2000
DOI: 10.1016/s0377-8398(00)00006-2
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Temperature influence on the carbon isotopic composition of Globigerina bulloides and Orbulina universa (planktonic foraminifera)

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Cited by 126 publications
(141 citation statements)
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References 66 publications
(106 reference statements)
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“…Laboratory measurements on the symbiont-barren planktonic foraminifer Globigerina bulloides show a decrease of δ 13 C foram by 0.11‰ per temperature increase of 1°C (Bemis et al, 2000), which is twice as large and opposite in sign compared to our results. Bemis et al (2000) hypothesise though that increasing temperatures induce higher respiration rates, which, in turn, introduce more depleted δ 13 C CO 2 near the shell. After conversion from CO 2 to HCO 3 − and CO 3 2− , this carbon is subsequently taken up during calcification, thus lowering δ 13 C foram .…”
Section: Temperaturecontrasting
confidence: 84%
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“…Laboratory measurements on the symbiont-barren planktonic foraminifer Globigerina bulloides show a decrease of δ 13 C foram by 0.11‰ per temperature increase of 1°C (Bemis et al, 2000), which is twice as large and opposite in sign compared to our results. Bemis et al (2000) hypothesise though that increasing temperatures induce higher respiration rates, which, in turn, introduce more depleted δ 13 C CO 2 near the shell. After conversion from CO 2 to HCO 3 − and CO 3 2− , this carbon is subsequently taken up during calcification, thus lowering δ 13 C foram .…”
Section: Temperaturecontrasting
confidence: 84%
“…Until consistent measurements emerge, we prefer the traditionally used fractionation factors of Mook (1986). Laboratory measurements on the symbiont-barren planktonic foraminifer Globigerina bulloides show a decrease of δ 13 C foram by 0.11‰ per temperature increase of 1°C (Bemis et al, 2000), which is twice as large and opposite in sign compared to our results. Bemis et al (2000) hypothesise though that increasing temperatures induce higher respiration rates, which, in turn, introduce more depleted δ 13 C CO 2 near the shell.…”
Section: Temperaturecontrasting
confidence: 61%
“…The observed Q 10 for respiration, 3.18, and the T A of 10,293uK are slightly higher than for tintinids (Verity 1985), microflagellates (Caron et al 1986), copepods (Vidal 1980), appendicularians (Lombard et al 2005), or euphausiids (Ross 1982); the Q 10 for these typically ranges between 1.5 and 2.8 in this temperature range. Our direct Q 10 estimates are also higher than previous ones calculated for foraminifera from indirect methods (based on the d 13 C of the shells), which give a Q 10 for respiration of between 2 and 2.75 (Ortiz et al 1996) and a Q 10 of ,1.6 for photosynthesis (Bemis et al 2000). Growth observations on foraminifera also give estimates of Q 10 of about 1.75 for O. universa (Caron et al 1987), and these estimates range from 2 to 9 for G. ruber, G. sacculifer, and O. universa (Bijma et al 1990).…”
Section: Discussioncontrasting
confidence: 62%
“…The high δ 13 C DIC values found close to the sea surface are assumed to be caused by high primary production, resulting in enrichment in 13 C (Fogel and Cifuentes, 1993): as 12 C is taken for photosynthesis, the water becomes enriched in 13 C. However, if no other processes would affect the incorporation of carbon into the calcite shells, the tests should also show the enrichment in 13 C. One possible explanation for the deviation in the upper ∼ 75 m could be the effect of high (near-surface) temperatures on the carbon isotope incorporation of the tests. Laboratory (Bemis et al, 2000) and field experiments (Jonkers et al, 2013) have shown that foraminiferal δ 13 C linearly decreases with increasing temperatures. However, in our data set the offsets measured between δ 13 C DIC and δ 13 C foraminifera have no correlation with in situ water temperatures.…”
Section: Carbon Isotope Values Of Dic and Foraminiferamentioning
confidence: 99%