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1.
2.
During a 14-month study of one group of woolly spider monkeys, or muriquis (Brachyteles arachnoides),at Fazenda Montes Claros, M. G., Brazil, the group used a home range of 168 ha. Day-range lengths averaged 1283 m and were longer in the wet season than in the dry season. An analysis of travel rates indicated that the group traveled faster on those days when they traveled farther. The availability of large patches of preferred food sources appears to affect daily movement patterns. Intraspecific comparisons, in addition to an apparent expansion of the study group’s home range as their group size has increased, suggest the importance of group size to muriqui range size. Interspecific comparisons between muriquis and sympatric brown howler monkeys suggest that locomotor adaptations are important to understanding species differences in ranging behavior.  相似文献   

3.
We investigated the ranging behaviour during the breeding season of 18 radiotracked little bustard (Tetrax tetrax) males, a disperse-lekking species inhabiting the cereal pseudo-steppes. The average kernel 95% home range was 60±50 ha and the average cluster 85% area was 17±17 ha. Range structure was as relevant as home range size for explaining the variation in the ranging behaviour of males, which could be partially explained by age, habitat quality and site. Ranging behaviour varied from males defending small and concentrated home ranges with high habitat quality, to males holding larger home ranges composed by several arenas. Our results suggest that social dominance and resource availability may affect ranging behaviour of males during the breeding season. Also, mating systems constraints may play a role on the use of space of males within the lekking ground. The ranging behaviour of a given male may be determined by a tendency to reduce and concentrate the home range as age and social status increase, and several fine-tuning mechanisms adjusting the ranging behaviour to the prevailing environmental or social factors on a given site and year.  相似文献   

4.
Seasonal fluctuation in food availability is a universal problem for wild animals. One common response to dietary changes is to modify ranging patterns. We studied the ranging pattern of one group (8–12 individuals) of red leaf monkeys (Presbytis rubicunda) in the lowland dipterocarp forest of Danum Valley, Borneo from December 2006 to December 2008. The seasonal availability of fruits varies significantly in this forest because of mast fruiting. We tested the hypothesis that changes in ranging pattern are linked with seasonal changes in diet in this species. We recorded activity, foods eaten, and location every 10 min from around 06:00 until 16:00 h, 5–10 days/mo. The home range size was 21.4 ha over the 25-mo study (95% kernel contour). There were no statistically significant relationships between feeding times on the four major nonexclusive dietary components (all species of seeds, all species of young leaves, young leaves of Spatholobus macropterus, and other species of young leaves) and either the home range (95% kernel contour) or the core area (50% kernel contour). The areas used in the seed-eating and non-seed-eating seasons overlapped to a large extent. The daily path length was 1160 ± 340 m (mean ± SD, range: 550–2140 m). Neither daily path length nor monthly mean travel rate was significantly related to feeding time on any of the four major dietary components. The group’s ranging patterns may be related to the unusual fallback strategy of this population, which depends on the young leaves of an abundant liana (S. macropterus), which are available in small patches. The monkeys need only a small home range because of the high abundance of these leaves. However, they range a relatively long distance because the patches of S. macropterus are easily depleted; thus the ranging distance does not decrease in non-seed-eating periods.  相似文献   

5.
Understanding the determinants of a species’ range use aids in understanding their ecological requirements, which in turn facilitates designing effective conservation strategies. The ranging behaviour of golden monkeys (Cercopithecus mitis kandti) in Mgahinga Gorilla National Park, Uganda was studied from January 2003 to February 2004 to establish habitat preferences. In each 0.25 ha grid cell in the group’s home range we quantified the basal area of food trees (n = 12,133 trees), measured bamboo (Arundinaria alpina) stems (n = 103,548), and estimated vine and shrub coverage. The evaluation of habitat preferences was facilitated by the fact that only five plant species, plus invertebrates (7.5%) constituted 96.4% of the group’s foraging effort; this included bamboo (59.9%), Maesa lanceolata (18.7%), Hypericum revolutum (6.8%), Galiniera saxifraga (2.1%) and Ilex mitis (1.4%). Phenology data were collected for all five food tree species, three vines, and two shrubs. Range use generally followed food tree basal area distribution and not the distribution of bamboo, with the abundance of M. lanceolata being more closely associated with home range use than any other food plant. Bamboo was ubiquitous in distribution and a vital year‐round resource for golden monkeys, which they combined with other food items to meet their nutritional requirements. Illegal bamboo or tree extraction both pose a serious threat to the conservation of the golden monkey, but activities that affect food tree abundance will likely have the most influence on monkey persistence.  相似文献   

6.
From March 1997 to February 1998, I investigated the activity patterns of 2 groups and the ranging patterns of 5 groups of eastern black-and-white colobus (Colobus guereza), aka guerezas, in the Kakamega Forest, Kenya. Guerezas at Kakamega spent more of their time resting than any other population of colobine monkeys studied to date. In addition, I recorded not one instance of intragroup aggression in 16,710 activity scan samples, providing preliminary evidence that intragroup contest competition may be rare or absent among guerezas at Kakamega. Mean daily path lengths ranged from 450 to 734 m, and home range area ranged from 12 to 20 ha, though home range area may have been underestimated for several of the study groups. Home range overlap was extensive with 49–83% of each group's range overlapped by the ranges of other groups. Despite the high level of home range overlap, the frequently entered areas (quadrats entered on 30% of a group's total study days) of any one group were not frequently entered by any other study group. Mean daily path length is not significantly correlated with levels of availability or consumption of any plant part item. Mean daily path length is also not significantly correlated with group size, though the largest group did have the longest mean daily path length. This finding suggests that intragroup scramble competition may have been rare or absent among guerezas at Kakamega except perhaps in the largest group, which was unusually large.  相似文献   

7.
I studied the ranging behavior of proboscis monkeys (Nasalis larvatus) at two sites in the Lower Kinabatangan Region of northern Borneo. I collected data on ranging behavior via scan sampling during group follows. Groups of Nasalis larvatus had ranges overlapping those of other groups in each area. I observed no territorial behavior. Groups of Nasalis larvatus occasionally swam across the Kinabatangan River, and frequently across its tributaries. The home range size of a focal one-male group (SU1) was 220.5 ha. The group traveled farther on days when the proportion of young leaves in the diet was higher. In addition, SU1 used particular areas when they fed on flowers and fruits. Apparently, rainfall and phenology did not influence ranging patterns.  相似文献   

8.
Ranging behaviour of a group of Red colobus monkeys, Colobus badius rufomitratus, on the Tana River, Kenya, is described. The main study group had a mean day journey of 603 in and an annual range area of 9 ha (measured in 0.25 ha quadrats). Relationships between ranging patterns and diet selection are sought on both spatial and temporal dimensions. Differential use of the annual range is related to the distribution of major food species, while the diversity of monthly ranging patterns is inversely related to the availability of young growth in the canopy. These findings lead to a discussion of why range areas at the Tana are much smaller than those reported from rain-forest sites.  相似文献   

9.
Many primates have to cope with a temporal scarcity in food availability that shapes their foraging strategies. Here we investigated the changes in diet, activity, and ranging behavior of a group of black-fronted titi monkeys (Callicebus nigrifrons) according to the availability of the main high-nutritional-density item in their diet and the foraging strategy adopted when this food is scarce. We monitored one habituated group using instantaneous scan sampling over 1 year (533 h of observation, 61 days) in a seasonal tropical forest fragment (245 ha). We simultaneously collected data on food availability with fruit traps. The titi monkeys consumed fleshy fruits, the main high-nutritional-density item of their diet, in accordance with its availability, and the availability of this item modulated the ingestion of vegetative plant parts, a relatively low-nutritional-density food. During high fleshy fruit availability, the titi monkeys consumed more fleshy fruits, flowers, and invertebrates. They also traveled more, but concentrated their activity in a central area of their home range. Conversely, during fleshy fruit scarcity, they increased the breadth of their diet, switching to one richer in seeds and vegetative plant parts, and with greater plant diversity. At the same time, they reduced most energy-demanding activities, traveling less and over shorter distances, but using their home range more broadly. Corroborating the optimal foraging theory, titi monkeys altered foraging strategies according to temporal food fluctuations and responded to low fleshy fruit availability by changing their diet, activity, and ranging behavior. The adoption of a low-cost/low-yield strategy allowed us to classify them as energy minimizers.  相似文献   

10.
A group of woolly monkeys (Lagothrix lagothricha), studied for 1,800 hr from June 1984 until September 1987 in the eastern Colombian Amazon, used a home range of about 760 ha, 90% of which overlapped the ranges of three other groups. Home range use varied throughout the year, correlating in part with variations in fruit production. The home range exhibited a nonexclusive “core area” in the floristically most diverse part of the home range, although the majority of the home range was entered at a much lower frequency. Within the study area woolly monkeys occurred at a density of 5.5 individuals/km2. The average day range was 2,880 m, and the average straight line distance between sleeping sites was 896 m. Day ranges differed significantly across months, but the only significant correlation tested was a positive relation with time spent “moving” in the activity budget. Comparisons with three other Amazonian sites where woolly monkeys have been studied reveal considerable variation. Soil fertility, plant community differences, and other factors seem to influence ranging patterns. © 1996 Wiley-Liss, Inc.  相似文献   

11.
Symptoms of psychological distress and disorder have been widely reported in people under quarantine during the COVID-19 pandemic; in addition to severe disruption of peoples’ daily activity and sleep patterns. This study investigates the association between physical-activity levels and sleep patterns in quarantined individuals. An international Google online survey was launched in April 6th, 2020 for 12-weeks. Forty-one research organizations from Europe, North-Africa, Western-Asia, and the Americas promoted the survey through their networks to the general society, which was made available in 14 languages. The survey was presented in a differential format with questions related to responses “before” and “during” the confinement period. Participants responded to the Pittsburgh Sleep Quality Index (PSQI) questionnaire and the short form of the International Physical Activity Questionnaire. 5056 replies (59.4% female), from Europe (46.4%), Western-Asia (25.4%), America (14.8%) and North-Africa (13.3%) were analysed. The COVID-19 home confinement led to impaired sleep quality, as evidenced by the increase in the global PSQI score (4.37 ± 2.71 before home confinement vs. 5.32 ± 3.23 during home confinement) (p < 0.001). The frequency of individuals experiencing a good sleep decreased from 61% (n = 3063) before home confinement to 48% (n = 2405) during home confinement with highly active individuals experienced better sleep quality (p < 0.001) in both conditions. Time spent engaged in all physical-activity and the metabolic equivalent of task in each physical-activity category (i.e., vigorous, moderate, walking) decreased significantly during COVID-19 home confinement (p < 0.001). The number of hours of daily-sitting increased by ~2 hours/days during home confinement (p < 0.001). COVID-19 home confinement resulted in significantly negative alterations in sleep patterns and physical-activity levels. To maintain health during home confinement, physical-activity promotion and sleep hygiene education and support are strongly warranted.  相似文献   

12.
I studied the ranging behavior of one group of L'Hoest's monkeys (Cercopithecus lhoesti) and one group of blue monkeys (C. mitis doggetti) in the Nyungwe Forest Reserve, Rwanda. This study is the first to examine the ranging behavior of the more terrestrial L'Hoest's monkeys. Fruits composed 47% of blue monkey diet and 24% of the L'Hoest's monkey diet; terrestrial herbaceous vegetation composed 35% of the diet of the latter. While overall abundance of fruit resources in the home range and overall proportion of fruit in the diet were not related to ranging behavior in either group, temporal and spatial availability of specific fruit species was related. Measures of ranging behavior indicated a more concentrated ranging pattern when fruit resources were scarce and dietary diversity increased and when fruit resources were abundant and the groups focused on a few abundant fruit species. Current hypotheses concerning primate ranging behavior suggest that frugivorous species are expected to have greater day ranges and larger home ranges than folivorous species, and invertebrate consumption is expected to produce a more wide-ranging pattern. However, the L'Hoest's monkey group, which was more folivorous and consumed fewer invertebrates, traveled greater daily distances, had a more diverse and longer ranging pattern, and had larger home range areas than the blue monkey group in every month of the study. Both species were highly selective of forest habitats; L'Hoest's monkeys used secondary forest, while blue monkeys preferred primary forest.  相似文献   

13.
In a year-long study, I investigated the ranging behavior of lowland woolly monkeys (Lagothrix lagotricha poeppigii) in a terra firma rainforest in Yasuní National Park, Ecuador, and examined the relationship between ranging, diet, food availability, and food patch use for this population. In Yasuní the total home range sizes for two social groups were 124 and 108 ha, which are much smaller than has been reported previously for Lagothrix elsewhere in its geographic distribution. The mean yearly day range estimates for these same groups were 1,792 m and 1,878 m, which are well within the range of variation previously reported. Ranging behavior was not correlated with the current habitat-wide abundance of ripe fruit, which comprises 76.3% of the yearly diet for this population, but was associated with one measure of likely insect prey abundance and with the availability of immature fruits, a minimal part of the diet. Specifically, one study group moved significantly greater distances during months of high likely insect prey abundance and when immature fruits were abundant. The second study group also traveled farther when likely insect prey abundance was high and when immature fruits were abundant, although the latter relationship only approached significance. This group also devoted significantly more of its daily activity budget to travel during these times. These results indicate that variation in ripe fruit abundance makes no meaningful contribution to explaining variation in ranging behavior for this population of woolly monkeys. Instead, the results raise the possibility that some aspects of the ranging behavior of frugivorous primates may be related to the availability of alternative food sources, such as animal prey, or to monitoring the phenological status of important fruit trees, rather than simply reflecting the degree of intragroup feeding competition.  相似文献   

14.
We studied the ranging behavior of a habituated group of black crested gibbons (Nomascus concolor jingdongensis) in a high, seasonal habitat on Mt. Wuliang, central Yunnan, China, between March 2005 and April 2006. Our results indicated that the total home range size for the study group was 129 ha, or 151 ha if the lacunae within the borders in which gibbons were not observed were included. This is a much bigger range size than that of other gibbon species. However, 69.7% of their activities occurred within 29 ha. The intensity of quadrant use was significantly correlated with the distribution of important food patches. The mean yearly daily path length was 1,391 m. Gibbons traveled farther when they spent more time feeding on fruit. To avoid often passing through ridges with little food, gibbons usually stayed in the same valley for successive days, and then moved on to another valley for another several days, which resulted in a concentrated ranging pattern.  相似文献   

15.
This is the first long-term, simultaneous, comparative study of three bamboo lemur species (Hapalemur griseus, H. aureus, and H. simus) at a site in southeastern-central Madagascar where they occur in sympatry. At Talatakely, Ranomafana National Park, the three Hapalemur spp. share overlapping home ranges. Hapalemur griseus has flexible group sizes, varying from three to nine individuals (n = 6). The home range of Hapalemur griseus averages 15 ha (n = 2). Hapalemur aureus forms family groups of 4 individuals (n = 3); they have a home range on average of 26 ha (n = 2). The single group of Hapalemur simus is composed of one or three adult males, two adult females, and their offspring; they occupy a home range of 62 ha. The three species of Hapalemur are year-round bamboo specialists: >88% of their diets consist of bamboo and grass in the Family Poaceae. Contrary to earlier findings, all three Hapalemur spp. consume the cynogenic parts—young leaf bases, young pseudopetioles, and young shoots—of the giant bamboo, Cathariostachys madagascariensis. They rely heavily on this plant, which comprises 72–95% of their diets. Hapalemur griseus and H. aureus consume similar proportions of bamboo vs. nonbamboo plants, though they differ in the species of bamboo they prefer. Hapalemur simus has the most distinct diet of the three bamboo lemurs. They exploit the young shoots of Cathariostachys madagascariensis during the austral summer rainy season, between November and April. From June to November, Hapalemur simus shifts its diet to eating the mature culm pith of Cathariostachys madagascariensis; the proportion of pith represented in their diet reaches a maximum of 89% in October. Seasonal availability of food resources, feeding competition, and factors related to body size may provide clues to the understanding of diet selection among the three sympatric Hapalemur spp.  相似文献   

16.
Capsule: Fledglings progressively increase their home range size and ranging behaviour as they age.

Aims: To examine the home range size and ranging behaviour of Bearded Vulture fledglings during the post-fledging dependence period and determine the onset of natal dispersal.

Methods: Post-fledging movements of three individuals were investigated in southern Africa using global positioning system (GPS) satellite telemetry which enabled home range sizes and distances travelled from the nest to be calculated.

Results: Fledglings increased their home range size from an average of 0.4–10 999?km2 (100% Minimum Convex Polygons) and 9.13–11 466?km2 (fixed 95% kernels) within the first six months post fledging. They also increased home range use as they aged with maximum daily distances travelled from the nest occurring between 98 and 136 days post fledging (when fledglings were aged between 222 and 262 days), after which time they dispersed from their natal area. Distances between fixes were highest during the dispersal period.

Conclusion: GPS satellite telemetry allows us to accurately demonstrate how fledglings progressively increase and use their home ranges as they age and undertake pre-dispersive exploratory flights. Results confirm the notion that juveniles disperse at the onset of the following breeding season and suggest that dispersal occurs earlier in the southern hemisphere.  相似文献   

17.
We collected systematic data on the home range and day ranges of one group of 57–63 muriquis (Brachyteles arachnoides hypoxanthus) at the Estação Biológica de Caratinga, Minas Gerais, Brazil from September 1998–July 1999, and compared them with similar data collected 15 years ago when the 23–27 individuals in the group traveled together as a cohesive unit. Home range size increased from 168 ha to 309 ha, reflecting an expansion into areas of the forest that were previously unutilized and consistent with the positive relationship predicted between group size and home range size. By contrast, muriquis exhibited remarkable seasonal and interannual stability in their day ranges. Day ranges, which were calculated from 144 days with 8 h of observation, averaged 1,313 ± 573 m (median = 1,206 m). Day ranges did not vary with the size of subgroups, defined as independent individuals that traveled with one another out of contact with other group members. Subgroups were significantly larger during the rainy season (mean = 41.8 ± 12.7, median = 46.0 individuals, n = 72) than the dry season (mean = 36.6 ± 13.25, median = 39.5 individuals, n = 72). Subgroups were also larger than the size of the entire group during the previous study, yet their day ranges are indistinguishable. The stability in muriqui day ranges is consistent with predictions for folivorous primates in which other indicators of intragroup feeding competition, such as female dominance relationships, are also absent. We attribute the transition from cohesive to fluid grouping patterns to limits on the number of individuals that can coordinate their movements when they spread out while foraging and suggest that seasonal differences in subgroup sizes without corresponding adjustments in day ranges reflect seasonal differences in the distribution of preferred foods coupled with the effects of reproductive seasonality on muriqui grouping patterns.  相似文献   

18.
We observed a unimale group (BE-Group) of proboscis monkeys (Nasalis larvatus) comprising an α-male, 6 adult females, and several immatures from May 2005 to May 2006. We followed the group for 2014 h along the Menanggul River, Sabah, Malaysia (118°30′E, 5°30′N). Observations focused mainly on ranging behavior. We determined availability and seasonal changes in plant species consumed by the members of the group by vegetation surveys in a 2.15-ha area along 200–500 m trails in the riverine forest. During the observation period, the group ranged ≤800 m from the riverbank, within a total range of 138.3 ha. The daily path length of the group ranged from 220 to 1734 m (mean, 799 m), and daily path length correlates negatively with fruit availability. The monkeys were apt to remain within a small range in fruit-abundant seasons. Because the monkeys preferred to feed on fruits of dominant plant species in the study area, their daily path length may decrease on days when they feed on fruits. The core areas of the group’s home range were along the river because the monkeys typically returned to riverside trees to sleep. The group most often used areas that were nearer the riverbank and where the availability of fruits was higher. The most frequently used grids were the ones where the group often had sleeping sites and crossed the river. Avoiding predation may be the main reason for river crossing and selecting particular sleeping sites; hence not only food availability but also the risk of predation appears to influence the ranging of the BE-Group.  相似文献   

19.
Group size and the distribution and quality of food resources are among the most important determinants of primate ranging behavior. In this study, I use the framework of the ecological constraints model to assess correlates of range size of a free-ranging group of bearded sakis (Chiropotes sagulatus). Bearded sakis are among the widest ranging neotropical primates, yet the lack of data from continuous forest populations has made understanding the factors influencing such large ranges difficult. I collected data on ranging behavior and diet during 44 full-day follows over 15 mo. The focal group used a home range of ca. 1000 ha and had daily path lengths of 2.8–6.5 km (mean?=?4.0 km). Daily path length did not significantly correlate with group size, patch quality, food availability, or the spatial distribution of feeding trees. Monthly home range size significantly positively correlated with group size and patch quality. The focal group had significantly shorter paths when ripe fruit consumption was higher and had more diverse diets, visited more food patches, and used larger monthly home ranges when they consumed a higher percentage of seeds. The results of this study, combined with other recent studies of Chiropotes in continuous forest, suggest that large home ranges (approaching 1000 ha) are characteristic of the genus. Although range size may be related to group size and food patch size, I suggest nutrient mixing and the need to balance the effects of seed secondary compounds as additional explanations for the large ranges of bearded sakis.  相似文献   

20.
Many primates exhibit behavioral flexibility which allows them to adapt to environmental change and different habitat types. The golden monkey (Cercopithecus mitis kandti) is a little-studied endangered primate subspecies endemic to the Virunga massif and the Gishwati forest in central Africa. In the Virunga massif, golden monkeys are mainly found in the bamboo forest, while in the Gishwati forest they live in mixed tropical montane forest. Here we describe and compare the diet of golden monkeys in both fragments. Over 24 consecutive months from January 2017 we used scan sampling to record feeding and ranging behavior of two Virunga groups and one Gishwati group totaling ca. 240 individuals. We also examined the phenology of bamboo and fruit trees, key seasonal food plant species for the monkeys. Golden monkeys fed on more than 100 plant species. The Virunga groups were mostly folivorous (between 72.8% and 87.16% of the diet) and fed mostly on young bamboo leaves and bamboo shoots, while 48.69% of the diet of the Gishwati group consisted of fruit from 22 different tree and shrub species. Bamboo shoots and fruit are seasonally available foods and were consumed regularly throughout the period when they were available. Despite being the smallest of the three study groups, the Gishwati group had a larger home range area (150.07 ha) compared to both Virunga groups (25.24 and 91.3 ha), likely driven by the differences in availability and distribution of fruit and bamboo in the habitats. Like other blue monkey subspecies, golden monkeys appear to have a flexible dietary strategy enabling them to adjust diet and ranging behavior to local habitats and available food resources. Additional studies and continuing conservation efforts are needed to better understand how variation in feeding and ranging ecology affects reproduction, population growth, and carrying capacity.  相似文献   

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