scholarly journals Hierarchical Functional Response of a Forager on a Wetland Landscape

2021 ◽  
Vol 9 ◽  
Author(s):  
Donald L. DeAngelis ◽  
Simeon Yurek ◽  
Stephen Tennenbaum ◽  
Hyo Won Lee
Keyword(s):  
Functional Response ◽  
Time Scale ◽  
Consumption Rate ◽  
Prey Consumption ◽  
Water Levels ◽  
Hierarchical Level ◽  
Short Time Scale ◽  
Functional Responses ◽  
Wetland Landscape ◽  
Wading Bird

We show that for some foragers the form that a functional response takes depends on the temporal and spatial scales considered. In representing the consumption rate of an organism, it may be necessary to use a hierarchy of functional responses. Consider, for example, a wading bird foraging in wetland landscape characterized by a spatial distribution of potential foraging sites, such as ponds. At the smallest time scale of minutes or hours, during which a wading bird is foraging within a single site, the functional response will reflect the local density of prey, as well as features of the site that affect the feeding rate, such as water depth. At this short time scale, which is determined by the giving up time of the wading bird in a particular site, prey density may be relatively constant. The food intake from a particular pond is then the product of the time spent before giving-up time and moving to another site and the rate of prey consumption at that site. A prey-centered functional response is most appropriate for describing the prey consumption rate. We propose that over the longer time scale of a day, during which a wading bird may visit several foraging sites, the type of functional response can be considered to be patch centered. That is, it is influenced by the spatial configuration of sites with available prey and the wading bird’s strategy of choosing among different sites and decisions on how long to stay in any given sites. Over the time scale of a day, if the prey densities stay relatively constant, the patch-centered functional response for a constant environment is adequate. However, on the longer time scale of a breeding season, in which changing water levels result in temporal changes in the availability of prey in sites, a third hierarchical level may be relevant. At that scale, the way in which the landscape pattern changes through time, and how the wading bird responds, influences the functional response. This hierarchical concept applies to a colony of breeding wading birds foraging in wetlands such as the Everglades.

scholarly journals Functional response of Harmonia axyridis preying on Acyrthosiphon pisum nymphs: the effect of temperature

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yasir Islam ◽  
Farhan Mahmood Shah ◽  
Xu Rubing ◽  
Muhammad Razaq ◽  
Miao Yabo ◽  
...  
Keyword(s):  
Functional Response ◽  
High Performance ◽  
Acyrthosiphon Pisum ◽  
Harmonia Axyridis ◽  
Effect Of Temperature ◽  
Functional Responses ◽  
Aphid Control ◽  
Host Aphid ◽  
Predator Foraging

AbstractIn the current study, we investigated the functional response of Harmonia axyridis adults and larvae foraging on Acyrthosiphon pisum nymphs at temperatures between 15 and 35 °C. Logistic regression and Roger’s random predator models were employed to determine the type and parameters of the functional response. Harmonia axyridis larvae and adults exhibited Type II functional responses to A. pisum, and warming increased both the predation activity and host aphid control mortality. Female and 4th instar H. axyridis consumed the most aphids. For fourth instar larvae and female H. axyridis adults, the successful attack rates were 0.23 ± 0.014 h−1 and 0.25 ± 0.015 h−1; the handling times were 0.13 ± 0.005 h and 0.16 ± 0.004 h; and the estimated maximum predation rates were 181.28 ± 14.54 and 153.85 ± 4.06, respectively. These findings accentuate the high performance of 4th instar and female H. axyridis and the role of temperature in their efficiency. Further, we discussed such temperature-driven shifts in predation and prey mortality concerning prey-predator foraging interactions towards biological control.

An Alternative Test Using Algal Cultures for Testing Chemicals for Toxicity

1993 ◽  
Vol 21 (2) ◽  
pp. 196-201
Author(s):  
Søren Achim Nielsen ◽  
Thomas Hougaard
Keyword(s):  
Size Distribution ◽  
Mitotic Activity ◽  
Time Scale ◽  
Test System ◽  
Short Time Scale ◽  
Toxic Substances ◽  
Alternative Test ◽  
Short Time ◽  
Algal Cultures ◽  
Test Cultures

An alternative test is presented, in which algal cultures are used for testing toxic substances. This test system is based on variations in the size distribution of cells in test cultures as a measurement of growth. Thus, inhibition of mitotic activity is used as a measurement for toxic effects. The test can be performed on a short time-scale and is very sensitive to even weak toxic doses.

scholarly journals Applying predator-prey theory to modelling immune-mediated, within-host interspecific parasite interactions

Parasitology ◽  
2010 ◽  
Vol 137 (6) ◽  
pp. 1027-1038 ◽  
Author(s):  
ANDY FENTON ◽  
SARAH E. PERKINS
Keyword(s):  
Functional Response ◽  
Interspecific Interactions ◽  
Parasite Load ◽  
Multiple Infections ◽  
Functional Responses ◽  
Predator Prey ◽  
Immune Activity ◽  
Parasite Communities ◽  
Immune Mediated ◽  
Predator Prey Models

SUMMARYPredator-prey models are often applied to the interactions between host immunity and parasite growth. A key component of these models is the immune system's functional response, the relationship between immune activity and parasite load. Typically, models assume a simple, linear functional response. However, based on the mechanistic interactions between parasites and immunity we argue that alternative forms are more likely, resulting in very different predictions, ranging from parasite exclusion to chronic infection. By extending this framework to consider multiple infections we show that combinations of parasites eliciting different functional responses greatly affect community stability. Indeed, some parasites may stabilize other species that would be unstable if infecting alone. Therefore hosts' immune systems may have adapted to tolerate certain parasites, rather than clear them and risk erratic parasite dynamics. We urge for more detailed empirical information relating immune activity to parasite load to enable better predictions of the dynamic consequences of immune-mediated interspecific interactions within parasite communities.

Effect of predation on the low-density dynamics of vendace: significance of the functional response

2001 ◽  
Vol 58 (10) ◽  
pp. 1909-1923 ◽  
Author(s):  
Outi Heikinheimo
Keyword(s):  
Functional Response ◽  
Brown Trout ◽  
Salmo Trutta ◽  
Dynamic Modelling ◽  
Perca Fluviatilis ◽  
Low Density ◽  
Functional Responses ◽  
Density State ◽  
Brown Trout Salmo Trutta ◽  
Stock Recruitment

During the past 20 years, there have been prolonged vendace (Coregonus albula) recessions in several Finnish lakes. Hypotheses have been proposed that predation by brown trout (Salmo trutta m. lacustris) or perch (Perca fluviatilis) on young-of-the-year vendace could prevent the recovery of the vendace stocks from a low-density state. In this study, dynamic modelling was applied to examine the effect of predation, assuming a dome-shaped spawning stock–recruitment relationship for vendace, type II or III functional responses to predation by brown trout and perch, and a constant rate of fishing. The results showed that the form of the functional response is crucial in determining the significance of the predation on vendace stocks that have a steep dome-shaped stock–recruitment relationship. In all cases, however, predation by perch had more effect than that by brown trout, probably due to perch occupying the pelagic zone when the vendace stock is sparse. This may make the mortality of vendace increase with decreasing population density (depensatory mortality) at certain density levels.

scholarly journals Permanence of Periodic Predator-Prey System with Functional Responses and Stage Structure for Prey

2008 ◽  
Vol 2008 ◽  
pp. 1-15 ◽  
Author(s):  
Can-Yun Huang ◽  
Min Zhao ◽  
Hai-Feng Huo
Keyword(s):  
Functional Response ◽  
Prey Species ◽  
Necessary Conditions ◽  
Stage Structure ◽  
Functional Responses ◽  
Predator Prey ◽  
Predator Prey Model ◽  
Prey System ◽  
Sufficient And Necessary Conditions ◽  
Holling Ii Functional Response

A stage-structured three-species predator-prey model with Beddington-DeAngelis and Holling II functional response is introduced. Based on the comparison theorem, sufficient and necessary conditions which guarantee the predator and the prey species to be permanent are obtained. An example is also presented to illustrate our main results.

Use of Functional Response Modeling to Evaluate the Effect of Temperature on Predation of Amblyseius swirskii (Acari: Phytoseiidae) Adults Preying on Tetranychus urticae (Acari: Tetranychidae) Nymphs

2021 ◽  
Author(s):  
Azadeh Farazmand ◽  
Masood Amir-Maafi
Keyword(s):  
Functional Response ◽  
Tetranychus Urticae ◽  
Attack Rate ◽  
Handling Time ◽  
Effect Of Temperature ◽  
Coefficient Of Determination ◽  
Temperature Threshold ◽  
Amblyseius Swirskii ◽  
Functional Responses ◽  
Wide Range

Abstract In this research, functional responses of Amblyseius swirskii Athias-Henriot preying on different Tetranychus urticae Koch nymphal densities (2, 4, 8, 16, 32, 64, and 128) were studied at eight constant temperatures (15, 20, 25, 27.5, 30, 32.5, 35 and 37.5°C) in a circular Petri dish (3-cm diameter × 1-cm height) under lab conditions. At all temperatures, the logistic regression showed a type II functional response. A nonlinear relationship was found between temperature and attack rate and the reciprocal of handling time. The reciprocal of handling time decreased exponentially with increasing temperature. In contrast, the attack rate grew rapidly with increasing temperatures up to an optimum, showing a decreasing trend at higher temperatures. In order to quantify the functional response of A. swirskii over a broad range of temperatures and to gain a better estimation of attack rate and handling time, a temperature-settled functional response equation was suited to our data. Our model showed that the number of prey consumed increased with rising prey density. Also, the predation rates increased with increasing temperatures but decreased at extremely high temperatures. Based on our model, the predation rate begins at the lower temperature threshold (11.73°C) and reaches its peak at upper temperature threshold (29.43°C). The coefficient of determination (R2) of the random predator model was 0.99 for all temperatures. The capability of A. swirskii to search and consume T. urticae over a wide range of temperatures makes it a good agent for natural control of T. urticae in greenhouses.

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