Artificially induced triploid male Rhodeus ocellatus ocellatus showed typic
al nuptial colorations, irrespective of spermiation. In milt from triploids
, abnormal spermatozoa (malformation of the head and mitochondrion, excessi
ve formation of the head, mitochondrion and flagellum, and no flagellum) oc
curred at 78.4% frequency. Spermatozoa with multiflagella were most common,
often with a saccate-like organ. Many triploid spermatozoa moved actively
as long as those of diploids (10.92 +/- 0.91 min = mean +/- S.D., P>0.05),
but did not advance like diploids, spinning around until movement ceased. T
he sperm density in triploids was <2% of that from diploids. In triploid te
stes, deformed and variously sized spermatids were often observed, and norm
al spermatids and spermatozoa were seldom recognized. The DNA content of tr
iploid spermatozoa varied greatly, compared with that of diploids. Peak of
sperm DNA content differed slightly between two triploid samples with two p
eaks at 1.5 n and 1.9 n (P<0.0001 in both), respectively. Triploids had the
greatest average sperm head diameter of 2.25 +/- 0.67 mu m (mean +/- S.D.)
, while that of diploids was 1.83 +/- 0.15 mu m (P = 0.002). In the fertili
zation test using the eggs of diploids (n = 1500, 30 trials), only one egg
developed. The embryo chromosome number was 60 (2.5 n) and the ploidy of sp
ermatozoa contributing to fertilization appears to be 1.5 n. The extremely
low fertility of triploid R. o. ocellatus spermatozoa seems to be caused by
the reduced motility and large head size of spermatozoa, and the low sperm
density of the milt. The ploidy of spermatozoa that are successful in fert
ilization is likely to be related to the distribution pattern in the DNA co
ntent of cells. (C) 1999 The Fisheries Society of the British Isles.