We identified sources of mapping inaccuracy during the construction of
RFLP linkage maps from one F-2 population and two F-1 microspore-deri
ved populations from the same cross of oilseed Brassica napus. The gen
etic maps were compared using a total of 145 RFLP marker loci includin
g 82 loci common to all three populations. In the process, we identifi
ed a series of mapping events that could lead to ambigous conclusions.
Superimposed restriction fragments could be mistaken as a single domi
nant restriction fragment in a F-2 population and, when analyzed as su
ch, would yield inaccurate linkage information. Residual heterozygosit
y in parental lines resulted in complicated allelic assignment and yie
lded subsequent difficulties in linkage determination. Loose and spuri
ous linkages occurred during mapping and were identified by comparing
maps derived from different populations. LOD scores and chi(2) test of
independence were compared for their capacity to detect loose linkage
s or generate spurious ones. Extreme segregation distortions towards t
he same parental allele also contributed to an additional source of sp
urious linkage. Small but significant segregation distortions resulted
in reduced estimates of the recombination fraction. The use of the sa
me 'probe x enzyme' combinations in doubled haploid populations allowe
d the identification of the correct allele assignment as well as loose
and spurious linkages. A translocation between two homoeologous linka
ge groups was observed. The consequences of such a chromosomal event a
s a source of error in mapping applications are discussed.