The Skutch (1949) Hypothesis that nest predation risk constrains parental nest activity has important implications for the evolution of parental care strategies, but the required conditions for the hypothesis to operate have been questioned. We found the necessary conditions existed in a montane tropical bird community where 95.4% of predation events (n = 456) occurred during daylight hours and almost all predators (n = 224) were visually oriented. Moreover, incubation strategies for 21 passerine species were explained by nest predation rates as proposed by the Skutch Hypothesis. Hourly rates of visits to the nest were lower among species with higher nest predation rates, and achieved in part by longer on- and off-bouts. Incubation attentiveness (percent of time incubating) does not necessarily affect parental nest activity and was not related to nest predation rates. Nest predation rates were greater in enclosed- than open-nesting species, counter to long-standing views. Moreover, nest predation was usually higher in the nestling period when parents were more actively visiting nests than during incubation for enclosed- but not open-nesting species. This increase in nest predation in the nestling period for enclosed-nesting species might indicate proximate predation responses to parental nest activity that underlie the evolutionary patterns. Adult mortality also can exert selection on evolved strategies. Following life history theory, annual adult mortality probability explained residual variation in incubation behaviors, while accounting for nest predation, with longer-lived species exhibiting lower nest activity and attentiveness. Ultimately, the conditions for the Skutch Hypothesis were clear and evolved behaviors suggest an important influence of natural selection by nest predation in this montane tropical bird community. At the same time, different patterns of nest predation between open- and enclosed-nesting species emphasize a need for further research into how parental nest activity interacts with nest type to affect predator detection of nests.
Offspring mortality varies dramatically among species with critical demographic and evolutionary ramifications, yet the causes of this variation remain unclear. Nests are widely used for breeding across taxa and thought to influence offspring mortality risk. Traditionally, more complex, enclosed nest structures are thought to reduce offspring predation by reducing the visibility of nest contents and muffling offspring sounds compared to open nests. Direct tests of the functional bases for nest structure influence on predation risk are lacking. We used experiments and 10 years of observational data to examine how nest structure influences nest predation risk in a diverse community of tropical songbirds. First, we examined how nest size was related to nest structure and nest predation rates across species. Second, we assessed how nest structure influences the detectability of nestling begging calls both in field and in laboratory settings. Finally, we examined how the acoustic properties of different nest structures influence nest predation risk. Specifically, we experimentally broadcast begging calls from open and enclosed nests to determine how auditory cues and nest structure interact to affect predation on plasticine and quail eggs. We also tested whether nest structure was associated with differences in nest predation rates between the incubation (no begging cues) and nestling (begging cues) stages. We found that enclosed nests are larger than open nests after accounting for adult size, and larger nests had increased predation rates. Moreover, enclosed nests did not consistently alter nestling begging calls in ways that reduce the likelihood of predation compared to open nests. Indeed, begging cues increased predation rates for enclosed but not open‐cup nests in our playback experiment, and nest predation rates showed greater increases after hatching in enclosed than open‐cup nests. Ultimately, enclosed nests do not necessarily provide greater predation benefits than open nests in contrast to long‐standing theory.
A free
- Award ID(s):
- 1656120
- NSF-PAR ID:
- 10458369
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Functional Ecology
- Volume:
- 33
- Issue:
- 10
- ISSN:
- 0269-8463
- Page Range / eLocation ID:
- p. 1973-1981
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Abstract -
Abstract Developmental responses can help young animals reduce predation risk but can also yield costs to performance and survival in subsequent life stages with major implications for lifetime fitness. Compensatory mechanisms may evolve to offset such costs, but evidence from natural systems is largely lacking.
In songbirds, increased nest predation risk should favour reduced provisioning, but also young that fledge (leave their nest) at an earlier age. Both responses can result in fledglings with shorter wings, reduced mobility and decreased survival. Young may compensate for shorter wings developmentally by reallocating resources towards feather development or behaviourally by adjusting flight kinematics or habitat use. However, underfed young may lack the capacity to express these phenotypes due to insufficient resources or an inability to adjust allocation of resources.
Using predation risk experiments and 29 years of observational field data, we test whether increased nest predation risk reduces flight performance and survival during the fledgling stage and explore potential mechanisms that might underlie these effects. We show that young from high‐risk nests did not leave the nest earlier on average, but wing growth was slower likely due to observed reductions in parental feeding rates. Wings were shorter in high‐risk nests when fledglings left the nest early. Yet, fledglings from high‐risk nests showed improved flight performance for a given wing length such that flight performance at fledging did not differ between young from high‐risk and low‐risk nests. Young from high‐risk nests may have offset the costs of shorter wings on flight performance by accelerating the emergence of flight feathers from their sheaths to reduce wing porosity, though evidence for this mechanism was mixed. Fledglings from high‐risk nests also selected habitat with denser woody vegetation compared with young from low‐risk nests.
Together, these developmental and behavioural responses seem to mitigate the expected effects of increased nest predation risk on fledgling survival. Ultimately, our results show that offspring predation risk can affect parental provisioning and offspring morphology without major implications for performance and survival in subsequent life stages.
A free
Plain Language Summary can be found within the Supporting Information of this article. -
Abstract Co‐parasitism is ubiquitous and has important consequences for the ecology and evolution of wild host populations. Studies of parasite co‐infections remain limited in scope, with few experimental tests of the fitness consequences of multiple parasites, especially in natural populations.
We measured the separate and combined effects of
Philornis seguyi nest flies and shiny cowbirdsMolothrus bonariensis on the fitness of a shared host, the chalk‐browed mockingbird (Mimus saturninus ) in Argentina.Using a two‐factor experimental approach, we manipulated the presence of nest flies and cowbirds in mockingbird nests and assessed their effects on mockingbird haemoglobin levels, begging and provisioning rates, body size, and fledging success. We also monitored rates of nest predation in relation to parasitism by flies and cowbirds.
Nest flies reduced the haemoglobin concentration, body size, and fledging success of mockingbirds, likely because mockingbirds did not compensate for parasitism by begging more or feeding their nestlings more. Cowbirds also reduced the fledging success of mockingbirds, even though they had no detectable effect on haemoglobin or body size. Nests with cowbirds, which beg more than mockingbirds, attracted more nest predators. There was no significant interaction between the effects of flies and cowbirds on any component of mockingbird fitness. The combined effects of nest flies and cowbirds were strictly additive.
In summary, we show that nest flies and cowbirds both reduce host fitness, but do not have interactive effects in co‐parasitized nests. Our results further suggest that predators exacerbate the effects of nest flies and cowbirds on their hosts. Our study shows that the fitness consequences of co‐parasitism are complex, especially in the context of community‐level interactions.
-
Abstract Predator fear effects influence reproductive outcomes in many species. In non‐urban systems, passerines often respond to predator cues by reducing parental investment, resulting in smaller and lighter nestlings. Since trophic interactions in urban areas are highly altered, it is unclear how passerines respond to fear effects in human‐altered landscapes. Nestlings of passerines in urban areas also tend to be smaller and lighter than their rural counterparts and are often exposed to high densities of potential predators yet experience lower per capita predation—the predation paradox. We suggest fear effects in urban habitats could be a significant mechanism influencing nestling condition in birds, despite lowered predation rates. We manipulated exposure of nesting birds to adult‐consuming predator risk in residential yards across a gradient of urbanization to determine the relative influence of urbanization and fear on nestling condition. We found nestlings had reduced mass in nests exposed to predator playbacks as well as in more urban areas. Despite lower per capita predation rates in urban areas, fear effects from increased predator densities may influence passerine fitness through reduced nestling condition. As urban development expands, biodiversity conservation hinges on a deeper mechanistic understanding of how urbanization affects reproductive outcomes.
-
Abstract The strategies by which animals allocate reproductive effort across their lifetimes vary, and the causes of variation in those strategies are actively debated. In birds, most research has focused heavily on variation in clutch size and fecundity, but incubation behaviour and other functionally related traits have received less attention. Variation in incubation period duration is notable because time‐dependent sources of clutch mortality should impose strong directional selection to minimize the incubation period. However, life‐history theory predicts multiple mechanisms by which inter‐ and intraspecific variation in incubation behaviours may be adaptive.
We conducted one of the first studies of intraspecific latitudinal variation in avian incubation behaviours across a large portion of a single species’ range. We placed motion‐activated nest cameras inside burrowing owl nests at five study sites to quantify variation in daily nest attentiveness, cumulative nest attendance and incubation period duration. We tested predictions of two alterative hypotheses that have been proposed to explain variation in incubation periods: the
parental risk tolerance hypothesis and theneonate quality hypothesis .Daily nest attentiveness, cumulative nest attendance and incubation period duration in burrowing owls were all positively correlated with latitude. Burrowing owls reduced their daily nest attentiveness at low latitudes and on days when the average nest temperature was within the range that is optimal for embryo development. Further, longer incubation periods were most strongly associated with greater cumulative nest attendance instead of reduced daily nest attentiveness.
These results support predictions of the
neonate quality hypothesis: longer incubation periods result from stronger selection on neonate quality rather than selection to reduce reproductive effort in response to low extrinsic mortality risk. However, some owls facultatively reduced their daily nest attentiveness, and this result supports the general hypothesis that incubation decisions reflect a trade‐off between reproduction and self‐maintenance, and that the optimal solution to that trade‐off varies systematically in response to latitudinal gradients in adult mortality.A free
Plain Language Summary can be found within the Supporting Information of this article.