Seagrass (Zostera marina L.) bed recolonisation after anoxia-induced full mortality

By M. Plus, J. Deslous-Paoli, Françoise Dagault. 2003

169 citations recorded by the source corpus.

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Citations in the corpus

Recolonization of Zostera marina following destruction caused by a red tide algal bloom: the role of new shoot recruitment from seed banks. (2007, background): “Recolonization of seagrass beds following destruction caused by various disturbances has been reported in many seagrass species (Peterken & Conacher 1997, Plus et al. 2003, Rasheed 2004, Olesen et al. 2004, Bernard et al. 2005).”
Vulnerability of Zostera marina seedlings to physical stress (2010, background): “Seedling survival varies between habitats from >80% yr–1, with complete recolonization in some areas (Plus et al. 2003, Lee et al. 2007), to between 0 and 5% yr–1 and much slower recolonization in most areas (Churchill 1983, Harrison 1993, Greve et al. 2005, Bos & van Katwijk 2007, Boese et al.…”
Epiphyte-cover on seagrass (Zostera marina L.) leaves impedes plant performance and radial O2 loss from the below-ground tissue (2015, background): “Over the past century, seagrasses have faced an alarming global decline, owing to both direct and indirect human interference (Robblee et al., 1991; Zieman et al., 1999; Seddon et al., 2000; Plus et al., 2003; Orth et al., 2006).”
Thalassia testudinum response to the interactive stressors hypersalinity, sulfide and hypoxia (2007, background): “Therefore, it is important to understand large-scale mortality events of meadow forming seagrass (Robblee et al., 1991; Seddon et al., 2000; Plus et al., 2003).”
The role of seedlings and seed bank viability in the recovery of Chesapeake Bay, USA, Zostera marina populations following a large-scale decline (2010, background): “Following these defoliation events, initial recruitment into the degraded areas occurred by seed germination from the sediment seed bank ( Plus et al., 2003; Greve et al., 2005).”
The potential role of plant oxygen and sulphide dynamics in die‐off events of the tropical seagrass, Thalassia testudinum (2005, background): “Sudden seagrass die-off has been reported in several parts of the world (Rask et al . 2000; Seddon et al . 2000; Plus et al . 2003 ).”
The ecological role of bivalve shellfish aquaculture in the estuarine environment: A review with application to oyster and clam culture in West Coast (USA) estuaries (2009, background): “In fact, both natural and human disturbances have been shown to enhance sexual reproduction in seagrass (Marba and Duarte, 1995; Peterken and Conacher, 1997; Plus et al., 2003; Olesen et al., 2004).”
Burial of seeds and seedlings by the lugworm Arenicola marina hampers eelgrass (Zostera marina) recovery (2011, background): “, 2006) and eelgrass recovery after large scale disturbance may occur exclusively from seeds (Greve et al., 2005; Lee et al., 2007; Plus et al., 2003).”
Sulphide intrusion in eelgrass (Zostera marina L.) (2004, background): “Zieman et al. 1999; Seddon et al. 2000; Plus, Deslous-Paoli & Degault 2003 ) which are conditions with a high risk of sulphide intrusion.”
Seed addition facilitates eelgrass recovery in a coastal bay system (2012, background): “…because seedling success rates are most easily documented in unvegetated sand, while their contribution to the maintenance of existing beds is not well understood (Olesen 1999), except in the case of recovery of gaps after a disturbance (Plus et al. 2003, Greve et al. 2005, Jarvis & Moore 2010).”
Seagrass reproductive effort as an ecological indicator of disturbance (2012, background): “However, sexual recruitment is the most important way to maintain genetic diversity of seagrass meadows (Ackerman, 2006), and can be critical for meadow maintenance in highly disturbed and extreme environments (Thayer et al., 1984; Peterken and Conacher, 1997; Marbà and Walker, 1999; Plus et al., 20”