The bug family Nabidae (Heteroptera) includes taxa showing either a low chromosome number 2n = 16 + XY or high chromosome numbers 2n = 26 or 32 + XY. In order to reveal the direction of karyotype evolution in the family, a molecular phylogeny of the family was created to reveal the taxon closest to the ancestral type and hence the ancestral karyotype. The phylogeny was based on a partial sequence of the 18S rDNA gene of both high and low chromosome number species belonging to the subfamilies Prostemmatinae and Nabinae. Phylogeny created by the Neighbour Joining method separated the subfamilies, Prostemmatinae and Nabinae, which form sister groups at the base of this phylogenetic tree, as well as within the Nabinae, tribes Nabini and Arachnocorini. Combining karyosystematic data with the phylogeny of the family indicated that the ancestral karyotype was a high chromosome number, consisting of 2n = 32 + XY. During the course of evolution changes have occurred both in meiotic behaviour of the sex chromosomes and in the number of autosomes. The direction of karyotype evolution was from a high to low autosome number. Abrupt decreases in the number of autosomes have occurred twice; firstly when the tribe Arachnocorini differentiated from the main stem in the subfamily Nabinae and secondly within the tribe Nabini, when within the genus Nabis 2n = 16 + XY species diverged from the 2n = 32 + XY species. A scheme of the sequence of events in karyotype evolution during the evolution of the Nabidae is presented.
The relative occurrence and seasonal abundance of aphidophagous predators (Insecta and Arachnida) were determined in alfalfa fields at two locations in the northeast Iberian Peninsula, using D-Vac and sweep-net sampling techniques. Among the insects, Heteroptera, Dermaptera, Neuroptera, Coleoptera and Diptera were found. The relative abundance of predators was similar at the two locations. Polyphagous predators were much more abundant than aphid specific species. Heteroptera were the most abundant order of insect predators: members of the Nabidae, Anthocoridae and Miridae were very common. Coleoptera were also abundant, represented mainly by the family Staphylinidae. Coccinellidae were less abundant and their occurrence coincided with maximum aphid presence. There was a low occurrence of other aphid-specific predators, i.e. Diptera: Syrphidae and Neuroptera: Chrysopidae. Arachnida varied between localities (from 35% to 65%). Over a five-year period, numerical responses by Orius spp., Nabis provencalis and Coccinellidae to aphids were found using polynomial regression models; however the abundance of predators was weakly explained by aphid abundance. Alfalfa, maize and winter cereals share similar aphid predator groups and these crops partially coincide in time, enabling the movement of predators among crops. The persistence of several predatory groups (Anthocoridae, Nabidae, Staphylinidae, Araneae) during most of the season suggests that alfalfa plays a major role as a reservoir of aphid predators.
As a part of ongoing cytogenetic studies on the bug family Nabidae (Heteroptera), the karyotypes and meiotic patterns of male Nabis (Aspilaspis) viridulus Spinola, 1837, N. (A.) indicus (Stål, 1873) (subfamily Nabinae) and Prostemma guttula (Fabricius, 1787) (subfamily Prostemmatinae) are described.
N. viridulus and N. indicus differ from P. guttula in their chromosome numbers, which are 2n = 32 + XY and 2n = 26 + XY, respectively, and behaviour of the sex chromosomes in male meiosis, which, respectively, show "distance pairing" and "touch-and-go pairing" in spermatocyte metaphase II. The karyotype of 2n = 34 and "touch-and-go pairing" are considered to be plesiomorphic characters in Nabidae. The evolutionary mechanisms that might underlie different chromosome numbers, the taxonomic significance of karyotype variation and the distribution of meiotic patterns in the family, are discussed.
In many insects, mate finding is mediated by volatile sex pheromones, but evidence in nabids is still fragmentary. The role of odour-mediated sexual attraction in two nabid species, Nabis pseudoferus and N. rugosus, was studied in a Y-tube olfactometer. Females of the two species were significantly attracted by odours of conspecifics males, and males of N. rugosus, but not of N. pseudoferus, were attracted by odours of conspecific females. Odours of conspecifics of the same gender were unattractive. These results suggest the existence of male pheromones in both species and a different female pheromone in N. rugosus.
The winter survival of three closely related univoltine heteropterans that overwinter as adults, Nabis rugosus, N. ericetorum and N. pseudoferus was investigated. After 150 days of low temperature treatment (3-5°C, 16L : 8D, r.h. 70-80%) more males than females died. The mortality rate ranged from 88.8 to 93.8% in males and from 54.2 to 60.7% in females. However, these sexual differences in mortality did not differ significantly across the three species and populations of different geographic origin. It remains a general question whether this considerable evolutionary stability in the sex-specific investment into reproduction and survival phylogenetically conserved or frequently evolves anew to similar levels in separated populations and species. In Nabis rugosus, the relative loss of body mass during overwintering was up to 37.8%. This reflects dramatic somatic costs of adult overwintering and indirectly supports the hypothesis that food supply during overwintering is important for some heteropteran predators. However, body mass before overwintering did not significantly explain the survival pattern in N. rugosus in either sex. The similar sex-specific survival rate of overwintering adult nabids regardless of species and geographic origin can be useful for studies on population dynamics of nabids in agroecosystems and biocontrol.