The hypothesis was intended to explain the constant (age-independent) extinction probability as observed in the paleontological record caused by co-evolution between competing species;[1] however, it has also been suggested that the Red Queen hypothesis explains the advantage of sexual reproduction (as opposed to asexual reproduction) at the level of individuals,[2] and the positive correlation between speciation and extinction rates in most higher taxa.
Collectively, these two observations suggest that the effective environment of any homogeneous group of organisms deteriorates at a stochastically constant rate.
[10][11] In all cases, sexual reproduction confers species variability and a faster generational response to selection by making offspring genetically unique.
In multi-host and multi-parasite coevolution, the Red Queen dynamics could affect what host and parasite types will become dominant or rare.
However, the assumption of the Red Queen hypothesis, that the primary factor in maintaining sexual reproduction is the generation of genetic variation does not appear to be generally applicable.
The relative rarity in nature of meiotic events that result from outcrossing is inconsistent with the idea that production of genetic variation is the main selective force maintaining meiosis in this organism (as would be expected by the Red Queen hypothesis).
[17][18] Further evidence for the Red Queen hypothesis was provided by observing long-term dynamics and parasite coevolution in a mixed sexual and asexual population of snails (Potamopyrgus antipodarum).
Contrary to expectation based on the Red Queen hypothesis, they found that the prevalence, abundance and mean intensity of mites in sexual geckos was significantly higher than in asexuals sharing the same habitat.
Critics of the Red Queen hypothesis question whether the constantly changing environment of hosts and parasites is sufficiently common to explain the evolution of sexual reproduction.
Otto and Gerstein[23] further stated that "it seems doubtful to us that strong selection per gene is sufficiently commonplace for the Red Queen hypothesis to explain the ubiquity of sex".
Parker[24] reviewed numerous genetic studies on plant disease resistance and failed to uncover a single example consistent with the assumptions of the Red Queen hypothesis.
In 2011, researchers used the microscopic roundworm Caenorhabditis elegans as a host and the pathogenic bacterium Serratia marcescens to generate a host–parasite coevolutionary system in a controlled environment, allowing them to conduct more than 70 evolution experiments testing the Red Queen hypothesis.
[30][31] The main idea is that aging is favored by natural selection since it allows faster adaptation to changing conditions, especially in order to keep pace with the evolution of pathogens, predators and prey.
Aesop[32] The predator-prey relationship can also be established in the microbial world, producing the same evolutionary phenomenon that occurs in the case of foxes and rabbits.
[34] A competing evolutionary idea is the court jester hypothesis, which indicates that an arms race is not the driving force of evolution on a large scale, but rather it is abiotic factors.
[35][36] The Black Queen hypothesis is a theory of reductive evolution that suggests natural selection can drive organisms to reduce their genome size.