The heterozygote superiority hypothesis for polymorphic color vision is not supported by long-term fitness data from wild neotropical monkeys.

The leading explanatory model for the widespread occurrence of color vision polymorphism in Neotropical primates is the heterozygote superiority hypothesis, which postulates that trichromatic individuals have a fitness advantage over other phenotypes because redgreen chromatic discrimination is useful for foraging, social signaling, or predator detection. Alternative explanatory models predict that dichromatic and trichromatic phenotypes are each suited to distinct tasks. To conclusively evaluate these models, one must determine whether proposed visual advantages translate into differential fitness of trichromatic and dichromatic individuals. We tested whether color vision phenotype is a significant predictor of female fitness in a population of wild capuchins, using longterm 26 years survival and fertility data. We found no advantage to trichromats over dichromats for three fitness measures fertility rates, offspring survival and maternal survival. This finding suggests that a selective mechanism other than heterozygote advantage is operating to maintain the color vision polymorphism. We propose that attention be directed to field testing the alternative mechanisms of balancing selection proposed to explain opsin polymorphism nichedivergence, frequencydependence and mutual benefit of association. This is the first indepth, longterm study examining the effects of color vision variation on survival and reproductive success in a naturallyoccurring population of primates.

Neutral indirect effects of mycorrhizal fungi on a specialist insect herbivore.

Arbuscular mycorrhizal (AM) fungi can indirectly affect insect herbivore performance by altering traits in their host plant. Typically, generalist herbivores are negatively affected by AM fungi, whereas specialists are positively affected. This is thought to be caused by differential abilities of specialists and generalists to tolerate and/or exploit plant secondary compounds, the prevalence of which may be related to mycorrhizal colonization. We performed a feeding experiment in which specialist sunflower beetle larvae (Zygogramma exclamationis Fabricius, Chrysomelidae) were fed on mycorrhizal or nonmycorrhizal common annual sunflower plants (Helianthus annuus L., Asteraceae). To determine the indirect effects of AM fungi on the sunflower beetle larvae, we measured insect survival and relative growth rate. We also measured leaf area eaten, which allowed relative growth rate to be broken down into two components: relative consumption rate and efficiency of conversion of ingested food. Contrary to several previous studies, we detected no indirect effects of mycorrhizal fungi on larval survival or on relative growth rate or its components. Small effect sizes suggest that this is nonsignificant biologically, as well as statistically, rather than merely an issue of statistical power. Our results support an emerging view that indirect effects of mycorrhizal fungi on insect herbivores may be complex and idiosyncratic. We suggest that future research should emphasize the effects of mycorrhizal fungi on individual plant traits and how these interact to affect insect performance.

Look before leaping: foraging selectivity of capuchin monkeys on acacia trees in Costa Rica.

Acacia trees in Costa Rica have an obligate mutualism with three species of Pseudomyrmex ants, which vigorously defend their host tree from insect and mammalian herbivores. Depending on the size and species of ant colony, individual acacia trees may be differentially protected. For animals able to discern between weakly and highly aggressive ant colonies, costs of ant stings from less active colonies might be offset by nutritional value acquired from feeding on acacia fruit or ant larvae in swollen thorns. We examined foraging selectivity of capuchin monkeys on acacia trees in Santa Rosa National Park, Costa Rica. We measured four characteristics of the acacia trees from which capuchins fed and of acacias immediately adjacent to those in which the monkeys fed: diameter at breast height (DBH), accessibility, species of closest tree and ant species present. We found that capuchins prefer to forage in acacias that are large and accessible. We also made two measurements of ant colony activity on each tree, one before and one after disturbing the ant colony. We found that the three species of mutualistic ants differ in baseline activity levels and that mutualistic ants are more active than non-mutualistic ant species found in acacia trees. We also found that capuchins foraged more frequently in trees colonized by non-mutualistic ants, but the explanatory value (r (2)) of this model was low. Furthermore, monkeys did not discriminate between acacias on the basis of baseline ant activity or the ant colony's response to disturbance. We conclude that these monkeys select acacia trees in which to forage based on characteristics of the trees rather than the ants. In addition, our study suggests that white-faced capuchins act as predators on the acacia ants but they probably benefit the dispersal and reproductive success of acacia trees. Capuchins may in fact function as an additional mutualistic partner for acacia trees via seed dispersal, but they must overcome the ants' defense of the trees to do so.

Arbuscular mycorrhizal fungi reduce the construction of extrafloral nectaries in Vicia faba.

Arbuscular mycorrhizal fungi (AMF) can alter the physiology and morphology of their host plant, and therefore may have indirect effects on insect herbivores and pollinators. We conducted this study to test the hypothesis that AMF can also affect insects involved in protection-for-food mutualisms. We examined the constitutive and inducible production of food rewards [extrafloral (EF) nectaries] in Vicia faba plants by manipulating the presence/absence of AMF and by simulating various levels of herbivory. Plants inoculated with AMF produced significantly fewer EF nectaries than uninoculated plants, even after accounting for differences in plant growth. In contrast to earlier studies, EF nectaries were not inducible: damaged plants produced significantly fewer EF nectaries than undamaged plants. Moreover, the effects of mycorrhizal and damage status on EF nectary production were additive. The reduction in EF nectaries in mycorrhizal plants potentially represents a mechanism for indirect effects of AMF on the protective insects that exploit EF nectaries as a food source (e.g., ants). Reduced reward size should result in reduced protection by ants, and could therefore be a previously unappreciated cost of the mycorrhizal symbiosis to host plants. However, the overall effect of AMF will depend upon the extent to which the reduction of EF nectaries affects the number and activity of ants and the extent to which AMF alter other aspects of host plant physiology. Our results emphasize the complexity of multitrophic interactions, particularly those that span belowground and aboveground ecology.

Predator-induced transgenerational phenotypic plasticity in the cotton aphid.

Transgenerational phenotypic changes, whereby offspring have an altered trait or a distinct alternate phenotype, frequently occur in response to increased maternal predation risk. The cotton aphid, Aphis gossypii (Glover), is unique, however, as offspring consist of four distinct phenotypes ("normal" light green apterae, "normal" dark green apterae, "dwarf" yellow apterae, and alatae), all with divergent life history patterns and resulting population dynamics. Here, we show that increased predation risk induces transgenerational phenotypic changes in cotton aphids. When exposed to search tracks from larval or adult convergent ladybird beetles, Hippodamia convergens Guerin-Meneville, cotton aphids produced greater numbers of winged offspring. In a subsequent experiment, apterous and alate individuals on clean plants were found to have primarily normal and dwarf offspring, respectively. We suggest that elevated predation risk may cause phenotypic changes in aphids over multiple generations, resulting in a more precipitous decline in herbivore populations than could be explained solely by increased predation rates.

Variation in the costs and benefits of mutualism: the interaction between yuccas and yucca moths.

Yucca moths are both obligate pollinators and obligate seed predators of yuccas. I measured the costs and net benefits per fruit arising for eight species of yuccas from their interaction with the yucca moth Tegeticula yuccasella. Yucca moths decrease the production of viable seeds as a result of oviposition by adults and feeding by larvae. Oviposition through the ovary wall caused 2.3-28.6% of ovules per locule to fail to develop, leaving fruit with constrictions, and overall, 0.6-6.6% of ovules per fruit were lost to oviposition by yucca moths. Individual yucca moth larvae ate 18.0-43.6% of the ovules in a locule. However, because of the number of larvae per fruit and the proportion of viable seeds, yucca moth larvae consumed only 0.0-13.6% of potentially viable ovules per fruit. Given both oviposition and feeding effects, yucca moths decreased viable seed production by 0.6-19.5%. The ratio of costs to (gross) benefits varied from 0% to 30%, indicating that up to 30% of the benefits available to yuccas are subsequently lost to yucca moths. The costs are both lower and more variable than in a similar pollinator-seed predator mutualism involving figs and fig wasps.There were differences between species of yuccas in the costs of associating with yucca moths. Yuccas with baccate fruit experienced lower costs than species with capsular fruit. There were also differences in costs between populations within species and high variation in costs between fruit within populations. High variability was the result of no yucca moth larvae being present in over 50% of the fruit in some populations, while other fruit produced up to 24 larvae. I present hypotheses explaining both the absence and high numbers of larvae per fruit.

Stability properties of 2-species models of mutualism: Simulation studies.

Most previous analyses of the stability properties of models of mutualism have emphasized the destabilizing effects of mutualism. However, these analyses can be shown to be based upon inappropriate assumptions, or to be applicable only for special cases of mutualism. In this paper three basic 2-species models of mutualism are presented and their six combinations are analyzed by computer simulation for their return time stability and persistence stability. Four out of six models show greater return time stability than an appropriate model without mutualism, and all models show higher persistence stability than the model without mutualism. It is argued that real biological systems can be related to the qualitative structure of each of the basic models of mutualism, and that therefore none of the basic models or their stability properties can be eliminated a priori as being inappropriate. The conclusion follows that while some kinds of mutualistic interactions may be relatively unstable, other mutualisms, probably representing the majority of cases, can be considered to be relatively stable. The limitations of these models and analyses are considered.