We quantify, compare, and generalize responses of experimental nutrient loadings (L N ) on planktonic community structure and function in coastal waters. Data were derived from three mesocosm experiments undertaken in Baltic (BAL), Mediterranean (MED), and Norwegian (NOR) coastal waters. A planktonic model with seven functional compartments and 30–32 different carbon flows fit to all three experiments was used as a framework for flow‐rate estimation and comparison. Flows were estimated on the basis of time series of measured biomass, some measured flows, and inverse modeling. Biomass and gross uptake rate of carbon of most groups increased linearly with increasing L N in the nutrient input range of 0–1 µmol N L −1 d −1 at all locations. The fate of the gross primary production (GPP) was similar in all systems. Autotrophic biomass varied by two orders of magnitude among locations, with the lowest biomass and response to nutrient addition in MED waters. The variation of GPP among sites was less than one order of magnitude. Mesozooplankton dominated by doliolids (Tunicata), but not those dominated by copepods, presumably exerted efficient control of the autotrophic biomass, thereby buffering responses of autotrophs to high nutrient input. Among the many factors that can modify the responses of autotrophs to nutrients, the time scale over which the enrichment is made and the precise mode of nutrient enrichment are important. We suggest a general concept that may contribute to a scientific basis for understanding and managing coastal eutrophication.
Abstract. The carbon burial in vegetated sediments, ignored in past assessments of carbon burial in the ocean, was evaluated using a bottom-up approach derived from upscaling a compilation of published individual estimates of carbon burial in vegetated habitats (seagrass meadows, salt marshes and mangrove forests) to the global level and a top-down approach derived from considerations of global sediment balance and a compilation of the organic carbon content of vegeatated sediments. Up-scaling of individual burial estimates values yielded a total carbon burial in vegetated habitats of 111 Tg C y-1. The total burial in unvegetated sediments was estimated to be 126 Tg C y-1, resulting in a bottom-up estimate of total burial in the ocean of 244 Tg C y-1, two-fold higher than estimates of oceanic carbon burial that presently enter global carbon budgets. The organic carbon concentrations in vegetated marine sediments exceeds by 2 to 10-fold those in shelf/deltaic sediments. Top-down recalculation of ocean sediment budgets to account for these, previously neglected, organic-rich sediments, yields a top-down carbon burial estimate of 197 Tg C y-1, with vegetated coastal habitats contributing about 50%. Even though vegetated carbon burial contribute about half of the total carbon burial in the ocean, burial represents a small fraction of the net production of these ecosystems, estimated at about 3031 Tg C y-1, suggesting that bulk of the benthic NEP must support excess respiration in other compartments, such as unvegetated sediments and the coastal pelagic compartment. The total excess organic carbon available to be exported to the ocean is estimated at between 769 to 3177 Tg C y-1, the bulk of which must be respired in the open ocean. Widespread loss of vegetated coastal habitats must have reduced carbon burial in the ocean by about 30 Tg C y-1, identifying the destruction of these ecosystems as an important loss of CO2 sink capacity in the biosphere.
Incubation (in vitro) and incubation-free (in situ) methods, each with their own advantages and limitations, have been used to derive estimates of net community metabolism in the oligotrophic subtropical gyres of the open ocean. The hypothesis that heterotrophic communities are prevalent in most oligotrophic regions is consistent with the available evidence and supported by scaling relationships showing that heterotrophic communities prevail in areas of low gross primary production, low chlorophyll a, and warm water, conditions found in the oligotrophic ocean. Heterotrophic metabolism can prevail where heterotrophic activity is subsidized by organic carbon inputs from the continental shelf or the atmosphere and from nonphotosynthetic autotrophic and mixotrophic metabolic pathways. The growth of the oli-gotrophic regions is likely to be tilting the metabolic balance of the ocean toward a greater prevalence of heterotrophic communities.
Mangroves have been converted and degraded for decades. Rates of loss have declined over the past decades, but achieving resilient coastlines requires both conservation and restoration. Here, we outline the challenges for the global restoration of mangroves and what actions could enhance restoration. Ambitious global targets for mangrove restoration, if successful, could deliver global benefits of carbon sequestration, fisheries production, biodiversity, and coastal protection. However, large-scale mangrove planting efforts have often failed, and smaller projects may not deliver landscape-scale benefits, even though they are more suited to community management. Solutions to achieving global targets include reducing risks of large projects and increasing the uptake and effectiveness of smaller projects. Sustainable mangrove restoration requires investment in capacity building in communities and institutions, and mechanisms to match restoration opportunities with prospective supporters and investors. Global reporting standards will support adaptive management and help fully understand and monitor the benefits of mangrove restoration.
The reduction in sea ice cover with Arctic warming facilitates the transit of ships through routes that are remarkably shorter than the traditional shipping routes. Automatic Identification System (AIS), ideally designed to avoid vessel collisions, transmits on vessel navigation information (currently 27 types of messages) such as name, position or speed, is a powerful data source to monitor the progress of Arctic shipping as the ice cover decreases. Based on the analysis of an online platform collecting shipping AIS data, we quantified the spatial distribution of shipping through the Arctic Ocean, its intensity and the temporal evolution, in relation to the area released by the sea ice area. Shipping through the Arctic Ocean is distributed spatially following a heavy-tailed distribution, implying heavy traffic through a limited Arctic area, with an exponent that depends on the vessel category. Fishing is the category with the largest spatial spread, with the width of shipping routes correlated with the proximal sea ice area. The time evolution of these routes is characterized by increasing extended periods of shipping activity through the year. AIS data offers valuable information on the activity of the international fleet worldwide. In the context of the new international agreements, it is a valuable source to monitor shipping, fishing and the potential impact in marine life among other aspects. Here we have focused on the Arctic shipping in recent years, which is rapidly growing, particularly around the Northeastern and Northwest Passage coastal routes, providing an opportunity for the design of shorter shipping routes and reduced greenhouse gas emissions from transport of goods, but at a risk of impacts on the Arctic ecosystem.
El siguiente articulo trata sobre un trabajo etnografico realizado en la Escuela de Combatientes del Ejercito de Liberacion Nacional en Colombia. La idea fue realizar un acercamiento a la preparacion de los aspirantes a guerrilleros y ver como este proceso construido social y simbolicamente se conforma como un rito de iniciacion. La metodologia utilizada en esta etnografia radica en la utilizacion del video como una herramienta de investigacion. De esta manera estamos frente a una etnografia de la comunicacion que combina la antropologia simbolica con la visual.
Abstract. The emerging field of blue carbon science is seeking cost-effective ways to estimate the organic carbon content of soils that are bound by coastal vegetated ecosystems. Organic carbon (Corg) content in terrestrial soils and marine sediments has been correlated with mud content (i.e. silt and clay), however, empirical tests of this theory are lacking for coastal vegetated ecosystems. Here, we compiled data (n = 1345) on the relationship between Corg and mud (i.e. silt and clay, particle sizes <63 μm) contents in seagrass ecosystems (79 cores) and adjacent bare sediments (21 cores) to address whether mud can be used to predict soil Corg content. We also combined these data with the δ13C signatures of the soil Corg to understand the sources of Corg stores. The results showed that mud is positively correlated with soil Corg content only when the contribution of seagrass-derived Corg to the sedimentary Corg pool is relatively low, such as in small and fast growing meadows of the genera Zostera, Halodule and Halophila, and in bare sediments adjacent to seagrass ecosystems. In large and long-living seagrass meadows of the genera Posidonia and Amphibolis there was a lack of, or poor relationship between mud and soil Corg content, related to a higher contribution of seagrass-derived Corg to the sedimentary Corg pool in these meadows. The relative high soil Corg contents with relatively low mud contents (i.e. mud-Corg saturation) together with significant allochthonous inputs of terrestrial organic matter could overall disrupt the correlation expected between soil Corg and mud contents. This study shows that mud (i.e. silt and clay content) is not a universal proxy for blue carbon content in seagrass ecosystems, and therefore should not be applied generally across all seagrass habitats. Mud content can only be used as a proxy to estimate soil Corg content for scaling up purposes when opportunistic and/or low biomass seagrass species (i.e. Zostera, Halodule and Halophila) are present (explaining 34 to 91% of variability), and in bare sediments (explaining 78% of the variability).
