2015
DOI: 10.1016/j.marmicro.2015.01.003
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Test morphology as a function of behavioral strategies — Inferences from benthic foraminifera

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Cited by 22 publications
(12 citation statements)
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“…Stable carbon and oxygen isotopes were measured at ZMT (Leibniz Centre for Tropical Marine Ecology) in Bremen, using a Finnigan MAT 253 ™ gas isotope ratio mass spectrometer with a Kiel IV automated carbonate preparation device (standard deviations of house standard: 0.02 ‰ for δ 13 C and 0.06 ‰ for δ 18 O), and at MARUM (Bremen), using a Finnigan MAT 251 ™ mass spectrometer with a Kiel I carbonate preparation device (standard deviations of house standard: 0.02 ‰ for δ 13 C and 0.03 ‰ for δ 18 O). The measurements were performed on two to eight tests (test size: 150-500 µm) of the epibenthic foraminifera Cibicides lobatulus (Ahrens et al, 1997;Dubicka et al, 2015) and the endobenthic foraminifera Nonionellina labradorica (Ahrens et al, 1997;Alve and Bernhard, 1995;Loubere and Rayray, 2016) for bottom water and pore water signals, respectively. Stable oxygen isotope values were corrected for a global ice volume effect (Waelbroeck et al, 2002) and adjusted for vital effects: +0.64 ‰ for C. lobatulus (Shackleton, 1974) and −0.2 ‰ for N. labradorica (Duplessy et al, 2005).…”
Section: Stable Isotope Measurementsmentioning
confidence: 99%
“…Stable carbon and oxygen isotopes were measured at ZMT (Leibniz Centre for Tropical Marine Ecology) in Bremen, using a Finnigan MAT 253 ™ gas isotope ratio mass spectrometer with a Kiel IV automated carbonate preparation device (standard deviations of house standard: 0.02 ‰ for δ 13 C and 0.06 ‰ for δ 18 O), and at MARUM (Bremen), using a Finnigan MAT 251 ™ mass spectrometer with a Kiel I carbonate preparation device (standard deviations of house standard: 0.02 ‰ for δ 13 C and 0.03 ‰ for δ 18 O). The measurements were performed on two to eight tests (test size: 150-500 µm) of the epibenthic foraminifera Cibicides lobatulus (Ahrens et al, 1997;Dubicka et al, 2015) and the endobenthic foraminifera Nonionellina labradorica (Ahrens et al, 1997;Alve and Bernhard, 1995;Loubere and Rayray, 2016) for bottom water and pore water signals, respectively. Stable oxygen isotope values were corrected for a global ice volume effect (Waelbroeck et al, 2002) and adjusted for vital effects: +0.64 ‰ for C. lobatulus (Shackleton, 1974) and −0.2 ‰ for N. labradorica (Duplessy et al, 2005).…”
Section: Stable Isotope Measurementsmentioning
confidence: 99%
“…The measurements were performed on two to eight tests (test size: 150-500 µm) of the epibenthic foraminifera Cibicides lobatulus (Ahrens et al, 1997;Dubicka et al, 2015) and the endobenthic foraminifera Nonionellina labradorica (Ahrens et al, 1997;Alve and Bernhard, 1995;Loubere and Rayray, 2016) for bottom water and pore water signals, respectively. Stable oxygen isotope values were corrected for a global ice volume effect (Waelbroeck et al, 2002) and adjusted for vital effects: +0.64 ‰ for C. lobatulus (Shackleton, 1974) and −0.2 ‰ for N. labradorica (Duplessy et al, 2005).…”
Section: Stable Isotope Measurementsmentioning
confidence: 99%
“…At about 80 kyr after the beginning of the PETM, large and flat Cibicidoides with coarse pores on the spiral side increased in relative abundance, an unusual feature for PETM assemblages [Thomas, 1998]. Possibly, these species resembled the living Cibicidoides wuellerstorfi [Lutze and Thiel, 1989] or Cibicidoides lobatulus [Dubicka et al, 2015;Gooday et al, 2015], living epifaunally attached to hard surfaces [Thomas, 1998]. These epifaunal species could not thrive during the phase of deep-sea ocean acidification during peak PETM, but they may have become abundant when currents were still too strong to allow reestablishment of the shallow infaunal suspension feeders [Schoenfeld, 2002] and corrosiveness declined.…”
Section: 1002/2015pa002837mentioning
confidence: 99%