Research Article

Persistent Copulation in Asexual Female   Potamopyrgus antipodarum: Evidence for Male Control with Size-Based Preferences

Table 1

Copulation frequency, shell length, and lineage age in asexual cultures.

CultureMean copulation frequency ± 1 SDMean shell length ± 1 SDLineage age 𝑁

Taylor a , b 0.13 ± 0.134.27 ± 0.33YOUNG14
Mapourika a 0.13 ± 0.184.32 ± 0.31OLD13
Denmark A 0.15 ± 0.104.30 ± 0.24OLD5
Duluth 0.16 ± 0.374.70 ± 0.22OLD4
Okareka a , b 0.18 ± 0.114.37 ± 0.58OLD15
Sarah a 0.19 ± 0.154.54 ± 0.50YOUNG14
Poerua0.24 ± 0.154.53 ± 0.21YOUNG14
Waikaremoana Lab 0.25 ± 0.154.65 ± 0.47OLD 19
Evelyn0.31 ± 0.164.67 ± 0.32YOUNG13
Waikaremoana Field 0.32 ± 0.154.65 ± 0.42OLD 19
Tarawera c 0.35 ± 0.155.09 ± 0.82OLD14
Taupo c 0.39 ± 0.215.60 ± 0.61OLD15
All females0.25 ± 0.174.67 ± 0.59159

Culture of origin (rank ordered by increasing copulation frequency), mean copulation frequency ± SD, mean shell length ± SD, lineage age, and number of individual asexual females used from each culture. “Young” indicates lineages derived from sexual ancestors <70,000 years ago, while “old” indicates lineages derived >500,000 years ago [23]. Denotes the only two population names that do not refer to lakes of origin in New Zealand; the ancestor of the Denmark A lineage was collected in Denmark in the early 1990s, and the ancestor of the Duluth lineage was collected in 2007 in Minnesota, USA from Lake Superior. Waikaremoana populations consist of multiple lineages of old asexuals. a Denotes cultures that differed significantly from Taupo in mean copulation frequency via Bonferroni-corrected chi-square comparisons. b Denotes significant differences in copulation frequency from Tarawera. c Taupo differed significantly in mean length from all cultures except Tarawera ( 𝑡 -tests). All differences are significant at 𝑃 < . 0 5 .