Elastic energy storage across speeds during steady-state hopping of desert kangaroo rats (Dipodomys deserti)

Small bipedal hoppers, including kangaroo rats, are thought to not benefit from substantial elastic energy storage and return during hopping. However, recent species-specific material properties research suggests that, despite relative thickness, the ankle extensor tendons of these small hoppers are considerably more compliant than had been assumed. With faster locomotor speeds demanding higher forces, a lower tendon stiffness suggests greater tendon deformation and thus a greater potential for elastic energy storage and return with increasing speed. Using the elastic modulus values specific to kangaroo rat tendons, we sought to determine how much elastic energy is stored and returned during hopping across a range of speeds. In vivo techniques were used to record tendon force in the ankle extensors during steady-speed hopping. Our data support the hypothesis that the ankle extensor tendons of kangaroo rats store and return elastic energy in relation to hopping speed, storing more at faster speeds. Despite storing comparatively less elastic energy than larger hoppers, this relationship between speed and energy storage offer novel evidence of a functionally similar energy storage mechanism, operating irrespective of body size or tendon thickness, across the distal muscle-tendon units of both small and large bipedal hoppers.

Plantar flexor muscles of kangaroo rats (D. deserti) shorten at a velocity to produce optimal power during jumping

During jumping by kangaroo rats, the musculotendon work contributions across all joints are not well understood. Namely, measures of external joint work do not provide information on the contributions from individual muscles or in-series elastic structures. In this study, we examined the functional roles of a major ankle extensor muscle, lateral gastrocnemius (LG), and of a major knee extensor muscle, vastus lateralis (VL), through in vivo sonomicrometry and electromyography techniques, during vertical jumping by kangaroo rats. Our data showed that both muscles increased shortening and activity with higher jumps. We found that knee angular velocity and VL muscle shortening velocity were coupled in time. In contrast, the ankle angular velocity and LG muscle shortening velocity were decoupled, and rapid joint extension near the end of the jump produced high power outputs at the ankle joint. Further, the decoupling of muscle and joint kinematics allowed the LG muscle to prolong the period of shortening velocity near optimal velocity (Vopt), which likely enabled the muscle to sustain maximal power generation. These observations were consistent with a LG tendon that is much more compliant than that of the VL.

Heterothermy as a mechanism to offset energetic costs of environmental and homeostatic perturbations

Environmental and biotic pressures impose homeostatic costs on all organisms. The energetic costs of maintaining high body temperatures (Tb) render endotherms sensitive to pressures that increase foraging costs. In response, some mammals become more heterothermic to conserve energy. We measured Tb in banner-tailed kangaroo rats (Dipodomys spectabilis) to test and disentangle the effects of air temperature and moonlight (a proxy for predation risk) on thermoregulatory homeostasis. We further perturbed homeostasis in some animals with chronic corticosterone (CORT) via silastic implants. Heterothermy increased across summer, consistent with the predicted effect of lunar illumination (and predation), and in the direction opposite to the predicted effect of environmental temperatures. The effect of lunar illumination was also evident within nights as animals maintained low Tb when the moon was above the horizon. The pattern was accentuated in CORT-treated animals, suggesting they adopted an even further heightened risk-avoidance strategy that might impose reduced foraging and energy intake. Still, CORT-treatment did not affect body condition over the entire study, indicating kangaroo rats offset decreases in energy intake through energy savings associated with heterothermy. Environmental conditions receive the most attention in studies of thermoregulatory homeostasis, but we demonstrated here that biotic factors can be more important and should be considered in future studies.

Conservation of endangered Tipton kangaroo rats (Dipodomys nitratoides nitratoides): status surveys, habitat suitability, and conservation recommendations

The Tipton kangaroo rat (Dipodomys nitratoides nitratoides; TKR) is listed as endangered both Federally and by the state of California due to profound habitat loss throughout its range in the southern San Joaquin Valley of California. Habitat loss is still occurring and critical needs for TKR include identifying occupied sites, quantifying optimal habitat conditions, and conserving habitat. Our objectives were to (1) conduct surveys to identify sites where TKR were extant, (2) assess habitat attributes on all survey sites, (3) generate a GIS-based model of TKR habitat suitability, (4) use the model to determine the quantity and quality of remaining TKR habitat, and (5) use these results to develop conservation recommendations. We surveyed for TKR on 44 sites by live-trapping and detected TKR on 15 sites. Sites with TKR tended to have larger alkali scalds and no obvious sign of past tilling compared to sites without TKR. Also, sites with TKR usually had relatively sparse ground cover and seepweed (Suaeda nigra) was present. The non-protected Heermann’s kangaroo rat (Dipodomys heermanni), a larger competitor, was either absent or present in relatively low numbers at sites with TKR, and when present its abundance was inversely related to that of TKR. Based on our habitat suitability modeling, an estimated 30,000 ha of moderately high or high quality TKR habitat and 60,000 ha of lower or medium quality habitat remain. However, habitat is still being lost and conversion of at least one survey site with TKR occurred during this project. Recommendations for TKR conservation are to (1) conduct additional TKR surveys on unsurveyed but suitable sites, (2) conserve suitable habitat on unprotected lands, (3) manage vegetation on occupied sites if necessary, (4) restore disturbed lands to increase suitability for TKR, and (5) research methods and conduct translocations of TKR to unoccupied sites with suitable habitat.

Conservation of threatened San Joaquin antelope squirrels: distribution surveys, habitat suitability, and conservation recommendations

The San Joaquin antelope squirrel (Ammospermophilus nelsoni: SJAS) is listed as Threatened pursuant to the California Endangered Species Act due to profound habitat loss throughout its range in the San Joaquin Desert in California. Habitat loss is still occurring and critical needs for SJAS include identifying occupied sites, quantifying optimal habitat conditions, and conserving habitat. Our objectives were to (1) conduct surveys to identify sites where SJAS were present, (2) assess habitat attributes on all survey sites, (3) generate a GIS-based model of SJAS habitat suitability, (4) use the model to determine the quantity and quality of remaining habitat, and (5) use these results to develop conservation recommendations. SJAS were detected on 160 of the 326 sites we surveyed using automated camera stations. Sites with SJAS typically were in arid upland shrub scrub communities where desert saltbush (Atriplex polycarpa) or jointfir (Ephedra californica) were the dominant shrubs, although shrubs need not be present for SJAS to be present. Sites with SJAS usually had relatively sparse ground cover with >10% bare ground and Arabian grass (Schismus arabicus) was the dominant grass. SJAS were more likely to occur on sites where kangaroo rats (Dipodomys spp.) were present and burrow abundance was greater, but SJAS were less likely to be present on sites with California ground squirrels (Otospermophilus beecheyi). Based on our habitat suitability model, an estimated 5,931 km2 of high or moderately high quality habitat and 4,753 km2 of lower quality habitat remain. To conserve SJAS, we recommend (1) conducting additional SJAS surveys on sites not surveyed but with suitable habitat, (2) conserving unprotected lands with suitable habitat, (3) managing vegetation on occupied sites if necessary, (4) restoring disturbed lands to increase suitability for SJAS, and (5) conducting translocations of SJAS to unoccupied sites with suitable habitat.

Modern extirpation of the Texas kangaroo rat, Dipodomys elator, in Oklahoma: changing land use and climate over a century of time as the road to eventual extinction

Surveys conducted during three years (2014-2017) provide the most extensive documentation to date for the possible presence of the Texas kangaroo rat (Dipodomys elator), a Tier II species considered to be of greatest conservation need, in seven counties in southwestern Oklahoma. The project encompassed 15 surveys on 93 nights; 266 localities were surveyed for a total of 9,094 trap nights and more than 32,428 km of paved and unpaved roads were surveyed for potential habitat and activity. No Texas kangaroo rats were captured or observed. However, 2,178 individuals of 17 mammal species were captured and individuals of 12 additional mammal species were collected and/or observed. New locality and natural history information for mammal species was obtained and six county records were recorded based on specimens and/or observations. Project results and historical information suggest that the Texas kangaroo rat (D. elator) is likely extirpated from the state of Oklahoma.

How to stick the landing: kangaroo rats use their tails to reorient during evasive jumps away from predators

Tails are widespread in the animal world and play important roles in locomotor tasks, such as propulsion, maneuvering, stability, and manipulation of objects. Kangaroo rats, bipedal hopping rodents, use their tail for balancing during hopping, but the role of their tail during the vertical evasive escape jumps they perform when attacked by predators has yet to be determined. Because we observed kangaroo rats swinging their tails around their bodies while airborne following escape jumps, we hypothesized that kangaroo rats use their tails to not only stabilize their bodies while airborne, but also to perform aerial re-orientations. We collected video data from free-ranging desert kangaroo rats (D. deserti) performing escape jumps in response to a simulated predator attack and analyzed the rotation of their bodies and tails in the yaw plane (about the vertical-axis). Kangaroo rat escape responses were highly variable. The magnitude of body re-orientation in yaw was independent of jump height, jump distance, and aerial time. Kangaroo rats exhibited a stepwise re-orientation while airborne, in which slower turning periods corresponded with the tail center of mass being aligned close to the vertical rotation axis of the body. To examine the effect of tail motion on body reorientation during a jump, we compared average rate of change in angular momentum. Rate of change in tail angular momentum was nearly proportional to that of the body, indicating that the tail reorients the body in the yaw plane during aerial escape leaps by kangaroo rats. Although kangaroo rats make dynamic 3D movements during their escape leaps, our data suggests that kangaroo rats use their tails to control orientation in the yaw plane. Additionally, we show that kangaroo rats rarely use their tail length at full potential in yaw, suggesting the importance of tail movement through multiple planes simultaneously.