Intertidal burrows of the air-breathing eel goby, <Emphasis Type="Italic">Odontamblyopus lacepedii</Emphasis> (Gobiidae: Amblyopinae)

Odontamblyopus lacepedii inhabits burrows in mudflats and breathes air at the surface opening. Investigations of the intertidal burrows using resin casting demonstrated a highly branched burrow system. The burrows are composed primarily of branching patterns of interconnected tunnels and shafts that communicate into two to seven surface openings. Bulbous chambers (i.e., dilated portions of the burrow) at branching sections of the tunnels or shafts are common features of the burrow. The presence of these chambers accords the fish adequate space to maneuver inside the burrow, and thus constant access to the surface. The combination of all burrow characteristics and previously reported variability in air breathing patterns are ostensibly of selective value for aerial predator avoidance during air breathing in O. lacepedii.     

Burrowing behaviour in the crayfish, Cambarus diogenes diogenes girard

The crayfish, Cambarus diogenes diogenesGirard (1852), spends most of its life cycle in individually constructed underground burrows. The architectural behavioral patterns and sequences with which adult C. d. diogenes excavate an underground chamber were evaluated. Two motor patterns (Pushing and Carrying) and three burrow stages (shallow depression, angular pit, and burrow with two openings) were identified. During the development of burrowing behaviour in juveniles, a third motor pattern (Fanning) occurred. While the three motor patterns are functional soon after hatching, crayfish may learn to orient the Carrying motor pattern for the most efficient excavation of a stage-3 burrow with two openings. The ground-water level determined the final structure of a burrow.     

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.     

Burrow structure and foraging costs in the fossorial rodent,Thomomys bottae

Summary A model for calculating the energy cost of burrowing by fossorial rodents is presented and used to examine the energetics of foraging by burrowing. The pocket gopher Thomomys bottae (Rodentia: Geomyidae) digs burrows for access to food. Feeding tunnels of Thomomys are broken into segments by laterals to the surface that are used to dispose of excavated soil. Energy cost of burrowing depends on both soil type and on burrow structure, defined by the length of burrow segments, angle of ascent of laterals, depth of feeding tunnels, and burrow diameter. In a desert scrub habitat, Thomomys adjust burrow segment length to minimize cost of burrowing. Observed segment lengths (mean=1.33 m) closely approximate the minimum-cost segment length of 1.22 m. Minimizing energy expended per meter of tunnel constructed maximizes efficiency of foraging by burrowing in the desert scrub. Burrow diameter and cost of burrowing increase with body size, while benefits do not, so foraging by burrowing becomes less enconomical as body size increases. Maximum possible body size of fossorial mammals depends on habitat productivity and energy cost of burrowing in local soils.     

Burrow behaviour,structure and utilization of the amphibious mudskipper Periophthalmus chrysospilos Bleeker, 1853 in the Mekong Delta

Burrows of fishes are important to their creators, but knowledge of burrowing behaviour, structure and utilization are poorly understood. We report the burrowing behaviour of the amphibious mudskipper, Periophthalmus chysospilos, from estuarine and coastal sites within the Mekong Delta (Vietnam). Activities at and around the burrow were observed over 12 months (April 2020 to March 2021). Burrow casts were recovered monthly to determine burrow structure and utilization in this species. Observations revealed that males excavate burrows with their mouths during the ebb tide. Burrows were J-, Y- and U-shaped, with 1–2 openings to the surface and a bulbous egg chamber. The burrow depth (BD) and total length (BL) varied with shape and site, but not season. The BD and BL ranged from 15.1 ± 0.9 to 18.6 ± 0.80 SE cm and from 22.1 ± 1.2 to 25.7 ± 1.0 SE (standard error of mean) cm, respectively. These results provide insights into the burrowing ability and better understand the ecology of these fishes in the Mekong Delta.Running head: Burrow behaviour, structure and utilization of Periophthalmus chrysospilos.     

Hidden burrow plugs and their function in the tiger beetle, Cosmodela batesi (Coleoptera, Cicindelidae)

Tiger beetle larvae excavate and live in underground burrows, whose openings they sometimes plug with soil. This study documents the burrow plugging behavior of the tiger beetle, Cosmodela batesi (Fleutiaux), in the field. We also tested the function of burrow plugs in the laboratory. In the field, C. batesi more frequently made a plug when it rained. Most larvae made plugs inside their burrows (rather than at the soil surface), and the use of an endoscope was necessary to detect these sub-surface plugs. In the laboratory, flooding was simulated by artificially introducing water into specially-made arenas. Water filled the entire burrow when there was no plug, whereas plugged burrows maintained air chambers inside. When a plug was broken with a wire, burrows filled up with water. The burrowing and plugging behavior described in this study is likely an important adaptation of C. batesi to its habitat.     

Seasonal variation of food and feeding in burrowing goby <Emphasis Type="Italic">Parapocryptes serperaster</Emphasis> (Gobiidae) at different body sizes

Diet composition and feeding habits of the burrowing fish Parapocryptes serperaster were investigated on different fish sizes across dry and wet seasons in the Mekong Delta, Vietnam. The gut length was positively related to fish length; the gut length was 1.57 ± 0.30 times the total length, which is in the range for omnivore (1–3). Detritus, algae and copepods were the main food items in the foregut. The diet composition showed seasonal and intraspecific variations in all fish sizes. The diet diversity varied with fish size and the dry-wet season pattern, and small fish had a higher diet diversity than large fish. The diet evenness index and Costello graphic analysis indicate that this goby is a generalist feeder and feeds mainly on detritus, followed by diatoms, and could obtain food from the bottom and the water column. The feeding intensity of P. serperaster was higher in the wet season than in the dry season, but was not significantly affected by fish size. The P. serperaster fed on Navicula spp. in the wet season, but on Nitzschia spp. in the dry season. The understanding of food and feeding habits of P. serperaster contributes to our knowledge on feeding adaptation of small-bodied bottom-dwelling gobies to the mud flat habitats in tropical monsoonal regions.     

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.     

Division of labor in the monogamous goby,Valenciennea longipinnis, in relation to burrowing behavior

Feeding and burrowing behavior of the monogamous gobiid fish,Valenciennea longipinnis, were studied on the coral reef at Sesoko Island, Okinawa, Japan. These fish usually live in pairs, the male and female feeding in close proximity to one another upon benthic animals and constructing several burrows cooperatively for purposes of shelter or spawning. Paired females fed more and burrowed less frequently than their mates. Because burrow maintenance was mostly conducted by the latter, the paired females performed work much less frequently than solitary females. Thus, the paired females may be able to allocate more energy toward egg production. The division of labor related to burrowing behavior in this species may be an effective way to increase reproductive success for both sexes. Moreover, the fameles burrowed even less frequently when paired with larger males, probably because burrowing ability may be correlated with mouth size in males. This is a likely reason for the preference of females to mate with larger males.     

Is communal burrowing or burrow sharing a benefit of group living in the lesser cavy <Emphasis Type="Italic">Microcavia australis</Emphasis>?

Burrow systems play an important role in the life of rodents in arid environments. The objectives of this study were to examine the hypothesis that group living is beneficial to the semifossorial rodent, and determine whether Microcavia australis (Geoffroy and d’Orbigny, 1833) burrows communally and/or shares burrow systems. I related the structure of burrow systems to the number of cavies inhabiting them, in two habitats with different soil hardness and different plant cover (El Leoncito and Ñacuñán). El Leoncito has a harsh climate, with lower plant density and softer soil than Ñacñuán. A total of 18 burrow systems were characterized at Ñacuñán, and 12 at El Leoncito. Social groups at El Leoncito have a higher number of individuals than at Ñacuñán, but the structure of burrow systems in softer soil is narrower (small area size), with fewer holes, less slope and depth of galleries, and with no relationship between the number of holes and burrow area. Therefore, considering the development of the burrow system as an indicator of the cost of burrowing, I conclude that communal burrowing to reduce the energetic cost of burrowing per capita is not the primary cause of cavy sociality. M. australis were not active diggers, because digging behaviour was rarely recorded at either site. Burrow systems of cavies persisted over the years of study, occupied by the same cavies and new offspring, and digging new burrow systems and tunnels was a relatively rare event at both sites. Under the burrow-sharing hypothesis, sociality could prevail in M. australis that regularly dig to build and maintain a burrow system which they use for a long time.     

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.     

The Tactile Communication between Cryptocentrus steinitzi (Pisces,Gobiidae) and Alpheus purpurilenticularis (Crustacea,Alpheidae)

The tactile alarm system between the symbiotic goby Cryptocentrus steinitzi and its burrowing shrimp partner Alpheus purpurilenticularis was investigated by underwater observations in the northern Red Sea. Warning signals by the goby which elicit the retreat of the shrimp into its burrow consist mainly of rapid tail flicks transmitted to the shrimp through its long antenna. No warning signals are given without that contact. The daily rhythm of the antennal contacts was described. Warning signals are emitted by the goby in a selective manner only in response to the approach of certain species of fish to the burrow entrance. The response of the shrimp to warning signals was described. The goby-shrimp communication system was used to study predator recognition in a series of controlled experiments. The sequence of the acts of the goby and shrimp was analyzed.     

Sociality in New World hystricognath rodents is linked to predators and burrow digging

The importance of predation and burrow digging in explainingthe evolution of sociality is generally unclear. We focusedon New World hystricognath rodents to evaluate three key predictionsof the predation hypothesis. First, large-bodied surface-dwellingspecies will be more vulnerable because they are more detectable;thus sociality should be associated with body size. Second,surface-dwelling, diurnal species would be more vulnerable topredators than nocturnal species; thus sociality should be associatedwith the evolution of diurnality. Third, species living in openhabitats will be more vulnerable; thus sociality should evolvein species living in open habitats. Regarding the importanceof burrows, we tested if species that dig burrows can benefitfrom communal labor; thus, sociality should be associated withburrow digging. All traits had significant phylogenetic signal,thus comparative analyses should explicitly address this. Ina comparative analysis on independent contrasts we found thatsociality was correlated with body size (larger species weremore social), diurnality (diurnal species were more social),and burrowing (burrowing species were more social), but we foundno effect of overhead plant cover of habitat on sociality inhystricognath rodents. Somewhat different results were foundwhen we analyzed the raw data. Taken together, our results providesupport for a link between predation risk, burrow digging, andsociality in this group.     

A comparison of crayfish burrow morphologies: Triassic and Holocene fossil,paleo‐ and neo‐ichnological evidence,and the identification of their burrowing signatures

The architectural and surficial morphologies of crayfish burrows from the Upper Triassic Chinle Formation and Holocene sediments were compared in order to determine: 1) if Triassic burrows could truly be attributed to crayfish activity; 2) how comparable the burrowing mechanisms are; and 3) whether or not a common set of burrowing signatures could be identified for both ancient and modern freshwater crayfish. Materials used in this study include burrows from the members of the Upper Triassic Chinle Formation, casts of modern burrows constructed by Procambarus clarkii Hobbs and Procambarus acutus acutus (Girard) in the laboratory, and casts of naturally constructed modern burrows of Cambarus diogenes di‐ogenes (Girard).

Triassic and Holocene crayfish burrow morphologies exhibit simple to complex architectures, varying degrees of branching, chamber, and chimney development. They also exhibit relatively textured surficial morphologies (bioglyphs) such as scrape and scratch marks, mud‐ and lag‐liners, knobby and hummocky surfaces, pleopod striae, and body impressions. Holocene crayfish construct distinctive burrows due to their conservative limb arrangement, functional morphology, and behavior with respect to environmental stimuli. Similarities between Holocene and Triassic crayfish burrows suggest that extant and Triassic crayfish employed identical burrowing mechanisms. Features of the surficial and architectural morphologies impart a distinctive signature to burrows of both ancient and modern freshwater burrowing crayfish.

Burrowing signatures of crayfish can be used to identify new and previously misinterpreted continental trace fossils. These are useful in studies of the paleohydrogeology, paleoclimatology and paleoecol‐ogy of burrow‐bearing deposits.     

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.     

Burrow architecture and digging activity in the Cape dune mole rat

While females are traditionally thought to invest more time and energy into parental care than males, males often invest more resources into searching and displaying for mates, obtaining mates and in male–male conflict. Solitary subterranean mammals perform these activities in a particularly challenging niche, necessitating energetically expensive burrowing to both search for mates and forage for food. This restriction presumably affects males more than females as the former are thought to dig longer tunnels that cover greater distances to search for females. We excavated burrow systems of male and female Cape dune mole rats Bathyergus suillus the, largest truly subterranean mammal, to investigate whether male burrows differ from those of females in ways that reflect mate searching by males. We consider burrow architecture (length, internal dimensions, fractal dimension of tunnel systems, number of nesting chambers and mole mounds on the surface) in relation to mating strategy. Males excavated significantly longer burrow systems with higher fractal dimensions and larger burrow areas than females. Male burrow systems were also significantly farther from one another than females were from other females' burrow systems. However, no sex differences were evident in tunnel cross-sectional area, mass of soil excavated per mound, number of mounds produced per unit burrow length or mass of soil excavated per burrow system. Hence, while males may use their habitat differently from females, they do not appear to differ in the dimensions of the tunnels they create. Thus, exploration and use of the habitat differs between the sexes, which may be a consequence of sex differences in mating behaviour and greater demands for food.     

Ecological Predictors of Range Areas and Use of Burrow Systems in the Diurnal Rodent, Octodon degus

Variation in animal space use patterns may be linked to numerous ecological factors affecting survival and reproduction. We examined the relationship between ecology and above‐ and below‐ground components of space use by Octodon degus, a semi‐fossorial rodent in Chile. We monitored the daytime minimum convex polygon and adaptive kernel range areas of 26 individuals and determined the number of burrow systems used by degus during night‐time radiotelemetry and trapping of burrow systems on two study grids at Rinconada de Maipú, a semi‐arid Matorral in central Chile. We quantified food biomass, soil hardness, distance to overhead vegetative cover, and density of burrow openings at putative nest burrows. Degus living on the grid with more shrub cover had larger range areas than degus living on the grid with less cover. The range areas of degus decreased with increasing distance from overhead vegetative cover. There was a weak (but statistically significant) negative relationship between the number of burrow systems used by degus and the distance to vegetative cover and density of burrow openings at burrow systems. Male and female degus had similar range areas. Our results suggest that overhead cover decreases the risk of predation to male and female degus. Degus probably balance the benefits of numerous burrow openings (reduced predation risk) with time and energy requirements of burrow construction and maintenance. Models of space use that consider the effect of multiple ecological variables should measure different dimensions of space use.     

Strategies of burrowing in soft muddy sediments by diverse polychaetes

Muddy sediments are elastic solids through which morphologically diverse animals extend burrows by fracture. Muddy sediments inhabited by burrowing infauna vary considerably in mechanical properties, however, and at high enough porosities, muds can be fluidized. In this study, we examined burrowing behaviors and mechanisms of burrow extension for three morphologically diverse polychaete species inhabiting soft muddy sediments. Worms burrowed in gelatin, a transparent analog for muddy sediments, and in natural sediments in a novel viewing box enabling visualization of behaviors and sediment responses. Individuals of Scalibregma inflatum and Sternaspis scutata can extend burrows by fracture, but both also extended burrows by plastic deformation and by combinations of fracture and plastic deformation. Mechanical responses of sediments corresponded to different burrowing behaviors in Scalibregma; direct peristalsis was used to extend burrows by fracture or a combination of plastic deformation and fracture, whereas a retrograde expansive peristaltic wave extended burrows by plastic deformation. Burrowing speeds differed between behaviors and sediment mechanical responses, with slower burrowing associated with plastic deformation. Sternaspis exhibited less variability in behavior and burrowing speed but did extend burrows by different mechanisms consistent with observations of Scalibregma. Individuals of Ophelina acuminata did not extend burrows by fracture; rather individuals plastically deformed sediments similarly to individuals of the related Armandia brevis. Our results extend the range of natural sediments in which burrowing by fracture has been observed, but the dependence of burrow extension mechanism on species, burrowing behavior, and burrowing speed highlights the need for better understanding of mechanical responses of sediments to burrowers.     

Small- and large-scale effect of the SW Atlantic burrowing crab Chasmagnathus granulatus on habitat use by migratory shorebirds

Here we address the question of whether the presence of the burrowing crabs Chasmagnathus granulatus affects small- and large-scale habitat use by migrant shorebirds. This crab is the dominant species in soft bare sediments and vegetated intertidal areas along the SW Atlantic estuaries (southern Brazil 28°S to the northern Argentinean Patagonia 42°S). They generate very extensive burrow beds in soft bottom intertidal areas. Our information shows that this burrowing crab affects the small-scale habitat use by shorebirds, given that shorebirds never walk through the funnel-shaped entrances of burrows. Given that crab burrow entrances occupy up to 40% of the intertidal area, there is a large decrease of available shorebird habitat in crab beds, restricting their activity to the spaces between the burrows. The southern migratory shorebird Charadrius falklandicus maximize the use of these areas by foraging closer to the burrows than the other bird species. Neotropical migrants, such as Calidris fuscicollis, Pluvialis squatarola and Tringa melanoleuca, used foraging paths that tended to maximize the distance from burrows, especially the distance to larger burrows. A field experiment showed that this was not necessarily due to a decrease in the availability of polychaetes near the crab burrows. A combination of landscape measurements and satellite images showed that crab beds covered up to 40% of the intertidal area of the Mar Chiquita coastal lagoon (37°40′S, Argentina), and nearly 100% of the intertidal area of the Bahia Blanca estuary (38°48′-39°25′S, Argentina). These two estuaries are located along the migratory flyway of Neotropical migratory shorebirds, but the Bahia Blanca estuary (area∼110,000 ha) shows a much lower shorebird diversity than Mar Chiquita (area∼4500 ha). The most common species in Bahia Blanca is the two-banded plover C. falklandicus, the species least affected by crabs at Mar Chiquita and which prefers to use high-density crab areas as foraging sites. The oystercatcher Haematopus palliatus was also most abundant in high-density crab areas, but they used these areas for resting. The abundances of preys varied during the study period and between the crab density areas, indicating that the use of these areas by birds is independent of crab density. However, burrowing crabs affect the depth distribution of polychaete and thus their availability to shorebirds. We suggest that this shorebirds-burrowing organism interaction could be generalized for other intertidal estuarine habitats.