{"id":34031,"date":"2025-08-31T03:50:22","date_gmt":"2025-08-31T03:50:22","guid":{"rendered":"https:\/\/www.europesays.com\/ie\/34031\/"},"modified":"2025-08-31T03:50:22","modified_gmt":"2025-08-31T03:50:22","slug":"future-directions-for-understanding-the-coevolution-of-life-and-oxygen","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ie\/34031\/","title":{"rendered":"Future directions for understanding the coevolution of life and oxygen"},"content":{"rendered":"<p>Defining an oxygenated world<\/p>\n<p>In order to constrain Earth System changes associated with environmental oxygen availability, a variety of proxies have been developed. These proxies are calibrated through careful laboratory-based investigations that determine specific redox sensitive chemical behaviours, alongside threshold calibrations derived from large datasets of modern and ancient depositional environments, where redox\/palaeoredox state is either known, or can be estimated using independent data (e.g., presence\/absence of fossil organisms inferred to have had high metabolic demands). After careful calibration, these proxies are then applied to suitable lithologies throughout the sedimentary rock record, and oxygen dynamics are reconstructed based on collations and collective interpretations of geochemical proxy data.<\/p>\n<p>Herein, experts were asked what proxies they preferred to use to define changes to Earth\u2019s surface oxygen concentrations through time (n\u2009=\u200949). Despite only 49 responses to this question, there are a total of 41 self-identified geochemists in the survey, meaning that this is likely a fair representation of experts in the field (Fig.\u00a0<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#Fig1\" rel=\"nofollow noopener\" target=\"_blank\">1<\/a>). To produce Fig.\u00a0<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#Fig1\" rel=\"nofollow noopener\" target=\"_blank\">1<\/a>, to ensure each respondent with one or more chosen proxies had a singular vote, weightings were applied where for each additional proxy their vote was partitioned in the figure; for example, if someone chose two proxies they had half a vote for each. Respondents who self-identified as having multiple disciplines also had their vote partitioned into the separate disciplines in Fig.\u00a0<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#Fig1\" rel=\"nofollow noopener\" target=\"_blank\">1<\/a> but this does not alter the overall total votes for the proxies. The raw data is available at <a href=\"https:\/\/doi.org\/10.6084\/m9.figshare.29591216.v1\" rel=\"nofollow noopener\" target=\"_blank\">https:\/\/doi.org\/10.6084\/m9.figshare.29591216.v1<\/a>.<\/p>\n<p><b id=\"Fig1\" class=\"c-article-section__figure-caption\" data-test=\"figure-caption-text\">Fig. 1: Current and future proxy development.<\/b><a class=\"c-article-section__figure-link\" data-test=\"img-link\" data-track=\"click\" data-track-label=\"image\" data-track-action=\"view figure\" href=\"https:\/\/www.nature.com\/articles\/s43247-025-02689-0\/figures\/1\" rel=\"nofollow noopener\" target=\"_blank\"><img decoding=\"async\" aria-describedby=\"Fig1\" src=\"https:\/\/www.europesays.com\/ie\/wp-content\/uploads\/2025\/08\/43247_2025_2689_Fig1_HTML.png\" alt=\"figure 1\" loading=\"lazy\" width=\"685\" height=\"432\"\/><\/a><\/p>\n<p><b>A<\/b> Geochemical proxies for constraining oxygenation through time, with preference allocated by expert respondents. <b>B<\/b> Proxies that may require further development, based on votes by expert respondents. Numbered proxies are listed in full in the Supplementary Information.<\/p>\n<p>The top four \u201cfavourite\u201d palaeoredox proxies were: MIF-S (&gt;14% of responses), redox sensitive element enrichments (RSEs) (&gt;12% of responses), cerium anomalies (&gt;11% of responses), and iron (Fe) speciation (&gt;7% of responses).<\/p>\n<p>As noted above, the loss of MIF-S has been used as a metric for defining the timing of the GOE for over two decades<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 7\" title=\"Farquhar, J., Bao, H. &amp; Thiemens, M. Atmospheric influence of Earth&#x2019;s earliest sulfur cycle. Science 289, 756&#x2013;758 (2000).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR7\" id=\"ref-link-section-d377369616e805\" rel=\"nofollow noopener\" target=\"_blank\">7<\/a> and constrains the point at which atmospheric oxygen rose across the 10\u22126 PAL threshold<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 10\" title=\"Zahnle, K. J., Claire, M. &amp; Catling, D. C. The loss of mass-independent fractionation in sulfur due to a Palaeoproterozoic collapse of atmospheric methane. Geobiology 4, 271&#x2013;283 (2006).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR10\" id=\"ref-link-section-d377369616e811\" rel=\"nofollow noopener\" target=\"_blank\">10<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 11\" title=\"Pavlov, A. A. &amp; Kasting, J. F. Mass-independent fractionation of sulfur isotopes in Archean sediments: strong evidence for an anoxic Archean atmosphere. Astrobiology 2, 27&#x2013;41 (2002).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR11\" id=\"ref-link-section-d377369616e814\" rel=\"nofollow noopener\" target=\"_blank\">11<\/a>. Based on the clear mechanistic interpretation for the loss of MIF-S, and consistent support for this interpretation based on independent multi-proxy records, it is considered as one of the defining characteristics, not only of the GOE, but as a benchmark for Earth\u2019s overall oxygen trajectory. Redox sensitive elements were also cited as a preferred palaeoredox proxy, and incorporate a suite of elements including molybdenum (Mo), vanadium (V), uranium (U), and rhenium (Re), whose absolute and relative enrichments (most commonly calculated as enrichment factors, or \u2018EFs\u2019, in fine grained siliciclastic rocks, e.g., shale) can be used to distinguish the dominant redox conditions of overlying waters that existed during deposition<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Tribovillard, N., Algeo, T. J., Lyons, T. W. &amp; Riboulleau, A. Trace metals as paleoredox and paleoproductivity proxies: an update. Chem. Geol. 232, 12&#x2013;32 (2006).\" href=\"#ref-CR39\" id=\"ref-link-section-d377369616e818\">39<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Bennett, W. W. &amp; Canfield, D. E. Redox-sensitive trace metals as paleoredox proxies: a review and analysis of data from modern sediments. Earth Sci. Rev. 204, 103175 (2020).\" href=\"#ref-CR40\" id=\"ref-link-section-d377369616e818_1\">40<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 41\" title=\"Li, S., Wignall, P. B. &amp; Poulton, S. W. Co-application of rhenium, vanadium, uranium and molybdenum as paleo-redox proxies: insight from modern and ancient environments. Chem. Geol. 674, 122565 (2025).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR41\" id=\"ref-link-section-d377369616e821\" rel=\"nofollow noopener\" target=\"_blank\">41<\/a>. Cerium anomalies (Ce\/Ce*), which also constitute one of the top four favourite proxies, are distinguished by enrichments or depletions in Ce relative to a specific rare Earth element (REE) profile<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 20\" title=\"Wallace, M. W. et al. Oxygenation history of the Neoproterozoic to early Phanerozoic and the rise of land plants. Earth Planet. Sci. Lett. 466, 12&#x2013;19 (2017).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR20\" id=\"ref-link-section-d377369616e825\" rel=\"nofollow noopener\" target=\"_blank\">20<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 42\" title=\"Tostevin, R. et al. Effective use of cerium anomalies as a redox proxy in carbonate-dominated marine settings. Chem. Geol. 438, 146&#x2013;162 (2016).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR42\" id=\"ref-link-section-d377369616e828\" rel=\"nofollow noopener\" target=\"_blank\">42<\/a>. Ce is readily adsorbed onto manganese oxides, and oxygen concentrations sufficient to oxidise reduced Mn can therefore lead to more efficient Ce removal from seawater, equating to a negative Ce\/Ce* anomaly (relative to the REE profile), most commonly recorded in early marine carbonate cements or carbonate sediments<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 20\" title=\"Wallace, M. W. et al. Oxygenation history of the Neoproterozoic to early Phanerozoic and the rise of land plants. Earth Planet. Sci. Lett. 466, 12&#x2013;19 (2017).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR20\" id=\"ref-link-section-d377369616e833\" rel=\"nofollow noopener\" target=\"_blank\">20<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 42\" title=\"Tostevin, R. et al. Effective use of cerium anomalies as a redox proxy in carbonate-dominated marine settings. Chem. Geol. 438, 146&#x2013;162 (2016).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR42\" id=\"ref-link-section-d377369616e836\" rel=\"nofollow noopener\" target=\"_blank\">42<\/a>. The fourth favourite palaeoredox proxy was Fe speciation. The Fe speciation protocol for modern sediments and ancient sedimentary rocks (commonly shales) has remained largely unchanged for almost 20 years<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 43\" title=\"Poulton, S. W. &amp; Canfield, D. E. Development of a sequential extraction procedure for iron: implications for iron partitioning in continentally derived particulates. Chem. Geol. 214, 209&#x2013;221 (2005).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR43\" id=\"ref-link-section-d377369616e840\" rel=\"nofollow noopener\" target=\"_blank\">43<\/a>, and is contingent upon the quantification of the proportion of total Fe (FeT) considered highly reactive (FeHR) to biological or abiological reduction under anoxic conditions. FeHR constitutes the sum of Fe in carbonates (Fecarb), oxides (Feox) and magnetite (Femag), which are operationally defined via a three step sequential extraction procedure, in addition to pyrite (Fepy), which is quantified via a separate extraction<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 43\" title=\"Poulton, S. W. &amp; Canfield, D. E. Development of a sequential extraction procedure for iron: implications for iron partitioning in continentally derived particulates. Chem. Geol. 214, 209&#x2013;221 (2005).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR43\" id=\"ref-link-section-d377369616e859\" rel=\"nofollow noopener\" target=\"_blank\">43<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 44\" title=\"Canfield, D. E., Raiswell, R., Westrich, J. T., Reaves, C. M. &amp; Berner, R. A. The use of chromium reduction in the analysis of reduced inorganic sulfur in sediments and shales. Chem. Geol. 54, 149&#x2013;155 (1986).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR44\" id=\"ref-link-section-d377369616e862\" rel=\"nofollow noopener\" target=\"_blank\">44<\/a>. All proxy datasets require thorough screening to determine the degree to which post-depositional conditions may have skewed geochemical data, and numerous articles have outlined best practices in the production and interpretation of Fe speciation data<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 45\" title=\"Poulton, S. W. The iron speciation paleoredox proxy. in Geochemical Tracers in Earth System Science (eds Lyons, T., Turchyn, W. A. &amp; Reinhard, C.) 1&#x2013;20 (Cambridge University Press, 2021).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR45\" id=\"ref-link-section-d377369616e866\" rel=\"nofollow noopener\" target=\"_blank\">45<\/a>.<\/p>\n<p>Experts were also asked what proxies they would like to see better developed in the future (n\u2009=\u200944). Responses to this question can be interpreted in several ways; either the expert considers their chosen proxy to require a more thorough calibration prior to widespread use (amounting to concern with regards to overinterpreting premature datasets or methodological\/analytical uncertainties), or that the expert believes that an underappreciated proxy is sufficiently novel to warrant more concerted development and application, or both. The top proxies that experts wish to see better developed are: redox sensitive elements (RSEs) (&gt;8% of responses), carbonate-bound iodine (&gt;13%), mass independent fractionation of oxygen isotopes (&gt;7%), trace metal isotopes (&gt;6%), and oxygen requirements of biology (&gt;4%).<\/p>\n<p>Only RSEs are found on both the favourite and further development lists, which may be due to the wide range of elements that can be grouped into this term, and ongoing research associated with the redox sensitivities and behaviours of specific elements. Carbonate-bound iodine has recently shown promise as a means to constrain shallow water oxygen concentrations in deep time, given that oxidised iodate is the only species of iodine that can be readily incorporated into the carbonate lattice<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 46\" title=\"Hardisty, D. S. et al. An iodine record of Paleoproterozoic surface ocean oxygenation. Geology 42, 619&#x2013;622 (2014).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR46\" id=\"ref-link-section-d377369616e880\" rel=\"nofollow noopener\" target=\"_blank\">46<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 47\" title=\"Lu, Z., Jenkyns, H. C. &amp; Rickaby, R. E. M. Iodine to calcium ratios in marine carbonate as a paleo-redox proxy during oceanic anoxic events. Geology 38, 1107&#x2013;1110 (2010).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR47\" id=\"ref-link-section-d377369616e883\" rel=\"nofollow noopener\" target=\"_blank\">47<\/a>. Mass independent fractionation of oxygen isotopes attempt to capture a transition in atmospheric pO2 driven by ozone formation<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Segura, A. et al. Ozone concentrations and ultraviolet fluxes on Earth-like planets around other stars. Astrobiology 4, 689&#x2013;708 (2003).\" href=\"#ref-CR48\" id=\"ref-link-section-d377369616e892\">48<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Gregory, B. S., Claire, M. W. &amp; Rugheimer, S. Photochemical modelling of atmospheric oxygen levels confirms two stable states. Earth Planet. Sci. Lett. 561, 116818 (2021).\" href=\"#ref-CR49\" id=\"ref-link-section-d377369616e892_1\">49<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 50\" title=\"Planavsky, N. J., Reinhard, C. T., Isson, T. T., Ozaki, K. &amp; Crockford, P. Large mass-independent oxygen isotope fractionations in mid-proterozoic sediments: evidence for a low-oxygen atmosphere? Astrobiology 20, 628&#x2013;636 (2020).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR50\" id=\"ref-link-section-d377369616e895\" rel=\"nofollow noopener\" target=\"_blank\">50<\/a>. Interpretations of O-MIF data have also been taken further, in attempts to constrain productivity dependence on pO2 and pCO2 estimates<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 51\" title=\"Crockford, P. W. et al. Triple oxygen isotope evidence for limited mid-Proterozoic primary productivity. Nature 559, 613&#x2013;616 (2018).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR51\" id=\"ref-link-section-d377369616e910\" rel=\"nofollow noopener\" target=\"_blank\">51<\/a>. The umbrella term \u2018trace metal isotopes\u2019 encapsulates a variety of elemental systems that, to describe in full, would be beyond the scope of this manuscript. As an example, Cr isotopes have been used over the past decade to constrain atmospheric O2 concentrations, given the sensitivity of Cr isotope fractionation to oxidative weathering and manganese cycling<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 52\" title=\"Frei, R., Gaucher, C., Poulton, S. W. &amp; Canfield, D. E. Fluctuations in Precambrian atmospheric oxygenation recorded by chromium isotopes. Nature 461, 250&#x2013;253 (2009).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR52\" id=\"ref-link-section-d377369616e916\" rel=\"nofollow noopener\" target=\"_blank\">52<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 53\" title=\"Bauer, K., Planavsky, N. J., Reinhard, C. T. &amp; Cole, D. B. in Elements in Geochemical Tracers in Earth System Science (eds Lyons, T., Turchyn, W. A. &amp; Reinhard, C.) 1&#x2013;20 (Cambridge University Press, 2021).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR53\" id=\"ref-link-section-d377369616e919\" rel=\"nofollow noopener\" target=\"_blank\">53<\/a>. Meanwhile, Mo isotopes can be used to constrain the extent of oceanic sulfidic conditions<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 54\" title=\"Kendall, B., Dahl, T. W. &amp; Anbar, A. D. The stable isotope geochemistry of molybdenum. Rev. Mineral. Geochem. 82, 683&#x2013;732 (2017).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR54\" id=\"ref-link-section-d377369616e924\" rel=\"nofollow noopener\" target=\"_blank\">54<\/a> and U isotopes can be used as a means to quantify the extent of oxic and anoxic global seafloor<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 55\" title=\"Lau, K. V., Romaniello, S. J. &amp; Zhang, F. in Elements in Geochemical Tracers in Earth System Science (eds Lyons, T., Turchyn, W. A. &amp; Reinhard, C.) (Cambridge University Press, 2019).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR55\" id=\"ref-link-section-d377369616e928\" rel=\"nofollow noopener\" target=\"_blank\">55<\/a>, due to the long residence time of these elements in the modern ocean. The variety of proxies that sit within the term \u2018trace metal isotopes\u2019 demonstrates that they must be extensively calibrated independently, but will provide more nuanced interpretations of depositional redox conditions when employed efficiently, and in concert. Additionally, research on the O2 requirements of animals may offer a more direct means by which to constrain oxygen concentrations in the water column, given that specific oxygen concentrations are required to sustain specific metabolisms. However, determining the precise oxygen requirements of these metabolisms demands both careful study under laboratory conditions<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 28\" title=\"Mills, D. B. et al. Oxygen requirements of the earliest animals. Proc. Natl. Acad. Sci. USA 111, 4168&#x2013;4172 (2014).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR28\" id=\"ref-link-section-d377369616e934\" rel=\"nofollow noopener\" target=\"_blank\">28<\/a>, as well as assumptions regarding the affinities and life habits of complex multicellular organisms preserved in the fossil record<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 42\" title=\"Tostevin, R. et al. Effective use of cerium anomalies as a redox proxy in carbonate-dominated marine settings. Chem. Geol. 438, 146&#x2013;162 (2016).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR42\" id=\"ref-link-section-d377369616e938\" rel=\"nofollow noopener\" target=\"_blank\">42<\/a>.<\/p>\n<p>Understanding the evidence across disciplines: is there a holistic view?<\/p>\n<p>Pieces of information are often misinterpreted during interdisciplinary communication. The Precambrian fossil record is rife in enigmatic fossils, many of which suffer an uncertain phylogenetic placement or even questioned biogenicity<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 56\" title=\"Cloud, P. Pseudofossils: a plea for caution. Geology 1, 123&#x2013;127 (1973).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR56\" id=\"ref-link-section-d377369616e950\" rel=\"nofollow noopener\" target=\"_blank\">56<\/a>. A specific example of a recent palaeontological finding that has been publicly refuted is the reassessment of a putative fossil from India that superficially resembled the Ediacaran organism Dickinsonia<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 57\" title=\"Retallack, G. J., Matthews, N. A., Masters, S., Khangar, R. G. &amp; Khan, M. Dickinsonia discovered in India and late Ediacaran biogeography. Gondwana Res. 90, 165&#x2013;170 (2021).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR57\" id=\"ref-link-section-d377369616e956\" rel=\"nofollow noopener\" target=\"_blank\">57<\/a> as the decaying impression of a modern beehive<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 58\" title=\"Meert, J. G., Pandit, M. K., Kwafo, S. &amp; Singha, A. Stinging news: &#x2018;Dickinsonia&#x2019; discovered in the Upper Vindhyan of India not worth the buzz. Gondwana Res. 117, 1&#x2013;7 (2023).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR58\" id=\"ref-link-section-d377369616e960\" rel=\"nofollow noopener\" target=\"_blank\">58<\/a>. However, published rebuttals are relatively uncommon, and in the majority of cases, uncertain or disputed fossils themselves tend to be largely ignored in subsequent scientific literature, without published critique. From the perspective of an exterior discipline (e.g., geochemistry), such lack of published critique may be interpreted as acceptance of the outdated perspective, especially if open cross-discipline communication is lacking. In sum, this highlights the necessity for active cross-discipline communication.<\/p>\n<p>Expert respondents were asked to self-categorise their primary discipline, and then to suggest which pieces of respective geochemical and palaeontological evidence are most often misinterpreted or misused. Experts who identified as palaeobiologists repeatedly outlined several instances of misinterpretation of the fossil record with regards to understanding the coevolution of life and oxygen (n\u2009=\u200934). Occurrences of stromatolites are often misinterpreted as direct evidence for the presence of cyanobacteria and thus onset of oxygenic photosynthesis (highest proportion of responses, c. 20%). This confusion likely derives from concerns with affinities of stromatolites in deep time. Recent microbialites, built largely by prokaryotic and eukaryotic photosynthesizers, are not always suitable analogues to Archean and Proterozoic ones<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 59\" title=\"Bosak, T., Knoll, A. &amp; Petroff, A. P. The meaning of stromatolites. Annu. Rev. Earth Planet Sci. 41, 21&#x2013;44 (2013).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR59\" id=\"ref-link-section-d377369616e970\" rel=\"nofollow noopener\" target=\"_blank\">59<\/a> and the metabolisms of ancient microbialite- and stromatolite-builders are not limited to oxygenic photosynthesis<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 60\" title=\"Bosak, T., Greene, S. E. &amp; Newman, D. K. A likely role for anoxygenic photosynthetic microbes in the formation of ancient stromatolites. Geobiology 5, 119&#x2013;126 (2007).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR60\" id=\"ref-link-section-d377369616e974\" rel=\"nofollow noopener\" target=\"_blank\">60<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 61\" title=\"Decraene, M. N. et al. Intense biogeochemical iron cycling revealed in Neoarchean micropyrites from stromatolites. Geochim. Cosmochim. Acta 312, 299&#x2013;320 (2021).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR61\" id=\"ref-link-section-d377369616e977\" rel=\"nofollow noopener\" target=\"_blank\">61<\/a>. A lack of, or poor, age constraints and\/or established affinity of Precambrian fossils are the second most often misinterpreted palaeontological evidence (&gt;17%), and may lead to confusion about the timing of the appearance of major lineages. This not only impacts evolutionary studies, but also our understanding of the coevolution of life and the changing environment. This is associated with the third most often misinterpreted palaeontological evidence; the interpretation of fossil biogenicity, especially of some Archean microfossils (&gt;14%). This response is likely driven by recent experimental studies that show inorganic growth of sulfur biomorphs with similar morphologies to early fossil cells<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 62\" title=\"Cosmidis, J. &amp; Templeton, A. S. Self-assembly of biomorphic carbon\/sulfur microstructures in sulfidic environments. Nat. Commun. 7, 12812 (2016).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR62\" id=\"ref-link-section-d377369616e981\" rel=\"nofollow noopener\" target=\"_blank\">62<\/a>. Beyond the Archean, the biogenicity of the Paleoproterozoic \u2018Francevillian biota\u2019<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 63\" title=\"El Albani, A. et al. Large colonial organisms with coordinated growth in oxygenated environments 2.1&#x2009;Gyr ago. Nature 466, 100&#x2013;104 (2010).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR63\" id=\"ref-link-section-d377369616e985\" rel=\"nofollow noopener\" target=\"_blank\">63<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 64\" title=\"El Albani, A. et al. The 2.1 Ga old francevillian biota: biogenicity, taphonomy and biodiversity. PLoS ONE 9, e99438 (2014).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR64\" id=\"ref-link-section-d377369616e988\" rel=\"nofollow noopener\" target=\"_blank\">64<\/a> are also specifically referred to (&gt;14% of responses). As an indicator of common scientific perspective, these expert responses identify areas of contention in deep time palaeontological research that might not always be obvious to external disciplines.<\/p>\n<p>Numerous geochemical data are also often misinterpreted, leading to an extensive list of proxies named by self-categorised experts in geochemistry (n\u2009=\u200947) including; carbon and oxygen isotopes (&gt;13% of responses), molecular biomarkers (&gt;11% of responses), iron speciation (&gt;9% of responses), trace metal concentrations (&gt;9% of responses), chromium, sulfur and metal isotopes (&gt;23% of responses in sum) and the S-MIF record (&gt;3% of responses). In addition to these, specific reference was made to the misinterpretation of local\/regional proxies as being informative of global environmental change (&gt;5% of responses). The diversity of proxies being reported either suggests poor intra-disciplinary communication or a common agreement that the majority of proxies require ongoing detailed study and continued calibration (e.g., incorporating novel laboratory or field-based insights). It is important to note, however, that a large proportion of oxygenation\/deoxygenation events are supported by a combination of proxies rather than relying on a single one.<\/p>\n<p>A further, broader question posed to respondents, asked what they deemed to be the most pressing questions in the field (total of 106 unique responses from 45 respondents). For example, one question that was commonly raised by respondent experts is how to better distinguish between local and global signatures, or \u2018how spatially representative is my geochemical dataset?\u2019 (&gt;16%). Specific responses highlighted the need to clarify local vs. global environmental drivers of oxygenation, as well as the extent of oxygen oases, throughout the Proterozoic. Several respondents also acknowledged that limited geological material exists with which to clarify a global understanding. Another pressing question that was repeatedly raised in the responses is how best to improve our proxy calibrations (&gt;16% of responses). Geochemical proxies used to constrain past environmental change rely on calibrations that rely on using observations in modern depositional environments or under controlled laboratory conditions, which attempt to recreate representative environments that may have existed in the geologic past. Given the likelihood of non-uniformitarian environmental conditions throughout much of Earth\u2019s history, it is necessary to continue investigating how these proxies behave in as many different chemical environments or depositional settings as possible. Furthermore, given that some ocean chemistries in the rock record are not available to study in nature today, theoretical or experimental studies are also required to supplement interpretations based on proxy data. The final, and potentially most pressing question, as defined by numerous experts, concerns whether or not O2 availability actually limits eukaryotic evolution, or indeed the timing, and pace, of early animal evolution (&gt;20% of responses). Current estimates of atmospheric O2 requirements for early eukaryotes are between 0.001% and 0.4% PAL<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 28\" title=\"Mills, D. B. et al. Oxygen requirements of the earliest animals. Proc. Natl. Acad. Sci. USA 111, 4168&#x2013;4172 (2014).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR28\" id=\"ref-link-section-d377369616e1005\" rel=\"nofollow noopener\" target=\"_blank\">28<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 29\" title=\"Mills, D. B. et al. Eukaryogenesis and oxygen in Earth history. Nat. Ecol. Evol. 6, 520&#x2013;532 (2022).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR29\" id=\"ref-link-section-d377369616e1008\" rel=\"nofollow noopener\" target=\"_blank\">29<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 65\" title=\"Leys, S. P. &amp; Kahn, A. S. Oxygen and the energetic requirements of the first multicellular animals. Integr. Comp. Biol. 58, 666&#x2013;676 (2018).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR65\" id=\"ref-link-section-d377369616e1011\" rel=\"nofollow noopener\" target=\"_blank\">65<\/a>. While the oldest eukaryotic fossils are found in ~1.63 Ga<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 66\" title=\"Miao, L., Yin, Z., Knoll, A., Qu, Y. &amp; Zhu, M. 1.63-billion-year-old multicellular eukaryotes from the Chuanlinggou Formation in North China. Sci. Adv. 10, &#010;                  https:\/\/doi.org\/10.1126\/sciadv.adk3208&#010;                  &#010;                 (2024).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR66\" id=\"ref-link-section-d377369616e1015\" rel=\"nofollow noopener\" target=\"_blank\">66<\/a> sedimentary rocks, some propose\u00a0O2 concentrations of this magnitude are thought to have been reached on Earth much later, sometime during the Neoproterozoic Era, further complicating potential linkages between environmental oxygenation and early evolution<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 1\" title=\"Lyons, T. W., Reinhard, C. T. &amp; Planavsky, N. J. The rise of oxygen in Earth&#x2019;s early ocean and atmosphere. Nature 506, 307&#x2013;315 (2014).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR1\" id=\"ref-link-section-d377369616e1022\" rel=\"nofollow noopener\" target=\"_blank\">1<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 2\" title=\"Lyons, T. W. et al. Co-evolution of early Earth environments and microbial life. Nat. Rev. Microbiol. 22, 572&#x2013;586 (2024).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR2\" id=\"ref-link-section-d377369616e1025\" rel=\"nofollow noopener\" target=\"_blank\">2<\/a> (Fig.\u00a0<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#Fig2\" rel=\"nofollow noopener\" target=\"_blank\">2<\/a>). Additional pressing questions arose repeatedly, including the timing of oxygenation events (&gt;10%), which require both better chronostratigraphic constraints as well as a more integrated use of geochemical proxies, and a more nuanced understanding of geochemical proxy interpretations. Importantly, each of these thematic questions still only received a maximum of 20% of responses, highlighting that the broad research community is approaching this prospect with a wide variety of methods.<\/p>\n<p><b id=\"Fig2\" class=\"c-article-section__figure-caption\" data-test=\"figure-caption-text\">Fig. 2: Summary of current understanding and intervals of time for future research.<\/b><a class=\"c-article-section__figure-link\" data-test=\"img-link\" data-track=\"click\" data-track-label=\"image\" data-track-action=\"view figure\" href=\"https:\/\/www.nature.com\/articles\/s43247-025-02689-0\/figures\/2\" rel=\"nofollow noopener\" target=\"_blank\"><img decoding=\"async\" aria-describedby=\"Fig2\" src=\"https:\/\/www.europesays.com\/ie\/wp-content\/uploads\/2025\/08\/43247_2025_2689_Fig2_HTML.png\" alt=\"figure 2\" loading=\"lazy\" width=\"685\" height=\"329\"\/><\/a><\/p>\n<p><b>A<\/b> Reported intervals of high priority according to experts (n\u2009=\u200937). Highest reported interval of priority occurs during the mid-late Tonian 800\u2013720\u2009Ma (timescale overlap of 14 individual responses). <b>B<\/b> Atmospheric oxygen throughout Earth history<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 2\" title=\"Lyons, T. W. et al. Co-evolution of early Earth environments and microbial life. Nat. Rev. Microbiol. 22, 572&#x2013;586 (2024).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR2\" id=\"ref-link-section-d377369616e1052\" rel=\"nofollow noopener\" target=\"_blank\">2<\/a>. <b>C<\/b> Global carbon isotope record based on a preliminary compilation<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 72\" title=\"Cramer, B. D. &amp; Jarvis, I. in Geologic Time Scale, 2020 (eds Gradstein, F. M., Ogg, J. G., Schmitz, M. D. &amp; Ogg, G. M.) 309&#x2013;343 (Elsevier, 2020).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR72\" id=\"ref-link-section-d377369616e1059\" rel=\"nofollow noopener\" target=\"_blank\">72<\/a>.<\/p>\n<p>Future directions<\/p>\n<p>This questionnaire offers a direct method of investigating and communicating a subsample of the current state of research and cross-disciplinary understanding in the Earth sciences. It also provides an opportunity for open communication and discussion regarding areas of future research that may advance, or challenge, the current paradigm. With this in mind, experts were asked what field-based, experimental and\/or modelling efforts they believed would be most interesting or useful going forward, to better understand the evolution of environmental oxygenation and its importance for the biosphere (total of 80 unique responses from 38 respondents). The most frequently requested items are listed in the Supplementary Information, but we expand on the most noted three here.<\/p>\n<p>The first recurring item calls for more isotope fractionation experiments, in order to better understand how isotope systems inform specific environmental changes (&gt;8%). As noted previously, this reiterates the widespread view that ongoing geochemical proxy calibration is essential.<\/p>\n<p>The second item calls for more accurate temporal calibration of the rock record, resulting in a higher precision temporal calibration of geochemical and fossil data (&gt;13%). Specifically, it is widely recognised that more data are required constrain age models for the Paleoproterozoic to early Neoproterozoic. The resulting dataset would ideally permit the calibration of geochemical and palaeontological information from mixed lithologies within a unified chronostratigraphic framework, or series of possible frameworks, each of which would be anchored in time by absolute ages derived from high-precision radiometric methods. Exploring alternative correlation frameworks may also help to discriminate between the relative likelihoods of alternative palaeogeographic reconstructions in deep time. In particular, more high-precision radiometric constraints are needed for time intervals of high research priority as identified by the survey responses (Fig.\u00a0<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#Fig2\" rel=\"nofollow noopener\" target=\"_blank\">2<\/a>).<\/p>\n<p>The third item calls for greater efforts to pursue global syntheses that demand interdisciplinary collaboration (&gt;6%). Numerous international initiatives that aim to collate sedimentary, geochemical and palaeontological data throughout Earth history are enhancing our ability to constrain aspects of the rock record with greater confidence over both longer and shorter timescales. These databases include the Sedimentary Geochemistry and Palaeoenvironments Project<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 67\" title=\"Farrell, &#xDA;C. et al. The sedimentary geochemistry and paleoenvironments project. Geobiology 19, 545&#x2013;556 (2021).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR67\" id=\"ref-link-section-d377369616e1091\" rel=\"nofollow noopener\" target=\"_blank\">67<\/a>, the North American MacroStrat database<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 68\" title=\"Segessenman, D. C. &amp; Peters, S. E. Macrostratigraphy of the Ediacaran System in North America. Geol. Soc. Am. 220, 399&#x2013;424 (2023).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR68\" id=\"ref-link-section-d377369616e1095\" rel=\"nofollow noopener\" target=\"_blank\">68<\/a>, and the growing Deeptime Digital Earth initiative (DDE, formerly known as the Geobiodiversity Database<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 69\" title=\"Stephenson, M. H., Cheng, Q., Wang, C., Fan, J. &amp; Oberh&#xE4;nsli, R. Progress towards the establishment of the IUGS Deep-time Digital Earth (DDE) programme. IUGS 43, 1057&#x2013;1062 (2020).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR69\" id=\"ref-link-section-d377369616e1099\" rel=\"nofollow noopener\" target=\"_blank\">69<\/a>), each of which not only collate data, but also facilitate large dataset interpretations by providing novel user interfaces and statistical methods for database interrogation.<\/p>\n<p>Experts were also asked what they believe to be the greatest remaining uncertainties in attempts to constrain the influence of evolving atmospheric and oceanic oxygen concentrations on life, throughout Earth history. The following items dominated responses, and summarise three key questions that captivate the research community, as a whole:<\/p>\n<p>(1) What environmental O2 concentration is required to facilitate the evolution of animal life?<\/p>\n<p>(2) What were the major mechanisms driving long-term changes in environmental O2?<\/p>\n<p>(3) What were the upper and lower limits of environmental O2 through time?<\/p>\n<p>Attempting to answer these questions demands interdisciplinary studies that interrogate large swathes of Earth history. However, the patchiness of the rock record in deep time often limits research during certain periods. With this in mind, experts were asked what intervals of the geologic record they believe to be priority targets for future sampling and investigation (Fig.\u00a0<a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#Fig2\" rel=\"nofollow noopener\" target=\"_blank\">2<\/a>). This revealed a notable interval of interest during the mid-Paleoproterozoic (c. 2.2\u20131.8 Ga), in the immediate aftermath of the GOE, encompassing the Lomagundi-Jatuli Event and the estimated origin of eukaryotes (per Betts et al.<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 24\" title=\"Betts, H. C. et al. Integrated genomic and fossil evidence illuminates life&#x2019;s early evolution and eukaryote origin. Nat. Ecol. Evol. 2, 1556&#x2013;1562 (2018).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR24\" id=\"ref-link-section-d377369616e1128\" rel=\"nofollow noopener\" target=\"_blank\">24<\/a>). Other target intervals include the late Mesoproterozoic (c. 1.3\u20131.0 Ga), coinciding with the radiation of eukaryotic lineages and the origin of multicellularity<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 70\" title=\"Butterfield, N. J. Bangiomorpha pubescens n. gen., n. sp.: implications for the evolution of sex, multicellularity, and the Mesoproterozoic\/Neoproterozoic radiation of eukaryotes. Paleobiology 26, 389&#x2013;404 (2000).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR70\" id=\"ref-link-section-d377369616e1132\" rel=\"nofollow noopener\" target=\"_blank\">70<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 71\" title=\"Sforna, M. C. et al. Intracellular bound chlorophyll residues identify 1 Gyr-old fossils as eukaryotic algae. Nat. Commun. 13, 146 (2022).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR71\" id=\"ref-link-section-d377369616e1135\" rel=\"nofollow noopener\" target=\"_blank\">71<\/a>, and the mid-late Tonian Period (c. 0.8\u20130.72 Ga) during eukaryotic diversification and the inception of climatic instability associated with the onset of the Sturtian Snowball Earth<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 26\" title=\"Brocks, J. J. et al. The rise of algae in Cryogenian oceans and the emergence of animals. Nature 548, 578&#x2013;581 (2017).\" href=\"http:\/\/www.nature.com\/articles\/s43247-025-02689-0#ref-CR26\" id=\"ref-link-section-d377369616e1139\" rel=\"nofollow noopener\" target=\"_blank\">26<\/a>.<\/p>\n<p>Overall, we hope this study promotes future interdisciplinary research and conversations that attempt to further our understanding of how the Earth became habitable for complex life. We believe that future conferences and workshops should continue to promote interdisciplinary research and conversations in order to address several of the topics highlighted herein. More specifically, we hope that the suggestions here concerning specific sedimentary intervals, geochemical analyses, and palaeobiological assessments, which together represent a community-wide perspective of themes that warrant further investigation, provide direction and support for continued research.<\/p>\n","protected":false},"excerpt":{"rendered":"Defining an oxygenated world In order to constrain Earth System changes associated with environmental oxygen availability, a variety&hellip;\n","protected":false},"author":2,"featured_media":34032,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[77],"tags":[26594,14697,18,26595,440,8101,910,19,17,133],"class_list":{"0":"post-34031","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-science","8":"tag-biogeochemistry","9":"tag-earth-sciences","10":"tag-eire","11":"tag-element-cycles","12":"tag-environment","13":"tag-evolution","14":"tag-general","15":"tag-ie","16":"tag-ireland","17":"tag-science"},"share_on_mastodon":{"url":"","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/posts\/34031","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/comments?post=34031"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/posts\/34031\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/media\/34032"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/media?parent=34031"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/categories?post=34031"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ie\/wp-json\/wp\/v2\/tags?post=34031"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}