Mixed Layer Heat Balance on Intraseasonal Time Scales in the Northwestern Tropical Atlantic Ocean*

2005 ◽  
Vol 18 (20) ◽  
pp. 4168-4184 ◽  
Author(s):  
Gregory R. Foltz ◽  
Michael J. McPhaden

Abstract Recent observations have shown evidence of intraseasonal oscillations (with periods of approximately 1–2 months) in the northern and southern tropical Atlantic trade winds. In this paper, the oceanic response to the observed intraseasonal wind variability is addressed through an analysis of the surface mixed layer heat balance, focusing on three locations in the northwestern tropical Atlantic where in situ measurements from moored buoys are available (14.5°N, 51°W; 15°N, 38°W; and 18°N, 34°W). It is found that local heat storage at all three locations is balanced primarily by wind-induced latent heat loss, which is the same mechanism that is believed to play a dominant role on interannual and decadal time scales in the region. It is also found that the intraseasonal wind speed oscillations are linked to changes in surface wind convergence and convection over the western equatorial Atlantic warm pool. These atmospheric circulation anomalies and wind-induced SST anomalies potentially feed back on one another to affect longer time-scale variability in the region.

2006 ◽  
Vol 19 (20) ◽  
pp. 5227-5252 ◽  
Author(s):  
Serena Illig ◽  
Boris Dewitte

Abstract The relative roles played by the remote El Niño–Southern Oscillation (ENSO) forcing and the local air–sea interactions in the tropical Atlantic are investigated using an intermediate coupled model (ICM) of the tropical Atlantic. The oceanic component of the ICM consists of a six-baroclinic mode ocean model and a simple mixed layer model that has been validated from observations. The atmospheric component is a global atmospheric general circulation model developed at the University of California, Los Angeles (UCLA). In a forced context, the ICM realistically simulates both the sea surface temperature anomaly (SSTA) variability in the equatorial band, and the relaxation of the Atlantic northeast trade winds and the intensification of the equatorial westerlies in boreal spring that usually follows an El Niño event. The results of coupled experiments with or without Pacific ENSO forcing and with or without explicit air–sea interactions in the equatorial Atlantic indicate that the background energy in the equatorial Atlantic is provided by ENSO. However, the time scale of the variability and the magnitude of some peculiar events cannot be explained solely by ENSO remote forcing. It is demonstrated that the peak of SSTA variability in the 1–3-yr band as observed in the equatorial Atlantic is due to the local air–sea interactions and is not a linear response to ENSO. Seasonal phase locking in boreal summer is also the result of the local coupling. The analysis of the intrinsic sustainable modes indicates that the Atlantic El Niño is qualitatively a noise-driven stable system. Such a system can produce coherent interdecadal variability that is not forced by the Pacific or extraequatorial variability. It is shown that when a simple slab mixed layer model is embedded into the system to simulate the northern tropical Atlantic (NTA) SST variability, the warming over NTA following El Niño events have characteristics (location and peak phase) that depend on air–sea interaction in the equatorial Atlantic. In the model, the interaction between the equatorial mode and NTA can produce a dipolelike structure of the SSTA variability that evolves at a decadal time scale. The results herein illustrate the complexity of the tropical Atlantic ocean–atmosphere system, whose predictability jointly depends on ENSO and the connections between the Atlantic modes of variability.


2009 ◽  
Vol 6 (4) ◽  
pp. 535-544 ◽  
Author(s):  
I. Hense ◽  
B. Quack

Abstract. The relative importance of potential source and sink terms for bromoform (CHBr3) in the tropical Atlantic Ocean is investigated with a coupled physical-biogeochemical water column model. Bromoform production is either assumed to be linked to primary production or to phytoplankton losses; bromoform decay is treated as light dependent (photolysis), and in addition either vertically uniform, proportional to remineralisation or to nitrification. All experiments lead to the observed subsurface maximum of bromoform, corresponding to the subsurface phytoplankton biomass maximum. In the surface mixed layer, the concentration is set by entrainment from below, photolysis in the upper few meters and the outgassing to the atmosphere. The assumed bromoform production mechanism has only minor effects on the solution, but the various loss terms lead to significantly different bromoform concentrations below 200 m depth. The best agreement with observations is obtained when the bromoform decay is coupled to nitrification (parameterised by an inverse proportionality to the light field). Our model results reveal a pronounced seasonal cycle of bromoform outgassing, with a minimum in summer and a maximum in early winter, when the deepening surface mixed layer reaches down into the bromoform production layer.


2015 ◽  
Vol 12 (7) ◽  
pp. 5559-5608 ◽  
Author(s):  
H. Hepach ◽  
B. Quack ◽  
S. Raimund ◽  
T. Fischer ◽  
E. L. Atlas ◽  
...  

Abstract. Halocarbons from oceanic sources contribute to halogens in the troposphere, and can be transported into the stratosphere where they take part in ozone depletion. This paper presents distribution and sources in the equatorial Atlantic from June and July 2011 of the four compounds bromoform (CHBr3), dibromomethane (CH2Br2), methyl iodide (CH3I) and diiodomethane (CH2I2). Enhanced biological production during the Atlantic Cold Tongue (ACT) season, indicated by phytoplankton pigment concentrations, led to elevated concentrations of CHBr3 of up to 44.7 pmol L−1 and up to 9.2 pmol L−1 for CH2Br2 in surface water, which is comparable to other tropical upwelling systems. While both compounds correlated very well with each other in the surface water,CH2Br2 was often more elevated in greater depth than CHBr3, which showed maxima in the vicinity of the deep chlorophyll maximum. The deeper maximum of CH2Br2 indicates an additional source in comparison to CHBr3 or a slower degradation of CH2Br2. Concentrations of CH3I of up to 12.8 pmol L−1 in the surface water were measured. In contrary to expectations of a predominantly photochemical source in the tropical ocean, its distribution was mostly in agreement with biological parameters, indicating a~biological source. CH2I2 was very low in the near surface water with maximum concentrations of only 3.7 pmol L−1, and the observed anticorrelation with global radiation was likely due to its strong photolysis. CH2I2 showed distinct maxima in deeper waters similar to CH2Br2. For the first time, diapycnal fluxes of the four halocarbons from the upper thermocline into and out of the mixed layer were determined. These fluxes were low in comparison to the halocarbon sea-to-air fluxes. This indicates that despite the observed maximum concentrations at depth, production in the surface mixed layer is the main oceanic source for all four compounds and has an influence on emissions into the atmosphere. The calculated production rates of the compounds yield 34 (CHBr3), 10 (CH2Br2), 21 (CH3I) and 384 (CH2I2) pmol m−3 h−1 in the whole mixed layer.


2012 ◽  
Vol 25 (10) ◽  
pp. 3583-3598 ◽  
Author(s):  
Jieshun Zhu ◽  
Bohua Huang ◽  
Zhaohua Wu

Abstract This study examines a mechanism of the interaction between the tropical Atlantic meridional and equatorial modes. To derive robust heat content (HC) variability, the ensemble-mean HC anomalies (HCA) of six state-of-the-art global ocean reanalyses for 1979–2007 are analyzed. Compared with previous studies, characteristic oceanic processes are distinguished through their dominant time scales. Using the ensemble empirical mode decomposition (EEMD) method, the HC fields are first decomposed into components with different time scales. The authors’ analysis shows that these components are associated with distinctive ocean dynamics. The high-frequency (first three) components can be characterized as the equatorial modes, whereas the low-frequency (the fifth and sixth) components are featured as the meridional modes. In between, the fourth component on the time scale of 3–4 yr demonstrates “mixed” characteristics of the meridional and equatorial modes because of an active transition from the predominant meridional to zonal structures on this time scale. Physically, this transition process is initiated by the discharge of the off-equatorial HCA, which is first accumulated as a part of the meridional mode, into the equatorial waveguide, which is triggered by the breakdown of the equilibrium between the cross-equatorial HC contrast and the overlying wind forcing, and results in a major heat transport through the equatorial waveguide into the southeastern tropical Atlantic. It is also shown that remote forcing from El Niño–Southern Oscillation (ENSO) exerts important influence on the transition from the equatorial to meridional mode and may partly dictate its time scale of 3–4 yr. Therefore, the authors’ results demonstrate another mechanism of the equatorial Atlantic response to the ENSO forcing.


2014 ◽  
Vol 119 (12) ◽  
pp. 8472-8494 ◽  
Author(s):  
Marcelo P. Curtarelli ◽  
Igor Ogashawara ◽  
Carlos A. S. Araújo ◽  
Enner H. Alcântara ◽  
João A. Lorenzzetti ◽  
...  

2015 ◽  
Vol 12 (21) ◽  
pp. 6369-6387 ◽  
Author(s):  
H. Hepach ◽  
B. Quack ◽  
S. Raimund ◽  
T. Fischer ◽  
E. L. Atlas ◽  
...  

Abstract. Halocarbons from oceanic sources contribute to halogens in the troposphere, and can be transported into the stratosphere where they take part in ozone depletion. This paper presents distribution and sources in the equatorial Atlantic from June and July 2011 of the four compounds bromoform (CHBr3), dibromomethane (CH2Br2), methyl iodide (CH3I) and diiodomethane (CH2I2). Enhanced biological production during the Atlantic Cold Tongue (ACT) season, indicated by phytoplankton pigment concentrations, led to elevated concentrations of CHBr3 of up to 44.7 and up to 9.2 pmol L−1 for CH2Br2 in surface water, which is comparable to other tropical upwelling systems. While both compounds correlated very well with each other in the surface water, CH2Br2 was often more elevated in greater depth than CHBr3, which showed maxima in the vicinity of the deep chlorophyll maximum. The deeper maximum of CH2Br2 indicates an additional source in comparison to CHBr3 or a slower degradation of CH2Br2. Concentrations of CH3I of up to 12.8 pmol L−1 in the surface water were measured. In contrary to expectations of a predominantly photochemical source in the tropical ocean, its distribution was mostly in agreement with biological parameters, indicating a biological source. CH2I2 was very low in the near surface water with maximum concentrations of only 3.7 pmol L−1. CH2I2 showed distinct maxima in deeper waters similar to CH2Br2. For the first time, diapycnal fluxes of the four halocarbons from the upper thermocline into and out of the mixed layer were determined. These fluxes were low in comparison to the halocarbon sea-to-air fluxes. This indicates that despite the observed maximum concentrations at depth, production in the surface mixed layer is the main oceanic source for all four compounds and one of the main driving factors of their emissions into the atmosphere in the ACT-region. The calculated production rates of the compounds in the mixed layer are 34 ± 65 pmol m−3 h−1 for CHBr3, 10 ± 12 pmol m−3 h−1 for CH2Br2, 21 ± 24 pmol m−3 h−1 for CH3I and 384 ± 318 pmol m−3 h−1 for CH2I2 determined from 13 depth profiles.


2019 ◽  
Vol 32 (13) ◽  
pp. 3899-3915 ◽  
Author(s):  
Ingo Richter ◽  
Takeshi Doi

Abstract The influence of sea surface temperature (SST) on interannual surface wind variability in the tropical Atlantic and Pacific is estimated using sensitivity experiments with the SINTEX-F GCM and the ensemble spread in a nine-member control simulation. Two additional estimates are derived for both SINTEX-F and the ERA-Interim reanalysis using regression analysis and singular value decomposition. All methods yield quite consistent estimates of the fraction of surface wind variability that is determined by SST and therefore potentially predictable. In the equatorial Atlantic, analysis suggests that for the period 1982–2014 approximately 2/3 of surface zonal wind variability in boreal spring and early summer is potentially predictable, while 1/3 is due to noise. Of the predictable component, up to about 35% may be driven from outside the tropical Atlantic, suggesting an important role for remote forcing and a diminished one for local feedbacks. In the northern tropical Atlantic, only 30% of boreal winter variability is predictable, most of which is forced from the Pacific. This suggests a minor role for local coupled air–sea feedbacks. For the equatorial Pacific, the results suggest high predictability throughout the year, most of which is due to local SST, with the tropical Atlantic only playing a minor role in boreal summer. In the tropical Atlantic, atmospheric internal variability is strongly dependent on the presence of deep convection, which, in turn, is related to mean SST. A similar, but weaker, state dependence of internal variability is evident in the tropical Pacific.


2021 ◽  
Author(s):  
François Counillon ◽  
Noel Keenlyside ◽  
Thomas Toniazzo ◽  
Shunya Koseki ◽  
Teferi Demissie ◽  
...  

AbstractWe investigate the impact of large climatological biases in the tropical Atlantic on reanalysis and seasonal prediction performance using the Norwegian Climate Prediction Model (NorCPM) in a standard and an anomaly coupled configuration. Anomaly coupling corrects the climatological surface wind and sea surface temperature (SST) fields exchanged between oceanic and atmospheric models, and thereby significantly reduces the climatological model biases of precipitation and SST. NorCPM combines the Norwegian Earth system model with the ensemble Kalman filter and assimilates SST and hydrographic profiles. We perform a reanalysis for the period 1980–2010 and a set of seasonal predictions for the period 1985–2010 with both model configurations. Anomaly coupling improves the accuracy and the reliability of the reanalysis in the tropical Atlantic, because the corrected model enables a dynamical reconstruction that satisfies better the observations and their uncertainty. Anomaly coupling also enhances seasonal prediction skill in the equatorial Atlantic to the level of the best models of the North American multi-model ensemble, while the standard model is among the worst. However, anomaly coupling slightly damps the amplitude of Atlantic Niño and Niña events. The skill enhancements achieved by anomaly coupling are largest for forecast started from August and February. There is strong spring predictability barrier, with little skill in predicting conditions in June. The anomaly coupled system show some skill in predicting the secondary Atlantic Niño-II SST variability that peaks in November–December from August 1st.


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