Landscape approaches to the analysis of aquatic ecosystems

1. In the mid-1970s, Hynes (1975) wrote eloquently about the complex interactions between aquatic and terrestrial systems. Central theories in stream ecology developed thereafter have dealt with the longitudinal flow of energy, materials and organisms in streams, and, with the exception of the flood pulse concept (Junk, Bayley & Sparks, 1989), have largely ignored areas outside the riparian zone. The structure of the upland and activities occurring there play a more important part than previously recognized in regulating community structure and ecosystem processes in streams.
2. These new perspectives are made possible by developments in hierarchy theory, patch dynamics, and the refinement of tools used to quantify spatial and temporal heterogeneity.
3. Geographical information systems (GIS), image processing technology and spatial statistical techniques allow quantitative assessment of lateral, longitudinal and vertical components of the landscape that interact at several spatial and temporal scales to influence streams. When GIS is used in concert with geostatistics, multivariate statistics, or landscape models, complex relationships can be elucidated and predicted.
4. To a certain extent, the tools discussed above have only automated functions that were previously performed manually. This suite of tools has improved the ability of aquatic ecologists to examine relationships and test theories over larger, more heterogeneous regions than were previously possible.
5. At the local, state and federal level, management and regulatory frameworks are currently being re-evaluated to incorporate this new perspective in resource management and policy decision making.
6. We will discuss current and future trends in technologies and tools used for aquatic ecosystem research, and the use of techniques as they are applied in these regional assessments are also discussed.     

A New Malaria Parasite Plasmodium (Sauramoeba) heischi in Skinks (Mabuya striata) from Nairobi, with a Brief Discussion of the Distribution of Malaria Parasites in the Family Scincidae

ABSTRACT. A new species of malaria parasite, Plasmodium (Sauramoeba) heischi , is described from African skinks (Mabuya striata). Eleven individuals of 90 specimens collected in Nairobi were found to be infected. The new parasite is a large species, characterized by spindle-shaped gametocytes, the female often with a subterminal nucleus. The schizonts produce up to 65 nuclei and cause great hypertrophy and distortion of the host cell. Although similar to P. (Sauramoeba) giganteum in dimensions and merozoite numbers, P. heischi is easily distinguished by gametocyte and schizont shapes.     

The Spontaneous Formation of Antheridia in Onoclea is not Blocked by Light

Onoclea sensibilis gametophytes were grown from spores on ashedsoil and agar to determine if the spontaneous formation of antheridiacan be blocked by light. Under most conditions, dark-grown gametophytesformed antheridia later than or at the same time as gametophytesgrown in the light. Under no circumstances was there a rapidonset of maleness in the dark. These results contradict thehypothesis that, in Onoclea, antheridiogen is required to inducemaleness because light inhibits the formation of antheridia.In the light, antheridia formed on heart-shaped thalli. In darkness,antheridia formed on filamentous gametophytes. The timing ofonset of maleness was affected by temperature and the presenceof sucrose. The effect of sucrose on the comparison betweenlight and dark treatments depended on both substrate and temperature Onoclea sensibilis, L., sensitive fern, fern gametophytes, sexuality, light-induced block     

Ecophenotypic strategies of dalmanellid brachiopods

General ecophenotypic patterns, of particular interest when they apply to all, or most, taxa of the group concerned, can never be demonstrated until after monophyletic taxa have been recognized, that is, until after the initial stages of phylogeny construction have been carried out. In criticizing certain dalmanellid phylogenies, and based in large part on a study of five 'species subgroups'. Hurst & Watkins (1978; Geologica et Palaeontologica 12 ) postulate ecophenotypic patterns for Isorthis , and Hurst (1978; Palaeontology 21 ) postulates general patterns of ecophenotypic variation for dalmanellid brachiopods. These patterns may be invalid for four reasons: (1) Univariate and 'bivariate' statistical analysis of the samples used to define the five subgroups reveals no significant differences between subgroups, or vertical trends, for the very morphological characters claimed to exhibit the ecophenotypic patterns; (2) Hurst & Watkins' discriminant function analysis contains procedural errors and its results are ambiguous; (3) several of the five subgroups represent mixtures of unrelated taxa; (4) in recognizing the alleged patterns, Hurst & Watkins ignored contrary evidence from many taxa (and from many dalmanellid studies). □ Brachiopoda, Dalmanellidae, Silurian, ecology, evolution, systematics.     

THE ORIGINS OF ADAPTIVE INTERSPECIFIC TERRITORIALISM

1. In order to understand fully the evolution of a behavioural trait one must not only consider whether it is adaptive in its present environment but also whether it originated as an adaptation to existing selective forces or as a fortuitous consequence of selection for a different role in other environments (i.e., as a pre-adaptation) or of selection for different traits (e.g., as a pleiotropic effect). In this paper interspecific territorialism is examined in species of humming-birds, sun-birds, tropical reef fishes, stingless bees, stomatopods, crayfish, and limpets as a means of determining its adaptiveness and its origins. 2. Humming-birds form complex assemblages with species sorted out among the available resources. Dominant species establish feeding territories where flowers provide sufficient nectar. A few large, dominant species, usually uncommon, are marauders on others' territories. Subordinate species establish territories where flowers are more dispersed or produce less nectar, or they fly a circuit from nectar source to nectar source when flowers are even more dispersed, a foraging pattern called ‘traplining’, or they steal nectar from the territorial species by being inconspicuous while foraging. Two species, Amazilia saucerottei and Selasphorus sasin, subordinate in one-to-one encounters, are able to take over rich resources by establishing several small territories within a territory of a dominant and forcing it to forage elsewhere. 3. Among humming-birds, territorial individuals attacked not only subordinate competitors but marauding humming-birds and some insects, which stayed in the territory and foraged at will, and seemingly inappropriate targets, such as non-competitors. This suggests that the stimulus for aggression is ‘any flying organism near the food resources’, regardless of its appearance. The behaviour rather than the identity of the intruder is the stimulus. 4. Sun-birds resemble humming-birds to the extent that dominants establish territories on rich nectar sources and subordinates establish territories on less rich nectar sources or steal from the territories of dominants. The diversity of foraging patterns is not so great as in humming-birds, perhaps because so few species of sun-birds have been studied. However, the advantage of territorialism has been measured in the sun-bird Nectarinia reichenowi. Individuals with territories lose much less nectar to competitors than do those without territories. 5. Field work on three species of tropical reef fishes involved a single aggressive species whose individuals attacked a wide range of species intruding on their territories. The stimulus for aggression in Pomacentrus jenkinsi seemed to be an “object moving through [its] territory”. As suggested for humming-birds, the stimulus is the behaviour rather than the identity of the intruder. 6. The relationships found in stingless bees, stomatopods, crayfish, and limpets are simpler. The dominant and subordinate species divide the resources in their habitat, the dominants' aggression preventing the subordinates from using resources that were otherwise available to them. 7. A general pattern emerges. Mutual interspecific territorialism occurs between species that (i) have different geographic ranges, (ii) occupy different habitats, or (iii) use different resources within the same habitat. Examples of two species holding separate territories on the same resources within the same habitat are rare and occur when the dominant species is rare relative to the available resources. These observations are contrary to the usual view that interspecific territorialism is an adaptation that permits co-existence of potential competitors within the same habitat. 8. Interspecific territorialism is sometimes adaptive and sometimes maladaptive, depending upon the species and the situation. 9. The general pattern of occurrence of the behaviour and the general nature of the stimulus for aggression, i.e., the behaviour rather than the identity of the intruder, suggest that interspecific territoriality is a fortuitous consequence of selection for intraspecific territorialism, the latter being not only an adaptation to the presence of conspecific competitors but a pre-adaptation to the presence of competitors of other species, should they occur.     

The RCE: a Riparian, Channel, and Environmental Inventory for small streams in the agricultural landscape

1. The Riparian, Channel and Environmental (RCE) Inventory has been developed to assess the physical and biological condition of small streams in the lowland, agricultural landscape. It consists of sixteen characteristics which define the structure of the riparian zone, stream channel morphology, and the biological condition in both habitats. 2. The inventory is based on the view that in landscapes where non-point source pollution and agriculture dominate, the environmental condition of small streams can be assessed by an appraisal of the physical condition of the riparian zone and stream channel. It is assumed that disturbance of this physical structure is a major cause for reduction of stream biological structure and function. This assumption is supported by a case study using fifteen Italian stream locations in which the RCE was found to be positively correlated to the benthic macroinvertebrate community as measured by the Extended Biotic Index (r = 0.80, P < 0.001) and the Shannon Diversity Index (r = 0.73; P < 0.001). 3. The inventory is designed for quick use to cover a large number of streams in a short period of time. When used it generates a numerical score which can be used to compare the physical and biological condition between different streams within a region. The numerical score is divided into five, colour-coded classes to facilitate use in streammonitoring programmes and to allow comparison with biological indices.     

Historical and Life History Factors in the Biogeography of Mayflies

SYNOPSIS. Cladistic analysis of mayflies suggests that dispersalwas very asymmetrical after the new land connection betweenNorth and South America. Twenty-one genera apparently movedfrom South to North and Central America, but there is good evidencefor only one North American genus moving into the south. Testablepredictions are possible once the boreal (Laurasian) or austral(Gondwanian) designations are made. For example, Paracloeodes,a genus of austral origin, was predicted to be found in SouthAmerica, and in North America in warm rivers north and eastof its known distribution. These predictions have been confirmed.Other characteristics of tropical mayflies, such as length oflarval period and emergence and mating patterns, may be usedto predict habitats and characteristics of present North Americangenera. Merger events and consequent dispersal of organismshave profound influences on distributional patterns, and fromsuch information, biologically useful generalities can be made.