Arid, mosaic environments during the Plio-Pleistocene transition and early hominin dispersals in northern Africa.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
04 Oct 2024
Historique:
received: 05 03 2024
accepted: 18 09 2024
medline: 5 10 2024
pubmed: 5 10 2024
entrez: 4 10 2024
Statut: epublish

Résumé

The earliest archaeological evidence from northern Africa dates to ca. 2.44 Ma. Nevertheless, the palaeoenvironmental setting of hominins living in this part of the continent at the Plio-Pleistocene transition remains poorly documented, particularly in comparison to eastern and southern Africa. The Guefaït-4 fossil site in eastern Morocco sheds light on our knowledge of palaeoenvironments in northern Africa. Our study reveals the oldest known presence of C

Identifiants

pubmed: 39366927
doi: 10.1038/s41467-024-52672-0
pii: 10.1038/s41467-024-52672-0
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8393

Informations de copyright

© 2024. The Author(s).

Références

Kingston, J. D. & Harrison, T. Isotopic dietary reconstructions of Pliocene herbivores at Laetoli: implications for early hominin paleoecology. Palaeogeogr. Palaeoclimatol. Palaeoecol. 243, 272–306 (2007).
doi: 10.1016/j.palaeo.2006.08.002
Ségalen, L., Lee-Thorp, J. A. & Cerling, T. Timing of C
pubmed: 17905413 doi: 10.1016/j.jhevol.2006.12.010
Levin, N. E., Simpson, S. W., Quade, J., Cerling, T. E. & Frost, S. R. Herbivore enamel carbon isotopic composition and the environmental context of Ardipithecus at Gona, Ethiopia. Spec. Pap. Geol. Soc. Am. 446, 215–235 (2008).
Bedaso, Z. K., Wynn, J. G., Alemseged, Z. & Geraads, D. Dietary and paleoenvironmental reconstruction using stable isotopes of herbivore tooth enamel from middle Pliocene Dikika, Ethiopia: implication for Australopithecus afarensis habitat and food resources. J. Hum. Evol. 64, 21–38 (2013).
pubmed: 23199576 doi: 10.1016/j.jhevol.2012.05.015
Cerling, T. E. et al. Dietary changes of large herbivores in the Turkana Basin, Kenya, from 4 to 1 Ma. Proc. Natl Acad. Sci. USA 112, 11467–11472 (2015).
pubmed: 26240344 pmcid: 4577203 doi: 10.1073/pnas.1513075112
Robinson, J. R., Rowan, J., Campisano, C. J., Wynn, J. G. & Reed, K. E. Late Pliocene environmental change during the transition from Australopithecus to Homo. Nat. Ecol. Evol. 1, 1–7 (2017).
doi: 10.1038/s41559-017-0159
Robinson, J. R., Rowan, J., Barr, W. A. & Sponheimer, M. Intrataxonomic trends in herbivore enamel δ
Lüdecke, T. et al. Dietary versatility of Early Pleistocene hominins. Proc. Natl Acad. Sci. USA 115, 13330–13335 (2018).
pubmed: 30530680 pmcid: 6310814 doi: 10.1073/pnas.1809439115
Lee-Thorp, J. et al. Isotopic evidence for an early shift to C
pubmed: 23150583 pmcid: 3528505 doi: 10.1073/pnas.1204209109
Zazzo, A. et al. Herbivore paleodiet and paleoenvironmental changes in Chad during the Pliocene using stable isotope ratios of tooth enamel carbonate. Paleobiology 26, 294–309 (2000).
doi: 10.1666/0094-8373(2000)026<0294:HPAPCI>2.0.CO;2
Lee-Thorp, J. A. & Sponheimer, M. Opportunities and constraints for reconstructing palaeoenvironments from stable light isotope ratios in fossils. Geol. Q. 49, 195–203 (2005).
Lee-Thorp, J. A., Sponheimer, M. & Luyt, J. Tracking changing environments using stable carbon isotopes in fossil tooth enamel: an example from the South African hominin sites. J. Hum. Evol. 53, 595–601 (2007).
pubmed: 17920103 doi: 10.1016/j.jhevol.2006.11.020
Lee-Thorp, J. A., Sponheimer, M., Passey, B. H., De Ruiter, D. J. & Cerling, T. E. Stable isotopes in fossil hominin tooth enamel suggest a fundamental dietary shift in the Pliocene. Philos. Trans. R. Soc. B Biol. Sci. 365, 3389–3396 (2010).
doi: 10.1098/rstb.2010.0059
Lehmann, S. B. et al. Stable isotopic composition of fossil mammal teeth and environmental change in southwestern South Africa during the Pliocene and Pleistocene. Palaeogeogr. Palaeoclimatol. Palaeoecol. 457, 396–408 (2016).
doi: 10.1016/j.palaeo.2016.04.042
Sahnouni, M. et al. 1.9-million- and 2.4-million-year-old artifacts and stone tool–cutmarked bones from Ain Boucherit, Algeria. Science 362, 1297–1301 (2018).
pubmed: 30498166 doi: 10.1126/science.aau0008
Cáceres, I. et al. Assessing the subsistence strategies of the earliest North African inhabitants: evidence from the Early Pleistocene site of Ain Boucherit (Algeria). Archaeol. Anthropol. Sci. 15, 87 (2023).
Gallotti, R. et al. First high resolution chronostratigraphy for the early North African Acheulean at Casablanca (Morocco). Sci. Rep. 11, 1–14 (2021).
doi: 10.1038/s41598-021-94695-3
Sala-Ramos, R. et al. Pleistocene and Holocene peopling of Jerada province, eastern Morocco: introducing a research project. Le peuplement humain pendant le Pléistocène et l’Holocène dans la province de Jerada, Maroc oriental: introduction d’un projet de recherche. Bull. d’Archéol. Marocaine 27, 27–40 (2022).
Larrasoaña, J. C., Roberts, A. P. & Rohling, E. J. Dynamics of Green Sahara Periods and their role in hominin evolution. PLoS ONE 8, e76514 (2013).
Larrasoaña, J. C. A review of West African monsoon penetration during Green Sahara Periods; implications for human evolution and dispersals over the last three million years. Oxford Open Clim. Chang. 1, 1–19 (2021).
Trauth, M. H., Larrasoaña, J. C. & Mudelsee, M. Trends, rhythms and events in Plio-Pleistocene African climate. Quat. Sci. Rev. 28, 399–411 (2009).
doi: 10.1016/j.quascirev.2008.11.003
Trauth, M. H. et al. Northern Hemisphere Glaciation, African climate and human evolution. Quat. Sci. Rev. 268, 107095 (2021).
Hennissen, J. A. I., Head, M. J., De Schepper, S. & Groeneveld, J. Dinoflagellate cyst paleoecology during the Pliocene–Pleistocene climatic transition in the North Atlantic. Palaeogeogr. Palaeoclimatol. Palaeoecol. 470, 81–108 (2016).
doi: 10.1016/j.palaeo.2016.12.023
Grant, K. M. et al. Organic carbon burial in Mediterranean sapropels intensified during Green Sahara Periods since 3.2 Myr ago. Commun. Earth Environ. 3, 1–9 (2022).
Cohen, A. S. et al. Plio-Pleistocene environmental variability in Africa and its implications for mammalian evolution. Proc. Natl Acad. Sci. USA 119, 1–7 (2022).
doi: 10.1073/pnas.2107393119
Patalano, R. et al. Microhabitat variability in human evolution. Front. Earth Sci. 9, 1–19 (2021).
doi: 10.3389/feart.2021.787669
Parés, J. et al. First magnetostratigraphic results in the Aïn Beni Mathar-Guefaït Basin, Northern High Plateaus (Morocco): the Pliocene-Pleistocene Dhar Iroumyane composite section. Geobios 76, 17–36 (2023).
doi: 10.1016/j.geobios.2023.01.004
Ramírez-Pedraza, I. et al. Multiproxy approach to reconstruct fossil primate feeding behavior: case study for macaque from the Plio-Pleistocene site Guefaït-4.2 (eastern Morocco). Front. Ecol. Evol. 11, 1011208 (2023).
Lee-Thorp, J., Thackeray, J. F. & van der Merwe, N. The hunters and the hunted revisited. J. Hum. Evol. 39, 565–576 (2000).
pubmed: 11102267 doi: 10.1006/jhev.2000.0436
Lee-Thorp, J. A., Sealy, J. C. & van der Merwe, N. J. Stable carbon isotope ratio differences between bone collagen and bone apatite, and their relationship to diet. J. Archaeol. Sci. 16, 585–599 (1989).
doi: 10.1016/0305-4403(89)90024-1
Sillen, A. & Lee-Thorp, J. A. Trace element and isotopic aspects of predator-prey relationships in terrestrial foodwebs. Palaeogeogr. Palaeoclimatol. Palaeoecol. 107, 243–255 (1994).
doi: 10.1016/0031-0182(94)90097-3
Levin, N. E., Cerling, T. E., Passey, B. H., Harris, J. M. & Ehleringer, J. R. A stable isotope aridity index for terrestrial environments. Proc. Natl Acad. Sci. USA 103, 11201–11205 (2006).
pubmed: 16840554 pmcid: 1544065 doi: 10.1073/pnas.0604719103
Blumenthal, S. A. et al. Aridity and hominin environments. Proc. Natl Acad. Sci. USA 114, 7331–7336 (2017).
pubmed: 28652366 pmcid: 5514716 doi: 10.1073/pnas.1700597114
Roberts, P. et al. Fossil herbivore stable isotopes reveal middle Pleistocene hominin palaeoenvironment in ‘Green Arabia’. Nat. Ecol. Evol. 2, 1871–1878 (2018).
Faith, J. T. Paleodietary change and its implications for aridity indices derived from δ
doi: 10.1016/j.palaeo.2017.11.045
Kohn, M. J. Predicting animal δ
doi: 10.1016/S0016-7037(96)00240-2
Kohn, M. J., Schoeninger, M. & Valley, J. W. Herbivore tooth oxygen isotope compositions: effect of diet and physiology. Geochim. Cosmochim. Acta 60, 3889–3896 (1996).
doi: 10.1016/0016-7037(96)00248-7
Belsky, A. J. et al. The effects of trees on their physical, chemical and biological environments in a semi-arid savanna in Kenya. J. Appl. Ecol. 26, 1005–1024 (1989).
doi: 10.2307/2403708
Ramírez-Pedraza, I. et al. Palaeoecological reconstruction of Plio-Pleistocene herbivores from the Ahl al Oughlam site (Casablanca, Morocco): insights from dental wear and stable isotopes. Quat. Sci. Rev. 319, 108341 (2023).
Liu, W., Yang, H. & Li, L. Hydrogen isotopic compositions of n-alkanes from terrestrial plants correlate with their ecological life forms. Oecologia 150, 330–338 (2006).
pubmed: 16977462 doi: 10.1007/s00442-006-0494-0
Hou, J., D’Andrea, W. J., MacDonald, D. & Huang, Y. Evidence for water use efficiency as an important factor in determining the δD values of tree leaf waxes. Org. Geochem. 38, 1251–1255 (2007).
doi: 10.1016/j.orggeochem.2007.03.011
Dodd, R. S. & Poveda, M. M. Environmental gradients and population divergence contribute to variation in cuticular wax composition in Juniperus communis. Biochem. Syst. Ecol. 31, 1257–1270 (2003).
doi: 10.1016/S0305-1978(03)00031-0
Castañeda, I. S., Werne, J. P., Johnson, T. C. & Filley, T. R. Late Quaternary vegetation history of southeast Africa: the molecular isotopic record from Lake Malawi. Palaeogeogr. Palaeoclimatol. Palaeoecol. 275, 100–112 (2009).
doi: 10.1016/j.palaeo.2009.02.008
Duan, Y. & He, J. Distribution and isotopic composition of n-alkanes from grass, reed and tree leaves along a latitudinal gradient in China. Geochem. J. 45, 199–207 (2011).
doi: 10.2343/geochemj.1.0115
Carr, A. S. et al. Leaf wax n-alkane distributions in arid zone South African flora: environmental controls, chemotaxonomy and palaeoecological implications. Org. Geochem. 67, 72–84 (2014).
doi: 10.1016/j.orggeochem.2013.12.004
Bush, R. T. & McInerney, F. A. Influence of temperature and C
doi: 10.1016/j.orggeochem.2014.12.003
Bray, E. E. & Evans, E. D. Distribution of n-paraffins as a clue to recognition of source beds. Geochim. Cosmochim. Acta 22, 2–15 (1961).
doi: 10.1016/0016-7037(61)90069-2
Castañeda, I. S. & Schouten, S. A review of molecular organic proxies for examining modern and ancient lacustrine environments. Quat. Sci. Rev. 30, 2851–2891 (2011).
doi: 10.1016/j.quascirev.2011.07.009
Diefendorf, A. F., Freeman, K. H., Wing, S. L. & Graham, H. V. Production of n-alkyl lipids in living plants and implications for the geologic past. Geochim. Cosmochim. Acta 75, 7472–7485 (2011).
doi: 10.1016/j.gca.2011.09.028
Jaeschke, A. et al. Influence of land use on distribution of soil n-alkane δD and brGDGTs along an altitudinal transect in Ethiopia: implications for (paleo)environmental studies. Org. Geochem. 124, 77–87 (2018).
doi: 10.1016/j.orggeochem.2018.06.006
Duan, Y. & Xu, L. Distributions of n-alkanes and their hydrogen isotopic composition in plants from Lake Qinghai (China) and the surrounding area. Appl. Geochem. 27, 806–814 (2012).
doi: 10.1016/j.apgeochem.2011.12.008
Jha, D. K. et al. Preservation of plant‐wax biomarkers in deserts implications for Quaternary environment and human evolutionary studies. J. Quat. Sci. 39, 349–358 (2024).
Ficken, K. J., Li, B., Swain, D. L. & Eglinton, G. An n-alkane proxy for the sedimentary input of submerged/floating freshwater aquatic macrophytes. Org. Geochem. 31, 745–749 (2000).
doi: 10.1016/S0146-6380(00)00081-4
Liu, H. & Liu, W. Concentration and distributions of fatty acids in algae, submerged plants and terrestrial plants from the northeastern Tibetan Plateau. Org. Geochem. 113, 17–26 (2017).
doi: 10.1016/j.orggeochem.2017.08.008
Van Geel, B. A palaeoecological study of Holocene peat bog sections in Germany and The Netherlands, based on the analysis of pollen, spores and macro and microscopic remains of fungi, algae, cormophytes and animals. Rev. Palaeobot. Palynol. 25, 1–120 (1978).
doi: 10.1016/0034-6667(78)90040-4
Benito-Calvo, A. et al. Geomorphological analysis using small unmanned aerial vehicles and submeter GNSS (Gara Soultana butte, High Plateaus Basin, Eastern Morocco). J. Maps 16, 459–467 (2020).
doi: 10.1080/17445647.2020.1773329
Parés, J. et al. Magnetostratigraphy of the sedimentary fill of the Aïn Beni Mathar-Guefaït Basin (High Plateau, E Morocco). In Proc. 2020 AGU Fall Meeting (2020).
Escoriza, D. & Comas, M. Is Hyalosaurus koellikeri a true forest lizard? Herpetol. Conserv. Biol. 10, 610–620 (2015).
Semprebon, G. M., Godfrey, L. R., Solounias, N., Sutherland, M. R. & Jungers, W. L. Can low-magnification stereomicroscopy reveal diet? J. Hum. Evol. 47, 115–144 (2004).
pubmed: 15337412 doi: 10.1016/j.jhevol.2004.06.004
Godfrey, L. R. et al. Dental use wear in extinct lemurs: evidence of diet and niche differentiation. J. Hum. Evol. 47, 145–169 (2004).
pubmed: 15337413 doi: 10.1016/j.jhevol.2004.06.003
Piñero, P. et al. Golunda aouraghei, sp. nov., the last representative of the genus Golunda in Africa. J. Vertebr. Paleontol. 39, 1–6 (2020).
Aulagnier, S. et al. Eliomys melanurus (amended version of 2016 assessment). IUCN Red List of Threatened Species 2021 e.T7619A197505035. https://doi.org/10.2305/IUCN.UK.2021-1.RLTS.T7619A197505035.en (2021).
Amori, G., Hutterer, R., Kryštufek, B. & Yigit, N. Eliomys munbyanus. IUCN Red List of Threatened Species 2022 e.T136469A22223369. https://doi.org/10.2305/IUCN.UK.2022-2.RLTS.T136469A22223369.en (2022).
Zhou, H., Helliker, B. R., Huber, M., Dicks, A. & Akçay, E. C
pubmed: 30401739 pmcid: 6255158 doi: 10.1073/pnas.1718988115
Cassola, F. Ctenodactylus gundi. IUCN Red List of Threatened Species 2022 e.T5792A22191625. https://doi.org/10.2305/IUCN.UK.2022-2.RLTS.T5792A22191625.en (2022).
De Bruijn, H. Superfamily Sciuroidea in The Miocene Land Mammals of Europe (eds Rössner, G. E. & Heissig, K.) 271–280 (Dr. Friedrich Pfeil, 1999).
Kryštufek, B., Mahmoudi, A., Tesakov, A. S., Matějů, J. & Hutterer, R. A review of bristly ground squirrels Xerini and a generic revision in the African genus Xerus. Mammalia 80, 521–540 (2016).
doi: 10.1515/mammalia-2015-0073
Pausas, J. G. Changes in fire climate in the easter Iberian Peninsula (Mediterranean Basin). Clim. Change 63, 337–350 (2004).
doi: 10.1023/B:CLIM.0000018508.94901.9c
Bunting, M. J., Gaillard, M. J., Sugita, S., Middleton, R. & Broström, A. Vegetation structure and pollen source area. Holocene 14, 651–660 (2004).
doi: 10.1191/0959683604hl744rp
Domingo, L. et al. Late Neogene and Early Quaternary paleoenvironmental and paleoclimatic conditions in Southwestern Europe: isotopic analyses on mammalian taxa. PLoS ONE 8, e63739 (2013).
Szabó, P. et al. Pliocene–Early Pleistocene continental climate and vegetation in Europe based on stable isotope compositions of mammal tooth enamel. Quat. Sci. Rev. 288, 107572 (2022).
doi: 10.1016/j.quascirev.2022.107572
Bocherens, H., Koch, P. L., Mariotti, A., Geraads, D. & Jaeger, J. J. Isotopic biogeochemistry (
doi: 10.2307/3515241
Fannin, L. D. et al. Carbon and strontium isotope ratios shed new light on the paleobiology and collapse of Theropithecus, a primate experiment in graminivory. Palaeogeogr. Palaeoclimatol. Palaeoecol. 572, 110393 (2021).
doi: 10.1016/j.palaeo.2021.110393
Duval, M. et al. The Plio-Pleistocene sequence of Oued Boucherit (Algeria): a unique chronologically-constrained archaeological and palaeontological record in North Africa. Quat. Sci. Rev. 271, 107116 (2021).
doi: 10.1016/j.quascirev.2021.107116
Ungar, P. S. & Sponheimer, M. The diets of early hominins. Science 334, 190–193 (2011).
pubmed: 21998380 doi: 10.1126/science.1207701
Levin, N. E., Haile-Selassie, Y., Frost, S. R. & Saylor, B. Z. Dietary change among hominins and cercopithecids in Ethiopia during the early Pliocene. Proc. Natl Acad. Sci. USA 112, 12304–12309 (2015).
pubmed: 26371308 pmcid: 4603467 doi: 10.1073/pnas.1424982112
Wynn, J. G. et al. Isotopic evidence for the timing of the dietary shift toward C
pubmed: 32839330 pmcid: 7486737 doi: 10.1073/pnas.2006221117
Lebatard, A. E. et al. Cosmogenic nuclide dating of Sahelanthropus tchadensis and Australopithecus bahrelghazali: Mio-Pliocene hominids from Chad. Proc. Natl Acad. Sci. USA 105, 3226–3231 (2008).
pubmed: 18305174 pmcid: 2265126 doi: 10.1073/pnas.0708015105
Stewart, K. M. Environmental change and hominin exploitation of C
pubmed: 25456823 doi: 10.1016/j.jhevol.2014.10.003
Zeller, E. et al. Human adaptation to diverse biomes over the past 3 million years. Science 380, 604–608 (2023).
pubmed: 37167387 doi: 10.1126/science.abq1288
Dart, R. Australopithecus africanus: the man-ape of South Africa. Nature 115, 195–199 (1925).
doi: 10.1038/115195a0
Coppens, Y. East side story: the origin of humankind. Sci. Am. 270, 88–95 (1994).
pubmed: 8197447 doi: 10.1038/scientificamerican0594-88
Potts, R. Environmental hypotheses of hominin evolution. Yearb. Phys. Anthropol. 41, 93–136 (1998).
doi: 10.1002/(SICI)1096-8644(1998)107:27+<93::AID-AJPA5>3.0.CO;2-X
Lupien, R. L. et al. A leaf wax biomarker record of early Pleistocene hydroclimate from West Turkana, Kenya. Quat. Sci. Rev. 186, 225–235 (2018).
doi: 10.1016/j.quascirev.2018.03.012
Mercader, J. et al. Earliest Olduvai hominins exploited unstable environments ~ 2 million years ago. Nat. Commun. 12, 3 (2021).
Plummer, T. W. et al. Expanded geographic distribution and dietary strategies of the earliest Oldowan hominins and Paranthropus. Science 566, 561–566 (2023).
doi: 10.1126/science.abo7452
Potts, R. et al. Increased ecological resource variability during a critical transition in hominin evolution. Sci. Adv. 6, 1–15 (2020).
doi: 10.1126/sciadv.abc8975
Foister, T., Tallavaara, M., Fortelius, M. & Wilson, O. E. Homo heterogenus: variability in Pleistocene Homo environments. Evol. Anthropol. 32, 373–385 (2023).
Peppe, D. J. et al. Oldest evidence of abundant C
pubmed: 37053309 doi: 10.1126/science.abq2834
Maslin, M. A. et al. East african climate pulses and early human evolution. Quat. Sci. Rev. 101, 1–17 (2014).
doi: 10.1016/j.quascirev.2014.06.012
Orlandi-Oliveras, G., Nacarino-Meneses, C. & Köhler, M. Dental histology of late Miocene hipparionins compared with extant Equus, and its implications for Equidae life history. Palaeogeogr. Palaeoclimatol. Palaeoecol. 528, 133–146 (2019).
doi: 10.1016/j.palaeo.2019.04.016
Domingo, M. S. et al. First radiological study of a complete dental ontogeny sequence of an extinct Equid: implications for Equidae life history and taphonomy. Sci. Rep. 8, 1–11 (2018).
doi: 10.1038/s41598-018-26817-3
Hoppe, K. A., Stover, S. M., Pascoe, J. R. & Amundson, R. Tooth enamel biomineralization in extant horses: implications for isotopic microsampling. Palaeogeogr. Palaeoclimatol. Palaeoecol. 206, 355–365 (2004).
doi: 10.1016/j.palaeo.2004.01.012
Nelson, S. V. Paleoseasonality inferred from equid teeth and intra-tooth isotopic variability. Palaeogeogr. Palaeoclimatol. Palaeoecol. 222, 122–144 (2005).
doi: 10.1016/j.palaeo.2005.03.012
van Dam, J. A. & Reichart, G. J. Oxygen and carbon isotope signatures in late Neogene horse teeth from Spain and application as temperature and seasonality proxies. Palaeogeogr. Palaeoclimatol. Palaeoecol. 274, 64–81 (2009).
doi: 10.1016/j.palaeo.2008.12.022
Koch, P. L., Tuross, N. & Fogel, M. L. The effects of sample treatment and diagenesis on the isotopic integrity of carbonate in biogenic hydroxylapatite. J. Archaeol. Sci. 24, 417–429 (1997).
doi: 10.1006/jasc.1996.0126
Tornero, C., Bǎlǎşescu, A., Ughetto-Monfrin, J., Voinea, V. & Balasse, M. Seasonality and season of birth in early Eneolithic sheep from Cheia (Romania): methodological advances and implications for animal economy. J. Archaeol. Sci. 40, 4039–4055 (2013).
doi: 10.1016/j.jas.2013.05.013
Yang, D. et al. Intra-tooth stable isotope analysis reveals seasonal dietary variability and niche partitioning among bushpigs/red river hogs and warthogs. Curr. Zool. https://doi.org/10.1093/cz/zoae007 (2024).
Hammer, Ø., Harper, D. A. & Ryan, P. D. Past: paleontological statistics software package for education and data analysis. Palaeontol. Electron. 4, 5–7 (2001).
Kaiser, T. M. & Schulz, E. Tooth wear gradients in zebras as an environmental proxy—a pilot study. Mitt. Hamb. Zool. Mus. Inst. 103, 187–211 (2006).
Rivals, F. & Solounias, N. Differences in tooth microwear of populations of caribou (Rangifer tarandus, Ruminantia, Mammalia) and implications to ecology, migration, glaciations and dental evolution. J. Mamm. Evol. 14, 182–192 (2007).
doi: 10.1007/s10914-007-9044-8
Solounias, N., Tariq, M., Hou, S., Danowitz, M. & Harrison, M. A new method of tooth mesowear and a test of it on domestic goats. Ann. Zool. Fenn. 51, 111–118 (2014).
doi: 10.5735/086.051.0212
Ackermans, N. L. et al. Dental wear proxy correlation in a long-term feeding experiment on sheep (Ovis aries). J. R. Soc. Interface 18, 20210139 (2021).
Rivals, F., Mihlbachler, M. C. & Solounias, N. Effect of ontogenetic-age distribution in fossil and modern samples on the interpretation of ungulate paleodiets using the mesowear method. J. Vertebr. Paleontol. 27, 763–767 (2007).
doi: 10.1671/0272-4634(2007)27[763:EOODIF]2.0.CO;2
Mihlbachler, M. C., Rivals, F., Solounias, N. & Semprebon, G. M. Dietary change and evolution of horses in North America. Science 331, 1178–1181 (2011).
pubmed: 21385712 doi: 10.1126/science.1196166
Franz-Odendaal, T. A. & Kaiser, T. M. Differential mesowear in the maxillary and mandibular cheek dentition of some ruminants (Artiodactyla). Ann. Zool. Fenn. 40, 395–410 (2003).
Teaford, M. F. & Oyen, O. J. Differences in the rate of molar wear between monkeys raised on different diets. J. Dent. Res. 68, 1513–1518 (1989).
pubmed: 2584518 doi: 10.1177/00220345890680110901
Grine, F. E. Dental evidence for dietary differences in Australopithecus and Paranthropus: a quantitative analysis of permanent molar microwear. J. Hum. Evol. 15, 783–822 (1986).
doi: 10.1016/S0047-2484(86)80010-0
King, T., Andrews, P. & Boz, B. Effect of taphonomic processes on dental microwear. Am. J. Phys. Anthropol. 108, 359–373 (1999).
pubmed: 10096686 doi: 10.1002/(SICI)1096-8644(199903)108:3<359::AID-AJPA10>3.0.CO;2-9
Micó, C. et al. Differentiating taphonomic features from trampling and dietary microwear, an experimental approach. Hist. Biol. 00, 1–23 (2023).
Uzunidis, A. et al. The impact of sediment abrasion on tooth microwear analysis: an experimental study. Archaeol. Anthropol. Sci. 13, 1–17 (2021).
doi: 10.1007/s12520-021-01382-5
Solounias, N. & Semprebon, G. M. Advances in the reconstruction of ungulate ecomorphology with application to early fossil equids. Am. Museum Novit. 3366, 1–49 (2002).
doi: 10.1206/0003-0082(2002)366<0001:AITROU>2.0.CO;2
Xafis, A., Nagel, D. & Bastl, K. Which tooth to sample? A methodological study of the utility of premolar/non-carnassial teeth in the microwear analysis of mammals. Palaeogeogr. Palaeoclimatol. Palaeoecol. 487, 229–240 (2017).
doi: 10.1016/j.palaeo.2017.09.003
Semprebon, G. M. & Rivals, F. Was grass more prevalent in the pronghorn past? An assessment of the dietary adaptations of Miocene to Recent Antilocapridae (Mammalia: Artiodactyla). Palaeogeogr. Palaeoclimatol. Palaeoecol. 253, 332–347 (2007).
doi: 10.1016/j.palaeo.2007.06.006
Rivals, F. MicrowearBivaR: a code to create tooth microwear bivariate plots in R (Versión 1). Zenodo https://doi.org/10.5281/zenodo.2587575 (2019).
Goeury, C. & de Beaulieu, J. L. À propos de la concentration du pollen à l’aide de la liqueur de Thoulet dans les sédiments minéraux. Pollen Spores 21, 239–251 (1979).
Burjachs, F., López Sáez, J. A. & Iriarte, M. J. Metodología arqueopalinológica in La Recogida de Muestras en Arqueobotànica: Objetivos y Propuestas Metodológicas (eds Buxó, R. & Piqué, R.) 9–16 (Museu d’Arqueologia de Catalunya, 2003).
Käärik, A., Keller, J., Kiffer, E., Perreau, J. & Reisinger, O. Atlas of Airborne Fungal Spores in Europe (Springer, 1983).
Jarzen, D. M. & Elsik, W. C. Fungal palynomorphs recovered from recent river deposits, Luangwa Valley, Zambia. Palynology 10, 35–60 (1986).
doi: 10.1080/01916122.1986.9989302
Van Geel, B. The application of fungal and algal remains and other microfossils in palynological analyses in Handbook of Holocene Palaeoecology and Palaeohydrology (ed. Berglund, B. E.) 497–505 (Wiley, 1986).
Moore, P. D., Webb, J. A. & Collinson, M. E. Pollen Analysis (Blackwell, 1991).
Reille, M. Pollen et Spores d’Europe et d’Afrique du Nord (Laboratoire de Botanique Historique et Palynologie, 1992).
Reille, M. Pollen et spores d’Europe et d’Afrique du Nord (Supplément 1) (Laboratoire de Botanique Historique et Palynologie, 1995).
Davis, O. K. & Shafer, D. S. Sporormiella fungal spores, a palynological means of detecting herbivore density. Palaeogeogr. Palaeoclimatol. Palaeoecol. 237, 40–50 (2006).
doi: 10.1016/j.palaeo.2005.11.028
Miola, A. Tools for non-pollen palynomorphs (NPPs) analysis: a list of Quaternary NPP types and reference literature in English language (1972–2011). Rev. Palaeobot. Palynol. 186, 142–161 (2012).
doi: 10.1016/j.revpalbo.2012.06.010
Loublier, Y. Application de l’Analyse Pollinique à l’Étude du Paléoenvironnement du Remplissage Würmien de la Grotte de L’Arbreda (Espagne). PhD dissertation, Université des Sciences e Techniques du Languedoc (1978).
Menail, A., Scharf, B. & Amarouayache, M. Living ostracods (Crustacea) from Algerian Sahara and High Plains: ecological data and new records. Zootaxa 5227, 501–530 (2023).
pubmed: 37044673 doi: 10.11646/zootaxa.5227.5.1
Meisch, C. Freshwater Ostracoda of Western and Central Europe (Süswasserfauna von Mitteleuropa) (Spektrum, 2000).
Fortelius, M. & Solounias, N. Functional characterization of ungulate molars using the abrasion-attrition wear gradient: a new method for reconstructing paleodiets. Am. Museum Novit. 3301, 1–36 (2000).
doi: 10.1206/0003-0082(2000)301<0001:FCOUMU>2.0.CO;2

Auteurs

Iván Ramírez-Pedraza (I)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain. ramirezpedrazaivan@gmail.com.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain. ramirezpedrazaivan@gmail.com.
isoTROPIC Research Group, Max Planck Institute of Geoanthropology, Jena, Germany. ramirezpedrazaivan@gmail.com.

Carlos Tornero (C)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Department of Prehistory, Autonomous University of Barcelona (UAB), Bellaterra, Spain.

Hassan Aouraghe (H)

Faculté des Sciences, Département de Géologie, Université Mohammed Premier, Oujda, Morocco.

Florent Rivals (F)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.
Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.

Robert Patalano (R)

isoTROPIC Research Group, Max Planck Institute of Geoanthropology, Jena, Germany.
Department of Biological and Biomedical Sciences, School of Health and Behavioral Sciences, Bryant University, Smithfield, USA.

Hamid Haddoumi (H)

Faculté des Sciences, Département de Géologie, Université Mohammed Premier, Oujda, Morocco.

Isabel Expósito (I)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.

Antonio Rodríguez-Hidalgo (A)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Consejo Superior de Investigaciones Científicas, Instituto de Arqueología (CSIC-Junta de Extremadura), Mérida, Spain.

Steffen Mischke (S)

Institute of Earth Sciences, University of Iceland, Reykjavík, Iceland.

Jan van der Made (J)

Consejo Superior de Investigaciones Científicas (CSIC), Museo Nacional de Ciencias Naturales, Departamento de Paleobiología, Madrid, Spain.

Pedro Piñero (P)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.

Hugues-Alexandre Blain (HA)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.

Patrick Roberts (P)

isoTROPIC Research Group, Max Planck Institute of Geoanthropology, Jena, Germany.
Department of Archaeology, Max Planck Institute of Geoanthropology, Jena, Germany.
School of Archaeology, University of Philippines, Diliman, Quezon City, Philippines.

Deepak Kumar Jha (DK)

Department of Archaeology, Max Planck Institute of Geoanthropology, Jena, Germany.

Jordi Agustí (J)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.
Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.

Christian Sánchez-Bandera (C)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.

Abdelkhalek Lemjidi (A)

Institut National des Sciences de l'Archéologie et du Patrimoine (INSAP), Rabat, Morocco.

Alfonso Benito-Calvo (A)

Centro Nacional de Investigación Sobre la Evolución Humana (CENIEH), Burgos, Spain.

Elena Moreno-Ribas (E)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.

Aïcha Oujaa (A)

Institut National des Sciences de l'Archéologie et du Patrimoine (INSAP), Rabat, Morocco.

Hicham Mhamdi (H)

Faculté des Sciences, Département de Géologie, Université Mohammed Premier, Oujda, Morocco.

Mohamed Souhir (M)

Faculté des Sciences, Département de Géologie, Université Mohammed Premier, Oujda, Morocco.

Al Mahdi Aissa (AM)

Faculté des Sciences, Département de Géologie, Université Mohammed Premier, Oujda, Morocco.

M Gema Chacón (MG)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.
UMR 7194-Histoire Naturelle de l'Homme Préhistorique (MNHN/CNRS/UPVD), Paris, France.

Robert Sala-Ramos (R)

Institut Català de Paleoecologia Humana i Evolució Social (IPHES-CERCA), Tarragona, Spain.
Departament d'Història i Història de l'Art, Universitat Rovira i Virgili (URV), Tarragona, Spain.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH