Calibration of the oxygen and clumped isotope thermometers for (proto-)dolomite based on synthetic and natural carbonates
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24 of 118 cited sources checked · 15 supported · 0 flagged · accuracy not yet measured
- Premisecitation
The phosphoric acid reaction of carbonate to CO2 produces a temperature-dependent isotopic fractionation whose temperature dependence is relatively well constrained for calcite but not for dolomite.
“The phosphoric acid reaction of the carbonate to CO 2 produces a temperature-dependent isotopic fractionation whose temperature dependence is relatively well constrained for calcite (e.g.Defliese et al., 2015;Murray et al., 2016;Petersen et al., 2019) but not for dolomite.”
Quote in the paperSubstantial claim1 of 3 sources checked - Findingreasoning
Recalculating the data from Müller et al. (2017a) with the new accepted ETH standard values of Bernasconi et al. (2018) and IUPAC parameters gives a difference in phosphoric acid fractionation between calcite and dolomite of 0.04‰.
“However, when recalculating the data from Müller et al. (2017a) with the new accepted ETH standard values of Bernasconi et al. (2018) calculated with the IUPAC parameters, rather than those of Meckler et al. (2014), the difference in phosphoric acid fractionation between calcite and dolomite becomes 0.04 ‰ (see Tables 4, S3).”
Quote in the paperSubstantial claim1 of 3 sources checked - Findingcitation
The natural dolomites from Lagoa Vermelha, Brazil all show the main dolomite reflections 104, 110 and 113 and the dolomite ordering reflections 015 and 021.
“The natural dolomites from Lagoa Vermelha, Brazil all show the main dolomite reflections 104, 110 and 113 at the corresponding 2θ space and the dolomite ordering reflections 015 and 021”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites Bradley et al., 1953
The Abstract and Additional information discuss dolomite powder diffraction and reflections affected by Ca–Mg ordering, but do not report measurements of dolomites from Lagoa Vermelha. Searches for the locality and the specified 104, 110, 113, 015, and 021 reflections found no passage establishing that all those samples show those peaks. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites Goldsmith and Graf, 1958 source
- cites Gregg et al., 2015 source
- Findingnone given
If the results of the proto-dolomites precipitated between 25 and 79°C of Fritz and Smith (1970) are corrected for the difference of their applied acid fractionation at 25°C, their calibration line is parallel to but slightly below (~1‰) the one of Vasconcelos et al. (2005).
“If the results of the proto-dolomites precipitated between 25 and 79 °C of Fritz and Smith (1970) are corrected for the difference of their applied acid fractionation at 25 °C, their calibration line is parallel to but slightly below (~1 ‰) the one of Vasconcelos et al. (2005).”
Quote in the paperSubstantial claim1 of 2 sources checked - Premisecitation
Simultaneous measurements of multiple dolomite standards with different bulk isotope composition, different degree of ordering and different Δ47 allow detection of differences due to scale compression, background correction or calculations to transfer isotope results to CDES.
“Simultaneous measurements of multiple dolomite standards with different bulk isotope composition, different degree of ordering and different Δ 47 allows to detect differences due to scale compression, background correction or calculations to transfer the isotope results to the CDES (see Bernasconi et al. (2018) for a detailed discussion of the advantages of carbonate standards).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Bernasconi et al. (2018) source
In “Carbonate Standards for Optimized Data Correction and Linkage to the ARF” (page unavailable), the paper explains that four carbonate standards can reveal background-correction errors and establish a transfer function to CDES; its regression slope also corrects scale compression. But those four standards are calcites, not dolomites, and the paper does not establish that standards with different degrees of dolomite ordering provide this diagnostic capability. The dolomites in Case III are used for an interlaboratory comparison. (LLM, conf=0.87)
Experimental — accuracy not yet measured
- Findingown data
The new (proto-)dolomite-specific Δ47-T calibration shows a clear offset of about 30 ppm in the temperature range 5 to 95°C relative to the calcite-specific calibration produced under identical conditions in the same laboratory (Bernasconi et al., 2018).
“The new (proto-)dolomite specific Δ 47 -T calibration shows a clear offset of about 30 ppm in the temperature range of 5 to 95 °C to the calcite specific calibration produced under identical conditions in the same laboratory (Bernasconi et al., 2018).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Bernasconi et al., 2018 source
In “Calculation of Δ47 and the Effect of the 17O Correction” (page unavailable), Bernasconi et al. report a reevaluated Δ47–temperature calibration covering 6–95°C. Our copy does not establish the claimed approximately 30 ppm offset from a (proto-)dolomite calibration or show that the two calibrations were produced under identical conditions. (LLM, conf=0.85)
Experimental — accuracy not yet measured
- Rests on an assumption: The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
- Premisenone given
Comparisons to other dolomite Δ47-fluid inclusion studies that used calcite-specific Δ47-T calibrations (Came et al., 2017; Honlet et al., 2017) are inconclusive.
“the inconclusive comparisons to other dolomite Δ 47 -fluid inclusion studies that used calcite specific Δ 47 -T calibrations (Came et al., 2017;Honlet et al., 2017)”
Quote in the paperSubstantial claim2 of 2 sources checked - Study design and conductcitation
Rodolo and Sansa were analyzed for Δ47 at MIT and reproduced well the results of the ETH laboratory.
“Rodolo and Sansa were also analyzed for their Δ 47 in the laboratory of the MIT with a Nu Perspective mass spectrometer coupled to a Nu Carb device by Kristin D. Bergmann and reproduced well the results of the ETH laboratory (see Bernasconi et al., 2018).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Bernasconi et al., 2018 source
- Findingown data§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonates
For the temperature range 25 to 220 °C, the linear Δ47-T relationship based on 289 individual measurements has an R2 of 0.864.
“For the temperature range 25 to 220 °C we obtain a linear Δ 47 -T relationship based on 289 individual measurements with R 2 of 0.864: = ± × + ± ° T 0.0428 0.0020 10 0.1481 0.0160 (T in Kelvin) CDES C 47 70 6 2”
Quote in the paperSubstantial claim- Rests on an assumption: Clumped isotope thermometry is solely temperature dependent.
- Findingreasoning§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonates
The oxygen isotope fractionation calibration for (proto-)dolomite formed in a wide temperature range from 25 to 350 °C is given by 10^3 ln α = 2.9923 ± 0.0557 × 10^6/T^2 - 2.3592 ± 0.4116.
“= ± × ± 10 2.9923 0.0557 10 T 2.3592 0.4116 3 CaMg carbonates Water 6 2”
Quote in the paperSubstantial claim0 of 2 sources checked - Findingown data§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonates
Applying a calcite Δ47-T relationship produced under identical laboratory conditions results in 3 to 16 °C colder calculated formation temperatures for dolomites with formation temperatures from 0 to 100 °C than using the (proto-)dolomite specific calibration presented here.
“Applying a calcite Δ 47 -T relationship produced under identical laboratory conditions results in 3 to 16 °C colder calculated formation temperatures for dolomites (with formation temperature from 0 to 100 °C) than using the (proto-)dolomite specific calibration presented here.”
Quote in the paperSubstantial claim- Rests on an assumption: Clumped isotope thermometry is solely temperature dependent.
- Findingown data§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonates
When including two isotopically scrambled dolomites at 1100 °C, the best fit is obtained with a third order polynomial temperature relationship with R2 = 0.924.
“When including two isotopically scrambled dolomites at 1100 °C, the best fit is obtained with a third order polynomial temperature relationship (R 2 = 0.924):”
Quote in the paperSubstantial claim- Rests on an assumption: Clumped isotope thermometry is solely temperature dependent.
- Findingnone given
No effect of the acid reaction length on the measured raw Δ47 values of the calcite standards was observed.
“no effect of the acid reaction length on the measured raw Δ 47 values of the calcite standards was observed.”
Quote in the paperNot a substantial claim - Findingown data
The shortest 140°C experiment Leeds 21 shows a Δ47 slightly bigger than the other samples synthesized at the same temperature.
“There is only the shortest 140 °C experiment Leeds 21 (the only proto-dolomite of the 140 °C samples) that shows a Δ 47 slightly bigger than the other samples synthesized at same temperature.”
Quote in the paperNot a substantial claim - Findingown data
All other Δ47 compositions for samples of a certain temperature match nicely.
“All the other Δ 47 compositions for the samples of a certain temperature match nicely.”
Quote in the paperSubstantial claim - Findingown data
The two natural dolomites heated to 1100°C show almost identical Δ47 CDES 70°C values: 0.230 ± 0.010‰ for Rodolo (H) and 0.228 ± 0.011‰ for Sansa (H).
“The two natural dolomites that where heated to 1100 °C to produce a stochastic isotope distribution were replicated much more and show almost identical Δ 47 CDES 70°C values with 0.230 ± 0.010 ‰ for Rodolo (H) and 0.228 ± 0.011 ‰ for Sansa (H).”
Quote in the paperSubstantial claim - Findingown data
For the synthetic dolomites equilibrated with solutions for variable times ranging from 1 to 12 weeks, a larger spread in results was obtained (70 °C samples: 21.86-23.23 ‰; 140 °C samples: 14.94-16.49 ‰; 220 °C samples: 9.66-13.05 ‰).
“For the synthetic dolomites that were equilibrated with the solutions for variable times ranging from 1 to 12 weeks, we obtained a larger spread in the results (70 °C samples: 21.86-23.23 ‰; 140 °C samples: 14.94-16.49‰; 220 °C samples: 9.66-13.05‰)”
Quote in the paperNot a substantial claim - Findingown data
No significant differences were observed between replicates untreated and treated with 10% H2O2.
“We did not observe any significant differences between replicates untreated and treated with 10% H 2 O 2”
Quote in the paperNot a substantial claim - Findingown data
The end products of the laboratory synthesis were determined to be (proto-)dolomite by X-ray diffraction.
“The end products were determined to be (proto-)dolomite by X-ray diffraction.”
Quote in the paperSubstantial claim- Rests on an assumption: Clumped isotope thermometry is solely temperature dependent.
- Findingown data
For the natural samples the dolomite-water oxygen isotope fractionation ranges tightly between 32.01 and 32.19 ‰.
“For the natural samples the fractionation ranges tightly between 32.01 and 32.19 ‰.”
Quote in the paperSubstantial claim - Findingown data
No trends were observed correlating conventional isotope scatter with differences in mineralogy and Δ47.
“We observed some scatter in the conventional isotopes, but we did not observe trends correlating with differences in the mineralogy and the Δ 47 .”
Quote in the paperSubstantial claim - Findingown data
The Δ47 CDES 70°C values range between 0.497 and 0.515‰ for samples synthesized at 70°C.
“the Δ 47 CDES 70°C values range between 0.497 and 0.515 ‰ for samples synthesized at 70 °C”
Quote in the paperSubstantial claim - Findingown data
Using only the (proto-)dolomites synthesized under controlled laboratory conditions (excluding heated dolomites and natural dolomites from Brazilian lagoon and Qatar), the oxygen isotope fractionation relative to water has a temperature dependence with R2 = 0.9862.
“Using only the (proto-)dolomites synthesized under controlled laboratory conditions without the two heated dolomites and the three natural dolomites from the Brazilian lagoon and from Qatar, we obtain a temperature dependence with R 2 = 0.9862 for the oxygen isotope fractionation relative to water”
Quote in the paperSubstantial claim - Findingown data
The Δ47 CDES 70°C values range between 0.311 and 0.348‰ for samples synthesized at 220°C.
“between 0.311 and 0.348 ‰ for the 220 °C samples”
Quote in the paperNot a substantial claim - Findingown data
The Δ47 of Rodolo dolomite is 0.632‰ with uncertainty ±0.006‰ at 95% CL.
“the Δ 47 of 0.632 ‰ is well constrained with an uncertainty of only ± 0.006 ‰ at the 95% Cl”
Quote in the paperSubstantial claim - Findingown data
There is no clear observable trend in the isotopes that correlates with the increasing degree of ordering.
“However, there is not clear observable trend in the isotopes that correlates with the increasing degree of ordering.”
Quote in the paperNot a substantial claim - Findingown data
The presence of ordering peaks in the natural samples and the 140 and 220°C samples is typical for poorly ordered to well-ordered, mostly stoichiometric dolomite.
“the presence of the ordering peaks in the natural samples, the 140 and 220 °C samples is typical for poorly ordered to well-ordered, in most cases stoichiometric or very close to stoichiometric dolomite.”
Quote in the paperSubstantial claim - Findingcitation
With the AC of 0.0380‰ from Murray et al. (2016), the calibration shifts down to about 8 ppm below Bonifacie et al. (2017).
“Whereas with the AC of 0.0380 ‰ from Murray et al. (2016), which observed a much steeper temperature relationship for dolomite compared to calcite, our calibration shifts down to about 8 ppm below the one of Bonifacie et al. (2017).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Findingown data
The dolomite-specific Δ47-T calibration shows an almost identical slope to the calibration of Bonifacie et al. (2017).
“Our dolomite specific Δ 47 -T calibration shows an almost identical slope as the calibration of Bonifacie et al. (2017)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
- Findingnone given
The linear regression for the dolomite-specific Δ47-T calibration for 70°C acid digestion fits the theoretical dolomite calibration better in the low temperature range.
“The linear regression for the dolomite specific Δ 47 -T calibration for 70 °C acid digestion fits the theoretical dolomite calibration better in the low temperature range.”
Quote in the paperNot a substantial claim - Findingreasoning
The combined 10^3 lnα Dolomite-Water -T relationship is: 10^3 ln α = (2.9923 ± 0.0557) × (10^6/T^2) + (2.3592 ± 0.4116).
“= ± × ± 10 ln 2.9923 0.0557 (10 /T ) 2.3592 0.4116 3 Dolomite Water 6 2”
Quote in the paperSubstantial claim - Findingcitation
Other studies, including ours, merged results from stoichiometric poorly to well-ordered dolomites formed above 140°C with results from proto-dolomites formed down to 70°C.
“Other studies, including ours, merged results from stoichiometric poorly to well-ordered dolomites formed at temperatures above 140 °C with results from proto-dolomites formed at temperatures down to 70 °C (experiments down to 80 °C in Horita, 2014).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Horita, 2014 source
- Findingcitation
Applying an acid fractionation correction of 0.0204‰ derived from Defliese et al. (2015), the dolomite calibration lies parallel with an offset of about 10 ppm above Bonifacie et al. (2017).
“Applying an acid fractionation correction (AC) of 0.0204 ‰ derived from Defliese et al. (2015), which observed no significant differences between dolomite and calcite, our dolomite calibration lies parallel with an offset of about 10 ppm above the one of Bonifacie et al. (2017) (see Fig. 7).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Findingown data
The average offset between the two sediment samples from Lagoa Vermelha and the two Brazilian lagoonal samples of Bonifacie et al. (2017) is approximately 0.029‰.
“The average offset between our two sediment samples from Lagoa Vermelha and their two Brazilian lagoonal samples (CVLV and CVBE of their Table 2) is approximately 0.029 ‰.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
- Findingown data
Our proto-dolomite samples formed at 70°C bridge the existing gap of the two datasets of Vasconcelos et al. (2005) and Horita (2014).
“On the other side our proto-dolomite samples formed at 70 °C bridge nicely the existing gap of the two datasets of Vasconcelos et al. (2005) and Horita (2014).”
Quote in the paperSubstantial claim0 of 2 sources checked - Findingown data
Despite different methods of forming (proto-)dolomites, differing degrees of ordering, and different acid digestion temperatures, the slopes of the two calibrations are statistically indistinguishable.
“Despite the different methods of forming (proto-)dolomites, the differing degrees of ordering and the different acid digestion temperatures used in the two studies, the slopes of our calibrations are statistically indistinguishable.”
Quote in the paperSubstantial claim - Findingown data
The two dolomite calibrations (this study and Winkelstern et al., 2016) are above the ETH calcite calibration.
“On Fig. 6 it is visible that the two dolomite calibrations are above the ETH calcite one”
Quote in the paperNot a substantial claim - Findingown data
The resulting Δ47-T relationship including the two heated dolomites is a third order polynomial fit that is largely identical to the theoretical dolomite calibration for 25°C acid reaction temperature of Guo et al. (2009).
“The resulting Δ 47 -T relationship is a third order polynomial fit that is largely identical to the theoretical dolomite calibration for 25 °C acid reaction temperature of Guo et al. (2009) displayed as grey dashed line in Fig. 8.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Guo et al., 2009 source
- Findingown data
A new (proto-)dolomite-water oxygen fractionation equation is valid for temperatures between 25 and 350°C, based on a compilation from samples from this study, Vasconcelos et al. (2005) and Horita (2014).
“We propose a new (proto-)dolomite-water oxygen fractionation equation valid for temperatures between 25 and 350 °C based on a compilation from samples from this study, Vasconcelos et al. (2005) and Horita (2014).”
Quote in the paperSubstantial claim0 of 2 sources checked- Rests on an assumption: The oxygen isotope fractionation data from this study, Vasconcelos et al. (2005) and Horita (2014) are directly comparable and can be combined into a single temperature relationship.
- Rests on an assumption: The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
- Findingnone given
NIST SRM 88b dolomite standard has a Δ47 CDES 70°C value of 0.522 ± 0.022 ‰.
“NIST SRM 88b dolomite standard (Δ 47 CDES 70°C of 0.522 ± 0.022 ‰)”
Quote in the paperNot a substantial claim - Findingown data
The slope of the new dolomite-specific Δ47-T calibration for 70°C acid digestion is statistically indistinguishable from the slope of the calibration of Bonifacie et al. (2017) produced at 90°C.
“The comparison of the new dolomite specific Δ 47 -T calibration of this study for 70 °C acid digestion with the calibration of Bonifacie et al. (2017) produced at 90 °C shows that the slope of the calibration is statistically indistinguishable”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bonifacie et al. (2017) source
- Rests on an assumption: The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
- Findingown data
The temperature relationship of Matthews and Katz (1977), corrected for the acid digestion factor of Rosenbaum and Sheppard (1986), lies slightly below the combined relationship of this study.
“As dashed grey line we also plotted the temperature relationship of Matthews and Katz (1977) (corrected for the acid digestion factor of Rosenbaum and Sheppard (1986) for consistent data treatment) lying slightly below our combined one.”
Quote in the paperNot a substantial claim0 of 2 sources checked - Findingnone given
The 30 ppm difference lies between the value predicted by Defliese et al. (2015) and the value predicted by Murray et al. (2016).
“The 30 ppm difference lies between the one predicted by Defliese et al. (2015) and the one by Murray et al. (2016).”
Quote in the paperNot a substantial claim0 of 2 sources checked - Findingown data
A new (proto-)dolomite-specific Δ47-T calibration for 70°C acid digestion covers a temperature range from 25 to 1100°C and is based on 22 different (proto-)dolomite samples formed at known temperatures, totaling 435 individual measurements.
“We propose a new (proto-)dolomite specific Δ 47 -T calibration for 70 °C acid digestion covering a temperature range from 25 to 1100 °C, based on 22 different (proto-)dolomite samples that formed at known temperatures and consists of a total of 435 individual measurements.”
Quote in the paperSubstantial claim- Rests on an assumption: The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
- Findingown data
The slopes of the dolomite and calcite calibrations are within uncertainties (0.0428 ± 0.0020 for dolomite vs. 0.0449 ± 0.0019 for calcite).
“The slopes of both calibrations are within uncertainties (0.0428 ± 0.0020 for dolomite vs. 0.0449 ± 0.0019 for calcite).”
Quote in the paperSubstantial claim - Findingown data
The slope of the new dolomite calibration is similar to those of calcites and siderites.
“and similar to calcites and siderites”
Quote in the paperSubstantial claim - Interpretationreasoning§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonates
The different phosphoric acid fractionation for Δ47 during acid digestion of dolomite compared to calcite causes additional uncertainties in Δ47 temperature estimates for dolomites analyzed in different laboratories using different acid digestion temperatures.
“This causes additional uncertainties in the Δ 47 temperature estimates for dolomites analyzed in different laboratories using different acid digestion temperatures.”
Quote in the paperSubstantial claim - Interpretationreasoning§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonates
Based on the similarity between the paper's results and two other recent studies (Vasconcelos et al., 2005 and Horita, 2014), a combination of the three datasets represents the most robust calibration for (proto-)dolomite formed in a wide temperature range from 25 to 350 °C.
“Based on the similarity between our results and two other recent studies (Vasconcelos et al., 2005 andHorita, 2014) we propose that a combination of the three datasets represents the most robust calibration for (proto-)dolomite formed in a wide temperature range from 25 to 350 °C.”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Two recent studies on the temperature dependence of the AFF for dolomite came to contrasting conclusions (Defliese et al., 2015; Murray et al., 2016).
“While earlier studies processed their Δ 47 measurements of different carbonate minerals with the same AFF as for calcite, two recent studies on the temperature dependence of the AFF for dolomite came to contrasting conclusions (Defliese et al., 2015;Murray et al., 2016).”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
In the ETH laboratory, dolomites and calcites are digested at 70 °C and at this temperature, a different dolomite-specific Δ47 acid fractionation is observed (Müller et al., 2017a).
“In the ETH laboratory, dolomites and calcites are digested at 70 °C and at this temperature, a different-dolomite specific Δ 47 acid fractionation is observed (Müller et al., 2017a).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The only study that determined the absolute Δ47 acid fractionation at 70°C using various carbonate minerals with a stochastic isotope distribution is Müller et al. (2017a).
“The only study which determined the absolute Δ 47 acid fractionation at 70 °C using various carbonate minerals with a stochastic isotope distribution is that of Müller et al. (2017a).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
The Rodolo dolomite Δ47 value gives a fluid source δ18O of +1.7 ± 0.04‰.
“and a fluid source with δ 18 O of +1.7 ± 0.04 ‰”
Quote in the paperNot a substantial claim - Interpretationreasoning
This suggests a slightly different (0.01‰) clumped isotope acid fractionation for dolomite and calcite at a specific temperature.
“This would suggest a slightly different (0.01 ‰) clumped isotope acid fractionation for dolomite and calcite at a specific temperature.”
Quote in the paperNot a substantial claim - Interpretationcitation
The difference between the intercepts of the dolomite and calcite calibrations produced at ETH can be explained by the difference in absolute Δ47 acid fractionation between calcite and dolomite of 0.029‰.
“The difference between the intercepts of the dolomite and calcite calibrations produced at the ETH can be explained by the differences in the absolute Δ 47 acid fractionation between calcite and dolomite of 0.029 ‰ (Müller et al., 2017a).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationcitation
Using the steeper temperature relationship of the acid fractionation for dolomite to project data to 25°C would lead to a larger difference to calcite at acid reaction temperatures below 90°C than using the Defliese et al. (2015) relationship.
“Thus, using the steeper temperature relationship of the acid fractionation for dolomite to project data to 25 °C would lead to a larger difference to calcite at acid reaction temperatures below 90 °C than what would be observed using the Defliese et al. (2015) relationship.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Defliese et al., 2015 source
- Study design and conductown data
Reproducibility of the measurements based on repeated measurements of an internal standard was better than 0.06 ‰.
“Reproducibility of the measurements based on repeated measurements of an internal standard was better than 0.06 ‰.”
Quote in the paperNot a substantial claim - Interpretationreasoning
A temperature of 32 ± 6 °C is assigned to the Qatar dolomite sample.
“Thus we assign a temperature of 32 ± 6 °C to this sample.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Illing et al., 1965
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Butler, 1969 source
- Interpretationreasoning
This is evidence that the clumped isotope composition of the (proto-)dolomites is in equilibrium with their actual formation temperature.
“This would be evidence that the clumped isotope composition of our (proto-)dolomites is in equilibrium to their actual formation temperature.”
Quote in the paperSubstantial claim - Study design and conductreasoning
Comparison of the new (proto-)dolomite calibration with the ETH calcite calibration (same instrumentation, same standards) allows exclusion of methodological artefacts and data processing differences.
“We start by comparing our new (proto-)dolomite calibration with the calcite calibration produced at ETH with the same instrumentation and normalized to the CDES using the same ETH-1,-2,-3,-4 calcite standards, thus we can exclude methodological artefacts and data processing differences (IUPAC parameters).”
Quote in the paperSubstantial claim - Study design and conductown data
The uncertainty of the oxygen isotope composition of the (proto-)dolomite samples varies between ± 0.03-0.44 ‰ at the 95% confidence level.
“The uncertainty of the oxygen isotope composition of the (proto-)dolomite samples varies between ± 0.03-0.44‰ at the 95% Cl”
Quote in the paperNot a substantial claim - Interpretationown data
With almost all dolomite ordering reflections expressed, the carbonate phase of LV 15 cm and LV 71 cm can be described as poorly ordered dolomite.
“With almost all dolomite ordering reflections expressed, the carbonate phase of LV 15 cm and LV 71 cm can be described as poorly ordered dolomite.”
Quote in the paperNot a substantial claim - Interpretationown data
Calcite and dolomite have to be treated separately when measured for clumped isotopes, especially when reacted with phosphoric acid at temperatures below 90°C due to the different phosphoric acid fractionation factor.
“Thus we conclude that calcite and dolomite have to be treated separately when measured for clumped isotopes, especially when reacted with phosphoric acid temperatures below 90 °C due to the different phosphoric acid fractionation factor.”
Quote in the paperSubstantial claim - Premisecitation
Müller et al. (2017a) showed that at 70°C the acid fractionation of dolomite is 29 ppm larger than that of calcite.
“This study showed that at 70 °C the acid fractionation of dolomite is 29 ppm larger than the one of calcite.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationown data
The significant difference between calcite and dolomite calibrations measured with the same methodology suggests that published estimates of temperatures of dolomite formation may have to be reevaluated.
“The significant difference we observe in this study between the calcite and dolomite calibration measured with the same methodology, therefore, suggest that published estimates of temperatures of dolomite formation may have to be reevaluated.”
Quote in the paperSubstantial claim - Interpretationown data
The Rodolo dolomite Δ47 value gives a temperature of 25 ± 2°C.
“giving a temperature of 25 ± 2 °C”
Quote in the paperNot a substantial claim - Interpretationreasoning
In contrast, the intercepts of the calibrations differ for different minerals due to differences in phosphoric acid fractionation.
“In contrast, the intercepts of the calibrations differ for the different minerals due to the difference in phosphoric acid fractionation.”
Quote in the paperSubstantial claim - Premisecitation
Bonifacie et al. (2017) obtained a linear regression of Δ47 CDES 90°C = (0.0428 ± 0.0033) × 10^6/T^2 + (0.1174 ± 0.0248).
“In their study Bonifacie et al. (2017) reacted 5 mg samples with 104% phosphoric acid in a common acid bath at 90 °C and obtained a linear regression of Δ 47 CDES 90°C = (0.0428 ± 0.0033) * 10 6 /T 2 + (0.1174 ± 0.0248).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
- Interpretationreasoning
Therefore, no or only minor differences are expected to an ideal ordered stoichiometric dolomite as found in the geologic record.
“Therefore we expect no or only minor differences to an ideal ordered stoichiometric dolomite as those found in the geologic record.”
Quote in the paperSubstantial claim - Interpretationreasoning
The direct comparison of published studies on the temperature dependency of oxygen isotope fractionation between dolomite and water is complicated by different studies using different phosphoric acid fractionation factors.
“The direct comparison of the published studies on the temperature dependency of the oxygen isotope fractionation between dolomite and water is complicated by the fact that different studies used different phosphoric acid fractionation factors.”
Quote in the paperSubstantial claim - Interpretationcitation
The offset between the dolomite and calcite calibration sets corresponds to the different absolute Δ47 acid fractionations of dolomite and calcite already observed in Müller et al. (2017a).
“The offset between the two calibration sets corresponds to the different absolute Δ 47 acid fractionations of dolomite and calcite already observed in Müller et al. (2017a).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Müller et al. (2017a)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
The offset of about 30 ppm corresponds to the dolomite isotope acid fractionation correction between 70°C and 90°C reaction.
“This offset corresponds to the dolomite isotope acid fractionation correction between 70 °C and 90 °C reaction.”
Quote in the paperSubstantial claim - Interpretationreasoning
The discrepancy in the intercept is due to poor understanding of the temperature dependence of the AFF for dolomite.
“due to poor understanding of the temperature dependence of the AFF for dolomite”
Quote in the paperSubstantial claim - Interpretationown data
All carbonates have a common calibration.
“indication that all carbonates have a common calibration.”
Quote in the paperSubstantial claim - Interpretationreasoning
This combined relationship makes poorly constrained extrapolations from calibrations based on high temperature dolomites to lower temperatures unnecessary.
“This makes poorly constrained extrapolations from calibrations based on high temperature dolomites to lower temperatures unnecessary.”
Quote in the paperSubstantial claim
- May combine two claims. 56
- Classified as probably not a substantial claim. 34
- The quote only partly states this claim. 6
May combine two claims.
PremisecitationA recalculation of Kele et al. (2015) by Bernasconi et al. (2018) showed that while the slope remained constant, the intercept decreased by 0.038 ‰.
“A recalculation of the Kele et al. (2015) by Bernasconi et al. (2018), however, showed that while the slope remained constant, the intercept decreased by 0.038 ‰.”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites Kele et al., 2015 source
The accepted manuscript describes Kele et al.’s isotope corrections and discusses calibration slopes, but it does not address a recalculation by Bernasconi et al. (2018). Searches for the claimed unchanged slope and 0.038‰ intercept decrease found no passage reporting that result. (LLM, conf=0.76)
Experimental — accuracy not yet measured - cites Bernasconi et al., 2018 source
Classified as probably not a substantial claim.
PremisecitationGeneral estimates for calcite or dolomite Δ47 blocking temperatures during cooling range between 200 and 300 °C, respectively (e.g. Bonifacie et al., 2017; Ryb et al., 2017).
“General estimates for calcite or dolomite Δ 47 blocking temperatures during cooling range between 200 and 300 °C, respectively (e.g.Bonifacie et al., 2017;Ryb et al., 2017).”
Quote in the paperSubstantial claim1 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationThe effect on recalculated temperatures in older publications is difficult to predict without a full recalculation that includes all heated and equilibrated gases measured with the samples.
“The effect on the recalculated temperatures in older publications is difficult to predict without a full recalculation that includes all heated and equilibrated gases measured with the samples (Petersen et al., 2019).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Petersen et al., 2019 source
May combine two claims.
Findingown dataThe slope of the new dolomite calibration (0.0428 ± 0.0020) is slightly shallower than the calcite calibration of Kele et al. (2015) recalculated in Bernasconi et al. (2018) (0.0449 ± 0.0019), but within uncertainties.
“Comparison with the calcite calibration of Kele et al. (2015) recalculated in Bernasconi et al. (2018) shows a slightly shallower slope within the uncertainties of each other (0.0428 ± 0.0020 vs. 0.0449 ± 0.0019).”
Quote in the paperSubstantial claim2 of 2 sources checked- cites Kele et al., 2015 source
- cites Bernasconi et al., 2018 source
The ‘Calculation of Δ47 and the Effect of the 17O Correction’ section reports a recalculated Kele et al. calibration slope of 0.0449, supporting the comparison’s cited value. It gives the uncertainty as ±0.001, however, not ±0.0019. The new dolomite slope is the citing paper’s own result, not a result attributed to Bernasconi et al. (LLM, conf=0.90)
Experimental — accuracy not yet measured
Classified as probably not a substantial claim. May combine two claims.
Study design and conductcitationIn this study the results are firmly anchored to the absolute reference frame using a calcite-based correction scheme using the widely distributed ETH Standards, which allows other laboratories to better compare the data to ours (Bernasconi et al., 2018).
“In addition, in this study we firmly anchor the results to the absolute reference frame using a calcite-based correction scheme using the widely distributed ETH Standards, which allows other laboratories to better compare the data to ours (Bernasconi et al., 2018).”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Bernasconi et al., 2018 source
May combine two claims.
InterpretationcitationComparison of calibrations established in different laboratories remains challenging due to lack of carbonate standards, pre-2016 data not calculated with Brand parameters, and different phosphoric acid fractionation factors.
“The comparison of calibrations established in different laboratories, however, remains challenging, because of many factors: the lack of carbonate standards to compare across laboratories, the fact that clumped isotope data pre-2016 are not calculated using the”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites Bernasconi et al., 2018 source
- cites Petersen et al., 2019 source
The Introduction (p. 4) says interlaboratory discrepancies remain, and Data Selection (p. 7) describes difficulties comparing early calibrations processed with older parameters. But the paper describes carbonate standards available across laboratories (p. 9), rather than a lack of them, and says differences in acid-digestion fractionation and correction parameters were eliminated as causes of the remaining disagreement (p. 19). It does not establish a pre-2016 cutoff for data calculated without Brand parameters. (LLM, conf=0.87)
Experimental — accuracy not yet measured
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationOrdered crystalline dolomite forms from an initial amorphous calcium-magnesium carbonate phase that first crystallizes to a non-stoichiometric proto-dolomite, and then transforms over hours to weeks, depending on the temperature, to fully ordered stoichiometric dolomite (Rodriguez-Blanco et al., 2015).
“Ordered crystalline dolomite forms from an initial amorphous calcium-magnesium carbonate phase that first crystallizes to a non-stoichiometric proto-dolomite, and that then transforms over hours to weeks, depending on the temperature, to fully ordered stoichiometric dolomite (Rodriguez-Blanco et al., 2015).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Rodriguez-Blanco et al., 2015 source
May combine two claims.
Findingown dataThe observed offset of the Daëron et al. (2019) calibration to the new (proto-)dolomite Δ47 temperature calibration is 0.04‰, very similar to the offset between absolute Δ47 acid fractionations of calcite and dolomite re-evaluated with IUPAC parameters.
“The observed offset of their calibration to our new (proto-)dolomite Δ 47 temperature calibration is with 0.04 ‰ very similar to the offset between the absolute Δ 47 acid fractionations of calcite and dolomite of Müller et al. (2017a) re-evaluated with the new IUPAC parameters in our study (see Table 4).”
Quote in the paperSubstantial claim1 of 2 sources checked- cites Daëron et al., 2019 source
Split into 2 atoms — 1 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 1 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured - cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAnother approach to overcome the difficulty of precipitating low temperature dolomites was the theoretical modelling of the dolomite-water oxygen isotope fractionation of Zheng (1999).
“Another approach to overcome the difficulty of precipitating low temperature dolomites was the theoretical modelling of the dolomite water oxygen isotope fractionation of Zheng (1999).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Zheng (1999) source
May combine two claims.
Findingown dataThe Winkelstern et al. (2016) dataset reevaluated in Petersen et al. (2019) for 75°C acid digestion is significantly different in slope (p = 0.0395) and intercept from the re-evaluated ETH calcite calibration dataset.
“the statistical evaluation of the Winkelstern et al. (2016) dataset reevaluated in Petersen et al. (2019) for 75 °C acid digestion is significantly different in slope (p value of 0.0395) and intercept to the re-evaluated ETH calcite calibration dataset.”
Quote in the paperNot a substantial claim1 of 2 sources checked- cites Winkelstern et al., 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Petersen et al., 2019 source
Section 3.4 (p. 15) confirms that Petersen et al. reprocessed Winkelstern data, and Section 3.7 (p. 18) reports tests of slope and intercept differences between calibration studies. Our copy does not report the claimed comparison with a re-evaluated ETH calcite calibration dataset or the slope p value of 0.0395; its mentions of ETH concern carbonate standards (p. 9). (LLM, conf=0.86)
Experimental — accuracy not yet measured
Classified as probably not a substantial claim.
PremisecitationBased on Fernandez et al. (2017), more samples covering a wider temperature range lead to more robust calibrations.
“Based on observations from the statistical evaluation of Fernandez et al. (2017) of existing Δ 47 -T calibrations that more samples covering a wider temperature range lead to more robust calibrations”
Quote in the paperSubstantial claim1 of 1 sources checked- cites Fernandez et al., 2017 source
Probably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningRegular analysis of dolomite standards would drastically reduce uncertainties arising from mineral-specific acid fractionation correction and from small differences in sample purification and data processing across laboratories.
“The regular analysis of dolomite standards would drastically reduce the uncertainties arising from mineral specific acid fractionation correction and uncertainties arising from small differences in sample purification procedures and data processing across laboratories (see also Bernasconi et al., 2018).”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites Bernasconi et al., 2018 source
The Outlook (page unavailable) says repeated carbonate-standard measurements can improve interlaboratory comparability across different acid-reaction and gas-purification systems, and recommends developing standards with different mineralogies, including dolomite. The data-correction section says carbonate normalization could eliminate uncertainty from temperature-dependent acid fractionation; Case III reports close agreement for one dolomite but a remaining difference for another. The paper does not establish that regular analysis of dolomite standards would *drastically* reduce mineral-specific fractionation and data-processing uncertainties across laboratories. (LLM, conf=0.85)
Experimental — accuracy not yet measured
May combine two claims.
Findingown dataThe XRD patterns of the samples synthesized at 220 °C clearly display all three dolomite ordering reflections and all of the analyzed samples are stoichiometric.
“Finally, the XRD patterns of the samples synthesized at 220 °C clearly display all three dolomite ordering reflections and all of the analyzed samples are stoichiometric.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe Δ47 value of sample Leeds 34 matches well the other 220°C samples and shows no sign of dis-equilibrium.
“(the Δ 47 value of sample Leeds 34 matches well the other 220 °C samples and shows no sign of dis-equilibrium)”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataAlthough the protodolomite samples synthesized at 70 °C show no 015 ordering reflection and their Mg content varied between 42 and 48%, their dissolution rate when exposed to 10% HCl or 104% phosphoric acid was much slower than that observed for a typical calcite or high Mg-calcite (15 mol% Mg).
“Although the protodolomite samples synthesized at 70 °C show no 015 ordering reflection and their Mg content varied between 42 and 48 %, their dissolution rate when exposed to 10% HCl or 104% phosphoric acid was much slower than what we observe for a typical calcite or high Mg-calcite (15 mol % Mg)”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Dolomieu, 1791
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Lumsden and Chimahusky, 1980 source
May combine two claims.
Findingown dataThe linear regression is well constrained, based on 289 individual measurements of 20 different samples formed at 5 different temperatures.
“The narrow 95% confidence interval envelope shows the well constrained linear regression that is based on 289 individual measurements of 20 different samples formed at 5 different temperatures.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe poorly ordered lacustrine Rodolo dolomite has δ13C VPDB of -3.71 ± 0.06‰ and δ18O VPDB of 2.77 ± 0.12‰.
“The poorly ordered lacustrine Rodolo dolomite has a δ 13 C VPDB of -3.71 ± 0.06 ‰ and a relatively high δ 18 O VPDB of 2.77 ± 0.12 ‰”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe natural sample from Qatar has a Mg content of 49.5%, all ordering peaks besides the 101 reflection are clearly visible, and the (015)/(110) ratio is 0.29.
“The natural sample from Qatar has a Mg content of 49.5 %, all ordering peaks, besides the 101 reflection, are clearly visible and the (015)/(110) ratio is with 0.29 slightly better expressed than the other two natural samples from Brazil”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe δ13C of Sansa and NIST SRM 88b are similar (1.45 ± 0.09‰ and 2.12 ± 0.10‰), but their oxygen isotope compositions differ (-3.56 ± 0.18‰ for Sansa and -7.09 ± 0.13‰ for NIST SRM 88b).
“Whereas their δ 13 C are similar (1.45 ± 0.09 ‰ and 2.12 ± 0.10 ‰), their oxygen isotope composition is different with -3.56 ± 0.18 ‰ for Sansa and -7.09 ± 0.13 ‰ for NIST SRM 88b.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe two diagenetic dolomites are more difficult to react with phosphoric acid compared to Rodolo, causing worse reproducibility among individual replicates, but their Δ47 values reproduce extremely well.
“The two diagenetic dolomites are more difficult to react with phosphoric acid compared to the Rodolo, which is the cause of the worse reproducibility amongst all individual replicates measured during one year (Table S2), however, the Δ 47 values reproduce extremely well.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe intercept of the calcite calibration is significantly lower, so the two calibrations do not overlap at their 95% confidence intervals.
“However, the intercept of the calcite calibration is significantly lower so that the two calibrations do not overlap at their 95% Cl's (Fig. 6).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataSamples crystallized at 140 °C exhibited the ordering reflections 015 and 021, but still lacked the 101 reflection, pointing to poorly ordered dolomite with (015)/(110) ratios between 0.14 and 0.21 and Mg content close to stoichiometric dolomite of 47.3 to 49.2%.
“Samples crystallized at 140 °C exhibited in their XRD pattern the ordering reflections of dolomite 015 and 021, but still lacked the 101 reflection pointing to poorly ordered dolomite with (015)/(110) ratios between 0.14 and 0.21 and Mg content close to stoichiometric dolomite of 47.3 to 49.2 %.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe Rodolo dolomite is stoichiometric, but the ordering reflections are moderately well expressed with (015)/(110) of 0.35.
“The Rodolo dolomite is stoichiometric, but the ordering reflections are moderately well expressed with (015)/ (110) of 0.35.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe two cold natural dolomite samples have similar oxygen isotope composition but distinct carbon isotope compositions (-8.32‰ for LV 15 cm and -10.21‰ for LV 71 cm).
“both samples have similar oxygen isotope composition, but their carbon isotope compositions are more distinct with -8.32 ‰ for the more shallow sample and -10.21‰ for the deeper one.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe 015 ordering reflection is much more expressed than for samples synthesized at lower temperatures, and the degree of ordering increases from 0.28 for the 2.1 week experiment (Leeds 34) up to around 0.4 for the 12 weeks experiments (Leeds 84-86).
“The 015 ordering reflection is much more expressed than for the samples synthesized at lower temperatures and the degree of ordering is increasing from 0.28 for the 2.1 week experiment (Leeds 34) up to around 0.4 for the 12 weeks experiments (Leeds 84-86 in Table 1).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe average Δ47 CDES 70°C values of the two cold natural dolomite calibration samples are 0.637‰ for LV 15 cm and 0.619‰ for LV 71 cm.
“The average Δ 47 CDES 70°C values of the two”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenThe δ13C VPDB and δ18O VPDB of the synthetic samples are quite similar to each other.
“The δ 13 C VPDB and δ 18 O VPDB of the synthetic samples are quite similar to each other”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataIn both Lagoa Vermelha samples the ordering reflection 015 is clearly smaller than the 110 reflection, with an ordering ratio (015)/(110) of 0.15 and 0.22 for LV 15 cm and LV 71 cm, respectively.
“In both samples the ordering reflection 015 is clearly smaller than the 110 reflection, with an ordering ratio (015)/(110) of 0.15 and 0.22 for LV 15 cm and LV 71 cm, respectively.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe dolomites NIST SRM 88b and Sansa are well-ordered and stoichiometric dolomites.
“The dolomites NIST SRM 88b and Sansa are well-ordered and stoichiometric dolomites (see Table 3).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataOur 70°C samples match well the temperature-dependent (proto-)dolomite water oxygen isotope fractionation of Horita (2014), whereas our samples at 140 and 220°C show more scatter.
“Whereas our 70 °C samples match well their temperature dependent (proto-)dolomite water oxygen isotope fractionation, our samples at 140 and 220 °C show more scatter.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Horita (2014) source
May combine two claims. The quote only partly states this claim.
FindingreasoningThe AC effectively needed to put the calibrations on the same level is approximately 0.030‰, between the values of Defliese et al. (2015) and Murray et al. (2016), corresponding to the observed offset between lagoonal proto-dolomite concretions.
“The AC effectively needed to put the calibrations on the same level is an AC of approximately 0.030 ‰, which is somewhere in between the values of Defliese et al. (2015), and that of Murray et al. (2016), and corresponds to the observed offset between our lagoonal proto-dolomite concretions and the ones of Bonifacie et al. (2017).”
Quote in the paperSubstantial claim0 of 3 sources checkedMay combine two claims.
Findingown dataFor Lagoa Vermelha, the upper sample (LV 15 cm) has Δ47 CDES 70°C of 0.637 ± 0.022‰ (16 replicates), while Bonifacie et al. (2017) obtained Δ47 CDES 90°C of 0.591 ± 0.022‰ (4 replicates) for their surface sample, an offset of 0.046‰.
“For a direct comparison between the two studies we can compare the natural samples of Lagoa Vermelha where we obtained a Δ 47 CDES 70°C of 0.637 ± 0.022 ‰ for the upper one (LV 15 cm, 16 replicates) and Bonifacie et al. (2017) obtained a Δ 47 CDES 90°C of 0.591 ± 0.022 ‰ (4 replicates) for their surface sample, an offset of 0.046 ‰.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
May combine two claims.
Findingown dataFrom Fig. 9, the new experimental data overlap with those of Vasconcelos et al. (2005) and Horita (2014), whereas the Matthews and Katz (1977) calibration is slightly below the data compilation over the entire temperature range.
“From Fig. 9 it appears that our new experimental data overlap with those of Vasconcelos et al. (2005) and Horita (2014), whereas the Matthews and Katz (1977) calibration is slightly below the data compilation over the entire temperature range.”
Quote in the paperSubstantial claim0 of 3 sources checkedMay combine two claims.
Findingown dataIn case of the 140°C samples, only the shortest experiment, protodolomite Leeds 21, matches Horita's data, whereas the others show larger fractionations.
“In case of the samples synthesized at 140 °C suspiciously only the one sample of the shortest experiment, the protodolomite Leeds 21 matches that data of Horita, whereas the others show larger fractionations.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Horita
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
The quote only partly states this claim.
Findingown dataSansa is a well-ordered stoichiometric dolomite with a Δ47 CDES 70°C value of 0.526 ± 0.014 ‰.
“the warmer well-ordered stoichiometric dolomite”
Quote in the paperSubstantial claimThe quote only partly states this claim.
FindingreasoningThere is a discrepancy in the intercept of the new dolomite calibration relative to the calibration of Bonifacie et al. (2017).
“However, there is a discrepancy in the intercept of the calibration”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bonifacie et al. (2017) source
- Rests on an assumption: The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
May combine two claims.
Findingnone givenThree possible reference materials are proposed that have a range of compositions and are available in large amounts for distribution.
“We propose three possible reference materials (XRD patterns displayed in Fig. 3 and Table 3) that have a range of compositions and are available in large amounts for distribution.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe new dolomite calibration has an identical slope but an offset of about 30 ppm relative to the calibration of Bonifacie et al. (2017) for 90°C acid digestion.
“This new dolomite calibration has identical slope but an offset of about 30 ppm to the one of Bonifacie et al. (2017) for 90 °C digestion.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bonifacie et al. (2017) source
- Rests on an assumption: The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
The quote only partly states this claim.
Findingown dataCombination of the datasets from this study, Horita (2014) and Vasconcelos et al. (2005) resulted in a linear relationship covering a temperature range from 25 to 350°C.
“Combination of these three datasets resulted in the black dashed line giving the displayed linear relationship and covers a temperature range from 25 to 350 °C.”
Quote in the paperSubstantial claim0 of 2 sources checked- Rests on an assumption: The oxygen isotope fractionation data from this study, Vasconcelos et al. (2005) and Horita (2014) are directly comparable and can be combined into a single temperature relationship.
May combine two claims. The quote only partly states this claim.
Findingown dataRodolo is a stoichiometric but poorly ordered dolomite with a Δ47 CDES 70°C value of 0.632 ± 0.006 ‰.
“the lacustrine low temperature dolomite”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationMüller et al. (2017a) also determined the acid fractionation for dolomite at 100 °C and observed that at this temperature it is smaller than that of calcite.
“In this study, Müller et al. (2017a) also determined the acid fractionation for dolomite at 100 °C and observed that at this temperature it is smaller than that of calcite supporting the findings of Murray et al. (2016).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Murray et al., 2016 source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMüller et al. (2017a) observed a significantly smaller acid fractionation for aragonite (0.172 ‰), compared to calcite (0.197 ‰) and dolomite (0.226 ‰) at 70 °C acid digestion temperature.
“In a study on the absolute Δ 47 acid fractionation at 70 °C acid digestion temperature, Müller et al. (2017a) moreover, observed a significantly smaller acid fractionation for aragonite (0.172 ‰), compared to calcite (0.197 ‰) and dolomite (0.226‰).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Classified as probably not a substantial claim.
Premisecitation§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonatesSome recent studies observed a different phosphoric acid fractionation for Δ47 during acid digestion of dolomite compared to calcite.
“some recent studies observed a different phosphoric acid fractionation for Δ 47 during acid digestion of dolomite compared to calcite.”
Quote in the paperSubstantial claim0 of 3 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationIt remains unclear how dolomite forms at Earth surface conditions and why it is so abundant during certain time intervals in the geological past.
“In spite of all the efforts it remains unclear how this mineral forms at Earth surface conditions and why it is so abundant during certain time intervals in the geological past”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Land, 1985 source
- cites Given and Wilkinson, 1987 source
- cites Spencer and Hardie, 1990
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Rests on an assumption: Dolomite is a very common carbonate mineral in ancient sediments, but is rarely found in modern environments.
- Rests on an assumption: The controls on dolomite formation are still debated after more than two centuries of research.
Probably not a substantial claim: may not pass S2 (checkable).
Interpretationreasoning§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonatesSimultaneous analyses of dolomite reference material will enable a much better comparison of published dolomite clumped and oxygen isotope data amongst different laboratories.
“In addition, the simultaneous analyses of dolomite reference material will enable a much better comparison of published dolomite clumped and oxygen isotope data amongst different laboratories.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
PremisecitationRecently two dolomite-specific Δ47-T calibrations were published (Winkelstern et al., 2016; Bonifacie et al., 2017) with the aim of eliminating additional uncertainties in the interpretation of dolomite clumped isotope temperatures.
“Recently two dolomite-specific Δ 47 -T calibrations were published (Winkelstern et al., 2016;Bonifacie et al., 2017) with the aim of eliminating additional uncertainties in the interpretation of dolomite clumped isotope temperatures.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Winkelstern et al., 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Bonifacie et al., 2017 source
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBonifacie et al. (2017) for 90 °C acid digestion revealed that the temperature relationship of dolomite is within error of the one of calcite based on a compilation of many different published laboratories carried out in the same study.
“On the other hand, Bonifacie et al. (2017) for 90 °C acid digestion revealed that the temperature relationship of dolomite is within error of the one of calcite based on a compilation of many different published laboratories carried out in the same study.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
Classified as probably not a substantial claim.
Premisenone givenFor dolomite, the temperature dependence of the acid fractionation correction factor (AFF) is still debated.
“For dolomite, however, the temperature dependence of the AFF is still debated.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationDefliese et al. (2015) observed similar temperature sensitivities for the AFF of dolomite and calcite.
“Whereas Defliese et al. (2015) observed similar temperature sensitivities for the AFF of dolomite and calcite”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Defliese et al., 2015 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationIn modern environments only few places of active (proto-)dolomite formation at the surface are known, and in most of these cases microorganisms have been shown to play an active or passive role.
“In modern environments only few places of active (proto-)dolomite formation at the surface are known and in most of these cases microorganisms have been shown to play an active or passive role”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Vasconcelos and McKenzie, 1997 source
- cites Wright, 1999 source
- cites Bontognali et al., 2010 source
- Rests on an assumption: Dolomite is a very common carbonate mineral in ancient sediments, but is rarely found in modern environments.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe results of Müller et al. (2017a) indicate that the Δ47 acid fractionations of dolomite and calcite seem to be identical at about 90 °C acid digestion temperature.
“Interestingly, the results of Müller et al. (2017a) indicate that the Δ 47 acid fractionations of dolomite and calcite seems to be identical at about 90 °C acid digestion temperature”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Müller et al., 2017a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Interpretationown data§ Calibration of the oxygen and clumped isotope thermometers for (proto-) dolomite based on synthetic and natural carbonatesThis study demonstrates the necessity to apply (proto-)dolomite specific Δ47-T relationships for accurate temperature estimates of dolomite formation, ideally done at identical acid digestion temperatures to avoid additional uncertainties introduced by acid digestion temperature corrections.
“This study demonstrates the necessity to apply (proto-)dolomite specific Δ 47 -T relationships for accurate temperature estimates of dolomite formation, ideally done at identical acid digestion temperatures to avoid additional uncertainties introduced by acid digestion temperature corrections.”
Quote in the paperSubstantial claim- Rests on an assumption: Clumped isotope thermometry is solely temperature dependent.
Classified as probably not a substantial claim.
PremisecitationMurray et al. (2016) observed a much steeper temperature sensitivity for the AFF of dolomite relative to calcite.
“Murray et al. (2016) observed a much steeper temperature sensitivity for the AFF of dolomite relative to calcite.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Murray et al., 2016 source
May combine two claims.
Interpretationown dataThere is no trend over the course of the experiments, and the rest of the samples record the designated temperatures.
“There is no trend over the course of the experiments to observe and it seems the rest of the samples records the designated temperatures.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductreasoningFor the measurement sequences of this dolomite study, the ETH calcite standards were treated identically to the unknown (proto-)dolomite samples with 1200 s reaction time.
“For the measurement sequences of this dolomite study, the ETH calcite standards were treated identically to the unknown (proto-)dolomite samples with 1200 s reaction time.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataAll uncertainties are reported at the 95% confidence level and range between 0.02 and 0.14 ‰ for δ13C VPDB, 0.04-0.54 ‰ for δ18O VPDB, 0.05-0.77 ‰ for δ47, and 0.010-0.054 ‰ for Δ47 CDES 70°C.
“All uncertainties are reported at the 95% Cl and range between 0.02 and 0.14 ‰ for δ 13 C VPDB , 0.04-0.54‰ for δ 18 O VPDB , 0.05-0.77‰ for δ 47 and 0.010-0.054‰ for Δ 47 CDES 70°C .”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationDefliese et al. (2015) determined that the temperature dependence of the acid fractionation factor for dolomite between 25 and 90°C is identical to that of calcite, whereas Murray et al. (2016) observed a significantly steeper temperature dependence for dolomite.
“For instance, Defliese et al. (2015) determined that temperature dependence of the acid fractionation factor for dolomite between 25 and 90 °C is identical to the one of calcite whereas Murray et al. (2016) observed a temperature dependence significantly steeper for dolomite.”
Quote in the paperNot a substantial claim0 of 2 sources checkedClassified as probably not a substantial claim.
PremisecitationThe dolomite from Qatar was interpreted to be a primary precipitate from the pore fluids and not a replacement of calcite or aragonite (Brauchli et al., 2016).
“This dolomite was interpreted to be a primary precipitate from the pore fluids and not a replacement of calcite or aragonite (Brauchli et al., 2016).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Brauchli et al., 2016 source
May combine two claims.
PremisecitationOriginal data in all publications before 2017 were not processed using the IUPAC parameters, which can lead to significant changes in calculated compositions.
“the original data in all publications before 2017 were not processed using the IUPAC parameters, which also can lead to significant changes in calculated compositions (Daëron et al., 2016).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Daëron et al., 2016 source
May combine two claims.
PremisecitationThe annual mean water temperature of Lagoa Vermelha is approximately 25 °C, and the recorded temperature in 20 cm sediment depth was 25.5 ± 5.7 °C from November 2011 till May 2015 (Do Nascimento, 2018).
“The annual mean water temperature of Lagoa Vermelha is approximately 25 °C, and the recorded temperature in 20 cm sediment depth was 25.5 ± 5.7 °C from November 2011 till May 2015 (Do Nascimento, 2018)”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Do Nascimento, 2018 source
May combine two claims.
PremisecitationThe cultures of Vasconcelos et al. (2005) produced a mixture of calcite and proto-dolomite; dissolving calcite with EDTA left an Mg-rich phase with the main d(104) XRD peak in the dolomite position, more resistant to dissolution than carbonate phases with lower Mg concentration.
“The cultures of Vasconcelos et al. (2005) produced a mixture of calcite and proto-dolomite and before measurement they dissolved the calcite with EDTA, thus the Mg rich phase that has the main d(104) XRD peak in the position of a dolomite, was more resistant to dissolution than all carbonate phases with lower Mg concentration.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Vasconcelos et al., 2005 source
May combine two claims.
PremisecitationThe study of Horita (2014) covers 80-350°C, whereas Vasconcelos et al. (2005) covers 25-45°C with a slightly more shallow temperature relationship.
“The study of Horita (2014) contains samples that cover a temperature range from 80 to 350 °C, whereas the study of Vasconcelos et al. (2005) covers a temperature range of 25 to 45 °C with a slightly more shallow temperature relationship.”
Quote in the paperSubstantial claim0 of 2 sources checkedThe quote only partly states this claim.
InterpretationcitationAn additional uncertainty in the comparison is that Bonifacie et al. (2017) was not corrected for IUPAC parameters, so the exact difference remains unclear until their data are recalculated.
“An additional uncertainty in this comparison is the fact that the Bonifacie et al. (2017) was not corrected for the”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationreasoningIn case of the 220°C samples, the two samples with larger oxygen isotope fractionation could be explained by inheritance of a more poorly ordered dolomite formed at lower temperature, or by the degree of ordering affecting oxygen isotope equilibrium with water.
“In case of the 220 °C the two samples with larger oxygen isotope fractionation could be explained by in two ways, first it could be that they inherited the isotope composition of a more poorly ordered dolomite (like sample Leeds 34, which we did exclude here) that formed at lower temperature during the heating stage of the experiment or that the degree of ordering affects the oxygen isotope”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataHowever, these two calibrations give very comparable results to the Matthews and Katz (1977) calibration, suggesting that proto- or poorly ordered dolomites have a very similar oxygen isotope fractionation to ordered dolomites.
“However, these two calibrations give very comparable results to the Matthews and Katz (1977) calibration, suggesting that the proto-or poorly ordered dolomites have a very similar oxygen isotope fractionation to ordered dolomites.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Matthews and Katz (1977) source
May combine two claims.
InterpretationreasoningCombining the results of the three studies (this study, Vasconcelos et al., 2005, Horita, 2014) derives a more accurate temperature dependence of the water-(proto-)dolomite oxygen isotope fractionation because it is based on more data points and covers 25-350°C.
“In spite of the possible limitations discussed above, we propose to combine the results of the three studies to derive a more accurate temperature dependence of the water-(proto-)dolomite oxygen isotope fractionation because it is based on more data points and covers a wide temperature range of 25 to 350 °C (see Fig. 9).”
Quote in the paperSubstantial claim0 of 2 sources checkedMay combine two claims.
InterpretationcitationThe offset of about 30 ppm between calcite and dolomite, and between siderite and calcite for siderites reacted at 70°C, shows the necessity to treat different minerals digested at 70°C differently than calcites.
“The offset of about 30 ppm between calcite and dolomite as well as the offset observed between siderite and calcite for the siderites reacted at 70 °C (van Dijk et al., 2019), however, shows the necessity to treat different minerals digested at 70 °C differently than calcites.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites van Dijk et al., 2019 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Premisenone givenThe XRD pattern of the (proto-)dolomites used in Horita (2014) are very similar to ours, although they used various carbonate seeds to synthesize the dolomites.
“The XRD pattern of the (proto-)dolomites used in Horita (2014) are very similar to ours, although they used various carbonate seeds to synthesize the dolomites.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Horita (2014) source
May combine two claims.
InterpretationreasoningApplying an acid fractionation correction for Δ47 analyses on dolomite can result in large uncertainties and produce erroneous temperature estimates.
“The above discussion shows that applying an acid fractionation correction for Δ 47 analyses on dolomite can result in large uncertainties and produce erroneous temperature estimates.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningAdditional measurement of various dolomite and calcite standards would enable a better and more direct data comparison to solve this discrepancy.
“Additional measurement of various dolomite and calcite standards would enable a better and more direct data comparison to solve this discrepancy.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningRegular analysis of dolomite standards would help correct for offsets between laboratories digesting carbonates at different reaction temperatures, allowing laboratories without their own temperature calibration to apply dolomite-specific Δ47-T calibrations with more confidence.
“Once more the regular analysis of dolomite standards would help to correct for offsets between laboratories digesting the carbonates at different reaction temperatures allowing laboratories without own temperature calibration the application of dolomite specific Δ 47 -T calibrations with more confidence.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningFor a dolomite formed at 25°C, using the calcite calibration would give 6°C colder temperatures; for one formed at 80°C, 12°C colder temperatures, impacting calculated δ18O of the fluid source.
“For example for a dolomite formed at 25 °C we would obtain 6 °C colder temperatures if calculated as a calcite and for one formed at 80 °C we would obtain 12 °C colder temperatures, which further impacts the calculated δ 18 O of the fluid source.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationAll of these studies faced the challenge that in the laboratory at temperatures below 100°C it becomes difficult to synthesize dolomite, although naturally occurring dolomite samples in most cases formed at lower temperatures.
“Unfortunately all of these studies faced the challenge that in laboratory at temperatures below 100 °C it becomes difficult to synthesize dolomite, although naturally occurring dolomite samples in most cases formed at lower temperatures (e.g. via mixing of fluids, as diagenetic replacement phase or biologically mediated primary precipitate, see Warren (2000) for a review).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Warren (2000) source
May combine two claims.
PremisecitationThe (proto-)dolomite specific Δ47-temperature calibration of Bonifacie et al. (2017) is based on 12 samples formed at 25-350°C with 67 individual measurements and includes one sample from Lagoa Vermelha and one from Brejo do Espinho.
“The (proto-)dolomite specific Δ 47 -temperature calibration of Bonifacie et al. (2017) is based on 12 different samples formed at temperatures between 25 and 350 °C with a total of 67 individual measurements and contains one sample from Lagoa Vermelha and another one of a neighbouring lagoon (Brejo do Espinho) that formed under similar conditions as the ones we used in this study.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bonifacie et al., 2017 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Interpretationnone givenThe observation that the 70°C acid digestion calibration (without AFF) lies on the theoretical line for 25°C acid digestion might be because they underestimate the dolomite-specific Δ47 acid fractionation or could be coincidence.
“On the other hand, the observation that our calibration for 70 °C acid digestion temperature (without AFF) lies on their theoretical line for 25 °C acid digestion might be due that they underestimate the dolomite specific Δ 47 acid fractionation or could be just coincidence.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
InterpretationreasoningThe only way to remove these uncertainties for dolomite measurements is the use of dolomite reference materials in addition to calcite standards used to transfer data to CDES.
“The only way to remove these uncertainties for dolomite measurements is the use of dolomite reference materials in addition to the calcite standards that are used to transfer the data to the CDES.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataTherefore, there is no difference in the temperature dependence of Δ47 between ordered stoichiometric dolomites and proto-dolomite, or if such differences exist, they are well below current analytical uncertainty.
“Therefore, we conclude that there is no difference in the temperature dependence of Δ 47 between ordered stoichiometric dolomites and so-called proto-dolomite, or, if such differences exist, they are well below the current analytical uncertainty.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationWe consider this a good indication that these phases, although not well ordered, are not very high magnesium calcites, but poorly ordered dolomites.
“We consider this a good indication that these phases, although not well ordered, are not very high magnesium calcites (Kaczmarek and Thornton, 2017), but poorly ordered dolomites.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Kaczmarek and Thornton, 2017 source
Classified as probably not a substantial claim.
PremisecitationMurray and Swart (2017) showed that for dolomite formed at 25°C, the calculated δ18O of the fluid source can vary by up to 3.6‰ depending on which calibration is used.
“In Fig. 1 they show that for dolomite formed at 25 °C the calculated δ 18 O of the fluid source can vary by up to 3.6 ‰ depending on which calibration is used.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Murray and Swart (2017) source
May combine two claims.
PremisecitationAn offset between the Δ47-T relationship of dolomite and calcite was predicted by theoretical calculations of Guo et al. (2009), but the offset was of opposite sign to what is observed experimentally.
“An offset between the Δ 47 -T relationship of dolomite and calcite was also predicted by theoretical calculations of Guo et al. (2009), however, the offset was of opposite sign of what we observe experimentally.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Guo et al., 2009 source
Probably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenA third explanation for the 220°C samples is that some solution leaked/evaporated, slightly enriching the remaining solution in 18O.
“A third explanation could be that some of the solution leaked/evaporated out of the experiment container slightly enriching the remaining solution in the heavier 18 O (these would be then the two samples matching Horita's data Leeds 84 and 85).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing). May combine two claims.
InterpretationreasoningThis would be valuable not only for clumped isotopes but also for oxygen isotopes, as there are also uncertainties in oxygen isotope fractionation with different preparation systems.
“This would be valuable not only for clumped isotopes but also for oxygen isotopes as well, as there are also uncertainties in oxygen isotope fractionation with different preparation systems.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisereasoningWhile proto-dolomites are not well ordered, they show properties that distinguish them from calcite.
“While these proto-dolomites are not well ordered, they show properties that distinguish them from calcite.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenFurther uncertainties might originate from the oxygen isotope analyses of the water when comparing studies published during almost half a century.
“Further uncertainties might originate from the oxygen isotope analyses of the water when comparing studies published during almost half a century.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenSansa is the product of diagenetic alteration of a primary early Triassic marine carbonate.
“which is the product of diagenetic alteration of a primary early Triassic marine carbonate (Table 3).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningOther unknown factors in sample preparation and/or data standardization are the cause for the discrepancy with Winkelstern et al. (2016).
“This points to other unknown factors in the sample preparation and/or data standardization as cause for the discrepancy.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
Dolomite is a very common carbonate mineral in ancient sediments, but is rarely found in modern environments.
“Dolomite is a very common carbonate mineral in ancient sediments, but is rarely found in modern environments.”
The paper relies on this without support.
The controls on dolomite formation are still debated after more than two centuries of research.
“Because of the difficulties in precipitating dolomite in the laboratory at low temperatures, the controls on its formation are still debated after more than two centuries of research.”
The paper relies on this without support.
Two important parameters to constrain the environment of dolomitization are the temperature of formation and the oxygen isotope composition of the fluid from which it precipitated.
“Two important parameters to constrain the environment of dolomitization are the temperature of formation and the oxygen isotope composition of the fluid from which it precipitated.”
The paper relies on this without support.
To improve models of dolomitization it is crucial to better characterize the temperature of formation and the composition of the fluid responsible for dolomite formation.
“To improve our models of dolomitization it is crucial to better characterize the temperature of formation and the composition of the fluid responsible for dolomite formation.”
The paper relies on this without support.
Clumped isotope thermometry is solely temperature dependent.
“Clumped isotope thermometry is a measure of the abundance of the 13 Ce 18 O bond within the carbonate mineral relative to its stochastic isotope distributions, which is solely temperature dependent.”
The paper relies on this without support.
The oxygen isotope fractionation data from this study, Vasconcelos et al. (2005) and Horita (2014) are directly comparable and can be combined into a single temperature relationship.
“Combination of these three datasets resulted in the black dashed line giving the displayed linear relationship and covers a temperature range from 25 to 350 °C.”
The paper relies on this without support.
The (proto-)dolomite samples used for calibration formed in isotopic equilibrium with their precipitation solutions.
“We propose a new (proto-)dolomite specific Δ 47 -T calibration for 70 °C acid digestion covering a temperature range from 25 to 1100 °C, based on 22 different (proto-)dolomite samples that formed at known temperatures and consists of a total of 435 individual measurements.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
There is a lack of consensus on optimal analytical conditions for different types of carbonate minerals, including calcite, dolomite, and magnesite, to determine their carbon and oxygen isotope compositions.
“Obviously, there is a lack of consensus on optimal analytical conditions for different types of carbonate minerals, including calcite, dolomite, and magnesite, to determine their carbon and oxygen isotope compositions (Table 2) (e.g., [14, 15, 22, 23, 24, 25, 26, 27, 28]).”
From Guidelines for Accurate and Precise Stable Isotope Analysis of Calcite, Dolomite, and Magnesite Using a Carbonate Device for Continuous Flow‐Isotope Ratio Mass Spectrometry (CF‐IRMS) (2025) · cites this paper as [28]
The Introduction and §4.1.2 describe disagreement over phosphoric-acid fractionation corrections for dolomite versus calcite, and §4.1.2 notes uncertainty in oxygen-isotope measurements across preparation systems. That supports a narrower concern about mineral-specific analytical conditions, chiefly for clumped and oxygen isotopes. The paper does not establish a lack of consensus for carbon-isotope analysis across calcite, dolomite, and magnesite; no page numbers were provided for these passages. (LLM, conf=0.84)
Experimental — accuracy not yet measuredDolomite non-InterCarb anchors measured here (SRM-88b and Rodolo) and in other studies (Defliese et al., 2015; Lucarelli et al., 2023; Müller et al., 2019; Murray et al., 2016; Upadhyay et al., 2021) have a relatively narrow range of Δ47 (0.52-0.63‰) and δ47 (-0.8-4.8‰; Figure S2).
“Dolomite non-InterCarb anchors measured here (SRM-88b and Rodolo) and in other studies (Defliese etal.,2015; Lucarelli etal.,2023; Müller etal.,2019; Murray etal.,2016; Upadhyay etal.,2021) have a relatively narrow range of Δ 47 (0.52-0.63‰) and δ 47 (-0.8-4.8‰; Figure S2 in Supporting InformationS1).”
From Re-Assessing the Need for Apatite- and Dolomite-Specific Calibrations of the Carbonate Clumped Isotope Thermometer (2024) · cites this paper as Müller et al., 2019
Section 3.4 and Table 3 report Δ47 values of 0.522‰ for NIST SRM 88b and 0.632‰ for Rodolo, matching the cited range when rounded. Our copy does not report δ47 values for these anchors or establish the claimed −0.8 to 4.8‰ range; its δ13C and δ18O values are different measurements. Page numbers were not available in the indexed passages. (LLM, conf=0.86)
Experimental — accuracy not yet measuredEasotope uses a 'moving-window' standardization approach, whereas D47crunch uses a pooled regression model of all analyses (anchors and unknowns); the moving-window approach is more appropriate for the Müller et al. (2019) data set given the distribution of InterCarb anchors.
“Easotope uses a 'moving-window' standardization approach, whereas D47crunch uses a pooled regression model of all analyses (anchors and unknowns); the moving-window approach is more appropriate for the Müller etal.(2019) data set given the distribution of InterCarb anchors.”
From Re-Assessing the Need for Apatite- and Dolomite-Specific Calibrations of the Carbonate Clumped Isotope Thermometer (2024) · cites this paper as Müller et al. (2019)
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredAll three studies concluded that dolomite ordering did not affect Δ47, but each study has a narrow range of ordering ratios that cannot be compared to each other without I-CDES standards.
“All three studies concluded that dolomite ordering did not affect Δ 47 , but each study has a narrow range of ordering ratios that cannot be compared to each other without I-CDES standards.”
From Re-Assessing the Need for Apatite- and Dolomite-Specific Calibrations of the Carbonate Clumped Isotope Thermometer (2024) · cites this paper as Müller et al., 2019
Section 4.1.3 concludes that differing degrees of dolomite ordering do not measurably change the temperature dependence of Δ47, within analytical uncertainty. Sections 4.1.3 and 4.3 recommend dolomite standards to improve inter-laboratory comparisons, but do not establish that all three studies reached this conclusion, that each had a narrow range of ordering ratios, or that their results cannot be compared without I-CDES standards. The paper discusses CDES, not I-CDES. (LLM, conf=0.86)
Experimental — accuracy not yet measuredThe temperature calibration of ref. 50 was used because it is based on 12 samples exhibiting a stronger correlation (R2 = 0.997), whereas the calibration of ref. 62 was based on only five samples with a modest correlation (R2 = 0.864).
“Because the temperature calibration of ref. 62 was based on only five samples exhibiting a modest correlation (R 2 = 0.864), we used the calibration of ref. 50, which is based on 12 samples exhibiting a stronger correlation (R 2 = 0.997).”
From Massive formation of early diagenetic dolomite in the Ediacaran ocean: Constraints on the "dolomite problem" (2020) · cites this paper as [62]
Section 3.3 reports R² = 0.864, as claimed, but says the calibration used 289 measurements of 20 samples formed at five temperatures—not five samples. The cited paper does not establish the stated sample count or R² for ref. 50. (LLM, conf=0.90)
Experimental — accuracy not yet measured
Two samples, originally from Müller et al. (2019), show up to ~20% greater dissolution in 90 min reaction time (Figure S4), suggesting incomplete dissolution of carbonate in 25 min.
“Two samples, originally from Müller etal.(2019), show up to ∼20% greater dissolution in 90min reaction time (Figure S4 in Supporting InformationS1), suggesting incomplete dissolution of carbonate in 25min.”
From Re-Assessing the Need for Apatite- and Dolomite-Specific Calibrations of the Carbonate Clumped Isotope Thermometer (2024) · cites this paper as Müller et al. (2019)
This observation corroborates the findings of Müller et al. (2019), who similarly saw no Δ47 effect of reaction time.
“This observation corroborates the findings of Müller etal.(2019), who similarly saw no Δ 47 effect of reaction time.”
From Re-Assessing the Need for Apatite- and Dolomite-Specific Calibrations of the Carbonate Clumped Isotope Thermometer (2024) · cites this paper as Müller et al. (2019)
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Rodolo fluid uncertainty differs by a factor of ten
MinorThe prose gives an uncertainty of ±0.04‰ for Rodolo's fluid oxygen-isotope value, while Table 3 gives ±0.4‰ for that value.
“a fluid source with δ 18 O of +1.7 ± 0.04 ‰.”
“| Rodolo | -3.71 ± 0.01 | 2.77 ± 0.02 | 0.632 ± 0.006 | 25 ± 2 | 1.7 ± 0.4 | 151 | 30.95 | 0.35 | 50.0 |”
Stated oxygen-isotope uncertainty range excludes Leeds 34
MinorThe prose places the upper uncertainty at ±0.44‰, whereas Table 2 reports ±0.54‰ for the oxygen-isotope composition of Leeds 34.
“The uncertainty of the oxygen isotope composition of the (proto-)dolomite samples varies between ± 0.03-0.44‰ at the 95% Cl”
“| Leeds 34 | 220 ± 2 | -7.45 ± 0.14 | -24.03 ± 0.54 | -16.95 ± 0.70 | 0.322 ± 0.054 | 6 |”
Reported 70 °C clumped-isotope range omits Leeds 6
MinorThe stated upper limit is 0.515‰, but Table 2 reports 0.523‰ for Leeds 6, a sample synthesized at 70 °C.
“the Δ 47 CDES 70°C values range between 0.497 and 0.515 ‰ for samples synthesized at 70 °C”
“| Leeds 6 | 70 ± 2 | -7.17 ± 0.03 | -14.90 ± 0.06 | -7.07 ± 0.06 | 0.523 ± 0.020 | 11 |”
Cites
Feinleib, M., & Zar, J. H. (1975) · Journal of the American Statistical Association · doi:10.2307/2285423 · Cited by 12,671 · see citing works
Compilation of stable isotope fractionation factors of geochemical interest
Friedman, I., & O'Neil, J. R. (1977) · Professional Paper · doi:10.3133/pp440kk · Cited by 2,646 · cited 4× · see citing works
“01110 for 25 °C from Friedman and O'Neil (1977). Further uncertainties might originate from the oxygen isotope analyses of the water when comparing studies published during almost half a century. In Fig. 9 we compiled the oxygen isotope fractionation between (proto-) dolomites and water of this study with the two most…”
BackgroundMethodInfluentialEquilibrium and nonequilibrium oxygen isotope effects in synthetic carbonates
Kim, S.-T., & O'Neil, J. R. (1997) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(97)00169-5 · Cited by 2,558 · see citing works
Dolomite: occurrence, evolution and economically important associations
Warren, J. (2000) · Earth-Science Reviews · doi:10.1016/s0012-8252(00)00022-2 · Cited by 1,435 · cited 2× · see citing works
“…temperatures below 100 °C it becomes difficult to synthesize dolomite, although naturally occurring dolomite samples in most cases formed at lower temperatures (e.g. via mixing of fluids, as diagenetic replacement phase or biologically mediated primary precipitate, see Warren (2000) for a review).”
BackgroundComparison of stable isotope reference samples
Coplen, T. B., Kendall, C., & Hopple, J. A. (1983) · Nature · doi:10.1038/302236a0 · Cited by 1,076 · see citing works
13C–18O bonds in carbonate minerals: a new kind of paleothermometer
Ghosh, P., Adkins, J., Affek, H., Balta, B., Guo, W., Schauble, E. A., Schrag, D., & Eiler, J. M. (2006) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2005.11.014 · Cited by 914 · see citing works
An isotopic study of siderites, dolomites and ankerites at high temperatures
Rosenbaum, J., & Sheppard, S. M. F. (1986) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(86)90396-0 · Cited by 827 · cited 3× · see citing works
“For δ18O we used an AFF of 1.009926 for dolomite (Rosenbaum and Sheppard, 1986).”
MethodInfluential“Clumped-isotope” geochemistry—The study of naturally-occurring, multiply-substituted isotopologues
Eiler, J. M. (2007) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2007.08.020 · Cited by 774 · see citing works
The Isotopic and Trace Element Geochemistry of Dolomite: The State of the Art
Land, L. S. (1980) · Concepts and Models of Dolomitization · doi:10.2110/pec.80.28.0087 · Cited by 664 · cited 1× · see citing works
“Complementary to microscopic methods, geochemical tools such as stable isotopes of oxygen, carbon or strontium were used to gain further insights in the environment or the “parental fluid” in which the mineral precipitated (e.g. Land, 1980; Wilson et al., 1990; Preto et al., 2015).”
Defining an absolute reference frame for ‘clumped’ isotope studies of CO2
Dennis, K. J., Affek, H. P., Passey, B. H., Schrag, D. P., & Eiler, J. M. (2011) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2011.09.025 · Cited by 627 · see citing works
Vasconcelos, C., & McKenzie, J. A. (1997) · Journal of Sedimentary Research · doi:10.1306/d4268577-2b26-11d7-8648000102c1865d · Cited by 620 · see citing works
The Origin of Massive Dolomite
Land, L. S. (1985) · Journal of Geological Education · doi:10.5408/0022-1368-33.2.112 · Cited by 614 · cited 1× · see citing works
“…remains unclear how this mineral forms at Earth surface conditions and why it is so abundant during certain time intervals in the geological past (Land, 1985; Given and Wilkinson, 1987; Spencer and Hardie, 1990; Chai et al., 1995; Hardie, 1996; Holland et al., 1996; Wright, 1997; Land, 1998;…”
BackgroundAbsolute18O content of standard mean ocean water
Baertschi, P. (1976) · Earth and Planetary Science Letters · doi:10.1016/0012-821x(76)90115-1 · Cited by 557 · see citing works
Ibáñez‐Sanz, G., Díez-Villanueva, A., Alonso, M. H., Rodríguez‐Moranta, F., Pérez‐Gómez, B., Bustamante, M., Martín, V., Llorca, J., Amiano, P., Ardanáz, E., et al. (2017) · Scientific Reports · doi:10.1038/srep46807 · Cited by 505 · see citing works
High precision measurements of 17 O/ 16 O and 18 O/ 16 O ratios in H 2 O
Barkan, E., & Luz, B. (2005) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.2250 · Cited by 493 · see citing works
Gregg, J. M., Bish, D. L., Kaczmarek, S. E., & Machel, H. G. (2015) · Sedimentology · doi:10.1111/sed.12202 · Cited by 480 · see citing works
Oxygen isotope fractionation in carbonate and sulfate minerals.
Zheng, Y.-F. (1999) · GEOCHEMICAL JOURNAL · doi:10.2343/geochemj.33.109 · Cited by 468 · cited 2× · see citing works
“Another approach to overcome the difficulty of precipitating low temperature dolomites was the theoretical modelling of the dolomite water oxygen isotope fractionation of Zheng (1999).”
BackgroundPassey, B. H., Levin, N. E., Cerling, T. E., Brown, F. H., & Eiler, J. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001824107 · Cited by 449 · see citing works
Measurement of ratios of total oxygen of carbonates
Sharma, T., & Clayton, R. N. (1965) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(65)90011-6 · Cited by 433 · see citing works
Oxygen isotope composition of the oceanic crust and its bearing on seawater
Muehlenbachs, K., & Clayton, R. N. (1976) · Journal of Geophysical Research Atmospheres · doi:10.1029/jb081i023p04365 · Cited by 413 · see citing works
Oxygen-Isotope Fractionations in Systems Containing Dolomite
Northrop, D. A., & Clayton, R. N. (1966) · The Journal of Geology · doi:10.1086/627153 · Cited by 405 · cited 1× · see citing works
“Some earlier studies produced dolomite at high temperatures> 100 °C and extrapolated their results to lower temperatures (Northrop and Clayton, 1966; Matthews and Katz, 1977).”
ResultLand, L. S. (1998) · Aquatic Geochemistry · doi:10.1023/a:1009688315854 · Cited by 396 · see citing works
Rapid Uplift of the Altiplano Revealed Through 13C-18O Bonds in Paleosol Carbonates
Ghosh, P., Garzione, C., & Eiler, J. (2006) · Science · doi:10.1126/science.1119365 · Cited by 382 · see citing works
Dolomite formation within microbial mats in the coastal sabkha of Abu Dhabi (United Arab Emirates)
BONTOGNALI, T. R. R., VASCONCELOS, C., WARTHMANN, R. J., BERNASCONI, S. M., DUPRAZ, C., STROHMENGER, C. J., & McKENZIE, J. A. (2010) · Sedimentology · doi:10.1111/j.1365-3091.2009.01121.x · Cited by 360 · cited 1× · see citing works
“been shown to play an active or passive role (e.g. Vasconcelos and McKenzie, 1997; Wright, 1999; Bontognali et al., 2010; Brauchli et al., 2016).”
BackgroundSelf-citationVasconcelos, C., McKenzie, J. A., Warthmann, R., & Bernasconi, S. M. (2005) · Geology · doi:10.1130/g20992.1 · Cited by 354 · cited 5× · see citing works
“(2017) used samples from the same Brazilian hypersaline lagoon (Vasconcelos and McKenzie, 1997) we have used as well as bacterially-mediated precipitated proto-dolomites that were originally used to calibrate the oxygen isotope fractionation between dolomite and the water (Vasconcelos et al., 2005).”
BackgroundMethodInfluentialSelf-citationWright, D. T. (1999) · Sedimentary Geology · doi:10.1016/s0037-0738(99)00037-8 · Cited by 314 · see citing works
Absolute isotopic abundance ratios and the accuracy of Δ47 measurements
Daëron, M., Blamart, D., Peral, M., & Affek, H. P. (2016) · Chemical Geology · doi:10.1016/j.chemgeo.2016.08.014 · Cited by 310 · see citing works
Bernasconi, S. M., Müller, I. A., Bergmann, K. D., Breitenbach, S. F. M., Fernandez, A., Hodell, D. A., Jaggi, M., Meckler, A. N., Millan, I., & Ziegler, M. (2018) · Geochemistry, Geophysics, Geosystems · doi:10.1029/2017gc007385 · Cited by 301 · see citing works
Self-citationOxygen and carbon isotope fractionation in the system dolomite–water–CO2 to elevated temperatures
Horita, J. (2014) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2013.12.027 · Cited by 298 · cited 11× · see citing works
“Their high temperature samples were synthesized by placing calcite or aragonite in Ca- Mg-(Na)-Cl solutions in stainless steel reactor vessels that were heated for several days at the corresponding experiment temperature of 100 to 350 °C (Horita, 2014 and Bonifacie et al., 2017).”
BackgroundMethodResultInfluentialStructural and compositional variations in some natural dolomites
Goldsmith, J. R., & Graf, D. L. (1958) · The Journal of Geology · doi:10.1086/626547 · Cited by 295 · see citing works
Guo, W., Mosenfelder, J. L., Goddard, W. A., & Eiler, J. M. (2009) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2009.05.071 · Cited by 262 · cited 7× · see citing works
“Ferry et al. (2011) on the other hand, used another approach: they added a correction factor of 0.02 ‰ and used the theoretical calibration of Guo et al. (2009) to calculate formation temperatures of dolomites.”
BackgroundMethodResultInfluentialKele, S., Breitenbach, S. F. M., Capezzuoli, E., Meckler, A. N., Ziegler, M., Millan, I. M., Kluge, T., Deák, J., Hanselmann, K., John, C. M., et al. (2015) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2015.06.032 · Cited by 261 · cited 8× · see citing works
“…included in this calibration, of many samples spread over a much wider temperature range than existing studies (analogues to the calibrations of Kele et al., 2015 (recalculated in Bernasconi et al., 2018); Kluge et al., 2015; Winkelstern et al., 2016 (recalculated in Petersen et al., 2019);…”
BackgroundMethodInfluentialSelf-citationOxygen isotope fractionation during the dolomitization of calcium carbonate
Matthews, A., & Katz, A. (1977) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(77)90249-6 · Cited by 260 · cited 7× · see citing works
“Some earlier studies produced dolomite at high temperatures> 100 °C and extrapolated their results to lower temperatures (Northrop and Clayton, 1966; Matthews and Katz, 1977).”
BackgroundMethodResultInfluentialButler, G. P. (1969) · Journal of Sedimentary Research · doi:10.1306/74d71be5-2b21-11d7-8648000102c1865d · Cited by 252 · see citing works
The isotopic composition of secondary dolomites
Fritz, P., & Smith, D. G. W. (1970) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(70)90056-6 · Cited by 247 · see citing works
John, C. M., & Bowen, D. (2016) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.7720 · Cited by 247 · see citing works
Meckler, A. N., Ziegler, M., Millán, M. I., Breitenbach, S. F. M., & Bernasconi, S. M. (2014) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6949 · Cited by 239 · see citing works
Self-citationMost Earth-surface calcites precipitate out of isotopic equilibrium
Daëron, M., Drysdale, R. N., Peral, M., Huyghe, D., Blamart, D., Coplen, T. B., Lartaud, F., & Zanchetta, G. (2019) · Nature Communications · doi:10.1038/s41467-019-08336-5 · Cited by 236 · see citing works
Bonifacie, M., Calmels, D., Eiler, J. M., Horita, J., Chaduteau, C., Vasconcelos, C., Agrinier, P., Katz, A., Passey, B. H., Ferry, J. M., et al. (2017) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2016.11.028 · Cited by 233 · cited 10× · see citing works
“Bonifacie et al., 2017; Ryb et al., 2017). However, from the observations of the heating study in Müller et al. (2017a) where calcites were scrambled at 1000 °C in two different heating devices and retained”
BackgroundMethodResultInfluentialSelf-citationSome hydrothermal syntheses of dolomite and protodolomite
Graf, D. L., & Goldsmith, J. R. (1956) · The Journal of Geology · doi:10.1086/626332 · Cited by 225 · see citing works
Petersen, S. V., Defliese, W. F., Saenger, C., Daëron, M., Huntington, K. W., John, C. M., Kelson, J. R., Bernasconi, S. M., Colman, A. S., Kluge, T., et al. (2019) · Geochemistry, Geophysics, Geosystems · doi:10.1029/2018gc008127 · Cited by 209 · cited 12× · see citing works
“…laboratory conditions (Kele et al., 2015) and the (proto-)dolomite dataset (n=37) for common acid bath digestion at 75 °C of Winkelstern et al. (2016), with the latter two being fully re-evaluated with the new IUPAC parameters in Bernasconi et al. (2018) and Petersen et al. (2019), respectively.”
BackgroundMethodResultInfluentialSelf-citationDolomite formation and biogeochemical cycles in the Phanerozoic
Burns, S. J., Mckenzie, J. A., & Vasconcelos, C. (2000) · Sedimentology · doi:10.1046/j.1365-3091.2000.00004.x · Cited by 201 · see citing works
Defliese, W. F., Hren, M. T., & Lohmann, K. C. (2015) · Chemical Geology · doi:10.1016/j.chemgeo.2014.12.018 · Cited by 190 · see citing works
Given, R. K., & Wilkinson, B. H. (1987) · Journal of Sedimentary Research · doi:10.1306/212f8cf1-2b24-11d7-8648000102c1865d · Cited by 190 · see citing works
High-precision measurements of 17O/16O and 18O/16O ratios in CO2.
Barkan, E., & Luz, B. (2012) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6400 · Cited by 187 · see citing works
Atomic weights of the elements 1995 (Technical Report)
Coplen, T. B. (1996) · Pure and Applied Chemistry · doi:10.1351/pac199668122339 · Cited by 187 · see citing works
Kelson, J. R., Huntington, K. W., Schauer, A. J., Saenger, C., & Lechler, A. R. (2017) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2016.10.010 · Cited by 177 · cited 1× · see citing works
“…minor differences to reported slopes of recent calcite calibrations (e.g. Bonifacie et al., 2017; Bernasconi et al., 2018; Breitenbach et al., 2018; Kelson et al., 2017; Peral et al., 2018; Daëron et al., 2019) or a new siderite calibration (van Dijk et al., 2019) strongly suggests that the slope…”
BackgroundBernasconi, S. M., Hu, B., Wacker, U., Fiebig, J., Breitenbach, S. F. M., & Rutz, T. (2013) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6490 · Cited by 166 · see citing works
Self-citationA revised calibration of the clumped isotope thermometer
Zaarur, S., Affek, H. P., & Brandon, M. T. (2013) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2013.07.026 · Cited by 163 · see citing works
A route for the direct crystallization of dolomite
Rodriguez-Blanco, J. D., Shaw, S., & Benning, L. G. (2015) · American Mineralogist · doi:10.2138/am-2015-4963 · Cited by 161 · cited 2× · see citing works
“described in Rodriguez-Blanco et al. (2015). Equimolar aqueous solutions of Na2CO3, CaCl2 and MgCl2 were mixed at room temperature, which led to an instantaneous precipitation of a white, gel-like solid confirmed by X-ray diffraction to be amorphous.”
BackgroundSelf-citationRelationship between Dolomite Nonstoichiometry and Carbonate Facies Parameters
Lumsden, D. N., & Chimahusky, J. S. (1980) · Concepts and Models of Dolomitization · doi:10.2110/pec.80.28.0123 · Cited by 161 · see citing works
A hydrothermal origin for isotopically anomalous cap dolostone cements from south China
Bristow, T. F., Bonifacie, M., Derkowski, A., Eiler, J. M., & Grotzinger, J. P. (2011) · Nature · doi:10.1038/nature10096 · Cited by 157 · see citing works
Kluge, T., John, C. M., Jourdan, A.-L., Davis, S., & Crawshaw, J. (2015) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2015.02.028 · Cited by 155 · cited 1× · see citing works
“…a much wider temperature range than existing studies (analogues to the calibrations of Kele et al., 2015 (recalculated in Bernasconi et al., 2018); Kluge et al., 2015; Winkelstern et al., 2016 (recalculated in Petersen et al., 2019); Bonifacie et al., 2017), the uncertainty of the linear…”
BackgroundFluid-Mineral Interactions: A Tribute to H. P. Eugster
Krauskopf, K. B. (1991) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(91)90147-w · Cited by 147 · see citing works
Müller, I., Fernandez, A., Radke, J., van Dijk, J., Bowen, D. A., Schwieters, J., & Bernasconi, S. (2017) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.7878 · Cited by 138 · see citing works
Self-citationCocker, J. D., Griffin, B. J., & Muehlenbachs, K. (1982) · Earth and Planetary Science Letters · doi:10.1016/0012-821x(82)90043-7 · Cited by 136 · see citing works
Hood, A. V. S., Wallace, M. W., & Drysdale, R. N. (2011) · Geology · doi:10.1130/g32119.1 · Cited by 133 · see citing works
Wilson, E. N., Hardie, L. A., & Phillips, O. M. (1990) · American Journal of Science · doi:10.2475/ajs.290.7.741 · Cited by 133 · see citing works
Direct physical evidence of dolomite recrystallization
Kaczmarek, S. E., & Sibley, D. F. (2014) · Sedimentology · doi:10.1111/sed.12119 · Cited by 131 · see citing works
Microbial Carbonates in Space and Time: Implications for Global Exploration and Production
Bosence, D. W. J., Gibbons, K., Heron, D. P. L., Morgan, W. A., Pritchard, T., & Vining, B. A. (2015) · Cited by 128 · see citing works
Kaczmarek, S. E., & Thornton, B. P. (2017) · Chemical Geology · doi:10.1016/j.chemgeo.2017.08.004 · Cited by 128 · see citing works
An automated method for ‘clumped-isotope` measurements on small carbonate samples
Schmid, T. W., & Bernasconi, S. M. (2010) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.4598 · Cited by 124 · see citing works
Self-citationFerry, J. M., Passey, B. H., Vasconcelos, C., & Eiler, J. M. (2011) · Geology · doi:10.1130/g31845.1 · Cited by 123 · see citing works
Self-citationDale, A., John, C. M., Mozley, P. S., Smalley, P. C., & Muggeridge, A. H. (2014) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2014.03.004 · Cited by 123 · see citing works
Updated calibration of the clumped isotope thermometer in planktonic and benthic foraminifera
Peral, M., Daëron, M., Blamart, D., Bassinot, F., Dewilde, F., Smialkowski, N., Isguder, G., Bonnin, J., Jorissen, F., Kissel, C., et al. (2018) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2018.07.016 · Cited by 113 · cited 2× · see citing works
“, 2019) and a common acid bath extraction line at 90 °C (Peral et al., 2018) for planktic and benthic foraminifera clearly lie below our new dolomite calibration by about 30 ppm, but with slopes that are within error of each other.”
BackgroundSynsedimentary diagenesis in a Cryogenian reef complex: Ubiquitous marine dolomite precipitation
Hood, A. V. S., & Wallace, M. W. (2012) · Sedimentary Geology · doi:10.1016/j.sedgeo.2012.02.004 · Cited by 112 · see citing works
Grauel, A.-L., Schmid, T. W., Hu, B., Bergami, C., Capotondi, L., Zhou, L., & Bernasconi, S. M. (2013) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2012.12.049 · Cited by 111 · cited 3× · see citing works
“This is because the sample size reduction allows to carry out high-resolution paleo-climate reconstructions (Grauel et al., 2013; Rodríguez-Sanz et al., 2017; Breitenbach et al., 2018; Leutert et al., 2019) or the study of complex diagenetic vein fabrics (Millán et al.”
BackgroundMethodResultSelf-citationvan Lith, Y., Vasconcelos, C., Warthmann, R., Martins, J. C. F., & McKenzie, J. A. (2002) · Hydrobiologia · doi:10.1023/a:1021323425591 · Cited by 111 · see citing works
Self-citationStevenson, E., Hermoso, M., Rickaby, R. E. M., Tyler, J. J., Minoletti, F., Parkinson, I. J., Mokadem, F., & Burton, K. W. (2013) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2013.11.043 · Cited by 105 · see citing works
Fernandez, A., Müller, I. A., Rodríguez‐Sanz, L., van Dijk, J., Looser, N., & Bernasconi, S. M. (2017) · Geochemistry, Geophysics, Geosystems · doi:10.1002/2017gc007106 · Cited by 101 · cited 2× · see citing works
“…of carbonates and the oxygen isotope composition of the fluid source (e.g. Ghosh et al., 2006a, 2006b; Eiler, 2007; Bristow et al., 2011; Ferry et al., 2011; Dale et al., 2014; Millán et al., 2016; Winkelstern and Lohmann, 2016; Rodríguez-Sanz et al., 2017; Suarez et al., 2017; Mangenot…”
BackgroundMethodInfluentialSelf-citationExperimental calibration of clumped isotope reordering in dolomite
Lloyd, M. K., Ryb, U., & Eiler, J. M. (2018) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2018.08.036 · Cited by 100 · cited 1× · see citing works
“These samples are important for a more accurate interpretation of natural dolomites that retained extremely hot temperature signals near magmatic intrusions (e.g. Lloyd et al., 2017; Ryb et al., 2017; Lloyd et al., 2018).”
BackgroundBerra, F., Jadoul, F., & Anelli, A. (2009) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/j.palaeo.2009.06.037 · Cited by 96 · see citing works
Clumped isotope analysis of carbonates: comparison of two different acid digestion techniques
Wacker, U., Fiebig, J., & Schoene, B. R. (2013) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6609 · Cited by 92 · see citing works
Shallow burial alteration of dolomite and limestone clumped isotope geochemistry
Winkelstern, I. Z., & Lohmann, K. C. (2016) · Geology · doi:10.1130/g37809.1 · Cited by 87 · cited 4× · see citing works
“Δ47-temperature relationship and the ones reported in Winkelstern et al. (2016) reevaluated in Petersen et al. (2019) and the one in Bonifacie et al.”
MethodInfluentialDetermining the Δ47 acid fractionation in dolomites
Murray, S. T., Arienzo, M. M., & Swart, P. K. (2016) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2015.10.029 · Cited by 83 · see citing works
Dolomitization and Limestone Diagenesis
Pray, L. C., & Murray, R. C. (1965) · SEPM (Society for Sedimentary Geology) eBooks · doi:10.2110/pec.65.07 · Cited by 83 · see citing works
García Del Cura, M. A., Calvo, J. P., Ordóñez, S., Jones, B. F., & Cañaveras, J. C. (2001) · Sedimentology · doi:10.1046/j.1365-3091.2001.00388.x · Cited by 81 · see citing works
Hu, B., Radke, J., Schlüter, H., Heine, F., Zhou, L., & Bernasconi, S. (2014) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6909 · Cited by 79 · see citing works
Self-citationSmeraglia, L., Bernasconi, S. M., Berra, F., et al. (2018) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2018.06.013 · Cited by 78 · see citing works
Self-citationThe importance of microbial mats for dolomite formation in the Dohat Faishakh sabkha, Qatar
Brauchli, M., McKenzie, J. A., Strohmenger, C. J., Sadooni, F., Vasconcelos, C., & Bontognali, T. R. R. (2016) · Carbonates and Evaporites · doi:10.1007/s13146-015-0275-0 · Cited by 74 · see citing works
Self-citationKaczmarek, S. E., & Sibley, D. F. (2007) · Journal of Sedimentary Research · doi:10.2110/jsr.2007.035 · Cited by 72 · see citing works
Mangenot, X., Gasparrini, M., Rouchon, V., & Bonifacie, M. (2017) · Sedimentology · doi:10.1111/sed.12427 · Cited by 70 · see citing works
Clumped isotope thermometry of calcite and dolomite in a contact metamorphic environment
Lloyd, M. K., Eiler, J. M., & Nabelek, P. I. (2017) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2016.10.037 · Cited by 68 · see citing works
Energetics of calcium-rich dolomite
Chai, L., Navrotsky, A., & Reeder, R. J. (1995) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(95)00011-9 · Cited by 67 · see citing works
Application of clumped isotope thermometry to benthic foraminifera
Piasecki, A., Bernasconi, S. M., Grauel, A., Hannisdal, B., Ho, S. L., Leutert, T. J., Marchitto, T. M., Meinicke, N., Tisserand, A., & Meckler, N. (2019) · Geochemistry, Geophysics, Geosystems · doi:10.1029/2018gc007961 · Cited by 66 · see citing works
Self-citationRodríguez-Sanz, L., Bernasconi, S., Marino, G., Heslop, D., Müller, I., Fernández, A., Grant, K., & Rohling, E. (2017) · Scientific Reports · doi:10.1038/s41598-017-16528-6 · Cited by 65 · see citing works
Self-citationClumped isotope fractionation during phosphoric acid digestion of carbonates at 70 °C
Müller, I. A., Violay, M. E. S., Storck, J.-C., Fernandez, A., van Dijk, J., Madonna, C., & Bernasconi, S. M. (2017) · Chemical Geology · doi:10.1016/j.chemgeo.2016.11.030 · Cited by 64 · see citing works
Self-citationA redetermination of absolute values for 17 R VPDB‐CO2 and 17 R VSMOW
Assonov, S. S., & Brenninkmeijer, C. A. M. (2003) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.1011 · Cited by 63 · see citing works
Wright, D. T. (1997) · Journal of Sedimentary Research · doi:10.1306/d42684f0-2b26-11d7-8648000102c1865d · Cited by 59 · see citing works
A CALIBRATED MEASUREMENT OF THE ATOMIC WEIGHT OF CARBON
Zhang, Q. (1990) · Cited by 57 · see citing works
Time scales of magma transport and mixing at Kīlauea Volcano, Hawai’i
Rae, A. S. P., Edmonds, M., Maclennan, J., et al. (2016) · Geology · doi:10.1130/g37800.1 · Cited by 57 · see citing works
Controls on Cyclic Formation of Quaternary Early Diagenetic Dolomite
McCormack, J., Bontognali, T. R. R., Immenhauser, A., & Kwiecien, O. (2018) · Geophysical Research Letters · doi:10.1002/2018gl077344 · Cited by 52 · see citing works
Self-citationPreto, N., Breda, A., Corso, J. D., Spötl, C., Zorzi, F., & Frisia, S. (2014) · Sedimentology · doi:10.1111/sed.12157 · Cited by 52 · see citing works
Murray, S. T., & Swart, P. K. (2017) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2017.02.021 · Cited by 52 · see citing works
Coupled Mg/Ca and clumped isotope analyses of foraminifera provide consistent water temperatures
Breitenbach, S. F. M., Mleneck-Vautravers, M. J., Grauel, A.-L., Lo, L., Bernasconi, S. M., Müller, I. A., Rolfe, J., Gázquez, F., Greaves, M., & Hodell, D. A. (2018) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2018.03.010 · Cited by 51 · see citing works
Self-citationKatz, A., Bonifacie, M., Hermoso, M., Cartigny, P., & Calmels, D. (2017) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2017.02.025 · Cited by 44 · see citing works
Huang, S., Huang, K., Jie, L., et al. (2014) · Petroleum Science · doi:10.1007/s12182-014-0316-7 · Cited by 44 · see citing works
Leutert, T. J., Sexton, P. F., Tripati, A., Piasecki, A. M., Ho, S. L., & Meckler, A. N. (2019) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2019.05.005 · Cited by 42 · see citing works
The clumped-isotope geochemistry of exhumed marbles from Naxos, Greece
Ryb, U., Lloyd, M. K., Stolper, D. A., & Eiler, J. M. (2017) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2017.04.026 · Cited by 41 · see citing works
Calibration of dolomite clumped isotope thermometry
Winkelstern, I. Z., Kaczmarek, S. E., Lohmann, K. C., & Humphrey, J. D. (2016) · Chemical Geology · doi:10.1016/j.chemgeo.2016.09.021 · Cited by 40 · see citing works
Bahniuk, A., McKenzie, J. A., Perri, E., Bontognali, T. R. R., Vögeli, N., Rezende, C. E., Rangel, T. P., & Vasconcelos, C. (2015) · Geological Society, London, Special Publications · doi:10.1144/sp418.11 · Cited by 37 · see citing works
Self-citationMillán, M. I., Machel, H. G., & Bernasconi, S. M. (2016) · Journal of Sedimentary Research · doi:10.2110/jsr.2016.6 · Cited by 35 · see citing works
Self-citationHonlet, R., Gasparrini, M., Muchez, P., Swennen, R., & John, C. M. (2018) · Terra Nova · doi:10.1111/ter.12326 · Cited by 32 · see citing works
van Dijk, J., Fernandez, A., Storck, J. C., White, T. S., Lever, M., Müller, I. A., Bishop, S., Seifert, R. F., Driese, S. G., Krylov, A., et al. (2019) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2019.03.018 · Cited by 29 · see citing works
Self-citationCame, R. E., Azmy, K., Tripati, A., & Olanipekun, B.-J. (2017) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2016.10.028 · Cited by 29 · see citing works
de Dolomieu, D., Carozzi, A. V., & Zenger, D. H. (1981) · Journal of Geological Education · doi:10.5408/0022-1368-29.1.4 · Cited by 21 · see citing works
CONTINENTAL PALEOTEMPERATURES FROM AN EARLY CRETACEOUS DOLOMITIC LAKE, GANSU PROVINCE, CHINA
Suarez, M. B., Ludvigson, G. A., González, L. A., & You, H. (2017) · Journal of Sedimentary Research · doi:10.2110/jsr.2017.31 · Cited by 18 · see citing works
Bernasconi, S. M. (1991) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-a-000611458 · Cited by 17 · see citing works
Self-citationA CALIBRATED MEASUREMENT OF THE ATOMIC WEIGHT OF CARBON
张青莲, & 李文军 (1990) · 中国科学通报:英文版 · Cited by 16 · see citing works
(1953) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign) · Cited by 16 · see citing works
On oxygen isotope fractionation in carbonate and sulfate minerals
Zheng, Y. (1998) · Chinese Science Bulletin · doi:10.1007/bf02891661 · Cited by 16 · see citing works
Energetics of calcium-rich dolomite
Chai, L. (1995) · Geochimica et Cosmochimica Acta · doi:10.1016/00167-0379(50)00119- · Cited by 6 · see citing works
Santilli do Nascimento, G. (2018) · ETH Zurich · doi:10.3929/ethz-b-000314300 · Cited by 5 · see citing works
Self-citationIsotopic and Trace-Element Geochemistry of Dolomite--State of the Art: ABSTRACT
Land, L. S. (1979) · AAPG Bulletin · doi:10.1306/c1ea5b4d-16c9-11d7-8645000102c1865d · Cited by 2 · see citing works
Flagged first, then by citations
6 of the 122 references couldn’t be matched to a known paper.
Research works printed but not linked: 5
- Holland, 1996, On the secular variations in the composition of Phanerozoic marine potash evaporates, Geology, 24, 993, 10.1130/0091-7613(1996)024<0993:OTSVIT>2.3.CO;2 · DOI · Paper page
- Illing, 1965, Penecontemporaneous dolomite in the Persian Gulf, vol. 13, 89
- Lehner, 1952, Zur Geologie des Gebietes der Denti della Vecchia, des M. Boglia, des M. Brè, und des Monte Salvatore bei Lugano, Eclogae Geol. Helv., 45, 86
- Spencer, 1990, Control of seawater composition by mixing of river waters and mid-ocean ridge hydrothermal brines, vol. 2, 409
- Zorn, 1971, Paläontologische, stratigraphische und sedimentologische Untersuchungen des Salvatoredolomits (Mitteltrias) der Tessiner Kalkalpen, vol. 91, 1
Cited by
Sorted by citations
Bernasconi, S. M., Daëron, M., Bergmann, K. D., Bonifacie, M., Meckler, A. N., Affek, H. P., Anderson, N., Bajnai, D., Barkan, E., Beverly, E., et al. (2021) · Geochemistry Geophysics Geosystems · doi:10.1029/2020gc009588 · Cited by 340 · see citing works
Self-citationAnderson, N. T., Kelson, J. R., Kele, S., Daëron, M., Bonifacie, M., Horita, J., Mackey, T. J., John, C. M., Kluge, T., Petschnig, P., et al. (2021) · Geophysical Research Letters · doi:10.1029/2020gl092069 · Cited by 323 · see citing works
“At high temperatures, theory predicts a non-linear 1/T2-Δ47 relationship (e.g., Guo et al., 2009; Hill et al., 2014), supported by recent empirical calibrations (e.g., Jautzy et al., 2020; Müller et al., 2019).”
BackgroundSelf-citationChang, B., Li, C., Liu, D., Foster, I., Tripati, A., Lloyd, M. K., Maradiaga, I., Luo, G., An, Z., She, Z., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916673117 · Cited by 152 · see citing works
“Currently published empirical calibration equations (Δ47-low temperature, 1 to 65 °C) have mostly been based on biogenic carbonates and inorganic synthetic calcites (18, 49, 59–61), and only two Δ47-temperature calibration equations for dolomite samples have been reported (50, 62).”
BackgroundUltramafic Rock Carbonation: Constraints From Listvenite Core BT1B, Oman Drilling Project
Beinlich, A., Plümper, O., Boter, E., Müller, I. A., Kourim, F., Ziegler, M., Harigane, Y., Lafay, R., Kelemen, P. B., & the Oman Drilling Project Science Team (2020) · Journal of Geophysical Research: Solid Earth · doi:10.1029/2019jb019060 · Cited by 88 · see citing works
“For the Δ47 temperature estimates of dolomite, we used the mineral specific Δ47‐temperature calibration of Müller et al. (2019) for 70 °C acid digestion temperature.”
MethodSelf-citationTemperature Dependence of Clumped Isotopes (∆ <sub>47</sub> ) in Aragonite
de Winter, N. J., Witbaard, R., Kocken, I. J., Müller, I. A., Guo, J., Goudsmit, B., & Ziegler, M. (2022) · Geophysical Research Letters · doi:10.1029/2022gl099479 · Cited by 52 · see citing works
“, 2006) and experimental studies disagree on a difference in acid fractionation factor (AFF) between calcite and aragonite (Guo et al., 2009; Müller et al., 2019; Petersen et al., 2019).”
Self-citationClumped isotope temperature calibration for calcite: Bridging theory and experimentation
Jautzy, J. J., Savard, M. M., Dhillon, R. S., Bernasconi, S. M., & Smirnoff, A. (2020) · Geochemical Perspectives Letters · doi:10.7185/geochemlet.2021 · Cited by 50 · see citing works
Self-citationBiogeochemical reappraisal of the freshwater–seawater mixing‐zone diagenetic model
Petrash, D. A., Bialik, O. M., Staudigel, P. T., Konhauser, K. O., & Budd, D. A. (2021) · Sedimentology · doi:10.1111/sed.12849 · Cited by 39 · see citing works
“In addition, there is large uncertainty regarding the actual δ18O fractionation factor between the fluid source and dolomite (Müller et al., 2019).”
BackgroundSabkha dolomite as an archive for the magnesium isotope composition of seawater
Shalev, N., Bontognali, T. R. R., & Vance, D. (2020) · Geology · doi:10.1130/g47973.1 · Cited by 39 · see citing works
Self-citationFracture dolomite as an archive of continental palaeo-environmental conditions
Baldermann, A., Mittermayr, F., Bernasconi, S. M., Dietzel, M., Grengg, C., Hippler, D., Kluge, T., Leis, A., Lin, K., Wang, X., et al. (2020) · Communications Earth & Environment · doi:10.1038/s43247-020-00040-3 · Cited by 33 · see citing works
Self-citationCurzi, M., Aldega, L., Billi, A., Boschi, C., Carminati, E., Vignaroli, G., Viola, G., & Bernasconi, S. M. (2024) · Earth-Science Reviews · doi:10.1016/j.earscirev.2024.104801 · Cited by 33 · see citing works
Self-citationGuo, Y., Deng, W., Liu, X., Kong, K., Yan, W., & Wei, G. (2021) · Marine Geology · doi:10.1016/j.margeo.2021.106513 · Cited by 30 · see citing works
Dietzel, M., Purgstaller, B., Kluge, T., Leis, A., & Mavromatis, V. (2020) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2020.02.032 · Cited by 28 · see citing works
Ternieten, L., Früh‐Green, G. L., & Bernasconi, S. M. (2021) · Journal of Geophysical Research Solid Earth · doi:10.1029/2021jb022712 · Cited by 27 · see citing works
Self-citationSánchez-Román, M., Gibert, L., Martín-Martín, J. D., van Zuilen, K., Pineda-González, V., Vroon, P., & Bruggmann, S. (2023) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2023.06.031 · Cited by 24 · see citing works
Clumped isotope acid fractionation factors for dolomite and calcite revisited: Should we care?
Lu, C., Murray, S. T., Koeshidayatullah, A., & Swart, P. K. (2021) · Chemical Geology · doi:10.1016/j.chemgeo.2021.120637 · Cited by 25 · see citing works
Ternieten, L., Früh‐Green, G. L., & Bernasconi, S. M. (2021) · Journal of Geophysical Research Solid Earth · doi:10.1029/2021jb021973 · Cited by 23 · see citing works
“Dolomite values are reported for a reaction temperature of 70°C, which is the same temperature used to establish the calibration (Müller et al., 2019), and calcites are projected to 25°C.”
MethodSelf-citationA Decrease to Low Carbonate Clumped Isotope Temperatures in Cryogenian Strata
Mackey, T., Jost, A. B., Creveling, J. R., & Bergmann, K. (2020) · AGU Advances · doi:10.1029/2019av000159 · Cited by 28 · see citing works
“…Mackey, A. B. Jost, J. R. Creveling, K. D. Bergmann Supervision: K. D. Bergmann Visualization: K. D. Bergmann Writing ‐ original draft: T. J. Mackey Writing – review & editing: T. J. Mackey, A. B. Jost, J. R. Creveling, K. D. Bergmann Müller et al., 2019, for discussion of dolomite calibrations).”
Li, H., Liu, X., Arnold, A., Elliott, B. M., Flores, R., Kelley, A. M., & Tripati, A. (2021) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2021.116840 · Cited by 23 · see citing works
Salomon, E., Rotevatn, A., Kristensen, T. B., Grundvåg, S., Henstra, G. A., Meckler, A. N., Albert, R., & Gerdes, A. (2020) · Solid Earth · doi:10.5194/se-11-1987-2020 · Cited by 23 · see citing works
Wang, R., Xiao, Y., Yu, K., Jones, B., Wu, L., Liang, F., Yang, Y., & Chang, B. (2022) · Sedimentary Geology · doi:10.1016/j.sedgeo.2021.106079 · Cited by 19 · see citing works
Amplified seasonality in western Europe in a warmer world
de Winter, N. D., Tindall, J., Johnson, A. L. A., Goudsmit-Harzevoort, B., Wichern, N., Kaskes, P., Claeys, P., Huygen, F., van Leeuwen, S. V., Metcalfe, B., et al. (2024) · Science Advances · doi:10.1126/sciadv.adl6717 · Cited by 21 · see citing works
Roberts, J. A. (2024) · Nature Geoscience · doi:10.1038/s41561-024-01490-6 · Cited by 16 · see citing works
Chang, B., Defliese, W. F., Li, C., Huang, J., Tripati, A., & Algeo, T. J. (2019) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.8678 · Cited by 17 · see citing works
Bernasconi, S. M., Daëron, M., Bergmann, K., Bonifacie, M., & Meckler, A. N. (2020) · doi:10.1002/essoar.10504430.4 · Cited by 14 · see citing works
Self-citationThermochemical oxidation of methane by manganese oxides in hydrothermal sediments
Huang, Q., Jiang, S., Pi, D.-H., Konhauser, K. O., Wen, X., Lu, L., & Yan, H. (2023) · Communications Earth & Environment · doi:10.1038/s43247-023-00891-6 · Cited by 16 · see citing works
Li, L., DeCelles, P. G., Kapp, P., Garzione, C. N., Quade, J., & Yanay, N. (2024) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2024.04.007 · Cited by 15 · see citing works
Anderson, N. T., Bonifacie, M., Jost, A. B., Siebert, J., Bontognali, T., Horita, J., Müller, I. A., Bernasconi, S. M., & Bergmann, K. D. (2024) · Geochemistry, Geophysics, Geosystems · doi:10.1029/2023gc011049 · Cited by 13 · see citing works
“An amorphous gel-like solid was precipitated from a room temperature mixture of equimolar solutions of Na 2 CO 3 , CaCl 2 , and MgCl 2 and followed by heating to the nominal temperature for between 1 day and 12 weeks (Müller et al., 2019).”
BackgroundMethodResultInfluentialSelf-citationHu, X., Müller, I. A., Zhao, A., Ziegler, M., Chen, Q., Han, L., & Shi, Z. (2021) · Chemical Geology · doi:10.1016/j.chemgeo.2021.120641 · Cited by 13 · see citing works
Self-citationDietzel, M., & Boch, R. (2024) · Geochemistry · doi:10.1016/j.chemer.2024.126206 · Cited by 14 · see citing works
Ryan, B. H., Petersen, S., Rivers, J. M., & Kaczmarek, S. E. (2023) · Journal of Sedimentary Research · doi:10.2110/jsr.2022.117 · Cited by 13 · see citing works
Clumped Isotope Temperatures of Coccolithophores From Global Sediment Traps
Clark, A. J., Jaggi, M., Bernasconi, S. M., Fiebig, J., & Stoll, H. M. (2025) · Paleoceanography and Paleoclimatology · doi:10.1029/2024pa005054 · Cited by 10 · see citing works
Self-citationAftabi, A., Atapour, H., & Mohseni, S. (2022) · Precambrian Research · doi:10.1016/j.precamres.2022.106740 · Cited by 11 · see citing works
Clumped isotopes in globally distributed Holocene coccoliths reveal their habitat depth
Mejía, L. M., Bernasconi, S. M., Zhang, H., Guitián, J., Fernández, Á., Hernández‐Almeida, I., Jaggi, M., Haghipour, N., & Stoll, H. M. (2023) · Earth and Planetary Science Letters · doi:10.1016/j.epsl.2023.118313 · Cited by 9 · see citing works
Self-citationDefliese, W., & Tripati, A. (2019) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.8666 · Cited by 6 · see citing works
Effects of mineralogy on Δ47 and Δ48 of carbonate-derived CO2 below analytical resolution
Bernecker, M., Bonifacie, M., Staudigel, P. T., Meijer, N., Siebert, J., Wehr, N., Haussühl, E., Bernasconi, S. M., Petrash, D. A., Dietzel, M., et al. (2025) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2025.06.004 · Cited by 9 · see citing works
Self-citationClark, A. J., Torres-Romero, I., Jaggi, M., Bernasconi, S. M., & Stoll, H. M. (2024) · Climate of the Past · doi:10.5194/cp-20-2081-2024 · Cited by 10 · see citing works
Self-citationBanerjee, S., Ghosh, P., Banerjee, Y., & Riding, R. (2023) · Chemical Geology · doi:10.1016/j.chemgeo.2023.121356 · Cited by 9 · see citing works
Curzi, M., Caracausi, A., Rossetti, F., Rabiee, A., Billi, A., Carminati, E., Aldega, L., Bernasconi, S. M., Boschi, C., Drivenes, K., et al. (2022) · Geochemistry Geophysics Geosystems · doi:10.1029/2022gc010474 · Cited by 9 · see citing works
Self-citationKirichenko, Y., Rickli, J., Bontognali, T. R. R., & Shalev, N. (2024) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2024.06.006 · Cited by 7 · see citing works
Self-citationTemperature dependence of clumped isotopes (∆47) in aragonitePreprint
de Winter, N. J., Witbaard, R., Kocken, I., et al. (2022) · doi:10.1002/essoar.10511492.1 · Cited by 7 · see citing works
Self-citationBarale, L., Bertok, C., D'Atri, A. R., Mantovani, A., Martire, L., Agostini, S., Bernasconi, S. M., Gerdes, A., & Ferrando, S. (2021) · Basin Research · doi:10.1111/bre.12594 · Cited by 7 · see citing works
Self-citationGuo, Y.-R., Kong, K., Liu, X., Deng, W.-F., & Wei, G.-J. (2024) · Chemical Geology · doi:10.1016/j.chemgeo.2024.122036 · Cited by 7 · see citing works
Fosu, B. R., Jautzy, J. J., Yong, W., & Secco, R. A. (2023) · Geochemistry Geophysics Geosystems · doi:10.1029/2023gc011047 · Cited by 6 · see citing works
“Furthermore, we note that the average value of ETH1-2 (heated at 600°C) used for standardization by Müller et al. (2019) for a 70°C acid digestion is 0.034‰ lower than the average Δ 47 value of their dolomites heated at 1100°C when the contrary would be expected.”
BackgroundMethodResultInfluentialPetrash, D. A., Roeser, P. A., Křı́bek, B., Staudigel, P. T., Bernecker, M., Jačková, I., Čejková, B., Kochergina, Y. V. E., Koubová, M., Křížová, Š., et al. (2025) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2025.08.025 · Cited by 5 · see citing works
Disi, Z. A. A., Bontognali, T. R. R., Sadooni, F., & Al-Kuwari, H. A. S. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.174714 · Cited by 5 · see citing works
Self-citationAn identity card for sabkha dolomite
Bontognali, T. R. R., Disi, Z. A. A., Dittrich, M., DiLoreto, Z. A., Barnasconi, S. M., Sadooni, F., & Al‐Kuwari, H. A. (2026) · The Depositional Record · doi:10.1002/dep2.70049 · Cited by 4 · see citing works
“…sabkhas are also important because they allow for precise measurement of physico-chemical and biological conditions associated with dolo-mite formation, making them ideal systems for calibrating geochemical proxies used in paleoclimatic reconstructions (Anderson et al., 2024; Müller et al., 2019).”
InfluentialSelf-citationGiorno, M., Bertok, C., Barale, L., et al. (2025) · Ore Geology Reviews · doi:10.1016/j.oregeorev.2025.106737 · Cited by 3 · see citing works
“Oxygen isotope values in Dol-2 on the other hand cluster around δ 18 O = (cid:0) 10 ‰ VPDB. Correcting this for the formation temperatures of Dol-2 (Giorno et al., 2022) using the equation of Müller et al. (2019), yields a δ 18 O SMOW value of the parent fluid of around + 2 ‰ .”
Self-citationLucca, A., Mittempergher, S., Balsamo, F., Cipriani, A., Cilona, A., & Storti, F. (2025) · Geosciences · doi:10.3390/geosciences15020035 · Cited by 3 · see citing works
El-Yamani, M. S., John, C. M., & Bell, R. (2024) · Marine and Petroleum Geology · doi:10.1016/j.marpetgeo.2024.106741 · Cited by 3 · see citing works
Coccolithophorids precipitate carbonate in clumped isotope equilibrium with seawater
Clark, A. J., Torres-Romero, I., Jaggi, M., Bernasconi, S. M., & Stoll, H. M. (2023) · doi:10.5194/egusphere-2023-2581 · Cited by 10 · see citing works
Self-citationSugawara, S., Fujiya, W., Kagi, H., Yamaguchi, A., & Hashizume, K. (2022) · ACS Omega · doi:10.1021/acsomega.2c03258 · Cited by 4 · see citing works
Li, R., Jones, B. H., Lu, C.-J., Chang, B., & Shao, L. (2026) · Sedimentary Geology · doi:10.1016/j.sedgeo.2026.107059 · Cited by 2 · see citing works
Kim, S., Kim, S., & Knyf, M. (2025) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.9958 · Cited by 2 · see citing works
“Obviously, there is a lack of consensus on optimal analytical conditions for different types of carbonate minerals, (2) (5) including calcite, dolomite, and magnesite, to determine their carbon and oxygen isotope compositions (Table 2) (e.g., [14, 15, 22, 23–28]).”
Matsumoto, R., Takeuchi, R., Nakagawa, H., et al. (2023) · The Journal of the Geological Society of Japan · doi:10.5575/geosoc.2023.0008 · Cited by 2 · see citing works
Salomon, É., Rotevatn, A., Kristensen, T. B., et al. (2020) · doi:10.5194/se-2020-72 · Cited by 2 · see citing works
Domed‐rim microbial polygons and their preservation potential
Blattmann, F. R., Eglinton, T. I., Haghipour, N., Rouwendaal, S. E., Bernasconi, S. M., Rivers, J. M., Dittrich, M., Disi, Z. A. A., Williford, K. H., Sadooni, F., et al. (2026) · The Depositional Record · doi:10.1002/dep2.70061 · Cited by 2 · see citing works
“The δ 13 C carb values from the DF site are, on average, comparable to those reported in the coastal sab-kha of Abu Dhabi, whereas the δ 18 O values of the DF and KAA are generally more positive (Bontognali et al., 2010; Müller et al., 2019).”
Self-citationGairola, G. S., Thiele, S. T., Khanna, P., Ramdani, A. I., Panara, Y., Patino, S., Swart, P. K., Gloaguen, R., & Vahrenkamp, V. (2026) · Scientific Reports · doi:10.1038/s41598-026-35353-4 · Cited by 2 · see citing works
“Multiple calibration equations have been proposed for temperature estimation in dolomites, differing in slope and resulting values 19,98,100,101,101 .”
Fosu, B. R., Jautzy, J. J., Petts, D. C., Clark, I., & Al, T. A. (2025) · Chemical Geology · doi:10.1016/j.chemgeo.2025.123189 · Cited by 1 · see citing works
Tanner, T., Rae, J. W. B., Hernández‐Almeida, I., et al. (2024) · doi:10.22541/essoar.171535711.15687939/v1 · Cited by 1 · see citing works
Self-citationAmplified seasonality in western Europe in a warmer worldPreprint
de Winter, N. J., Tindall, J. C., Johnson, A. L. A., et al. (2023) · doi:10.31223/x5h986 · Cited by 1 · see citing works
Clumped isotopes in globally distributed Holocene coccoliths reveal their habitat depthPreprint
Mejía, L. M., Bernasconi, S. M., Zhang, H., Guitián, J., Fernández, Á., Hernández‐Almeida, I., Jaggi, M., Haghipour, N., & Stoll, H. M. (2023) · doi:10.31223/x5qs8w
Self-citationClumped Isotope Signatures of Dolomites as Reservoir Rocks, Southeast Anatolia
Atasoy, D., Geçer, A., AKTOSUN, A., & Büyükutku, A. G. (2022) · Afyon Kocatepe University Journal of Sciences and Engineering · doi:10.35414/akufemubid.1105170 · Cited by 1 · see citing works
Zhao, J., Yan, C., Liu, S., et al. (2022) · Magazine of Concrete Research · doi:10.1680/jmacr.20.00306 · Cited by 1 · see citing works
BayClump: Bayesian Calibration and Temperature Reconstructions for Clumped Isotope ThermometryPreprint
Román‐Palacios, C., Carroll, H. M., Arnold, A., Gan, Q., & Tripati, A. (2022) · doi:10.1002/essoar.10507995.2 · Cited by 1 · see citing works
Norouzi, S., Adabi, M. H., & Kaczmarek, S. E. (2026) · Sedimentary Geology · doi:10.1016/j.sedgeo.2026.107187
Thermal history reconstruction of deep diverse lithology in Tarim Basin, Northwest China
Chang, J., Li, D., Nan-sheng, Q., & Li, C.-X. (2026) · Petroleum Science · doi:10.1016/j.petsci.2026.08.014
McCormick, C. A., Jones, B., Olsen, E. K., & Ingalls, M. (2026) · Geochemistry Geophysics Geosystems · doi:10.1029/2026gc013142
“Unlike the traditional δ 18 O paleothermometer, carbonate clumped isotope temperatures (TΔ 47 ; Anderson et al., 2021; Bonifacie et al., 2017; Müller et al., 2019; Swart et al., 2019) are independent of the fluid composition and, when paired with δ 18 O DOL measurements, allow δ 18 O FLUID to be…”
Hydrothermal perturbation controls clumped isotope heterogeneity in deep-buried carbonates
Guo, Y., Guo, Y., Hu, J., Deng, W., & Wei, G. (2026) · Chemical Geology · doi:10.1016/j.chemgeo.2026.123552 · Cited by 1 · see citing works
Müller, M., Bernasconi, S. M., Picotti, V., & Hemingway, J. (2026) · The Depositional Record · doi:10.1002/dep2.70060
Self-citationMüller, I. A., Rijkes, D., Judd, E. J., Hamers, M., Plümper, O., Jagt, J. W. M., & Ziegler, M. (2025) · Cretaceous Research · doi:10.1016/j.cretres.2025.106258
Self-citationMarchegiano, M., Ziegler, M., Bialik, O., & Vleeschouwer, D. D. (2025) · Geology · doi:10.1130/g53550.1 · Cited by 1 · see citing works
Clumped isotope thermometry determines diagenetic origin of the crystalline dolomitePreprint
Hou, J., Zhu, G., Li, H. M., & 王丽珍 (2025) · Research Square · doi:10.21203/rs.3.rs-7244432/v1
Clumped isotope temperatures of coccolithophores from global sediment trapsPreprint
Clark, A. J., Jaggi, M., Bernasconi, S. M., et al. (2024) · doi:10.22541/essoar.173042174.40363194/v1
Self-citationClark, A. J. (2024) · doi:10.5194/egusphere-2023-2581-ac2
Clark, A. J. (2024) · doi:10.5194/egusphere-2023-2581-ac1
Comment on egusphere-2023-2581
Clark, A. J., Torres-Romero, I., Jaggi, M., et al. (2024) · doi:10.5194/egusphere-2023-2581-rc2
Self-citationPing, H., Deng, W., Chen, H., Guo, Y., Kong, K., Yang, X., & Liu, J. (2024) · Marine and Petroleum Geology · doi:10.1016/j.marpetgeo.2024.106773
Comment on egusphere-2023-2581
Clark, A. J., Torres-Romero, I., Jaggi, M., et al. (2024) · doi:10.5194/egusphere-2023-2581-rc1
Self-citationNew Experimental Constraints on Clumped Isotope Bond Reordering in DolomitePreprint
Petschnig, P., Looser, N., Hemingway, J., Schmidt, M. W., & Bernasconi, S. M. (2023) · doi:10.22541/essoar.169945121.15752377/v1
Self-citationLucca, A., Mittempergher, S., Balsamo, F., Cipriani, A., Bernasconi, S. M., Cilona, A., & Storti, F. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4462936
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Self-citation
- Authors
- Müller, I. A., Rodriguez-Blanco, J. D., Storck, J.-C., do Nascimento, G. S., Bontognali, T. R. R., Vasconcelos, C., Benning, L. G., & Bernasconi, S. M.
- Affiliations
- Utrecht University (NL)
- ETH Zurich (CH)
- University of Basel (CH)
- University of Leeds (GB)
- Corresponding author
- Müller, Inigo A.
- ORCID
- Venue
- Chemical Geology
- Publisher
- Elsevier BV
- Published
- 2019-10
- Volume
- 525
- Pages
- 1-17
- ISSN
- 0009-2541 (ISSN-L)
- OpenAlex
- W2958233285
- Cited by
- 77
- References
- 122
- Citations by year
- 2026: 10 · 2025: 10 · 2024: 16 · 2023: 10 · 2022: 8 · 2021: 12 · 2020: 9 · 2019: 2
- FWCI
- 6.08
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Chemical Geology (acceptedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
- BORIS (University Library Bern) (submittedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- edoc (University of Basel) (submittedVersion)
- Publication Database GFZ (GFZ German Research Centre for Geosciences) (submittedVersion)
- Utrecht University Repository (Utrecht University) (submittedVersion)
- Funders
- Marie Curie
- Helmholtz-Zentrum Potsdam - Deutsches GeoForschungsZentrum GFZ
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Stratigraphy of Fossils
- Physical Sciences › Earth and Planetary Sciences › Atmospheric Science › Geology and Paleoclimatology Research
- Physical Sciences › Earth and Planetary Sciences › Geophysics › Geological and Geochemical Analysis
- Keywords
- carbonate clumped isotopes, oxygen isotopes, dolomitization, dolomite precipitation, carbonate mineralogy, isotopic scrambling, paleoclimate proxies, diagenesis, authigenic dolomite
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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