Monitoring bee populations: are eusocial bees attracted to different colours of pan trap than other bees?

Declines in pollinator populations have made monitoring pollinators, in particular bees, increasingly important. There is general agreement among practitioners that using a mix of trap colours is important, but the empirical evidence to support this is scattered. During studies of bees in forestry cutovers, large differences were noted in capture rate among white, blue, and yellow pan traps. Pooled data from collections in cutovers and commercial cranberry fields demonstrated significant differences in the effect of trap colour, with the largest numbers captured in white traps, and the fewest in yellow, but only for the genus Bombus Latreille (Hymenoptera: Apidae). The colour preference was consistent with the spectral sensitivity of Bombus, and the visible reflectance spectra of the traps. A literature review suggested that among eusocial bees, Apis Linnaeus (Hymenoptera: Apidae) are more attracted to white traps and Bombus are more attracted to blue traps, while non-eusocial bees with a variety of social structures are more attracted to yellow. Among the non-eusocial bees, Halictidae were somewhat attracted to blue, while Andrenidae were not. This supports the common practice of using white, blue, and yellow traps when surveying bees to ensure adequate taxonomic representation.     

Bacillus DNA in fossil bees: an ancient symbiosis?

We report here the isolation of DNA from abdominal tissue of four extinct stingless bees (Proplebeia dominicana) in Dominican amber, PCR amplification of a 546-bp fragment of the 16S rRNA gene from Bacillus spp., and their corresponding nucleotide sequences. These sequences were used in basic local alignment search tool searches of nonredundant nucleic acid data bases, and the highest scores were obtained with 16S rRNA sequences from Bacillus spp. Phylogenetic inference analysis by the maximum-likelihood method revealed close phylogenetic relationships of the four presumed ancient Bacillus sequences with Bacillus pumilus, B. firmus, B. subtilis, and B. circulans. These four extant Bacillus spp. are commonly isolated from abdominal tissue of stingless bees. The close phylogenetic association of the extracted DNA sequences with these bee colonizers suggests that a similar bee-Bacillus association existed in the extinct species P. dominicana.     

Environment or kin: whence do bees obtain acidophilic bacteria?

As honey bee populations decline, interest in pathogenic and mutualistic relationships between bees and microorganisms has increased. Honey bees and bumble bees appear to have a simple intestinal bacterial fauna that includes acidophilic bacteria. Here, we explore the hypothesis that sweat bees can acquire acidophilic bacteria from the environment. To quantify bacterial communities associated with two species of North American and one species of Neotropical sweat bees, we conducted 16S rDNA amplicon 454 pyrosequencing of bacteria associated with the bees, their brood cells and their nests. Lactobacillus spp. were the most abundant bacteria in many, but not all, of the samples. To determine whether bee-associated lactobacilli can also be found in the environment, we reconstructed the phylogenetic relationships of the genus Lactobacillus. Previously described groups that associate with Bombus and Apis appeared relatively specific to these genera. Close relatives of several bacteria that have been isolated from flowers, however, were isolated from bees. Additionally, all three sweat bee species associated with lactobacilli related to flower-associated lactobacilli. These data suggest that there may be at least two different means by which bees acquire putative probiotics. Some lactobacilli appear specific to corbiculate apids, possibly because they are largely maternally inherited (vertically transmitted). Other lactobacilli, however, may be regularly acquired from environmental sources such as flowers. Sweat bee-associated lactobacilli were found to be abundant in the pollen and frass inside the nests of halictids, suggesting that they could play a role in suppressing the growth of moulds and other spoilage organisms.     

Why do leafcutter bees cut leaves? New insights into the early evolution of bees

Stark contrasts in clade species diversity are reported across the tree of life and are especially conspicuous when observed in closely related lineages. The explanation for such disparity has often been attributed to the evolution of key innovations that facilitate colonization of new ecological niches. The factors underlying diversification in bees remain poorly explored. Bees are thought to have originated from apoid wasps during the Mid-Cretaceous, a period that coincides with the appearance of angiosperm eudicot pollen grains in the fossil record. The reliance of bees on angiosperm pollen and their fundamental role as angiosperm pollinators have contributed to the idea that both groups may have undergone simultaneous radiations. We demonstrate that one key innovation--the inclusion of foreign material in nest construction--underlies both a massive range expansion and a significant increase in the rate of diversification within the second largest bee family, Megachilidae. Basal clades within the family are restricted to deserts and exhibit plesiomorphic features rarely observed among modern bees, but prevalent among apoid wasps. Our results suggest that early bees inherited a suite of behavioural traits that acted as powerful evolutionary constraints. While the transition to pollen as a larval food source opened an enormous ecological niche for the early bees, the exploitation of this niche and the subsequent diversification of bees only became possible after bees had evolved adaptations to overcome these constraints.     

Spider signals: are web decorations visible to birds and bees?

We are becoming increasingly aware of animal communication outside the range of human sensitivity. Web decorations are silk structures used by orb-web spiders to deceive prey and predators. However, despite the level of interest in these structures, their visibility to prey and predators has never, to our knowledge, been objectively assessed. Here, we use spectrophotometric analyses to show that the decorations of all five tested spider species are visible to honey bees and birds over short and long distances. Furthermore, the discoid decorations of one species may provide some protection against arthropod predators. However, these decorations are inefficient at camouflaging the spider against birds, despite the overlap between the spider's body and web decoration.     

Floral constancy in bumble bees: handling efficiency or perceptual conditioning?

Individual bees often prefer flowers of the same species that they are already foraging on, and other individual bees prefer other flowers. This floral constancy has classically been explained as a learned behavior by which bees avoid wasting time switching between handling techniques. Choice trails were given to Bombus vagans workers that were freely foraging in mixed and pure fields of Trifolium pratense, T. repens, Viccia cracca, and Prunella vulgaris. Contrary to expectation, (1) bees showed if anything a stronger preference for their flower type in pure fields where they lacked experience than in a mixed field where they had had the opportunity to learn, (2) there was greater constancy in a mixed field of the two morphologically similar Trifolium species than in a mixed field of the morphologically disparate T. pratense and P. vulgaris, and (3) bees were more willing to switch between flowers of distinct morphologies when the colors were similar than between flowers of distinct colors when the morphologies were similar. We suggest that constancy is due to some form of perceptual conditioning whereby individual bees become temporarily sensitized to one or a few floral cues.     

Orchard pollination in Capitol Reef National Park,Utah, USA. Honey bees or native bees?

Capitol Reef National Park in central Utah, USA surrounds 22 managed fruit orchards started over a century ago by Mormon pioneers. Honey bees are imported for pollination, although the area in which the Park is embedded has over 700 species of native bees, many of which are potential orchard pollinators. We studied the visitation of native bees to apple, pear, apricot, and sweet cherry over 2 years. Thirty species of bees visited the flowers but, except for pear flowers, most were uncommon compared to honey bees. Evidence that honey bees prevented native bees from foraging on orchard crop flowers was equivocal: generally, honey bee and native bee visitation rates to the flowers were not negatively correlated, nor were native bee visitation rates positively correlated with distance of orchards from honey bee hives. Conversely, competition was tentatively suggested by much larger numbers of honey bees than natives on the flowers of apples, apricots and cherry; and by the large increase of native bees on pears, where honey bee numbers were low. At least one-third of the native bee species visiting the flowers are potential pollinators, including cavity-nesting species such as Osmia lignaria propinqua, currently managed for small orchard pollination in the US, plus several fossorial species, including one rosaceous flower specialist (Andrena milwaukiensis). We suggest that gradual withdrawal of honey bees from the Park would help conserve native bee populations without decreasing orchard crop productivity, and would serve as a demonstration of the commercial value of native pollinators.     

Representation of conspecific song by chickadees: Comparisons among embedded ‘fee bees’

Captive black-capped chickadees (Parus atricapillus) were presented with normal (2-note) and lengthened (3-note) songs to investigate how note number and order are represented. Normal fee bee (FB) song was embedded in four different 3-note sequences containing an additional fee (F) or bee (B). Latency to vocalize after playback varied with the position, but not the type of added note, (i.e. slower responses to BFB and FFB than to FBF and FBB). Latency did not differ appreciably between normal (2-note) and these 3-note songs. The presence of normal 2-note song in each 3-note song may override note count. Our results provide further evidence that chickadees represent the absolute temporal location of the first, but not the last note of conspecific song.     

Why do bees turn back and look?

The timing of learning of colour and shape of the food source, as well as of near-by landmarks, was examined exploiting a behaviour described recently, the Turn Back and Look behaviour (TBL): Bees departing from a novel food source after feeding turn around to view it at a short distance (Figs. 2, 3) before departing for the hive. They repeat this behaviour on several successive visits, termed the TBL phase (Fig. 5). To examine the function of the TBL, I trained individual bees in 4 different modes. In the first 3 they could view a food source or a landmark of a particular colour or shape during (i) arrival as well as departure, (ii) only arrival, and (iii) only departure; in the final mode (iv) the bees viewed one colour (or shape) on arrival, and another on departure. At the end of the TBL phase, the bees were tested by offering them a choice between the visual stimulus to which they were trained (modes i–iii) and a different (novel) one, or between the stimulus viewed on arrival and that viewed on departure (mode iv). The test results show that learning after feeding (while performing the TBL), i.e. backward conditioning, occurs regardless of whether the colour (Fig. 6, Fig. 10a) or shape (Fig. 7) of the food source, or the colour (Fig. 10b), shape (Fig. 11), and position (Fig. 12) of a near-by landmark is considered. Bees trained in mode (iv) preferred the stimulus learned on arrival over that learned on departure in almost all cases. However, a stimulus viewed exclusively on departure (mode iii) was often learned as well as when it was viewed exclusively on arrival (mode ii) (Figs. 10a, 11, 12), or both on arrival and departure (mode i) (Fig. 6). The finding that the timing of learning can be manipulated suggests that it is not based on hard wired predispositions to learn particular visual cues on arrival, and others on departure.     

The nested structure of marine cleaning symbiosis: is it like flowers and bees?

In a given area, plant-animal mutualistic interactions form complex networks that often display nestedness, a particular type of asymmetry in interactions. Simple ecological and evolutionary factors have been hypothesized to lead to nested networks. Therefore, nestedness is expected to occur in other types of mutualisms as well. We tested the above prediction with the network structure of interactions in cleaning symbiosis at three reef assemblages. In this type of interaction, shrimps and fishes forage on ectoparasites and injured tissues from the body surface of fish species. Cleaning networks show strong patterns of nestedness. In fact, after controlling for species richness, cleaning networks are even more nested than plant-animal mutualisms. Our results support the notion that mutualisms evolve to a predictable community-level structure, be it in terrestrial or marine communities.     

Butterflies & wild bees: biology teachers’ PCK development through citizen science*

Citizen science is a rapidly growing emerging field in science and it is gaining importance in education. Therefore, this study was conducted to document the pedagogical content knowledge (PCK) of biology teachers who participated in a citizen science project involving observation of wild bees and identification of butterflies. In this paper, knowledge about how these biological methods can be taught to students is presented. After two years in the project, four teachers were interviewed and their PCK was captured in the form of content representations (CoRes) and Pedagogical and Professional-Experience Repertoires (PaP-eRs). These results can help future citizen science projects to link their activities to the school curriculum. But not only success can be reported: although one of the project team’s aims was to make the Nature of Science accessible to the teachers and students in the course of the project, the teachers did not take this aspect into account. This paper discusses the possible reasons and proposes various strategies for improving citizen science in the context of school biology learning.     

Buzz-pollination in Neotropical bees:genus-dependent frequencies and lack of optimal frequency for pollen release

Over 50 genera of bees release pollen from flower anthers using thoracic vibrations,a phenomenon known as buzz-pollination.The efficiency of this process is directly affected by the mechanical properties of the buzzes,namely the duration,amplitude,and frequency.Nonetheless,although the effects of the former two properties are well described,the role of buzz frequency on pollen release remains unclear.Furthermore,nearly all of the existing studies describing vibrational properties of natural buzz-pollination are limited to bumblebees(Bombus)and carpenter bees(Xvlocopa)constraining our current understanding of this behavior and its evolution.Therefore,we attempted to minimize this shortcoming by testing whether flower anthers exhibit optimal frequency for pollen release and whether bees tune their buzzes to match these(optimal)frequencies.If true,certain frequencies will trigger more pollen release and lighter bees will reach buzz frequencies closer to this optimum to compensate their smaller buzz amplitudes.Two strategies were used to test these hypotheses:(i)the use of(artificial)vibrational playbacks in a broad range of buzz frequencies and amplitudes to assess pollen release by tomato plants(Solarium Ivcopersicum L.)and(ii)the recording of natural buzzes of Neotropical bees visiting tomato plants during pollination.The playback experiment indicates that although buzz frequency does affect pollen release,no optimal frequency exists for that.In addition,the recorded results of natural buzz-pollination reveal that buzz frequencies vary with bee genera and are not correlated with body size.Therefore,neither bees nor plants are tuned to optimal pollen release frequencies.Bee frequency of buzz-pollination is a likely consequence of the insect flight machinery adapted to reach higher accelerations,while flower plant response to buzz-pollination is the likely result of its pollen granular properties.     

Longer tongues and swifter handling: why do more bumble bees (Bombus spp.) than honey bees (Apis mellifera) forage on lavender (Lavandula spp.)?

相似文献   

How do bees learn and recognize visual patterns?

The basic task of perceptual systems is the recognition and localization of objects. The central nervous system has to solve these problems on the basis of the excitation patterns of sensory nerves, in spite of the fact that these provide only ambiguous information about objects. Two processing principles seem to be fundamental for an efficient formation of object representations: the extraction of characteristic features and the ability to assess similarities between different objects. This article reviews investigations in which different training paradigms were applied in order to explore the honeybee's capacities to learn and recognize visual patterns. One aim of these experiments is to assess whether insects use similar processing mechanisms as vertebrates, for instance human beings. By comparing the computational performance of perceptual systems in animals with different evolutionary history we can hope to learn more about the operation of basic rules in nervous systems. “The messages which the brain receives have not the least similarity with the stimuli. They consist in pulses of given intensities and frequencies, characteristic for the transmitting nerve-fiber, which ends at a definite place of the cortex. ... From this information it produces the image of the world by a process which can metaphorically be called a consummate piece of combinatorial mathematics: it sorts out of the maze of indifferent and varying signals, invariant shapes and relations which form the world of ordinary experience.” Max Born (1949) Received: 4 October 1997 / Accepted in revised form: 26 August 1998     

Patterns of size variation in bees at a continental scale: does Bergmann's rule apply?

Body size latitudinal clines have been widley explained by the Bergmann's rule in homeothermic vertebrates. However, there is no general consensus in poikilotherms organisms in particular in insects that represent the large majority of wildlife. Among them, bees are a highly diverse pollinators group with high economic and ecological value. Nevertheless, no comprehensive studies of species assemblages at a phylogenetically larger scale have been carried out even if they could identify the traits and the ecological conditions that generate different patterns of latitudinal size variation. We aimed to test Bergmann's rule for wild bees by assessing relationships between body size and latitude at continental and community levels. We tested our hypotheses for bees showing different life history traits (i.e. sociality and nesting behaviour). We used 142 008 distribution records of 615 bee species at 50 × 50 km (CGRS) grids across the West Palearctic. We then applied generalized least squares fitted linear model (GLS) to assess the relationship between latitude and mean body size of bees, taking into account spatial autocorrelation. For all bee species grouped, mean body size increased with higher latitudes, and so followed Bergmann's rule. However, considering bee genera separately, four genera were consistent with Bergmann's rule, while three showed a converse trend, and three showed no significant cline. All life history traits used here (i.e. solitary, social and parasitic behaviour; ground and stem nesting behaviour) displayed a Bergmann's cline. In general there is a main trend for larger bees in colder habitats, which is likely to be related to their thermoregulatory abilities and partial endothermy, even if a ‘season length effect’ (i.e. shorter foraging season) is a potential driver of the converse Bergmann's cline particularly in bumblebees.