2020
DOI: 10.1016/j.earscirev.2020.103326
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Proteinaceous corals as proxy archives of paleo-environmental change

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Cited by 8 publications
(8 citation statements)
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“…The review ends with a reflection of outstanding challenges and opportunities over the coming decades of innovation (Section 6). To complement recent reviews of paleoclimate studies across a diversity of long‐lived reef‐building (Sadler et al, 2014) and proteinaceous (Williams, 2020) coral genera, this review will focus primarily on Porites spp. corals, which remain the most extensively utilized genera for paleoclimate studies.…”
Section: Introductionmentioning
confidence: 99%
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“…The review ends with a reflection of outstanding challenges and opportunities over the coming decades of innovation (Section 6). To complement recent reviews of paleoclimate studies across a diversity of long‐lived reef‐building (Sadler et al, 2014) and proteinaceous (Williams, 2020) coral genera, this review will focus primarily on Porites spp. corals, which remain the most extensively utilized genera for paleoclimate studies.…”
Section: Introductionmentioning
confidence: 99%
“…A few factors make reef‐building corals a particularly powerful archive of past climate variability: (1) annual density banding patterns (Knutson et al, 1972), relatively rapid growth (~0.3–2 cm/year, depending on the species), and fine‐scale milling techniques permit annual or even sub‐annual reconstructions of past climate (hereafter “high‐resolution”); (2) annual density banding patterns, combined with advances in radiometric dating techniques (see Section 3.6) permit chronological uncertainties on the order of only a few years or less for well‐dated chronologies; and (3) well‐preserved colonies of living (modern) and sub‐fossil (hereafter “fossil,” Figure 1) samples fill critical gaps in both the spatial and temporal coverage of climate information from the global tropics (Lough, 2010). Several reviews have discussed the rich history of coral paleoclimate studies, including an in‐depth discussion of the commonly utilized proxies for paleo‐temperature (δ 18 O, Sr/Ca) and coral growth (density, extension, and calcification) (Barnes & Lough, 1996; Corrège, 2006; Felis & Pätzold, 2003; Gagan et al, 2000; Grottoli & Eakin, 2007; Jones et al, 2009; Lough, 2004, 2008, 2010; Lough & Cantin, 2014; Lough & Cooper, 2011; Sadler et al, 2014; Williams, 2020), as well as novel geochemical proxies (Saha et al, 2016).…”
Section: Introductionmentioning
confidence: 99%
“…Bromine is a known structural (organically-bound) component of proteinaceous deepsea coral skeletons and is present in the form of a halogenated scleroprotein (Nowak et al, 2009;Williams et al, 2006), namely bromotyrosine and dibromotyrosine (Ehrlich, 2019). As such, the proteinaceous skeletons of deep-sea corals contain some of the largest concentrations of halogens (specifically Br and I) in a biological material (Nowak et al, 2009;Williams, 2020). Interestingly, these concentrations vary throughout the deep-sea coral skeletons and thus must be controlled by their biological availability (Juárez-de la Rosa et al, 2007;Prouty et al, 2011;Williams, 2020;Williams and Grottoli, 2011).…”
Section: Brominementioning
confidence: 99%
“…As such, the proteinaceous skeletons of deep-sea corals contain some of the largest concentrations of halogens (specifically Br and I) in a biological material (Nowak et al, 2009;Williams, 2020). Interestingly, these concentrations vary throughout the deep-sea coral skeletons and thus must be controlled by their biological availability (Juárez-de la Rosa et al, 2007;Prouty et al, 2011;Williams, 2020;Williams and Grottoli, 2011). Considering Br is predominantly present in seawater in a dissolved phase and is accumulated in large proportions by black corals, it seems unlikely the coral would source Br from any minor particulate phase -such as POM.…”
Section: Brominementioning
confidence: 99%
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