SEXUAL DIMORPHISM OF SHELL SHAPE AND GROWTH OF VILLOSA VILLOSA (WRIGHT) AND ELLIPTIO ICTERINA (CONRAD) (BIVALVIA: UNIONIDAE)

Shell shape and growth of two unionacean species, Villosa villosaand Elliptio icterina, are analyzed with univariate and multivariatetechniques. The relationship of shape variables to size variablesis examined. Under the lognormal assumption, parametric testsof these allometric relationships are valid. Variables describingthe ventro-posterior region of the shell are shown to be thebest of those tested for discriminating between the sexes ofboth species regardless of statistical method. Neither speciesexhibits size sexual dimorphism. Shape sexual dimorphism ofV. villosa is constant during adult growth, but the more subtledimorphism of E. icterina changes as adults continue to grow. (Received 20 January 1986;     

Prevention of potato top-roll by aphicide and its effect on leaf area and photosynthesis

In a field of potatoes, top-roll, which is induced by the aphid Macrosiphum euphorbiae feeding on the leaves, was restricted to two rows of plants which accidentally received no phorate aphicide granules at planting. The photo-synthetic rate per unit leaf area and the ground cover of top-rolled leaves were respectively 50% and 20% less than those of normal plants which may account for the smaller yields of affected plants observed in previous experiments.     

TWO TYPES OF SENSORY PANELS OR ARE THERE MORE?

The purpose of this article is to discuss the issues associated with selecting assessors for sensory panels. It develops the argument that although there are many variations in the detail of how assessors are selected, all panels can be considered as either (1) selecting respondents to measure ingredient concentrations via perceptions or (2) selecting respondents to represent the response that would be obtained from a wider consumer population. The validity of the data collected, i.e., the extent to which the data collected measures what was originally intended, depends on the detail of how assessors were selected as well as a number of other factors.     

NEMATOCYSTS OF THE SEA ANEMONE METRIDIUM

Six types of nematocysts and their nematocytes in tentaclesand acontia of the sea anemone Metridium senile fimbriatum werestudied by electron microscopy. Microbasic b-mastigophores, microbasic amastigophores, and basitrichshave one fundamental feature in common: a straight, complexly-foldedshaft with dense spines pointing apically. An additional resemblancebetween a b-mastigophore and a basitrich is the possession ofa long, narrow, coiled thread bearing spines. An amastigophoreis characterized by a short, looped, unspined thread and a cup-shapedgranular matrix. Atrich and holotrich nematocysts have a coiled, spined tubeof uniform diameter which lies in an evenly granular matrixfilling the entire capsule. The above five nematocysts have three flaps at the apex of thecapsule which open upon discharge, and each nematocyte possessesa flagellum with which is associated one or two centrioles anda striated rootlet. The long rootlet of the b-mastigophorebearingnematocyte passes through a circular band of fibrils surroundingthe neck region of the capsule, and the short rootlet of theatrich lies in a dense fibrous sheath surrounding all but theapex of the capsule. The spirocyst differs from the other nematocysts in having athin, ridged, singlewalled capsule; an inverted tube containingbundles of tubules; an apical disk covered only by a thin layerof granular material and the nematocyst membrane; and the absenceof a flagellum in its nematocyte. Theories of excitation and mechanism of discharge of nematocystsand the function of spirocysts are discussed in the light ofthis and other recent studies of the fine structure of nematocysts.Special attention is drawn to the probable role of the foldsin the walls of shaft and thread in increasing the length ofthe tube upon discharge.     

Evidence for long-distance dispersal in a sedentary passerine, Gymnorhina tibicen (Artamidae)

Australian magpies (Gymnorhina tibicen) are group-living birds found across much of mainland Australia. Adults commonly remain in a breeding territory until death. Young of the year either remain on the natal (birth) site or are forced by their parents to disperse. Observational studies in south-eastern Australia suggest that most dispersing juveniles settle within 7 km of their natal territory. Therefore, despite potential for considerable gene flow (via flight), social organization predisposes magpies towards local population structuring. In this study, we measured genetic variation at both nuclear (allozyme) and mitochondrial loci and found evidence of substantial gene flow over very large distances (up to 1599 km). Thus, some juvenile magpies may disperse much greater distances than was previously thought. For mtDNA, geographic and genetic distance were strongly correlated, consistent with a pattern of isolation by distance. Therefore, although female gene flow is substantial it is apparently geographically restricted over large distances, in approximately a stepping-stone fashion. We conclude that a strong relationship between gene flow and geographic distance can develop even over large distances if populations have experienced no major historical disturbances to gene flow.     

Sandhill Crane Abundance and Nesting Ecology at Grays Lake,Idaho

Abstract: We examined population size and factors influencing nest survival of greater sandhill cranes (Grus canadensis tabida) at Grays Lake National Wildlife Refuge, Idaho, USA, during 1997–2000. Average local population of cranes from late April to early May, 1998–2000, was 735 cranes, 34% higher than that reported for May 1970–1971. We estimated 228 (SE = 30) nests in the basin core (excluding renests), 14% higher than a 1971 estimate. Apparent nest success in our study (x̄ = 60%, n = 519 nests) was lower than reported for Grays Lake 30–50 years earlier. Daily survival rates (DSRs) of all nests averaged 0.9707 (41.2%). The best model explaining nest survival included year and water depth and their interaction. Nest survival was highest (DSR = 0.9827) in 1998 compared with other years (0.9698-0.9707). Nest survival changed little relative to water depth in 1998, when flooding was extensive and alternative prey (microtines) irrupted, but declined markedly with lower water levels in 2000, the driest year studied. Hypotheses relating nest survival to vegetation height, land use (idle, summer grazing, fall grazing), and date were not supported. In a before-after-control-impact design using 12 experimental fields, nest survival differed among years but not among management treatments (idle, fall graze, fall burn, and summer—graze—idle rotation), nor was there an interaction between year and treatments. However, DSRs in fall-burn fields declined from 0.9781 in 1997–1998 to 0.9503 in 1999–2000 (posttreatment). Changes in the predator community have likely contributed to declines in nest success since the 1950s and 1970s. Our results did not support earlier concerns about effects of habitat management practices on crane productivity. Nest survival could best be enhanced by managing spring water levels. Managers should continue censuses during late April to evaluate long-term relationships to habitat conditions and management.     

Metabolic rate in diapause and nondiapause brown locust eggs correlated with embryonic development

Insects use dormancy to survive adverse conditions. Brown locust Locustana pardalina (Walk.) eggs offer a convenient model to study dormancy (diapause and quiescence), which contributes to their survival under arid conditions. The metabolic rates of developing nondiapause, diapause and quiescent eggs are compared in the present study using closed‐system respirometry. The embryo becomes committed to continue development and hatch or to enter diapause 6 days after the eggs are placed on moist soil. The metabolic rate of nondiapause eggs increases exponentially until hatching, whereas that of diapause eggs is low and stable. The metabolic rate of diapause laboratory eggs (1.9 ± 0.6 µL CO₂ mg^?1 h^?1) is significantly higher than that of field eggs (0.5 ± 0.3 µL CO₂ mg^?1 h^?1), although the ranges of metabolic rate overlap and the embryos are all in late anatrepsis. The metabolic rate of quiescent eggs is similar to that of diapause eggs but decreases with time. Low metabolic rates during arrested development allow eggs to persist over long periods before hatching.