scholarly journals Hind foot drumming: morphological adaptations of the muscles and bones of the hind limb in three African mole‐rat species

2019 ◽  
Vol 235 (4) ◽  
pp. 811-824 ◽  
Author(s):  
L. Sahd ◽  
N. C. Bennett ◽  
S. H. Kotzé
2015 ◽  
Vol 97 (1) ◽  
pp. 211-233 ◽  
Author(s):  
Margaret Liu ◽  
Shawn P. Zack ◽  
Lynn Lucas ◽  
Darien Allen ◽  
Rebecca E. Fisher

Abstract The ringtail ( Bassariscus astutus ) is a widely distributed small carnivorous mammal (Procyonidae) in Mexico and the southwestern United States. As in other procyonids, the ringtail is capable of rotating its hind foot to allow headfirst descent of vertical substrates. The osteological correlates of this process, termed hind foot reversal, are well documented, but potential myological correlates have never been investigated. We present the 1st detailed study of the muscular anatomy of the hind limb of B. astutus , including the 1st muscle maps of the pelvis and pes of any procyonid. Comparison of the hind limb myology of the ringtail with other arctoid carnivorans, including taxa incapable of hind foot reversal, indicates that the muscles responsible for the action of reversal do not differ significantly between nonreversing forms and taxa capable of partial or full reversal. This suggests that specific myological adaptations are not necessary to achieve hind foot reversal. However, increased development of the digital flexors, which maintain a grip while body mass is supported by the hind limb, may characterize taxa that make use of reversed postures. The hind limb myology of members of Procyonidae does not strongly support either morphological or molecular hypotheses of relationship, in part because relatively few differences among members of the family can be documented.


Author(s):  
Eliot Goldfinger

Kangaroo characteristics: Forelimb small; has five digits with strong claws. Large, powerful hind limb with long, strong, narrow foot. Muscular thigh; muscle mass of lower leg positioned on upper half, toward knee. In foot, large fourth and smaller fifth digits transmit force during locomotion; first digit missing, small digits two and three bound together by skin. Long tail, thick at base, used for body support at rest and balance during hopping. Fast locomotion is by leaping with hind limbs only. Walking: Hind limbs, forelimbs, and tail in contact with ground at various times. Sitting: Body rests on entire foot and tail; arms hang loosely. Pouch in female opens forward, supported by two long, thin bones. Sea lion characteristics: Webbed flipper-like forefoot and hind foot. Front flipper thicker on front edge. Skin of flipper extends past tips of toe bones, supported by individual cartilages attached to ends of toe bones. Noticeable claws on three middle toes of hind foot; other claws tiny and inconspicuous. Front flipper triangular; hind flipper rectangular. Hind limb can be advanced forward—can walk, but thigh and lower leg encased in skin of abdomen (seals can’t walk—their hind limbs permanently extended backward). Elbow also enclosed in body skin, but forearms are free. Body streamlined (torpedo-shaped) for swimming. Thick insulating blubber layer between skin and muscles. Thick, flexible, muscular neck. Pelvis and femur small. Sternum has forward projection. Small external ears present (absent in seals). Ears and slit-like nostrils can be closed under water. Short, stubby tail. Very short hair; fur much darker when wet. Body uniform in color (no spots). Males larger than females. Closely related to terrestrial carnivores. Pinniped is not scientific classification, but means “fin footed.”


New data on the greater mole-rat’s biology in the territory of the Regional landscape park «Velikoburlutskyi steppe” (Kharkiv region, Ukraine) concerning nutrition, burrow structure and social structure are presented. The greater mole-rat has only one litter consisting of 1–3 pups during the year. Contrary to the prevailing general opinion that mole-rats lead solitary way of life we have found cohabitation of a female, a male and their young of the current year at three of the seven areas of our study. Young mole-rats settle in a new place at the end of June – early July. They can be found above ground often at this time. In the greater mole-rat population from the Regional Park “Velikoburlutskyi steppe” males are characterized by the body length of 220–260 mm, by hind foot length of 27–30 mm, by the body weight of 219–520 g. For adult females the average body length is 200–250 mm, the hind foot length is about 26–30 mm, the body weight ranges from 284 to 409.6 g. Many greater mole-rat specimens on the forehead or occiput have an individual light spot (yellowish-white) or a white longitudinal strip by which we can identify individuals at repeated catching. Eating the underground parts of plants, the mole-rat makes very long tunnels conducting by them horizontally and closely to the surface and throwing along them the large piles of soil (up to 0.5 m in diameter). Soil emissions marking feeding tunnels had a base diameter of up to 50–60 cm. In the nest part of the hole the number of habitable chambers and chambers for stocks can be up to 10, and they are located at the depth of 3.5 m. Digging activity of the mole-rat grows in late March – early April and in the autumn at the end of September – early October. We have repeatedly noted the appearance of emissions in the winter during the thaw. Mole-rats harm the agriculture with their digging activity (damage cultivated areas, digging under the plants and so on); in addition, mole-rats sometimes directly eat potato tubers, onion and other root vegetables. The total weight of one mole-rat stock can reach 16 kg. In one of burrows excavated by us near the vegetable gardens of locals in Nesterivka village of Velikoburlukskyi district in Kharkiv region we found 8 kg of potatoes, 4 kg of carrots, 3 kg of greater burdock roots, 0.6 kg of couch grass roots.


Author(s):  
William P. Jollie

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.


Sign in / Sign up

Export Citation Format

Share Document