In this study we examine differences in the occurrence of life history stages of the destructive fish ectoparasite Argulus foliaceus (L., 1758) on eight fish species (stickleback, rudd, roach, gudgeon, bream, tench, crucian carp and common carp) sampled from a mixed-species recreational fishing lake on nine occasions during late spring and summer. Total numbers of A. foliaceus, as well as the number of larval, juvenile and adult parasite stages, from each fish were recorded along with the fish species. Lice generally exhibited an aggregated distribution approximating a negative binomial distribution. Significant differences in the prevalence, intensity and intensity frequency distribution were observed between life history stages and between host species. In general, all life history stages of A. foliaceus exhibited an over-dispersed distribution. However, larval lice did show some degree of aggregation particularly within the stickleback samples. Infection data for parasite larval stages suggested that sticklebacks are more likely to be infected than other host species. For adult lice, however, carp appeared to be the main host. We propose that A. foliaceus infection characteristics are predominantly determined by the level of host exposure to the parasite and its life history stages (larval, juvenile and adult) rather than by an innate difference in host susceptibility related to individual host factors such as immune responses. We conclude that host exposure is determined by the parasite-host behavioural interplay related to species-specific ecology and behavioural traits such as microhabitat preference and normal swimming speed.
With biocrusts playing a cardinal role in C and N fixation in arid zones, information regarding the factors that determine their limits of growth is of uttermost importance for the study of ecosystem structure and function. This is also the case in the western Negev dunefields, where although abundant on the sandy surfaces, biocrusts are scarce on finegrained (mainly loessial) sediments, termed playas. In the Nizzana research site (NRS), visibly distinct surfaces, with and without biocrusts were noted within a single playa. In an attempt to characterize these distinct surfaces, a set of random measurements were carried out, which included measurements of crack density, microrelief and chlorophyll content of the upper 0-1 cm. Following a cluster analysis, four distinct types of surfaces (hereafter habitats) were defined, one with substantial amount of chlorophyll content which can be regarded as biocrust (P4), and three non-crusted surfaces (P1- P3). Within each type, two 50 cm-deep pits were dug and the pH, electrical conductivity (EC) and fine (silt and clay) content (FC) of samples collected at 1-5, 5-10, 10-20, 20-30, 30-40 and 40-50 cm-depth were analyzed. In addition, periodical moisture measurements were carried out (in pairs) to a depth of 0-20 cm at each surface type during 2013/14. All non-crusted habitats (P1-P3) were characterized by loessial subsurface sediments. Conversely, P4 was either characterized by loessial subsurface sediments (and in this case it was characterized by a slightly concave surface) or having a sandy subsurface (at ~5-10 cm depth). While the non-crusted surfaces exhibited low moisture content, P4 exhibited deeper and higher moisture content explained either by the more sandy sediments or by lower water loss through runoff. The findings point to the close link between surface and subsurface properties and indicate that water availability may explain biocrust establishment and growth also at the loessial playa surfaces. Biocrusts may thus serve as bioindicators for habitats with high moisture content.
We prove identities involving sums of Legendre and Jacobi polynomials. The identities are related to Green’s functions for powers of the invariant Laplacian and to the Minakshisundaram-Pleijel zeta function.