Morphological and physiological features indicate Metriorhynchidae as the only group of crocodylomorphs with a pelagic lifestyle. Some of these features have evolved convergently in several clades of tetrapods secondarily adapted to aquatic life. One striking feature of metriorhynchids as compared to other crocodylomorphs is the morphology of the pelvic region (i.e., ventrally deflected sacral ribs and reduced pelvic girdle), which increases significantly the depth of this region. This morphology, as a whole, resembles that of other viviparous Mesozoic marine reptiles not phylogenetically related to metriorhynchids. We tested two alternative hypotheses of reproductive strategies in this clade: oviparity vs. viviparity. Given the lack of direct evidence supporting one or the other, we explored the use of evidence that may disconfirm either of these hypotheses. Using this counter-inductive approach, we found no cases contradicting viviparity in metriorhynchids, except for their phylogenetic position as archosaurs. A survey of reproductive modes amongst amniotes depicts the evolutionary plasticity of the transition to viviparity, and a widespread occurrence among tetrapods secondarily adapted to a marine life. Assuming oviparity for metriorhynchids implies egg-laying out of the water. However, their postcranial morphology (i.e., features of fore and hind limbs, pelvic girdle, and tail) contradicts this possibility. In this context, we rejected oviparity for metriorhynchids.

Offspring size and performance in invertebrates often decrease with maternal age or as a response to seasonal environment. In viviparous ectoparasites maternal provision may wholly determine offspring performance outside the host. The viviparous deer ked (Lipoptena cervi), an ectoparasite of cervids, breeds from autumn to spring. We reared deer ked pupae through the reproductive period to investigate whether offspring size and performance vary according to maternal age and offspring environment. We expected that, in autumn, young females would produce the largest offspring to ensure that early-born pupae would survive a long period of winter diapause, and that offspring size would decrease with maternal age and decreasing diapause length. Diapause was associated with a significant weight loss, which reduced survival through post-diapause development. It was thus surprising that the early-born offspring were the smallest, and that size and survival (eventually) increased towards the spring. The variability among offspring in the length of off-host period seems to be an important component of life-history evolution in this ectoparasite, and should be studied further. Unexpected seasonal variation in the offspring size of this blood-feeding ectoparasite may result from changes in female resources due to weakening host condition as the winter progresses.

Off-host stages of temperate parasites must cope with low temperatures. Cold tolerance is often highest in winter, as a result of diapause and cold acclimation, and low during the active summer stages. In some blood-feeding ectoparasites, offspring provisioning determines cold tolerance through all the non-feeding, off-host stages. Large size increases survival in the cold, but so far seasonal variation in within-female offspring size has not been associated with offspring cold tolerance. The deer ked (Lipoptena cervi) reproduces on cervids from autumn to spring. Newborn pupae drop off the host, facing frosts without any acclimation. We examined cold tolerance through 4 seasons and from birth to adulthood by means of short- and long-term frost exposure. We expected females to produce more tolerant offspring in winter than in spring. Large spring pupae survived prolonged frosts better than did small winter pupae. Thus more tolerant offspring were not produced when the temperature outside the host is at its lowest. Unexpectedly, the freezing points were −20°C or below all year round. We showed that high cold tolerance is possible without acclimation regardless of life stage, which presumably correlates with other survival characteristics, such as the starvation resistance of free-living ectoparasites.

A description is given of the external morphology of a single young caecilian (gymnophionan) amphibian from the North Pare Mountains, Tanzania, referable to Scolecomorphus vittatus (Boulenger, 1895). This is the smallest known free-living Scolecomorphus, and it is characterized by many remarkable features previously unrecorded for any life-history stage of any caecilian. The cheeks have conspicuous, posteroventrally divergent paraoral processes that border a concavity on the ventral surface of the snout. The mandibles are very flexible about their articulation with the cranium, and they have a broader curvature than the upper jaw. The dentition is heterogeneous, with adult-like monocusped teeth in single rows, but also some supernumerary teeth, some of which are bicornute. The posterior parts of the paraoral processes bear a small number of monocuspid teeth that lie outside, and project away from, the mouth. The nuchal region of the body bears a distinctive concavity on the underside of the throat, bordered by longitudinal ridges that terminate in fleshy nipples. All of these features are unknown in adult Scolecomorphus, and many are unique for caecilians, and they suggest a highly distinctive life-history stage. The discovery and description of this specimen adds substantially to the currently meagre information on the life history of scolecomorphids and of the diversity of caecilian reproductive biology. Two modes of viviparity in caecilians are identified, with S. vittatus resembling the caeciliid Geotrypetes in giving birth to small altricial young that seem to require extended post-parturition parental care.

Viviparous gyrodactylid monogeneans which are detached from their host may form an important source of infection in fish communities. This is particularly significant for these ectoparasites which have no specific free-living stage and where transmission usually occurs through transfer of adult parasites when fish come into close contact. In this study, in vitro survival of Gyrodactylus gasterostei was correlated with changes in tissue ultrastructure of parents and their embryos during detachment and following return to a host. At 10 °C, detached worms survived for up to 89 h (50% survival = 20 h) with mortality influenced by both age-independent and age-dependent factors. The gastrodermis of attached, fed parasites is syncytial and contains a variety of vesicles and feeding vacuoles. However, following detachment and starvation, degenerative changes occur within the gastrodermis, eventually leading to marked damage to the embryo/s. When starved worms reattached to a fish, they began browsing on host epithelial cells within 1 min and ultrastructural evidence for phagocytic activity in the gastrodermis was detected after 5 min. Putative waste vacuoles increased in abundance after 5–30 min on the new host, coinciding with the reappearance of electron-dense vesicles and possibly indicating completion of the first intracellular cycle of digestion. Parental feeding directly influenced the normal cyclical maturation and regression of the uterine lining between births. In extreme cases, starvation led to detached parasites (6·1%) aborting their embryos. However, even short periods off the host influenced development and survival of embryos, suggesting that temporary interruption of nutrient flow to the embryo can significantly affect gyrodactylid reproductive rates.

Reproductive success of Gyrodactylus salaris from River Lierelva was compared experimentally on 3 stocks of salmon (12·5°C±0·2). Isolated fish from 2 susceptible Norwegian stocks (Rivers Lier and Alta) and 1 resistant Baltic stock of salmon (River Neva) were infected with a single gravid worm in order to record the temporal sequence of births and age at death of individual parasites. Establishment success (proportion of worms surviving to give birth) was generally low and mortality high, but significantly fewer worms survived on Neva (45% with mean survival of 3·5 days) compared to Alta and Lier fish (60%, mean survival 7·9 and 5·2 days, respectively). There was a dramatic difference in parasite fecundity between the host stocks: only 2 births occurred on Neva fish compared to third and fourth births on both Alta and Lier hosts. The timing of the first birth was more variable on Neva hosts and was significantly extended (mean 2·3 days) relative to that on Alta and Neva fish (1·8 days). However, timing of the second birth did not vary on any of the 3 salmon stocks. Age-specific mortality and fecundity data are consistent with exponential population growth of G. salaris on Alta and Lier fish but eventual extinction on Neva hosts. This is the first demonstration that gyrodactylids maintained on different host stocks exhibit variations in fecundity, development and mortality, which may in turn account for the variable virulence noted when G. salaris infects different salmonid hosts.

An alternative to the cold-climate model for the evolution of viviparity is that the impetus for the initial transition from oviparity to viviparity is not an increase in the duration of egg retention but a shift in the location of nests to more superficial and thus warmer locations in the soil profile as temperature declines with increasing altitude or latitude. Shallower nest placement, however, would lead to increased egg mortality as a result of physiological stress or predation, and enhanced egg mortality would thus provide the initial benefit of extended egg retention. To test this hypothesis, I examined the thermal biology of three species of Sceloporus lizards living at high altitudes: S. virgatus (1800 m), S. aeneus (2800 m), and S. bicanthalis (3200 m). The oviparous S. virgatus and S. aeneus females laid eggs at depths of 6 and 2 cm, and mean body/nest temperatures were 24.6/25.2 °C and 19.9/20.8 °C, respectively. Because the initial increment in the duration of egg retention is presumably short, females of these oviparous species cannot initially keep their eggs appreciably warmer than they would be in nests. In contrast, mean temperatures of simulated nests (17.6 °C) of the viviparous S. bicanthalis were similar to the 17 °C low temperature threshold for development, and temperatures in some nests fell below freezing at night and rose to lethal levels during the day. Mean body temperatures of S. bicanthalis females were 20.1 °C; eggs retained during the entire developmental period would hatch 17 days sooner than they would if laid in a nest. Extended egg retention at the highest elevation site would thus provide two benefits: reduced mortality of eggs and accelerated development relative to that in a nest. These benefits, however, accrue because of the initial shift of nests from deeper to more superficial depths in the soil profile.

The taxonomic distribution and evolution of viviparity in Diptera is critically reviewed. The phenomenon ranges from ovoviviparity (eggs deposited at an advanced stage of embryonic development; larva emerges immediately after deposition), through viviparity (larva hatches inside female before deposition) to pupiparity (offspring deposited as pupa). Some Diptera are known to be facultatively viviparous, which is hypothesized to be a step towards the evolution of obligate viviparity. Obligate viviparity is found to comprise unilarviparity (single large larva in maternal uterus) which evolved many times independently, the rare oligolarviparity (more than one but not more than 12 larvae) and multilarviparity (large numbers of developing eggs or larvae in uterus) which is typical for the two largest clades of viviparous Diptera. Unilarviparity is either lecithotrophic (developing larva nourished by yolk of egg) or pseudo-placental (larva nourished by glandular secretions of mother). Viviparity has clearly evolved on many separate occasions in Diptera. It is recorded in 22 families, and this review identifies at least 61 independent origins of viviparity. Six families appear to have viviparity in their ground-plan. Some families have a single evolution of viviparity, others multiple evolutions. Guimaraes' model for the evolution of viviparity in Diptera is tested against phylogenetic information and the adaptive significance of viviparity is reviewed in detail. Possible correlations with life-history parameters (coprophily, parasitism, breeding in ephemeral plant parts, malacophagy and adult feeding habits – especially haematophagy) are analysed critically, as are potential advantages (shorter larval life, less investment in yolk by mother, protection of vulnerable stages, better access to breeding substrates, predation on competitors). Morphological constraints, adaptations and exaptations are reviewed, including the provision of an incubation space for the egg(s), the positioning of the egg(s) in the uterus, and maternal glands. The main morphological adaptations include greater egg size, reduction of egg respiratory filaments, thinning of chorion, modified larval respiratory system and mouthparts, and instar skipping. Female morphology and behaviour is particularly strongly modified for viviparity. The terminalia are shortened, the vagina is more muscular and tracheated, and the ovaries of unilarviparous species have a reduced number of ovarioles with alternate ovulation. Many of the final conclusions are tentative, and a plea is made for more detailed morphological and experimental study of many of the viviparous species. Viviparity in Diptera provides a fascinating example of multiple parallel evolution, and a fertile field for future research.

Constraints on time and energy suggest that animals often will have to forgo one activity in favour of another. In the field, gravid garter snakes, Thamnophis elegans, eat little or nothing, especially late in pregnancy. In addition, they spend considerable time basking, presumably to aid development of their progeny. Apparently, therefore, a conflict exists between feeding and behaviours related to gestation. Alternatively, low feeding levels in the field might reflect reduced ability to catch food while gravid, or anorexia, attributable either to reduced space in the gut or to physiological suppression of appetite. In this study, by supplying abundant food in the laboratory, we test the hypothesis that gravid females are anorexic; we also examine the interactions among feeding, thermoregulation and reproductive condition. Typically, gravid females, whether fed or not, spent most of their time at the warm end of a gradient, as did fed non-gravid snakes; unfed non-gravid females spent significantly less time at the warm end. However, gravid snakes, even when presented with food ad libitum, ate less than non-gravid snakes, suggesting that they are anorexic while pregnant. Feeding and thermoregulatory behaviours of gravid females changed around the time of parturition (increased feeding, reduced warming rate). Comparable changes are seen in animals in the field, and are correlated with changes in movement pattern. Evidently, the tendency to eat little food is carried over into the laboratory, even when apparent proximate causes of the behaviour are removed. Although we cannot distinguish clearly between the two potential causes of anorexia, the evidence slightly favours physiological suppression of appetite. Physiological suppression of appetite while gravid would ensure that the urge to forage rather than thermoregulate does not diminish the chances of present reproductive success. By contrast, non-gravid snakes, faced with a shortage of food, lower their body temperature and reduce their metabolic costs.

Functional diversities associated with structural polymorphism involving oedymery and gynaecoidy among males and major and minor forms in females, with or without alary polymorphs appear typical of many mycophagous Tubulifera. Notable is the occurrence of reproductive polymorphism resulting in oviparity, ovoviviparity, and viviparity among individuals of the same species reflecting both gross as well as histological profiles.

While alary polymorphism tends to result in ovarian diversities in some species, the combination of this feature with gynaecoidy and oedymery among Tubulifera results in a variety of mating combinations and variations in egg output. Information presented pertains to the mating patterns in mycophagous and sporophagous species in relation to the degree of polymorphism and reproductive efficiency in terms of oviposition rates. The considerably higher longevity of the oedymerous males as compared to gynaecoids adds further to the reproductive efficiency of the oedymeres. Size assortive mating is very evident, with females tending to reject males smaller than them, and with males competing for larger females in this intrasexual rivalry.