Polymorphic populations are often considered as intermediate stages of speciation. Bluegill sunfish (Lepomis macrochirus) from Lake Waban, Wellesley, MA have diverged into two ecomorphs based on their diet, occupied habitat and morphology. Littoral bluegills are generalist feeders that consume a variety of aquatic invertebrates. Pelagic bluegills feed primarily on Daphnia. We aimed to understand if suction pressure generation, prey capture behaviors and pharyngeal jaw morphology differed between the littoral and pelagic ecomorphs feeding on three prey types. Littoral and pelagic bluegills showed similar feeding kinematics and peak pressure, however, significant differences were observed among prey types within an ecomorph. Feeding events on brine shrimp were slower and accompanied by less negative pressure for both ecomorphs. Littoral bluegills varied their use of ram among prey types, however, pelagic bluegills (zooplankton specialists) did not. Similar to previous studies, when presented with different prey items both dietary generalists and specialists varied equally in most aspects of their feeding behaviors. However, pelagic bluegills (dietary specialists) did not vary in their approach behaviors. Despite the lack of differences in trophic morphology among the individuals sampled here, the prey approach behaviors of dietary specialists appears to be fixed in pelagic bluegills. This result deemphasizes the importance of suction during feeding and places more importance on prey approach behaviors.
Temperature can have profound impacts on fitness‐related activities in fishes. Feeding is an ecologically relevant task which is controlled by muscle function. Consequently, in ectotherms, muscle function and feeding kinematics can be altered by temperature. This study investigated the effect of decreasing temperature on the feeding kinematics of the northern most labrid in the Western Atlantic. During winter, cunner (Tautogolabrus adspersus) enter a state of extended torpor in order to conserve energy when water temperatures drop below ~10°C. We hypothesized that feeding kinematics would be slower at lower temperatures especially those associated with torpor (≤10°C). Additionally, we hypothesized that prey type will elicit different feeding behaviors. Feeding events on sandworms and Asian shore crabs were recorded at 5, 10, 15 and 20°C. Fish held at 5°C had slower opening and closing jaw velocities while using more ram than the other temperature treatments. No differences were detected between prey types. For both prey types, the temperature treatment which consistently induced torpor (5°C) slowed oral jaw movements, which likely forced cunner to rely more on ram than suction to capture prey. Torpor temperatures appeared to have less of an effect on feeding than on metabolic rate, steady swimming capabilities and muscle function, suggesting some compensatory mechanisms of feeding musculature in cunner.
The goal for this project was to re-examine key morphological characters hypothesized to differentiate Gila intermedia, Gila robusta and Gila nigra and outline methods better suited for making species designations based on morphology. Using a combination of meristic counts, morphological measurements and geometric morphometrics, morphological dissimilarities were quantified among these three putative species. Traditional meristic counts and morphological measurements (i.e. distances between landmarks) were not useful for species identification. Geometric morphometrics, however, identified differences among species, while also suggesting an effect of geographic location on morphological variation. Using canonical variate analysis for the 441 fish sampled in this study, geometric morphometrics accurately predicted true group membership 100% of the time for G. nigra, 97% of the time for G. intermedia and 91% of the time for G. robusta. These results suggest that geometric morphometric analysis is necessary to identify morphological differences among the three species. Geometric morphometric analysis used in this study can be adopted by management officials as a tool to classify unidentified individuals.
Although the majority of teleost fishes possess a fused lower jaw (or mandible), some lineages have acquired a secondary joint in the lower jaw, termed the intramandibular joint (IMJ). The IMJ is a new module that formed within the already exceptionally complex teleost head, and disarticulation of two bony elements of the mandible potentially creates a "double-jointed" jaw. The apparent independent acquisition of this new functional module in divergent lineages raises a suite of questions. (1) How many teleostean lineages contain IMJ-bearing species? (2) Does the IMJ serve the same purpose in all teleosts? (3) Is the IMJ associated with altered feeding kinematics? (4) Do IMJ-bearing fishes experience trade-offs in other aspects of feeding performance? (5) Is the IMJ used to procure prey that are otherwise unavailable? The IMJ is probably under-reported, but has been documented in at least 10 lineages within the Teleostei. Across diverse IMJ-bearing lineages, this secondary joint in the lower jaw serves a variety of functions, including: generating dynamic out-levers that allow fish to apply additional force to a food item during jaw closing; allowing fish to "pick" individual prey items with pincer-like jaws; and facilitating contact with the substrate by altering the size and orientation of the gape. There are no consistent changes in feeding kinematics in IMJ-bearing species relative to their sister taxa; however, some IMJ-bearing taxa produce very slow movements during the capture of food, which may compromise their ability to move prey into the mouth via suction. Despite diversity in behavior, all IMJ-bearing lineages have the ability to remove foods that are physically attached to the substrate or to bite off pieces from sessile organisms. Because such prey cannot be drawn into the mouth by suction, the IMJ provides a new mechanism that enables fish to obtain food that otherwise would be unavailable.
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