The autotetraploid model proposed by R.C. Jackson and colleagues distinguishes autotetraploids from segmental allotetraploids in that the frequencies of late prophase I circle and chain quadrivalents and bivalents are predictable in autoploids while they are not predictable in segmental alloploids because the degree of genome divergence is generally unknown. Included among the tenets upon which the autotetraploid model is based are that 1) there is one synaptic initiation site per chromosome arm; 2) any chromosome arm has an equal probability of synapsing with any other homologous arm; and 3) synapsis in one arm is independent of synapsis in the opposite arm. This model predicts that for four homologous chromosomes, a quadrivalent will be formed 2/3 of the time and two bivalents will be formed 1/3 of the time during the pairing stage of mid-prophase I when the synaptonemal complex (SC) is formed. Natural tetraploid populations of Machaeranthera pinnatifida ( =Happlopappus spinulosus) (Asteraceae) (2n=4x=16) occurring along the Arkansas River in south-central Colorado were previously established to be autotetraploid based on the application of the autotetraploid model to late prophase I meiotic configuration frequencies. The objective of the current study was to determine if the tenets above hold true by analyzing synapsis in M. pinnatifida autotetraploids using the synaptonemal complex spreading technique. The quadrivalent frequency from SCs was 0.69, which is not significantly different from the 0.67 expected. There were no significant differences in quadrivalent frequencies among the four chromosomes. Contrary to the expectation based on the autotetraploid model of one partner switch per quadrivalent, we observed a range of 1-4 partner switches with an overall mean of 1.56. This suggests that the number of synaptic initiations is greater than two per chromosome and questions one of the primary tenets of the autoploid model.

Key words: autotetraploid, chromosomes, Machaeranthera pinnatifida, meiosis, polyploid, synaptonemal complex