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Late Quaternary micromammals and the precipitation history of the southern Cape, South Africa: response to comments by F. Thackeray, Quaternary Research 95, 154–156

Published online by Cambridge University Press:  12 May 2020

J. Tyler Faith*
Affiliation:
Natural History Museum of Utah, University of Utah, Salt Lake City, Utah84108, USA Department of Anthropology, University of Utah, Salt Lake City, Utah84112, USA
Brian M. Chase
Affiliation:
Institut des Sciences de l'Evolution-Montpellier (ISEM), University of Montpellier, Centre National de la Recherche Scientifique (CNRS), EPHE, IRD, Montpellier, France
D. Margaret Avery
Affiliation:
Iziko South African Museum, Cape Town, 8000South Africa
*
*Corresponding author E-mail address: [email protected] (J.T. Faith).
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Abstract

Type
Letter to the Editor
Copyright
Copyright © University of Washington. Published by Cambridge University Press, 2020

INTRODUCTION

We appreciate Thackeray's (Reference Thackeray2020) comments on our recent examination of late Quaternary micromammals from the southern Cape of South Africa (Faith et al., Reference Faith, Chase and Avery2019). Focusing on the well-sampled sequence from Boomplaas Cave, we argued—controversially in Thackeray's (Reference Thackeray2020) opinion—that the micromammals indicated a transition from a relatively humid last glacial maximum (LGM) to a more arid Holocene. This is at odds with earlier interpretations of the region's climate history (e.g., Avery, Reference Avery1982; Deacon et al., Reference Deacon, Deacon, Scholtz, Thackeray, Brink and Vogel1984; Deacon and Lancaster, Reference Deacon and Lancaster1988), though it is now supported by a growing body of evidence (e.g., Faith, Reference Faith2013a, Reference Faith2013b; Chase et al., Reference Chase, Chevalier, Boom and Carr2017, Reference Chase, Faith, Mackay, Chevalier, Carr, Boom, Lim and Reimer2018; Engelbrecht et al., Reference Engelbrecht, Marean, Cowling, Potts, Engelbrecht, Nkoana and O'Neill2019). We welcome this opportunity to clarify a few points raised by Thackeray (Reference Thackeray2020) and to further elaborate on our original interpretations.

MOISTURE AVAILABILITY, PRECIPITATION, AND TEMPERATURE

In Faith et al. (Reference Faith, Chase and Avery2019), our analysis and interpretation focused specifically on moisture availability (humidity/aridity). As defined in the paper, this variable is determined by precipitation relative to evapotranspiration. While it is common to conflate moisture availability with rainfall amount, as Thackeray (Reference Thackeray2020) has in his comment, this leads to confusion, as rainfall amount is only one factor determining moisture availability. As discussed by Chevalier and Chase (Reference Chevalier and Chase2016), moisture availability is largely determined by the combination of precipitation and temperature, through its influence on evapotranspiration. Thus, our interpretation of relatively humid conditions during the LGM at Boomplaas Cave should not be equated as implying relatively higher rainfall, as Thackeray (Reference Thackeray2020) has inferred.

To be clear, a relatively humid LGM could result from greater precipitation, cooler temperatures, or a combination of both. There is no question that cooler temperatures during the LGM would have contributed to greater moisture availability by reducing evapotranspiration (as suggested by Chase et al., Reference Chase, Chevalier, Boom and Carr2017, Reference Chase, Faith, Mackay, Chevalier, Carr, Boom, Lim and Reimer2018), but whether this was accompanied by higher or lower precipitation cannot be ascertained from our analysis. Indeed, we are skeptical that any analysis of faunal community composition can inform directly on rainfall amount sensu stricto, when it is moisture availability that determines habitat structure and the availability of the key resources (e.g., forage, standing water) on which faunas depend (Faith and Lyman, Reference Faith and Lyman2019). Faith et al. (Reference Faith, Chase and Avery2019) focused on moisture availability precisely because most organisms (both floral and faunal) are influenced by moisture availability rather than by rainfall amount—as a given amount of precipitation can have vastly different environmental consequences depending on how much of it is lost through evapotranspiration (e.g., Chevalier and Chase, Reference Chevalier and Chase2016).

A SEMIARID CLIMATE

Thackeray (Reference Thackeray2020) observes that in our ordination of modern and fossil micromammal samples, the LGM assemblage from member GWA at Boomplaas Cave plots adjacent to several modern assemblages characterized by a semiarid climate. The emphasis Thackeray (Reference Thackeray2020) places on “semiarid” throughout his letter implies that some clarification is necessary, because the implication is that a semiarid LGM is inconsistent with our original interpretations. It is not. Following the United Nations National Environment Programme classification scheme (UNEP, 1997), a “semiarid” climate is characterized by mean annual precipitation (MAP) equal to 20%–50% of mean annual evapotranspiration (MAE), or aridity index (AI = MAP/MAE) values of 0.2 to 0.5. Boomplaas Cave today is at the lower limit of semiarid (AI = 0.24), yet the modern samples flagged by Thackeray (Reference Thackeray2020) are characterized by much greater moisture availability, with AI values of 0.43 to 0.48. Though not discussed by Thackeray (Reference Thackeray2020), the GWA assemblage also plots close to modern samples characterized by a “dry subhumid” climate (AI values of 0.5 to 0.65), further emphasizing its similarity to modern environments with greater moisture availability than the contemporary Boomplaas environment. Thus, the proximity of GWA to these semiarid and dry subhumid assemblages is fully consistent with our previous observation of a relatively humid LGM.

CUTTING THROUGH THE CONFUSION

Resolving the paleoclimatic history of the southern Cape has proven challenging in part due to a combination of seemingly contradictory lines of evidence (e.g., Avery, Reference Avery1982, Reference Avery2004) together with conflicting interpretations of the evidence (e.g., Deacon et al., Reference Deacon, Deacon, Scholtz, Thackeray, Brink and Vogel1984; Chase and Meadows, Reference Chase and Meadows2007; Faith, Reference Faith2013a; Faith et al., Reference Faith, Chase and Avery2019; Thackeray, Reference Thackeray2020). These conflicts arise because many of the key archives provide only indirect—and at times uncertain—proxies for the climate variables in question. Indeed, many characterizations of the LGM as a time of harsh and arid conditions are based on ambiguous evidence (reviewed in Chase and Meadows, Reference Chase and Meadows2007), and this is particularly true of the records from Boomplaas Cave (see discussion in Faith, Reference Faith2013a). For example, focusing on the micromammals, Avery (Reference Avery1982) once argued that low taxonomic diversity during the LGM was indicative of arid conditions, though she later showed that diversity was a poor predictor of precipitation (Avery, Reference Avery1999). Thackeray's (Reference Thackeray1987) interpretation of an arid LGM was based on a micromammal-derived index that is only weakly correlated with precipitation (r 2 = 0.35), implying that it is strongly influenced by other (currently unknown) environmental parameters. Likewise, elevated frequencies of the bush Karoo rat (Myotomys unisulcatus) during the LGM have also been interpreted as indicative of aridity (Avery, Reference Avery1982; Deacon et al., Reference Deacon, Deacon, Scholtz, Thackeray, Brink and Vogel1984; Thackeray, Reference Thackeray1987)—most recently by Thackeray (Reference Thackeray2020)—yet this species occurs at similar if not higher abundances in environments that are considerably more humid than Boomplaas Cave is today (Supplementary Table 1 in Faith et al., Reference Faith, Chase and Avery2019).

Because the reconstruction of paleoclimatic changes from the mammalian fossil record is fraught with potential pitfalls, confidence in the interpretations is enhanced when there is consistency between multiple independent lines of evidence (Faith and Lyman, Reference Faith and Lyman2019). Our interpretations provide just that. In Faith et al. (Reference Faith, Chase and Avery2019), we emphasized the broad similarities between our record of moisture availability and that provided by isotopic analysis of the Seweweeksport hyrax middens (Chase et al., Reference Chase, Chevalier, Boom and Carr2017, Reference Chase, Faith, Mackay, Chevalier, Carr, Boom, Lim and Reimer2018), located in a similar environment ~70 km west of Boomplaas. Also important is that the nearby Cango Cave speleothem (~3 km east of Boomplaas) shows a hiatus from the late glacial to the middle Holocene, signaling a lack of drip water availability (Vogel, Reference Vogel1983; Talma and Vogel, Reference Talma and Vogel1992). Deacon et al. (Reference Deacon, Deacon, Scholtz, Thackeray, Brink and Vogel1984) struggled to reconcile this with their interpretations of an arid LGM transitioning to a humid Holocene, though the timing of the hiatus closely matches what we infer to be the most arid portion of the Boomplaas Cave sequence (Faith et al., Reference Faith, Chase and Avery2019). In addition, a recent climate simulation suggests that the region would have received greater rainfall during the LGM relative to the present (Engelbrecht et al., Reference Engelbrecht, Marean, Cowling, Potts, Engelbrecht, Nkoana and O'Neill2019). In our view, the consistency within all of these records tips the scale in favor of the emerging understanding of the southern Cape's climate history—the transition from the LGM to the Holocene was characterized by increased aridity.

ACKNOWLEDGMENTS

Though we may not agree on this issue, we thank Francis Thackeray for his collegiality and for his efforts to better understand the late Quaternary climates of South Africa.

References

REFERENCES

Avery, D.M., 1982. Micromammals as palaeoenvironmental indicators and an interpretation of the late Quaternary in the southern Cape Province, South Africa. Annals of the South African Museum 85, 183374.Google Scholar
Avery, D.M., 1999. A preliminary assessment of the relationship between trophic variability in southern African Barn owls Tyto alba and climate. Ostrich 70, 179186.CrossRefGoogle Scholar
Avery, D.M., 2004. Size variation in the common molerat Cryptomys hottentotus from southern Africa and its potential for palaeoenvironmental reconstruction. Journal of Archaeological Science 31, 273282.CrossRefGoogle Scholar
Chase, B.M., Chevalier, M., Boom, A., Carr, A.S., 2017. The dynamic relationship between temperate and tropical circulation systems across South Africa since the last glacial maximum. Quaternary Science Reviews 174, 5462.CrossRefGoogle Scholar
Chase, B.M., Faith, J.T., Mackay, A., Chevalier, M., Carr, A.S., Boom, A., Lim, S., Reimer, P.J., 2018. Climatic controls on later Stone Age human adaptation in Africa's southern Cape. Journal of Human Evolution 114, 3544.CrossRefGoogle ScholarPubMed
Chase, B.M., Meadows, M.E., 2007. Late Quaternary dynamics of southern Africa's winter rainfall zone. Earth-Science Reviews 84, 103138.CrossRefGoogle Scholar
Chevalier, M., Chase, B.M., 2016. Determining the drivers of long-term aridity variability: a southern African case study. Journal of Quaternary Science 31, 143151.CrossRefGoogle Scholar
Deacon, H.J., Deacon, J., Scholtz, A., Thackeray, J.F., Brink, J.S., 1984. Correlation of palaeoenvironmental data from the Late Pleistocene and Holocene deposits at Boomplaas Cave, southern Cape. In: Vogel, J.C. (Ed.), Late Cainozoic Palaeoclimates of the Southern Hemisphere. Balkema, Rotterdam, pp. 339351.Google Scholar
Deacon, J., Lancaster, N., 1988. Late Quaternary Palaeoenvironments of Southern Africa. Oxford University Press, New York.Google Scholar
Engelbrecht, F.A., Marean, C.W., Cowling, R., Potts, A.J., Engelbrecht, C., Nkoana, R., O'Neill, D., et al. ., 2019. Downscaling Last Glacial Maximum climate over southern Africa. Quaternary Science Reviews 226, 105879.CrossRefGoogle Scholar
Faith, J.T., 2013a. Taphonomic and paleoecological change in the large mammal sequence from Boomplaas Cave, Western Cape, South Africa. Journal of Human Evolution 65, 715730.CrossRefGoogle Scholar
Faith, J.T., 2013b. Ungulate diversity and precipitation history since the Last Glacial Maximum in the Western Cape, South Africa. Quaternary Science Reviews 68, 191199.CrossRefGoogle Scholar
Faith, J.T., Chase, B.M., Avery, D.M., 2019. Late Quaternary micromammals and the precipitation history of the southern Cape, South Africa. Quaternary Research 91, 848860.CrossRefGoogle Scholar
Faith, J.T., Lyman, R.L., 2019. Paleozoology and Paleoenvironments: Fundamentals, Assumptions, Techniques. Cambridge University Press, Cambridge.CrossRefGoogle Scholar
Talma, A.S., Vogel, J.C., 1992. Late Quaternary palaeotemperatures derived from a speleothem from Cango Caves, Cape Province, South Africa. Quaternary Research 37, 203213.CrossRefGoogle Scholar
Thackeray, J.F., 1987. Late Quaternary environmental changes inferred from small mammalian fauna, southern Africa. Climatic Change 10, 285305.CrossRefGoogle Scholar
Thackeray, J.F., 2020. Late Quaternary micromammals and the precipitation history of the southern Cape, South Africa—comment to the published paper by Faith et al., Quaternary Research 91 (2019), 848860. Quaternary Research 95, 154–156.Google Scholar
[UNEP] United Nations Environment Programme, 1997. World Atlas of Desertification. 2nd ed.United Nations Environment Programme, London.Google Scholar
Vogel, J.C., 1983. Isotopic evidence for the past climates and vegetation of southern Africa. Bothalia 14, 391394.CrossRefGoogle Scholar