Burrow utilization by yellowedge grouper,Epinephelus flavolimbatus,in the northwestern Gulf of Mexico

Synopsis Submersible dives were made on a site in the Gulf of Mexico 160 km southeast of Galveston, Texas in September 1984. Both yellowedge, Epinephelus flavolimbatus, and snowy grouper, E. niveatus, were observed utilizing shelter around rock ridge habitats. The yellowedge grouper also sought shelter within three types of burrows cut into soft sediment. Many of these burrows were significant excavations consisting of large trenches 7–8 m long, 2–3 m wide, and 1–1.5 m deep. Burrows were found in depths from 265 to 290 m. Tilefish, Lopholatilus chamaeleonticeps, also occur at this site, usually inhabiting the characteristic vertical burrows already described for this species. In four daytime submersible transects covering a linear distance of over 13000 m, we observed a total of 66 yellowedge groupers. Twenty-five were in burrows, 39 among rocks, and two over open bottom. It is suggested that this species may have an advantage over congeners that utilize only rocky habitat for cover. It may also compete for shelter with tilefish at depths where the two species overlap.Contribution No. 696, Harbor Branch Foundation, Inc. and Contribution No. 733, The University of Texas Marine Science Institute.     

Parental care and reproductive behavior of the clown goby, <Emphasis Type="Italic">Microgobius gulosus</Emphasis>, with observations on predator interactions

Describe reproductive behavior and mating system of the clown goby from field observations. Clown gobies exhibit a loosely haremic mating system. Pairs construct burrows at the base of cattails, the roots of which provide structural support and a spawning substrate. Larger males monopolize multiple burrows, each with an individual female. After spawning, males camouflage burrow entrances with sand and females brood developing young for 4 days. Males continue to guard the covered nests in 50% of observed brooding periods. Burrows are also used as shelter from predators. Both sexes confront intruders but only males exhibit a distinct color response to juvenile blue crabs, Callinectes sapidus, the most significant predator. The male color response appeared to mimic the color of adult blue crabs, a known predator of juvenile crabs, perhaps acting as a deterrent. The presence of the predatory blue crab may require one parent to perform deterrent displays, promoting female care in this mating system.     

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.     

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     

Cost-effectiveness of five burrow fumigants for managing black-tailed prairie dogs

We evaluated the cost-effectiveness of two solid form burrow fumigants (aluminum phosphide and gas cartridges) and three pressurized gas–liquid burrow fumigants (methyl bromide, chloropicrin, and a methyl bromide–chloropicrin mixture) for managing black-tailed prairie dogs (Cynomys ludovicianus). Fifty-two variable-sized plots, including 25 treatment and 25 control burrows, were established within 13 prairie dog colonies in central Nebraska during spring 1989. Each group of 25 treatment burrows was fumigated with one of the five fumigants according to label directions or manufacturer recommendations. All five fumigants reduced burrow activity 95–98%, as measured by a plugged burrow technique. No significant differences in efficacy (P=0.453) were detected among the five treatments. Total costs for materials and labor for the aluminum phosphide and gas cartridges, excluding application equipment, were twice ($75.00 to $96.88 ha⁻¹) the cost of the pressurized gas–liquid fumigants ($37.67 to $41.76 ha⁻¹). Costs for the application equipment were considerably higher for the pressurized materials. Each treatment required labor for burrow plugging, which accounted for 50–75% of the total cost. None of the products tested met all requirements of a proposed selection criteria for fumigants.     

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.     

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.     

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.     

Spatial structure of a leaf-removing crab population in a mangrove of North-Brazil

The leaf-removing decapod crab, Ucides cordatus plays a key role as ecological engineer in Brazilian mangrove ecosystems. We analyzed the spatial distribution of a specific population at two different scales to observe how individual behavior could alter spatial population structure. First, we conducted a spatial point pattern analysis of the burrow entrances and the Rhizophora mangle prop roots on the mangrove floor at a scale of few meters. Secondly, we analyzed at a large scale (10–100 m) the potential effects of surface elevation, light intensity, prop root coverage, species of neighboring tree (R. mangle, Laguncularia racemosa, Avicennia germinans) and pneumatophore density on the size and number of burrow entrances. At the same large scale, we conducted an analysis of clustering of the crabs around the R. mangle trees. At small scale, the burrow entrances, although aggregated around the prop roots, showed a regularly spaced distribution (∼25 cm) signaling an intraspecific competition among the crabs. At large scale, crabs preferred to install their burrows at an intermediate level of surface elevation and prop root coverage, and in R. mangle-dominated areas. At the same kind of habitats, the largest burrows, and thus potentially the largest crabs, were found in higher number than on other habitats. The R. mangle-dominated areas preference was confirmed by an aggregating around R. mangle trees in R. mangle-dominated forest, but only of large individuals in L. racemosa-dominated forest. These observations lead us to the definition of a preferred habitat for U. cordatus. Competition leading to the small-scale regular patterns was proposed as an explanation for exclusion of smaller crabs from preferred habitats seen at large scale. We hypothesize that this preferred habitat might explain at regional scale the variation of U. cordatus importance in Neotropical mangroves.     

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.     

A small sensor for detecting animal burrows and monitoring burrow water conductivity

An electrical conductivity probe for measuring ground conductivity is described. The probe measures bulk ground conductivity in situ and can assist in locating animal burrows on a centimeter scale and in monitoring conductivity of burrow waters over long period of times. It is shown how burrow caves are located by their conductivity contrast relative to the soil. The conductivity of the water in a burrow cave 70cm under the swamp surface has been recorded over 15 days. The conductivity dropped during/after periods of significant rainfall, and rapidly increased during tidal inundation of the swamp. At times with neither freshwater nor saltwater input through the openings of the burrow on the surface, the conductivity slowly increased presumably due to diffusion of salt through the burrow walls. The diffusion constant was estimated to be 2×10^–9m²/s, being comparable to previously determined diffusion constants for diffusion of salt within the substrate.     

Spawning dynamics of orange roughy,Hoplostethus atlanticus,in mid-slope waters of New Zealand

Synopsis The social and reproductive biology of the sand tilefish,Malacanthus plumieri (Malacanthidae), was studied at Glover's Reef, Belize, where this species occurs in colonies over sand-rubble flats. Individuals each occupy a home burrow refuge and a surrounding home range. Home range overlap among adjacent fish of the same sex is low, and individuals defend exclusive use of much of their home range against all conspecifics except mates (i.e., territoriality). Areas defended by males overlap the territories of up to 6 females; and male territory area is positively related to the number of female residents. Males maintain dominance over females within their territories by aggression, including intervention into some female disputes. Females spawn pelagically-dispersed eggs as frequently as every day. Each female spawns near her burrow, almost exclusively with the male whose defended area encompasses her territory (harem polygyny). Tilefish colonies therefore consist of a mosaic of female territories over which adjacent male territories are superimposed. Histological evidence and observation of behavioral sex change in one female revealed thatM. plumieri is capable of protogynous sex reversal. Females did not change sex in response to removal of one male. Occurrence of small transitional fish indicates that the onset of sex change is controlled by factors other than size-related social hierarchies within harems or colonies.     

Size-dependent Mating Behaviours of Male Sand-bubbler Crab,Scopimera globosa: Alternative Tactics in the Life History

Factors leading to the separation of mating behaviours were investigated in the sand-bubbler crab, Scopimera globosa. The crabs mated on the surface (surface copulation, SC) and underground (UC). UC males were large (old) whilst SC males were small (young). Burrowless females bred in the UC males' burrows. These females accepted UC in exchange for access to a burrow. UC occurred much more frequently than SC in the burrow area in which females oviposited. Most SC occurred in the water-saturated area affording a rich diet. SC was accepted by most large and small females in both areas and most UC by small females in the burrow area. SC was an alternative to UC for males in that there was a size dependence between types of copulation. These two mating behaviours involved different degrees of interaction with neighbouring males. Males attempting to carry a female to their burrows for UC were more often disturbed by other males than were males attempting SC. In the interaction for both UC and SC, larger males were likely to resist the disturbances. UC males needed their own burrows, but these burrows were not enlarged before mating. UC males have a higher paternity of eggs than SC males, because SC males' sperm is often displaced by other males. Thus, UC was a behaviour with relatively higher costs and benefits for male crabs than SC behaviour. Alternative mating behaviours in male S. globosa are conditional, and explained by intrasexual interactions and a male life history strategy with a trade-off between growth and reproduction. It is not likely that the size dependence of male mating behaviour is caused by mate preference of females for UC males in the burrow area.     

Ontogenetic shift in susceptibility to predators in juvenile northern abalone, Haliotis kamtschatkana

Predation has been suggested as a major cause of juvenile mortality in benthic marine invertebrates. However, the extent to which juveniles are susceptible to predators is unknown for most species, and it remains unclear to what extent ontogenetic shifts in susceptibility to predators are common among marine invertebrates. This study examined the northern abalone Haliotis kamtschatkana, a species listed as threatened in British Columbia, Canada. Our goals were to characterize the diversity and abundance of species that prey on juvenile abalone and determine if abalone experience an ontogenetic shift in susceptibility to predators. Juvenile H. kamtschatkana were found to be susceptible to a broad variety of predators: 14 of the 37 potential predator species to which we offered juvenile abalone (≤ 28 mm shell length (SL)) consumed at least one juvenile abalone. Four of those species (three crabs and one seastar) consumed ≥ 10% of the juvenile abalone that were offered in the laboratory. These species were present at field sites where abalone are found, indicating that they have the potential to be significant predators of juvenile H. kamtschatkana in the wild. The most abundant predators were small crabs, especially Lophopanopeus bellus (black-clawed crabs) and Scyra acutifrons (sharp-nosed crabs). Juvenile H. kamtschatkana also experienced a pronounced ontogenetic shift in susceptibility to predators. The risk of predation for juvenile H. kamtschatkana decreased rapidly with increasing body size, especially over the 12–13 mm SL size range. Susceptibility remained low beyond 13 mm SL, indicating relatively low and unchanging levels of predation risk once the individual reaches this size. Although abalone are susceptible to several species during the first 1–2 years of life, predator effects on juvenile abalone abundance and microhabitat use may largely be attributable to the influence of only 1 or 2 predator species that can only kill abalone < 13 mm SL.     

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。     

Paradoxical selective feeding on a low-nutrient diet: why do mangrove crabs eat leaves?

Sesarmid crabs dominate Indo West-Pacific mangroves, and consume large amounts of mangrove litter. This is surprising, since mangrove leaves have high tannin contents and C/N ratios that far exceed 17, normally taken as the maximum for sustainable animal nutrition. This paradox has led to the hitherto untested hypothesis that crabs let leaves age in burrows before consumption, thereby reducing tannin content and C/N ratio. We excavated burrows of Neosarmatium meinerti within high-shore Avicennia marina mangroves, and investigated whether burrow leaves had C, N or C/N values significantly different from those of senescent leaves. Leaves were found in <45% of burrows, mostly only as small fragments, and N concentrations and C/N ratios of burrow leaves never varied significantly from senescent leaves. The leaf-ageing hypothesis was therefore not supported. In the field N. meinerti and Sesarma guttatum fed on sediment in 76% and 66-69% of observations, respectively, and on leaves in <10% of observations. Sediments from two A. marina mangroves had a mean C/N ratio of 19.6. Our results, and the literature, show that mangrove leaves are unlikely to fulfil the N requirements of crabs, whether or not leaf ageing takes place. Sediment detritus could be a richer source of N, as shown by lower C/N ratios and regular ingestion by crabs. By fragmenting leaves crabs may be elevating the nutritional quality of the substrate detritus.     

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.     

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.     

Evaluation of the sample size used for the rapid bioassessment of rivers using macroinvertebrates

Experiments were designed to investigate selective predation by medium (40–55 mm carapace width: CW) and large (55–70 mm CW) Carcinus maenas when feeding on four bivalves of contrasting shell morphology. Size-selection was examined by presenting individual crabs with a wide size range of Mytilus edulis, Ostrea edulis, Crassostrea gigas and Cerastoderma edule. Medium-sized crabs preferred mussels 5–15 mm shell length (maximum shell dimension: SL) and cockles 5–10 mm SL, whereas large crabs preferred mussels 15–25 mm and cockles 10–20 mm SL. Crabs generally showed no preference for any particular size of either oyster species. Species-selection was examined by presenting individual crabs with paired combinations of the four bivalves in various proportions. When offered mussels and oysters simultaneously, both size categories of crabs consistently selected mussels, and food choice was independent of prey relative abundance. By contrast, C. maenas selected mussels and cockles as expected by the frequency in which each size category of crab encountered the preferred size ranges of prey. Crab preference clearly paralleled the rank order of prey profitability, which in turn was mainly determined by prey biomass, suggesting that active selection takes place at some point of the predation cycle. Experiments with epoxy resin models showed that initial reluctance of crabs to attack oysters was not associated with the ultimate energy reward. Moreover, they suggest that foraging decisions are partly based on evaluations of overall prey shape and volume, and that the minimum dimension of the shell constitutes an important feature which crabs recognise and associate with prey value.     

Direct evidence of a mesopelagic fish,Melanostigma atlanticum (Zoarcidae) spawning within bottom sediments

Synopsis Adult Melanostigma atlanticum were observed living 15 to 32 cm deep within sediment box cores from 350 m depth in the Laurentian Trough of the Maritime Estuary of the St. Lawrence. The fish were found in fluid pockets or burrows of brown-coloured (oxygenated) silty clay within the anoxic zone of the sediment. In August 1983, four individuals (3 male and 1 female) were recovered from pockets located 15 and 32 cm below the sediment surface. All specimens were greater than 100 mm in length, had empty stomachs, and the female carried no eggs. In July 1985, 6 individuals (1 male and 5 females) were found in a head to tail arrangement within a single burrow at 18–20 cm depth. Three of the females carried eggs, while two appeared to have already released their eggs. A cluster of about 50 large eggs, some of which appeared to have been fertilized, was also found in the burrow. Most of the stomachs were empty, but one contained two copepods, another a proceroid cestode, and others contained between 4–22 parasitic hemiurid trematodes. These observations indicate that burrowing into bottom sediments is important in the reproductive behaviour of M. atlanticum.