Impactos del ENSO en la biogeoquímica del sistema de afloramiento frente a Perú central, febrero 2013 - diciembre 2015

El ecosistema de afloramiento frente a Perú, tiene características que le confieren propiedades únicas y relevantes en el contexto regional y global. Entre sus propiedades biogeoquímicas se destaca la presencia de i) una alta productividad consecuencia de aguas ricas en nutrientes, ii) una extensa y somera Zona de Mínimo Oxígeno (ZMO) y iii) un alto reciclaje y pérdida de nitratos, asociado a los procesos de productividad como a la remineralización de la materia orgánica. Todas estas características están inmersas en una alta variabilidad temporal, observándose cambios significativos a escala interanual asociados con el ciclo ENSO y su fase cálida El Niño y fría La Niña. En este contexto, desde el año 2013, la DGIOCC de IMARPE desarrolla el proyecto “Estudio integrado del Afloramiento Costero frente a Perú Central”, con la finalidad de caracterizar el afloramiento costero, sus forzantes y sus características físico- químicas y biológicas en una gradiente costa-océano. En este artículo, se presentan resultados de las condiciones químicas del afloramiento frente a Callao, poniendo en evidencia el impacto del ciclo El Niño Oscilación del Sur (ENSO) que se desarrolló entre los años 2013 y 2015.p.2-6IMARP

Strong and Dynamic Benthic-Pelagic Coupling and Feedbacks in a Coastal Upwelling System (Peruvian Shelf)

Monthly time-series data (1998–2009) of bottom water oxygen, nitrate and nitrite concentrations from the outer shelf (150 m water depth) in the oxygen minimum zone offshore Peru were coupled to a layered biogeochemical sediment model to investigate benthic-pelagic coupling over multi-annual time scales. The model includes the mineralization of four reactive pools of particulate organic carbon (POC) with lifetimes of 0.13, 1.3, 20, and 1700 year that were constrained using empirical data. Total POC rain rates to the seafloor were derived from satellite based estimates of primary production. Solute fluxes and concentrations in sediment porewater showed highly dynamic behavior over the course of a typical year. Conversion of fixed N to N2 by denitrification varied from 1.1 mmol m−2 d−1 of N in winter to 1.8 mmol m−2 d−1 of N in summer with a long term mean N loss for the shelf of 1.5 mmol m−2 d−1 of N. Fixed N loss across the whole time-series agreed very well with a previously-published vertically-integrated sediment model for coupling the benthic and pelagic N cycle in regional and global models. Dissimilatory nitrate reduction to ammonium (DNRA) emerges as a major process in the benthic N cycle, producing on average 1.9 mmol m−2 d−1 of ammonium: more than twice the rate of ammonification of organic nitrogen. The model predicts sulfide emissions from the sediment of up to 1 mmol m−2 d−1 when POC rain rate exceeds 20 mmol m−2 d−1, in agreement with past observations of benthic sulfide fluxes and sulfide plume distributions in the water column. This study demonstrates that sediments on the Peruvian shelf are not static repositories that are independent of changes taking place in the water column. Our results strongly suggest the shelf sediments must exert an important feedback on biogeochemical processes in the overlying waters, and should be considered in regional model studies

Dissolved Organic Matter Cycling in the Coastal Upwelling System Off Central Peru During an “El Niño” Year

The Peruvian upwelling system (PUS) is among the most productive regions in the ocean, with high rates of primary production and an intense oxygen minimum zone (OMZ). The main perturbation of this system is associated to “El Niño” (EN), which affects water mass distribution and reduces primary production. Previous studies in the PUS provided first insights into the dynamics of dissolved organic matter (DOM), but high-resolution studies involving the molecular characterization of the DOM pool to reveal the processes that affect the carbon cycle in this highly productive system are lacking. We characterized the molecular composition of solid-phase extractable DOM (SPE-DOM) in the coastal upwelling system off Central Peru and linked it to specific processes that affect DOM cycling. Seasonal sampling (April, August, and December) was carried out off Central Peru (12°S) during 2015, a low productivity year marked by EN conditions. The DOM molecular composition was obtained via Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). Solid-phase extractable dissolved organic carbon (SPE-DOC) concentrations showed significant differences (p < 0.05) between the water masses present off central Peru. In order to explore if changes in SPE-DOC concentrations were the result of water mass mixing, we applied a conservative mixing (CM) model. The model revealed a non-conservative behavior of SPE-DOC and allowed us to identify two distinct groups of samples with increased and decreased SPE-DOC concentrations, respectively, and one group of samples inside the CM range. Differences in environmental parameters characterizing these groups were in accordance with respective processes associated to production and degradation of SPE-DOC. The trends observed for molecular parameters revealed the imprint of processes related to DOM production and DOM degradation, both biotic (microbial degradation) and abiotic (photodegradation). Our study suggests that even under low productivity conditions like EN, there is an active cycling of the DOM pool off central Peru

Oxygen Variability During ENSO in the Tropical South Eastern Pacific

The Oxygen Minimum Zone (OMZ) of the Tropical South Eastern Pacific (TSEP) is one of the most intensely deoxygenated water masses of the global ocean. It is strongly affected at interannual time scales by El Niño (EN) and La Niña (LN) due to its proximity to the equatorial Pacific. In this work, the physical and biogeochemical processes associated with the subsurface oxygen variability during EN and LN in the period 1958–2008 were studied using a regional coupled physical-biogeochemical model and in situ observations. The passage of intense remotely forced coastal trapped waves caused a strong deepening (shoaling) of the OMZ upper limit during EN (LN). A close correlation between the OMZ upper limit and thermocline depths was found close to the coast, highlighting the role of physical processes. The subsurface waters over the shelf and slope off central Peru had different origins depending on ENSO conditions. Offshore of the upwelling region (near 88°W), negative and positive oxygen subsurface anomalies were caused by Equatorial zonal circulation changes during LN and EN, respectively. The altered properties were then transported to the shelf and slope (above 200 m) by the Peru-Chile undercurrent. The source of nearshore oxygenated waters was located at 3°S−4°S during neutral periods, further north (1°S−1°N) during EN and further south (4°S−5°S) during LN. The offshore deeper (<200–300 m) OMZ was ventilated by waters originating from ~8°S during EN and LN. Enhanced mesoscale variability during EN also impacted OMZ ventilation through horizontal and vertical eddy fluxes. The vertical eddy flux decreased due to the reduced vertical gradient of oxygen in the surface layer, whereas horizontal eddy fluxes injected more oxygen into the OMZ through its meridional boundaries. In subsurface layers, remineralization of organic matter, the main biogeochemical sink of oxygen, was higher during EN than during LN due to oxygenation of the surface layer. Sensitivity experiments highlighted the larger impact of equatorial remote forcing with respect to local wind forcing during EN and LN

Aerobic Microbial Respiration In Oceanic Oxygen Minimum Zones

Oxygen minimum zones are major sites of fixed nitrogen loss in the ocean. Recent studies have highlighted the importance of anaerobic ammonium oxidation, anammox, in pelagic nitrogen removal. Sources of ammonium for the anammox reaction, however, remain controversial, as heterotrophic denitrification and alternative anaerobic pathways of organic matter remineralization cannot account for the ammonium requirements of reported anammox rates. Here, we explore the significance of microaerobic respiration as a source of ammonium during organic matter degradation in the oxygen-deficient waters off Namibia and Peru. Experiments with additions of double-labelled oxygen revealed high aerobic activity in the upper OMZs, likely controlled by surface organic matter export. Consistently observed oxygen consumption in samples retrieved throughout the lower OMZs hints at efficient exploitation of vertically and laterally advected, oxygenated waters in this zone by aerobic microorganisms. In accordance, metagenomic and metatranscriptomic analyses identified genes encoding for aerobic terminal oxidases and demonstrated their expression by diverse microbial communities, even in virtually anoxic waters. Our results suggest that microaerobic respiration is a major mode of organic matter remineralization and source of ammonium (~45-100%) in the upper oxygen minimum zones, and reconcile hitherto observed mismatches between ammonium producing and consuming processes therein

Giant Hydrogen Sulfide Plume in the Oxygen Minimum Zone off Peru Supports Chemolithoautotrophy

In Eastern Boundary Upwelling Systems nutrient-rich waters are transported to the ocean surface, fuelling high photoautotrophic primary production. Subsequent heterotrophic decomposition of the produced biomass increases the oxygen-depletion at intermediate water depths, which can result in the formation of oxygen minimum zones (OMZ). OMZs can sporadically accumulate hydrogen sulfide (H2S), which is toxic to most multicellular organisms and has been implicated in massive fish kills. During a cruise to the OMZ off Peru in January 2009 we found a sulfidic plume in continental shelf waters, covering an area >5500 km2, which contained ~2.2×104 tons of H2S. This was the first time that H2S was measured in the Peruvian OMZ and with ~440 km3 the largest plume ever reported for oceanic waters. We assessed the phylogenetic and functional diversity of the inhabiting microbial community by high-throughput sequencing of DNA and RNA, while its metabolic activity was determined with rate measurements of carbon fixation and nitrogen transformation processes. The waters were dominated by several distinct γ-, δ- and ε-proteobacterial taxa associated with either sulfur oxidation or sulfate reduction. Our results suggest that these chemolithoautotrophic bacteria utilized several oxidants (oxygen, nitrate, nitrite, nitric oxide and nitrous oxide) to detoxify the sulfidic waters well below the oxic surface. The chemolithoautotrophic activity at our sampling site led to high rates of dark carbon fixation. Assuming that these chemolithoautotrophic rates were maintained throughout the sulfidic waters, they could be representing as much as ~30% of the photoautotrophic carbon fixation. Postulated changes such as eutrophication and global warming, which lead to an expansion and intensification of OMZs, might also increase the frequency of sulfidic waters. We suggest that the chemolithoautotrophically fixed carbon may be involved in a negative feedback loop that could fuel further sulfate reduction and potentially stabilize the sulfidic OMZ water

Global perspectives on observing ocean boundary current systems

Ocean boundary current systems are key components of the climate system, are home to highly productive ecosystems, and have numerous societal impacts. Establishment of a global network of boundary current observing systems is a critical part of ongoing development of the Global Ocean Observing System. The characteristics of boundary current systems are reviewed, focusing on scientific and societal motivations for sustained observing. Techniques currently used to observe boundary current systems are reviewed, followed by a census of the current state of boundary current observing systems globally. The next steps in the development of boundary current observing systems are considered, leading to several specific recommendations.Fil: Todd, Robert E.. Woods Hole Oceanographic Institution; Estados UnidosFil: Chavez, Francisco. Monterey Bay Aquarium Research Institute; Estados UnidosFil: Clayton, Sophie. Old Dominion University; Estados UnidosFil: Cravatte, Sophie E.. Centre National de la Recherche Scientifique. Institut de Recherche pour le Développement; Francia. Universite de Toulouse; FranciaFil: Goes, Marlos P.. University of Miami; Estados UnidosFil: Graco, Michelle I.. Instituto del Mar del Peru; PerúFil: Lin, Xiaopei. Ocean University of China; ChinaFil: Sprintall, Janet. University of California; Estados UnidosFil: Zilberman, Nathalie V.. University of California; Estados UnidosFil: Archer, Matthew. California Institute of Technology; Estados UnidosFil: Arístegui, Javier. Universidad de Las Palmas de Gran Canaria; EspañaFil: Balmaseda, Magdalena A.. European Centre for Medium-Range Weather Forecasts; Reino UnidoFil: Bane, John M.. University of North Carolina; Estados UnidosFil: Baringer, Molly O.. Atlantic Oceanographic and Meteorological Laboratory ; Estados UnidosFil: Barth, John A.. State University of Oregon; Estados UnidosFil: Beal, Lisa M.. University of Miami; Estados UnidosFil: Brandt, Peter. Geomar-Helmholtz Centre for Ocean Research Kiel; AlemaniaFil: Calil, Paulo H.. Universidade Federal do Rio Grande; BrasilFil: Campos, Edmo. Universidade de Sao Paulo; BrasilFil: Centurioni, Luca R.. University of California; Estados UnidosFil: Chidichimo, María Paz. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Ministerio de Defensa. Armada Argentina. Servicio de Hidrografía Naval; ArgentinaFil: Cirano, Mauro. Universidade Federal do Rio de Janeiro; BrasilFil: Cronin, Meghan F.. National Oceanic and Atmospheric Administration. Pacific Marine Environmental Laboratory; Estados UnidosFil: Curchitser, Enrique N.. Rutgers University; Estados UnidosFil: Davis, Russ E.. University of California; Estados UnidosFil: Dengler, Marcus. Geomar-Helmholtz Centre for Ocean Research Kiel; AlemaniaFil: DeYoung, Brad. Memorial University of Newfoundland; CanadáFil: Dong, Shenfu. University of Miami; Estados UnidosFil: Escribano, Ruben. Universidad de Concepción; ChileFil: Fassbender, Andrea J.. Monterey Bay Aquarium Research Institute; Estados Unido

Factors controlling plankton community production, export flux, and particulate matter stoichiometry in the coastal upwelling system off Peru

Eastern boundary upwelling systems (EBUS) are among the most productive marine ecosystems on Earth. The production of organic material is fueled by upwelling of nutrient-rich deep waters and high incident light at the sea surface. However, biotic and abiotic factors can modify surface production and related biogeochemical processes. Determining these factors is important because EBUS are considered hotspots of climate change, and reliable predictions of their future functioning requires understanding of the mechanisms driving the biogeochemical cycles therein. In this field experiment, we used in situ mesocosms as tools to improve our mechanistic understanding of processes controlling organic matter cycling in the coastal Peruvian upwelling system. Eight mesocosms, each with a volume of ∼55 m3, were deployed for 50 d ∼6 km off Callao (12∘ S) during austral summer 2017, coinciding with a coastal El Niño phase. After mesocosm deployment, we collected subsurface waters at two different locations in the regional oxygen minimum zone (OMZ) and injected these into four mesocosms (mixing ratio ≈1.5 : 1 mesocosm: OMZ water). The focus of this paper is on temporal developments of organic matter production, export, and stoichiometry in the individual mesocosms. The mesocosm phytoplankton communities were initially dominated by diatoms but shifted towards a pronounced dominance of the mixotrophic dinoflagellate (Akashiwo sanguinea) when inorganic nitrogen was exhausted in surface layers. The community shift coincided with a short-term increase in production during the A. sanguinea bloom, which left a pronounced imprint on organic matter C : N : P stoichiometry. However, C, N, and P export fluxes did not increase because A. sanguinea persisted in the water column and did not sink out during the experiment. Accordingly, export fluxes during the study were decoupled from surface production and sustained by the remaining plankton community. Overall, biogeochemical pools and fluxes were surprisingly constant for most of the experiment. We explain this constancy by light limitation through self-shading by phytoplankton and by inorganic nitrogen limitation which constrained phytoplankton growth. Thus, gain and loss processes remained balanced and there were few opportunities for blooms, which represents an event where the system becomes unbalanced. Overall, our mesocosm study revealed some key links between ecological and biogeochemical processes for one of the most economically important regions in the oceans

Global variability in seawater Mg:Ca and Sr:Ca ratios in the modern ocean

Seawater Mg:Ca and Sr:Ca ratios are biogeochemical parameters reflecting the Earth–ocean–atmosphere dynamic exchange of elements. The ratios’ dependence on the environment and organisms' biology facilitates their application in marine sciences. Here, we present a measured single-laboratory dataset, combined with previous data, to test the assumption of limited seawater Mg:Ca and Sr:Ca variability across marine environments globally. High variability was found in open-ocean upwelling and polar regions, shelves/neritic and river-influenced areas, where seawater Mg:Ca and Sr:Ca ratios range from ∼4.40 to 6.40 mmol:mol and ∼6.95 to 9.80 mmol:mol, respectively. Open-ocean seawater Mg:Ca is semiconservative (∼4.90 to 5.30 mol:mol), while Sr:Ca is more variable and nonconservative (∼7.70 to 8.80 mmol:mol); both ratios are nonconservative in coastal seas. Further, the Ca, Mg, and Sr elemental fluxes are connected to large total alkalinity deviations from International Association for the Physical Sciences of the Oceans (IAPSO) standard values. Because there is significant modern seawater Mg:Ca and Sr:Ca ratios variability across marine environments we cannot absolutely assume that fossil archives using taxa-specific proxies reflect true global seawater chemistry but rather taxa- and process-specific ecosystem variations, reflecting regional conditions. This variability could reconcile secular seawater Mg:Ca and Sr:Ca ratio reconstructions using different taxa and techniques by assuming an error of 1 to 1.50 mol:mol, and 1 to 1.90 mmol:mol, respectively. The modern ratios’ variability is similar to the reconstructed rise over 20 Ma (Neogene Period), nurturing the question of seminonconservative behavior of Ca, Mg, and Sr over modern Earth geological history with an overlooked environmental effect