Wild populations of a small neotropical primate, Geoffroy's tamarin (Saguinus geoffroyi), were studied through 30-s instantaneous observational sampling to identify different canopy habitats used by this tamarin. Tree and shrub canopies were sampled in randomly selected plots and in nearby plots that tamarins were observed to use in the forests of Agua Clara, Panama (28 d, 59 100-m2 plots, 32.25 h of tamarin observations, 27 tamarins in total), and in the nearby forests of Barro Colorado Island (49 d, 29 100-m2 plots, 29.6 h of tamarin observations, 14 tamarins in total). Light penetration through the canopy, ambient temperature and humidity, presence of other primates, stem diameters, plant life-forms, distribution of woody flora, abundance of fleshy fruits and arthropods typically consumed by tamarins and abundance of thorny vegetation and biting arthropods in plots used by tamarins were compared with control plots. Habitats used by tamarins had significantly shorter distances between adjacent tree canopies and between canopies and the ground. There was a random distribution of large insects and fleshy fruits that tamarins are known to eat. Habitat selection by tamarins may not be influenced by spiny vegetation, but tamarins may avoid areas with abundant hooked thorns and blood-sucking arthropods. Mobility along runways in various tiers of a rain-forest canopy may be of primary importance, with local abundance of food being a secondary consideration in habitat selection by this small primate.

The morphology and taxonomy of a new species of otoplanid (Plathelminthes: Rhabditophora: Proseriata) is discussed. Otoplana proxima sp. nov., collected at Marina di Bibbona (Livorno), presents the typical morphological peculiarities of the subfamily Otoplaninae, but clearly differs from the previously described species with regard to the organization of the genital organs. The new flatworm appears more similar to Otoplana intermedia, but differs sharply in its body length and male copulatory organ made up of 23–24 pliable spines (42–70 μm long) characterized by a forked tip and a canaliculated proximal end.

Siphonotretid brachiopod distribution in the Lower Ordovician of the Prague Basin is described and discussed; the new species Alichovia cometa is established. The preservation and distribution of the group indicate a preference for shallow-water offshore, high-energy environments: siphonotretids are abundant shelly fossils in the shallower-water, mostly marginal sites of the basin but are absent in the deeper parts. Their environmental limits were complementary to those of the graptolites; siphonotretids co-occur with epiplanktonic graptolites at only a few localities. Deeper offshore deposits with biramose dichograptids and diverse, generally delicate benthic dendroids lack siphonotretids. Indeed, siphonotretids were intolerant to dysoxia and preferred a well-aerated siliciclastic, firm sea floor in the shallower parts of the basin. They were tolerant to suspended coarser detritus, using their spines which functioned as an effective sieve. The density and ramification of spines indicate three sifting strategies. Suggested life styles above the seabed on elevated surfaces (algae, sponges, dendroids) are not supported by direct evidence. They more likely lived within more supple and soft matrices (sponges, tufts of algae) stabilised by their spines, with the spinose basket maintaining free space for inhalant and exhalant currents.

Parasitism often influences the phenotype of individuals. Many of the resulting changes are due to changes in resource allocation that come with infection. Here we examine the effect of a trematode parasite on the shape and defence morphology of a New Zealand freshwater snail, Potamopyrgus antipodarum. The trematode Microphallus sp. asexually produces hundreds of metacercarial cysts in the snail. The length, width and 2-dimensional area of each snail were measured. Snails were also assessed for their degree of spininess. Snails were dissected to determine gender, brooding condition and parasitism. Snails infected with Microphallus sp. were found to be significantly less spiny than uninfected snails. Microphallus-infected snails were also found to have a significantly greater width to length ratio at larger sizes than their uninfected counterparts. These trends could be explained in at least 3 ways. (1) Infection causes the snails to not produce spines and to become wider. (2) Spiny and narrower snails are more likely to die when they become infected. (3) Spiny and narrower snails are more resistant to infection. The changes in phenotype observed are unlikely to be adaptive for either the host or parasite and probably represent physiological by-products of the host-parasite relationship.

Aristiform spines of the rodents Niviventer fulvescens, Maxomys surifer, Hoplomys gymnurus and 17 species of Proechimys (representing both recognized subgenera and all nine species groups) were studied qualitatively using scanning electron microscopy (SEM) and quantitatively by measuring seven linear dimensions. SEM was used to examine spine tips, bases, longitudinal furrows and cross sections. Spines of the murid rodents N. fulvescens and M. surifer differed from those of the echimyid rodents H. gymnurus and Proechimys spp. in possessing a smaller base with a longer, narrower neck, scaled rather than ridged longitudinal furrows, and a solid internal core and large lacunae at the spine margins. Spines of H. gymnurus differed from those of Proechimys spp. in being considerably more robust with a stout neck at the base, an abruptly-tapering tip and a dense inner layer with a series of smaller lacunae at the spine margins. A factor analysis of spine measurements revealed major differences among N. fulvescens, M. surifer, H. gymnurus, the Proechimys subgenus Trinomys and the nine Proechimys species groups within the subgenus Proechimys. However, all Proechimys species groups clustered closely together. A discriminant function analysis of the nine Proechimys species groups provided generally limited discriminatory power. Although spines are distinct at the generic and subgeneric levels, spines may possess limited diagnostic structure at the level of species within the subgenus Proechimys.

Increased shoot growth has recurrently been recorded following real or simulated shoot browsing, although responses may vary between different woody species. We investigated morphological responses to simulated dry-season browsing on Colophospermum mopane, Acacia tortilis, Grewia flava, Peltophorum africanum and Ziziphus mucronata, which differ in growth rate, occurrence of spines and use by mammalian herbivores. Treatment groups included a control, four clipping intensities and cutting at ground level. Responses were monitored during the following growth season on three annual shoots, located in the bottom, middle and top height interval, on each sapling. All five species showed compensatory growth responses, although no obvious relation was found between the strength of responses and growth rate or natural browsing pressure. The general pattern was an increased shoot length, shoot diameter, number of lateral shoots and shoot biomass with increased clipping intensity. These responses are probably an effect of the reduction of competing growing points and disrupted apical dominance. Growth responses were stronger in shoots with higher location on the sapling, which may reflect the pressure on saplings to attain a certain height to avoid browsing, reproduce and increase resistance to fire. We found no evidence of the number of spines being an induced defence in either of the two spinescent species studied.

Xenacanthids were a very successful group of elasmobranchs that ranged from the Lower Carboniferous to the Upper Triassic. The history of discovery of the xenacanthids, which is closely connected with the history of coal prospecting in England, began with the finding of the type specimen of Xenacanthus laevissimus in the Westphalian B of the West Midlands. In this first review of British Carboniferous xenacanthids, the number of taxa, mainly erected during Victorian times, is reduced to 14 species distributed among six genera. Determinable remains are recorded from at least 96 localities in the British Isles. Unique characteristics of the Dinantian Diplodoselache suggest that the lineage to which this taxon belongs marks a dead end in xenacanthid evolution. This investigation also shows that the Pendleian Dicentrodus, formerly described as Cladodus, belongs to the xenacanthids. The occurrence of Orthacanthus cf. kounoviensis in the Pennines, also known from the German Saar-Nahe basin, the Saale depression and from Bohemia, indicates a faunal exchange between these intramontainous basins during the Carboniferous. The genus Triodus is identified from British deposits for the first time. A cladistic analysis of the xenacanthids suggests that they evolved from phoebodontid elasmobranchs. This analysis also confirms separation of the Middle Devonian Antarctilamna from a relationship with xenacanthid sharks.

Fragmentary remains of a vascular sporophyte from the Rhynie Chert are described as a new genus and species, Trichopherophyton teuchansii. The plant, which is characterised by the possession of unicellular spinous hairs, exarch xylem and laterally attached, marginally dehiscent sporangia, is assigned to the Zosterophyllophytina, but lack of information on the arrangement of sporangia prevents its more precise positioning within the subdivision. Unusual features include the combination of circinate tips to axes with almost terete xylem strands, and the lack of a thick-walled outer cortical zone. Associated axes, lacking spinous hairs, but having papillate or rhizoid-like epidermal emergences, are interpreted as likely rhizomes of Trichopherophyton. Features, such as unicellular spinous hairs, rhizoid-like emergences, circinate tipsand parenchymatous cortex are considered in relation to the functioning and growth of aplant inhabiting an early Devonian wetland.

1. Under laboratory conditions (25 to 27°C), female Cydia ptychora (Meyrick) laid an average of 44 eggs. 2. The egg incubation period was 5 days, while the larval developmental period lasted 7 to 10 days, and the pupal period 12 days. Thus, the total developmental period (egg to adult) lasted 24 to 27 days. The adult longevity averaged 10 days (13 to 15 days). 3. Descriptions of the different life stages and setal maps of the different larval instars are provided.