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Isotopes of calcium
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| Standard atomic weight Ar°(Ca) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Calcium (20Ca) has 26 known isotopes, ranging from 35Ca to 60Ca. There are five stable isotopes (40Ca, 42Ca, 43Ca, 44Ca and 46Ca), plus one isotope (48Ca) with such a long half-life that it is for all practical purposes stable. The most abundant isotope, 40Ca, as well as the rare 46Ca, are theoretically unstable on energetic grounds, but their decay has not been observed. Calcium also has a cosmogenic isotope, 41Ca, with half-life 99,400 years. Unlike cosmogenic isotopes that are produced in the air, 41Ca is produced by neutron activation of solid 40Ca in rock and soil. Most of its production is in the upper metre of the soil column, where the cosmogenic neutron flux is still strong enough. The most stable artificial isotopes are 45Ca with half-life 162.61 days and 47Ca with half-life 4.536 days. All other calcium isotopes have half-lives of minutes or less.
Stable 40Ca comprises about 97% of natural calcium and is mainly created by nucleosynthesis in stars (alpha process). Similarly to 40Ar, however, some atoms of 40Ca are radiogenic, created through the radioactive decay of 40K. While K–Ar dating has been used extensively in the geological sciences, the prevalence of 40Ca in nature initially impeded the proliferation of K-Ca dating in early studies, with only a handful of studies in the 20th century. Modern techniques using increasingly precise Thermal-Ionization (TIMS) and Collision-Cell Multi-Collector Inductively-coupled plasma mass spectrometry (CC-MC-ICP-MS) techniques, however, have been used for successful K–Ca age dating[4][5] similar in method to Rb-Sr dating, as well as determining K losses from the lower continental crust[6] and for source-tracing calcium contributions from various geologic reservoirs.[7][8]
Stable isotope variations of calcium (most typically 44Ca/40Ca or 44Ca/42Ca, denoted as 'δ44Ca' and 'δ44/42Ca' in delta notation) are also widely used across the natural sciences for a number of applications, ranging from early determination of osteoporosis[9] to quantifying volcanic eruption timescales.[10] Other applications include: quantifying carbon sequestration efficiency in CO2 injection sites[11] and understanding ocean acidification,[12] exploring both ubiquitous and rare magmatic processes, such as formation of granites[13] and carbonatites,[14] tracing modern and ancient trophic webs including in dinosaurs,[15][16][17] assessing weaning practices in ancient humans,[18] and a plethora of other emerging applications.
List of isotopes
[edit]
| Nuclide |
Z | N | Isotopic mass (Da)[19] [n 1] |
Half-life[1] [n 2] |
Decay mode[1] [n 3] |
Daughter isotope [n 4] |
Spin and parity[1] [n 5][n 6] |
Natural abundance (mole fraction) | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Normal proportion[1] | Range of variation | ||||||||||||||||||
| 35Ca | 20 | 15 | 35.00557(22)# | 25.7(2) ms | β+, p (95.8%) | 34Ar | 1/2+# | ||||||||||||
| β+, 2p (4.2%) | 33Cl | ||||||||||||||||||
| β+ (rare) | 35K | ||||||||||||||||||
| 36Ca | 20 | 16 | 35.993074(43) | 100.9(13) ms | β+, p (51.2%) | 35Ar | 0+ | ||||||||||||
| β+ (48.8%) | 36K | ||||||||||||||||||
| 37Ca | 20 | 17 | 36.98589785(68) | 181.0(9) ms | β+, p (76.8%) | 36Ar | 3/2+ | ||||||||||||
| β+ (23.2%) | 37K | ||||||||||||||||||
| 38Ca | 20 | 18 | 37.97631922(21) | 443.70(25) ms | β+ | 38K | 0+ | ||||||||||||
| 39Ca | 20 | 19 | 38.97071081(64) | 860.3(8) ms | β+ | 39K | 3/2+ | ||||||||||||
| 40Ca[n 7] | 20 | 20 | 39.962590850(22) | Observationally stable[n 8] | 0+ | 0.9694(16) | 0.96933–0.96947 | ||||||||||||
| 41Ca | 20 | 21 | 40.96227791(15) | 9.94(15)×104 y | EC | 41K | 7/2− | Trace[n 9] | |||||||||||
| 42Ca | 20 | 22 | 41.95861778(16) | Stable | 0+ | 0.00647(23) | 0.00646–0.00648 | ||||||||||||
| 43Ca | 20 | 23 | 42.95876638(24) | Stable | 7/2− | 0.00135(10) | 0.00135–0.00135 | ||||||||||||
| 44Ca | 20 | 24 | 43.95548149(35) | Stable | 0+ | 0.0209(11) | 0.02082–0.02092 | ||||||||||||
| 45Ca | 20 | 25 | 44.95618627(39) | 162.61(9) d | β− | 45Sc | 7/2− | ||||||||||||
| 46Ca | 20 | 26 | 45.9536877(24) | Observationally stable[n 10] | 0+ | 4×10−5 | 4×10−5–4×10−5 | ||||||||||||
| 47Ca | 20 | 27 | 46.9545411(24) | 4.536(3) d | β− | 47Sc | 7/2− | ||||||||||||
| 48Ca[n 11][n 12] | 20 | 28 | 47.952522654(18) | 5.6(10)×1019 y | β−β−[n 13][n 14] | 48Ti | 0+ | 0.00187(21) | 0.00186–0.00188 | ||||||||||
| 49Ca | 20 | 29 | 48.95566263(19) | 8.718(6) min | β− | 49Sc | 3/2− | ||||||||||||
| 50Ca | 20 | 30 | 49.9574992(17) | 13.45(5) s | β− | 50Sc | 0+ | ||||||||||||
| 51Ca | 20 | 31 | 50.96099566(56) | 10.0(8) s | β− | 51Sc | 3/2− | ||||||||||||
| 52Ca | 20 | 32 | 51.96321365(72) | 4.6(3) s | β− (>98%) | 52Sc | 0+ | ||||||||||||
| β−, n (<2%) | 51Sc | ||||||||||||||||||
| 53Ca | 20 | 33 | 52.968451(47) | 461(90) ms | β− (60%) | 53Sc | 1/2−# | ||||||||||||
| β−, n (40%) | 52Sc | ||||||||||||||||||
| 54Ca | 20 | 34 | 53.972989(52) | 90(6) ms | β− | 54Sc | 0+ | ||||||||||||
| 55Ca | 20 | 35 | 54.97998(17) | 22(2) ms | β− | 55Sc | 5/2−# | ||||||||||||
| 56Ca | 20 | 36 | 55.98550(27) | 11(2) ms | β− | 56Sc | 0+ | ||||||||||||
| 57Ca | 20 | 37 | 56.99296(43)# | 8# ms [>620 ns] | 5/2−# | ||||||||||||||
| 58Ca | 20 | 38 | 57.99836(54)# | 4# ms [>620 ns] | 0+ | ||||||||||||||
| 59Ca | 20 | 39 | 59.00624(64)# | 5# ms [>400 ns] | 5/2−# | ||||||||||||||
| 60Ca | 20 | 40 | 60.01181(75)# | 2# ms [>400 ns] | 0+ | ||||||||||||||
| 61Ca[21][n 15] | 20 | 41 | 61.02041(86)# | 1# ms | 1/2−# | ||||||||||||||
| This table header & footer: | |||||||||||||||||||
- ^ ( ) – Uncertainty (1σ) is given in concise form in parentheses after the corresponding last digits.
- ^ Bold half-life – nearly stable, half-life longer than age of universe.
- ^
Modes of decay:
EC: Electron capture
n: Neutron emission p: Proton emission - ^ Bold symbol as daughter – Daughter product is stable.
- ^ ( ) spin value – Indicates spin with weak assignment arguments.
- ^ # – Values marked # are not purely derived from experimental data, but at least partly from trends of neighboring nuclides (TNN).
- ^ Heaviest observationally stable nuclide with equal numbers of protons and neutrons
- ^ Believed to undergo double electron capture to 40Ar with a half-life no less than 9.9×1021 y
- ^ Cosmogenic nuclide
- ^ Believed to undergo β−β− decay to 46Ti
- ^ Primordial radionuclide
- ^ Believed to be capable of undergoing triple beta decay with very long partial half-life
- ^ Lightest nuclide known to undergo double beta decay
- ^ Theorized to also undergo β− decay to 48Sc with a partial half-life exceeding 1.1+0.8
−0.6×1021 years[20] - ^ Discovery of this isotope is unconfirmed
Calcium-48
[edit]
Calcium-48 is a doubly magic nucleus with 28 neutrons; unusually neutron-rich for a light primordial nucleus. It decays via double beta decay with an extremely long half-life of about 5.6×1019 years, though single beta decay is also theoretically possible. This decay can analyzed with the sd nuclear shell model, and it is more energetic (4.27 MeV) than any other double beta decay.[22] It is used as a precursor for neutron-rich[23] and superheavy[24] isotopes.
Calcium-60
[edit]Calcium-60 is the heaviest known isotope as of 2020[update].[1] First observed in 2018 at Riken alongside 59Ca and seven isotopes of other elements,[25] its existence suggests that there are additional even-N isotopes of calcium up to at least 70Ca, while 59Ca is probably the last bound isotope with odd N.[26] Earlier predictions had estimated the heaviest even isotope to be at 60Ca, and 59Ca unbound.[25]
In the neutron-rich region, N = 40 becomes a magic number, so 60Ca was considered early on to be a possibly doubly magic nucleus, as is observed for the 68Ni isotone.[27][28] However, subsequent spectroscopic measurements of the nearby nuclides 56Ca, 58Ca, and 62Ti instead predict that it should lie on the island of inversion known to exist around 64Cr.[28][29]
See also
[edit]Daughter products other than calcium
References
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- ^ Pogge von Strandmann, Philip A. E.; Burton, Kevin W.; Snæbjörnsdóttir, Sandra O.; Sigfússon, Bergur; Aradóttir, Edda S.; Gunnarsson, Ingvi; Alfredsson, Helgi A.; Mesfin, Kiflom G.; Oelkers, Eric H.; Gislason, Sigurður R. (2019-04-30). "Rapid CO2 mineralisation into calcite at the CarbFix storage site quantified using calcium isotopes". Nature Communications. 10 (1): 1983. doi:10.1038/s41467-019-10003-8. ISSN 2041-1723. PMC 6491611. PMID 31040283.
- ^ Fantle, Matthew S.; Ridgwell, Andy (2020-08-05). "Towards an understanding of the Ca isotopic signal related to ocean acidification and alkalinity overshoots in the rock record". Chemical Geology. 547 119672. Bibcode:2020ChGeo.54719672F. doi:10.1016/j.chemgeo.2020.119672. ISSN 0009-2541.
- ^ Antonelli, Michael A.; Yakymchuk, Chris; Schauble, Edwin A.; Foden, John; Janoušek, Vojtěch; Moyen, Jean-François; Hoffmann, Jan; Moynier, Frédéric; Bachmann, Olivier (2023-04-15). "Granite petrogenesis and the δ44Ca of continental crust". Earth and Planetary Science Letters. 608 118080. doi:10.1016/j.epsl.2023.118080. hdl:20.500.11850/603069. ISSN 0012-821X.
- ^ admin (December 2023). "Calcium isotope fractionation during melt immiscibility and carbonatite petrogenesis | Geochemical Perspectives Letters". Geochemical Perspectives Letters. 28 (28): 13–19. doi:10.7185/geochemlet.2338. Retrieved 2024-10-16.
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- ^ Hassler, A.; Martin, J. E.; Amiot, R.; Tacail, T.; Godet, F. Arnaud; Allain, R.; Balter, V. (2018-04-11). "Calcium isotopes offer clues on resource partitioning among Cretaceous predatory dinosaurs". Proceedings of the Royal Society B: Biological Sciences. 285 (1876) 20180197. doi:10.1098/rspb.2018.0197. ISSN 0962-8452. PMC 5904318. PMID 29643213.
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- ^ Tarasov, O. B.; Sherrill, B. M.; Dombos, A. C.; Fukushima, K.; Gade, A.; Haak, K.; Hausmann, M.; Kahl, D.; Kaloyanov, D.; Kwan, E.; Matthews, H. K.; Ostroumov, P. N.; Portillo, M.; Richardson, I.; Smith, M. K.; Watters, S. (4 September 2025). "Discovery of new isotopes in the fragmentation of Se 82 and insights into their production". Physical Review C. 112 (3) 034604. doi:10.1103/573p-7fjp.
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- ^ a b Tarasov, O. B.; Ahn, D. S.; Bazin, D.; et al. (11 July 2018). "Discovery of 60Ca and Implications For the Stability of 70Ca". Physical Review Letters. 121 (2) 022501. doi:10.1103/PhysRevLett.121.022501. PMID 30085743.
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Further reading
[edit]External links
[edit]Isotopes of calcium
View on GrokipediaOverview
Known isotopes and stability
Calcium has 26 known isotopes, with mass numbers ranging from Ca to Ca.[4] The stable isotopes of calcium are those for which no radioactive decay has been observed: Ca, Ca, Ca, Ca, Ca, and Ca.[5] Stability among calcium isotopes generally follows nuclear pairing rules, where even-even nuclei (with even numbers of both protons and neutrons) exhibit greater stability compared to neighboring odd-A isotopes. Neutron-rich calcium isotopes beyond a neutron number of display reduced stability, attributed to the erosion of the neutron shell closure as one moves further from stability.[6][7] The primary decay mode for neutron-rich calcium isotopes is decay: while proton-rich isotopes predominantly decay via electron capture () or emission.[1]Natural occurrence and production
Calcium isotopes are primarily synthesized through stellar nucleosynthesis processes in massive stars and supernovae. The dominant isotope, ^{40}Ca, which constitutes over 96% of natural calcium, is mainly produced during explosive oxygen and silicon burning in core-collapse supernovae of Type II. This process occurs in the final stages of massive star evolution, where high temperatures and densities facilitate alpha-particle captures on lighter nuclei like ^{16}O and ^{28}Si, leading to the buildup of ^{40}Ca. Lighter stable isotopes such as ^{42}Ca and ^{43}Ca also arise from similar explosive burning stages, while ^{46}Ca is predominantly formed via the slow neutron-capture process (s-process) in asymptotic giant branch stars, and ^{48}Ca originates from neutron-rich environments in Type Ia supernovae or electron-capture supernovae. The radioactive isotope ^{41}Ca, with a half-life of approximately 99,400 years, is produced cosmogenically through spallation reactions induced by high-energy cosmic rays interacting with ^{40}Ca and other target nuclei in Earth's atmosphere and extraterrestrial materials like meteorites. In the atmosphere, galactic cosmic rays fragment calcium atoms, generating trace amounts of ^{41}Ca that subsequently incorporate into sediments and ice cores, serving as a proxy for cosmic ray flux variations over time. In meteorites, such as iron meteorites like Grant and Estherville, ^{41}Ca production occurs via spallation on iron and calcium, with saturation activities around 24 dpm/kg, and is influenced by shielding depth and exposure duration to cosmic rays. On Earth, primordial ^{48}Ca traces back to the early solar system, incorporated into calcium-aluminum-rich inclusions (CAIs) as the first condensates formed around 4.567 billion years ago, reflecting heterogeneous nucleosynthetic contributions from Type Ia supernovae. However, its natural abundance is negligible at about 0.187%, dwarfed by ^{40}Ca, due to incomplete mixing of presolar material in the solar nebula. Heavier isotopes like ^{60}Ca, which lies near the neutron drip line, are not found in nature and are artificially produced using particle accelerators through projectile fragmentation or multinucleon transfer reactions on heavy targets, enabling studies of nuclear structure at facilities such as the National Superconducting Cyclotron Laboratory. Geochemically, calcium isotopes exhibit subtle variations between Earth's mantle and crust, driven by planetary differentiation and mantle metasomatism. Mid-ocean ridge basalts (MORB), representing upper mantle-derived melts, have a uniform δ^{44/40}Ca value of +0.84 ± 0.03‰, while certain mantle sources for alkaline rocks and carbonatites show lighter compositions (δ^{44/40}Ca down to +0.58‰), attributed to volatile-rich lithologies like carbonated peridotites or K-richterite-bearing metasomes that fractionate isotopes during partial melting. These mantle-crust distinctions arise from incomplete homogenization during accretion and subsequent recycling, with minimal fractionation during magmatic differentiation at mid-ocean ridges.Stable isotopes
Abundances and variations
Calcium has six stable isotopes in its natural composition: ^{40}Ca, ^{42}Ca, ^{43}Ca, ^{44}Ca, ^{46}Ca, and ^{48}Ca. The standard atomic weight of calcium is 40.078(4), reflecting these isotopic proportions determined through mass-spectrometric measurements. The accepted natural abundances, based on the IUPAC Commission on Isotopic Abundances and Atomic Weights (CIAAW), are as follows:| Isotope | Mass (u) | Natural abundance (atom %) |
|---|---|---|
| ^{40}Ca | 39.9625909(2) | 96.941(156) |
| ^{42}Ca | 41.958618(1) | 0.647(23) |
| ^{43}Ca | 42.958766(2) | 0.135(10) |
| ^{44}Ca | 43.955482(2) | 2.086(110) |
| ^{46}Ca | 45.95369(2) | 0.004(3) |
| ^{48}Ca | 47.9525229(6) | 0.187(21) |
Applications in stable isotope tracing
Stable calcium isotopes, particularly 42Ca, 44Ca, 46Ca, and 48Ca, serve as non-radioactive tracers in mass spectrometry-based studies to quantify calcium absorption, retention, and metabolic pathways in humans.[13] These isotopes are administered orally or intravenously in enriched forms, allowing researchers to track their incorporation into biological compartments without ethical concerns over radiation exposure.[14] High-precision techniques like thermal ionization mass spectrometry or inductively coupled plasma mass spectrometry enable detection of isotopic ratios in urine, blood, or feces, providing insights into bioavailability from dietary sources.[13] In nutritional research, stable calcium isotopes are employed to evaluate true fractional calcium absorption (TFCA) and utilization, especially in vulnerable populations such as infants and adolescents. For instance, dual-tracer methods using oral 46Ca and intravenous 44Ca have demonstrated absorption rates of 50-60% in premature infants, with retention influenced by intake levels rather than feed concentration.[14] Studies in adolescents have revealed ethnic variations in absorption, such as higher TFCA in African American youth compared to Caucasian peers, highlighting dietary and physiological factors affecting bone mineralization.[13] These approaches avoid the need for prolonged fecal collections by relying on 24-hour urine sampling, improving feasibility in pediatric cohorts.[13] Clinical applications extend to assessing bone health and conditions like osteoporosis through isotopic dosing protocols. Double-tracer techniques with 42Ca (intravenous) and 46Ca (oral) measure kinetic parameters of calcium turnover, informing interventions for maximizing peak bone mass and preventing age-related loss.[13] In osteoporosis research, enriched 42Ca and 44Ca have been used to link TFCA with urinary calcium excretion and vitamin D status, showing correlations that guide therapeutic strategies in at-risk adults.[15] Such methods support long-term monitoring of bone calcium balance, as isotopic signatures persist without decay, facilitating repeated dosing in chronic studies.[16] In environmental science, 44Ca/40Ca ratios (expressed as δ44/40Ca) trace calcium cycling in ecosystems and reconstruct paleoclimate conditions. Riverine δ44/40Ca values, averaging 0.88‰, reflect inputs from silicate (0.94‰) and carbonate (0.60‰) weathering, modulated by biosphere processes like vegetation uptake and biomass degradation.[17] These ratios enable quantification of non-steady-state fluxes in catchments, where biotic recycling can shift signatures by tenths of a permil over timescales less than 10,000 years.[17] For paleoclimate reconstruction, δ44/40Ca in marine carbonates and foraminifera proxies past seawater chemistry, linking continental weathering to ocean anoxia events or aragonite-calcite sea transitions across geological epochs.[18] Seawater's heavy δ44/40Ca (1.92 ± 0.20‰) serves as a baseline for interpreting global Ca fluxes.[17] The primary advantages of stable calcium isotopes over radioactive tracers include the absence of radiation risk, making them ideal for pediatric, pregnant, and long-term human studies, as well as the ability to use multiple isotopes simultaneously without regulatory hurdles or disposal costs.[16] Unlike short-half-life radioisotopes, stable variants like 46Ca remain detectable indefinitely, supporting kinetic modeling over extended periods without ethical limitations.[19] For calcium specifically, no suitable radioisotope exists for routine tracing, positioning stable isotopes as the preferred tool for precise, safe bioavailability assessments.[16]Radioactive isotopes
Long-lived isotopes
Long-lived isotopes of calcium are defined as radioactive nuclides with half-lives exceeding years, enabling their persistence over geological or astronomical timescales. The sole significant example is Ca, which undergoes 100% electron capture decay to the ground state of K, with a half-life of years.[20] This decay mode produces characteristic X-rays and Auger electrons from the K-shell of potassium, but no gamma rays, making direct detection challenging without specialized techniques.[20] Ca is primarily produced cosmogenically via neutron capture on abundant Ca by cosmic-ray-induced neutrons in the upper atmosphere or surface rocks, resulting in trace abundances on Earth (typically Ca/Ca ratios around to ). It can also be generated artificially in nuclear reactors or particle accelerators through neutron irradiation of calcium targets. Detection of Ca at ultratrace levels relies on accelerator mass spectrometry (AMS), which ionizes samples as negative calcium fluoride molecules to suppress isobaric interference from K, achieving sensitivities down to one Ca atom per to calcium atoms.[21] Alternative methods, such as atom-trap trace analysis (ATTA), enable single-atom counting by laser manipulation but are less commonly applied.[22] These isotopes contribute to geochronology by serving as chronometers for processes spanning years, particularly in astrophysics where Ca acts as an extinct radionuclide in meteoritic calcium-aluminum-rich inclusions (CAIs), revealing the timing of early solar system formation and nucleosynthetic origins with initial Ca/Ca ratios of (though recent studies suggest possibly lower values around ).[23][24] No other calcium isotopes qualify as long-lived.Short-lived isotopes
Short-lived isotopes of calcium are radioactive nuclides with half-lives shorter than 1000 days, typically produced artificially for scientific applications rather than occurring naturally. These isotopes span a range from proton-rich to neutron-rich variants, with decay half-lives varying from milliseconds to several months. They are primarily generated through nuclear reactions in accelerators or reactors, enabling their use in short-term experiments due to their rapid decay.[25] Production of these isotopes commonly involves neutron activation of stable calcium targets in nuclear reactors, where thermal or fast neutrons capture to form neutron-rich species like ^{45}Ca and ^{47}Ca via reactions such as ^{44}Ca(n,γ)^{45}Ca. For proton-rich isotopes such as ^{39}Ca, charged particle bombardment in cyclotrons is employed, using protons or other light ions on lighter targets to induce (p,n) or similar reactions. These methods allow tailored yields for laboratory-scale production, with cross-sections optimized for specific energies to minimize impurities.[26][27] Decay characteristics of short-lived calcium isotopes depend on their neutron-to-proton imbalance: neutron-rich isotopes predominantly undergo β^- decay, emitting electrons and antineutrinos to form scandium daughters, while proton-rich ones favor β^+ decay or electron capture (EC), producing potassium daughters. Key examples include ^{45}Ca, with a half-life of 162.7 days, decaying 100% via β^- to ^{45}Sc (spin and parity 7/2^-), and ^{47}Ca, half-life 4.54 days, also 100% β^- to ^{47}Sc (7/2^-). Shorter-lived variants, such as ^{39}Ca (half-life 0.86 s, 100% β^+ to ^{39}K, spin 3/2^+) and ^{49}Ca (half-life 8.72 min, 100% β^- to ^{49}Sc, spin 3/2^-), illustrate the extremes, with decay energies around 0.26–4 MeV facilitating detection in experiments.[25][28]| Isotope | Half-life | Decay mode | Daughter | Spin/Parity |
|---|---|---|---|---|
| ^{39}Ca | 0.86 s | β^+ (100%) | ^{39}K | 3/2^+ |
| ^{45}Ca | 162.7 d | β^- (100%) | ^{45}Sc | 7/2^- |
| ^{47}Ca | 4.54 d | β^- (100%) | ^{47}Sc | 7/2^- |
| ^{49}Ca | 8.72 min | β^- (100%) | ^{49}Sc | 3/2^- |
