The occupation of artificial burrows by Helice tridens (De Haan) and the length of its stay

The mud-crab Helice tridens (De Haan) influences the cycling of matter in salt-marsh ecosystems through its burrowing activity. If the crabs occupy and stay in their burrows for a short time, their burrowing activity will be great, since they will continuously construct new burrows. Therefore, investigation of the relation between the crabs and their burrows is considered to be important. In the present study, the relation between pipes as a form of artificial burrow and their occupation by the crab was analyzed. A close relationship was recognized between the diameter of the pipe opening and the carapace width of the crab which occupied the pipe, while pipes with a length shorter than the depth of the crab burrows were hardly occupied. These results indicate that the diameter and length of an artificial burrow affects the likelihood of its occupation by this species of crab. The length of the crab's stay in this type of artificial burrow was generally 1 day. This result may be related to the field observation that newly made burrows frequently collapse due to water current occurring through tidal action after the crabs have left.     

Human disturbance as a cause of bias in ecological indicators for sandy beaches: Experimental evidence for the effects of human trampling on ghost crabs (Ocypode spp.)

Human pressures on coastlines are increasing globally, particularly on urban beaches where maintenance of sand budgets and erosion control are the main focus of current shoreline management. By contrast, biological attributes are rarely considered and few, if any, ecological indicators are routinely monitored on beaches. Abundance of ghost crabs (genus Ocypode) generally responds predictably to human stressors, and is thus a potentially suitable ecological indicator for beaches. The crabs construct burrows with a single, prominent opening at the surface, and population sizes are commonly estimated by counting the number of these burrow openings. While such ‘burrow counts’ are attractive as a low-cost and simple monitoring technique, they may violate a key performance criterion of indicators: not to be overly sensitive to expected sources of interference. On urban beaches such interference is human trampling and, consequently, we evaluated its influence on the performance of burrow counts. The effects of short-term, intense human trampling on numbers and sizes of crab burrows were measured in a series of impact experiments, in which pedestrian trampling was repeatedly applied over 5 h on 4 consecutive days. Burrow counts were highly sensitive to interference from short-term trampling disturbance, which can substantially bias population estimates inferred from such counts. Importantly, burrow densities recovered overnight and apparent shifts in entrance size structures recorded immediately after the trampling impacts were also no longer evident on the following day. Thus, short-term trampling shifted parameter estimates without significant biological effects underpinning such changes—a clear case of bias. Although crab density and size structure are susceptible to artefacts caused be human trampling, they remain valuable indicators for sandy beaches, if interference by pedestrians is small in field measurements or can be accommodated in numerical analyses.     

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.     

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.     

Size as a Factor Influencing the Ownership of Copulation Burrows by the Ghost Crab (Ocypode ceratophthalmus)

On Cousin Island, Seychelles, male ghost crabs mostly constructed their copulation burrows around new moon. The burrows were sited below the high tide mark and therefore only lasted until washed away by the incoming tide. Large males were able to defeat small males in contests for burrows and so, to reduce the risk of eviction, small males built their burrows later on the ebbing tide than large males, after the period when fights for burrows were most frequent. There was also evidence that small males built their burrows on stretches of beach presumed to be inferior, because the burrow density was lower.     

Number of ghost crab burrows does not correspond to population size

Ghost crabs are distributed worldwide on sandy beaches, and several studies have associated the number of ghost crab burrows with the levels of anthropogenic impacts on the beaches under study. However, our results show that the use of ghost crab Ocypode quadrata burrows to assess levels of anthropogenic impacts on sand beaches may not be accurate, as previously thought, because the number of burrows does not represent an estimate of the population size. In addition, we propose three hypotheses to explain the extremely low number of individuals/number of burrows ratio: the “secret chamber”, the “multiple openings”, and the “one crab, several burrows” hypotheses. We also observed an unusual sex ratio.     

The burrow structure of the European rabbit (Oryctolagus cuniculus L.)

Samples of rabbit burrows were excavated and measured at four areas around Edinburgh. Of these, 31 burrows over 2 m long were analysed for internal structural relationships and the effect of soil composition and slope of the ground on their form. Seven variables were measured for each burrow—total length, number of entrance holes, number of junctions, number of ends, average length of sections between holes, junctions and ends, average depth and maximum depth. There are three main trends in burrow variation—size, an inverse relationship between relative number of holes and average depth, and an inverse relationship between average section length and relative number of junctions. Burrows in sand have relatively fewer holes and junctions, longer element lengths, a higher average depth and three times the enclosed volume per hole. Burrows dug into slopes have a higher average depth. Areas differed significantly in the relative number of holes and junctions, and average depth. It was concluded that an apparently complex structure could be summarized in terms of relatively few components. The chief of these, size, was largely independent of the soil and site characteristics, whereas the remaining two were dependent on the soil in which the burrow was dug. This may have implications for the ecology and behaviour of rabbits in different areas, and is relevant to the success of some rabbit control procedures such as burrow fumigation and warren ripping.     

How do goannas find sea turtle nests?

Squamate reptiles rely heavily on visual and chemical cues to detect their prey, so we expected yellow‐spotted goannas (Varanus panoptes) which are predators of sea turtle nests on mainland beaches in northern Australia would use these cues to find sea turtle nests. Ghost crabs (Ocypode ceratophthalmus and Ocypode cordimanus) are also common on Australian sea turtle nesting beaches and frequently burrow into sea turtle nests. However, the potential for ghost crab burrowing activity at sea turtle nests to signal the location of a nest to goannas has not been investigated. Here, we used camera traps and presence of tracks at nests to record goanna activity around selected nests during the incubation period and 10 days after hatchling turtles emerged from their nests. We also recorded the number of ghost crab burrows around nests to evaluate ghost crab activity. Our results indicated that nest discovery by goannas was independent of nest age, but that the nest visitation rate of goannas and crabs increased significantly after a nest had been opened by a goanna or after hatchlings had emerged from the nest. There was no apparent connection between ghost crab burrows into a nest and the likelihood of that nest being predated by goannas.     

Comparative Burrow Architectures of Resident Fiddler Crabs (Ocypodidae) in Indian Sundarban Mangroves to Assess Their Suitability as Bioturbating Agents

Excavation of burrows by fiddler crabs (genus Uca) is an important component in mangrove ecosystem functioning. This bioturbation activity can be measured by analysing the burrow architecture of these crabs. The aim of the present study is to describe and evaluate inter specific differences in the burrow morphologies of four species of fiddler crabs (Uca rosea, Uca triangularis, Uca dussumieri and Uca vocans) using polyester resin casts of the burrows. For each of the species, sex and carapace width (CW; mm) were determined for all the individuals. Three burrow morphological characters viz. burrow diameter (BD; mm), total burrow depth (TBD; mm) and burrow volume (BV; cm³) were considered during the study. Density of each species throughout the year was also assessed. For all the species BD and BV were higher in case of males compared to the females and they showed significant positive correlation with the CW of the burrow inhabitants. The amount of sediment excavated by each crab was evaluated in terms of BV. Among all the studied species, U. rosea was established as the most potent bioturbative candidate in the studied mangrove due to their greater density and moderate ability to excavate burrow.     

Determinants of between‐year burrow re‐occupation in a colony of the European bee‐eater Merops apiaster

Re‐occupation of existing nesting burrows in the European bee‐eater Merops apiaster has only rarely – and if so mostly anecdotically – been documented in the literature record, although such behavior would substantially save time and energy. In this study, we quantify burrow re‐occupation in a German colony over a period of eleven years and identify ecological variables determining reuse probability. Of 179 recorded broods, 54% took place in a reused burrow and the overall probability that one of 75 individually recognized burrows would be reused in a given subsequent year was estimated as 26.4%. This indicates that between‐year burrow reuse is a common behavior in the study colony which contrasts with findings from studies in other colonies. Furthermore, burrow re‐occupation probability declined highly significantly with increasing age of the breeding wall. Statistical separation of within‐ and between‐burrow effects of the age of the breeding wall revealed that a decline in re‐occupation probability with individual burrow age was responsible for this and not a selective disappearance of burrows with high re‐occupation probability over time. Limited duty cycles of individual burrows may be caused by accumulating detritus or decreasing stability with increasing burrow age. Alternatively, burrow fidelity may presuppose pair fidelity which may also explain the observed restricted burrow reuse duty cycles. A consequent next step would be to extend our within‐colony approach to other colonies and compare the ecological circumstances under which bee‐eaters reuse breeding burrows.     

Burrow construction and behavior of tilefish,Lopholatilus chamaeleonticeps,in Hudson Submarine Canyon

Synopsis During 22 daylight submersible dives in August 1979 numerous juvenile and adult tilefish, Lopholatilus chamaeleonticeps, were observed in and around vertical burrows in the clay substrate of portions of Hudson submarine canyon in depths from 110–230 m. The size and shape of the burrows varied considerably with the smallest juveniles occupying simple vertical shafts in the substrate. Larger fish were found in much larger burrows (up to 4–5 m in diameter and at least 2–3 m deep) that were funnel shaped in cross-section with the upper conical portions containing numerous smaller burrows of associated crabs. The range of burrow sizes observed suggests a regular sequence of burrow construction by tilefish and the associated crabs. Both juvenile and adult tilefish swam into the burrows head first and exited tail first. This behavior, which would preclude the possibility of ambushing prey, and evidence of predation by sharks and other tilefish, suggests that the burrow is a refuge from predators.Tilefish burrows appear to serve as a focus for biological activity. Species associated with the burrows included galatheid crabs, Cancer sp., Acanthocarpus alexandri, Homarus americanus, Heliocolenus dactylopterus and Conger oceanicus. Tilefish may play an important role in structuring outer continental shelf communities. They physically shape their environment and probably have significant biological interactions with the species that associate with their burrows.     

The Contribution of Crab Burrow Excavation to Carbon Availability in Surficial Salt-marsh Sediments

Geomorphology, vegetation and tidal fluxes are usually identified as the factors introducing variation in the flushing of particulate organic matter (POM) from tidal marshes to adjacent waters. Such variables may, however, be insufficient to explain export characteristics in marshes inhabited by ecosystem engineers that can alter the quantity and quality of POM on the marsh surface that is subject to tidal flushing. In this study we evaluated the balance between transfer of buried sedimentary organic carbon (C) to the marsh surface due to crab excavation (measured from the mounds of sediment excavated from burrows) and outputs of C from the surface due to sediment deposition within crab burrows (estimated from sediment deposited within PVC burrow mimics), in a Southwestern Atlantic salt marsh supporting dense (approximately 70 ind m⁻²) populations of the crab Chasmagnathus granulatus. C excavation by crabs was much greater than deposition of C within crab burrow mimics. Per area unit estimates of the balance between these two processes indicated that crabs excavated 5.98 g m⁻² d⁻¹ and 4.80 mg m⁻² d⁻¹ of total and readily (10 d) labile C, respectively. However, sediments excavated by crabs showed a significantly lower content of both total and readily-labile C than sediment collected in burrow mimics. This indicates that ecosystem engineering by burrowing crabs causes a net decrease in the concentration of C in the superficial sediment layers and, thus, an overall decrease in the amount of C that can be washed out of the marsh by tidal action. Incorporating the in situ activities of ecosystem engineers in models of marsh export should enhance understanding of the function of marshes in estuarine ecosystems.     

瑶山鳄蜥洞穴的生态学初步研究

通过对广西昭平鳄蜥的洞穴采用封堵法和坐标法进行研究表明,植被盖度和洞穴之间呈现明显的正相关性.调查中共测量洞穴124个,其深度在18～132cm之间.在鳄蜥活动时间的分配上,洞穴占据了近1/3,故洞穴是其生命活动的一个重要条件.鳄蜥喜欢选择深邃弯曲的石缝、石洞或树洞居住或越冬,洞穴内湿度较大但不被水浸泡,隐蔽程度高、避光,洞口常有较密的植被.     

Activity patterns, feeding and burrowing behaviour of the crab Ucides cordatus (Ucididae) in a high intertidal mangrove forest in North Brazil

Activity patterns, feeding and burrowing behaviour of the economically important semi-terrestrial mangrove crab Ucides cordatus (Ucididae, L. 1763) was studied in a high intertidal Rhizophora mangle forest stand in Bragança, North Brazil. Video observations in the rainy and dry season were conducted over 24 h cycles at different lunar phases to investigate the behaviour of these litter-feeding crabs outside their burrows. During the rainy season, crabs stayed inside their burrows for 79% and 92% of the time during day and night, respectively. Time spent for feeding, burrowing and other activities outside their burrows was significantly longer during the day with 9.9% (night: 1.7%) and at waning and waxing moon with 9% (full and new moon: 0.9%). At neap tides (no tidal inundation) foraging and feeding activities outside burrows were clearly light-dependent, increasing at dawn and decreasing at dusk. Highest activities during daytime relate to the visual localisation of food. During the dry season, crabs spent less time inside burrows at neap tides than during the rainy season (80% and 91%, respectively). However, time spent for feeding activities was similar during both seasons. During almost all observation periods crabs collected leaf litter, but rarely fed on it outside burrows. At neap tides nearly all available litter was collected, suggesting that the U. cordatus population is litter-limited during these times. At spring tides (regular tidal inundation) the surface activity of U. cordatus was tide-dependent. Crabs closed their burrow entrances 2-3 h before flooding and re-emerged as soon as the tide retreated. During the day, burrow maintenance was the second most frequent behaviour after feeding. Agonistic interactions were regularly observed and were mainly related to burrow defence. The mean foraging radius of the crabs was only 19 cm (max: 1 m) underneath high Rhizophora mangle trees where crab densities were high. The results point to a high competition for burrows and show that U. cordatus is territorial. It is concluded that several exogenous factors, in particular light, leaf litter availability, flooding of burrows and the presence of conspecifics are important in controlling the crabs' activity patterns.     

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.     

Burrow morphology and dynamics of mudshrimp in Asian soft shores

Mudshrimps are important soft shore bioturbators but research on the ecology of tropical species has received less attention when compared with their temperate counterparts. The mudshrimp Austinogebia edulis is common on Asian soft shores and lives in burrows for its entire adult life. Epoxy resin casting of A. edulis burrows showed that they were approximately Y-shaped, with an upper U-part and the lower central shaft part. The burrows had two openings extending to the surface; the mean distance between the two openings was 11.0 cm in Hong Kong and 26.4 cm in Taiwan. Openings of the burrows had small chimneys. The tunnels of the burrows were circular, narrow and with a smooth surface (tunnel diameter corresponded to shrimp carapace width). Each burrow was inhabited by a single shrimp and burrows were inter-connected during the mating and reproductive season. Each burrow had four to 12 spherical chambers, which were free of detritus. The chambers were thought to be used for suspension feeding, current generation and as turning points. The depth of burrows was up to 1.1 m. Multivariate analysis on various burrow parameters showed that burrows collected on a mud flat in Taiwan were deeper, had a wider distance between the openings and a larger volume than burrows collected from a sandy shore in Hong Kong, suggesting that burrow architecture is variable between shore types. Burrow architecture, however, did not vary between tidal levels, seasons and shrimp density on the shores in Hong Kong, indicating that the burrows were quite stable within the substratum and were not affected by environmental and biological factors.     

The response of meiofauna and microphytobenthos to engineering effects of fiddler crabs on a subtropical intertidal sandflat

Fiddler crabs are key bioturbators on tidal flats. During their intense bioturbation process, they manipulate large amounts of sediment, altering the physical state of existing materials. We investigated whether different types of sediment bioturbation produced by fiddler crabs modulate meiofaunal assemblages and microphytobenthic content. We hypothesized that sedimentary structures produced by burrowing (the burrow itself and the excavation pellets) and feeding (feeding pellets) generate different microenvironments compared with areas without apparent signs of fiddler crab disturbance, affecting both meiofauna and microphytobenthos, independent of the sampling period. Our results indicate that the engineering effects of burrow construction and maintenance and the engineering effects of fiddler crab foraging modulate meiofaunal assemblages in different ways. Overall, meiofauna from burrows and excavation pellets was more abundant and diverse than at control sites, whereas feeding pellets contained poor meiofaunal assemblages. By contrast, only foraging effects were detected on microphytobenthos; independent of the sampling period, Chl a and phaeopigment content were higher in the feeding pellets, but similar among burrows, excavation pellets and control sites. The present study demonstrates that the different engineering effects of fiddler crabs are an important source of habitat heterogeneity and a structuring agent of meiofaunal assemblages on subtropical tidal flats.     

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     

Burrow structure and use in the sand fiddler crab, Uca pugilator (Bosc)

Uca pugilator, the sand fiddler crab, constructs two kinds of burrows in protected, sandy upper-intertidal and supratidal substrates on the west coast of Florida. Temporary burrows are built and used as a refuge by non-breeding crabs during high tide periods and at night when crabs cease feeding in the intertidal zone. Breeding burrows are constructed and defended by courting males and are the site of mating, oviposition and the incubation of eggs by females. Up to three ovigerous females may be accommodated in a single breeding burrow, each female sequestered in a separate terminal chamber. The construction and defence of burrows specialized for breeding may be an adaptive response by males to the preferences females exhibit when selecting a breeding site.     

The validity of burrow counting in estimating the densities of Chiromantes dehaani and Ilyoplax deschampsi in tidal flat at Yangtze Estuary

It has been confirmed that the crabs play significant roles in the structure and function of coastal wetland ecosystems, such as mangroves and salt marshes. However it is not easy to estimate the abundance and density of burrowing crabs effectively, thus a further understanding of roles of crabs in these ecosystems has been lagged. Some studies have discussed the suitability of several census techniques, such as burrow counting method in estimating crab density in mangroves. The validities of burrow counting method and other census techniques in estimating crab density, however, has not been tested in salt marshes, especially where vegetation are dense. In this study, we tested the validity of burrow counting method in estimating the densities of Chiromantes dehaani and Ilyoplax deschampsi in tidal flat with dense vegetation of Phragmites australis and Zizania aquatica at Yangtze Estuary through comparing densities estimated by the burrow counting method and the excavation. Burrow counting averagely underestimated the density of C. dehaani by 15% and the degree of underestimation varied among vegetations and habitats (from an overestimate by 23% to underestimate by 41%). Burrow counting averagely overestimated the density of I. deschampsi by 43% and the degree of overestimate varied from 0% to 133% depending on the vegetations and habitats. The percentage of occupied burrows and the number of crabs sharing one burrow were important factors influencing the validity of estimating crab density through burrow counting method.