Almond are among the most consumed tree nuts and used in a variety of food products. Recent almond butter recalls due to potential contamination of Listeria monocytogenes highlight the need to control L. monocytogenes in almond products. The objectives of this study were to examine the stability of L. monocytogenes in almond meal during extended storage and analyze thermal resistance of L. monocytogenes in almond meal of controlled moisture contents or water activity (a w) using thermal death time (TDT) cells and thermal water activity (TWA) cells, respectively. L. monocytogenes maintained a stable population in almond meal for 44-48 weeks at 4 • C regardless of a w ; however, we observed about 1.69 and 2.14 log 10 colony-forming units (CFU)/g reduction of L. monocytogenes in a w 0.25 and 0.45 almond meal over 44 to 48 weeks of storage at 22 • C. Under all test conditions using either TDT or TWA cells, the inactivation kinetics of L. monocytogenes in almond meal fitted the log-linear model well; thermal resistance of L. monocytogenes in almond meal was inversely related to the a w of samples. D 75-/D 80-values of L. monocytogenes in a w 0.25 and 0.45 almond meal obtained using TDT cells were 47.6/22.0 versus 17.2/11.0 min, respectively. D 80-, D 85-, and D 90-values of L. monocytogenes in a w 0.25 almond meal obtained using TWA cells were 59.5 ± 2.1, 27.7 ± 0.7, and 13.2 ± 1.1 min, respectively, in contrast to 22.0 ± 1.1, 10.6 ± 0.2, and 4.6 ± 0.4 min obtained using TDT cells. The z-value of L. monocytogenes in a w 0.25 almond meal was not affected by TWA and TDT cell type (15.4-15.5 • C), whereas zvalue of L. monocytogenes in a w 0.45 almond meal was 10 • C higher than that in a w 0.25 almond meal. This study contributes to our understanding of L. monocytogenes in nuts and impacts of a w on the development of thermal resistance in low-moisture foods.