Effects of different water storage procedures on the dissolved Fe concentration and isotopic composition of chemically contrasted waters from the Amazon River Basin†. (1st October 2015)
- Record Type:
- Journal Article
- Title:
- Effects of different water storage procedures on the dissolved Fe concentration and isotopic composition of chemically contrasted waters from the Amazon River Basin†. (1st October 2015)
- Main Title:
- Effects of different water storage procedures on the dissolved Fe concentration and isotopic composition of chemically contrasted waters from the Amazon River Basin†
- Authors:
- Mulholland, Daniel S.
Poitrasson, Franck
Boaventura, Geraldo R. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm7368-sec-0001" sec-type="section"> <title>Rationale</title> <p>Although recent studies have investigated the Fe isotopic composition of dissolved, colloidal and particulate phases from continental and oceanic natural waters, few efforts have been made to evaluate whether water sample storage and the separation of different pore‐size fractions through filtration can cause any change to the Fe isotopic compositions. The present study investigates the possible biases introduced by different water storage conditions on the dissolved Fe concentration and isotopic composition of chemically different waters.</p> </sec> <sec id="rcm7368-sec-0002" sec-type="section"> <title>Methods</title> <p>Water samples were collected from an organic‐rich river and from mineral particulate‐rich rivers. Filtered and unfiltered water samples were stored either at room temperature or frozen at –18°C in order to assess possible biases due to (i) different water storage temperature, and (ii) storage of bulk (unfiltered) vs filtered water. Iron isotope measurements were performed by Multicollector Inductively Coupled Plasma Mass Spectrometry with a Thermo Electron Neptune instrument, after Fe purification using anion‐exchange resins.</p> </sec> <sec id="rcm7368-sec-0003" sec-type="section"> <title>Results</title> <p>Our data reveal that bulk water storage at room temperature without filtration produces<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm7368-sec-0001" sec-type="section"> <title>Rationale</title> <p>Although recent studies have investigated the Fe isotopic composition of dissolved, colloidal and particulate phases from continental and oceanic natural waters, few efforts have been made to evaluate whether water sample storage and the separation of different pore‐size fractions through filtration can cause any change to the Fe isotopic compositions. The present study investigates the possible biases introduced by different water storage conditions on the dissolved Fe concentration and isotopic composition of chemically different waters.</p> </sec> <sec id="rcm7368-sec-0002" sec-type="section"> <title>Methods</title> <p>Water samples were collected from an organic‐rich river and from mineral particulate‐rich rivers. Filtered and unfiltered water samples were stored either at room temperature or frozen at –18°C in order to assess possible biases due to (i) different water storage temperature, and (ii) storage of bulk (unfiltered) vs filtered water. Iron isotope measurements were performed by Multicollector Inductively Coupled Plasma Mass Spectrometry with a Thermo Electron Neptune instrument, after Fe purification using anion‐exchange resins.</p> </sec> <sec id="rcm7368-sec-0003" sec-type="section"> <title>Results</title> <p>Our data reveal that bulk water storage at room temperature without filtration produces minor changes in the dissolved Fe isotopic composition of mineral particulate‐rich waters, but significant isotopic composition changes in organic‐rich waters. In both cases, however, the impact of the different procedures on the Fe concentrations was strong. On the other hand, the bulk water stored frozen without filtration produced more limited changes in the dissolved Fe concentrations, and also on isotopic compositions, relative to the samples filtered in the field. The largest effect was again observed for the organic‐rich waters.</p> </sec> <sec id="rcm7368-sec-0004" sec-type="section"> <title>Conclusions</title> <p>These findings suggest that a time lag between water collection and filtration may cause isotopic exchanges between the dissolved and particulate Fe fractions. When it is not possible to filter the samples in the field immediately after collection, the less detrimental approach is to freeze the bulk water sample until filtration, to reduce isotopic artifacts. Copyright © 2015 John Wiley &amp; Sons, Ltd.</p> </sec> </abstract> … (more)
- Is Part Of:
- Rapid communications in mass spectrometry. Volume 29:Number 21(2015)
- Journal:
- Rapid communications in mass spectrometry
- Issue:
- Volume 29:Number 21(2015)
- Issue Display:
- Volume 29, Issue 21 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 21
- Issue Sort Value:
- 2015-0029-0021-0000
- Page Start:
- 2102
- Page End:
- 2108
- Publication Date:
- 2015-10-01
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/rcm.7368 ↗
- Languages:
- English
- ISSNs:
- 0951-4198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7254.440000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4125.xml