Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
PLoS One
2012 Jan 01;711:e49396. doi: 10.1371/journal.pone.0049396.
Show Gene links
Show Anatomy links
Trophic cascades induced by lobster fishing are not ubiquitous in southern California kelp forests.
Guenther CM
,
Lenihan HS
,
Grant LE
,
Lopez-Carr D
,
Reed DC
.
Abstract
Fishing can trigger trophic cascades that alter community structure and dynamics and thus modify ecosystem attributes. We combined ecological data of sea urchin and macroalgal abundance with fishery data of spiny lobster (Panulirus interruptus) landings to evaluate whether: (1) patterns in the abundance and biomass among lobster (predator), sea urchins (grazer), and macroalgae (primary producer) in giant kelp forest communities indicated the presence of top-down control on urchins and macroalgae, and (2) lobster fishing triggers a trophic cascade leading to increased sea urchin densities and decreased macroalgal biomass. Eight years of data from eight rocky subtidal reefs known to support giant kelp forests near Santa Barbara, CA, USA, were analyzed in three-tiered least-squares regression models to evaluate the relationships between: (1) lobster abundance and sea urchin density, and (2) sea urchin density and macroalgal biomass. The models included reef physical structure and water depth. Results revealed a trend towards decreasing urchin density with increasing lobster abundance but little evidence that urchins control the biomass of macroalgae. Urchin density was highly correlated with habitat structure, although not water depth. To evaluate whether fishing triggered a trophic cascade we pooled data across all treatments to examine the extent to which sea urchin density and macroalgal biomass were related to the intensity of lobster fishing (as indicated by the density of traps pulled). We found that, with one exception, sea urchins remained more abundant at heavily fished sites, supporting the idea that fishing for lobsters releases top-down control on urchin grazers. Macroalgal biomass, however, was positively correlated with lobster fishing intensity, which contradicts the trophic cascade model. Collectively, our results suggest that factors other than urchin grazing play a major role in controlling macroalgal biomass in southern California kelp forests, and that lobster fishing does not always catalyze a top-down trophic cascade.
Figure 1. Map of study area along 55 km of Southern California coast.Black dots mark annual transect sites from July 2001 through July 2008 for the Santa Barbara Coastal LTER. Grey polygons mark the 8 trapping areas around LTER sites where commercial lobster fishermen reported daily effort and catch. Mean polygon area was 1.23 km2 with the largest being 2.8 km2 and the smallest 0.44 km2. Abbreviations and numbers of transects sampled at each site are as follows (AHND = Arroyo Hondo, 2 transects; AQUE = Arroyo Quemado, 6 transects; NAPL = Naples, 7 transects; IVEE = Isla Vista, 2 transects; GOLB = Goleta Beach 2 transects; ABUR = Arroyo Burro, 2 transects; MOHK = Mohawk, 2 transects; CARP = Carpinteria, 7 transects).
Figure 2. Relationships among lobster catch (a proxy for lobster abundance), urchins, and macroalgae.Lobster catch [legal-sized (≥83 mm carapace length) lobsters only] in number of individuals caught in traps km−2, urchin density, and total macroalgal biomass at each of the eight sites from 2001–2008. Macroalgae consisted of non-calcareous species, including giant kelp Macrocystis pyrifera. Data for lobster catch were not recorded in 2005 for Goleta Bay, and in 2001 and 2002 for Carpinteria Reef. Note the differences in scale for urchin density at Carpinteria Reef.
Figure 3. Relationships among trophic levels and lobster fishing intensity.Data represent the mean values for the eight sites shown in Figure 2, each datum pooled across all eight years (2001–2008) (excluding the missing few data described in Figure 2). (A) Urchin density as a function of fishing intensity, measured as the mean daily number of lobster traps pulled (“sampled”) per km−2 of each fishing polygon (see Figure 1). (B) Total macroalgal biomass as a function of urchin density. (C) Macroalgal biomass as a function of fishing intensity.
Arkema,
Direct and indirect effects of giant kelp determine benthic community structure and dynamics.
2009, Pubmed
Arkema,
Direct and indirect effects of giant kelp determine benthic community structure and dynamics.
2009,
Pubmed
Cowen,
The effects of sheephead (Semicossyphus pulcher) predation on red sea urchin (Strongylocentrotus franciscanus) populations: an experimental analysis.
1983,
Pubmed
,
Echinobase
Crowder,
Sustainability. Resolving mismatches in U.S. ocean governance.
2006,
Pubmed
Estes,
Killer whale predation on sea otters linking oceanic and nearshore ecosystems.
1998,
Pubmed
,
Echinobase
Gorman,
Land-to-sea connectivity: linking human-derived terrestrial subsidies to subtidal habitat change on open rocky coasts.
2009,
Pubmed
Halpern,
Strong top-down control in southern California kelp forest ecosystems.
2006,
Pubmed
Hughes,
Catastrophes, phase shifts, and large-scale degradation of a Caribbean coral reef.
1994,
Pubmed
Jackson,
Historical overfishing and the recent collapse of coastal ecosystems.
2001,
Pubmed
Kay,
Collaborative assessment of California spiny lobster population and fishery responses to a marine reserve network.
2012,
Pubmed
Ling,
Overfishing reduces resilience of kelp beds to climate-driven catastrophic phase shift.
2009,
Pubmed
,
Echinobase
Menge,
Coastal oceanography sets the pace of rocky intertidal community dynamics.
2003,
Pubmed
Pace,
Trophic cascades revealed in diverse ecosystems.
1999,
Pubmed
Pearse,
Ecological role of purple sea urchins.
2006,
Pubmed
,
Echinobase
Reed,
Wave disturbance overwhelms top-down and bottom-up control of primary production in California kelp forests.
2011,
Pubmed
,
Echinobase
Reed,
Density derived estimates of standing crop and net primary production in the giant kelp Macrocystis pyrifera.
2009,
Pubmed
Sale,
Critical science gaps impede use of no-take fishery reserves.
2005,
Pubmed
Salomon,
Cascading effects of fishing can alter carbon flow through a temperate coastal ecosystem.
2008,
Pubmed
,
Echinobase
Shears,
Marine reserves demonstrate top-down control of community structure on temperate reefs.
2002,
Pubmed
,
Echinobase
Shears,
Context-dependent effects of fishing: variation in trophic cascades across environmental gradients.
2008,
Pubmed
,
Echinobase
Steneck,
Human influences on coastal ecosystems: does overfishing create trophic cascades?
1998,
Pubmed