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1. |
Dispersal Dynamics of the Bivalve Gemma Gemma in a Patchy Environment |
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Ecological Monographs,
Volume 65,
Issue 1,
1995,
Page 1-20
John A. Commito,
Carol A. Currier,
Laura R. Kane,
Kathleen A. Reinsel,
Irene M. Ulm,
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摘要:
The purpose of this study was to analyze the dispersal dynamics of the ovoviviparous bivalve Gemma gemma (hereafter referred to as Gemma) in an environment disturbed by the pit—digging activities of horseshoe crabs, Limulus polyphemus. Gemma broods its young and has no planktonic larval stage, so all dispersal is the result of juvenile and adult movement. Animal movement was measured using natural crab pits, hand—dug simulated crab pits, and cylindrical bottom traps in the intertidal zone at Tom's Cove, Virginia, USA. This study demonstrated that horseshoe crabs create localized patches with reduced densities of Gemma, that all sizes and ages of Gemma quickly disperse into these low density patches, and that the mechanism of dispersal is passive bedload and suspended load transport. Freshly excavated natural pits had significantly lower Gemma densities than did undisturbed background sediment, but there were no significant differences in total density of other species, number of species, and species diversity (H'). Equitability (J') was greater in pits than in controls because of the reduced abundance of Gemma, the numerically dominant species. Newly dug simulated crab pits also had significantly lower Gemma densities than controls and returned to control levels by the next day. Density recovery trajectories for individually marked pits showed consistent responses in summer and fall, but not in winter when low Gemma abundance resulted in greater variability among pits. Significant positive correlations between the volume of sediment and the number of Gemma collected per bottom trap support the hypothesis that Gemma dispersal is a passive transport phenomenon. Assuming no active, density—dependent movement, the product of the Gemma density frequency distribution in undisturbed background sediment and the frequency distribution of sediment volume collected per trap created a predicted Gemma frequency distribution in traps that matched the actual distribution. Absolute dispersal rates and relative dispersal rates (absolute dispersal rate divided by background density in undisturbed sediment) into pits and traps were greater in summer than winter. Dispersal rate results suggest that increased horseshoe crab disturbance in summer may cause an increase in Gemma transport. Because Gemma individuals are dispersed by hydrodynamic action, it was expected that small, young individuals would be most easily transported in the bedload. There was, however, little evidence that movement into pits and traps was size— or age—selective. Most recent benthic dispersal research has focused on the large—scale movement and settlement patterns of invertebrate larvae. The results from this study illustrate that dispersal of bottom—dwelling juveniles and adults plays an important role in regulating the local distribution and abundance of Gemma. Previous workers have shown that young Gemma live in dense aggregations and that growth and fecundity are reduced at such high densities, leading to population crashes. This study demonstrated a mechanism by which Gemma disperses into low—density patches where intraspecific competition may be mitigated, possibly resulting in enhanced individual reproductive success and population fitness.
ISSN:0012-9615
DOI:10.2307/2937157
出版商:Ecological Society of America
年代:1995
数据来源: WILEY
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2. |
Indirect Effects in Marine Rocky Intertidal Interaction Webs: Patterns and Importance |
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Ecological Monographs,
Volume 65,
Issue 1,
1995,
Page 21-74
Bruce A. Menge,
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摘要:
To determine the patterns of occurrence and importance of indirect effects relative to direct effects in natural communities, I analyzed experimentally based studies from 23 rocky intertidal habitats. The vehicle of analysis was the construction of interaction webs, or the subset of species in food webs involved in strong interactions. The analysis focused on indirect effects involving changes in abundance, or interaction chains, since little information was available on other types of indirect effects (behavioral, chemical response, environmental). As expected, number of direct (= strong) interactions, indirect effects, interaction sequences producing indirect effects, and types of indirect effects (e.g., keystone predation, apparent competition, etc.) all increased with web species richness. Less expected, when these measures were adjusted to a per species basis, positive relationships with species richness were still observed for all measures but the number of types. In other words, with increasing web diversity, each species interacted strongly with more species, was involved in more indirect effects, and was part of more interaction pathways. The analysis identified 83 subtypes of indirect effect, including the seven previously identified types. Many of the 76 additional types could be reclassified into the seven types if the original definitions of these "classic" types were expanded to include interactions having similar effects but differing in the specific mechanism (e.g., both interference competition and inhibition of recruitment [preemption] have negative effects involving a spatial resource). Two new types of indirect effect, termed "apparent predation" and "indirect defense" were also identified, producing a total of 9 general types of indirect effect divided among 565 specific indirect effects. Of these, keystone predation (35%) and apparent competition (25%) were most common and exploitation competition (2.8%) was least common in these webs. Two methods of analysis suggested that indirect effects accounted for °40% of the change in community structure resulting from manipulations, with a range of 24—61%. The proportion of change due to indirect effects was constant with web species richness, indicating that strong direct interactions and indirect effects produce roughly the same level of alteration of community structure regardless of the level of web complexity. Several potential artifacts and biases were evaluated. Most importantly, neither variation in level of taxonomic resolution nor intensity of experimentation varied significantly with web size (species richness). Despite a bias toward manipulation of consumers over manipulation of basal species, some predator—initiated indirect effect types were scarce while some basal species—initiated types were common. While the frequency of exploitation competition may have been underestimated, it is unlikely that the frequency of this indirect effect would change dramatically: changes due to this effect should have been detected in many of the studies and reported; and the most intensively studied individual webs did not report frequencies differing much from the average. This analysis suggests investigators effectively identified and first manipulated those species responsible for most indirect effects and that more experiments added decreasing numbers of indirect effects. Moreover, the frequencies and importance of indirect effects may be more predictable than expected on the basis of theory.
ISSN:0012-9615
DOI:10.2307/2937158
出版商:Ecological Society of America
年代:1995
数据来源: WILEY
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3. |
Sea Otters and Kelp Forests in Alaska: Generality and Variation in a Community Ecological Paradigm |
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Ecological Monographs,
Volume 65,
Issue 1,
1995,
Page 75-100
James A. Estes,
David O. Duggins,
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摘要:
Multiscale patterns of spatial and temporal variation in density and population structure were used to evaluate the generality of a three—trophic—level cascade among sea otters (Enhydra lutris), invertebrate herbivores, and macroalgae in Alaska. The paradigm holds that where sea otters occur herbivores are rare and plants are abundant, whereas when sea otters are absent herbivores are relatively common and plants are rare. Spatial patterns were based on 20 randomly placed quadrats at 153 randomly selected sites distributed among five locations with and four locations without sea otters. Both sea urchin and kelp abundance differed significantly among locations with vs. without sea otters in the Aleutian Islands and southeast Alaska. There was little (Aleutian Islands) or no (southeast Alaska) overlap between sites with and without sea otters, in plots of kelp density against urchin biomass. Despite intersite variation in the abundance of kelps and herbivores, these analyses demonstrate that sea otter predation has a predictable and broadly generalizable influence on the structure of Alaskan kelp forests. The percent cover of algal turf and suspension feeder assemblages also differed significantly (although less dramatically) between locations with and without sea otters. Temporal variation in community structure was assessed over periods of from 3 to 15 yr at sites in the Aleutian Islands and southeast Alaska where sea otters were 1) continuously present, 2) continuously absent, or 3) becoming reestablished because of natural range expansion. Kelp and sea urchin abundance remained largely unchanged at most sites where sea otters were continuously present or absent, the one exception being at Torch Bay (southeast Alaska), where kelp abundance varied significantly through time and urchin abundance varied significantly among sites because of episodic and patchy disturbances. In contrast, kelp and sea urchin abundances changed significantly, and in the expected directions, at sites that were being recolonized by sea otters. Sea urchin biomass declined by 50% in the Aleutian Islands and by nearly 100% in southeast Alaska following the spread of sea otters into previously unoccupied habitats. In response to these different rates and magnitudes of urchin reduction by sea otter predation, increases in kelp abundance were abrupt and highly significant in southeast Alaska but much smaller and slower over similar time periods in the Aleutian Islands. The different kelp colonization rates between southeast Alaska and the Aleutian Islands appear to be caused by large—scale differences in echinoid recruitment coupled with size—selective predation by sea otters for larger urchins. The length of urchin jaws (correlated with test diameter, r2= 0.968) in sea otter scats indicates that sea urchins<15—20 mm test diameter are rarely eaten by foraging sea otters. Sea urchin populations in the Aleutian Islands included high densities of small individuals (<20 mm test diameter) at all sites and during all years sampled, whereas in southeast Alaska similarly sized urchins were absent from most populations during most years. Small (<30—35 mm test diameter) tetracycline—marked urchins in the Aleutian Islands grew at a maximum rate of °10 mm/yr; thus the population must have significant recruitment annually, or at least every several years. In contrast, echinoid recruitment in southeast Alaska was more episodic, with many years to perhaps decades separating significant events. Our findings help explain regional differences in recovery rates of kelp forests following recolonization by sea otters.
ISSN:0012-9615
DOI:10.2307/2937159
出版商:Ecological Society of America
年代:1995
数据来源: WILEY
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4. |
Avian Life History Evolution in Relation to Nest Sites, Nest Predation, and Food |
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Ecological Monographs,
Volume 65,
Issue 1,
1995,
Page 101-127
Thomas E. Martin,
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摘要:
Food limitation is generally thought to underlie much of the variation in life history traits of birds. I examined variation and covariation of life history traits of 123 North American Passeriformes and Piciformes in relation to nest sites, nest predation, and foraging sites to examine the possible roles of these ecological factors in life history evolution of birds. Annual fecundity was strongly inversely related to adult survival, even when phylogenetic effects were controlled. Only a little of the variation in fecundity and survival was related to foraging sites, whereas these traits varied strongly among nest sites. Interspecific differences in nest predation were correlated with much of the variation in life history traits among nest sites, although energy trade—offs with covarying traits also may account for some variation. For example, increased nest predation is associated with a shortened nestling period and both are associated with more broods per year, but number of broods is inversely correlated with clutch size, possibly due to an energy trade—off. Number of broods was much more strongly correlated with annual fecundity and adult survival among species than was clutch size, suggesting that clutch size may not be the primary fecundity trait on which selection is acting. Ultimately, food limitation may cause trade—offs between annual fecundity and adult survival, but differences among species in fecundity and adult survival may not be explained by differences in food abundance and instead represent differing tactics for partitioning similar levels of food limitation. Variation in fecundity and adult survival is more clearly organized by nest sites and more closely correlated with nest predation; species that use nest sites with greater nest predation have shorter nestling periods and more broods,yielding higher fecundity, which in turn is associated with reduced adult survival. Fecundity also varied with migratory tendencies; short—distance migrants had more broods and greater fecundity than did neotropical migrants and residents using similar nest sites. However, migratory tendencies and habitat use were confounded, making separation of these two effects difficult. Nonetheless, the conventional view that neotropical migrants have fewer broods than residents was not supported when nest site effects were controlled.
ISSN:0012-9615
DOI:10.2307/2937160
出版商:Ecological Society of America
年代:1995
数据来源: WILEY
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