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Isotopes of calcium
Isotopes of calcium
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Isotopes of calcium (20Ca)
Main isotopes[1] Decay
Isotope abun­dance half-life (t1/2) mode pro­duct
40Ca 96.9% stable
41Ca trace 9.94×104 y ε 41K
42Ca 0.647% stable
43Ca 0.135% stable
44Ca 2.09% stable
45Ca synth 162.61 d β 45Sc
46Ca 0.004% stable
47Ca synth 4.536 d β 47Sc
48Ca 0.187% 5.6×1019 y ββ 48Ti
Standard atomic weight Ar°(Ca)

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

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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 ββ[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:
  1. ^ ( ) – Uncertainty (1σ) is given in concise form in parentheses after the corresponding last digits.
  2. ^ Bold half-life – nearly stable, half-life longer than age of universe.
  3. ^ Modes of decay:
    EC: Electron capture



    n: Neutron emission
    p: Proton emission
  4. ^ Bold symbol as daughter – Daughter product is stable.
  5. ^ ( ) spin value – Indicates spin with weak assignment arguments.
  6. ^ # – Values marked # are not purely derived from experimental data, but at least partly from trends of neighboring nuclides (TNN).
  7. ^ Heaviest observationally stable nuclide with equal numbers of protons and neutrons
  8. ^ Believed to undergo double electron capture to 40Ar with a half-life no less than 9.9×1021 y
  9. ^ Cosmogenic nuclide
  10. ^ Believed to undergo ββ decay to 46Ti
  11. ^ Primordial radionuclide
  12. ^ Believed to be capable of undergoing triple beta decay with very long partial half-life
  13. ^ Lightest nuclide known to undergo double beta decay
  14. ^ Theorized to also undergo β decay to 48Sc with a partial half-life exceeding 1.1+0.8
    −0.6
    ×1021 years[20]
  15. ^ Discovery of this isotope is unconfirmed

Calcium-48

[edit]
About 2 g of calcium-48

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.[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

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References

[edit]

Further reading

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Calcium (₂₀Ca) is a chemical element with twenty-six known isotopes, ranging in mass number from ³⁵Ca to ⁶⁰Ca, of which six are considered stable due to their indefinite half-lives or extremely long radioactive decay periods exceeding the age of the universe: ⁴⁰Ca, ⁴²Ca, ⁴³Ca, ⁴⁴Ca, ⁴⁶Ca, and ⁴⁸Ca (as of 2025). In naturally occurring calcium, the isotopic composition is dominated by ⁴⁰Ca at 96.941% abundance, followed by ⁴⁴Ca at 2.086%, ⁴²Ca at 0.647%, ⁴⁸Ca at 0.187%, ⁴³Ca at 0.135%, and ⁴⁶Ca at 0.004%. The remaining isotopes are radioactive, with half-lives varying from milliseconds for the heaviest (e.g., ⁵²Ca at 4.6 seconds) to very long durations for lighter ones like ⁴¹Ca (102,000 years, decaying via to ⁴¹K). Notable radioactive isotopes include ⁴⁵Ca (half-life 162.7 days, β⁻ decay to ⁴⁵Sc), which is widely used in biological and to study and formation. Stable heavier isotopes such as ⁴²Ca, ⁴⁴Ca, ⁴⁶Ca, and ⁴⁸Ca are employed in clinical and nutritional studies to trace calcium absorption and bioavailability, particularly in populations like postmenopausal women and children. Additionally, ⁴⁸Ca serves as a target projectile in experiments to synthesize superheavy elements by bombarding lead or targets.

Overview

Known isotopes and stability

Calcium has 26 known isotopes, with mass numbers ranging from 35^{35}Ca to 60^{60}Ca. The stable isotopes of calcium are those for which no radioactive decay has been observed: 40^{40}Ca, 42^{42}Ca, 43^{43}Ca, 44^{44}Ca, 46^{46}Ca, and 48^{48}Ca. 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 N=28N=28 display reduced stability, attributed to the erosion of the N=28N=28 neutron shell closure as one moves further from stability. The primary decay mode for neutron-rich calcium isotopes is β\beta^- decay: ACaASc+e+νˉe^{A}\mathrm{Ca} \to ^{A}\mathrm{Sc} + e^{-} + \bar{\nu}_{e} while proton-rich isotopes predominantly decay via electron capture (ACa+eA1K+νe^{A}\mathrm{Ca} + e^{-} \to ^{A-1}\mathrm{K} + \nu_{e}) or β+\beta^+ emission.

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 reactions induced by high-energy s interacting with ^{40}Ca and other target nuclei in Earth's atmosphere and like meteorites. In the atmosphere, galactic s fragment calcium atoms, generating trace amounts of ^{41}Ca that subsequently incorporate into sediments and ice cores, serving as a proxy for flux variations over time. In meteorites, such as iron meteorites like Grant and Estherville, ^{41}Ca production occurs via on iron and calcium, with saturation activities around 24 dpm/kg, and is influenced by shielding depth and exposure duration to s. On , 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 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 and mantle . 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 . These mantle-crust distinctions arise from incomplete homogenization during accretion and subsequent , with minimal during magmatic differentiation at mid-ocean ridges.

Stable isotopes

Abundances and variations

Calcium has six isotopes in its natural composition: ^{40}Ca, ^{42}Ca, ^{43}Ca, ^{44}Ca, ^{46}Ca, and ^{48}Ca. The 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:
IsotopeMass (u)Natural abundance (atom %)
^{40}Ca39.9625909(2)96.941(156)
^{42}Ca41.958618(1)0.647(23)
^{43}Ca42.958766(2)0.135(10)
^{44}Ca43.955482(2)2.086(110)
^{46}Ca45.95369(2)0.004(3)
^{48}Ca47.9525229(6)0.187(21)
These values represent the terrestrial standard and have been refined over time through improved techniques, with the 2003 IUPAC review incorporating data from multiple laboratories to reduce uncertainties. Natural variations in calcium isotopic abundances arise primarily from mass-dependent processes. In biological systems, significant fractionation occurs during the of in organisms such as and coccolithophores, where the resulting biominerals are depleted in heavier isotopes relative to the source material by up to 1-2‰ in δ^{44}Ca notation. exhibits a uniform isotopic composition that is enriched in heavier isotopes compared to continental weathering inputs, with δ^{44}Ca values around +1.8‰ relative to bulk , maintained by the long of calcium (approximately 1 million years) and continuous biogenic cycling. In meteorites, isotopic variations of up to 2.5‰ in ^{40}Ca/^{44}Ca ratios have been observed, attributed to early solar system processes like and in calcium-aluminum-rich inclusions. Precise measurement of these abundances and variations relies on thermal ionization mass spectrometry (TIMS) and multi-collector (MC-ICP-MS), often employing double-spike techniques with ^{42}Ca/^{48}Ca to correct for instrumental fractionation. Historical refinements, such as those in the 1978 and 1997 IUPAC evaluations, have progressively lowered uncertainties by addressing matrix effects and standardizing reference materials like NIST SRM 915a. The radioactive isotope ^{41}Ca contributes negligibly to the total calcium inventory, with a natural abundance of approximately 10^{-15} atom fraction in terrestrial materials, primarily from cosmogenic production via on ^{40}Ca. This trace level is detectable only through ultrasensitive methods like (AMS) or atom-trap trace analysis.

Applications in stable isotope tracing

Stable calcium isotopes, particularly 42Ca, 44Ca, 46Ca, and 48Ca, serve as non-radioactive tracers in -based studies to quantify calcium absorption, retention, and metabolic pathways in humans. These isotopes are administered orally or intravenously in enriched forms, allowing researchers to track their incorporation into biological compartments without ethical concerns over . High-precision techniques like mass spectrometry or enable detection of isotopic ratios in , , or , providing insights into from dietary sources. 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. 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 mineralization. These approaches avoid the need for prolonged fecal collections by relying on 24-hour sampling, improving feasibility in pediatric cohorts. Clinical applications extend to assessing bone health and conditions like 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. In osteoporosis research, enriched 42Ca and 44Ca have been used to link TFCA with urinary calcium excretion and status, showing correlations that guide therapeutic strategies in at-risk adults. Such methods support long-term monitoring of bone calcium balance, as isotopic signatures persist without decay, facilitating repeated dosing in chronic studies. In , 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 (0.94‰) and (0.60‰) , modulated by processes like uptake and degradation. 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. For paleoclimate reconstruction, δ44/40Ca in marine carbonates and proxies past chemistry, linking continental to ocean anoxia events or aragonite-calcite transitions across geological epochs. 's heavy δ44/40Ca (1.92 ± 0.20‰) serves as a baseline for interpreting global Ca fluxes. 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. Unlike short-half-life radioisotopes, stable variants like 46Ca remain detectable indefinitely, supporting kinetic modeling over extended periods without ethical limitations. For calcium specifically, no suitable radioisotope exists for routine tracing, positioning stable isotopes as the preferred tool for precise, safe bioavailability assessments.

Radioactive isotopes

Long-lived isotopes

Long-lived isotopes of calcium are defined as radioactive nuclides with half-lives exceeding 10410^4 years, enabling their persistence over geological or astronomical timescales. The sole significant example is 41^{41}Ca, which undergoes 100% electron capture decay to the ground state of 41^{41}K, with a half-life of 99,400±1,50099{,}400 \pm 1{,}500 years. 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. 41^{41}Ca is primarily produced cosmogenically via on abundant 40^{40}Ca by cosmic-ray-induced neutrons in the upper atmosphere or surface rocks, resulting in trace abundances on (typically 41^{41}Ca/40^{40}Ca ratios around 101510^{-15} to 101410^{-14}). It can also be generated artificially in nuclear reactors or particle accelerators through neutron of calcium targets. Detection of 41^{41}Ca at ultratrace levels relies on (AMS), which ionizes samples as negative calcium fluoride molecules to suppress isobaric interference from 41^{41}, achieving sensitivities down to one 41^{41}Ca atom per 101510^{15} to 101710^{17} calcium atoms. Alternative methods, such as atom-trap trace analysis (ATTA), enable single-atom counting by laser manipulation but are less commonly applied. These isotopes contribute to by serving as chronometers for processes spanning 10510^5 years, particularly in where 41^{41}Ca acts as an extinct in meteoritic calcium-aluminum-rich inclusions (CAIs), revealing the timing of early solar system formation and nucleosynthetic origins with initial 41^{41}Ca/40^{40}Ca ratios of (1.41±0.14)×108(1.41 \pm 0.14) \times 10^{-8} (though recent studies suggest possibly lower values around 10910^{-9}). 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. 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. 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 daughters, while proton-rich ones favor β^+ decay or (EC), producing 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.
IsotopeHalf-lifeDecay modeDaughterSpin/Parity
^{39}Ca0.86 sβ^+ (100%)^{39}K3/2^+
^{45}Ca162.7 dβ^- (100%)^{45}Sc7/2^-
^{47}Ca4.54 dβ^- (100%)^{47}Sc7/2^-
^{49}Ca8.72 minβ^- (100%)^{49}Sc3/2^-
In settings, these isotopes serve as tracers in chemical and biological studies, leveraging their emission properties for tracking calcium dynamics over short timescales; detailed applications, such as in bone metabolism, are covered under ^{45}Ca. Their brief persistence limits long-term environmental impact but requires prompt handling post-production.

Notable isotopes in research

Calcium-41

Calcium-41 (41Ca^{41}\mathrm{Ca}) is a cosmogenic radioisotope of calcium, produced primarily by the interaction of cosmic rays with calcium nuclei in the Earth's atmosphere and extraterrestrial materials. It possesses an atomic mass of 40.9622783(4) u and decays via to the ground state of 41K^{41}\mathrm{K}, with a (Q-value) of 0.421 MeV. The isotope's was refined in 2012 to 99,400 ± 1,500 years through precise measurements of enriched samples using and beta-spectrometry. First identified in the through experiments on 40Ca^{40}\mathrm{Ca}, 41Ca^{41}\mathrm{Ca} has since become a key tracer due to its long , enabling studies over timescales beyond those accessible by shorter-lived isotopes like 14C^{14}\mathrm{C}. Detection of 41Ca^{41}\mathrm{Ca} relies on ultra-sensitive techniques capable of measuring isotopic ratios as low as 41Ca/Ca1015^{41}\mathrm{Ca}/\mathrm{Ca} \approx 10^{-15}, far below natural abundances. (AMS) is the primary method, accelerating ions to high energies to separate and count rare isotopes while suppressing interferences from stable calcium. Recent advances in 2023 have introduced magneto-optical trapping (MOT) within atom-trap trace analysis (ATTA), where individual 41Ca^{41}\mathrm{Ca} atoms are selectively captured using on the 423-nm transition and detected via , achieving sensitivities down to 101710^{-17} ratios and enabling single-atom counting in small samples. These methods require to convert calcium to or forms for , with backgrounds minimized through isobar suppression. In , 41Ca^{41}\mathrm{Ca} serves as a long-term tracer for turnover, particularly in research. Administered as a tracer dose, the 41Ca:Ca^{41}\mathrm{Ca}:\mathrm{Ca} ratio is monitored in urine or serum over years to quantify and formation rates, providing integrated measures of skeletal health unresponsive to short-term fluctuations. This approach has revealed altered dynamics in postmenopausal women and responses to interventions like dietary soy , offering superior sensitivity over traditional biomarkers. For radiometric dating, 41Ca^{41}\mathrm{Ca} enables age determination of bones spanning 50,000 to 1,000,000 years, bridging the gap between 14C^{14}\mathrm{C} (up to ~50 ka) and longer-lived methods like 10Be^{10}\mathrm{Be}. By measuring the decay of cosmogenically produced 41Ca^{41}\mathrm{Ca} accumulated during an organism's lifetime, AMS-dated samples from archaeological contexts provide insights into and migration. In extraterrestrial applications, 41Ca^{41}\mathrm{Ca} facilitates cosmogenic exposure dating of meteorites, recording flux histories and aiding reconstruction of events through short-lived signatures in early solar system materials.

Calcium-45

Calcium-45 (⁴⁵Ca) is a radioactive of calcium with an atomic mass of 44.956186 ± 0.000001 u. It undergoes pure β⁻ decay to scandium-45 (⁴⁵Sc), with a maximum beta energy of 0.257 MeV and no accompanying gamma emission. The of ⁴⁵Ca is 162.61 days, making it suitable for experiments spanning several months. Production of ⁴⁵Ca primarily occurs through on stable ⁴⁴Ca in nuclear reactors, via the reaction ⁴⁴Ca(n,γ)⁴⁵Ca. This method yields high-specific-activity material, and the isotope is commercially available from specialized suppliers for research purposes. As a primary radioactive tracer for calcium dynamics, has been employed since the 1940s in to investigate calcium absorption and in humans, animals, and . Key applications include quantifying intestinal calcium uptake in dietary studies, tracking formation and resorption in metabolic disorders, and assessing dynamics such as absorption in crops. It has also been used to evaluate calcium binding in detergents and systems, providing insights into sequestration efficiency. In plant biology, ⁴⁵Ca tracing reveals translocation patterns from to foliage, aiding optimization of strategies for uptake. Detection of ⁴⁵Ca relies on its low-energy beta emission, which necessitates for accurate measurement due to poor penetration in Geiger-Müller counters. Safety considerations are critical because of its long in , approximately 50 years, leading to prolonged retention and potential concerns for internal exposure. The effective , combining physical decay and biological retention, is about 163 days, but bone-seeking behavior requires strict handling protocols to minimize uptake risks.

Calcium-48

Calcium-48 (48^{48}Ca) is a stable of calcium with an atomic mass of 47.952523 u, comprising 20 protons and 28 neutrons, making it the heaviest stable isotope of the element. It occurs naturally with an abundance of 0.187%, rendering it scarce compared to the dominant 40^{40}Ca isotope. Due to its low natural prevalence, 48^{48}Ca is typically enriched for research purposes using methods such as atomic vapor (AVLIS) or liquid , which exploit differences in atomic or molecular properties to achieve high isotopic purity up to 97%. As a doubly magic nucleus—with closed proton shell at Z=20 and neutron shell at N=28—48^{48}Ca exhibits enhanced nuclear stability, reflected in its high of 8.666 MeV per . In nuclear physics, 48^{48}Ca serves as a key benchmark for testing theoretical models of nuclear structure and forces. Its strong binding arises from the magic configuration, which minimizes energy and resists deformation. A longstanding puzzle regarding its magnetic dipole (M1) transition strength—where experimental measurements conflicted with shell-model predictions— was resolved in 2024 through ab initio calculations performed on the Frontier supercomputer. These quantum many-body simulations, using the in-medium similarity renormalization group method, accurately reproduced the dominant resonant M1 state at 10.23 MeV excitation energy, confirming a transition strength of B(M1) ≈ 0.12 μ_N² and highlighting the role of three-nucleon forces in neutron-rich systems. Such computations provide stringent tests of nuclear interactions, bridging microscopic theories with observable properties like electromagnetic responses. 48^{48}Ca plays a pivotal role in synthesizing superheavy elements due to its neutron-rich nature, which facilitates fusion with targets to form more stable isotopes near the predicted . A landmark example is its use in the 2004 experiment bombarding 244^{244}Pu with 48^{48}Ca ions, producing (element 116) via the reaction 48^{48}Ca + 244^{244}Pu → ^{292}Lv^* → ^{288}Lv+4n,withobserveddecaychainsconfirmingthesynthesis.Additionally,parityviolating[electronscattering](/page/Electronscattering)experiments,suchastheCREXcollaborationatJeffersonLabin2022,measuredthe[neutron](/page/Neutron)skinthicknessofLv + 4n, with observed decay chains confirming the synthesis. Additionally, parity-violating [electron scattering](/page/Electron_scattering) experiments, such as the CREX collaboration at Jefferson Lab in 2022, measured the [neutron](/page/Neutron) skin thickness of ^{48}$Ca to be 0.121 ± 0.026 fm, a thinner value than many models predicted, offering insights into the isovector sector of nuclear forces and constraints on the equation of state for stars. Isotopic anomalies in meteoritic materials further underscore 48^{48}Ca's astrophysical significance. Primitive chondrites exhibit excesses of 48^{48}Ca, correlated with anomalies in 50^{50}Ti and 54^{54}Cr, which are interpreted as signatures of heterogeneous from supernovae. These excesses, up to several epsilon units (ε48^{48}Ca ≈ +2 to +5), suggest input from electron-capture supernovae or core-collapse events that produced neutron-rich calcium isotopes, later incorporated into the solar system's .

Calcium-60

Calcium-60 (^{60}Ca) is the heaviest known of calcium, consisting of 20 protons and 40 neutrons, and represents a key neutron-rich nucleus near the limits of nuclear stability. It was discovered in 2018 through projectile fragmentation reactions at the Radioactive Beam Factory (RIBF) at , , where a 345 MeV/ ^{70}Zn beam was directed onto a target, yielding a production cross-section of approximately 0.11(7) pb for ^{60}Ca. This has no natural occurrence and is produced solely in laboratory settings as an artificial . Its is theoretically estimated at around 60.001 u based on ab initio nuclear models, though direct mass measurements remain unavailable due to its fleeting existence. The ground-state spin and parity of ^{60}Ca are predicted to be 0^+, consistent with expectations for an even-even nucleus, while its decay proceeds primarily via β^- emission to scandium-60 (^{60}Sc). Experimental measurements have not been achieved, but theoretical calculations using continuum shell-model approaches estimate a of approximately 2 ms, with a β-decay branching ratio dominated by transitions to low-lying states in the daughter nucleus. Earlier predictions suggested a shorter of about 0.3 ms, highlighting uncertainties in modeling the β-strength function for such exotic systems. Production of ^{60}Ca relies on high-energy reactions to access its extreme neutron-to-proton ratio. In addition to fragmentation at facilities like RIBF, multi-nucleon transfer (MNT) reactions using stable or radioactive beams in the A ≈ 40–60 mass range at energies around 1.5 MeV/nucleon offer a complementary approach, as explored in simulations for neutron-rich isotope synthesis. Future experiments at facilities such as GSI/ are anticipated to enhance production yields through advanced MNT setups with heavy targets, potentially enabling detailed . Theoretically, ^{60}Ca serves as a critical probe for neutron-rich shell structure beyond the N=32 subshell closure, testing the persistence of calcium's Z=20 magic number amid strong tensor-force effects from neutron excess. Ab initio coupled-cluster calculations reveal large neutron-^{60}Ca scattering lengths, indicative of a possible neutron halo and Efimov physics in the ^{60}Ca–n–n three-body system, where universal low-energy correlations emerge due to resonant two-body interactions. Studies from 2013 further correlate observables in this system with the two-neutron separation energy of ^{62}Ca, providing benchmarks for ab initio predictions of the neutron drip line. Discrepancies between ab initio methods, which place the drip line at ^{60}Ca, and energy-density functional approaches, suggesting stability up to ^{70}Ca, underscore ^{60}Ca's role in resolving the island of inversion extension and nuclear binding trends near N=40.

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