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Virginia Institute of Marine Science

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I tested the importance of both total cover and cover quality to the foraging ability of large Fundulus heteroclitus fish in tanks. Total cover was measured as the combined areas of all the individual structures, viewed as shadows. I divided total cover by the bottom area of the tank to form C-t/A(t), an index that measures the total amount of structure available in a given area for prey to hide behind. Cover quality was measured as the width of each individual structure divided by the width of the individual prey organism (C-w/P-w). This index measures how visible a prey organism is when hiding behind an individual structure. Both of these complexity indices are dimensionless and potentially applicable to any habitat type and habitat scale. I predicted that prey survivorship should increase hyperbolically with increasing C-t/A(t), because increasing the amount of structure within a habitat increases the amount of the habitat blocked off from detection, but with diminishing returns. Past experiments demonstrated that increased C-t/A(t) does increase prey survivorship, but the shape of the relationship was unclear. I also predicted that prey survivorship should increase hyperbolically with increasing C-w/P-w. I predicted this by simulating a prey organism hiding behind a flat structure being viewed by a predator from all potential angles. In this simple simulation, the 'average amount of the prey hidden from view' increased hyperbolically with increasing C-w/P-w, to an asymptote of 0.5. 1 performed 2 experiments to test these ideas, In the first, I kept C-t/A(t) constant between treatments and varied the width of the individual structures relative to the width of shrimp prey Paleomonetes spp. In the second experiment, I kept the inter-structural space widths nearly constant between treatments and varied C-t/A(t). The prey for the second experiment were mobile amphipods. I tested the hypothesis that survivorship and treatment were independent using log-linear models for both experiments. I found that there was no significant difference in survivorship between treatments for the C-w/P-w, experiment, and there was a significant difference in survivorship between treatments for the C-t/A(t) experiment. The relationship between C-t/A(t) and prey survivorship appeared to increase hyperbolically, as predicted. Finally, I used the results of the C-t/A(t) experiment, and results from a past study, to form a modeled regression equation of the survivorship surface for large F. heteroclitus feeding on amphipods for various levels of C-t/A(t) and Sp/Pr (inter-structural space size/predator width). This equation was highly significant, and fit the data well. In this regression, amphipod survivorship increased hyperbolically with increasing C-t/A(t), and decreased sigmoidally with increasing Sp/Pr.




amphipods; complexity; cover; dimensionless index; Fundulus heteroclitus; habitat structure; Paleomonetes spp.