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  • American Geophysical Union  (109)
  • 2010-2014  (66)
  • 1985-1989  (43)
  • 1
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 10 (2009): Q05008, doi:10.1029/2009GC002429.
    Description: A method is presented for precisely measuring all five noble gases and their isotopic ratios in water samples using multiple programmed multistage cryogenic traps in conjunction with quadrupole mass spectrometry and magnetic sector mass spectrometry. Multiple automated cryogenic traps, including a two-stage cryotrap used for removal of water vapor, an activated charcoal cryotrap used for helium separation, and a stainless steel cryotrap used for neon, argon, krypton, and xenon separation, allow reproducible gas purification and separation. The precision of this method for gas standards is ±0.10% for He, ±0.14% for Ne, ±0.10% for Ar, ±0.14% for Kr, and ±0.17% for Xe. The precision of the isotopic ratios of the noble gases in gas standards are ±1.9‰ for 20Ne/22Ne, ±2.0‰ for 84Kr/86Kr, ±2.5‰ for 84Kr/82Kr, ±0.9‰ for 132Xe/129Xe, and ±1.3‰ for 132Xe/136Xe. The precision of this method for water samples, determined by measurement of duplicate pairs, is ±1% for He, ±0.9% for Ne, ±0.3% for Ar, ±0.3% for Kr, and ±0.2% for Xe. An attached magnetic sector mass spectrometer measures 3He/4He with precisions of ±0.1% for air standards and ±0.14% for water samples.
    Description: We are grateful for support by the National Science Foundation Chemical Oceanography program (OCE-0221247), by the Department of Defense (graduate fellowship to RHRS), and by the Woods Hole Oceanographic Institution (postdoctoral fellowship for B.B.).
    Keywords: Noble gas ; Oceanography ; Mass spectrometry ; Seawater ; Isotope ; Cryogenic
    Repository Name: Woods Hole Open Access Server
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  • 2
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 114 (2009): C11020, doi:10.1029/2009JC005396.
    Description: Air-sea gas exchange is an important part of the biogeochemical cycles of many climatically and biologically relevant gases including CO2, O2, dimethyl sulfide and CH4. Here we use a three year observational time series of five noble gases (He, Ne, Ar, Kr, and Xe) at the Bermuda Atlantic Time series Study (BATS) site in tandem with a one-dimensional upper ocean model to develop an improved parameterization for air-sea gas exchange that explicitly includes separate components for diffusive gas exchange and bubble processes. Based on seasonal timescale noble gas data, this parameterization, which has a 1σ uncertainty of ±14% for diffusive gas exchange and ±29% for bubble fluxes, is more tightly constrained than previous parameterizations. Although the magnitude of diffusive gas exchange is within errors of that of Wanninkhof (1992), a commonly used parameterization, we find that bubble-mediated exchange, which is not explicitly included by Wanninkhof (1992) or many other formulations, is significant even for soluble gases. If one uses observed saturation anomalies of Ar (a gas with similar characteristics to O2) and a parameterization of gas exchange to calculate gas exchange fluxes, then the calculated fluxes differ by ∼240% if the parameterization presented here is used compared to using the Wanninkhof (1992) parameterization. If instead one includes the gas exchange parameterization in a model, then the calculated fluxes differ by ∼35% between using this parameterization and that of Wanninkhof (1992). These differences suggest that the bubble component should be explicitly included in a range of marine biogeochemical calculations that incorporate air-sea gas fluxes.
    Description: Funding from the National Science Foundation Chemical Oceanography program (OCE-0221247 and OCE-0623034).
    Keywords: Air-sea gas exchange ; Noble gas ; Bubbles
    Repository Name: Woods Hole Open Access Server
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  • 3
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 12 (2011): Q08001, doi:10.1029/2011GC003617.
    Description: Isotope systematics of basalts provide information on the distribution of mantle components and the length scale of mantle heterogeneity. To obtain this information, high data and sampling density are crucial. We present hafnium and neodymium isotope data on more than 400 oceanic volcanics. Over length scales of several hundred to over one thousand kilometers hafnium and neodymium isotopes of mid-ocean ridge basalts are correlated and form an array of parallel trends on a global scale. On a larger scale these domains differ in the amount of highly depleted mantle material with radiogenic hafnium and neodymium isotope ratios. Compared to the Atlantic and Indian Ocean basins the asthenosphere of the Pacific basin seems to have a more uniform and a less radiogenic Hf isotopic composition for a given Nd isotopic composition. The parallel arrays of mid-ocean ridge basalts provide strong constraints on the makeup of the MORB mantle and are evidence for the presence of a highly depleted and highly radiogenic neodymium and hafnium component. This component, because of its highly depleted character, is unrecognized in the strontium-neodymium-lead isotope systems alone. Alternatively, the parallel arrays can have an ancient origin of systematic variations in the degree of depletion. Each array then represents the variations in this fossil melting regime. Individual ocean island basalt suites display different slopes in hafnium-neodymium isotope space, which are also best explained by varying amounts of highly residual mantle rather than isotopic differences in enriched mantle components as previously invoked. The ocean island basalt arrays diverge at the depleted end and project to radiogenic compositions that are similar to those of the asthenosphere through which they travel. This is strong evidence that the plume material interacts with its surrounding mantle as it ascends. The isotopic compositions of the ocean island and ridge basalts suggest that their systematics are influenced by a heretofore unrecognized depleted component.
    Description: This work was supported by NSF grants EAR 0635864 and OCE0648484 to V.S. and OCE0351437 to S.H.
    Keywords: MORB ; Hafnium ; Isotopes ; Neodymium
    Repository Name: Woods Hole Open Access Server
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  • 4
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 10 (2009): Q03006, doi:10.1029/2008GC002324.
    Description: We report 87Sr/86Sr and 143Nd/144Nd data on clinopyroxenes recovered from 10 ocean island lavas from three different hot spots (Samoa, Society, and Cook-Austral island chains). The clinopyroxenes recovered from eight of the 10 lavas analyzed in this study exhibit 87Sr/86Sr disequilibrium with respect to the host lava. The 87Sr/86Sr ratios in clinopyroxene separates are 95–3146 ppm (0.0095–0.31%) different from their respective host whole rocks. Clinopyroxenes in three lavas have 143Nd/144Nd ratios that are 70–160 ppm (0.007–0.016%) different from the host lavas. The 87Sr/86Sr and 143Nd/144Nd disequilibrium in one lava (the oldest lava considered in this study, Mangaia sample MGA-B-47) can be attributed to posteruptive radiogenic ingrowth, but the isotope disequilibrium in the other, younger lavas cannot be explained by this mechanism. In five of the lava samples, two populations of clinopyroxene were isolated (black and green, separated by color). In four out of five of these samples, the 87Sr/86Sr ratios of the two clinopyroxene populations are isotopically different from each other. In addition to 87Sr/86Sr disequilibrium, the two clinopyroxene populations in one of the lavas (Tahaa sample TAA-B-26) have 143Nd/144Nd ratios that are ∼100 ppm different from each other. Given the resilience of clinopyroxene to seawater alteration and the likelihood that the Sr and Nd isotope composition of fresh clinopyroxene separates provides a faithful record of primary magmatic compositions, the clinopyroxene-clinopyroxene isotope disequilibrium in these four lavas provides strong evidence that a mechanism other than seawater alteration has generated the observed isotopic disequilibrium. This study confirms the isotopic diversity in ocean island lavas previously observed in olivine-hosted melt inclusions. For example, the Sr isotopic variability previously observed in olivine-hosted melt inclusions is mirrored by the isotopic diversity in clinopyroxenes isolated from many of the same Samoan lavas. The isotopic data from melt inclusions and clinopyroxenes are not consistent with shallow assimilation of sediment or with entrainment of xenocrystic clinopyroxene from the oceanic crust or upper mantle. Instead, the data are interpreted as reflecting isotopic heterogeneity in the mantle sources of the lavas. The isotopic diversity in clinopyroxenes and melt inclusions suggests that a single lava can host components derived from isotopically diverse source regions.
    Description: NSF grant EAR-0509891 to SRH is gratefully acknowledged.
    Keywords: Clinopyroxene ; Melt inclusion ; Mantle geochemistry ; Sr-87/Sr-86 ; Nd-143/Nd-144 ; Trace elements
    Repository Name: Woods Hole Open Access Server
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  • 5
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2012. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 117 (2012): C05012, doi:10.1029/2010JC006856.
    Description: The triple oxygen isotopic composition of dissolved oxygen (17Δ) is a promising tracer of gross oxygen productivity (P) in the ocean. Recent studies have inferred a high and variable ratio of P to 14C net primary productivity (12–24 h incubations) (e.g., P:NPP(14C) of 5–10) using the 17Δ tracer method, which implies a very low efficiency of phytoplankton growth rates relative to gross photosynthetic rates. We added oxygen isotopes to a one-dimensional mixed layer model to assess the role of physical dynamics in potentially biasing estimates of P using the 17Δ tracer method at the Bermuda Atlantic Time-series Study (BATS) and Hawaii Ocean Time-series (HOT). Model results were compared to multiyear observations at each site. Entrainment of high 17Δ thermocline water into the mixed layer was the largest source of error in estimating P from mixed layer 17Δ. At both BATS and HOT, entrainment bias was significant throughout the year and resulted in an annually averaged overestimate of mixed layer P of 60 to 80%. When the entrainment bias is corrected for, P calculated from observed 17Δ and 14C productivity incubations results in a gross:net productivity ratio of 2.6 (+0.9 −0.8) at BATS. At HOT a gross:net ratio decreasing linearly from 3.0 (+1.0 −0.8) at the surface to 1.4 (+0.6 −0.6) at depth best reproduced observations. In the seasonal thermocline at BATS, however, a significantly higher gross:net ratio or large lateral fluxes of 17Δ must be invoked to explain 17Δ field observations.
    Description: We acknowledge support from Center for Microbial Oceanography Research and Education (CMORE) (NSF EF-0424599) and NOAA Global Carbon Program (NA 100AR4310093). BL thanks the USA-Israel Binational Science Foundation for supporting his project at BATS.
    Description: 2012-11-08
    Keywords: Bermuda Atlantic Time-series ; Hawaii Ocean Time-series ; Primary production ; Triple oxygen isotopes
    Repository Name: Woods Hole Open Access Server
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  • 6
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 12 (2011): Q07025, doi:10.1029/2010GC003438.
    Description: The volcanic origin of the Samoan archipelago can be explained by one of three models, specifically, by a hot spot forming over a mantle plume, by lithospheric extension resulting from complex subduction tectonics in the region, or by a combination of these two processes, either acting sequentially or synchronously. In this paper, we present results of 36 high-resolution 40Ar/39Ar incremental heating age analyses for the initial (submarine) phase of Samoan volcanoes, ranging from 13.2 Ma for the westernmost Samoan seamounts to 0.27 Ma in the eastern Samoan volcanic province. Taken as a whole, our new age data point to a hot spot origin for the shield-building volcanism in the Samoan lineament, whereby seamounts younger than 5 Ma are consistent with a model of constant 7.1 cm/yr plate motion, analogous to GPS measurements for the Pacific Plate in this region. This makes our new 40Ar/39Ar ages of the submarine basalts all older compared to recent absolute plate motion (APM) models by Wessel et al. (2008), which are based on the inversion of twelve independent seamount trails in the Pacific relative to a fixed reference frame of hot spots and which predict faster plate motions of around 9.3 cm/yr in the vicinity of Samoa. The Samoan ages are also older than APM models by Steinberger et al. (2004) taking into account the motion of hot spots in the Pacific alone or globally. The age systematics become more complicated toward the younger end of the Samoan seamount trail, where its morphology bifurcates into two en echelon subtracks, termed the VAI and MALU trends, as they emanate from two eruptive centers at Vailulu'u and Malumalu seamount, respectively. Spaced ∼50 km apart, the VAI and MALU trends have distinct geochemical characters and independent but overlapping linear 40Ar/39Ar age progressions since 1.5 Ma. These phenomena are not unique to Samoa, as they have been observed at the Hawaiian hot spot, and can be attributed to a geochemical zoning in its underlying mantle source or plume. Moreover, the processes allowing for the emergence of two distinct eruptive centers in the Samoan archipelago, the stepped offset of these subtracks, and their slight obliqueness with respect to the overall seamount trail orientation may very well be controlled by local tectonics, stresses, and extension, also causing the rejuvenated volcanism on the main islands of Savai'i, Upolu, and Tutuila since 0.4 Ma.
    Description: Financial support is provided by NSF‐OCE 0002875 and NSF‐OCE 0351437.
    Keywords: Ar-40/Ar-39 geochronology ; Seamounts ; Pacific plate ; Hot spots ; Intraplate volcanism ; Zoned mantle plume
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  • 7
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2004. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 19 (2004): PA4031, doi:10.1029/2004PA001084.
    Description: Using Secondary Ion Mass Spectrometry (SIMS) ion microprobe techniques, we generated annual Sr/Ca cycles with subweekly resolution from chunks of Porites coral retrieved from a Tahiti barrier reef drill core (149°W, 17°S), representing the period 13,650 to 13,100 years B.P. The centers of pristine skeletal septa were selectively targeted with a 10 μm diameter ion beam spot, avoiding adjacent pore spaces occupied by secondary aragonite needles. Applying a Sr/Ca–sea surface temperature (SST) calibration equation derived from modern Tahiti Porites having the same low growth rate as the fossil specimens, we obtained SSTs ∼0.5°–1.5°C cooler during the Bølling-Allerod relative to the present day, with no significant change in seasonality. On the contrary, we estimate that analysis of bulk samples would yield excessively cool Sr/Ca-based SST estimates due to the occupation by secondary aragonite crystals of up to 50% of the skeletal pore space in the ancient samples. We find that growth rate effects on coral Sr/Ca further depress the apparent mean annual derived SSTs (by 〉3°C) and amplify the apparent seasonality by selectively enhancing wintertime cooling. Our microscale analysis of pristine skeleton and application of an appropriate growth-dependent calibration yield Sr/Ca-derived SSTs that are in good agreement with those derived from Mg/Ca ratios of calcitic foraminifera which indicate a continuous postglacial warming of the western tropical Pacific, in phase with the warming of the tropical Atlantic.
    Description: Funds for this study were provided by NSF MG&G award number OCE-0241075.
    Keywords: Tropical Pacific ; Sea surface temperature ; Bølling-Allerod ; Coral Sr/Ca ; Ion microprobe ; Diagenesis
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  • 8
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2008. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 9 (2008): Q04003, doi:10.1029/2007GC001651.
    Description: We report 238U-230Th-226Ra-210Pb-210Po, 232Th-228Ra and 235U-231Pa measurements for a suite of 14 geologically and geochemically well-characterized basaltic samples from the Samoan volcanoes Vailulu'u, Malumalu, and Savai'i. Maximum eruption ages based on the presence of parent-daughter disequilibria indicate that Vailulu'u is magmatically productive with young lavas (〈8 Ka) resurfacing both its summit crater and lower flanks. 210Pb and 210Po measurements indicate that several flows have erupted within its summit crater in the past 100 years, with the newest observed flow being erupted in November of 2004. For lavas which have eruption ages that are demonstrably young, relative to the half-lives of 230Th, 231Pa, and 226Ra, we interpret their 238U -230Th, 235U-231Pa and 230Th - 226Ra disequilibria in terms of the magmatic processes occurring beneath the Samoan Islands. (230Th/238U) 〉 1 indicates that garnet is required as a residual phase in the magma sources for all these lavas. The large range of (238U/232Th) and (230Th/232Th) is attributed to long-term source variation. The Samoan basalts are all alkaline basalts and show significant 230Th and 231Pa excesses but limited variability, indicating that they have been derived by small but similar extents of melting. Their (230Th/238U), (231Pa/235U) and Sm/Nd fractionation are consistent with correlations among other ocean island basalt suites (particularly Hawaii) which show that (230Th/238U) and (231Pa/235U) of many OIBS can be explained by simple time-independent models. Interpretation of the 226Ra data requires time-dependent melting models. Both chromatographic porous flow and dynamic melting of a garnet peridotite source can adequately explain the combined U-Th-Ra and U-Pa data for these Samoan basalts. Several young samples from the Vailulu'u summit crater also exhibit significant 210Pb deficits that reflect either shallow magmatic processes or continuous magma degassing. In both cases, decadal residence times are inferred from these 210Pb deficits. The young coeval volcanism on Malumalu and Vailulu'u suggests the Samoa hot spot is currently migrating to the northeast due to dynamic interaction with the Tonga slab.
    Description: Support for this research was provided by NSF grants EAR-9909473 (KWWS), EAR-0509891 (SRH), EAR- 0609670 (MKR) and EAR-0504362 (MKR).
    Keywords: U-series disequilibria ; Samoa ; Eruption ages
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  • 9
    Publication Date: 2022-05-26
    Description: Author Posting. © American Geophysical Union, 2008. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geochemistry Geophysics Geosystems 9 (2008): Q04027, doi:10.1029/2007GC001876.
    Description: We report evidence for a global Ti, Ta, and Nb (TITAN) enriched reservoir sampled by ocean island basalts (OIBs) with high 3He/4He ratios, an isotopic signature associated with the deep mantle. Excesses of Ti (and to a lesser degree Nb and Ta) correlate remarkably well with 3He/4He in a data set of global OIBs, demonstrating that a major element signature is associated with the high 3He/4He mantle. Additionally, we find that OIBs with high 3He/4He ratios have moderately radiogenic 187Os/188Os (〉0.135). The TITAN enrichment and radiogenic 187Os/188Os in high 3He/4He OIBs indicate that they are melts of a mantle domain that hosts a nonprimitive (nonchondritic) component. The observation of TITAN enrichment in the high 3He/4He mantle may be important in balancing the Earth's budget for the TITAN elements. Understanding the origin of the TITAN enrichment is important for constraining the evolution of the enigmatic high 3He/4He mantle domain.
    Description: Funds for helium measurements were provided by NSF-OCE to M.D.K. Funds for major and trace element analyses were provided by NSF-EAR 0509891 to S.R.H.
    Keywords: He-3/He-4 ; FOZO ; PHEM ; C ; OIB ; Eclogite
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  • 10
    Publication Date: 2022-05-26
    Description: Author Posting. © American Geophysical Union, 2010. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 24 (2010): GB4001, doi:10.1029/2009GB003651.
    Description: Net community production (NCP) and gross primary production (GPP) are two key metrics for quantifying the biological carbon cycle. In this study, we present a detailed characterization of NCP and GPP in the western equatorial Pacific during August and September 2006. We use continuous measurements of dissolved gases (O2 and Ar) in the surface water in order to quantify NCP at subkilometer scale resolution. We constrain GPP in discrete samples using the triple isotopic composition of O2. We find the average NCP in the western equatorial Pacific is 5.9 ± 0.9 mmol O2 m−2 d−1 (equivalent to 1.5 ± 0.2 mol C m−2 yr−1 with error estimates reflecting 1σ confidence levels) and the average GPP is 121 ± 34 mmol O2 m−2 d−1 (equivalent to 32 ± 9 mol C m−2 yr−1). The measurements reveal significant spatial variability on length scales as small as 50 km. The NCP/GPP ratio is 5.7% ± 1.8%. We also present results for NCP and GPP in the coastal area off Papua New Guinea and for GPP in the central Pacific along the equator.
    Description: This work was supported by the NSF Chemical Oceanography and the Office of Polar Programs, by the NOAA climate and global change program (fellowship to RHRS), and by Princeton University (Hess fellowship to RHRS).
    Keywords: Production ; Triple oxygen isotopes ; Equatorial pacific
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