The Ultrastructure of the Glandular Trichomes of Solanum tuberosum

The potato plant has two types of glandular trichomes whichwere investigated by electron microscopy. One type has a eight celled globular head on a neck cell anda stalk cell Each glandular cell has many rather large vacuoles,a large nucleus, many ribosomes and mitochondria, a few Golgibodies, and darkly coloured, often irregular plastids (chloroplasts).The plastids are mostly located near the axial cell wall borderinga large central intercellular space filled with secretion materialThe plastids are assumed to participate in the formation ofthe secretion material, which reacts positively to esterasetests. The outer wall is covered by a thin cuticle. The other type has a club-shaped multicellular head on a singlestalk cell. The cytoplasmic features in the cells are similarto those of the globular-headed trichome, except that they possesslarge central vacuoles and randomly distributed plastids. Centricendoplasmic reticulum has been observed in young cells. Intercellularspaces develop between the cells and into the outer wall, whichis thus split into two. Whereas the older glandular cells reactpositively to tests for esterase, the secretion material itselfis pectinaceous and reacts negatively. The outer wall is cutinizedand covered by a cuticle. Solanum tuberosum L., potato, glandular trichomes, ultrastructure     

Vibration and sound communication in solitary bees and wasps

ABSTRACT. Females of solitary bees ( Colletes cunicularius L.) and of digger wasps ( Bembix rostrata L.) produce buzzing sounds and are known to secrete volatile odours when digging their way from the subterranean nests to the soil surface. The odours allow patrolling males to determine the approximate position of the digging virgin female. The buzzes are measured as substrate-borne sound (soil buzz vibrations) and as air-borne sound (soil buzz sounds). Play-back experiments suggest that the soil buzzes are used by the males as additional cues for localization. Faint buzz sounds are emitted regularly by the male during genital contact in copulation. They may serve to change the receptivity of the female. Intense and broadband buzz sounds are produced by bees of either sex, if restrained from moving, perhaps serving to deter predators.     

A PORTABLE DIGITAL SOUND EMITTER FOR INTERACTIVE PLAYBACK OF ANIMAL VOCALISATIONS

ABSTRACT

A new portable digital sound emitter (DSE) for normal and interactive playback of sound signals in the field and in the laboratory is described together with two examples of applications of the DSE in interactive field experiments. The DSE may be loaded with a broad spectrum of digitised sounds, e.g. artificial signals or natural animal vocalisations, and it is controlled via the keyboard of a portable PC running a dedicated program. This program, which can be tailored to support a vast number of different demands, enables the experimenter to start and stop the analog output from the DSE at any time and to choose freely between the available sounds and playback modes. The use of the DSE for interactive playback experiments therefore is only limited by the ability of the operator to perceive the vocalisations of the participating animal and to operate the keyboard of the PC.     

When similar beginnings lead to different ends: Constraints and diversity in cirripede larval development

Summary

Cirripedes are fascinating models for studying both functional constraints and diversity in larval development. Adult cirripedes display an amazing variation in morphology from sessile suspension feeders that still retain many crustacean characters to parasites that have lost virtually all arthropod traits. In contrast, cirripede larval development follows a common scheme with pelagic larvae comprising a series of nauplii followed by a cyprid. Variations are mostly concerned with whether or not the nauplii are feeding and the degree of abbreviation of development, culminating in species where the larvae hatch as cyprids. The cypris larvae are very similar among the ingroups of the Cirripedia, but interesting variations occur in structures used for substrate location and attachment. The cyprid is specialized to both swim through the water and actively explore the substratum by walking on the antennules and using an array of sensory organs in search for a suitable site to attach. This unique morphology and behavior of the cyprid have enabled the Cirripedia to colonize widely different habitats ranging from hard rock to soft animal tissue. Yet, the cyprid can metamorphose into juveniles as different as a setose feeding barnacle and the vermiform stages of the parasitic forms. This emphasizes the importance of the cyprid as one of the key features for the evolutionary success of the Cirripedia.     

Spatially patterned guild structure in larval parasitoids of cyclically outbreaking winter moth populations

1. Wide temporal fluctuations in host abundance are a potential source of instability and stochasticity in the spatiotemporal population dynamics of associated parasitoid species. Within parasitoid guilds (i.e. parasitoids with similar modes of host utilisation), a conceivable outcome is guild organisation according to a lottery model, in which guild members attain local dominance by colonising previously emptied habitats during increasing host density, before other guild members. In the spatial dimension, an expected manifestation of such dynamics is variable guild structure even across homogeneous habitats. 2. We examined the extent of large‐scale spatial patterning of guild characteristics in larval parasitoid wasps associated with cyclically outbreaking populations of the geometrid moth Operophtera brumata in northern Fennoscandia. The study was performed at the onset of the crash‐phase of the geometrid's outbreak cycle, along a 70‐km transect in costal northern Norway, characterised by largely homogeneous environmental conditions, except for a small climatic gradient. 3. There was a distinct large‐scale spatial turnover in dominance among the major parasitoid groups (i.e. guild structure) in O. brumata along the transect, whereas the total prevalence rate of the guild and its diversity showed no consistent variation. Guild structure was unrelated to host density. 4. Although group‐specific responses to a slight spatial climatic gradient cannot be rejected as a causal mechanism, we conclude that our results are consistent with the expectation from large‐scale stochastic extinction‐recolonisation dynamics among functionally equivalent parasitoids relying on a host with strongly cyclic population fluctuations.     

Wolf Movement Patterns: a Key to Estimation of Kill Rate?

Abstract: To estimate wolf (Canis lupus) kill rates from fine-scale movement patterns, we followed adult wolves in 3 territories of the Scandinavian wolf population using Global Positioning Systems (GPS) during the winters of 2001–2003. The resulting 6 datasets of 62–84 study days gave a total of 8,747 hourly GPS positions. We visited clusters of positions in the field on average 8.8 days after positioning and found moose (Alces alces) killed by wolves during the study period on 74 (8%) of the 953 clusters. The number of positions and visits to a cluster, their interaction, and the proportion of afternoon positions were significant fixed effects in mixed logistic-regression models predicting the probability of a cluster containing a wolf-killed moose. The models, however, displayed a poor goodness-of-fit and were not a suitable tool for estimating kill rates from positioning data alone. They might be used to reduce fieldwork by excluding unlikely clusters, although the reduction was not substantial. We discuss proximate factors (i.e., human disturbance and access to prey) as well as ultimate factors (i.e., social organization, intra-guild dominance, and litter size) as potential causes of the observed high temporal and spatial variation in prey-handling. For similar future kill-rate studies, we recommend increasing field efforts and shortening positioning intervals.     

Predation on Moose Calves by European Brown Bears

Abstract: In North America, brown bears (Ursus arctos) can be a significant predator on moose (Alces alces) calves. Our study in Sweden is the first in which brown bears are the only predator on moose calves. Bears and moose occurred at densities of about 30/1,000 km² and 920/1,000 km², respectively, and bears killed about 26% of the calves. Ninety-two percent of the predation took place when calves were <1 month old. Bear predation was probably additive to other natural mortality, which was about 10% in areas both with and without bears. Females that lost their calves in spring produced more calves the following year (1.54 calves/F) than females that kept their calves (1.11 calves/F), which reduced the net loss of calves due to predation to about 22%.