Seasonal Changes in Glycogen Level and Size of Pinealocytes of the White-Footed Mouse, Peromyscus leucopus: A Semiquantitative Histochemical Study

1984 ◽  
Vol 1 (2) ◽  
pp. 163-174 ◽  
Author(s):  
T. Kachi ◽  
W.B. Quay
1995 ◽  
Vol 73 (2) ◽  
pp. 243-252 ◽  
Author(s):  
Terry L. Derting ◽  
Edward B. Noakes III

Changes in gut capacity may be important for a species adapting to increased energy requirements or decreased food quality in a seasonal environment. We conducted a comparative study of seasonal changes in gut capacity in two rodent species with diets of different types. Although the lengths and masses of gut organs differed between species within a season, the species did not differ in the types of gut changes that occurred from summer to winter. All organs except the colon had significantly heavier wet and dry masses in winter than in summer. No significant differences in organ lengths, volumes, or surface areas occurred with season. Increased mass of the small intestine was due to large increases in the mass of the mucosa and smaller increases in the mass of the serosa. In winter, Microtus pennsylvanicus had significantly lower body mass than in summer. Peromyscus leucopus had no change in body mass in winter but may have used torpor as an energy-conservation mechanism. Energy-conservation adaptations in each species may have minimized the need for large changes in the gut organs.


1978 ◽  
Vol 51 (3) ◽  
pp. 289-299 ◽  
Author(s):  
G. Robert Lynch ◽  
F. Daniel Vogt ◽  
Harvey R. Smith

2003 ◽  
Vol 117 (2) ◽  
pp. 184 ◽  
Author(s):  
Erin Stewart Lindquist ◽  
Charles F. Aquadro ◽  
Deedra McClearn ◽  
Kevin J. McGowan

Field identification of the White-footed Mouse (Peromyscus leucopus noveboracensis) and Long-tailed Deer Mouse (Peromyscus maniculatus gracilis) is difficult because of their similar external morphology. Peromyscus were sampled by live-trapping during a five-year period (1992-1996) at the Arnot Teaching and Research Forest, Van Etten, New York and identified to species by electrophoresis of their salivary amylase. No electromorphs were shared between P. leucopus and P. maniculatus, thus permitting unambiguous species identification of individuals. Means and ranges of four external measurements (ear, head-body, hind-foot, and tail) and tail to head-body ratio were determined for amylase-genotyped live mice. Although some body measurements did differ on average between the two species (ear, head-body, and tail for adults; hind-foot and tail for juveniles), the ranges of these overlap considerably. When the four external measurements (excluding the tail to head-body ratio) were used to construct two discriminant-function equations, they yielded correct identification of 80% of the adult P. l. noveboracensis and P. m. gracilis assessed excluding juveniles, and 71% of adult and juvenile mice combined. The function reported here allows partial field identification, but genetic analysis remains the only reliable field method for differentiation between live P. l. noveboracensis and P. m. gracilis. Includes erratum for a figure in this article.


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