Camilla Crifò, J. Berrío, A. Boom, D. Giraldo-Cañas, L. Bremond
{"title":"A paleothermometer for the northern Andes based on C3–C4 grass phytoliths","authors":"Camilla Crifò, J. Berrío, A. Boom, D. Giraldo-Cañas, L. Bremond","doi":"10.1017/pab.2022.44","DOIUrl":null,"url":null,"abstract":"Abstract. Grass-dominated ecosystems cover ∼40% of Earth's terrestrial surface, with tropical grasses accounting for ∼20% of global net primary productivity. C3 (cool/temperate) and C4 (tropical and subtropical) grass distribution is driven primarily by temperature. In this work, we used phytolith assemblages collected from vegetation plots along an elevation and temperature gradient in the northern Andes (Colombia and Ecuador) to develop a paleothermometer for the region. To accomplish this, we created a transfer function based on the inverse relationship between mean annual temperature (MAT) and the phytolith-based climatic index (Ic), which is the proportion of C3 over C4 grass phytoliths (GSSCP). To evaluate how accurately the index reflects C4–C3 grass abundance in vegetation plots, we compared it with semiquantitative floristic estimates of C4–C3 grass abundance. To further evaluate the 1 – Ic index as a proxy for C4–C3 grass abundance, we compared it with corresponding δ13C values (an independent proxy for C4–C3 vegetation). Results indicate that (1) GSSCP assemblages correctly estimate C4–C3 grass abundance in vegetation plots; (2) the Ic index outperforms the δ13C record in estimating C4–C3 grass abundance, even in open-vegetation types; and (3) our Ic index–based model accurately predicts MAT. This new calibrated proxy will help improve paleotemperature reconstructions in the northern Andes since at least the emergence and spread of C4 grasses in the region during the late Miocene.","PeriodicalId":54646,"journal":{"name":"Paleobiology","volume":"49 1","pages":"414 - 430"},"PeriodicalIF":2.6000,"publicationDate":"2023-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Paleobiology","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.1017/pab.2022.44","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIODIVERSITY CONSERVATION","Score":null,"Total":0}
引用次数: 0
Abstract
Abstract. Grass-dominated ecosystems cover ∼40% of Earth's terrestrial surface, with tropical grasses accounting for ∼20% of global net primary productivity. C3 (cool/temperate) and C4 (tropical and subtropical) grass distribution is driven primarily by temperature. In this work, we used phytolith assemblages collected from vegetation plots along an elevation and temperature gradient in the northern Andes (Colombia and Ecuador) to develop a paleothermometer for the region. To accomplish this, we created a transfer function based on the inverse relationship between mean annual temperature (MAT) and the phytolith-based climatic index (Ic), which is the proportion of C3 over C4 grass phytoliths (GSSCP). To evaluate how accurately the index reflects C4–C3 grass abundance in vegetation plots, we compared it with semiquantitative floristic estimates of C4–C3 grass abundance. To further evaluate the 1 – Ic index as a proxy for C4–C3 grass abundance, we compared it with corresponding δ13C values (an independent proxy for C4–C3 vegetation). Results indicate that (1) GSSCP assemblages correctly estimate C4–C3 grass abundance in vegetation plots; (2) the Ic index outperforms the δ13C record in estimating C4–C3 grass abundance, even in open-vegetation types; and (3) our Ic index–based model accurately predicts MAT. This new calibrated proxy will help improve paleotemperature reconstructions in the northern Andes since at least the emergence and spread of C4 grasses in the region during the late Miocene.
期刊介绍:
Paleobiology publishes original contributions of any length (but normally 10-50 manuscript pages) dealing with any aspect of biological paleontology. Emphasis is placed on biological or paleobiological processes and patterns, including macroevolution, extinction, diversification, speciation, functional morphology, bio-geography, phylogeny, paleoecology, molecular paleontology, taphonomy, natural selection and patterns of variation, abundance, and distribution in space and time, among others. Taxonomic papers are welcome if they have significant and broad applications. Papers concerning research on recent organisms and systems are appropriate if they are of particular interest to paleontologists. Papers should typically interest readers from more than one specialty. Proposals for symposium volumes should be discussed in advance with the editors.