Identification of a Triterpenoid Saponin from a Crucifer, Barbarea vulgaris, as a Feeding Deterrent to the Diamondback Moth, Plutella xylostella

Larvae of the diamondback moth, Plutella xylostella, a crucifer specialist, refuse to feed on a crucifer, Barbarea vulgaris, because of the presence of a feeding deterrent, which is extractable with chloroform. We isolated a feeding deterrent from B. vulgaris leaves, by successive fractionations with silica-gel, ODS, i.e., C₁₈ reversed phase, and Sephadex LH-20 column chromatographies, and ODS-HPLC, guided by a bioassay for feeding deterrent activity. The structure of the compound was determined to be a monodesmosidic triterpenoid saponin, 3-O-[O--D-glucopyranosyl-(14)--D-glucopyranosyl]-hederagenin, based on FAB-MS, ¹H- and ¹³C-NMR spectra, and hydrolysis experiments. When the compound was applied to cabbage leaf disks at greater than 0.18 g/mm², consumption of the disks by third instars was less than 11% of control disks treated with the solvent alone. Furthermore, all first instars died on the disks treated with the same concentrations. Because the concentration of the compound in the fresh leaves of B. vulgaris was comparable to the effective dose in the cabbage leaf disk tested, we conclude that the unacceptability of B. vulgaris to P. xylostella larvae is primarily due to this saponin.     

Identification of Volatile Synomones, Induced by Nezara viridula Feeding and Oviposition on Bean spp., That Attract the Egg Parasitoid Trissolcus basalis

Bean plants (Vicia faba L. and Phaseolus vulgaris L.) damaged by feeding activity of Nezara viridula (L.) (Heteroptera: Pentatomidae), and onto which an egg mass had been laid, produced volatiles that attracted the egg parasitoid Trissolcus basalis (Wollaston) (Hymenoptera: Scelionidae). Extracts of volatiles of broad bean and French bean plants induced by adults of N. viridula as a result of their feeding activity, oviposition activity, and feeding and oviposition activity combined were analyzed by gas chromatography-mass spectrometry (GC-MS), and tested in Y-tube olfactometer bioassays as attractants for T. basalis females. In extracts from undamaged leguminous plants, green-leaf volatiles were absent or scarcely detected, and monoterpenes and sesquiterpenes were present at trace levels. No significant differences were detected in the profiles of volatiles of undamaged plants, and undamaged plants on which bugs were allowed only to lay eggs. In contrast, feeding and oviposition by adults of N. viridula induced in both leguminous plants a significant increase in terpenoids such as linalool, (E)-beta-caryophyllene, (E,E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene, and (3E)-4,8-dimethyl-1,3,7-nonatriene, which was induced only in French bean plants. Quantitative comparisons revealed increased levels of (E)-beta-caryophyllene in extracts from feeding-damaged plants with N. viridula egg masses compared to feeding-damaged plants without egg masses. In Y-tube olfactometer bioassays, T. basalis females were attracted by extracts of both leguminous plants only when N. viridula adults were allowed to feed and oviposit upon them. Fractionation of extracts of volatiles from broad bean plants with N. viridula feeding damage and egg masses yielded two fractions. but only the fraction containing (E)-beta-caryophyllene was attractive to the egg parasitoid. These findings indicate that N. viridula feeding and oviposition induce leguminous plants to produce blends of volatiles that are characterized by increased amounts of (E)-beta-caryophyllene, and these blends attract female T. basalis. The role of (E)-beta-caryophyllene as a potential synomone for T. basalis is discussed.     

Spring migration of damson-hop aphid,Phorodon humuli (Homoptera,Aphididae), and summer host plant-derived semiochemicals released on feeding

Behavioral studies using an olfactometer demonstrated that spring migrants of the damson-hop aphid,Phorodon humuli, respond to semiochemicals released by spring migrants feeding on hop leaves. Samples of the total volatiles released on feeding were analyzed by coupled gas chromatographysingle cell recording techniques and showed the presence of several active components. Three compounds were identified, using coupled gas chromatography-mass spectrometry, as methyl salicylate, (E)-2-hexenal and-caryophyllene. These three compounds elicited responses from separate olfactory receptors on the antenna. In the olfactometer, both (E)-2-hexenal and-caryophyllene gave positive responses from spring migrants, and a mixture of the two compounds in the natural ratio was more attractive than (E)-2-hexenal alone. Addition of methyl salicylate eliminated the response to the active binary mixture.     

Cardenolides fromErysimum cheiranthoides: Feeding deterrents toPieris rapae larvae

Larvae of the cabbage butterfly,Pieris rapae, refuse to feed on the wild mustard,Erysimum cheiranthoides, due to the presence of alcoholextractable deterrents. The active components were extracted inton-BuOH, and this extract was separated into four fractions (I–IV) by reverse-phase HPLC. Fractions III and IV retained the feeding deterrent activity. The activity of fraction III was found to be due to the cardenolide diglycosides 1 and 2, which were previously reported as oviposition deterrents for gravidP. rapae butterflies. Three active compounds were isolated from fraction IV by column chromatography on silica gel followed by reverse-phase HPLC. These compounds were identified as a monoglycoside, digitoxigenin 3-O--D-glucoside (4), and two diglycosides, glucodigigulomethyloside (5) and glucodigifucoside (6). An additional cardenolide isolated from fraction II was identified as cheirotoxin (7). All compounds were identified by UV, NMR (¹H and¹³C), and mass spectrometry, as well as hydrolysis experiments. The feeding deterrent activity of these compounds was compared with that of related commercially available chemicals and other compounds isolated fromE. cheiranthoides.     

Isolation of the diterpenoids, ent-kauran-16alpha-ol and ent-atisan-16alpha-ol, from sunflowers, as oviposition stimulants for the banded sunflower moth, Cochylis hospes

Two diterpenoid alcohols, ent-kauran-16-ol (1) and ent-atisan-16-ol (2), were isolated from pre bloom (R3-R4 stage) sunflower heads as oviposition stimulants for the banded sunflower moth, Cochylis hospes. Fractionation of a sunflower head extract, by normal-phase flash column chromatography, resulted in an early eluting fraction exhibiting significant activity in an egg-laying bioassay. Compounds 1 and 2, along with ent-trachyloban- 19-oic acid (3) and ent-kaur-16-en-19-oic acid (4), were isolated as the major components of this fraction and identified by their NMR and mass spectra. The purified compounds were individually tested for ovipositional activity in dose-response bioassays. In these bioassays, compounds 1 and 2 gave linear dose responses, with increasing numbers of eggs laid as the dosage of either increased. Compounds 3 and 4 failed to stimulate significant egg-laying at any of the dosages tested. A factorial design bioassay, using compounds 1 and 2, showed that 1 was relatively more stimulatory than 2, and that there was no synergistic effect on oviposition when the two compounds were combined.     

Quantification of Invertase Activity in Ants Under Field Conditions

Invertases (EC 3.2.1.26) are hydrolases that cleave sucrose into the monosacccharides, glucose, and fructose. They play a central role in carbohydrate metabolism of plants and animals. Methods presented so far to quantify invertase activity in ants or other animals have been hampered by the variability in both substrates and products of the enzymatic reaction in animals whose carbohydrate metabolism is highly active. Our method is based on a spectrophotometric quantification of the kinetics of glucose release. We first obtained an equilibrium state summarizing reactions of any carbohydrates and enzymes that are present in the extract. Sucrose was then added to quantify invertase activity as newly released glucose. Invertase activities differed significantly among species of ants. Variances were lowest among individuals from the same colony and highest among different species. When preparations were made from ants of the same species, invertase activity was linearly related to the number of ants used for extraction. Our method does not require ants to be kept on specific substrates prior to the experiment, or expensive or large equipment. It, thus, appears suitable for dealing with a broad range of physiological, ecological, and evolutionary questions.     

Catalytic properties of new Cu based catalysts containing Zr and/or V for methanol synthesis from a carbon dioxide and hydrogen mixture

Pure unsupported copper is a poor catalyst for CH₃OH synthesis from CO₂+H₂ when it is compared to Cu coprecipitated with Zr or Zr+V in which case its selectivity and yield in methanol are strongly enhanced. The two Zr and V components added to pure Cu are shown to be textural promoters towards zerovalent Cu which participate to the building of the active sites. Methanol formation on these catalysts is a structure insensitive reaction with respect to the metallic Cu dosed by N₂O surface decomposition.     

Chemistry and Defensive Efficacy of Secretion of Burrowing Bug (Sehirus cinctus cinctus)

Adult Sehirus cinctus cinctus emit a volatile secretion from their metathoracic scent glands when tactually stimulated. We identified the volatile components by gas chromatography, high-performance liquid chromatography, and mass spectrometry. The secretion of both sexes contained (1R)-(+)--pinene, (1S)-(–)--pinene, -myrcene, (R)-(+)-limonene, and -terpinolene. Two additional compounds were found in only female secretions: (E)-2-hexenyl acetate and (E)-2-octenal. We also tested the defensive capability of this insect by offering it to various predators. Anoles, starlings, and a killdeer rejected S. c. cinctus after an initial sampling. These findings suggest that the secretion plays a defensive role.     

Polyimides based on “multiring” flexible diamines

The five benzene rings-containing (hereafter for convenience, referred to as five-ringrd) diamines ad-bis[4-(4-aminophenoxy)phenyl]-1,4 (or 1,3)-diisopropylbenzene (p- or m-3) were prepared by a nucleophilic substitution of ,-bis(4-hydroxyphenyl)-1, 4 (or 1,3)-diisopropylbenzene (p- or m-1) with p-chloronitrobenzene in the presence of K₂CO₃ and then hydro-reduced. The polyimides were synthesized from diamine 3 and various aromatic dianhydrides via the two-stage procedure that include ring-opening polyaddition in DMAc to give poly(amic acid)s, followed by thermal conversion to polyimides. The poly(amic acid)s had inherent viscosities of 0.63–1.54 dL/g depending on the dianhydrides used. Almost all the poly(amic acid)s could be solution-cast and thermally converted into transparent, flexible, and tough polyimide films. These polyimides have glass transition temperatures in the range of 186–290°C and almost no weight loss up to 500°C in air or nitrogen atmosphere. The polyimide obtained from pyromellitic dianhydride and diamine m-3 showed two endothermic peaks of 270 and 300°C on the diagram of differential scanning calorimetry (DSC), and the other polyimides showed no endotherms on their DSC traces.     

Platinum impregnated zeolite β as a reforming catalyst

It is shown that Pt impregnated zeolite has a high reforming capability for naphthenic feeds such as methylcyclopentane and methylcyclohexane, which are transformed in aromatic and cyclic saturated multibranched molecules with higher octane numbers. The temperature plays a major role in these reactions. The cycloolefinic intermediates produced by the dehydrogenation of the feed molecules are alkylated with the carbonium ions produced by the ring opening of other feed molecules. The disproportionation of the alkylated compounds is suggested to be responsible for the enlargement of the feed molecules. This disproportionation, the isomerization of the cycloolefinic intermediates, and some cracking particularly for methylcyclohexane, are proposed to be responsible for the product distribution under the present conditions.     

Stereospecific antennal response by red turpentine beetle,Dendroctonus valens to chiral monoterpenes from ponderosa pine resin

The antennal response ofDendroctonus valens to host monoterpenes from the resin of ponderosa pine was studied using the electroantennogram (EAG) technique. Male and female beetles were given a single dose of each of 11 different monoterpenes. Response amplitude to the different compounds did not vary between sexes and was generally well correlated with results from field attraction studies. Response to (S)-(–)--pinene was greatest. The relative amplitude of the responses to the (R)-(+) and (S)-(–) enantiomers of a-pinene, however, were reversed from their relative attractiveness in the field. A dose-response study was conducted for the (R)-(+) and (S) -(–) enantiomers of a-pinene, plus a reciprocal differential saturation test with successive doses of first one enantiomer of-pinene and then the other. Comparison of EAG traces suggests different receptors for the two stereoisomers of-pinene. Differential saturation curves suggest that while one set of receptors may respond to both enantiomers, some receptors respond only to the (S)-(–) enantiomer.     

Chiral specificity in responses by the bark beetleDendroctonus valens to host kairomones

The attraction of the red turpentine beetle,Dendroctonus valens, to the resin volatiles of its host,Pinus ponderosa, is elicited by three chiral monoterpenes. In field assays response was greatest to (S)-(–)--pinene; 92% (S)-(–)--pinene found inP ponderosa resin was not attractive. However, 75% (R)-(+)--pinene, which occurs inPinus lambertiana, a sympatric host ofD. valens, was attractive. (S)-(–)--Pinene interrupted response to (R)-(+)--pinene. (S)-(+)-3-Carene from both hosts was attractive at the (R)-(+)--pinene level. Three sympatric coniferous nonhosts each have the same attractive monoterpenes but produce less resin. These studies demonstrate the importance of chirality of host compounds in the host finding behavior of this bark beetle.     

Attraction of the Larval Predator Elater ferrugineus to the Sex Pheromone of Its Prey, Osmoderma eremita, and Its Implication for Conservation Biology

Elater ferrugineus is a threatened click beetle inhabiting old hollow trees. Its larvae consume larvae of other saproxylic insects including the threatened scarab beetle Osmoderma eremita. Recently, (R)-(+)-gamma-decalactone was identified as a male-produced sex pheromone of O. eremita. Here we present evidence that E. ferrugineus adults use this odor as a kairomone for location of their prey. In field trapping experiments, significantly more trapping events of E. ferrugineus beetles were observed in Lindgren funnel traps baited with (R)-(+)-gamma-decalactone than in control traps (20 vs. 1, respectively). Analyses of headspace collections from E. ferrugineus beetles indicate that the predator itself does not produce the substance. Both sexes were attracted to the prey pheromone. suggesting that E. ferrugineus males use the odor as an indirect cue for location of mates or of the tree hollows, which make up their habitat. When compared to pitfall traps, the Lindgren system was significantly more effective in trapping E. ferragineus, and no difference could be established for O. eremita, showing the high potential to use odor-based systems to catch both species. We suggest that (R)-(+)-gamma-decalactone could be used as a master signal in monitoring programs for these vulnerable beetle species. which are both regarded as indicators of the associated insect fauna of the threatened habitat of old hollow trees.     

Ontogeny of Alarm Pheromone Secretion in Pea Aphid, Acyrthosiphon pisum

When attacked by a predator, an aphid may secrete a droplet of fluid from its cornicles containing a volatile alarm pheromone component, (E)--farnesene. This study investigated both qualitative and quantitative aspects of alarm pheromone production in the pea aphid, Acyrthosiphon pisum. The best predictor of cornicle droplet emission was reproductive phase, rather than instar, as prereproductive aphids were more likely to secrete cornicle droplets than either reproductive or postreproductive individuals. Analogously, alarm pheromone amounts were highest in prereproductive aphids. (E)--Farnesene quantities (mean ± SE) increased significantly from first instar (1.5 ± 0.6 ng) to second instar (11.2 ± 3.7 ng) and did not significantly change during third (12.8 ± 3.0 ng) or fourth instars (11.0 ± 3.7 ng). Alarm pheromone amounts then decreased significantly in adults (4.8 ± 2.3 ng). We suggest that prereproductive aphids have been selected to produce higher levels of pheromone because of their more clustered colony structure and higher levels of predation, as compared with adult aphids.     

Protein-precipitating capacity of tannins inShorea (Dipterocarpaceae) seedling leaves

The protein-precipitating capacities of tanniferous extracts from immature and mature leaves of threeShorea spp. (Dipterocarpaceae) seedlings were measured by an adaptation of Goldstein and Swain's -glucosidase precipitation assay. Protein precipitation by the extracts was not correlated with total phenolics (Folin-Denis assay) or proanthocyanidin content (BuOH-HCl assay) as measured in an earlier study. Extracts ofS. maxwelliana mature leaves had much lower protein-precipitating capacity than those ofS. acuminata andS. leprosula, but fewer insect species feed on and cause less damage to the foliage ofS. maxwelliana compared with the other species' foliage. Immature leaf extracts ofS. leprosula andS. acuminata had substantial protein-precipitating capacities which in the latter species exceeded that of its mature leaf extracts. Leaf extracts precipitated less protein when initial protein concentration was reduced, although not limiting, but no effect or the reverse effect occurred with quebracho tannin and tannic acid. Problems in the characterization of foliage astringency and the interpretation of its role as a potential antiherbivore defense are discussed.     

Transesterification of β-Keto Esters Catalysed by Basic Porous Material

-keto esters have been successfully transesterified with primary, secondary, tertiary, allylic and alkynic alcohols in good yields using TBD anchored on MCM support for the first time. The hybrid solid base catalyst can be recycled several times with consistent activity.     

Allelochemical Potential of Callicarpa acuminata

The allelochemical potential of Callicarpa acuminata (Verbenaceae) was investigated by using a biodirected fractionation study as part of a long-term project to search for bioactive compounds among the rich biodiversity of plant communities in the Ecological Reserve El Eden, Quintana Roo, Mexico. Aqueous leachate, chloroform-methanol extract, and chromatographic fractions of the leaves of C. acuminata inhibited the root growth of test plants (23-70%). Some of these treatments caused a moderate inhibition of the radial growth of two phytopathogenic fungi, Helminthosporium longirostratum and Alternaria solani (18-31%). The chloroform-methanol (1:1) extract prepared from the leaves rendered five compounds: isopimaric acid (1), a mixture of two diterpenols [sandaracopimaradien-19-ol (3) and akhdarenol (4)], alpha-amyrin (5), and the flavone salvigenin (6)]. The phytotoxicity exhibited by several fractions and the full extract almost disappeared when pure compounds were evaluated on the test plants, suggesting a synergistic or additive effect. Compounds (4), (5), and the semisynthetic derivative isopimaric acid methyl ether (2) had antifeedant effects on Leptinotarsa decemlineata. Compound 5 was most toxic to this insect, followed by (2), (4), and (6) with moderate to low toxicity. No correlation was found between antifeedant and toxic effects on this insect, suggesting that different modes of action were involved. All the test compounds were cytotoxic to insect Sf9 cells while (6), (4), and (1) also affected mammalian Chinese Hamster Ovary (CHO) cells. Compound 5 showed the strongest selectivity against insect cells. This study contributes to the knowledge of the defensive chemistry and added value of C. acuminata.     

Sex attractant pheromone of the red-shouldered stink bug Thyanta pallidovirens: a pheromone blend with multiple redundant components

The male-produced sex pheromone of the red-shouldered stink bug, Thyanta pallidovirens (Stål) (Hemiptera: Pentatomidae) consists of a blend of methyl (E2,Z4,Z6)-decatrienoate (E2,Z4,Z6–10:COOMe), and the sesquiterpenes (+)-curcumene, (–)-zingiberene, and (–) --sesquiphellandrene. In laboratory bioassays, sexually mature males attracted sexually mature females but not males, and females did not attract either sex. Extracts of volatiles collected from sexually mature males contained compounds not present in extracts from females or sexually immature males, and male-produced extract was attractive to females. Biological activity was lost when the extract was fractionated, indicating that the pheromone consisted of at least two components having different chemical properties. Individually, pheromone components were not attractive to females, but E2,Z4,Z6–10:COOMe in combination with at least one of the three male-produced sesquiterpenes was attractive. The presence of more than one sesquiterpene in the blend did not increase attraction, indicating redundancy in the pheromone signal. Male extract was as attractive as a blend reconstructed from synthesized compounds, indicating all biologically active components had been identified. In bioassays conducted at dusk in a 1- × 1- × 1-m screen field cage, females were attracted to synthetic pheromone lures. In field trials, adult female T. pallidovirens were attracted to pheromone-baited traps in relatively low numbers. The profile of volatiles released by sexually mature males of a congeneric species, Thyanta accerra custator McAtee, was remarkably similar to that of male T. pallidovirens, with the exception that the former species produced (E)-2-decenal, a compound that was not found in T. pallidovirens extracts.     

Response of the Seven-spot Ladybird to an Aphid Alarm Pheromone and an Alarm Pheromone Inhibitor is Mediated by Paired Olfactory Cells

Electrophysiological responses of adult seven-spot ladybirds, Coccinella septempunctata, to (E)--farnesene, an aphid alarm pheromone, and (–)--caryophyllene, a plant-derived alarm pheromone inhibitor, were investigated by recording from single olfactory cells (neurons) on the antenna. Cells having high specificity for each of the two compounds were identified. Furthermore, these two cell types were frequently found in close proximity, with a larger amplitude consistently recorded for the cell responding specifically to (E)--farnesene. Preliminary behavioral studies in a two-way olfactometer showed that walking adults were significantly attracted to (E)--farnesene; this activity was inhibited with increasing proportions of (–)--caryophyllene. The possible ecological significance of colocation or pairing of olfactory cells for semiochemicals with different behavioral roles is discussed.     

Additional male mediterranean fruitfly (Ceratitis capitata wied.) Attractants from Angelica seed oil (Angelica archangelica L.)

Two sesquiterpene hydrocarbons, -copaene and -ylangene, were isolated from bioactive fractions of angelica seed oil and were shown by field bioassays to be attractive to the male Mediterranean fruit fly. Their relative attractiveness, compared with the(+)-and (–)--copaene enantiomers, are: (+)--copaene>angelica -copaene>angelica -ylangene>(–)--copaene. The enantiomer ratios for the two compounds are: -copaene, 61.4% (+), 38.6% (–); -ylangene, 91.9% (+), 8.1% (–).trans--Bergamotene was also isolated from the same fractions, but in sufficient quantity for bioassay [enantiomer ratio: 95.7% (+), 4.3% (–)].