Farine and Aplin (1) question the validity of our study reporting group-specific social dynamics in chimpanzees (2). As alternative to our approach, Farine and Aplin advance a "prenetwork permutation" methodology that tests against random assortment (3). We appreciate Farine and Aplin's interest and applied their suggested approaches to our data. The new analyses revealed highly similar results to those of our initial approach. We further dispel Farine and Aplin's critique by outlining its incompatibility to our study system, methodology, and analysis. First, when we apply the suggested prenetwork permutation to our proximity dataset, we again find significant population-level differences in association rates, while controlling for population size [as derived from Farine and Aplin's script (4); original result, P < 0.0001; results including prenetwork permutation, P < 0.0001]. Furthermore, when we exchange "population size" for "density" (i.e., population size/enclosure size) in our analyses, as suggested by Farine and Aplin, we continue to find strong evidence for population-level differences in association rates [generalized linear mixed model (GLMM) with population size, P < 0.0001; GLMM with density, P < 0.0001]. Interestingly, whereas population size significantly explains variation in association indices (P = 0.012; see ref. 2), density does not (P = 0.912), indicating that chimpanzees intentionally navigate their social world. Here, we note that this argument is consistent with decades of previous research that has shown that chimpanzees are intentional animals who selectively associate rather than "bump into" their conspecifics (5-8), even in small zoo enclosures (9, 10). Second, we address the incorrect assumptions integrated into Farine and Aplin's simulation approach. Farine and Aplin's rule for deriving "proximity" from the simulated data bears no resemblance to the heuristic used in our original study (2). Where Farine and Aplin