Phylogenetic Analysis of the Socioecology of Neotomine-Peromyscine Rodents

This chapter focuses on the breeding systems of Neotomine-Peromyscine rodents. There are three specific objectives to this chapter. First, we describe the patterns for major Neotomine-Peromyscine clades using data collected from the literature (table 6.1). Second, we examine data from the literature on the following breeding behaviors: male spacing, female spacing, relative intersexual home range/territory size, paternal care, and juvenile dispersal patterns. We examine breeding behavior data in a phylogenetic framework to test if any phylogenetic patterns emerge in the observed variation in these breeding behaviors and if relationships occur among these behaviors. Third, we examine in a phylogenetic framework whether dietary, physiological, or life-history characteristics of the taxa are able to explain the observed variation in these breeding behaviors

Alternative reproductive tactics in females: the case of size polymorphism in ant queens

Alternative reproductive tactics are common in males but rather rare in females. In this respect, ants are apparently an interesting exception. Ant queens can either start a new colony on their own or utilize the work force of existing colonies for dependent colony founding. As the success of these different options depends on body reserves of the queens, the finding of two different classes of alate queens in some ant species that differ only in size strongly suggests alternative modes of reproduction. Studies of queen size polymorphism from a number of ant species differ in scope and also in their results. Nevertheless, across taxa evidence exists that small queens found dependently while their larger conspecifics found colonies on their own. However, in most cases it is not clear whether the small queens exploit unrelated colonies (intraspecific “social parasitism”) or return to their natal colonies. In some ant species the queen size polymorphism might constitute an evolutionary transition to either interspecific social parasitism or a mor-phologically more pronounced queen polymorphism linked to dispersal. In others, queen size polymorphism might be a stable phenomenon. Although it is important in this context whether queen size polymorphism is caused by a genetic polymorphism or phenotypic plasticity, so far no conclusive evidence about proximate mechanisms of size determination has been presented. Some considerations are made about the question why female alternative reproductive tactics correlated with morphological adaptations are comparatively widespread in ants

A female caste specialized for the production of unfertilized eggs in the ant Crematogaster smithi

In colonies of the North American ant Crematogaster smithi “large workers” occur which are morphologically intermediate between winged queens and small workers and appear to be specialized for the production of unfertilized eggs. In queenless colonies these eggs may develop into males, but most of them are eaten in colonies containing a queen. We discuss the possible significance of this new type of female

A new type of exocrine gland and its function in mass recruitment in the ant Cylindromyrmex whymperi (Formicidae: Cerapachinae)

Workers of the ant Cylindromyrmex whymperi display mass trail recruitment. Bioassays show that the trail pheromone originates from a unique gland between abdominal sternites 6 and 7. The gland has a hitherto unknown structural organization. Upon leaving the secretory cell, the duct cell widens to form a sclerotized pear-shaped reservoir chamber, lined with multiple duct cells. Each duct thus forms a miniature reservoir for the secretions of each single secretory cell, a novel structural arrangement in exocrine glands of social Hymenoptera

Support for the reproductive ground plan hypothesis of social evolution and major QTL for ovary traits of Africanized worker honey bees (Apis mellifera L.)

Background The reproductive ground plan hypothesis of social evolution suggests that reproductive controls of a solitary ancestor have been co-opted during social evolution, facilitating the division of labor among social insect workers. Despite substantial empirical support, the generality of this hypothesis is not universally accepted. Thus, we investigated the prediction of particular genes with pleiotropic effects on ovarian traits and social behavior in worker honey bees as a stringent test of the reproductive ground plan hypothesis. We complemented these tests with a comprehensive genome scan for additional quantitative trait loci (QTL) to gain a better understanding of the genetic architecture of the ovary size of honey bee workers, a morphological trait that is significant for understanding social insect caste evolution and general insect biology. Results Back-crossing hybrid European x Africanized honey bee queens to the Africanized parent colony generated two study populations with extraordinarily large worker ovaries. Despite the transgressive ovary phenotypes, several previously mapped QTL for social foraging behavior demonstrated ovary size effects, confirming the prediction of pleiotropic genetic effects on reproductive traits and social behavior. One major QTL for ovary size was detected in each backcross, along with several smaller effects and two QTL for ovary asymmetry. One of the main ovary size QTL coincided with a major QTL for ovary activation, explaining 3/4 of the phenotypic variance, although no simple positive correlation between ovary size and activation was observed. Conclusions Our results provide strong support for the reproductive ground plan hypothesis of evolution in study populations that are independent of the genetic stocks that originally led to the formulation of this hypothesis. As predicted, worker ovary size is genetically linked to multiple correlated traits of the complex division of labor in worker honey bees, known as the pollen hoarding syndrome. The genetic architecture of worker ovary size presumably consists of a combination of trait-specific loci and general regulators that affect the whole behavioral syndrome and may even play a role in caste determination. Several promising candidate genes in the QTL intervals await further study to clarify their potential role in social insect evolution and the regulation of insect fertility in general

Differences in Ultrasonic Vocalizations between Wild and Laboratory California Mice (Peromyscus californicus)

BACKGROUND: Ultrasonic vocalizations (USVs) emitted by muroid rodents, including laboratory mice and rats, are used as phenotypic markers in behavioral assays and biomedical research. Interpretation of these USVs depends on understanding the significance of USV production by rodents in the wild. However, there has never been a study of muroid rodent ultrasound function in the wild and comparisons of USVs produced by wild and laboratory rodents are lacking to date. Here, we report the first comparison of wild and captive rodent USVs recorded from the same species, Peromyscus californicus. METHODOLOGY AND PRINCIPAL FINDINGS: We used standard ultrasound recording techniques to measure USVs from California mice in the laboratory (Peromyscus Genetic Stock Center, SC, USA) and the wild (Hastings Natural History Reserve, CA, USA). To determine which California mouse in the wild was vocalizing, we used a remote sensing method that used a 12-microphone acoustic localization array coupled with automated radio telemetry of all resident Peromyscus californicus in the area of the acoustic localization array. California mice in the laboratory and the wild produced the same types of USV motifs. However, wild California mice produced USVs that were 2-8 kHz higher in median frequency and significantly more variable in frequency than laboratory California mice. SIGNIFICANCE: The similarity in overall form of USVs from wild and laboratory California mice demonstrates that production of USVs by captive Peromyscus is not an artifact of captivity. Our study validates the widespread use of USVs in laboratory rodents as behavioral indicators but highlights that particular characteristics of laboratory USVs may not reflect natural conditions

Finding the Missing Honey Bee Genes: Lessons Learned from a Genome Upgrade

Background: The first generation of genome sequence assemblies and annotations have had a significant impact upon our understanding of the biology of the sequenced species, the phylogenetic relationships among species, the study of populations within and across species, and have informed the biology of humans. As only a few Metazoan genomes are approaching finished quality (human, mouse, fly and worm), there is room for improvement of most genome assemblies. The honey bee (Apis mellifera) genome, published in 2006, was noted for its bimodal GC content distribution that affected the quality of the assembly in some regions and for fewer genes in the initial gene set (OGSv1.0) compared to what would be expected based on other sequenced insect genomes.Results: Here, we report an improved honey bee genome assembly (Amel_4.5) with a new gene annotation set (OGSv3.2), and show that the honey bee genome contains a number of genes similar to that of other insect genomes, contrary to what was suggested in OGSv1.0. The new genome assembly is more contiguous and complete and the new gene set includes ~5000 more protein-coding genes, 50% more than previously reported. About 1/6 of the additional genes were due to improvements to the assembly, and the remaining were inferred based on new RNAseq and protein data.Conclusions: Lessons learned from this genome upgrade have important implications for future genome sequencing projects. Furthermore, the improvements significantly enhance genomic resources for the honey bee, a key model for social behavior and essential to global ecology through pollination

Size-dimorphism in the queens of the North American ant Leptothorax rugatulus (Emery)

With recent findings of an unexpected variability in the reproductive behaviour of ant sexuals, their morphology has become an area of major evolutionary interest (Heinze and Tsuji, 1995). Here we report on the occurrence of two queen morphs in Leptothorax rugatulus (Hym., Formi-cidae): Microgynes (small queens), exceeding worker-size only marginally, and macrogynes, which are, typically for the subgenus Myrafant, about twice as big as their workers. The frequency distribution of queen-size is clearly bimodal, in contrast to worker- and male-size. The average size of queens is highly correlated with the size of daughters in field-collected colonies, whereas within colonies no correlation between the average queen-size and the size of workers or males exists. This gives additional support that size-dimorphism is due to a specific, transmissible size reduction of the microgynes which could be based on genetics, the environment or both. This reduction is quasi-isometric, with a slightly smaller thorax-to-head ratio in microgynes, and scanning electron microscopy does not reveal any significant degeneration of the pterothorax, ocelli or number of ommatidia. The frequency of microgynes at different sample sites is highly variable, correlating well with the prevailing social structure in the respective subpopulations. Indeed, the majority of macrogynes is found in monogynous colonies, while microgynes abound in polygynous ones, which is strong evidence for an alternative dispersal tactic. However, the expected correlation to altitude or latitude was not found and further investigations are needed to reveal proximate and ultimate causes of this prevalent polymorphism between two types of female ant reproductives