Genetic and social structure of the queen size dimorphic ant Leptothorax cf. andrei

1. The study of queen polymorphisms can provide insight into the evolution of alternative life histories in ants. In this paper, results of morphological, social and genetic investigations of the newly discovered queen size dimorphism in Leptothorax cf. andrei are presented. 2. Queens had a bimodal size distribution, and were classified as large (macrogynes) or small (microgynes) queens. Despite their small size, microgynes had a fully developed external flight apparatus and a functional reproductive tract. 3. Queen morphology was not correlated with colony social structure, and the relatedness among nestmate queens was high, indicating secondary polygyny by re‐adoption of related queens (daughters) into existing colonies. 4. The distribution of microsatellite alleles indicated that there is a genetic separation between macro‐ and micro‐gynes but the two morphs belong to the same species. 5. The results support the hypothesis that microgyny in Leptothorax has not evolved as a specialisation to inter‐ or intra‐specific social parasitism but rather is an adaptation to alternative dispersal behaviour.     

Optimal length distribution of termite tunnel branches for efficient food search and resource transportation

Subterranean termites excavate branching tunnels for searching and transporting food in soil. Experimentally, the length distribution of the branch tunnels, P(L), was characterized by the exponentially decaying function, P(L)  exp(−L) with a branch length exponent of  = 0.15. To evaluate the significance of this value, we used a lattice model to simulate tunnels of the Formosan subterranean termite, Coptotermes formosanus Shiraki in featureless soil and computed the ratio of energy gain for obtained food to loss for transporting food for a given time, γ for various simulated tunnel patterns with the different values of . In simulation, the γ was maximized at 0.15 <  < 0.20 for the number of primary tunnels N = 6, 8, and 10. Our results indicate that tunnels with branch length distributions similar to those derived from empirical tunnel patterns result in tunnels made up of highly efficient paths to search and transport resources.     

Evolution of alternative foraging tactics driven by water temperature and physiological constraints in an amphibious snake

Amphibious predatory ectotherms live and forage in two environments (aquatic and terrestrial) that can drastically differ in temperature means and variance across space and time. The locomotor performance of ectotherms is known to be strongly affected by temperature. However, how differences in water temperature may drive the evolution of alternative foraging tactics in amphibious animals remains poorly understood. Fish‐eating Viperine snakes Natrix maura occur from high altitude cold water streams to warm shallow lakes, and employ two main feeding strategies: sentinel foraging (underwater sit‐and‐wait behaviour) and active foraging (fish chasing). Using 272 juvenile snakes we measured: the performance kinetics of diving and swimming in a wide range of water temperatures; basal metabolic levels in relation to body temperature; and the type of foraging mode expressed in water‐temperature‐acclimated snakes. Individual swimming performances increased with testing temperature (10, 15, 20, 25 or 30 °C). Apnoea time followed an opposite trend however, plausibly reflecting the fact that oxygen demands are related to the metabolic rate of ectotherms. That is, snake heart rates increased with body temperature. Snakes acclimated to 10 °C water mostly displayed sentinel foraging. By contrast, 20 °C and 30 °C water‐acclimated snakes were extremely active fish chasers. Individual apnoea times at the various testing temperatures were all correlated; as were individual swimming speeds. There was however no clear relationship between an individual's ability to hold its breath and its ability to swim, suggesting that both performance traits may be the target of different selective pressures. Fast swimming speed and long breath holding abilities are likely key determinants of both foraging success and predatory evasion, although in a context dependent manner. Active swimming foraging is likely to be advantageous in warm water (> 20 °C), while sentinel foraging appears better suited to cold water (< 14 °C). The physiological aspects of foraging tactics of amphibious snakes combined with field and laboratory observations support the idea that physiological and environmental constraints may generate shifts in habitat use and associated foraging tactics in amphibious ectotherms. Avenues for further research are discussed. © 2015 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, 115 , 411–422.     

Interaction between descending input and thoracic reflexes for joint coordination in cockroach. II Comparative studies on tethered turning and searching

Tethered cockroaches turn from unilateral antennal contact using asymmetrical movements of mesothoracic (T2) legs (Mu and Ritzmannin J Comp Physiol A 191:1037–1054, 2005). During the turn, the leg on the inside of the turn (the inside T2 leg) has distinctly different motor patterns from those in straight walking. The transformation from walking to inside leg turning could be triggered by descending commands that alter a few critical reflexes that start a cascade of physical changes in leg movement or posture, leading to further alterations. This hypothesis has two implications: First, the descending activities must be able to influence thoracic reflexes. Second, one should be able to initiate the turning motor pattern in the absence of descending signals by mimicking a point farther down in the reflex cascade. We addressed the first implication in the companion paper. To examine the second implication, we compared kinematics and motor activities of the T2 leg during searching with that of inside leg turning. The reaching movements made during searching were found to be similar to the movements made by the inside leg during turning. Moreover, even after disconnecting the brain from the thoracic ganglia the reaching movements were similar. This observation is consistent with the second implication from the hypothesis.     

Bioaffinity purification of NADP(+)-dependent dehydrogenases: studies with alcohol dehydrogenase from Thermoanaerobacter brockii.

This study describes the development and application of a bioaffinity chromatographic system for the one-step purification of an NADP(+)-dependent secondary alcohol dehydrogenase from the obligate anaerobe, Thermoanaerobacter brockii (TBADH, EC 1.1.1.2). The general approach is based upon improving the selectivity of immobilized cofactor derivatives (general ligand approach to bioaffinity chromatography) through using soluble enzyme-specific substrate analogues in irrigants to promote biospecific adsorption (the kinetic locking-on tactic). Specifically, the following is described: Evaluation of 8'-azo-linked, C(8)-linked, N(1)-linked, and N(6)-linked immobilized NADP(+) derivatives for use with the kinetic locking-on strategy for bioaffinity purification of TBADH; evaluation of 2', 5'-ADP as a stripping ligand for TBADH bioaffinity purifications using an 8'-azo-linked immobilized NADP(+) derivative in the locking-on mode; and application of the developed bioaffinity chromatographic system to the purification of TBADH from a crude cellular extract. Surprizingly, of the four immobilized NADP(+) derivatives investigated, only the 8'-azo-linked immobilized NADP(+) derivative proved effective for TBADH affinity purification when used in conjunction with pyrazole (a competitive inhibitor of TBADH activity) as the locking-on ligand. This is in contrast to other NADP(+)-dependent dehydrogenases where the immobilized N(6)-linked cofactor proved to be suitable. While the one-step purification of TBADH to electrophoretic homogeneity is described in the present study (92% yield), results from the model chromatographic studies point to improvements that could be made to the immobilized cofactor derivative to improve its suitability for TBADH bioaffinity purification and to facilitate future large scale protein purification operations.     

Calling and Duetting Behavior in the Leafhopper <Emphasis Type="Italic">Balclutha incisa</Emphasis> (Hemiptera: Cicadellidae: Deltocephalinae): Opportunity for Female Choice?

Male Balclutha incisa (Cicadellidae: Deltocephalinae) produces substrate-borne signals as well as sounds produced by wing fluttering. Males produce 6 signal types that are associated with different behavioral activities: (i) cleaning, (ii) calling, (iii) precopulatory, (iv) copulation, (v) postcopulatory behavior, and (vi) aggression. Within each category signals have a high degree of stereotypy in regard to their temporal structure. Females produce two kinds of signals: (i) a duetting signal in response to the male, and (ii) an introductory or preparatory signal before the main signal. The sexes duet, with the female placing its signal immediately after the first two components of the males call, with an interval of some 136 ms. We discuss the role of the male calls in attracting females and the importance of the duet in maintaining a temporary pair-bond.     

The evolution of intraspecific variation in social organization

Many species show intraspecific variation in their social organization (IVSO), which means the composition of their social groups can change between solitary living, pair living, or living in groups. Understanding IVSO is important because it demonstrates species resilience to environmental change and can help us to study ultimate and proximate reasons for group living by comparing solitary and group‐living individuals in a single species. It has long been realized that the environment plays a key role in explaining the occurrence of IVSO. IVSO is expected to have evolved in variable environments and can thus be a key adaptation to environmental change. It has previously been suggested that four different mechanisms relying on the environment exist that can lead to IVSO: environmental disrupters, genetic differentiation, developmental plasticity, and social flexibility. All four mechanisms depend on the environment such that focusing only on environmental factors alone cannot explain IVSO. Importantly, only three represent evolved mechanisms, while environmental disrupters leading to the death of important group members induce nonadaptive IVSO. Environmental disrupters can be expected to cause IVSO even in species where IVSO is also an adaptive response. Here, we focus on the questions of why IVSO occurs and why it evolved. To understand IVSO at the species level, it is important to conduct continuous long‐term studies to differentiate between nonadaptive and adaptive IVSO. We predict that IVSO evolves in environments that vary in important ecological variables, such as rainfall, food availability, and population density. IVSO might also depend on life history factors, especially longevity. IVSO is predicted to be more common in species with a short life span and that breed only for one breeding season, being selected to respond optimally to the prevailing environmental situation. Finally, we emphasize the importance of accounting for IVSO when studying social evolution, especially in comparative studies, as not every species can be assigned to one single form of social organization. For such comparative studies, it is important to use data based on the primary literature.     

Foraging behavior of Ural owls (Strix uralensis) in a patchy environment: The importance of acquired information

How the allocation of searching investiment by Ural owls (Strix uralensis) in a patchy and fluctuating environment is affected by prior information was experimentally studied. The owls searched among four patches, two with prey and two without prey. During the five days, the positions of two prey patches were randomly assigned daily (random treatment) and for the other five days, they were fixed (fixed treatment). In experiment I, the sequence of treatments was from random to fixed. In experiment II, the sequence of treatments was reversed. The choice of prey present patch was affected by acquired information which owls acquired during one night (short term), a treatment period (medium term), and throughout the experiment run (long term). They predicted the positions of the prey patches, to some extent, in the first choice in one night in the fixed treatment by the experience of previous days. The searching time per visit was also affected by previous information. Owls searched prey patches longer than empty patches. In the random treatment, the giving up time in prey patches was variable, while in the fixed treatment, it was longer and fixed. Although owls could use information on the environment where they had searched to make a decision of foraging behavior, they were not able to choose prey patches accurately. The information which was acquired during the treatment period and throughout the experiment run affected the gain from prey. The changes in gain were not caused by the encounter rate but by the proportion of attack success.     

Dimorphic male midshipman fish: reduced sexual selection or sexual selection for reduced characters?

In most taxa with male dimorphisms, some males are large inbody size with exaggerated secondary sexual characters (exaggeratedmorph), whereas other males in the same population are smalland have reduced secondary sexual characters (reduced morph).What selective pressures cause male dimorphisms? Reduced morphologiesmay result when a) some males develop a morphology that, inthe absence of sexual selection pressures for an exaggeratedmorphology, reduces energetic and developmental costs and/orb) some males opt for an alternative morphology that does wellat an alternative behavioral tactic such as cuckoldry. The 2mechanisms could act together, but each alone is theoreticallysufficient to drive dimorphisms. Here, we tested hypothesis"b" (sexual selection for reduced characters) in the plainfinmidshipman fish, Porichthys notatus. Behavioral plasticity betweenterritoriality and cuckoldry in an exaggerated male morph (typeI) allows for a direct comparison of cuckoldry by exaggeratedmorph males to cuckoldry by reduced morph (type II) males. Comparedwith type I cuckolders, type II cuckolders were able to remainnear the nest for longer periods before being chased by theterritorial type I male, suggesting that the reduced type IImorphology allows type II males to prolong the time before attackby territorial males. Combined with other studies showing arole of sexual selection in maintaining the exaggerated morph,the data support the "sexual selection for reduced characters"hypothesis and elucidate how sexual selection can act in differentways on different males to maintain 2 male morphologies withina single species.