The return of the giants: ecological effects of an increasing elephant population

Northern Botswana and adjacent areas, have the world's largest population of African elephant (Loxodonta africana). However, a 100 years ago elephants were rare following excessive hunting. Simultaneously, ungulate populations were severely reduced by decease. The ecological effects of the reduction in large herbivores must have been substantial, but are little known. Today, however, ecosystem changes following the increase in elephant numbers cause considerable concern in Botswana. This was the background for the "BONIC" project, investigating the interactions between the increasing elephant population and other ecosystem components and processes. Results confirm that the ecosystem is changing following the increase in elephant and ungulate populations, and, presumably, developing towards a situation resembling that before the reduction of large herbivores. We see no ecological reasons to artificially change elephant numbers. There are, however, economic and social reasons to control elephants, and their range in northern Botswana may have to be artificially restricted.     

Excess nitrogen deposition: issues for consideration

This paper briefly reviews some major mechanisms by which deposition of inorganic N compounds from the atmosphere could be damaging forest and natural ecosystems. Twelve issues which needed further discussion or research were identified. These were: has N deposition increased; what is a N-saturated ecosystem; can the time of onset of N saturation be predicted; can fertiliser experiments simulate the effects of atmospheric deposition; are there relationships between N input and N leaching; is N deposition leading to acidification; does high N input lead to toxicity symptoms in trees; does N input increase tree susceptibility to stress; does N input induce nutrient deficiency; does increasing N affect natural plant communities; what are the effects on aquatic ecosystems; can a 'critical load' for protection of ecosystems be defined? There is a brief critical discussion of each issue. It is concluded that there is not enough understanding of ecosystem function to define a critical load objectively, but that limits can be defined for some ecosystems.     

Diving behaviour of gentoo penguins,Pygoscelis papua; factors keeping dive profiles in shape

The foraging ecology of seven Gentoo penguins,Pygoscelis papua, breeding at Ardley Island, Antarctica was studied using animal-attached devices which recorded swimming speed, heading and dive depth. Reconstruction of the foraging routes by vectorial analysis of the data indicated that at no time did the birds forage on the sea bed. Swimming speed was relatively constant at 1.7 m s^-1, but rates of descent and ascent in the water column during dives increased with increasing maximum dive depth due to changes in descent and ascent angles. The amount of time spent discending and ascending in the water column increased with maximum dive depth as did the duration spent at the point of maximum depth. Dive profiles were essentially either U-shaped (flat-bottomed dives), or V-shaped (bounce dives). Development of a model based on simple probability theory indicated that the optimal dive profile to maximize the chances of prey acquisition depends on vertical prey distribution and on the visual capabilities of the birds with respect to descent and ascent angles.     

Upper temperature tolerances of Tellina tenuis and T. fabula

The upper lethal tolerances of Tellina tenuis da Costa and T. fabula Gmelin were studied under a variety of temperature regimes in which both short-term and long-term mortality were noted; these included steady temperatures, acclimation at a steady temperature then exposure to a steady tempeature, and acclimation at gradually increasing temperatures. T. tenuis alone was also tested for variation in mortality rate according to the date of collection or to the size (i.e., age) of the mollusc. The results suggested that T. tenuis was consistently more tolerant than T. fabula, and that the difference in tolerance was around 5 C°. Both species readily acclimated to higher temperatures after steady temperature acclimation, but not under a regime of gradually increasing temperature. There was no significant, variation in the mortality rate of T. tenuis with season or age. It is suggested that, since the difference in temperature tolerance is not reflected in their respective geographical distributions, there may be some other stage in their life cycle, e.g. the larvae, which is equally susceptible to temperature extremes. The difference in tolerance is, however, reflected in their respective littoral and sublittoral distributions.     

Foraging strategies and prey encounter rate of free-ranging Little Penguins

There is little information on the effort put into foraging by seabirds, even though it is fundamental to many issues in behavioural ecology. Recent researchers have used changes in the underwater cruising speed of penguins to allude to prey ingestion since accelerations are thought to reflect the encounter and pursuit of prey. In this study, we attached minute accelerometers, to determine flipper beat frequency as a proxy for prey pursuit, to Little Penguins Eudyptula minor foraging in shallow waters in Western Australia. During diving, Little Penguins flapped continuously and at a regular pace of 3.16 Hz while descending the water column and throughout the bottom phase of most dives. However, the frequency and amplitude of wingbeats increased transitorily, reaching 3.5–5.5 Hz, during some dives indicating prey pursuit. Pursuit phases lasted a mean of 2.9±3.3 s and occurred principally during the bottom phases of dives (75.4%). Most dives in all birds (86%) had a clear square-shaped depth profile indicating feeding activity near the seabed in the shallow waters of the bays. Hourly maximum depth, time spent underwater, percentage of dives with pursuit events and catch per unit effort showed an overall increase from zero at ca. 0500 h to a maximum during the hours around mid-day before decreasing to zero by 1900 h. During pursuit phases, Little Penguins headed predominantly downward, probably using the seabed to assist them in trapping their prey. In the light of our results, we discuss depth use by Little Penguins and their allocation of foraging effort and prey capture success as a function of environmental conditions.     

Functional mechanisms underlying cetacean distribution patterns: hotspots for bottlenose dolphins are linked to foraging

Many studies have shown that the distribution of cetaceans can be closely linked to habitat, but the underlying function of the preferred habitats often remains unclear. Only when behavioural observations are made in relation to habitat types can functional mechanisms behind the habitat use be revealed. Within the range of a bottlenose dolphin (Tursiops truncatus) population off NE Scotland, dolphins show clear preferences for several discrete areas. If the observed patterns of distribution are related to foraging, we predict that behaviour patterns shown by dolphins would reflect this relationship. In this study we identify behaviours of dolphins at the water surface that were related to feeding events, evaluate whether the patterns of distribution were related to foraging and whether they were related the local submarine habitat characteristics. To investigate whether visible surface evidence of foraging behaviour varied spatially, we analysed data collected from 104 regular boat-based surveys made within the Moray Firth, NE Scotland, between 1990 and 2000. To determine whether underlying bathymetry had any influence on the surface behaviour of dolphins, a land-based observation study was carried out in the populations core region of use. The results of this study show that feeding behaviour by dolphins was significantly higher in areas used intensively by dolphins. Furthermore, there were clear relationships between feeding events and the submarine habitat characteristics; certain forms of feeding occur primarily over steep seabed gradients, and in deeper waters during June and July. These results quantitatively support the hypothesis that the distinctive patterns of distribution shown by these dolphins are related to foraging behaviour or opportunities, and that submarine habitat characteristics may be a significant factor in the foraging efficiency of dolphins. Future work should focus on collecting detailed information on the distribution patterns of prey within the study area to allow direct comparisons between predator and prey distributions.Communicated by J.P. Thorpe, Port Erin     

Dynamic model for the assessment of radiological exposure to marine biota

A generic approach has been developed to simulate dynamically the uptake and turnover of radionuclides by marine biota. The approach incorporates a three-compartment biokinetic model based on first order linear kinetics, with interchange rates between the organism and its surrounding environment. Model rate constants are deduced as a function of known parameters: biological half-lives of elimination, concentration factors and a sample point of the retention curve, allowing for the representation of multi-component release. The new methodology has been tested and validated in respect of non-dynamic assessment models developed for regulatory purposes. The approach has also been successfully tested against research dynamic models developed to represent the uptake of technetium and radioiodine by lobsters and winkles. Assessments conducted on two realistic test scenarios demonstrated the importance of simulating time-dependency for ecosystems in which environmental levels of radionuclides are not in equilibrium.     

Diving deep in a foraging hotspot: acoustic insights into bottlenose dolphin dive depths and feeding behaviour

To exploit resources in their environment, odontocete cetaceans have evolved sophisticated diving abilities to allow effective foraging. However, data on the diving behaviour and underwater foraging behaviour remains limited. This study made use of echolocation clicks and other calls to study the diving behaviour of bottlenose dolphins. Dolphins used the full water column and consistently dived to depths of around 50 m, close to the seabed. However, the majority of their time appeared to be spent within the surface layers of the water column. In addition, by localising calls that have been associated with prey capture events (Janik, Proc R Soc Lond Ser B 267:923–927, 2000a), it appeared that certain forms of feeding behaviour occurred primarily at depths of between 20 and 30 m. Furthermore, data on the depth of clicks made before and after these feeding calls suggested that during the minute before the calls, dolphins were consistently diving from the surface to depths close to the seabed, and were subsequently returning to the surface after the calls. This passive acoustic technique proved an accurate method for studying the depth distribution of dolphin vocalisations. By exploiting the natural sounds made by these wild odontocetes, this investigation provided a previously unavailable perspective on the the 3D nature of bottlenose dolphins foraging behaviour. It confirmed that while the dolphins spent the majority of time close to the surface, the full water column was exploited during foraging events.