Social polymorphism in the sweat bee <Emphasis Type="Italic">Lasioglossum (Evylaeus) baleicum</Emphasis> (Cockerell) (Hymenoptera,Halictidae) in Hokkaido,northern Japan

Summary The life cycle and social behaviour of the sweat bee Lasioglossum (Evylaeus) baleicum (Cockerell) was investigated in two geographically separate populations in Hokkaido, northern Japan. Colonies were excavated throughout the brood rearing season from an aggregation in Nishioka forest park, Sapporo, and near Kawakita in eastern Hokkaido during 2000 and 2001. The Nishioka population produced two discrete broods during the year and was weakly eusocial; 57% of workers were mated and 28% exhibited some ovarian development, 12–16% of the first brood was male, and workers were on average 4.5% smaller than their respective queen. In contrast, the population at Kawakita was solitary, and produced a single brood per year with an unbiased sex ratio. In addition however, there were some solitary colonies in the Nishioka population and evidence of a partial second brood in some colonies at Kawakita, suggesting differences between the populations are not fixed and that this species is truly socially polymorphic. L. (E.) baleicum is a member of the fulvicorne species group, which includes other examples of social polymorphic species as well as solitary and eusocial species, though this is the only species of this group so far known to exhibit a solitary/non-delayed eusocial polymorphism. Recent studies suggest that social polymorphism has both genetic and environmental influences, raising questions as to the relative import of each.     

Characterization of microsatellite loci from the solitary sweat bees Lasioglossum leucozonium and Lasioglossum oenotherae (Hymenoptera,Halictidae)

Microsatellite loci were isolated from two solitary sweat bees: the polylectic Lasioglossum leucozonium (10 loci) and the oligolectic Lasioglossum oenotherae (9 loci) (Hymenoptera, Halictidae). All loci were polymorphic with high observed heterozygosities (0.07–0.75 for L. leucozonium; 0.06–0.92 for L. oenotherae). These loci will be used to study the consequences of diet specialization on the population and conservation genetics of bees.     

Microsatellite loci for the eusocial Lasioglossum malachurum and other sweat bees (Hymenoptera,Halictidae)

Sweat bees (family Halictidae) comprise a numerous and diverse group that are arguably among the most socially labile of all insect taxa. Given the lack of highly variable markers for eusocial species of the family, we developed a suite of dinucleotide and trinucleotide markers for one of its members, the Eurasian Lasioglossum malachurum, and used them to amplify DNA from other halictids. Loci were highly variable in L. malachurum and amplified DNA from many other halictids.     

Lasioglossum (Dialictus) tenax (Sandhouse) (Hymenoptera: Halictidae) as a solitary sweat bee

Summary Nine nests ofLasioglossum (Dialictus) tenax were excavated near Calgary, Alberta, Canada over a time period encompassing the entire brood production period in 1988. Each nest contained a maximum of one active adult female, nest productivity peaked in mid July, protandry was noted and no significant size difference between foundresses and the earlier emerging females was detected. These data suggest that this species is solitary. These results are compared with data for the sympatrically nesting eusocial speciesL. (D.) laevissimum.     

Taxonomic notes on Lasioglossum (Lasioglossum) subopacum (Smith) and L. (L.) okinawa Ebmer et Maeta (Hymenoptera, Halictidae) from Asia

Lasioglossum (Lasioglossum) subopacum (Smith) is recorded from the Korean Peninsula for the first time. Lasioglossum (Lasioglossum) okinawa Ebmer et Maeta from Japan is ranked to a subspecies of Lasioglossum (Lasioglossum) subopacum judging from the characteristics of the male. The male of Lasioglossum (Lasioglossum) subopacumokinawa is described for the first time. Some bionomical notes of both subspecies are presented.     

Invasion of Nests of Lasioglossum imitatum by a Social Parasite,Paralictus asteris (Hymenoptera: Halictidae)

Paralictus asteris Mitchell is a socially parasitic sweat bee that invades nests and becomes the dominant reproductive in colonies of a phylogenetically related host, Lasioglossum (Dialictus) imitatum (Smith). The parasite has a greatly enlarged quadrate head, with elongate scythe-like mandibles, and other morphological modifications apparently associated with a parasitic lifestyle. Nevertheless, the parasite did not forcefully enter nests. Host guards adopted a defensive posture at the nest entrance when they contacted a dead, frozen parasite, suggesting that they recognized the intruders as parasites. Living parasites, however, only sometimes induced this guarding response, while in other cases parasites entered host nests without obvious signs of aggression from the guard. Guards also responded aggressively to both frozen and living conspecifics from other nests, but were not aggressive to living or frozen nest-resident conspecifics, suggesting that the cues used for recognition of both unrelated conspecifics and parasites are chemical ones. More than one parasite can invade and occupy a nest, and successful invasion was not influenced by whether a parasitic female was mated or had developed ovaries.     

The population genetics of a solitary oligolectic sweat bee, Lasioglossum (Sphecodogastra) oenotherae (Hymenoptera: Halictidae)

Strong evidence exists for global declines in pollinator populations. Data on the population genetics of solitary bees, especially diet specialists, are generally lacking. We studied the population genetics of the oligolectic bee Lasioglossum oenotherae, a specialist on the pollen of evening primrose (Onagraceae), by genotyping 455 females from 15 populations across the bee's North American range at six hyper-variable microsatellite loci. We found significant levels of genetic differentiation between populations, even at small geographic scales, as well as significant patterns of isolation by distance. However, using multilocus genotype assignment tests, we detected 11 first-generation migrants indicating that L. oenotherae's sub-populations are experiencing ongoing gene flow. Southern populations of L. oenotherae were significantly more likely to deviate from Hardy-Weinberg equilibrium and from genotypic equilibrium, suggesting regional differences in gene flow and/or drift and inbreeding. Short-term N(e) estimated using temporal changes in allele frequencies in several populations ranged from approximately 223 to 960. We discuss our findings in terms of the conservation genetics of specialist pollinators, a group of considerable ecological importance.     

Phylogeny of the bee genus Lasioglossum (Hymenoptera: Halictidae) based on mitochondrial COI sequence data

The bee genus Lasioglossum Curtis is a model taxon for studying the evolutionary origins of and reversals in eusociality. This paper presents a phylogenetic analysis of Lasioglossum species and subgenera based on a data set consisting of 1240 bp of the mitochondrial cytochrome oxidase I (COI) gene for seventy-seven taxa (sixty-six ingroup and eleven outgroup taxa). Maximum parsimony was used to analyse the data set (using paup *4.0) by a variety of weighting methods, including equal weights, a priori weighting and a posteriori weighting. All methods yielded roughly congruent results. Michener’s Hemihalictus series was found to be monophyletic in all analyses but one, while his Lasioglossum series formed a basal, paraphyletic assemblage in all analyses but one. Chilalictus was consistently found to be a basal taxon of Lasioglossum sensu lato and Lasioglossum sensu stricto was found to be monophyletic. Within the Hemihalictus series, major lineages included Dialictus + Paralictus, the acarinate Evylaeus + Hemihalictus + Sudila and the carinate Evylaeus + Sphecodogastra. Relationships within the Hemihalictus series were highly stable to altered weighting schemes, while relationships among the basal subgenera in the Lasioglossum series (Lasioglossum s.s., Chilalictus, Parasphecodes and Ctenonomia) were unclear. The social parasite of Dialictus, Paralictus, is consistently and unambiguously placed well within Dialictus, thus rendering Dialictus paraphyletic. The implications of this for understanding the origins of social parasitism are discussed.     

Ontogenetic patterns of volatiles identified in Dufour's gland extracts from queens and workers of the primitively eusocial halictine bee,Lasioglossum malachmum (Hymenoptera: Halictidae)

Summary Ontogenetic patterns of volatile compounds identified in Dufour's gland extracts from queens and workers of the primitively eusocial sweat beeLasioglossum malachurum (K.) were compared. Only young unmated queens showed high proportions of isopentenyl esters, while macrocyclic lactones were dominant in old breeding queens, spring queens, and workers. In young queens the relative and absolute amounts of volatiles changed one day after mating. A discriminant analysis revealed significant differences in odor patterns of unmated and mated young queens. The fat body was the largest in young females, while eggs could be recorded only in breeding queens. Possible functions of different odor components in the investigated female groups are discussed.     

Lasiocepsin, a novel cyclic antimicrobial peptide from the venom of eusocial bee Lasioglossum laticeps (Hymenoptera: Halictidae)

In the venom of eusocial bee Lasioglossum laticeps, we identified a novel unique antimicrobial peptide named lasiocepsin consisting of 27 amino acid residues and two disulfide bridges. After identifying its primary structure, we synthesized lasiocepsin by solid-phase peptide synthesis using two different approaches for oxidative folding. The oxidative folding of fully deprotected linear peptide resulted in a mixture of three products differing in the pattern of disulfide bridges. Regioselective disulfide bond formation significantly improved the yield of desired product. The synthetic lasiocepsin possessed antimicrobial activity against both Gram-positive and -negative bacteria, antifungal activity against Candida albicans, and no hemolytic activity against human erythrocytes. We synthesized two lasiocepsin analogs cyclized through one native disulfide bridge in different positions and having the remaining two cysteines substituted by alanines. The analog cyclized through a Cys8-Cys25 disulfide bridge showed reduced antimicrobial activity compared to the native peptide while the second one (Cys17-Cys27) was almost inactive. Linear lasiocepsin having all four cysteine residues substituted by alanines or alkylated was also inactive. That was in contrast to the linear lasiocepsin with all four cysteine residues non-paired, which exhibited remarkable antimicrobial activity. The shortening of lasiocepsin by several amino acid residues either from the N- or C-terminal resulted in significant loss of antimicrobial activity. Study of Bacillus subtilis cells treated by lasiocepsin using transmission electron microscopy showed leakage of bacterial content mainly from the holes localized at the ends of the bacterial cells.     

Geographical patterns of mitochondrial DNA variation in Apis mellifera iberiensis (Hymenoptera: Apidae)

An extensive survey of mitochondrial haplotypes in honeybee colonies from the Iberian Peninsula has corroborated previous hypotheses about the existence of a joint clinal variation of African (A) and west European (M) evolutionary lineages. It has been found that the Iberian Peninsula is the European region with the highest haplotype diversity (12 haplotypes detected of the M lineage and 10 of the A lineage). The frequency of A haplotypes decreases in a SW-NE trend, while that of M haplotypes increases. These results are discussed in relation to hypotheses about the African origin of Apis mellifera and an early colonization of west Europe during intermediate Pleistocene glaciation events, followed by a regional differentiation. The extant pattern of haplotype frequency and distribution seems to be influenced at a regional scale by adaptation to local climatic conditions and the mobile beekeeping that has become a large-scale practice during the last decades. Other previous anthropogenic influences (Greek, Roman and Arab colonizations) are thought to be of minor importance in present day populations.     

Segregation of temporal and spatial distribution between kleptoparasites and parasitoids of the eusocial sweat bee, Lasioglossum malachurum (Hymenoptera: Halictidae, Mutillidae)

Cuckoo bees and velvet ants use different resources of their shared host bees, the former laying eggs on the host pollen stores and the latter on immature stages. We studied the activity patterns of the cuckoo bee Sphecodes monilicornis and the velvet ant Myrmilla capitata at two nesting sites of their host, the social digger bee Lasioglossum malachurum , over a 3 year period. Due to the difference in host exploitation, we expected different temporal patterns of the two natural enemies as well as a positive spatial association with host nest density for both species. At a daily level, S. monilicornis was more abundant between 10.00 and 15.00 h, while M. capitata was most active in the early morning and late afternoon; both species activities were independent from host provisioning activity. The activity of cuckoo bees was in general positively correlated with the density of open host nests (but not with the total number of nests), while that of velvet ants was rarely correlated with this factor. Sphecodes monilicornis was seen both attacking the guard bees and directly entering into the host nests or digging close to nest entrances, while M. capitata only gained access to host nests through digging. We conclude that the temporal and spatial segregation between the two species may be, at least partially, explained both by the different resources exploited and by the different dynamics of host interactions.     

Phylogeny of eusocial Lasioglossum reveals multiple losses of eusociality within a primitively eusocial clade of bees (Hymenoptera: Halictidae)

We performed a phylogenetic analysis of the species, species groups, and subgenera within the predominantly eusocial lineage of Lasioglossum (the Hemihalictus series) based on three protein coding genes: mitochondrial cytochrome oxidase I, nuclear elongation factor 1alpha and long-wavelength rhodopsin. The entire data set consisted of 3421 aligned nucleotide sites, 854 of which were parsimony informative. Analyses by equal weights parsimony, maximum likelihood, and Bayesian methods yielded good resolution among the 53 taxa/populations, with strong bootstrap support and high posterior probabilities for most nodes. There was no significant incongruence among genes, and parsimony, maximum likelihood, and Bayesian methods yielded congruent results. We mapped social behavior onto the resulting tree for 42 of the taxa/populations to infer the likely history of social evolution within Lasioglossum. Our results indicate that eusociality had a single origin within Lasioglossum. Within the predominantly eusocial clade, however, there have been multiple (six) reversals from eusociality to solitary nesting, social polymorphism, or social parasitism, suggesting that these reversals may be more common in primitively eusocial Hymenoptera than previously anticipated. Our results support the view that eusociality is hard to evolve but easily lost. This conclusion is potentially important for understanding the early evolution of the advanced eusocial insects, such as ants, termites, and corbiculate bees.     

Flagellar Sensilla of Sphecodes Bees (Hymenoptera, Halictidae)

The antenna of Sphecodes bees were investigated as regards the type and distribution of the sensilla. Eleven species originating from Sweden were used. Totally 325 specimens were studied. The distribution of sensilla placodea and sensilla trichodea on the antennal segments were studied in the light stereomicroscope. One to three antennae per species were also examined by SEM. The following types of sensilla were found: s. placodea; pit organs; s. campaniformia; s. basiconica; s. trichodea A, B and CD; and setae. The distribution of sensilla, especially s. placodea and s. trichodea A, was found to be species-specific in the male sex and their diagnostic value in taxonomy is stressed. In the female sex no specific characteristics were found, although two groups could be distinguished.     

Nesting biology of tropical solitary and social sweat bees,Lasioglossum (Dialictus) figueresi Wcislo andL. (D.) aeneiventre (Friese) (Hymenoptera: Halictidae)

Summary The nesting biology of a mainly solitary bee,Lasioglossum (Dialictus) figueresi, is compared with that of a possible relative and mainly eusocial bee,L. (D.) aeneiventre. These bees nest in the ground in highly disturbed areas in the Meseta Central of Costa Rica. Information is provided on social organization, male production, diel and seasonal activity patterns, pollen utilization, natural enemies and nest architecture. L. (D.) figueresi nests within aggregations in vertical earthen banks, and 80–90 % of females are solitary during the nest-provisioning phase. Social nests contain two (or rarely three) females which may be either equal or unequal in reproductive status (i.e. mated with developed ovaries or not). Solitary nests and two-female nests do not experience different rates of parasitism. Mid-way through the dry season, females cease provisioning at a time when otherL. (Dialictus) remain active. Females typically remain within their nests, although they occasionally forage for nectar. This behavior is similar of that of spring gynes of temperate eusocial species. The egg-to-adult developmental rate ofL. (D.) figueresi is unusually slow for halictine bees, however, so that all the adult females die before their brood eclose in April and May, precluding overlap of generations. The eclosed offspring remain in open cells within their natal nests until mid-June, when both males and females emerge to mate. These newly mated females either establish new nests or re-use old ones. L. (D.) aeneiventre nests within aggregations in horizontal ground or in vertical banks. A foundress female digs a nest at the beginning of the dry season, although some re-activate old nests. Foundress nests develop into colonies with various kinds of social organization. In contrast toL. (D.) figueresi, L. (D.) aeneiventre is active nearly all year round, except during periods of heavy rain, and produces up to three broods per year.Sweat bees (Hymenoptera: Halictinae) are a socially heterogeneous group of mainly ground-nesting bees which are abundant world-wide. Intra-specific variation in social behavior is prevalent both within and among populations, presumably indicating social and environmental control of behavioral modifications (see e.g. Sakagami and Munakata, 1972; Eickwort, 1986; Packer, 1990; Yanega, 1988; reviewed in Michener, 1990). The initial stages of hymenopteran social evolution are represented by solitary individuals and those in undifferentiated societies, yet their biology is not well known, as is true for the numerous tropical halictine species or populations (see Michener, 1990).The subgenusDialictus ofLasioglossum is a primarily New World group of several hundred species (Moure and Kurd, 1987). These bees are monotonously similar in structure and appearance, yet diverse in social behavior. FemaleLasioglossum (Dialictus) figueresi are usually solitary, and structurally are very similar to their social relativeL. (D.) aeneiventre (Wcislo, 1990 a). The systematic placement of these species with respect to otherL. (Dialictus) is uncertain, but they have no obvious affinities to other recognized species groups (G. C. Eickwort, pers. comm.). Unusual morphological features, such as large size, yellowish wings and pubescence, and features of the genital organs, may indicate thatL. (D.) figueresi is the more derived of the pair, and may therefore be secondarily solitary, as is known for other sweat bees (Packer, 1991).     

A new species of Microsphecodes from Jamaica (Hymenoptera, Halictidae)

A new species of the cleptoparasitic bee genus Microsphecodes Eickwort and Stage (Halictinae: Halictini) is described and figured from a male and female collected in Jamaica. Microsphecodes xaymacensis Engel, sp. n., is distinguished from its congeners on the basis of integumental coloration and sculpturing, and form of the male pygidial plate and genitalia.     

Colony social organization of <Emphasis Type="Italic">Lasioglossum malachurum</Emphasis> Kirby (Hymenoptera,Halictidae) in southern Greece

Summary We studied the nesting and social biology of two aggregations of the obligately eusocial halictine bee Lasioglossum malachurum at Agios Nikolaos Monemvasias (ANM) in southern Greece. Observations and nest excavations carried out from May to June 2000, revealed social and demographic variation between aggregations and years at ANM, as well as notable differences between these and other European populations. In southern Greece, the colony cycle includes multiple broods: the first two broods comprise only workers, whereas the third brood comprises workers, males, and gynes. Although pleometrosis is unknown in other populations, in the ANM region, as many as 10% of nests have more than one foundress. Newly emerged workers and gynes exhibit non-overlapping size distributions, but a few queens are worker-sized, indicating that workers occasionally overwinter and become foundresses. Although the vast majority of workers are unmated and most exhibit no ovarian development, an increase in worker ovarian development at the time of male production suggests that many males may develop from worker-laid eggs. Worker reproduction seems to be inhibited by the presence of queens, and annual variation in queen mortality may underlie annual variation in worker ovarian development. Across Europe, the major demographic and social differences among L. malachurum populations are in the number of worker broods and the extent of worker ovarian development. This contrasts with the results of a principal components analysis of social traits among 15 social L. (Evylaeus) populations, which shows that interspecific social variation is defined by the proportion of males in the early brood, the proportion of workers mated, queen-worker size dimorphism, gyne overwintering locale, and the proportion of workers with developed ovaries.Received 17 June 2002; revised 16 January 2002; accepted 27 January 2003.