Do changing moisture levels during incubation influence phenotypic traits of hatchling snakes (Tropidonophis mairii, Colubridae)?

Phenotypic traits (e.g., size, strength, speed) of hatchlings in many reptile species are influenced by hydric conditions in the nest. Previous experiments have focused on comparisons between eggs maintained under constant (but different) conditions, but eggs in natural nests frequently experience strong temporal shifts in soil water content during incubation. Keelback snakes (Tropidonophis mairii) in the Australian wet-dry tropics nest over most of the year, so early nests experience decreasing water availability during development, late nests experience increases, and others (midyear) remain stable in this respect. We mimicked these three conditions and incubated 54 eggs (nine from each of six clutches) in a split-clutch design to maintain the same average water content but with differing trajectories through incubation. The experimental treatments significantly affected the total amount of water taken up by the eggs (and thus final egg mass), but incubation periods were unaffected. Hatchling size but not strength showed minor but statistically significant effects of incubation regimes. The ability of keelback eggs to take up excess water whenever it becomes available (either early or late in development) and to retain it even when conditions change buffers embryogenesis effectively (but not completely) against fluctuations in soil water conditions.     

The effect of canopy closure on chimpanzee nest abundance in Lagoas de Cufada National Park,Guinea-Bissau

The present study aimed to gather baseline information about chimpanzee nesting and density in Lagoas de Cufada Natural Park (LCNP), in Guinea-Bissau. Old and narrow trails were followed to estimate chimpanzee density through marked-nest counts and to test the effect of canopy closure (woodland savannah, forest with a sparse canopy, and forest with a dense canopy) on nest distribution. Chimpanzee abundance was estimated at 0.79 nest builders/km², the lowest among the areas of Guinea-Bissau with currently studied chimpanzee populations. Our data suggest that sub-humid forest with a dense canopy accounts for significantly higher chimpanzee nest abundance (1.50 nests/km of trail) than sub-humid forest with a sparse canopy (0.49 nests/km of trail) or woodland savannah (0.30 nests/km of trail). Dense-canopy forests play an important role in chimpanzee nesting in the patchy and highly humanized landscape of LCNP. The tree species most frequently used for nesting are Dialium guineense (46 %) and Elaeis guineensis (28 %). E. guineensis contain nests built higher in the canopy, while D. guineense contain nests built at lower heights. Nests observed during baseline sampling and replications suggest seasonal variations in the tree species used for nest building.     

Potential influences of climate and nest structure on spotted owl reproductive success: a biophysical approach

Many bird species do not make their own nests; therefore, selection of existing sites that provide adequate microclimates is critical. This is particularly true for owls in north temperate climates that often nest early in the year when inclement weather is common. Spotted owls use three main types of nest structures, each of which are structurally distinct and may provide varying levels of protection to the eggs or young. We tested the hypothesis that spotted owl nest configuration influences nest microclimate using both experimental and observational data. We used a wind tunnel to estimate the convective heat transfer coefficient (h(c)) of eggs in 25 potential nest configurations that mimicked 2 nest types (top-cavity and platform nests), at 3 different wind speeds. We then used the estimates of h(c) in a biophysical heat transfer model to estimate how long it would take unattended eggs to cool from incubation temperature (～36°C) to physiological zero temperature (PZT; ～26°C) under natural environmental conditions. Our results indicated that the structural configuration of nests influences the cooling time of the eggs inside those nests, and hence, influences the nest microclimate. Estimates of time to PZT ranged from 10.6 minutes to 33.3 minutes. Nest configurations that were most similar to platform nests always had the fastest egg cooling times, suggesting that platform nests were the least protective of those nests we tested. Our field data coupled with our experimental results suggested that nest choice is important for the reproductive success of owls during years of inclement weather or in regions characterized by inclement weather during the nesting season.     

Using artificial nests to explore predation by introduced predators inhabiting alpine areas in New Zealand

Abstract

Many bird species endemic to alpine New Zealand are now at critically low densities and restricted in range, making predator‐prey research difficult. We used artificial nests in the Borland Valley, Fiordland National Park, to investigate (1) which introduced species is the most frequent nest predator in the two habitats, (2) whether nest survival differs between habitats, and (3) the utility of artificial nests for guiding conservation management. We used different types of artificial nest in 2 different years and undertook a calibration study of the two types. In 2003, survival of artificial nests containing wax eggs and chicken eggs was high in both habitats. In 2004, survival of artificial nests containing plastilina eggs and chicken eggs was low in both habitats, but was higher in alpine grassland compared with beech forest. Stoats and possums were the most frequent predators (36 and 22% respectively of artificial plastilina nests in alpine grassland and high‐altitude beech forest combined); these percentages did not vary significantly between habitats. Given the low density and sparse distribution of vulnerable species in much of New Zealand, data from artificial nests can be a useful tool for studying predation in these remote and difficult habitats, or at least, preferable to ignorance. However, the type of artificial nest used can strongly affect the rate at which they are destroyed.     

Different nest predator guild associated with egg size in the Patagonian temperate forest

Capsule: Studies of nest predation using artificial nests need to consider the effect of egg size on the types of predator that are detected.

Aims: To estimate the nest predation rate in the Patagonian temperate forest and evaluate the influence of egg size on predator guild.

Methods: On different plant species, we placed 108 nests each containing eggs of either Atlantic Canary Serinus canaria or Common Quail Coturnix coturnix, and a model clay egg of equal size to the real egg. Nest predators were identified from the marks left on the clay eggs or by videos recorded using camera traps.

Results: 86% of the nests were predated. Birds, mainly Chimango Caracara Milvago chimango, were the main nest predators. A marsupial, the Monito del Monte Dromiciops gliroides, and rodents also contributed to nest predation. Nest predation rates were similar for both egg sizes but the nest predator guild was different. Birds and rodents preyed on both eggs but the Monito del Monte consumed mainly small eggs.

Conclusion: Egg size did not influence the rate of nest predation but, instead, affected the nest predator guild. Consequently, in order to avoid underestimating the impacts of small predators, egg size should be considered in studies of nest predation.     

Predation on artificial nests in relation to forest type: contrasting the use of quail and plasticine eggs

Previous studies of avian nest predation have focused on how human-induced changes in the landscape influence the frequency of predation However, natural variation in the abundance of predators due to their choice of habitat can also influence predation rate To determine if predation on artificial nests was influenced by forest stand type, we placed ground and shrub nests containing quail and plasticine eggs in contiguous coniferous, mixedwood and deciduous stands in the southern boreal mixedwood forest of central Canada Nest predators were identified using remotely triggered cameras and marks left in plasticine eggs, while the relative abundance of nest predators such as squirrels and corvids were estimated using acoustic-visual surveys Using the fate of quail eggs to calculate predation rate, we found that predation was significantly higher in coniferous (67%) than in deciduous (17%) or mixedwood (25%) forest, with similar predation on ground (37%) and shrub (29%) nests Using plasticine eggs to calculate predation rate, nests in coniferous forest still suffered higher rates of predation, although predation rates were 15–20% higher, and ground nests suffered significantly higher rates of predation than shrub nests Quail eggs seemed to suffer lower rates of predation because small mammals were unable to penetrate the shell, but could leave marks on plasticine eggs The higher predation rate in coniferous forest was likely caused by higher abundance of red squirrels Tamiasciurus hudsonicus , the presence of fishers Martes pennanti and a simplified understory which may have made it easier for predators to find nests relative to the deciduous and mixedwood forest Plasucine eggs provide new insights into nest predation by identifying predation events by smaller predators such as mice that are missed when using quail eggs     

Nest orientation of the Spotted Barbtail, <Emphasis Type="Italic">Premnoplex brunnescens</Emphasis>, is strongly correlated with stream flow

The placement and orientation of bird nests may strongly influence reproductive success. For many species, nest orientation is related to the cardinal directions and has to do with prevailing winds or solar exposure. Nest orientation differs among species in different environments, variously cooling or warming nests to maintain a nest microclimate optimal for successful development of eggs and young. The Spotted Barbtail (Premnoplex brunnescens) builds mossy, enclosed nests along shaded streams in Neotropical cloud forests. It shows a unique pattern of nest orientation, whereby nests are oriented in relation to the direction of water flowing below the nest entrance, rather than compass bearing. Nests face in one of three directions in relation to the stream: downstream, upstream, or perpendicular to the flow of the water. I discuss the ability of various hypotheses to explain this pattern in the context of factors affecting nest orientation in other species. While the reasons for this pattern of orientation remain unclear, orientation is likely driven by the need to create and maintain an optimal internal nest microclimate.     

Removal of seeds from Neotropical frugivore droppings

In a Costa Rican rain forest, the majority of tree and shrub species have their seeds dispersed by vertebrates. Over a third of the species' seeds are of a size accessible to, and primarily carried away by, ants. Frugivorous bird droppings come in sizes from a few seeds to over a thousand, with number of seeds isometric with bird body mass. Dropping size decreases as seeds are scattered by rain. Larger droppings produced from fruits ofMiconia affinis (Melastomataceae) are discovered and recruited to more by ants, with a diverse guild of 22 ant species carrying away the seeds. Droppings with 64 and 16 seeds were used by a subset of the ant community exploiting 4-seed droppings, likely due to resource defense by aggressive species. Seeds in the smallest droppings stood the smallest chance of being removed. Although soil-nesting ants of the tribe Attini were the primary removers of seeds in this forest, a third of removal was by ants living in ephemeral litter nests. Seeds ofM. affinis were found in litter ant nests in 8 of 28 1-m² plots, suggesting that seed rain was not highly localized. Since litter nests are common, contain few seeds/nest and are often abandoned by their ants, litter ants may be the best candidates for ant-plant dispersal mutualisms.     

Effects of Edge Habitat and Nest Characteristics on Depredation of Artificial Nests in Fragmented Australian Tropical Rainforest

Variation in nest predation levels associated with rainforest fragmentation (edge effects) was assessed in Australia's Wet Tropics bioregion. Artificial nests were placed in the forest understorey at seven edge sites where continuous forest adjoined pasture, seven interiors (about 1 km from the edge), and six linear riparian forest remnants (50–100 m wide) that were connected to continuous forest. Four nest types were also compared, representing different combinations of two factors; height (ground, shrub) and shape (open, domed). At each site, four nests of each type, containing one quail egg and two model plasticine eggs, were interspersed about 15 m apart within a 160 m transect during September–October 2001. Predators were identified from marks on the plasticine eggs. The overall depredation rate was 66.5% of 320 nests' contents damaged over a three-day period. Large rodents, especially the rat Uromys caudimaculatus, and birds, especially the spotted catbird Ailuroedus melanotis, were the main predators. Mammals comprised 56.5% and birds 31.0% of predators, with 12.5% of unknown identity. The depredation rate did not vary among site-types, or between open and domed nests, and there were no statistically significant interactions. Nest height strongly affected depredation rates by particular types of predator; depredation rates by mammals were highest at ground nests, whereas attacks by birds were most frequent at shrub nests. These effects counterbalanced so that overall there was little net effect of nest height. Mammals accounted for 78.4% of depredated ground nests and birds for at least 47.4% of shrub nests (and possibly up to 70.1%). The main predators were species characteristic of rainforest, rather than habitat generalists, open-country or edge specialists. For birds that nest in the tropical rainforest understorey of the study region, it is unlikely that edges and linear remnants presently function as ecological population sinks due to mortality associated with increased nest predation.     

Different nest predator faunas and nest predation risk on ground and shrub nests at forest ecotones: an experiment and a review

This study examined predator faunas of artificial ground and shrub nests and whether nest predation risk was influenced by nest site, proximity to forest edge, and habitat structure in 38 grassland plots in south-central Sweden. There was a clear separation of predator faunas between shrub and ground nests as identified from marks in plasticine eggs. Corvids accounted for almost all predation on shrub nests whereas mammals mainly depredated ground nests. Nest predation risk was significantly greater for shrub than for ground nests at all distances (i.e. 0, 15 and 30 m) from the forest edge. However, nest predation risk was not significantly related to distance to forest edge, but significantly increased with decreasing distance to the nearest tree. Different corvid species robbed nests at different distances from the forest edge, with jays robbing nests closest to edges. We conclude that the relationship between the predation risk of grassland bird nests and distance to the forest edge mainly depends on the relative importance of different nest predator species and on the structure of the forest edge zone. A review of published articles on artificial shrub and ground nest predation in the temperate zone corroborated the results of our own study, namely that shrub nests experienced higher rates of depredation in open habitats close to the forest edge and that avian predators predominantly robbed shrub nests. Furthermore, the review results showed that predation rates on nests in general are highest <50 m inside the forest and lower in open as well as forest interior habitats (≥50 m from the edge). Received: 16 March 1998 / Accepted: 30 July 1998     

Breeding biology of Eared Quetzals in the Sierra Madre Occidental, Mexico

ABSTRACT.   Eared Quetzals ( Euptilotis neoxenus ), a threatened species, are one of the least studied trogons in Mexico. We monitored 29 Eared Quetzal nests in the Chihuahuan portion of the Sierra Madre Occidental from 1998 to 2003. All nests were in tree cavities, and the mean tree and nest cavity heights ( N = 14) were 16.9 ± 7.8 m and 11.4 ± 4.1 m, respectively. The mean clutch size was 2.8 ± 0.9 eggs ( N = 28), the incubation period lasted 22 d ( N = 1), and nestling periods ranged from 29 to 31 d ( N = 5). Both adults incubated eggs and fed nestlings. Of 80 eggs, 70 hatched (87.5%) and 67 of 70 young fledged (95.7%). Twenty-five of 29 nests (86.2%) produced at least one fledgling. One nest was predated, and two failed when nest trees fell. Higher rates of nest predation have been reported for other species of trogons. However, fewer potential predators, such as snakes and mammals, are present in the Sierra Madre than in tropical zones where most trogon species occur. In addition, antipredator behaviors, including nestlings with calls resembling a snake and nests with an unpleasant odor, may contribute to the high nesting success. The main limiting factors for Eared Quetzals in the northern Chihuahua may be competition for cavities with other secondary cavity-nesters, and the failure of nests when snags fall.     

Environmentally induced variation in body size of turtles hatching in natural nests

Eggs from three snapping turtles (Chelydra serpentina) were divided between two natural nests in a factorial experiment assessing the role of the nest environment as a cause for variation in body size and energy reserves of hatchlings at our study site in northcentral Nebraska. Nest # 1 was located in an unshaded area on the south side of a high sandhill, whereas nest #2 was located in an unshaded area on level ground. Eggs in nest #1 increased in mass over the course of incubation, with eggs at the bottom of the nest gaining more mass than eggs nearer to the surface. In constrast, eggs in nest #2 lost mass during incubation, with eggs at the bottom declining less in mass than eggs at the top of the cavity. Hatchlings from nest #1 were much larger (but contained smaller masses of unused yolk) than hatchlings from nest #2. Additionally, eggs from the lower layers in both nests tended to produce larger hatchings (but with smaller masses of unused yolk) than eggs from the upper layers. Thus, ecologically important variation in body size and nutrient reserves of hatchling snapping turtles results from variation in the environment among and within nests.     

Threat-sensitive Nest Preferences in Male Upland Bullies,Gobiomorphus breviceps

A male's ability to acquire and defend a nest site against competitors is an important requirement for successful breeding in many fish species. In the upland bully Gobiomorphus breviceps (Eleotridae), not all males are successful in gaining ownership of nesting rocks; therefore, male-male competition may be important in nest acquisition. Although larger nests have the potential to hold more eggs, in nature there is a preferred nest size well below the maximum available. I found that in over 88% of dyadic contests, the larger male was successful in acquiring the single nesting site provided. When males were individually given a choice of two artificial nest rocks, they consistently preferred the larger nest. These results suggest that larger males have the ability to occupy the largest nests. In the presence of a trout predator, males preferred nests with three closed sides 93% of the time. This preference disappeared when the threat was a conspecific. This shows that while males were choosing the larger nests their decisions were also threat-sensitive.     

Community-wide patterns of parasitism of a host “generalist” brood-parasitic cowbird

The brown-headed cowbird (Molothrusater) is a generalist obligate brood parasite. Despite intensive study and growing concern over the negative impact of cowbird parasitism on populations of many hosts, very little is known about the factors influencing community-wide patterns of cowbird parasitism. Using systematic nest searches, nest parasitism was studied over two breeding seasons at a study site in northeastern Illinois encompassing grassland, forest-edge, and forest habitat, supporting a diverse avian community. Parasitism was observed for 18 out of 34 altricial bird species found nesting at the study site. A total of 299 cowbird eggs and nestlings were found in 191 of a total of 593 nests. Analyses revealed several ecological and behavioral factors associated with frequency of parasitism and the resulting distribution of cowbird eggs. Much higher frequencies of parasitism were found in edge and forest habitats than in grassland. Within the edge habitat, open nests were parasitized significantly more often than cavity nests. Among open nests in the edge habitat, the two largest species were never parasitized. Host behavior, particularly egg-ejection behavior, was associated with a reduced observed frequency of parasitism, but at least three species known to eject cowbird eggs were sometimes parasitized. For six common hosts capable of rearing cowbirds, we found no correlation between level of parasitism and host nest-survivorship, suggesting that fine-grained assessments of host quality by female cowbirds do not influence patterns of parasitism among acceptable host species, or that differences in host quality are not great and/or predictable enough for such fine-grained assessments. Our results suggest that when a variety of possible nests are available, the level of parasitism on a particular species is a balance between a␣cowbird's preference for a particular species and the effectiveness of host species' defenses. A conceptual model was developed that incorporates the observed correlation of cowbird eggs or nestlings with habitat, nest-type, host species' body mass, and host behavioral defenses. Additional community-wide studies of cowbird parasitism will test if this model is applicable to other avian communities. Received: 20 December 1996 / Accepted: 17 May 1997     

Analysis of the nest environment of tuatara Sphenodon punctatus

Water potential and temperature were monitored in 20 natural nests of tuatara, Sphenodon punctatus , through 12 months of incubation on Stephens Island, New Zealand. Tuatara nest in rookeries in open pasture, in sites that often are more than 100m from residential burrows located beneath the closed canopy of native bush. Nest tunnels are approximately 197 mm long, 73mm wide, and 45mm high, and have a slightly expanded chamber at the end. Eggs are generally deposited in 1-3 layers in the terminal chamber. The top eggs are 30-155mm below the soil surface, and an air space of as much as 20 mm may exist between the uppermost egg and the top of the chamber. Each nest receives an average of 8.6 eggs that imbibe water and swell during incubation. Only 48% of eggs have hatched or are still alive 12 months after oviposition. Survival by embryos is higher in moist nests than in dry ones. Variation in temperature in nests has only a small influence on survival, and this influence may be mediated indirectly by effects of temperature on the water exchanges experienced by incubating eggs. Water potentials in the soil of closed canopy forest on Stephens Island are high enough to support embryogenesis, but temperatures are too low. Thus, females leave the forest to nest in areas where soil temperatures are suitable for incubation.     

Costs and response to conspecific brood parasitism by colonial red-breasted mergansers

Costs of conspecific brood parasitism (CBP) are expected to be influenced by a species’ life history traits. Precocial birds lay large clutches, and clutches that have been enlarged by CBP can affect host fitness through a longer incubation period, displaced eggs, and lower hatching success. We examined costs and response to CBP by hosts in a population of colonial red-breasted mergansers (Mergus serrator; n?=?400 nests over 8 years) within which 29% of parasitized clutches were enlarged considerably (≥?15 eggs). Length of the incubation period did not increase with clutch size. The mean number of eggs displaced from a parasitized nest during incubation (2.8) was 2×?greater than at an unparasitized nest (1.4). Hatching success declined by 2% for each additional egg in the nest. Thus, for a nest with?≥?15 eggs, one or more fewer host eggs hatch relative to an unparasitized nest with the same number of host eggs, assuming equal probability of success for all eggs. Hosts were 40% more likely to desert nests receiving 2 or 6 experimental eggs relative to unparasitized control nests, although it is unknown whether hens deserting a nest renested elsewhere. Our study indicates that costs of CBP to hosts during nesting may be limited to those red-breasted mergansers incubating the largest clutches (≥?15 eggs), and it raises questions about the adaptive significance of deserting a parasitized clutch.     

Forest fragmentation and avian nest predation in forested landscapes

Summary The size of forest fragments, the use of land bordering fragments, and the distance of nests from an edge all affect the frequency of predation upon bird nests in Maine (USA), an area where the forest has been fragmented by roads, but not significantly reduced in area. We placed artificial nests containing quail eggs in forests of different sizes and at various distances from the edge to test which of these factors was most important in describing predation. Predation was greatest in small tracts surrounded completely by land. Large areas and those bordered on at least one side by a large water body had lower predation rates. This suggests that influx of predators from nearby habitats may be responsible for much of the nest predation in forest fragments.     

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.     

Intraspecific nest parasitism in the grey starling (Sturnus cineraceus)

We studied intraspecific nest parasitism in the grey starling (Sturnus cineraceus) in 1992 and 1993. We used three criteria to detect nest parasitism: (i) the appearance of more than one egg per day while the host was laying; (ii) the appearance of extra eggs after the host completed its clutch; and (iii) the appearance of eggs which were of a different shape, size and color to other eggs in the clutch. There were 290 nests (157 nests in 1992; 133 nests in 1993) in which the clutch was completed early (clutches initiated before May 10). Twenty-nine (1992) and 32 (1993) nests contained at least one parasitic egg. Parasitic eggs hatched if they were laid during the laying period and early in the incubation period of their host, and a few of them fledged. Fledging success of parasitic eggs was not different from that of eggs in non-parasitized nests if parasitic eggs were laid during the host's laying period. However, fledging success of all parasitic eggs was fewer than that of eggs in non-parasitized nests. By comparison, fledging success of parasitized nests was not a great as that of non-parasitized nests.     

Forest fragmentation relaxes natural nest predation in an Afromontane forest

Nest predation is widely regarded as a major driver underlying the population dynamics of small forest birds. Following forest fragmentation and the subsequent invasion by species from non-forested landscape matrices, shifts in predator communities may increase nest predation near forest edges. However, effects of human-driven habitat change on nest predation have mainly been inferred from studies with artificial nests, despite being regarded as poor surrogates for natural ones. We studied variation in predation rates, and relationships with timing of breeding and characteristics of microhabitats and fragments, on natural white-starred robin Pogonocichla stellata nests during three consecutive breeding seasons (2004–2007) in a Kenyan fragmented cloud forest. More than 70% of all initiated nests were predated during each breeding season. Predation rates nearly quadrupled between the earliest and the latest nests within a single breeding season, increased with distance to the forest edge, and decreased with the edge-to-area ratio of forest fragments. These spatial relationships oppose the traditional perception of edge and fragmentation effects on nest predation, but are in line with results from artificial nest experiments in other East African forests. In case of inverse edge and fragmentation effects on nest predation, such as shown in this study, species that tolerate edges for breeding may be affected positively, rather than negatively, by forest fragmentation, while the opposite can be expected for species restricted to the forest interior. The possibility of inverse edge effects, and its conservation implications, should therefore be taken into account when drafting habitat restoration plans.