Compilation of stable isotope fractionation factors of geochemical interest
Open accessAbstract
Phase equilibrium relations of the common rock-forming oxides except water, by G
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- Findingnone given
The I.A.E.A. SMOW water has been analyzed in many laboratories and its oxygen isotope composition has been found identical to the originally defined SMOW within ±0.05 per mil.
“This latter SMOW has been analyzed in many laboratories, and the oxygen isotope composition has been found by many investigators to be identical to the originally defined SMOW within the limits of analytical uncertainty (±0.05°/oo)-”
Quote in the paperNot a substantial claim - Findingown data
Several recent determinations of the CO2-H2O fractionation factor at 25°C indicate that the factor is probably larger than 1.0407.
“However, several recent determinations of this factor indicate that the factor is probably larger than 1.0407 (table 2).”
Quote in the paperSubstantial claim - Findingnone given
The δO18 value of NBS-28 reported from several laboratories indicates a range between 9.5 and 9.9.
“The SO18 value of NBS-28 reported to the authors from several laboratories indicate a range between 9.5 and 9.9.”
Quote in the paperNot a substantial claim - Findingcitation
Recent determinations indicate that the δ value of NBS-21 is closer to −28.10.
“Recent determinations indicate that the latter value is closer to-28.10 (Mook, 1971;Letolle, 1971;F. C. Tan, unpub. data, 1973;J. D. Gleason and I. Friedman, unpub. data, 1973).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites Mook, 1971 source
- cites Letolle, 1971
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites F. C. Tan, unpub. data, 1973
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Findingreasoning
When results of deuterium analyses of the four I.A.E.A. standard waters were compared, significant discrepancies in δD were apparent.
“When the results of deuterium analyses of the four I.A.E.A. standard waters were compared several years ago, significant discrepancies in 8 D were apparent.”
Quote in the paperNot a substantial claim
- Findingnone given
The average of all published analyses of the CO2-H2O fractionation factor at 25°C, excepting the value 1.0424 (Staschewski, 1964), is 1.0412.
“NOTE.The average of all the published analyses, excepting the value of 1.0424 (Staschewski, 1964), is 1.0412.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Staschewski, 1964
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Findingreasoning
If the acid fractionation factor of 1.01109 is used for dolomite, the dolomite-calcite fractionation value becomes +2.3.
“If the acid fractionation factor of 1.01109 is used for dolomite, this value becomes +2.3.”
Quote in the paperNot a substantial claim - Findingreasoning
The constant dolomite-calcite fractionation of +3.1 in the temperature range 25° to 79°C is calculated from data on synthesized protodolomites, using the acid fractionation factor of 1.01025 for both carbonates.
“The constant dolomite-calcite fractionation of +3.1 in the temperature range 25° to 79°C is calculated from data on synthesized protodolomites, using the acid fractionation factor of 1.01025 for both carbonates.”
Quote in the paperNot a substantial claim - Findingcitation
The plagioclase-magnetite curves formulated by Anderson, Clayton, and Mayeda (1971) are virtually identical to those shown in the figure.
“The plagioclase-magnetite curves formulated by Anderson, Clayton, and Mayeda (1971) are virtually identical to those shown in the figure.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Anderson, Clayton, and Mayeda (1971)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The correct statement about Craig (1961) is that the δO18 value of CO2 produced by reaction of 100 percent H3PO4 with PDB calcite at 25°C is +0.22 per mil relative to CO2 equilibrated at 25°C with SMOW water.
“The correct statement should have been that the SO 18 value of the CO 2 produced by reaction of 100 percent H 3 PO4 with PDB calcite at 25°C is +0.22 per mil relative to CO2 equilibrated at 25°C with SMOW water.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Craig (1961)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
For perfect gases, ln α varies as 1/T^2 and 1/T in the high- and low-temperature limits, respectively.
“For perfect gases, In a varies as 1/T2 and 1/T in the high-and low-temperature limits, respectively (Bigeleisen and Mayer, 1947).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Bigeleisen and Mayer, 1947 source
- Study design and conductreasoning
It is impossible, owing to present limitations of mass spectrometry, to determine a CO2-H2O fractionation factor as large as ~1.04 with an accuracy of more than ±0.0004.
“Although it is possible to determine this factor with a precision of ±0.0001, it is impossible, owing to the present limitations of mass spectrometry, to determine a factor as large as this with an accuracy of more than ±0.0004 (approximately 1 percent of the difference in 5 between the CO2 and H2O.”
Quote in the paperSubstantial claim - Premisecitation
Apparent differences in δO18 of a carbonate sample can arise depending on temperature of the acid reaction, procedure used to remove organic material, carbonate to acid ratio, and grain size of the carbonate.
“Apparent differences in 8 O 18 of a carbonate sample can arise, depending, for example, on (1) temperature of the acid reaction, (2) procedure used to remove organic material (Emiliani, 1966), (3) carbonate to acid ratio (Fontes and others, 1965), and, (4) grain size of the carbonate (Fritz and Fontes, 1966).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites Emiliani, 1966 source
- cites Fontes and others, 1965
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Fritz and Fontes, 1966
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationreasoning
The differences in δD among the I.A.E.A. standard waters were attributed to the use of incorrect mass spectrometer correction factors by some investigators.
“The differences were attributed to the use of incorrect mass spectrometer correction factors by some investigators.”
Quote in the paperNot a substantial claim - Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-H2O(l) at 0°C is 3.1.
“5 H2O(s)-H2O(l)........ | | 0 | 3.1 | ..... | O'Neil (1968).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites O'Neil (1968) source
- Premisecitation
The measured fractionation factor 10^3 ln α for CO2(g)-CO2(l) at 30°C is -0.06.
“| | 30 | -.06 | | | |”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Grootes, Mook, and Vogel (1969) source
- Premisecitation
For molybdenite-galena, 10^3 ln α = 1.3(10^6 T^-2) - 0.80.
“Suvorova (1974). Experimental: A, Molybdenite-galena 103 lna = 1.3(106T-2)-0.80”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Suvorova (1974)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-2.5 M NaCl at -10°C is 2.2.
“6 H20(s)-2.5 M NaCl. | | -10 | 2.2 | ..... | Stewart (1974).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Stewart (1974) source
- Interpretationreasoning
Even at present state of knowledge, geologically reasonable temperatures are usually inferred from stable isotope relations.
“but even at our present state of knowledge, geologically reasonable temperatures are usually inferred.”
Quote in the paperSubstantial claim - Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-H2O(g) at -10°C is 12.6.
“| | | -10 | 12.6 | ..... | ......do.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsuo and Matsubaya (1969) source
- Premisecitation
For molybdenite-pyrite, 10^3 ln α = 0.48(10^6 T^-2) - 0.75.
“C, Molybdenite-pyrite 103 lna = 0.48(106T-2)-0.75”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Suvorova (1974)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-H2O(g) at -20°C is 13.4.
“| | | -20 | 13.4 | ..... | ......do.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsuo and Matsubaya (1969) source
- Premisecitation
For molybdenite-sphalerite, 10^3 ln α = 0.71(10^6 T^-2) - 0.15, calculated for 400° to 750°C.
“B, Molybdenite-sphalerite 103 lna = 0.71(106T-2)-0.-15. Calculated: (400° to 750°C).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Suvorova (1974)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Interpretationnone given
The data given in Bottinga (1968a) has more internal consistency than the carbon dioxide(g)-graphite data given in Bottinga (1969b).
“Although carbon dioxide(g)-graphite is given in Bottinga (1969b), the data given in Bottinga (1968a) has more internal consistency”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Bottinga (1968a)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Bottinga (1969b)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
For molybdenite-pyrrhotite, 10^3 ln α = 0.65(10^6 T^-2) - 1.65.
“E, Molybdenite-pyrrhotite 103 lna = 0.65(106T-2)-1.65.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Suvorova (1974)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The measured fractionation factor 10^3 ln α for CO2(g)-CO2(l) at 0°C is -0.42.
“1 1 CO2(g)-CO2( 1 ) Continued | 0 | -0.42 | -0.58 | Grootes, Mook, and Vogel (1969).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Grootes, Mook, and Vogel (1969) source
- Premisecitation
The measured fractionation factor 10^3 ln α for CO2(g)-CO2(l) at 10°C is -0.32.
“| | 10 | -.32 | | | |”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Grootes, Mook, and Vogel (1969) source
- Interpretationreasoning
The uncertainty in the CO2-H2O fractionation factor at 25°C has serious implications both in relating oxygen isotope standards and in comparing experimentally determined oxygen isotope fractionation factors.
“The uncertainty in the CO2-H2O fractionation factor at 25°C has serious implications both in relating oxygen isotope standards and in comparing experimentally determined oxygen isotope fractionation factors.”
Quote in the paperSubstantial claim - Interpretationnone given
Of the minerals investigated, calcite has shown the most consistent oxygen isotope results among several investigations, including equilibrations with water and with carbon dioxide.
“Of the minerals investigated, calcite has shown the most consistent oxygen isotope results among several investigations, including equilibrations with water and with carbon dioxide.”
Quote in the paperNot a substantial claim - Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-H2O(g) at -5°C is 12.2.
“| | | -5 | 12.2 | ...... ......do.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsuo and Matsubaya (1969) source
- Study design and conductown data
The curve in Figure 33 is constructed from fractionations between coexisting calcite and dolomite in marbles, calibrated by the Mg-calcite solvus thermometer.
“This curve is constructed from fractionations between coexisting calcite and dolomite in marbles, calibrated by the Mg-calcite solvus thermometer.”
Quote in the paperNot a substantial claim - Premisecitation
For molybdenite-chalcopyrite, 10^3 ln α = 0.72(10^6 T^-2) - 0.70.
“D, Molybdenite-chalcopyrite 103 lna = 0.72(106T-2)-0.70”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Suvorova (1974)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Premisecitation
The measured fractionation factor 10^3 ln α for CO2(g)-CO2(l) at 20°C is -0.21.
“| | 20 | -.21 | | | |”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Grootes, Mook, and Vogel (1969) source
- Premisecitation
The calculated fractionation factor 10^3 ln α for CO2(g)-CO2(l) at 0°C is -0.58.
“1 1 CO2(g)-CO2( 1 ) Continued | 0 | -0.42 | -0.58 | Grootes, Mook, and Vogel (1969).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Grootes, Mook, and Vogel (1969) source
- Study design and conductreasoning
In this compilation, all curves with the exception of those of Bottinga and Javoy (1973) have been recalculated to the newly proposed value of α (1.0412).
“In the compilation published herein, all the curves with the exception of those of Bottinga and Javoy (1973) have been recalculated to the newly proposed value of a (1.0412).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bottinga and Javoy (1973) source
- Study design and conductown data
The curve in Figure 26 is constructed from fractionations between coexisting calcite and dolomite in marbles, calibrated by the Mg-calcite solvus thermometer.
“This curve is constructed from fractionations between coexisting calcite and dolomite in marbles, calibrated by the Mg-calcite solvus thermometer.”
Quote in the paperNot a substantial claim - Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-H2O(g) at 0°C is 11.8.
“7 H20(s)-H20(g)........ | | 0 | 11.8 | ...... Matsuo and Matsubaya (1969).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsuo and Matsubaya (1969) source
- Premisecitation
The fractionation factor 10^3 ln α for H2O(s)-H2O(g) at -15°C is 13.0.
“| | | -15 | 13.0 | ..... | ......do.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Matsuo and Matsubaya (1969) source
- May combine two claims. 14
- Classified as probably not a substantial claim. 27
- The quote only partly states this claim. 2
May combine two claims.
Findingnone givenThe per mil fractionation 10^3 ln α is very well approximated by Δ = δ_A − δ_B; subtracting δ values is an excellent approximation to the per mil fractionation and identical within analytical error for values of both Δ's and δ's less than about 10.
“That is, merely subtracting S values will be an excellent approximation to the per mil fractionation and identical to it within the limits of analytical error for values of both A 's and 6 's, which are less than about 10.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationRecent measurements by Coplen and Clayton (1973) on a high-resolution mass spectrometer have verified Craig's δD results; Coplen and Clayton's δD for NBS-1A is −183.0 ± 0.5.
“Recent measurements by Coplen and Clayton (1973) on a high-resolution mass spectrometer (Hs”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Coplen and Clayton (1973) source
May combine two claims.
FindingcitationThe I.A.E.A. sample of water called SMOW is not identical in D/H ratio to the defined SMOW; Coplen and Clayton (1973) report a δD value of −1.2.
“The I.A.E.A. sample of water called SMOW has been analyzed in several laboratories and is not identical in D/H ratio to the defined SMOW.Coplen and Clayton (1973), for example, report a 8D value of -1.2.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Coplen and Clayton (1973) source
May combine two claims.
Findingown dataFriedman found differences in δD as high as 8 per mil among 4 separate samples of NBS-1 received over the past 20 years; therefore some interlaboratory differences may depend on the batch of NBS-1 standard utilized.
“Friedman has recently measured the hydrogen isotope compositions of 4 separate samples of NBS-1 that he received over the past 20 years and found differences in 8D as high as 8°/oo.Therefore some of the interlaboratory differences observed may depend on the batch of NBS-1 standard utilized.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingreasoningTo relate δO18 values of calcite on the PDB and SMOW scales, δSMOW = 1.03086 δPDB + 30.86 and δPDB = 0.97006 δSMOW − 29.94, based on fractionation factors at 25°C: 1.0412 for CO2-H2O, 1.01025 for H3PO4-liberated CO2 from calcite, and 1.00022 for H3PO4-liberated CO2 from PDB-CO2 in equilibrium with SMOW.
“To relate 8 O 18 values of calcite on the PDB and SMOW scales, the following expressions are used: 8 sMow=1 -030868 PDB + 30.86, and 8 PDB=0.970068SMOW-29.94.These relationships are based on the following fractionation factors at 25°C: 1.0412 for CO2-H2O, 1.01025 for H 3PO4-liberated CO2 from calcite and, 1.00022 for H 3PO4-liberated CO2 from PDB-CO2 in equilibrium with SMOW.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Findingnone givenThere is some indication that random and significant variations in δO18 exist between different samplings of the main storage vessels of the NBS water standards.
“There is some indication that random and significant variations in 5O18 exist between different samplings of the main storage vessels of the NBS water standards.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Findingnone givenSodium and potassium feldspar have identical isotopic properties within the limits of analytical uncertainty.
“NOTE.Sodium and potassium feldspar have identical isotopic properties within the limits of analytical uncertainty.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Findingnone givenPotassium feldspar has isotopic properties identical to albite within the limits of analytical error.
“Potassium feldspar has isotopic properties identical to albite within the limits of analytical error.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThe crossover point (10^3 ln α = 0) occurs at 130°C, and there is a reversal at 425°C (10^3 ln α = -48).
“The crossover point (10s Ina = 0) occurs at 130°C, and there is a reversal at 425°C 10s In a--48).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenAdditional data on these systems by O'Neil and Truesdell (written commun., 1976) are in agreement with those of Sofer and Gat (1972) and of Taube (1954).
“Additional data on these systems by O'Neil and Truesdell (written commun., 1976) are not shown but are in agreement with those of Sofer and Gat (1972) and of Taube (1954).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites O'Neil and Truesdell (written commun., 1976)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Sofer and Gat (1972)
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites Taube (1954) source
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenThe crossover point in Figure 31 is at 192°C.
“Note the crossover point at 192°C.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Findingnone givenMuscovite and paragonite have identical isotopic properties within the limits of analytical uncertainty.
“NOTE.Muscovite and paragonite have identical isotopic properties within the limits of analytical uncertainty.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductreasoningIn oxygen isotope analysis of carbonates, identical physical and chemical conditions must be operative during preparation of standard and sample so that systematic errors will cancel.
“In the oxygen isotope analysis of carbonates, identical physical and chemical conditions must be operative during preparation of standard and sample so that systematic errors will cancel.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationEquilibrium fractionation factors between species of geochemical interest have been determined directly by laboratory experiments, by calculations using statistical thermodynamics, and inferred from regularities in stable isotope ratios of natural materials.
“Equilibrium fractionation factors that measure the distribution of a rare stable isotope between two species have been determined directly by laboratory experiments and also by calculations using the methods of statistical thermodynamics.They have also been inferred from regularities in the stable isotope ratios of natural materials.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Urey (1947) source
May combine two claims.
PremisecitationThe δ values given by Craig (1957) for NBS-20 and NBS-21 are −1.06 and −27.79, respectively.
“The 8 values given by Craig (1957) for these standards are -1.06 and -27.79, respectively.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Craig (1957) source
May combine two claims.
Study design and conductreasoningThe H3+ contribution to the mass 3 beam cannot be determined precisely; when this contribution is large (>10 percent), the correction may result in incorrect δ values.
“The H3 + contribution to the mass 3 beam cannot be determined precisely.Consequently, when this contribution is large ( > 10 percent), the correction may result in incorrect 8 values.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningAs geothermometers, stable isotope fractionation factors continue to show considerable promise for a variety of geologic environments.
“As geothermometers, stable isotope fractionation factors continue to show considerable promise for a variety of geologic environments.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationnone givenThe two curves for quartz-magnetite are similar and the slope for this important system is fairly certain.
“It is encouraging that the two curves are so similar and that the slope for this important system is fairly certain.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenThe curve in Figure 20 should show a reversal of slope at low temperature similar to that shown by the magnetite-water system.
“This curve should show a reversal of slope at low temperature similar to that shown by the magnetite-water system.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningThere is enough consistency in the natural data to warrant future investigations aimed at reconciling some of the discrepancies in the experimental data.
“There is enough consistency in the natural data to warrant future investigations aimed at reconciling some of the discrepancies in the experimental data.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenSome discrepancies among the experimental curves are undoubtedly the result of nonequilibrium or kinetic isotope effects, which can often be difficult to recognize.
“However, some of the discrepancies among the experimental curves are undoubtedly the result of nonequilibrium or kinetic isotope effects, which can often be difficult to recognize.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThe curve in Figure 26 is based on measurements at only two temperatures, 350° and 400°C.
“This curve is based on measurements at only two temperatures, 350° and 400°C.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenSulfur hexafluoride has some advantages over sulfur dioxide for sulfur isotopic analysis.
“Sulfur hexafluoride has some advantages over sulfur dioxide for sulfur isotopic analysis.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). The quote only partly states this claim.
Study design and conductown dataThe curve in Figure 27 is a least-squares fit to the authors' data.
“This curve is a least-squares fit to the authors' data.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductnone givenTemperatures can be read to ±0.5°C on some curves and to ±5°C on others.
“Temperatures can be read to ±0.5°C on some curves and to ±5°C on others.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenThe expressions in Figure 2 are independent of the standard used.
“The expressions are independent of the standard used.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenThe calculated fractionation factors for gaseous systems are among the most reliable factors presented here.
“The calculated fractionation factors for gaseous systems are among the most reliable factors presented here.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenExcept for the feldspars and micas, rutile, and magnetite, the factor 1.0407 was used in the determination of the isotopic compositions of the waters used in all the experiments.
“Except for the feldspars and micas (O'Neil and Taylor, 1967Taylor, , 1969)), rutile (Addy and Garlick, 1974), and magnetite (Bertenrath and Friedrichsen, 1975) the factor 1.0407 was used in the determination of the isotopic compositions of the waters used in all the experiments.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites O'Neil and Taylor, 1967
- cites Addy and Garlick, 1974 source
- cites Bertenrath and Friedrichsen, 1975
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
Interpretationnone givenThe quartz-magnetite pair is potentially the most useful, and certainly the most sensitive, pair for oxygen isotope thermometry.
“The quartz-magnetite pair is potentially the most useful, and certainly the most sensitive, pair for oxygen isotope thermometry”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe curves proposed by Bottinga and Javoy (1973, 1974) are self-consistent and take into account much of the experimental work and theoretical considerations.
“The curves proposed by Bottinga andJavoy (1973, 1974) are presented, inasmuch as they are self-consistent and take into account much of the experimental work and theoretical considerations.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Bottinga and Javoy (1973, 1974)
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). The quote only partly states this claim.
Study design and conductnone givenThe curve in Figure 4 is an extrapolation of lower temperature data.
“This is an extrapolation of their lower temperature data.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing).
InterpretationreasoningPresenting all these data together uncritically calls attention to the problem areas that require resolution.
“Presenting all these data together uncritically calls attention to the problem areas that require resolution.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenThe Solenhofen Limestone standard is too fine grained to be a good and lasting standard.
“The Solenhofen Limestone standard is actually too fine grained to be a good and lasting standard.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningSome systems have been examined more thoroughly than others in the original references.
“It is clear from reading the details given in the original references that some systems have been examined more thoroughly than others.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone given8W is incorrectly defined in the original paper (Longinelli and Nutti, 1973).
“NOTE.8 W is incorrectly defined in the original paper.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Longinelli and Nutti (1973)
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).
Study design and conductnone givenFractionations (10^3 ln α) can normally be read to ±0.2 per mil from the curves.
“Fractionations (103lna) can normally be read to ±0.2 per mil.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S4 (based).
Premisenone givenThe mass spectrometric corrections for sulfur dioxide are large.
“The mass spectrometric corrections for sulfur dioxide are large”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductreasoningThe curves have been extrapolated beyond the temperature ranges investigated and even beyond the range of stability of some minerals, to provide rough estimates when no other information is available.
“The curves have been extrapolated beyond the temperature ranges investigated and even beyond the range of stability of some minerals.This was done to provide rough estimates when no other information is available.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Interpretationnone givenStable isotope relations are somewhat obscured by experimental difficulties and nonequilibrium effects.
“The stable isotope relations are somewhat obscured by experimental difficulties and nonequilbrium effects”
Quote in the paperSubstantial claim
The authors state this as an assumption.
The fractionation at 25°C is 40.37 for the CO2-H2O system.
“The data have been plotted assuming that the fractionation at 25°C is 40.37.”
The authors state this as an assumption.
For purposes of geothermometry, Δ_quartz-illmenite = 0.95 Δ_quartz-magnetite.
“Based on natural data, it is commonly assumed for purposes of geothermometry that Aquam-illimenite = 0.95 Aquartz.magnetite .”
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?
The paleotemperature under which calcite precipitated is interpreted to have occurred between approximately 13°C and ±33°C.
“the paleotempertaure under which the calcite have precipitated is interpreted to have occurred between approximately 13˚C to ±33˚C (from analyzed samples; see calculation above).”
From Isotopes (<sup>13</sup>C and <sup>18</sup>O) Geochemistry of Lower Triassic Montney Formation, Northeastern British Columbia, Western Canada (2017) · cites this paper as [35]
Figure 2 provides carbonate–water paleotemperature equations that could be used to calculate a calcite precipitation temperature. It does not report the claimed range of approximately 13°C to ±33°C for the citing paper’s analyzed samples; the citing sentence says that range comes from its own calculation. The indexed passages provide no page number for Figure 2. (LLM, conf=0.84)
Experimental — accuracy not yet measuredThe pattern of δ18O depletion with depth is consistent with temperature-dependent δ18O depletion on carbonate minerals at elevated temperatures.
“This pattern is consistent with temperature-dependent δ 18 O depletion on carbonate minerals at elevated temperatures [103-105].”
From Clumped Isotope Reordering and Kinetic Differences in Co-Hosted Calcite and Dolomite Minerals throughout Burial Diagenesis and Exhumation (2023) · cites this paper as [104]
Paleotemperature of precipitation of calcite during the Lower Triassic Period in the study area is approximately 32°C.
“Therefore, paleotemperature of precipitation of calcite during the Lower Triassic Period in the study area is ~32˚C.”
From Isotopes (<sup>13</sup>C and <sup>18</sup>O) Geochemistry of Lower Triassic Montney Formation, Northeastern British Columbia, Western Canada (2017) · cites this paper as [35]
Figure 2 presents a carbonate–water paleotemperature scale, but it does not report a precipitation temperature for the citing study area. Searches for “Lower Triassic,” “study area,” and “32°C” found no passage establishing the claimed site-specific estimate. (LLM, conf=0.76)
Experimental — accuracy not yet measuredAnoxic conditions generate high alkalinity, which increases total dissolved carbon that causes calcite to precipitate from pore-water, thereby biasing carbon isotope towards light δ13C PDB values during early diagenesis.
“The anoxic condition generate high alkalinity, which increases the total dissolved carbon that causes calcite to precipitate from pore-water, thereby biased towards light δ 13 C PDB values during early diagenesis [35].”
From Isotopes (<sup>13</sup>C and <sup>18</sup>O) Geochemistry of Lower Triassic Montney Formation, Northeastern British Columbia, Western Canada (2017) · cites this paper as [35]
The CARBON section (page not provided) identifies PDB as a carbon-isotope reporting standard, and the figure listings describe carbon-13 fractionation factors. Neither addresses the claimed sequence from anoxic conditions through increased alkalinity and pore-water calcite precipitation to light δ13C values during early diagenesis. Searches for anoxic conditions, alkalinity, pore water, and diagenesis found no passage establishing that mechanism. (LLM, conf=0.75)
Experimental — accuracy not yet measured
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“This pattern suggests an inverse correlation between Keq[3866] and the atomic number of the cation, as is also observed in O/O and C/C partitioning between carbonates and other phases (e.g. Sheppard and Schwarcz, 1970; Friedman and O’Neil, 1977; Sommer and Rye, 1978; Grossman and Ku, 1986; Chacko et al., 2001).”
BackgroundResultPan, Y., & Dong, P. (1999) · Ore Geology Reviews · doi:10.1016/s0169-1368(99)00022-0 · Cited by 480 · 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
“These authors apparently synthesized VHMC and therefore have not improved the understanding of the dolomite-water fractionation factor (Friedman & O’Neil, 1977).”
BackgroundBöhlke, J. K., Mroczkowski, S. J., & Coplen, T. B. (2003) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.1123 · Cited by 465 · see citing works
A stable isotope aridity index for terrestrial environments
Levin, N. E., Cerling, T. E., Passey, B. H., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604719103 · Cited by 466 · see citing works
Equilibrium Oxygen, Hydrogen and Carbon Isotope Fractionation Factors Applicable to Geologic Systems
Chacko, T., Cole, D. R., & Horita, J. (2001) · Reviews in Mineralogy and Geochemistry · doi:10.2138/gsrmg.43.1.1 · Cited by 462 · see citing works
Oxygen isotope variations in phosphate of biogenic apatites, IV. Mammal teeth and bones
Luz, B., & Kolodny, Y. (1985) · Earth and Planetary Science Letters · doi:10.1016/0012-821x(85)90047-0 · Cited by 452 · see citing works
Brasier, M. D., & Lindsay, J. F. (1998) · Geology · doi:10.1130/0091-7613(1998)026 · Cited by 243 · see citing works
Rowley, D. B., Pierrehumbert, R. T., & Currie, B. S. (2001) · Earth and Planetary Science Letters · doi:10.1016/s0012-821x(01)00324-7 · Cited by 441 · see citing works
“Conversion of N(18)OCc PDB to N(18)Op SMOW is based on equilibrium, temperature-dependent fractionation between carbonate and water [72] where temperatures and 1c deviations of T derived from the model at the current elevation of each sample is used.”
BackgroundBreecker, D. O., Sharp, Z. D., & McFadden, L. D. (2009) · Geological Society of America Bulletin · doi:10.1130/b26413.1 · Cited by 429 · see citing works
Tremaine, D. M., Froelich, P. N., & Wang, Y. (2011) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2011.06.005 · Cited by 395 · see citing works
“3), while calculations of Frisia et al. (2011) demonstrate a cave air-CO2 contribution to drip water DIC on the order of 25–30%.”
BackgroundHydrogen generation from mantle source rocks in Oman
Neal, C., & Stanger, G. (1983) · Earth and Planetary Science Letters · doi:10.1016/0012-821x(83)90144-9 · Cited by 405 · see citing works
An interactive code (NETPATH) for modeling NET geochemical reactions along a flow PATH, version 2.0
Plummer, L. N., Prestemon, E. C., & Parkhurst, D. L. (1994) · doi:10.3133/wri944169 · Cited by 408 · see citing works
Cenozoic dolomites of carbonate islands: their attributes and origin
Budd, D. A. (1997) · Earth-Science Reviews · doi:10.1016/s0012-8252(96)00051-7 · Cited by 403 · see citing works
Capezzuoli, E., Gandin, A., & Pedley, M. H. (2013) · Sedimentology · doi:10.1111/sed.12075 · Cited by 403 · see citing works
“…when coupled with a d18O water composition estimate, palaeotemperatures can be obtained from the water–bicarbonate oxygen isotope equilibrium fractionation value (Halas & Wolacewicz, 1982, as an alternative to employing the water-travertine equilibrium fractionation of Friedman & O’Neil, 1977).”
Wang, Y., & Cerling, T. E. (1994) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/0031-0182(94)90100-7 · Cited by 403 · see citing works
Jaffrés, J. B. D., Shields, G. A., & Wallmann, K. (2007) · Earth-Science Reviews · doi:10.1016/j.earscirev.2007.04.002 · Cited by 398 · see citing works
“Similarly, the equation for calcite was determined as 1000⁎ ln(αcalcite-water)=2.78⁎10 6T−2− 2.89 (Friedman and O'Neil, 1977).”
BackgroundInfluentialOxygen and carbon isotope fractionations between CO2 and calcite
Chacko, T., Mayeda, T. K., Clayton, R. N., & Goldsmith, J. R. (1991) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(91)90452-b · Cited by 387 · see citing works
The influence of microhabitats on the carbon isotopic composition of deep‐sea benthic foraminifera
McCorkle, D. C., Keigwin, L. D., Corliss, B. H., & Emerson, S. (1990) · Paleoceanography · doi:10.1029/pa005i002p00161 · Cited by 382 · see citing works
Swart, P. K., Burns, S. J., & Leder, J. J. (1991) · Chemical Geology: Isotope Geoscience section · doi:10.1016/0168-9622(91)90055-2 · Cited by 382 · see citing works
Phosphoric acid fractionation factors for calcite and aragonite between 25 and 75 °C: Revisited
Kim, S.-T., Mucci, A., & Taylor, B. E. (2007) · Chemical Geology · doi:10.1016/j.chemgeo.2007.08.005 · Cited by 374 · see citing works
“The 1000lnαCO2(ACID)–carbonate value for aragonite was initially determined by Sharma and Clayton (1965), and later revised by Friedman and O'Neil (1977) to 10.29 (±0.06; n=2) at 25 °C.”
BackgroundMethodResultInfluentialUranium-series Chronology and Environmental Applications of Speleothems
Richards, D. A. (2003) · Reviews in Mineralogy and Geochemistry · doi:10.2113/0520407 · Cited by 385 · see citing works
Stable isotope analysis of multiple carbonate samples using selective acid extraction
Al‐Aasm, I. S., Taylor, B. E., & South, B. C. (1990) · Chemical Geology Isotope Geoscience section · doi:10.1016/0168-9622(90)90020-d · Cited by 371 · see citing works
Fouke, B. W., Farmer, J. D., Marais, D. J. D., Pratt, L. M., Sturchio, N. C., Burns, P. C., & Discipulo, M. (2000) · Journal of Sedimentary Research · doi:10.1306/2dc40929-0e47-11d7-8643000102c1865d · Cited by 363 · see citing works
“The individual fractionation factors (Friedman and O'Neil 1977) are ␣ f ϭ C f /C g , ␣ b ϭ C b /C g , ␣ d ϭ C d /C g (g ϭ gaseous CO 2 , f ϭ dissolved CO 2 ϩ H 2 CO 3 , b ϭ dissolved HCO 3 Ϫ , d ϭ dissolved CO 3 2Ϫ ).”
Dettman, D. L., Reische, A. K., & Lohmann, K. C. (1999) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(99)00020-4 · Cited by 358 · see citing works
Oxygen isotope partitioning between phosphate and carbonate in mammalian apatite
Bryant, J. D., Koch, P. L., Froelich, P. N., Showers, W., & Genna, B. J. (1996) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(96)00308-0 · Cited by 353 · see citing works
Stable Isotope-Based Paleoaltimetry
Rowley, D. B., & Garzione, C. N. (2007) · Annual Review of Earth and Planetary Sciences · doi:10.1146/annurev.earth.35.031306.140155 · Cited by 355 · see citing works
Geochemistry and origin of formation brines from the Paris Basin, France
Fontes, J. C., & Matray, J. (1993) · Chemical Geology · doi:10.1016/0009-2541(93)90068-t · Cited by 354 · see citing works
Vasconcelos, C., McKenzie, J. A., Warthmann, R., & Bernasconi, S. M. (2005) · Geology · doi:10.1130/g20992.1 · Cited by 354 · see citing works
Coplen, T. B. (2007) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2007.05.028 · Cited by 347 · see citing works
Watson, E. B. (2004) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2003.10.003 · Cited by 340 · see citing works
Carbon and oxygen isotope fractionation in scleractinian corals: a review
Swart, P. K. (1983) · Earth-Science Reviews · doi:10.1016/0012-8252(83)90076-4 · Cited by 341 · see citing works
Calculation of oxygen isotope fractionation in metal oxides
Yong-fei, Z. (1991) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(91)90105-e · Cited by 337 · see citing works
Kieffer, S. W. (1982) · Reviews of Geophysics · doi:10.1029/rg020i004p00827 · Cited by 332 · see citing works
Garzione, C. N., Quade, J., DeCelles, P. G., & English, N. B. (2000) · Earth and Planetary Science Letters · doi:10.1016/s0012-821x(00)00252-1 · Cited by 326 · see citing works
“1 We use the equation of Friedman and O'Neil [55] instead of the more recently published equation by Kim and O'Neil [56]”
BackgroundMethodInfluentialYakir, D., & Wang, X. (1996) · Nature · doi:10.1038/380515a0 · Cited by 326 · see citing works
Andrews, J. A., & Schlesinger, W. H. (2001) · Global Biogeochemical Cycles · doi:10.1029/2000gb001278 · Cited by 325 · 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
A humid climate state during the Palaeocene/Eocene thermal maximum
Bowen, G. J., Beerling, D. J., Koch, P. L., Zachos, J. C., & Quattlebaum, T. (2004) · Nature · doi:10.1038/nature03115 · Cited by 320 · see citing works
Greinert, J., Bohrmann, G., & Suess, E. (2011) · Geophysical monograph · doi:10.1029/gm124p0099 · Cited by 320 · see citing works
“Whereas carbon isotopes reflect the carbon source, oxygen isotopes are effected by the formation temperature, the isotopic composition of the source water and the respective fractionation of the carbonate phases [Friedman and O'Neil, 1977].”
BackgroundBijma, J., Spero, H. J., & Lea, D. W. (1999) · Springer eBooks · doi:10.1007/978-3-642-58646-0_20 · Cited by 322 · see citing works
Stuart, F. M., Burnard, P. G., Taylor, R. P., et al. (1995) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(95)00300-2 · Cited by 311 · see citing works
Affek, H. P., Bar-Matthews, M., Ayalon, A., Matthews, A., & Eiler, J. M. (2008) · Geochimica et Cosmochimica Acta · doi:10.1016/j.gca.2008.06.031 · Cited by 306 · see citing works
Environment of formation and styles of volcanogenic massive sulfides: The Iberian Pyrite Belt
Tornos, F. (2005) · Ore Geology Reviews · doi:10.1016/j.oregeorev.2004.12.005 · Cited by 306 · see citing works
Proskurowski, G., Lilley, M. D., Kelley, D. S., & Olson, E. J. (2006) · Chemical Geology · doi:10.1016/j.chemgeo.2005.11.005 · Cited by 299 · see citing works
“We extrapolate the experimentally derived geothermometer equations to accommodate the low-temperature Lost City samples, a treatment similar to the one published in Friedman and O'Neil (1977).”
MethodMass transfer and carbon isotope evolution in natural water systems
Wigley, T. M. L., Plummer, L. N., & Pearson, F. J. (1978) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(78)90108-4 · Cited by 302 · see citing works
Oxygen 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 · see citing works
Stable isotope mass balance of lakes: a contemporary perspective
Gibson, J. J., Birks, S. J., & Yi, Y. (2015) · Quaternary Science Reviews · doi:10.1016/j.quascirev.2015.04.013 · Cited by 294 · see citing works
“Analogous to marine studies (Emiliani, 1955; Shackleton and Opdyke, 1973) stratigraphic changes in d18O in the lacustrine environment were initially attributed largely to changes in lake or air temperature (Eicher and Siegenthaler, 1976) and interpreted based on the understanding of the temperature dependence of isoto…”
BackgroundAn interactive code (NETPATH) for modeling NET geochemical reactions along a flow PATH
Plummer, L. N., Prestemon, E. C., & Parkhurst, D. L. (1991) · doi:10.3133/wri914078 · Cited by 295 · see citing works
“Friedman and O'Neil (1977) give an extensive review of literature values of a.”
BackgroundKursinski, E. R., Hajj, G. A., Bertiger, W. I., et al. (1996) · Science · doi:10.1126/science.271.5252.1107 · Cited by 290 · see citing works
Naehr, T., Eichhubl, P., Orphan, V. J., Hovland, M. T., Paull, C. K., Ussler, W., Lorenson, T. D., & Greene, H. G. (2007) · Deep Sea Research Part II Topical Studies in Oceanography · doi:10.1016/j.dsr2.2007.04.010 · Cited by 286 · see citing works
“Our calculations of equilibrium formation temperatures or pore water isotopic compositions are based on equations by Friedman and O’Neil (1977) for Mg-calcite, Hudson and Anderson (1989) for aragonite, and Irwin (1980) for protodolomite and dolomite.”
MethodThe formation of caliche in soils of the Mojave Desert, California
Schlesinger, W. H. (1985) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(85)90191-7 · Cited by 286 · see citing works
von Grafenstein, U., Erlernkeuser, H., & Trimborn, P. (1999) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/s0031-0182(98)00180-1 · Cited by 285 · see citing works
Fleitmann, D., Burns, S. J., Neff, U., et al. (2003) · Quaternary Research · doi:10.1016/s0033-5894(03)00086-3 · Cited by 285 · see citing works
“Whereas DFI values directly reflect the isotopic composition of paleogroundwater, 18O values must be calculated from measured 18OC values using the calcite-water fractionation equation (103ln 2.78(106T 2) 2.89; Friedman and O’Neil, 1977), assuming a cave air temperature between 25° and 27°C.”
MethodInfluentialKlein, R. T., Lohmann, K. C., & Thayer, C. W. (1996) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(96)00232-3 · Cited by 279 · see citing works
Carothers, W. W., Adami, L. H., & Rosenbauer, R. J. (1988) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(88)90302-x · Cited by 282 · see citing works
Oxygen isotope variations in phosphate of biogenic apatites, II. Phosphorite rocks
Shemesh, A., Kolodny, Y., & Luz, B. (1983) · Earth and Planetary Science Letters · doi:10.1016/0012-821x(83)90101-2 · Cited by 281 · see citing works
An Isotopic Study of Paleosol Carbonates from Olduvai Gorge
Cerling, T. E., & Hay, R. L. (1986) · Quaternary Research · doi:10.1016/0033-5894(86)90044-x · Cited by 279 · see citing works
Mullis, J., Jean Dubessy, A., Poty, B., & O’Neil, J. R. (1994) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(94)90008-6 · Cited by 278 · see citing works
Self-citationThe Cenomanian–Turonian boundary at Eastbourne (Sussex, UK): a proposed European reference section
PAUL, C. R. C., Lamolda, M. A., Mıtchell, S. F., et al. (1999) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/s0031-0182(99)00009-7 · Cited by 275 · see citing works
“01025 was used (Friedman and O’Neil, 1977): R samples were reacted at 50oC and an acid fractionation factor of 1.”
MethodInfluentialMao, J., Wang, Y., Li, H., Pirajno, F., Zhang, C., & Wang, R. (2007) · Ore Geology Reviews · doi:10.1016/j.oregeorev.2007.01.003 · Cited by 274 · see citing works
Oxygen isotope fractionation in quartz, albite, anorthite and calcite
Clayton, R. N., Goldsmith, J. R., & Mayeda, T. K. (1989) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(89)90015-x · Cited by 272 · see citing works
Delaney, M. L., Bé, A. W. H., & Boyle, E. A. (1985) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(85)90284-4 · Cited by 266 · see citing works
Curtis, C. D., Coleman, M. L., & Love, L. G. (1986) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(86)90085-2 · Cited by 264 · see citing works
Zazzo, A., Lécuyer, C., & Mariotti, A. A. (2003) · Geochimica et Cosmochimica Acta · doi:10.1016/s0016-7037(03)00278-3 · Cited by 265 · see citing works
Oxygen 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 · see citing works
Truesdell, A. H., Nathenson, M., & Rye, R. O. (1977) · Journal of Geophysical Research Atmospheres · doi:10.1029/jb082i026p03694 · Cited by 259 · see citing works
Stable isotope stratigraphy and paleoclimatology of the Paleogene Bighorn Basin (Wyoming, USA)
Koch, P., Zachos, J., & Dettman, D. (1995) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/0031-0182(94)00107-j · Cited by 279 · see citing works
Hildreth, W., Christiansen, R. L., & O'Neil, J. R. (1984) · Journal of Geophysical Research Atmospheres · doi:10.1029/jb089ib10p08339 · Cited by 251 · see citing works
Self-citationStable isotopic compositions of precipitation in China
Liu, J., Song, X., Yuan, G., et al. (2014) · Tellus B · doi:10.3402/tellusb.v66.22567 · Cited by 247 · see citing works
“where a2 and a18 are temperature dependent (Friedman and O’Neil, 1977; Criss, 1999):”
BackgroundRicketts, R. D., Johnson, T. C., Brown, E. T., Rasmussen, K. A., & Romanovsky, V. V. (2001) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/s0031-0182(01)00339-x · Cited by 244 · see citing works
δ18O and δ13C values of modern brachiopod shells
Carpenter, S. J., & Lohmann, K. C. (1995) · Geochimica et Cosmochimica Acta · doi:10.1016/0016-7037(95)00291-7 · Cited by 242 · see citing works
Currie, B. S., Rowley, D. B., & Tabor, N. J. (2005) · Geology · doi:10.1130/g21170.1 · Cited by 242 · see citing works
Middle to Late Paleozoic Atmospheric CO <sub>2</sub> Levels from Soil Carbonate and Organic Matter
Mora, C. I., Driese, S. G., & Colarusso, L. A. (1996) · Science · doi:10.1126/science.271.5252.1105 · Cited by 239 · see citing works
“A number of studies report an increase in the 8'3C of marine inorganic carbon (marine carbonate rocks) from 0 per mil in the Late Silurian to 6 per mil in the Early Permian (I 1); the 8'3C of atmospheric CO2 is thus predicted to parallel this trend, with values -7 per mil more negative (12).”
BackgroundAn integrated chemical and stable‐isotope model of the origin of Midocean Ridge Hot Spring Systems
Bowers, T. S., & Taylor, H. P. (1985) · Journal of Geophysical Research Atmospheres · doi:10.1029/jb090ib14p12583 · Cited by 239 · see citing works
Rosales, I., Quesada, S., & Robles, S. (2004) · Palaeogeography Palaeoclimatology Palaeoecology · doi:10.1016/s0031-0182(03)00686-2 · Cited by 238 · see citing works
- Authors
- Friedman, I., & O'Neil, J. R.
- Venue
- Professional Paper
- Publisher
- US Geological Survey
- Published
- 1977
- ISSN
- 1044-9612 (ISSN-L)
- 2330-7102
- OpenAlex
- W1547907389
- Cited by
- 2,646
- References
- 43
- Citations by year
- 2026: 14 · 2025: 51 · 2024: 43 · 2023: 57 · 2022: 65 · 2021: 85 · 2020: 111 · 2019: 94 · 2018: 86 · 2017: 85 · 2016: 79 · 2015: 84 · 2014: 70 · 2013: 82 · 2012: 82
- Type
- report
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- USGS professional paper (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Inorganic Chemistry › Radioactive element chemistry and processing
- Physical Sciences › Environmental Science › Waste Management and Disposal › Chemical Synthesis and Characterization
- Physical Sciences › Environmental Science › Environmental Chemistry › Methane Hydrates and Related Phenomena
- Keywords
- stable isotope fractionation, isotope fractionation factors, geochemistry, cosmochemistry, Earth composition, chemical elements
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