Orientation of crustacean burrows

Most arthropod burrows show a marked preferred orientation: they are not random in alignment. A recent burrow made by Jaxea nocturna Nardo is compared to three fossil burrows from the Austrian Tertiary. In each system very steep and very flat burrow sections can be distinguished. In three cases, including the Recent one, flat burrow sections dominate in length. In all burrow sections the distribution of trend angles is also not uniform but indicate preferred directions. In those cases where two mean vectors exist their position is nearly orthogonal, in systems with three mean vectors they form angles of nearly 60°. A relationship between these preferred directions to coastline orientation and current direction is likely.     

Homing in fiddler crabs (Uca lactea annulipes and Uca vomeris : Ocypodidae)

Fiddler crabs emerge from burrows on intertidal sand- and mudflats to feed during low tide. In the species studied here (Uca lactea annulipes, Uca vomeris) a crab normally wanders no more than about 1 m away from its burrow and, when frightened, dashes back along a straight line to take cover. Feeding crabs tend to move sideways, without changing orientation, along paths radiating from the burrow. When they move along circumferential paths they adjust their orientation so that one side continues to point towards the burrow. The crabs do not need to see the burrow in order to stay aligned with the home vector, and they are not misled by a dummy hole close to their own burrow unless they have come to within about 10 cm of it. The home runs of crabs end within a few centimeters of a burrow that is covered with a sheet of sandpaper and then give way to search runs, centred upon a position slightly short of the burrow location. Feeding crabs can be displaced on sandpapers and their subsequent home runs end at a position where the burrow would be, had there been no displacement. Landmarks close to the burrow do not influence the home runs of displaced crabs. Crabs that are rotated on a sheet of sandpaper, counter-turn to keep their original orientation constant. Fiddler crabs thus employ path integration with external compass information and close range visual guidance for homing. Accepted: 11 May 1998     

Location of long‐term communal burrows of a threatened arid‐zone lizard in relation to soil and vegetation

The great desert skink (Liopholis kintorei) of the Egerniinae subfamily (Reptilia: Scincidae) is a communal burrowing lizard that inhabits arid spinifex grasslands in central Australia. Great desert skink activity is centred in and around the burrows which are inhabited for many years. However, it is not known whether skinks select burrow sites with specific attributes or how continuing occupancy of burrows is influenced by the surrounding habitat; especially post‐fire, when plant cover is reduced. Here, we test whether great desert skink burrows in areas burnt 2 years previously and in longer unburnt areas are associated with particular habitat attributes, and whether there are differences between occupied and recently abandoned burrow sites. Vegetation composition, cover and soil surface characteristics at 56 established great desert skink burrows, including occupied and recently unoccupied burrows, were compared with 56 random nearby non‐burrow control sites. Burrow sites had higher plant cover compared with the surrounding landscape in both recently burnt and longer unburnt areas and were more likely to be associated with the presence of shrubs. Soil stability and infiltration were also higher at burrow sites. However, we found no evidence that burrows with lower cover were more likely to be abandoned. Our results suggest that great desert skinks may actively select high cover areas for burrow construction, although differences between burrow and control sites may also partly reflect local changes to plant cover and composition and soil properties resulting from burrow construction and long‐term habitation of a site. Further research should determine if burrows with shrubs or higher plant cover provide greater protection from predators, more structural stability for burrow construction, increased prey abundance or other benefits. We recommend that maintenance of areas with relatively higher plant cover be prioritized when managing great desert skink habitat.     

Application of morphologic burrow interpretations to discern continental burrow architects: Lungfish or crayfish?

A methodology for trace fossil identification using burrowing signatures is tested by evaluating ancient and modern lungfish and crayfish burrows and comparing them to previously undescribed burrows in a stratigraphic interval thought to contain both lungfish and crayfish burrows. Permian burrows that bear skeletal remains of the lungfish Gnathorhiza, from museum collections, were evaluated to identify unique burrow morphologies that could be used to distinguish lungfish from crayfish burrows when fossil remains are absent. The lungfish burrows were evaluated for details of the burrowing mechanism preserved in the burrow morphologies together forming burrowing signatures and were compared to new burrows in the Chinle Formation of western Colorado to test the methodology of using burrow signatures to identify unknown burrows.

Permian lungfish aestivation burrows show simple, nearly vertical, unbranched architectures and relatively smooth surficial morphologies with characteristic quasi‐horizontal striae on the burrow walls and vertical striae on the bulbous terminus. Burrow lengths do not exceed 0.5 m. In contrast, modern and ancient crayfish burrows exhibit simple to highly complex architectures with highly textured surficial morphologies. Burrow lengths may reach 4 to 5 m.

Burrow morphologies unlike those identified in Gnathorhiza aestivation burrows were found in four burrow groups from museum collections. Two of these groups exhibit simple architectures and horizontal striae that were greater in sinuosity and magnitude, respectively. One of these burrows contains the remains of Lysoro‐phus, but the burrow surface reveals no reliable surficial characteristics. It is not clear whether Lysorophus truly burrowed or merely occupied a pre‐existing structure. The other two groups exhibit surficial morphologies similar to those found on modern and ancient crayfish burrows and may provide evidence of freshwater crayfish in the Permian.

Burrows from the Upper Triassic Chinle Formation in western Colorado exhibit simple to moderately complex architectural morphologies, ranging from predominantly vertical, unbranched, with little or no chamber development to predominantly vertical, few branches, and with minor chamber development. Surficial burrow morphologies are moderate to highly textured. The burrows have scrape marks, scratch marks, mud and lag‐liners, knobby surfaces, pleopod striae, and body impressions.

Although no fossil remains of the burrowing organism were found within or associated with the Chinle burrows from western Colorado, the similarity of architectural and surficial burrow morphologies to those in the Chinle of Canyonlands, Utah and to modern crayfish burrows, clearly indicates that the Colorado burrows are the product of burrowing crayfish rather than lungfish. Evaluation of burrowing signatures preserved in the architectural and surficial burrow morphologies is a very useful tool to compare and contrast Chinle burrows from different regions on the Colorado Plateau. Documentation of crayfish burrows in the Chinle of Utah and Colorado strongly suggests that other large‐diameter Chinle burrows elsewhere on the Colorado Plateau and in stratigraphically equivalent units may also be the product of crayfish activity.     

Burrow Architecture of the Ghost Crab Ocypode ceratophthalma on a Sandy Shore in Hong Kong

The ghost crab Ocypode ceratophthalma (Pallas) creates burrows of variety shapes at different ages. Juveniles (mean carapace length 11 mm) produced shallow J-shaped burrows, which incline vertically into the substratum (mean depth 160 mm). Larger crabs (17–25 mm carapace length) have Y-shaped and spiral burrows (mean depth 361 mm). These Y-shaped burrows have a primary arm, which extends to the surface forming the opening, and a secondary arm which terminates in a blind spherical ending. The two arms join in a single shaft and end with a chamber at the base. The secondary arms and chambers are believed to be used for mating or as a refuge from predation. The spiral burrows have spiral single channel ending in a chamber. Older crabs (mean carapace length 32.6 mm) had simple, straight single tube burrows, which inclined into the substratum at mean of 73° and had a mean depth of 320 mm. During summer daytime periods, the burrows shelter the crabs from heat and desiccation stress. The sand surface temperature at the burrow opening was ~48 °C but temperatures inside the burrows can drop to 32 °C at a depth of 250 mm. Variation in the burrow architecture with crab age appears to be related to the crab’s behaviour. Juvenile crabs have smaller gill areas and move out of the burrows regularly to renew their respiratory water and, as a result, they do not need a deep burrow. Larger crabs, in contrast, can tolerate prolonged periods without renewing their respiratory water and therefore create deeper and more complex burrows for mating and refuges.     

Depth of artificial Burrowing Owl burrows affects thermal suitability and occupancy

Many organizations have installed artificial burrows to help bolster local Burrowing Owl (Athene cunicularia) populations. However, occupancy probability and reproductive success in artificial burrows varies within and among burrow installations. We evaluated the possibility that depth below ground might explain differences in occupancy probability and reproductive success by affecting the temperature of artificial burrows. We measured burrow temperatures from March to July 2010 in 27 artificial burrows in southern California that were buried 15–76 cm below the surface (measured between the surface and the top of the burrow chamber). Burrow depth was one of several characteristics that affected burrow temperature. Burrow temperature decreased by 0.03°C per cm of soil on top of the burrow. The percentage of time that artificial burrows provided a thermal refuge from above‐ground temperature decreased with burrow depth and ranged between 50% and 58% among burrows. The percentage of time that burrow temperature was optimal for incubating females also decreased with burrow depth and ranged between 27% and 100% among burrows. However, the percentage of time that burrow temperature was optimal for unattended eggs increased with burrow depth and ranged between 11% and 95% among burrows. We found no effect of burrow depth on reproductive success across 21 nesting attempts. However, occupancy probability had a non‐linear relationship with burrow depth. The shallowest burrows (15 cm) had a moderate probability of being occupied (0.46), burrows between 28 and 40 cm had the highest probability of being occupied (>0.80), and burrows >53 cm had the lowest probability of being occupied (<0.43). Burrowing Owls may prefer burrows at moderate depths because these burrows provide a thermal refuge from above‐ground temperatures, and are often cool enough to allow females to leave eggs unattended before the onset of full‐time incubation, but not too cool for incubating females that spend most of their time in the burrow during incubation. Our results suggest that depth is an important consideration when installing artificial burrows for Burrowing Owls. However, additional study is needed to determine the possible effects of burrow depth on reproductive success and on possible tradeoffs between the effects of burrow depth on optimal temperature and other factors, such as minimizing the risk of nest predation.     

Estimation of N2 fixation based on differences in the natural abundance of 15N among freshwater N2-fixing and non-N2-fixing algae

The hypothesis that small mammal burrows can increase the amount of water infiltrating into the soil profile was tested. The amount of water added to the soil profile from spring recharge in areas adjacent to ground squirrel (Spermophilus townsendii and S. elegans) burrows was compared to nearby areas without burrows. Recharge amounts in burrow areas were significantly higher than nonburrow areas. An average of 21% more of the winter precipitation infiltrated into the soil near burrows. The amount of recharge was also found to be positively related to burrow density. Burrows also affected the distribution of the recharge by adding significantly more water to the deeper portions (>50 cm) of the soil profile.     

Development of an index of abundance for pygmy rabbit populations

The pygmy rabbit (Brachylagus idahoensis) is a cryptic, burrowing lagomorph of conservation concern for which an efficient method to monitor populations is needed for conservation planning. We developed an index of abundance based on density of active burrow systems at 7 sites (57.2–118.5 ha) in east central Idaho. We conducted censuses of burrow systems and used mark-resight surveys of 80 radio-collared individuals to estimate density of rabbits. At 5 sites, we also used a second method to estimate rabbit numbers based on presence of tracks in snow around burrow systems. We evaluated patterns of burrow use by individuals and examined the relationship between vegetation structure and density of rabbits. Density of active burrow systems varied from 0.19 to 3.46 per ha, and density of rabbits ranged from 0.02 to 0.46 per ha. Number of burrow systems used by individuals increased with density of available burrows, which supported a nonlinear relationship between abundance of burrows and rabbits. Population density increased curvilinearly with density of active burrows accounting for >75% of the variation (r² = 0.79) in population estimates across sites. We documented a positive relationship between visual obstruction of vegetation and density of rabbits across 6 of the study sites. Our results suggest that density of burrows can serve as an index for monitoring changes in abundance of pygmy rabbits in east central Idaho and that this index also might be useful for monitoring changes in relative abundance over time at other locations. To assess abundance at larger spatial scales or across different regions, the index should be calibrated under regional conditions and site-level covariates should be evaluated. © 2011 The Wildlife Society.     

高原鼠兔有效洞穴密度对高山嵩草群落及其主要种群空间分布特征的影响

高原鼠兔(Ochotona curzoniae)有效洞穴密度变化会引发高山嵩草(Kobresia pygmaea)草甸植物群落及其种群分布格局发生变化。采用野外调查法研究了高原鼠兔有效洞穴密度对高山嵩草群落特征及其主要种群分布格局的影响。结果表明:随高原鼠兔有效洞穴密度增加,高山嵩草草甸植物群落的优势种没发生明显变化,部分伴生种发生更替;高度、盖度、多样性指数和均匀度指数呈现降低态势;地上生物量和丰富度指数变化不明显;高山嵩草和矮火绒草(Leontopodium nanum)种群的盖度、密度以及生物量均呈现降低态势,而达乌里秦艽(Gentiana dahurica)和小花草玉梅(Anemone rivularis var.flore-minors)种群的盖度、密度和生物量呈增加趋势。高山嵩草和矮火绒草的种群分布格局从8个/625m2和14个/625m2的聚集分布分别变为34个/625m2时的均匀分布和随机分布,达乌里秦艽和小花草玉梅种群从8个/625m2和14个/625m2的随机分布变为23个/625m2和34个/625m2时的聚集分布,这说明高原鼠兔有效洞穴密度变化改变了高山嵩草群落的特征和主要植物种群的空间分布格局,而对应群落特征和种群分布格局改变的有效洞穴密度为14个/625m2和23个/625m2。     

The magnetic compass orientation of the burrows of the Damara mole-rat Cryptomys damarensis (Bathyergidae)

In response to reports claiming that part of the ability of mole-rats (Bathyergidae) to orientate with respect to the geomagnetic field involves orientation of their burrow systems in a southward direction, we measured the orientation of burrows of the Damara mole-rat, Cryptomys damarensis , in the Kalahari Desert. It was found that burrow orientation was not significantly different from that expected for a random distribution of compass orientations.     

The Biology of a Subtropical Population of Halictus ligatus Say (Hymenoptera; Halictidae)

The ability of Manx shearwaters (Puffinus puffinus) to locate their nesting burrows at night was investigated using observation and experiments. Shearwaters walking to their burrows did so at random with respect to the wind direction, and did not vocalize, suggesting that visual cues are important to successful burrow homing. Experiments to test whether vision, audition or olfaction functioned in guiding birds back to burrows supported this conclusion.     

Obligate crayfish burrow use and core habitat requirements of crawfish frogs

Crawfish frogs (Lithobates areolatus) have experienced declines across large portions of their former range. These declines are out of proportion to syntopic wetland-breeding amphibian species, suggesting losses are resulting from unfavorable aspects of non-breeding upland habitat. Crawfish frogs get their common name from their affinity for crayfish burrows, although the strength of this relationship has never been formally assessed. We used radiotelemetry to address 4 questions related to upland burrow dwelling in crawfish frogs: 1) what burrow types are used and how do they function to affect crawfish frog survivorship; 2) what are the physical characteristics and habitat associations of crawfish frog burrows; 3) what are the home range sizes of crawfish frogs when burrow dwelling; and 4) where are crawfish frog burrows situated with respect to breeding wetlands? We tracked crawfish frogs to 34 burrows, discovered another 7 occupied burrows, and therefore report on 41 burrows. Crawfish frogs exclusively occupied crayfish burrows as primary burrows, which they inhabited for an average of 10.5 months of the year. With one exception, crawfish frogs also used crayfish burrows as secondary burrows—temporary retreats occupied while exhibiting breeding migrations or ranging forays. Burrows were exclusively located in grassland habitats, although crawfish frogs migrated through narrow woodlands and across gravel roads to reach distant grassland primary burrow sites. Home range estimates while inhabiting burrows were 0.05 m² (the area of the burrow entrance plus the associated feeding platform) or 0.01 m³ (the estimated volume of their burrow). Crawfish frog burrows were located at distances up to 1,020 m from their breeding wetlands. To protect crawfish frog populations, we recommend a buffer (core habitat plus terrestrial buffer) of at least 1.2 km around each breeding wetland. Within this buffer, at least 3 critical habitat elements must be present: 1) extensive grasslands maintained by prescribed burning and/or logging, 2) an adequate number of upland crayfish burrows, and 3) no soil disturbance of the sort that would destroy crayfish burrow integrity. © 2012 The Wildlife Society.     

Influence of age and environmental factors on burrow-making behavior of the short-tailed cricket,Anurogryllus muticus (De Geer) (Orthoptera: Gryllidae)

For the short-tailed cricket, Anurogryllus muticus, burrow-making behavior is essential. All nymphal instars construct burrows, but in the adult stage the rate of burrowing behavior is age dependent. Increases in photophase and light intensity stimulate burrowing, and the explicit negative phototaxis is correlated with the cricket's inability to exist under dry conditions. Ingestion of substrate during burrow construction may serve to acquire additional moisture. There is no evidence of burrow recognition, and crickets can construct a burrow when needed. The natural distribution of burrows at the plot investigated on Moorea supports the notion thatA. muticus builds burrows where the preferred food plantAlysicarpus vaginalis is most abundant. By minimizing the traveling distance to food sources when foraging they can retreat to their burrow again.     

Burrow defense behaviors in a sand-bubbler crab, Scopimera globosa, in relation to body size and prior residence

The burrow defense behaviors in a sand-bubbler crab, Scopimera globosa, living on a tidal flat, were experimentally examined. Body size and prior residence influenced the results of struggles for the burrows, and large individuals or the burrow owners won in most cases when the intruders were not significantly larger than the owners. Most large owners defended their burrows by directly fighting their opponents. On the other hand, small owners defended their burrows in three different ways. (1) Owners fought directly against same-sized or smaller intruders. For larger intruders, (2) most owners returned to their burrows when the owner was nearer to the burrow than the intruder (returning behavior), and (3) owners sat motionless when the intruder was nearer to the burrow than the owner (sitting behavior). Success ratios of the three types of burrow defense were 38.2%, 88.5%, and 100%, respectively. It was considered that sitting behavior of the cryptically colored S. globosa has evolved because intruders cannot see motionless owners and consequently cannot detect the owner's burrow. Received: October 6, 2000 / Accepted: January 22, 2001     

Nesting activity,breeding success and colony size for the Wedge-tailed Shearwater Puffinus pacificus on Heron Island

Abstract The Capricorn Group of islands in Australia's Great Barrier Reef Marine Park sustains one of the world's largest breeding populations of the Wedge-tailed Shearwater Puffinus pacificus. Heron Island, a 13.5 ha coral cay which supports tourist and research station leases as well as a national park, is the third largest nesting island in the group. Sample censuses of breeding burrows were conducted each year between 1985 and 1990 and a further survey was completed in 1993. These returned estimates of between 13 264±1387 and 16 337±1545 active burrows (Y±SE). Burrow densities within each of the habitats monitored showed no significant trends between years, although there were large differences in burrow density between habitats. There were roughly the same number of burrows in the developed (west) and national park (east) halves of the cay. A miniature video camera system (burrowscope), which allowed nesting chambers at the ends of burrows to be inspected, was used in 1989, 1990 and 1993. This demonstrated that around half the burrows were occupied by incubating birds. Variations were found in the distribution of incubating birds between habitats, although this did not remain constant between the years. In the 1993 season, breeding activity was traced from the burrow establishment to fledging stage. Fifty-one per cent of burrows were used for breeding (eggs laid), 77% of eggs hatched and 80% of chicks produced a fledgling. Overall breeding success for the island was estimated at 61%. In 1993 the area designated as Buildings was found to have significantly lower hatching success compared with natural habitats. Most mortality occurred at the egg stage; however, in the Fringe habitat, mortality was highest at the chick stage. Previous surveys have estimated the breeding population from burrow counts. It now appears that only about 30% of such burrows produce fledglings.     

Selection of food patches by sympatric herbivores in response to concealment and distance from a refuge

Small herbivores face risks of predation while foraging and are often forced to trade off food quality for safety. Life history, behaviour, and habitat of predator and prey can influence these trade‐offs. We compared how two sympatric rabbits (pygmy rabbit, Brachylagus idahoensis; mountain cottontail, Sylvilagus nuttallii) that differ in size, use of burrows, and habitat specialization in the sagebrush‐steppe of western North America respond to amount and orientation of concealment cover and proximity to burrow refuges when selecting food patches. We predicted that both rabbit species would prefer food patches that offered greater concealment and food patches that were closer to burrow refuges. However, because pygmy rabbits are small, obligate burrowers that are restricted to sagebrush habitats, we predicted that they would show stronger preferences for greater cover, orientation of concealment, and patches closer to burrow refuges. We offered two food patches to individuals of each species during three experiments that either varied in the amount of concealment cover, orientation of concealment cover, or distance from a burrow refuge. Both species preferred food patches that offered greater concealment, but pygmy rabbits generally preferred terrestrial and mountain cottontails preferred aerial concealment. Only pygmy rabbits preferred food patches closer to their burrow refuge. Different responses to concealment and proximity to burrow refuges by the two species likely reflect differences in perceived predation risks. Because terrestrial predators are able to dig for prey in burrows, animals like pygmy rabbits that rely on burrow refuges might select food patches based more on terrestrial concealment. In contrast, larger habitat generalists that do not rely on burrow refuges, like mountain cottontails, might trade off terrestrial concealment for visibility to detect approaching terrestrial predators. This study suggests that body size and evolutionary adaptations for using habitat, even in closely related species, might influence anti‐predator behaviors in prey species.     

长江口芦苇和互花米草盐沼湿地蟹类洞穴分布特征及主要影响因子

蟹类洞穴是蟹类在潮间带盐沼生存、繁衍的特征性结构,具有重要的生态功能。洞穴分布特征及其影响因子的分析,是深入探讨蟹类及其洞穴的生态系统功能的重要基础。2015年10月,在崇明北滩单一芦苇(Phragmites australis)群落,单一互花米草(Spartina alterniflora)群落和芦苇-互花米草混合群落3种典型生境中,对蟹类洞穴的分布特征及其相关的大型底栖动物、植被、沉积物等的特征参数进行了调研与分析。结果表明,生境类型差异对蟹类洞穴分布特征及相关生境因子具有重要影响。蟹类洞穴的分布密度和开口直径在不同生境间存在显著差异(P0.05),且单一芦苇群落生境内洞穴密度要显著高于单一互花米草群落生境(P0.05),洞穴开口直径在单一互花米草生境要显著高于单一芦苇生境(P0.05);大型底栖动物生物量、密度、植物地下部分生物量在不同生境间差异不显著(P0.05),而植株密度、活植株高度、植物地上部分生物量以及沉积物含水率、p H、氧化还原电位在不同生境间存在显著差异(P0.05)。沉积物中值粒径,总氮含量和总碳含量在不同生境间的差异随深度不同会发生变化。不同生境主要生境因子的差异是导致蟹类洞穴分布特征不同的根本原因;蟹类洞穴分布特征受多个生境因子的综合作用。筛选的生境因子的组合虽然与洞穴分布特征具有显著相关性,但相关系数较小。未来研究中需要拓展生境因子涵盖范围,加强多因子综合作用分析。     

Microhabitat and rhythmic behavior of tiger beetle Callytron yuasai okinawense larvae in a mangrove forest in Japan

Mangrove forests are regularly flooded by tides at intervals of approximately 12.4 h (tidal rhythm). Larvae of the tiger beetle Callytron yuasai okinawense in a mangrove forest made shallow burrows in mounds up to 1 m in height constructed by the mud lobster Thalassina anomala. No larval burrows were observed on the forest floor, which was very muddy even during low tide. Some larvae plugged the burrow openings before they were submerged at high tide. The mean interval between consecutive burrow plugging events was 12.37 h, which is similar to the period of tidal cycles. Nine out of 30 larvae plugged the burrow openings even when the burrows did not become submerged. Plugging behavior may be governed by an endogenous biological clock, or may be a response to exogenous information about tidal level (e.g. moisture seeping through the ground).     

Kangaroo Rats Remodel Burrows in Response to Seasonal Changes in Environmental Conditions

Burrow architecture enhances important animal functions such as food storage, predator avoidance, and thermoregulation. Occupants may be able to maximize fitness by remodeling burrows in response to seasonal changes in climate and predation risk. My objective was to examine how banner‐tailed kangaroo rats (Dipodomys spectabilis) modify the number of burrow entrances in response to seasonal conditions. For 3 yr, I monitored fluctuations in number of burrow entrances in kangaroo rat mounds. Individual kangaroo rats continually remodeled mounds in response to seasonal conditions. Compared to summer, mounds in winter had approximately 50% fewer entrances and plugged entrances were common. Monthly differences in number of entrances were closely linked with seasonal changes in soil temperature and precipitation. Number of entrances decreased as soil temperature and precipitation declined. Changes in burrow entrances likely reflect seasonal differences in the relative importance of burrow functions. Fewer burrow entrances during winter would create a warmer microclimate by reducing convective heat loss in mounds, resulting in thermoregulatory savings for occupants. During the summer, thermoregulatory costs of kangaroo rats are low, but risk of seed cache spoilage and predation from snakes increases. Adding burrow entrances after large summer rainfall events would increase the evaporation rate within mounds, reducing spoilage of seed caches. More burrow entrances would also reduce predation risk in the summer by providing additional escape routes.     

Effects of an invasive species on refuge‐site selection by native fauna: The impact of cane toads on native frogs in the Australian tropics

Invasive species can induce shifts in habitat use by native taxa: either by modifying habitat availability, or by repelling or attracting native species to the vicinity of the invader. The ongoing invasion of cane toads (Rhinella marina) through tropical Australia might affect native frogs by affecting refuge‐site availability, because both frogs and toads frequently shelter by day in burrows. Our laboratory and field studies in the wet‐dry tropics show that native frogs of at least three species (Litoria tornieri, Litoria nasuta and Litoria dahlii) preferentially aggregate with conspecifics, and with (some) other species of native frogs. However, the frogs rarely aggregated with cane toads either in outdoor arenas or in standardized experimental burrows that we monitored in the field. The native frogs that we tested either avoided burrows containing cane toads (or cane toad scent) or else ignored the stimulus (i.e. treated such a burrow in the same way as they did an empty burrow). Native frogs selected a highly non‐random suite of burrows as diurnal retreat sites, whereas cane toads were less selective. Hence, even in the absence of toads, frogs do not use many of the burrows that are suitable for toads. The invasion of cane toads through tropical Australia is unlikely to have had a major impact on retreat‐site availability for native frogs.