Morphological variation and mating compatibility within the mealybugs Pseudococcus calceolariae and P. similans (Hemiptera: Pseudococcidae), and a new synonymy

A laboratory study of isolines of Pseudococcus calceolariae (Maskell) and P. similans (Lidgett) collected from Hawke's Bay and Auckland, two widely separated regions in the North Island of New Zealand, threw doubt on the validity of the defining characters of these species. For P. similans, the number and position of oral rim tubular ducts varied widely and sometimes fell outside the defined limits for the species, and characteristic ‘stout abdominal setae’ were lost in the F₁ generation. The morphological characters that separate one species from the other were manipulated by changing the temperature at which the mealybugs developed, such that cohorts of F₁ sisters reared in the laboratory contained phenotypes of both P. calceolariae and P. similans. No impediments were found to breeding among populations of P. calceolariae and P. similans from Hawke's Bay and Auckland. All combinations of crosses between virgin females and males produced viable progeny. Those reared at 16°C laid more eggs than those reared at 23°C. The data did not suggest the existence of cryptic or sibling species, and contrasted with experiments elsewhere which quite clearly showed species incompatibility of closely related mealybugs. Examination of 160 ‘wild’ specimens of P. calceolariae from New Zealand, Australia and California (U.S.A.) and P. similans from New Zealand and Australia showed a morphological continuum from one species to the other. It is concluded that P. calceolariae and P. similans merely represent the phenotypic extremes of one widely polymorphic species, with the morphological characters of individual adults determined by the microenvironment in which they developed. Pseudococcus calceolariae is thus the senior synonym of P. similans.     

Observer-rated ataxia: rating scales for assessment of genetic differences in ethanol-induced intoxication in mice.

Identification of genetic and physiological mechanisms underlying a drug's or mutation's effects on motor performance could be aided by the existence of a simple observation-based rating scale of ataxia for mice. Rating scales were developed to assess ataxia after ethanol (2.75, 3.0, and 3.25 g/kg) in nine inbred mouse strains. Each scale independently rates a single behavior. Raters, blinded to dose, scored four behaviors (splay of hind legs, wobbling, nose down, and belly drag) at each of four time points after injection. The severities of hind leg splaying and wobbling were quantifiable, whereas nose down and belly dragging were expressed in all-or-none fashion. Interrater reliabilities were substantial (0.75 0 at some time), but all doses were equally effective. Incidence of nose down and belly dragging behaviors increased strain dependently after ethanol, but strains did not differentially respond to dose. Ethanol-induced splaying was modestly, and negatively, genetically correlated with wobbling. Nose down and belly dragging tended to be associated with splaying and wobbling at later times. Four distinct ataxia-related behaviors were sensitive to ethanol. Strains differed in ethanol sensitivity for all measures. Modest strain mean correlations among behaviors indicate that these behaviors are probably under control of largely different genes and that ataxia rating scales should rate separate behaviors on discrete scales.