Flirting with danger: predation risk interacts with male condition to influence sexual display

Sexual signaling coevolves with the sensory systems of intended receivers; however, predators may be unintended receivers of sexual signals. Conspicuous aerial displays in some species may place males at high risk of predation from eavesdropping predators. There are three different hypotheses to explain how signaling males can deal with increased predation risk: (1) males invest in survival by decreasing signal conspicuousness; (2) males invest in reproduction by increasing signal conspicuousness; and (3) male response is condition-dependent according to his residual reproductive value. Here, we used blue-black grassquits (Volatinia jacarina) to test these hypotheses, asking whether males modify leap displays under different levels of predation risk. Grassquit males develop an iridescent nuptial plumage and spend considerable time emitting a multimodal signal: while leaping from a perch, males clap their wings above their heads and emit a high-pitched short song. We exposed males to predator and nonpredator playbacks while video recording their displays. We found interactions between predation risk and 2 male condition variables (ectoparasite infestation and proportion of nuptial plumage coverage) that influenced display behavior. Less parasitized males and those with higher proportion of nuptial plumage showed no change in display behavior, while more parasitized males and those with lower proportion of nuptial plumage increased the vigor of displays under predation risk. In other words, males with low residual reproductive value increased reproductive effort when there was a high risk of extrinsic death. Our study provides some empirical support for the terminal investment hypothesis.

Age affects escape behavior by the zebra-tailed lizard (Callisaurus draconoides) more strongly than in other lizards

Prey of different ages may exhibit differences in escape behavior, including flight initiation distance (FID – predator-prey distance when escape begins) and distance fled before stopping (DF). Escape theory predicts FID and, in some circumstance, DF, based on trade-offs between conflicting cost of not fleeing (predation risk) and cost of fleeing (primarily opportunities to enhance fitness lost by fleeing). The prey’s expected lifetime fitness when an encounter begins also affects escape decisions. Because hatchling and adult lizards may differ in ways that affect all three of these factors, a priori prediction of age differences is not possible without measurements of all three. In a field study I found that hatchling zebra-tailed lizards (Callisaurs draconoides) had much shorter FID and DF than adults. These relationships were not affected by distance to refuge, which did not differ between ages, and refuge use was infrequent. The findings agree with those of all but one previous study of age differences, suggesting that hatchling lizards typically have shorter FID and DF than adults because they 1) assess risk as being lower due to lower attractiveness to or detectability by predators, lack of experience or greater maneuverability, 2) have greater opportunity cost due to the need for rapid growth and good body condition before winter, and possibly 3) have lower residual reproductive value due to higher mortality rate than adults. Effects of age and size are confounded, and smaller size may be the major reason for the shorter FID and distance fled of hatchlings.

The influence of male age and simulated pathogenic infection on producing a dishonest sexual signal

In recent years, studies have shown that reproductive effort decelerates in response to pathogenic infection. If infection substantially reduces a host's residual reproductive value (RRV), however, then an acceleration of effort may instead occur (e.g. terminal investment). Reproductive acceleration would theoretically allow hosts to maintain or exaggerate their sexual signal upon infection. This would create a deceptive message from the perspective of the chooser, who may unwittingly copulate with an infected mate to their detriment. Using the cricket Allonemobius socius , we assessed the potential for reduced RRV to accelerate male reproductive effort and create a dishonest signal. RRV was manipulated through male age and simulated pathogenic insult. Reproductive effort was measured as calling song energetics, mating success, latency to mate and nuptial gift size. We show that males adopted either an accelerated or decelerated reproductive strategy upon infection, and that this decision was probably mediated by RRV. Moreover, males who accelerated their effort produced a dishonest signal by increasing their song energetics while providing fewer paternal resources (i.e. smaller gifts). Our study is one of the few to document the existence of dishonest signals and relate dishonesty to a potential reduction in female fitness, underscoring the conflict inherent in sexual reproduction.

Effects of stage in incubation, time in season, and proportion of original clutch remaining on nest desertion by house sparrows, Passer domesticus

Life history theory predicts that individuals should maximize their fitness by balancing current investment in offspring versus future prospects for reproduction. Faced with reduction of their current clutch, birds should desert if the prospective opportunity would increase inclusive fitness more than continued investment in the reduced clutch. I studied nest desertion in response to clutch reduction by house sparrows (Passer domesticus) to determine if continuing investment in a reduced clutch differs based on proportion of original clutch remaining, stage in incubation, and ordinal date. Nests were reduced to two eggs early or late in incubation over two complete breeding seasons. Of 150 nests manipulated, 36 were deserted. Nests were more likely to be deserted when reduction occurred earlier in incubation, earlier in the season, and with a smaller proportion of original clutch remaining. This suggests that both time and brood size are used to assess the tradeoffs between current and future investment. However, near the end of the breeding season, the proportion of original clutch remaining and stage in incubation were less important, and low desertion was likely associated with a lack of re-nesting opportunities in the current season. Therefore, whether to desert or continue investing in a reduced clutch is a function of offspring reproductive value (RV) when there is opportunity for re-nesting in the same season. However, near the end of the season the decision is based on the residual reproductive value (RRV) of parents.