Respiratory Response to Periodic Emergence in Intertidal Molluscs

SYNOPSIS: The ratio of aerial: aquatic was computed for species of intertidal molluscs.This ratio was <1 for sub- and lower littoral species suggestingpartial anaerobiosis in air and >1 for high littoral archeogastropodssuggesting high metabolic demands in air. ratios were near unity for meso- and neogastropodspecies regardless of zonation. Littoral fringe mesogastropodshad ratios <1 reflecting reduced activity on emergence. Amajor gastropod adaptation to increasing emergence is reductionof ctenidium surface area and formation of a mantle cavity lung.Mid- and high littoral pulmonates with both a mantle cavitylung and secondary gills have ratios near unity. In contrast, littoral fringe pulmonates withoutsecondary gills are partially anaerobic in water. Emerged lowand mid-littoral bivalves close the valves, are almost entirelyanaerobic, have ratios 0.14:1and conserve energy by greatly reducing metabolic demand inair. In contrast, emerged high littoral bivalves remain aerobicby periodic gaping and mantle cavity ventilation. Such behaviorssupport an aerobic metabolism while minimizing evaporative waterloss. Aerial gas exchange prevents anaerobic end-product accumulationand, with a reduction in energy demand, allows efficient energystore utilization during prolonged emergence.     

The Physiological Ecology of the Zebra Mussel, Dreissena polymorpha, in North America and Europe

SYNOPSIS. The zebra mussel, Dreissena polymorpha (Pallas), wasintroduced into North America in 1986. Initial North American(N.A.) studies suggested that physiological responses variedbetween N.A. and European populations. However, literature reviewindicates agreement on most aspects of physiological adaptationincluding: respiratory responses; hypoxia/anoxia tolerance;salinity limits; emersion tolerance; freezing resistance; environmentalpH limits; calcium limits; starvation responses; and bioenergeticpartitioning. The main differences among N.A. and European musselsappear to be elevated upper thermal limits and temperaturesfor optimum growth among N.A. populations. N.A. zebra musselsprobably originated from the northern shore of the Black Seain the warmest portion of the mussel's European range. However,most European physiological data come from northern Europe wherepopulations may be adapted to colder temperatures. Alternatively,N.A. research suggests that mussels may have a capacity forseasonal temperature acclimatization such that responses recordedin warmer N.A. waters may be different from those recorded innorthern Europe even after short-term laboratory acclimation.Studies of genetic variation and physiological response amongEuropean and N.A. D. polymorpha populations are required toelucidate the basis for physiological differentiation. Recentlyevolved D. polymorpha has poor resistance adaptations comparedto unionacean and sphaeriid bivalves with longer freshwaterfossil histories. Poor resistance adaptations make it less suitedfor stable habitats, instead, its high fecundities, early maturity,and rapid growth are adaptations to unstable habitats whereextensive resistance adaptations are of little value.     

Why grow up? A perspective on insect strategies to avoid metamorphosis

1. Insects with complete metamorphosis (holometaboly) are extremely successful, constituting over 60% of all described animal species. Complete metamorphosis confers significant advantages because it enables organisms to optimise life‐history components through temporal partitioning, and thereby to exploit multiple ecological niches. Yet holometaboly can also impose costs, and several lineages have evolved life cycle modifications to avoid complete metamorphosis. 2. In this review, we discuss different strategies that have evolved that result in the loss of complete metamorphosis (type I and type II paedomorphosis). In addition, the ecological pressures and developmental modifications that facilitate this avoidance are considered, as well as the importance of life cycle complexity in life‐history evolution. 3. Interestingly, only female holometabolous insects have entirely avoided complete metamorphosis, and it is always the ancestrally juvenile morphology that is retained. These findings point to a strong sex‐biased trade‐off between investment in reproduction and development. While the loss of complete metamorphosis in females has occurred independently on several occasions across holometabolous insects, only a small number of species possessing this ability have been described. 4. Thus, complete metamorphosis, which originated only once in insects, appears to have been almost fully retained. This indicates that significant modifications to the holometabolan metamorphic ground plan are highly constrained, and suggests that the transition to complete metamorphosis is evolutionarily irreversible.     

EFFECTS OF TEMPERATURE ON CHRONIC HYPOXIA TOLERANCE IN THE NON-INDIGENOUS BROWN MUSSEL, PERNA PERNA (BIVALVIA: MYTILIDAE) FROM THE TEXAS GULF OF MEXICO

Effects of temperature (15°, 20° and 25°C), O₂ partialpressure (P_O2=0, 1, 2, 4, and 6 kPa), and individual size(12–79 mm shell length; SL) on survivorship of specimensof the non-indigenous, marine, brown mussel, Perna perna, fromTexas were investigated to assess its potential distributionin North America. Its hypoxia tolerance was temperature-dependent,survivorship being significantly extended at lower temperaturesunder all tested lethal P_O2. Incipient tolerated P_O2 was 4 and6 kPa at 15 and 20°C, respectively, with >50% mortalityoccurring at 25°C at all tested levels of hypoxia. P_O2 hadless of an effect on survival of hypoxia than temperature. At25°C, survivorship was not different over a P_O2 range of0–2 kPa and increased only at 4 and 6 kPa. Survivorshipwas size-dependent. Median survival times increased with increasingSL in anoxia and P_O2=1 kPa, but at 2, 4 and 6 kPa,smaller individuals survived longer than larger individuals.With tolerance levels similar to other estuarine bivalve species,P. perna should withstand hypoxia encountered in estuarine environments.Thus, its restriction to intertidal rocky shores may be dueto other parameters, particularly its relatively low temperaturetolerance. (Received 26 January 2004; accepted 31 March 2005)     

Behavioral and Physiological Responses to Emersion in Freshwater Bivalves

SYNOPSIS. Littoral lentic and shallow lotic freshwater habitatsare unpredictable in periodicity and duration of shore emersion.As a result, freshwater bivalves have evolved extensive capacitiesto withstand prolonged emersion. Valve movement behaviors allowemersed bivalves to control rate of water loss while maintainingat least partial aerial gas exchange; these behaviors are affectedby environmental variables such as temperature and relativehumidity. Aerial oxygen uptake is associated directly with valveventilatory behaviors and mantle edge exposure. Such behaviorsare often phasic, indicative of oxygen "debt" payment. Lackingeffective hemolymph buffer, respiratory acidosis during emersionis compensated by shell carbonate stores allowing hemolymphP_CO2 to rise to levels facilitating diffusion of CO₂ to theenvironment. During emersion, hemolymph calcium can increasefour fold while Na and Cl are tightly regulated. Ammonia productionceases in emersed bivalves. It resumes on reimmersion, indicativeof heavy reliance on non-protein catabolism during emersion.Some emersion adaptations of freshwater species appear to bemodifications of those displayed by intertidal and estuarinebivalves, while others appear independently evolved to allowsurvival of the extreme emersion periods associated with lifein shallow freshwaters.     

Genetic structure of introduced swamp buffalo subpopulations in tropical Australia

High densities of introduced herbivores can damage sensitive ecosystems, increase the risk of extinction of native biota, and host and spread disease. An essential step in managing large ‘feral’ animal populations is to quantify how they use habitats so that management interventions, such as culling, can be targeted to reduce densities and to minimize migration into areas from which animals have been removed. An effective method to quantify animal movements is by measuring landscape‐scale genetic population structure. We describe the genetic population structure of one of Australia's more destructive introduced mammals – the Asian swamp buffalo (Bubalus bubalis). We collected 524 skin samples from buffalo across their range in the Northern Territory of Australia. Allelic diversity in the Northern Territory population was low compared to those reported from populations in their native Asian habitats. The Australian population is tentatively made of three subpopulations; Melville Island, Eastern Arnhem and Central‐Western Arnhem populations. The Melville Island population is represented by a single cluster, while the Eastern Arnhem population has three clusters and the Central‐Western Arnhem population seven clusters. We found some support for isolation by distance across all the sampled populations, but little evidence for this relationship when comparing the two well‐mixed mainland meta‐populations. Despite their small founder populations and limited genetic variation, the persistence of buffalo in Australia has likely been aided by release from high predation, parasitism and disease typical of their native habitats.