Thresholds of irradiance for seagrass Posidonia oceanica meadow metabolism

Meadows of the endemic seagrass Posidonia oceanica are threatened in the Mediter- ranean due to a general deterioration of the light environment that becomes critical when light irradiance is insufficient to meet the carbon requirements of the system. Here, we conduct a 3 wk, in situ shading experiment (8 levels plus controls) to determine the threshold of irradiance for bal- anced metabolism in a shallow P. oceanica meadow and further assess the recovery of the system 1 wk later. Reduced light irradiance decreased the net community production of the meadow, which may turn negative (i.e. respiration exceeded gross community primary production) under 338 μE m −2 s −1 . Shading throughout the experiment did not appear to cause sustained physiologi- cal damage to the system since values of net community production after the cessation of shading were similar to pre-experimental, ambient levels. Sediment acid volatile sulfide pools ranged between 0.002 and 0.058 mol m −2 across shading treatments, and the highest pools were observed in the most shaded sediments. At high light impairment, meristematic cell divisions were low, and carbohydrate content in young rhizomes decreased throughout the experiment. Eight days after the cessation of shading, reduced rhizome carbohydrate stores and elevated sediment sulfide lev- els still persisted in the previously intensively shaded areas. The present study provides evidence of resistance and resilience of the seagrass Posidonia oceanica to light impairment for short (3 wk) periods of time. Although the compensation irradiance of the system varied by ~2-fold, it provides a quantitative estimate of the irradiance threshold at which seagrass meadows may shift from being coastal carbon sinks to CO2 sources.

[1]  J. Fourqurean,et al.  Novel methodology for in situ carbon dioxide enrichment of benthic ecosystems , 2011 .

[2]  O. Serrano,et al.  Seasonal response of Posidonia oceanica to light disturbances , 2011 .

[3]  N. Marbà,et al.  Seagrass community metabolism: Assessing the carbon sink capacity of seagrass meadows , 2010 .

[4]  J. Romero,et al.  Nutrient status, plant availability and seasonal forcing mediate fish herbivory in temperate seagrass beds , 2010 .

[5]  Kathryn McMahon,et al.  Interactive effects of timing, intensity and duration of experimental shading on Amphibolis griffithii , 2009, Marine Ecology Progress Series.

[6]  Núria Marbà,et al.  Mediterranean warming triggers seagrass (Posidonia oceanica) shoot mortality , 2009 .

[7]  M. Verlaque,et al.  Regression of Mediterranean seagrasses caused by natural processes and anthropogenic disturbances and stress: a critical review , 2009 .

[8]  C. Duarte,et al.  Dissolved organic matter release in a Posidonia oceanica meadow , 2009 .

[9]  C. Duarte,et al.  LOW IMPACT OF HURRICANE KATRINA ON SEAGRASS COMMUNITY STRUCTURE AND FUNCTIONING IN THE NORTHERN GULF OF MEXICO , 2009 .

[10]  N. Marbà,et al.  Effects of sediment sulfides on seagrass Posidonia oceanica meristematic activity , 2008 .

[11]  V. Pasqualini,et al.  Effects of experimental reduction of light and nutrient enrichments (N and P) on seagrasses: a review , 2008 .

[12]  Jason P. Stutes,et al.  Benthic metabolism across a gradient of anthropogenic impact in three shallow coastal lagoons in NW Florida , 2007 .

[13]  Núria Marbà,et al.  Testing the predictive power of seagrass depth limit models , 2007 .

[14]  Christopher J. Madden,et al.  Thalassia testudinum response to the interactive stressors hypersalinity, sulfide and hypoxia , 2007 .

[15]  P. Lavery,et al.  Effects of experimental reduction of light availability on the seagrass Amphibolis griffithii , 2007 .

[16]  N. Marbà,et al.  The relationship between seagrass (Posidonia oceanica) decline and sulfide porewater concentration in carbonate sediments , 2007 .

[17]  N. Marbà,et al.  Iron Additions Reduce Sulfide Intrusion and Reverse Seagrass (Posidonia oceanica) Decline in Carbonate Sediments , 2007, Ecosystems.

[18]  Javier Romero,et al.  Impact of the brine from a desalination plant on a shallow seagrass (Posidonia oceanica) meadow , 2007 .

[19]  N. Marbà,et al.  Seagrass Beds and Coastal Biogeochemistry , 2007 .

[20]  C. Duarte,et al.  Light regulation of benthic sulfate reduction rates mediated by seagrass (Thalassia testudinum) metabolism , 2006 .

[21]  T. Binzer,et al.  Community photosynthesis of aquatic macrophytes , 2006 .

[22]  Xabier Irigoien,et al.  Scaling the metabolic balance of the oceans. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[23]  C. Duarte,et al.  Organic carbon metabolism and carbonate dynamics in a Mediterranean seagrass (Posidonia oceanica), meadow , 2006 .

[24]  S. Enríquez,et al.  Form-function analysis of the effect of canopy morphology on leaf self-shading in the seagrass Thalassia testudinum , 2005, Oecologia.

[25]  N. Marbà,et al.  Light-dependence of the metabolic balance of a highly productive Philippine seagrass community , 2005 .

[26]  N. Marbà,et al.  Direct evidence of imbalanced seagrass (Posidonia oceanica) shoot population dynamics in the Spanish Mediterranean , 2005 .

[27]  James W. Fourqurean,et al.  The potential role of plant oxygen and sulphide dynamics in die‐off events of the tropical seagrass, Thalassia testudinum , 2005 .

[28]  Growth-form Light Form-function analysis of the effect of canopy morphology on leaf self-shading in the seagrass Thalassia testudinum , 2005 .

[29]  B. Delille,et al.  Whole-system metabolism and CO2 fluxes in a Mediterranean Bay dominated by seagrass beds (Palma Bay, NW Mediterranean) , 2004 .

[30]  C. Duarte,et al.  Community metabolism and carbon budget along a gradient of seagrass (Cymodocea nodosa) colonization , 2004 .

[31]  N. Marbà,et al.  Sulfur cycling and seagrass (Posidonia oceanica) status in carbonate sediments , 2003 .

[32]  M. Pace,et al.  The Limits to Models in Ecology , 2003 .

[33]  N. Marbà,et al.  Carbon and nitrogen translocation between seagrass ramets , 2002 .

[34]  J. Middelburg,et al.  Carbon and nutrient deposition in a Mediterranean seagrass (Posidonia oceanica) meadow , 2002 .

[35]  J. Romero,et al.  Effects of in situ experimental shading on the Mediterranean seagrass Posidonia oceanica , 2001 .

[36]  J. Romero,et al.  Annual metabolic carbon balance of the seagrass Posidonia oceanica: the importance of carbohydrate reserves , 2001 .

[37]  B. Jørgensen,et al.  Anoxic incubation of sediment in gas-tight plastic bags: a method for biogeochemical process studies , 2000 .

[38]  Carlos M. Duarte,et al.  Seagrass Biomass And Production: A Reassessment , 1999 .

[39]  R. Zimmerman,et al.  Resource allocation and sucrose mobilization in light-limited eelgrass Zostera marina , 1999 .

[40]  F. Roland,et al.  Rapid and precise determination of dissolved oxygen by spectrophotometry: Evaluation of interference from color and turbidity , 1999 .

[41]  W. Dennison,et al.  Effects of light deprivation on the survival and recovery of the seagrass Halophila ovalis (R.Br.) Hook , 1999 .

[42]  J. Gattuso,et al.  CARBON AND CARBONATE METABOLISM IN COASTAL AQUATIC ECOSYSTEMS , 1998 .

[43]  C. Duarte,et al.  Patterns in leaf herbivory on seagrasses , 1998 .

[44]  J. Romero,et al.  Effects of pH on seagrass photosynthesis: a laboratory and field assessment , 1997 .

[45]  K. Dunton,et al.  Seasonal photosynthetic patterns of the seagrass Thalassia testudinum in the western Gulf of Mexico , 1997 .

[46]  K. Dunton,et al.  Effect of in situ light reduction on the maintenance, growth and partitioning of carbon resources in Thalassia testudinum banks ex König , 1997 .

[47]  Carlos M. Duarte,et al.  Submerged aquatic vegetation in relation to different nutrient regimes , 1995 .

[48]  C. Heip,et al.  Production and consumption of biological particles in temperate tidal estuaries , 1995 .

[49]  G. Gong,et al.  Determination of dissolved oxygen in seawater by direct spectrophotometry of total iodine , 1993 .

[50]  B. Jørgensen,et al.  Measurement of bacterial sulfate reduction in sediments: Evaluation of a single-step chromium reduction method , 1989 .

[51]  B. Osborne,et al.  Light and Photosynthesis in Aquatic Ecosystems. , 1985 .

[52]  Bo Barker J⊘rgensen A comparison of methods for the quantification of bacterial sulfate reduction in coastal marine sediments: III. Estimation from chemical and bacteriological field data , 1978 .

[53]  Joel D. Cline,et al.  SPECTROPHOTOMETRIC DETERMINATION OF HYDROGEN SULFIDE IN NATURAL WATERS1 , 1969 .

[54]  A. Willis,et al.  The estimation of carbohydrates in plant extracts by anthrone. , 1954, The Biochemical journal.