Predator size and prey size: presumed relationship in the mantid Hierodula coarctata Saussure

1976 ◽  
Vol 54 (10) ◽  
pp. 1760-1764 ◽  
Author(s):  
C. S. Holling ◽  
R. L. Dunbrack ◽  
L. M. Dill
Keyword(s):  
Body Weight ◽  
Prey Size ◽  
Cube Root ◽  
Interspecific Relationship ◽  
Predator Prey ◽  
Mantis Shrimp ◽  
Predator Size ◽  
Size Relationship ◽  
Tibia Length

Measurements of tibia length and tibial hook angle were used to calculate optimum prey size in 714 specimens of the mantid Hierodula coarctata. These values were then regressed on the cube root of dry body weight to derive a presumed predator–prey size relationship for the species. Energetic arguments are advanced to account for the observed relationship. An interspecific relationship is also demonstrated for three species of mantids and two species of mantis shrimp (stomatopod crustaceans).

Feeding behaviour of predatory larvae of Atherix lantha Webb (Diptera: Athericidae)

1994 ◽  
Vol 72 (10) ◽  
pp. 1695-1699 ◽  
Author(s):  
Fiona F. Hunter ◽  
Astrid K. Maier
Keyword(s):  
Feeding Behaviour ◽  
Prey Species ◽  
Prey Size ◽  
Prey Type ◽  
Predator Prey ◽  
Size Classes ◽  
Predator Size ◽  
Oxygenated Water

Larvae of Atherix lantha Webb (Diptera: Athericidae) are piercing – sucking predators. Predator–prey experiments were conducted in beakers containing gravel substrates and airstone-oxygenated water. The predator:prey ratio used in all experiments was 5:5. One prey type was tested at a time. Prey tested included large and small heptageniid mayflies, hyalellid amphipods, and hydropsychid caddisflies. The effect of predator size was examined using two size classes of A. lantha larvae. Large A. lantha consumed more mayflies than did small A. lantha. However, amphipod mortality was the same with large as with small A. lantha. The effect of prey size on predation success was tested using two size classes of mayflies. Statistically, small A. lantha fed on equal numbers of small and large mayflies, whereas large A. lantha consumed more large than small mayflies. Data for species-wise comparisons are only available for small A. lantha; according to our results, hydropsychid caddisflies (average mortality (m) = 0.5346) are more vulnerable to predation than are hyalellid amphipods (m = 0.2041) and heptageniid mayflies (m = 0.1135–0.1813). However, the mortality of large mayflies caused by large A. lantha larvae (m = 0.5375) is the same as that of caddisflies caused by small A. lantha larvae. Thus, the vulnerability of prey species depends, in part, on predator size.

scholarly journals Atlantic cod and snow crab predator–prey size relationship in the Gulf of St. Lawrence, Canada

2008 ◽  
Vol 363 ◽  
pp. 227-240 ◽  
Author(s):  
D Chabot ◽  
B Sainte-Marie ◽  
K Briand ◽  
JM Hanson
Keyword(s):  
Atlantic Cod ◽  
Prey Size ◽  
Snow Crab ◽  
Predator Prey ◽  
Size Relationship

scholarly journals The mechanics of predator–prey interactions: First principles of physics predict predator–prey size ratios

2018 ◽  
Vol 33 (2) ◽  
pp. 323-334 ◽  
Author(s):  
Sébastien M. J. Portalier ◽  
Gregor F. Fussmann ◽  
Michel Loreau ◽  
Mehdi Cherif
Keyword(s):  
First Principles ◽  
Prey Size ◽  
Predator Prey

scholarly journals The impact of large terrestrial carnivores on Pleistocene ecosystems

2015 ◽  
Vol 113 (4) ◽  
pp. 862-867 ◽  
Author(s):  
Blaire Van Valkenburgh ◽  
Matthew W. Hayward ◽  
William J. Ripple ◽  
Carlo Meloro ◽  
V. Louise Roth
Keyword(s):  
Prey Size ◽  
Habitat Degradation ◽  
Terrestrial Ecosystems ◽  
Growth Data ◽  
Predator Prey ◽  
Body Sizes ◽  
Population Sizes ◽  
Potential Impact ◽  
The Impact ◽  
Ground Sloths

Large mammalian terrestrial herbivores, such as elephants, have dramatic effects on the ecosystems they inhabit and at high population densities their environmental impacts can be devastating. Pleistocene terrestrial ecosystems included a much greater diversity of megaherbivores (e.g., mammoths, mastodons, giant ground sloths) and thus a greater potential for widespread habitat degradation if population sizes were not limited. Nevertheless, based on modern observations, it is generally believed that populations of megaherbivores (>800 kg) are largely immune to the effects of predation and this perception has been extended into the Pleistocene. However, as shown here, the species richness of big carnivores was greater in the Pleistocene and many of them were significantly larger than their modern counterparts. Fossil evidence suggests that interspecific competition among carnivores was relatively intense and reveals that some individuals specialized in consuming megaherbivores. To estimate the potential impact of Pleistocene large carnivores, we use both historic and modern data on predator–prey body mass relationships to predict size ranges of their typical and maximum prey when hunting as individuals and in groups. These prey size ranges are then compared with estimates of juvenile and subadult proboscidean body sizes derived from extant elephant growth data. Young proboscideans at their most vulnerable age fall within the predicted prey size ranges of many of the Pleistocene carnivores. Predation on juveniles can have a greater impact on megaherbivores because of their long interbirth intervals, and consequently, we argue that Pleistocene carnivores had the capacity to, and likely did, limit megaherbivore population sizes.

scholarly journals Successful escape of bombardier beetles from predator digestive systems

2018 ◽  
Vol 14 (2) ◽  
pp. 20170647 ◽  
Author(s):  
Shinji Sugiura ◽  
Takuya Sato
Keyword(s):  
Ecological Factors ◽  
Laboratory Conditions ◽  
Predator Size ◽  
Size Relationship ◽  
Chemical Spray

Some prey animals can escape from the digestive systems of predators after being swallowed. To clarify the ecological factors that determine the success of such an escape, we investigated how the bombardier beetle Pheropsophus jessoensis escapes from two toad species, Bufo japonicus and B . torrenticola , under laboratory conditions. Pheropsophus jessoensis ejects a hot chemical spray from the tip of the abdomen when it is attacked. Although all toads swallowed the bombardier beetles, 43% of the toads vomited the beetles 12–107 min after swallowing them. All the vomited beetles were still alive and active. Our experiment showed that P . jessoensis ejected hot chemicals inside the toads, thereby forcing the toads to vomit. Large beetles escaped more frequently than small beetles, and small toads vomited the beetles more frequently than large toads. Our results demonstrate the importance of the prey–predator size relationship in the successful escape of prey from inside a predator.

scholarly journals A novel method optimizing the normalization of cardiac parameters in small animal models: the importance of dimensional indexing

2019 ◽  
Vol 316 (6) ◽  
pp. H1552-H1557 ◽  
Author(s):  
Quint A. J. Hagdorn ◽  
Guido P. L. Bossers ◽  
Anne-Marie C. Koop ◽  
Arnold Piek ◽  
Tim R. Eijgenraam ◽  
...  
Keyword(s):  
Body Weight ◽  
Animal Models ◽  
Animal Experiments ◽  
Three Dimensional ◽  
Small Animal ◽  
Left Ventricular ◽  
Heart Weight ◽  
Small Animal Models ◽  
Rats And Mice ◽  
Tibia Length

For indexing cardiac measures in small animal models, tibia length (TL) is a recommended surrogate for body weight (BW) that aims to avoid biases because of disease-induced BW changes. However, we question if indexing by TL is mathematically correct. This study aimed to investigate the relation between TL and BW, heart weight, ventricular weights, and left ventricular diameter to optimize the current common practice of indexing cardiac parameters in small animal models. In 29 healthy Wistar rats (age 5–34 wk) and 116 healthy Black 6 mice (age 3–17 wk), BW appeared to scale nonlinearly to TL1 but linearly to TL3. Formulas for indexing cardiac weights were derived. To illustrate the effects of indexing, cardiac weights between the 50% with highest BW and the 50% with lowest BW were compared. The nonindexed cardiac weights differed significantly between groups, as could be expected ( P < 0.001). However, after indexing by TL1, indexed cardiac weights remained significantly different between groups ( P < 0.001). With the derived formulas for indexing, indexed cardiac weights were similar between groups. In healthy rats and mice, BW and heart weights scale linearly to TL3. This indicates that not TL1 but TL3 is the optimal surrogate for BW. New formulas for indexing heart weight and isolated ventricular weights are provided, and we propose a concept in which cardiac parameters should not all be indexed to the same measure but one-dimensional measures to BW1/3 or TL1, two-dimensional measures to BW2/3 or TL2, and three-dimensional measures to BW or TL3. NEW & NOTEWORTHY In healthy rats and mice, body weight (BW) scales linearly to tibia length (TL) to the power of three (TL3). This indicates that for indexing cardiac parameters, not TL1 but TL3 is the optimal surrogate for BW. New formulas for indexing heart weight and isolated ventricular weights are provided, and we propose a concept of dimensionally consistent indexing. This concept is proposed to be widely applied in small animal experiments.

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