scholarly journals Size-dependent visual predation risk and the timing of vertical migration: An optimization model

2002 ◽  
Vol 47 (4) ◽  
pp. 925-933 ◽  
Author(s):  
Alex De Robertis
2000 ◽  
Vol 45 (8) ◽  
pp. 1838-1844 ◽  
Author(s):  
Alex De Robertis ◽  
Jules S. Jaffe ◽  
Mark D. Ohman

1998 ◽  
Vol 76 (10) ◽  
pp. 1878-1884 ◽  
Author(s):  
Edward P Levri

Foraging behavior can be influenced by such factors as predation risk, individual size, and parasite infection. Snails (Potamopyrgus antipodarum) placed in tanks with large rocks were exposed to four types of water: (1) water with crushed snails, (2) water from a tank in which fish (Gobiomorphus cotidianus) were fed only trout chow, (3) water from a tank where the fish were also fed snails, and (4) plain water. Snails could respond by moving to the top of rocks (where algal food was present) or to the bottom of rocks (where the predation risk was lower). The snails responded to fish chemicals by moving to the bottom of rocks. The response was dependent on snail size and fish diet. Smaller snails moved to the bottom of rocks more than larger snails did. Trematode-infected snails were found on top of the rocks more than other classes of snails, but infected snails still moved to the bottom of rocks in response to the fish predator. Snails eaten by fish in the field tend to be smaller than snails in the overall available population. Thus, snails that are more vulnerable to predation respond more intensely to the odor of fish by moving to the bottom of rocks. This size-dependent response to fish appears to be independent of the occurrence of trematode infection.


Oikos ◽  
2004 ◽  
Vol 104 (1) ◽  
pp. 109-121 ◽  
Author(s):  
Pär Byström ◽  
Jens Andersson ◽  
Lennart Persson ◽  
André M. De Roos

2007 ◽  
Vol 64 (12) ◽  
pp. 1747-1760 ◽  
Author(s):  
Espen Strand ◽  
Geir Huse

We investigate the trade-offs associated with vertical migration and swimming speed of Atlantic cod (Gadus morhua) using an adaptive individual-based model. Simulations with varying distribution and occurrence of prey, with and without swimbladder constraints, and visual predation were performed. Most simulations resulted in cod migrations between the bottom and pelagic zones. In simulations with high probability of encountering pelagic prey, the cod spent the daytime in the pelagic zone, moving to the bottom to feed only when no pelagic prey were encountered. At night the cod stayed in the pelagic zone to attain neutral buoyancy. In simulations with low occurrence of pelagic prey or high visual predation pressure, the cod remained at the bottom feeding on the consistently present benthic prey. If the pelagic prey occurred far above the sea floor or there were no benthic prey, the cod abandoned all bottom contact. The study thus predicts that the probability of encountering energy-rich pelagic prey is the key factor in driving vertical migration in adult cod. Buoyancy regulation is further shown to be an important constraint on vertical migration.


2021 ◽  
Vol 17 (2) ◽  
pp. 20200810
Author(s):  
Laura Hobbs ◽  
Neil S. Banas ◽  
Jonathan H. Cohen ◽  
Finlo R. Cottier ◽  
Jørgen Berge ◽  
...  

The predation risk of many aquatic taxa is dominated by visually searching predators, commonly a function of ambient light. Several studies propose that changes in visual predation will become a major climate-change impact on polar marine ecosystems. The High Arctic experiences extreme seasonality in the light environment, from 24 h light to 24 h darkness, and therefore provides a natural laboratory for studying light and predation risk over diel to seasonal timescales. Here, we show that zooplankton (observed using acoustics) in an Arctic fjord position themselves vertically in relation to light. A single isolume (depth-varying line of constant light intensity, the value of which is set at the lower limit of photobehaviour reponses of Calanus spp. and krill) forms a ceiling on zooplankton distribution. The vertical distribution is structured by light across timescales, from the deepening of zooplankton populations at midday as the sun rises in spring, to the depth to which zooplankton ascend to feed during diel vertical migration. These results suggest that zooplankton might already follow a foraging strategy that will keep visual predation risk roughly constant under changing light conditions, such as those caused by the reduction of sea ice, but likely with energetic costs such as lost feeding opportunities as a result of altered habitat use.


Hydrobiologia ◽  
2008 ◽  
Vol 614 (1) ◽  
pp. 321-327 ◽  
Author(s):  
Meryem Beklioglu ◽  
Ayse Gul Gozen ◽  
Feriha Yıldırım ◽  
Pelin Zorlu ◽  
Sertac Onde

2000 ◽  
Vol 57 (S3) ◽  
pp. 38-50 ◽  
Author(s):  
Geraint Tarling ◽  
Michael Burrows ◽  
Jack Matthews ◽  
Reinhard Saborowski ◽  
Friedrich Buchholz ◽  
...  

An optimisation model was developed to examine the effect of predation risk and environmental conditions on the diel vertical migration (DVM) of adult northern krill (Meganyctiphanes norvegica). Model predictions were compared in two locations with contrasting environmental conditions, the Clyde Sea and the Kattegat. The model was constructed from a combination of parameterised functions and empirical field data obtained during summer conditions. Parameter matrices were set up to cover the entire water column over a 24-h period. The first matrix contained values for "net energy gain," which incorporated empirical data on temperature-dependent respiration, copepod and phytoplankton abundance, and a functional response model for feeding rate. The second matrix expressed the risk of encountering a generalised visual (fish) predator as a function of light levels. The optimisation procedure sought a path through depth and time such that the energy gain was equal to the amount necessary to grow, produce eggs, and moult, while the risk of predation was minimised. The model predicted DVM in both the Clyde Sea and the Kattegat. Sensitivity analyses showed that the predicted DVM pattern was mainly driven by food and predation risk, with temperature effects on metabolic costs having a minor effect.


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