http://lod.bco-dmo.org/id/dataset/820063
eng; USA
utf8
dataset
Highest level of data collection, from a common set of sensors or instrumentation, usually within the same research project
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
2020-08-04
ISO 19115-2 Geographic Information - Metadata - Part 2: Extensions for Imagery and Gridded Data
ISO 19115-2:2009(E)
Vanadium isotope data from globally representative sediments that have a range of bottom water oxygen conditions
2020-08-04
publication
2020-08-04
revision
Marine Biological Laboratory/Woods Hole Oceanographic Institution Library (MBLWHOI DLA)
2020-08-13
publication
https://doi.org/10.26008/1912/bco-dmo.820063.1
Jeremy D. Owens
Florida State University
principalInvestigator
Sune G. Nielsen
Woods Hole Oceanographic Institution
principalInvestigator
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
publisher
Cite this dataset as: Owens, J., Nielsen, S. (2020) Vanadium isotope data from globally representative sediments that have a range of bottom water oxygen conditions. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2020-08-04 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.820063.1 [access date]
Dataset Description: <p>This dataset includes the first vanadium isotope data from globally representative sediments that have a range of bottom water oxygen conditions.</p>
<p><strong>Note:&nbsp;</strong>Data other than V isotopes were obtained in previous studies and references for this work can be found in the published work of Wu et al., 2020. Cells with "nd" indicate that data was not available or obtained.</p> Methods and Sampling: <p><strong>Methodology:</strong><br />
This work analyzed V isotope composition of previously collected sediments from a global network that have a range of bottom water oxygen conditions. Below is a description of the methods used for the samples collected by various cruises.</p>
<p>Twenty-two pelagic sediment samples from various localities around the globe were investigated in this study. A total of thirteen samples were analyzed from the Pacific Ocean at water depths of 3500–5800 m, four samples were analyzed from the Indian Ocean at water depths of 4400–5200 m, four samples were analyzed from the Atlantic Ocean at water depths of 3300–6000 m, and one sample was analyzed from the Arctic Ocean at water depths of 4041 m. All the samples are distal from any known marine hydrothermal vent field and thus should not include a hydrothermal signature. Sediment lithologies consist predominantly of oxidized fine-grained pelagic clay ranging from light to dark brown or greenish-gray in color, with various carbonate and calcareous ooze contents. Dried sediments were collected from cores housed in the sediment repository of Woods Hole Oceanographic Institution (WHOI) and from the U.S. GEOTRACES East Pacific Zonal Transect (EPZT GP16). These samples are bulk powders from the top portions (0–10 cm) of cores.</p>
<p>Sediment samples from the continental margin off Namibia in the eastern South Atlantic were collected as part of the RV Meteor expeditions M57/2. The core samples were collected on a continental slope transect with water depths between 605 and 2470 m. The bottom water oxygen contents of the sample locations are from 150 to 220 µM. The sediments in the Eastern Cape Basin are characterized by low input of terrigenous matter and high biogenic contents. The high amounts of organic matter (up to 9% for the analyzed V isotope sites) in the sediments are due to high water column primary production on the shelf and lateral transport of organic carbon from the shelf to the slope. The sediments off Namibia analyzed here are all core top sediments from 0 to 5 cm.</p>
<p>Sediment samples from the Argentine Basin in the western South Atlantic were collected during R/V Meteor expedition M78/3. The predominantly terrigenous material in this region is delivered from the numerous fluvial tributaries along the coast of Argentina and Uruguay and transported further downslope via gravity-controlled mass flows. The core samples were collected east of the Rio de la Plata mouth from water depths between 58 m and 4273 m, forming a transect from shelf to deep basin. The sediments from the Argentine Basin analysis here are from core depths between 5 to 45 cm.</p>
<p>Samples from the Peruvian Margin in this study were mostly from a transect along 11°S during the RV Meteor cruise M77-1 in November 2008. In addition, some Peruvian Margin sediment samples were collected during the U.S. GEOTRACES East Pacific Zonal Transect (EPZT GP16) and R/V Moana Wave cruise 87 leg 08. High oxygen demand within the water column leads to a perennial oxygen minimum zone (OMZ) that impinges on the continental shelf/ slope between 50 and 500 m water depth. Thirteen sediment cores were analyzed from the continental shelf to deep slope at water depths between 85 and 2025 m, which transects from the reducing OMZ to the deeper oxic seafloor with bottom water oxygen contents from 1.5 mM to 93.4 µM. The Peruvian Margin samples analyzed were from core depths between 0 to 35 cm.</p>
<p>Sediment samples from the deepest portion (594 m water depth) of the Santa Barbara Basin were collected in 2001 as part of the CALMEX cruise (R/V New Horizon in November 2001). The Santa Barbara Basin is a shallow, near-shore basin off southern California with a sill depth of approximately 475 m. Below the basin sill depth of 475 m, the water column is characterized by limited exchange with waters outside of the basin, thus the circulation within the basin is restricted resulting in low bottom water oxygen concentrations, typically &lt; 5 µM, though the concentration can vary on seasonal timescales The core samples were collected at the center of the basin with bottom water oxygen contents near-zero (1 µM). The Santa Barbara Basin samples analyzed here include the core top sediment (0–3 cm) to shallow depths (10–11 cm).</p>
<p>Sediment samples from the Cariaco Basin were collected in 1990 as part of the PLUME Leg 7 Cruise (R/V Thomas Washington). The Cariaco Basin is the second-largest euxinic (anoxic and sulfidic water column) marine basin in the modern ocean. Below 300 m water depth, the basin is euxinic due to a combination of limited deepwater renewal and high surface productivity supplying organic matter that promotes microbial respiration, oxygen depletion, and the accumulation of hydrogen sulfide. Seven separate box core top samples (0–1 cm) from around the Cariaco basin including both sub-basins were collected. All of the Cariaco sediment samples measured in this study were collected below the permanent chemocline (sulfidic portion) at water depths between 400 and 1350 m.</p>
<p><strong>Sampling and analytical procedures:</strong><br />
Sample dissolution:<br />
Samples were dissolved using bulk digestion and leaching methods. Both methods were carried out to ensure that the V isotope analyses captured the authigenic values, especially given the limited enrichment for some of the samples (e.g. differences between the bulk and leach methods). For the bulk digestion, sediment samples for V isotope analysis were ashed overnight at 600°C to remove organic phases. Ashed sediment powders were then completely digested with a multi-acid HF–HNO₃–HCl procedure using trace metal clean acids. All materials were completely dissolved in 0.8 N HNO₃ prior to purification using ion exchange column chemistry.</p>
<p>The leach technique was applied to extract authigenic V. For the organic carbon-rich sediments, splits of sediment were leached in a Teflon Savillex vial with 3 mL of 3 N HNO₃ for 12–16 hours at room temperature with constant agitation using a shaking table. These samples were then centrifuged, and the supernatant was collected and placed in a new clean Savillex vial and dried. During the collection of the supernatant, care was taken to avoid the solid phase siliciclastic materials; additionally, HF was avoided to ensure the limited dissolution of siliciclastic minerals. Several high-purity acid treatments (aqua regia, conc. HNO₃) were added to each vial to completely oxidize any organic matter that might have been present. Samples were then dissolved with 0.8 N HNO₃ prior to ion exchange column chemistry. To validate this leaching method, the leaching method was performed on United States Geological Survey (USGS) shale standards SCo-1 and SDO-1 with 1 N HNO₃ concentrations. Splits of the leach solution were also taken for elemental analysis.</p>
<p>For the oxic pelagic sediments, we applied the well-established extraction technique for oxide dissolution to obtain the isotopic analysis of the authigenic V. One aliquot of the pelagic sediments was reacted in 10 mL 25% acetic acid + 1 N hydroxylamine hydrochloride solution at 90°C for three hours, and each sample was agitated every 30 minutes. The supernatant was removed from the detrital particles, treated with 8 N HNO₃ and then dissolved with 0.8 N HNO₃ prior to ion exchange column chemistry.</p>
<p>Vanadium Purification:<br />
The purification of V was conducted with a four-step ion exchange procedure by coupling cation-and anion-exchange columns. Briefly, samples were first loaded on a cation resin AG50W-X12 (200–400 mesh) and major cations Al, Ti, and Na were eluted with 0.8 N HNO₃ + 0.1 N HF and 0.8 N HNO₃. V was then eluted and collected with 1.2 N HNO₃. The major cations Fe, Mg and Ca do not leave the resin by the time all of the V is eluted, thus the procedure separates all major cations except for K. The anion exchange resin AG1-X8 (200–400 mesh) was subsequently applied to remove all the residual matrix elements from V as described in Nielsen et al. (2011). The anion column was performed twice in order to quantitatively remove any residual Ti and Cr. In-between each column, samples were evaporated and refluxed in aqua regia overnight at 135°C to remove potential organic material leached from the resin, evaporated again, and redissolved in the next solution. The yield of the entire V column chemistry procedure is within error of 100%. Samples were re-dissolved in 1 mL 2% HNO₃ prior to elemental and isotopic analysis. Total procedural blanks (from sample dissolution/leach to instrumental analysis) were &lt; 2 ng, which is negligible compared with the amount of V extracted from each sample (2-6 mg).</p>
<p>Instrumental Configuration:<br />
Instrument measurements were performed at the National High Magnetic Field Laboratory at Florida State University (FSU) using a Thermo Scientific Neptune Multicollector-Inductively Coupled Plasma-Mass Spectrometer (MC-ICP-MS). Measurements were performed on the flat-topped shoulder on the lower mass side of the overlapping V and molecular interference peaks in medium-resolution mode (resolution &gt; 4000) to resolve all interfering molecular species representing combinations of C, N, O, S, Ar and Cl (such as ³⁶Ar¹⁴N+, ³⁶Ar¹⁶O+, and ³⁸Ar¹⁴N+). To obtain the highest possible V transmission efficiency, solutions were introduced with a desolvating nebulizer system (Aridus II) and Jet sample and Ni X-skimmer cones were also applied. The typical sensitivity of ⁵¹V under such configuration was 1.5–2.5 nA/ppm.</p>
Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1434785 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1434785
Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1624895 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1624895
completed
Jeremy D. Owens
Florida State University
850-644-5018
1800 E. Paul Dirac Drive
Tallahassee
FL
32310
USA
jdowens@fsu.edu
pointOfContact
Sune G. Nielsen
Woods Hole Oceanographic Institution
CRPG, CNRS, Université de Lorraine 15 rue Notre Dame des Pauvres
54501 Vandoeuvre lès Nancy
France
sune.nielsen@univ-lorraine.fr
pointOfContact
asNeeded
Dataset Version: 1
Unknown
Site
Location_Name
Latitude
Longitude
Water_Depth
Bottom_Water_O2
Sediment_Depth
d51VBulk
two_sd_d51VBulk
n_d51VBulk
TOC_pcnt
Bulk_Al_pcnt
Bulk_Fe_pcnt
Bulk_Mn_pcnt
Bulk_Ti_ppm
Bulk_V_ppm
d51VLeach
two_sd_d51VLeach
n_d51VLeach
Leach_Al_pcnt
Leach_Ti_ppm
Leach_V_ppm
Thermo Neptune multi-collector ICP-MS
theme
None, User defined
site
latitude
longitude
depth
dissolved Oxygen
depth below seafloor
Vanadium
numb_obs
total organic Carbon
Aluminum
Iron
Manganese
Titanium
featureType
BCO-DMO Standard Parameters
Inductively Coupled Plasma Mass Spectrometer
instrument
BCO-DMO Standard Instruments
otherRestrictions
otherRestrictions
Access Constraints: none. Use Constraints: Please follow guidelines at: http://www.bco-dmo.org/terms-use Distribution liability: Under no circumstances shall BCO-DMO be liable for any direct, incidental, special, consequential, indirect, or punitive damages that result from the use of, or the inability to use, the materials in this data submission. If you are dissatisfied with any materials in this data submission your sole and exclusive remedy is to discontinue use.
Fingerprinting and Calibrating Low Oxygen Conditions Using Vanadium Isotopes
https://osprey.bco-dmo.org/project/775701
Fingerprinting and Calibrating Low Oxygen Conditions Using Vanadium Isotopes
<p><em>NSF Award Abstract:</em><br />
Discovering, testing, and developing chemical proxies (relic materials) in marine sediments that reveal how strongly or weakly oxidizing near-surface environmental conditions were in the Earth's geological past are immensely important for understanding interactions between ocean chemistry, biological evolution and extinctions, and climate. To date scientists do not have a proxy for low but non-zero oxygen conditions -- the sort of conditions that are likely to have dominated in biologically important periods of Earth history. In this project, researchers will study the relationship between bottom water oxygen concentration and the isotopes of the trace metal vanadium (V) in a range of oxygen conditions in the modern ocean. Based on pilot data, theoretical calculations and dissolved seawater V concentrations they believe that stable V isotope ratios of core top sediments will correlate systematically over a range of bottom water oxygen conditions. By analyzing these materials, the research team expects to establish the relationship between V isotopes and bottom water oxygen concentrations. Given the importance of chemical proxies to quantify past climate change, the results of this study will be of great importance to the modern and paleoceanographic community, as well as for modelers to better understand a broad range of oxygen variability in Earth history.</p>
<p>Although recent investigations have provided a wealth of information about the redox conditions of the ancient oceans, there is a significant gap in understanding low oxygen conditions throughout Earth history. Therefore, it is important to develop new paleoredox proxies that can provide additional and complementary knowledge about ocean redox conditions during these important periods of Earth history. In this study, scientists will analyze bulk sediments and their organic and ferromanganese mineral fractions to investigate the V isotopic variability within the various sedimentary components. (These samples comprise organic rich to ferromanganese rich sediments due to a range in bottom water oxygen concentrations.) Reconstructing marine low oxygen conditions using vanadium isotopes would fill a void in the paleoredox proxy toolbox. Developing, calibrating, and fingerprinting the V isotopic variability in modern sediments is required to be able to apply vanadium isotopes as an accurate paleoredox proxy.</p>
Vanadium Isotopes
largerWorkCitation
project
eng; USA
oceans
-120.03
170.387
-39.491
53.525
2020-08-04
0
BCO-DMO catalogue of parameters from Vanadium isotope data from globally representative sediments that have a range of bottom water oxygen conditions
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
http://lod.bco-dmo.org/id/dataset-parameter/820071.rdf
Name: Site
Units: unitless
Description: <p>Site name</p>
http://lod.bco-dmo.org/id/dataset-parameter/820072.rdf
Name: Location_Name
Units: unitless
Description: <p>Location name</p>
http://lod.bco-dmo.org/id/dataset-parameter/820073.rdf
Name: Latitude
Units: decimal degrees North
Description: <p>Latitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/820074.rdf
Name: Longitude
Units: decimal degrees East
Description: <p>Longitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/820075.rdf
Name: Water_Depth
Units: meters (m)
Description: <p>Water depth to the sediment where the sample was collected</p>
http://lod.bco-dmo.org/id/dataset-parameter/820076.rdf
Name: Bottom_Water_O2
Units: micromolar (uM)
Description: <p>Measured and published bottom water oxygen in micromoles</p>
http://lod.bco-dmo.org/id/dataset-parameter/820077.rdf
Name: Sediment_Depth
Units: centimeters
Description: <p>Sediment sample depth below the seafloor (BSF)</p>
http://lod.bco-dmo.org/id/dataset-parameter/820078.rdf
Name: d51VBulk
Units: per mil (‰)
Description: <p>Measured bulk V isotope value</p>
http://lod.bco-dmo.org/id/dataset-parameter/820079.rdf
Name: two_sd_d51VBulk
Units: per mil (‰)
Description: <p>2 standard deviation error from all analyses of d51VBulk</p>
http://lod.bco-dmo.org/id/dataset-parameter/820080.rdf
Name: n_d51VBulk
Units: unitless
Description: <p>Number of isotope analyses for d51VBulk</p>
http://lod.bco-dmo.org/id/dataset-parameter/820081.rdf
Name: TOC_pcnt
Units: weight percent
Description: <p>Quantified bulk total organic carbon in weight percent</p>
http://lod.bco-dmo.org/id/dataset-parameter/820082.rdf
Name: Bulk_Al_pcnt
Units: weight percent
Description: <p>Quantified bulk aluminum concentration in weight percent</p>
http://lod.bco-dmo.org/id/dataset-parameter/820083.rdf
Name: Bulk_Fe_pcnt
Units: weight percent
Description: <p>Quantified bulk iron concentration in weight percent</p>
http://lod.bco-dmo.org/id/dataset-parameter/820084.rdf
Name: Bulk_Mn_pcnt
Units: weight percent
Description: <p>Quantified bulk manganese concentration in weight percent</p>
http://lod.bco-dmo.org/id/dataset-parameter/820085.rdf
Name: Bulk_Ti_ppm
Units: parts per million (ppm)
Description: <p>Quantified bulk titanium concentration in parts per million</p>
http://lod.bco-dmo.org/id/dataset-parameter/820086.rdf
Name: Bulk_V_ppm
Units: parts per million (ppm)
Description: <p>Quantified bulk vanadium concentration in parts per million</p>
http://lod.bco-dmo.org/id/dataset-parameter/820087.rdf
Name: d51VLeach
Units: per mil (‰)
Description: <p>Measured leach V isotope value</p>
http://lod.bco-dmo.org/id/dataset-parameter/820088.rdf
Name: two_sd_d51VLeach
Units: per mil (‰)
Description: <p>2 standard deviation error from all analysis of d51VLeach</p>
http://lod.bco-dmo.org/id/dataset-parameter/820089.rdf
Name: n_d51VLeach
Units: unitless
Description: <p>Number of isotope analysis for d51VLeach</p>
http://lod.bco-dmo.org/id/dataset-parameter/820090.rdf
Name: Leach_Al_pcnt
Units: weight percent
Description: <p>Quantified leached aluminum concentration in weight percent</p>
http://lod.bco-dmo.org/id/dataset-parameter/820091.rdf
Name: Leach_Ti_ppm
Units: parts per million (ppm)
Description: <p>Quantified leached titanium concentration in parts per million</p>
http://lod.bco-dmo.org/id/dataset-parameter/820092.rdf
Name: Leach_V_ppm
Units: parts per million (ppm)
Description: <p>Quantified leached vanadium concentration in parts per million</p>
GB/NERC/BODC > British Oceanographic Data Centre, Natural Environment Research Council, United Kingdom
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
9861
https://darchive.mblwhoilibrary.org/bitstream/1912/26065/1/dataset-820063_sedimentary-v-isotope-signatures__v1.tsv
download
https://doi.org/10.26008/1912/bco-dmo.820063.1
download
onLine
dataset
<p><strong>Methodology:</strong><br />
This work analyzed V isotope composition of previously collected sediments from a global network that have a range of bottom water oxygen conditions. Below is a description of the methods used for the samples collected by various cruises.</p>
<p>Twenty-two pelagic sediment samples from various localities around the globe were investigated in this study. A total of thirteen samples were analyzed from the Pacific Ocean at water depths of 3500–5800 m, four samples were analyzed from the Indian Ocean at water depths of 4400–5200 m, four samples were analyzed from the Atlantic Ocean at water depths of 3300–6000 m, and one sample was analyzed from the Arctic Ocean at water depths of 4041 m. All the samples are distal from any known marine hydrothermal vent field and thus should not include a hydrothermal signature. Sediment lithologies consist predominantly of oxidized fine-grained pelagic clay ranging from light to dark brown or greenish-gray in color, with various carbonate and calcareous ooze contents. Dried sediments were collected from cores housed in the sediment repository of Woods Hole Oceanographic Institution (WHOI) and from the U.S. GEOTRACES East Pacific Zonal Transect (EPZT GP16). These samples are bulk powders from the top portions (0–10 cm) of cores.</p>
<p>Sediment samples from the continental margin off Namibia in the eastern South Atlantic were collected as part of the RV Meteor expeditions M57/2. The core samples were collected on a continental slope transect with water depths between 605 and 2470 m. The bottom water oxygen contents of the sample locations are from 150 to 220 µM. The sediments in the Eastern Cape Basin are characterized by low input of terrigenous matter and high biogenic contents. The high amounts of organic matter (up to 9% for the analyzed V isotope sites) in the sediments are due to high water column primary production on the shelf and lateral transport of organic carbon from the shelf to the slope. The sediments off Namibia analyzed here are all core top sediments from 0 to 5 cm.</p>
<p>Sediment samples from the Argentine Basin in the western South Atlantic were collected during R/V Meteor expedition M78/3. The predominantly terrigenous material in this region is delivered from the numerous fluvial tributaries along the coast of Argentina and Uruguay and transported further downslope via gravity-controlled mass flows. The core samples were collected east of the Rio de la Plata mouth from water depths between 58 m and 4273 m, forming a transect from shelf to deep basin. The sediments from the Argentine Basin analysis here are from core depths between 5 to 45 cm.</p>
<p>Samples from the Peruvian Margin in this study were mostly from a transect along 11°S during the RV Meteor cruise M77-1 in November 2008. In addition, some Peruvian Margin sediment samples were collected during the U.S. GEOTRACES East Pacific Zonal Transect (EPZT GP16) and R/V Moana Wave cruise 87 leg 08. High oxygen demand within the water column leads to a perennial oxygen minimum zone (OMZ) that impinges on the continental shelf/ slope between 50 and 500 m water depth. Thirteen sediment cores were analyzed from the continental shelf to deep slope at water depths between 85 and 2025 m, which transects from the reducing OMZ to the deeper oxic seafloor with bottom water oxygen contents from 1.5 mM to 93.4 µM. The Peruvian Margin samples analyzed were from core depths between 0 to 35 cm.</p>
<p>Sediment samples from the deepest portion (594 m water depth) of the Santa Barbara Basin were collected in 2001 as part of the CALMEX cruise (R/V New Horizon in November 2001). The Santa Barbara Basin is a shallow, near-shore basin off southern California with a sill depth of approximately 475 m. Below the basin sill depth of 475 m, the water column is characterized by limited exchange with waters outside of the basin, thus the circulation within the basin is restricted resulting in low bottom water oxygen concentrations, typically &lt; 5 µM, though the concentration can vary on seasonal timescales The core samples were collected at the center of the basin with bottom water oxygen contents near-zero (1 µM). The Santa Barbara Basin samples analyzed here include the core top sediment (0–3 cm) to shallow depths (10–11 cm).</p>
<p>Sediment samples from the Cariaco Basin were collected in 1990 as part of the PLUME Leg 7 Cruise (R/V Thomas Washington). The Cariaco Basin is the second-largest euxinic (anoxic and sulfidic water column) marine basin in the modern ocean. Below 300 m water depth, the basin is euxinic due to a combination of limited deepwater renewal and high surface productivity supplying organic matter that promotes microbial respiration, oxygen depletion, and the accumulation of hydrogen sulfide. Seven separate box core top samples (0–1 cm) from around the Cariaco basin including both sub-basins were collected. All of the Cariaco sediment samples measured in this study were collected below the permanent chemocline (sulfidic portion) at water depths between 400 and 1350 m.</p>
<p><strong>Sampling and analytical procedures:</strong><br />
Sample dissolution:<br />
Samples were dissolved using bulk digestion and leaching methods. Both methods were carried out to ensure that the V isotope analyses captured the authigenic values, especially given the limited enrichment for some of the samples (e.g. differences between the bulk and leach methods). For the bulk digestion, sediment samples for V isotope analysis were ashed overnight at 600°C to remove organic phases. Ashed sediment powders were then completely digested with a multi-acid HF–HNO₃–HCl procedure using trace metal clean acids. All materials were completely dissolved in 0.8 N HNO₃ prior to purification using ion exchange column chemistry.</p>
<p>The leach technique was applied to extract authigenic V. For the organic carbon-rich sediments, splits of sediment were leached in a Teflon Savillex vial with 3 mL of 3 N HNO₃ for 12–16 hours at room temperature with constant agitation using a shaking table. These samples were then centrifuged, and the supernatant was collected and placed in a new clean Savillex vial and dried. During the collection of the supernatant, care was taken to avoid the solid phase siliciclastic materials; additionally, HF was avoided to ensure the limited dissolution of siliciclastic minerals. Several high-purity acid treatments (aqua regia, conc. HNO₃) were added to each vial to completely oxidize any organic matter that might have been present. Samples were then dissolved with 0.8 N HNO₃ prior to ion exchange column chemistry. To validate this leaching method, the leaching method was performed on United States Geological Survey (USGS) shale standards SCo-1 and SDO-1 with 1 N HNO₃ concentrations. Splits of the leach solution were also taken for elemental analysis.</p>
<p>For the oxic pelagic sediments, we applied the well-established extraction technique for oxide dissolution to obtain the isotopic analysis of the authigenic V. One aliquot of the pelagic sediments was reacted in 10 mL 25% acetic acid + 1 N hydroxylamine hydrochloride solution at 90°C for three hours, and each sample was agitated every 30 minutes. The supernatant was removed from the detrital particles, treated with 8 N HNO₃ and then dissolved with 0.8 N HNO₃ prior to ion exchange column chemistry.</p>
<p>Vanadium Purification:<br />
The purification of V was conducted with a four-step ion exchange procedure by coupling cation-and anion-exchange columns. Briefly, samples were first loaded on a cation resin AG50W-X12 (200–400 mesh) and major cations Al, Ti, and Na were eluted with 0.8 N HNO₃ + 0.1 N HF and 0.8 N HNO₃. V was then eluted and collected with 1.2 N HNO₃. The major cations Fe, Mg and Ca do not leave the resin by the time all of the V is eluted, thus the procedure separates all major cations except for K. The anion exchange resin AG1-X8 (200–400 mesh) was subsequently applied to remove all the residual matrix elements from V as described in Nielsen et al. (2011). The anion column was performed twice in order to quantitatively remove any residual Ti and Cr. In-between each column, samples were evaporated and refluxed in aqua regia overnight at 135°C to remove potential organic material leached from the resin, evaporated again, and redissolved in the next solution. The yield of the entire V column chemistry procedure is within error of 100%. Samples were re-dissolved in 1 mL 2% HNO₃ prior to elemental and isotopic analysis. Total procedural blanks (from sample dissolution/leach to instrumental analysis) were &lt; 2 ng, which is negligible compared with the amount of V extracted from each sample (2-6 mg).</p>
<p>Instrumental Configuration:<br />
Instrument measurements were performed at the National High Magnetic Field Laboratory at Florida State University (FSU) using a Thermo Scientific Neptune Multicollector-Inductively Coupled Plasma-Mass Spectrometer (MC-ICP-MS). Measurements were performed on the flat-topped shoulder on the lower mass side of the overlapping V and molecular interference peaks in medium-resolution mode (resolution &gt; 4000) to resolve all interfering molecular species representing combinations of C, N, O, S, Ar and Cl (such as ³⁶Ar¹⁴N+, ³⁶Ar¹⁶O+, and ³⁸Ar¹⁴N+). To obtain the highest possible V transmission efficiency, solutions were introduced with a desolvating nebulizer system (Aridus II) and Jet sample and Ni X-skimmer cones were also applied. The typical sensitivity of ⁵¹V under such configuration was 1.5–2.5 nA/ppm.</p>
Specified by the Principal Investigator(s)
<p><strong>Data processing:</strong><br />
Sample analysis protocols follow standard-sample bracketing procedures. The 10¹⁰Ω resistor is applied to monitor ⁵¹V, while other concerned isotopes (⁴⁹Ti, ⁵⁰V, ⁵²Cr, ⁵³Cr) are monitored with conventional 10¹¹Ω resistors to accommodate the large natural isotope abundance differences of V (⁵¹V/⁵⁰V = 400). While the chemical purification nearly quantitatively separates Ti and Cr from V, minor amounts of ⁵⁰Ti and ⁵⁰Cr remain in solution which can dramatically affect the analysis on ⁵¹V/⁵⁰V ratio, especially for low V concentration measurements. Therefore, analysis of the ⁴⁹Ti/⁵¹V and ⁵³Cr/⁵¹V ratios are needed and should be less than 0.00005 to properly correct for interferences of ⁵⁰Cr and ⁵⁰Ti. Here we use the procedure described by Nielsen et al. (2011) and Wu et al. (2016) to correct the raw data for any potential interferences. Briefly, 50 ng/g Cr and 50 ng/g Ti standard solutions were analyzed every time the mass spectrometer was tuned to calculate the mass bias coefficients. The obtained mass bias coefficients were then used to calculate the true ⁵⁰Ti and ⁵⁰Cr ion beam that was subtracted from the total signal on mass 50.</p>
<p>Vanadium isotopic data are reported in conventional δ notation in permil relative to AA (δ⁵¹V = ((⁵¹V/⁵⁰V)<sub>sample</sub> /⁵¹V/⁵⁰V)<sub>AA</sub> – 1) × 1,000). Each data analysis was run with 40 cycles of 4.194 s integrations for each cycle and baseline calibration was run before each analysis. Each sample was bracketed by measurements of the AA solution to obtain an average value and stability of the instrument for the highest quality control. After the evaluation of two samples, a solution standard, BDH, was measured to ensure the performance and stability of the analysis on the MC-ICP-MS. The in-house isotope BDH standard was a 1000 µg/g V standard solution, which has an isotope composition of δ⁵¹V= -1.2‰ based on analyses in several different labs worldwide. The errors for V isotope results of each sample are reported in two standard deviations relative to the average value (2SD). Measurements of BDH in this study gave an average δ⁵¹V = -1.19 ± 0.10‰ (2sd, n = 121). The USGS igneous rocks reference materials BCR-2, BIR-1, and AGV-2 were processed through the same ion-exchange procedures and δ⁵¹V values are in agreement with literature values. The uncertainties of δ⁵¹V for reference materials are better than ± 0.12‰ (2SD), representing the long-term external reproducibility of the data in this study.</p>
<p><strong>BCO-DMO Processing:</strong><br />
- moved site names into a column;<br />
- modified parameter names;<br />
- replaced 'NA'&nbsp;with 'nd' (no data);<br />
- converted latitude and longitude to decimal degrees.</p>
Specified by the Principal Investigator(s)
asNeeded
7.x-1.1
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
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Thermo Neptune multi-collector ICP-MS
Thermo Neptune multi-collector ICP-MS
PI Supplied Instrument Name: Thermo Neptune multi-collector ICP-MS Instrument Name: Inductively Coupled Plasma Mass Spectrometer Instrument Short Name:ICP Mass Spec Instrument Description: An ICP Mass Spec is an instrument that passes nebulized samples into an inductively-coupled gas plasma (8-10000 K) where they are atomized and ionized. Ions of specific mass-to-charge ratios are quantified in a quadrupole mass spectrometer. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB15/