牙齿如何记录和减弱季节信号

IF 2.6 1区 地球科学 Q1 ANTHROPOLOGY Journal of Archaeological Science Pub Date : 2024-12-28 DOI:10.1016/j.jas.2024.106148
Daniel R. Green , Tanya M. Smith , Gerry Olack , Ian S. Williams , Paul Tafforeau , Albert S. Colman , Kevin T. Uno
{"title":"牙齿如何记录和减弱季节信号","authors":"Daniel R. Green ,&nbsp;Tanya M. Smith ,&nbsp;Gerry Olack ,&nbsp;Ian S. Williams ,&nbsp;Paul Tafforeau ,&nbsp;Albert S. Colman ,&nbsp;Kevin T. Uno","doi":"10.1016/j.jas.2024.106148","DOIUrl":null,"url":null,"abstract":"<div><div>Variability of oxygen isotopes in environmental water is recorded in tooth enamel, providing a record of seasonal change, dietary variability, and mobility. Physiology dampens this variability, however, as oxygen passes from environmental sources into blood and forming teeth. We showcase two methods of high resolution, 2-dimensional enamel sampling, and conduct modeling, to report why and how environmental oxygen isotope variability is reduced in animal bodies and teeth. First, using two modern experimental sheep, we introduce a sampling method, die-saw dicing, that provides high-resolution physical samples (n = 109 and 111 sample locations per tooth) for use in conventional stable isotope and molecular measurement protocols. Second, we use an ion microprobe to sample innermost enamel in an experimental sheep (n = 156 measurements), and in a Pleistocene orangutan (n = 176 measurements). Synchrotron and conventional μCT scans reveal innermost enamel thicknesses averaging 18 and 21 μm in width. Experimental data in sheep show that compared to drinking water, oxygen isotope variability in blood is reduced to 70–90 %; inner and innermost enamel retain between 36 and 48 % of likely drinking water stable isotope range, but this recovery declines to 28–34 % in outer enamel. 2D isotope sampling suggests that declines in isotopic variability, and shifted isotopic oscillations throughout enamel, result from the angle of secretory hydroxyapatite deposition and its overprinting by maturation. This overprinting occurs at all locations including innermost enamel, and is greatest in outer enamel. These findings confirm that all regions of enamel undergo maturation to varying degrees and confirm that inner and innermost enamel preserve more environmental variability than other regions. We further show how the resolution of isotope sampling — not only the spatial resolution within teeth, but also the temporal resolution of water in the environment — impacts our estimate of how much variation teeth recover from the environment. We suggest inverse methods, or multiplication by standard factors determined by ecology, taxon, and sampling strategy, to reconstruct the full scale of seasonal environmental variability. We advocate for combined inverse modeling and high-resolution sampling informed by the spatiotemporal pattern of enamel formation, and at the inner or innermost enamel when possible, to recover seasonal records from teeth.</div></div>","PeriodicalId":50254,"journal":{"name":"Journal of Archaeological Science","volume":"175 ","pages":"Article 106148"},"PeriodicalIF":2.6000,"publicationDate":"2024-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"How teeth record and attenuate seasonal signals\",\"authors\":\"Daniel R. Green ,&nbsp;Tanya M. Smith ,&nbsp;Gerry Olack ,&nbsp;Ian S. Williams ,&nbsp;Paul Tafforeau ,&nbsp;Albert S. Colman ,&nbsp;Kevin T. Uno\",\"doi\":\"10.1016/j.jas.2024.106148\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Variability of oxygen isotopes in environmental water is recorded in tooth enamel, providing a record of seasonal change, dietary variability, and mobility. Physiology dampens this variability, however, as oxygen passes from environmental sources into blood and forming teeth. We showcase two methods of high resolution, 2-dimensional enamel sampling, and conduct modeling, to report why and how environmental oxygen isotope variability is reduced in animal bodies and teeth. First, using two modern experimental sheep, we introduce a sampling method, die-saw dicing, that provides high-resolution physical samples (n = 109 and 111 sample locations per tooth) for use in conventional stable isotope and molecular measurement protocols. Second, we use an ion microprobe to sample innermost enamel in an experimental sheep (n = 156 measurements), and in a Pleistocene orangutan (n = 176 measurements). Synchrotron and conventional μCT scans reveal innermost enamel thicknesses averaging 18 and 21 μm in width. Experimental data in sheep show that compared to drinking water, oxygen isotope variability in blood is reduced to 70–90 %; inner and innermost enamel retain between 36 and 48 % of likely drinking water stable isotope range, but this recovery declines to 28–34 % in outer enamel. 2D isotope sampling suggests that declines in isotopic variability, and shifted isotopic oscillations throughout enamel, result from the angle of secretory hydroxyapatite deposition and its overprinting by maturation. This overprinting occurs at all locations including innermost enamel, and is greatest in outer enamel. These findings confirm that all regions of enamel undergo maturation to varying degrees and confirm that inner and innermost enamel preserve more environmental variability than other regions. We further show how the resolution of isotope sampling — not only the spatial resolution within teeth, but also the temporal resolution of water in the environment — impacts our estimate of how much variation teeth recover from the environment. We suggest inverse methods, or multiplication by standard factors determined by ecology, taxon, and sampling strategy, to reconstruct the full scale of seasonal environmental variability. We advocate for combined inverse modeling and high-resolution sampling informed by the spatiotemporal pattern of enamel formation, and at the inner or innermost enamel when possible, to recover seasonal records from teeth.</div></div>\",\"PeriodicalId\":50254,\"journal\":{\"name\":\"Journal of Archaeological Science\",\"volume\":\"175 \",\"pages\":\"Article 106148\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-12-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Archaeological Science\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0305440324002164\",\"RegionNum\":1,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ANTHROPOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Archaeological Science","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0305440324002164","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ANTHROPOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

在牙釉质中记录了环境水中氧同位素的变化,提供了季节变化、饮食变化和流动性的记录。然而,当氧气从环境来源进入血液并形成牙齿时,生理抑制了这种变异性。我们展示了两种高分辨率、二维珐琅质采样的方法,并进行了建模,以报告动物身体和牙齿中环境氧同位素变异性减少的原因和方式。首先,我们使用两只现代实验羊,介绍了一种采样方法,即模锯切,该方法提供了高分辨率的物理样本(n = 109和111个样本位置),用于传统的稳定同位素和分子测量方案。其次,我们使用离子探针对一只实验绵羊(n = 156次测量)和一只更新世猩猩(n = 176次测量)的最内层牙釉质进行取样。同步加速器和常规μCT扫描显示最内层的牙釉质厚度平均为18 μm和21 μm。绵羊的实验数据表明,与饮用水相比,血液中的氧同位素变异性降低到70 - 90%;内层和最内层的牙釉质保留了可能饮用水稳定同位素范围的36 - 48%,但外层牙釉质的这种恢复下降到28 - 34%。二维同位素采样表明,珐琅质中同位素变异性的下降和同位素振荡的转移是由分泌羟基磷灰石沉积的角度和成熟的套印造成的。这种叠印发生在所有位置,包括最内层的珐琅,最外层的珐琅。这些发现证实了牙釉质的所有区域都经历了不同程度的成熟,并证实了内层和最内层的牙釉质比其他区域保留了更多的环境变异性。我们进一步展示了同位素采样的分辨率——不仅是牙齿内部的空间分辨率,还有环境中水的时间分辨率——如何影响我们对牙齿从环境中恢复多少变化的估计。我们建议采用逆方法,或通过由生态、分类单元和采样策略决定的标准因子相乘,来重建季节环境变化的全尺度。我们提倡结合逆建模和高分辨率采样,根据牙釉质形成的时空模式,并在可能的情况下,在内部或最内部的牙釉质,以恢复牙齿的季节性记录。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
How teeth record and attenuate seasonal signals
Variability of oxygen isotopes in environmental water is recorded in tooth enamel, providing a record of seasonal change, dietary variability, and mobility. Physiology dampens this variability, however, as oxygen passes from environmental sources into blood and forming teeth. We showcase two methods of high resolution, 2-dimensional enamel sampling, and conduct modeling, to report why and how environmental oxygen isotope variability is reduced in animal bodies and teeth. First, using two modern experimental sheep, we introduce a sampling method, die-saw dicing, that provides high-resolution physical samples (n = 109 and 111 sample locations per tooth) for use in conventional stable isotope and molecular measurement protocols. Second, we use an ion microprobe to sample innermost enamel in an experimental sheep (n = 156 measurements), and in a Pleistocene orangutan (n = 176 measurements). Synchrotron and conventional μCT scans reveal innermost enamel thicknesses averaging 18 and 21 μm in width. Experimental data in sheep show that compared to drinking water, oxygen isotope variability in blood is reduced to 70–90 %; inner and innermost enamel retain between 36 and 48 % of likely drinking water stable isotope range, but this recovery declines to 28–34 % in outer enamel. 2D isotope sampling suggests that declines in isotopic variability, and shifted isotopic oscillations throughout enamel, result from the angle of secretory hydroxyapatite deposition and its overprinting by maturation. This overprinting occurs at all locations including innermost enamel, and is greatest in outer enamel. These findings confirm that all regions of enamel undergo maturation to varying degrees and confirm that inner and innermost enamel preserve more environmental variability than other regions. We further show how the resolution of isotope sampling — not only the spatial resolution within teeth, but also the temporal resolution of water in the environment — impacts our estimate of how much variation teeth recover from the environment. We suggest inverse methods, or multiplication by standard factors determined by ecology, taxon, and sampling strategy, to reconstruct the full scale of seasonal environmental variability. We advocate for combined inverse modeling and high-resolution sampling informed by the spatiotemporal pattern of enamel formation, and at the inner or innermost enamel when possible, to recover seasonal records from teeth.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Archaeological Science
Journal of Archaeological Science 地学-地球科学综合
CiteScore
6.10
自引率
7.10%
发文量
112
审稿时长
49 days
期刊介绍: The Journal of Archaeological Science is aimed at archaeologists and scientists with particular interests in advancing the development and application of scientific techniques and methodologies to all areas of archaeology. This established monthly journal publishes focus articles, original research papers and major review articles, of wide archaeological significance. The journal provides an international forum for archaeologists and scientists from widely different scientific backgrounds who share a common interest in developing and applying scientific methods to inform major debates through improving the quality and reliability of scientific information derived from archaeological research.
期刊最新文献
I walk an ancient road: A straightforward methodology for analyzing intra- and inter-regional connectivity systems along Roman Frontier Zones (c. 1st—5th century AD) Combining ATR far- and mid-infrared spectroscopy to distinguish native Australian plant exudates for cultural heritage analysis Editorial Board Origins of medieval lead glass ornaments in Central Europe in the light of lead isotopic analysis of finds from Wrocław and Sypniewo (Poland) Spatial analysis of Amazonian Dark Earth formation supports an anthropic origin at the Caldeirão site, Brazil
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1