scholarly journals Mechanisms Controlling the Annual Cycle of Precipitation in the Tropical Atlantic Sector in an Atmospheric GCM*

2004 ◽  
Vol 17 (24) ◽  
pp. 4708-4723 ◽  
Author(s):  
M. Biasutti ◽  
D. S. Battisti ◽  
E. S. Sarachik

Abstract A set of AGCM experiments is used to study the annual cycle of precipitation in the region surrounding the tropical Atlantic Ocean. The experiments are designed to reveal the relative importance of insolation over land and the (uncoupled) SST on the annual cycle of precipitation over the tropical Atlantic Ocean, Africa, and the tropical Americas. SST variations impact the position of the maritime ITCZ by forcing the hydrostatic adjustment of the atmospheric boundary layer and changes in surface pressure and low-level convergence. The condensation heating released in the ITCZ contributes substantially to the surface circulation and the maintenance of the SST-induced ITCZ anomalies. The remote influence of SST is felt in equatorial coastal areas and the Sahel. The circulation driven by condensation heating in the maritime ITCZ extends to the coastal regions, thus communicating the SST signal onshore. Conversely, the Sahel responds to variations in SST through boundary layer processes that do not involve the maritime ITCZ. The atmospheric response to changes in subtropical SST is advected inland and forces changes in sea level pressure and low-level convergence across a large part of tropical Africa. The impact of local insolation on continental precipitation can be explained by balancing net energy input at the top of the atmospheric column with the export of energy by the divergent circulation that accompanies convection. Increased insolation reduces the stability of the atmosphere in the main continental convection centers, but not in monsoon regions. Insolation over land impacts the intensity of the maritime ITCZ via its influence on precipitation in Africa and South America. Reduced land precipitation induces the cooling of the Atlantic upper troposphere and the enhancement of convective available potential energy in the maritime ITCZ.

2007 ◽  
Vol 7 (14) ◽  
pp. 3933-3956 ◽  
Author(s):  
A. Stickler ◽  
H. Fischer ◽  
H. Bozem ◽  
C. Gurk ◽  
C. Schiller ◽  
...  

Abstract. We present a comparison of different Lagrangian and chemical box model calculations with measurement data obtained during the GABRIEL campaign over the tropical Atlantic Ocean and the Amazon rainforest in the Guyanas, October 2005. Lagrangian modelling of boundary layer (BL) air constrained by measurements is used to derive a horizontal gradient (≈5.6 pmol/mol km−1) of CO from the ocean to the rainforest (east to west). This is significantly smaller than that derived from the measurements (16–48 pmol/mol km−1), indicating that photochemical production from organic precursors alone cannot explain the observed strong gradient. It appears that HCHO is overestimated by the Lagrangian and chemical box models, which include dry deposition but not exchange with the free troposphere (FT). The relatively short lifetime of HCHO implies substantial BL-FT exchange. The mixing-in of FT air affected by African and South American biomass burning at an estimated rate of 0.12 h−1 increases the CO and decreases the HCHO mixing ratios, improving agreement with measurements. A mean deposition velocity of 1.35 cm/s for H2O2 over the ocean as well as over the rainforest is deduced assuming BL-FT exchange adequate to the results for CO. The measured increase of the organic peroxides from the ocean to the rainforest (≈0.66 nmol/mol d−1) is significantly overestimated by the Lagrangian model, even when using high values for the deposition velocity and the entrainment rate. Our results point at either heterogeneous loss of organic peroxides and/or their radical precursors, underestimated photodissociation or missing reaction paths of peroxy radicals not forming peroxides in isoprene chemistry. We calculate a mean integrated daytime net ozone production (NOP) in the BL of (0.2±5.9) nmol/mol (ocean) and (2.4±2.1) nmol/mol (rainforest). The NOP strongly correlates with NO and has a positive tendency in the boundary layer over the rainforest.


2007 ◽  
Vol 7 (2) ◽  
pp. 4781-4855 ◽  
Author(s):  
A. Stickler ◽  
H. Fischer ◽  
H. Bozem ◽  
C. Gurk ◽  
C. Schiller ◽  
...  

Abstract. We present a comparison of different Lagrangian and steady state box model runs with measurement data obtained during the GABRIEL campaign over the tropical Atlantic Ocean and the rainforest in the Guyanas, October 2005. Lagrangian modelling of boundary layer (BL) CO constrained by measurements of reactive trace gases and radiation is used to derive a horizontal gradient (≈5.6 pmol/mol km−1) of this compound from the ocean to the rainforest (east to west). This is significantly smaller than that derived from the measurements (16–48 pmol/mol km−1), indicating that photochemical production from organic precursors alone cannot explain the observed strong gradient. It appears that HCHO is overestimated by the Lagrangian and "steady state" models, which include dry deposition but not exchange with the free troposphere (FT). The relatively short lifetime of HCHO (50–100 min) implies substantial BL-FT exchange. The mixing-in of FT air affected by African and South American biomass burning at an estimated rate of 0.12 h−1 increases the CO and lowers the HCHO mixing ratios, leading to a better agreement with measurements. A 24 h mean deposition velocity of 1.35 cm/s for H2O2 over the ocean as well as over the rainforest is deduced assuming BL-FT exchange adequate to the results for CO. The measured increase of the organic peroxides from the ocean to the rainforest (≈0.66 nmol/mol d−1) is significantly overestimated by the Lagrangian model, even when using high values for the deposition velocity and the entrainment rate. Our results point at either heterogeneous loss of organic peroxides and/or their radical precursors or a missing reaction path of peroxy radicals not forming peroxides in isoprene chemistry. We calculate a mean integrated daytime net ozone production (NOP) in the BL of (0.2±5.9) nmol/mol (ocean) and (2.4±2.1) nmol/mol (rainforest). The NOP strongly correlates with NO and shows a positive tendency in the boundary layer over the rainforest.


2006 ◽  
Vol 19 (23) ◽  
pp. 6153-6169 ◽  
Author(s):  
Lisan Yu ◽  
Xiangze Jin ◽  
Robert A. Weller

Abstract The present study used a new net surface heat flux (Qnet) product obtained from the Objective Analyzed Air–Sea Fluxes (OAFlux) project and the International Satellite Cloud Climatology Project (ISCCP) to examine two specific issues—one is to which degree Qnet controls seasonal variations of sea surface temperature (SST) in the tropical Atlantic Ocean (20°S–20°N, east of 60°W), and the other is whether the physical relation can serve as a measure to evaluate the physical representation of a heat flux product. To better address the two issues, the study included the analysis of three additional heat flux products: the Southampton Oceanographic Centre (SOC) heat flux analysis based on ship reports, and the model fluxes from the National Centers for Environmental Prediction–National Center for Atmospheric Research (NCEP–NCAR) reanalysis and the 40-yr European Centre for Medium-Range Weather Forecasts (ECMWF) Re-Analysis (ERA-40). The study also uses the monthly subsurface temperature fields from the World Ocean Atlas to help analyze the seasonal changes of the mixed layer depth (hMLD). The study showed that the tropical Atlantic sector could be divided into two regimes based on the influence level of Qnet. SST variability poleward of 5°S and 10°N is dominated by the annual cycle of Qnet. In these regions the warming (cooling) of the sea surface is highly correlated with the increased (decreased) Qnet confined in a relatively shallow (deep) hMLD. The seasonal evolution of SST variability is well predicted by simply relating the local Qnet with a variable hMLD. On the other hand, the influence of Qnet diminishes in the deep Tropics within 5°S and 10°N and ocean dynamic processes play a dominant role. The dynamics-induced changes in SST are most evident along the two belts, one of which is located on the equator and the other off the equator at about 3°N in the west, which tilts to about 10°N near the northwestern African coast. The study also showed that if the degree of consistency between the correlation relationships of Qnet, hMLD, and SST variability serves as a measure of the quality of the Qnet product, then the Qnet from OAFlux + ISCCP and ERA-40 are most physically representative, followed by SOC. The NCEP–NCAR Qnet is least representative. It should be noted that the Qnet from OAFlux + ISCCP and ERA-40 have a quite different annual mean pattern. OAFlux + ISCCP agrees with SOC in that the tropical Atlantic sector gains heat from the atmosphere on the annual mean basis, where the ERA-40 and the NCEP–NCAR model reanalyses indicate that positive Qnet occurs only in the narrow equatorial band and in the eastern portion of the tropical basin. Nevertheless, seasonal variances of the Qnet from OAFlux + ISCCP and ERA-40 are very similar once the respective mean is removed, which explains why the two agree with each other in accounting for the seasonal variability of SST. In summary, the study suggests that an accurate estimation of surface heat flux is crucially important for understanding and predicting SST fluctuations in the tropical Atlantic Ocean. It also suggests that future emphasis on improving the surface heat flux estimation should be placed more on reducing the mean bias.


2021 ◽  
Author(s):  
Arthur Prigent ◽  
Joke F. Lübbecke ◽  
Tobias Bayr ◽  
Mojib Latif ◽  
Christian Wengel

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