A permanent snow cover for several months is typical for large parts of Norway, Sweden and Finland. Snow layers thicker than about 20 cm insulate the soil surface and stabilize the ground temperature close to 0°C. Many ground-living invertebrates are active at this temperature in the subnivean air space. From this "base camp", some invertebrates migrate upwards to use the snow as a substrate. The intranivean fauna consists of springtails (Collembola) and mites (Acari) that are small enough to move within the narrow pores between snow crystals. The supranivean fauna consists of various invertebrates that are active on the snow surface. Some of them are Collembola that have migrated through the snow layers. However, most of them are larger insects and spiders which migrate between the subnivean and supranivean habitats following air channels which are naturally created along tree stems, bushes etc. penetrating the snow. Likewise, certain Chironomidae and Plecoptera, hatching from winter-open rivers and brooks, are active on the snow surface. The supranivean arthropod fauna has the following characteristics: 1. It is a weather dependent assemblage of species, coming and going with changes in air temperature, cloud cover, and wind. Below ca. -6°C animals are absent, but at temperatures around or above zero, many groups can be simultaneously active on snow. 2. The snow surface fauna shows phenological changes throughout the winter, as certain species and groups are mainly active during certain months. 3. Some invertebrates are highly specialized and take advantage of the snow surface as an arena in their life cycle. Examples are Hypogastrura socialis (Collembola), and the two wingless insects Chionea sp. (Diptera: Limoniidae) and Boreus sp. (Mecoptera). They use the smooth snow surface for efficient migration. Chionea sp. and Boreus sp. lay their eggs during the snow-covered period, while H. socialis migrates to create new colonies. The cold tolerant spider Bolephthyphantes index is unique in constructing webs in small depressions on the snow, to catch migrating Collembola. Various adaptations for using the snow as a substrate are discussed. Besides physiological and morphological adaptations, snow surface arthropods show special behavioural adaptations. Most conspicuous is the ability of several Collembola species to navigate during migration, using the position of the sun for orientation. Furthermore, in Collembola and Mecoptera, jumping as an original mechanism to escape predators has independently evolved into a migrating mechanism. An evolutionary potential exists for more invertebrate groups to take advantage of snow as a substrate in their life cycle. For instance, several more cold tolerant spiders might evolve the ability to catch migrating Collembola on snow.
Palaearctic species of the genus Gymnophora are reviewed. Four new species, G. amurensis sp. n., G. gornostaevi sp. n., G. perpropinqua sp. n., and G. victoria sp. n., are described from the European Russia, Middle Asia, and Russian Far East. Females of two other species from the Far East are described under code letters. G. laciniata Michailovskaya, 1997 is synonymised under G. prescherweberae Disney, 1997. Lectotypes of G. arcuata (Meigen, 1839) and G. verrucata (Schmitz, 1929) are designated. The latter species is redescribed. Palaearctic females of G. nigripennis demonstrate wide variation of taxonomically important features and may, in fact, represent a group of closely related species. One female of G. nigripennis, which has been caught alive, is recorded to be infected with fungi.
A fauna of quill mites of the subfamily Picobiinae (Acari: Syringophilidae) associated with African birds is revised. Two new monotypic genera are proposed, Gunabopicobia gen. n. for Picobia zumpti Lawrence, 1959 and Lawrencipicobia gen. n. for Picobia poicephali Skoracki et Dabert, 2002. These new genera differ from other genera of the subfamily by the following features: in females of Gunabopicobia, propodonotal setae vi are situated anterior to the level of setae ve; the narrow lateral propodonotal shields bear bases of setae vi, ve, si and se; the bases of setae 1a-1a are coalesced; the genital setae and the opisthosomal lobes are absent; the leg I with full set of solenidia and apodemes I are devoid of the thorn-like protuberances in the middle part. In females of Lawrencipicobia, the bases of setae 1a-1a are not coalesced; the propodonotal shield is entire; the genital setae are present; legs I are with full set of solenidia. Additionally, two new species belonging to Picobia Haller, 1878 are described, Picobia illadopsae sp. n. parasitising Illadopsis rufipennis (Sharpe) (Passeriformes: Pellorneidae) in Kenya and Picobia phoenicuri sp. n. infecting Phoenicurus moussieri (Olphe-Galliard) in Tunisia. The following species are redescribed, Columbiphilus alectoris (Fain, Bochkov et Mironov, 2000), Lawrencipicobia poicephali (Skoracki et Dabert, 2001) comb. n. and Picobia phoeniculi (Fain, Bochkov et Mironov, 2000). The key to the genera of the Picobiinae is provided.
As apex predators with a regulating effect on interspecific competitors and prey demographics, monitoring of spotted hyaena (Crocuta crocuta) population trends can provide a reliable indicator of ecosystem health. However, the ability of current survey techniques to monitor carnivore densities effectively are increasingly questioned. This has led recent studies to advocate increased application of spatial capture-recapture (SCR) methods to estimate population density for large carnivores. We reviewed the literature regarding methods used to estimate population density for spotted hyaena since 2000. Our review found that SCR methods are underutilised for estimating spotted hyaena density, with only eight published studies (13% of articles assessed) using an SCR approach. Call-in surveys were the most frequently used method, featuring in 47% of studies. However, 63% of studies that used call-in surveys could not estimate a site-specific calibration index. The calibration index estimates the distance and rate at which the focal species responds to audio lures and, as response rates are impacted by site-specific ecological and environmental factors, studies that could not calibrate this index are likely inaccurate. Further application of SCR techniques will allow more robust estimation of spotted hyaena density, reducing uncertainty and potential overestimation that limit inference from existing survey methods.
Flies of the Colocasiomyia toshiokai species group depend exclusively on inflorescences/infructescences of the aroid tribe Homalomeneae. The taxonomy and reproductive biology of this group is reviewed on the basis of data and samples collected from Southeast Asia. The species boundaries are determined by combining morphological analyses and molecular species delimitation based on sequences of the mitochondrial COI (cytochrome c oxidase subunit I) gene. For the phylogenetic classification within this species group, a cladistic analysis of all the member species is conducted based on 29 parsimony-informative, morphological characters. As a result, six species are recognised within the toshiokai group, including one new species, viz. C. toshiokai, C. xanthogaster, C. nigricauda, C. erythrocephala, C. heterodonta and C. rostrata sp. n. Various host plants are utilised by these species in different combinations at different localities: Some host plants are monopolized by a single species, while others are shared by two or three species. C. xanthogaster and C. heterodonta cohabit on the same host plant in West Java, breeding on spatially different parts of the spadix. There is a close synchrony between flower-visiting behaviour of flies and flowering events of host plants, which indicate an intimate pollination mutualism.
In the present study, we review the known zoogonid cercariae, summarise their life-cycles and first intermediate host distributions, and present a new cercaria, Cercaria capricornia XI (Digenea: Zoogonidae), which was found in one of three nassariid gastropods, Nassarius olivaceus (Bruguière), surveyed in the intertidal zone in the Capricornia region of Central Queensland, Australia. Morphological data and molecular analysis of the ITS2 rDNA region support placement of this cercaria in the family Zoogonidae but do not allow any further resolution of its identity. There are now fifteen cercariae described as belonging to the Zoogonidae; thirteen of these, including the present species, infect neogastropods as first intermediate hosts and two use vetigastropods. This study reinforces the pattern that the Nassariidae is by far the most commonly reported family for the Zoogonidae. Given its richness we predict that the Nassariidae will prove to harbour many more zoogonid species.
Traditionally, the Microsporidia were primarily studied in insects and fish. There were only a few human cases of microsporidiosis reported until the advent of AIDS, when the number of human microsporidian infections dramatically increased and the importance of these new pathogens to medicine became evident. Over a dozen different kinds of microsporidia infecting humans have been reported. While some of these infections were identified in new genera (Enterocytozoon, Vittaforma), there were also infections identified from established genera such as Pleistophora and Encephalitozoon. The genus Pleistophora, originally erected for a species described from fish muscle, and the genus Encephalitozoon, originally described from disseminated infection in rabbits, suggested a link between human infections and animals. In the 1980's, three Pleistophora sp. infections were described from human skeletal muscle without life cycles presented. Subsequently, the genus Trachipleistophora was established for a human-infecting microsporidium with developmental differences from species of the genus Pleistophora. Thus, the existence of a true Pleistophora sp. or spp. in humans was put into question. We have demonstrated the life-cycle stages of the original Pleistophora sp. (Ledford et al. 1985) infection from human muscle, confirming the existence of a true Pleistophora species in humans, P. ronneafiei Cali et Takvorian, 2003, the first demonstrated in a mammalian host. Another human infection, caused by a parasite from invertebrates, was Brachiola algerae (Vavra et Undeen, 1970) Lowman, Takvorian et Cali, 2000. The developmental stages of this human muscle-infecting microsporidium demonstrate morphologically what we have also confirmed by molecular means, that B. algerae, the mosquito parasite, is the causative agent of this human skeletal muscle infection. B. algerae had previously been demonstrated in humans but only in surface infections, skin and eye. The diagnostic features of B. algerae and P. ronneafiei infections in human skeletal muscle are presented. While Encephalitozoon cuniculi has been known as both an animal (mammal) and human parasite, the idea of human microsporidial infections derived from cold-blooded vertebrates and invertebrates has only been suggested by microsporidian phylogeny based on small subunit ribosomal DNA sequences but has not been appreciated. The morphological data presented here demonstrate these relationships. Additionally, water, as a link that connects microsporidial spores in the environment to potential host organisms, is diagrammatically presented.
Ten species of Cixiidae, formerly placed in Trirhacus Fieber, 1875, are redescribed and one additional species is described. They belong to seven genera: Trirhacus s. str. with T. setulosus Fieber, 1876 (type species), T. dubiosus Wagner, 1959, T. biokovensis Dlabola, 1971 and T. peloponnesiacus sp. n., Apartus gen. n. with A. michalki (Wagner, 1948) comb. n. (type species) and A. wagnerianus (Nast, 1965) comb. n., Nanocixius Wagner, 1939 stat. n. with N. discrepans (Fieber, 1876) comb. n., Neocixius Wagner, 1939 stat. n. with N. limbatus (Signoret, 1862) comb. n., Sardocixius gen. n. with S. formosissimus (Costa, 1883) comb. n., Simplicixius gen. n. with S. trichophorus (Melichar, 1914) comb. n. and Sphaerocixius Wagner, 1939 stat. n. with S. globuliferus (Wagner, 1939) comb. n. The phylogenetic relationships of these genera to other Cixiidae are briefly discussed and a key to the genera of European Cixiidae is provided.
European species of the genus Phradis Förster, 1869 are reviewed. A new species from Spain, Phradis mediterraneus sp. n., is described and illustrated. A key to all 24 European species and data on distribution and biology of these species are provided.