Troop size and human-modified habitat affect the ranging patterns of a chacma baboon population in the cape peninsula, South Africa

Differences in group size and habitat use are frequently used to explain the extensive variability in ranging patterns found across the primate order. However, with few exceptions, our understanding of primate ranging patterns stems from studies of single groups and both intra- and inter-specific meta-analyses. Studies with many groups and those that incorporate whole populations are rare but important for testing socioecological theory in primates. We quantify the ranging patterns of nine chacma baboon troops in a single population and use Spearman rank correlations and generalized linear mixed models to analyze the effects of troop size and human-modified habitat (a proxy for good quality habitat) on home range size, density (individuals/km(2) ), and daily path length. Intrapopulation variation in home range sizes (1.5-37.7 km(2) ), densities (1.3-12.1 baboons/km(2) ), and daily path lengths (1.80-6.61 km) was so vast that values were comparable to those of baboons inhabiting the climatic extremes of their current distribution. Both troop size and human-modified habitat had an effect on ranging patterns. Larger troops had larger home ranges and longer daily path lengths, while troops that spent more time in human-modified habitat had shorter daily path lengths. We found no effect of human-modified habitat on home range size or density. These results held when we controlled for the effects of both a single large outlier troop living exclusively in human-modified habitat and baboon monitors on our spatial variables. Our findings confirm the ability of baboons, as behaviorally adaptable dietary generalists, to not only survive but also to thrive in human-modified habitats with adjustments to their ranging patterns in accordance with current theory. Our findings also caution that studies focused on only a small sample of groups within a population of adaptable and generalist primate species may underestimate the variability in their respective localities.     

The Macrobenthos of Sites within Prince William Sound,Alaska, Prior to the Exxon Valdez Oil Spill

Benthic fauna within three bays (Rocky and Zaikof Bays, and Port Etches) of outer Prince William Sound, Alaska are examined. The data represent the only detailed benthic faunal information available for the period prior to a major oil spill by the tanker Exxon Valdez within the Sound. The spatial distribution of fauna determined by classification and ordination resulted in eight station groups. Stepwise multiple discriminant analysis demonstrated a relationship between station groups, sediment grain size and nitrogen. Major faunal differences were observed within Rocky and Zaikof Bays between 1982 and 1990. The faunal differences between the two time periods demonstrate the extreme temporal variability that might be expected within Prince William Sound. The study serves as a cautionary note to avoid conclusions about the effects of disturbance to the benthos on a single data set. An explanation for temporal differences within the bays is presented.     

Retardation of bone development in the Koshima troop of Japanese macaques

Retardation of bone development was observed in the Koshima troop of free ranging Japanese macaques. In the control group, epiphyseal unions of appendicular long bones generally started to close at about 4 yrs of age and were completed at about 8 or 9 yrs of age. Limb bone unions of the Koshima troop, however, started to close at about 9 yrs of age and completely closed at about 15 yrs of age. In the epiphyseal unions of trunk and girdle bones, the Koshima troop again showed a retardation of closure compared with the control group. Until long bones reached their full length, that is, until about 15 yrs of age, their size was small in the Koshima troop compared with the control group, though the sample size of the Koshima troop was small. After 15 yrs of age, however, many osteometrical measurements of the Koshima troop were nearly the same as controls. A prolonged growing duration compensated for the slow growth and allowed them to become as large as controls. This prolongation may be an adaptation in response to small size during the developmental period. In some parts of the body, however, Koshima macaques failed to reach the adult size of controls. Males were less likely than females to reach full size. Causes of the retardation and small size in the Koshima troop are discussed, but they remain open to further studies.     

Does troop size of wild Japanese macaques influence birth rate and infant mortality in the absence of predators?

For the wild Japanese macaques of Yakushima and Kinkazan Islands, we analyzed the relationship between the troop size or the number of adult females of each troop, infant/adult female ratio (IFR; crude birth rate), and infant mortality (IM) in habitats with no predators. In Yakushima, IFR was positively correlated to troop size and the number of adult females. In Kinkazan, however, IFR tended to decrease with the number of adult females. This difference may be due to the difference in troop size; i.e. in Yakushima, where troop size was small, IFR may increase with that of troop size, because a relatively larger troop is likely to the advantage in intertroop competition. In Kinkazan, where troop size was large, however, IFR is likely to decrease with troop size, because intratroop competition may increase. Thus, the present data roughly supportWrangham's model of the social structure of female-bonded primates, and suggests that there is an optimal troop size for birth rate (BR). On the other hand, there was no clear correlation between IM and the troop size or number of adult females of each troop.     

Effect of habitat fragmentation on the genetic diversity and structure of peripheral populations of beech in Central Italy

Fragmentation can affect the demographic and genetic structure of populations near the boundary of their biogeographic range. Higher genetic differentiation among populations coupled with lower level of within-population variability is expected as a consequence of reduced population size and isolation. The effects of these 2 factors have been rarely disentangled. Given their high gene flow, anemophilous forest trees should be more affected, in terms of loss of genetic diversity, by small population size rather than geographic isolation alone. We studied the impact of distance from the main range (a measure of isolation) and reduced population size on the within-population and among population components of genetic variability. We assayed 11 isozyme loci in a total of 856 individuals in 27 marginal populations of European beech (Fagus sylvatica L.) in Central Italy. Populations were divided into 3 groups with an increasing level of fragmentation. In the most fragmented group, the within-population genetic variability was slightly smaller and the among population differentiation significantly larger than in the other 2 groups. Isolation-by-distance was lost when only pairs of populations involving at least one from the most fragmented group were considered and maintained in the other groups. These results support the role of random genetic drift having a larger impact on the most fragmented group, whereas gene flow seems to balance genetic drift in the 2 less fragmented ones. Given that average distance from the main range is not different between the intermediate and the most fragmented group, but average population size is smaller, we can conclude that gene flow is effective, even at relatively long distances, in balancing the effect of fragmentation if population size is not too small.     

Effects of Group Membership and Size Distribution within a Group on Growth Rates of Juvenile Sablefish Anoplopoma fimbria

Group membership can confer both advantages and disadvantages to growth in juvenile fishes. The balance between costs and benefits of social interactions can shift depending on such factors as the composition of the group (density and size disparity) and the availability of food. We examined the effect of these factors on absolute growth and growth depensation in juvenile sablefish, Anoplopoma fimbria. Increasing density and increasing size disparity had little influence on absolute growth rates of juvenile sablefish and the effects of these social factors were not modified by ration level. In experiments testing density effects, absolute growth did not differ among groups of 1, 3, or 10 fish held at high rations, but at low rations single fish exhibited a different pattern of size-dependent growth compared to fish in groups. In experiments testing disparity effects, absolute growth did not differ between groups with an even size distribution and groups with a mixed size distribution. The relative size of an individual within a group, i.e., small, medium, or large, also did not modify growth, despite evidence of higher chasing behavior in mixed size distributions. Although the growth of small fish was not diminished in the presence of large fish, negative impacts of size disparity were expressed in high levels of cannibalism, which occurred in 42% of groups with a mixed size distribution. Significant growth depensation over time occurred in the density experiment, but not in the size disparity experiment, possibly due to the shorter duration of the latter experiment. We suggest that growth depensation was generated by individual variability in growth capacity rather than social effects on growth rates. Schooling behavior, measured by group cohesion indices, increased with fish size and was higher in groups with an even vs. a mixed size distribution. These results for sablefish are consistent with other schooling species in which growth variability is determined by exploitative competition and/or genetic variability in growth capacity rather than interference competition.     

Sociological study on the troop fission of wild

During the period from June to July 1983, the Hanyama-A troop of wild non-provisioned Japanese monkeys on Yakushima Island began to show signs of troop fission. Adult females together with their infants and juveniles subdivided into two groups, the Hanyama-K group and Hanyama-M group. After the subdivision, all of the troop males were observed vacillating between these two female groups. During the mating season, non-troop males were also observed moving around the two female groups. After this mating season, one of these non-troop males was found to have entered and become the alpha male in one of the groups, while higher-ranking adult males of the original troop settled into the other group. Each fissioned group was strongly considered to be composed of either high-ranking matrilines or low-ranking matrilines as observed previously in provisioned troops. The dominance relation between the two fissioned groups indicated that dominance rank reversal between these two female kin groups must have occurred during the course of subdivision of the troop. However, different from most previous cases of troop fission, there was no indication that males ever participated in the subdivision of the original female group. This was disrupted not as a result of males' involvement, but only as a result of antagonism among females, which initiated the troop fission. The main factor which appeared to determine when and in which fission group males eventually settled was the competition between the troop males' coalition and non-troop males and their ability to monopolize females. The present process of troop fission suggests a dual strategy between males and females (Wrangham, 1979, 1980) even in the society of Japanese macaques.     

Spatial and temporal population structure of sea trout at the Island of Gotland, Sweden, delineated from mitochondrial DNA

In a study of the genetic relationships among 879 anadromous brown trout Salmo trutta from 13 streams at the Island of Gotland, Sweden, using RFLP analysis of a mitochondrial DNA segment (NADH dehydrogenase-1 gene), six haplotypes were detected. Significant genetic divergence was observed among streams as well as between cohorts within streams. Approximately 8–9% of the total variation was due to differences between populations, and 4–5% was explained by differences between cohorts within populations. The female effective population size ( N _ef) was assessed from temporal haplotype frequency differences between consecutive cohorts; the estimated average N _ef over all populations was just below 30, suggesting that these populations were effectively quite small. With such small effective sizes the populations are expected to loose genetic variability quickly, but the observed levels do not appear particularly low. This indicates that female migration between streams occurs. The observed level of differentiation does not support the presumption that a particular pre-smolt migratory behaviour observed in Gotland streams, with large portions of fry leaving for the sea soon after hatching, results in a reduced homing ability. From a conservation management perspective the Gotland brown trout streams should be regarded as a population system where the vitality and survival of brown trout in one stream is dependent on the opportunity of contact and exchange of individuals from other streams.     

Experimental design and the outcome and interpretation of diversity–stability relations

The nature of the relationship between diversity and stability has become the subject of intense research effort over the last few decades as the role of diversity as a major driver of ecosystem functioning and stability has come to the forefront of ecological interest. Here, we present a meta‐analysis of the impact of twelve experimental design factors on the strength and direction of relations between biotic richness and temporal variability at both the aggregate community‐ and population‐level. Based on 35 studies that report 59 community‐level and 36 population‐level relations, our results show that biotic richness has a highly general stabilizing effect on community properties that are only marginally affected by the nuances of experimental design. In contrast, experimental design factors have a highly significant effect on mean effect sizes and the resulting interpretation of relations between richness and population‐level variability. The strongest dichotomous effect was observed based on the method of calculating the response variable, such that when population variability was calculated as the mean variability of populations across all replicates, biotic richness showed a negative (stabilizing) mean effect size. In contrast, when population variability was calculated on a per replicate basis, biotic richness showed a positive (destabilizing) mean effect size. This latter result suggests that a renewed focus on the mechanisms by which populations can be stabilized (and destabilized) by diversity is needed.     

Skull morphometry of Pygoscelis (Sphenisciformes): inter and intraspecific variations

Morphological diversity of 47 pygoscelid skulls was tested empirically through geometric morphometrics approach. Using 14 landmarks, shape is analyzed independently of other aspects of the body form. The shape disparity within and between the three living species of Pygoscelis is explored as well as how the structure of the skull is related to food preferences. Comparison of the three mean configurations of the species suggests that differences among groups are small relative to the variability within each group. However, some differences at the posterior portion of the braincase are indicated. Sexual dimorphism within each species is not noticeable. Comparison with a piscivorous species (Spheniscus humboldti) shows two cranial patterns: pygoscelid type with wide nasal gland depression limited by well-marked edges, shallow temporal fossae, and a poorly developed temporal nuchal crest; the second type represented by Spheniscus humboldti with laterally open nasal gland depression, deep temporal fossae, and a well-developed temporal nuchal crest.     

Predation, group size and mortality in a cooperative mongoose, Suricata suricatta

1. In social mammals where group members cooperate to detect predators and raise young, members of small groups commonly show higher mortality or lower breeding success than members of large ones. It is generally assumed that this is because large group size allows individuals to detect or repel predators more effectively but other benefits of group size may also be involved, including reduced costs of raising young and more effective competition for resources with neighbouring groups.
2. To investigate the extent to which predation rate affects survival, we compared mortality rates in two populations of suricates ( Suricata suricatta ), one living in an area of high predator density (Kalahari Gemsbok Park) and one living in an area of relatively low predator density (neighbouring ranchland). Most aspects of feeding ecology and growth (including time spent feeding, daily weight gain, growth, adult body weight, breeding frequency and neonatal mortality) were similar in the two populations. In contrast, mortality of animals over 3 months old was 1·7 times higher in the Park than on ranchland.
3. Mortality of juveniles between emergence from the natal burrow and 6 months of age was higher in small groups than large ones in the Park but significantly lower in small groups than large ones on ranchland. Adult mortality declined in larger groups in both areas.
4. The tendency for survival to be low in small groups had far-reaching consequences for the risk of group extinction. During a year of low rainfall in the Park, all groups of less than nine animals became extinct and population density declined to around a third of its initial level. We argue that high group extinction rates are to be expected in species where survival declines in small groups and mortality rates are high.     

Group Composition of Guinea Baboons (<Emphasis Type="Italic">Papio papio</Emphasis>) at a Water Place Suggests a Fluid Social Organization

Baboon social systems are among the most studied in primates. Solid knowledge of the hamadryas and savannah baboon systems has accumulated, leading to a dichotomic view of baboon social systems. Hamadryas baboons live in multilayered troops based on 1-male units whereas savannah baboons live in multimale multifemale groups based on a network of related females. Less attention has been paid to their West African congenerics, the Guinea baboons, Papio papio. To fill this gap, in 2007 we initiated a long-term study of a baboon troop ranging in the Niokolo Koba National Park in southeastern Senegal. Earlier studies suggested a tendency for a multilayered social system in Guinea baboons, similar to the hamadryas baboon organization. Therefore, as a first approach to analyzing variability in party size and composition, we observed members of the troop crossing an open area from a fixed point for 3 mo during the dry and wet seasons. We counted individuals and recorded changes in composition of both arriving and departing parties. Party size and composition were highly variable on both a daily and a seasonal basis; 45.9% of the arriving parties changed in composition while crossing the open area, either splitting into smaller parties or fusing into larger ones, suggesting a fluid organization. Our data support the existence of neither a hamadryas baboon-like multilayered social organization nor a stable medium-sized multimale multifemale group as in savannah baboons. In light of our data we may need to revise the dichotomic view of baboon social systems and include space for greater variability of their social systems.     

Density dependence constrains mean growth rate while enhancing individual size variation in stream salmonids

The objective of this study was to elucidate the effects of density dependence on the individual size variation of brown trout (Salmo trutta) juveniles. Recruitment (the abundance of the youngest juveniles in May when they were 2 months old); the mean size attained by those individuals in September (6 months old) and the corresponding size variability around the mean size quantified with the coefficient of variation (CV) were examined in 22 year-classes at seven sites of two contrasting tributaries of the Rio Esva drainage (north-western Spain). Both mean size and CV tended to be site-specific but density dependence in the form of recruitment dependence affected both mean size and CV: the mean size depicted negative power relationships with increased recruitment whereas the CV increased positively with increased recruitment. However, this pattern differed among sites. At two out of seven sites, there was no obvious relationship between the mean size and recruitment. The CV increased positively with increased recruitment at all sites, although at several sites the CV described linear relationships and at others described power relationships. As a consequence, the stronger effects of density dependence on mean size occurred at low densities with minor effects at high densities, whereas density dependence operated on CV with continuous effects within the whole range of recruitment variation except at several sites where lower effects occurred at high densities. Thus, the occurrence, shape and intensity of competitive interactions underlying density dependence as a major cause of size variation differed across temporal and spatial scales.     

Responses of a transplanted troop of Japanese macaques (Macaca fuscata) to bobcat (Lynx rufus) predation

A series of encounters between a transplanted troop of Japanese monkeys (Macaca fuscata) and one or more bobcats (Lynx rufus) is described. One incident of predation was observed and four additional cases assumed. Reactions of identified individuals and groups of monkeys as well as general troop reactions are noted. The effects of breeding season behavior, troop size, differences in mother care, behavior of the bobcat, and the structure of the south Texas environment are explored. After the observed predation incident, intervention by the researchers affected the behavior of the monkeys and the bobcat, and reduced encounters.     

Age-related differences in the performance, diffusion, and maintenance of stone handling, a behavioral tradition in Japanese macaques

Identifying the sources of behavioral diversity in non-human primates is vital to understanding the evolution of human behavior. Stone handling (SH, hereafter) is a form of object play consisting of the manipulation of stones by performing various behavioral patterns. This behavior is socially transmitted from generation to generation in Japanese macaques (Macaca fuscata), as a behavioral tradition. SH behavior in particular may reflect on the origin and evolution of stone-tool material culture. The objective of this study was to assess how group size, age structure, and age- and sex-related differences may account for the substantial intra- and inter-troop variations in SH reported in ten troops of Japanese macaques. Our results supported the hypothesis that patterns of variation in SH across troops reflected variability in group size and composition in age classes. We found that troop size was correlated with the proportion of troop members exhibiting SH simultaneously. The effect of troop size on the synchronized performance of SH may reveal the contagious nature of play. Our results suggest that the age structure of the group may affect the diffusion of SH. As predicted by the surplus energy hypothesis, a major functional hypothesis about play, intra-group variation in SH reflected more age- than sex-related differences. SH mainly occurred and was more frequent in younger than in older individuals, whereas no significant sex differences were found. SH episodes were shorter, more vigorous, and SH patterns were more diverse and less complex in immature than in mature individuals. The present findings reveal that age-related factors and group size may constrain the performance, diffusion, and maintenance of SH within a troop. Contrary to most other socially transmitted stone-tool using behaviors in non-human primates and early hominids, there is no optimal SH pattern. Provided some form of social learning, the non-adaptive nature of SH may allow particular SH pattern preferences to emerge at the group level. Our findings urge the use of an inter-populational comparative approach based on multivariate analyses when addressing the question of the evolution of behavioral traditions in primate and human populations.     

The variable social organization of hanuman langurs(Presbytis entellus), infanticide,and the monopolization of females

Data from 24 wild populations of hanuman langurs (Presbytis entellus)in south Asia are used to test hypotheses seeking to explain variation in troop structure and the incidence of infanticide. The occurrence of infanticide is associated with a one-male troop structure and not with a high density. The density, predation, and economic-advantage hypotheses, as explanations for the occurrence of one-male and multimale troops, are not supported by the review. However, the monopolization hypothesis is not contradicted; the number of adult males per troop is significantly correlated with troop size and with the number of adult females per troop. Therefore it is suggested that a one-male troop structure will arise if a male is able to monopolize a group of females, a multimale troop if he cannot. One-male troops may predispose to infanticide because of high variance in male mating success and high intermale competition between groups rather than within troops. If female dispersion determines troop structure, it is speculated that females could manipulate males to form a multimale society if the advantages in terms of infant survival and intertroop conflict exceeded the costs in terms of not producing infanticidal “sexy sons.”     

Neocortical development and social structure in primates

The relationships between the relative size of the neocortex and differences in social structures were examined in prosimians and anthropoids. The relative size of the neocortex (RSN) of a given congeneric group in each superfamily of primates was measured based on the allometric relationships between neocortical volume and brain weight for each superfamily, to control phylogenetic affinity and the effects of brain size. In prosimians, “troop-making” congeneric groups (N=3) revealed a significantly larger RSN than solitary groups (N=6), and there was a significant, positive correlation between RSN and troop size. In the case of anthropoids, polygynous/frugivorous groups (N=5) revealed a significantly larger RSN than monogynous/frugivorous groups (N=8). Furthermore, a significant, positive correlation between RSN and troop size was found for frugivorous congeneric groups of the Ceboidea. These results suggest that neocortical development is associated with differences in social structure among primates.     

On the fission of troops of Japanese monkeys

The troop fission of Japanese monkeys has been observed in 11 troops, and the total number of fissions observed numbered 22. Examined cases of fission relative to season, amount of food, troop size and socionomic sex ratio of the main troop and to individuals that acted as nucleus in forming a branch troop and females, exhibited variance, not being uniform. But inquiry into troop fission as seen from the standpoint of the mechanism maintained by Japanese monkeys' society indicated (1) troop fission checks the growth of troop size and increases the socionomic sex ratio of the main troop, (2) troop fission is an effective mechanism for the maintenance of class structure among adult males, and (3) the possibility that troop fission functions to check inbreeding.Thus, it must be said in general that troop fission, along with single desertions of males, plays a very important role as one mechanism for the maintenance of the society of Japanese monkey. However, the branch troop is often composed of a large number of males and a small number of females; in short, it is under very difficult conditions that a branch troop starts on its way to becoming a fully established Japanese monkey troop.The troop fission is an effective mechanism for the maintenance of the main troop, but not too effective for that of the branch troop.It cannot be said that there are abundant data on troop fission of primates other than Japanese monkey. But, from limited data, we can find various forms of troop fission according to each species, and it may be ultimately related to the maintenance mechanism of the primate society.     

津巴布韦奇马尼马尼人工松林中狒狒分布型和结群大小与树木剥皮的关系

本研究调查了人工松林中狒狒结群大小和家区面积与树木剥皮率的关系。于2003年9月至2004年8月间每月对每个狒狒结群进行5天观察,采用足迹计数法统计狒狒结群大小,对不同结群狒狒家区内具有新旧剥皮的树木数进行统计,以方差分析和回归分析狒狒结群大小和家区面积与树木剥皮之间的关系。结果表明:定居和访问松林的狒狒结群分布型不受结群和家区大小的影响而与季节有关。树木剥皮与狒狒结群大小和家区面积均无相关性,特别是雨季更是如此,揭示狒狒对树木剥皮不是对食物和水源短缺的反应。树木剥皮具有很大的月份间变异,与狒狒群定居和访问利用松林亦无相关。树木剥皮率与狒狒结群大小的关系说明树木剥皮是由于狒狒结群中少数个体的偶然剥皮行为造成的。     

Feeding Competition and Group Size in Alouatta pigra

Researchers consider group size in primates to be determined by complex relationships among numerous ecological forces. Antipredator benefits and better resource defense are the primary pressures for large groups. Conversely, intragroup limited food availability, can result in greater intragroup feeding competition and individual energy expenditure in larger groups, creating energetic advantages for individuals in small groups and placing an upper limit group size. However, the extent to which food availability constrains group size remains unclear for many species, including black howlers (Alouatta pigra), which ubiquitously live in small social groups (≤10 individuals). We studied the relationship between group size and 2 key indices of feeding competition—day journey length and activity budgets—in 3 groups of wild Alouatta pigra at a hurricane-damaged site in Belize, Central America. We controlled for differences in food availability between home ranges (food tree density) and compared both indicators of feeding competition directly with temporal variation in food availability for each group. Our results show no consistent association between resource availability, group size, and either index of competition, indicating that feeding competition does not limit group size at the site—i.e., that larger groups can form without increased costs of feeding competition. The results support the search for other explanations, possibly social ones, for small group size in the primates, and we conclude with suggestions and evidence for such alternative explanations.