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Life History of the Kangaroo Rat · Charles Taylor Vorhies — chapter 5 of 11 · ~2,026 words · public domain

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One individual in a laboratory cage, which had not yet been given a nest box, busied itself in broad daylight in carrying its grain supply into the darkest corner of the cage. When a nest box is supplied the individual will retreat into its dark shelter, and will only come forth after darkness has fallen unless forcibly ejected, but will store the food supplied.

In another case an animal escaped while being handled, and sought refuge behind a built-in laboratory table, where it could not be recovered without tearing out the table. For four days and nights it had the run of the laboratory. On the first night of its freedom it found and entered a burlap bag of grass seed that had been taken from a mound. A trail of seed and chaff next morning showed that it had been busily engaged in making its new quarters comfortable with bedding and food. After four nights of freedom it was captured alive in a trap, and later it was found that it had moved from the corner behind the table to the space beneath a near-by drawer, where it had stored about 2 quarts of the grass seed and a handful of the oatmeal used for trap bait.

BREEDING HABITS.

Observations on breeding habits have consisted mainly in taking records from the females trapped at all seasons of the year throughout the course of the investigation, and from examinations made during poisoning operations, and yet from this source the number of pregnant females taken or of young discovered is disappointingly small. The records indicate a breeding period of considerable length, extending from January to August, inclusive. It is possible that the length of the period may be increased by a second litter from the earliest breeding females in summer, but the large percentage of nonpregnant or nonbreeding animals which occurs throughout the season would indicate a wide variation in the time of breeding of different individuals.

Trapping in February and March for the purpose of securing greater numbers of female specimens, begun with the idea that these months were most likely to be the breeding months, has invariably yielded an unsatisfactory number of nonbreeding specimens and males. Unfortunately, the numbers of females secured in some months were not sufficient to be significant if worked out in percentages of breeding and nonbreeding individuals, and this, coupled with the fact that the importance of recording carefully all nonbreeders was not at first recognized, makes it impossible to tabulate such information reliably. The total of females taken in April, for example, is only 3, of which 1 was breeding; while in June, during the course of poisoning operations, 45 females were examined, of which 21 were breeding.

Five breeding females were taken in January, all during the last three days of the month. One of these was a suckling female, the young of which were secured alive and were probably at least a week old when taken. This must have been exceptionally early for young, since of a number of adult kangaroo rats taken during the first week of January none have been found to be breeding. Two records from Vernon Bailey are as follows: May 19-June 8, 1903, young specimen in nest (Santa Rosa, N. Mex.); June 12, 1889, one female, two embryos (Oracle, Ariz.).

The considerable proportion (which we believe to be more than 50 per cent) of nonbreeding females taken during all those months in which breeding has been found to occur may also indicate an extended period of breeding, with a small percentage breeding at any one time. This period also furnishes ample time for the rearing of two litters a year by some females, but we have no evidence as to the occurrence of two litters. Young of the year, practically grown, are taken during and after the month of April.

The mammae are arranged in three pairs, pectoral, 1/1; inguinal, 2/2.

Kangaroo rats are among those rodents in which the vagina becomes plugged with a rather solid material, translucent, and of the consistency of a stiff gelatine, after copulation. This must occur very soon after coitus, since in those individuals taken in this condition no definite evidence of the beginning of development of embryos could be detected by examination.

The length of the gestation period of spectabilis is unknown. The young are born naked, a fact inferred by failure to find any fetus showing noticeable hair development, and from the conditions observed in such young as have been seen. A suckling female was taken by Vorhies, January 31, 1920, and her den immediately excavated in the hope of securing the young. Two juveniles were found in a special nest chamber (see p. 30). These were estimated to be perhaps two weeks old. A serious effort was made to raise the little animals by feeding milk with a pipette and keeping them warm with a hot water bottle, but they survived only 10 days, without the eyes having opened. The uneven temperature as well as the character of the food was probably responsible for their deaths. On February 3 they were measured and weighed, with the following results:

--------------------------------------------------- | | Measurements (in millimetres). | Weight |------------------------------- | (in | Total | Tail | Hind | grams). | length. | vertebrae. | foot. ---------|---------|---------|------------|-------- No. 1 | 13.3 | 90 | 38 | 24 No. 2 | 12.6 | 93 | 38 | 24 ---------------------------------------------------

At this stage the young were partially clothed with a coat of fine velvety fur, more especially on the bodies, the tails being still nearly naked. The body color was dark plumbeous, just the color of the dark underfur of the adult, or a shade darker, while the characteristic white markings of the adult stood out sharply as pinkish-white areas against the dark background (see Pl. IX, Fig. 2, at p. 32). The proportions were much as in the adult, except that the tails were relatively much shorter and the feet relatively longer.

Only one other record of young is at hand, that by Bailey, who secured the young after capture of a suckling female at Santa Rosa, N. Mex. In this case the litter contained only one. This was squeaking when found, but was not large enough to crawl away. Its eyes and ears were closed, and its soft, naked skin was distinctly marked with the pattern of the adult, the colors being as given for the other two. This juvenile lived only a week. Young less than half grown were not trapped or noted in our poisoning operations outside the dens.

Kangaroo rats, if spectabilis be representative, reproduce at a slow rate as compared with many other small rodents. We have records of 67 females with embryos or scars showing the number produced, and of the two litters of young described above. Of the 69 females thus recorded, 15, or 21.7 per cent, had but one offspring each; 52, or 75.3 per cent, but two each; while only 2 individuals, or 2.9 per cent, had three. Three young is the maximum litter recorded. This, taken in connection with the protracted breeding season and lack of sure evidence of the production of two broods a year, gives a surprisingly low rate of reproduction, indicating relative freedom from inimical factors.

Our breeding records for merriami are fewer than for spectabilis, but are very similar in every way so far as they go, both as to the time of year and number of young.

FOOD AND STORAGE.

Dipodomys s. spectabilis does not hibernate, so must prepare for unfavorable seasons by extensive storage of food materials. There are two seasons of the year, in southeastern Arizona at least, when storage of food takes place, namely, in spring, during April or May, and in fall, from September to November, the latter being the more important. For the periods between, the animal must rely largely on stored materials. Not infrequently a season of severe drought precludes the possibility of any storage. The summer and fall of 1918 was such a season on the Range Reserve (Pl. II, Fig. 2). If food stores are inadequate at such a time the kangaroo rats must perish in considerable numbers. Fisher found many deserted mounds in the vicinity of Dos Cabezos, Ariz., in June, 1894, which may be accounted for in this way. In 1921 Vorhies found all mounds within 4 or 5 miles of Albuquerque, N. Mex., deserted by spectabilis, resulting probably from overgrazing by sheep and goats during a succession of dry years. In the arid Southwest natural selection probably favors the animals with the largest food stores, and it is not surprising that the storing habit has been developed to a remarkable degree.

Some stored material is likely to be found at any time of year in any mound examined, the largest quantity usually in fall and winter, the smallest in July or August (Table 1, dens 1, 2, 14, and 24). Amounts found by different observers vary from a few ounces to several quarts or pecks, and stored materials taken from 22 mounds on the Range Reserve vary in weight from 5 to 4,127 grams (more than 9 pounds). This is exceeded by one lot from New Mexico, which totaled 5,750 grams (12.67 pounds). It is fairly evident that in seasons of scanty forage for stock the appropriation of such quantities of grass seeds and crowns and other grazing materials by numerous kangaroo rats may appreciably reduce the carrying capacity of the range. Studies of cheek-pouch contents and food stores taken from dens show that the natural food of spectabilis consists principally of various seeds and fruits, particularly the seeds of certain grasses. The study of burrow contents has been especially illuminating and valuable.

All of the stored material from 22 dens on the Range Reserve and from 2 near Albuquerque, N. Mex., has been saved and analyzed as to species as carefully as the conditions of storage would permit. Within the mound the food stored is usually more or less segregated by plant species, though the stores of material of any one kind may be found in several places through the mound, and often the material is mixed. In the latter case the quantities of the various species can only be estimated, but in the former the species may be kept separate by the use of several bags for collecting the seeds, and a fairly accurate laboratory weighing can be made later. Very frequently, the explanation of this separation of species lies in the different seasons of ripening, but sometimes where two species are ripe at the same time near the mound, one is worked upon for a time to the exclusion of the other. The one kind is often packed in tightly against the other, but with a very abrupt change in the character of the material.

A number of the more interesting and representative results of the weighing and analyses of burrow contents are presented herewith in tabular form. The data for each den, or lot, shows in grams the quantity of stored material removed and the best estimate it was possible to make of the percentages or weights of the various species. When the weight was less than 5 grams, the mere trace of the species frequently is indicated in the following tables by the abbreviation "Tr."

TABLE 1.--Analyses of plants stored by Dipodomys spectabilis spectabilis Merriam, obtained from examination of representative dens (all except Den 24 from U. S. Range Reserve, near the Santa Rita Mountains, Ariz.).

DEN 1.

February 7, 1918. Burrow typical, located on bank of wash in partially denuded grass-land, Bouteloua rothrockii and weed type; soil sandy; burrow photographed in section (Pl. VII, Fig. 1).

Species stored. Grams.

Bouteloua rothrockii 2,205 Bouteloua aristidoides (B. eriopoda and B. rothrockii, Tr.) 1,445 Plantago ignota 442 Eriogonum polycladon 35 ----- Total 4,127

Four species of plants represented in burrow contents (Pl. VII, Fig. 2). Maximum quantity for single burrow in series of 22 from Range Reserve.

DEN 2.

March 9, 1918. Surroundings overgrazed and partially restored by complete protection. Red soil, with much coarse rough gravel and stone.

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