Hatching and viability of rotifer diapausing eggs collected from pond sediments

1. Planktonic rotifers inhabiting variable environments produce diapausing eggs that accumulate in the sediment of lakes and ponds, forming egg banks that may withstand adverse periods. A common assumption in zooplankton diapausing egg bank studies is to count as viable all eggs in the sediment that look healthy. This assumption should be challenged by asking how effectively ‘healthy‐looking’ eggs represent viable eggs. 2. In this study, viability of more than 1100 ‘healthy‐looking’ diapausing eggs belonging to the Brachionus plicatilis species complex was assessed in a laboratory hatching experiment. Eggs were collected at different depths from sediment cores obtained from 15 ponds located in coastal and inland areas of Eastern Spain. 3. Only approximately one half of the ‘healthy‐looking’ diapausing eggs hatched after incubation in experimental conditions. Almost all the hatchlings (99.4%) survived to maturity. The proportion of ‘healthy‐looking’ diapausing eggs that hatched varied among areas and among ponds within area, and substantially declined with sediment depth. Most of the hatchlings (88%) were obtained from the uppermost 2 cm of sediment. ‘Healthy‐looking’ eggs from upper sediment layers hatched after significantly shorter incubation times than eggs recovered from deeper layers. 4. Both decreased hatching success and increased incubation time for hatching with sediment depth suggest that older ‘healthy‐looking’ eggs are less responsive to hatching stimuli and could become unviable. However, the strong correlation found between the number of ‘healthy‐looking’ eggs and the number of hatchlings indicates that the abundance of ‘healthy‐looking’ eggs is a good index of egg bank viability.     

Response of diapausing eggs hatching to changes in temperature and the presence of fish kairomones

It has been hypothesized that the production of diapausing eggs in Daphnia can be induced by fish kairomones. A population of Daphnia could survive severe predation using this predator avoidance strategy. However, in changing environments, diapausing eggs experience various temperature conditions, and hatchlings at emergence may be exposed to the same predation risks as their mothers. Therefore, staying in diapause or an immediate response upon hatching to available environmental information could be important for hatchling survival. For this study, we investigated the impact of water temperature (10, 15, 20, and 25°C) in the presence and absence of fish kairomones (Lepomis macrochirus) on the hatching success of resting eggs (D. galeata). Results show that no diapausing eggs hatched at the lowest temperature (10°C), and the highest hatch percentage occurred at 15°C. Although higher water temperatures reduced hatching success, diapausing eggs hatched more quickly. The number of hatchlings was significantly higher after exposure to fish kairomones, and this was more noticeable at higher temperatures (20 and 25°C). The present results suggest that the diapausing eggs were produced as a predator avoidance strategy in Daphnia; however, the presence of fish works as a positive signal to increase hatchlings when the diapausing stage is terminated.     

Ecology of hatching size for marine snails

Summary Chances for survival increase as a snail grows, and the resulting size-specific survival curve dictates hatching size. Related species tend to hatch at the same size, reflecting similarities in ecological roles. Hatching size depends upon macrohabitat and microhabitat among the Muricidae. Thais emarginata hatches large enough to escape from a major predator (the hermit crab) of newly hatched T. lamellosa. However, Thais hatching sizes reflect a general trend for upper shore muricids to hatch larger than lower shore ones, rather than a response to predators. A given volume of yolk will yield the same volume of hatchlings (regardless of hatching type or number of hatchlings) for all prosobranchs, including those whose embryos feed on nurse eggs. Therefore, no hatchlings are inflated more than others to make them less attractive to predators.     

Hatching of cladoceran resting eggs: temperature and photoperiod

Summary 1. We identified temperature and photoperiod conditions under which the hatching of 45 cladoceran species could be elicited. Identification of appropriate hatching cues is of primary importance for the exploration of the ties between active and diapausing stages.
2. Incubation temperature affected the hatching success of resting eggs isolated from Danish, Belgian/Dutch and Spanish sediments. In general, most hatchlings and species were retrieved at 15 °C. Danish and Belgian/Dutch resting eggs hatched more successfully under a long day photoperiod than in continuous illumination.
3. Most species could be retrieved after incubation of resting eggs isolated from a limited amount of sediment (0.4 kg) under a single, well chosen combination of temperature and photoperiod. Processing additional sediment samples under seven more incubation regimes only allowed detection of 21% (Spain) to 34% (Denmark) more species.
4. The incubation period for resting eggs to hatch was strongly influenced by incubation temperature. Our results show that hatching experiments aimed at assessing cladoceran species richness and conducted at 15 °C should be continued for a period of at least 2 weeks, after which a random subset of hatchlings (e.g. n  = 100) can be selected from the total hatchling assemblage.     

The hatching time of Locusta migratoria under outdoor conditions: role of temperature and adaptive significance

The present study investigates the time of hatching of the migratory locust Locusta migratoria using egg pods that are artificially buried in the soil under outdoor conditions. Most eggs hatch in the mid‐morning, with a peak between 11.00 and 12.00 h, and none hatch before 09.00 or after 16.00 h. Furthermore, most egg pods complete hatching within a day, although some take 2 or 3 days, and egg hatching is interrupted by rain. There are no large differences in hatching time from May to September. Laboratory experiments in which the eggs are exposed to temperatures simulating outdoor conditions show that soil temperature is the main factor controlling hatching activity. The increase in temperature in the morning appears to trigger egg hatching, as confirmed by laboratory experiments, which may explain the similar hatching times between seasons. The seasonal patterns of temperature variation and hatching time suggest that the hatching time of L. migratoria eggs may be adjusted to allow the hatchlings to be exposed to high temperatures in the afternoon so that they can harden their bodies quickly.     

The coadaptation of female morphology and offspring size: a comparative analysis in crickets

Few studies of invertebrates have considered combinations of morphological and life history traits in the context of the evolution of reproductive strategies. Cricket species that exploit habitats harsh with respect to egg survival have evolved a long ovipositor, presumably because laying deep in the soil reduces egg mortality. Yet hatchling mortality increases with laying depth, and the ability of hatchlings to climb through the soil increases with egg size. Thus a conflict may exist between survival of the egg and that of the hatchling, inducing a positive covariation between egg size and ovipositor length across species evolving under contrasting selective habitats. We used the phylogenetic autocorrelation method and a path analysis to assess whether egg size coevolved with ovipositor length across 40 species of crickets, and whether egg size was affected by body size or ecological factors that influence egg mortality. Body size and ovipositor length were affected by taxonomic association, whereas common ancestry had no significant effect on egg size, diapausing strategy, and oviposition preference for soil types. The path model indicated that 29.11% of the variance in egg size was explained by independent evolution. As expected, ovipositor length was positively correlated with egg size, and species diapausing in the egg stage produced larger eggs than crickets diapausing in the nymphal stage or with no diapause. Ovipositor length and diapausing strategy were the first and second most important traits, respectively, in term of the proportion of variance in egg size explained by specific values. These results support the hypothesis that the ability of hatchlings to climb through the soil, and variation in diapause strategies, are general selective factors affecting the evolution of egg size in crickets. Phylogeny explained 51.01% of the variance in egg size. Egg size in a current cricket species, however, was not directly determined by egg size in its ancestor. Instead, it was strongly related to the phylogenetic values of body size and ovipositor length. Such indirect phylogenetic effects of body size and ovipositor length may have arisen because clades originating from ancestors with different ovipositor lengths experienced different selective pressures on egg size. Recelived: 13 October 1995 / Accepted: 30 September 1996     

Temperature‐mediated trade‐offs and changes in life‐history integration in two slipper limpets (Gastropoda: Calyptraeidae) with planktotrophic development

Intraspecific variation in egg size and hatching size, and the genetic and environmental trade‐offs that contribute to variation, are the basis of the evolution of life histories. The present study examined both univariate and multivariate temperature‐mediated plasticity of life‐history traits, as well as temperature‐mediated trade‐offs in egg size and clutch size, in two planktotrophic species of marine slipper limpets, Crepidula. Previous work with two species of Crepidula with large eggs and lecithotrophic development has shown a significant effect of temperature on egg size and hatching size. To further examine the effect of temperature on egg size in Crepidula, the effects of temperature on egg size and hatching size, as well as the possible trade‐offs with other the life‐history features, were examined for two planktotrophic species: Crepidula incurva and Crepidula cf. marginalis. Field‐collected juveniles were raised at 23 or 28 °C and egg size, hatching size, capsules/brood, eggs/capsule, time to hatch, interbrood interval, and final body weight were recorded. Consistent with results for the lecithotrophic Crepidula, egg size and hatching size decreased with temperature in the planktotrophic species. The affects of maternal identity and individual brood account for more than half of the intraspecific variation in egg size and hatching size. Temperature also showed a significant effect on reproductive rate, with time to hatch and interbrood interval both decreasing with increasing temperature. However, temperature had contrasting effects on the number of offspring. Crepidula cf. marginalis has significantly more eggs/capsule and therefore more eggs per brood at 28 °C compared to 23 °C, although capsules/brood did not vary with temperature. Crepidula incurva, on the other hand, produced significantly more capsules/brood and more eggs per brood at the lower temperature, whereas the number of eggs/capsule did not vary with temperature. The phenotypic variance–covariance matrix of life‐history variables showed a greater response to temperature in C. incurva than in C. cf. marginalis, and temperature induced trade‐offs between offspring size and number differ between the species. These differences suggest that temperature changes as a result of seasonal upwelling along the coast of Panama will effect the reproduction and evolution of life histories of these two co‐occurring species differently. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.     

Bergmann's rule: a biophysiological rule examined in birds

The most studied ecogeographic rule is Bergmann's rule, but aspects of the original paper are often presented incorrectly even though Bergmann (1847) is explicitly cited. The goal of this paper is to 1) summarize the contents of Bergmann's paper, supported by direct translations, and 2) to discuss the main issues surrounding Bergmann's rule based on Bergmann's intentions and early definitions of the rule. Although Bergmann himself never formulated an explicit rule, based on Bergmann's (1847) intentions and early definitions of Bergmann's rule, Bergmann's rule is: “Within species and amongst closely related species of homeothermic animals a larger size is often achieved in colder climates than in warmer ones, which is linked to the temperature budget of these animals.” Bergmann (1847) assumed that the surface area of an animal is a measure for heat dissipation and an animal's volume a measure of its heat production. As body size increases, an animal's surface area increases less than its volume; however, modifications in morphology and behaviour will also influence the temperature budget. Bergmann hypothesized that when everything but size is equal, the smaller animals should live in warmer areas. This was supported by empirical data on > 300 bird species belonging to 86 genera. Recommendations for use of the term Bergmann's rule include 1) inclusion of a thermoregulatory mechanism, 2) application only to homoeothermic animals, 3) but to any taxonomic group, 4) tests of the rule should test the assumption that larger animals have to produce less heat to increase body temperatures, and 5) future authors should either go back to the original publication (Bergmann 1847) when referring to it or simply not cite it at all. Synthesis Based on Bergmann's (1847) intentions and early definitions, Bergmann's rule is: “Within species and amongst closely related species of homeothermic animals a larger size is often achieved in colder climates than in warmer ones, which is linked to the temperature budget of these animals.” Recommendations for use of the term Bergmann's rule include 1) inclusion of a thermoregulatory mechanism, 2) application only to homoeothermic animals, 3) and to any taxonomic group, 4) tests of the rule should examine whether larger animals have to produce less heat to increase body temperatures, and 5) authors should go back to the original publication (Bergmann 1847) when referring to it.     

Physiological control of water flux in conifers

Summary Pre-hatching developmental times for prosobranch gastropods are greatly influenced by temperature and taxonomic affinity. If the data used here (including all available data from the Muricacea) are a representative sample, then reasonably accurate estimates of developmental time can be obtained for most prosobranchs knowing only temperature and taxon. Times are also significantly affected by egg or hatching size. Correlations between developmental time and hatching form are probably accounted for by egg size. Prehatching periods are little, if at all, longer for metamorphosed hatchlings than for swimming hatchlings; in any event, differences are small relative to typical free swimming periods. Therefore, the planktonic period is a substantial addition to the total pre-juvenile period. Many embryos die before hatching. More would survive if development were faster; development is, therefore, prolonged at a measurable selective cost. Factors promoting extended developmental periods should be evaluated with these costs in mind. For example, providing much of the yolk as nurse-eggs may allow a species to have a large hatching size and at the same time a relatively brief developmental time.     

Temperature‐mediated plasticity and genetic differentiation in egg size and hatching size among populations of Crepidula (Gastropoda: Calyptraeidae)

Offspring size is a key characteristic in life histories, reflecting maternal investment per offspring and, in marine invertebrates, being linked to mode of development. Few studies have focused explicitly on intraspecific variation and plasticity in developmental characteristics such as egg size and hatching size in marine invertebrates. We measured over 1000 eggs and hatchlings of the marine gastropods Crepidula atrasolea and Crepidula ustulatulina from two sites in Florida. A common‐garden experiment showed that egg size and hatching size were larger at 23 °C than at 28 °C in both species. In C. ustulatulina, the species with significant genetic population structure in cytochrome oxidase I (COI), there was a significant effect of population: Eggs and hatchlings from the Atlantic population were smaller than those from the Gulf. The two populations also differed significantly in hatchling shape. Population effects were not significant in C. atrasolea, the species with little genetic population structure in COI, and were apparent through their marginal interaction with temperature. In both species, 60–65% of the variation in egg size and hatching size was a result of variation among females and, in both species, the population from the Atlantic coast showed greater temperature‐mediated plasticity than the population from the Gulf. These results demonstrate that genetic differentiation among populations, plastic responses to variation in environmental temperature, and differences between females all contribute significantly to intraspecific variation in egg size and hatching size. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 489–499.     

Deterioration patterns in diapausing egg banks of Brachionus (Müller, 1786) rotifer species

Rotifers are cyclical parthenogens that produce sexual diapausing eggs at some stage in their life cycle. These eggs are encysted embryos that remain viable for extended periods in lake and pond sediments, thus acting as an egg bank with many ecological and evolutionary consequences. Despite its importance to rotifer evolution, there are no studies on resting egg deterioration and associated processes in natural environments. In this study, more than 4000 diapausing eggs of species from the Brachionus plicatilis complex, which includes several closely related cryptic species, were collected from different sediment depths in 15 ponds in eastern Spain and were classified according to three features thought to be related to their viability: shell integrity, embryo size, and embryo colour. A positive association was found between embryo size and hatching success in those eggs having an intact shell. Diapausing eggs that showed good shell integrity and no more than a 25% reduction of multinuclear embryo maximum size were classified as healthy and 98.9% hatched. Darkening of diapausing egg embryo was an indicator of viability loss. A decreasing frequency of healthy-looking diapausing eggs was observed with increasing sediment depth, although some exceptions were found.     

Shallow water ray-finned marine fishes follow Bergmann’s rule

Understanding the interspecific variation in body size across macroclimatic gradients has been of paramount importance to naturalists and biogeographers. Bergmann’s rule, which describes a trend of increasing body size polewards, is arguably the best-known ecogeographical rule in terrestrial environments but remains largely unexplored in the marine realm. In this study we tested Bergmann's rule in marine ray-finned fishes (Pisces, Actinopterygii), analyzing the relationship between body size and latitude in 5662 species. To examine possible underlying mechanisms, we adopted a cross-species approach to evaluate the association of body size with four predictors: Sea Surface Temperature, Net Primary Productivity, Salinity, and Human impact. We analyzed the relationships between body size and environmental and anthropogenic variables building mixed linear models, which considered the taxonomic structure in the data. We conducted complementary analyses dividing the data into five latitudinal bands. Actinopterygii showed a clear Bergmannian pattern, with the largest species observed in temperate regions, being the first global analysis on ray-finned fishes showing a pattern consistent with Bergmann’s rule. Sea Surface Temperature and Net Primary Productivity were the best predictors, in accordance with the time to sexual maturity and resource availability hypotheses. Our analyses based on latitudinal bands showed a differential response of body size to the environment, with temperature, salinity and human impact more strongly associated with size variation at cold environments. These results agree with previous studies on Bergmann’s rule for terrestrial ectothermic, freshwater and marine fishes. Our findings suggest that temperature rise in the ocean and growing human impact may have effects on the distribution of body size, thus altering ecosystem functioning. Fundamental differences often assumed to exist between marine and terrestrial systems are not so evidently reflected in the emergence of large-scale body size gradients.     

Wasp predation and wasp-induced hatching of red-eyed treefrog eggs

Eggs often suffer high levels of predation and, compared with older animals, embryos have few options available for antipredator defence. None the less, hatchlings can escape from many predators to which eggs are vulnerable. I studied early hatching as an antipredator defence of red-eyed treefrog embryos, Agalychnis callidryas, in response to egg predation by social wasps (Polybia rejecta). Red-eyed treefrogs attach their eggs to vegetation overhanging water, where they are exposed to arboreal and aerial predators. Wasps attacked half the egg clutches and killed almost a quarter of the eggs I monitored at a natural breeding site in Panama. Hatching tadpoles fall into the water, where they face aquatic predators. As predicted from improved survival of older hatchlings with aquatic predators, most undisturbed eggs hatched relatively late. However, many younger embryos directly attacked by wasps hatched immediately. Embryos attacked by wasps hatched as much as a third younger than the peak undisturbed hatching age, and most hatching embryos escaped. Thus hatching is an effective defence against wasp predation, and plasticity in hatching stage allows embryos to balance risks from stage-specific egg and larval predators. Wasp-induced hatching is behaviourally similar to the snake-induced hatching previously described in A. callidryas, but occurs in fewer eggs at a time, congruent with the scale of the risk. Individual embryos hatch in response to wasps, which take single eggs, whereas whole clutches hatch in response to snakes, which consume entire clutches. Embryos of A. callidryas thus respond appropriately to graded variation in mortality risks. Copyright 2000 The Association for the Study of Animal Behaviour.     

The balance between predictions and evidence and the search for universal macroecological patterns: taking Bergmann’s rule back to its endothermic origin

Geographical variation in environmental temperatures is expected to impose clinal phenotypic selection that results in the expression of large-scale gradients of body mass variation within animal clades. Body size is predicted to increase with increasing latitude and elevation, and hence, with decreasing temperature, a pattern broadly known as Bergmann’s rule. However, empirical observations are highly conflicting. Whilst most studies support this prediction in endotherms (birds and mammals), analyses conducted on ectotherms often fail to report this pattern. Does it reduce the validity of this macroecological rule? Since the original formulation of Bergmann’s rule only involved endothermic organisms, I argue that the controversy is not a consequence of its predictive power, but a result of the later inclusion of ectotherms as part of the prediction. Here, I propose that the common conception of Bergmann’s rule maintained for half a century is changed back to its original definition restricted to endotherms. This temperature–size relationship might therefore consolidate as a well-established macroecological rule if its original formulation is respected. Finally, I develop these claims on my initial suggestion that Bergmann’s rule should be recognized as the evolutionary outcome of a general process with no phylogenetic scale distinction of species or populations, being equally applicable amongst and within species.     

Temporal dispersal: ecological and evolutionary aspects of zooplankton egg banks and the role of sediment mixing

Zooplankton egg banks are the accumulation of diapausing embryosof planktonic animals buried in the sediments of many aquaticecosystems. These eggs, which are analogous life history stagesto the seeds of many plants, can survive in a ready-to-hatchstate for periods ranging from a few years to greater than acentury. Their presence in ponds, lakes and near-shore marineenvironments has substantial implications for understandingtrajectories of ecological and evolutionary change. When thesediments of lakes are structured in historical sequence, diapausingeggs extracted from different sediment ages can provide a meansof studying past changes in community or population-geneticstructure. A completely different aspect of egg banks derivesfrom the fact that hatching of diapausing eggs can influence,through what can be thought of as temporal dispersal, populationand community response to environmental change. Eggs hatchingfrom diapause introduce to current environments species or genotypeslaid at times in the distant past. In addition, egg banks createextended generation overlap that can play an important rolein maintaining diversity in a fluctuating environment when differenttypes (species or genotypes) are favored at different times.These distinct aspects of egg banks (i.e., their direct impacton ecological and evolutionary processes versus their usefulnessin reconstructing historical changes), are potentially in conflictbecause for old eggs to hatch, the sediments must be at leastpartially mixed. This same mixing, however, degrades the accuracyof the historical record. Both aspects are possible, however,even within a single lake when sediment-mixing intensity isspatially heterogeneous.     

Effect of plasticity in hatching on duration as a precompetent swimming larva in the nudibranch Phestilla sibogae

Abstract. Plasticity in hatching can balance risks of benthic and pelagic development and thereby affect the extent of larval dispersal. Veligers of the nudibranch Phestilla sibogae hatched from their individual capsules if the encapsulated embryos were scattered from a torn gelatinous egg ribbon. Hatching occurred as early as day 4 at 23°–25°C. The early hatchlings lacked a propodium, swam, and were not yet competent to settle and metamorphose. Hatching may be induced by predation: crabs consumed egg ribbons, and a portunid crab, caught in the act of tearing an egg ribbon, scattered encapsulated embryos. Undisturbed egg masses hatched as late as 9–11 d at 23°–25°C, or as early as 8 d in a trial at 26°C. Late hatchlings had a well-developed propodium, and 20–100% metamorphosed within a day of exposure to the inducer from the nudibranch's coral prey. A few metamorphosed nudibranchs were found within hatching egg masses. Thus, the veligers can hatch so late that many are competent to metamorphose or so early that the obligate planktonic period can last 4 or more days. An attack by a predator means the benthic habitat is dangerous for the embryos, and swimming is presumably the safer option. In the absence of disturbance, the veligers hatch when ready or nearly ready to settle.     

Bergmann′s rule in mammals: a cross‐species interspecific pattern

Although Bergmann’s rule – stating that among closely related species, the bigger ones will inhabit the colder climates/higher latitudes – was formulated for inter‐specific comparisons, most analyses that tested this pattern in mammals were on an intra‐specific level. To date, no large‐scale taxonomy‐driven cross‐species evaluation of the pattern predicted by Bergmann exists. Here we show, in a dataset comprising 3561 mammal species from 26 orders, that while there is no significant correlation between latitude and body mass using conventional methods, this correlation is highly significant when the phylogenetic structure of the dataset is accounted for, thus supporting Bergmann’s claim that the rule only applies to closely related species. Analyses of different subsets indicate that the Bergmann’s rule is evident across a variety of latitude ranges. In many taxonomic subsets, when analysed alone, there is no significant correlation between body mass and latitude. In combination with both the significant relationship in the overall dataset and with results of intra‐specific analyses from the literature, this suggests that Bergmann’s rule describes a fundamental principle within mammals, but that its expression has been modified by a variety of factors during mammalian diversification yet to be resolved.     

Effect of nesting environment on incubation temperature and hatching success of Morelet's crocodile (Crocodylus moreletii) in an urban lake of Southeastern Mexico

Incubation temperature is an important aspect in terms of biological performance among crocodiles, and several controlled experiments have demonstrated a significant relationship between incubation temperature, success in hatching and survival of hatchlings. However, a few studies have tested these relationships in the wild. The objective of this study was to determine the relationship of nest characteristics and environment (hatch year, nest basal area and height, clutch size, distance to shore line, and vegetation cover), to incubation temperature and hatching success among Morelet's crocodile (Crocodylus moreletii). The study was carried out during the nesting seasons of Morelet's crocodile, from 2007 to 2009 in the Laguna de Las Ilusiones, an urban lake located in Villahermosa, Tabasco, Mexico. We physically characterized 18 nests and inserted a temperature data logger in each nest chamber. At the end of the nesting season and prior to hatching, we recovered the crocodile eggs and data loggers and calculated hatching success, under laboratory conditions. We related the environmental variables of the nest with the mean and fluctuation (standard deviation) of nest temperature, using linear models. We also related the environmental variables affecting the nest, to mean nest temperature and fluctuation in incubation temperature and to hatching success, using linear models. Although we found differences in incubation temperature between nests, mean incubation temperature did not differ between years, but there were differences in nest thermal fluctuation between years. The mean incubation temperature for 11 nests (61.1%) was lower than the suggested Female–Male pivotal temperature (producing 50% of each sex) for this species, and all hatchlings obtained were males. There were no differences in clutch size between years, but hatching success varied. Our study indicates that hatching success depends on certain environmental variables and nest conditions to which the eggs are subjected, including season, nest size and clutch size. We also discuss the importance of the fluctuation of incubation temperature on hatching success and sex determination.     

An Intercontinental Analysis of Climate-Driven Body Size Clines in Reptiles: No Support for Patterns, No Signals of Processes

Climatic gradients impose clinal selection on animal ecological and physiological performance, often promoting geographic body size clines. Bergmann’s rule predicts that body size increases with decreasing environmental temperatures given the need to retain body-heat through adjustments of body-mass-to-surface-area ratio. This prediction generally holds for endotherms, but remains controversial for ectotherms. An alternative interpretation, the ‘resource rule’, suggests that food abundance, primary productivity and precipitation (which, unlike temperature, do not necessarily correlate with geography), drive body size clines. We investigate geographic variation in body size within 65 species of lizards and snakes (squamates) based on an intercontinental dataset (6,500+ specimens belonging to 56 Israeli species, and multiple populations of nine Liolaemus species from Argentina and Chile). Bergmann’s rule is only rarely supported by our data (in four species, 6 %), whereas six species (9 %) follow its converse (hence, it is unsupported in 94 % of cases). Similarly, size increases with resource abundance in only 12 species (18 %). Therefore, although neither of the rules is supported, factors suggested by the resource rule are better predictors of body size than temperature. Surprisingly, we show that some measures of the extent of a species’ climatic envelope do not affect the likelihood of it showing a size-climate relationship. We conclude that negative size-temperature associations are an exception rather than a generality among squamates.     

A comparison of methods for incubating zooplankton diapausing eggs from sediment of endorheic pans in the Free State,South Africa

Determining the composition of zooplankton in endorheic pans can be challenging, and live sampling of these microcrustaceans does not give a true indication of their species diversity and abundance. The incubation of zooplankton diapausing eggs can assist in determining their diversity and abundance. In this study the efficacy of two incubation methods – isolation and non-isolation – was tested using samples taken in 2013 from five endorheic pans in the Free State province, South Africa. The non-isolation incubation method made use of distilled water in the hatching experiments, whereas the Onbé–Marcus isolation incubation method, using 1:5 v/v ADAM medium/water, was adapted and applied to samples to isolate the diapausing eggs. The isolation method provided hatchlings at a higher rate than that of the non-isolation method, but subsequent removal and identification of the hatchlings was challenging. In particular, the success of the isolation method was putatively related to sediment grain size composition. Some difficulties were also noted in using the non-isolation method in the hatching and growing of anostracans.