Marion K. Bamford

Microstratigraphic evidence of in situ fire in the Acheulean strata of Wonderwerk Cave, Northern Cape province, South Africa

The ability to control fire was a crucial turning point in human evolution, but the question when hominins first developed this ability still remains. Here we show that micromorphological and Fourier transform infrared microspectroscopy (mFTIR) analyses of intact sediments at the site of Wonderwerk Cave, Northern Cape province, South Africa, provide unambiguous evidence—in the form of burned bone and ashed plant remains—that burning took place in the cave during the early Acheulean occupation, approximately 1.0 Ma. To the best of our knowledge, this is the earliest secure evidence for burning in an archaeological context.

Early evidence of San material culture represented by organic artifacts from Border Cave, South Africa

Recent archaeological discoveries have revealed that pigment use, beads, engravings, and sophisticated stone and bone tools were already present in southern Africa 75,000 y ago. Many of these artifacts disappeared by 60,000 y ago, suggesting that modern behavior appeared in the past and was subsequently lost before becoming firmly established. Most archaeologists think that San hunter–gatherer cultural adaptation emerged 20,000 y ago. However, reanalysis of organic artifacts from Border Cave, South Africa, shows that the Early Later Stone Age inhabitants of this cave used notched bones for notational purposes, wooden digging sticks, bone awls, and bone points similar to those used by San as arrowheads. A point is decorated with a spiral groove filled with red ochre, which closely parallels similar marks that San make to identify their arrowheads when hunting. A mixture of beeswax, Euphorbia resin, and possibly egg, wrapped in vegetal fibers, dated to ∼40,000 BP, may have been used for hafting. Ornaments include marine shell beads and ostrich eggshell beads, directly dated to ∼42,000 BP. A digging stick, dated to ∼39,000 BP, is made of Flueggea virosa. A wooden poison applicator, dated to ∼24,000 BP, retains residues with ricinoleic acid, derived from poisonous castor beans. Reappraisal of radiocarbon age estimates through Bayesian modeling, and the identification of key elements of San material culture at Border Cave, places the emergence of modern hunter–gatherer adaptation, as we know it, to ∼44,000 y ago.

Early hominin diet included diverse terrestrial and aquatic animals 1.95 Ma in East Turkana, Kenya

The manufacture of stone tools and their use to access animal tissues by Pliocene hominins marks the origin of a key adaptation in human evolutionary history. Here we report an in situ archaeological assemblage from the Koobi Fora Formation in northern Kenya that provides a unique combination of faunal remains, some with direct evidence of butchery, and Oldowan artifacts, which are well dated to 1.95 Ma. This site provides the oldest in situ evidence that hominins, predating Homo erectus, enjoyed access to carcasses of terrestrial and aquatic animals that they butchered in a well-watered habitat. It also provides the earliest definitive evidence of the incorporation into the hominin diet of various aquatic animals including turtles, crocodiles, and fish, which are rich sources of specific nutrients needed in human brain growth. The evidence here shows that these critical brain-growth compounds were part of the diets of hominins before the appearance of Homo ergaster/erectus and could have played an important role in the evolution of larger brains in the early history of our lineage.

Middle Stone Age bedding construction and settlement patterns at Sibudu, South Africa

Early humans constructed sleeping mats from local plants, including some with insecticidal properties. The Middle Stone Age (MSA) is associated with early behavioral innovations, expansions of modern humans within and out of Africa, and occasional population bottlenecks. Several innovations in the MSA are seen in an archaeological sequence in the rock shelter Sibudu (South Africa). At ~77,000 years ago, people constructed plant bedding from sedges and other monocotyledons topped with aromatic leaves containing insecticidal and larvicidal chemicals. Beginning at ~73,000 years ago, bedding was burned, presumably for site maintenance. By ~58,000 years ago, bedding construction, burning, and other forms of site use and maintenance intensified, suggesting that settlement strategies changed. Behavioral differences between ~77,000 and 58,000 years ago may coincide with population fluctuations in Africa.

The diet of Australopithecus sediba

Specimens of Australopithecus sediba from the site of Malapa, South Africa (dating from approximately 2 million years (Myr) ago) present a mix of primitive and derived traits that align the taxon with other Australopithecus species and with early Homo. Although much of the available cranial and postcranial material of Au. sediba has been described, its feeding ecology has not been investigated. Here we present results from the first extraction of plant phytoliths from dental calculus of an early hominin. We also consider stable carbon isotope and dental microwear texture data for Au. sediba in light of new palaeoenvironmental evidence. The two individuals examined consumed an almost exclusive C3 diet that probably included harder foods, and both dicotyledons (for example, tree leaves, fruits, wood and bark) and monocotyledons (for example, grasses and sedges). Like Ardipithecus ramidus (approximately 4.4 Myr ago) and modern savanna chimpanzees, Au. sediba consumed C3 foods in preference to widely available C4 resources. The inferred consumption of C3 monocotyledons, and wood or bark, increases the known variety of early hominin foods. The overall dietary pattern of these two individuals contrasts with available data for other hominins in the region and elsewhere.

Jurassic–Early Cretaceous Gondwanan homoxylous woods: a nomenclatural revision of the genera with taxonomic notes

The homoxylous fossil woods occurring in the Gondwanan continents of South America, Australia, Africa, India and Antarctica during the Jurassic and Early Cretaceous period are considered here. Original descriptions of the genera and wherever possible, the type material, have been consulted. Applying the rules of the International Code of Botanical Nomenclature, the generic names of the homoxylous woods have been revised from a nomenclatural point of view. According to this review, out of 31 generic names used for woods from the given time interval and area, 6 are illegitimate later nomenclatural synonyms, 1 is a later homonym, and 5 can be considered as taxonomical synonyms. Moreover, 9 genera have been used erroneously. We propose one new generic name (Protaxodioxylon n. gen.) and elsewhere we will propose for conservation, with a conserved type one of the illegitimate names and one of the taxonomic synonyms. As a result, we consider that there are only eighteen generic names correctly quoted for the Jurassic-Early Cretaceous of Gondwana, and we provide a taxonomic key for the corresponding genera. This revision is the first step in systematically comparing northern and southern hemisphere woods.

Taphonomic Trends of Macrofloral Assemblages Across the Permian–Triassic Boundary, Karoo Basin, South Africa

Abstract The terrestrial crisis that reportedly parallels the P/Tr marine mass extinction is based mainly on Northern Hemisphere microfloral assemblages and Southern Hemisphere Gondwanan macrofloral collections. It is well established that taphonomic filters control the ultimate collectable fossil assemblage in any depositional regime. Recognition and comparison of isotaphonomic assemblages are critical before conclusions can be drawn about evolutionary trends over time. Such an approach has been taken in the investigation of pre-boundary, trans-boundary, and post-boundary plant-fossil assemblages in the Karoo Basin, South Africa. Fourteen stratigraphic sections were evaluated in the Balfour and Normandien formations (Lower Beaufort Group), Katberg Formation, and overlying Burgersdorp Formation (Upper Beaufort Group). These include previously published (e.g., Bulwer, Bethulie, Carlton Heights, Wapadsberg, Commando Drift) as well as newly discovered (e.g., Clouston Farm) localities, and span the Late Permian to Middle Triassic. Fossiliferous intervals were characterized with respect to their sedimentology and plant taphonomy, and bulk collections were made at several stratigraphic levels for future evaluation of floristic and plant-insect associational trends. The depositional regimes and plant taphonomic character of assemblages change through time. Much of the Lower Beaufort Group is characterized by parautochthonous assemblages within oxbow-lake channel fills. Below the P/Tr boundary, these are replaced by allochthonous assemblages, poorly preserved in lateral-accretion deposits and barforms of relatively shallow fluvial nature. Allochthonous assemblages within the same fluvial context continue across the boundary into the earliest Triassic (Palingkloof Member and Katberg Formation, and typify the Middle Triassic where scour-and-fill structures preserve plant debris. Based on the literature, parautochthonous assemblages reappear in the Upper Triassic Molteno Formation. Hence, the change in taphonomic regime to poorly preserved allochthonous assemblages (dispersed, fragmentary adpressions) at the critical interval on either side of the P/Tr extinction event, but not coincident with, requires extreme caution when interpreting global patterns from these data. Additionally, the presence of plant fossils in the Early Triassic provides evidence for a vegetated landscape during a time when sedimentation patterns are interpreted to be the result of a land-plant die-off.

Is the vertebrate-defined Permian-Triassic boundary in the Karoo Basin, South Africa, the terrestrial expression of the end-Permian marine event?

The end-Permian extinction records the greatest ecological catastrophe in Earth history. The vertebrate fossil record in the Karoo Basin, South Africa, has been used for more than a century as the standard for understanding turnover in terrestrial ecosystems, recently claimed to be in synchrony with the marine crisis. Workers assumed that systematic turnover at the Dicynodon assemblage zone boundary, followed by the appearance of new taxa directly above the base of the Lystrosaurus assemblage zone, is the continental expression of the end-Permian event and recovery. To test this hypothesis, we present the first highprecision age on strata close to the inferred Permian-Triassic boundary. A U-Pb isotope dilution–thermal ionization mass spectrometry zircon age of 253.48 ± 0.15 Ma (early Changhsingian) is from a silicified ash layer ~60 m below the current vertebrate-defined boundary at Old Lootsberg Pass (southern South Africa). This section yields newly discovered plants and vertebrates, and is dominated by a normal polarity signature. Our collective data suggest that the Dicynodon-Lystrosaurus assemblage zone boundary is stratigraphically higher than currently reported, and older than the marine extinction event. Therefore, the turnover in vertebrate taxa at this biozone boundary probably does not represent the biological expression of the terrestrial end-Permian mass extinction. The actual Permian-Triassic boundary in the Karoo Basin is either higher in the Katberg Formation or is not preserved. The currently accepted model of the terrestrial ecosystem response to the crisis, both in this basin and its extension globally, requires reevaluation.

Landscape distribution of Oldowan stone artifact assemblages across the fault compartments of the eastern Olduvai Lake Basin during early lowermost Bed II times.

The density and composition of Oldowan stone artifact assemblages deposited during the first ca. 20,000 years of lowermost Bed II times show a recurrent pattern of variation across recognized synsedimentary faults that compartmentalized landscapes of the eastern Olduvai Lake Basin. When active, the faults created minor topographic relief. The upthrown fault footwalls accumulated assemblages with relatively high densities of artifacts, including types retaining potential usefulness, particularly volcanic flaked pieces, manuports, pounded pieces, and split cobbles. Values for these assemblage characteristics decline toward the lower-lying hangingwall of the fault compartments, accompanied by an increase in the proportionate weight of artifact assemblages comprising quartzite, particularly flaking shatter and potentially useful detached pieces. Values reverse once again at faults, either on the downthrown, hangingwall side or on the upthrown side. The patterns are stronger for the volcanic components of the artifact assemblages than for the quartzite components, reflecting the additional influence of distance from the local source on quartzite assemblage characteristics reported previously. The landscape distributions of artifact assemblages are consistent with a landscape-fault model in which minor fault-induced topographic relief at times created a mosaic of vegetation environments repeated within each of the three fault compartments of the lake margin and distal alluvial fan. The fault-compartmentalized landscape model is currently supported only by sediment thickness and facies changes across synsedimentary faults, but it provides predictions for spatial variation in the cover abundance of trees, freshwater reservoirs and associated distributions of resources and hazards associated with stone artifact use and discard that can be tested if sample sizes of key paleoenvironmental indicators are increased.

Diversity of the Woody Vegetation of Gondwanan Southern Africa

Abstract The flora of Gondwanan southern Africa is represented in the rock record by micro-fossils, macro-fossils and petrified woods. All these types of fossils are seldom preserved together in any one particular facies because of taphonomic and preservational biases. In order to obtain as accurate a picture as possible of the woody vegetation, both the fossil woods and other macroplant fossils, such as leaf impressions, fructifications and cuticle, of woody plants, have been correlated. This was done for each Formation in the Karoo Supergroup in order to illustrate the changes in diversity of woody vegetation over time. Sediments of the Karoo Supergroup represent the terrestrial fossil record of the period Upper Carboniferous to the Lower Cretaceous when Africa finally separated from South America. In the Upper Carboniferous to Lower Permian (Dwyka Formation) there are at least five described genera of woods from South Africa and Namibia. Early to Middle Permian woods (Ecca Group) are a little more diverse with six genera, representing the glossopterids, cordaitaleans and possibly other seed fern groups. Late Permian to Early Triassic (Beaufort Group) woods show very little change in diversity in spite of the major floral and biotic turnover evident from the rest of the fossil record. Although the Late Triassic (Molteno Formation) macro-flora has been shown to be an example of explosive diversification, the generally poorly preserved woods do not reflect this. Lower Jurassic fossils (Clarens Formation) are also poorly preserved but have araucarian characteristics. Early Cretaceous woods represent the Araucariaceae, Cheirolepidiaceae and Podocarpaceae with a number of species. The diversity of the woods has not changed as much as the rest of the floral components in southern Africa from the Late Carboniferous to the Early Cretaceous. Possible reasons for this apparent stasis are the conservative nature of wood, functional restrictions, limitations of suitable conditions for petrifications and the fact that very little research has been done on southern African woods.