Maastrichtian island in the central European Basin—new data inferred from palynofacies analysis and inoceramid stratigraphy

The palynological study and palynofacies analysis supported by size analysis of opaque phytoclasts and diversity indexes for particulate organic matter in stratigraphically well-constrained (inoceramid biostratigraphy) sections is applied in monotonous Upper Cretaceous carbonate-siliciclastic sediments of southern Poland. Integrated data allow for the estimation of the proximity of an uplifted area from the studied sections. For the first time in palynofacies analysis, both Simpson’s Index of Diversity (1 ? D) and Shannon’s index are used for organic matter distribution providing a comprehensive understanding of a proximal–distal trend in a sedimentary basin. Cluster analysis allowed grouping the samples within proximal to distal shelf zones. The size analysis of opaque woody phytoclasts is used to extrapolate the distance from the source area. Palynofacies analysis indicates the existence of an uplifted area (probably connected with “Kukernitz Island”) in the Holy Cross part of the Danish-Polish Trough during the Maastrichtian. The presented results improve contemporary paleogeographical interpretations for this part of the Late Cretaceous central European Basin. The youngest Maastrichtian deposits of the Miechów Synclinorium are described, based on inoceramids which are of early Late Maastrichtian age.     

Specialized shell-breaking crab claws in Cretaceous seas

Here we report on a large brachyuran crab species from the Late Cretaceous of Mexico that has claws indicative of highly specialized shell-breaking behaviour. This crab possessed dimorphic claws (the right larger than the left), armed with several broad teeth, including a curved tooth structure found at the base of the movable finger of the right claw. The curved tooth is similar to the one observed on claws of many living durophagous crabs that use it as a weapon to peel, crush or chip the edges of hard-shelled prey, particularly molluscs. These morphological traits suggest that specialized shell-breaking crab predators had evolved during the Cretaceous, which contradicts previous findings supporting an Early Cenozoic origin for specialized shell crushers within the brachyuran clade.     

Predatory asteroids and the decline of the articulate brachiopods

Various causes, such as increased predation pressure, the lack of planktotrophic larvae, a 'resetting' of diversity, increased competition from benthic molluscs and the decline of the Palaeozoic fauna, have been suggested to explain the failure of the brachiopods to reradiate following the Permo-Triassic mass extinction. Increased predation pressure has hitherto appeared improbable, because typical predators of brachiopods, such as teleostean fish, brachyuran crabs and predatory gastropods, did not undergo major radiation until the late Mesozoic and early Cenozoic. However, new evidence strongly suggests that one important group of predators of shelly benthic organisms, the asteroids, underwent a major radiation at the beginning of the Mesozoic. Although asteroids appeared in the early Ordovician, they remained a minor element of the marine benthos during the Palaeozoic acme of the brachiopods. However, these early asteroids lacked four important requirements for active predation on a bivalved epifauna: muscular arms (evolved in the early Carboniferous); suckered tube feet, a flexible mouth frame and an eversible stomach (all evolved in the early Triassic). Thus radiation of the Subclass Neoasteroidea coincided with both their improved feeding capability and the decline of the articulates. The asteroids were the only group of predators of brachiopods that underwent a major adaptive radiation in the earliest Mesozoic. The asteroids may therefore have contributed to inhibiting a Mesozoic reradiation of the brachiopods. Epifaunal species lacking a muscular pedicle may have been particularly vulnerable. Unlike bivalve molluscs, modern brachiopods show only a limited range of adaptations to discourage asteroid predation. □ Asteroidea, Brachiopoda, evolution, predation, functional morphology.     

Environmental stress and diagenetic modifications in inoceramids and belemnites from the Upper Cretaceous James Ross Basin, Antarctica

Summary New petrographic and isotopic data from inoceramid bivalve shells and belemnite rostra from the lower Campanian and belemnite rostra from the mid-upper Maastrichtian of the Marambio Group, James Ross Basin, Antarctica are presented. Most of the inoceramid data were processed from shell fragments of the large formAntarcticeramus rabotensis (Crame and Luther) at the stratigraphic level marking the extinction of the inoceramids in the James Ross Basin (uppermost early Campanian-basal late Campanian). Standard transmitted light microscopy and cathodoluminescence (CL) studies in thin sections ofA. rabotensis show clear evidence of environmental stress, which is reflected as marked growth breaks in the shell banding of this large inoceramid bivalve. At Redonda Point, CL and the mean oxygen isotopic value (δ¹⁸O=-3.11‰ 3 (PDB); n=11; t°=25.4°C) indicate a varied degree of diagenetic modification, but without any evidence of neomorphism along the prismatic microstructures. Early Campanian belemnite rostra are much less diagenetically modified (at the Brandy Bay section; and the Santa Marta section; δ¹⁸O=-0.50‰ (PDB); n=5; t°=14.0°C and 3 δ¹⁸O=-0.94‰ (PDB); n=21; t°=15.8°C) and are non luminescent 3 except for localized, organic-rich bands. The mean oxygen isotopic value for mid-late Maastrichtian belemnite rostra (at the Seymour Island section; δ¹⁸O=-0.11‰ 3 (PDB); n=5; t°=12.5°C) indicates a substantial drop in the sea-water paleotemperature, suggesting a causal relationship between the early extinction of the inoceramid bivalves in high latitudes of the Southern Hemisphere and the falling sea-water temperature.     

Maria Helena Ribeiro Hessel: Lower Turonian inoceramids from Sergipe, Brazil: systematics, stratigraphy and palaeoecology

Abstract: Lower Turonian inoceramid bivalves are described from the Sergipe Basin in northeastern Brazil, and a palaeoecological analysis of the region is attempted. The principal locality, Retiro 26, comprises a sequence of 35 m of the Cotinguiba Limestone Formation. Various unconformities occur in the sequence. The formation is inferred to have been deposited in an outer shelf environment of a subtropical shallow sea, with oscillating water depth, occasional strong bottom currents and ephemeral reductions of the oxygen level. The inoceramids show some endemism. Two inoceramid associations are recognized: the Mytiloides mytiloides and the Mytiloides hercynicus associations. Four new species of divergently ornamented inoceramids are described and referred to the new genus Rhyssomytiloides . Two new species of Sergipia and some previously known species of Mytiloides and Rhyssomytiloides are also described.     

Selective predation,parasitism, and trophic cascades in a bluegill–<Emphasis Type="Italic">Daphnia</Emphasis>–parasite system

As disease incidence increases worldwide, there is increased interest in determining the factors controlling parasitism in natural populations. Recently, several studies have suggested a possible role of predation in reducing parasitism, but this idea has received little experimental attention. Here, I present the results of an experiment in which I manipulated predation rate in large field enclosures to test the effects of predation on parasitism using a bluegill predator–Daphnia host–yeast parasite system. Based on previous work showing high bluegill sunfish selectivity for infected over uninfected Daphnia, I anticipated that predators would reduce infection levels. Contrary to expectations, predation did not reduce infection prevalence. Instead, there were large epidemics in all treatments, followed by reductions of host density to very low levels. As Daphnia density decreased, phytoplankton abundance increased and water clarity decreased, suggesting a parasite-driven trophic cascade. Overall, these results suggest that selective predation does not always reduce infection prevalence, and that parasites have the potential to drastically reduce host densities even in the presence of selective predators. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Shell utilization,predation pressure,and thermal stress in panamanian hermit crabs: An interoceanic comparison

Shell preference patterns of two common hermit crabs from hard bottom reef flats on the Caribbean coast of Panama are examined in relation to the predation pressures and physical stresses of their habitat. Clibanarius antillensis Stimpson lives in the high intertidal habitat and minimizes exposure to predators by seeking refuge during high tides. It prefers high-spired shells which maximize protection from thermal stress. Calcinus tibicen Herbst avoids tidal emersion and prefers low-spired shells which enhance resistance to the predators common on Caribbean reef flats.The results are compared with similar results from the tropical eastern Pacific Bay of Panama. Shell-crushing predation on Caribbean hermit crabs is suggested to differ quantitatively and qualitatively from predation on hermit crabs in the Bay of Panama. Predation on hermit crabs in the Bay of Panama is more intense and effects larger individuals than predation on Caribbean reef flat hermit crabs. In addition, shell-crushing predation on hermit crabs in the Bay of Panama is primarily from teleost fish predators (Diodon spp.), while predation on Caribbean hermit crabs is primarily by bottom-dwelling crustaceans.Differences in predation pressures and tidal regimes between the Caribbean and Pacific coasts of Panama are reflected in the shell preferences and behavior of hermit crabs from the two areas.     

Release from Parasites as Natural Enemies: Increased Performance of a Globally Introduced Marine Crab

Introduced species often seem to perform better than conspecifics in their native range. This is apparent in the high densities they may achieve or the larger individual sizes they attain. A prominent hypothesis explaining the success of introduced terrestrial species is that they are typically free of or are less affected by the natural enemies (competitors, predators, and parasites) they encounter in their introduced range compared to their native range. To test this hypothesis in a marine system, we conducted a global assessment of the effect of parasitism and predation on the ecological performance of European green crab populations. In Europe, where the green crab is native, crab body size and biomass were negatively associated with the prevalence of parasitic castrators. When we compared native crab populations with those from introduced regions, limb loss (an estimator of predation) was not significantly lower in introduced regions, parasites infected introduced populations substantially less and crabs in introduced regions were larger and exhibited a greater biomass. Our results are consistent with the general prediction that introduced species suffer less from parasites compared to populations where they are native. This may partly explain why the green crab is such a successful invader and, subsequently, why it is a pest in so many places.     

Does cowbird parasitism increase predation risk to American redstart nests?

Brood parasitism and nest predation are major causes of reproductive failure for many bird species nesting in fragmented landscapes. While brood parasites and predators may act independently, they could also interact if brood parasites increase the likelihood that predators detect nests. In this study, we examined the interaction between cowbird parasitism and nest predation in a 10 year study on 466 American redstart Setophaga ruticilla nests in central Alberta, Canada. We used advanced nest survival models to examine the support for three mechanisms that might lead to a positive correlation between brood parasitism and nest predation: 1) the presence of a cowbird nestling might increase the detection of the nest by predators, 2) nests with lower cover are more likely to be detected by both cowbirds and predators, and 3) cowbirds and predators may co-occur in landscapes of similar structure. Twelve percent of nests were parasitized and those nests had a 16–19% higher rate of failure due to predators compared to unparasitized nests. Daily nest predation rates increased during the nestling stage for both groups, but more strongly for parasitized nests. Loud begging by the cowbird nestling and/or higher parental feeding rates for the cowbird may have increased nest detectability to predators. Brood parasitism and nest predation were also positively related to forest cover, indicating landscape level effects were influential. Most nest predators were forest species and we suspect cowbirds responded positively to forest cover because of the increased abundance of songbird hosts. Nest-site features had less of an impact on nest predation or brood parasitism, although nests with higher overhead cover were less susceptible to predators. Our study shows how multiple mechanisms, particularly the behavioral effects of the brood parasite nestling and landscape structure, can lead to a positive relationship between nest predation and brood parasitism.     

Parallel and nonparallel behavioural evolution in response to parasitism and predation in Trinidadian guppies

Natural enemies such as predators and parasites are known to shape intraspecific variability of behaviour and personality in natural populations, yet several key questions remain: (i) What is the relative importance of predation vs. parasitism in shaping intraspecific variation of behaviour across generations? (ii) What are the contributions of genetic and plastic effects to this behavioural divergence? (iii) And to what extent are responses to predation and parasitism repeatable across independent evolutionary lineages? We addressed these questions using Trinidadian guppies (Poecilia reticulata) (i) varying in their exposure to dangerous fish predators and Gyrodactylus ectoparasites for (ii) both wild‐caught F0 and laboratory‐reared F2 individuals and coming from (iii) multiple independent evolutionary lineages (i.e. independent drainages). Several key findings emerged. First, a population's history of predation and parasitism influenced behavioural profiles, but to different extent depending on the behaviour considered (activity, shoaling or boldness). Second, we had evidence for some genetic effects of predation regime on behaviour, with differences in activity of F2 laboratory‐reared individuals, but not for parasitism, which had only plastic effects on the boldness of wild‐caught F0 individuals. Third, the two lineages showed a mixture of parallel and nonparallel responses to predation/parasitism, with parallel responses being stronger for predation than for parasitism and for activity and boldness than for shoaling. These findings suggest that different sets of behaviours provide different pay‐offs in alternative predation/parasitism environments and that parasitism has more transient effects in shaping intraspecific variation of behaviour than does predation.     

Durophagous predation on scaphitid ammonoids in the Late Cretaceous Western Interior Seaway of North America

This study is the first to report a trend of predation intensity on scaphitid ammonoids from the Turonian to the Maastrichtian (Late Cretaceous) on the basis of analysis of ventral shell breakage in large samples from the US Western Interior Province. Analysis of 835 adult specimens revealed ventral shell breakage in 50 specimens. In most of the damaged specimens, the breakage occurred in a preferred position at the rear part of the body chamber. Ventral breakage is rare in the Turonian specimens, whereas it is common in the Campanian and Maastrichtian specimens. The shell diameter of adult scaphitid ammonoids tends to increase with time. The position of the breakage and the absence of repairs indicate that the ventral breakage resulted from lethal predation. Based on the incidence of breakage and the size and shape of the breaks, possible predators include fish, reptiles and cephalopods such as Placenticeras, Eutrephoceras and coleoids. Our statistical analysis of ventral shell breakage indicates that the incidence of lethal predation increased in conjunction with an increase in adult shell size, suggesting that the body size of the prey was an important factor in predator–prey interactions. In addition, the predatory damage is more extensive in larger adults.     

水稻种植密度和生育期对三化螟卵天敌种群及其效益的影响

研究结果表明,水稻种植密度和生育期对三化螟Scirpophaha incertulas卵的天敌种群及其捕食串和寄生率有显著的影响。捕食性天敌和某些寄生蜂的种群密度随种植密度的增加和生育期的增长而增加,但啮小蜂和赤眼蜂对种植密度的反应不明显。螟卵捕食串随种植密度的增加和生育期的增长而增加。但螟卵寄生率则相反：种植密度低、生育期早,卵寄生率高,且差异显著。种植密度和生育期不仅影响了单种寄生蜂的寄生率,而且也影响了螟卵寄生蜂种类的多少。在种植密度低的地块和水稻生长初期,卵块通常有3种寄生蜂出现,而在密度高的地块和生长末期,卵块通常没有寄生蜂或仅有赤眼蜂出现。虽然卵捕食和卵寄生都是三化螟卵的重要控制因素,但由天敌所造成的卵死亡率则随种植密度的增加或生育期的延长而下降。     

Mosasaur predation on a nautiloid from the Maastrichtian Pierre Shale,Central Colorado,Western Interior Basin,United States

Mosasaurs were common predators on the ammonites that inhabited the upper water column of the Late Cretaceous Western Interior epicontinental seaway of North America. Mosasaurs developed predictable behaviour patterns for feeding on ammonite prey. There are no previous reports of mosasaur predation on the much less common Cretaceous nautiloids, possibly because of the prey's predominantly deep, epibenthic habitat, as deduced from modern Nautilus life habits. A single specimen of the highly inflated nautiloid, Eutrephoceras dekayi (Conrad), prey to a small adult mosasaur, likely Platycarpus, Prognathodon or Mosasaurus, is reported herein from the Pierre Shale of Colorado in the Early Maastrichtian biozone of Baculitesgrandis transitional to the biozone of B. clinolobatus. The nautiloid was killed in the same manner as described previously for discoid ammonites (Placenticeras, Sphenodiscus) from coeval strata in the USA and Canada.     

Climate Change and Trophic Response of the Antarctic Bottom Fauna

Background

As Earth warms, temperate and subpolar marine species will increasingly shift their geographic ranges poleward. The endemic shelf fauna of Antarctica is especially vulnerable to climate-mediated biological invasions because cold temperatures currently exclude the durophagous (shell-breaking) predators that structure shallow-benthic communities elsewhere.

Methodology/Principal Findings

We used the Eocene fossil record from Seymour Island, Antarctic Peninsula, to project specifically how global warming will reorganize the nearshore benthos of Antarctica. A long-term cooling trend, which began with a sharp temperature drop ∼41 Ma (million years ago), eliminated durophagous predators—teleosts (modern bony fish), decapod crustaceans (crabs and lobsters) and almost all neoselachian elasmobranchs (modern sharks and rays)—from Antarctic nearshore waters after the Eocene. Even prior to those extinctions, durophagous predators became less active as coastal sea temperatures declined from 41 Ma to the end of the Eocene, ∼33.5 Ma. In response, dense populations of suspension-feeding ophiuroids and crinoids abruptly appeared. Dense aggregations of brachiopods transcended the cooling event with no apparent change in predation pressure, nor were there changes in the frequency of shell-drilling predation on venerid bivalves.

Conclusions/Significance

Rapid warming in the Southern Ocean is now removing the physiological barriers to shell-breaking predators, and crabs are returning to the Antarctic Peninsula. Over the coming decades to centuries, we predict a rapid reversal of the Eocene trends. Increasing predation will reduce or eliminate extant dense populations of suspension-feeding echinoderms from nearshore habitats along the Peninsula while brachiopods will continue to form large populations, and the intensity of shell-drilling predation on infaunal bivalves will not change appreciably. In time the ecological effects of global warming could spread to other portions of the Antarctic coast. The differential responses of faunal components will reduce the endemic character of Antarctic subtidal communities, homogenizing them with nearshore communities at lower latitudes.     

A reconsideration of the origins of the 'typical' Cretaceous inoceramid calcitic hinge plate in the light of new ultrastructural observations from some Jurassic 'inoceramids'

Abstract:  Marked differences occur between the hinge plates of Jurassic and Upper Cretaceous British 'inoceramid' species. Albian and Upper Cretaceous inoceramids had the poiriform calcite hinge plate with closely spaced resiliifers that is widely associated with this extinct bivalve family. The whole structure was dominated by compressible ligament. Jurassic species, in contrast, had an ultrastructurally less familiar aragonite hinge plate with widely spaced resiliifers and a ligament reminiscent of Isognomon with equally spaced elastic and compressional components. The wider taxonomic relationships of the Inoceramidae still remain uncertain, although the majority of the evidence links the family to the Pterioida. This study, however, suggests that the ancestral inoceramid did not necessarily have a calcitic hinge plate, but rather that a Jurassic 'inoceramid' species could have been developing such a structure via an aragonite precursor. Observations on British Kimmeridgian 'inoceramid' specimens indicate that calcite was being incorporated into the aragonite hinge plate by these times. Structures in the ligamentat of Jurassic species suggest that the fundamental change in mineralogy was initiated by valve architectural modification at the byssal notch, linked to inoceramid epifaunalism. Worldwide poor preservation of Lower Cretaceous inoceramids makes it very difficult to further prove this hypothesis via intermediate evolutionary stages leading to the fully poiriform calcite hinge plate observed in Albian and Upper Cretaceous species of Inoceramidae.     

Predation by blue crabs, Callinectes sapidus, on rapa whelks, Rapana venosa: possible natural controls for an invasive species?

Blue crabs Callinectes sapidus are voracious predators in Chesapeake Bay and other estuarine habitats. The rapa whelk Rapana venosa is native to Asian waters but was discovered in Chesapeake Bay in 1998. This predatory gastropod grows to large terminal sizes (in excess of 150 mm shell length (SL)) and has a thick shell that may contribute to an ontogenetic predation refuge. However, juvenile rapa whelks in Chesapeake Bay may be vulnerable to predation by the blue crab given probable habitat overlap, relative lack of whelk shell architectural defenses, and the relatively large size of potential crab predators. Feeding experiments using three size classes of blue crab predators in relation to a size range of rapa whelks of two different ages (Age 1 and Age 2) were conducted. Blue crabs of all sizes tested consumed Age 1 rapa whelks; 58% of all Age 1 whelks offered were eaten. Age 2 rapa whelks were consumed by medium (67% of whelks offered were eaten) and large (70% of whelks offered were eaten) blue crabs but not by small crabs. The attack methods of medium and large crabs changed with whelk age and related shell weight. Age 1 whelks were typically crushed by blue crabs while Age 2 whelk shells were chipped or left intact by predators removing prey. Rapa whelks less than approximately 35 mm SL are vulnerable to predation by all sizes of blue crabs tested. Rapa whelk critical size may be greater than 55 mm SL in the presence of large blue crabs indicating that a size refugia from crab predation may not be achieved by rapa whelks in Chesapeake Bay until at least Age 2 or Age 3. Predation by blue crabs on young rapa whelks may offer a natural control strategy for rapa whelks in Chesapeake Bay and other estuarine habitats along the North American Atlantic coast.     

Crab shell-crushing predation and gastropod architectural defense

The shell-breaking behavior of the crabs Ozius verreauxii Saussure 1853 and Eriphia squamata, Stimpson 1859 from the Bay of Panama is described. The master claws of both these crabs are well designed for breaking shells. Small shells, relative to the size of a crab predator, are crushed by progressively breaking off larger segments of a shell's apex, while larger shells are peeled by inserting a large dactyl molar into the aperture of a shell and progressively chipping away the lip of the shell.

Heavy gastropod shells are shown to be less vulnerable to crab predators than lighter shells, and narrow shell apertures and axial shell sculpture are demonstrated to be architectural features that deter crab predation. The incidence of architectural features which deter crab predation appears to be higher for smaller gastropod species than for larger gastropods which are too large for most crab predators. Large fish predators prey upon both gastropods and shell-crushing crabs. To avoid fish predators, both these prey groups seek refuge under rocks when covered by the tide. Fish predation thus appears to enforce a close sympatry between smaller gastropods and their crab predators.     

Predation by gulls on crabs in rocky intertidal and shallow subtidal zones of the Gulf of Maine

Most organisms in intertidal areas are marine in origin; many have distributions that extend into the subtidal zone. Terrestrial predators such as mammals and birds may exploit these animals during low tide and can have considerable effects on intertidal food webs. Several studies have shown that avian predators are capable of reducing densities of sessile and slow-moving intertidal invertebrates but very few studies have considered avian predation on mobile invertebrate predators such as crabs. In this study, we investigated predation by Great Black-backed Gulls (Larus marinus Linnaeus) on three species of crabs (Cancer borealis Stimpson, Cancer irroratus Say, and Carcinus maenas Linnaeus). The study was at Appledore Island, ME (a gull breeding island) and 8 other sites throughout the Gulf of Maine, including breeding islands and mainland sites. On Appledore Island, intertidal and subtidal zones provided over one-third of prey remains found at gull nests, and crabs were a substantial proportion (∼ 30% to 40%) of the total remains. Similarly, collections of prey remains from intertidal areas indicated that crabs were by far the most common marine prey. C. borealis was eaten far more often and C. irroratus and C. maenas less often than expected at each site. Comparing numbers of carapaces to densities of crabs in low intertidal and shallow subtidal zones at each site, we estimated that gulls remove between 15% and 64% of C. borealis during diurnal low tides. The proportion of C. borealis eaten by gulls was independent of proximity to a gull colony. Approximately 97% of the outer coast of Maine is within 20 km of a breeding island. Thus, a lot of gull predation on crabs may occur throughout the Gulf of Maine during summer months. Crabs are important predators of other invertebrates; if predation by gulls reduces the number of crabs in intertidal and shallow subtidal areas, gulls may have important indirect effects on intertidal food webs.     

Revealing the role of predator interference in a predator–prey system with disease in prey population

Predation on a species subjected to an infectious disease can affect both the infection level and the population dynamics. There is an ongoing debate about the act of managing disease in natural populations through predation. Recent theoretical and empirical evidence shows that predation on infected populations can have both positive and negative influences on disease in prey populations. Here, we present a predator–prey system where the prey population is subjected to an infectious disease to explore the impact of predator on disease dynamics. Specifically, we investigate how the interference among predators affects the dynamics and structure of the predator–prey community. We perform a detailed numerical bifurcation analysis and find an unusually large variety of complex dynamics, such as, bistability, torus and chaos, in the presence of predators. We show that, depending on the strength of interference among predators, predators enhance or control disease outbreaks and population persistence. Moreover, the presence of multistable regimes makes the system very sensitive to perturbations and facilitates a number of regime shifts. Since, the habitat structure and the choice of predators deeply influence the interference among predators, thus before applying predators to control disease in prey populations or applying predator control strategy for wildlife management, it is essential to carefully investigate how these predators interact with each other in that specific habitat; otherwise it may lead to ecological disaster.     

Native species vulnerability to introduced predators: testing an inducible defense and a refuge from predation

To manage the impacts of biological invasions, it is important to determine the mechanisms responsible for the effects invasive species have on native populations. When predation by an invader is the mechanism causing declines in a native population, protecting the native species will involve elucidating the factors that affect native vulnerability. To examine those factors, this study measured how a native species responded to an introduced predator, and whether the native response could result in a refuge from predation. Predation by the green crab, Carcinus maenas, has contributed to the decline in numbers of native soft-shell clams, Mya arenaria, and efforts to eradicate crabs have proven futile. We tested how crab foraging affected clam burrowing, and how depth in the sediment affected clam survival. Clams responded to crab foraging by burrowing deeper in the sediment. Clams at shallow depths were more vulnerable to predation by crabs. Results suggest soft-shell clam burrowing is an inducible defense in response to green crab predation because burrowing deeper results in a potential refuge from predation by crabs. For restoring the native clam populations, tents could exclude crabs and protect clams, but when tents must be removed, exposing the clams to cues from foraging crabs should induce the clams to burrow deeper and decrease vulnerability. In general, by exposing potential native prey to cues from introduced predators, we can test how the natives respond, identify whether the response results in a potential refuge, and evaluate the risks to native species survival in invaded communities.