A great diversity of unicellular and invertebrate organisms swim along a helical path, but it is not well understood how asymmetries in the body shape or the movement of propulsive structures affect a swimmer’s ability to perform the body rotation necessary to move helically. The present study found no significant asymmetries in the body shape of ascidian larvae (Distaplia occidentalis) that could operate to rotate the body during swimming. By recording the three-dimensional movement of free-swimming larvae, it was found that the tail possessed two bends, each with constant curvature along their length. As these bends traveled posteriorly, the amplitude of curvature changes was significantly greater in the concave-left direction than in the concave-right direction. In addition to this asymmetry, the tail oscillated at an oblique angle to the midline of the trunk. These asymmetries generated a yawing moment that rotated the body in the counterclockwise direction from a dorsal view, according to calculations from hydrodynamic theory. The tails of resting larvae were bent in the concave-left direction with a curvature statistically indistinguishable from the median value for tail curvature during swimming. The flexural stiffness of the tails of larvae, measured in three-point bending, may be great enough to allow the resting curvature of the tail to have an effect on the symmetry of kinematics. This work suggests that asymmetrical tail motion is an important mechanism for generating a yawing moment during swimming in ascidian larvae and that these asymmetries may be caused by the tail’s bent shape. Since helical motion requires that moments also be generated in the pitching or rolling directions, other mechanisms are required to explain fully how ascidian larvae generate and control helical swimming.
Organisms spanning great phylogenetic diversity and a wide range of body sizes swim along a helical path. Helical swimming has been observed in unicellular swimmers with cilia (e.g. Paramecium caudatum, Loxodes rostrum) (Jennings, 1901) and flagella (e.g. Tubularia crocea spermatozoa) (Miller and Brokaw, 1970) (Chlamydomonas reinhardtii) (Boscov and Feinleib, 1979). Many marine invertebrate larvae use cilia to swim helically (e.g. chordate lancelet larvae) (Stokes, 1997) (sponge planula) (Bergquist et al., 1970) (mollusc veligers) (Jonsson et al., 1991) (echinoderm doliolaria) (Mladenov and Chia, 1983), and ascidian larvae follow a helical path by propelling themselves by tail undulation (Grave, 1920). Helical swimming also occurs in vertebrates that swim by undulating their bodies but have undeveloped or impaired spatial orientation. For example, early-stage larvae of the frog Xenopus laevis are thought to swim helically because they have undeveloped vestibular organs, and late-stage larvae can be made to swim helically by ablating their vestibular organ (Roberts et al., 2000). Ullén et al. (Ullén et al., 1995) caused adult lamprey Lampetra fluviatilis to swim helically by ablating their vestibular organ, thereby demonstrating that at least some vertebrates swim helically when they lack the sensory feedback necessary to control body rotation.
To move along a curvilinear trajectory such as a helix, an organism must rotate its body as it moves forward (see Crenshaw et al., 2000). An organism’s weight, buoyancy and swimming hydrodynamics have all been hypothesized to generate the moments (i.e. torques) for rotation and the forces for forward movement (Young, 1995). Moments can be generated by hydrodynamics from asymmetries either in the body shape of swimmers or in the motion of their propulsive structures. Such mechanisms appear to play a role in the helical swimming of Tubularia crocea spermatozoa, which beat their flagella with asymmetrical undulations (Miller and Brokaw, 1970). Jennings (Jennings, 1901) suggested that helical swimming in many microorganisms is generated by asymmetrical body shapes. Knight-Jones (Knight-Jones, 1954) implied a hydrodynamic mechanism for body rotation when he reported that metachronal waves in ciliary beating are directed at an oblique angle to the long axis of the body in a diversity of metazoans that swim helically. Although these studies suggest a variety of mechanisms for helical swimming, two fundamental questions remain untested: (i) do morphological and kinematic asymmetries generate moments that act to rotate the body during helical swimming, and (ii) how are kinematic asymmetries generated?
The present study addresses these questions by testing hypotheses about the mechanics of helical swimming in ascidian larvae. Swimming plays a brief but important role in the ecology of this relatively large group of urochordates (ascidians include around 3000 species) (Jeffery, 1997). Larvae disperse in the ocean for a duration ranging from a few minutes (e.g. Botrylloides sp.) (Worcester, 1994) to 10 days (e.g. Ascidia mentula) (Svane, 1984) and do not feed. After this dispersal phase, larvae metamorphose into a sessile juvenile form. Therefore, helical swimming in the larval phase is the only opportunity for locomotion in the life cycle of an individual.
Both morphological and kinematic asymmetries have been hypothesized to enable ascidian larvae to swim along a helical trajectory. Grave (Grave, 1920) suggested that the subtle depression on the left side of the trunk of Aplidium constellatum larvae contributes to the generation of their right-handed (i.e. clockwise when viewed from the rear) helical trajectory. The tail fin of Aplidium constellaum is thought to twist during swimming undulations and thereby cause the body to rotate (Mast, 1921). The tail of many species has been observed to bend to one side of the body when at rest (Berrill, 1950). If the flexural stiffness of the larval tail is substantial, then this asymmetry in shape could cause an asymmetry in motion that may help to rotate the body. Furthermore, if the tail stiffness resists tail bending more in one direction than the other, then further kinematic asymmetry should result.
Ascidian larvae are well suited for this investigation because their tail motion when freely swimming is easier to observe than the patterns of movement by the fields of cilia used by many other helical swimmers (e.g. bivalve veligers) (Jonsson et al., 1991) (ciliated metazoans) (Knight-Jones, 1954) (microorganisms) (Jennings, 1901). The study species, Distaplia occidentalis, is abundant in Northern California, USA, and is reproductively active for a long period during the summer and autumn. The larvae of Distaplia occidentalis possess a visibly dark ocellus and a light trunk, which makes it possible to measure the body orientation in three dimensions from video sequences. Furthermore, larvae of D. occidentalis are relatively large (mean body length 3.50mm), so tail stiffness could be measured more easily than in smaller larvae.
By measuring the body shape of resting larvae, the flexural stiffness of the tail and the motion of the body during swimming, I tested the following hypotheses: (i) that the trunk and tail fin possess morphological asymmetries; (ii) that the tail undulates with an asymmetrical kinematic pattern; (iii) that the flexural stiffness provides greater resistance to deflection in one direction than the other; and (iv) that kinematic asymmetries generate moments that act to rotate the body.
Materials and methods
In the months of August and September in 1999, Distaplia occidentalis (Bancroft) were collected from floating docks at the Spud Point Marina in Bodega Bay, CA, USA, in water that was between 11 and 16°C. Colonies were transported within 2h to a cold room at the University of California, Berkeley, CA, USA, where they were held at temperatures between 13 and 17°C. To stimulate release of larvae, colonies were exposed to bright artificial light after being kept in darkness overnight (Cloney, 1987). Released larvae were placed in an aquarium that was cooled with a water bath at 15°C. Within 2h of release, one of three experiments was conducted on an individual larva. A larva was (i) videotaped while swimming, (ii) photographed while resting or (iii) used for measurements of tail flexural stiffness. All experiments were conducted within 4 days of collection of the adult colony.
Digital still images of resting larvae from dorsal and lateral views were captured by computer (7100/80 PowerPC Macintosh with Rasterops 24XLTV frame grabber) using a video camera (Sony, DXC-151A) mounted on a dissecting microscope (Nikon, SMZ-10A). Images of the body shape were measured using NIH Image software (version 1.62) on an Apple Macintosh G3 computer. These images had a spatial resolution of 640×480 pixels, with each pixel representing a square with sides measuring approximately 7μm.
All morphometric measurements were made relative to the body’s midline. In the trunk, this midline was defined as the axis running through the center of intersection of the trunk with the tail and the center of the three adhesive papillae at the anterior end of the trunk (Fig.1). To test for dorso-ventral morphological asymmetries, the distance between the dorsal margin of the trunk and the midline was compared with the distance between the ventral margin and the midline at 20 equally spaced longitudinal positions. At each of these trunk positions, the distance between the right margin of the trunk and the midline was compared with the distance between the left margin and the midline as a measure of bilateral symmetry (Fig.2).
The larval tail is composed of a cellular portion, containing the notochord, muscle and nerve cells, and the extracellular tail fin made of tunic tissue (Burighel and Cloney, 1997). The midline of the tail at each longitudinal position was centered between the left, right, dorsal and ventral margins of the cellular region. To test for dorso-ventral asymmetries in the tail fin, the distance from the midline to the dorsal margin was compared with the distance from the midline to the ventral margin at 10 equally spaced longitudinal positions.
The curvature of the tail of resting larvae was measured to determine whether larvae are consistently bent towards the same side of the body. Resting curvature was measured as the mean value of discrete measures of curvature (see Fig.1B) at all tail positions. The present study considers the side of the tail with the nerve cord to be in the dorsal direction (as in Burighel and Cloney, 1997) for the trunk and tail (this is not always the convention for ascidian larvae) (e.g. Cavey and Cloney, 1972).
Swimming larvae were filmed simultaneously with two digital high-speed video cameras recording at 500framess−1 (Redlake PCI Mono/100S Motionscope, 320×280 pixels per camera, each equipped with a 50mm macro lens (in the arrangement described by Crenshaw, 1991). The cameras were directed in perpendicular directions and both were focused on a small volume (1cm3) of water in the center of an aquarium (3cm×3cm×6cm). Larvae were illuminated from the side with two fiber-optic lamps (Cole Parmer 9741-50). The aquarium was built with a separate outer chamber into which chilled water flowed from a water bath equipped with a thermostat (VWR Scientific, 1166) to maintain a water temperature of approximately 15°C. Larvae generally swam in the vertical direction and passively sank to the bottom of the tank when resting. As in most species of ascidian larvae, swimming could be stimulated by briefly dimming the illuminators (the ‘shadow response’) (Grave, 1941). Once initiated, swimming behavior continued with the lights on and ceased after larvae arrived at the water’s surface.
The three-dimensional swimming movements of the trunk and tail were acquired and analyzed with custom-designed computer programs. Since the trunk was assumed to be rigid, its motion was described by changes in the position of a point in the center of the three anterior papillae and a second point at the intersection of the trunk and tail (Fig.1B). The coordinates of both points were manually selected with an Apple PowerMac G3 with NIH Image software (version 1.62). Using the same procedure, the movement of the ocellus was tracked to later reconstruct the body axes in the analysis stage. Since larvae were the brightest figures (i.e. the pixels with the lowest values) in the video frames, the silhouette of the tail could be traced automatically. The midline of the tail was found by ‘dissolving’ its silhouette (see Russ, 1999) to a line with a width of 1 pixel with a custom-designed macro in NIH Image. A second macro found between 5 and 20 coordinate pairs (X and Z) along the midline’s length in one video frame, then referred to the corresponding video frame recorded by the other camera to find matching coordinates in the third dimension (Y). This acquisition of three-dimensional coordinates was completed for every frame of video for a period of approximately 1s (500 video frames) in sequences in which larvae appeared to swim vertically along a straight helical trajectory.
The tail kinematics were analyzed in four stages: (i) the coordinates of unequal number and spacing in the camera’s frame of reference were transformed into 20 evenly spaced points in the frame of reference of the body, (ii) the shape of the midline of the tail was described using the angle between the trunk and the tail (trunk angle) and a curvature function for each instant of time, (iii) changes in tail midline shape and trunk angle with time were described and (iv) asymmetries in this kinematic pattern were tested. These four stages are described below in detail.
Stage 1: transforming midline coordinates into evenly spaced points in the body’s frame of reference
The first stage in the kinematic analysis transformed the variable number of coordinates describing the tail midline (described above) into 20 evenly spaced points for each instant of time. Programs for this analysis were written with Matlab software (version 5.2, Mathworks). The positions of points along the length of the tail were calculated by measuring the sum of the distances between points. To describe the relationships between tail position and each of the three spatial dimensions with a continuous expression, coefficients describing a fifth-order polynomial were found by least-squares approximation for each spatial dimension. Polynomials of the fifth order were the lowest order that described the shape of the tail well. Equidistant coordinate points were found by solving these functions for 20 tail positions at equal intervals. The result was a description of 19 tail segments of equal length in three-dimensional space. To ensure against operator error and smoothing errors, two-dimensional projections of these coordinates were plotted back on the original video frames for verification. Swimming sequences were discarded if coordinate points were not aligned with the midline of the body. This criterion combined with the relatively brief duration that individuals remained within view of both cameras restricted the analysis to a single tail-beat cycle per individual.
Using methodology described by Craig (Craig, 1989), the body’s frame of reference was defined for larvae using the three coordinate points describing the trunk’s position. The origin of the body’s coordinate system was defined as the intersection point between the tail and trunk, and the anterio-posterior axis was defined by the line between this point and the center of the papillae at the anterior end of the trunk. Using the position of the ocellus within the trunk measured in resting individuals, the lateral and dorso-ventral axes were reconstructed. Tail coordinates in the camera’s frame of reference were then transformed into coordinates relative to the body’s frame of reference.
Stage 2: describing tail midline shape
By observing the swimming of ascidian larvae, it was apparent that conventional methods for kinematic description would not suffice. The classical kinematic analyses for fish swimming (e.g. Lighthill, 1975; Webb et al., 1984) were insufficient because (i) no simple axis of progression (e.g. the straight path of a swimming fish) (McHenry et al., 1995) exists for swimmers following a three-dimensional curvilinear trajectory, (ii) the curvature of the tail was so great that it could not be described by a function with a single independent variable in Cartesian space and (iii) symmetrical kinematics could not be assumed. Therefore, coordinates describing tail shape in single video frames were described by the angle between the trunk and the tail (trunk angle) and curvature (κ) as a function of tail position. For these measurements, the discrete form of curvature was used (see Fig.1B).
Brokaw (Brokaw, 1965) found that the shape of the flagellum of bull spermatozoa during swimming was better described by a series of adjoining semi-circles than by conventional kinematic equations (e.g. Gray and Hancock, 1955). As is characteristic of circles, these semi-circular portions of the tail were constant in curvature along their length. The tail shape of D. occidentalis may also be described by bends of constant curvature, one bent to the right and another bent to the left of the body (Fig.3A,C,E). Therefore, tail shape at a single instant of time may be described by one concave-left curvature (κCL), one concave-right curvature (κCR) and the position along the body’s length (s) where the semi-circles intersect, which is the inflection point (si). The following equation shows how curvature varies as a function of tail position:
This expression means that, in the first half of a tail beat (t<0.5), tail curvature, κ(s,t), anterior to the inflection point (s<si) is equal to κCR, but is equal to κCL posterior to the inflection point (s>si). In the second half of the tail beat (t>0.5), tail curvature equals κCL anterior to (s<si) and κCR posterior to (s>si) the inflection point. This pattern of curvature is illustrated for two instants of time in Fig.3, in which concave-right curvatures are positive in sign and concave-left curvatures are negative. Trunk angle (θ), a variable that completed the description of body shape, is the angle between the trunk’s midline and the first anterior segment of the tail (Fig.1B).
The following equations were used to translate the midline shape variables (θ, κCL, κCR and si) into a series of coordinate points that could be compared with the data:
where Δs is tail segment length and n is the tail segment number. These equations calculate the position of the posterior end of segment n. These relationships show that the position of the end of the first tail segment (n=1) is dependent on the trunk angle θ. The curvature at the intersection of each segment pair (sn) affects the position of all segments posterior to it. By trial and error, values for θ, then anterior curvature (κCL or κCR), then the inflection point (si) and then posterior curvature (κCL or κCR) were selected on the basis of the visual closeness of fit between the curve that they described and the data. Fig.3 illustrates the midline data and the curves that describe their shape.
Stage 3: measuring shape changes over time
After determining values for the midline shape variables (θ, κCL, κCR and si) for each instant in time at 2ms intervals, the next objective was to describe how these variables changed with time. An equation describing how each variable changed with time was created (see Results), and the values for parameters in these equations were found using a non-linear least-squares algorithm (Matlab version 5.2, Mathworks). Although the exact form of these equations could not be predicted, their parameters were apparent from qualitative observation of the swimming motion. The inflection point si was expected to travel down the tail at some wave speed ε. Trunk angle θ appeared to vary periodically with time and was therefore expected to oscillate above and below a value β with an amplitude equal to αθ. Since tail curvature has been shown to oscillate with time in swimming fish (e.g. Katz and Shadwick, 1998), it was expected that the amplitude of changes in concave-left curvature (αCL) and concave-right curvature (αCR) could be measured.
Stage 4: testing for kinematic asymmetries
Asymmetries in undulatory motion were described by how each of the variables describing midline shape (θ, κCL, κCR and si) changed with time. Three sources of asymmetry were hypothesized and tested (see below). (i) As observed in the turning maneuvers of the eel Anguilla rostrata (Gray, 1933), the speed with which waves travel down the tail may vary with time. Wave speed ε was hypothesized to be different between the first and second halves of the tail-beat cycle. (ii) An asymmetry would also result if the trunk angle oscillated around a non-zero baseline value (β). (iii) Unequal values for the amplitude of curvature changes between the concave-left (αCL) and concave-right (αCR) sides should also cause asymmetry.
Tail bending stiffness
To address whether tails resist deflection more in one direction than the other, three-point bending tests were conducted using the general approach taken by Adams et al. (Adams et al., 1990) for Xenopus laevis embryonic notochords. A beam of known stiffness was pushed against the lateral surface of the tail to place it in bending. This beam, which was composed of silver, was 5cm in length and 100μm in diameter. The two static points held in opposition to the beam were placed 0.4mm apart. All lateral deflections of both the silver beam and the portion of tail in bending were kept below 10% of their length in order not to violate the assumptions of low-deflection beam theory. This theory uses the following equation to calculate flexural stiffness from a three-point bending test (Adams et al., 1990):
where EI is the flexural stiffness, F is the force that the tip of the silver beam exerted on the tail, l is the length of the portion of the tail between the two supports and δ is the lateral deflection of the tail resulting from the load.
Kinematics and morphometrics alone can only provide qualitative hypotheses for their effect on the mechanics of swimming. The hydrodynamic model of Jordan (Jordan, 1992) was used to calculate a quantitative prediction of the turning moments generated by the kinematics and morphometrics measured for D. occidentalis. This model is appropriate for the size and swimming speed range of ascidian larvae, where both viscous and inertial forces are important to their hydrodynamics. Reynolds number (Re) represents the ratio of inertial to viscous forces and it is calculated as:
where U is the swimming speed, L is a characteristic length (taken as the distance between the anterior margin of the trunk and the posterior margin of the tail) and ν is the kinematic viscosity. The mean ±1 s.d. Re calculated for D. occidentalis larvae was 92.9±20 (N=11; see Table1).
Jordan (Jordan, 1992) modeled the hydrodynamic forces generated by swimming at intermediate Reynolds’ numbers (1<Re<1000) by body undulation for the chaetognath Sagitta elegans. According to this blade-element model, the force acting on a segment of the tail is the vector sum of the acceleration reaction (i.e. ‘reactive forces’, Freactive), and the quasi-steady forces acting normal and tangential to the segment (i.e. ‘resistive forces’, Fresistive). The following equations were used to calculate the instantaneous force (Ftotal) acting on a tail segment:
where ρ is the density of water, A is the surface area of the tail segment, Cn and Ct are the respective normal and tangential force coefficients, Vn and Vt are the normal and tangential components of velocity for the segment, n̂ is the unit vector normal to the surface of the tail segment, n̂ is the unit vector tangential to the surface of the tail segment and m is the mass of water accelerated by the tail segment, known as the added mass. A unit vector has a magnitude of 1 and, in this case, points in the normal or tangential direction of a tail segment with respect to the global (i.e. inertial) frame of reference (Thomas and Finney, 1980). Added mass was calculated using the method described by Lighthill (Lighthill, 1975) for each tail segment:
where Δs is the length and h is the height of the tail segment (the distance between the dorsal and ventral margins of the fin). Acceleration of a tail segment was calculated as the component of the discrete changes in velocity in the direction normal to the tail’s surface (ΔVn) divided by change in time (Δt). The following equations for the normal and tangential force coefficients were used (Jordan, 1992):
Since larvae swam steadily, the conventional measure of Re for undulatory swimmers (equation 5) was used instead of the method of Jordan (Jordan, 1992), which calculates Re for each instant of time.
The forces and moments generated by each tail segment were calculated using the measured morphometrics of the tail (see above) and the kinematics from the body’s frame of reference (see above) for each instant of time. The origin of this coordinate system was positioned at the intersection of the tail and the trunk, a point I will refer to as the center of body. The total moment around the center of body was equal to the sum of all moments generated by tail segments. To assess whether the kinematics generated greater moments in one direction than the other, the mean value of total moments during left-directed half tail beats was compared with the mean value during right-directed half tail beats. These calculations were executed with Matlab (version 5.2, Mathworks) software running on a computer (IBM Thinkpad 760XD).
Statistical tests were used to detect asymmetries in body morphology, kinematics, turning moments and the bending stiffness of the tail. A Kolomogorov–Smirnov test was used to test the normality of data (Sokal and Rohlf, 1995). When samples were found not to be normally distributed (i.e. Kolomogorov–Smirnov test, P<0.05), the median and range were reported. The assumption of normality was avoided when comparing samples by using a non-parametric Mann–Whitney U-test. Samples were considered significantly different if the Mann–Whitney U-test found P<0.05 (Sokal and Rohlf, 1995). Normally distributed samples (i.e. Kolomogorov–Smirnov test, P>0.05) were reported by their mean and standard deviation. These distributions were considered significantly different if a Student’s t-test found P<0.05. Since no data could be assumed to have a normal distribution, data are illustrated in the figures by their median, range, quartiles and outliers rather than by their mean and standard deviation.
Symmetry of the trunk and tail fin
In the trunk, no significant differences were detected between the distances from the left margin of the body to the midline and from the right margin to the midline (Mann–Whitney U-test, P>0.05, N=18; Fig.2A). Comparisons between the distances from the midline to the dorsal margin of the larva and the distances from the midline to the ventral margin were also not significantly different at any position along the length of the trunk or tail (Mann–Whitney U-test, P>0.05, N=18; Fig.2B). These data suggest that the bodies of larvae are symmetrical with respect to the midline in all individuals (N=18). Although symmetrical, the tails of all larvae were bent in the concave-left direction, as illustrated by the individual shown in Fig.1 (measurements of resting tail curvature given below).
Symmetry of the undulatory motion
An example of the changes with time in the shape of the midline of the tail in a swimming larva is illustrated in Fig.3. Changes in concave-left curvature (κCL), concave-right curvature (κCR), the position of the inflection point (si) and the trunk angle (θ) were described by the following functions of time (Fig.4):
The data used to test the three possible sources of kinematic asymmetry are shown in Fig.5. The amplitude of concave-left curvature (median 0.68radmm−1, range 0.41radmm−1, N=11) is significantly different (Mann–Whitney U-test, P≪0.001, N=11; Fig.5A) from concave-right curvature in the same tail beat (median 0.42radmm−1, range 0.40radmm−1, N=11), and this difference generates asymmetry in the motion of the tail. The ratio of αCL to αCR is a measure of kinematic asymmetry; a value of 1 corresponds to no asymmetry due to curvature differences. Because it is often more convenient to measure maximum values of curvature than the amplitude of curvature changes, the ratio of αCL to αCR for swimming sequences was compared with the ratio of maximum curvature in the concave-left (κCLmax) and the concave-right (κCRmax) directions for the same sequences. These ratios were found to be statistically indistinguishable (unpaired two-tailed t-test, P=0.624), as represented by the following relationship:
The ratio αCL to αCR (1.9±0.8, mean ±1 s.d.,N=11) was greater than 1 in all larvae (Kolomogorov–Smirnov, P>0.05), which means that the maximum curvature on the concave-left side was greater than the curvature on the concave-right side. Trunk angle oscillated around a baseline value (β) that was significantly less than zero (Fig.5C) (Kolomogorov–Smirnov, P>0.05; mean ±1 s.d. −0.13±0.08rad; one-tailed t-test, P<0.001, N=11), meaning that the trunk is generally bent in the concave-left direction. Wave speed (ε), in contrast, did not appear to be a source of kinematic asymmetry because it was not significantly different between the left-directed (median 8.3mms−1, range 47.5mms−1, N=11) and right-directed (median 42.2mms−1, range 37.5mms−1, N=11) halves of the tail beat and therefore cannot cause any asymmetries (Mann–Whitney U-test, P=0.49, N=11; Fig.5B).
To summarize these results, the tails of larvae moved with asymmetries that resulted in the tail bending more towards to the left than towards the right (Fig.3, Fig.4, Fig.5). Two parameters describe these asymmetries: curvature amplitude and baseline trunk angle. Curvature amplitude was greater in the concave-left than in the concave-right direction. Baseline trunk angle was found to be significantly less than zero, which means that the tail oscillated at an oblique angle towards the left of the midline of the trunk.
The median tail curvature measured over the tail-beat cycle was compared with the tail curvature of resting larvae. The median value was chosen because, unlike the mean, its value does not vary with the speed of tail motion. There was no significant difference between the tail curvature of resting larvae and the median value for tail curvature in swimming larvae (both samples normally distributed: Kolomogorov–Smirnov test, P>0.05; two-tailed, unpaired t-test, P=0.964, N=11; Fig.6C).
Flexural stiffness of the tail
Larval tail bending stiffness did not require more force to deflect the tail in one direction than in the other (Fig.7). This result refutes the hypothesis that an asymmetry in flexural stiffness causes the kinematic asymmetries observed. Although stiffness in some individuals was greater in the concave-left direction than the concave-right direction (e.g. Fig.7A), concave-left stiffness (median 0.29×10−13Nm2, range 2.01×10−13Nm2, N=13) was generally not significantly different (Mann–Whitney U-test, P=0.419, N=13) from concave-right stiffness (median 0.40×10−13Nm2, range 1.08×10−13Nm2, N=13; Fig.7B) among larvae.
Turning moments predicted from the kinematic asymmetries
The hydrodynamic model of Jordan (Jordan, 1992) for intermediate-Re swimming was used to formulate predictions for the turning moments generated by the kinematic patterns observed for D. occidentalis larvae (Fig.8). The time-averaged mean moment (1.75×10−9±0.12×10−9Nm, mean ±1 s.d.,N=11) for the kinematics of single tail beats was significantly greater than zero and therefore acted in the counterclockwise direction (Kolomogorov–Smirnov test, P>0.05; one-tailed, unpaired t-test, P=0.019). This result supports the hypothesis that the kinematic asymmetries observed (Fig.3, Fig.4, Fig.5) act as a mechanism to rotate the body.
Generation of kinematic asymmetries
The similarity between median tail curvature during swimming and the tail curvature of larvae at rest (Fig.6) suggests that the shape of the resting tail may affect the symmetry of tail midline kinematics. However, if the muscle stress required to bend the tail is negligible compared with the stress that the muscles are capable of generating, then it is unlikely that the resting shape of the tail affects the swimming motion. The data presented here for the flexural stiffness of the tail (Fig.7) may be used to estimate the muscle stress required to bend the tail.
If a larva were to bend its tail by isometric contraction of its muscles on one side, then the moment generated at any point along the tail’s length should be resisted by a moment generated by the flexural stiffness of the tail. This situation is modeled in the relationship below, in which the symbols on the left represent the moment generated by the muscles and the symbols on the right represent the moment generated by the passive properties of the tail (Denny, 1988):
where the product of muscle force (Fm) and the distance (z) between the neutral axis and the muscle’s center is equal and opposite to the product of the curvature of the tail (κ) and its flexural stiffness (EI). Since muscle force is the product of muscle stress (σ) and the cross-sectional area of the muscle (Sm), it follows that:
To estimate the isometric muscle stress necessary to bend the tail, values for z (9.3×10−6m) and Sm (3.3×10−11m) were measured from the transverse section of a D. occidentalis tail pictured in Fig.2 of Cavey and Cloney (Cavey and Cloney, 1972). Using the absolute value of the largest value for κCLmax (2.5×103radm−1) (Table1) and the maximum value for EI (2.2×10−13Nm2) (Fig.7) recorded in the present study, a high boundary of σ equals 1800kPa. By the same calculation, using the smallest values for κCRmax (0.7×103radm−1) and EI (5.0×10−15Nm2), a low boundary for σ equals 11kPa. For comparison, maximum isometric stress for invertebrate muscle ranges between 100 and 1000kPa (Daniel, 1995), but there are no published values for ascidians. These rough estimates suggest that the stress required simply to bend the tail is at least 10% of the maximum stress that the muscle can generate. Since animals generally generate muscle stresses much lower than isometric values during steady locomotion (Full, 1997), it is likely that a much larger fraction of the total force generated by the muscles is used just to bend the tail. It is therefore plausible that the flexural stiffness measured (Fig.7) is great enough that the resting curvature of the tail affects the symmetry of swimming kinematics.
The mechanics of helical swimming
Although the results presented here emphasize the importance of kinematic asymmetries to the hydrodynamics of swimming in D. occidentalis larvae, this mechanism alone is insufficient to explain the dynamics of helical swimming. If the tail fin does not twist during swimming, the asymmetry in lateral undulations described here (Fig.5) should result in swimming along a circular, not helical, trajectory. Tail motion in the frontal plane only generates forces within that plane and moments perpendicular to that plane (Fig.9A). Assuming a dorso-ventrally oriented tail fin, this means that kinematic asymmetries in lateral undulation can act only as a mechanism for generating a yawing moment.
To swim along a helix, a larva must generate pitching or rolling moments in addition to a yawing moment. These moments may be generated by the buoyancy force and the weight of the body (Fig.9B). Buoyancy acts at the body’s center of volume, and weight acts at its center of mass. If the body is composed of tissue of uniform density, the center of mass and center of volume would occur at the same point. Depending on the relative magnitudes of the body’s buoyancy and weight, these forces will tend to accelerate the body down in the direction of gravity or up towards the water’s surface. It is likely that combining the hydrodynamics of swimming with the weight and buoyancy of a body of uniform density could generate pitching or rolling moments. However, these moments would be greater if the body’s tissues were not of uniform density. For example, if the anteriorly positioned otolith organ was more dense than the rest of the body, then the center of mass should be anterior to the center of volume. In this case, the distance between the center of mass and the center of buoyancy would create a moment arm that could generate a pitching moment, as shown in Fig.9B. This ‘non-uniform-density model’ has been suggested to play a role in the geotaxic behavior of a variety of marine invertebrate larvae (Chia et al., 1984). This mechanism has been proposed for generating moments in the helical swimming of both bivalve larvae (Jonsson et al., 1991) and frog tadpoles (Roberts et al., 2000), but it remains to be integrated with hydrodynamic mechanisms in any system.
It is possible that the kinematic asymmetries described here could contribute to the generation of rolling or pitching moments if the tail fin were to twist while it undulates. Twisting along the longitudinal axis of the tail could occur if the notochord and muscle cells were not sufficiently stiff in torsion or if the dorsal half of the fin had a different flexibility from that of the ventral half. A twist in the tail fin could direct some of the hydrodynamic force out of the frontal plane of the body and, thereby, generate a moment arm for rolling or pitching rotation. Unfortunately, the video recordings for the present study did not have a spatial resolution great enough to observe twisting in the tail fin. However, in the few video frames in which the fin was visible, no twisting in the tail fin could be seen.
Helical versus straight swimming
Crenshaw (Crenshaw, 1993) suggested that organisms having single light-sensing organs with poor directional sensitivity may orient to light by swimming along a helical trajectory. This mechanism, known as helical klinotaxis, may facilitate phototaxis in ascidian larvae (Svane and Young, 1989), which have one ocellus. Alternatively, swimming along a straight trajectory requires the body to be stabilized against body rotation. This would probably be difficult for ascidian larvae because they possess no paired appendages for swimming and they are often found in turbulent environments (Berrill, 1950). Although helical swimming may not bestow ascidian larvae with greater speed, efficiency and maneuverability than straight swimming, it does appear to make oriented swimming possible despite a limited sensory and motor capacity. It seems plausible that high-performance larval swimming may be less important in the life history of an ascidian than sufficient phototaxis with a minimal morphological investment.
In summary, the results presented here suggest that swimming D. occidentalis larvae generate yawing moments by moving their tails asymmetrically (Fig.8). Both the angle between the trunk and the tail (i.e. trunk angle; Fig.1) and the tail curvature cause the tail to bend towards the left during swimming (Fig.3, Fig.4). This asymmetry is predicted by hydrodynamic theory to generate moments that should be great enough to rotate the body (Fig.8) and therefore contribute to helical swimming. The flexural stiffness of the tail (Fig.7) may be great enough that kinematic asymmetries are caused by the bent shape of the resting tail (Fig.6).
List of symbols
A surface area of a tail segment
Cn normal force coefficient
Ct tangential force coefficient
EI flexural stiffness
f tail-beat frequency
Fm muscle force
Freactive reactive force on a tail segment
Fresistive resistive force on a tail segment
Ftotal total force on a tail segment
h height of a tail segment
l length of the tail in three-point bending
L body length
m added mass of a tail segment
n tail segment number
n̂ unit vector normal to a tail segment’s surface
Re Reynolds number
s position along length of body
si position of inflection point on the body
Sm cross-sectional area of muscle mass
n̂ unit vector tangential to a tail segment’s surface
U swimming speed
Vn normal component of tail segment velocity
Vt tangential component of tail segment velocity
z distance from the tail midline to the center of muscle mass
αCL amplitude of concave-left curvature changes during swimming
αCR amplitude of concave-right curvature changes during swimming
αθ amplitude of trunk angle changes during swimming
β baseline of periodic changes in trunk angle
ν kinematic viscosity
δ deflection of the tail
Δs length of a tail segment
Δφ angular flexion between neighboring segments
ε wave speed of inflection point propagation
θ trunk angle
κ curvature of a tail segment
κ̅ mean curvature over the length of the tail
κCL concave-left curvature
κCLmax maximum concave-left curvature
κCR concave-right curvature
κCRmax maximum concave-right curvature
κ̅M̅ median tail curvature measured over a tail-beat cycle
ρ water density
σ muscle stress
I would like to thank M. Koehl for her guidance, H. Crenshaw for enlightening me about helical kinematics, E. Azizi for technical assistance, W. Getz for his comments on the manuscript and the Berkeley Biomechanics Group for general input. This research was supported with an NSF predoctoral fellowship and grants-in-aid of research from the Society for Integrative and Comparative Biology and Sigma Xi. Additional support came from National Science Foundation Grant OCE-9907120 to M. A. R. Koehl and the Office of Naval Research Grant N00014-98-0775 to M. A. R. Koehl.