Population Characteristics and Phenology of a Franklin Ground Squirrel (Spermophilus franklinii) Colony in Alberta, Canada

1973 ◽  
Vol 90 (2) ◽  
pp. 334 ◽  
Author(s):  
Jan O. Murie
Keyword(s):  
Ground Squirrel ◽  
Population Characteristics ◽  
Spermophilus Franklinii

scholarly journals Distribution, Abundance, and Habitat Associations of Franklin’s Ground Squirrel (Spermophilus franklinii Sabine 1822)

2007 ◽  
Vol 38 (1-6) ◽  
pp. 1-58 ◽  
Author(s):  
J. J. Huebschman
Keyword(s):  
Tallgrass Prairie ◽  
Ground Squirrel ◽  
Management Strategies ◽  
Geographic Range ◽  
Habitat Associations ◽  
The Body ◽  
Spermophilus Franklinii ◽  
Conservation Concern ◽  
Franklin's Ground Squirrel ◽  
Dispersal Events

To better inform conservation and management strategies directed at Franklin’s ground squirrel, Spermophilus franklinii, I reviewed published and unpublished accounts of the squirrel’s distribution, abundance, and principally, habitat associations. I present the body of literature on S. franklinii and include portions of original accounts to avoid potential bias from paraphrasing. A consensus of the literature indicates that S. franklinii is most frequently associated with habitat characterized by a mixture of grassy and woody vegetation, referred to as savanna-like or parkland habitat. Moreover, S. franklinii has had an affinity for this type of habitat throughout its geographic range in recent, historic, and even prehistoric times. This is in contrast to a view of the species as primarily associated with tallgrass prairie habitat. As indicated in the literature, populations of S. franklinii are subject to marked fluctuations, which probably are influenced by local disturbances in addition to regular dispersal events. In the southern part of its geographic range, S. franklinii is currently limited in its occurrence principally to roadside and railroad right-of-ways. In these southern regions S. franklinii is justifiably of conservation concern. I suggest that more detailed surveys for the species (such as those that have recently occurred in Illinois and Missouri) take place in Iowa and Kansas.

Scanning Electron Microscopy and X-Ray Analyses of Dental Tissues from a Hibernator

1976 ◽  
Vol 34 ◽  
pp. 178-179
Author(s):  
M. L. Zimny ◽  
A. C. Haller
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Body Temperature ◽  
Ground Squirrel ◽  
Alveolar Bone ◽  
X Ray ◽  
Dental Tissues ◽  
Bone Minerals ◽  
Apical Tooth ◽  
Scanning Electron

During hibernation the ground squirrel is immobile, body temperature reduced and metabolism depressed. Hibernation has been shown to affect dental tissues varying degrees, although not much work has been done in this area. In limited studies, it has been shown that hibernation results in (1) mobilization of bone minerals; (2) deficient dentinogenesis and degeneration of alveolar bone; (3) presence of calculus and tears in the cementum; and (4) aggrevation of caries and pulpal and apical tooth abscesses. The purpose of this investigation was to study the effects of hibernation on dental tissues employing scanning electron microscopy (SEM) and related x-ray analyses.

Retrospective Diagnosis of Pontocerebellar Hypoplasia Type 1B in a Family with Two Deceased Newborn Children

2020 ◽  
Author(s):  
Irena Bradinova ◽  
Silvia Andonova ◽  
Alexey Savov
Keyword(s):  
Clinical Signs ◽  
Final Diagnosis ◽  
Population Based ◽  
Neuromuscular Disorder ◽  
Population Characteristics ◽  
High Risk Population ◽  
Pontocerebellar Hypoplasia ◽  
Clinical Genetic ◽  
Retrospective Diagnosis ◽  
Newborn Children

AbstractPontocerebellar hypoplasia type 1B is a severe autosomal recessive neurologic disorder characterized by a combination of cerebellar and spinal motor neuron degeneration beginning at birth. Pontocerebellar hypoplasia type 1B is caused by mutations in EXOSC3 gene. High prevalence of the p.Gly31Ala mutation was found recently, especially in the Roma ethnic minority. We present a young Bulgarian Roma family with two deceased newborn children manifesting severe neuromuscular disorder including severe muscle weakness, respiratory distress, and multiple joint contractures. Based on the clinical signs and family's population characteristics, DNA testing for the previously described EXOSC3 in Bulgarian Roma mutation c.92G > C; p.Gly31Ala was performed on blood samples of both parents and they were found to be heterozygous carriers. This finding indirectly confirmed the diagnosis of pontocerebellar hypoplasia type B in the deceased offspring. Knowledge of population-specific molecular bases of genetic conditions was the key to final diagnosis in the presented family. Designing of population-based clinical-genetic panels may be a powerful diagnostic tool for patients with such origin. Preconception carrier screening in high-risk population groups is a feasible option to discuss.

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