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Read Ebook: Mammals of Mesa Verde National Park Colorado by Anderson Sydney

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On February 20 in Prater Canyon Ranger Markley noticed that prairie dogs were active although about three feet of snow lay on the ground. Between April 15 and May 15 approximately 500 prairie dogs were in Prater Canyon above Lower Well; through field glasses 350 were counted. Young were first noted in Prater Canyon on July 12. Quaintance and Lloyd White had under observation two bulky nests of the red-tailed hawk in the tops of tall Douglas firs in side draws of Prater Canyon. Quaintance found near the rimrock a quarter of a mile from the prairie-dog town the skeletons of two prairie dogs between a sliver of a dead pinyon branch and the branch itself. Another skeleton lay on a dead limb fifteen feet from the ground. A red-tailed hawk once was observed to swoop down, seize a prairie dog and fly down the canyon. The four colonies found in the Park were in Prater Canyon, in Morfield Canyon, in the east fork of School Section Canyon, and in Whites Canyon. The last two were smaller colonies than the first two.

Prairie dogs were observed away from these colonies. On June 20 a young prairie dog ran into a culvert on the Knife Edge Section of the road. Others were observed on the north side of the road, at the head of the east prong of School Section Canyon, on the road west of Park Point, and on the road at the head of Long Canyon five miles from the nearest known colony in the Park. Possibly this last individual came from the Montezuma Valley north of the Park. Mr. Prater, after whom Prater Canyon is named, homesteaded on the Mesa Verde in 1899. He informed Quaintance that prairie dogs were present in Morfield Canyon prior to 1900 but were not in Prater Canyon in 1899. Prater said he drowned out a few that came into Prater Canyon before 1914. In 1942, Chief Ranger Faha wrote in his Annual Animal Census Report that he had interviewed an old time resident who stated that prairie dogs were not present on the Mesa Verde until about 1905 or 1906 and that Helen Morfield, the daughter of Judge Morfield who homesteaded in Morfield Canyon, brought the first prairie dogs on the Mesa Verde. Estimates of the prairie-dog population in the Annual Animal Census Reports for 1935 through 1941 were: 1935--800, 1936--650, 1937--650, 1938--650, 1939--no report, 1940--1500 and increasing, 1941--slight decrease. After 1942 more adequate records were kept by Chief Ranger Wade and other Park Service personnel.

On August 9, 1943, occupied burrows of prairie dogs were found to be thinly scattered down Prater Canyon from the head of the canyon at the Maintenance Camp to a point about one hundred feet below the lower well. The largest concentration was in the vicinity of the upper well near Prater's Cabin. Little new digging that would indicate a spreading population was noticed. Seemingly desirable, but unoccupied, habitat extended at least two miles south of the inhabited area. In Morfield Canyon, burrows were found from a point one hundred yards north of the fence at the south boundary of Section 17, south for a mile and one-half to a point one-third of a mile into Section 29. The greatest concentration was in the vicinity of Morfield Well. South of this point the burrows were found only along the narrow dry sides of the canyon and in sage-covered areas at slightly higher elevations than the rest of the floor of the canyon. Seemingly desirable habitat extended at least three miles to the south and one mile to the north of the occupied area. The report of the study in 1943 concluded with the statement that artificial control by poisoning would be unwise and unnecessary. Requests were being made at that time to exterminate prairie dogs in the Park on the basis of the unproved assumption that prairie dogs move from the Park to surrounding range land where extermination was then being attempted by poisoning.

On August 10, 1944, no occupied burrows were found in Whites Canyon or the east fork of School Section Canyon. A heavy rain on August 9 made accurate count of occupied burrows possible. In Prater Canyon the occupied area extended 200 feet south of the area occupied in 1943. In Morfield Canyon no change had occurred. North of the fence in Morfield Canyon 130 occupied burrows were counted. More than one hole, if judged to be part of the same burrow system, were counted as one. The vegetation within the colony had continued to improve in spite of the large population of prairie dogs.

On August 8 and 14, 1945, although a careful search was made, the only prairie dogs found in Prater Canyon were living in one burrow fifty yards from the Maintenance Camp. In Morfield Canyon the colony had decreased. Occupied burrows were found on the west side of the canyon near the fence and above the well , and below the well on the west side . The total population in both canyons was estimated to be 100, compared with 800 in the preceding year. The ground-water table was thought to be rising, and vegetation was increasing.

On August 12, 1946, two prairie dogs were observed in Prater Canyon, one near the Maintenance Camp, and the other a mile to the south. In Morfield Canyon 18 occupied burrows were found north of the fence and 36 below the well, in the same two areas occupied in 1945.

On August 12, 1947, two animals were seen at one of the localities occupied a year earlier in Prater Canyon, and three burrows were occupied. In Morfield Canyon 119 occupied burrows were counted. At least 12 dens occupied by badgers were present in 1946, and four in 1947.

On August 9, 1948, no evidence of living prairie dogs was found in Prater Canyon. In Morfield Canyon 45 burrows were counted north of the fence. The grass had been increasing in abundance for several years.

On August 18, 1949, no evidence of living prairie dogs was found in either canyon. In 1951 five prairie dogs were said to have been seen in Prater Canyon in June and July. No other observations have been recorded.

Both the history of the prairie dogs and the history of the viewpoint of people toward them are interesting. Individual views have ranged from a desire to exterminate all the prairie dogs to a desire to leave them undisturbed by man.

In review: The early history of prairie dogs on the Mesa Verde is not well documented but reports are available of the absence of prairie dogs before settlement by white men, and of introductions of prairie dogs. Other reports indicate that prairie dogs have been observed far from established colonies; therefore natural invasion may account for the establishment of prairie dogs on the Mesa. Grazing of moderate to heavy intensity by livestock continued in Morfield Canyon until 1941. Cessation of grazing and above average precipitation were accompanied by increased growth of vegetation in the colonies of prairie dogs. Mr. Wade has suggested that flooding of burrows by ground water drove prairie dogs from some lower parts of the floors of the canyons, and that increased vegetation favored predators, primarily badgers and coyotes, which further reduced the population. The abruptness of the decline, especially in Prater Canyon, is consistent with the theory that some epidemic disease occurred. This possibility was considered at the time of the decline, and a Mobile Laboratory of the United States Public Health Service spent from June 5 to June 25, 1947, in the Park collecting rodents and their fleas for study. The primary concern was plague, which had been detected in neighboring states. No evidence of plague or of tularemia was reported after study of 494 small rodents obtained from 13 localities in the Park. Only six prairie dogs were studied. The negative report does not prove that tularemia or some other disease was not a factor in the decimation of the colony in Prater Canyon the year before.

If prairie dogs were able to survive primarily because of over-grazing by domestic animals, future introductions may fail. If disease was the major factor in their disappearance, reintroductions may succeed.

Spermophilus lateralis lateralis Golden-mantled Ground Squirrel

Spermophilus variegatus grammurus Rock Squirrel

Specimen number 7893/507 had 360 Purshia seeds in its cheek-pouches according to a note on the label. On July 18, 1960, I found a young male rock squirrel dead on the road a mile north of headquarters that had 234 pinyon seeds in its cheek-pouches. Young, recorded as "half-grown," have been observed in May and July. The first appearance may be as early as January. In 1950, D. Watson thought that they did not hibernate, except for a few days when the weather was stormy. I observed a rock squirrel in August in the public campground at Park Headquarters sitting on its haunches on a branch of a juniper some twelve feet from the ground and eating an object held in its forefeet. The rock squirrel ranges throughout the Park in all habitats.

Eutamias minimus operarius Merriam Least Chipmunk

Five of the fourteen specimens of known sex are females, all of which were taken in August and September, and none of which is recorded as having contained embryos. The skulls of the eight August-taken specimens also suggest that young are born in late spring or early summer: the largest skull had well-worn teeth that might indicate an age of more than one year; four others had complete adult dentitions that were barely worn; and three had not yet acquired complete adult dentitions.

Eutamias quadrivittatus hopiensis Merriam Colorado Chipmunk

Thomomys bottae aureus J.A. Allen Botta's Pocket Gopher

In the Park, pocket gophers occur both on mesa tops and in canyons. Most of the localities listed above and others at which mounds were seen are areas of disturbance such as the old burn on Wetherill Mesa, the rights of way for roads, the river valley, and the grazed floor of Prater Canyon. Little evidence of pocket gophers was found on unusually rocky slopes, steep slopes, or in stands of pinyon and juniper or in relatively pure stands of oak-brush. In addition to workability of the soil, the presence of herbaceous plants, many of them weedy annuals, is probably the most important factor governing the success of pocket gophers in a local area. No female was recorded to have contained embryos, but two had enlarged uteri or placental scars. This fact and the capture of nine half-grown individuals indicate breeding prior to late August when most specimens were trapped.

Dipodomys ordii longipes Ord's Kangaroo Rat

Kangaroo rats have been seen crossing the highway in the Park less than one mile from the Park entrance by Jean Pinkley.

Castor canadensis concisor Warren and Hall Beaver

In 1935 Quaintance and White spent June 16 to June 20 in the Mancos River Bottoms at the mouth of Weber Canyon, looking for sign of fresh beaver work. They found none. Annual Animal Census Reports include the following information based on patrols along the Mancos River at the east boundary of the Park: 1937--estimate 4 beaver present, 1938--8, 1941--numerous bank burrows, 1942--uncommon, 1944--uncommon, 1945--most concentrated at southeast corner, 1946--runs and two small dams seen , 1947--only in 1-1/2 miles north of boundary with Ute Reservation, 1949--two separate colonies , 1950--none, owing to drouth and diversion of water upstream completely drying the river at times, 1951--none, 1953--present, 1955--present. On the Mancos River, 6200 ft., in late August, 1956, sign of beaver was abundant, numerous trees had been cut but none within a week, and a bank den was found on the west side of the river extending back 50 feet from the stream and caved in at three places. In 1959 dens were still present.

Reithrodontomys megalotis aztecus J.A. Allen Western Harvest Mouse

Peromyscus boylii rowleyi Brush Mouse

The specimens were taken in August, September, and November. One adult female trapped on September 10, 1958, had six embryos.

Peromyscus crinitus auripectus Canyon Mouse

Peromyscus maniculatus rufinus Deer Mouse

The most abundant mammal is the ubiquitous deer mouse. Series of specimens taken in August , in September , and in November make possible the following comparisons of age, reproductive conditions, and molts.

Molt was observed in some individuals no longer having juvenal pelage; some new pelage was observed on the skins of seven mice collected in August. Each of these was in category 4 or 5 and probably had been born in the previous calendar year. These seven molting individuals make up nearly 17 per cent of 42 individuals that had completed the juvenal to postjuvenal molt. In November, 80 per cent of individuals that had previously obtained their postjuvenal or adult pelage were molting. These mice were in age-categories 3, 4, and 5. Some of the individuals in category 3 were developing new hair beneath a relatively unworn bright pelage that I judge to be an adult pelage rather than a postjuvenal pelage. If this judgment be correct and if the relatively unworn dentition means that these animals are young of the year, we must conclude that individuals born in early summer may molt from juvenal to postjuvenal, then to adult pelage, and finally in the autumn into another adult pelage. Other individuals, six in number and of categories 2 and 3, are simultaneously completing the juvenal to postjuvenal molt and beginning the postjuvenal to adult molt. The juvenal to postjuvenal molt begins, as has been described by various authors, along the lateral line and proceeds dorsally and ventrally and anteriorly and posteriorly, and the last patch to lose the gray juvenal color is the top of head and nape, or less frequently the rump. In some individuals a gray patch on the nape remained but emerging hair was not apparent; perhaps the molt had been halted just prior to completion. The progressing band of emerging hair is narrow in most specimens but in some up to one-fifth of the circumference of the body has hair at the same degree of emergence. Subsequent molts, both from postjuvenal to adult pelage and between adult pelages, are less regular in point, or points, of origin, width of progressing molt, and amount of surface molting at one time. Half or more of the dorsum is oftentimes involved in the same stage of molt at once. In some specimens the molt begins along the lateral line, and in others in several centers on the sides. In some skins distinct lines of molt are visible without parting the hair, and in some others the molt is patchy in appearance. Growth of new hair is apparent at various times of the year as a result of injury such as that caused by bot fly larvae, cuts, scratches, or bites of other mice. Abrasion, wear, irritation by ectoparasites, and other kinds of injury to the skin may play a part in the development of a patchy molt. Both breeding and molting are sources of considerable stress, and the delay of the peak of molting activity until November when breeding activity has decreased seems of benefit to the mice. A change in the ratio of young mice to old mice between August and November was noted. In August, 29 per cent of the population is composed of old mice, and in November only 6 per cent. This change results from birth of young as well as death of old mice, but may indicate that a mouse in November has less than one chance in ten of being alive the following November. Some females born early in the reproductive season breed in their first summer or autumn. For example, a female of category 2, taken on August 12, and probably in postjuvenal pelage, had placental scars. Undoubtedly the young of the year contribute to the breeding population, especially late in the season.

In Figure 3 the proportion of females bearing embryos in August, September, and November is shown. Of the females trapped in August, 11 of 32 that were more than 144 mm. in total length contained embryos; an additional 14 females were lactating or possessed placental scars or enlarged uteri. Therefore, approximately 80 per cent of the larger females were reproducing in August. In September two females were pregnant and an additional sixteen of the 44 females examined showed other evidence of reproduction; these eighteen females make up 41 per cent of those more than 144 mm. in total length. The only reproductive data available for November pertain to the presence or absence of embryos. No female was pregnant although 35 females more than 144 mm. in total length were examined. Some of the skins show prominent mammae indicative of recent nursing, and juveniles less than a month old were taken. The reproductive activity of deer mice on the Mesa Verde seems to be greatly reduced in autumn.

Peromyscus difficilis nasutus Rock Mouse

Peromyscus truei truei Pinyon Mouse

In August three females were pregnant or lactating, or both. None of seven adult females taken in November was pregnant.

Neotoma cinerea arizonae Merriam Bushy-tailed Wood Rat

Neotoma mexicana inopinata Goldman Mexican Wood Rat

The Mexican wood rat is the most common species of wood rat on the Mesa Verde. The two specimens from Spruce Tree Lodge obtained by R.B. Finley on September 2, 1949, are young individuals.

Ondatra zibethicus osoyoosensis Muskrat

D. Watson reported that he has seen muskrat tracks many times along the Mancos River. He also relates a report received from Chief Ranger Wade and D.A. Spencer who saw a muskrat, no doubt a wanderer, on the Knife Edge Road on a cold winter night. These men, both reliable observers, stopped and saw the muskrat at a distance of two feet, where it took shelter under a power shovel parked beside the road. Reports of dens seen along the Mancos River are available for 1944, 1945, 1946, and 1947.

Microtus longicaudus mordax Long-tailed Vole

Microtus mexicanus mogollonensis Mexican Vole

Microtus montanus fusus Hall Montane Vole

Erethizon dorsatum couesi Mearns Porcupine

I saw no other porcupine in the Park.

In 1935, C.W. Quaintance took special notice of porcupines because of the possibility, then being considered, of their being detrimental to habitat conditions thought to be favorable to wild turkeys. Porcupines were suspected of killing ponderosa pine, which occurred in only a few places, and which was thought to be necessary for wild turkeys. Porcupines were recorded as follows: one found dead on the road at the North Rim on March 16; one killed in oak brush along the North Rim; one killed between April 15 and May 15; oak brush damaged by porcupines in Soda Canyon below the well; one seen on July 4 on the Poole Canyon Trail; one seen at the foot of the Mesa on June 26; one seen by Lloyd White in Moccasin Canyon on June 27; and one seen by Mrs. Sharon Spencer on July 1 in Prater Canyon. After four months on the Mesa Verde, Quaintance concluded that there were not so many porcupines as had been expected and that there were more ponderosa pines than had been expected.

The general policy in regard to porcupines from 1930 to 1946 was to kill them because they eat parts of trees. In at least the following years porcupines were killed: 1930, 1933, 1935, 1940, 1943, 1944, and 1946. The largest number reported killed in one year is 71 in 1933 when a crew of men was employed for this purpose. The amount of effort devoted to killing porcupines varied from year to year. The most frequently voiced alarm was that the scenic value of the areas along the entrance highway and near certain ruins was being impaired. The direst prediction was that all pine trees on the Mesa Verde were doomed to extinction in the near future. The last prediction has not come to pass, nor has this extinction occurred in the past thousand years and more during which pine trees and porcupines have existed together on the Mesa Verde.

In 1946 the studies of Spencer, Wade, and Fitch began. Much effort was expended in obtaining and dating scars for analysis, and the interesting results mentioned above were the reward. Also many porcupines were captured alive and marked with ear-tags so that they could be recognized later. For example, in the winter of 1946 and 1947, 117 were marked in Soda Canyon. A decline in numbers in recent years reduced the impetus for continuation of the study by reducing the results obtained for each day spent searching for porcupines. Information obtained on movements of porcupines relative to season and weather conditions in these studies may be summarized and published later. Data regarding ratio of young to adult animals from year to year are also of interest.

The effect of a porcupine on a single tree is often easy to assess. The effect of a fluctuating population of porcupines on a mixed forest is not so easy to assess, but is of more intrinsic interest. It is desirable that studies designed to evaluate the latter effect continue while the population remains low and also when the next cyclic increase begins. Publication of Spencer's results would be a major step forward.

Cahalane mentions the difficulty that has been experienced in protecting aesthetically desirable trees around cliff dwellings. Perhaps in a local area removal of porcupines is sometimes warranted, but control of the porcupine seems undesirable to me, as a general policy, because one purpose of a National Park is to preserve natural conditions and that implies naturally occurring changes.

What is needed is continued careful study of the ecological relationships of animals and of plants. National parks provide, to the extent that they are not disturbed or "controlled," especially favorable places for studies of this sort.

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