<p>Bars depict standard deviation across sampled quadrats. Data are from the 11 sites surveyed between September and December 2011 (sites 1–4, 6, 10, 14, 16, 18, 23, 24). The shaded area denotes the impacted region, in which we found zero individuals at all sites surveyed after the event (n = 5).</p
<p>Data represent the number of urchins per 1.3 m <sup>2</sup> on the exposed substrate as determine...
Dataset: Sea urchin density Galápagos IslandsSea urchin (E. galapagensis) densities showed high vari...
In 1983–1984, an unknown waterborne pathogen caused the mass mortality of long-spined sea urchin (Di...
<p>Data are shown by depth class, and represent counts (mean ± SE) in transects surveyed before (gre...
<p>(A) A large tidepool outside the impact zone (site 4), with a dense population of live <i>Strongy...
<p>Survey data describing densities of Strongylocentrotus purpuratus (purple sea urchin) in subtidal...
<p>Data are shown for surveys before the 2011 mass mortality (2001–2010) and after (2012). In the in...
<p>Spatial distribution within each landscape area (L1, L2 and L3) of the final predation rate and t...
Abstract: Recent reports indicate that populations of the black sea urchin Diadema antillarum are sl...
In 1983-1984, a mass mortality caused a Caribbean-wide, >95% population reduction of the echinoid gr...
Mass mortalities in natural populations, particularly those that leave few survivors over large spat...
The 1983-1984 die-off of the long-spined sea urchin Diadema antillarum stands out as a catastroph...
Two-decade-long monitoring studies at Europe\u27s first statutory marine reserve—Lough Hyne in SW Ir...
Mass mortality of echinoids is well documented, and has potentially profound effects on benthic comm...
The 1983-1984 die-off of the long-spined sea urchin Diadema antillarum stands out as a catastrophic ...
<p>Data represent the number of urchins per 1.3 m <sup>2</sup> on the exposed substrate as determine...
Dataset: Sea urchin density Galápagos IslandsSea urchin (E. galapagensis) densities showed high vari...
In 1983–1984, an unknown waterborne pathogen caused the mass mortality of long-spined sea urchin (Di...
<p>Data are shown by depth class, and represent counts (mean ± SE) in transects surveyed before (gre...
<p>(A) A large tidepool outside the impact zone (site 4), with a dense population of live <i>Strongy...
<p>Survey data describing densities of Strongylocentrotus purpuratus (purple sea urchin) in subtidal...
<p>Data are shown for surveys before the 2011 mass mortality (2001–2010) and after (2012). In the in...
<p>Spatial distribution within each landscape area (L1, L2 and L3) of the final predation rate and t...
Abstract: Recent reports indicate that populations of the black sea urchin Diadema antillarum are sl...
In 1983-1984, a mass mortality caused a Caribbean-wide, >95% population reduction of the echinoid gr...
Mass mortalities in natural populations, particularly those that leave few survivors over large spat...
The 1983-1984 die-off of the long-spined sea urchin Diadema antillarum stands out as a catastroph...
Two-decade-long monitoring studies at Europe\u27s first statutory marine reserve—Lough Hyne in SW Ir...
Mass mortality of echinoids is well documented, and has potentially profound effects on benthic comm...
The 1983-1984 die-off of the long-spined sea urchin Diadema antillarum stands out as a catastrophic ...
<p>Data represent the number of urchins per 1.3 m <sup>2</sup> on the exposed substrate as determine...
Dataset: Sea urchin density Galápagos IslandsSea urchin (E. galapagensis) densities showed high vari...
In 1983–1984, an unknown waterborne pathogen caused the mass mortality of long-spined sea urchin (Di...