| Sex | Original record | Record(s) of recapture | ||||
| Date | Snout-vent length, millimeters | Weight, grams | Date | Snout-vent length, millimeters | Weight, grams | |
| ♂ | Aug. 17, 1959 | 223 | 5.3 | Sept. 12, 1960 | 503 | 42 |
| ♀ | Oct. 26, 1959 | 278 | 10 | Oct. 26, 1959 | 566 | 55 |
| ♀ | Nov. 2, 1959 | 340 | 18 | May 11, 1961 | 582 | 65 |
| ♀ | Nov. 10, 1959 | 348 | 13.7 | June 20, 1961 | 733 | 127 |
| ♀ | Oct. 19, 1952 | 361 | 15.3 | Oct. 9, 1953 | 620 | 68 |
| ♂ | May 9, 1953 | 368 | 17 | May 13, 1954 | 609 | 84 |
| ♀ | April 16, 1950 | 328 | 142 | Oct. 10, 1950 | 603 | 78.2 |
| ♀ | May 17, 1956 | 358 | 15.2 | Oct. 6, 1956 | 575 | 52 |
| ♂ | Nov. 1, 1953 | 330 | 11 | May 21, 1955 | 674 | 92 |
Though covering a wide size-range, the young of the year entering hibernation are still a distinct size group, not yet overlapping that of the next older group of young. Growth during the first year of life is best shown by the individuals in [Table 12], all of which were marked either before their first hibernation or soon after emerging from it, and were recaptured either the following autumn, or in spring soon after emerging from a second hibernation.
These records indicate that the young racers at the time of their second hibernation have grown to a snout-vent length of well over 500 millimeters, but less than 700 millimeters, and a weight of more than 40 grams but less than 100 grams. Other racers marked in the first few weeks of life were recaptured after two or more seasons of growth, and indicate the sizes that may be expected in young adults from two to five years old, as shown in [Table 13].
Table 13. Growth of Racers Marked at an Age of Less Than One Year
and Recaptured in Their Second, Third or Fourth Years
| Sex | Original record | Record(s) of recapture | ||||||
| Date | Snout-vent length in mm. | Weight in grams | Probable age in months | Date | Snout-vent length mm. | Weight in grams | Probable age in months | |
| ♂ | Nov. 12, 1952 | 342 | .... | 21/2 | May 20, 1955 | 702 | 110 | 33 |
| ♂ | Nov. 1, 1953 | 330 | 11 | 2 | Aug. 16, 1956 | 780 | 162 | 351/2 |
| ♂ | Nov. 12, 1953 | 293 | .... | 21/2 | May 14, 1956 | 634 | 96 | 321/2 |
| Oct. 13, 1956 | 689 | 110 | 371/2 | |||||
| ♂ | April 15, 1955 | 320 | 13 | 91/2 | June 8, 1958 | 740 | 118 | 45 |
| ♂ | Oct. 2, 1955 | 348 | 18 | 1 | May 22, 1958 | 728 | 120 | 33 |
| May 21, 1960 | 795 | 130 | 57 | |||||
| ♂ | June 25, 1959 | 378 | 10 | 10 | June 30, 1960 | 590 | 60 | 22 |
| June 7, 1961 | 705 | 123 | 33 | |||||
| ♂ | Nov. 1, 1953 | 330 | 11 | 2 | Aug. 25, 1957 | 805 | 183 | 48 |
Unlike young of the year, racers in their second autumn were trapped in large numbers. By this time all were large enough to be caught in the traps of quarter-inch wire mesh, and they were the most abundant size group. Many that were marked at this stage were recaptured after intervals of months or years, showing the trend of growth. Some of these snakes in their second autumn already had overtaken the more retarded third-year individuals. The two age classes cannot be separated with certainty. Selected records of individuals that were almost certainly second-year young at the time they were marked are presented in [Table 14].
Table 14. Growth of Young Racers That Were Marked Near the Time of Their Second Hibernation
| Sex | Original record | Record(s) of recapture | ||||||
| Date | Snout-vent length in mm. | Weight in grams | Probable age in months | Date | Snout-vent length in mm. | Weight in grams | Probable age in months | |
| ♂ | Oct. 6, 1960 | 595 | 80 | 13 | July 23, 1961 | 650 | 70 | 23 |
| ♂ | Oct. 13, 1950 | 525 | 52.6 | 131/2 | Oct. 2, 1951 | 675 | 105 | 25 |
| ♂ | Nov. 2, 1950 | 545 | 55.6 | 14 | Oct. 24, 1951 | 670 | 100 | 26 |
| ♂ | Sept. 2, 1957 | 522 | 57 | 12 | Oct. 14, 1958 | 690 | 103 | 251/2 |
| ♂ | Oct. 17, 1953 | 558 | 47 | 131/2 | May 10, 1955 | 718 | .... | 32 |
| ♂ | Nov. 14, 1956 | 587 | 57 | 141/2 | May 20, 1958 | 728 | 100 | 521/2 |
| June 17, 1959 | 880 | 219 | 641/2 | |||||
| ♂ | Sept. 7, 1959 | 533 | 45 | 12 | June 6, 1961 | 740 | 112 | 33 |
| ♂ | Oct. 17, 1959 | 558 | 56 | 131/2 | July 21, 1960 | 625 | 63 | 221/2 |
| June 7, 1961 | 670 | 95 | 33 | |||||
| ♂ | Oct. 16, 1952 | 577 | 62.0 | 131/2 | May 31, 1955 | 809 | 160 | 45 |
| May 11, 1956 | 855 | 144.3 | 561/2 | |||||
| ♂ | Oct. 11, 1950 | 570 | 65.9 | 131/2 | July 11, 1956 | 820 | 193.6 | 821/2 |
| ♂ | Oct. 14, 1953 | 560 | 52 | 131/2 | June 29, 1958 | 794 | 256 | 70 |
| ♂ | Oct. 6, 1950 | 563 | 55.8 | 13 | Sept. 28, 1958 | 907 | 243 | 109 |
| ♂ | Oct. 14, 1953 | 523 | 44 | 131/2 | May 19, 1959 | 818 | 190 | 801/2 |
| May 17, 1960 | 850 | 211 | 921/2 | |||||
| ♂ | Oct. 13, 1953 | 521 | 50.1 | 131/2 | May 13, 1958 | 814 | 166.4 | 441/2 |
| June 3, 1959 | 826 | 165 | 47 | |||||
| ♂ | Nov. 5, 1953 | 512 | 34 | 14 | May 22, 1958 | 847 | 135 | 69 |
| ♀ | Aug. 11, 1953 | 534 | 39.2 | 111/2 | Sept. 18, 1954 | 670 | 143 | 241/2 |
| ♀ | Oct. 14, 1949 | 588 | 55.2 | 131/2 | Oct. 11, 1950 | 713 | 114.0 | 251/2 |
| ♀ | Oct. 6, 1950 | 570 | 60.4 | 13 | Oct. 11, 1951 | 783 | 174 | 251/2 |
| ♀ | Oct. 31, 1953 | 582 | 58 | 14 | Oct. 5, 1954 | 860 | 195 | 25 |
| ♀ | Oct. 21, 1959 | 588 | 63 | 131/2 | May 7, 1961 | 730 | 120 | 32 |
| ♀ | May 14, 1960 | 506 | 34 | 201/2 | Oct. 26, 1960 | 690 | 90 | 26 |
| ♂ | Oct. 22, 1960 | 527 | 45 | 131/2 | Oct. 7, 1961 | 620 | 74 | 25 |
| ♂ | May 3, 1960 | 530 | 48 | 20 | May 16, 1961 | 700 | 110 | 321/2 |
| ♂ | May 27, 1961 | 535 | 40 | 21 | Oct. 25, 1961 | 672 | 98 | 26 |
From the records in [Table 14] and many more like them, average and extreme sizes for progressively older age groups were estimated. Even racers that were already of adult size when they were marked were tentatively identified with one or another age group, and their records of subsequent growth were used. Most of the records show that the females grow more rapidly than the males, and are, on the average, larger at any given age.