The few publications discussing growth in turtles express conflicting views as to the exact mode of growth of epidermal laminae. Carr (1952:22) briefly discussed growth of turtle scutes in general and stated that eccentric growth results from an entirely new laminal layer forming beneath, and projecting past the edges of the existing lamina. Ewing (1939) found the scutes of T. carolina to be the thickest at the areola and successively thinner in the following eight annual zones of growth; parts of scutes formed subsequent to the ninth year varied irregularly in thickness. He stated that epidermal growth took place at the margins of the laminae rather than over their entire under-surfaces.
It is evident that the mode of scutular growth described by Carr (loc. cit.) applies to emyid turtles that shed the epidermal laminae more or less regularly (for example, Chrysemys and Pseudemys). In these aquatic emyids a layer of the scute, the older portion, periodically becomes loose and exfoliates usually in one thin, micalike piece; since the loosened portion of the scute corresponds in size to the scute below, it must be concluded that a layer of epidermis is shed from the entire upper surface of the scute, including the area of new epidermal growth. Box turtles ordinarily do not shed the older parts of their scutes; the areola and successively younger portions of the lamina remain attached to the shell until worn off. The appearance of a single unworn scute, especially one of the centrals or the posterior laterals, closely resembles a low, lopsided pyramid.
Examination of parasagittal sections of scutes revealed that they were composed of layers, the number of layers varying with the age of the scute. A scute from a hatchling consists of one layer. A scute that shows a single season of growth has two layers; a new layer is added in each subsequent season of growth. Stratification is most evident in the part of the scute that was formed in the first three or four seasons and becomes increasingly less distinct in newer parts of the scute. It may further be understood that scutes grow in the manner described by Carr (loc. cit.).
When the epidermal laminae are removed, a sheet of tough, pale grayish tissue remains firmly attached to the bones of the shell beneath. This layer probably includes, or consists of, germinal epithelium. Contrasting pale and dark areas of the germinal layer correspond to the pattern of markings on the scute removed.
Fig. 8. The second central scute from a juvenal T. o. ornata (KU 16133) in its third full season of growth. A) Entire scute from above (× 2½); dashed line shows portion removed in parasagittal section. B) Diagonal view of section removed from scute in "A" (× 43∕8, thickness greatly exaggerated) showing layers of epidermis formed in successive seasons of growth. Each layer ends at a major growth-ring (M 1-3) that was formed during hibernation; minor growth-rings (m), formed in the course of the growing season, do not result from the formation of a new layer of epidermis. Note the granular texture of the areola (a); the smooth zone between the areola and M1 shows amount of growth in the season of hatching. |
Growth of epidermal laminae is presumably stimulated by growth of the bony shell. As the bone grows, the germinal layer of the epidermis grows with it. When growth ceases at the beginning of hibernation, the thin edges of the scutes are slightly down-turned where they enter the interlaminal seams ([Fig. 8]). When growth is resumed in spring, the germinal layer of the epidermis, rather than continuing to add to the edge of the existing scute, forms an entirely new layer of epidermis. The new layer is thin and indistinct under the oldest part of the scute but becomes more distinct toward its periphery. Immediately proximal to the edge of the scute, the new layer becomes greatly thickened, and, where it passes under the edge, it bulges upward, recurving the free edge of the scute above. At this time the formation of a major growth-ring is completed. The newly-formed epidermis, projecting from under the edges of the scute, is paler and softer than the older parts of the scute; the presence or absence of areas of newly formed epidermis enables one to determine quickly whether a turtle is growing in the season in which it is captured. There is little actual increase in thickness of the scute after the first three or four years of growth. The epidermal laminae are therefore like low pyramids only in appearance. This appearance of thickness is enhanced by the contours of bony shell which correspond to the contours of the scutes.
Minor growth-rings differ from major growth-rings in appearance and in origin. Ewing (op. cit.: 91) recognized the difference in appearance and referred to minor growth-rings as "pseudoannual growth zones." Minor growth-rings result from temporary cessations of growth that occur in the course of the growing season, not at the onset of hibernation. They are mere dips or depressions in the surface of the scute. The occurrence of minor growth-rings indicates that interruptions in growth of short duration do not result in the formation of a new layer of epidermis. Slowing of growth or its temporary cessation may be caused by injuries, periods of quiescence due to dry, hot, or cold weather, lack of food, and possibly by physiological stress, especially in females, in the season of reproduction. Minor growth-rings that lie immediately proximal to major growth-rings ([Pl. 22, Fig. 2]), are the result of temporary dormancy in a period of cold weather at the end of a growing season, followed by nearly normal activity in a warmer period before winter-long hibernation is begun. Cagle (1946:699) stated that sliders (Pseudemys scripta elegans) remaining several weeks in a pond that had become barren of food would stop growing and develop a growth-ring on the epidermal laminae; he did not indicate, however, whether these growth-rings differ from those formed during hibernation.
In species that periodically shed scutes a zone of fracture develops between the old and new layers of the scute as each new layer of epidermis is formed, and the old layer is shed. Considering reptiles as a group, skin shedding is of general occurrence; the process in Pseudemys and Chrysemys differs in no basic respect from that in most reptiles. Retention of scutes in terrestrial emyids and in testudinids is one of many specializations for existence on land. Retention of scutes protects the shell of terrestrial chelonians against wear. Some box turtles were observed to have several scutes of the carapace in the process of exfoliation but no exfoliation was observed on the plastron. Exfoliation ordinarily occurred on the scutes of the carapace that were the least worn; the exfoliating portion included the areola and the three or four oldest (first formed) layers of the scute. The layer of scute exposed was smooth and had yellow markings that were only slightly less distinct than those on the portion that was exfoliating.
Wear on the shell of a box turtle reduces the thickness of scutes, as does the shedding of scutes in the aquatic emyids mentioned. It is noteworthy that any of the layers in the scute of a box turtle can form the cornified surface of the scute when the layers above it wear away or are shed.