Biology subjects

Wang, W. W.-Y.

Publications and source records attributed to Wang, W. W.-Y..

3 recordsLinked to original sources

bioRxiv2026

Similar fertility losses in response to heat are followed by distinct recovery trajectories across seven Drosophila species

Heat-induced sterility is widespread across ectotherm species, yet its underlying mechanisms remain poorly understood. In mated females, thermal stress can disrupt female reproductive physiology while also affecting sperm stored within the reproductive tract, making the mechanisms of fertility loss difficult to distinguish. Here, we investigated the extent and recovery dynamics of female heat-induced fertility loss across seven Drosophila species. We tracked fertility after acute heat exposure, tested whether remating restored fertility, quantified stored sperm in two closely related species, and examined whether reproductive thermal sensitivity covaried with adult heat tolerance. We found that heat exposure reduced egg-hatching success in all seven species, but recovery differed among species. Fertility recovered within several days in most species, whereas D. simulans showed persistent declines and D. melanogaster showed limited recovery. Remating restored or maintained fertility in both species. Stored sperm declined through time in both D. simulans and D. mauritiana, but D. mauritiana retained more sperm at later sampling points, consistent with their contrasting patterns of fertility decline and maintenance. Across species, greater adult heat tolerance was associated with smaller immediate reductions in fertility, but not with cumulative reproductive loss across subsequent days. Together, these findings show that similar initial fertility losses can lead to markedly different recovery trajectories and highlight the importance of comparative, multi-species approaches that integrate female physiology, sperm-storage dynamics, mating behavior, and whole-organism thermal tolerance when assessing reproductive resilience to climate warming.

ecology↗

bioRxiv2026

No adaptive plasticity in the heat tolerance of lizard sperm

O_LIAdaptive phenotypic plasticity can help organisms cope with global warming by increasing their heat tolerance, yet most research has focused on whole-organism traits. Much less is known about thermal plasticity at the gamete level despite increasing evidence that reproduction, and particularly sperm function, is especially sensitive to heat. C_LIO_LIWe tested for plasticity in sperm heat tolerance in two ways: via male thermal acclimation (pre-ejaculate stage) and via sperm cell heat hardening (post-ejaculate stage) in brown anole lizards (Anolis sagrei). We also measured plasticity in several other sperm and ejaculate traits in response to male thermal acclimation. C_LIO_LITo test for effects of male thermal acclimation, adult males were exposed to one of two ecologically realistic, fluctuating temperature regimes that either mimic cool spring conditions or projected future summer conditions for eight weeks. Throughout this period, we repeatedly measured sperm heat tolerance (LT50), baseline motility, and sperm count. We also measured sperm morphology at the end of thermal acclimation. We predicted that males in the warmer treatment would produce more heat tolerant sperm. C_LIO_LITo test for post-ejaculate heat hardening, we compared the heat tolerance of ejaculated sperm that either did or did not experience a high but non-lethal temperature prior to heat tolerance measurement. C_LIO_LIWe found no plasticity in sperm heat tolerance due to either male thermal acclimation or sperm cell heat shock. Long-term thermal acclimation of males did not increase sperm heat tolerance, nor change motility, sperm count, or sperm morphology. We also found no evidence for post-ejaculate heat hardening, as exposing sperm cells to mild sublethal heat shock did not enhance sperm heat tolerance. C_LIO_LIOur results indicate that gametic traits have limited capacity for plastic adjustment to thermal stress, which is broadly consistent with the low levels of thermal plasticity found for whole-organism thermal tolerance across ectotherms. This highlights the vulnerability of reproductive traits to rising temperatures and the importance of evolutionary and behavioral responses to buffer organisms from climate change. C_LI

ecology↗

bioRxiv2024

The heat sensitivity of sperm in the lizard Anolis sagrei

The heat sensitivity of reproduction is a critical determinant of population persistence under climate change. However, the heat sensitivity of gametes is poorly known relative to adults. We developed a method to measure the heat tolerance of lizard sperm cells, and used the method to test several aspects of sperm cell thermal biology in the brown anole lizard (Anolis sagrei). We estimated the repeatability of sperm traits by measuring heat tolerance and baseline motility of ejaculated sperm from the same individuals multiple times over 21 days. To investigate co-adaptation of sperm and adult thermal traits, we tested for a correlation between sperm heat tolerance and the heat tolerance of adults that produced them. Furthermore, we tested for effects of episodic heat stress experienced by males on sperm performance. Sperm heat tolerance and motility were both repeatable, consistent with evolutionary potential, though there was clear evidence for environmental effects on these traits as well. Contrary to the expectation of thermal co-adaptation, we found no correlation between sperm and adult heat tolerance. A single, episodic extreme heat event experienced by adult males immediately impaired sperm motility, consistent with detrimental effects of adult heat stress on stored sperm. Our study adds to the mounting evidence that sperm are heat-sensitive and represent a vulnerability to global warming, but also suggest evolutionary potential for thermal adaptation at the gamete level. Summary statementThis study investigates gamete heat sensitivity in lizards, revealing heat tolerance and repeatability in sperm thermal traits. These findings are essential for understanding reproductive responses to climate change.

zoology↗