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1.
J. P. Croxall 《Ibis》1976,118(3):333-346
Mixed-species flocks of birds feeding on insects were observed mainly in forest in Sarawak at a time of year when insect availability is known to be near its annual minimum. The approximate individual and specific composition of most flocks were noted. Twenty-six species occurring in 25% of flocks were regarded as occasional members, 15 species occurring in 40% of flocks being classed as regular members. Recording species' feeding behaviour was the main priority and few observations of inter- and intra-specific interactions within the flock, horizontal distribution or vertical stratification were made, although the last proved to be of potential significance. From the analysis of feeding behaviour two groups of species were distinguished. The larger group contained those usually having an exclusive common feeding pattern and showing very little overlap with the other such species. Fewer species used a wide range of feeding methods, all of which were shared with other species, but the least overlap was with other members of the same category. The observed composition of these flocks, in terms of regular members, might be interpreted as ensuring a low level of inter-specific competition and it is suggested that the less specialized foragers may occur in the flocks by utilizing the ‘gaps’ between, and absences of, specialists. The possible advantages of membership of mixed-species flocks are briefly considered and the likelihood of the selective advantage in any situation being the result of a balance of factors emphasized. In the apparent absence of regular potential predators the existence of these flocks is interpreted primarily as an adaptation for augmenting available insect food, particularly perhaps at critical times of year, by flushing insects as a result of the foraging activities of flock members. It is suggested that the varied responses of insects on being disturbed coupled with the different and fairly specialized feeding techniques of the birds could ensure benefit for all members of the flock.  相似文献   

2.
P. W. GREIG-SMITH 《Ibis》1978,120(3):284-297
Mixed-species flocks of birds were observed during the wet season (July to September 1975) in savanna woodland in Ghana. Thirty-four flocks contained birds of 56 species in 20 families, including insectivorous, granivorous, and nectarivorous species, using a wide range of foraging methods. Only two species occurred in more than half the flocks. There was no correlation between the number of flocks joined by a species and its abundance in the community. Among insectivores, but not granivores, the species which joined most flocks were those which habitually occurred in the largest single-species groups. All stages of breeding activity were represented by the various members. Some species joined flocks only while these were passing through their territories. Of the two species which were present most frequently, there were no differences between mixed and single-species flocks for Eremomela pusilla, but Parus leucomelas foraged and called on more occasions in mixed flocks than single-species flocks, though the rates of foraging and calling were related only to the number of P. leucomelas present. Groups of P. leucomelas appeared to initiate some flocks by attraction due to their conspicuous wing-bars, active movement, and loud calls. Black-and-white species joined them first, followed by birds of other plumage patterns. The advantages of mixed flocking are thought to be connected with finding patches of the food of bark- and foliage-searching insectivores, which were the only species regularly seen foraging in the flocks. Because of dry season burning which leaves small unburnt patches of savanna, these insect species may share a common, patchy distribution. Birds may also gain protection from predators, and some species probably gain no advantages. The species composition and behaviour of flocks previously recorded elsewhere in African savannas are similar to the Ghana flocks.  相似文献   

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IMITATIVE FORAGING IN MIXED-SPECIES FLOCKS OF SEYCHELLES BIRDS   总被引:1,自引:0,他引:1  
P. W. GREIG-SMITH 《Ibis》1978,120(2):233-235
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The feeding ecology of three Costa Rican finches occurring in mixed flocks, Tiaris olivacea, Sporophila aurita corvina and Sporophila torquella , was investigated by measuring both behavioural and ecological variables. Observations on foraging height, rate of hopping and pecking rate, as well as the identity, proximity and number of nearest neighbours were recorded. In addition the duration of all feeding and perching episodes were timed. Comparisons were also made between the abundances of food items (grass seeds) consumed and those potentially available for consumption.
The analysis of variance of the feeding behaviour revealed that the presence or absence of neighbouring birds, whether of the same or different species, influenced the duration of feeding bouts more significantly than did either differences in habitat or species-characteristic behaviour. In addition the dietary comparisons revealed overlap in both species and size of seed consumed. Such similarities suggest that these species are not partitioning fields in the classical sense.
We propose that the increase in the duration of the feeding bout associated with the presence of mixed species aggregations leads to increased feeding efficiency and is the result of intra- and inter-specific social learning. Certainly flocking is often advantageous, since searching in a group facilitates finding clumped resources; mixed species flocking, by increasing exposure to a diversity of foraging places and patterns, can further augment feeding efficiency.  相似文献   

7.
A. Guillet 《Ostrich》2013,84(4):252-255
Guillet, A. 1979. Aspects of the foraging behaviour of the Shoebill. Ostrich 50:252-255.

The foraging behaviour of the Shoebill Balaeniceps rex. in relation to the bird's habitat and morphology, is described. The Shoebill preys on fish in shallow water, and uses platforms of floating vegetation as fishing sites. The Shoebill's behaviour in stalking, detecting and capturing prey is compared with foraging techniques used by herons and storks. The Shoebill uses a peculiar and complicated technique, called “collapsing”, for capturing prey.  相似文献   

8.
Barbara K.  Snow 《Ibis》1966,108(2):265-280
From 25 September to 8 October 1963 daily observations were made on a group of Flightless Cormorants Nannopterum harrisi nesting on the west side of Albemarle Island in the Galápagos. Flightless Cormorants are apparently bottom-feeders, and confined to shallow coasts at the western end of the Galapagos Archipelago where there is an upwelling of cold nutrient-rich water. There is no reason to suppose that they are declining in numbers. Males are very much larger than females, the size difference between the sexes being greater than in other species of cormorants. Courtship behaviour, nest-building and mating are described. The earliest phases of courtship take place on the water, later phases at the nest-site. Homologies are traced with other cormorant species. In contrast to other members of the family, allopreening apparently does not occur. Both sexes incubate and care for the young. Observations on families of different ages over the 12-day period allowed the development of the young to be traced up to the age of about 40 days. Egg-laying takes place in most months of the year, with a peak in April-June and perhaps a second peak about October. Observations on birds colour-ringed on an earlier visit suggested that individuals do not breed more than once in the year. Nesting success appeared to be very low in 1963.  相似文献   

9.
Herholdt, J.J., Kemp, A.C. & Du Plessis, D. 1996. Aspects of the breeding status and ecology of the Bateleur and Tawny Eagle in the Kalahari Gemsbok National Park. Ostrich 67:126-137.

The nesting success at 13 nesting territories of Bateleur Terathopius ecaudatus and 19 nesting territorites of Tawny Eagle Aquila rapax was monitored for seven successive years (1988–1994) in a protected area in the Kalahari desert of South Africa. On average Bateleurs laid one year in two (51/95 pair-years) and fledged 0.33 young/pair/year (31/95). Tawny Eagles laid, on average, in two out of three years (66/105), and fledged 0.4 young/pair/year (42/105). Most Bateleurs laid eggs in January and February, while Tawny Eagles mostly laid from May to June. Almost all Bateleur and Tawny Eagle nesting territories located were in the Acacia erioloba savanna in the dry Auob and Nossob riverbeds. Bateleur nesting territories were spaced at intervals of 7.2 km (2.5–14.6 km; n = 9) along the Nossob River. Tawny Eagle nesting territories were spaced at intervals of 17.6 km (6.1–32.7 km) in the Nossob River and 11.3 km (8–14 km) in the Auob River respectively. A total of 13 Bateleur and 30–40 Tawny Eagle nesting territories (27 known active nesting territories) respectively occurred in the Kalahari Gemsbok National Park during the study period. There was evidence of a 13% decline in active nesting territories of Bateleur during the seven year study, and at least a 40% decline over the previous 10 years. Vacated nesting territories were not reoccupied. There was no safe buffer zone around the Kalahari Gemsbok National Park and persecution in the adjacent farmlands, when foraging Bateleur from the protected Park enter these areas, as well as nesting site disturbance, could have been part of the reason for this decline. Poisoned and suspected poisoned Bateleurs have been found in the Park during the study period. There was no obvious decline in active Tawny Eagle nesting territories.  相似文献   

10.
S. J. J. F. Davies 《Ibis》1963,105(1):76-98
Part 1.
Some action patterns of the Magpie Goose are clearly ritualized as signal actions, whilst others, although not so ritualized, are none the less characteristic of particular moods of the bird. It is considered that the action patterns form a simple language such that individual geese are aware and can often anticipate the actions of other geese.
Particular attention is given to fighting actions, which appear on the second day of a goose's life, and to "concerting", at first a threat display but later also used in pair maintenance, where it appears very similar in function to the triumph display of true geese.
Part 2.
The family, comprising the reproductive group and its offspring, is the fundamental entity in Magpie Goose flocks. Males may be paired to one or two females, but they dominate their mates and offspring and defend a "territory" around them from other geese.
Magpie Goose flocks are built up of families, each of which acts independently except in an alarm situation, when the flock acts as an entity. Flocks build up at feeding, roosting and watering sites, and although constant in location are probably composed of a different combination of families each day. The flock behaviour of Magpie Geese closely parallels that of the true geese.
No alarm stimuli have been found which are innately recognized by Magpie Geese. The fact that alarm stimuli are learnt, taken with the unstable nature of the flocks, suggests that it may be very difficult to produce a "magic wand" which effectively scares the birds from rice crops.  相似文献   

11.
EXPERIMENTS ON THE LIMITATION OF BIRD NUMBERS BY TERRITORIAL BEHAVIOUR   总被引:2,自引:0,他引:2  
(1) This paper examines removal and other experimental studies on the role of territorial behaviour in the limitation of bird densities. Experimental design is discussed, as are the types of conclusions that can be drawn. (2) Experiments have been conducted on more than 40 species from a wide range of taxonomic groups. Most provided evidence for density limitation, probably mediated by territorial behaviour, and for the existence of a non-territorial sector able to take territories when territory owners were removed or when additional habitat was made available. Experiments in the breeding season indicated that some surplus birds, although younger on average then territorial birds, were sexually mature and able to breed when given the chance. In some species, replacement birds bred less well than other territorial birds, but in other species no difference was apparent between the two groups. (3) Other experiments indicated that, while density was limited by territorial behaviour in good habitats, this was not the case in poor habitats, and that some individuals would move from poor to good habitat when territory owners were removed from good habitat. (4) In some species, non-territorial birds of breeding age were present in the population despite the existence of vacant territorial sites, while in others replacements were observed on good territories but not on poor ones. The implications were that site quality influenced whether settlement, defence and breeding occurred, and that some individuals had more stringent site requirements than others. In some seabirds' sites in the centre of a colony were more attractive than sites on the edges. (5) Many land-bird species that have been studied show two peaks of territorial activity each year, in autumn and in spring, and a limitation on breeding density can occur at either or both seasons, depending on conditions. (6) The fact that densities of many bird species fluctuate greatly from year to year is not inconsistent with the limitation of density by territorial behaviour. Several mechanisms are apparent through which density might be limited by territorialism at different levels in different years, so that surplus non-territorial birds are present in years of low territorial density, as well as in years of high territorial density. (7) Experiments have shown that density is limited by the presence of territorial birds, in some species at different levels in different areas or years. The next step is to find whether density is regulated by the presence of territorial birds over a period of years in a density-dependent manner. For this, observational data are required to find whether the proportion of birds that is excluded by territorial behaviour each year varies with the total number available for settlement. Such studies can be made only on species in which non-territorial birds can be counted accurately, as well as territorial ones.  相似文献   

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哈萨克斯坦北部轮藻植物的分布与生态学研究   总被引:1,自引:0,他引:1  
哈萨克斯坦北部已发现26种轮藻植物,其中以Kockchetav丘陵地区最为丰富。轮藻植物生长的盐度范围为0.2—44.9g/L,一般生长于盐度不超过1—5(8)g/L的淡水或微咸水环境。在盐度高达41.1—44.9g/L的水体中,仅发现Lamprothamnium papulosum。轮藻植物生长的最大水深为7m,多数种生长的水深不超过1m。轮藻生长的主要底质类型为砂及粉砂质。一些种类如Chara kirghisorum,C.glopbularis,C.tomentosa和Nitellopsis obtusa构成稳定的植被,而其它种类构成湖区周期性干涸环境中短时间生长的水生大型植物群落的一部分。  相似文献   

16.
通过试验分析,结果得出,油菜菌核病菌生长温度范围在0~34℃之间,23℃以下菌丝生长速度与温度呈正相关,25℃以上则呈负相关,23~25℃最适宜,菌丝和菌核致死温度分别为45℃和75℃.该菌对酸碱度适应范围很广,PH1~14范围内只在PH_1条件下不能生长,其最适PH值为5~6。病菌利用铵态氮源能力最强,硝态氮源次之,不能利用亚硝态氮;对氨基酸利用能力以精氨酸最强,其次是酪氨酸、天门冬氨酸和谷氨酸,赖氨酸最差。植株内精氨酸和赖氨酸比值大的白菜型油菜“黄鳝籽”病情扩展最快。  相似文献   

17.
Alan C. Kemp 《Ostrich》2013,84(2-3):61-68
Kemp, A. C. 1995. Aspects of the breeding biology and behaviour of the Secretarybird Sagittarius serpentarius near Pretoria, South Africa. Ostrich 66: 61–68.

Secretarybirds in three adjacent territories were monitored from 1977 to 1988 on grass- and croplands near Pretoria, South Africa. Most observations of breeding biology and behaviour confirmed or extended previous studies. There was no correlation between pairs in occupancy of territory, productivity or development periods of young: this confirms the flexible breeding abilities which are unusual for such a large bird. Some aspects of breeding biology (egg shape and texture, watering of chicks) and behaviour (Wings open and Up-down greeting displays) may be homologous with storks and important in understanding the phylogeny and evolution of the Sagitariidae and other diurnal raptors.  相似文献   

18.
J. P. Croxall 《Ibis》1977,119(2):113-146
Fifty species of insectivorous warblers Sylviidae, flycatchers Muscicapidae and whistlers Pachycephalidae were studied in primary rainforest at various localities in New Guinea. The structure of the various forest types is described and the birds' feeding ecology and behaviour analysed by recognizing three main foraging techniques and five horizontal and three vertical basic structural divisions of the habitats. Altitudinal ranges of the species are assessed to determine potential co-existence and they are divided into lowland and lower montane groups (either side of the main avifaunal discontinuity at 1500 m) with a third small group occurring in both areas and a fourth group of 12 lower montane species that occur also in the structurally much simpler Upper Montane forest. The feeding behaviour and ecology of the species within each major habitat are compared, with particular attention to taxonomically related and ecologically similar species. Other important considerations—additional behavioural differences, notable morphological distinctions, altitudinal separation of ranges within the habitat—are also noted. The likely importance of differences in foraging behaviour and feeding sites for reducing competition between related species is amply demonstrated, members of several pairs and groups of species have nearly mutually exclusive preferences. The overall pattern of habitat utilization is, however, extremely complex with nearly all stations used, in a variety of ways, by several species and there are many instances of substantial similarity between pairs of species, often involving congeners. The calculation of information theory derived indices of foraging diversity and overlap enables more general comparisons between the altitudinally graded habitats to be made and differences related to current ideas on tropical species diversity. Between Lowland and Lower Montane forest there is a fairly general trend of reduction in foraging diversity and decrease in the mean overlap between species in many genera and groups. The 12 species that continue into the simpler Upper Montane forest show very significantly reduced foraging diversity (compared with their values in lower montane forest) and also less overlap, indicating a different relationship between these species in the absence of the other Lower Montane forest birds. Together these results suggest that the most tropical (i.e., lowland) species show greatest overlap but do not necessarily have smaller niches. In progressively higher habitats there is a bias to the disappearance of generalist (high diversity index) species. These mainly use flycatcher-gleaning techniques supporting suggestions that the increase in insectivorous species in the tropics is partly due to exploitation of feeding strategies related to hovering. Habitat and ecological factors influencing this are assessed. The importance of altitudinal isolating mechanisms is also discussed and, amongst the species studied, both on average and in specific cases, those with the greatest similarities in foraging behaviour and ecology are segregated altitudinally and do not co-exist. It is suggested, however, that substantial overlap between many co-existing tropical species may not be abnormal, but rather an adaptation for ensuring maximum efficiency of habitat utilization in the prevailing environmental conditions of tropical rainforest.  相似文献   

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