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The scent gland secretion of an undetermined species of Prionostemma from Costa Rica was analyzed by gas chromatography–mass spectrometry and shown to consist of medium-chain carboxylic acids (mainly octanoic acid) and a ß-hydroxy-carboxylic acid, eventually identified as myrmicacin (= (R)-3-hydroxydecanoic acid). While scent gland secretions in harvestmen have traditionally been considered to be products of de novo synthesis, we here provide evidence for the unusual case of sequestration-derived scent gland constituents: at least myrmicacin appears to be sequestered from leaf-cutter ants that constitute a part of the prey of the Prionostemma-species herein investigated. This is the first report on the scent gland chemistry of the sclerosomatid subfamily Gagrellinae as well as on a possible sequestration mechanism in harvestmen. [ABSTRACT FROM AUTHOR]

Atta mexicana is a polyphagous insect that can exploit a wide range of plant species to cultivate its main food source, the symbiotic fungus Leucoagaricus gongylophorus. In the present study, we evaluated the foraging rate of A. mexicana workers among leaves of three favored and three rejected plant species under laboratory conditions. In addition, we conducted a phytochemical characterization of leaves of these six plant species. Ants preferred leaf discs of Rosa × alba, Trema micrantha and Styrax glabrescens, but rejected those of Coffea arabica, Citrus reticulata and Psidium guajava. In a second behavioral experiment using plant extracts, the results suggest that in the case of C. reticulata, rejection was not due chemical composition, but may have been due to different foliar attributes that could modulate the ant's foraging preferences in this species. Alkaloids, phenols, flavonoids, and tannins were present at different concentrations in all six plant species. Furthermore, C. arabica leaves presented significantly higher concentrations of alkaloids and this species, together with P. guajava, exhibited the highest concentration of phenols. Rejected plant species showed high concentrations of chlorogenic acid, (−)-epicatechin, quercetin-3, 4-di-O-glucoside (in C. arabica); shikimic acid, ellagic acid and (−)-epicatechin (in P. guajava), and scopoletin (in C. reticulata). Some of the identified compounds have been shown to possess antifungal effects and/or to dissuade leaf-cutter ants from defoliation. We discuss the likely implications on foraging on such plant species by A. mexicana, and on the growth of its symbiotic fungus. [ABSTRACT FROM AUTHOR]

While the chemistries of scent gland secretions from a few selected species of three families of Cyphophthalmi, namely Sironidae, Pettalidae, and Stylocellidae, have already been reported and found to consist of complex blends of naphthoquinones and methyl ketones, nothing is known about the other families. We here report on the secretions of Metasiro savannahensis Clouse and Wheeler (Zootaxa 3814:177–201, 2014), a first representative of the family Neogoveidae. The secretions from males, females and one juvenile were extracted and analyzed by gas chromatography–mass spectrometry. Twenty-five compounds were identified, all of which belong to the chemical classes of naphthoquinones and methyl ketones, confirming a hypothesized chemical uniformity of cyphophthalmid exudates. One major naphthoquinone compound, however, was new for cyphophthalmids and for arthropod exocrine secretions in general: a methyljuglone isomer, 6-methyljuglone (= 6-MJ; iupac name: 5-hydroxy-6-methyl-1,4-naphthoquinone), amounted for about 20% of the secretion and was eventually identified by synthesis. Hydroxy-naphthoquinones and their derivatives are known to possess a variety of antibiotic effects, probably enhancing the antimicrobial/antifungal potential of the Metasiro-secretion. Currently, without further data on neogoveids, the compound represents a chemical autapomorphy of M. savannahensis, and—just as the strange chloro-naphthoquinones of Sironidae and Pettalidae—adds to the repertoire of unusual naphthoquinone compounds across the Cyphophthalmi. [ABSTRACT FROM AUTHOR]

How foraging trails are formed and the chemical communication between individual ants is well known. However, communication between partners in mutualistic relationships, such as the leaf-cutting ants (LCA) and their symbiotic fungus, is less studied. There is a feedback mechanism that operates in LCA colonies, with the fungus garden communicating its condition to the ants, most probably using chemicals. We discuss the literature on the chemistry of the LCA-forage-fungus system starting from selection of plants and its effect on the fungus garden. We suggest, using chemical examples, how the fungus might communicate with attendant ants and suggest areas for future research into this fascinating and complex system. [ABSTRACT FROM AUTHOR]

The homologous and phylogenetically old scent glands of harvestmen—also called defensive or repugnatorial glands—represent an ideal system for a model reconstruction of the evolutionary history of exocrine secretion chemistry (“phylogenetic chemosystematics”). While the secretions of Laniatores (mainly phenols, benzoquinones), Cyphophthalmi (naphthoquinones, chloro-naphthoquinones, methyl-ketones) and some Eupnoi (naphthoquinones, ethyl-ketones) are fairly well studied, one open question refers to the still largely enigmatic scent gland chemistry of representatives of the suborder Dyspnoi and the relation of dyspnoan chemistry to the remaining suborders. We here report on the secretion of a nemastomatid Dyspnoi, Nemastoma triste, which is composed of straight-chain methyl-ketones (heptan-2-one, nonan-2-one, 6-tridecen-2-one, 8-tridecen-2-one), methyl-branched methyl-ketones (5-methyl-heptan-2-one, 6-methyl-nonan-2-one), naphthoquinones (1,4-naphthoquinone, 6-methyl-1,4-naphthoquinone) and chloro-naphthoquinones (4-chloro-1,2-naphthoquinone, 4-chloro-6-methyl-1,2-naphthoquinone). Chemically, the secretions of N. triste are remarkably reminiscent of those found in Cyphophthalmi. While naphthoquinones are widely distributed across the scent gland secretions of harvestmen (all suborders except Laniatores), methyl-ketones and chloro-naphthoquinones arise as linking elements between cyphophthalmid and dyspnoan scent gland chemistry. [ABSTRACT FROM AUTHOR]

The winter firefly ( Ellychnia corrusca) is common throughout the eastern United States and Canada. It is notable among fireflies (Coleoptera: Lampyridae) for its adult activity during the winter and early spring months, and for its lack of a light-producing organ. Multiple lines of evidence suggest that E. corrusca is chemically protected, specifically its unusual phenology which results in prolonged exposure to predators, its aposematic coloration, its reflex bleeding upon disturbance, and its relatedness to toxic firefly genera. Chemical investigation of this species revealed the presence of large quantities (>500 μg/beetle) of steroidal pyrones known as lucibufagins. The structures of these lucibufagins were determined using 1D and 2D NMR spectroscopy along with UHPLC-HRMS. Four of these compounds were previously detected in fireflies of the genus Photinus, while the remaining four, which contain a highly modified D-ring of the steroid core, are previously unknown. Analysis of reflex bleeding showed that the hemolymph contained the lucibufagins and that it was primarily released via a band of cuticular pores along the costal margin of the elytra. In addition, our analysis of the eggs, larva, and pupa established that all immature stages possess lucibufagins, thus representing the first instance of a firefly species for which all life stages have been investigated chemically. [ABSTRACT FROM AUTHOR]

In case of disturbance, the phalangiine harvestman Rilaena triangularis (Eupnoi, Phalangiidae) emits a directed jet from large prosomal scent ('defensive') glands. The pungent-smelling secretion was analyzed by gas chromatography-mass spectrometry and found to contain mainly 1,4-benzoquinone along with 1,4-naphthoquinone and caprylic (=octanoic) acid. While various alkylated benzoquinones are characteristic for the scent gland secretions of many grassatorean Laniatores, this is the first incidence of benzoquinone-based chemical defense in palpatorean harvestmen. [ABSTRACT FROM AUTHOR]

Delphastus catalinae (Horn) is a predatory ladybird beetle (Coccinellidae) commonly used as a biocontrol agent against greenhouse infestation by whiteflies. It belongs to the basal subfamily Microweisinae, a group for which chemical defenses have not been previously investigated. The larval and pupal stages of D. catalinae possess minute secretory hairs that produce droplets containing compounds of both isoprenoid and polyketide origin. Bioassays with the predatory ant Crematogaster lineolata showed both the larval and pupal secretions to be deterrent. Moreover, isolated secretion components, from both classes of compounds, displayed antipredator activity against the ant. Experiments with D. catalinae larvae fed isotopically labeled glucose showed C-incorporation into both categories of compounds within the pupal secretion, demonstrating that these antipredator compounds, which differ from the typical nitrogenous defensive molecules of coccinellids, are biosynthesized endogenously. This suggests that the wide use of alkaloids by more derived coccinellids may have arisen after their divergence from the more basal Microweisinae. [ABSTRACT FROM AUTHOR]

While considerable knowledge on the chemistry of the scent gland secretions from the opilionid suborders Laniatores and Cyphophthalmi has been compiled, it is the Palpatores (Eupnoi and Dyspnoi) where chemical data are scarce. In particular, the Dyspnoi have remained nearly unstudied, mainly due to their reported general reluctance to release secretions as well as to the phenomenon of production of insoluble-and inaccessible-solid secretion. We here show that at least certain nemastomatid Dyspnoi, namely all three species of genus Carinostoma, indeed produce a volatile secretion, comprising octan-3-one, 6-methyl-5-hepten-2-one and acetophenone in species-specific combinations. In all Carinostoma spp., these volatiles are embedded in a semi-volatile, naphthoquinone matrix (mainly 1,4-naphthoquinone and 6-methyl-1,4-naphthoquinone). In detail, acetophenone and traces of naphthoquinones characterize the secretions of Carinostoma carinatum. A mixture of octan-3-one, 6-methyl-5-hepten-2-one and large amounts of naphthoquinones were found in C. elegans, and 6-methyl-5-hepten-2-one together with small amounts of naphthoquinones in the secretions of C. ornatum. So far, exclusively naphthoquinones had been reported from a single dyspnoan hitherto studied, Paranemastoma quadripunctatum. [ABSTRACT FROM AUTHOR]

Abstract  The curculionid beetle Naupactus bipes (Germar, 1824) (Coleoptera: Curculionidae: Brachycerinae) has shown feeding preference for leaves of Piper gaudichaudianum, demonstrating an unexpected specificity for an insect considered to be a generalist. The leaves of P. gaudichaudianum contain the prenylated chromenes gaudichaudianic acid (4, major compound) and its methyl ester (5) in addition to a chromene (3) lacking one prenyl residue. In addition to 4, roots contain the chromone methyl ester (1) and methyl taboganate (2, major compound). Feeding on roots, larvae of N. bipes sequester exclusively the root-specific compounds 1 and 2. Adult beetles sequester the leaf-specific chromenes 3 and 4, but were found to also contain compounds 1 and 2 that are absent in leaves. Therefore, it is suggested that 1 and 2 are sequestered by larvae and can be found in the body of adult insects after long-term storage. In addition, 3 and 4, the major compounds in leaves were found to be associated with the eggs. [ABSTRACT FROM AUTHOR]

Summary.  Beetles of the family Lycidae have long been known to be chemically protected. We present evidence that North American species of the lycid genera Calopteron and Lycus are rejected by thrushes, wolf spiders, and orb-weaving spiders, and that they contain a systemic compound that could account, at least in part, for this unacceptability. This compound, a novel acetylenic acid that we named lycidic acid, proved actively deterrent in feeding tests with wolf spiders and coccinellid beetles. Species of Lycuscommonly figure as models of mimetic associations. Among their mimics are species of the cerambycid beetle genus Elytroleptus, remarkable because they prey upon the model lycids. We postulated that by doing so Elytroleptus might incorporate the lycidic acid from their prey for their own defense. However, judging from analytical data, the beetles practice no such sequestration, explaining why they remain relatively palatable (in tests with wolf spiders) even after having fed on lycids. Chemical analyses also showed the lycids to contain pyrazines, such as were already known from other Lycidae, potent odorants that could serve in an aposematic capacity to forestall predatory attacks. [ABSTRACT FROM AUTHOR]

Lucidota atra, a diurnal firefly, shares possession of defensive steroids (lucibufagins or LBGs) with nocturnal fireflies of the genus Photinus. Photinus are protected against predators by their LBGs, but not against fireflies of the genus Photuris, the so-called firefly femmes fatales, which prey upon Photinus, thereby acquiring LBGs for their own defense. We propose that L. atra may have been prompted evolutionarily to become diurnal by the opportunity to avoid, thereby, being hunted by Photuris. Indeed, L. atra, if offered to Photuris, were eagerly devoured by the latter, which sequestered their LBG’s. In feeding on L. atra, Photuris may be driven by a gustatory affinity for LBGs. Persistent nocturnality might therefore have put L. atra at risk vis à vis Photuris. Diurnality freed the firefly from that risk, without compromising its defended status with respect to other predators. Possession of LBGs may in fact account for L. atra’s unacceptability to birds and spiders. [ABSTRACT FROM AUTHOR]

Female Photuris fireflies contain defensive chemicals of two types. They sequester steroidal pyrones (lucibufagins) from male fireflies of the genus Photinus that they eat, and themselves produce the defensive betaine N-methylquinolinium 2-carboxylate. Chemical analyses of Photuris eggs showed that females that fed on Photinus males endow their eggs with both lucibufagin and the betaine, while those that did not feed on Photinus lay eggs that contain betaine, but virtually no lucibufagin. Photuris females collected in the field during the Photinus flight season laid eggs that invariably contained betaine, but lucibufagin only at times. Predation experiments showed that Photuris eggs are essentially unacceptable to larvae of a coccinellid beetle ( Harmonia axyridis) and an ant ( Leptothorax longispinosus), but moderately acceptable to an earwig ( Forficula auricularia). When applied experimentally to palatable insect eggs, lucibufagin proved deterrent to these three predators, while the betaine proved deterrent to the ant and coccinellid larva only. Both types of defensive compound decreased egg predation in the field. By endowing their eggs with both exogenous and endogenous chemicals, Photuris females are essentially “maximizing their options”– when feeding on Photinus, their eggs are doubly protected, but they are not entirely defenseless when the females are unable to procure lucibufagin. [ABSTRACT FROM AUTHOR]

Female Photuris fireflies sequester defensive steroidal pyrones (lucibufagins) from male fireflies of the genus Photinus. Lucibufagin analyses of Photuris females and Photinus ignitus males show that the lucibufagin mixtures of predator and prey differ in their composition. Analyses of whole body extracts showed that P. ignitus males contain a mixture of eight non-glycosylated lucibufagins, composed mostly of compounds with two oxygenated positions in the steroidal A-ring (C-3, C-5). After feeding on P. ignitus males, Photuris females contain six major lucibufagins. Three of these compounds are not present in the prey, including the novel lucibufagin glycoside 5β,11α-dihydroxy-12-oxo-3β-O-β-D-xylopyranosylbufalin, and two other lucibufagins with a trioxygenated A-ring (C-2, C-3, C-5). These results indicate that Photuris females transform the sequestered lucibufagins both by glycosylation and oxidation, which could affect the systemic transportability of these compounds due to an increase in their polarity. [ABSTRACT FROM AUTHOR]

Chemical communication plays a very important role in the lives of many social insects. Several different types of pheromones (species-specific chemical messengers) of ants have been described, particularly those involved in recruitment, recognition, territorial and alarm behaviours. Properties of pheromones include activity in minute quantities (thus requiring sensitive methods for chemical analysis) and specificity (which can have chemotaxonomic uses). Ants produce pheromones in various exocrine glands, such as the Dufour, poison, pygidial and mandibular glands. A wide range of substances have been identified from these glands. [ABSTRACT FROM AUTHOR]