ABSTRACT
Mallard ducks are capable of performing a wide range of behaviors including nearly vertical takeoffs from both terrestrial and aquatic habitats. The hindlimb plays a key role during takeoffs from both media. However, because force generation differs in water versus on land, hindlimb kinematics and muscle function are likely modulated between these environments. Specifically, we hypothesize that hindlimb joint motion and muscle shortening are faster during aquatic takeoffs, but greater hindlimb muscle forces are generated during terrestrial takeoffs. In this study, we examined the hindlimb kinematics and in vivo contractile function of the lateral gastrocnemius (LG), a major ankle extensor and knee flexor, during takeoffs from water versus land in mallard ducks. In contrast to our hypothesis, we observed no change in ankle angular velocity between media. However, the hip and metatarsophalangeal joints underwent large excursions during terrestrial takeoffs but exhibited almost no motion during aquatic takeoffs. The knee extended during terrestrial takeoffs but flexed during aquatic takeoffs. Correspondingly, LG fascicle shortening strain, shortening velocity and pennation angle change were greater during aquatic takeoffs than during terrestrial takeoffs because of the differences in knee motion. Nevertheless, we observed no significant differences in LG stress or work, but did see an increase in muscle power output during aquatic takeoffs. Because differences in the physical properties of aquatic and terrestrial media require differing hindlimb kinematics and muscle function, animals such as mallards may be challenged to tune their muscle properties for movement across differing environments.
INTRODUCTION
Navigating between terrestrial and aquatic environments presents a challenge for animals because differences in solid and fluid properties change the demands for generating propulsive forces for locomotion. As a result, movement across these media likely requires differing kinematics and muscle function (Kamel et al., 1996; Biewener and Gillis, 1999; Biewener and Corning, 2001; Gillis and Blob, 2001; Foster et al., 2018). In particular, previous studies have reported differences in hindlimb kinematics and muscle function between walking and surface swimming in ducks (Biewener and Corning, 2001; Carr, 2008; Provini et al., 2012a).
Mallards, Anas platyrhynchos Linnaeus 1758, are dabbling ducks that readily move between water and land, and their behavioral repertoire includes nearly vertical takeoffs in both environments (Raikow, 1973). Consequently, it is likely that mallards also face the challenge of modulating hindlimb movement and muscle function during takeoff depending on the takeoff medium, particularly because the hindlimb contributes to the first part of takeoff when the body is still in contact with the substrate. Previous work on terrestrial takeoff has examined takeoffs from solid surfaces by focusing on distal hindlimb kinematics and substrate reaction forces (Earls, 2000; Tobalske et al., 2004; Berg and Biewener, 2010; Provini et al., 2012b; Chin and Lentink, 2017; Crandell et al., 2018) or wing musculature (Williamson et al., 2001). Others have considered avian behaviors at the water's surface, including paddle-assisted flight (Norberg and Norberg, 1971; Gough et al., 2015), mating displays (Clifton et al., 2015), hydroplaning (Aigeldinger and Fish, 1995) and steaming (Gough et al., 2015). However, no previous studies have examined how vertical takeoff varies between water and land, and none have reported hindlimb muscle function or the kinematics of proximal joints (hip and knee) during takeoff. Therefore, our goal here was to compare the hindlimb kinematics and in vivo function of the lateral gastrocnemius (LG), a major ankle extensor and knee flexor (Biewener and Corning, 2001; Clifton et al., 2018), in response to differences in propulsive requirements for aquatic versus terrestrial takeoffs in mallard ducks.
Similar to other tetrapods that use their hindlimbs for jumping, in many avian species the hindlimbs play an important role in flight takeoff. When taking off from the ground or a perch, birds extend their legs as the wings unfold, with the first downstroke of the wings occurring late in hindlimb extension or after the feet have left the ground or perch (Earls, 2000; Provini et al., 2012b). Depending on the species, the hindlimbs are responsible for 59–100% of the body's velocity at the time of toe-off (Earls, 2000; Tobalske et al., 2004; Berg and Biewener, 2010; Provini et al., 2012b; Chin and Lentink, 2017), with the remainder made up by an active upstroke or rotations of the body (Provini et al., 2012b). Because birds take off from a variety of substrates, takeoff performance may be compromised if behaviors are not adjusted to substrate properties (Crandell et al., 2018). Substrate compliance can affect jumping kinematics, with more compliant substrates linked to lower takeoff velocities and larger joint excursions (Giatsis et al., 2004; Astley et al., 2015; Crandell et al., 2018). Waterfowl face perhaps the most disparate tasks of taking off from both terrestrial and aquatic environments. Consequently, adjusting their kinematics to water and land may present challenges for hindlimb muscle tuning.
How locomotor forces are produced necessarily differs between aquatic and terrestrial environments, and these differences can lead to changes in limb kinematics and muscle shortening. On land, an animal's limbs and body are supported and accelerated by ground reaction forces, which are directly proportional to the force produced by skeletal muscles, whereas in water, hydrodynamic forces produced by propulsive appendages (in this case, the duck's feet) accelerate the body and depend on the foot's relative velocity squared (drag force) and on the acceleration of the added mass of fluid displaced by the foot (acceleration reaction force; Daniel, 1984; Biewener and Patek, 2018). Consequently, in order to increase hydrodynamic forces, the duck's feet must be moved faster (hypothesis 1, H1), requiring greater muscle shortening and contraction velocities (H2). This has particular importance for the function of ankle extensors, such as the LG, which power foot motion. Although active modulation could result in higher hindlimb joint velocities and muscle shortening velocities, the increased compliance of a fluid versus solid substrate can also result in larger limb excursions under a given applied force (Hsieh, 2003; Giatsis et al., 2004), potentially contributing to higher joint excursions and muscle shortening velocities.
How much propulsive force is required differs between terrestrial and aquatic habitats. On land, force must be generated both to support an animal's body weight and to accelerate the body. In contrast, in water, body weight support is reduced or eliminated because of an animal's buoyancy. However, during aquatic takeoffs, the force required to launch the body is increased by the water's resistance to the bird exiting the water (drag on the body, surface tension) and by water entrained in a bird's plumage, increasing its effective body mass. Nevertheless, we expect that buoyancy will dominate relative to these other forces, resulting in higher forces being required for terrestrial takeoffs (H3). Consistent with this, many animals produce higher forces and increase muscle activation on land versus in water (Kamel et al., 1996; Biewener and Gillis, 1999; Gillis and Biewener, 2000; Gillis and Blob, 2001; Foster et al., 2018), although this pattern does not universally hold (Gillis and Blob, 2001). Of most relevance to this study, previous work has shown that the mallard LG produces higher stresses (i.e. force/fiber cross-sectional area) during walking than during surface swimming (Biewener and Corning, 2001).
Thus, we hypothesized that mallard hindlimb kinematics and LG force production would change with takeoff substrate, specifically by producing (H1) greater hindlimb joint extension velocities and (H2) greater muscle shortening velocities during aquatic takeoffs to generate the required hydrodynamic forces, while producing (H3) greater hindlimb muscle forces during terrestrial takeoffs to accelerate the body and support body weight. Because these differing demands for force versus velocity likely impact hindlimb muscle function, an animal's ability to balance these demands is of particular interest given that skeletal muscles are well known to exhibit a tradeoff between their force and velocity contractile properties (Hill, 1938; McMahon, 1984; Lieber, 1992; Biewener and Patek, 2018). In this study, differences between terrestrial and aquatic takeoffs in mallard ducks were examined by measuring hindlimb kinematics of both proximal and distal joints and in vivo function of the LG, a major ankle extensor that generates foot motion during both aquatic and terrestrial locomotion.
MATERIALS AND METHODS
Animals and training
Wild-caught (n=8) and farm-raised (n=4) mallard ducks (Table S1) were fed ad libitum and housed in an indoor–outdoor enclosure with both terrestrial and aquatic areas. Experiments were performed during May–November. This period includes a full molt of the primary feathers in late summer that typically renders the ducks flightless for a few weeks. Animals were only studied during times when they had flight ability, either prior to molt or after the feathers had regrown. All animal procedures were approved by Harvard University's Institutional Animal Care and Use Committee under protocol number 20-09. Wild birds were collected under Massachusetts Division of Fisheries & Wildlife Permits 011.15SCB, 007.17SCB and 093.18SCB and U.S. Fish & Wildlife Permit MB005348-0.
Birds were trained in the flight arena, a long hall with high ceilings. Training involved first acclimating the birds to two areas: the takeoff area – either a platform (0.6×0.4 m) for terrestrial takeoffs or an acrylic water tank (1×1×0.25 m depth) for aquatic takeoff – and the landing area at the other end of the hall. Birds were rewarded with treats (millet) and withdrawal of the researcher when they remained in either location. Researcher approach encouraged the birds to move from the takeoff area to the landing area. A small barrier placed at the front of the platform or tank encouraged vertical takeoffs (Fig. S1A). The barrier height was gradually increased after successful practice trials at previous heights. During all experiments, animals were placed on or guided to the takeoff area. After a period of acclimation (30 s to 2 min), birds were encouraged to take off by researcher approach, although some birds took off spontaneously. Following takeoff, birds rested in the landing area or were returned to the takeoff area for a rest period of 1–5 min.
Animals trained in the flight arena readily translated their training to takeoffs in the X-ray setup, where they took off from the same platform for terrestrial takeoffs as for the light video and from a smaller tank (0.66×0.4×0.3 m depth) for aquatic takeoffs (Fig. S1B). To avoid researcher exposure to the X-ray beam, motion of a glove attached to a long rod was used as a takeoff stimulus.
Kinematics
Timing
We used kinematic parameters to determine when the ‘power stroke’ of takeoff commenced and ended. All time-varying data, including in vivo LG recordings, are plotted relative to the kinematic power stroke, where time=0 is the beginning and time=1 is the end of takeoff power stroke. For terrestrial takeoffs, the first forward and/or upward motion of the body was considered the start of takeoff, with the end of takeoff being when the toe left the ground (i.e. toe-off). For aquatic takeoffs, we considered the first movement of the foot caudally and/or inferiorly as the start of takeoff. During aquatic takeoffs, the webbing of the foot collapses prior to the foot leaving the water, at which point the foot likely no longer contributes to powering takeoff as it is drawn forward in the water. We therefore considered collapse of the webbing to be the end of the aquatic takeoff power stroke. Although normalized time was used to compare relative timing of kinematics and measures of muscle function, real time (in s) was used for calculating durations and velocities (joint motion duration, joint angular velocities, muscle shortening velocities and muscle power).
Ankle and metatarsophalangeal joint
Takeoffs were elicited in the flight arena, as described above. We used high-speed light video to measure movement of the externally visible portions of the leg (distal tibiotarsus, tarsometatarsus and foot; Fig. 1A; Movie 1; N=5 individuals, n=15 trials, three trials per individual for each takeoff substrate). Takeoffs were recorded at 250 frames s−1 (shutter 1–1.5 ms) using IDT NR5-S1 cameras (Integrated Design Tools, Inc., Pasadena, CA, USA) equipped with Nikon AF Nikkor 24–85 mm zoom lenses (Nikon Inc., Melville, NY, USA). We used a wand of known length to calibrate the 3D space using easyWand5 (Theriault et al., 2014). The tip of the toes, metatarsophalangeal (MTP) joint, ankle and the distal tibiotarsus (Fig. 1A) were marked with white latex and black marker pen, and these points were digitized using DLTdv6 (Hedrick, 2008) to calculate MTP and ankle joint angles. Note that in the example movie (Movie 1), the camera view is oblique rather than perfectly perpendicular as two cameras with an oblique lateral view were used to capture 3D kinematics (Fig. S1A).
Hip and knee
We used videoradiography to examine the proximal joints for each type of takeoff (N=3 individuals, n=6 trials, two trials per individual for each condition) because these joints are not visible or well-identified using light video. We recorded lateral view X-ray images from a C-arm (Model 9400, OEC-Diasonics Inc.; modified by Radiological Imaging Services) using a high-speed Photron Fastcam 1024 PCI camera (Photron USA, Inc., San Diego, CA, USA; 500 frames s−1, shutter 1 ms). These images were de-distorted using a grid and XMALab (v.1.4.0; Knörlein et al., 2016).
For terrestrial takeoffs, we performed a 2D analysis using anatomical landmarks to identify the synsacrum, hip, knee and ankle, so that hip and knee joint angles could be calculated (Fig. 1B). However, the water tank used for aquatic takeoffs was sufficiently large that the X-ray beam could not penetrate the water, blocking views of the knee and ankle joints. However, the synsacrum and proximal femur were above the water line and thus visible on X-ray video. We combined light video using the IDT cameras (125 frames s−1) synchronized with the X-ray video to calculate the location and angle of the knee (Fig. 1C). Using a metal calibration object in view of both the light and X-ray videos, the light video of the distal leg was aligned with the X-ray recordings of the proximal leg. 3D coordinates from the light video were then projected onto a plane parallel to the X-ray plane. The X-ray recordings yielded locations for the synsacrum and hip, and the direction of the femur. The light video recordings yielded the location of the ankle and the direction of the tibiotarsus. The locations and angle of the knee were then calculated using these digitized points and measured lengths of the femur and tibiotarsus (Fig. 1C).
Splay correction for X-ray analysis
The splay correction allowed our otherwise 2D analysis to more accurately determine the hip and knee angles. Although unaccounted for out-of-plane motion could produce errors in our measured knee and hip angles, these errors are likely to be small (i.e. a 10 deg change in the splay angle would result in <1 deg error in the observed angular excursions of the hip and knee joints) and are unlikely to produce the changes in kinematic patterns that we observed (see Results).
Filtering
To account for digitizing errors, raw kinematics traces were smoothed in Python (v.3.7) by applying a 4th order low-pass Butterworth filter with a cutoff frequency of 20 Hz for the hip, knee and ankle joints and 50 Hz for the MTP joint. Kinematics time scales were normalized to the duration of the power stroke, and the data were interpolated in 100 time steps during the power stroke to average across trials and individuals.
In vivo muscle measurements
Surgery
In vivo LG function was measured during aquatic and terrestrial takeoffs in N=10 individuals. We anesthetized (via mask induction) the animals using a 1–2% isoflurane:oxygen gas mixture. Three 2.0 mm sonomicrometry crystals (Sonometrics Corporation, London, ON, Canada) were implanted in the LG, one at each end of a mid-belly fascicle and one proximal to, but in-line with, the crystal at the superficial end of the fascicle (Fig. 1D). The crystals and lead wires were secured with 5-0 silk suture (Ethicon, Cincinnati, OH, USA). This configuration of crystals allowed us to measure length changes along the fascicle and calculate pennation angle using the law of cosines (Fig. 1D). We also implanted silver fine wire hook electrodes (0.1 mm, with 0.5 mm exposed tips and 2–3 mm spacing, California Fine Wire Company, Grover Beach, CA, USA) to obtain electromyography (EMG) recordings. An E-shaped tendon buckle was sutured in place on the LG portion of the gastrocnemius tendon, proximal to where the medial gastrocnemius (MG) tendon joins with the LG tendon to form the common tendon (Fig. 1D). The tendon buckle design followed Biewener and Corning (2001) and was built by mounting a strain gauge (Type FLA-1-11, Tokyo Sokki Kenkyujo Co., Ltd, Tokyo, Japan) on the middle arm of an E-shaped piece of 1 mm thick stainless steel. After soldering 36 gauge lead wires and insulating with oven-cured epoxy (AE-10, Micromeasurements Group, Inc., Raleigh, NC, USA), the transducer was subsequently coated with polyurethane M-coat A (Micromeasurements Group, Inc.) to minimize tissue reaction. All transducer lead wires were passed subcutaneously where they emerged to an external custom-designed 12 pin miniature connector that was secured to the animal's back with 2-0 Vicryl sutures (Ethicon) between the wings. This connector location allowed us to disconnect the birds from the cables between recording bouts and ensured that the connectors and cables did not inhibit motion of the wings or feet.
Data collection
Birds were permitted to recover from surgery overnight. Animals were administered flunixin (4 mg kg−1, intramuscularly to the pectoralis) every 12 h for the duration of the experiment following surgery (2–3 days). After recovery, animals were recorded performing terrestrial and aquatic takeoffs; takeoffs were elicited as described in ‘Animals and training’ above. Signals were transmitted from the animal's back connector via ∼8 m shielded multi-lead cable to recording equipment located outside of the flight arena. The sonomicrometry signals were recorded using a Sonometrics Digital Ultrasonic Measurement System (TR-USB Series 8) and sonoLAB data acquisition software (Sonometrics Corporation). The tendon buckle signal was passed through a bridge amplifier (Vishay Instruments, Raleigh, NC, USA), and the EMG signals were passed through Grass P-511 Series amplifiers (Grass Instruments, West Warwick, RI, USA) before being recorded at 5000 Hz by a BIOPAC MP150 data acquisition system (BIOPAC Systems, Inc., Goleta, CA, USA) using the accompanying AcqKnowledge software (v.4.1.1). High-speed light videos of the takeoffs were also recorded as described above. A voltage pulse trigger that illuminated an LED light in the cameras' field of view was used to synchronize across software programs and video. This resulted in synchronized kinematics (MTP and ankle joints) and LG force, EMG, fascicle length and pennation angle. Because of the challenging nature of the experiments, not all data were obtained for all individuals. A list of animals used and the data collected from each is provided in Table S1.
Following data collection, animals were euthanized, and the hindlimb was dissected. The tendon force buckle was calibrated by removing the common gastrocnemius tendon from the ankle, distal to the thick fibrocartilage pad. Kevlar thread (DuPont de Nemours, Inc.) was tied proximal to the fibrocartilage pad and attached to a calibrated piezoelectric force transducer (model 9203, Kistler Instrument Corporation, Amherst, NY, USA) or an ergometer lever arm (Aurora Scientific Inc., Aurora, ON, Canada). By first freezing the aponeurosis with liquid nitrogen and then pulling on the instrumented tendon or by activating the muscle, we simultaneously recorded the tendon buckle voltage output with the force transducer or lever arm output to obtain dynamic calibrations of tendon force; least-squares linear regression fits had r2>0.94 (P<0.05). Following calibration, we dissected the hindlimb to confirm the alignment of the sonomicrometry crystals and to measure resting LG fascicle length, resting pennation angle and muscle mass. The muscle was bisected along the muscle midline, revealing the locations of the implanted sonomicrometry crystals. Length measurements were made with calipers to a precision of 0.1 mm and angles were measured with a swing arm protractor. The distance between the crystals (inter-crystal distance) and the full length of the fascicle in which the crystals were implanted (resting fascicle length) were measured. In order to calculate a mean fascicle length and pennation angle, measurements were taken at 3–6 midline fascicles distributed along the proximo-distal axis of the muscle.
Data processing
Sonomicrometry crystals were implanted mid-belly to record from as large a portion of the LG muscle's fascicle length as possible (Fig. 1). Measurements of fascicle strain were obtained from the fascicle segment recordings. Resting fascicle length and inter-crystal distance were measured post-mortem, and we multiplied the ratio of these distances (fascicle length/inter-crystal distance) to convert the sonomicrometry output to fascicle length. Fascicle strain was calculated as (instantaneous length−resting length)/resting length. Fascicle shortening velocity was calculated from smoothed (4th order low-pass Butterworth filter with 30 Hz cutoff) fascicle length data over the duration of shortening and normalized by resting fascicle length to L s−1.
Muscle–tendon force was filtered using a 4th order low-pass Butterworth filter with a cutoff frequency of 20 Hz. Muscle physiological cross-sectional area (PCSA in cm2) was calculated as [cos(α)×m]/(ρ×lfas) where α is the pennation angle (Fig. 1D), m is muscle mass (kg), ρ is density (assumed to be 1.06×10−3 kg cm−3) and lfas is fascicle length (cm). Muscle stress (kPa) was calculated by dividing force by PCSA. Muscle work (J) was calculated as the area under the force versus fascicle length curve for the portion of takeoff when both force was being produced and the fascicles were shortening. Work was converted to mass-specific work by dividing by muscle mass. Average mass-specific muscle power was calculated as work/(time×muscle mass).
Statistics
Statistical tests were performed in R (v.3.6.0). All reported values are means±s.e.m., with significance based on α=0.05. We first obtained the average of all measurements for each individual and then plotted and performed statistical tests on the individual averages, which allowed us to account for the different number of trials per individual and permitted paired comparisons between aquatic and terrestrial takeoffs. Prior to performing t-tests, normality was verified using a Shapiro–Wilk test. If this assumption was not violated (P>0.05), we compared the aquatic and terrestrial takeoffs using one-tailed t-tests. If the normality assumption was violated (Shapiro–Wilk P<0.05), we instead used a one-tailed, Wilcoxon non-parametric test. Kinematics were compared using paired tests. LG measurements were compared using unpaired tests. For a subset of animals, we recorded from the LG during both aquatic and terrestrial takeoffs. For some measures with sufficient samples with paired data, we also tested for differences using paired, one-tailed t-tests or Wilcoxon tests, as appropriate, to take into consideration large differences between individuals. All figures display data from all individuals and report paired statistics for kinematics and unpaired statistics for LG measures; any statistics that result from paired tests for LG measures are indicated in the text.
RESULTS
Kinematics during terrestrial versus aquatic takeoffs
The kinematics of aquatic versus terrestrial takeoffs differed substantially (Movie 1). Qualitatively, during terrestrial takeoffs, leg extension coincided with wing upstroke and there was very little overlap with wing downstroke. Many, but not all, terrestrial takeoffs were preceded by a countermovement, where the wings remained folded, legs were very flexed and the head was drawn near the body by flexing the neck. The neck began to extend as the wings unfolded and the body angle shifted from horizontal to vertical. Neck extension and shifts in body angle continued throughout the remainder of takeoff. As the legs began to extend, the wings were elevated dorsally and cranially in upstroke. At the point of toe-off, the wings changed direction and were depressed ventrally and slightly caudally for downstroke, the neck was fully extended and the body angle was nearly vertical. In contrast, during aquatic takeoffs, leg extension coincided with ventral depression of the tail and wing downstroke. Prior to takeoff, the legs were drawn to a very flexed position such that the foot was parallel with and very near to the water's surface. The wings were drawn cranially. The wings were oared through the water with ventral and caudal motion, nearly synchronously with the extension of the leg and ventral depression of the tail. As in terrestrial takeoff, the neck extended and the body angle shifted from horizontal to nearly vertical throughout the takeoff. The wings, tail and legs reached their final position quickly to propel the bird out of the water; once clear of the water, the wings were elevated dorsally and flapping commenced. The feet also paddled once clear of the water, occasionally striking the water at the surface or, if the water was cleared, cycling mid-air.
Power stroke duration of aquatic takeoffs (0.13±0.018 s) did not differ significantly (P=0.087; Table 1) from terrestrial takeoffs (0.16±0.012 s). Because each limb joint only moves during a portion of the power stroke (Fig. 2), we also compared the duration of motion for each joint, with motion onset based on when joint angular velocity exceeded zero (or fell below zero for the knee during aquatic takeoffs) and motion ending when velocity returned to zero. No significant differences were found for the duration of joint motion between aquatic and terrestrial takeoffs for any of the joints measured (P>0.05; Fig. 3A, Table 1).
Hindlimb kinematics of individual joints differed between terrestrial and aquatic takeoffs. Terrestrial takeoffs involved extension of all hindlimb joints (Fig. 2). In contrast, during aquatic takeoffs, hip (Figs 2A and 3B) and MTP (Figs 2D and 3B) joint angles changed very little; angular excursions at these joints were significantly lower than for terrestrial takeoffs (Table 1), resulting in significantly lower angular velocities at these joints during aquatic takeoffs (Fig. 3C, Table 1). The direction of knee motion reversed, with the knee being extended during terrestrial takeoffs but flexed during aquatic takeoffs. This change in direction resulted in significantly different knee angular excursions (Figs 2B and 3B, Table 1) and velocities (Fig. 3C, Table 1), although the magnitudes of the excursion (P=0.370) and velocity (P=0.450) were not different. The ankle underwent a larger angular excursion during aquatic versus terrestrial takeoffs (Figs 2C and 3B, Table 1), but no significant difference was observed in ankle extension angular velocity (Fig. 3C, Table 1).
LG function during terrestrial versus aquatic takeoffs
Average time-varying patterns of LG fascicle strain, fascicle shortening velocity, pennation angle and stress for aquatic and terrestrial takeoff trials are shown in Fig. 4. Representative traces from an individual with nearly complete datasets are shown in Fig. S2, including activation (EMG). A terrestrial trial from a second individual is also displayed, demonstrating the variation in the timing of force production among individuals (Fig. S2). The rapid lengthening of the LG fascicle prior to takeoff (Fig. S2A) corresponds to a countermovement (example in Movie 1). However, because not all animals used a large countermovement, this lengthening pattern was not observed in the LG strain pattern averaged across individuals (Fig. 4A). Similarly, the shortening observed prior to force production for the example terrestrial takeoff (Fig. S2A, black traces) was not observed across all individuals (Fig. 4A; Fig. S2A, gray traces), and we suspect this shortening results from a shift in body orientation that flexes the knee in preparation for takeoff during this trial. Note that LG fascicles operate at greater strains during aquatic takeoffs due to the extremely flexed position of the ankle joint and, on average, LG stress is higher prior to terrestrial takeoffs as a result of weight support (Fig. 4). Normalized timing of pennation angle change [terrestrial (T): n=6; aquatic (A): n=5], fascicle shortening (T: n=7; A: n=6), force production (T: n=5; A: n=4) and EMG activity (T: n=6, A: n=2) are shown in Fig. 5A. When comparing the onset and ending of each of these measures, we found that LG fascicle shortening (P=0.022) and force production (P=0.004) began earlier and force production ended earlier (P=0.043) during terrestrial takeoffs. All other timing parameters, including the onset and ending time of LG pennation angle change and EMG activity, the ending time for fascicle shortening, and the duration of all four measures, did not differ significantly with takeoff medium (P>0.05).
The range of LG fascicle strain used during terrestrial versus aquatic takeoffs is shown in Fig. 5B. When comparing data from all animals (T: n=7; A: n=6), the maximum strain (T: −0.05±0.08; A: 0.15±0.08) and minimum strain (T: −0.27±0.07; A: −0.26±0.06) did not significantly differ between aquatic and terrestrial takeoffs (maximum strain: P=0.059, minimum strain: P=0.223), but both maximum (P=0.016) and minimum fascicle strain (P=0.006) were significantly greater during aquatic takeoffs when based on paired t-tests (n=5). In addition, the magnitude of LG shortening strain was significantly lower (P=0.011) for terrestrial (0.22±0.07) compared with aquatic (0.41±0.06) takeoffs (Fig. 6B). Given the similar shortening durations (Fig. 5A), LG fascicle shortening velocity was also significantly greater (P=0.004) during aquatic (4.12±0.82 L s−1, n=6) versus terrestrial (1.41±0.17 L s−1, n=6) takeoffs (Fig. 6C). Pennation angle change (Fig. 6D) was significantly larger during aquatic takeoffs than terrestrial takeoffs when compared using a paired t-test (difference: 4±1 deg, P=0.018, n=4), although this difference was not observed when using an unpaired t-test and all animals (P=0.127; T: 10±2 deg, n=7; A: 15±4 deg, n=4).
There was no significant difference in the LG stress during terrestrial (79±12 kPa) versus aquatic (53±15 kPa) takeoffs (P=0.116; T: n=4, A: n=4; Fig. 6A). LG mass-specific work (T: 8±1 J kg−1; A: 15±5 J kg−1) did not differ significantly between media (P=0.1); however, there was a significant difference (P=0.05) in average muscle power output (T: 43±3 W kg−1; A: 172±72 W kg−1; sample sizes for work and power T: n=3, A: n=3; Fig. 6E,F).
DISCUSSION
Animals that regularly move between aquatic and terrestrial environments must be able to manage the different physical properties of fluids and solids. On land, ground reaction forces are used to support or accelerate an animal's body and are proportional to the forces produced by an animal's muscles. However, in water, propulsive forces are hydrodynamic and depend on the square of the velocity of the body part moving through the water. We therefore expected to see differences in both hindlimb kinematics and muscle function of mallards to accommodate differences in environment during takeoff. Specifically, we hypothesized that (H1) hindlimb joints would move at higher angular velocities during aquatic versus terrestrial takeoffs, that (H2) higher angular velocities at the ankle joint would be powered by higher LG shortening velocities, and that (H3) the LG would produce greater forces during terrestrial than aquatic takeoffs. We did not find support for the hypothesis that mallard hindlimb joints move at higher angular velocities in water (H1; Fig. 3C); however, we did observe substantial differences between the kinematics of aquatic versus terrestrial takeoffs. Of particular interest, the knee reversed its motion from flexion during aquatic takeoffs to extension during terrestrial takeoffs with, unexpectedly, no change in ankle angular velocity (Figs 2 and 3). The change in knee kinematics reflects the underlying difference in LG muscle function, which shortens at higher velocities during aquatic takeoffs than during terrestrial takeoffs (H2; Fig. 6C). Finally, although two of the three animals for which we have paired data produced greater muscle stress during terrestrial compared with aquatic takeoffs, overall, the difference in LG muscle stress was not significant (Fig. 6A) and failed to support our hypothesis regarding LG force (H3).
Takeoff kinematic patterns and implications for muscle length change
One way to address the challenge of moving on or through media with differing properties is through different kinematics. Changes in kinematics represent a combination of active control and passive interactions with the environment (Gillis and Biewener, 2000).
Our study of takeoff performance, facilitated by X-ray video analysis, confirms changes in mallard hindlimb kinematics, particularly at the knee, between the two media. The knee joint reverses its direction of rotation, extending during terrestrial takeoffs but flexing during aquatic takeoffs (Figs 2, 3 and 7). The overall excursion and angular velocity for each type of takeoff are the same but in opposite directions. Knee extension causes cranial motion of the foot while knee flexion and extension at the hip, ankle and MTP joints cause caudal motion (Fig. 7). Thus, knee flexion during aquatic takeoffs contributes to caudal motion of the foot in the water caused by ankle extension, rather than opposing it (Fig. 7), allowing the knee and ankle joints to work together to enhance foot motion. Similarly, aquatic specialist frog species tend to reduce knee extension during swimming to prevent it from counteracting the propulsive foot motion induced by ankle extension (Richards, 2010). We expect that the change in knee joint rotation was the result of active control, acting to increase foot velocity and hydrodynamic force production. Knee extensors almost certainly contribute to terrestrial takeoff by helping to accelerate the body's center of mass off the ground. Knee flexors (including the LG) likely contribute to knee motion during aquatic takeoff but not terrestrial takeoff. Although the LG is active during both aquatic and terrestrial takeoffs, antagonist activity of knee extensors could prevent the LG from causing knee flexion during terrestrial takeoff.
Unexpectedly, the ankle joint exhibited similar kinematics between aquatic and terrestrial takeoffs (Figs 2 and 3). Although angular excursion of the ankle differed significantly between the two media, the difference was much lower than we observed for the other joints, and ankle angular velocity did not differ significantly. Although this result might suggest that the LG and other muscles driving ankle extension would exhibit similar contractile patterns across both types of takeoff, because the LG crosses both the knee and ankle joints, the reversal in knee motion for aquatic versus terrestrial takeoffs profoundly impacts LG contractile function. During terrestrial takeoffs, the LG shortens to extend the ankle, but this is opposed by knee extension (Fig. 7), resulting in more limited LG shortening and reduced velocity during terrestrial takeoffs (Fig. 6). In contrast, because the knee flexes during aquatic takeoffs, LG shortening is greater and occurs with higher velocity to contribute to knee flexion as well as ankle extension (Fig. 7).
Changes in the kinematics of the MTP and hip joint between terrestrial and aquatic takeoffs likely alter the roles played by the muscles acting at these joints. Both joints undergo large excursions during terrestrial takeoffs but experience almost no angle change during aquatic takeoffs (Figs 3, 7). The MTP first flexes, as the more proximal joints extend, and then extends rapidly at the end of takeoff from land (Fig. 2). For aquatic takeoffs, MTP motion is negligible, as the joint is held close to 180 deg, allowing the foot and tarsometatarsus to act as a propulsive paddle. Being held rigid during a power stroke seems to be a characteristic pattern of MTP kinematics for aquatic locomotion, as it is also observed during surface swimming, when flexion of the MTP joint only occurs during the recovery stroke (Provini et al., 2012a). The hip joint, which exhibits large extensions during terrestrial takeoff, also undergoes little motion during aquatic takeoffs. This pattern is also consistent with other types of avian locomotion, in which the hip undergoes large excursions during walking but is relatively stationary during surface swimming (Carr, 2008; Provini et al., 2012a). These hip kinematic patterns are reflected in the length change patterns of hip extensor muscles, which undergo more shortening during walking than during swimming (Carr, 2008). Thus, although we did not measure muscle function at these joints, we would predict that muscles acting at the hip and MTP joints also change roles between aquatic and terrestrial takeoff, with terrestrial takeoffs requiring greater muscle shortening compared with aquatic takeoffs, which would require nearly isometric contractions to stabilize these joints.
LG stress, work and power
Unexpectedly, we observed no significant differences in LG muscle stress or work but did see a significant difference in muscle power output in our in vivo recordings across takeoff media (Fig. 6). The small sample size for these variables may have contributed to our inability to distinguish differences that, in fact, exist for muscle stress and work. That muscle work did not differ was perhaps less surprising, given that the increase in muscle shortening during aquatic takeoffs was balanced by a decrease in LG force for two out of the three animals for which paired results were obtained. However, the decrease in LG force observed for most animals was not enough to offset the increase in LG shortening velocity, resulting in significantly higher LG power during aquatic takeoffs.
It is interesting to consider how a demanding task like takeoff can be managed by a major leg extensor muscle, such as the LG, which must accommodate differing contractile lengths and velocities depending on the medium in, or on, which the animal moves. Both force–length and force–velocity effects (McMahon, 1984; Lieber, 1992; Biewener and Patek, 2018) would decrease the force-generating ability of the LG muscle during aquatic takeoffs. Given that LG stress did not decrease significantly, it seems likely that increased neural recruitment compensated for force–length and force–velocity effects. However, our limited success in obtaining paired EMG recordings of the LG in multiple individuals across both takeoff behaviors (Table S1) prevented us from confirming this.
LG pennation angle changes and muscle gearing
When pennate muscles contract, their fibers can rotate, changing their pennation angle. Fascicle shortening and rotation, therefore, can both contribute to whole-muscle shortening (Brainerd and Azizi, 2005; Azizi et al., 2008). The ratio of muscle velocity to fascicle velocity defines a muscle's gear ratio, which has been shown to change in relation to changes in muscle force requirements during shortening contractions (Azizi et al., 2008). Muscle gear ratios are predicted to be higher under low force behaviors, allowing for higher whole-muscle shortening velocities, and lower during high-force behaviors, keeping the fascicles' force more aligned with the line of action of the muscle (Azizi et al., 2008). Consequently, we hypothesized that terrestrial takeoffs would involve lower muscle gear ratios to favor greater force generation, whereas aquatic takeoffs would favor increased gear ratios to enhance whole-muscle shortening velocity. Although we did not see a difference in normalized muscle force, or stress, we did observe larger changes in LG pennation angle, consistent with a higher gear ratio, during aquatic takeoffs versus terrestrial takeoffs when compared using a paired t-test (Fig. 6).
Implications of moving between water and land
Animals that regularly move between environments face the challenge of using the same propulsive structures and muscles in media having very different physical properties. As made obvious by their webbed feet and waddling gait, many waterfowl, such as mallards, exhibit specializations for swimming that are thought to have compromised their walking ability (Biewener and Corning, 2001; Provini et al., 2012a) and increased the energetic cost of terrestrial locomotion relative to that of other birds (Pinshow et al., 1977; Griffin and Kram, 2000; Nudds et al., 2010).
As previously discussed, force production varies between environments. On land, animals need to support body weight as well as generate ground reaction forces to accelerate the body. In water, animals produce hydrodynamic forces, which depend on the speed of the propulsive structure (drag) and the acceleration of the added mass of fluid displaced by the structure (Daniel, 1984). Thus, we predicted that muscle force production would be higher during terrestrial locomotion and joint angular and muscle-shortening velocities would be higher during aquatic locomotion. These hypotheses are consistent with previous comparisons of kinematically similar behaviors where higher muscle EMG activity (Kamel et al., 1996; Biewener and Gillis, 1999; Gillis and Biewener, 2000; Gillis and Blob, 2001; Foster et al., 2018) and higher impulses (Nauwelaerts and Aerts, 2003) are observed during terrestrial locomotion, while faster limb movements are observed during aquatic behaviors (Wilkinson, 2014; Clifton et al., 2015).
That our results do not support these hypotheses is likely a result of their simplicity. For example, we expected the demand for hydrodynamic force would be lower because body weight is supported by buoyancy. However, when moving through water, the ducks also experience other sources of energy loss and demand for force. For example, when taking off from water, the ducks would need to produce force to compensate for drag experienced by the body or accelerating the extra mass of water entrained in the feathers. In addition, as the foot moves faster and hydrodynamic force increases, larger muscle force will be required to balance hydrodynamic force. Thus, velocity and force must simultaneously increase during aquatic locomotion (Richards, 2011), as evidenced by our observation of higher LG power (i.e. force×velocity) during aquatic versus terrestrial takeoffs (Fig. 6).
Another important difference between moving on land versus water is the compliance of water relative to the rigid terrestrial takeoff platform used in our study. Differences in compliance can affect kinematics and performance. For example, takeoff velocity was lower on more compliant substrates for frogs (Astley et al., 2015; Reynaga et al., 2019), birds (Crandell et al., 2018) and humans (Giatsis et al., 2004). When jumping from the water column, frogs extended their legs faster than during terrestrial jumps (Wilkinson, 2014) and frogs that reduced slip of their feet during aquatic jumps had higher jump heights (Nauwelaerts et al., 2004). More compliant, dissipative substrates, such as sand, also require more mechanical work and incur a higher energetic cost to walk and run over (Lejeune et al., 1998). The higher compliance of a fluid substrate and the resulting ‘slip’ of the propulsive appendage relative to the fluid also results in a loss of mechanical energy (Hsieh, 2003; Li et al., 2012; Astley et al., 2015; Reynaga et al., 2019), and compromises the ability of animals to store elastic energy (Li et al., 2012; Reynaga et al., 2019). Because slip (motion of the appendage relative to the fluid) represents energy loss, animals need to produce additional work (Hsieh, 2003; Li et al., 2012) through larger joint excursions or higher forces.
In order to account for differences between environments, ducks are not limited to only changing hindlimb kinematics. Ducks and other waterfowl use their wings and tail to assist foot propulsion during aquatic behaviors, including during vertical takeoffs (Williamson et al., 2001). Although characterizing the contributions of the wings and tail to aquatic takeoff is beyond the scope of the current study, they are clearly key to achieving vertical takeoff in mallards. In fact, the wings and feet working in unison is a common strategy for birds moving at the water's surface and has been described for behaviors like taxiing prior to takeoff or paddle-assisted flight (Norberg and Norberg, 1971; Gough et al., 2015), and hydroplaning and/or steaming (Aigeldinger and Fish, 1995; Gough et al., 2015). An inverse dynamics study pairing ground reaction forces (measured using a force plate) and fluid dynamic forces (measured using PIV), although challenging to carry out, could elucidate the relative contributions of the hindlimbs, wings and tail during takeoff. Although not the focus of the current study, preliminary results demonstrated a strong but not significant relationship between ground reaction force and LG stress (r2=0.88, P=0.06; Fig. S3), suggesting that LG function plays an important role in terrestrial and, we would argue, aquatic takeoffs.
Linked to the kinematic differences they produce, changes in muscle function also facilitate movement in different media. Based on the knee kinematics we observed for aquatic versus terrestrial takeoffs, it is clear that changes in motor coordination patterns must occur, altering the timing of when and which muscles are activated (i.e. knee flexors versus extensors). Differential recruitment of LG synergists could also play a role. Biewener and Corning (2001) observed that the mallard MG and LG have similar force contributions during walking but the MG generates much less force than the LG during swimming. This suggests that increased MG recruitment may account for the additional force needed to accelerate the body during terrestrial takeoffs, which could explain why we found no significant change in LG stress between terrestrial and aquatic takeoffs.
Because muscle force is maximized over a limited range of length changes and shortening velocities, changes in these parameters could limit force, work and power production. The LG exhibited higher shortening velocities during aquatic takeoffs than during terrestrial takeoffs, which likely compromises its force production for a given amount of muscle recruitment, requiring the recruitment of more fibers and more energy expenditure to produce similar forces. We also observed that the LG operated over longer fascicle lengths and generated force over a broader range of strains during aquatic takeoffs than for terrestrial takeoffs (Fig. 5B), suggesting length-dependent shifts in its force-generating ability. Mapping the LG's in vivo muscle use patterns during aquatic and terrestrial takeoff to muscle force–length and force–velocity properties would allow us to determine whether these changes in strain and shortening velocity involve a tradeoff in muscle force production.
Conclusions
Locomotion on or through different environments places demands on the mechanisms by which animals generate propulsive forces that require changes in both motor behavior and muscle function. We found that hindlimb kinematics and the function of at least one key propulsive muscle (LG) change between terrestrial and aquatic takeoffs. Because aquatic takeoffs require larger and faster fascicle length changes, LG muscle function is likely altered by changes in neural activation as well as by its intrinsic force–length and force–velocity properties, which may be compensated by differential recruitment of other leg muscles or other parts of the body that assist in propulsion. This study highlights the challenges animals face when moving through or on different media and how muscle function may be tuned across behaviors.
Acknowledgements
We are grateful for the help we received with data collection and analysis, including from Konow Lab at UMass Lowell (especially Dr Nicolai Konow and Alexandra Collias), Dr Chris Tijs, Kathryn Gillespie, Kamryn Hoag, Dr Jennifer Carr and Jacob Freedman. We appreciate the helpful comments we received from Dr Tom Roberts on an earlier draft of the manuscript. We are also grateful for the assistance we received from Ken Wilcox and Pedro Ramirez for help building the experimental setup and providing animal care, respectively, and from the rest of the Concord Field Station community.
Footnotes
Author contributions
Conceptualization: K.R.T.-B., A.A.B.; Methodology: K.R.T.-B., A.A.B.; Formal analysis: K.R.T.-B.; Investigation: K.R.T.-B., A.A.B.; Resources: A.A.B.; Data curation: K.R.T.-B.; Writing - original draft: K.R.T.-B.; Writing - review & editing: K.R.T.-B., A.A.B.; Visualization: K.R.T.-B.; Supervision: A.A.B.; Project administration: K.R.T.-B.; Funding acquisition: K.R.T.-B., A.A.B.
Funding
This work was supported by Harvard University’s Department of Organismic & Evolutionary Biology, including through dissertation research funding and the Robert A. Chapman Memorial Scholarship for Vertebrate Locomotion (K.R.T.-B.).
Data availability
Data are available on figshare at doi:10.6084/m9.figshare.12654506.
References
Competing interests
The authors declare no competing or financial interests.