Foraging is one of the most important endeavors undertaken by animals, and it has been studied intensively from both mechanistic-empirical and optimal foraging perspectives. Planktivorous fish make excellent study organisms for foraging studies because they feed frequently and in a relatively simple environment. Most optimal foraging studies of planktivorous fish have focused, either on diet choice or habitat selection and have assumed that these animals used a cruise search foraging strategy. We have recently recognized that white crappie do not use a cruise search strategy (swimming continuously and searching constantly) while foraging on zooplankton but move in a stop and go pattern, searching only while paused. We have termed thissaltatory search. Many other animals move in a stop and go pattern while foraging, but none have been shown to search only while paused. Not only do white crappie search in a saltatory manner but the components of the search cycle change when feeding on prey of different size. When feeding on large prey these fish move further and faster after an unsuccessful search than when feeding on small prey. The fish also pause for a shorter period to search when feeding on large prey. To evaluate the efficiency of these alterations in the search cycle, a net energy gain simulation model was developed. The model computes the likelihood of locating 1 or 2 different size classes of zooplankton prey as a function of the volume of water scanned. The volume of new water searched is dependent upon the dimensions of the search volume and the length of the run. Energy costs for each component of the search cycle, and energy gained from the different sized prey, were assessed. The model predicts that short runs produce maximum net energy gains when crappie feed on small prey but predicts net energy gains will be maximized with longer runs when crappie feed on large prey or a mixed assemblage of large and small prey. There is an optimal run length due to high energy costs of unsuccessful search when runs are short and reveal little new water, and high energy costs of long runs when runs are lengthy. The model predicts that if the greater search times observed when crappie feed on small prey are assessed when they feed on a mixed diet of small and large prey, net energy gained is less than if small prey are deleted from the diet. We believe the model has considerable generality. Many animals are observed to move in a saltatory manner while foraging and some are thought to search only while stationary. Some birds and lizards are, known to modify the search cycle in a manner similar to white crappie.

Many species of fish exhibit metamorphosis in which dramatic external transformations occur as a consequence of coordinated changes in gene expression within an organism. Because postembryonic development and change appears to be the rule rather than the exception in teleost fish species, we view metamorphosis as one of many developmental strategies in fish which have continued plasticity as a common theme. Metamorphic changes are manifested in the visual system by modification of photoreceptor peak sensitivity, rod photoreceptor cell addition, and retinal reorganization. These changes correspond to significant changes in the natural habitat of the animal and in its visual capabilities as demonstrated behaviorally. Thyroxine is the main metamorphic hormone as has also been found in amphibia. The sequence of metamorphic events occur in all teleosts, but they are compressed in time in direct developing animals suggesting that such animals might prove useful for understanding the evolution of metamorphosis in fish. It seems likely that rod photoreceptors may have evolved in conjunction with the change from larval to juvenile stage through metamorphosis in indirect developing fishes. During evolution, the contraction and/or loss of the larval stage has resulted in earlier appearance of rod photoreceptors during development although they always arise later than cone photoreceptors. This ontogenetic developmental sequence supports Walls's (1942) proposal that cones are phylogenetically older than rods and suggests that rods may have evolved several times.

Predators are often categorized as either cruise or ambush feeding strategists. We present evidence that white crappie (Pomoxis annularis) are neither. Instead, the crappie swim intermittently and search only when stationary. If the crappie searched while swimming, one would expect the run speeds to be slower than the pursuit speeds, but no difference was found between these two measurements. Assuming that prey are located while swimming, a foreshortening of runs prior to pursuit would also be expected, but again, none was detectable. The duration of the search pause appears to be related to the detectability of the prey. Crappie also search during the pause immediately following the attack and ingestion of a prey item. The observation that the probabilities of detecting and pursuing a prey following a run or an attack do not differ significantly supports this conclusion. Also, the duration of the pause following a run or attack does not differ significantly over a wide range of temperatures. If these views are correct, white crappie could not forage optimally by either deleting located prey items from the diet or minimizing handling time. What they appear to be doing is creatively managing their search time.

The habitat occupied by larval winter flounder (Pseudopleuronectes americanus) differs considerably in light regime from that of the adult. To understand how the visual system has adapted to such changes, photoreceptor spectral absorbance was measured microspectrophotometrically in premetamorphic and postmetamorphic specimens of winter flounder. Before metamorphosis, larval flounder retinas contain only one kind of photoreceptor which is morphologically cone-like with peak absorbance at 519 nm. After metamorphosis, the adult retina has three types of photoreceptors: single cones, double cones, and rods. The visual pigment in single cones has a peak absorbance at X max = 457 nm, the double cones at X max = 531 and 547 nm, and the rod photoreceptors at X max = 506 nm. Double cones were morphologically identical, but the two members contained either different (531/547 nm) or identical pigments (531/531 nm). The latter type were found only in the dorsal retina. The measured spectral half-bandwidths (HBW) were typical of visual pigments with chromophores derived from vitamin A! with the possible exception of the long-wavelength absorbing pigment in double cones which appeared slightly broader. Because the premetamorphic pigment absorbance has a different X max than those of the postmetamorphic pigments, different opsin genes must be expressed before and after metamorphosis.

Winter flounder (Pseudopleuronectes americanus) are hatched as bilaterally symmetric larvae which live near the ocean surface. At metamorphosis, they become laterally compressed, one eye migrates to the opposite side of the head, and they live the remainder of their lives lying on their blind side on the ocean floor. The present study characterizes and quantifies retinal cell distribution throughout the larval period and contrasts it with the adult retina. Based on light- and electron-microscopic analyses, retinas of larval flounder contain only a single cone-like photoreceptor type, arranged in a hexagonal array. In contrast, after metamorphosis, the adult retina has three types of photoreceptors: rods, single cones, and double cones. Rod photoreceptors are numerous in the ventral retina and decrease in density dorsad. The cone photoreceptor density, in contrast to rods, is higher in the dorsal retina decreasing ventrad. Adult cone photoreceptors are arranged in a square mosaic with four double cones surrounding one single cone. The differences in larval and adult retinal morphology reflect the distinctly different habitat each occupies.