Volatile components from the mandibular glands of the turtle ants, Cephalotes alfaroi and Cephalotes cristatus

GC–MS analysis of whole head extracts from the turtle ants, Cephalotes alfaroi and Cephalotes cristatus, showed that 4-heptanone and 4-heptanol were the major volatile components in the mandibular glands. 4-Heptanone and 4-heptanol have rarely been identified in mandibular gland secretions from other ant genera. Thus, these compounds may be chemotaxonomic markers for the genus Cephalotes, since they have been identified in the mandibular glands from all members of this genus that have been investigated to date. Minor components identified in the whole head extracts of these ants were 3-methyl-1-butanol, 3-heptanone, 3-hexanol, 2- and 3-methylbutanoic acids, 2-methyl-4-heptanone, 2-phenylethanol and phenol. To our knowledge, this is the first time that 2-methyl-4-heptanone and phenol have been reported in the mandibular gland secretion from any Formicid.     

Alarm behaviour in Eciton army ants

The effective communication of alarm can be critical for social animals so that they are able to deal with threats posed by predators and competitors. In the case of many of the most ecologically dominant, large‐colony ant species, these alarm responses are aggressive and coordinated by alarm pheromones, produced generally from the mandibular glands. In the present study, the alarm behaviour of two Neotropical army ant species is examined, the swarm raiding Eciton burchellii (Westwood) and the column raiding Eciton hamatum (Fabricius). Both species exhibit aggressive alarm responses in response to crushed heads, suggesting that the alarm pheromone is indeed produced by the mandibular glands in these ants. The most abundant component of the mandibular gland secretion, 4‐methyl‐3‐heptanone (10 µL on a rubber septum), stimulates a substantial alarm response, although this is less than the response to a single crushed head. This suggests that 4‐methyl‐3‐heptanone may be an alarm‐stimulating compound in Eciton. The alarm response of E. burchellii involves more workers than that of E. hamatum, although major workers play a much greater role in the response of the latter species. The differences in the alarm response of the two closely‐related species may relate to their foraging strategies, with E. burchellii relying more on quantity rather than the caste of ants responding and possibly using alarm pheromones for offensive as well as defensive functions.     

Contents of the exocrine glands of the ant subfamily Cerapachyinae

The chemistry of the exocrine glands of three species of the small and little-known ant subfamily Cerapachyinae has been examined for the first time. The mandibular glands of Cerapachys jacobsoni contained acetophenone and skatole, but some individuals contained, in addition, 4-methyl-3-heptanone and 3-octanol. The mandibular glands of the new species, presently known as Cerapachys sp. 15 of FI contained 4-methyl-3-heptanone, as the major substance but also 4-methyl-3-heptanol, methyl 6-ethylsalicylate, and traces of 4,5-dimethyl-4-hexen-3-one and homomanicone. The Dufour glands of C. jacobsoni contained a mixture of higher aldehydes, acetates and other esters, with a small amount of hydrocarbons, all in the range C₁₁–C₂₀. The Dufour glands of Cylindromyrmex whymperi contained a mixture of long-chain epoxides, the second ant species to display them. The sternal glands of C. whymperi contain a recruitment pheromone, but only partial identification of the contents was possible. The venom glands of all three species were devoid of volatile material. The Dufour glands of Cerapachys sp. 15 of FI and the mandibular glands of C. whymperi had no detectable volatile contents.     

Chemical Taxonomy of Economically Important Tyrophagus Mites (Acariformes,Acaridae)

Rosefuran and perillene were isolated from the opisthonotal glands secretion of the Tyrophagus neiswanderi mite. A facile synthesis of the former was accomplished by the lithiation of 3-methyl- furan with butyllithium-tetramethylethylenediamine, and a subsequent reaction with 3-methyl-2- butenylbromide. A mixture of rosefuran, 4-methyl-2-(3-methyl-2-butenyl)-furan and 3-methyl-2,5-bis- (3-methyl-2-butenyl)-furan was obtained in a high yield. The occurrence of these and other recently identified monoterpenoids, namely, α- and β-acaridial and 2,3-epoxyneral, is discussed relative to the CP-Sil 19 CB column profiles as worthy for the identification of economically important mites of the genus Tyrophagus, which is a difficult but essential task for the successful application of the species-specific alarm pheromones in the management of these pests.     

Social Insect Pheromones: Their Chemistry and Function

Exocrine secretions of social insects are often characterizedby extraordinarily complex mixtures of natural products. Thus,chemical communication in social insects must be interpretedin terms of signals generated by multicomponent systems, theindividual constituents of which can affect the informationalcontent of the message. Alarm pheromones have been identified chiefly in three subfamiliesof ants and their distribution appears to be chemosystematicallysignificant. Myrmicine genera emphasize 3-alkanones as alarmreleasers, whereas methyl ketones, primarily of terpenoidalorigin, are widely utilized as alarm pheromones in the subfamilyDolichoderinae. Formicine species may employ formic acidas analarm pheromone in addition to the compounds produced in themandibular and Dufour's glands. The mandibular gland pheromonesare chiefly acyclic monoterpene aldehydes (e.g., citronellal)which are relatively low boiling compounds. Higher boiling n-alkanesare produced in the Dufour's glands and may serve as more persistentreleasers of alarm behavior. Alarm pheromones as well as thecaste-specific pheromones of male bees and ants, probably alsoserve as defensive products. In many cases it is likely thatpheromones were originally utilized as defensive compounds andtheir communicative function is a secondary development.     

Two Odorant-Binding Proteins Mediate the Behavioural Response of Aphids to the Alarm Pheromone (E)-?-farnesene and Structural Analogues

Background

Aphids are agricultural pests of great economical interest. Alternatives to insecticides, using semiochemicals, are of difficult applications. In fact, sex pheromones are of little use as aphids reproduce partenogenetically most of the time. Besides, the alarm pheromone, (E)-ß-farnesene for a great number of species, is difficult to synthesize and unstable in the environment. The search for novel semiochemicals to be used in population control can be efficiently approached through the study of the olfactory system at the biochemical level. Recently odorant-binding proteins (OBPs) have been shown to play a central role in olfactory recognition, thus becoming the target of choice for designing new semiochemicals.

Methodology/Principal Findings

To address the question of how the alarm message is recognised at the level of OBPs, we have tested 29 compounds, including (E)-ß-farnesene, in binding assays with 6 recombinant proteins and in behaviour experiments. We have found that good repellents bind OBP3 and/or OBP7, while non repellents present different spectra of binding. These results have been verified with two species of aphids, Acyrthosiphon pisum and Myzus persicae, both using (E)-ß-farnesene as the alarm pheromone.

Conclusions

Our results represent further support to the idea (so far convincingly demonstrated only in Drosophila) that OBPs are involved in decoding the chemical information of odorants and pheromones, and for the first time provide such evidence in other insect species and using wild-type insects. Moreover, the data offer guidelines and protocols for the discovery of potential alarm pheromones, using ligand-binding assays as a preliminary screening before subjecting selected compounds to behaviour tests.     

A comparison of mandibular gland volatiles from ants of the bull horn acacia,Acacia collinsii

GC–MS analyses of dichloromethane extracts of the mandibular glands from three obligate symbiotic Psuedomyrmex ant species of Acacia collinsii from Costa Rica: Pseudomyrmex flavicornis (synonym Pseudomyrmex belti), Psuedomyrmex spinicola, and Psuedomyrmex nigrocincta, showed distinct differences in the 16 ketones, 15 alcohols, 2 aldehydes and 2 carboxylic acids that were identified. Different compounds were the major component from each species: P. flavicornis, 3-octanone; P. spinicola, 4-methyl-3-heptanone; and P. nigrocincta, 3-methyl-2-hexanol. The secretion of P. flavicornis contained 10 compounds not found in the other species, including the two terpene alcohols, citronellol and geraniol. The secretions of P. spinicola and P. nigrocincta had 12 compounds in common, that were not found in P. flavicornis' secretion. The similarity of the mandibular gland secretion of P. spinicola and P. nigrocincta may indicate that they are more closely related to each other than either is to P. flavicornis. The components from the mandibular gland of Crematogaster rochai, another ant associated with this acacia, are 2- and 3-methylbutanoic acid, 3-octanone, 3-octanol, 6-methyl-3-octanol and 3-nonanone.     

Isolation, identification, synthesis and biological activity of volatile compounds from the heads of Atta ants

S-(+)-4-methyl-3-heptanone has been identified as the principal alarm pheromone of Atta texana and Atta cephalotes. Both enantiomers of 4-methyl-3-heptanone have been synthesized and their biological activities have been compared on both species of ants. Comparison of the geometric averages of response ratios, at threshold concentration levels on A. texana, showed S-(+)-4-methyl-3-heptanone to be about 100 times more active than the (?) enantiomer. A similar analysis also showed no inhibition of the activity of S-(+)-4-methyl-3-heptanone by the (?) enantiomer. A less rigorous study on A. cephalotes showed S-(+)-4-methyl-3-heptanone to be about 210 times more active than R-(?)-4-methyl-3-heptanone.Both ant species produce 3-octanone, possible trace amounts of 3-octanol, and both diastereomers of 4-methyl-3-heptanol. A. texana also produces (+)-2-heptanol, 2-heptanone, and 3-heptanol. A. cephalotes contains trace amounts of 2-heptanone.     

Temporal Response of Foragers and Guards of Two Stingless Bee Species to Cephalic Compounds of the Robber Bee <Emphasis Type="Italic">Lestrimelitta niitkib</Emphasis> (Ayala) (Hymenoptera,Apidae)

Lestrimelitta spp. are stingless bees that steal food and nesting materials from other highly social bees to survive. Though most of their victim species respond, either aggressively or submissively, to cephalic components of Lestrimelitta, little is known about if such response changes at some point during extended periods of exposure. Moreover, potential synergistic effects due to a mixture of victim’s alarm/defense pheromones and Lestrimelitta mandibular pheromones, like in an actual attack, have not been examined so far. In this paper, we investigated the response of two species of non-robber stingless bees, Scaptotrigona mexicana (Guérin) and Tetragonisca angustula (Latreille), to (a) cephalic compounds from crushed heads of nestmates, (b) cephalic compounds of Lestrimelitta niitkib (Ayala), and (c) a mixture of (a) and (b). We found that even though T. angustula did not react to nestmates’ crushed head, its response towards L. niitkib cephalic compounds was stronger and lasted longer than that of S. mexicana. Interestingly, the addition of crushed heads of the non-robber species to L. niitkib crushed heads caused no significant increase in the alarm response of both species. It may be that the absence of an alarm pheromone in T. angustula made this species more receptive to extraneous odors, which is not the case for S. mexicana; however, more species must be studied to elucidate any pattern regarding the absence/presence of alarm pheromones and the corresponding response to intruders’ pheromones.     

Multiple functions of fire ant Solenopsis invicta mandibular gland products

Alarm pheromones of social insects are best known for their role in the defence and maintenance of colony integrity. Previous studies with the fire ant Solenopsis invicta Buren (Hymenoptera: Formicidae) demonstrate that the mandibular glands of workers (sterile females) and male and female sexuals produce an alarm pheromone, 2‐ethyl‐3,6‐dimethylpyrazine. The function of alarm pheromones in worker ants is well understood and divergent from the function of these compounds in the winged sexual forms. The present study quantifies the amount of pyrazine in the mandibular glands from male and female alate sexuals, as well as queens. Pyrazine production in female alates starts in the late pupal stage and increases until they reach mating flight‐ready maturity; however, after mating flight participation, the pyrazine level declines by >50%. Interestingly, mature male alates lose >85% of their mandibular gland pyrazine during mating flight activity. The results of the present study indicate that male and female sexuals use mandibular gland secretions for mating flight initiation and during mating flights. Furthermore, the ontogeny of mandibular gland products (pyrazine as the marker) from newly‐mated queens to mature colony queens shows a more than two‐fold increase in the amount of pyrazine by 6 months after mating. However, this is followed by a decline to trace amounts in mature colony queens (>2 years old), suggesting a function for mandibular gland products during colony development. Multifunctional use of social insect pheromones is well documented and data are reported in the present study suggesting new roles for mandibular gland products in fire ants.     

Reactions of five species of stingless bees to some volatile chemicals and to other species of bees

Trigona pectoralis and T. mexicana attacked when volatile chemicals that have been identified from their heads were presented at the nest entrance; mixtures approximating the composition of the head extracts elicited stronger reactions than did any of the single chemicals. Alarm pheromones of T. pectoralis occur in approximately equal concentrations in the mandibular glands and the remainder of the heads; other alarm pheromones occur in small concentrations in the abdomen. Three other species of stingless bees gave defensive reactions when presented with the mixture of chemicals, with some of the single chemicals, with living or freshly killed T. pectoralis, or with the heads of that species. Living or freshly killed Lestrimelitta limao, which are known to live by robbing other bees, elicited strong defence reactions from all species; citral, the major volatile component of the head extract of L. limao, gave similar results. Variations in the strength of reactions of bees to other species and to a wide variety of volatile chemicals led to the conclusion that bees probably learn to recognize the odour of other species that rob from their nests, and that the pheromones of the robbing species are allomones that recruit the victims to the defence of the nest. It is postulated that the reactions to some of the chemicals developed because the bees had been exposed to enemies that contained the chemicals. It is often impossible to decide whether the reactions of bees to a chemical result from an inability to distinguish the chemical from some other, or from the properties and usual origin of the chemical itself.Some of the problems that arise from the reactions of the bees, and particularly from their reactions to 2-heptanone, geraniol, and benzoic acid, are discussed.     

The volatile components of the mandibular gland secretion of workers of the ants Myrmica lobicornis and Myrmica sulcinodis

The mandibular glands of workers of M. lobicornis produce a mixture of 3-alkanones and 3-alkanols in the C₆–C₁₀ carbon chain length range, in addition to nanogram amounts of acetone, ethanal and 2-methylpropanal. Ethological studies have shown that the three major constituents, 3-octanol, 3-octanone and 3-decanol, are also the major pheromonally active components. When presented together they stimulate an alarm response in the workers similar to that induced by a worker's crushed head.In M. sulcinodis the mandibular gland secretion is composed of a mixture of the same ketones and alcohols, but in different proportions.     

Sink or swim: a test of tadpole behavioral responses to predator cues and potential alarm pheromones from skin secretions

Chemical signaling is a vital mode of communication for most organisms, including larval amphibians. However, few studies have determined the identity or source of chemical compounds signaling amphibian defensive behaviors, in particular, whether alarm pheromones can be actively secreted from tadpoles signaling danger to conspecifics. Here we exposed tadpoles of the common toad Bufo bufo and common frog Rana temporaria to known cues signaling predation risk and to potential alarm pheromones. In both species, an immediate reduction in swimming activity extending over an hour was caused by chemical cues from the predator Aeshna cyanea (dragonfly larvae) that had been feeding on conspecific tadpoles. However, B. bufo tadpoles did not detectably alter their behavior upon exposure to potential alarm pheromones, neither to their own skin secretions, nor to the abundant predator-defense peptide bradykinin. Thus, chemicals signaling active predation had a stronger effect than general alarm secretions of other common toad tadpoles. This species may invest in a defensive strategy alternative to communication by alarm pheromones, given that Bufonidae are toxic to some predators and not known to produce defensive skin peptides. Comparative behavioral physiology of amphibian alarm responses may elucidate functional trade-offs in pheromone production and the evolution of chemical communication.     

Lipophilic C-methylflavonoids with no B-ring oxygenation in Metrosideros species (Myrtaceae)

Five unusual C-methylflavonoids lacking B-ring oxygenation (2′,4′-dihydroxy-3′,5′-dimethyl-6′-methoxychalcone, 2′,4′-dihydroxy-3′-methyl-6′-methoxychalcone, 2′,6′-dihydroxy-3′-methyl-4′-methoxychalcone, 2′-hydroxy-3′-methyl-4′,6′-dimethoxychalcone and 5,7-dihydroxy-6,8-dimethylflavanone) were found for the first time in Metrosideros excelsa. The flavanone was the major constituent in leaves, whereas 2′,6′-dihydroxy-3′-methyl-4′-methoxychalcone dominated all other aerial plant parts studied. Other Metrosideros species were investigated for these five flavonoids. C₁₉–C₃₆ aldehydes and C₂₂–C₃₂ alcohols were also identified from the dried seed capsules of M. excelsa.     

The fatty acid and sterol composition of two marine dinoflagellates

The fatty acid, sterol and chlorophyll pigment compositions of the marine dinoflagellates Gymnodinium wilczeki and Prorocentrum cordatum are reported. The fatty acids of both algae show a typical dinoflagellate distribution pattern with a predominance of C₁₈, C₂₀ and C₂₂ unsaturated components. The acid 18:5ω3 is present at high concentration in these two dinoflagellates. G. wilczeki contains a high proportion (93.4%) of 4-methyl-5α-stanols including 4,23,24-trimethyl-5α-cholest-22E-en-3β-ol (dinosterol), dinostanol and 4,23,24-trimethyl-5α-cholest-7-en-3β-ol reported for the first time in dinoflagellates. The role of this sterol in the biosynthesis of 5α-stanols in dinoflagellates is discussed. P. cordatum contains high concentrations of a number of δ ²⁴⁽²⁸⁾-sterols with dinosterol, 24-methylcholesta-5,24(28)-dien-3β-ol, 23,24-dimethylcholesta-5,22E-dien-3β-ol, 4,24-dimethyl-5α-cholest-24(28)-en-3β-ol and a sterol identified as either 4,23,24-trimethyl- or 4-methyl-24-ethyl-5α-cholest-24(28)-en-3β-ol present as the five major components. The role of marine dinoflagellates in the input of both 4-methyl- and 4-desmethyl-5α-stanols to marine sediments is discussed.     

Formic acid and saturated hydrocarbons as alarm pheromones for the ant Formica rufa

Releasers for the most intense, the fast-running, phase of the alarm behaviour were studied in worker ants of the formicine ant Formica rufa. The investigation was performed with a new technique in which the intensity and the duration of the behaviour pattern were measured in an objective and automatic way.Workers of formicine ants eiect a mixture of formic acid and the secretion from Dufour's gland against an enemy. The secretion from this gland in F. rufa consists of a great number of substances, 39 of which have been identified. The dominating substances form a homologous series of aliphatic, saturated hydrocarbons. Some of these hydrocarbons as well as the formic acid are alarm pheromones. The behavioural threshold value for one of these compounds, decane, was lower than 5.10¹³ molecules cm^?3 air. The threshold value for formic acid was estimated to 7.10¹⁵ molecules cm^?3 air. Formic acid and undecane are shown to belong to different reaction groups. The hydrocarbons, on the other hand, seem to affect the same kind of acceptor or receptor.The total intensity and duration of the alarm behaviour released by formic acid and one hydrocarbon are additive if the two substances are combined in a stimulus. A combination of two hydrocarbons and formic acid release a stronger behaviour than one hydrocarbon with formic acid even when the two stimuli contain the same number of molecules. The hydrocarbons have a combined effect and their relative concentrations regulate the intensity and duration of the alarm behaviour.     

Alarm pheromones of the Attini: Their phylogenetic significance

The volatile components present in the mandibular glands of a number of species of the attine genera Cyphomyrmex (1 species), Trachymyrmex (3 species), and Acromyrmex (2 species) were investigated and compared with those present in Atta. The extracts were found to consist of mixtures of a number of compounds. All but one of these mixtures contained some or all of the following compounds: 3-octanone, 4-methyl-3-heptanone, 3-octanol, and 4-methyl-3-heptanol. The behavioural responses of Trachymyrmex and Cyphomyrmex workers to these compounds were tested. A common chemical heritage based on 3-ketones and 3-alcohols appeared to exist among the genera studied. The chemical data were compared with an accepted phylogeny of these genera to see whether it supported the phylogeny.     

Crystal structure of Sol I 2: a major allergen from fire ant venom

Sol i 2 is a potent allergen from the venom of red imported fire ant, which contains allergens Sol i 1, Sol i 2, Sol i 3, and Sol i 4 that are known to be powerful triggers of anaphylaxis. Sol i 2 causes IgE antibody production in about one-third of individuals stung by fire ants. Baculovirus recombinant dimeric Sol i 2 was crystallized as a native and selenomethionyl-derivatized protein, and its structure has been determined by single-wavelength anomalous dispersion at 2.6 Å resolution. The overall fold of each subunit consists of five helices that enclose a central hydrophobic cavity. The structure is stabilized by three intramolecular disulfide bridges and one intermolecular disulfide bridge. The nearest structural homologue is the sequence-unrelated odorant binding protein and pheromone binding protein LUSH of the fruit fly Drosophila, which may suggest a similar biological function. To test this hypothesis, we measured the reversible binding of various pheromones, plant odorants, and other ligands to Sol i 2 by the changes in N-phenyl-1-naphthylamine fluorescence emission upon binding of ligands that compete with N-phenyl-1-naphthylamine. The highest binding affinity was observed for hydrophobic ligands such as aphid alarm pheromone (E)-β-farnesene, analogs of ant alarm pheromones, and plant volatiles decane, undecane, and β-caryophyllene. Conceivably, Sol i 2 may play a role in capturing and/or transporting small hydrophobic ligands such as pheromones, odors, fatty acids, or short-living hydrophobic primers. Molecular surface analysis, in combination with sequence alignment, can explain the serological cross-reactivity observed between some ant species.     

Myrcene: A precursor of pheromones in Ips beetles

Males of Ips spp. produced the pheromones ipsdienol (2-methyl-6-methylene-2,7-octadien-4-ol) and/or ipsenol (2-methyl-6-methylene-7-octen-4-ol) when exposed to vapours of myrcene, a monoterpene present in their hosts (Pinus spp.). Ips grandicollis and Ips calligraphus require feeding before metabolizing the myrcene, whereas Ips avulsus and Ips paraconfusus produce some pheromone without prior feeding. Topical treatment with ipsdienol results in ipsenol production in both fed and unfed I. paraconfusus males but only in fed I. gradicollis males. I. calligraphus males, which do not produce ipsenol in nature, did not produce any with the topical treatment regardless of prior conditioning. It is concluded that myrcene can serve as a precursor for these terpene alcohols and suggested that ipsenol is produced by the reduction of ipsdienol. Furthermore, the biosynthesis of these pheromones appears to be under some form of control in certain species, with the stimulus for production occurring upon feeding.     

The response of grass-cutting ants to natural and synthetic versions of their alarm pheromone

The responses of the grass‐cutting ants Atta bisphaerica (Forel) and Atta capiguara (Gonçalves) to the main components of their alarm pheromones were examined in simple field bioassays. Both species react most strongly to 4‐methyl‐3‐heptanone, which causes the full range of alarm behaviour and a large increase in the number of individuals near the sources. In later experiments with A. capiguara, this increase was found to be due primarily to attraction, with some arrestment also occurring. The ant response to 4‐methyl‐3‐heptanone was compared with that to crushed heads and to that with whole ants with crushed heads. The pheromone 4‐methyl‐3‐heptanone by itself stimulates the same level of attraction as crushed heads, but results in far less alarm behaviour and arrests fewer ants. Whole ants with crushed heads attract a greater number of ants than the other sources and also cause more alarm behaviour. Bodies alone attract ants, but do not result in alarm behaviour. The main component in both species is the same, supporting the view that alarm pheromones lack species specificity. However, it appears that other components may also be important either as synergists of the main compound, or by stimulating behaviours that would not be observed in its absence.