Effects of size and temperature on mud crab,Panopeus herbstii,predation on hard clams,Mercenaria mercenaria

Predation byPanopeus herbstii onMercenaria mercenaria was significantly affected by temperature, and the size of predators and prey items. LargerP. herbstii opened more clams and preyed more successfully on larger clams than did smaller crabs. Increase in seed clam size and decrease in water temperature significantly reduced predation. Clam size appeared to be more important than crab satiation in reducing predation rate. Planting larger seed clams in cooler months should help to improve clam survival by reducing the impact ofP. herbstii in culture operations.     

Feeding habits of red drum (Sciaenops ocellatus) in Galveston Bay, Texas: Seasonal diet variation and predator-prey size relationships

Feeding habits, seasonal diet variation, and predator size-prey size relationships of red drum (Sciaenops ocellatus) were investigated in Galveston Bay, Texas through stomach contents analysis. A total of 598 red drum ranging from 291–763 mm total length were collected and their stomach contents analyzed during fall 1997 and spring 1998. The diet of red drum showed significant seasonal patterns, and was dominated by white shrimp (Penaeus setiferus) during fall and gulf menhaden (Brevoortia patronus) during spring. Blue crab (Callinectes sapidus) was an important component of red drum diets during both seasons. Significant differences existed between prey types consumed during fall and spring as red drum diet reflected seasonal variation in prey availability. Predictive regression equations were generated to estimate original carapace width of blue crabs from several measurements taken from carapace fragments recovered in red drum stomachs. Regressions were highly significant (r²>0.97) and increased the number of blue crabs with size information nearly three fold. Predator size-prey size relationships were determined for red drum feeding on white shrimp, gulf menhaden, and blue crab. Although regression slopes were statistically significant, prey sizes increased only slightly with increasing red drum size. Comparisons of prey sizes consumed by red drum with sizes occurring in the field indicate that red drum feed in nearshore shallow water habitats, which serve as nursery areas for many juvenile fishes and crustaceans. Our findings demonstrate that red drum feed on several prey species of commercial and recreational value and may have important effects on estuarine community structure.     

Reduction of sea star predation by the burrowing response of the hard clam Mercenaria mercenaria (Mollusca: Bivalvia)

The hard clam Mercenaria mercenaria burrows deeper into the sediment when the predaceous sea star, Asterias forbesi is present. The supposition that this increase in burial depth represents an escape response designed to reduce predation was tested experimentally by regulating clam burial depth through manipulation of the amount of sediment available for burial. Mercenaria maintained at zero depth were eaten by Asterias at greater rates than those held at ordinary burial depths (2.5–3.0 cm). These clams in turn were eaten at greater rates than those maintained at escape depths (4.0–4.5 cm). The results unambiguously establish an anti-predator function for the burrowing response, as well as underscoring the protective function of the fossorial habit. They are not confounded by behavioral predator food preferences, inherent differences between prey species, or debilitating side effects of preventing prey from escaping. Mechanisms by which the burrowing response may reduce predation are discussed and observations on the unreported clam-digging behavior of Asterias forbesi are presented.     

Intertidal distribution and feeding habits of the mud crab,Eurytium limosum

Average summer densities of the xanthid crab,Eurytium limosum, in an intertidal salt marsh on Sapelo Island, Georgia were in the range of 7.5 to 80.0 individuals m^?2. Crab densities were lowest in wet, lowlying marsh and highest in well-drained creekbank and mussel mound habitats. An analysis of crab stomach contents indicated that feeding occurred mostly around high tide, especially at night. Although the diet included some plant material,Eurytium limosum is primarily predatory and consumed crabs, polychaetes, ostracods, bivalves, and snails. In the laboratory, under simulated low-tide field conditions, both small (11–15 mm carapace width) and large (20–37 mm CW)Eurytium could capture and consume young killifish (Fundulus heteroclitus). Large crabs consumed the entire size range (7–19 mm total length) of larval/juvenile fish offered, but small crabs did not prey upon fish >11.5 mm TL. The potential importance ofE. limosum as a predator on young killifish may not be realized in the field because alternative prey are available and the crabs feed primarily at high tide, when young killifish are dispersed in the water column and are less vulnerable to benthic predators.     

Effects of a photosynthesis inhibitor,atrazine, on the salt-marsh fiddler crab,Uca pugnax (Smith)

Atrazine (2-chloro-4-ethylamino-6-isopropylamine-s-triazine) concentrations of 1,000 ppm either killed or eliminated the escape response (considered to be analogous to death) ofUca pugnax in laboratory experiments in August 1977. Adverse effects were observed at concentrations as low as 100 ppm and the severity was dependent on size and sex of the crab. However, in subsequent experiments, each with a new group of crabs, the effects of atrazine became smaller and smaller until a November experiment when no deleterious effects were observed even when exposed to 1,000 ppm. Experiments in August, 1978 confirmed the data obtained 1 year earlier. Ecological and physiological considerations of this seasonal variation in response are discussed. Crabs fed for 20 days with detritus wetted with 10^?4 M atrazine were not adversely affected. Crabs exposed to a single application of 0, 100, 1,000, and 10,000 ppm atrazine in the field and in microecosystems were adversely affected only by the 10,000-ppm rate. Toxicity of atrazine to the larval stage of the crab was not investigated.     

Faunal colonization of artificial seagrass plots: The importance of surface area versus space size relative to body size

An index of structural habitat complexity was devised: the average inter-structural space size within a habitat/the width of the prey organism of concern (Sp/Py). Prey survivorship should be low at Sp/Py<1 as the prey will be effectively excluded from using the habitat as refuge (they cannot maneuver through the spaces). At Sp/Py near to 1, survivorship should be high, as the spaces within the habitat are ideal for the prey and their predators are excluded (assuming they are larger than the prey). As Sp/Py increases, prey survivorship should drop rapidly until reaching a lower plateau where no predators are excluded by the structure. Sp/Py is dimensionless, and is potentially applicable across different scales and habitat types. Some of the predictions of this model were tested using artificial seagrass plots deployed in a seagrass bed in the York River, Virginia. The plots had 5 different structural treatments: control (a base with no ribbon), low, medium and high densities, as well as a heterogeneous treatment (composed of 1/3 low, medium and high density in a single treatment). The abundance of 2 mobile fauna size classes (<3.5 mm width and 3.5 to 9.5 mm width) and total species richness were compared among the different density treatments. The abundance of the smaller fauna increased with increasing density, and this response was proportional to the total surface area of the plots. The small fauna apparently did not respond to the smaller, ideal space sizes associated with the higher density plots. The larger fauna responded to the treatments as well, with the highest abundances occurring in the heterogeneous and high density treatments. The larger fauna did not respond to the structure proportional to the surface area within the plots, and its is possible that they responded to the inter-structural space sizes appropriate to their body sizes, although the results do not clearly support this conclusion. The different treatments did not affect species richness when the effect of total abundance on richness was controlled.     

Optimal benthic macrofaunal sampling protocol for detecting differences among four habitats in Willapa Bay,Washington, USA

As part of an effort to estimate estuarine habitat values with respect to ecological indicators of benthic macrofaunal community condition, an optimal (effective and least costly) sampling protocol (sample unit size [area x depth], sieve mesh size, and sample number [n]) was determined. The goal was to use four ecological indicators (number of species, abundance, biomass, and fish and crab prey abundance) to detect differences among four intertidal habitats in Willapa Bay, Washington, United States. The four habitats were eelgrass (Zostera marina), Atlantic cordgrass (Spartina alterniflora), mud shrimp (Upogebia pugettensis), and ghost shrimp (Neotrypaea californiensis). Four sample unit areas (0.005, 0.010, 0.015, and 0.020 m²), two sample unit depths (0–5 and 0–10 cm), and two sieve mesh sizes (1.0 and 0.5 mm) were evaluated. The optimal sampling protocol was defined as the least costly protocol capable of reliably (statistical power, 1?β≥0.80) detecting significant (α=0.05) differences among ≥4 of the 6 pairwise habitat contrasts by ANOVA on all four ecological indicators. The relative cost of each sampling protocol was estimated as a direct function of the sample unit size and number and the cost-in-processing-time ratios of 1 (5 cm deep):1.7 (10 cm deep) and 1 (≥1.0 mm macrofauna size fraction); 2.5 (≥0.5 mm macrofauna size fraction), which were taken from previous studies. The optimal sampling protocol was 15–20, 0.01-m²×5-cm deep, 0.5-mm mesh samples per habitat.     

Predation on soft-shell clams,Mya arenaria,by the common mummichog,Fundulus heteroclitus

Invertebrate predation has been cited as the major factor determining post-settling survival of the soft-shell clam, Mya arenaria. Feeding studies on common mummichogs, Fundulus heteroclitus, in Essex Bay, Massachusetts, from July 1976 to June 1978 showed soft-shell clams to be an important diet item in fish greater than 55 mm TL. Biweekly quantitative seining from 16 April to 24 September 1977 revealed predation peaks in the spring and fall corresponding to March–April and June–July spawning periods for M. arenaria. In spring and fall 1977 and spring 1978, 38.5% of the male and 52.8% of the female mummichogs sampled over 55 mm TL averaged 6.77 and 7.32 clams per stomach respectively. The maximum number of clams per stomach was 49 (108 mm female), and 47 (100 mm male). Quantitative seining at low tide yielded mummichog densities from 0.35 to 6.04 fish/m². Combining mummichog density estimates with soft-shell clam predation data gave a possible consumption of 546,000 M. arenaria per km low tide shoreline per day during peak predation periods. Results indicate mummichog predation may equal or exceed invertebrate predation as a major cause of small (<12 mm) soft-shell clam mortality in the Gulf of Maine.     

Comparison of intertidal habitat use and growth rates of two northern Puget Sound cohorts of 0+ age Dungeness crab,Cancer magister

Density, habitat use, and growth of intertidal 0+ age Dungeness crabs, Cancer magister, were examined at five northern Puget Sound (Washington, USA) sites between June 1984 and September 1987. Sampling was conducted biweekly during settlement, from June to September, and approximately monthly or bimonthly thereafter. Northern Puget Sound Dungeness crab populations appear to be largely supported by recruitment from inland parental stocks, but a smaller proportion of recruits originate from coastal or oceanic stocks, as evidenced by earlier settlement and larger size of the first instar. Settlement of Dungeness crabs in inland waters typically peaked in August, and interannual variation in year-class strength at settlement (measured as intertidal density) was low relative to that reported for coastal crab populations. Spatial and interannual differences in settlement densities were mediated by high postsettlement mortality, which varied inversely with habitat complexity. Seasonal densities were highest in mixed sand and gravel with an overstory of attached or drift macroalgae, intermediate in eelgrass (Zostera marina), and lowest on open sand. Postsettlement growth rates corresponded to seasonal water temperatures and were greatest for the coastal cohort that settled in May and June. This cohort was larger as first juvenile instars (7.2 mm carapace width, CW) and grew rapidly at summer temperatures in excess of 15°C to a size (>30 mm CW) that allowed emigration from intertidal to subtidal areas by September. The late summer cohort settled in August at 5.3 mm CW and soon after was subjected to decreasing autumn water temperatures. There crabs experienced little growth while over wintering in the intertidal, but growth rates increased in March, and the crabs emigrated in April and May, approximately 10 mo after settlement.     

Sedimentary geochemistry of hydrothermal vents in Guaymas Basin,Gulf of California,Mexico

Surface sediments from 4 contrasting environmental settings in the Southern Trough of Guaymas Basin were analysed to determine their texture, total organic matter (TOM), P (TP), and N (TN) content as well as the spatial variation in their C:N:P atomic ratios in hydrothermally altered sediments. Particle size analysis revealed a marked spatial heterogeneity among sites. Cores taken at Beggiatoa bacterial mats and at clam fields contained significant silt and clay content, while those obtained near venting sites had sand and gravel as the main components because no fine sedimentary materials are deposited at these sites. Fine grain sediments were common farther away from vents. High levels of organic C (3.4 to 12.4%) were recorded in the upper 8 cm but no clear trends of decreasing TOC with depth were noted. The presence of hydrothermally generated petroleum in some cores increased the organic C content between 8 and 12 cm. TN was generally high (456.3–4356 μg/g) and sustained a significant correlation with TOM (r=0.834, P<0.005). TP is essentially of lithogenic origin and reached concentrations greater than those normally reported in productive coastal areas (1165 μg/g) in the Gulf of California. A marked increase with depth was noted for this parameter. High C:N:P atomic ratios were estimated. These had vertical and horizontal gradients decreasing in the upper 4 cm, and then slightly increasing in intermediate strata. Organic matter enrichment at venting sites results in high C:N:P ratios (2130:25:1–2692:57:1) which are 5-fold greater than the values estimated at sedimentary environments where Beggiatoa or vesicomyd clams are predominant.     

Habitat use,temporal abundance variability,and diet of blue crabs from a New Jersey estuarine system

In a long-term, spatially comprehensive beam trawl survey of the Navesink River-Sandy Hook Bay estuary, the blue crabCallinectes sapidus was one of the most abundant species. Seasonal changes in abundance were evident, with low abundances in summer followed by peak abundances in the fall, after juveniles recruited to the estuary. We saw no long-term trends in abundance during the 5 yr study. Location in the navesink River or Sandy Hook Bay explained most of the variance in abundance within any one survey. In diet analyses, we found evidence of cannibalism in all seasons, but in the size range of crabs caught in this study (10–180 mm), we did not find a relationship between cannibalism and juvenile crab abundance. Within surveys, crabs divided into 20 mm size categories showed no sizerelated differences in location within the estuary or among 7 habitat types examined (algae bed, amphipod bed, beach, channel, marsh edge, mid-depth, and sandbar). Channels and sandbars tended to exhibit lower crab abundance than other habitats. Shallow habitats with and without cover were equally preferred by juvenile blue crabs, implying that the presence of structure was not critical. Spatial models of crab abundance (<- 80 mm carapace width) to environmental data were fit from several seasons of intensive sampling in the Navesink River-Sandy Hook Bay estuary between summer 1996 and spring 1998. These models indicated that fine-grained sediments, tmmperature, depth, and salinity were good indicators of crab abundance in spring, summer, and fall. Using these spatial models and environmental data collected in subsequent seasons (summer 1998−fall 1999), we were able to predict blue crab abundance in the river as evidenced by significant correlations between predicted and observed abundances. For the size range of crabs examined here, physical conditions may be as important as structural habitat types or cannibalism in determining habitat use in northerly estuaries.     

Comparison of spawning seasons,age, growth rates,and food of two sympatric species of searobins,Prionotus carolinus and Prionotus evolans,from Long Island Sound

Prionotus carolinus and Prionotus evolans were collected from many locations within Long Island Sound in 1971–1973, and in 1976–1977. Data from earlier collections in Block Island Sound (1943–1945) were also included. A total of 1751 specimens, 960 P. carolinus and 791 P. evolans was examined within these two time periods. Both species entered the Sound in April and spawned during June and July. P. evolans appeared to spawn slightly earlier in summer than P. carolinus. Adults began to leave the Sound after spawning and were usually absent after November. Young-of-the-year were taken regularly from August to November and, occasionally in water over 20 m deep, into February when the bottom water temperature was 1.4°C. At the end of the first growing seasons both species exhibited large variations in standard lengths. Back-calculations from scale annuli measurements indicated that linear growth rates during the juvenile years were similar in both species. However, P. evolans was considerably heavier than P. carolinus. During adulthood P. evolans was not only longer and heavier than P. carolinus, but lived longer. Growth rates are described by the following equations: P. carolinus L_t+1=9.60+0.68 (L_t), and p. evolans L_t+1=7.70+0.80 (L_t). Both species were opportunistic feeders, and crustaceans were clearly the dominant group of prey. Young-of-the-year, between 3–6 cm, ate copepods. As they grew they ate larger prey, such as Neomysis americana, Diastylis quadrispinosus, various species of amphipods of small sizes, and juvenile Crangon septemspinosus. Older fish ate larger sizes of these same prey, a number of species of crabs, juvenile Homarus americanus, and Squilla empusa. Occasionally they ate polychaetes, molluscs, and juvenile fish. Partitioning of the resources of Long Island Sound by these two species appeared to be by prey size. P. evolans ate prey that, on the average, were slightly larger than those eaten by P. carolinus. Furthermore, P. evolans ate a greater amount of nektonic species than P. carolinus, which appeared to prefer benthonic invertebrates.     

Predation and Functional Responses of Carcinus maenas and Cancer magister in the Presence of the Introduced Cephalaspidean Philine orientalis

An increasing number of examples suggest that interactions among introduced species are ecologically important and relevant to the management of invaded systems. We investigated the potential for the introduced cephalaspidean sea slug Philine orientalis to interfere with the feeding of the introduced European green crab (Carcinus maenas) and the native Dungeness crab (Cancer magister). We observed co-occurrence of crab species and P. orientalis at field sites in Bodega Harbor and Tomales, San Pablo, and San Francisco Bays. In laboratory and field experiments, we determined whether crab feeding was suppressed by P. orientalis and the duration of this suppression for individual crabs. We also used foraging response models to explore changes in the feeding rate of crabs with varying densities of P. orientalis and small bivalve prey. We found that P. orientalis deterred predation by green and Dungeness crabs on small clams in laboratory feeding trials, but not in field experiments with green crabs and P. orientalis. Foraging models predicted that P. orientalis would only affect crab feeding in the field under specific conditions of crab, P. orientalis, and prey densities. These foraging models bridged an important gap between lab and field experiments and allowed us to predict how changes in species abundances at two trophic levels might alter the importance of crab suppression by P. orientalis.     

Quantifying Tidal Movements of the Shore Crab <Emphasis Type="Italic">Carcinus maenas</Emphasis> on to Complex Epibenthic Bivalve Habitats

Many subtidal predators undertake regular tidal migrations into intertidal areas in order to access abundant prey. One of the most productive habitats in soft bottom intertidal systems is formed by beds of epibenthic bivalves such as blue mussels (Mytilus edulis) and Pacific oysters (Crassostrea gigas). In the Dutch Wadden Sea, these bivalves might face substantial predation pressure by the shore crab (Carcinus maenas), which increased considerably in numbers during the last 20 years. However, the quantification of this species on bivalve beds is challenging, since most methods common for quantifying animal abundance in marine habitats cannot be used. This study investigated the potential of two methods to quantify the abundance of C. maenas on 14 epibenthic bivalve beds across the Dutch Wadden Sea. The use of the number of crabs migrating from subtidal towards intertidal areas as a proxy of abundance on bivalve beds yielded unreliable results. In contrast, crabs caught with traps on the beds were correlated with the abundance assessed on the surrounding bare flats by beam trawl and therefore provided usable results. The estimates, however, were only reliable for crabs exceeding 35 mm in carapace width (CW). The application of these estimates indicated that crab abundances on bivalve beds were influenced by the biogenic structure. Beds dominated by oysters attracted many large crabs (> 50-mm CW), whereas abundances of medium-sized crabs (35–50-mm CW) showed no relationship to the oyster occurrence. The combination of traps and trawls is capable of quantifying crab abundance on bivalve beds, which offers the possibility to study biotic processes such as predator-prey interactions in these complex structures in more detail.     

Transport of juvenile gem clams (Gemma gemma) in headland wake

Accumulation of bivalve recruits in the bottom convergence at the center of coastal eddies has been suggested as a possible mechanism resulting in locally abundant adult populations. We investigated transport of juvenile gem clams (Gemma gemma) in a headland wake to determine whether they accumulated, and where. Velocity measurements during three flood tides showed that a wake consistently formed, but that flow speeds were too slow to transport juvenile clams to the eddy center. Instead, the clams were deposited just inside the wake perimeter, where shear velocities decreased to levels below critical erosion velocities of the clams. This result demonstrated that accumulation in a coastal flow separation can occur even in the absence of a well-defined eddy or a strong bottom convergence. Juvenile gem clams were carried, probably as bedload, to regions in the wake dominated by sediments with similar grain sizes, rather than similar fall velocities, suggesting that bedload transport was particularly dependent on particle diameter in this flow regime. Adult gem clam populations tended to be locally abundant in regions receiving transported juveniles, but clam transport on any specific flood tide was not sufficient to fully predict the adult distributions.     

Seasonal and spatial distribution of the Carolina marsh clamPolymesoda caroliniana (Bosc) in a Mississippi tidal marsh

The abundance of the marsh clamPolymesoda caroliniana at four stations on a Mississippi tidal marsh was followed from February 1977 through April 1978. The stations varied with respect to inundation time and vegetative cover. The largest population was found in an area flooded 12% of the year (136 individuals per m²) and in an area flooded 3.2% of the year (126 individuals per m²). However, the latter area contained no large clams (>25.5 mm). Smaller populations were found in the upper reaches of a tidal creek draining the marsh (68 individuals per m²) and in an area flooded 5.8% of the year (73 individuals per m²). The average abundance of the clams on the marsh was 100 per m². At least three recruitment periods were apparent. In laboratory studies, clams larger than 15 mm survived longer than 30 days without water. Clams smaller than 12 mm survived less than 6 days without water. Several decapods (Callinectes sapidus, Uca longisignalis, andSesarma reticulatum) consumed clams smaller than 10 mm but were unable to eat larger clams under laboratory conditions.Polymesoda caroliniana may be important to the functioning of the marsh by removing large quantities of particulate matter from flooding water.     

Water quality variation and clam growth: Is pH really a non-issue in estuaries?

A tandem deployment system was used to critically evaluate relationships between important water chemistry parameters (pH, salinity, dissolved oxygen) and biotic performance based on clam growth. The effects of environmental conditions on growth of juvenile clams,Mercenaria mercenaria, were determined after 7-day field deployments in cages at reference sites from 1998 to 2000. Continuous measurements of the overlying water chemistry parameters were monitored by deploying an in situ water quality instrument (Hydrolab Datasonde) at the same time. While salinity was identified as an important determinant of clam growth over wide salinity ranges (10–35‰), pH was also found to be a very important parameter, especially in low-salinity regimes (<25‰). Average pH measurements ranged from 7.2 to 7.8; minimal pHs ranged from 6.9 to 7.6. The results indicated that when average pH levels fell below 7.5 or minimum pH levels fell below 7.2, growth rates were <50% that of clams deployed under higher pH conditions. Estuarine systems are generally perceived as being well-buffered so pH is frequently assumed to be unimportant, but our results suggest that pH levels can decline in estuarine systems to levels that can adversely affect biological responses. The potential impacts on biological resources of even moderate decreases in pH, particularly in systems that naturally tend to have lower pH conditions, may be more important than previously realized.     

Genetic variation in the soft-shelled Clam,Mya arenaria

Genetic variability for two popula-tions, Maine and Maryland, of the soft-shelled clam,Mya arenaria, was estimated from electrophoretic anal-yses of whole clams. Polymorphism (12.5% in Maine and 16.7% in Maryland clams) and heterozygosity per individ-ual (4.6% in Maine and 6.6% in Maryland) were low for the two populations based on 40 loci in Maine and 42 loci in MarylandMya.     

Distribution, morphology, and origin of sedimentary furrows in cohesive sediments, Southampton Water

Patches of sedimentary furrows are developed at several locations in the cohesive estuarine sediments of Southampton Water (water depth 1–12 m). These furrows apparently result from short periods of erosion followed by long periods of deposition. Although all the furrows are similar, regularly spaced, parallel troughs, 0.5–15 m wide aligned with the dominant current, furrows in different patches have different characteristics. In some areas furrow width is 1/5–1/15 of furrow spacing (termed ‘narrow’), whereas in other areas furrow width is about 1/2 of the spacing (termed ‘wide’). Narrow furrows have developed where sediment accumulation rates are greater than 3–6 cm yr^?1; wide furrows where accumulation rates are lower. Cockle shells, and other coarse sediments, concentrated on the furrow floors and on floors of smaller (2–10 cm wide) minifurrows, play an important role in furrow formation and evolution as they act to widen the furrows when mobilized during current episodes. Uniform sedimentation across the profile during slack periods tends to narrow the furrow. Some of the larger furrows have remained in the same position for 12 years, while mini-furrows have duration scales of a few months or less. Well-developed furrows are also found in a recently dredged channel. Bedforms similar to those described here may be preserved in the sedimentary record. While no analogues to the larger furrows are presently known, minifurrows may be morphologically similar to the ‘gutter casts’ described from ancient rocks.     

Blue crab,<Emphasis Type="Italic">Callinectes sapidus</Emphasis>, response to the invasive common reed,<Emphasis Type="Italic">Phragmites australis</Emphasis>: Abundance,size, sex ratio,and molting frequency

Much effort has been directed recently at restoring marshes, by the removal of the invasive common reed,Phragmites australis, yet it is not clear how fish and invertebrates have responded either to the invasion ofPhragmites or to marsh restoration. The blue crab,Callinectes sapidus, uses marsh habitats during much of its benthic life. We investigated the response of blue crabs toPhragmites invasion and restoration efforts by comparing crab abundance (catch per unit effort), mean size and size frequency distribution, sex ratio, and molting of crabs in three physically similar areas differing in marsh vegetation;Spartina-dominated,Phragmites-dominated, and a treated area (Phragmites removed and now dominated bySpartina) in one marsh in the upper portion of Delaware Bay. Field sampling occurred monthly (April to November) from 1999 to 2001 using replicate daytime otter trawls in large marsh creeks. Crabs were categorized by carapace width into recruits (<30 mm), juveniles (30–115 mm), and adults (>115 mm). Juveniles dominated the system, representing 69.4% of all crabs. Similar monthly increases in mean size and molting patterns during the growing season (May–August) occurred inSpartina (natural and treated sites) andPhragmites sites suggesting that, subtidal habitats, used for molting, in these areas do not differ. More juveniles in the feeding molt stage (i.e., intermolt) than in other molt stages and more recruits predominantly in the feeding molt stage than adults were inSpartina, suggesting differences in the marsh surfaces used as feeding habitats withSpartina being preferred. Sex ratios of each life history stage were skewed towards males, but this was related to the low salinity of Alloway Creek, rather than marsh surface vegetation. Our results suggest that marsh surface vegetation influences the way blue crabs use marsh surface habitats, thus restoration efforts focusing on changing vegetation type may have a positive influence on blue crabs.