Abstract:A recent study on wild male Mediterranean fruit flies [Papadopoulos, N.T., Katsoyannos, B.I., Kouloussis, N.A., Carey, J.R., Müller, H.-G., Zhang, Y., 2004. High sexual signalling rates of young individuals predict extended life span in male Mediterranean fruit flies. Oecologia 138,[127][128][129][130][131][132][133][134] provided evidence that intense sexual signalling (calling behavior) is associated with longer life span. We demonstrate here an approach based on functional data analysis methodology for pred… Show more
“…The existence of non-calling males is not fully understood yet and may be caused by male – male aggression or by genetic factors (Shelly, 2000). It appears that age and time of the day can also affect the emission of pheromone (Flath et al, 1993; Papadopoulos et al, 1998; Papadopoulos et al, 2004; Zhang et al, 2006; Neto et al, 2009). It is known that frequently calling males usually achieve higher mating success (Shelly, 2000).…”
Although age-based effects on the reproductive success of males have been reported in several animal taxa the cost of aging on male mating success in lekking species has not been fully explored. We used the Mediterranean fruit fly, a lekking species, to investigate possible cost of aging on male reproductive success. We performed no choice and choice mating tests to test the hypothesis that aging does not affect the mating performance (mating success in conditions lacking competition) or the mating competitiveness (mating success against younger rivals) of males. The mating probability of older males decreased significantly when competing with younger males. Aging gradually reduced the mating performance of males but older males were still accepted as mating partners in conditions lacking competition. Therefore, older males are capable of performing the complete repertoire of sexual performance but fail to be chosen by females in the presence of young rivals. Older males achieved shorter copulations than younger ones, and female readiness to mate was negatively affected by male age. Older and younger males transferred similar amount of spermatozoids to female spermathecae. Females stored spermatozoids asymmetrically in the two spermathecae regardless the age of their mating partner. Aging positively affected the amount of spermatozoids in testes of both mated and non mated males. No significant differences were observed on the amount of spermatozoids between mated and non mated males.
“…The existence of non-calling males is not fully understood yet and may be caused by male – male aggression or by genetic factors (Shelly, 2000). It appears that age and time of the day can also affect the emission of pheromone (Flath et al, 1993; Papadopoulos et al, 1998; Papadopoulos et al, 2004; Zhang et al, 2006; Neto et al, 2009). It is known that frequently calling males usually achieve higher mating success (Shelly, 2000).…”
Although age-based effects on the reproductive success of males have been reported in several animal taxa the cost of aging on male mating success in lekking species has not been fully explored. We used the Mediterranean fruit fly, a lekking species, to investigate possible cost of aging on male reproductive success. We performed no choice and choice mating tests to test the hypothesis that aging does not affect the mating performance (mating success in conditions lacking competition) or the mating competitiveness (mating success against younger rivals) of males. The mating probability of older males decreased significantly when competing with younger males. Aging gradually reduced the mating performance of males but older males were still accepted as mating partners in conditions lacking competition. Therefore, older males are capable of performing the complete repertoire of sexual performance but fail to be chosen by females in the presence of young rivals. Older males achieved shorter copulations than younger ones, and female readiness to mate was negatively affected by male age. Older and younger males transferred similar amount of spermatozoids to female spermathecae. Females stored spermatozoids asymmetrically in the two spermathecae regardless the age of their mating partner. Aging positively affected the amount of spermatozoids in testes of both mated and non mated males. No significant differences were observed on the amount of spermatozoids between mated and non mated males.
“…In addition, Carey (2003) has noted that males exhibit a characteristic supine behavior prior to death. Current male calling behavior in medflies may also be used to predict remaining lifespan (Zhang et al 2006). These observations suggest a physiological decline prior to death that may exhibit its effects in a variety of characters, not just female fecundity.…”
There is now a significant body of research that establishes the deceleration of mortality rates in late life and their ultimate leveling off on a late-life plateau. Natural selection has been offered as one mechanism responsible for these plateaus. The force of natural selection should also exert such effects on female fecundity. We have already developed a model of female fecundity in late life that incorporates the general predictions of the evolutionary model. The original evolutionary model predicts a decline in fecundity from a peak in early life, followed by a plateau with non-zero fecundity in late life. However, in Drosophila there is also a well-defined decline in fecundity among dying flies, here called the "death spiral". This effect produces heterogeneity between dying and non-dying flies. Here a hybrid evolutionary heterogeneity model is developed to accommodate both the evolutionary plateau prediction and the death spiral. It is shown that this evolutionary heterogeneity model gives a much better fit to late-life fecundity data.
“…In this experiment we measured WBF at 5 days of age conditioned on an individual fly's lifespan. This approach to determining the correlation between biological function at a particular age and longevity has previously been used to study functional aging in flies, for example, to determine the rate of egg laying at a particular age conditioned on lifespan (Carey et al 2005), effects of the onset of dietary restrictions on subsequent longevity (Mair et al 2003;Vaupel et al 2003), and association between the intensity of a male fly's sexual signaling (e.g., calling behavior) and lifespan (Papadopoulos et al 2004;Zhang et al 2006). Figure 5 shows results of this experiment.…”
Section: Wbf Measured At 5 Days Of Age Conditioned On Lifespanmentioning
Methuselah is a Drosophila mutant with a 35% increased lifespan. We examined the robustness of methuselah's sensorimotor abilities in tethered flight as a function of age in experiments designed to test visuomotor synchronization and phototaxis in simulated flight. A total of 282 flies from different age groups (4 hours to 70 days) and genotypes (mth and w1118) were individually tethered under an infrared laser-sensor system that digitally recorded wing-beat frequency (WBF). We found that mth has a higher average WBF throughout most of its lifespan compared to parental control flies (w1118) and develops flight ability at a younger age. Its WBF at late life, however, is not significantly different than that of its parental control line. We further found that mth entrains during flight to motion of a visual grating significantly better than its parental line. These findings suggest that the mth gene not only delays chronological aging but enhances sensorimotor abilities critical to survival during early and middle, but not late life.
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