British Museum

The origin of living Homo sapiens has once again been the subject of much debate. Genetic data on present human population relationships and data from the Pleistocene fossil hominid record are used to compare two contrasting models for the origin of modern humans. Both genetics and paleontology support a recent African origin for modern humans rather than a long period of multiregional evolution accompanied by gene flow.

The chlorites form an extensive isostructural series with a high degree of isomorphous substitution, within which it has always been difficult to define or delimit species; until recently, owing to the lack of adequate X-ray studies; several structurally distinct species were included with the group, further complicating the problem. The group comprises aluminosilicates of magnesium and iron (ferrous and ferric); a few contain appreciable amounts of chromium, nickel, or manganese, and one (pennantite) contains manganese as a major constituent. The first step towards the understanding of the relations of the chlorites was taken by G. Tschermak (1890, 1891), who divided them into two groups: the orthochlorites, with compositions between (Mg,Fe") 2 Al 2 SiO 5 (OH) 4 and (Mg,Fe") 2 Si 2 O 5 (OH) 4 , and the leptochlorites, with compositions not explicable on this basis, and in general richer in trivalent ions (often including considerable Fe"′) relative to silicon and divalent ions. The two orthochlorite end-members have the composition of amesite and serpentine respectively, but it is now known that neither of these two minerals has the chlorite structure.

Abstract Generic and familial concepts of the Ascidae Voigts and Oudemans (= Blattisociidae Garman, Aceosejidae Baker and Wharton) are reviewed and modified from a world standpoint. The postembryonic developments of chaetotactic and external morphological features of the body and appendages are discussed. Twenty-two genera in three subfamilies are recognized, keyed, and defined: Arctoseius Thor, Iphidozercon Berlese, Xenoseius nov., and Zerconopsis Hull in the Arctoseiinae Evans; Cheiroseius Berlese and Platyseius Berlese in the Platyseiinae Evans; Aceodromus Muma, Antennoseius Berlese, Arctoseiodes Willmann, Asca Heyden, Blattisocius Keegan, Diseius nov., Gamasellodes Athias-Henriot, Hoploseius Berlese, Lasioseius Berlese, Leioseius Berlese, Melichares Hering, Neojordensia Evans, Proctolaelaps Berlese, Protogamasellus Karg, Rhinoseius Baker and Yunker, and Zercoseius Berlese in the Ascinae Voigts and Oudemans.Newly synonymized genera are Hyattella Krantz under Lasioseius , Mucroseius Lindquist and Orolaelaps DeLeon under Melichares , Garmaniella Westerboer under Proctolaelaps , and Tropicoseius Baker and Yunker under Rhinoseius . Genera removed from the Ascidae include Africoseius Krantz, Digamasellus Berlese, Laelaptoseius Womersley, and Zygoseius Berlese. Modified systems of nomenclature based on holotrichous Gamasina are introduced and applied to setae on the dorsum of the idiosoma and on the venter of the opisthosoma.

A revolution is occurring in the pursuit of ethnography as the development world changes its focus from topdown intervention to a grassroots participatory perspec-The Development tive. The time has come for anthropology, with growing demands for its skills and insights in development, to of Indigenous consolidate its place, fostering the potential of the new relationship and building on its maligned applied tradition (Haile 1996, Rew 1992). The focus of the revolution Knowledge is the appearance, within the broad context of the recent participatory approach to development (Chambers,

The mathematical analysis of bimodal distributions is very complex. Karl Pearson (1894) investigated the problem and developed equations for the purpose; but found them unsolvable as the ‘majority [of the relations] lead to exponential equations the solution of which seems more beyond the wit of man than that of a numerical equation even of the ninth order’. He did indeed evolve an equation of this order and used it to analyse a few bimodal distributions, but the arithmetic involved was very laborious. Later he (Pearson, 1914) gives a table for ‘Constants of normal curve from moments of tail about stump ’which, as he describes in the introduction, occasionally permits a rough analysis of a distribution which is known to be bimodal. This method is much more rapid than the solution of the nonic equation, but ‘owing to the paucity of material in tails and corresponding irregularity there will be large probable errors’. Gottschalk (1948) discusses the question and shows that inthe special case where the bimodal distribution is symmetrical comparatively simple solutions can be found.

Summary A criterion for comparing diversity is offered based on dominance patterns involving all the proportional species abundances. The method is applied by plotting percentage cumulative abundance curves. This can reveal that some assemblages cannot be compared in terms of diversity or equitability and that intrinsic diversity indices cannot under these circumstances be relied upon. The behaviour and interpretation of these dominance curves under different circumstances is explored using examples from macrobenthic and marine nematode studies. Dominance curves are also compared with Sanders' rarefaction curves and the relative advantages discussed. It is recommended that these graphical methods be routinely applied to marine biological data before calculating more complex diversity or equitability indices.

SUMMARY In spite of a considerable literature on fruit‐eating, the general evolutionary implications of fruit as a source of food for birds have been neglected. A preliminary attempt is made to explore the evolutionary and ecological consequences of fruit‐eating, considered as a mutual interaction between parent plant and dispersal agent. The relationship considered is that obtaining between fleshy fruits and the “legitimate” fruit‐eating birds which digest the fleshy part of the fruit and void the seed intact. Evolutionary aspects of seed‐eating are also briefly discussed. The “strategies” adopted by fruits for dispersal by birds result in the production of abundant food supplies which are easy of access and exploitable by many species of birds. By contrast, the predation of birds on insects leads to a heterogeneous, sparse and cryptic food supply, to exploit which many different hunting techniques are necessary. Two important evolutionary developments in birds are attributed to these differences in food supply: there tend to be more species in families of insectivorous than of frugivorous birds, and lek behaviour in tropical forest has evolved in predominantly frugivorous birds. The seasonal succession of fruits in temperate latitudes is discussed, and contrasted with the situation in the tropics, using examples from Europe and Trinidad. In general, the succession of ripe fruits in Europe seems to be adapted to the seasonal shifts of the bird populations, and the more nutritious fruits tend to have a more southerly distribution and to ripen later than the more succulent fruits. In the tropics the distinction between nutritious and succulent fruits seems to be largely one of habitat. The constant succession of ripe fruits throughout the year in the tropics probably depends on competition for dispersal by frugivorous birds, which thus ensure the maintenance of their own food supply. This may be regarded as a symbiosis at the level of the ecosystem.

Biologists are still trying to grasp the global dimensions of the phylum Arthropoda and its major class the Insecta, in spite of the fact that over a million species of arthropods have been described. The canopy of rain forest trees is believed by many to hold the key to the immense diversity of insects. In recent years the use of knock-down insecticides to sample insects from rain forest canopy has revealed information on the canopy's arthropod inhabitants and community structure. The sampling techniques involved are outlined and data reviewed on taxonomic and guild structure, species abundance, body size and biomass of insects, and the faunal similarity of trees. Calculations by Erwin (1982), based on knock-down insecticide studies of the beetle fauna of one species of Central American tree, suggest there may be 30 million species of tropical forest arthropods. Reanalysis of these calculations, using additional data, produces a range of possible estimates from about 10 to 80 million. The unknown range of plant host-specificities of tropical insects is the main weakness of this method of calculation. Assessment of the faunal importance of the canopy in relation to that of other rain forest biotopes requires comparative quantitative studies. The preliminary results of one such simple study suggest that over 42 million arthropods may be found in a hectare of Seram rain forest (at the time of study), and that 70% occur in the soil and leaf litter and 14% in the canopy. They also suggest that Collembola and Acarina are the dominant groups in this hectare, and that there are as many ants as all the other insects (excluding Collembola).

Anopheles gambiae complex mosquitoes are present throughout tropical Africa and its offshore islands. Recent work has shown that at least 6 cryptic or “sibling” species are involved. They comprise 2 salt-water species, A. melas and A. merus, 3 freshwater species—provisionally known as species A, B, and C, and a mineralwater species known as species D. Artificial inter-species crosses yield sterile hybrid males. Rarity of hybridization in nature proves the reproductive isolation and valid genetic barriers between these 6 species. Morphological identification of most individuals of both saltwater and the mineralwater species is possible for larvae and adult females, using meristic features and other variable dimensions and ratios. Differential identification of the 3 freshwater species relies almost completely on cytotaxonomic methods. Species A and B occur together in most areas, extending southwards to sub-tropical latitudes and eastward to Mauritius. Proportions of mixed A-B populations may depend directly or indirectly on relative humidity, with A favoured when nocturnal humidities approach saturation. Species B is often absent from areas of highest humidity, but thrives in relatively arid savannas and steppes. Species C and D have relict distributions. Both saltwater species are coastal: melas in West Africa and merus in East Africa and larger islands except Zanzibar; merus also spreads inland. Apart from species C, which is always zoophilic, all members of the complex are proven or probable vectors of human malaria and filariasis, but with some wide contrasts in their levels of vectorial efficiency. Transmission of some arboviruses (Tataguine, O'nyong-nyong) is associated with species B, and perhaps with A also. Species B may transmit setariasis of cattle; melas and merus may also carry enzootic filariae. Much of the confusing ecophenotypic plasticity of A. gambiae sensu lato is attributable to the differential biological characteristics of these 6 species with their dissimilar geographical distributions, behavioural contrasts and asynchronous population dynamics. Shifts in the species balance occur regularly between A and B and between freshwater and saltwater populations. Species C does not interchange so much with B under natural conditions, but may survive at high densities after control of A or B. Additional versatility is caused by genetic polymorphism in some of the species, notably B. This species is the most widespread, and individual females tend to be either endophilic or exophilic, anthropophagic or zoophagic, early biters or late biters, and doubtless other alternatives, according to the arrangement of their floating chromosome inversions. Control measures have to be considered separately for each of the sibling species. House spraying with residual insecticides against endophilic species A is possibly sufficient to break disease transmission (assuming favourable response of ancillary vectors) and even to eradicate A completely. Efficacy of this method against other species in the complex is reduced by their exophily, which can be enhanced by behaviouristic avoidance due to the extremely low threshold of irritability exhibited by gambiae s.l. adults in general. Genetic polymorphism of species B may lead to true behaviouristic resistance. Larvicidal control of species A and B is beneficial, but made operationally difficult by their tendency to utilize temporary breeding-sites. Effectiveness of DDT and cyclodiene insecticides is further limited by the development of physiological insecticide resistance by species A and B. Adequate control of both saltwater species, and probably the mineralwater species also, can be attained by antilarval measures. Prospects of reduction of malaria and filariasis where melas, merus and species A and D are principal vectors may be much better than many people imagine. Widespread prevalence and inherent resilience of species B represents an insurmountable public health obstacle at present. Continued research may provide new control methods for integrated use against these mosquitoes. Concepts such as seeding breeding sites with pathogenic microsporidians or fungi, releasing sterile hybrid males or chemosterilized males, and other even more elaborate genetic control techniques, may be of special relevance to control of gambiae complex mosquitoes and diseases they transmit.

Summary The most profitable ways of collecting chalcids are discussed, namely by sweeping, suction sampler, beating, pyrethrum spray, rearing, Malaise traps, yellow pan traps, suction traps, pitfall traps and extraction from leaf litter or grass tussocks. Methods of preserving chalcids are also outlined, with particular emphasis on storing all unmounted material dry rather than in alcohol. The techniques of sweeping, card mounting specimens and slide preparation are described in detail.

The Oxford Radiocarbon Accelerator Unit (ORAU) has used an ultrafiltration protocol to further purify gelatin from archaeological bone since 2000. In this paper, the methodology is described, and it is shown that, in many instances, ultrafiltration successfully removes low molecular weight contaminants that less rigorous methods may not. These contaminants can sometimes be of a different radiocarbon age and, unless removed, may produce erroneous determinations, particularly when one is dating bones greater than 2 to 3 half-lives of 14 C and the contaminants are of modern age. Results of the redating of bone of Late Middle and Early Upper Paleolithic age from the British Isles and Europe suggest that we may need to look again at the traditional chronology for these periods.

(Uploaded by Plazi from the Biodiversity Heritage Library) No abstract provided.

Hypotheses of homology are the basis of comparative morphology and comparative molecular biology. The kinds of homologous and nonhomologous relations in classical and molecular biology are explored through the three tests that may be applied to a hypothesis of homology: congruence, conjunction, and similarity. The same three tests apply in molecular comparisons and in morphology, and in each field they differentiate eight kinds of relation. These various relations are discussed and compared. The unit or standard of comparison differs in morphology and in molecular biology; in morphology it is the adult or life cycle, but with molecules it is the haploid genome. In morphology the congruence test is decisive in separating homology and nonhomology, whereas with molecular sequence data similarity is the decisive test. Consequences of this difference are that the boundary between homology and nonhomology is not the same in molecular biology as in morphology, that homology and synapomorphy can be equated in morphology but not in all molecular comparisons, and that there is no detected molecular equivalent of convergence. Since molecular homology may reflect either species phylogeny or gene phylogeny, there are more kinds of homologous relation between molecular sequences than in morphology. The terms paraxenology and plerology are proposed for two of these kinds--respectively, the consequence of multiple xenology and of gene conversion.

Ongoing debates about the emergence of modern human behavior, however defined, regularly incorporate observations from the later part of the southern African Middle Stone Age and emphasize the early appearance of artifacts thought to reflect symbolic practice. Here we report a large sample of 270 fragments of intentionally marked ostrich eggshell from the Howiesons Poort at Diepkloof Rock Shelter, Western Cape, South Africa. Dating from approximately 60,000 years ago, these pieces attest to an engraving tradition that is the earliest reliable evidence of what is a widespread modern practice. These abstract linear depictions were made on functional items (eggshell containers), which were curated and involved in daily hunter-gatherer life. The standardized production of repetitive patterns, including a hatched band motif, suggests a system of symbolic representation in which collective identities and individual expressions are clearly communicated, suggesting social, cultural, and cognitive underpinnings that overlap with those of modern people.

These specially commissioned essays offer a radical and fresh appraisal of how ancient Greek art was looked at, written about and discussed in antiquity. The first section focuses on fifth-century culture, examining painted pottery, architecture and sculpture, and theatrical uses of set-piece descriptions. The second section turns to Hellenistic culture and literary artists' self-conscious exploration of new conditions of viewing and writing about viewing in epigrams, books on travel, and accounts of imaginary museums.

Concern about biodiversity loss has led to increased public investment in conservation. Whereas there is a widespread perception that such initiatives have been unsuccessful, there are few quantitative tests of this perception. Here, we evaluate whether rates of biodiversity change have altered in recent decades in three European countries (Great Britain, Netherlands and Belgium) for plants and flower visiting insects. We compared four 20-year periods, comparing periods of rapid land-use intensification and natural habitat loss (1930-1990) with a period of increased conservation investment (post-1990). We found that extensive species richness loss and biotic homogenisation occurred before 1990, whereas these negative trends became substantially less accentuated during recent decades, being partially reversed for certain taxa (e.g. bees in Great Britain and Netherlands). These results highlight the potential to maintain or even restore current species assemblages (which despite past extinctions are still of great conservation value), at least in regions where large-scale land-use intensification and natural habitat loss has ceased.

Porotic hyperostosis is currently considered to be one of several stress markers available for assessing the health and nutritional status of past human populations. The present study questions one of the basic assumptions underlying its use; that is, that the occurrence of porotic hyperostosis in an individual represents an episode of anemia that was current or had occurred within a relatively short period prior to death. A synthesis of data from a Romano-British site Poundbury Camp, anthropological and clinical studies, and information on bone physiology suggests that lesions of porotic hyperostosis seen in adults are most probably representative of a childhood episode of anemia. Lesions seen in adults are the result of bone changes occurring in the growth period that have not undergone complete remodelling. This viewpoint has implications for future interpretation of data on porotic hyperostosis obtained from skeletal collections.

Summary The ability to shed (autotomize) all or part of the tail, usually in response to predator attack, and often to subsequently regenerate it is widespread in lizards and amphisbaenians and also occurs in a few snakes and in the tuatara. Most species possess a sophisticated intravertebral autotomy mechanism which seems to be primitive in the Squamata. This appears to have been independently lost in members of many groups, but some agamids and snakes have regained the ability to shed their tails by a simpler intervertebral means and a number of agamids have also redeveloped tail regeneration as well. Breakable tails are used to evade capture in two main ways: by enabling reptiles to break away from predators that have grasped them by the tail and by providing a distraction which deflects the attention of the attacker away from the vulnerable head and body. It is argued that loss of caudal autotomy has occurred when the costs of tail shedding outweigh its benefits. Likely costs include the expense of regrowing the tail and the loss of a variety of possible tail functions that may cause partial incapacitation, at least until the tail regenerates. Benefits of autotomy are liable to be low if predation is rare, if the animal is able to protect itself effectively in other ways, if it is too slow to evade further pursuit after the tail is shed, or if the tail is small or unpalatable and consequently not likely to distract a predator. Benefit variation may well be greater than cost variation and therefore more important in initiating the loss of autotomy mechanisms. Many taxa that do not shed the tail appear to conform to the above interpretation, but in some cases, such as the Platynota, Agamidae and Chamaeleonidae, lack of intravertebral autotomy may reflect the history of these groups rather than being a direct result of present ecological pressures. The distribution of intervertebral autotomy in the Agamidae suggests that it may have evolved only in rather special circumstances where tail fragility is advantageous even in the absence of the ability to regenerate. Restriction of autotomy planes to the tail-base, so that the whole organ is lost, a condition found in a number of relatively slow-moving geckoes, is interpreted as a means of ensuring that enough of the tail is shed to distract a predator from further pursuit. The stimulus necessary to induce autotomy can vary rapidly in individual lizards and at least some of these changes probably maximize the effectiveness of the tail-shedding mechanism. Differences in the readiness with which all or part of the tail is shed exist between species and are likely to reflect the balance of costs and benefits in particular cases. Variations in incidence of broken tails between species and populations may be due to such differences in fragility but many other factors may play a part, including the age structure of samples, incidence of unsuccessful attacks by predators and ability to evade predators after autotomy. There is a clear tendency for climbing lizards, especially those living on rock surfaces, to have higher incidences of broken tails than ground-dwelling species, perhaps because the tail is usually less important in locomotion in the first group. Many lizards possess conspicuously coloured tails and tail movements that seem likely to help distract attention from the head and body. Conspicuous tail colouring is more frequent and often better developed in young animals, which tend to be more vulnerable than adults, and in active species from open habitats where crypsis may not always be very effective. Conspicuous tails usually have contrasting light and dark areas in nocturnal forms but are often a single bright colour in diurnal ones, probably reflecting the visual capacities of their respective predators. The predominance of blue tails in day-active species may be because this colour is striking close to but not very arresting at a distance, so it may not attract predators from far away while still drawing their attention at close quarters.

Transparent high lead and tin‐opacified lead‐alkali glazes have been extensively used throughout Europe and the Near East from their first appearance in the Roman era and the tenth‐ to eleventh‐century Islamic world, respectively, up until the present day. Using, to a large extent, information which is widely scattered through a diverse range of literature, the methods employed in the production of these two glaze types are first outlined and their merits are then compared with those of alkali glazes in terms of ease of preparation of the glaze mixture, ease of application of the glaze, ease of firing, cost of production, glaze‐body fit and visual appearance. The principal advantages of transparent high lead glazes as compared to alkali glazes are shown to be ease of preparation and application of the glaze suspension, low susceptibility to glaze ‘crazing’ and ‘crawling’ and high, optical brilliance. Factors that influence the choice of tin‐opacified lead‐alkali glazes include ease of production of tin oxide by melting tin and lead metals together; a reduced risk of reduction of lead oxide to lead metal and consequent blackening of the glaze; and, again, low susceptibility to ‘crazing’ and ‘crawling’. Limits of current knowledge regarding these two glaze types and requirements for future research are outlined.

A method has been developed for calculating characteristic fluorescence corrections in all cases involving K and L lines, based on the formula derived by Castaing for the case of one K line exciting another K line. A modification to the original formula is proposed, which takes into account more recent work on K line intensities; also some simplifications are suggested which enable corrections to be calculated quickly. Measurements of the relative intensities of K and L lines have been carried out to provide the necessary data for calculating corrections for fluorescence involving K and L lines.