Distribution of Pirhemocyton Chatton & Blanc and other, Possibly Related, Infections of Poikilotherms

SYNOPSIS. Data for host and geographic distribution are listed for Pirhemocyton and for apparently similar infections of poikilothermic vertebrates. The list was compiled from published accounts of Pirhemocyton, Toddia, Cytamoeba, Bertarellia , Piscine erythrocytic necrosis, Immanoplasma, Haematractidium, Sauroplasma, Sauromella, Serpentoplasma, Tunetella, Haemohormidium and unnamed infections. New records are included for Pirhemocyton and Haematractidium. The probability that some may be viruses and not protozoa is discussed; Haematractidium is shown by electron microscopy to be a eukaryote whereas Immanoplasma is not a eukaryote.     

Species of street tree is important for southern hemisphere bird trophic guilds

Abstract Urban environments are highly modified with unique assemblages of bird species. Much of the research on urban bird assemblages comes from the northern hemisphere. Southern hemisphere bird assemblages differ from northern hemisphere assemblages in that they contain a large proportion of nectarivores. In this study we focus on bird use of street trees in Australia. We investigate the relative influence of tree species (plane tree, Platanus x acerifolia; red gums, Eucalyptus camaldulensis; jacaranda, Jacaranda mimosifolia; bottlebrush, Callistemon citrinus), season and the environment surrounding street trees, on the abundance and species richness of birds in Adelaide, South Australia. Our study considers birds in terms of granivore, nectarivore and insectivore trophic guilds. Nectarivores accounted for the greatest proportion of observations, in terms of abundance, in each of the tree species investigated. Species of street tree was a significant influence on bird use of the trees for all birds and each dietary guild. Red gums were used more than the other tree species by nectarivores, while plane trees were used more than the other trees by insectivores. Use of the tree species by granivores varied with the season. The measures of the environment surrounding street trees were largely unimportant with the exception of traffic for nectarivores in some cases. Urban avifauna use street trees and the species of tree will strongly influence its use by birds. However, the pattern of use of street tree species varied at different times of year and differed between different trophic guilds of birds. The dominance of nectarivores in the southern avifauna will likely produce different patterns of urban environment use to northern hemisphere avifaunas.     

A note on the use of dextran in blood cultures monitored by conductance methods

The incorporation of dextran into broth for the detection of bacteraemia by conductance monitoring is recommended to eliminate the effect of sedimenting blood cells which may mask early signals from bacteria. Broth containing ten times the recommended concentration of dextran was tested with a wide range of bacteria without demonstrating any reduction in growth or rate of change of conductance.     

Responses of High Arctic wet sedge tundra to climate warming since 1980

The global climate is changing rapidly and Arctic regions are showing responses to recent warming. Responses of tundra ecosystems to climate change have been examined primarily through short‐term experimental manipulations, with few studies of long‐term ambient change. We investigated changes in above‐ and belowground biomass of wet sedge tundra to the warming climate of the Canadian High Arctic over the past 25 years. Aboveground standing crop was harvested from five sedge meadow sites and belowground biomass was sampled from one of the sites in the early 1980s and in 2005 using the same methods. Aboveground biomass was on average 158% greater in 2005 than in the early 1980s. The belowground biomass was also much greater in 2005: root biomass increased by 67% and rhizome biomass by 139% since the early 1980s. Dominant species from each functional group (graminoids, shrubs and forbs) showed significant increases in aboveground biomass. Responsive species included the dominant sedge species Carex aquatilis stans, C. membranacea, and Eriophorum angustifolium, as well as the dwarf shrub Salix arctica and the forb Polygonum viviparum. However, diversity measures were not different between the sample years. The greater biomass correlated strongly with increased annual and summer temperatures over the same time period, and was significantly greater than the annual variation in biomass measured in 1980–1983. Increased decomposition and mineralization rates, stimulated by warmer soils, were likely a major cause of the elevated productivity, as no differences in the mass of litter were found between sample periods. Our results are corroborated by published short‐term experimental studies, conducted in other wet sedge tundra communities which link warming and fertilization with elevated decomposition, mineralization and tundra productivity. We believe that this is the first study to show responses in High Arctic wet sedge tundra to recent climate change.     

Growth and survivorship as proximate causes of sexual size dimorphism in peninsula dragon lizards Ctenophorus fionni

Males and females differ in body size in many animals, but the direction and extent of this sexual size dimorphism (SSD) varies widely. Males are larger than females in most lizards of the iguanian clade, which includes dragon lizards (Agamidae). I tested whether the male larger pattern of SSD in the peninsula dragon lizard, Ctenophorus fionni, is a result of sexual selection for large male size or relatively higher mortality among females. Data on growth and survivorship were collected from wild lizards during 1991–1994. The likelihood of differential predation between males and females was assessed by exposing pairs of male and female lizards to a predator in captivity, and by comparing the frequency of tail damage in wild‐caught males and females. Male and female C. fionni grew at the same rate, but males grew for longer than females and reached a larger asymptotic size (87 mm vs. 78 mm). Large males were under‐represented in the population because they suffered higher mortality than females. Predation may account for some of this male‐biased mortality. The male‐biased SSD in C. fionni resulted from differences in growth pattern between the sexes. The male‐biased SSD was not the result of proximate factors reducing female body size. Indeed SSD in this species remained male‐biased despite high mortality among large males. SSD in C. fionni is consistent with the ultimate explanation of sexual selection for large body size in males.