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Ebook has 208 lines and 75745 words, and 5 pages

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Introduction 351

Materials, Methods, and Acknowledgments 352

Paleontology of the Genus 355

Relationships, Distribution, and Speciation 356

Annotated List of Specific and Subspecific Names 369

Characters of Taxonomic Worth 371

Nongeographic Variation 376

Check-List of the Species and Subspecies of the Genus Zapus 382

Genus Zapus 382

Artificial Key to the Species of the Genus Zapus 384

Systematic Accounts of Species and Subspecies 385

Tables of Measurements 455

Literature Cited 466

INTRODUCTION

The jumping mice are widely distributed over northern North America, occurring as far north as the Arctic Circle and as far south as Georgia, Missouri, Oklahoma, New Mexico, Arizona, and central California. In some years these small rodents are locally common in moist places that are either grassy or weedy; the jumping mice are notable for the much enlarged hind legs and the exceptionally long tail.

Members of the Genus as a whole have received no serious comprehensive taxonomic attention in the 54 years since Preble's revisionary work. In this time 15 new names have been proposed, mostly for subspecies, and only a few attempts have been made at grouping related named kinds.

MATERIALS, METHODS, AND ACKNOWLEDGMENTS

The present report is based on a study of approximately 3,600 specimens that were assembled at the Museum of Natural History of the University of Kansas or that were examined at other institutions. Most of these specimens are stuffed skins with skulls separate. Skulls without skins, skins without skulls, entire skeletons, and separately preserved bacula are included as a part of the total. Almost every specimen is accompanied by an attached label, which bears place and date of capture, name of collector, external measurements, and sex.

Specimens used in the study of geographic variation were arranged by season of capture and according to geographic location; then they were segregated as to sex, and, under each sex, by age. Next, individual variation was measured in comparable samples of like age, sex, season, and geographic origin. Finally, comparable materials were arranged geographically in order to determine variations of systematic significance.

The only external measurements used were total length, length of tail, and length of hind foot; these measurements were recorded by the collectors on the labels attached to the skins. Height of the ear was not used since it was not recorded by many of the collectors.

The baculum has a characteristic size and shape according to the species, and the following significant measurements of the structure were taken:

In the descriptions of color the capitalized color terms refer to those in Ridgway . Any color term that does not have the initial letter capitalized does not refer to any one standard.

In the description of the subspecies the two sexes are treated as one because no significant secondary sexual variation was found. Only fully adult specimens of age groups 3 to 5, as defined on pages 377 and 388, have been considered.

Unless otherwise indicated, specimens are in the University of Kansas Museum of Natural History. Those in other collections are identified by the following abbreviations:

AMNH. American Museum of Natural History. CAS. California Academy of Science. CM. Carnegie Museum. Chic. AS. Chicago Academy of Science. Clev. MNH. Cleveland Museum of Natural History. LMH. Collection of Lawrence M. Huey. JKJ. Collection of J. Knox Jones, Jr. CMNH. Colorado Museum of Natural History. FM. Chicago Museum of Natural History. HM. Hastings Museum, Hastings, Nebraska. ISC. Iowa State College. MCZ. Museum of Comparative Zoology. MO. University of Missouri Museum of Zoology. MVZ. Museum of Vertebrate Zoology, Berkeley, Calif. NMC. National Museum of Canada. NGFP. Nebraska Game, Forestation, and Parks Commission. NCS. North Carolina State College. OHIO. Ohio Wildlife Research Unit, Ohio State University. OKLA. Oklahoma Agricultural and Mechanical College. PM. Provincial Museum of British Columbia. ROM. Royal Ontario Museum of Zoology. SDM. San Diego Natural History Museum. SITC. Southern Illinois Teachers College. USBS. United States Biological Surveys Collection. USNM. United States National Museum. UCM. University of Colorado Museum. UIM. University of Illinois Museum of Natural History. UM. University of Michigan Museum of Zoology. UU. University of Utah Museum of Zoology.

The species are arranged from least to most progressive, and the subspecies are arranged alphabetically.

The synonymy for each subspecies includes first a citation to the earliest available name then one citation to each name combination that has been applied to the subspecies and, finally, any other especially important references.

Marginal records of occurrence for each subspecies are shown on the maps by means of hollow circles and these localities are listed in clockwise order beginning with the northernmost locality. If more than one of these localities lies on the line of latitude that is northernmost for a given subspecies the western-most of these is recorded first. Marginal localities have been cited in a separate paragraph at the end of the section on specimens examined in the account of a subspecies. Localities that are not marginal are shown on the maps by solid black circles. Localities that could not be represented on the distribution map because of undue crowding or overlapping of symbols are italicized in the lists of specimens examined and in the lists of marginal records.

The localities of capture of specimens examined are recorded alphabetically by state or province, and then by county in each state or province. Within a county the specimens are recorded geographically from north to south. The word "County" is written out in full when the name of the county is written on the label of each specimen listed for that county, but the abbreviation "Co." is used when one specimen or more here assigned to a given county lacks the name of the county on the label.

PALEONTOLOGY OF THE GENUS

RELATIONSHIPS, DISTRIBUTION, AND SPECIATION

Relationships in the Subfamily Zapodinae

The subfamily Zapodinae is known from Pliocene and Pleistocene deposits of North America and now occurs over much of northern North America and in Szechuan and Kansu, China. The living species occur among grasses and low herbs in damp or marshy places both in forested areas and in plains areas.

EAR OSSICLES.--The auditory ossicles are of three types which differ only slightly. These ossicles possibly are more conservative than some other structures because the ossicles are not so much affected by the molding influence of the environment.

In the region between the Rocky Mountains and the present Cascade Range and the Sierra Nevada, the flora became semidesert, which presumably made most of this region uninhabitable for jumping mice. The aridity probably induced local concentration into boreal montane islands, thus possibly displacing the populations of the two species that were in contact.

ANNOTATED LIST OF SPECIFIC AND SUBSPECIFIC NAMES

CHARACTERS OF TAXONOMIC WORTH

The individual hair of the underfur is cylindrical and tapers abruptly at each end; it is short, thin, flexible, and usually is bicolored on the back and sides of the mouse. The apical zone is yellow-brown and the proximal part is whitish or grayish, which gradually darkens to near black subapically.

The width of a hair in the underfur is of no taxonomic significance, in that individual variation exceeds that between species.

The pelage of juveniles is usually finer and softer than the pelage of adults. The lateral and dorsal bands are not so conspicuously marked in young animals, and individual hairs are not so long or so wide as in adult animals.

Preble and Howell remark as to the noticeable difference between pelages of spring and early fall. The pelage in spring is described as bright and fresh whereas that in fall is dull and worn. Actually both bright and worn pelages can occur in any one population at any one time. Some newly molted individuals are in fresh unworn pelage; some individuals, which are molting, are in ragged, worn pelage; and other individuals perhaps could be found to represent intermediate stages.

Three measurements--length, transverse diameter at the base, and transverse diameter at the tip--are easily obtained and are diagnostic. The bacula of all species are somewhat curved. The measurement of length used by me does not represent the actual length of the bone, but instead the chords of the arcs involved.

NONGEOGRAPHIC VARIATION

A knowledge of variation resulting from age, individual, or secondary sexual differences, as opposed to geographic variation between two or more populations of a single species is important in determining the reliability of taxonomic characters.

Age Variation

TEETH.--The teeth provide a valuable standard for age determination in that they wear at a measurable rate. The molars erupt in sequence from front to back, and wear shows first on M1 and last on M3. The peglike permanent P4, of which I have not seen the deciduous precursor, receives wear at the same time that the molars are being worn. Wear proceeds at approximately the same rate in the teeth of both the upper jaws and lower jaws.

In order to be more nearly certain that specimens used in making racial comparisons were comparable as to age, six age-groups were established, from youngest to oldest. These groups were based on the degree of wear on the occlusal surface of the upper cheek-teeth, and are as follows: group 1, in which M1 and M2 have not reached full and equal height and show no occlusal wear, and M3 has not erupted or is just breaking through the alveolus; group 2, in which M1 and M2 have reached full and equal height and show slight wear, and M3 may be almost or quite equal in height to M1 and M2 and, when equal, sometimes shows slight wear; group 3, in which M1 and M2 show wear on all cusps but cusps are visible, and M3 shows slight wear; group 4, in which P4 shows slight wear, M1 has cusps and re-entrant folds between cusps mostly gone, M2 shows considerable wear but re-entrant folds are visible, and M3 has most re-entrant folds and cusps gone; group 5, in which P4 shows considerable wear, M1 has cusps completely worn away, M2 has re-entrant folds and cusps worn away, and M3 lacks occlusal pattern except for one or two lakes; group 6, in which all upper cheek-teeth are without occlusal pattern.

These groupings are based on continuously variable features, and, therefore, when the teeth are at certain stages of wear a specimen is difficult to place in one of two groups.

Age group 1 and 2 include juvenal and subadult animals. Animals of age groups 3 through 6 are considered adult. Individuals of age groups 3 through 5, including as they do the great majority of the adult population, were the only age classes used in measuring geographic variation.

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.

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