Studies of Sociosexual Interactions in Rats in an Externally Valid Procedure: Are They Relevant for Understanding Human Sexual Behavior?

When a prolonged observation of groups of rats in a seminatural environment is used as testing procedure, different behavioral patterns are shown compared with what observed in a pair housed in a small cage. Males and females copulate simultaneously, they show a promiscuously and random copulatory pattern. Females remain completely receptive from the first lordosis displayed in the period of behavioral estrus until the last. There is no reduction in paracopulatory behaviors and no increase in rejections towards the end of estrus. Female paracopulatory behavior and receptivity change in a most abrupt way at both initiation and termination of behavioral estrus. It appears that, in the seminatural environment, males copulate in bouts, and males do not pursue the females unless they are fully receptive. Non-sexual, social behavior including affiliative and nonaffiliative interaction among rats is rather unrelated to sexual activities in both sex.

Copulatory pattern and behavior in a semi-captive population of Eld’s deer

Male copulatory patterns, female multiple copulation and male post-copulatory guarding were studied in Eld’s deer Cervus eldi in Datian National Nature Reserve, China. Mating behavior in 18 females and 11 males from a group of 61 semi-captive Eld’s deer were observed. The majority (55.8%) of copulations occurred between 15:00–19:00 h. The ejaculatory mount was preceded by an average of 5.1 prior mounts. Successful copulation consisted of a single thrust with ejaculation during one intromission, with no lock. This copulatory pattern is classified as pattern No. 15 (no lock, no intravaginal thrusting, single intromission, and multiple ejaculation) and No. 16 (no lock, no intravaginal thrusting, single intromission, and single ejaculation) under Dewsbury’s scheme (1972) and as No. 16 (no lock, no thrusting, single and brief intromission) under Dixson’s classification (1998). Copulation frequency was 1.5 ± 0.9 times for males/ females with the same female/male per day. The duration of the final mount, which included ejaculation, was brief (3.4 ± 1.3 s), and ejaculation usually terminated copulation. Eleven females copulated more than once in this study: three of them copulated with several males (multi-male copulations) and the remainder copulated with a single male (repeated copulations). Our results indicate that some female Eld’s deer may seek multiple copulations to be a strategy to improve the genetic quality of their offspring or to avoid harassment. Post-copulatory guarding of females by males followed all copulations, with dominant males guarding for significantly longer than subordinate males. Dominant males appear to be more effective at post-copulatory guarding than subordinate males. Subordinate males engaged in a quicker pre-copulatory phase to improve their chances of finishing copulation before being forced to accede to dominant males.

MONOZYGOTIC VS. DIZYGOTIC TWIN BEHAVIOR IN ARTIFICIAL MOUSE TWINS

ABSTRACT Adult inbred mice of an isogenic strain (AKR/NHan or C57BL/6J Han) differ in social (sexual and agonistic), emotional and psychomotoric behavior, depending on the kind of manipulation to which they were subjected at an early ontogenetic stage. Monozygotic twins (MZT) from eight-cell stages halved and transferred to uterine foster mothers were compared with dizygotic twins (DZT) from nonreduced but transferred eight-cell stages and with naturally born animals (NBA). Generally, early embryonic conditions predict the behavioral characteristics of the adult animals to a high degree. The MZT are motorially less active, less emotional, less aggressive and less socially interested than DZT and NBA. In tests of spontaneous social behavior (allogrooming, anogenital licking, mounting, fighting), as well as in tests for emotionality (open field: crossed fields and defecation), these behavioral patterns occurred less frequently in MZT than in DZT; the NBA were mostly intermediate. The copulatory pattern of male MZT differs from that of male DZT by a shortage of intromission latency and duration; furthermore, MZT pairs do not build up a steady rank order in competitive copulation tests, as opposed to DZT and NBA pairs. In a test for psychomotoric behavior (swimming), the MZT prefer "floating" as a survival strategy, wheras the DZT and NBA prefer "adult swimming." Therefore, it can be concluded that these behavioral differences may be caused by the particular psychosocial environment in which the twins grow up or may be due to early prenatal peculiarities, such as inadequate synchronization of the developmental status of uterus and embryo.