"[9] Adaptive differences that distinguish races can accumulate even with substantial gene flow and clinal (rather than discrete) habitat variation.
[20] If the races are sufficiently different or if they have been tested to show little genetic connection regardless of phenotype, two or more groups/races can be identified as subspecies or (in botany, mycology, and phycology) another infraspecific rank, and given a name.
Ernst Mayr wrote that a subspecies can be "a geographic race that is sufficiently different taxonomically to be worthy of a separate name.
For example, in 2008, two populations of the brown planthopper (Nilaparvata lugens) in the Philippines, one adapted to feeding on rice, and another on Leersia hexandra grass, were reclassified from races into "two distinct, but very closely allied, sympatric species", based on poor survival rate when given the opposite food source, barriers to hybridization between the populations, uniform preference for mating between members of the same population, differences in mating sounds, oviposition variances, and other distinguishable characteristics.
Although historically the term has been used inconsistently by plant pathologists, the modern trend is to use race to refer to "groups of host genotypes permitting characterization of virulence"[23] (in simpler terms: grouping the parasitic fungi into races based on how strongly they affect particular host plants).
[17][24] A 2004 literature review of this issue concluded that "race identification is important for basic research and is especially important for the commercial seed industry", but was seen as having little utility in horticulture for choosing specific cultivars, because of the rapidity with which the local pathogen population can change geographically, seasonally, and by host plant.