Barr (1979) pointed out thatLignieraandPolymyxacannot be distinguished by their sporosori, but can, however, by their sporangial states.Karyotypic analysisrevealed that the two species ofPolymyxahave 30 synaptonemal complexes in pachynema whereas the formerLigniera verrucosa(nowPseudoligniera verrucosa) has 38.
Personal Comments
I thought that comparing the two species ofPolymyxawith aLignierawould be a good test of how well karyotyping with synaptonemal complexes could be used to characterize various plasmodiophorids. My opportunity to collect samples ofP.betaecame when I was visiting Stefan Buczacki at the then National Vegetable Research Station (NVRS) in Wellesbourne UK in 1982. He helped me make contact with Ian MacFarlane at Rothamsted Research Station in Harpenden, Hertfordshire UK.
Anyone familiar with the plasmodiophorids would recognized thatIan MacFarlanehad contributed to much of the fundamental information we had about the plasmos. For me it was an honor to visit him at Rothamsted and have him provide some of his sugar beet infected withP.betae. Ian was a very gracious host for the day and provided a wealth of information about his early work with the plasmodiophorids.
Ian and Stefan both introduced me to Bill Byford and Phil Payne atBroom's Barnnear Bury St Edmunds in Suffolk. In addition to showing me the ins and outs of research into sugar beet, they treated me to lunch at a delightful country pub not far from the station. They also provided plants infected withP.betae.
The roots of sugar beet infected withP.betaewere prepared for transmission electron microscopy at NVRS, but it was not until I returned to Ohio that I had time to serial section transitional sporogenic plasmodia to determine the karyotypes.
Once I returned to Ohio, Donald Barr, then at the Biosystematics Research Institute in Ottawa, Ontario, sent me a sample of dried roots of wheat that were infected withP.graminis. I used techniques for growing infected wheat on sand with nutrient solutions learned from Ian MacFarlane in his work with sugar beet.
Both species ofPolymyxawere beautiful in the prepared specimens. The synaptonemal complexes were better defined than those ofPlasmodiophorabrassicae, but the nuclei were larger and required more serial sections to completely make it through one nucleus. The material looked so good that I used 15 serial sections of a synaptonemal complex inP.betaefor an illustration of the technique for karyotyping inZoosporic Fungi in Teaching and Research, edited by M. S. Fuller and A. Jaworski, 1987.
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