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1.
In this paper we study optimal animal movement in heterogeneous environments consisting of several food patches in which animals trade-off energy gain versus predation risk. We derive a myopic optimization rule describing optimal animal movements by fitness maximization assuming an animal state is described by a single quantity (such as weight, size, or energy reserves). This rule predicts a critical state at which an animal should switch from a more dangerous and more profitable patch to a less dangerous and less profitable patch. Qualitatively, there are two types of behavior: either the animal switches from one patch to another and stays in the new patch for some time before it switches again, or the animal switches between two patches instantaneously. The former case happens if animal state growth is positive in all patches, while the latter case happens if animal state growth is negative in one patch. In particular, this happens if one patch is a refuge. We consider in detail two special cases. The first one assumes a linear animal state growth while the second assumes a saturating animal state growth described by the von Bertalanffy curve. For the first model the proportion of time spent in the more profitable and more risky patch increases with profitability of this patch when state growth is positive in both patches. On contrary, if state growth is negative in the less profitable and safer patch, animals spend proportionally less time in the more profitable and more risky patch as its profitability increases. As a function of the predation risk in the more profitable patch the time spent there proportionally decreases. When animal state growth is described by the saturating curve, time spent in the more risky patch is a hump-shaped curve if state growth is positive in both patches. Our results extend the mu/f rule, which predicts that animals should behave in such a way as to minimize mortality risk to resource intake ratio.  相似文献   

2.
The exploitation of food resources by the German cockroach, Blattella germanica (L.) (Dictyoptera: Blattellidae) was investigated experimentally in relation to distance from shelters and depletion of neighbouring food patches. In addition, the dynamics of exploitation of a patch were analysed. Observations were made after dark in a public swimming baths building and each one lasted 3 h. Food patches were placed in rows, at different distances from the shelters. The number of cockroaches in food dishes, in a 20 cm diameter circle round each food dish and in a 60 cm diameter circle round this first circle were recorded.Food items nearest the shelters were exploited first. Exploitation of row 2 and of row 3 food items started later, after row 1 food patches had been depleted. Under these conditions, the moment a food patch was exploited was related to its distance from shelter. Exploitation of food patches occurred in a step-by-step manner, one patch attracting animals when a nearby patch had been depleted, and not following a model of ideal free distribution.Although our experimental food patches were exploited in relation to their distance from shelter, we were able to demonstrate that distance did not influence the dynamics of exploitation of a food item. The mean number of cockroaches on a food patch, whatever its spatial position, increased regularly, reached a maximum at t=–10 min, and then decreased rapidly after all the food had been completely consumed, at t=0 min. The mean number of animals in the 20 cm diameter circle round a food source peaked at t=0 min, then decreased rapidly. This area appeared to be a transit area. The mean number of animals in a 60 cm diameter circle round the food source peaked later, and then decreased slowly. Animals remained in this area longer than in the area closer to the food dish, but their presence there was concomitant with the depletion of the food box.  相似文献   

3.
Recent insights suggest that predators should include (mildly) toxic prey when non-toxic food is scarce. However, the assumption that toxic prey is energetically as profitable as non-toxic prey misses the possibility that non-toxic prey have other ways to avoid being eaten, such as the formation of an indigestible armature. In that case, predators face a trade-off between avoiding toxins and minimizing indigestible ballast intake. Here, we report on the trophic interactions between a shorebird (red knot, Calidris canutus canutus) and its two main bivalve prey, one being mildly toxic but easily digestible, and the other being non-toxic but harder to digest. A novel toxin-based optimal diet model is developed and tested against an existing one that ignores toxin constraints on the basis of data on prey abundance, diet choice, local survival and numbers of red knots at Banc d''Arguin (Mauritania) over 8 years. Observed diet and annual survival rates closely fit the predictions of the toxin-based model, with survival and population size being highest in years when the non-toxic prey is abundant. In the 6 of 8 years when the non-toxic prey is not abundant enough to satisfy the energy requirements, red knots must rely on the toxic alternative.  相似文献   

4.
长白山北坡岳桦种群结构及动态分析   总被引:40,自引:1,他引:40  
以“空间代时间”的方法 ,以种群径级结构代替年龄结构 ,采用静态生命表、生存分析和空间格局分析方法 ,探讨了长白山北坡不同海拔分布的岳桦种群的结构和动态规律。结果表明 ,在海拔 180 0、190 0和 2 0 0 0m ,随海拔升高 ,岳桦种群密度增大 ,径级分布范围减小 ,种群存活曲线由DeeveyⅡ型过渡到DeeveyⅠ型 ,种群由稳定型过渡为增长型 ,说明岳桦种群由低海拔向高海拔 ,群落处于不同的演替和发展阶段。而且随着岳桦径级的增大 ,其分布格局由集群分布过渡到随机分布。  相似文献   

5.
1. Both resources and natural enemies can influence the distribution of a herbivore. The ideal free distribution predicts that herbivores distribute themselves to optimise utilisation of resources. There is also evidence of herbivores seeking out refuges that reduce natural enemy attack (enemy‐free space). Which of these theories predominates in a thistle–tephritid Terellia ruficauda (Diptera: Tephritidae)–parasitoid interaction is examined. 2. The plant, Cirsium palustre, had a contagious distribution approximated by the negative binomial distribution. Terellia ruficauda foraged preferentially and oviposited on isolated plants although its larvae gained neither nutritional benefit nor reduced natural enemy pressure from such behaviour. 3. Parasitoids of T. ruficauda foraged and oviposited more frequently on isolated than on crowded T. ruficauda, resulting in inverse density‐dependent parasitoid attack at all spatial scales examined. Neither the herbivore nor natural enemies distributed themselves according to the predictions of the ideal free distribution and the herbivore did not oviposit to reduce natural enemy attack. 4. Extrapolating from the theoretical predictions of the ideal free distribution and enemy‐free space to the field requires considerable caution. Terellia ruficauda and its parasitoids appear to select their oviposition sites to spread the risk of losses through factors (e.g. mammal herbivory) that may damage dense clusters of C. palustre.  相似文献   

6.
7.

Background and Aims

This study considers the spatial structure of patchy habitats from the perspective of plants that forage for resources by clonal growth. Modelling is used in order to compare two basic strategies, which differ in the response of the plant to a patch boundary. The ‘avoiding plant’ (A) never grows out of a good (resource-rich) patch into a bad (resource-poor) region, because the parent ramet withdraws its subsidy from the offspring. The ‘entering plant’ (E) always crosses the boundary, as the offspring is subsidized at the expense of the parent. In addition to these two extreme scenarios, an intermediate mixed strategy (M) will also be tested. The model is used to compare the efficiency of foraging in various habitats in which the proportion of resource-rich areas (p) is varied.

Methods

A stochastic cellular automata (CA) model is developed in which habitat space is represented by a honeycomb lattice. Each cell within the lattice can accommodate a single ramet, and colonization can occur from a parent ramet''s cell into six neighbouring cells. The CA consists of two layers: the population layer and the habitat. In the population layer, a cell can be empty or occupied by a ramet; in the habitat layer, a cell can be good (resource-rich) or bad (resource-poor). The habitat layer is constant; the population layer changes over time, according to the birth and death of ramets.

Key Results

Strategies M and E are primarily limited by patch distance, whereas A is more sensitive to patch size. At a critical threshold of the proportion of resource-rich areas, p = 0·5, the mean patch size increases abruptly. Below the threshold, E is more efficient than A, whilst above the threshold the opposite is true. The mixed strategy (M) is more efficient than either of the pure strategies across a broad range of p values.

Conclusions

The model predicts more species/genotypes with the ‘entering’ strategy, E, in habitats where resource-rich patches are scattered, and more plants with the ‘avoiding’ strategy, A, in habitats where the connectivity of resource-rich patches is high. The results suggest that the degree of physiological integration between a parent and an offspring ramet is important even across a very short distance because it can strongly influence the efficiency of foraging.  相似文献   

8.
Dynamics of the buried seeds and plant population of two dominant weeds, viz.,Emilia sonchifolia (Linn.) DC. andRichardsonia pilosa HBK were studied in the crop fields of Meghalaya, north-east India during radish and maize cropping and intervening fallow periods. The total buried seed population ofR. pilosa was always larger than that ofE. sonchifolia, but the germinable fraction was invariably greater in the latter. A major portion (39–41%) of the viable (germinable+dormant) seed population in both weeds was confined to the surface soil layer (0–5 cm). The viable seed population ofE. sonchifolia peaked during April, while that ofR. pilosa showed two peaks (during August and December). The survival pattern and half-lives of seedling cohorts showed, some differences in the two weed species, but both being summer annuals, their populations behaved in a similar manner by showing higher seedling recruitment (K) and survivorship (p) rates in the summer crop (maize) than in the winter crop (radish). However, the density of plants that could attain adulthood was significantly higher inE. sonchifolia thanR. pilosa which might have resulted in greater seed input of the former to the soil leading to its greater abundance in the crop fields.  相似文献   

9.
Optimal foraging theory has entered a new phase. It is not so much tested as used. It helps behavioural ecologists discover the nature of the information in an animals brain. It helps population ecologists reveal coefficients of interaction and their patterns of density-dependent variation. And it helps community ecologists examine niche relationships. In our studies on two species of Negev desert gerbil, we have taken advantage of the second and third of these functions. Both these gerbils prefer semi-stabilized dune habitat, and both altered their selective use of this habitat and stabilized sand according to experimental changes we made in their populations. Their changes in selectivity agree with a type of optimal foraging theory called isoleg theory. Isoleg theories provide examples of dipswitch theories – bundles of articulated qualitative predictions – that are easier to falsify than single qualitative predictions. By linking behaviour to population dynamics through isoleg theory, we were able to use the behaviour of the gerbils to reveal the shapes of their competitive isoclines. These have the peculiar non-linear shapes predicted by optimal foraging theory. Finally, when owl predation threatens, the behaviour of Gerbillus allenbyi reveals the shape of their victim isocline. As has long been predicted by predation theory and laboratory experiments, it is unimodal.  相似文献   

10.
Global Red List data on mammals, birds and plants for over 100non-island nations are used to identify the impact of area, endemism, humanpopulation, and many other social variables (urbanized population,human-dominated land, national wealth, % land protected) on proportions ofthreatened species among nations. Human population size and, especially,proportion of endemic species emerge as the strongest correlates of proportionof threatened species in nations. Area tends to increase both human populationand proportion of endemics and thus increases the proportion of threatenedspecies. Increasing wealth is associated with increased relative threat inmammals and plants. Proportion of land protected is significantly associatedwith decreased relative threat in mammals and birds.  相似文献   

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14.
Warming could strongly stabilize or destabilize populations and food webs by changing the interaction strengths between predators and their prey. Predicting the consequences of warming requires understanding how temperature affects ingestion (energy gain) and metabolism (energy loss). Here, we studied the temperature dependence of metabolism and ingestion in laboratory experiments with terrestrial arthropods (beetles and spiders). From this data, we calculated ingestion efficiencies (ingestion/metabolism) and per capita interaction strengths in the short and long term. Additionally, we investigated if and how body mass changes these temperature dependencies. For both predator groups, warming increased metabolic rates substantially, whereas temperature effects on ingestion rates were weak. Accordingly, the ingestion efficiency (the ratio of ingestion to metabolism) decreased in all treatments. This result has two possible consequences: on the one hand, it suggests that warming of natural ecosystems could increase intrinsic population stability, meaning less fluctuations in population density; on the other hand, decreasing ingestion efficiencies may also lead to higher extinction risks because of starvation. Additionally, predicted long‐term per capita interaction strengths decreased with warming, which suggests an increase in perturbation stability of populations, i.e., a higher probability of returning to the same equilibrium density after a small perturbation. Together, these results suggest that warming has complex and potentially profound effects on predator–prey interactions and food‐web stability.  相似文献   

15.
Rapid larval growth in insects may be selected for by rapid ephemeral phenological changes in food resources modifying the structure of phenotypic and genetic (co)variation in and among individual traits. We studied the relative effects of three processes which can modify expression of additive genetic and nongenetic variation in traits. First, natural selection tends to erode genetic variation in fitness-related traits. Second, there may be high variance even in traits closely coupled with fitness, if these traits are themselves products of variable lower level traits. Third, traits may be canalized by developmental processes which reduce phenotypic variation. Moreover, we investigated the phenotypic and genetic role played by the underlying traits in attaining simultaneously both large size and short development time. We measured phenotypic and genetic (co)variation in several pre- and post-ingestive foraging traits, growth, development rate, development time and size, together forming a hierarchical network of traits, in the larvae of a flush feeding geometrid, Epirrita autumnata. Rapid larval growth rate and high pupal mass are closely related to fitness in E. autumnata. Traits closely associated with larval growth displayed low levels of additive genetic variation, indicating that genetic variability may have been exhausted by selection for rapid growth. The body size of E. autumnata, in spite of its close correlation with fitness, exhibited a significant additive genetic variation, possiblye because caterpillar size is the outcome of many underlying heritable traits. The low level traits in the hierarchical net, number (indicating larval movements) and size of feeding bouts in leaves, relative consumption rate and efficiency of conversion of ingested food, displayed high levels of residual variation. High residual variation in consumption and physiological ability to handle leaf material resulted from their flexibility which reduced variation in growth rate, i.e. growth rate was canalized. We did not detect a trade-off between development time and final size. On the contrary, large pupal masses were attained by short larval periods, and this relationship was strongly genetically determined, suggesting that both developmental time and final size are expressions of the same developmental process (vigorous growth) and the same genes (or linkage disequilibrium).  相似文献   

16.
By varying the time spent searching for food, parasitoids modifytheir expected lifespan, and therefore their total lifetimereproductive success. Using a stochastic dynamic approach, wedefine the best choice between searching for food and searchingfor hosts as a function of the state of the parasitoid and theavailability of food when hosts and food are found in differentparts of the environment A first model deals with the influenceof food availability and survivorship conditions on the behaviorof a single parasitoid. Our results suggest that under conditionsof very low food availability, parasitoids should never searchfor food. When food availability is moderate, parasitoids shouldnot wait until their reserves are low before searching for food.When food is abundant and survivorship is independent of foodconsumption, parasitoids should search for food only when theirreserves are almost exhausted. They should not wait so longif survivorship depends on the energy reserves. By finding thestate-dependent ideal free distribution for a population ofparasitoids, we are able to predict their distribution betweenthe feeding area and the host living area at equilibrium. Theproportion of parasitoids in each area is altered by the numberof competitors and interference. Finally, the model predictsthat optimal time sharing between food searching and host searchingmay promote the stability of the host-parasitoid system.  相似文献   

17.
    
Understanding the drivers underlying fluctuations in the size of animal populations is central to ecology, conservation biology, and wildlife management. Reliable estimates of survival probabilities are key to population viability assessments, and patterns of variation in survival can help inferring the causal factors behind detected changes in population size. We investigated whether variation in age‐ and sex‐specific survival probabilities could help explain the increasing trend in population size detected in a small, discrete population of bottlenose dolphins Tursiops truncatus off the east coast of Scotland. To estimate annual survival probabilities, we applied capture–recapture models to photoidentification data collected from 1989 to 2015. We used robust design models accounting for temporary emigration to estimate juvenile and adult survival, multistate models to estimate sex‐specific survival, and age models to estimate calf survival. We found strong support for an increase in juvenile/adult annual survival from 93.1% to 96.0% over the study period, most likely caused by a change in juvenile survival. Examination of sex‐specific variation showed weaker support for this trend being a result of increasing female survival, which was overall higher than for males and animals of unknown sex. Calf survival was lower in the first than second year; a bias in estimating third‐year survival will likely exist in similar studies. There was some support first‐born calf survival being lower than for calves born subsequently. Coastal marine mammal populations are subject to the impacts of environmental change, increasing anthropogenic disturbance and the effects of management measures. Survival estimates are essential to improve our understanding of population dynamics and help predict how future pressures may impact populations, but obtaining robust information on the life history of long‐lived species is challenging. Our study illustrates how knowledge of survival can be increased by applying a robust analytical framework to photoidentification data.  相似文献   

18.
Tripleurospermum perforatum is an invasive weedy species which exhibits strong over-compensating density dependence. Interactions between density-dependent survival, probability of flowering and fecundity were modelled and their impact on the population dynamics were examined. When only fecundity was density-dependent, the dynamics were similar to those observed in the model containing all three density-dependent terms. Density-dependent survival was a stabilizing process when acting in combination with density-dependent fecundity and probability of flowering; removing density-dependent survival from the model produced two-point cycles. The addition of a seed bank was also stabilizing. Simulations of control strategies at different life-history stages indicated that full control would be difficult due to the strong over-compensating density dependence, with severe reductions in fecundity and late season survival necessary in order to reduce equilibrium seed density and biomass.  相似文献   

19.
Pre-dispersal seed predation may have important effects on population dynamics and trait evolution in plants. In this review, we first present a conceptual framework of the strength of pre-dispersal seed predation and its variation in space and time. We consider the interaction between plants and their seed predators to be “strong” when it affects plant population dynamics or causes changes in plant trait–fitness relationships, and “weak” when it has no such effects, and propose ways of how to adequately assess these effects. Second, we review the ecological literature between 1991 and 2005 to evaluate documented effects of pre-dispersal seed predation on plants and draw five major conclusions. (1) Pre-dispersal seed predation rates are usually low but sometimes high, and show a considerable variation in space and time. (2) Direct evidence suggests that pre-dispersal seed predation can have a significant effect on recruitment and plant population growth rate. Accumulating evidence of seed-limited recruitment suggests that such effects are common. (3) Pre-dispersal seed predation affects selection on several plant traits, such as flowering phenology and flower number, which are usually interpreted mainly in the context of plant–pollinator interactions. (4) The patterns of variation in the interactions between plants and pre-dispersal seed predators suggest that geographic selection mosaics may be common. (5) Although there are numerous studies estimating seed predation, there are still rather few studies that have aimed at examining the interaction explicitly in terms of effects on plant population dynamics and trait selection. From these we know that seed predators can have important, and often variable, effects on plant population dynamics and trait evolution. However, it still remains to assess how important they are across study systems and relative to other aspects of the plant's biotic and abiotic environment.  相似文献   

20.
    
Using diffusion processes, I model stochastic individual growth, given exogenous hazards and starvation risk. By maximizing survival to final size, optimal life histories (e.g. switching size for habitat/dietary shift) are determined by two ratios: mean growth rate over growth variance (diffusion coefficient) and mortality rate over mean growth rate; all are size dependent. For example, switching size decreases with either ratio, if both are positive. I provide examples and compare with previous work on risk‐sensitive foraging and the energy–predation trade‐off. I then decompose individual size into reversibly and irreversibly growing components, e.g. reserves and structure. I provide a general expression for optimal structural growth, when reserves grow stochastically. I conclude that increased growth variance of reserves delays structural growth (raises threshold size for its commencement) but may eventually lead to larger structures. The effect depends on whether the structural trait is related to foraging or defence. Implications for population dynamics are discussed.  相似文献   

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