Effects of environmental parameters on the oxygen consumption of four marine invertebrates: a comparative factorial study

The oxygen consumption curves of two decapod crustaceans (Palaemon serratus, Penaeus monodon) and two prosobranch molluscs (Trunculariopsis trunculus, Nassarius mutabilis) have been detected in the entire pO₂ interval from 0 to 160 mmHg, under different conditions of temperature and salinity. From the experimental curves, physiological parameters such as the initial oxygen consumption velocity, the Q ₁₀ values and the oxygen independence indices have been measured. The latter parameters have been obtained using normalised plots which allow their better evaluation. The effects of temperature, salinity and oxygen partial pressure on the oxygen-consumption features have been studied using a factorial experimental plan which allows measurement of the effects of each experimental variable as well as the effects of synergistic interactions between different variables. Received: 27 March 2000 / Accepted: 13 November 2000     

Trail and recruitment pheromones in Camponotus socius (Hymenoptera: Formicidae)

Summary. Worker ants of Camponotus socius employ multicomponent signals during group recruitment to food sources and nest emigrations. The chemical signals consist of trail orientation pheromones that originate from the hindgut. Two components that elicit trail orientation behavior were identified: (2S,4R,5S)-2,4-dimethyl-5-hexanolide and 2,3-dihydro-3,5-dihydroxy-6-methylpyran-4-one. Although both compounds release trail following behavior, in choice tests the former compound is preferred significantly. The major recruitment signal appears to be formic acid discharged from the poison gland. Compounds identified in the Dufour gland secretions do not seem to be involved in the recruitment process.     

Spray mechanism of crepidogastrine bombardier beetles (Carabidae; Crepidogastrini)

Summary.   The defensive glandular apparatus of primitive bombardier beetles of the tribe Crepidogastrini (Carabidae) is described for the first time. As exemplified by two African species (Crepidogaster ambreana and C. atrata), the apparatus conforms to the basic bombardier plan, in that the glands are bicompartmented and the secretion is quinonoid (it contains 1,4-benzoquinones and hydrocarbons), hot, and discharged audibly. In a number of morphological respects the crepidogastrine apparatus resembles that of the classical bombardiers of the tribe Brachinini (rather than that of bombardiers of the paussoid lineage), reinforcing the view, already held on taxonomic grounds, that the Crepidogastrini and Brachinini are closely related. That the Crepidogastrini may be primitive relative to Brachinini is underscored by the finding that, unlike brachinines, crepidogastrines do not pulse their secretory emissions. Moreover, they discharge their secretion as a mist, rather than forcibly in the form of jets. Received 22 May 2001; accepted 29 May 2001.     

Boundaries and Corridors as a Continuum of Ecological Flow Control: Lessons from Rivers and Streams

Abstract: Landscape boundaries and corridors are areas of small spatial extent relative to their large effects on ecological flows. The trend in ecological literature is to treat corridors and boundaries as separate phenomena on the landscape. This approach, however, misses a fundamental aspect they have in common: their strong influence on ecological flows. Corridors and boundaries exist at opposite ends of a permeability gradient, differing in their effects on rates and direction of flow. The position of landscape structures along this permeability gradient depends on attributes of both the flow and of the structure itself. We discuss boundaries and corridors in terms of mover specificity, scale, and effects on different levels of ecological organization, using rivers and streams to illustrate our points. We predict which structures will act as boundaries or corridors and at what spatial and temporal scales they are likely to be relevant. Considering the function of landscape structures across the boundary-corridor continuum will provide researchers and managers with a more complete, holistic viewpoint and will allow better strategies to attain conservation goals.     

State Intervention to Protect Endangered Species: Why History and Bad Luck Matter

Abstract: Illegal exploitation threatens the survival of many species, and anti-poaching legislation ("protection on paper") does not protect species. State enforcement is needed to support and supplement the formal status of endangered species, but state enforcement can be a source of instability leading to the demise of species if ad hoc rules are followed blindly. We demonstrate this with a model of poaching, wildlife, and government wildlife enforcement, but our findings apply more generally. Crucial assumptions of the dynamic model are that both poaching and enforcement effort increase or decrease whenever poaching effort and enforcement are relatively profitable or unprofitable activities, respectively. We found that multiple steady states may characterize the system's equilibrium. Depending on initial populations, the initial extent of state involvement, and random events, animal populations may be severely depleted or unexpectedly built up during transition phases. Our findings highlight the importance of history and luck in protecting endangered species.