What determines the way of deposition of excavated soil

Subterranean rodents continuously extend their burrow systems primarily in search of food, which has an important impact on the ecosystem in which they live. Excavated soil may be pushed either into aboveground mounds or into tunnels underground. Factors affecting the amount of burrowing and the preference of aboveground or underground soil deposition are, nevertheless, little known. We investigated the influence of food supply, soil hardness, and the animal’s body mass on the mode of soil deposition in ten burrow systems of free ranging silvery mole-rats Heliophobius argenteocinereus Peters, 1846. In each burrow system, we estimated the volume of backfilled tunnels and the volume of soil deposited aboveground. The highest amount of variation in these parameters was explained by the interaction of food supply and soil hardness. The ratio of the volume of backfilled tunnels to the volume of mounds was not significantly dependent on any of the explanatory variables. The proportion of backfilled tunnels decreased with the increasing volume of the complete burrow system. We propose that both low food supply and soft soil lead to an increased amount of burrowing, which results in a larger volume of soil deposited both above ground and under ground over a given period of time.     

Accurate quantification of the influence of benthic macro- and meio-fauna on the geometric properties of estuarine muds by micro computer tomography

This paper describes the novel application of high resolution micro computer tomography (microCT) to the quantification of the properties of marine biogenic structures. CT scanning has been used to examine sediments in the past but the resolution of most previous techniques has been dependent upon commercial medical CT scanners which only have a slice thickness of ≥ 0.625 mm. In addition adequate software has not previously been available to rapidly quantify all the properties of biogenic structures. The microCT technique developed here used a standard core sample of estuarine sediment and new software was developed to calculate the axial variation of the following burrow parameters: number, diameter, volume, surface area and density. The increased resolution has resulted in the first quantification of meiofaunal burrow structures.A test core has shown, as an example, that the total volume of burrows created by macrofaunal organisms decreased from 827 mm³, within the top 15 mm of the core, to 204.2 mm³ at a depth 60 -75 mm within the core. Total burrow surface area decreased from 1883 mm² to 512 mm², for these depth ranges, respectively and burrow diameter ranged from 2.37-2.58 mm, remaining fairly constant between depths. Meiofaunal burrow structures decreased from 1.3-0.1 mm³ within the top 6 mm of the core with burrow surface area decreasing from 33.52-3.4 mm². Again, burrow diameter remained relatively constant, ranging from 0.23-0.25 mm.Quantification to this resolution is required to identify the impact of infaunal organisms on factors such as oxygen penetration, vertical and horizontal (across burrow walls) gradients in redox conditions and chemical/nutrient speciation and flux. The quantification of these burrow properties will improve the ability to examine the interrelationships between chemical, physical and biological processes and their role in ecological functioning. The present study indicates that there is potential for further development of this software to allow more detailed analysis of burrow structures and surface features including parameters such as burrow length, shape and sediment surface roughness.     

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.     

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.     

Passive irrigation and functional morphology of crustacean burrows in a tropical mangrove swamp

Flushing measurements and a resin cast of a burrow inhabited by Sesarma messa and Alpheus cf macklay were taken from a Rhizophoraspp. forest. The burrow had 9 openings and occupied a swamp surface area of 0.64 m². Passive irrigation of the burrow was investigated by recording change in conductivity of burrow water in a chamber 45 cm below the swamp surface during tidal inundation of the swamp. The chamber was completely flushed within approximately one hour, i.e. by a single tidal event. Burrow morphology was determined by means of resin casting. The investigated burrow was of discrete structure, with an overall depth of 1.2 m and a total volume of 68 l, i.e. ca. 9% of the volume of swamp soil. The below ground surface area of chambers and tunnels was 3.8 m². The mean and maximum chamber/tunnel diameter was 7 cm and 11 cm respectively. The soil in the close vicinity of the burrow was extensively penetrated by roots, and any two parts of the burrow were located no further than 20 cm away from each other. By reducing diffusion distances within the soil and by being well flushed, the burrows provide an efficient mechanism for removal of excess salt accumulated in the soil around mangrove roots due to exclusion.     

哈尔滨郊区人为鼠疫疫源地蚤类种群动态分析

1982～1999年对黑龙江省哈尔滨郊区人为鼠疫疫源地达乌尔黄鼠Spermophilus dauricus巢蚤、体蚤、洞干蚤指数和染蚤率进行了调查和分析。共获蚤9种,其中方形黄鼠蚤松江亚种Citellophius tesquorum sungaris是优势种(89.39%),其次为二齿新蚤Neopsylla bidentatiformis (10.37%)。3类蚤指数、染蚤率的均值差异均显著(P<0.01)。巢蚤与体蚤指数相关显著(P<0.05)。巢蚤指数∶体蚤指数∶洞干蚤指数≈650∶140∶1; 巢染蚤率∶体染蚤率∶洞干染蚤率≈165∶88∶1。     

Home-Range Dynamics in a Solitary Subterranean Rodent

Despite an important role of subterranean rodents as ecosystem engineers, their belowground mobility is poorly documented. It is supposed that their underground burrow systems, once established, are relatively stable because of high-energy costs of digging. We chose the silvery mole-rat, Heliophobius argenteocinereus (Bathyergidae, Rodentia) from mesic Afrotropics as a representative of solitary subterranean rodents to investigate how, and how fast these rodents process their established burrow systems. We combined radio-tracking of individual animals with subsequent mapping of their burrow systems, and we developed a new method for assessing the rate of burrowing. Mole-rats continuously rebuilt their burrow systems; they excavated approx. 0.7 m of new tunnels per day and backfilled on average 64% of all tunnels. On average, every 32 d they established a new nest. They often completely backfilled newly excavated peripheral burrows, while other parts of their burrow systems were more permanent. Their home-ranges were dynamic and continuously shifted in space. Burrow system processing continued even in the advanced dry season, when soil is difficult to work.     

Environmental factors affecting the spawning burrow selection by the gobiid Valenciennea longipinnis

Spawning burrow selection by the longfinned goby Valenciennea longipinnis was studied in the near-shore moat on coral reefs, Okinawa, Japan. The gobies make several burrows within their home range, and spawn in one of them. To examine the factors important for spawning burrow selection three characteristics were investigated: current strength, burrow length and effect of underground water on the burrow. Among the burrows, pairs tended to spawn in a larger burrow irrespective of their body sizes. Most of the other non-spawning burrows were too small for a pair to stay together, because hard substrata may prevent the fish from excavating and shaping the burrow as they like. Moreover, pairs preferred to spawn in burrows where the underground water was oozing out, probably because the male's parental burden will decrease due to the higher dissolved oxygen concentration in such burrows. Although current strength may affect a water-exchange in a V. longipinnis burrow in relation to water-exchange function of a mound, it did not affect the spawning burrow selection because of the smaller velocity difference among the burrows relative to the daily fluctuation of tidal current.     

Recognition of burrow's olfactory signature in blue petrels, Halobaena caerulea: an efficient discrimination mechanism in the dark

Previous work has shown that blue petrels need olfaction to home. We investigated whether they also recognize an olfactory signature of their own nest. We performed T-maze experiments in which maze arms were connected with the subject bird's burrow and with the burrow of a conspecific neighbour. Of 23 birds, 16 were able to recognize the arm leading to their own burrow. In a second experiment, we positioned the maze in front of the subject's burrow but the maze arms were closed and did not enter the burrow. Consequently, no burrow odours could be sensed by the bird. In this case, 85% of birds (17 of 20) failed to choose, suggesting that petrels were not motivated to choose by positional cues in the absence of odour cues. We explored this idea further by performing a homing experiment whereby homing birds had to relocate an artificially displaced burrow entrance. Blue petrels homed, ignoring the natural burrow entrance and using the new artificial one. The ability to smell their own burrow allows blue petrels to return to the colony at night and to find the correct nest.     

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.     

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     

Use of burrow entrance flaps to minimise interference to Chatham petrel (

The Chatham petrel (Pterodroma axillaris) is an endangered species, restricted to a single population on South East Island, Chatham Islands. The key threat to breeding success is loss of chicks as a result of interference by broad-billed prions (Pachyptila vittata) prospecting for burrows for their oncoming breeding season. The effectiveness in decreasing interference using an artificial burrow entrance flap was investigated. The flap exploits behavioural differences between the species. Chatham petrels have a high incentive to push through a flap due to their investment in their burrow and chick, while prospecting prions are influenced by ease of access when searching for potential burrows. This trial found 90% of Chatham petrels entered their burrows through the artificial flap. Flaps acted as barriers to broad-billed prions, where 22% entered the burrow through the flap (P <0.01) compared to the control burrows. Artificial burrow flaps have the potential to provide a low cost, low labour strategy for protecting the known breeding population of Chatham petrels.     

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     

The underground life of the oriental mole cricket: an analysis of burrow morphology

The underground life of the oriental mole cricket Gryllotalpa orientalis has been investigated by studying the structure of its burrows under different environmental situations and in different seasons. The different uses of different burrow types and their advantages and disadvantages have been examined. The total length, number of tunnels and combination of burrow types varied from a simple tunnel to a more complex one with branches at various angles to the surface, burrow types being divided roughly into shallow horizontal or deep vertical ones. In horizontal burrows, the branching structure was well developed in various directions. It is notable that the vertical burrows of G. orientalis were occupied by only one individual. Both vertical and horizontal burrows were used for foraging: vertical burrows for plants with subterranean stems and horizontal burrows for creeping plants. Vertical burrows were also used for hiding from predators, resting, moulting and overwintering, whereas horizontal burrows were used for escaping from predators and as mating routes. Egg chambers were constructed beside horizontal burrows, and calling burrows were constructed as part of horizontal burrows. Based on their current requirements, mole crickets continuously modify their burrow structures or change burrowing sites.     

Influence of sediment characteristics on density and distribution of Ocypodoid crab burrows (superfamily: Ocypodoidea) along the coastal areas of Pakistan

Crabs belong to the superfamily Ocypodoidea are a significant component of benthic fauna and considered as ecosystem engineers because of their dynamic role as an active burrower in mangrove and estuarine environment. The current investigation was to evaluate the crab burrow density, diameter and total area of burrow opening along the coast of Pakistan. The variations in burrow properties and their relation to sediment characteristics were also evaluated to recognize the most influencing variables of sediments that effects on crab burrows. All crab burrow and sediment characteristics differed significantly (p < 0.05) among the monitoring sites. Regression analysis showed that crab density was significantly correlated with burrow density (P < 0.001). Moreover, burrow density was noticed significantly greater (p < 0.05) than crab density. Pearson correlation analysis reveals that moisture, porosity, organics, sand and mean grain size observed as most influencing the features of sediment to determine the ecological functioning of crab burrows in mangrove and mudflats of Pakistan.     

The activity of a subterranean small mammal alters Afroalpine vegetation patterns and is positively affected by livestock grazing

Subterranean rodents can act as ecosystem engineers by shaping the landscape due to soil perturbation and herbivory. At the same time, their burrow density is affected by environmental conditions, vegetation and anthropogenic factors. Disentangling this complex interplay between subterranean rodents and their environment remains challenging. In our study, we analysed the interplay of abiotic conditions, vegetation patterns and human land-use and the burrow density of the giant root-rat (GRR; Tachyoryctes macrocephalus), a subterranean rodent endemic to the Afroalpine ecosystem of the Bale Mountains in south-east Ethiopia. Specifically, we examined the effects of GRR on plant species richness and vegetation cover and vice-versa, and how these reciprocal effects might be modulated by temperature, habitat wetness and grazing. Our results showed that increasing GRR burrow density led to decreased vegetation cover, and that effects of GRR on vegetation cover were slightly stronger than vice-versa. Considering the reciprocal causation models, we found that increasing plant species richness led to increased GRR burrow density, while GRR burrow density decreased as vegetation cover increased. Increases in habitat wetness and livestock grazing intensity also directly led to increased GRR burrow density. Our results stress the importance of subterranean ecosystem engineers on vegetation and highlight the vulnerability of these complex interactions to human activity.     

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.     

Microvertebrates preserved in mammal burrows from the Holocene of the Argentine Pampas: a taphonomic and paleoecological approach

Microvertebrates are a major component of many assemblages recovered from the Quaternary of the Argentine Pampas. The main goal of this paper is to analyse the taphonomic history of a Holocene microfossil bonebed, recovered from the infilling of a burrow. Evidences suggest the plains vizcacha Lagostomus maximus as the putative producer of the burrow. The assemblage includes individuals belonging to different taxa of mammals (marsupials and rodents) and reptiles (snakes). Taphonomic features suggest that the accumulation inside the burrow was related to flooding processes in the plain. The burrow was a natural trap that favoured the accumulation and preservation of remains corresponding to individuals from different sources. According to the taphonomic evidence, some individuals (Lagostomus maximus, Lestodelphys halli and Serpentes indet.) died inside the burrow, whereas others (Microcavia australis, Reithrodon auritus and Ctenomys sp.) died outside the burrow, and after a time of being exposed on the surface their remains were transported by surface run-offs into the burrow. The record of Lestodelphys halli and Serpentes indet. in the burrow produced by Lagostomus maximus could be related to a circumstantial use. Mammal burrows are a significant taphonomic mode for the late Cenozoic of the Argentine Pampas.     

Activity periods and energetic reserves of the brown lemming in northern Alaska

Radiotelemetry provided data on the activity periods of brown lemmings Lemmus sibiricus in northern Alaska. Activity inside the burrow and inactivity outside the burrow usually occurred in short episodes (<3 min), whereas periods of activity outside the burrow and inactivity inside the burrow were more prolonged and appeared to be associated with foraging (outside) and sleeping (inside). Energetic reserves for lemmings entering a burrow consisted of body fat and undigested gut contents, which allowed minimal survival times of 8.6 ± 2.3 h (mean ± 1 S.E.). Nevertheless, lemmings usually left their burrows within 40 min of entering, at which time their stomachs would be at least two-thirds empty. Activity patterns of lemmings appear to change in response to predators, weather and nutritional requirements. We argue that lemmings seek to minimize the time spent foraging rather than to maximize the net energy gain while foraging.     

The effects of location and design on the diffusion of respiratory gases in mammal burrows

To investigate the constraints placed on the location and design of mammal burrows by the resident mammal's need for an adequate exchange of respiratory gases with the free atmosphere, we constructed several simple mathematical models for the steady-state diffusion of these gases in sterile burrow-soil systems. In this exchange, diffusion through the soil is of prime importance. Openings of narrow tunnels further than three body lengths from a mammal have a negligible effect on its respiratory microenvironment. Since only a short length of a narrow tunnel around the mammal is of importance in this exchange we may confine attention to design and siting criteria for a discrete chamber containing the mammal.The porosity of the soil in which a burrow chamber is sited and the volume of the burrow chamber have strong and moderate effects respectively on the rate of gas exchange between a resident mammal and the free atmosphere. The depth of the burrow chamber, beyond two chamber diameters, has only a weak effect on this transfer. Soil temperature within the thermoneutral zone of the resident mammal has a weak effect on this transfer, but below the thermoneutral zone, where temperature modifies the rate of consumption (production) of respiratory gas, the effect is strong. Concentrations of respiratory gas in the burrow chamber approach free-atmosphere values when soil porosity, soil temperature, and chamber volume increase and burrow depth decreases.Large mammals are more restricted in the design and siting of burrows than small mammals. Our models indicate that normothermic eutherian mammals with masses much in excess of 0·5 kg are precluded from an indefinite occupation of deep burrows in most field situations. In considering the limitations to our models, several avenues for expanding a mammal's respiratory space are suggested.