The Canary Islands CTZ region: Ecosystem response to the interplay between upwelling filaments, eddies and island wakes
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The Canary Islands CTZ region: Ecosystem response to the interplay between upwelling filaments, eddies and island wakes Javier Arístegui1, Eric D. Barton2, Pablo Sangrá1, Evan Mason1 1Facultad de Ciencias del Mar, Universidad de Las Palmas de Gran Canaria, Spain NASE 2Instituto de Investigaciones Marinas de Vigo, CSIC, Spain CTZ
Outline ! Zonal gradients along the Coastal Transition Zone ! The island-lee region: convergence and divergence fronts ! The eddy field south of the islands ! Biological response to cyclonic and anticyclonic eddies NASE ! Interactions between eddies and filaments CTZ ! Role of eddies in carbon export ! Tracking filaments: frontal structures and temporal evolution ! Modelling the mesoscale and submesocale in the Canary region ! Conclusions and way forward
The Coastal Transition Zone region Madeira ! Transition zone between the eutrophic waters of NASE the Canary Current Coastal Region and the C. Ghir oligotrophic waters of the North Atlantic Subtropical Gyre (NASE) Canary Islands ! Region of intense mesoscale & submesoscale C. Jubi variability, and filament-eddy exchanges CTZ C. Bojador ! Represents a significant carbon source and offshore pump to the open ocean C. Blanc Africa SST
P The range of variation in P-E parameters is of E the same magnitude as ranges observed in basin-scale studies in the Atlantic Ocean. ! : 0.03 – 0.053 (mixed layer) Pm : 0.60 – 13.02 (mixed layer) P Basterretxea and Arístegui 2000, MEPS E
28.5 Gran Canaria Fuerteventura 28.0 Latitude (N) 27.5 Prochlorococcus Pigment biomarkers 20 21 17 Haptophytes 25.64 44.10 19 18 14 Pelagophytes 27.0 41 Diatoms 42 Africa 12 Integrated values (mg m-2) Prasinophytes 18 19 37 38 39 40 Cryptophytes 26.5 10 Temperature (ºC) 8 16.0 15.5 15.0 14.5 14.0 13.5 13.0 6 Longitude (W) 4 Station numbers 18 19 37 38 39 40 41 42 2 max. 3.5 0 18 19 37 38 39 40 41 42 50 Coastal-ocean replacement of diatoms d e pth (m ) DCM 100 by smaller phytoplankton 150 200
Summer Strong upwelling Larger phytoplankton Spring Weaker upwelling More phytoplankton …but smaller Baltar et al. 2009, PiO
Cyclonic Eddy ! Wakes at the lee of the islands ! Cyclonic eddies Wake ! Anticyclonic eddies Filament ! Upwelling filaments Anticyclonic Eddy The NW Africa-Canary CTZ region represents an exceptional laboratory to study oceanographic processes at mesoscale and submesoscale!
Night Night Day Evening-Night CE Warm wake: diurnal heating cycle Weak variability with semi-diurnal period Barton et al. 2000, JGR
Night Night Day Evening-Night CE Trichodesmium Warm wake: diurnal heating cycle Phaeocystis-like Accumulation of positive-buoyant phytoplankton Barton et al. 2000, JGR
Wind rows AVHRR sea surface temperature SAR: wind shear boundaries Field wind from SAR backscatter intensity Barton et al. 2000, JGR
Trade Winds Ekman transport Ekman transport
Section 1 Section 2 Leeward Leeward Convergent and divergent frontal regions (with upwelling and downwelling of 10-20 m d-1) are generated by the wind shear zones extending from the flanks of the island Basterretxea et al. 2002, DSR
Section 1 Section 2 Leeward Leeward Convergent and divergent frontal regions (with upwelling and downwelling of 10-20 m d-1) are generated by the wind shear zones extending from the flanks of the island Basterretxea et al. 2002, DSR
The eddy field south of the Canary Islands C F C !Island eddies are formed by the combination of flow-perturbation A F and Ekman pumping forced at the A C C wind-shearing zones A F A C A !Interaction between island-eddies F and the coastal jet may induce the C A A development of upwelling filaments C. Bojador A F SST C A F August, 1999 C : Cyclonic eddy A : Anticyclonic eddy F : Upwelling filament
Biological consequences of cyclonic eddies D’ D Eddy center 50 100 150 200 Total chlorophyll a (!g l-1) Depth (m) 20 40 60 80 100 Fucoxanthin (ng l-1) 20 40 60 80 100 Divinyl chlorophyll a (!g l-1) Cyclonic eddies inject nutrients into the euphotic zone, increasing primary production and promoting changes in plankton community structure Barton et al. 1998, PiO
Biological consequences of cyclonic eddies F CE AE
Biological consequences of cyclonic eddies Nitrate (uM) 16.2 16.0 15.8 15.6 15.4 15.2 15.0 F CE AE
Biological consequences of cyclonic eddies F CE AE
Contribution of cyclonic eddies to nitrate fluxes Cyclonic eddies contribute as much as coastal upwelling to nitrogen fluxes Barton et al. 1998, PiO
Biological consequences of anticyclonic eddies! Canary Islands Cyclonic Eddy Anticyclonic Eddy CZCS Chlorophyll Anticyclonic island-eddies entrain and transport chlorophyll-rich upwelling waters Arístegui et al., 1997, DSR
Biological consequences of anticyclonic eddies! Anticyclonic eddies accumulate and sink down organic matter in their cores, increasing respiration rates Arístegui et al., 2003, AME
Frontal regions between eddies: POM distribution! Accumulation of POC at interface layers In the deep ocean
Frontal regions between eddies! 66 66 70 70 More than 6 times increase in Bacteria at Station 66… (front between CE and AE)
Frontal regions between eddies! H/L 64 65 0,0 0,2 0,4 0,6 0,8 1,0 1,2 66 0 67 100 68 69 200 70 300 71 72 Depth (m) 400 73 74 500 75 600 76 77 700 78 800 79 80 900 81 82 1000 83 …but they are mostly Low Nucleic-Acid Bacteria (less active?)
POC (!M) Canary Islands 2 C. Juby 8 32 22 14 C. Bojador Africa SeaWIFS Chlorophyll C. Blanc How important is the contribution of eddies to the global carbon export ? (both to the deep ocean and to the open ocean)
Propagation of a SWESTY (Pingree, 1994 ) SWESTY: anticyclonic Shallow subtropical subducting WEStward-propagating eddY Sangrá et al., 2009, DSR
31 Jul
Sedimentation of Chla Centre of filament Perihery of filament Sea Surface Temperature (21 Aug 2009)
6 4 Sedimentation of Chla Centre of filament Perihery of filament Sea Surface Temperature (21 Aug 2009)
!" ,,)-'("*.*#/'"*)&00. 1)23#$)4"'5"'6 !"#$%&'()*&'(&+ Filament poleward front convergence #" !"#$%&'###()"*+,-./0)1223) Compression of planetary vorticity tubes anticyclone
D4 D3 D6 D5 D2 D1
D4 D3 D6 D5 D2 D1 Microplankton Nanoplankton Picoplankton
D4 D3 D6 D5 D2 D1
Cape Guir, 1992 C. Juby, 1999 mmolO2 m-2 d-1 mmolO2 m-2 d-1 P/R P/R GP/R >1 GP/R
Cyclonic Eddy SST August 1993 Wake Filament Anticyclonic Eddy Near surface currents Zooplankton biomass 28.5 N 28.0 27.5 27.0 26.5 Chlorophyll a Neritic larvae Barton et. al. 1998 26.0
NW Africa UW Filaments Canary Is. Year Catches Larvae Catches 1993 Sardina pilchardus S. pilchardus S. pilchardus 1999 Engraulis encrasicolus E. encrasicolus E. encrasicolus Sardinella aurita S. aurita S. aurita 2001 Sardina pilchardus S. pilchardus S. pilchardus ( ! ) Moyano et al. 2009, Fish Ocean
! Large domain " 10 years " 11–km resolution " Includes open Strait of Gibraltar ! Intermediate domain " 6 years " 5-km resolution ! Small domain " 2 years " 1-1.5-km resolution
! Develop a ROMS configuration for the Canary Island region " ROMS: 3D, primitive equation, hydrostatic model (Shcheptekin & McWilliams, 2005) ! Study the evolution and generation mechanisms of eddies and upwelling filaments " Topographic forcing " Wind forcing
1.5-km domain: Compare low vs. high resolution wind Climatological wind stress forcing Atmospheric model (MM5) Mason et al. (in prep)
Vorticity-1-km resolution. 1-km domain embedded within a 3 Km domain Side boundary forcing:TS climatology with geostrophic velocities 25-km SCOW wind stress climatology and COADS surface fluxes Mason et al. (in prep)
Conclusions & Way Forward ! The Canary region is an excellent laboratory to study the influence of submesoscale ocean dynamics on the marine ecosystem and biogeochemical cycles ! The interplay between (island) eddies and upwelling filaments enhance production and may export coastal enriched water to the open ocean through POC sedimentation and transport by an eddy corridor ! Little is known about the effects and global magnitude of submesoscale dynamics on transient productivity and carbon fluxes events ! Novel instrumentation (e.g autonomous vehicles and drifters with new generation of optical sensors) and processes-oriented studies at the submesoscale are necessary to understand the mechanisms of carbon production, exchange and transport in CTZ ! ROMS does good job of reproducing submesoscale variability in response to both topographic and wind forcing ! Biogeochemical ROMS modules should be incorporated to address productivity and carbon fluxes in the region
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