Home About us Contact
|
Home About us Contact | ||
|
|
||
Swimming Mode (swimming + mode)
Selected AbstractsEffect of light and predator abundance on the habitat choice of plant-attached zooplanktonFRESHWATER BIOLOGY, Issue 3 2007LEENA NURMINEN Summary 1. The diurnal variations in the habitat choice of the periodically plant-attached cladoceran Sida crystallina together with light environment and predator abundance were studied. 2. The density of S. crystallina attached to floating leaves of Nuphar lutea increased between 18:00 and 20:00 hours, when light intensity underneath the leaves was temporarily increased, and decreased again when light intensity declined. A proportion of S. crystallina remained in the swimming mode underneath the leaves even during daylight, indicating that the water column sheltered by the leaves is safer than the open water. 3. In the water adjacent to the leaves, the density of S. crystallina increased steeply in the dark. The increase was not accompanied by a decrease in S. crystallina attached to plant leaves, indicating that the nocturnal increment in the open water density of S. crystallina was due to migration from daytime refuges other than floating leaves. 4. Sida crystallina was most intensively consumed by perch (Perca fluviatilis). Predation threat by fish had weaker effects on the density of S. crystallina attached to plant leaves than on cladocerans in the adjacent water. Cladocerans underneath floating plant leaves, whether attached or not, are probably less vulnerable to fish predation than those outside the leaf cover. 5. The results suggested that light intensity is the proximate factor regulating the attachment of zooplankton to the lower surfaces of floating macrophyte leaves. Light intensity has a positive effect on the density of S. crystallina attached to the floating leaves and a negative effect on density in the water. Predation threat by fish has a strong effect on the migration of zooplankters into the open water habitat. [source] Jordan's and other ecogeographical rules, and the vertebral number in fishesJOURNAL OF BIOGEOGRAPHY, Issue 3 2008R. M. McDowall Abstract Aim, To explore variation in the number of vertebrae in fishes in the context of Jordan's rule and other ecogeographical rules. Location, Global. Methods, The study is based on literature review. Results, The number of vertebrae varies very widely across the diversity of fishes. Jordan's rule states that vertebral number increases with latitude, and this is widely attributed to ambient temperatures during ontogeny of individual fishes. However, the number of vertebrae may depend on both the ontogenetic environment and inheritance. Diverse other aspects of fish development and ecology are suggested as influencing vertebral number, including fish size, phyletic position, body shape and swimming mode. Main conclusions, The number of different factors that influence the number of vertebrae in fishes makes for highly complex patterns of variation, and means that unravelling causes is difficult. The question needs to be addressed at the population/species/species group scale; moreover, the lack of discrimination between environmental and inherited causes of variation adds to the complexity. [source] The musculotendinous system of an anguilliform swimmer: Muscles, myosepta, dermis, and their interconnections in Anguilla rostrataJOURNAL OF MORPHOLOGY, Issue 1 2008Nicole Danos Abstract Eel locomotion is considered typical of the anguilliform swimming mode of elongate fishes and has received substantial attention from various perspectives such as swimming kinematics, hydrodynamics, muscle physiology, and computational modeling. In contrast to the extensive knowledge of swimming mechanics, there is limited knowledge of the internal body morphology, including the body components that contribute to this function. In this study, we conduct a morphological analysis of the collagenous connective tissue system, i.e., the myosepta and skin, and of the red muscle fibers that sustain steady swimming, focusing on the interconnections between these systems, such as the muscle-tendon and myosepta-skin connections. Our aim is twofold: (1) to identify the morphological features that distinguish this anguilliform swimmer from subcarangiform and carangiform swimmers, and (2) to reveal possible pathways of muscular force transmission by the connective tissue in eels. To detect gradual morphological changes along the trunk we investigated anterior (0.4L), midbody (0.6L), and posterior body positions (0.75L) using microdissections, histology, and three-dimensional reconstructions. We find that eel myosepta have a mediolaterally oriented tendon in each the epaxial and hypaxial regions (epineural or epipleural tendon) and two longitudinally oriented tendons (myorhabdoid and lateral). The latter two are relatively short (4.5,5% of body length) and remain uniform along a rostrocaudal gradient. The skin and its connections were additionally analyzed using scanning electron microscopy (SEM). The stratum compactum of the dermis consists of ,30 layers of highly ordered collagen fibers of alternating caudodorsal and caudoventral direction, with fiber angles of 60.51 ± 7.05° (n = 30) and 57.58 ± 6.92° (n = 30), respectively. Myosepta insert into the collagenous dermis via fiber bundles that pass through the loose connective tissue of the stratum spongiosum of the dermis and either weave into the layers of the stratum compactum (weaving fiber bundles) or traverse the stratum compactum (transverse fiber bundles). These fiber bundles are evenly distributed along the insertion line of the myoseptum. Red muscles insert into lateral and myorhabdoid myoseptal tendons but not into the horizontal septum or dermis. Thus, red muscle forces might be distributed along these tendons but will only be delivered indirectly into the dermis and horizontal septum. The myosepta-dermis connections, however, appear to be too slack for efficient force transmission and collagenous connections between the myosepta and the horizontal septum are at obtuse angles, a morphology that appears inadequate for efficient force transmission. Though the main modes of undulatory locomotion (anguilliform, subcarangiform, and carangiform) have recently been shown to be very similar with respect to their midline kinematics, we are able to distinguish two morphological classes with respect to the shape and tendon architecture of myosepta. Eels are similar to subcarangiform swimmers (e.g., trout) but are substantially different from carangiform swimmers (e.g., mackerel). This information, in addition to data from kinematic and hydrodynamic studies of swimming, shows that features other than midline kinematics (e.g., wake patterns, muscle activation patterns, and morphology) might be better for describing the different swimming modes of fishes. J. Morphol., 2008. © 2007 Wiley-Liss, Inc. [source] Fish functional design and swimming performanceJOURNAL OF FISH BIOLOGY, Issue 5 2004R. W. Blake Classifications of fish swimming are reviewed as a prelude to discussing functional design and performance in an ecological context. Webb (1984a, 1998) classified fishes based on body shape and locomotor mode into three basic categories: body and caudal fin (BCF) periodic, BCF transient (fast-starts, turns) and median and paired fin (MPF) swimmers. Swimming performance and functional design is discussed for each of these categories. Webb hypothesized that specialization in any given category would limit performance in any other. For example, routine MPF swimmers should be penalized in BCF transient (fast-start propulsion). Recent studies offer much support for Webb's construct but also suggest some necessary amendments. In particular, design and performance compromises for different swimming modes are associated with fish that employ the same propulsor for more than one task (coupled, e.g. the same propulsor for routine steady swimming and fast-starts). For example, pike (BCF transient specialist) achieve better acceleration performance than trout (generalist). Pike steady (BCF periodic) performance, however, is inferior to that of trout. Fish that employ different propulsors for different tasks (decoupled, e.g. MPF propulsion for low-speed routine swimming and BCF motions for fast-starts) do not show serious performance compromises. For example, certain MPF low-speed swimmers show comparable fast-start performance to BCF forms. Arguably, the evolution of decoupled locomotor systems was a major factor underlying the adaptive radiation of teleosts. Low-speed routine propulsion releases MPF swimmers from the morphological constraints imposed by streamlining allowing for a high degree of variability in form. This contrasts with BCF periodic swimming specialists where representatives of four vertebrate classes show evolutionary convergence on a single, optimal ,thunniform' design. However, recent experimental studies on the comparative performance of carangiform and thunniform swimmers contradict some of the predictions of hydromechanical models. This is addressed in regard to the swimming performance, energetics and muscle physiology of tuna. The concept of gait is reviewed in the context of coupled and decoupled locomotor systems. Biomimetic approaches to the development of Autonomous Underwater Vehicles have given a new context and impetus to research and this is discussed in relation to current views of fish functional design and swimming performance. Suggestions are made for possible future research directions. [source] The musculotendinous system of an anguilliform swimmer: Muscles, myosepta, dermis, and their interconnections in Anguilla rostrataJOURNAL OF MORPHOLOGY, Issue 1 2008Nicole Danos Abstract Eel locomotion is considered typical of the anguilliform swimming mode of elongate fishes and has received substantial attention from various perspectives such as swimming kinematics, hydrodynamics, muscle physiology, and computational modeling. In contrast to the extensive knowledge of swimming mechanics, there is limited knowledge of the internal body morphology, including the body components that contribute to this function. In this study, we conduct a morphological analysis of the collagenous connective tissue system, i.e., the myosepta and skin, and of the red muscle fibers that sustain steady swimming, focusing on the interconnections between these systems, such as the muscle-tendon and myosepta-skin connections. Our aim is twofold: (1) to identify the morphological features that distinguish this anguilliform swimmer from subcarangiform and carangiform swimmers, and (2) to reveal possible pathways of muscular force transmission by the connective tissue in eels. To detect gradual morphological changes along the trunk we investigated anterior (0.4L), midbody (0.6L), and posterior body positions (0.75L) using microdissections, histology, and three-dimensional reconstructions. We find that eel myosepta have a mediolaterally oriented tendon in each the epaxial and hypaxial regions (epineural or epipleural tendon) and two longitudinally oriented tendons (myorhabdoid and lateral). The latter two are relatively short (4.5,5% of body length) and remain uniform along a rostrocaudal gradient. The skin and its connections were additionally analyzed using scanning electron microscopy (SEM). The stratum compactum of the dermis consists of ,30 layers of highly ordered collagen fibers of alternating caudodorsal and caudoventral direction, with fiber angles of 60.51 ± 7.05° (n = 30) and 57.58 ± 6.92° (n = 30), respectively. Myosepta insert into the collagenous dermis via fiber bundles that pass through the loose connective tissue of the stratum spongiosum of the dermis and either weave into the layers of the stratum compactum (weaving fiber bundles) or traverse the stratum compactum (transverse fiber bundles). These fiber bundles are evenly distributed along the insertion line of the myoseptum. Red muscles insert into lateral and myorhabdoid myoseptal tendons but not into the horizontal septum or dermis. Thus, red muscle forces might be distributed along these tendons but will only be delivered indirectly into the dermis and horizontal septum. The myosepta-dermis connections, however, appear to be too slack for efficient force transmission and collagenous connections between the myosepta and the horizontal septum are at obtuse angles, a morphology that appears inadequate for efficient force transmission. Though the main modes of undulatory locomotion (anguilliform, subcarangiform, and carangiform) have recently been shown to be very similar with respect to their midline kinematics, we are able to distinguish two morphological classes with respect to the shape and tendon architecture of myosepta. Eels are similar to subcarangiform swimmers (e.g., trout) but are substantially different from carangiform swimmers (e.g., mackerel). This information, in addition to data from kinematic and hydrodynamic studies of swimming, shows that features other than midline kinematics (e.g., wake patterns, muscle activation patterns, and morphology) might be better for describing the different swimming modes of fishes. J. Morphol., 2008. © 2007 Wiley-Liss, Inc. [source] | ||||||||||