pablo Bay core is consistent with the imposition of drastic source control measures four these constituents in 1970 and 1977 respectively. The observed decline in DDT and PCB levels towards the surface of both cores is consistent with a dramatic drop in the input of these pollutants once the effect of sediment resuspension and mixing is taken into account.

California↗

USGS1997

A120 yr record of widespread contamination from mining of the Iberian pyrite belt

A metal-enriched seawater plume entering the western Mediterranean Sea through the Strait of Gibraltar originates 300 km to the west in the Rio Tinto estuary of southwestern Spain. Mining of Rio Tinto ore, one of the largest metal-rich sulfide deposits in the world, started well before Roman times. Contemporary Rio Tinto waters draining the region are highly acidic (pH 2.5) with dissolved cadmium, zinc, and copper concentrations 10 5 −10 6 times higher than in uncontaminated surface water of the Gulf of Cadiz. Two dated sediment cores from the Spanish continental shelf show that metal inputs to the region increased with the onset of intensive mining activities during the second half of the 19th century. Although the impact of mining may have decreased over the past few decades, the Tinto river and estuary remain highly contaminated.

Geology↗

USGS1996

Cadmium in the California Current system: Tracer of past and present upwelling

Over 100 samples were collected off the west coast of North America during 1991–1993 to determine the relation between wind‐driven upwelling and nearshore concentrations of dissolved silicate (Si), phosphate (P), and cadmium (Cd). Highly enriched in deep water offshore, these constituents are sensitive indicators of upwelling. Coastal water was sampled from the shore in January and June 1992 at 12 sites distributed between 36° and 48°N latitude. In January the composition of nearshore water along this transect was fairly uniform: 5–15 μmol/kg for Si, 0.5 to 1.0 μmol/kg for P, and 0.1–0.3 nmol/kg for Cd. In June, elevated concentrations of Si (30 μmol/kg), P (2.0 μmol/kg), and Cd (0.6 nmol/kg) revealed a region of intense upwelling between 38° and 40°N. The pattern is broadly consistent with meridional gradients in coastal upwelling calculated from the long‐term mean of alongshore winds compiled from ship reports. Nearshore water was also collected biweekly to monthly at two sites 3 km apart near San Francisco Bay (37.5°N) during 1991–1993. The variability seen in the time series suggests that the composition of nearshore water integrates the effect of alongshore winds over timescales of several weeks. Seasonal variations in Si (5–50 μmol/kg), P (0.5–2.5 μmol/kg), and Cd (0.1–0.8 nmol/kg) concentrations were consistent with upwelling during spring and summer. Maximum Si, P, and Cd concentrations reached in May 1991 were consistent with advection to the very nearshore region from a depth of about 300 m relative to a vertical profile at a distance of 200 km from the coast. Nearshore Si, P, and Cd concentrations were reduced relative to 1991 in 1992, and, to a lesser extent, in 1993 due to weaker upwelling linked to the warm phase of the El Niño‐Southern Oscillation. During periods of weaker upwelling or downwelling, variations in P, Si, and Cd concentrations became uncoupled. There is a good correlation between the coastal Cd time series near San Francisco Bay (37.5°N) and a second order polynomial function of the upwelling index of Bakun [1975] at 36°N, filtered with a 30‐day running mean ( r 2 = 0.71, n = 39). The index is a daily estimate of coastal upwelling calculated from 6‐hourly mean atmospheric pressure distributions at 36°N. From this function and a record of daily upwelling indices, we infer a range of annually averaged coastal Cd concentrations of at least 0.3–0.5 nmol/kg since 1967. Cd/Ca ratios in shells of foraminifera from San Francisco Bay suggest that average coastal Cd concentrations 3500–4500 years ago were at the upper end of this range.

Journal of Geophysical Research C: Oceans↗

USGS1996

Ventilation changes in the northeast Pacific during the last deglaciation

Under present climate conditions, convection at high latitudes of the North Pacific is restricted to shallower depths than in the North Atlantic. To what extent this asymmetry between the two ocean basins was maintained over the past 20 kyr is poorly known because there are few unambiguous proxy records of ventilation from the North Pacific. We present new data for two sediment cores from the California margin at 800 and 1600 m depth to argue that the depth of ventilation shifted repeatedly in the northeast Pacific over the course of deglaciation. The evidence includes benthic foraminiferal Cd/Ca, 18 O/ 16 O, and 13 C/ 12 C data as well as radiocarbon age differences between benthic and planktonic foraminifera. A number of features in the shallower of the two cores, including an interval of laminated sediments, are consistent with changes in ventilation over the past 20 kyr suggested by alternations between laminated and bioturbated sediments in the Santa Barbara Basin and the Gulf of California [ Keigwin and Jones , 1990; Kennett and Ingram , 1995; Behl and Kennett , 1996]. Data from the deeper of the two California margin cores suggest that during times of reduced ventilation at 800 m, ventilation was enhanced at 1600 m depth, and vice versa. This pronounced depth dependence of ventilation needs to be taken into account when exploring potential teleconnections between the North Pacific and the North Atlantic.

Paleoceanography and Paleoclimatology↗

USGS1993

Trace metals (Cd, Cu, Ni, and Zn) and nutrients in coastal waters adjacent to San Francisco Bay, California

Samples collected in December 1990 and July 1991 show that dissolved Cd, Cu, Ni, and Zn distributions in the Gulf of the Farallones are dominated by mixing of two end-members: (1) metal-enriched San Francisco Bay water and (2) offshore California Current water. The range of dissolved metal concentrations observed is 0.2–0.9 nmol kg −1 for Cd, 1–20 nmol kg −1 for Cu, 4–16 nmol kg −1 for Ni, and 0.2–20 nmol kg −1 for Zn. Effective concentrations in fresh water discharged into San Francisco Bay during 1990–1991 (estimated by extrapolation to zero salinity) are 740–860 μmol kg −1 for silicate, 21–44 μmol kg −1 for phosphate, 10–15 nmol kg −1 for Cd, 210–450 nmol kg −1 for Cu, 210–270 nmol kg −1 for Ni, and 190–390 nmol kg −1 for Zn. Comparison with effective trace metal and nutrient concentrations for freshwater discharge reported by Flegal et al. (1991) shows that input of these constituents to the northern reaches of San Francisco Bay accounts for only a fraction of the input to Gulf of the Farallones from the estuary system as a whole. The nutrient and trace metal composition of shelf water outside a 30-km radius from the mouth of the estuary closely resembles that of California Current water further offshore. In contrast to coastal waters elsewhere, there is little evidence of Cd, Cu, Ni, and Zn input by sediment diagenesis in continental shelf waters of California.

Estuaries↗