Anguillicola australiensis (Johnston et Mawson, 1940) is widespread and common in Anguilla reinhardtii Steidachner in rivers and dams of eastern Queensland, Australia, having been found in nine out of ten localities. Overall prevalence was 50% and maximum local prevalence reached 77.7%. The parasite never attained high levels of abundance and maximum adult abundance never exceeded 3.22 or intensity 10. Adults were overdispersed throughout the eel populations and abundance was unrelated to eel or swimbladder size. The greater part of the adult population was composed of immature parasites. The occurrence of larvae in the swimbladder wall was erratic and unrelated to the size of the adult population. Larvae were never abundant and the great majority were damaged by a host response. It appears that parasites either pass through the swimbladder wall rapidly and moult to adults or if delayed are destroyed. There was no indication that a paratenic host was involved in the life cycle. There was no evidence that adult parasites had any local pathogenic effects on their hosts. The population biology of Anguillicola australiensis in its natural host Anguilla reinhardtii appears to be far more similar to those of other Pacific species of Anguillicola in Anguilla japonica in China and Japan than to A. crassus in Anguilla anguilla in Europe or Japan. This latter host-parasite combination appears to be the exception not the rule. It is suggested that the lack of pathogenicity of A. australiensis may reflect a long period of host-parasite co-evolution and/or lower transmission rates resulting in lower parasite population densities.
Haemogregarina bigemina Laveran et Mesnil, 1901 was examined in marine fishes and the gnathiid isopod, Gnathia africana Barnard, 1914 in South Africa. Its development in fishes was similar to that described previously for this species. Gnathiids taken from fishes with H. bigemina, and prepared sequentially over 28 days post feeding (d.p.f.), contained stages of syzygy, immature and mature oocysts, sporozoites and merozoites of at least three types. Sporozoites, often five in number, formed from each oocyst from 9 d.p.f. First-generation merozoites appeared in small numbers at 11 d.p.f., arising from small, rounded meronts. Mature, second-generation merozoites appeared in large clusters within gut tissue at 18 d.p.f. They were presumed to arise from fan-shaped meronts, first observed at 11 d.p.f. Third-generation merozoites were the shortest, and resulted from binary fission of meronts, derived from second-generation merozoites. Gnathiids taken from sponges within rock pools contained only gamonts and immature oocysts. It is concluded that the development of H. bigemina in its arthropod host illustrates an affinity with Hemolivia and one species of Hepatozoon. However, the absence of sporokinetes and sporocysts also distances it from these genera, and from Karyolysus. Furthermore, H. bigemina produces fewer sporozoites than Cyrilia and Desseria, although, as in Desseria, Haemogregarina (sensu stricto) and Babesiosoma, post-sporogonic production of merozoites occurs in the invertebrate host. The presence of intraerythrocytic binary fission in its fish host means that H. bigemina is not a Desseria. Overall it most closely resembles Haemogregarina (sensu stricto) in its development, although the match is not exact.
Saliva-activated transmission of Borrelia afzelii Canica, Nato, du Merle, Mazie, Baranton et Postic, 1993 was demonstrated using salivary gland extract (SGE) from Ixodes ricinus (L., 1758) ticks and C3H mice. Injection of Borrelia spirochaetes together with SGE increased the level of bacteraemia and accelerated the appearance of bacteria in the urinary bladder, compared with the injection of spirochaetes alone. More I. ricinus nymphs became infected when feeding on mice inoculated with B. afzelii plus SGE. Analysis of cytokines produced by cells of draining lymph nodes from SGE-treated mice showed a suppression of proinflammatory cytokines IFN-γ, IL-6 and GM-CSF following a transient upregulation in comparison with the control mice infected without SGE.
The present study is focusing on the transmission of the monogenean ectoparasite Gyrodactylus salaris Malmberg, 1957, a major pathogen on natural populations of Norwegian Atlantic salmon, Salmo salar L. In laboratory experiments the transmission rate of G. salaris after direct host to host contact was positively correlated with water temperature (1.2, 4,7 and 12.2°C). The transmission of detached G. salaris in the planktonie drift was studied in field experiments where salmon parr were individually isolated for 24 hours in small wire mesh cages suspended in the water column. Ten out of 157 salmon parr (prevalence 6.4%, mean intensity 1.0) contracted G. salaris infections after this exposure. Furthermore, 200 uninfected marked salmon parr were released into the same area of the river. After 24 and 48 hours, respectively 18 and 19 marked parr were caught by electro-fishing. The prevalence of G. salaris was 44.4% (mean intensity 1.9) after 24 hours, rising to 57.9% (mean intensity 2.3) after 48 hours. Gyrodactylids have no specific transmission stage or swimming ability, but detached G. salaris drifting in the water column were found to infect salmon parr. However, the transmission rate was markedly higher to free-living fish, suggesting that transmission routes such as indirect transmission from the substrate or direct contact transmission from infected live and/or dead fish, are relatively more important than transmission by drifting detached parasites.
At present, chlorophyll meters are widely used for a quick and nondestructive estimate of chlorophyll (Chl) contents in plant leaves. Chl meters allow to estimate the Chl content in relative units - the Chl index (CI). However, using such meters, one can face a problem of converting CI into absolute values of the pigment content and comparing data acquired with different devices and for different plant species. Many Chl meters (SPAD-502, CL-01, CCM-200) demonstrated a high degree of correlation between the CI and the absolute pigment content. A number of formulas have been deduced for different plant species to convert the CI into the absolute value of the photosynthetic pigment content. However, such data have not been yet acquired for the atLEAF+ Chl meter. The purpose of the present study was to assess the applicability of the atLEAF+ Chl meter for estimating the Chl content. A significant species-specific exponential relationships between the atLEAF value (corresponding to CI) and extractable Chl a, Chl b, Chl (a+b) for Calamus dioicus and Cleistanthus sp. were shown. The correlations between the atLEAF values and the content of Chl a, Chl b, and Chl (a+b) per unit of leaf area was stronger than that per unit of dry leaf mass. The atLEAF value- Chl b correlation was weaker than that of atLEAF value-Chl a and atLEAF value-Chl (a+b) correlations. The influence of light conditions (Chl a/b ratio) on the atLEAF value has been also shown. The obtained results indicated that the atLEAF+ Chl meter is a cheap and convenient tool for a quick nondestructive estimate of the Chl content, if properly calibrated, and can be used for this purpose along with other Chl meters., E. V. Novichonok, A. O. Novichonok, J. A. Kurbatova, E. F. Markovskaya., and Obsahuje seznam literatury