Difference between revisions of "Isotopes of carbon"

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| 12 (by definition)<ref group="note" name="C-12">The [[relative atomic mass]] of [[carbon-12]] is exactly twelve [[atomic mass unit]]s, without any [[measurement uncertainty]], by the definition of the atomic mass unit.</ref>
 
| 12 (by definition)<ref group="note" name="C-12">The [[relative atomic mass]] of [[carbon-12]] is exactly twelve [[atomic mass unit]]s, without any [[measurement uncertainty]], by the definition of the atomic mass unit.</ref>
 
| 0.9893(8)
 
| 0.9893(8)
−
| 0.9885–0.9902
+
| 0.988 53–0.990 37
 
|-
 
|-
 
| <sup>13</sup>C
 
| <sup>13</sup>C
 
| 13.003 354 837 78(98)
 
| 13.003 354 837 78(98)
 
| 0.0107(8)
 
| 0.0107(8)
−
| 0.0115–0.0098
+
| 0.011 47–0.009 63
 
|-
 
|-
−
| colspan=4 | References:<ref name="IUPAC2000">{{IUPAC atomic weight review 2000}}.</ref><ref name="AME"/><ref name="TICE">{{IUPAC isotopic compositions 1997}}.</ref>
+
| colspan=4 | References:<ref name="IUPAC2000">{{IUPAC atomic weight review 2000}}.</ref><ref name="AME"/><ref name="TICE">{{TICE 2001}}.</ref>
 
|-
 
|-
 
|}
 
|}
 
The standard [[atomic weight]] of carbon has been fixed at its current value since 1995.<ref name="IUPAC2000"/> The range of natural [[isotopic composition]]s makes a more precise standard value unobtainable, and some terrestrial geological specimens may show compositions outside of the normal range.<ref name="IUPAC2000"/> Natural amounts of [[carbon-14]] (''x''&nbsp;<&nbsp;10<sup>−12</sup>) are insignificant in the calculation of atomic weight.<ref name="IUPAC2000"/>
 
The standard [[atomic weight]] of carbon has been fixed at its current value since 1995.<ref name="IUPAC2000"/> The range of natural [[isotopic composition]]s makes a more precise standard value unobtainable, and some terrestrial geological specimens may show compositions outside of the normal range.<ref name="IUPAC2000"/> Natural amounts of [[carbon-14]] (''x''&nbsp;<&nbsp;10<sup>−12</sup>) are insignificant in the calculation of atomic weight.<ref name="IUPAC2000"/>
  
−
Carbon-13 is systematically depleted in samples of biological origin (compared to atmospheric [[carbon dioxide]] and most [[Carbonate mineral|carbonate rocks]]) due to a [[kinetic isotope effect]] that is particularly pronounced in [[Photosynthesis|photosynthetic reactions]].<ref group="note">Marine organisms that obtain carbonate from sea water to construct exoskeletons do not show the depletion of <sup>13</sup>C ''in the exoskeletons'': indeed, when such exoskeletons become carbonate rocks, they often show anomalously ''high'' amount fractions of <sup>13</sup>C, an indication that the carbon did not pass through a photosynthetic pathway.</ref> The effect is strongest in [[C4-Pathway|C<sub>4</sub>-plants]], which are predominant in tropical and subtropical climates, and measurements of carbon isotopic compositions are important in [[geochemistry]], [[paleoclimatology]] and [[paleoceanography]]. Such measurements have also attracted interest for detecting cases of "doping" in sport:<ref>{{citation | first1 = Rodrigo | last1 = Aguilera | first2 = Caroline K. | last2 = Hatton | first3 = Don H. | last3 = Catlin | title = Detection of Epitestosterone Doping by Isotope Ratio Mass Spectrometry | journal = Clin. Chem. | volume = 48 | pages = 629–36 | year = 2002 | pmid = 11901061}}.</ref><ref>{{citation | journal = J. Steroid Biochem. Mol. Biol. | year = 2009 | volume = 115 | issue = 3–5 | pages = 107–14 | title = Drug testing data from the 2007 Pan American Games: ''δ''<sup>13</sup>C values of urinary androsterone, etiocholanolone and androstanediols determined by GC/C/IRMS | last1 = Aguilera | first1 = Rodrigo | last2 = Chapman | first2 = Thomas E. | last3 = Pereira | first3 = Henrique | last4 = Oliveira | first4 = Giselle C. | last5 = Illanes | first5 = Renata P. | last6 = Fernandes | first6 = Telma F. | last7 = Azevedo | first7 = Débora A. | last8 = Aquino Neto | first8 = Francisco | doi = 10.1016/j.jsbmb.2009.03.012}}.</ref> steroid hormones produced by biotechnological methods would be expected to have higher amount fractions of <sup>13</sup>C than those produced by an athlete's body.<ref group="note">It was shown by Aguilera, Hatton & Catlin (2002) that their 2002 samples of artificial [[epitestosterone]] had significantly (''P''&nbsp;<&nbsp;0.0001) lower ''δ''<sup>13</sup>C values than natural epitestosterone from human urine.</ref>
+
Carbon-13 is systematically depleted in samples of biological origin (compared to atmospheric [[carbon dioxide]] and most [[Carbonate mineral|carbonate rocks]]) due to a [[kinetic isotope effect]] that is particularly pronounced in [[Photosynthesis|photosynthetic reactions]].<ref group="note">Marine organisms that obtain carbonate from sea water to construct exoskeletons do not show the depletion of <sup>13</sup>C ''in the exoskeletons'': indeed, when such exoskeletons become carbonate rocks, they often show anomalously ''high'' amount fractions of <sup>13</sup>C, an indication that the carbon did not pass through a photosynthetic pathway.</ref> The effect is slightly weaker (but still significant) in [[C4-Pathway|C<sub>4</sub>-plants]], which are predominant in tropical and subtropical climates, and measurements of carbon isotopic compositions are important in [[geochemistry]], [[paleoclimatology]] and [[paleoceanography]].<ref>{{IUPAC IAV 2002}}.</ref> Such measurements have also attracted interest for detecting cases of "doping" in sport:<ref>{{citation | first1 = Rodrigo | last1 = Aguilera | first2 = Caroline K. | last2 = Hatton | first3 = Don H. | last3 = Catlin | title = Detection of Epitestosterone Doping by Isotope Ratio Mass Spectrometry | journal = Clin. Chem. | volume = 48 | pages = 629–36 | year = 2002 | pmid = 11901061}}.</ref><ref>{{citation | journal = J. Steroid Biochem. Mol. Biol. | year = 2009 | volume = 115 | issue = 3–5 | pages = 107–14 | title = Drug testing data from the 2007 Pan American Games: ''δ''<sup>13</sup>C values of urinary androsterone, etiocholanolone and androstanediols determined by GC/C/IRMS | last1 = Aguilera | first1 = Rodrigo | last2 = Chapman | first2 = Thomas E. | last3 = Pereira | first3 = Henrique | last4 = Oliveira | first4 = Giselle C. | last5 = Illanes | first5 = Renata P. | last6 = Fernandes | first6 = Telma F. | last7 = Azevedo | first7 = Débora A. | last8 = Aquino Neto | first8 = Francisco | doi = 10.1016/j.jsbmb.2009.03.012}}.</ref> steroid hormones produced by biotechnological methods would be expected to have higher amount fractions of <sup>13</sup>C than those produced by an athlete's body.<ref group="note">It was shown by Aguilera, Hatton & Catlin (2002) that their 2002 samples of artificial [[epitestosterone]] had significantly (''P''&nbsp;<&nbsp;0.0001) lower ''δ''<sup>13</sup>C values than natural epitestosterone from human urine.</ref>
  
−
The [[primary standard]] for the isotopic composition of carbon is Pee Dee Belemnite (PDB), a fossile marine carbonate from the Pee Dee Formation, South Caroline, USA:<ref name="IAEA">{{citation | first1 = R. | last1 = Gonfiantini | first2 = W. Stichler | first3 = K. | last3 = Rozanski | contribution = Standards and intercomparison materials distributed by the International Atomic Energy Agency for stable isotope measurements | title = Reference and intercomparison materials for stable isotopes of light elements | url = http://www.iaea.org/programmes/aqcs/pdf/tecdoc_0825.pdf | year = 1995 | location = Vienna | publisher = International Atomic Energy Agency | id = IAEA-TECDOC-825 | pages = 13–29}}.</ref> as with most carbonate rocks, this has a relatively high amount franction of <sup>13</sup>C, and so most ''δ''<sup>13</sup>C values are negative. Supplies of standard PDB have long been been exhausted, so modern measurements of isotopic composition are referred to a secondary standard, NBS&nbsp;19, a crushed [[marble]] of unknown geographical origin that is also referred to as "TS-limestone".<ref>{{citation | title = NBS 19, TS-Limestone | url = http://curem.iaea.org/catalogue/SI/SI_002190000.html | publisher = International Atomic Energy Agency | accessdate = 2010-03-14}}.</ref> NBS&nbsp;19 forms the basis of the V-PDB (for "Vienna PDB") scale of ''δ''<sup>13</sup>C, which is designed to give equivalent ''δ''<sup>13</sup>C values to the older PDB scale: NBS&nbsp;19 has a defined value of ''δ''<sup>13</sup>C&nbsp;= +1.95‰ on the V-PDB scale. A two-point scale based on NBS&nbsp;19 and LSVEC, a [[lithium carbonate]] standard with a very low ''δ''<sup>13</sup>C value, has also been proposed.<ref>{{citation | last1 = Coplen | first1 = Tyler B.| last2 = Brand | first2 = Willi A. | last3 = Gehre | first3 = Matthias | last4 = Gröning | first4 = Mannfred | last5 = Meijer | first5 = Harro A. J. | last6 = Toman | first6 = Blaza | last7 = Verkouteren | first7 = R. Michael | year = 2006 | title = New Guidelines for ''δ''<sup>13</sup>C Measurements | journal = Anal. Chem. | volume = 78 | issue = 7 | pages = 2439–41 | doi = 10.1021/ac052027c}}.</ref>
+
The [[primary standard]] for the isotopic composition of carbon is Pee Dee belemnite (PDB), a fossile marine carbonate from the Pee Dee Formation, South Carolina, USA:<ref name="IAEA">{{citation | first1 = R. | last1 = Gonfiantini | first2 = W. | last2 = Stichler | first3 = K. | last3 = Rozanski | contribution = Standards and intercomparison materials distributed by the International Atomic Energy Agency for stable isotope measurements | title = Reference and intercomparison materials for stable isotopes of light elements | url = http://www.iaea.org/programmes/aqcs/pdf/tecdoc_0825.pdf | year = 1995 | location = Vienna | publisher = International Atomic Energy Agency | id = IAEA-TECDOC-825 | pages = 13–29}}.</ref> as with most carbonate rocks, this has a relatively high amount franction of <sup>13</sup>C, and so most ''δ''<sup>13</sup>C values are negative. Supplies of standard PDB have long been been exhausted, so modern measurements of isotopic composition (since about 1985) are referred to a secondary standard, NBS&nbsp;19, a crushed [[marble]] of unknown geographical origin that is also referred to as "TS-limestone".<ref>{{citation | title = NBS 19, TS-Limestone | url = http://curem.iaea.org/catalogue/SI/SI_002190000.html | publisher = International Atomic Energy Agency | accessdate = 2010-03-14}}.</ref> NBS&nbsp;19 forms the basis of the V-PDB (for "Vienna PDB") scale of ''δ''<sup>13</sup>C, which is designed to give equivalent ''δ''<sup>13</sup>C values to the older PDB scale: NBS&nbsp;19 has a defined value of ''δ''<sup>13</sup>C&nbsp;= +1.95‰ on the V-PDB scale. A two-point scale based on NBS&nbsp;19 and L-SVEC, a [[lithium carbonate]] standard with a very low ''δ''<sup>13</sup>C value, has also been proposed.<ref name="Stichler">{{citation | first = W. | last = Stichler | contribution = Interlaboratory Comparison of New Materials for Carbon and Oxygen Isotope Ratio Measurements | title = Reference and intercomparison materials for stable isotopes of light elements | url = http://www.iaea.org/programmes/aqcs/pdf/tecdoc_0825.pdf | year = 1995 | location = Vienna | publisher = International Atomic Energy Agency | id = IAEA-TECDOC-825 | pages = 67–74}}.</ref><ref>{{citation | last1 = Coplen | first1 = Tyler B.| last2 = Brand | first2 = Willi A. | last3 = Gehre | first3 = Matthias | last4 = Gröning | first4 = Mannfred | last5 = Meijer | first5 = Harro A. J. | last6 = Toman | first6 = Blaza | last7 = Verkouteren | first7 = R. Michael | year = 2006 | title = New Guidelines for ''δ''<sup>13</sup>C Measurements | journal = Anal. Chem. | volume = 78 | issue = 7 | pages = 2439–41 | doi = 10.1021/ac052027c}}.</ref>
  
 
{| class="wikitable"
 
{| class="wikitable"
 
! Standard
 
! Standard
 +
! Material
 
! ''δ''<sup>13</sup>C (PDB)
 
! ''δ''<sup>13</sup>C (PDB)
 
! ''δ''<sup>13</sup>C (V-PDB)
 
! ''δ''<sup>13</sup>C (V-PDB)
Line 40: Line 41:
 
|-
 
|-
 
| PDB
 
| PDB
 +
| belemnite
 
| '''0‰'''
 
| '''0‰'''
−
| 0‰
+
| —
 
| 0.011 2372(300)
 
| 0.011 2372(300)
−
| 0.011 11(3)
+
| 0.011 112(29)
−
| 12.011 15(3)
+
| 12.011 15(29)
 
| align=center | <ref>{{citation | first = Harmon | last = Craig | title = Isotopic standards for carbon and oxygen and correction factors for mass-spectrometric analysis of carbon dioxide | journal = Geochim. Cosmochim. Acta | volume = 12 | issue = 1–2 | pages = 133–49 | year = 1957 | doi = 10.1016/0016-7037(57)90024-8}}.</ref>
 
| align=center | <ref>{{citation | first = Harmon | last = Craig | title = Isotopic standards for carbon and oxygen and correction factors for mass-spectrometric analysis of carbon dioxide | journal = Geochim. Cosmochim. Acta | volume = 12 | issue = 1–2 | pages = 133–49 | year = 1957 | doi = 10.1016/0016-7037(57)90024-8}}.</ref>
 +
|-
 +
| ''V-PDB''
 +
| ''virtual''
 +
| —
 +
| '''0‰'''
 +
| 0.011 180
 +
| 0.011 057
 +
| 12.011 09
 +
| align=center | <ref name="Chang">{{citation | first1 = T.-L. | last1 = Chang | first2 = W. | last2 = Li | journal = Chin. Sci. Bull. | volume = 35 | pages = 290–96 | year = 1990}}.</ref>
 
|-
 
|-
 
| NBS 19
 
| NBS 19
 +
| [[calcite]]
 
| —
 
| —
 
| '''+1.95‰'''
 
| '''+1.95‰'''
−
|  
+
| 0.011 202(29)
−
|  
+
| 0.011 078(28)
−
|  
+
| 12.011 12(28)
−
| align=center | <ref>{{citation | first1 = T.-L. | last1 = Chang | first2 = W. | last2 = Li | journal = Chin. Sci. Bull. | volume = 35 | pages = 290–96 | year = 1990}}.</ref>
+
| align=center | <ref name="Chang"/>
 
|-
 
|-
−
| LSVEC
+
| L-SVEC
 +
| [[Lithium carbonate|Li<sub>2</sub>CO<sub>3</sub>]]
 
| —
 
| —
 
| −46.479(150)‰
 
| −46.479(150)‰
−
|  
+
| 0.010 660
−
|  
+
| 0.010 548
−
|  
+
| 12.010 58
 +
| align=center | <ref name="IAEA"/><ref name="Stichler"/>
 +
|-
 +
| IAEA-CO-1
 +
| [[calcite]]
 +
| —
 +
| +2.480(25)‰
 +
| 0.011 208
 +
| 0.011 084
 +
| 12.011 12
 +
| align=center | <ref name="Stichler"/>
 +
|-
 +
| IAEA-CO-8
 +
| [[calcite]]
 +
| —
 +
| −5.749(63)‰
 +
| 0.011 116
 +
| 0.010 994
 +
| 12.011 03
 +
| align=center | <ref name="Stichler"/>
 +
|-
 +
| IAEA-CO-9
 +
| [[Barium carbonate|Ba<sub>2</sub>CO<sub>3</sub>]]
 +
| —
 +
| −47.119(149)‰
 +
| 0.010 654
 +
| 0.010 548
 +
| 12.010 58
 +
| align=center | <ref name="Stichler"/>
 +
|-
 +
| USGS 24
 +
| [[graphite]]
 +
| —
 +
| −15.994(105)‰
 +
| 0.011 002
 +
| 0.010 882
 +
| 12.010 92
 +
| align=center | <ref name="Stichler"/>
 +
|-
 +
| NBS 22
 +
| [[oil]]
 +
| —
 +
| −29.739(124)‰
 +
| 0.010 848
 +
| 0.010 732
 +
| 12.010 77
 +
| align=center | <ref name="IAEA"/>
 +
|-
 +
| IAEA-CH-7
 +
| [[polythene]]
 +
| —
 +
| −31.826(114)‰
 +
| 0.010 825
 +
| 0.010 709
 +
| 12.010 74
 +
| align=center | <ref name="IAEA"/>
 +
|-
 +
| IAEA-C-6
 +
| [[sucrose]]
 +
| —
 +
| −10.431(126)‰
 +
| 0.011 064
 +
| 0.010 943
 +
| 12.010 98
 
| align=center | <ref name="IAEA"/>
 
| align=center | <ref name="IAEA"/>
 +
|-
 +
| colspan=8 | The isotopic compositions of some [[standard reference material]]s for carbon isotope analysis.<br/>Values in bold are fixed by definition.
 
|-
 
|-
 
|}
 
|}
  
−
The highest reported ''δ''<sup>13</sup>C value is +37.5‰ [''n''(<sup>13</sup>C)/''n''(<sup>12</sup>C)&nbsp;= ; ''x''(<sup>13</sup>C)&nbsp;= 0.011 466; ''A''<sub>r</sub>(C)&nbsp;= 12.011 50] for dissolved carbonate in marine sediment pore water,<ref>{{citation | first1 = George E. | last1 = Claypool | first2 = Charles N. | last2 = Threlkeld | first3 = Paul N. | last3 = Mankiewicz | first4 = Michael A. | last4 = Arthur | first5 = Thomas F. | last5 = Anderson | contribution = Isotopic Composition of Interstitial Fluids and Origin of Methane in Slope Sediment of the Middle America Trench, Deep Sea Drilling Project Leg 84 | url = http://www.deepseadrilling.org/84/volume/dsdp84_24.pdf | title = Initial Reports of the Deep Sea Drilling Project | volume = 84 | pages = 683–91 | year = 1985 | doi = 10.2973/dsdp.proc.84.124.1985}}.</ref> while the lowest reported value is −130.3‰ [''n''(<sup>13</sup>C)/''n''(<sup>12</sup>C)&nbsp;= ; ''x''(<sup>13</sup>C)&nbsp;= 0.009 629; ''A''<sub>r</sub>(C)&nbsp;= 12.009 66] for a sample of [[crocetane]] recovered from the ocean bottom at cold seeps in the northern Pacific Ocean.<ref>{{citation | first1 = Marcus | last1 = Elvert | first2 = Erwin | last2 = Suess | first3 = Jens | last3 = Greinert | first4 = Michael J. | last4 = Whiticar | title = Archaea mediating anaerobic methane oxidation in deep-sea sediments at cold seeps of the eastern Aleutian subduction zone  | journal = Org. Geochem. | year = 2000 | volume = 31 | issue = 11 | pages = 1175–87 | doi = 10.1016/S0146-6380(00)00111-X}}.</ref>
+
The highest reported ''δ''<sup>13</sup>C value is +37.5‰ [''n''(<sup>13</sup>C)/''n''(<sup>12</sup>C)&nbsp;= 0.011 599; ''x''(<sup>13</sup>C)&nbsp;= 0.011 466; ''A''<sub>r</sub>(C)&nbsp;= 12.011 50] for dissolved carbonate in marine sediment pore water,<ref>{{citation | first1 = George E. | last1 = Claypool | first2 = Charles N. | last2 = Threlkeld | first3 = Paul N. | last3 = Mankiewicz | first4 = Michael A. | last4 = Arthur | first5 = Thomas F. | last5 = Anderson | contribution = Isotopic Composition of Interstitial Fluids and Origin of Methane in Slope Sediment of the Middle America Trench, Deep Sea Drilling Project Leg 84 | url = http://www.deepseadrilling.org/84/volume/dsdp84_24.pdf | title = Initial Reports of the Deep Sea Drilling Project | volume = 84 | pages = 683–91 | year = 1985 | doi = 10.2973/dsdp.proc.84.124.1985}}.</ref> while the lowest reported value is −130.3‰ [''n''(<sup>13</sup>C)/''n''(<sup>12</sup>C)&nbsp;= 0.009 723; ''x''(<sup>13</sup>C)&nbsp;= 0.009 629; ''A''<sub>r</sub>(C)&nbsp;= 12.009 66] for a sample of [[crocetane]] recovered from the ocean bottom at cold seeps in the northern Pacific Ocean.<ref>{{citation | first1 = Marcus | last1 = Elvert | first2 = Erwin | last2 = Suess | first3 = Jens | last3 = Greinert | first4 = Michael J. | last4 = Whiticar | title = Archaea mediating anaerobic methane oxidation in deep-sea sediments at cold seeps of the eastern Aleutian subduction zone  | journal = Org. Geochem. | year = 2000 | volume = 31 | issue = 11 | pages = 1175–87 | doi = 10.1016/S0146-6380(00)00111-X}}.</ref>
  
 
==Radiologically significant isotopes==
 
==Radiologically significant isotopes==
Line 75: Line 153:
 
! <u>Energy</u><br/>MeV
 
! <u>Energy</u><br/>MeV
 
! Weighted mean<br/>energies/MeV
 
! Weighted mean<br/>energies/MeV
 +
! <u>Dose eq.</u><br/>µSv/MBq
 
! Daughter<br/>nuclide
 
! Daughter<br/>nuclide
 
! Ref.
 
! Ref.
Line 83: Line 162:
 
| 0.3856(4)
 
| 0.3856(4)
 
| rowspan=4 | γ, X: 1.02<br/>β, Auger: 0.385
 
| rowspan=4 | γ, X: 1.02<br/>β, Auger: 0.385
−
| rowspan=4 | {{nuclide|Z=5|A=11}} (stable)
+
| rowspan=4 align=center | 4
−
| rowspan=4 | <ref>{{citation | title = ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for <sup>11</sup>C | url = http://www.nndc.bnl.gov/useroutput/11c_mird.html | publisher = National Nuclear Data Center | accessdate = 2010-03-13}}.</ref><ref>{{citation | first = F. | last = Ajzenberg-Selove | year = 1990 | title = Energy levels of light nuclei ''A'' = 11–12 | journal = Nucl. Phys. A | volume = 506 | issue = 1 | pages = 1–158 | doi = 10.1016/0375-9474(90)90271-M}}.</ref>
+
| rowspan=4 | {{nuclide|Z=5|A=11|link=yes}} (stable)
 +
| rowspan=4 | <ref>{{citation | title = ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for <sup>11</sup>C | url = http://www.nndc.bnl.gov/useroutput/11c_mird.html | publisher = National Nuclear Data Center | accessdate = 2010-03-13}}.</ref><ref>{{citation | first = F. | last = Ajzenberg-Selove | year = 1990 | title = Energy levels of light nuclei ''A'' = 11–12 | journal = Nucl. Phys. A | volume = 506 | issue = 1 | pages = 1–158 | doi = 10.1016/0375-9474(90)90271-M}}.</ref><ref>{{citation | title = PET Studies with Carbon-11 Radioligands in Neuropsychopharmacological Drug Development | url = http://www.balazs-gulyas.hu/pdf/2001/Halldin_Gulyas_Farde_2001.pdf | first1 = Christer | last1 = Halldin | first2 = Balázs | last2 = Gulyás | first3 = Lars | last3 = Farde | journal = Curr. Pharm. Des. | year = 2001 | volume = 7 | issue = 18 | pages = 1907–29 | doi = 10.2174/1381612013396871}}.</ref>
 
|-
 
|-
 
| γ<sup>±</sup> (2×99.759%)
 
| γ<sup>±</sup> (2×99.759%)
Line 100: Line 180:
 
| 0.049 47
 
| 0.049 47
 
| β: 0.049 47
 
| β: 0.049 47
−
| {{nuclide|Z=7|A=14}} (stable)
+
|
 +
| {{nuclide|Z=7|A=14|link=yes}} (stable)
 
| <ref>{{citation | title = ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for <sup>14</sup>C | url = http://www.nndc.bnl.gov/useroutput/14c_mird.html | publisher = National Nuclear Data Center | accessdate = 2010-03-13}}.</ref><ref>{{citation | first = F. | last = Ajzenberg-Selove | year = 1991 | title = Energy levels of light nuclei ''A'' = 13–15 | journal = Nucl. Phys. A | volume = 523 | issue = 1 | pages = 1–196 | doi = 10.1016/0375-9474(91)90446-D}}.</ref>
 
| <ref>{{citation | title = ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for <sup>14</sup>C | url = http://www.nndc.bnl.gov/useroutput/14c_mird.html | publisher = National Nuclear Data Center | accessdate = 2010-03-13}}.</ref><ref>{{citation | first = F. | last = Ajzenberg-Selove | year = 1991 | title = Energy levels of light nuclei ''A'' = 13–15 | journal = Nucl. Phys. A | volume = 523 | issue = 1 | pages = 1–196 | doi = 10.1016/0375-9474(91)90446-D}}.</ref>
 
|-
 
|-
 
|}
 
|}
 +
 +
===Carbon-11===
 +
{{main|Carbon-11}}
 +
 +
===Carbon-14===
 +
{{main|Carbon-14}}
  
 
==All isotopes==
 
==All isotopes==
Line 295: Line 382:
 
{{reflist|2}}
 
{{reflist|2}}
  
−
[[Category:Isotopes of carbon|*]]
+
[[Category:Isotopes of carbon| ]]
  
 
{{CC-BY-3.0}}
 
{{CC-BY-3.0}}

Latest revision as of 16:29, 23 September 2010

Carbon has two stable, naturally occurring isotopes, carbon-12 and carbon-13. There is also a naturally-occuring radioactive isotope, carbon-14 (t½ = 5700 years), that is formed by the action of cosmic rays on the Earth's atmosphere. Carbon-11 is an artificial isotope used in positron emission tomography (PET), a medical imaging technique.

Atomic weight

Ar(6C) = 12.0107(8)
Isotope Mass/u Amount
fraction 		Normal
range
12C 12 (by definition)[note 1] 0.9893(8) 0.988 53–0.990 37
13C 13.003 354 837 78(98) 0.0107(8) 0.011 47–0.009 63
References:[1][2][3]

The standard atomic weight of carbon has been fixed at its current value since 1995.[1] The range of natural isotopic compositions makes a more precise standard value unobtainable, and some terrestrial geological specimens may show compositions outside of the normal range.[1] Natural amounts of carbon-14 (x < 10−12) are insignificant in the calculation of atomic weight.[1]

Carbon-13 is systematically depleted in samples of biological origin (compared to atmospheric carbon dioxide and most carbonate rocks) due to a kinetic isotope effect that is particularly pronounced in photosynthetic reactions.[note 2] The effect is slightly weaker (but still significant) in C4-plants, which are predominant in tropical and subtropical climates, and measurements of carbon isotopic compositions are important in geochemistry, paleoclimatology and paleoceanography.[4] Such measurements have also attracted interest for detecting cases of "doping" in sport:[5][6] steroid hormones produced by biotechnological methods would be expected to have higher amount fractions of 13C than those produced by an athlete's body.[note 3]

The primary standard for the isotopic composition of carbon is Pee Dee belemnite (PDB), a fossile marine carbonate from the Pee Dee Formation, South Carolina, USA:[7] as with most carbonate rocks, this has a relatively high amount franction of 13C, and so most δ13C values are negative. Supplies of standard PDB have long been been exhausted, so modern measurements of isotopic composition (since about 1985) are referred to a secondary standard, NBS 19, a crushed marble of unknown geographical origin that is also referred to as "TS-limestone".[8] NBS 19 forms the basis of the V-PDB (for "Vienna PDB") scale of δ13C, which is designed to give equivalent δ13C values to the older PDB scale: NBS 19 has a defined value of δ13C = +1.95‰ on the V-PDB scale. A two-point scale based on NBS 19 and L-SVEC, a lithium carbonate standard with a very low δ13C value, has also been proposed.[9][10]

Standard Material δ13C (PDB) δ13C (V-PDB) n(13C)/n(12C) x(13C) Ar(C) Ref.
PDB belemnite 0‰ — 0.011 2372(300) 0.011 112(29) 12.011 15(29) [11]
V-PDB virtual — 0‰ 0.011 180 0.011 057 12.011 09 [12]
NBS 19 calcite — +1.95‰ 0.011 202(29) 0.011 078(28) 12.011 12(28) [12]
L-SVEC Li2CO3 — −46.479(150)‰ 0.010 660 0.010 548 12.010 58 [7][9]
IAEA-CO-1 calcite — +2.480(25)‰ 0.011 208 0.011 084 12.011 12 [9]
IAEA-CO-8 calcite — −5.749(63)‰ 0.011 116 0.010 994 12.011 03 [9]
IAEA-CO-9 Ba2CO3 — −47.119(149)‰ 0.010 654 0.010 548 12.010 58 [9]
USGS 24 graphite — −15.994(105)‰ 0.011 002 0.010 882 12.010 92 [9]
NBS 22 oil — −29.739(124)‰ 0.010 848 0.010 732 12.010 77 [7]
IAEA-CH-7 polythene — −31.826(114)‰ 0.010 825 0.010 709 12.010 74 [7]
IAEA-C-6 sucrose — −10.431(126)‰ 0.011 064 0.010 943 12.010 98 [7]
The isotopic compositions of some standard reference materials for carbon isotope analysis.
Values in bold are fixed by definition.

The highest reported δ13C value is +37.5‰ [n(13C)/n(12C) = 0.011 599; x(13C) = 0.011 466; Ar(C) = 12.011 50] for dissolved carbonate in marine sediment pore water,[13] while the lowest reported value is −130.3‰ [n(13C)/n(12C) = 0.009 723; x(13C) = 0.009 629; Ar(C) = 12.009 66] for a sample of crocetane recovered from the ocean bottom at cold seeps in the northern Pacific Ocean.[14]

Radiologically significant isotopes

Isotope Half life Decay mode Energy
MeV 		Weighted mean
energies/MeV 		Dose eq.
µSv/MBq 		Daughter
nuclide 		Ref.
11C 1223.1(12) s
(20.39(2) min) 		β+ (99.759(15)%) 0.3856(4) γ, X: 1.02
β, Auger: 0.385 		4 115B (stable) [15][16][17]
γ± (2×99.759%) 0.5110
X (ec) (0.0002%) 1.0 × 10−4
K-Auger (0.241(15)%) 1.7 × 10−4
14C 5.70(3) × 103 a β− (100%) 0.049 47 β: 0.049 47 147N (stable) [18][19]

Carbon-11

Main article: Carbon-11

Carbon-14

Main article: Carbon-14

All isotopes

Symbol Z(p) N(n) Mass/u Excess energy
MeV 		Binding energy/A
MeV 		β−-decay energy
MeV 		Spin Half life Decay mode,
proportion
Excitation energy/MeV
8C 6 2 8.037 675(25) 35.094(23) 3.0978(29) — 0 2.0(4) zs 2p (100%)
9C 6 3 9.031 0367(23) 28.9105(21) 4.337 48(24) — (−3⁄2) 126.5(9) ms β+ (100%)
10C 6 4 10.016 853 23(43) 15.698 68(40) 6.032 041(40) −23.10(40) 0 19.290(12) s β+ (100%)
11C 6 5 11.011 433 61(102) 10.650 34(95) 6.676 370(86) −13.653(46) −3⁄2 20.39(2) min β+ (100%)
12C 6 6 12 (by definition)[note 1] 0 (by definition)[note 1] 7.680 144 −17.338 08(100) 0 STABLE
13C 6 7 13.003 354 837 78(98) 3.125 011 29(91) 7.469 849 −2.220 47(27) −1⁄2 STABLE
14C 6 8 14.003 241 9887(41) 3.019 8931(38) 7.520 319 0.156 476(4) 0 5.70(3) × 103 a β− (100%)
15C 6 9 15.010 5992(86) 9.873 14(80) 7.100 169(53) 9.771 71(80) +1⁄2 2.449(5) s β− (100%)
16C 6 10 16.014 7013(38) 13.6941(36) 6.922 05(22) 8.0105(44) 0 747(8) ms β− (100%)
17C 6 11 17.022 5861(187) 21.0388(174) 6.557 62(102) 13.167(23) (+3⁄2) 193(5) ms β− (100%)
18C 6 12 18.026 759(32) 24.926(30) 6.425 75(167) 11.812(35) 0 92(2) ms β− (100%)
19C 6 13 19.034 805(106) 32.421(98) 6.1179(52) 16.559(99) (+1⁄2) 46.2(23) ms β− (100%)
20C 6 14 20.040 32(26) 37.56(24) 5.9587(120) 15.79(25) 0 16(3) ms β− (100%)
21C 6 15 21.049 34(54)# 45.96(50)# 5.659(24)# 20.71(51)# +1⁄2# <30 ns ?n
22C 6 16 22.057 20(97)# 53.28(90)# 5.436(41)# 21.24(92)# 0 6.2(13) ms β− (100%)
Values marked # are estimated from systematic trends rather than experimentally measured.
Spins quoted in parentheses are uncertain in value and/or parity.
Sources: Except as otherwise noted,
isotopic masses and associated energies are taken from the AME 2003 dataset;[2]
nuclear spins and decay properties are taken from NUBASE 2003.[20]

Notes and references

Notes

  1. ↑ 1.0 1.1 1.2 The relative atomic mass of carbon-12 is exactly twelve atomic mass units, without any measurement uncertainty, by the definition of the atomic mass unit.
  2. ↑ Marine organisms that obtain carbonate from sea water to construct exoskeletons do not show the depletion of 13C in the exoskeletons: indeed, when such exoskeletons become carbonate rocks, they often show anomalously high amount fractions of 13C, an indication that the carbon did not pass through a photosynthetic pathway.
  3. ↑ It was shown by Aguilera, Hatton & Catlin (2002) that their 2002 samples of artificial epitestosterone had significantly (P < 0.0001) lower δ13C values than natural epitestosterone from human urine.

References

  1. ↑ 1.0 1.1 1.2 1.3 Atomic weights of the elements. Review 2000. Pure Appl. Chem., 75 (6), 683–800. DOI: 10.1351/pac200375060683.
  2. ↑ 2.0 2.1 Wapstra, A. H.; Audi, G.; Thibault, C. The AME2003 atomic mass evaluation (I). Evaluation of input data, adjustment procedures. Nucl. Phys. A 2003, 729, 129–336. DOI: 10.1016/j.nuclphysa.2003.11.002. Wapstra, A. H.; Audi, G.; Thibault, C. The AME2003 atomic mass evaluation (II). Tables, graphs, and references. Nucl. Phys. A 2003, 729, 337–676. DOI: 10.1016/j.nuclphysa.2003.11.003. Data tables.
  3. ↑ Böhlke, J. K.; de Laeter, J. R.; De Bièvre, P.; Hidaka, H.; Peiser, H. S.; Rosman, K. J. R.; Taylor, P. D. P. Isotopic Compositions of the Elements, 2001. J. Phys. Chem. Ref. Data 2005, 34 (1), 57–67. DOI: 10.1063/1.1836764.
  4. ↑ Coplen, T. B.; Böhlke, J. K.; De Bièvre, P.; Ding, T.; Holden, N. E.; Hopple, J. A.; Krouse, H. R.; Lamberty, A., et al. Isotopic Abundance Variations Of Selected Elements. Pure Appl. Chem. 2002, 74 (10), 1987–2017. DOI: 10.1351/pac200274101987.
  5. ↑ Aguilera, Rodrigo; Hatton, Caroline K.; Catlin, Don H. Detection of Epitestosterone Doping by Isotope Ratio Mass Spectrometry. Clin. Chem. 2002, 48, 629–36. PMID 11901061.
  6. ↑ Aguilera, Rodrigo; Chapman, Thomas E.; Pereira, Henrique; Oliveira, Giselle C.; Illanes, Renata P.; Fernandes, Telma F.; Azevedo, Débora A.; Aquino Neto, Francisco Drug testing data from the 2007 Pan American Games: δ13C values of urinary androsterone, etiocholanolone and androstanediols determined by GC/C/IRMS. J. Steroid Biochem. Mol. Biol. 2009, 115 (3–5), 107–14. DOI: 10.1016/j.jsbmb.2009.03.012.
  7. ↑ 7.0 7.1 7.2 7.3 7.4 Gonfiantini, R.; Stichler, W.; Rozanski, K. Standards and intercomparison materials distributed by the International Atomic Energy Agency for stable isotope measurements. In Reference and intercomparison materials for stable isotopes of light elements; International Atomic Energy Agency: Vienna, 1995; pp 13–29. IAEA-TECDOC-825, <http://www.iaea.org/programmes/aqcs/pdf/tecdoc_0825.pdf>.
  8. ↑ NBS 19, TS-Limestone; International Atomic Energy Agency, <http://curem.iaea.org/catalogue/SI/SI_002190000.html>. (accessed 14 March 2010).
  9. ↑ 9.0 9.1 9.2 9.3 9.4 9.5 Stichler, W. Interlaboratory Comparison of New Materials for Carbon and Oxygen Isotope Ratio Measurements. In Reference and intercomparison materials for stable isotopes of light elements; International Atomic Energy Agency: Vienna, 1995; pp 67–74. IAEA-TECDOC-825, <http://www.iaea.org/programmes/aqcs/pdf/tecdoc_0825.pdf>.
  10. ↑ Coplen, Tyler B.; Brand, Willi A.; Gehre, Matthias; Gröning, Mannfred; Meijer, Harro A. J.; Toman, Blaza; Verkouteren, R. Michael New Guidelines for δ13C Measurements. Anal. Chem. 2006, 78 (7), 2439–41. DOI: 10.1021/ac052027c.
  11. ↑ Craig, Harmon Isotopic standards for carbon and oxygen and correction factors for mass-spectrometric analysis of carbon dioxide. Geochim. Cosmochim. Acta 1957, 12 (1–2), 133–49. DOI: 10.1016/0016-7037(57)90024-8.
  12. ↑ 12.0 12.1 Chang, T.-L.; Li, W. Chin. Sci. Bull. 1990, 35, 290–96.
  13. ↑ Claypool, George E.; Threlkeld, Charles N.; Mankiewicz, Paul N.; Arthur, Michael A.; Anderson, Thomas F. Isotopic Composition of Interstitial Fluids and Origin of Methane in Slope Sediment of the Middle America Trench, Deep Sea Drilling Project Leg 84. In Initial Reports of the Deep Sea Drilling Project, 1985; Vol. 84, pp 683–91. doi:10.2973/dsdp.proc.84.124.1985, <http://www.deepseadrilling.org/84/volume/dsdp84_24.pdf>.
  14. ↑ Elvert, Marcus; Suess, Erwin; Greinert, Jens; Whiticar, Michael J. Archaea mediating anaerobic methane oxidation in deep-sea sediments at cold seeps of the eastern Aleutian subduction zone. Org. Geochem. 2000, 31 (11), 1175–87. DOI: 10.1016/S0146-6380(00)00111-X.
  15. ↑ ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for 11C; National Nuclear Data Center, <http://www.nndc.bnl.gov/useroutput/11c_mird.html>. (accessed 13 March 2010).
  16. ↑ Ajzenberg-Selove, F. Energy levels of light nuclei A = 11–12. Nucl. Phys. A 1990, 506 (1), 1–158. DOI: 10.1016/0375-9474(90)90271-M.
  17. ↑ Halldin, Christer; Gulyás, Balázs; Farde, Lars PET Studies with Carbon-11 Radioligands in Neuropsychopharmacological Drug Development. Curr. Pharm. Des. 2001, 7 (18), 1907–29. doi:10.2174/1381612013396871, <http://www.balazs-gulyas.hu/pdf/2001/Halldin_Gulyas_Farde_2001.pdf>.
  18. ↑ ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for 14C; National Nuclear Data Center, <http://www.nndc.bnl.gov/useroutput/14c_mird.html>. (accessed 13 March 2010).
  19. ↑ Ajzenberg-Selove, F. Energy levels of light nuclei A = 13–15. Nucl. Phys. A 1991, 523 (1), 1–196. DOI: 10.1016/0375-9474(91)90446-D.
  20. ↑ Audi, G.; Bersillon, O.; Blachot, J.; Wapstra, A. H. The NUBASE evaluation of nuclear and decay properties. Nucl. Phys. A 2003, 729, 3–128. doi:10.1016/j.nuclphysa.2003.11.001, <http://amdc.in2p3.fr/nubase/Nubase2003.pdf>.
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