Wu, Z., Huang, N. E., Wallace, J. M., Smoliak, B. V., & Chen, X. (2011). On the time-varying trend in global-mean surface temperature.
Clim Dyn, 37(3-4), 759–773.
Zhang, M., Wu, Z., & Qiao, F. (2018). Deep Atlantic Ocean Warming Facilitated by the Deep Western Boundary Current and Equatorial Kelvin Waves.
J. Climate, 31(20), 8541–8555.
Abstract: Increased heat storage in deep oceans has been proposed to account for the slowdown of global surface warming since the end of the twentieth century. How the imbalanced heat at the surface has been redistributed to deep oceans remains to be elucidated. Here, the evolution of deep Atlantic Ocean heat storage since 1950 on multidecadal or longer time scales is revealed. The anomalous heat in the deep Labrador Sea was transported southward by the shallower core of the deep western boundary current (DWBC). Upon reaching the equator around 1980, this heat transport route bifurcated into two, with one continuing southward along the DWBC and the other extending eastward along a narrow strip (about 4 degrees width) centered at the equator. In the 1990s and 2000s, meridional diffusion helped to spread warming in the tropics, making the eastward equatorial warming extension have a narrow head and wider tail. The deep Atlantic Ocean warming since 1950 had overlapping variability of approximately 60 years. The results suggest that the current basinwide Atlantic Ocean warming at depths of 1000-2000 m can be traced back to the subsurface warming in the Labrador Sea in the 1950s. An inference from these results is that the increased heat storage in the twenty-first century in the deep Atlantic Ocean is unlikely to partly account for the atmospheric radiative imbalance during the last two decades and to serve as an explanation for the current warming hiatus.
Zhang, M., Zhang, Y., Shu, Q., Zhao, C., Wang, G., Wu, Z., et al. (2018). Spatiotemporal evolution of the chlorophyll a trend in the North Atlantic Ocean.
Sci Total Environ, 612, 1141–1148.
Abstract: Analyses of the chlorophyll a concentration (chla) from satellite ocean color products have suggested the decadal-scale variability of chla linked to the climate change. The decadal-scale variability in chla is both spatially and temporally non-uniform. We need to understand the spatiotemporal evolution of chla in decadal or multi-decadal timescales to better evaluate its linkage to climate variability. Here, the spatiotemporal evolution of the chla trend in the North Atlantic Ocean for the period 1997-2016 is analyzed using the multidimensional ensemble empirical mode decomposition method. We find that this variable trend signal of chla shows a dipole pattern between the subpolar gyre and along the Gulf Stream path, and propagation along the opposite direction of the North Atlantic Current. This propagation signal has an overlapping variability of approximately twenty years. Our findings suggest that the spatiotemporal evolution of chla during the two most recent decades is part of the multidecadal variations and possibly regulated by the changes of Atlantic Meridional Overturning Circulation, whereas the mechanisms of such evolution patterns still need to be explored.
Zhu, J., Huang, B., & Wu, Z. (2012). The Role of Ocean Dynamics in the Interaction between the Atlantic Meridional and Equatorial Modes.
J. Climate, 25(10), 3583–3598.
Zou, M., Xiong, X., Wu, Z., Li, S., Zhang, Y., & Chen, L. (2019). Increase of Atmospheric Methane Observed from Space-Borne and Ground-Based Measurements.
Remote Sensing, 11(8).
Abstract: It has been found that the concentration of atmospheric methane (CH4) has rapidly increased since 2007 after a decade of nearly constant concentration in the atmosphere. As an important greenhouse gas, such an increase could enhance the threat of global warming. To better quantify this increasing trend, a novel statistic method, i.e. the Ensemble Empirical Mode Decomposition (EEMD) method, was used to analyze the CH4 trends from three different measurements: the mid-upper tropospheric CH4 (MUT) from the space-borne measurements by the Atmospheric Infrared Sounder (AIRS), the CH4 in the marine boundary layer (MBL) from NOAA ground-based in-situ measurements, and the column-averaged CH4 in the atmosphere (X-CH4) from the ground-based up-looking Fourier Transform Spectrometers at Total Carbon Column Observing Network (TCCON) and the Network for the Detection of Atmospheric Composition Change (NDACC). Comparison of the CH4 trends in the mid-upper troposphere, lower troposphere, and the column average from these three data sets shows that, overall, these trends agree well in capturing the abrupt CH4 increase in 2007 (the first peak) and an even faster increase after 2013 (the second peak) over the globe. The increased rates of CH4 in the MUT, as observed by AIRS, are overall smaller than CH4 in MBL and the column-average CH4. During 2009-2011, there was a dip in the increase rate for CH4 in MBL, and the MUT-CH4 increase rate was almost negligible in the mid-high latitude regions. The increase of the column-average CH4 also reached the minimum during 2009-2011 accordingly, suggesting that the trends of CH4 are not only impacted by the surface emission, however that they also may be impacted by other processes like transport and chemical reaction loss associated with [OH]. One advantage of the EEMD analysis is to derive the monthly rate and the results show that the frequency of the variability of CH4 increase rates in the mid-high northern latitude regions is larger than those in the tropics and southern hemisphere.