Cited by 172Paleontology and Stratigraphy of FossilsGeology and Paleoclimatology ResearchGeological formations and processes

The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.

Stable oxygen and carbon isotope compositional fields for skeletal and diagenetic components in New Zealand Cenozoic nontropical carbonate sediments and limestones: A synthesis and review

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Nelson, Campbell S., Smith, Abigail M.·1996·New Zealand Journal of Geology and Geophysics

Abstract

The stable oxygen isotope composition (δ 18 O) of a precipitated carbonate depends mainly on the isotope composition, salinity, and temperature of the host fluid, whereas the stable carbon isotope composition (δ 13 C) reflects the source of CO 2 for precipitation, such as meteoric or sea water, shell dissolution, or various biochemical origins, including microbial oxidation of organic matter and methane. Despite the potentially complex array of controls, natural waters tend to show a characteristic range of isotope values which in turn are mimicked or tracked by the carbonate minerals precipitated from them. Consequently, plots of δ 18 O versus δ 13 C for carbonate materials can help identify their depositional and/or diagenetic environment(s). Here we compile isotope results for about 800 samples of carbonate skeletons, bulk sediments, fossils, limestones, cements, concretions, and veins spanning a range of ages (latest Cretaceous to modern) and locations in temperate‐region New Zealand. Despite some overlap, the isotope values for 21 defined categories of carbonate materials tend to group in discrete regions of the δ 18 O‐δ 13 C diagram, thereby providing important insights about their origin. New Zealand modern skeletal shelf carbonates plot in a distinctly different field from their tropical counterparts because of their heavier δ 18 O and narrower range of δ 13 C values, in accord with their nontropical bryomol skeletal facies. Cements in New Zealand temperate limestones are predominantly of burial or, more rarely, meteoric origin, but their nontropical heritage based solely on isotope composition becomes blurred and eventually lost as diagenesis proceeds. In common with many other global examples, siderite, calcite, and dolomite concretions have developed during shallow burial in a range of freshwater to marine depositional settings, the carbon originating mainly from early diagenetic, bacterially mediated reactions involving the decomposition of organic matter in bottom sediments. A summary δ 18 O‐δ 13 C diagram showing mean and standard‐deviation isotope values for the various New Zealand carbonate categories will form a basis for comparing and interpreting other carbonate materials and deposits.

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Crossref · 10.1080/00288306.1996.9514697

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Research works printed but not linked: 15

  1. Anderson J. M., 1984, The sedimentology and diagenesis of an Oligocene carbonate sequence (Nile Group), Westport to Punakaiki
  2. Burns D. A., 1980, Aspects of the stable isotope geochemistry of some New Zealand sediments
  3. Devereux I., 1967, Oxygen isotope paleotemperature measurements on New Zealand Tertiary fossils, New Zealand journal of science, 10, 988
  4. Gage M. 1957.The geology of the Waitaki subdivision New Zealand Geological Survey bulletin 55.
  5. Harris G. J., 1986, Aspects of carbonate diagenesis of nontropical-latitude shelf limestones of the late Paleogene Te Kuiti Group, South Auckland region, New Zealand
  6. Haywick D. W. N., 1990, Stratigraphy, sedimentology, palaeo-ecology and diagenesis of the Petane Group (Plio-Pleistocene) in the Tangoio block, central Hawke's Bay, New Zealand
  7. Hendy C. H., 1969, The isotopic geochemistry of speleothems and its application to the study of past climates
  8. Lohmann K. C., 1983, New ideas and methods for exploration for carbonate reservoirs
  9. Middleton H. A., 1989, Nature and origin of concretionary materials in predominantly non-marine to marginal-marine deposits of the early Tertiary Te Kuiti Group, South Auckland
  10. Milliman J. D., 1974, Marine carbonates
  11. Morrison J. O., 1986, Geochemistry of Recent marine invertebrates, Geoscience Canada, 13, 237
  12. Nelson C. S., 1968, Sedimentology of redeposited calcareous and glauconitic beds at Pahaoa, south-east Wellington, Transactions of The Royal Societv of New Zealand, 6, 45
  13. Nelson C. S., 1993, Compendium of stable oxygen and carbon isotope data for the late Quaternary interval of deep-sea cores from the New Zealand sector of the Tasman Sea and Southwest Pacific Ocean, 87
  14. Smith A. M., 1992, Aspects of the sedimentology of New Zealand bryozoans: a contribution to the temperate shelf carbonate model
  15. Weber J. N., 1968, Comparison of 13C/I2C and 18O/ I6O in the skeletal ealcite of Recent and fossil echinoids, Journal of paleontology, 42, 37

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Metadata

Authors
Nelson, C. S., & Smith, A. M.
Affiliations
University of Waikato (NZ)
Venue
New Zealand Journal of Geology and Geophysics
Publisher
Wiley
Published
1996-03
Volume
39
Issue
1
Pages
93-107
ISSN
  • 0028-8306 (ISSN-L)
  • 1175-8791
OpenAlex
W2156055143
Cited by
172
References
63
Citations by year
2026: 6 · 2025: 10 · 2024: 10 · 2023: 9 · 2022: 11 · 2021: 17 · 2020: 12 · 2019: 16 · 2018: 9 · 2017: 8 · 2016: 6 · 2015: 6 · 2014: 2 · 2013: 4 · 2012: 7
FWCI
1.07
Type
journal article
Language
en
Open access
Locations
  • New Zealand Journal of Geology and Geophysics (publishedVersion)
  • Research Commons (University of Waikato) (submittedVersion)
Funders
  • University of Waikato
  • University of Tasmania
Topics
  • Physical Sciences › Earth and Planetary Sciences › Paleontology › Paleontology and Stratigraphy of Fossils
  • Physical Sciences › Earth and Planetary Sciences › Atmospheric Science › Geology and Paleoclimatology Research
  • Physical Sciences › Earth and Planetary Sciences › Earth-Surface Processes › Geological formations and processes
Keywords
stable oxygen isotopes, stable carbon isotopes, carbonate diagenesis, carbonate cement, siderite concretions, burial diagenesis, meteoric water, limestone

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