Life History and Ecology of the Five-lined Skink, Eumeces fasciatus Part 5

Widely different incubation periods have been recorded in the literature and the variation probably is not due to temperature alone. n.o.ble and Mason (1933:4) recorded incubation periods for six females from the same locality, and evidently kept under the same laboratory conditions, as 47, 41, 36, 29, 29, and 27 days. Despite the wide difference in incubation time, all six clutches hatched within a 12-day period from July 5-17. It seems improbable that differences in temperature account for the 20-day disparity between maximum and minimum incubation time, in these females kept under similar conditions. Cagle (1940:229) recorded an even shorter incubation period for one kept in the laboratory, which laid eggs on June 30; hatching occurred on July 23 and 24. Retention of eggs in the oviduct by females kept under unnatural conditions would partly explain their late laying and the short incubation period of their clutches. Such ability to retain eggs in the oviduct while their development proceeds would not be especially surprising in _E.

fasciatus_ since its congener _E. lynxe_ of the highlands in southern Mexico is normally ovoviviparous (Hartweg, 1931:61; Taylor, 1936:171).

Cagle did not determine incubation time for any of the natural nests found, but evidently in all of them laying occurred earlier than in the single female brought to the laboratory while still gravid. All the eggs in natural nests found by him were brought to the laboratory and most of them were hatched. Cagle remarked: "The fact that these 26 nests hatched within a period of nine days seemingly indicates that the egg laying period extends over not more than two weeks."

In the present study no incubation periods so short as those recorded by n.o.ble and Mason, and Cagle, were observed. Incubation times were recorded for clutches both in the laboratory and in the field, but for most of the clutches only approximate incubation periods were recorded.

Failure to record the exact date of laying or of hatching, or both resulted from attempts to avoid frequent disturbance of females in their nests, which might have caused them to desert.

One clutch of eggs laid in a terrarium probably on June 17, 1951--possibly a day or two earlier--hatched on July 30, after an incubation of about 44 days. Another clutch, found in a terrarium on July 17, 1951, was estimated to have been laid about a week earlier, judging from the average length (11.8 mm.) and average weight (.55 gm.) of the eggs. These eggs hatched on August 9, a little more than three weeks after their discovery. A clutch found in the field on June 25, 1951, evidently recently laid (average length 12 mm., weight .45 gm.), hatched 41 days later, on August 5. Another clutch found in a terrarium on July 17, 1951, was estimated to have been laid ten days or two weeks before, as the average length was 12.7 mm. The eggs hatched on August 7, three weeks after their discovery. On June 25, 1951, an incomplete clutch of three eggs was found with a female which still had an unlaid egg. The three eggs probably had been laid the same day or the day before. They were kept in the laboratory and weighed and measured at intervals until July 28, 33 days after their discovery when both those that remained were accidentally punctured and found to have nearly full term fetuses. In the field a nest which contained only a gravid female on June 24, 1951, had a clutch of eggs already mud stained and slightly enlarged on June 29. The most probable date of laying was June 26. On August 6 the eggs had all hatched but several young were still in the nest. Probably most hatched on August 5. The incubation time was hence approximately 40 days.

On June 21, 1951, a natural nest was found with eggs already somewhat enlarged (12.5 8 mm.) and mud stained. This nest was checked from time to time in the next few weeks, and after 39 days, on July 30, it was found that all the eggs had recently hatched, but six young were still in the nest cavity.

Another nest was found on June 24, 1951, with the eggs already markedly enlarged (14 8 mm.) indicating that laying must have been several days earlier--probably well over a week. Hatching occurred approximately 34 days later, probably on July 28, since on July 26 there was no sign that hatching was imminent, and on July 30 only the empty dried eggsh.e.l.ls remained in the nest.

The incubation time approximated six weeks for those nests with most complete records. Under wet and stormy weather conditions such as prevailed in 1951, this may have been the normal incubation period, but in warmer and drier years incubation time is shortened.

In the five-lined skink each adult female normally produces one clutch of eggs annually. The size of the clutch produced is subject to individual variation, and is influenced by the age, size and condition of the female. Geographic variation in clutch size might also be expected. Data were obtained from breeding females killed and dissected, from counts of eggs found in natural nests in the field, and from clutches of eggs laid by females kept in captivity. For the total of 115 recorded clutches represented by the combined data from all these sources, the average number of eggs per clutch was 9.5.

In many females dissected for the purpose of obtaining egg counts, ovulation had not yet occurred. The ovarian eggs present in each of these females included two main size groups, the larger ones in process of maturing and evidently destined for deposition in the current season, and minute, immature ones. A few of intermediate size were always present, however, resulting in uncertainty as to the size of the clutch being produced, especially when development had not proceeded far. Even when the larger eggs formed a fairly distinct size group, some usually were well below maximum size. Relatively high counts of clutches were obtained from these examinations of enlarged ovarian eggs. Evidently development frequently is arrested, and resorption may occur before ovulation. As a result the numbers of ovarian eggs developing are a poor indication of actual clutch size. A series of gravid females were obtained and examined after ovulation; the numbers of eggs in their oviducts probably indicates accurately the sizes of their clutches.

Gravid females taken from their nest burrows and kept in the laboratory in containers with loose damp soil soon excavated new burrows and deposited clutches. Many natural nests were found in the field, and the egg counts obtained from them provided further data concerning clutch size. Although most of these clutches probably had their full complements of eggs, others certainly had sustained losses to predators, or to the females themselves, which may eat some of the eggs. Therefore the average number found is erroneously low. Some of the natural nests found may have contained two or more clutches or parts of them, and the higher counts obtained from natural nests therefore are also questionable.

For different sets of data on clutch size, numbers were as follows:

Table 6. Size of Clutch.

=================+===========+============+===========+=========+========= Number of Standard SOURCE OF SAMPLE clutches Mean deviation Maximum Minimum -----------------+-----------+------------+-----------+---------+--------- Early ovarian 25 11.4 .46 2.28 20 5 Late ovarian, uterine, or laid in captivity 56 9.16 .21 1.85 15 4 In natural nests 34 8.82 .32 1.85 16 4 -----------------+-----------+------------+-----------+---------+---------

On the average, larger females produce more eggs per clutch than do smaller females. Of 49 females for which measurements were recorded, and which had uterine or large ovarian eggs, 31 were 70 mm. or more in snout-vent length. These 31, mostly or entirely old adults, averaged 9.9 eggs per clutch, whereas 18 others that were 69 mm. or less in snout-vent length, and that must have been mainly or entirely newly matured adults in their first breeding season, averaged only 7.8 eggs per clutch.

Smith (1946:350) states that in the northern part of the range of this skink there is some indication of decrease in size of clutches. This is not well shown by published records. For the southern states, most of the published records of clutch size are by authors who did not clearly distinguish between the three kinds of five-lined skinks, and there is some doubt as to which species is involved in each record. For 56 clutches reported upon from north of approximately lat.i.tude 37, I obtain a slightly higher figure than for 11 clutches from south of this line. Geographic trends are, of course, obscured by individual variation, and perhaps by abnormal clutches produced by individuals kept in captivity.

In Table 7, the figures marked with asterisks pertain to clutches that might have belonged to skinks of the species _E. laticeps_ or _E.

inexpectatus_ since they were recorded in regions where _laticeps_ and in some cases, _inexpectatus_ also, occurs along with _fasciatus_. If these questionable clutches are excluded the remaining 55, definitely of _fasciatus_, average 8.48 eggs per clutch, whereas the 12 questionable clutches average 8.42. Both figures are close to the average of 8.82 .32 eggs for the 34 natural nests recorded in the present study. For the total of 1661 eggs of 182 clutches, from the combined sample of all available records for clutches found in the present study or reported upon in the literature, the average egg number is 9.13.

[Ill.u.s.tration: FIG. 10. Correlation between size of female and number of eggs in clutch; females in their first breeding season, mostly less than 72 mm. in snout-vent length, produce smaller clutches, on the average, than do larger and older females, but there is extensive overlap.]

To sum up the available information on clutch size, the number of eggs is most typically 9, 10, or 11 and is more in large old females, than in small, newly matured females. In natural nests, even in those that are successful, there is often some loss of eggs, which are eaten by predators, or by the female herself, with the result that the egg counts made by various observers average somewhat lower than the numbers actually produced. The loss during incubation cannot be measured readily since it is almost certainly sharply increased by the disturbance entailed in observing nests. Exposing nests, even momentarily, for observation, may result in compacting of the surrounding soil, desiccation, temporary or permanent desertion by the female, and exposure to predation. Some indication of the incidence of loss during incubation might be obtained by counting and measuring the eggs in newly found nests and correlating numbers with size (indicating the length of time incubated).

Table 7.--Numbers of Eggs Per Clutch, Time of Occurrence, Laying Dates and Hatching Dates, as Reported in the Literature by Various Authors.

==========+==============+===============+=========+=============+==========+============= Numbers AUTHOR of eggs Date recorded Natural Laying date Hatching Locality per clutch nest date ----------+--------------+---------------+---------+-------------+----------+------------- Allard 7* .... Yes .... .... Northern Georgia Bishop 8* .... Yes .... .... Breathitt Co., Kentucky Blanchard 9* .... .... .... .... Tennessee Burt 6; 11 May, and Yes June 12, .... Douglas June 18, 1926 1926 Co., Kansas Burt 9*, 9*, June 25 to Yes .... .... Arkansas 9*, 10* July 13, 1926 Ashville, Burt 8* June 6, 1933 Yes .... .... North Carolina Burt 8* June 28, 1934 Yes .... .... Scott, Mississippi Burt 6* July 7, 1933 Yes .... .... Emma, Georgia Burt 6* July 8, 1933 Yes .... .... Elk River, Alabama Cagle Average 9.16 in 26 July Elkville, nests (6-15) June-July Yes June 30 23-24 Illinois Conant 7, 9, 10, July 27, 11, 13 .... .... .... July 27 Ohio Dunn 12* .... .... .... Aug. 9 Evans and First Arden, Roecker 6, 7 .... Yes .... week of Ontario Sept. Fitch 9 July 22, 1947 Yes .... .... Vernon (field Parish, notes) Louisiana McCauley 3; 20 in 3 other nests July 5 August combined .... Yes and 6 30 Maryland n.o.ble and 2, 5, 5, May 23, 27, July 5, Anderson Mason 6, 7, 8, 8 .... No 31; June 6, 5, 6, 7, Co., 6, 13, 20 9, 17 Kansas Ruthven 6, 6, 8, 9, 11, 13, 14 .... Yes .... .... Michigan Smith 9 .... Yes .... .... Ohio ----------+--------------+---------------+---------+-------------+----------+-------------

BROODING

Lizards and snakes of several different families, are known to brood their clutches of eggs, although the great majority of oviparous forms do not do so. The brooding habit is perhaps best known in _Eumeces fasciatus_, and has been described by many authors. By far the most thorough account is that of n.o.ble and Mason (1933) who observed and experimented upon seven females that laid clutches of eggs in captivity.

These females, kept in separate terraria, excavated nest burrows for reception of their clutches, and remained with them throughout the time of incubation. There were three characteristic brooding postures; curved in a semicircle around the clutch, in an S-shaped figure extending among them, or lying straight, either over or among the eggs. The brooding females, taken quietly from their nests without disturbing them, were found to have temperatures averaging .4C. higher than the nests.

Evidently normal room temperatures were maintained in the laboratory where the terraria were kept. The females occasionally left their nests, especially in late afternoon, to wander about the terraria, and to bask in sunlight. While basking, their temperatures averaged 2.7C. higher than the nest temperatures. The authors suggested that an important function of the brooding female was to transfer warmth from absorbed sunlight to the eggs. They state: "In nature the importance of the mother's body heat in the incubation of the eggs probably varies greatly with the type of nesting site selected." They suggest that in clutches deposited in logs or stumps beneath a thin layer of bark exposed to direct sunlight the need for warming by the female would be less.

My own observations do not support the idea that brooding by the female serves to hasten the development of the eggs. Both in the laboratory and in natural nests, clutches deserted by disturbed females hatched and the hatching was not unduly delayed. In the field, females were never observed to bask in the sun beside their nest burrows, and seemingly left them infrequently even to feed. When a female was caught in her nest burrow, her temperature nearly always approximated that of the surrounding earth with which she was in contact. The temperature in each nest depends primarily upon its situation. When the immediate vicinity of the nest receives direct sunlight, the eggs are warmed without the aid of the female, but when there is no sunlight the temperature is much lower. In order to maintain an appreciably higher nest temperature the female would have to make frequent trips to spots perhaps several feet or several yards away to find sunlight. Upon returning to the nest, her body heat would be quickly dissipated into the eggs and the surrounding damp soil. She would need to shuttle back and forth almost continually between the nest and a spot exposed to suns.h.i.+ne. Cloudy weather often preventing the warming of the eggs by absorption of solar heat prevails during much of the incubation season, in the region of the present study, and probably to an even greater extent throughout the range as a whole.

n.o.ble and Mason state (_op. cit._:9) that while in some non-brooding kinds of lizards the eggs are actually damaged by turning, the female _fasciatus_ frequently turns her eggs and moves the whole clutch about in the nest cavity. On returning to their nests the experimental females each invariably touched one or more eggs with their tongues as an olfactory test. Eggs of other kinds of lizards not of the genus _Eumeces_, and sh.e.l.lacked eggs of _fasciatus_, or paraffin models of them, ordinarily were discarded immediately after a single touch of the tongue. Eggs of other individuals of the species, and even the eggs of _Eumeces laticeps_ were accepted as part of the brood. Any of the experimental females would quickly retrieve one of her eggs moved a short distance outside the nest cavity. Even if the whole clutch of eggs were scattered about, the female would, over a period of hours, gather the eggs and return them to the nest cavity. This movement of the eggs is accomplished by rolling or pus.h.i.+ng them in a loop of the body or tail, or, less frequently, by grasping an egg in the jaws, lifting it, and gently placing it in a new position. Even if the females were blindfolded, they were still able to retrieve scattered eggs, but one in which the tongue tip was experimentally removed showed no further interest in its eggs, presumably having lost the capacity to recognize them by olfactory test.

In the present study clutches unattended by females were observed to sustain heavy losses, both in the laboratory and in the field, and no doubt the attending female performs important functions other than that of warming the eggs. In the damp or wet nest cavity, the eggs tend to adhere to each other and to the earth walls and floor, and become sealed to such surfaces as a result of partial drying, reducing the amount of surface exposed to the air and probably hindering respiration. An eggsh.e.l.l sealed in prolonged contact with the soil tends to rot with the result that it is easily ruptured, and even if it is not broken there is the likelihood of fungi or microorganisms gaining entry and killing the embryo. In many of the eggs that were handled to obtain measurements and weight, rupturing of sh.e.l.ls occurred. The sh.e.l.ls are tough and elastic to the extent that even when eggs being handled were accidentally dropped on the floor on several occasions, no damage to them resulted. However, slight friction on the sh.e.l.l was sometimes sufficient to puncture one. Particles of sharp rock from the nest cavity may adhere to the sh.e.l.l, and result in rupturing, perhaps at weak spots where prolonged contact with the soil has caused deterioration. The female tends to keep her eggs in a compact cl.u.s.ter, s.h.i.+fting their position frequently so that no part of an eggsh.e.l.l adheres to its surroundings long enough for rotting to occur, and most of the surface of each egg is exposed to the air.

Another important function of the brooding female seems to be that of altering the nest burrow and s.h.i.+fting the eggs so that the effects of unfavorable weather are minimized. The usual response to warm and dry weather is deepening of the nest burrow. A cavity originally in loose soil on the underside of a flat rock, having the eggs in contact with the rock surface, may be displaced downward. The female excavates loose soil from the floor of the burrow and packs it on the top and sides, until the eggs are two or even three inches underground, in a cavity different in position and shape from the original one, although derived from it by gradual stages. In many instances, however, no such response to drying was observed. Probably extensive alteration of the nest burrow no longer is possible after drying of the soil has progressed beyond a certain stage as these skinks are not strong diggers. In some nests that were examined frequently, with resulting desertions by the attending females, the outlines of the cavities became indistinct and the soil around them became dry and packed. In heavy rains, when nest burrows are partly flooded, the females move the eggs to avoid their being submerged. The extent of the female's activity within the nest burrow is suggested by the glazed condition of the earth walls and floor, and by the mottled appearance which the eggsh.e.l.ls soon acquire as a result of being slid and dragged about in the nest cavity.

Still another important function of the female is to dampen the nest burrow to prevent desiccation of the eggs. Even in dry weather, females taken from nests almost invariably voided water in relatively large quant.i.ties. They drink dew or other available water, and may void the contents of the bladder to moisten the nest cavity, as on numerous occasions, when nests were exposed by raising flat rocks covering them, part of the chamber was seen to be recently watered, and distinctly moister than the surrounding soil.

n.o.ble and Mason (_op. cit._:16-19) found that brooding females, in the laboratory, would vigorously defend their eggs against small enemies, including mice and lizards and the smaller kinds of snakes that were tested. The female watched alertly as the intruder approached, and attempted to bite it if it came too near or touched an egg. The females failed to defend their nests against persons and against a large blacksnake; when confronted with such a threat, the female would run from her nest cavity to hide. Cagle (1940:228) stated that the brooding females found by him stayed in the nests even when the logs in which they were situated were chopped open with an ax, and that the skinks would attempt to bite when touched with the finger.

In the present study, females whose nests were exposed never made any active attempt to defend them. Many darted away and hid as soon as they were exposed. In other instances, especially when the nest cavity was only partly exposed, from one side, the female cowered back against the inner wall, opening her mouth in threat if closely approached. If further molested she might then attempt to escape. In brooding females a tendency to sluggishness, and an affinity for the eggs delayed the usually speedy escape reactions. The temperature of the female was ordinarily lower than it would have been in the open or on the underside of a flat rock, and this also tended to slow her reactions. Gravid females when exposed in nest cavities that still contain no eggs are similarly sluggish and reluctant to leave differing little or none in behavior from those that have laid their clutches. Usually the female was found with her body encircling the eggs, holding them together in a compact cl.u.s.ter in the center of the nest cavity. The eggs rest in contact with the loose soil on the floor of the cavity, with each other, and with the female's body in the case of the outer ones of the cl.u.s.ter.

Normal brooding habits proved to be difficult to follow because the females were easily disturbed. In many instances those that had excavated nest burrows, but had not yet laid, deserted the nests after the disturbance involved in raising the sheltering rock. Females that had already laid before discovery of their nests were somewhat less inclined to desert, but many did so.

On numerous occasions, at the time of year when most females are gravid and are staying in nest burrows, I have discovered well formed nest burrows empty and seemingly deserted, with no female in evidence nearby. In some instances the female may have been out foraging or basking although she was not seen, and in other instances the female may have been killed by a predator or eliminated by some other accident.

However, it seems that gravid females frequently do desert their original nest burrows, for one cause or another, and excavate new ones.

Such desertions were noted many times in the females observed on the study area, where the disturbance from my own activities in raising the sheltering rocks may have caused s.h.i.+fts, but it was probably not the sole motivation. One female s.h.i.+fted approximately 120 feet, to excavate her second nest burrow in a site that was damper and more heavily shaded than the first site. This was in the notably dry summer of 1952. Most of the favorite sites under flat rocks in open situations, that were used in 1950 and 1951, were not occupied in 1952 or 1953, although several females did use them for original excavations, which were deserted before laying, as drought conditions developed. In the summers of 1952 and 1953 nests were difficult to find, and those discovered were on the average deeper and better protected than those found in other years.

As compared with other North American lizards in general, _Eumeces fasciatus_ is notable for the relatively exposed and superficial situations chosen as nesting sites. However, it occurs in a climate of high humidity; in contrast, the great majority of our lizards live in arid climates where the eggs are in much greater danger of desiccation, and require better shelter to maintain the humidity at a sufficiently high level. Accounts in the literature and observations in the present study indicate that these skinks exercise a wide range of choice of nesting sites. Ruthven (1911:264) stated that in northern Michigan nests were usually in decaying logs; occasional nests were found in burrows in sand, but invariably decaying wood was present in or around at least part of the nest.

Blanchard (1922) mentions a nest in Tennessee that may have been made by either this species or _E. laticeps_ "in a hollow in a dead willow tree about fifteen feet from the ground buried in the loose, damp, rotted wood." n.o.ble and Mason (_op. cit._:16) quote Blanchard (_in litt._) that in northern Michigan _fasciatus_ nests in logs that are exposed to sunlight. Conant (1951:31) stated that several clutches of eggs found in Ohio were an inch to six inches beneath the upper surface of the log or stump which sheltered them. Evans and Roecker (1951:70) record finding two incubating females inside rotten pine logs, in Ontario. Cagle, studying this species near Elkville, Illinois, in oak-hickory woods, found 25 natural nests of which three were in loose soil among the roots of a fallen tree, another was under loose bark of a log, and the remainder were all in cavities of partly decayed logs. Bishop (1926:119) recorded finding a female with a clutch of eggs beneath damp boards at Quicksand, Breathitt County, Kentucky.

In the present study, more than one hundred natural nests were found, of which just one (containing two clutches of eggs) was in decaying wood beneath the bark of an old log. All other nests were beneath rocks. On the University of Kansas Natural History Reservation, where most of the nests were found, the policy is not to tear apart decaying logs; therefore the nests probably present in such situations were not ordinarily found. On several occasions groups of hatchlings were seen on logs within which they probably had hatched. In the area of the study, however, decaying logs are scarce. The hardwood forests consist mostly of young trees that are second growth on cutover areas or pioneer on areas that were previously gra.s.sland. Because of frequent cutting there are few old mature trees, and logs have not acc.u.mulated on the forest floor. In northeastern Kansas, nesting in logs is comparatively rare. On wooded slopes and the edges of level hilltops, the flat limestone rocks that are often abundant provide preferred nesting sites. Even on collecting trips off the Reservation, where stumps and logs could be torn apart and searched, flat rocks were found to provide the main source of nesting sites. These nest rocks varied from less than an inch in thickness to nine inches or more, and from a few inches in diameter to three feet or more. Some were resting loosely on the surface of the soil and others were deeply sunken, on one side. Some were in situations exposing them to nearly the maximum amount of suns.h.i.+ne whereas others were in sites nearly always shaded. The varied character of the nesting sites chosen demonstrated a wide range of tolerance for temperature, moisture, and other factors, in the gravid and brooding female and in the developing embryo.

As already mentioned, n.o.ble and Mason (_op. cit._:9-10) noted that females would accept and brood the eggs of other individuals just as readily as their own, and several writers have reported gregarious nesting habits, with two or more females occupying either the same nest cavity, or separate cavities that were in close proximity. For instance, Cagle wrote that among the small logs he found to contain nests, four logs each contained one nest, five each contained two nests, and two each contained three nests, while three other nests were found within an eight inch square area in loose soil among tree roots. McCauley (1939:93) in Maryland found three females brooding clutches of eggs, which totaled 20, and which were so near together that there was uncertainty as to which clutch certain eggs belonged in.

The gregarious nesting habit may be of benefit in permitting maximum utilization of choice nesting sites, where such sites are in short supply in an environment otherwise favorable. Also, the gregarious tendencies make possible more continuous guarding of the eggs against such natural enemies as can be repulsed by the female, since each female occasionally interrupts her brooding to bask or forage.

Many of the nests that I found were in close proximity to others. Often two nests, and sometimes even three, were found beneath the same rock, and sometimes a distance of only two or three inches intervened between the separate clutches. It seemed, however, that in almost every instance each female had excavated a separate nest chamber originally. In some instances adjacent nest chambers communicated with each other.

On July 13, 1948, a communal nest was discovered beneath loose bark of a decaying elm log. There were 22 eggs in the combined clutch, and there were two females in the vicinity. The bark was raised on several different days to examine the eggs, and one or both females always were found with the eggs.

On June 10, 1949, at the pond rock pile, a flat rock was turned and an unusual nesting aggregation consisting of a minimum of eight females, and probably more than ten, was found. The nests were somewhat disturbed by movement of the rock. The ground beneath was honeycombed with tunnels connecting the flask-shaped nest cavities, which were in part open to the rock surface on their upper sides. Clutches of eggs numbered 13, 12, 11, 8, and 6 (the last attended by a female which appeared to be still distended with several more unlaid eggs). Of five other females taken, two had laid and three were still gravid. Of the five clutches, two had eggs noticeably larger than those in the other three, and with their sh.e.l.ls mottled brown from adhering earth. These nest cavities were about half an inch deep and two to three inches wide. The females were released as soon as they had been examined. One female moved about over the nest areas exposed, and evinced interest in a lone egg which had become separated from the others. She moved up to it, standing high off the ground, with her head turned at right angles to her body as if preparing to push the egg forward in the angle thus formed, and tested it with her tongue, but then she became alarmed and left the vicinity.

The flat rock was lowered over the nests again with a minimum of disturbance.

On July 9, 1949, the flat rock covering the nests was raised again. Most of the eggs had hatched. Two broods of hatchlings were still in their respective nest cavities, and one entire clutch had not begun to hatch although its incubation was nearly completed. Three eggs of _Scincella laterale_ were found mixed with the _Eumeces_ eggs. One of these was opened to verify their ident.i.ty; the other two hatched a few days later in the laboratory.

The following selected excerpts from my field notes, setting forth histories of several nests, so far as they were known, give some idea of the types of nesting sites chosen, the behavior of the females, and the hazards to which the eggs are exposed.

No. 1. At corner of pond rock pile.

June 21, 1951. Female escaped when rock was turned. One egg measured 12.5 8 mm., mud-stained.

June 22, 1951. Nest not in evidence when rock was turned; digging into loose soil beneath to a depth of about an inch I exposed the eggs but did not disturb them further.

July 23, 1951. When rock was turned, female did not attempt to escape, but withdrew to far corner of nest cavity; when caught she voided a large scat which seemed to consist mainly of _Ceuthophilus_ remains. Largest eggs in the clutch were 18 10 mm. but two were noticeably smaller, and all were heavily coated with dried mud.

July 30, 1951. Six young in the nest cavity, still not fully active; all of them were heavily coated with dried mud.