Ontogenetic niche feeding partitioning in juvenile of white sea catfish Genidens barbus in estuarine environments, southern Brazil

Author(s):  
Manuel Mendoza-Carranza ◽  
João Paes Vieira

Ontogenetic diet changes (prey species richness and size) in juveniles of white sea catfish (Genidens barbus) were tested in three southern Brazilian estuaries: Mampituba (29°12′S), Tramandaí (30°02′S), Chuí (33°44′S). Cluster analysis revealed that white sea catfish juvenile populations in the three estuaries are composed of two feeding groups. These two feeding groups are coincident with a bimodal size–age distribution of the juveniles of white sea catfish. In small catfish (5 to 10 cm TL) copepods were the most numerous prey (Chuí = 86.66%N, Tramandaí = 85.52%N and Mampituba = 52.34%N). In large catfish (10 to 20 cm TL) the most abundant and frequent prey was fish (Chuí: 73.19%N and 74.56%FO; Tramandaí: 85.92%N and 73.33%FO; Mampituba: 52.34%N and 61.54%FO). The Morisita overlap index among small and large fish was low in all estuaries; high values of Morisita's similarity index were observed among same size catfish groups. In all cases, no differences were observed among prey bio-volume curves of same size predator groups (small, F = 0.41, P = 0.65; large, F = 2.19, P = 0.11). In all estuaries, prey size increased significantly with increasing predator size. The 90th regression quantile estimated with most precision the predator–prey size relationship.

1994 ◽  
Vol 72 (10) ◽  
pp. 1695-1699 ◽  
Author(s):  
Fiona F. Hunter ◽  
Astrid K. Maier

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.


1970 ◽  
Vol 48 (6) ◽  
pp. 1229-1240 ◽  
Author(s):  
R. Stewart Anderson

Experimental studies on Diaptoimus shoshone, D. arcticus, D. nevadensis, Cyclops bicuspidatus thomasi, C. vernalis, and Branckinecta gigas show that these predatory species can capture and eat many prey species of various sizes. B. gigas probably combines raptorial with filter feeding and can eat 150 or more smaller crustaceans per day. Adult D. shoshone, D. arcticus, and D. nevadensis eat up to 12 or more cyclopoids or diaptomids per day. Rotifers are also preferred prey. Predation rates are inversely proportional to prey size. Cannibalism probably causes the uniformity in body size and instar of predaceous diaptomids in some populations, C. vernalis and C. b. thomasi can eat six or more prey animals daily, depending on the size of the prey. Predaceous diaptomids and cyclopoids will eat the same prey species at rates which are influenced more by hunger than by abundance of prey. Furthermore, each species is a potential predator on the other, where the role of predator or prey is determined by the relative size or instar of the two groups. Hence, codominance of the zooplankton by predaceous diaptomid and cyclopoid species is unlikely.


1999 ◽  
Vol 202 (15) ◽  
pp. 2083-2089 ◽  
Author(s):  
H. Malli ◽  
L. Kuhn-Nentwig ◽  
H. Imboden ◽  
W. Nentwig

Previous experimental studies have shown that neotropical wandering spiders (Cupiennius salei) inject more venom when attacking larger crickets. It has been postulated that this is a consequence of predator-prey interactions during envenomation, which increase in intensity with the size of a given prey species. The present study was designed to test this hypothesis using anaesthetized crickets of different sizes that were moved artificially. Cupiennius salei was found (1) to inject more venom the greater the intensity of the struggling movement of the crickets (prey size kept constant); (2) to inject more venom the longer the duration of the struggling movement of the crickets (prey size and intensity of movement kept constant); and (3) to inject equal amounts into crickets of different size (duration and intensity of movement kept constant). These results indicate that C. salei alters the amount of venom it releases according to the size and motility of its prey. Venom expenditure depends mainly on the extent of the interactions with the prey during the envenomation process, whereas prey size is of minor significance. The regulation of venom injection in concert with behavioural adaptations in response to various types of prey minimizes the energetic cost of venom production, thus increasing the profitability of a given prey item.


Author(s):  
Xavier Lambin

The dependency of mustelid demographic rates on prey abundance has the potential to cause a strong coupling between predator-prey populations. Data on mustelid dynamics show that such strong reciprocal interactions only materialise in some restricted conditions. Bite-size mustelid predators searching for scarce, depleted prey expose themselves to increased risk of predation by larger predators of small mammal that are themselves searching for similar prey species. As voles or muskrats become scarcer, weasels and mink searching for prey over larger areas become increasingly exposed to intra-guild predation, unless they operate in a habitat refuge such as the sub-nivean space. Where larger predators are sufficiently abundant or exert year-round predation pressure on small mustelids, their impact on mustelids may impose biological barrier to dispersal that are sufficient to weaken the coupling between small mustelids and their rodent prey, and thus impose a degree of top down limitation on mustelids.


1986 ◽  
Vol 64 (11) ◽  
pp. 2624-2633 ◽  
Author(s):  
Peter F. Major ◽  
Lawrence M. Dill ◽  
David M. Eaves

Three-dimensional interactions between grouped aerial predators (frontal discs of aircraft engines), either linearly arrayed or clustered, and flocks of small birds were studied using interactive computer simulation techniques. Each predator modelled was orders of magnitude larger than an individual prey, but the prey flock was larger than each predator. Expected numbers of individual prey captured from flocks were determined for various predator speeds and trajectories, flock–predator initial distances and angles, and flock sizes, shapes, densities, trajectories, and speeds. Generally, larger predators and clustered predators caught more prey. The simulation techniques employed in this study may also prove useful in studies of predator–prey interactions between schools or swarms of small aquatic prey species and their much larger vertebrate predators, such as mysticete cetaceans.The study also provides a method to study problems associated with turbine aircraft engine damage caused by the ingestion of small flocking birds, as well as net sampling of organisms in open aquatic environments.


2010 ◽  
Vol 2010 ◽  
pp. 1-12
Author(s):  
Xiangzeng Kong ◽  
Zhiqin Chen ◽  
Li Xu ◽  
Wensheng Yang

We propose and study the permanence of the following periodic Holling III predator-prey system with stage structure for prey and both two predators which consume immature prey. Sufficient and necessary conditions which guarantee the predator and the prey species to be permanent are obtained.


2008 ◽  
Vol 2008 ◽  
pp. 1-15 ◽  
Author(s):  
Can-Yun Huang ◽  
Min Zhao ◽  
Hai-Feng Huo

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.


2012 ◽  
Vol 102 (2) ◽  
pp. 131-137 ◽  
Author(s):  
Marta J. Cremer ◽  
Pedro C. Pinheiro ◽  
Paulo C. Simões-Lopes

The present study provides information about the diet of sympatric populations of small cetaceans in the Babitonga Bay estuary. This is the first study on the diet of these species in direct sympatry. The stomach contents of seven Guiana dolphins Sotalia guianensis and eight franciscanas Pontoporia blainvillei were analyzed. The prey of both cetaceans was mostly teleost fishes, followed by cephalopods. We identified 13 teleost fishes as part of the diet of the franciscanas, and 20 as part of the diet of Guiana dolphins. Lolliguncula brevis was the only cephalopod recorded, and was the most important prey for both cetaceans. Stellifer rastrifer and Gobionellus oceanicus were also important for franciscana, so as Mugil curema and Micropogonias furnieri were important for Guiana dolphins. Stellifer rastrifer and Cetengraulis edentulus were the fishes with the highest frequency of occurrence for franciscana (50%), while Achirus lineatus, C. edentulus, S. brasiliensis, Cynoscion leiarchus, M. furnieri, M. curema, Diapterus rhombeus, Eugerres brasilianus and G. oceanicus showed 28.6% of frequency of occurrence for Guiana dolphins. Franciscanas captured greater cephalopods than the Guiana dolphins in both total length (z= -3.38; n= 40; p< 0.05) and biomass (z = -2.46; n = 40; p<0.05). All of the prey species identified occur inside the estuary, which represents a safe habitat against predators and food availability, reinforcing the importance of the Babitonga Bay for these cetacean populations.


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

2015 ◽  
Vol 113 (4) ◽  
pp. 862-867 ◽  
Author(s):  
Blaire Van Valkenburgh ◽  
Matthew W. Hayward ◽  
William J. Ripple ◽  
Carlo Meloro ◽  
V. Louise Roth

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.


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