8 research outputs found
Shifts in caterpillar biomass phenology due to climate change and its impact on the breeding biology of an insectivorous bird
Timing of reproduction has major fitness consequences, which can only be understood when the phenology of the food for the offspring is quantified. For insectivorous birds, like great tits (Parus major), synchronisation of their offspring needs and abundance of caterpillars is the main selection pressure. We measured caterpillar biomass over a 20-year period and showed that the annual peak date is correlated with temperatures from 8 March to 17 May. Laying dates also correlate with temperatures, but over an earlier period (16 March – 20 April). However, as we would predict from a reliable cue used by birds to time their reproduction, also the food peak correlates with these temperatures. Moreover, the slopes of the phenology of the birds and caterpillar biomass, when regressed against the temperatures in this earlier period, do not differ. The major difference is that due to climate change, the relationship between the timing of the food peak and the temperatures over the 16 March – 20 April period is changing, while this is not so for great tit laying dates. As a consequence, the synchrony between offspring needs and the caterpillar biomass has been disrupted in the recent warm decades. This may have severe consequences as we show that both the number of fledglings as well as their fledging weight is affected by this synchrony. We use the descriptive models for both the caterpillar biomass peak as for the great tit laying dates to predict shifts in caterpillar and bird phenology 2005–2100, using an IPCC climate scenario. The birds will start breeding earlier and this advancement is predicted to be at the same rate as the advancement of the food peak, and hence they will not reduce the amount of the current mistiming of about 10 days. [KEYWORDS: Climate change ; Fitness ; Great tit ; Phenology ; Timing of reproduction]
Nesting habitat requirements and nestling diet in the Mediterranean populations of Crested Tits Lophophanes cristatus
Most bird species show specific habitat requirements for breeding and feeding. We studied the pattern of
habitat occupation, nestling diet and breeding performance of Crested Tits Lophophanes cristatus in a “typical” (coniferous)
and an “atypical” (Holm Oak Quercus ilex) forest in eastern Spain during 2005–2007. We aimed to determine which
microhabitat characteristics in the Holm Oak forest could account for the presence of Crested Tits, and checked whether
the nestling diet in the Holm Oak forest resembled that obtained in the pine forest. Vegetation maps were produced
using GIS from observations made in the field (tree species, tree and shrub cover). Nestling diet was recorded through
video surveillance. Crested Tits bred in mature, low-density areas in the pine forest. Those breeding in the Holm Oak
forest built their nests in areas including pine trees and avoided densely forested areas. Birds breeding in the pine forest
started laying by mid-April and the average clutch size was 5 eggs. In the Holm Oak forest, birds started laying by
the end of April and average clutch size was also 5 eggs. Fledglings weighed around 12 g in both forests. Nestling diet,
prey size and feeding frequency by the parents did not vary between the forests. The main prey types consumed were
Lepidoptera larvae and Diptera.
Predicting adaptation of phenology in response to climate change, an insect herbivore example
Climate change has led to an advance in phenology in many species. Synchrony in phenology between different species within a food chain may be disrupted if an increase in temperature affects the phenology of the different species differently, as is the case in the winter moth egg hatch–oak bud burst system. Operophtera brumata (winter moth) egg hatch date has advanced more than Quercus robur (pedunculate oak) bud burst date over the past two decades. Disrupted synchrony will lead to selection, and a response in phenology to this selection may lead to species genetically adapting to their changing environment. However, a prerequisite for such genetic change is that there is sufficient genetic variation and severe enough fitness consequences. So far, examples of observed genetic change have been few. Using a half-sib design, we demonstrate here that O. brumata egg-hatching reaction norm is heritable, and that genetic variation exists. Fitness consequences of even a few days difference between egg hatch and tree bud opening are severe, as we experimentally determined. Estimates of genetic variation and of fitness were then combined with a climate scenario to predict the rate and the amount of change in the eggs' response to temperature. We predict a rapid response to selection, leading to a restoration of synchrony of egg hatch with Q. robur bud opening. This study shows that in this case there is a clear potential to adapt – rapidly – to environmental change. The current observed asynchrony is therefore not due to a lack of genetic variation and at present it is unclear what is constraining O. brumata to adapt. This kind of model may be particularly useful in gaining insight in the predicted amount and rate of change due to environmental changes, given a certain genetic variation and selection pressure.
Across and within-forest effects on breeding success in Mediterranean Great Tits Parus major
Forest type and habitat structure can have profound effects on different aspects of avian life histories. These effects may, however, strongly differ across and within forests that vary in vegetation composition and structure, especially when an ancient forest has been replaced by a new forest. To test for these differences in effect, we studied Great Tit Parus major life-history traits (280 first clutches) in two Mediterranean evergreen forests during 2005–07: an ancient Holm Oak Quercus ilex and a reforested pine forest. A comparison between
forests revealed that females breeding in the Holm Oak forest started laying one week later, and produced larger clutches and broods both at hatching and at fledging. Chicks raised in the Holm Oak forest also fledged in better condition. Within forests, however, the reproductive success was not higher for pairs breeding in nestboxes surrounded by oaks within the pine forest, and also reproductive success was not lower in nestboxes surrounded by pines within oak forest. Instead, vegetation maturity around nestboxes, rather than tree species
composition, affected hatching success. Surprisingly, hatching success was higher in nestboxes surrounded by immature vegetation. We suggest that this may be due to a lower nest predation rate in nestboxes surrounded by immature vegetation, compared to nestboxes surrounded by mature vegetation. We suggest that different factors appear to affect variation in breeding success in Mediterranean Great Tits comparing across forests (e.g. food availability) vs. within a forest (e.g. nest predation).
Evolutionary response of the egg hatching date of a herbivorous insect under climate change
Under changing climatic conditions, species need to adapt to their new environment. Genetic adaptation is crucial to prevent population extinction1 but examples where climate change leads to genetic changes in wild populations have been few2, 3. The synchronization between the timing of egg hatching of a herbivorous insect, the winter moth (Operophtera brumata), and the seasonal bud burst of its food plant, oak (Quercus robur), has been disrupted by climate change4 and a quantitative genetic model predicts that selection will delay the egg hatching date5. Here we show, using both long-term observational data and experiments, that the egg hatching date has changed genetically, resulting in closer synchrony with oak bud burst. The observed rate of change matches the predicted rate of change of one day per year. Hence, altered selection pressures, caused by environmental change, result in a rapid adaptive response in insect phenology. These genetic changes in a key life-history trait in this herbivorous insect therefore seem to be fast enough to match the climate-change-induced advancement of their host phenology
Evolutionary response of the egg hatching date of a herbivorous insect under climate change
Under changing climatic conditions, species need to adapt to their new environment. Genetic adaptation is crucial to prevent population extinction1 but examples where climate change leads to genetic changes in wild populations have been few2, 3. The synchronization between the timing of egg hatching of a herbivorous insect, the winter moth (Operophtera brumata), and the seasonal bud burst of its food plant, oak (Quercus robur), has been disrupted by climate change4 and a quantitative genetic model predicts that selection will delay the egg hatching date5. Here we show, using both long-term observational data and experiments, that the egg hatching date has changed genetically, resulting in closer synchrony with oak bud burst. The observed rate of change matches the predicted rate of change of one day per year. Hence, altered selection pressures, caused by environmental change, result in a rapid adaptive response in insect phenology. These genetic changes in a key life-history trait in this herbivorous insect therefore seem to be fast enough to match the climate-change-induced advancement of their host phenology.
Genetic variation in cue sensitivity involved in avian timing of reproduction
1.Annual variation in the timing of avian reproduction is associated with predictive cues related to ambient temperature. Understanding how these cues affect timing, and estimating the genetic variation in sensitivity to these cues, is essential to predict the micro-evolutionary changes in timing which are needed to adapt to climate change. 2.We carried out a 2-year experiment with great tits Parus major of known genetic background, which were kept in pairs in climate-controlled aviaries with simulated natural photoperiod and exposed to a seasonal change in temperature, where the two treatments differed by 4 °C. We recorded the dates of laying the first and last eggs and timing of moult, as well as physiological proxies associated with reproduction: plasma luteinizing hormone (LH), prolactin, and gonadal size at four-weekly intervals. 3.The temperature treatments did not affect first-egg dates, nor gonadal growth or plasma LH and prolactin concentrations. However, birds terminated egg laying, regressed their testes and started their moult earlier at higher temperatures. 4.There were marked family differences in both the start of egg laying, with sisters from early laying maternal families laying early, and in the termination of laying, indicating that there is heritable variation in sensitivity to cues involved in timing. 5.Our experiment, the first to use genetically related individuals in an experimental design with a natural change in photoperiod and biologically realistic temperature differences, thus shows that genetic adaptation in cue sensitivity is possible, essential for species to be able to adapt to a warming world
Genetic variation in cue sensitivity involved in avian timing of reproduction
1.Annual variation in the timing of avian reproduction is associated with predictive cues related to ambient temperature. Understanding how these cues affect timing, and estimating the genetic variation in sensitivity to these cues, is essential to predict the micro-evolutionary changes in timing which are needed to adapt to climate change.
2.We carried out a 2-year experiment with great tits Parus major of known genetic background, which were kept in pairs in climate-controlled aviaries with simulated natural photoperiod and exposed to a seasonal change in temperature, where the two treatments differed by 4 °C. We recorded the dates of laying the first and last eggs and timing of moult, as well as physiological proxies associated with reproduction: plasma luteinizing hormone (LH), prolactin, and gonadal size at four-weekly intervals.
3.The temperature treatments did not affect first-egg dates, nor gonadal growth or plasma LH and prolactin concentrations. However, birds terminated egg laying, regressed their testes and started their moult earlier at higher temperatures.
4.There were marked family differences in both the start of egg laying, with sisters from early laying maternal families laying early, and in the termination of laying, indicating that there is heritable variation in sensitivity to cues involved in timing.
5.Our experiment, the first to use genetically related individuals in an experimental design with a natural change in photoperiod and biologically realistic temperature differences, thus shows that genetic adaptation in cue sensitivity is possible, essential for species to be able to adapt to a warming world.