Clutch size versus clutch interval: life history strategies in the colour-polymorphic pygmy grasshopper Tetrix subulata

Theory posits that reproduction carries a cost in terms either of future fecundity, growth or survival. Different life history strategies may evolve in response to different external sources of mortality. In ectothermic organisms, such as insects and reptiles, reproductive characteristics may also vary due to effects of differences in body temperature on activity and physiological performance. In this study, female pygmy grasshoppers [Tetrix subulata (L.) Orthoptera: Tetrigidae] belonging to four different colour morphs were maintained under two different temperatures, and data on reproductive life history traits were used to test for costs of reproduction, plasticity of reproductive characteristics in response to temperature and variation among colour morphs in reproductive strategies. The results revealed that average clutch size decreased progressively from the first to third clutch, and that females producing relatively large clutches displayed a greater reduction (in both absolute and relative terms) in the number of eggs to the following clutch, as expected from the hypothesis that present reproduction negatively affects future fecundity. Great expenditure on present reproduction also negatively influenced the time to next clutch:the decrease in mean clutch size with clutch number was associated with a reduction in inter-clutch interval, and clutch interval increased with clutch size across individuals within colour morphs. Females maintained in a warm environment were more likely to oviposit, laid their first clutch earlier, produced more clutches and had shorter intervals between sequential clutchesthan females in a cold environment, suggesting that differences in body temperature may contribute to variation in reproductive performance within and among natural populations. A comparison among colour morphs maintained under identical conditions suggested that females belonging to certain morphs produce relatively large clutches at the expense of fewer clutches per unit time. However, experimental data revealed no difference in relative fat content between dark and pale individuals maintained either in sun-exposed outdoor enclosures (where they were unable to increase their body temperature by basking) or in shaded enclosures. This suggest that the divergence in life history strategies among colour morphs may reflect a response to morph-specific differences in adult survival imposed by visually searching predators, rather than being due to the effects of differences in body temperature.     

Activity and weight loss in relation to solar radiation in the polymorphic land snail Cepaea nemoralis

Shell spectral reflectance, activity and weight loss in the land snail Cepaea nemoralis were examined to test whether solar radiation has different effects on the behavioural and physiological responses of different morphs. A uniform area from the empty shells of different morphs was cut and a spectrophotometer was used to measure the spectral reflectance at wavelengths from 220 nm to 800 nm. Snails were put into cages made of mesh hardware cloth, and their activities were observed from dawn onwards on two hot, dry days. Weight loss of snails under shade and under direct sunlight was also measured.
The results show that unbanded morphs reflect more light than five-banded ones, but the yellow morphs reflect only a little more than pink morphs. Five-banded morphs became inactive more quickly than unbanded ones from dawn onwards, but the differences in activity patterns were not significant between pink and yellow morphs. There are significant differences in percent weight loss between snails placed under direct sunlight and under shade. The weight loss of different morphs under shade was not statistically different. But when exposed to sunlight, five-banded morphs lost more weight than pink and yellow unbanded morphs.
Because of their lower reflectance of solar radiation, the five-banded morphs are, in a hot, arid climate, at a selective disadvantage compared to unbanded morphs. However, they can avoid such selective disadvantage by actively seeking a shaded area, as all other morphs do in the field. Such behavioural habitat selection could help the maintenance of genetic polymorphisms in natural populations.     

Colour polymorphism and thermal capacities in Theba pisana (O.F. Müller 1774)

Several land snail species are highly polymorphic regarding their shell colouration. This polymorphism has been related to predatory effects as well as climatic reasons, assuming that dark morphs benefit from being more cryptic and therefore less prone to predation, whereas pale morphs are at an advantage under solar radiation, as they are suspected to heat up less. However, the assumption of different thermal capacities of these morphs is based on experiments with little standardisation or little environmental relevance. In this study, we aimed at measuring thermal capacities of two different morphs (pale versus dark-brown banded) of the Mediterranean land snail Theba pisana, applying a standardised and environmentally relevant test set-up, in order to prove whether darker morphs indeed do heat up more than lighter coloured morphs. We did not find any differences in the thermal capacity of the different morphs and conclude that thermal capacity of the shell is predominantly defined by its material rather than its coloration. These results are discussed with regard to previous studies on thermal characteristics of different land snail morphs and correlations between climate and morph distribution.     

Humidity and seasonality drives body size patterns in males of the bush cricket Isophya rizeensis Sevgili, 2003 （Orthoptera： Tettigoniidae： Phaneropterinae）

Two primary patterns of body size variation have been recorded in ectotherms in relation to latitudinal/altitudinal shifts. In some, body size increases with increasing latitude/altitude whereas, in others, body size decreases with increasing latitude/altitude. This clinal variation is generally assumed to be caused by local adaptation to environmental conditions however the selective variable（s） （temperature, humidity, diet quality, etc.） is still heavily debated. Here we investigate geographic variation in body size of dark and pale color morphs of males of the bush-cricket lsophya rizeensis collected from 15 locations along an elevation gradient ranging from 350 to 2 500 m. Using an information theoretical approach we evaluate the relative support of four different hypotheses （the temperature size rule, the moisture gradient hypothesis, the seasonal constraint hypothesis, and the primary productivity hypothesis） explaining body size variation along the altitudinal gradient. Body size variation in pale color morphs showed a curvilinear relationship with altitude while dark color morphs showed no variation in body size. Body size variation in pale color morphs was highly correlated with precipitation and temperature seasonality values thus giving strong support for the moisture gradient and seasonal constraint hypothesis. Our results reinforce the importance of gradients in humidity and seasonality over temperature in the creation of altitudinal body size clines and the role of selection for resistance to stress factors in the establishment of these clines. Whether a body size cline is observed or not might also depend on the phenotypic properties of the individuals, like coloration.     

Heating properties of morphs of the mangrove snail Littoraria pallescens

The rate of heating and the temperature attained after 10 and 20 min have been examined for shells of the yellow, dark and orange morphs of the mangrove leaf snail Littoraria pallescens. Under the experimental conditions used, heating from 20 to 40C took 5–10 min and thereafter the temperature remained roughly constant for up to 20 min. This represents temperature conditions which the animals are likely to experience in the wild. Large shells heat more slowly than small ones and reach lower temperatures. At around 40C yellows are on average 1.5C cooler than the dark morph, and orange individuals lie between. This difference could account for the observed difference between morphs in their choice of preferred leaf surface. Besides differing in colour, yellows are thinner and less heavy than dark shells, which probably contributes to the fact that they arc less robust.     

Perch color preference in juvenile green tree pythons,Chondropython viridis

Green tree pythons, Chondropython viridis, are polymorphic for color as juveniles, commonly being primarily yellow or brown until becoming mostly green at about 1 year of age. We tested the hypothesis that the different morphs arose as a result of selection for differential background matching, yellow morphs selecting light-colored backgrounds, and brown morphs selecting dark-colored backgrounds. Twelve yellow and eight brown morphs were placed repeatedly in individual testing enclosures and allowed to choose between black and white or yellow and brown halves of a t-perch. Trials showed that both color morphs preferred dark over light perches. We tentatively suggest that individuals chose dark-colored perches for purposes of concealment. © 1994 Wiley-Liss, Inc.     

An experimental study of the multiple effects of brown trout Salmo trutta on the bioenergetics of two Arctic charr Salvelinus alpinus morphs

This study investigated the importance of competition with brown trout Salmo trutta as a driver of the morphological and behavioural divergence of two morphs of Arctic charr Salvelinus alpinus. The morphs originated from two lakes differing in absence or presence of the competitor. The bioenergetics and behaviour of S. alpinus were quantified in replicate experimental enclosures (mean volume: 150 m(3) ) stocked with 15 S. alpinus of one morph or the other and in the absence or presence of nine S. trutta. The presence of S. trutta decreased growth rate, affected food consumption and increased activity costs in S. alpinus, but provided little support for the hypothesis that competition with S. trutta is a major driver of the divergence of the two S. alpinus morphs. Both morphs responded similarly in terms of mean growth and consumption rates per enclosure, but the association between individual morphology and growth rate reversed between allopatric and sympatric enclosures. While the activity patterns of the two morphs were unaffected by the presence of S. trutta, their swimming speed and activity rate differed. Since the profound differences in the structure of the physical habitat of the source lakes provided a more likely explanation for the difference observed among these two morphs than interspecific competition, it is hypothesized that physical habitat may sometimes be a significant driving force of the phenotypic divergence.     

Brown tawny owls moult more flight feathers than grey ones

The mechanisms by which melanin‐based colour polymorphism can evolve and be maintained in wild populations are poorly known. Theory predicts that colour morphs have differential sensitivity to environmental conditions. Recently it has been proposed that colour polymorphism covaries genetically with intrinsic and behavioural properties. Plumage moult is a costly and crucial somatic maintenance function in birds. We used a long‐term data set consisting of 761 observations on 307 individuals captured between 1985 and 2010 to examine differences in partial flight feather moult between grey (pale) and brown (pheomelanic dark) colour morphs of the tawny owl. We find that the brown morph consistently moult more primary flight feathers than the grey morph whereas there is no clear difference between colour morphs in the moulting of secondary feathers. Contrary to expectations, the difference in the number of moulted flight feathers between the morphs was independent of environmental conditions, as quantified by the abundance of prey. We discuss the potential physiological and behavioural causes for and costs of the observed difference in maintenance functions between colour morphs.     

Coevolution of color pattern and thermoregulatory behavior in polymorphic pygmy grasshoppers Tetrix undulata

Ectothermic organisms, such as insects and reptiles, rely on external heat sources to control body temperature and possess physiological and behavioral traits that are temperature dependent. It has therefore been hypothesised that differences in body temperature resulting from phenotypic properties, such as color pattern, may translate into selection against thermally inferior phenotypes. We tested for costs and benefits of pale versus dark coloration by comparing the behaviors (i.e., basking duration and bouts) of pygmy grasshopper (Tetrix undulata) individuals exposed to experimental situations imposing a trade-off between temperature regulation and feeding. We used pairs consisting of two full-siblings of the same sex that represented different (genetically coded) color morphs but had shared identical conditions from the time of fertilization. Our results revealed significant differences in behavioral thermoregulation between dark and pale individuals in females, but not in males. Pale females spent more time feeding than dark females, regardless of whether feeding was associated with a risk of either hypothermia or overheating. In contrast, only minor differences in behavior (if any) were evident between individuals that belonged to the same color morph but had been painted black or gray to increase and decrease their heating rates. This suggests that the behavioral differences between individuals belonging to different color morphs are genetically determined, rather than simply reflecting a response to different heating rates. To test for effects of acclimation on behaviors, we used pairs of individuals that had been reared from hatchlings to adults under controlled conditions in either low or high temperature. The thermal regime experienced during rearing had little effect on behaviors during the experiments reported above, but significantly influenced the body temperatures selected in a laboratory thermal gradient. In females (but not in males) preferred body temperature also varied among individuals born to mothers belonging to different color morphs, suggesting that a genetic correlation exists between color pattern and temperature preferences. Collectively, these findings, at least in females, are consistent with the hypothesis of multiple-trait coevolution and suggest that the different color morphs represent alternative evolutionary strategies.     

Shell-banding polymorphism of the land snail Xeropicta vestalis along the coastal plain of Israel

Along the coastal plain of Israel, shell darkness of the polymorphic land snail Xeropicta vestalis is positively related to the extent of perennial vegetation. It is not related to rain, temperature, geographic position or darkness of the ground.
White shells reflect more radiation than dark ones do, and therefore in Israel's coastal plain, where solar radiation is very strong, they are favoured. Perennial vegetation, where it occurs, shields the snails from the sun by absorbing radiation, so that snails amongst them can afford to be darker, and thus more cryptic. Hence, the more perennial vegetation in the habitat, the darker the shells.
Also during the Pleistocene, when temperatures were 5–10°C lower than today, the shells of the coastal plain were as pale as recent ones are. The distribution of a snail-predator, Gerbillus allenbyi , which is restricted to sandy biotopes where perennial bushes occur, and which was absent from Israel during the Pleistocene, could perhaps explain the distribution of X. vestalis morphs, both today and in the past.     

Polymorphic snails on varied backgrounds

The general matching of shell colours to background colours seen in terrestrial gastropods implies that, as in insects, visual predation is an important factor which has a long term directional effect. Polymorphism in snails is associated with background heterogeneity, but the causal relation of polymorphism to heterogeneity is not obvious. Predation could maintain polymorphism if predators are frequency dependent in their choice of prey. However, the appropriate predator behaviour does not depend directly on background heterogeneity. An indirect contribution could be that the heterogeneity serves to lower the signal:noise ratio during the predation process. Background heterogeneity could have a direct effect if the background provided specific elements mimicked by the morphs. The remaining diversity could aid the process by lowering the signal:noise ratio. Polymorphism could be maintained if there was frequency-dependent niche selection on the part of prey. Background diversity would then be directly involved. It is necessary that there should be independent control of numbers in the different niches. In warm conditions the niche selection could come about because darker morphs, which gain more radiant heat than paler ones, will move to more cryptic sites by seeking the shade. For morph frequences to approach equilibrium values closely it is necessary for the alleles controlling the polymorphism to exhibit dominance. Differences in received energy could make pale morphs disadvantageous compared with dark ones at low temperatures but advantageous at high ones. In spatially varied temperature conditions a polymorphism could be generated without predation. Density-dependent selection is again required.     

Daily flight activity of the western flower thrips (Thysan., Thripidae) in nectarine orchards in British Columbia, Canada

Abstract:   Hourly flight patterns of western flower thrips, Frankliniella occidentalis (Pergande) (Thysan., Thripidae) were assessed over a 24 h period in two nectarine orchards located in the Similkameen Valley, British Columbia, on 13 separate occasions between March and October 1994. The numbers of western flower thrips (male or female, dark or pale morphs) trapped per hour at between four to eight heights (0.25–2.00 m) were compared with temperature, wind speed, time of year and location of trap placement. Traps were placed within orchards, at the border of orchards and adjacent wild land, and within wildlands. Temperature and wind speed thresholds are defined, although the effect of wind speed varied with height of flight. Height of flight was affected by both the height of prevalent vegetation and temperature, with mean height of flight increasing linearly with temperature. Numbers of thrips in flight decreased with height of sticky trap from the ground. The pale morph was generally more common than the dark morph of western flower thrips. Males were not present until after emergence of the first generation in May, and were found at an approximate ratio of 4 : 1 (F : M) for the rest of the year. There were no differences between sexes or morphs of western flower thrips for location, height or daily patterns of flight.     

Genetic divergence between sympatric Arctic charr Salvelinus alpinus morphs in Gander Lake,Newfoundland: roles of migration,mutation and unequal effective population sizes

A suite of 10 microsatellite loci was used to examine genetic divergence between two sympatric morphs of Arctic charr Salvelinus alpinus (‘dark’ and ‘pale’) inhabiting Gander Lake, Newfoundland. Results can be summarized as follows: (1) the morphs are strongly reproductively isolated – gene flow–migration estimates were consistently low in long and short‐term evolutionary timescales of analysis; (2) intermorph divergence based on allele size (R_ST) was significantly larger than those based on allele state (θ) implying a cumulative effect of stepwise‐like mutations; (3) historical (coalescent) and current (linkage disequilibrium) point estimates of effective population size (N_e) were consistently higher for dark than for pale S. alpinus. The first and second findings lend support to the hypothesis that divergence between forms may have preceded the last glacial period (ending c. 12 000 years bp ). The third finding argues for significant differences in habitat quantity and quality between morphs, which were emphasized in a previous study. Overall, these analyses underscore the importance of genetic assessment and monitoring in the conservation of fish diversity, with emphasis on ‘rare’ or under‐represented forms among temperate species pairs.     

Effect of the enclosure on carriers' body weight loss in the cotton-top tamarin (Saguinus oedipus)

Infant carrying in cotton-top tamarins is a costly activity that results in weight loss by the fathers and helpers. However, to date, measures of carrying costs have been obtained in small indoor enclosures. We studied body weight changes in adult and subadult individuals from eight large groups (n > 5) for 9 weeks after the birth of infants. Four groups were housed in large indoor/outdoor enclosures (42 m(2) x 3.3 m high), and four were housed in small indoor enclosures (12 m(2) x 2.4 m high). All of the individuals were weighed regularly at least three times a week. Reproductive males lost more weight in the big indoor/outdoor enclosures (mean=6.51%) than in the small indoor ones, as did male adult helpers (mean=5.59%) and female adult helpers (mean=4.4%). Still-growing subadult individuals also lost weight in the big indoor/outdoor enclosures (mean=3.17%), although the differences did not reach significance (P=0.07). These results support the hypothesis that cotton-top tamarins living in more natural settings experience higher weight loss than those housed under less-natural conditions.     

Salamander predation and vertical distributions of zooplankton

SUMMARY. 1. The impact of different predation regimes of zooplanktivorous larval tiger salamanders, Ambystoma tigrinum nebulosum , on the vertical temporal distributions of Daphnia pulex, Diaptomus nudus and larval Chaoborus flavicans was studied in limnetic enclosures in a pond in east-central Arizona. Zooplankton densities were monitored 1-2 h before sunset, at sunset, and 1-2 h after sunset at three depths (0-0.4, 1.0 and 2.0 m) in four salamander treatments (0, 20, 40 salamanders per enclosure, and unenclosed limnetic areas).
2. Densities and body size of Daphnia pulex were consistently greater in salamander-free enclosures than in other treatments. More Daphnia were generally nearer the surface (0-1.0 m) than along the bottom before and at sunset than after sunset in enclosures without salamanders. After sunset, Daphnia was by far most dense along the bottom. Densities were uniform among depths and sample times in treatments with salamanders. Salamanders moved throughout the water column. Frequencies of D. pulex spined morphs (with prominent dorsal crest) did not differ among salamander treatments.
3. Chaoborus densities were positively correlated with D. pulex distributions among depths and sample times in treatments. Spatio-temporal distributions of Chaoborus were influenced more by their daphnid prey than by risk of predation from larval salamanders.
4. Densities of Diaptomus nudus were highest in open water controls and lowest in enclosures without salamanders. Diaptomus was generally more dense between 0 and 1 m than at 2.0 m depths in all treatments, and vertical distributions were not dependent on salamander density.     

Pale and dark dichromatism related to microhabitats in a herbivorous tanganyikan cichlid fish,Telmatochromis temporalis

Dichromatism and habitat utilization of a small herbivorous cichlid fish,Telmatochromis temporalis, were studied in a littoral rocky area of Lake Tanganyika. Individuals of both sexes had either pale or dark body coloration that did not change for long periods. Both sexes defended territories from consexuals, and a male had a harem of several females. Pale fish had territories in exposed areas and dark fish in shaded ones. Larger fish were dominant over smaller consexuals and occupied well-illuminated areas. When pale and dark fish were kept in areas with shaded and lighted backgrounds, respectively, they changed body colour within a few weeks. When pale fish were in well-illuminated areas and dark ones in shaded areas, they were cryptic. BecauseTelmatochromis temporalis are very vulnerable prey in coastal areas, dichromatism may function as antipredator camouflage.     

Tests of hypotheses on predation as a factor maintaining polymorphic melanism in coastalplain fox squirrels (Sciurus niger L.)

Fox squirrels ( Sciurus niger ) in the south-eastern U.S. coastal plain differ from those in the rest of the species' range by having black heads with white nose and ears. Postcranially on the dorsum, they also show interindividual colour variation, ranging from all-light agouti to all-black non-agouti. I present results of experiments undertaken to test whether the evolution of these pigmentary features can be attributed to interactions with predators. Comparative static crypsis (when the squirrels are still) was tested by determining how well specimens of the squirrel morphs matched their backgrounds in terms of intensity (brightness) distributions and patch size. Comparative dynamic effects (when the squirrels are moving) were tested using captive red-tailed hawks ( Buteo jamaicensis ) and models of the fox squirrel morphs. Results indicated that morphs of coastal-plain fox squirrels with all-light backs are better static matches to unburned backgrounds than are the darker morphs with which they coexist. Against fire-blackened backgrounds, fox squirrel morphs with intermediate and all-black backs are better intensity matches than those with all-light backs, but the dark morphs are not better patch-length matches than light morphs. The superiority of dark morphs in intensity matching for a short time after a fire does not seem sufficient to account for their long-term maintenance. Hawks responded more slowly to moving fox squirrel models with intermediate amounts of black on the back than to all-light or all-dark morphs; this result suggests a possible factor that would favour retention of genes for dorsal blackness in the coastal-plain population. Patchy black and white heads appear to promote static crypsis of south-eastern fox squirrels, and hawks reacted more slowly to moving squirrel models with such colouration than to those with plain heads.     

Immune defence,a possible nonvisual selective factor behind the industrial melanism of moths (Lepidoptera)

It is generally believed that industrial melanism in Lepidoptera is mainly caused by differential predation by birds. In polluted areas, melanic individuals are favoured by natural selection because they are better camouflaged than pale moths on lichen‐free and sooty tree trunks. In this article, we show that, in the black arches moth (Lymantria monacha), melanic morphs have a stronger encapsulation response than pale morphs against nylon monofilament implants. This indicates that the melanic and pale morphs differ in the strength of their immune defence. The same chemical precursors and their end product, melanin pigment, are involved in the encapsulation response and in the external coloration. Thus, it seems that there may be two possible, not mutually exclusive, explanations for the frequency changes observed in the industrial melanism of moths. The dominant gene causes an increase in the amount of melanin pigment and its precursors. This increase causes two changes: an intensified immune defence as a form of improved encapsulation ability of foreign objects, and the well‐known protective dark coloration (a case of relational pleiotropy). It seems possible that industrial melanism is a by‐product of selection on the strength of immunity. In the field, these pleiotropic aspects are exceedingly difficult to distinguish from each other, and the factors may even be compensatory. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99 , 831–838.     

Pollination and reproductive success of two colour variants of a deceptive orchid, Dactylorhiza maculata (Orchidaceae)

Polymorphism in petal colour is common in deceptively pollinated plant species. Most of the deceptively pollinated orchids are food frauds, and in most of them, the deception is not mimetic. These plants have conspicuously coloured flowers which they use as the main attractant of naive pollinators. In a field experiment, we studied the response of bumblebees and other types of flower visitors to colour differences between experimentally paired plants of Dactylorhiza maculata , a nectarless food-deceptive species. In addition, pollen removal, an estimate of male fitness, and fruit production, an estimate of female fitness, were measured in the two colour variants. We found a trend of bumblebee preference for the dark-coloured flowers, but other flower visitors (as a group) showed no preference for any colour variant. No difference was found in the reproductive success between the two colour variants of D. maculata. The lack of a difference in reproductive success between plants with pale and dark inflorescences, despite the observed trend of bumblebee preference for dark inflorescences, suggests that there is some balancing factor in the pollination of the pale inflorescences. An excess of visits by some nocturnal species (or a group of species) which favours the pale colour of D. maculata inflorescences or an excess of visits during day time by some flower visitors other than bumblebees preferring the pale inflorescences over dark ones may form such a balancing factor.     

Melanin‐based colour polymorphism responding to climate change

Climate warming leads to a decrease in biodiversity. Organisms can deal with the new prevailing environmental conditions by one of two main routes, namely evolving new genetic adaptations or through phenotypic plasticity to modify behaviour and physiology. Melanin‐based colouration has important functions in animals including a role in camouflage and thermoregulation, protection against UV‐radiation and pathogens and, furthermore, genes involved in melanogenesis can pleiotropically regulate behaviour and physiology. In this article, I review the current evidence that differently coloured individuals are differentially sensitive to climate change. Predicting which of dark or pale colour variants (or morphs) will be more penalized by climate change will depend on the adaptive function of melanism in each species as well as how the degree of colouration covaries with behaviour and physiology. For instance, because climate change leads to a rise in temperature and UV‐radiation and dark colouration plays a role in UV‐protection, dark individuals may be less affected from global warming, if this phenomenon implies more solar radiation particularly in habitats of pale individuals. In contrast, as desertification increases, pale colouration may expand in those regions, whereas dark colourations may expand in regions where humidity is predicted to increase. Dark colouration may be also indirectly selected by climate warming because genes involved in the production of melanin pigments confer resistance to a number of stressful factors including those associated with climate warming. Furthermore, darker melanic individuals are commonly more aggressive than paler conspecifics, and hence they may better cope with competitive interactions due to invading species that expand their range in northern latitudes and at higher altitudes. To conclude, melanin may be a major component involved in adaptation to climate warming, and hence in animal populations melanin‐based colouration is likely to change as an evolutionary or plastic response to climate warming.