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Quimby's data indicate that some mice produce litters at the age of approximately 2 months, when four-fifths grown. Therefore, sexual maturity is not always synonymous with morphological maturity.

In specimens assigned to age groups 1 and 2 the length of the body averaged 70 and 74.8 mm, respectively. The individuals of both groups are less than 13 weeks old if we assume that growth proceeds at the same rate in Michigan as it does in Minnesota.

In the specimens from Michigan of age groups 3, 4, 5, and 6 the average length of the body is 80.9, 83.7, 89.0, and 83.6, respectively.

According to Quimby , the pinna of the ear at birth is small and folded over the external auditory meatus. The length of the ear increases proportionately more than any other external dimension after the first four weeks of growth.

If the average length of the ear of adults is 14.7 mm, the animals from Michigan in age groups 1 and 2 are 91.8 per cent and 96.5 per cent as large as adults.

TABLE 1.--Average Dimensions for Specimens of Z. h. hudsonius of Various Ages .

From these data, concerning growth of external parts, it seems that: growth is most rapid during the four weeks following parturition; specimens from Michigan, assigned to age groups 1 and 2 on the basis of tooth wear, are less fully developed and probably younger than mice from Minnesota, with a known age of 13 weeks; individuals with sufficient wear on the teeth to be placed in age group 3, if they were obtained in the late fall, may be young from the first litters of the year or, if they were obtained in early spring, may be at least one year old; individuals in age groups 4, 5, and 6 are at least one year old.

SKULL.--The post-embryonic development of the skull is rapid. Animals in age groups 1 and 2 have skulls which average more than 80 per cent of the size that is here considered adult . The actual increase in size of certain cranial elements for various age groups is given in table 2.

The incisive foramina in age group 1 are short , broad , and taper to a point at each end. In age group 2 the foramina have elongated and are less pointed posteriorly, but there is no change in breadth. In age groups 3, 4, 5, and 6 the foramina become progressively longer , have a relatively constant breadth , and become more nearly truncate anteriorly.

TABLE 2.--Average and Extreme Measurements of Skulls of Six Age-groups in Specimens of Zapus hudsonius from Michigan.

Individual Variation

Individual variation in the occlusal pattern of the molariform teeth is slight. In several specimens, however, the re-entrant fold is absent from the lingual surface of M1. Teeth in addition to the normal number were recorded for five specimens. In all instances they are in the upper dentition and usually at the posterior end of the maxillary tooth-row. In each of four specimens , there is only a single additional tooth. One individual possessed two extra molars, one in each maxillary tooth-row. The extra teeth vary in size from those which are only slightly smaller than the adjacent normal molars to those which are simple, peglike structures. In four of the five animals the extra teeth are posterior to the normal M3; in the fifth the added tooth is anteriormedial to M3.

TABLE 3.--Coefficients of Variation for Dimensions of Corresponding Parts of the Skull of Three Species of Zapus. The Specimens of Zapus hudsonius are from Menominee and Keweenaw counties, Michigan, the Zapus princeps are from the Vicinity of Encampment, Wyoming, and the Zapus trinotatus from Huntingdon, British Columbia.

The size and shape of certain cranial elements vary individually even between right and left sides of the same animal. The paired parietal bones in some animals are nearly square and identical. In other animals these bones are approximately equal and straight on three sides with the fourth side forming an anterolateral projection; this projection may be slightly or greatly produced, and opposite elements in a single individual differ in this respect.

The interparietal also is variable; the lateral arms may be blunted and not included in the fusion of the squamosal, parietal, and occipital elements, or the interparietals may be elongated and fused with these elements. Posterior and anterior borders of the interparietal may be straight, produced anteriorly, produced posteriorly, or produced anteriorly and posteriorly.

There is frequently variation in the degree of taper of the nasals. They may be parallel sided, narrowed distally, or narrowed proximally. There is some variation in the degree of inflation, in the size, and in the shape of the frontal bones. The anterior surface of the postpalatal notch varies individually and may be truncate, anteriorly convex, or anteriorly concave.

Individual variation in the color of the pelage of animals that are in the same stage of molt or non-molt is by my observation slight. The presence of oil in the hair results in a false impression of sleekness and seemingly darker pigmentation. Abnormal white-spotting dorsally occurs as does yellow and melanistic coat color. These mutations are considered in the discussion concerning pelage.

Secondary Sexual Variation

TABLE 4.--Mean Measurements for Adult Male and Female Z. hudsonius of Age Group 2 and Per Cent Difference of Females to Males .

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EXTERNAL CHARACTERS.--Muriform in general appearance; forelimbs small, short; hind limbs greatly developed; hind feet long and narrow; tail tapering, attenuate, subcylindrical; head long and mouse-shaped; eyes small and situated midway between nose and ear; external ear somewhat longer than surrounding hair and provided with antitragal flap which can cover external auditory meatus, and in company with tragus completely close opening; upper lip without median groove; internal cheek-pouches well developed and opening at corners of mouth; mystacial vibrissae conspicuous; supercilliary vibrissae few; genal tuft absent; teats normally eight and arranged in pairs ; anterior and posterior pairs frequently undeveloped; general pelage coarse; color of pelage varies somewhat in different species but always follows single basic pattern of broad dorsal band of some shade of brown or brownish-yellow darkened with brownish-black, sides of a lighter tone and slightly streaked with brownish-black, underparts snow-white, sometimes suffused with color of the sides and usually separated from color of sides by sharp line of clear brownish-yellow; backs of forefeet and hind feet grayish-white; tail distinctly bicolor, dark brown above and yellowish-white below; ears dark and narrowly edged with light color.

CRANIAL CHARACTERS.--Skull short in relation to width, deep relative to other dimensions, somewhat convex; delicate, papery, without strong angularity; braincase relatively unexpanded; antorbital foramen obliquely oval and transmits masseter muscle of great size; foramen in inferior ramus of zygomatic process of maxillary for passage of superior maxillary branch of trigeminal nerve small; zygomata not wide-spreading; underside of zygoma nearly horizontal, upper edge anteriorly rises prominently owing to extension of jugal upward along maxillary; jugal and lachrymal in contact; one ramus of zygomatic process of maxilla arises directly above other; rostrum thick basally and relatively attenuate distally; ends of nasals project noticeably beyond incisors; premaxillaries develop strong alveolar plate separating superior incisors for half their length; palatal bones shortened posteriorly, free edge often concave; incisive foramina long, broad, and separated by bulbose bony septum; mastoid bullae absent; auditory bullae short and transversely placed; postorbital process never present; parietals nearly square, sometimes emarginate in front; angle of mandible flattened and bent inward; coronoid process weak, acute, and slopes strongly upward.

DENTAL CHARACTERS.--Dental formula

upper incisors short, compressed, curved backward, and strongly grooved; lower incisors slender, curved backward, and ungrooved; both upper and lower incisors deep orange or yellow; four upper cheek-teeth present; premolar small, single rooted and, sometimes, non-functional; upper molars tri-rooted, sub-hypsodont, and with occlusal surface non-cuspidate ; enamel pattern, much complicated, consisting of one main re-entrant fold lingually and four re-entrant folds labially; three lower molars, bi-rooted, sub-hypsodont, flat crowned, with two outer and four inner re-entrant folds.

POSTCRANIAL CHARACTERS.--Neck short and weak; atlas large; axis separate from atlas; remaining cervical vertebrae also free; thoracic and lumbar vertebrae strongly built; posterior lumbars with enlarged neural and anteriorly directed transverse processes; sacral vertebrae as in murids; caudal vertebrae variable in number ; clavicle long, slender, uniformly curved, convex outwardly; scapula with supraspinous and infraspinous fossae of equal size; forelimbs short, approximately half as long as hind limbs; hind limbs elongate, slender; femur with third trochanter; tibia and fibula fused slightly distal to middle of former; five elongate, separate metatarsals .

ARTIFICIAL KEY TO THE SPECIES OF THE GENUS ZAPUS

A?. Baculum with tip lanceolate and tip less than 0.43 mm wide; underfur with medullary pattern square or rectangular; but, if rectangular, cuticular scales large; coronoid process short and broad, angle of divergence from condyle narrow; angle of mandible turned inward and small to medium; pterygoid fossae usually narrow; skull not broad in relation to length; premolars without crescentine fold on occlusal surface.

SYSTEMATIC ACCOUNTS OF SPECIES AND SUBSPECIES

GEOGRAPHIC VARIATION

There are four subspecies currently recognized, all of which are confined to the Pacific coastal region of North America . The features that vary geographically are external size, color of pelage , and dimensions of certain cranial structures .

External size is smallest in the southernmost geographic race and largest in the northernmost geographic race . This decrease in size from north to south is clinal and is in keeping with Bergman's Rule which postulates that within one species the smallest individuals occur in the warmer parts of its geographic range.

NATURAL HISTORY

Svihla and Svihla heard captive animals make squeaking noises when fighting. On several occasions captive animals made a drumming noise by rapidly beating the tail against a resonant body such as the bottom of a tin can.

Concerning hibernation, Bailey remarks that animals of this species in Oregon, become fat in early autumn and lay down excess adipose tissue under the skin, over the muscles, and in the abdominal cavity. Svihla and Svihla noted that captives from the Olympic Peninsula, Washington, gained weight in September and October and became extremely fat. With the additional weight they were more listless and drowsy, often spending days curled up in the hibernating position with the head between the hind legs and the long tail curled completely over the head and body. Warmth aroused the animals to activity, but when the temperature dropped they again hibernated. Flahaut reported the discovery on February 23, 1939, at Henderson Inlet, South Bay, Thurston County, Washington, of two nest cavities inhabited by jumping mice that were hibernating. The nests, four inches apart and 30 inches below the surface of the ground, were approximately five inches in diameter and made of shredded paper. Both mice were dormant, covered by nesting materials and curled up in the aforementioned hibernating posture. Dalquest writes that in the lowlands of Washington this species disappears by late July but that in the mountains it remains active until the middle of September. Edson records an individual taken on April 20 from its place of hibernation beneath the roots of a decaying stump. This animal quickly roused in the warm mid-afternoon sun but became dormant again when the temperature dropped to 45? F. It seems that animals near the end of hibernation become active on warm days and return to the torpid state on cold ones.

GEOGRAPHIC VARIATION

There are 11 subspecies recognized, most of which are in the mountains of the western United States and southwestern Canada. There is geographic variation in color, relative proportions of external parts , and shape and size of the skull.

External dimension as a whole decreases from north to south, although not uniformly. For example, the smallest individuals are of the southernmost geographic subspecies , but the largest are of the subspecies that is near the geographic center of the range for the species. In the skull there is geographic variation in the length and shape of the zygomata, size and shape of the incisive foramina, alignment of maxillary tooth-rows, size and shape of auditory bullae, position of the postpalatal notch in relation to M3, and the presence or absence and size of the medial projection on the inferior ramus of the zygomatic process of the maxillary.

NATURAL HISTORY

According to Hollister and Davis , jumping mice are for the most part nocturnal, but occasionally they are seen by day in tall grass.

Embryos in 25 pregnant females averaged 5 . The mammae of the female are arranged in four pairs .

BRITISH COLUMBIA: Vermilion Crossing, Kootenay, 1 ; Paradise Mine, 3 ; Crows Nest Pass, 4450 ft., 3 ; Newgate, 10 .

ALBERTA: 4 mi. N Marinville, 2; Blindman River, 1 ; Camrose, 1 ; Red Deer River, 1 ; Didsbury, Little Red Deer River, 1 ; Kananaskis Valley, 7000 ft., 1 ; High River, 2 ; Lodge Creek, 2 .

MANITOBA: Shoal Lake, 6 ; Oak Lake, 4 ; Aweme, 7 .

ALASKA: Taku River, 1 .

YUKON: Rose River, mile 95 on Canol Road, 1 .

GEOGRAPHIC VARIATION

Color of the pelage varies, as a general rule, from dark-backed, dull-sided individuals in the northern parts of the geographic range of the species to light-backed, bright-sided individuals in the southern parts of the range.

Seemingly there is no clinal variation in the several qualitative features of the cranium, for instance in the shape of the auditory bullae, shape of the incisive foramina, and shape of the postpalatal notch. On the other hand, the dimensions of the entire skull show that the larger crania are of the northernmost subspecies and the smaller of the southernmost subspecies.

NATURAL HISTORY

Concerning the use of the tail as a balancing organ, G. S. Miller describes the behavior of a jumping mouse from which the tail had been severed by the sickle of a mowing machine. "When I approached, it made violent efforts to escape, but the moment it was launched in the air, its body, deprived of its balancing power, turned end over end so that it was as likely as not to strike the ground facing the direction from which it had come."

From the foregoing reports on hibernation sites it is evident that well drained areas are utilized. Sheldon remarks that the burrows used for hibernating are dug in a bank or some place from which the rain water and melted snow probably drains off.

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