Male parental care and its adaptive significance in a neotropical frog

In the Puerto Rican frog Eleutherodactylus coqui, parental care is performed exclusively by males, and consists of attending the eggs and hatchlings at a terrestrial oviposition site. The two major behavioural components of parental care are egg brooding and nest defence against conspecific egg cannibals. Defence behaviour includes aggressive calling, biting, sustained biting, wrestling, and blocking directed against nest intruders. Parental care lasts from oviposition to hatching (17–26 days) and often for several days after hatching. During pre-hatching development, males are present in their nests 97.4% of the time during the day and 75.8% of the time at night. A large portion of this time is spent brooding eggs. In a field experiment, males were removed from their nests and the fate of clutches was monitored. Compared to control clutches (males not removed), experimental clutches had significantly lower hatching success and suffered significantly greater mortality from desiccation and cannibalism. Hence, parental care yields significant benefits to male fitness via increased offspring survival.     

Plant architecture affects periodical cicada oviposition behavior on native and non‐native hosts

Variation in plant quality provides a basis for oviposition site selection for a variety of insects. Of the plant traits that influence plant–insect interactions, plant architecture has received little attention despite its putative role in modulating oviposition behavior. In a common garden comprised of native and non‐native plant species, we assessed how host plant architecture and identity influenced the oviposition behavior of 17‐year periodical cicadas (Homoptera: Cicadidae: Magicicada). On each host, we quantified the availability of branches suitable for oviposition and compared those measures with the branches used by ovipositing cicadas. Using this approach, we determined how the structural attributes of plants (i.e. branch diameter, length and incline) affected oviposition site selection. We then related cicada oviposition preferences to offspring performance by quantifying egg hatching success. On each host species, cicadas selectively used broader and longer branches for oviposition, suggesting that branch architecture provides a basis for oviposition behavior irrespective of plant identity. Broader and longer branches were more abundant on native than on non‐native hosts in our study, contributing to greater oviposition loads among the native species. Egg hatching success was similar among native and non‐native hosts. However, it is possible that the use of native plants for oviposition could enhance offspring output because native hosts generally contained more viable eggs per egg nest and more egg nests per plant. While previous accounts of cicada oviposition preferences have focused on differences in oviposition loads among hosts, our evaluation of within‐host branch selection by ovipositing cicadas helps to clarify oviposition preferences at a higher resolution and demonstrates that plant architecture provides an important basis for oviposition behavior. Furthermore, because branch structure can differ substantially among host species, our results suggest that periodical cicadas may be sensitive to the changes in plant composition that often result from non‐native plant invasions.     

Factors affecting piping plover hatching success on Long Island,New York

Low hatching success may limit progress towards reaching productivity goals for Atlantic Coast piping plover (Charadrius melodus) recovery, despite management strategies to protect eggs from predators and decrease human disturbance of birds on nests. We measured piping plover hatching success on Eastern Long Island beaches and identified the major causes of egg failure to better understand why eggs that were otherwise intact (not depredated or destroyed by tidal flooding) failed to hatch. We documented egg and nest fates, dissected contents of unhatched eggs to determine viability, and recorded human and predator activity near a subset of plover nests on Suffolk County Parks properties. The low hatching success we recorded (0.60) in 2006 and 2007 would require higher chick survival rates than are typically observed for piping plovers to meet recovery targets for productivity. Few eggs showed signs of poor viability and overall egg hatchability was comparable to other ground nesting birds. Most egg failure was due to either depredation at unexclosed nests or nest abandonment by adults. The best predictor of nest abandonment was the maximum number of red fox tracks (Vulpes vulpes) counted on nearby transects (β = −1.16, 95% CI: −2.0 to −0.3) and we found evidence that plovers abandoned eggs in response to predation risk (e.g., a fox circling a nest exclosure). Adults from abandoned nests may have deserted eggs or been depredated. In either case, intact and viable eggs were abandoned. Nest abandonment was not related to human activity near nests, which were buffered from human disturbance by symbolic string fencing. Our results suggest that depredation and nest abandonment (e.g., desertion or death of adults) due to predator disturbance, not human disturbance or poor egg viability, contributed to the low hatching success we recorded. Active predator removal in addition to modification of predator exclosure use and design may be necessary to prevent direct (egg depredation) and indirect (nest abandonment) negative effects of predators on hatching success. © 2010 The Wildlife Society.     

Effects of Shiny Cowbird Molothrus bonariensis parasitism on different components of House Wren Troglodytes aedon reproductive success

Avian brood parasites, including cuckoos and cowbirds, have multiple negative effects on their hosts. We analysed the effects of Shiny Cowbird Molothrus bonariensis parasitism on different components (e.g. egg losses, hatching success, chick survival and nest abandonment) of House Wren Troglodytes aedon reproductive success. We also conducted an experiment to discriminate between two mechanisms that may reduce hatching success in parasitized clutches: lower efficiency of incubation due to the increase in clutch volume and disruption of host incubation by the early hatching of Cowbirds. Egg puncturing by Shiny Cowbirds reduced host clutch size at hatching by 10–20%, and parasitized nests had a decrease in hatching success of 40–80%. Egg losses and hatching failures were positively associated with the intensity of parasitism. Brood reduction was greater in parasitized nests, but the growth rate of the chicks that fledged was similar to that in unparasitized nests. The combined effects of egg losses, hatching failures and brood reduction decreased the number of fledged chicks by 80%. In addition, egg puncturing increased the likelihood of nest abandonment by Wrens. Experimental data showed that hatching failures occurred when there was a combination of: (1) an increase in the volume of the clutch by the addition of the Cowbird egg without removal of host eggs, and (2) the addition of the Cowbird egg before the onset of incubation. This was relatively common in House Wren nests, as Cowbirds generally parasitize before the onset of incubation. Our results indicate that Shiny Cowbird parasitism imposes a major impact on House Wrens, as it affects all components of the Wren's reproductive success.     

Extreme host specificity by Microdon mutabilis (Diptera: Syrphiae), a social parasite of ants

Larvae of the syrphid fly Microdon mutabilis are social parasites which live up to two years, feeding on ant brood in nests of Formica lemani ants. We questioned why M. mutabilis is extremely localized when its host is widespread and abundant. Like endoparasitic diseases, social parasites must penetrate formidable defences before ''infecting'' their hosts. This occurs during the egg stage of M. mutabilis: females are sedentary and oviposit at F. lemani nest entrances, which workers treat as part of their nest, leaving the thin-shelled eggs vulnerable to attack for 10 to 14 days before hatching. We describe experiments which show a strong maternal effect in M. mutabilis. New-laid eggs had > 95% survival when introduced to the individual ant colony that reared each mother fly or to its close neighbours, but survival declined as a sigmoidal logistic function of distance from the mother nest, with F. lemani colonies from 2 and 30 km away killing 80 and > 99% of eggs, respectively, within 24 h. Attacks on eggs also increased in proportion to the delay before introduction to laboratory nests. We suggest that they may be coated with a mimetic chemical disguise that lasts for three to four days after oviposition. The results indicate extreme local adaptation by an M. mutabilis population not simply to one species of host, but to an individual host population and possibly to local strains or family groups within an F. lemani population. This conclusion is discussed in terms of virulence, transmission and coevolution in parasitic diseases.     

The effect of short-term weather fluctuations on temperatures inside lizard nests, and on the phenotypic traits of hatchling lizards

Can short‐term stochastic variation in local weather conditions modify the thermal conditions inside lizard nests, and thus (potentially) the developmental rates, hatching success, and phenotypic traits of hatchlings from these nests? This hypothesis requires that (i) natural nests are poorly buffered thermally, such that ambient regimes affect temperatures inside the nest, and (ii) short‐term thermal variations modify attributes of the offspring. Field data on natural nests of the sub‐alpine skink Bassiana duperreyi confirm the existence of this first effect, and laboratory experiments substantiate the latter. Exposure to warmer‐than‐usual temperatures for 2 wéeks during the 9‐ to 16‐wéek incubation period doubled hatching success, and significantly modified hatchling phenotypes (hatching dates, offspring size and locomotor performance). The proportion of development completed prior to this exposure influenced the degrée of response. Exposure to a brief ‘window’ of higher‐than‐usual temperatures soon after oviposition had more effect on hatching time, egg survival and hatchling phenotypes than if the exposure occurred later in development. Thus, minor variations in weather conditions during incubation may have substantial effects on reptile populations.     

Function of egg punctures by Shiny Cowbirds in parasitized and nonparasitized Creamy‐bellied Thrush nests

ABSTRACT Avian brood parasites usually remove or puncture host eggs. Several hypotheses have been proposed to explain the function of these behaviors. Removing or puncturing host eggs may enhance the efficiency of incubation of cowbird eggs (incubation‐efficiency hypothesis) or reduce competition for food between cowbird and host chicks in parasitized nests (competition‐reduction hypothesis) and, in nonparasitized nests, may force hosts to renest and provide cowbirds with new opportunities for parasitism when nests are too advanced to be parasitized (nest‐predation hypothesis). Puncturing eggs may also allow cowbirds to assess the development of host eggs and use this information to decide whether to parasitize a nest (test‐incubation hypothesis). From 1999 to 2002, we tested these hypotheses using a population of Creamy‐bellied Thrushes (Turdus amaurochalinus) in Argentina that was heavily parasitized by Shiny Cowbirds (Molothrus bonariensis). We found that 56 of 94 Creamy‐bellied Thrush nests (60%) found during nest building or egg laying were parasitized by Shiny Cowbirds, and the mean number of cowbird eggs per parasitized nest was 1.6 ± 0.1 (N= 54 nests). At least one thrush egg was punctured in 71% (40/56) of parasitized nests, and 42% (16/38) of nonparasitized nests. We found that cowbird hatching success did not differ among nests where zero, one, or two thrush eggs were punctured and that the proportion of egg punctures associated with parasitism decreased as incubation progressed. Thus, our results do not support the incubation‐efficiency, nest‐predation, or test‐incubation hypotheses. However, the survival of cowbird chicks in our study was negatively associated with the number of thrush chicks. Thus, our results support the competition‐reduction hypothesis, with Shiny Cowbirds reducing competition between their young and host chicks by puncturing host eggs in parasitized nests.     

Breeding pattern and nest guarding in Sicyopterus lagocephalus, a widespread amphidromous Gobiidae

Amphidromous gobies are usually nest spawners. Females lay a large number of small eggs under stones or onto plant stems, leaves or roots while males take care of the clutch until hatching. This study investigates the breeding pattern and paternal investment of Sicyopterus lagocephalus in a stream on Reunion Island. In February 2007 and January 2010, a total of 170 nests were found and the presence of a goby was recorded at 61 of them. The number of eggs in the nests ranged from 5,424 to 112,000 with an average number of 28,629. We showed that males accepted a single female spawning in the nest and cared for the eggs until hatching. The probability for a nest to be guarded increased with the number of eggs within it, suggesting that paternal investment depends on a trade-off between the reproductive value of the current reproduction and future nesting events. We showed that large nest stones were occupied by large males (TL >80 mm), whereas smaller males (TL <50 mm) were found under smaller cobbles, probably because of male–male competition for available nests. Our results suggest that the male’s choice relies upon a similarity to the female size, while the female’s choice was based on both body and nest stone sizes.     

Maternal and environmental effects on offspring phenotypes in an oviparous lizard: do field data corroborate laboratory data?

A vast literature suggests that maternal factors and egg incubation conditions have substantial effects on offspring phenotypes in oviparous species. However, many studies that evaluate these effects have relied on experimental conditions that are rarely, if ever, encountered under natural conditions. To address this issue, we evaluated relationships among maternal factors, natural nest conditions, egg development in the field, and the resultant offspring phenotypes in a lizard with temperature-dependent sex determination, the jacky dragon (Amphibolurus muricatus, Agamidae). Many, but not all, of the relationships shown in our field-based study corroborate results from laboratory-based experiments. Offspring body size was affected primarily by egg size at oviposition, as well as by water uptake by eggs, rather than by environmental variables measured within the nest. Date of oviposition was related to offspring growth rate and body size prior to the onset of winter; this relationship is likely mediated through an influence on the timing of hatching. Nest temperature generated substantial variation in egg survival; nests that experienced higher temperatures and higher thermal fluctuations suffered relatively high egg mortality. Contrary to results from laboratory incubation, however, nest temperature did not predict offspring sex ratios. Hence, although many results from this field study corroborate those from the laboratory, caution is needed when extrapolating laboratory-incubation results to field conditions. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Male body size and brooding success under natural conditions in the freshwater Japanese goby, Rhinogobius sp. OR (orange type)

Males of the Japanese goby Rhinogobius sp. OR (orange type) establish nests under stones in streams. They provide care to egg masses until hatching. We carried out field observations and a field experiment in a natural stream to examine the effect of male body size on brooding success. An experiment excluding guarding males indicated that their presence has a positive effect on nest defense. Field data showed that male body size was positively correlated with the size of the egg mass that was initially found at the nest. Furthermore, a sequential increase in egg mass size seen in the nests of larger males indicated that multiple females spawned during a single breeding cycle of larger males. To examine male brooding success, two dependent variables, egg mass persistence (days from initial egg mass to disappearance or hatching) and hatching success were analyzed. The results indicated that the variation found in both dependent variables was significantly explained by two independent variables, namely, initial egg-mass size and the number of matings. It is also suggested that male body size indirectly influenced brooding success through positive correlations with these independent variables.     

Effect of Temperature on Pratylenchus penetrans Development

Reproduction and development of Pratylenchus penetrans were studied on genetically transformed ladino clover roots. Solitary females developing on transformed roots in nutrient gellan gum medium (pH 5.5) deposited 1.2, 1.5, 1.6, 1.8, and 2.0 eggs per day at the respective temperatures of 17, 20, 25, 27, and 30 °C. The number of eggs deposited was highly correlated with temperature. A reduction in egg-laying rates at the start of hatching was observed at all temperatures. Juvenile mortality was higher at 17 °C (50.4%), 20 °C (50.3%), and 30 °C (58.4%) than at 25 °C (34.6%) and 27 °C (37.6%). Life-cycle (egg deposition to egg deposition) duration was 46, 38, 28, 26, and 22 days at the respective temperatures. The developmental zero degrees (°C) and the effective accumulative temperatures (degree-days) required for hatching, female emergence, and onset of oviposition (completion of one generation) of P. penetrans were estimated to be 2.7 and 200, 4.2 and 548, and 5.1 and 564, respectively. Pratylenchus penetrans reproduces over a wide range of temperatures.     

Artificial incubation of eggs of the green iguana (Iguana iguana)

Successful hatching of large numbers of artificially incubated eggs from the green iguana, Iguana iguana, are reported. Gravid females were captured at a nesting site in Summit Gardens, Soberania, Parque Nacional, Panama, and released into an enclosure with an artificial nesting area. Females dug their own tunnels and nest chambers or used artificial nest chambers for egg deposition. Eggs (n = 829) from 21 clutches were removed from the nests and artificially incubated. Average hatching success per clutch was 94.6% and the mean clutch incubation time was 92.1 days. A distinct odor was noticed in the incubation containers several days before the eggs began to hatch. At this time, the substrate layer was removed exposing the top surface of all eggs, and the eggs desiccated to some degree prior to hatching. High incubation temperature, hydric conditions, and egg arrangement are all implicated as contributing factors in low hatching success in previous studies using artificial incubation techniques.     

Age-specific nest-site preference and success in eiders

Variation in nest concealment is puzzling given the expected strong selection for safe nest sites. Selecting a concealed nest may decrease the risk of clutch predation but hinder parents from escaping predators, providing a possible solution to this paradox. Because the relative value of current versus future reproduction may vary with breeder age or state, nest concealment may also vary as a function of these attributes. We tested four predictions of the female and clutch safety trade-off hypothesis in eiders (Somateria mollissima): (1) nest concealment is negatively related to escape possibilities, (2) our capture rate of females is higher in covered nests, (3) egg predation is higher in open nests, and (4) overall nest success is unrelated to nest habitat. We also analysed nest microhabitat preferences and nest success relative to breeder age and body condition, controlling for nest spatial centrality. As expected, nest concealment and potential escape angle were negatively related, and capture by us, indicating female predation vulnerability, increased with nest cover. Clutch size was smaller in open nests, suggesting higher partial clutch predation, while it was larger among experienced and good-condition breeders. The probability of successful hatching was unrelated to nest habitat, positively associated with breeder experience, and negatively associated with hatching date. Experienced females selected more concealed and centrally located nests without sacrificing potential escape angles. The age-specific spatial distribution of nests on islands was unrelated to nest initiation dates, indicating no apparent competition. The age-specific preference of eiders for concealed nests may reflect declining reproductive value with age or confidence in surviving despite selecting a concealed nest. The apparently positive relationship between female age and survival and fecundity in eiders refutes the former alternative. Individual improvement in choosing safe nest sites, coupled with differential survival of individuals performing well, most likely explains age-specific nest-site preference and success.     

5. FIELD OBSERVATIONS,NORTHERN PROVINCE,NORTHERN RHODESIA

Cooper, J. 1986. Biology of the Bank Cormorant, Part 4: Nest construction and characteristics. Ostrich 57: 170–179.

Bank Cormorants Phalacrocorax neglectus construct their nests of material gathered by diving. Males undertake diving bouts of approximately 3–5 min, made up of several dives lasting on average 28 s. Nest material is gathered throughout the breeding cycle: number of diving bouts per day varies from a mean of 7,6 during pre-egg laying to 1,5 bouts per day when rearing young in the nest. Nest building recommences within 24 h of loss of nest due to storms. Both sexes occasionally steal nest material from the nests of neighbours. Bank Cormorants sometimes defecate onto their nests. This is assumed to make the nests better able to withstand rough seas. Nest construction takes approximately 34 d, a period similar to that of other ground-nesting species of cormorants. Construction of a nest in 34 d represents 238 diving bouts of a total duration of 18 h. Nests are heavy (up to 6 kg) and are made up primarily of seaweed. Feathers, sticks and artificial material are also incorporated into the nest. Bank Cormorant nests are large (up to 54 litres in total volume). Nests do not change significantly in size between egg laying and hatching. Nests in which at least one egg hatches are larger in all dimensions measured than those in which no eggs hatch. Nests are larger at the time of laying of repeat clutches than at the time of laying the first clutch. The Bank Cormorant's seaweed nest has enabled it to breed on bare offshore rocks where no nest material exists. The species' large nest is a necessary prerequisite for successful breeding close to the sea.     

THE BIRDS OF LANGEBAAN LAGOON

Data are presented on breeding success of Red Bishops (Euplectes orix) collected over four breeding seasons at a colony in the Addo Elephant National Park, Eastern Cape, South Africa. Overall hatching and fledging success were 53.8% and 26.0% of all eggs laid, respectively, and the overall mean number of fledglings per breeding attempt was 0.77. Hatching and fledging success varied significantly among seasons, with both clutch and brood losses due to predation being the main reason for the observed differences. Hatching success also differed significantly among clutch sizes, being highest for four-egg clutches (63.2%), intermediate for three-egg clutches (55.5%) and lowest for two-egg clutches and five-egg clutches (33.2% and 34.3%, respectively). However, fledging success was not significantly different among clutch sizes. The mean number of fledglings per breeding attempt was 0.44 for two-egg clutches, 0.80 for three-egg clutches, 1.10 for four-egg clutches, and 0.57 for five-egg clutches. The height of accepted nests (i.e.nests in which at least one egg was laid) was significantly lower than the height of nests not accepted. In addition, accepted nests in which eggs hatched and young fledged were significantly lower than accepted nests in which no eggs hatched and no young fledged. These overall effects of nest height on nest acceptance and hatching and fledging success were, however, due only to nests built above water, since no such effects were found when nests built above ground (i.e.on dry land) were analysed separately. I detected no effect of nest coverage on the probability of a nest being accepted, nor was there any effect of nest coverage on hatching or fledging success. Nests above water were significantly more likely to be accepted than nests above ground; however, hatching and fledging success of nests that were accepted did not differ significantly between nests built above water and those built above ground.     

Nest Sanitation as the Evolutionary Background for Egg Ejection Behaviour and the Role of Motivation for Object Removal

Higher interclutch colour variation can evolve under the pressure of brood parasitism to increase the detection of parasitic eggs. Nest sanitation could be a prerequisite for the evolution of anti-parasite defence in terms of egg ejection. In this respect, we used nest sanitation behaviour as a tool to identify: i) motivation and its underlying function and, ii) which features provoke ejection behaviour. Therefore, we experimentally tested whether size, colour or shape may influence ejection behaviour using artificial flat objects. We found a high interclutch variation in egg colouration and egg size in our tree sparrow (Passer montanus) population. Using colour and size we were in fact able to predict clutch affiliation for each egg. Our experiments further revealed the existence of direct anti-parasite behaviours and birds are able to recognise conspecific eggs, since only experimentally-deposited eggs have been removed. Moreover, experiments with different objects revealed that the motivation of tree sparrows to remove experimental objects from their nests was highest during egg laying for objects of varying size, most likely because of parasitism risk at this breeding stage. In contrary, motivation to remove white objects and objects with edges was higher during incubation stage as behavioural patterns connected to hatching started to emerge. The fact that rejection rate of our flat objects was higher than real egg ejection, suggests that egg ejection in tree sparrows and probably more general in small passerines, to be limited by elevated costs to eject eggs with their beaks. The presence of anti-parasite behaviour supports our suggestion that brood parasitism causes variation in egg features, as we have found that tree sparrows can recognise and reject conspecific eggs in their clutch. In conclusion, in tree sparrows it seems that nest sanitation plays a key role in the evolution of the removal of parasitic eggs.     

Influence of nest-floor slope on the nest choice of laying hens

Group nests in alternative housing systems for laying hens primarily fulfil the hen's needs for seclusion and protection. Commercial nests used in Switzerland are built according to the provisions of the Swiss Animal Welfare Legislation. However, nest types can differ in aspects, such as floor slope, that could have an impact on egg-laying behaviour. Floor slope has to be designed so that eggs roll away without breaking and so that hens feel comfortable laying their eggs. In commercial nests, the slope is usually between 12% and 18%. The aim of this study was to investigate the effect of floor slope on the hen's nest preference and laying behaviour. We predicted that hens would prefer nests with a lower sloped floor for evolutionary reasons and for reasons related to comfort.Eight pens, each with 17-18 white laying hens (LSL), were equipped with two roll-away nests (0.54 m²) having different floor slopes (12% and 18%). Eggs were collected each day (from approximately 20 weeks of age until 28 weeks of age); the number of eggs in each nest and on the floor of the pens was recorded. Behaviour inside the nest was filmed for two consecutive days during the main egg-laying time from the second hour to the fifth hour (4 h) after lights came on in week 27/28. The following data were recorded: number of hens in each nest, the nest visits/egg number ratio, the number of sitting events, the body alignment of hens sitting in the nest and the number and duration of nest visits. Data were analysed with a repeated-measures ANOVA. There was no difference between the numbers of eggs in the two nests, but more hens were counted in nests with a 12% slope (p = 0.027). The ratio between the number of nest visits and number of eggs did not differ significantly between the nests. However, we counted more sitting events in the nest with 12% slope (p = 0.007). The percentage of body alignment towards the back (p = 0.044) and towards the front (p = 0.028) of the nest differed between the nests. Furthermore, for nest visits lasting between 10 and 90 min, we found significant differences in the total number of nest visits (p = 0.039). For visits in this range of duration, we also found significant differences for nest visits with sitting (p = 0.025) and for the number of nest visits with egg laying (p = 0.049). All of these differences favoured the 12% nest.Both nests were generally accepted by the hens. However, because of the higher number of hens counted in the 12% nest and the higher amounts of nest visits and sitting events found in these nests, we recommend to use nests with a floor slope of 12% rather than 18%.     

Nest sanitation behavior does not increase the likelihood of parasitic egg rejection in herring gulls

Birds’ behavioral response to brood parasitism can be influenced not only by evolution but also by context and individual experience. This could include nest sanitation, in which birds remove debris from their nests. Ultimately, nest sanitation behavior might be an evolutionary precursor to the rejection of parasitic eggs. Proximately, the context or experience of performing nest sanitation behavior might increase the detection or prime the removal of parasitic eggs, but evidence to date is limited. We tested incubation-stage nests of herring gulls Larus argentatus to ask whether nest sanitation increased parasitic egg rejection. In an initial set of 160 single-object experiments, small, red, blocky objects were usually rejected (18 of 20 nests), whereas life-sized, 3D-printed herring gull eggs were not rejected whether red (0 of 20) or the olive-tan base color of herring gull eggs (0 of 20). Next, we simultaneously presented a red, 3D-printed gull egg and a small, red block. These nests exhibited frequent nest sanitation (small, red block removed at 40 of 48 nests), but egg rejection remained uncommon (5 of those 40) and not significantly different from control nests (5 of 49) which received the parasitic egg but not the priming object. Thus, performance of nest sanitation did not shape individuals’ responses to parasitism. Interestingly, parents were more likely to reject the parasitic egg when they were present as we approached the nest to add the experimental objects. Depending on the underlying mechanism, this could also be a case of experience creating variation in responses to parasitism.     

Variation in incubation effort during egg laying in the Mountain Bluebird and its association with hatching asynchrony

Females in many bird species reportedly begin incubation prior to clutch completion, but the nature of such incubation and the degree to which it varies among females remains undescribed for almost all species. We used continuous recording of nest‐cup temperatures to document incubation effort during egg laying at 57 Mountain Bluebird (Sialia currucoides) nests in a high‐elevation Wyoming population. We then asked whether such effort predicted the degree to which eggs hatch asynchronously. Although substantial egg heating could begin abruptly late in laying (previously reported as the norm for this species) or even after clutch completion, we found that most (>90%) females began incubation gradually, engaging in a few (usually 1–8), brief (<10 min) bouts of heating on the day they laid their first or second egg. Thereafter, females varied markedly in when they increased incubation effort and by how much. The onset of nocturnal incubation also varied, with females beginning to incubate at night after laying their prepenultimate, penultimate, or last egg and not always initially incubating through the night. As an index of the total amount of heat applied to eggs during laying, we calculated the cumulative number of degrees by which nest‐cup temperatures exceeded the threshold temperature required for embryonic development. This value varied by more than 150‐fold between nests and explained >50% of the variation in hatching asynchrony. Our results thus provide strong support for the widely held, but rarely tested, assumption that parent birds can have substantial control over the degree of hatching asynchrony by varying the amount of incubation done prior to clutch completion.     

Impact of nest relocation on the reproductive success of Loggerhead Turtles,Caretta caretta,in the Göksu Delta,Turkey (Reptilia: Cheloniidae)

When the nests of marine turtles are at a risk of inundation, relocation of the nests are often used in the conservation measures. Here, I determined the effect of nest relocation on Loggerhead Turtle (Caretta caretta) egg hatching success during the 2013 and 2014 nesting seasons in the Göksu Delta, Mersin, Turkey. I compared natural and relocated clutches, including those relocated before and after inundation, and evaluated 102 (94.6%) and 63 (81.1%) of survived nests in 2013 and 2014 respectively. Relocated nests experienced a 30% decrease in hatching success and a more prolonged incubation period compared to nests left in situ. Egg failure in nests relocated before and after inundation was similar in early-stage embryos, whereas it was three-fold higher in mid-stage embryos and two-fold lower in late-stage embryos. Thus, there was no significant difference in overall hatching success between the two relocation types. Moreover, there was no effect of delayed relocation of nests after inundation on hatching success. Possible impacts specific to the nesting site should be considered and explored before using nest relocation as a conservation tool. The relocation approach is recommended for nests at a high risk of inundation when the loss of nests is inevitable.