The capitate of Australopithecus afarensis and A. africanus

The capitates of Australopithecus afarensis (AL 288-lw and AL 333–40) and A. africanus (TM 1526) have the identical combination of modern pongid, modern hominid, and unique characteristics. These traits include the combination of a length that is proximodistally shortened (Homo sapiens-like), a facet for the second metacarpal that is distolaterally facing (unique), the reduced styloid process on the third metacarpal (pongidlike), a dorsally placed trapezoid facet (pongidlike), mediolaterally constricted metacarpal III facet (pongidlike), a prominent palmar beak (pongidlike), a single elongated facet for the second metacarpal (H. sapiens-like), a waisted neck (pongidlike), and a reduced amount of “cupping” in the third metacarpal facet (H. sapiens-like). In overall shape the bones are more like H. sapiens than other extant hominids, although they are uniquely different. The two A. afarensis capitates provide no evidence that there are two postcranial morphotypes at Hadar. Available evidence shows that A. afarensis and A. africanus are strikingly similar postcranially. The morphological differences between the capitate of Australopithecus and H. sapiens may relate to the retention of climbing ability and an absence of certain grip capabilities in these early hominids.     

Dental development in South African australopithecines. Part I: Problems of pattern and chronology

It is well known that humans take about twice as long as apes to mature. The traditional view that such delayed maturation was already present in australopithecines has been called into question during the past several years. We have approached this problem by looking at patterns of dental development in gracile and robust australopithecines from South Africa and comparing them to patterns found in extant humans and apes. We have employed both 2 and 3 dimensional computed tomography in our research. The dental growth patterns in these two australopithecine morphs differ, particularly in M1/I1 development. The robust australopithecines are more humanlike and the gracile australopithecines more apelike in this feature (“humanlike” and “apelike” are not used in any taxonomic sense). Pattern and chronology of dental development must be considered separately. Several major problem areas for future research are identified, most of which revolve around the issue of intra- versus interspecific variation.     

Some comments on coordinate-free and scale-invariant methods in morphometrics

The unusual strategy for comparing biological shapes is to use some kind of superimposition of the two forms under study and then look at the "residuals" as the shape change. In this paper, I take a careful look at this general strategy and point out some subtle but inherent and important pitfalls. Additionally an alternative approach based on Euclidean Distance Matrix representation is presented. It is applicable to two- as well as three-dimensional objects.     

Snail predation by larvae of Sepedon scapularis Adams (Diptera: Sciomyzidae), a potential biocontrol agent of snail intermediate hosts of schistosomiasis in South Africa

Malacophagous larvae of the fly Sepedon scapularis Adams were shown experimentally to be effective predators of three species of aquatic pulmonate snails tested as prey: Bulinus africanus (Krauss) an important intermediate host of Schistosoma haematobium (Bilharz), Bulinus tropicus (Krauss) and the invasive species Physa acuta Draparnaud. Survival of S. scapularis larvae from instar to instar was negatively affected by the size of prey snails, since larvae tended to be asphyxiated by the mucous secretions of the snails, or by the larval hydrofuge hairs becoming entangled in snail faeces. In experiments to test the choice of S.scapularis larvae for different species and sizes of snails, B.africanus was significantly disfavoured compared with the other two snail species. Small snails (< 3 mm) were more frequently killed by all three larval instars of S.scapularis. First instars killed few, if any, large snails (> 7 mm), whereas second and third instars preyed effectively on all sizes of snails. Third instars killed significantly more snails than younger instars. For larvae offered only one species of snail as prey, the mean total number of snails killed per larva during its entire development was 49 B.africanus, 45 B.tropicus or 34 P.acuta. It is concluded that S.scapularis is potentially useful as a biological control agent for use against indigenous Bulinus and exotic Physa snails.     

Chimpanzee variation facilitates the interpretation of the incisive suture closure in South African Plio-Pleistocene hominids

For a better understanding of early hominid growth patterns, we need to compare skeletal maturation among humans and chimpanzees. This study provides new data on variation of the incisive suture closure in extant species to facilitate the understanding of growth patterns among South African Plio-Pleistocene hominids. The complete anterior closure of the incisive suture occurs early during human life, mostly before birth. In contrast, in chimpanzees a complete anterior closure occurs mostly after the eruption of either the first permanent molars (pygmy chimpanzees) or the third molars (common chimpanzees). The first aim of this study is to test whether the patterns of closure of both the anterior and palatal components of the incisive suture in chimpanzees accurately mirror their polytypism by investigating 720 museum specimens of known geographical origin. Then we use the data gleaned from the incisive suture closure in chimpanzees to determine whether there are different growth patterns among South African Plio-Pleistocene hominids and to interpret them. Results about the pattern of incisive suture closure are consistent with the differences among chimpanzees as revealed by molecular data. Thus, the variation in chimpanzee patterns of incisive suture closure facilitates the interpretation of morphology in South African fossil hominids. In Australopithecus (Paranthropus) robustus as compared to Australopithecus africanus, the complete anterior closure and, probably, the complete palatal closure of the incisive suture occurs during early life in the same way as they occur in humans. Moreover, the closure pattern observed on Stw 53, a supposed early Homo from Sterkfontein Member 5, is similar to that seen in A. africanus and in chimpanzees. Thus, with respect to the anterior component of the incisive suture, A. africanus and Stw 53 retain the primitive feature for which A. (P.) robustus and Homo share the derived character state. Finally, it is worth noting that the Taung child does not show the robust condition. Am J Phys Anthropol 105:121–135, 1998. © 1998 Wiley-Liss, Inc.     

Paleopediatrics: Or when did human infants really become human?

Modern human children take about twice as long as their closest biological relative, the chimpanzee, to mature. One standard explanation for the evolution of “delayed maturation” at an early stage of human evolution is that it provided the time necessary for immature individuals to learn complex skills, most notably those relating to tool-making abilities. However, after comparing dental maturational profiles of early hominids from South Africa (who apparently did make and use stone tools) (Susman [1994] Science 265:1570–1573) to those of extant humans and chimpanzees, we find no evidence to document an association between “delayed maturation” and tool-making abilities in the early stages of human evolution. This also suggests that the assumed association between prolonged childhood dependency and other behaviors often associated with the advent of tool-making such as cooperative hunting, food sharing, home bases, sexual division of labor, etc., is also suspect. Instead, we must look for other, or additional, selective pressures for the evolution of “delayed maturation,” which may postdate the australopithecine radiation. © 1995 Wiley-Liss, Inc.     

Re-appraisal of the stratigraphy and determination of new U-Pb dates for the Sterkfontein hominin site, South Africa

Sterkfontein Caves is the single richest early hominin site in the world with deposits yielding one or more species of Australopithecus and possible early Homo, as well as an extensive faunal collection. The inability to date the southern African cave sites accurately or precisely has hindered attempts to integrate the hominin fossil evidence into pan-African scenarios about human evolutionary history, and especially hominin biogeography. We have used U-Pb and U-Th techniques to date sheets of calcium carbonate flowstone inter-bedded between the fossiliferous sediments. For the first time, absolute age ranges can be assigned to the fossil-bearing deposits: Member 2 is between 2.8 ± 0.28 and 2.6 ± 0.30 Ma and Member 4 between 2.65 ± 0.30 and 2.01 ± 0.05 Ma. The age of 2.01 ± 0.05 Ma for the top of Member 4 constrains the last appearance of Australopithecus africanus to 2 Ma. In the Silberberg Grotto we have reproduced the U-Pb age of ∼2.2 Ma of for the flowstones associated with StW573. We believe that these deposits, including the fossil and the flowstones, accumulated rapidly around 2.2 Ma. The stratigraphy of the site is complex as sediments are exposed both in the underground chambers and at surface. We present a new interpretation of the stratigraphy based on surface mapping, boreholes logs and U-Pb ages. Every effort was made to retain the Member system, however, only Members 2 and 4 are recognized in the boreholes. We propose that the deposits formally known as Member 3 are in fact the distal equivalents of Member 4. The sediments of Members 2 and 4 consisted of cone-like deposits and probably never filled up the cave. The U-Th ages show that there are substantial deposits younger than 400 ka in the underground cave, underlying the older deposits, highlighting again that these cave fills are not simple layer-cakes.