<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Balkenius, A.</style></author><author><style face="normal" font="default" size="100%">Bisch-Knaden, S.</style></author><author><style face="normal" font="default" size="100%">Hansson, B.S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Interaction of visual and odour cues in the mushroom body of the hawkmoth Manduca sexta</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Experimental Biology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">BRAIN</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">MUSHROOM BODY</style></keyword><keyword><style  face="normal" font="default" size="100%">NEUROLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">OLFACTION</style></keyword><keyword><style  face="normal" font="default" size="100%">PETUNIA</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword><keyword><style  face="normal" font="default" size="100%">VISION</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2009</style></year></dates><volume><style face="normal" font="default" size="100%">212</style></volume><pages><style face="normal" font="default" size="100%">535-541</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;The responses to bimodal stimuli consisting of odour and colour were recorded using calcium-sensitive optical imaging in the mushroom bodies of the hawkmoth &lt;em&gt;Manduca sexta&lt;/em&gt;. The results show that the activity in the mushroom bodies is influenced by both olfaction and vision. The interaction between the two modalities depends on the odour and the colour of the visual stimulus. A blue stimulus suppressed the response to a general flower scent (phenylacetaldehyde). By contrast, the response to a green leaf scent (1-octanol) was enhanced by the presence of the blue stimulus. A green colour had no influence on these odours but caused a marked increase in the response to an odour component (benzaldehyde) of the hawkmoth-pollinated &lt;em&gt;Petunia axillaris&lt;/em&gt;.&amp;quot;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><section><style face="normal" font="default" size="100%">535</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Dahake, A.</style></author><author><style face="normal" font="default" size="100%">Jain, P.</style></author><author><style face="normal" font="default" size="100%">Vogt, C.C.</style></author><author><style face="normal" font="default" size="100%">Kandalaft, W.</style></author><author><style face="normal" font="default" size="100%">Stroock, A.D.</style></author><author><style face="normal" font="default" size="100%">Raguso, R.A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A signal-like role for floral humidity in a nocturnal pollination system</style></title><secondary-title><style face="normal" font="default" size="100%">Nature Communications</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">ADULT FEEDING</style></keyword><keyword><style  face="normal" font="default" size="100%">ADULT MORPHOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">ANATOMY</style></keyword><keyword><style  face="normal" font="default" size="100%">ANTENNAE</style></keyword><keyword><style  face="normal" font="default" size="100%">DATURA</style></keyword><keyword><style  face="normal" font="default" size="100%">ELECTROANTENNOGRAM</style></keyword><keyword><style  face="normal" font="default" size="100%">FLORAL HUMIDITY</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">PHYSIOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATION</style></keyword><keyword><style  face="normal" font="default" size="100%">SENSILLA</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword><keyword><style  face="normal" font="default" size="100%">STOMATA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">12/2022</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1038/s41467-022-35353-8</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">7773</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;Previous studies have considered floral humidity to be an inadvertent consequence of nectar evaporation, which could be exploited as a cue by nectarseeking pollinators. By contrast, our interdisciplinary study of a nightblooming flower, &lt;em&gt;Datura wrightii&lt;/em&gt;, and its hawkmoth pollinator, &lt;em&gt;Manduca sexta&lt;/em&gt;, reveals that floral relative humidity acts as a mutually beneficial signal in this system. The distinction between cue- and signal-based functions is illustrated by three experimental findings. First, floral humidity gradients in &lt;em&gt;Datura &lt;/em&gt;are nearly ten-fold greater than those reported for other species, and result from active (stomatal conductance) rather than passive (nectar evaporation) processes. These humidity gradients are sustained in the face of wind and are reconstituted within seconds of moth visitation, implying substantial physiological costs to these desert plants. Second, the water balance costs in &lt;em&gt;Datura &lt;/em&gt;are compensated through increased visitation by &lt;em&gt;Manduca &lt;/em&gt;moths, with concomitant increases in pollen export.We show that moths are innately attracted to humid flowers, even when floral humidity and nectar rewards are experimentally decoupled. Moreover, moths can track minute changes in humidity via antennal hygrosensory sensilla but fail to do so when these sensilla are experimentally occluded. Third, their preference for humid flowers benefits hawkmoths by reducing the energetic costs of flower handling during nectar foraging. Taken together, these findings suggest that floral humidity may function as a signal mediating the final stages of floral choice by hawkmoths, complementing the attractive functions of visual and olfactory signals beyond the floral threshold in this nocturnal plant-pollinator system.&amp;quot;&lt;/p&gt;
</style></abstract><section><style face="normal" font="default" size="100%">7773</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Fouelifack-Nintidem, B.</style></author><author><style face="normal" font="default" size="100%">Yetchom-Fondjo, J.A.</style></author><author><style face="normal" font="default" size="100%">Tsekane, S.J.</style></author><author><style face="normal" font="default" size="100%">Ngamaleu-Siewe, B.</style></author><author><style face="normal" font="default" size="100%">Kenne, E.L.</style></author><author><style face="normal" font="default" size="100%">Biawa-Kagmegni, M.</style></author><author><style face="normal" font="default" size="100%">Tuekam-Kowa, P.S.</style></author><author><style face="normal" font="default" size="100%">Yomon, A.K.</style></author><author><style face="normal" font="default" size="100%">Kentsop-Tsafong, R.M.</style></author><author><style face="normal" font="default" size="100%">Dim-Mbianda, A.M.</style></author><author><style face="normal" font="default" size="100%">Kenne, M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Diversity and abundance of pest insects associated with Solanum aethiopicum Linnaeus, 1756 (Solanaceae) in Balessing (West-Cameroon)</style></title><secondary-title><style face="normal" font="default" size="100%">American Journal of Entomology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">CAMEROON</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">PEST</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANUM</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09/2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">70-91</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;Despite chemical treatments, all development stages of &lt;em&gt;Solanum aethiopicum&lt;/em&gt; Linnaeus, 1756 plants are damaged in the field by insects in Balessing locality (West-Cameroon). During ecological surveys conducted from July to October 2020 in 11 plots presenting four development stages: seedlings (St1), fruit setting plants (St2), flowering phase plants (St3), and fruiting phase plants (St4). Insects active on stems, leaves, flowers and fruits, were captured, identified and the community structure was characterized. Abundance of each species and the part of the plant attacked were noted. Specimens were stored in vials containing 70&amp;deg; alcohol while immature insects were reared in the laboratory till the adult emergence. A total of 155 specimens collected in the field belonged to four orders, 13 families and 22 species. Lepidoptera and Hemiptera were most abundant (38.7% and 34.8% of the total collection respectively). Coleoptera and Orthoptera were least abundant (14.2% and 12.3% respectively). In the laboratory rearing, two Lepidoptera emerged from reared caterpillars: the Crambidae (&lt;em&gt;Leucinodes orbonalis&lt;/em&gt; Guenee, 1854) and the Noctuidae [&lt;em&gt;Helicoverpa armigera&lt;/em&gt; (H&amp;uuml;bner, 1808)]. This gives a total of four orders, 14 families, 22 genera and 23 species associated with eggplant plants. In the field, plants were damaged by three borer species (13.0%) [&lt;em&gt;Phrissotrichum grenieri &lt;/em&gt;(Desbrochers, 1875) (Coleoptera, Brentidae),&lt;em&gt; Le. orbonalis &lt;/em&gt;(Lepidoptera, Crambidae) and&lt;em&gt; H. armigera&lt;/em&gt; (Lepidoptera, Noctuidae)], by five phytophagous pest species (21.7%) [&lt;em&gt;Lagria villosa&lt;/em&gt; (Fabricius, 1781) (Coleoptera, Tenebrionidae), &lt;em&gt;Leptoglossus occidentalis&lt;/em&gt; Heidemann, 1910 (Hemiptera, Coreidae), &lt;em&gt;Manduca sexta&lt;/em&gt; Linnaeus, 1763 (Lepidoptera, Sphingidae), &lt;em&gt;Sphaerocoris annulus&lt;/em&gt; (Fabricius, 1775) (Hemiptera, Scutelleridae) and &lt;em&gt;Taphronota ferruginea &lt;/em&gt;(Fabricius, 1781) (Orthoptera, Pyrgomorphidae)], three sap-feeding species (13.0%) [&lt;em&gt;Dysdercus volkeri&lt;/em&gt; (Schmidt, 1932) (Hemiptera, Pyrrhocoridae), &lt;em&gt;Edessa rufomarginata&lt;/em&gt; (De Geer, 1773) (Hemiptera, Pentatomidae) and &lt;em&gt;Gonocerus acuteangularis &lt;/em&gt;(Goeze, 1778) (Hemiptera, Coreidae)] and 12 species of unknown pest-status. We recorded 11 pest species (47.8% of the total species richness) [six (26.1%) non-native and five (21.7%) native species]. Coleoptera presented a high number of species (34.8%) followed by Hemiptera (30.4%), Orthoptera (21.7%) and Lepidoptera (13.0%). Lepidoptera Crambidae (38.1%) was the most represented, followed by Hemiptera Pentatomidae (14.1%), Orthoptera Acrididae (10.2%), Hemiptera Coreidae and Hemiptera Pyrrhocoridae (7.7% respectively), Hemiptera Scutelleridae (5.2%), Coleoptera Tenebrionidae (5.1%), Coleoptera Chrysomelidae (4.5%), Orthoptera Pyrgomorphidae (3.9%) and Coleoptera Brentidae (1.3%). Three families (Carabidae, Sphingidae and Scarabeidae) were rare (&amp;lt;1% of the total collection). Chemicals were not efficient in Balessing, since entomofauna associated with eggplant plants remained diverse and consisted mostly of alien species. The situation calls for more research on the bio-ecology of the recorded pests with further goal of developing sustainable management strategies to reduce yield losses.&amp;quot;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><section><style face="normal" font="default" size="100%">70</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bing, J.</style></author><author><style face="normal" font="default" size="100%">Li, X.</style></author><author><style face="normal" font="default" size="100%">Haverkamp, A.</style></author><author><style face="normal" font="default" size="100%">Baldwin, I.T.</style></author><author><style face="normal" font="default" size="100%">Hansson, B.S.</style></author><author><style face="normal" font="default" size="100%">Knaden, M.</style></author><author><style face="normal" font="default" size="100%">Yon, F.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Variation in Manduca sexta pollination-related floral traits and reproduction in a wild tobacco plant</style></title><secondary-title><style face="normal" font="default" size="100%">Frontiers in Ecolology and Evolution</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">FLORAL MORPHOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">FLORAL SCENT</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">NICOTIANA</style></keyword><keyword><style  face="normal" font="default" size="100%">PHENOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">PHYSIOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATION</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATOR SPECIFICITY</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword><keyword><style  face="normal" font="default" size="100%">TRAITS</style></keyword><keyword><style  face="normal" font="default" size="100%">USA</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">9</style></volume><pages><style face="normal" font="default" size="100%">680463</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;Most flowering plants depend on animal pollination for successful sexual reproduction. Floral signals such as color, shape, and odor are crucial in establishing this (often mutualistic) interaction. Plant and pollinator phenotypes can vary temporally but also spatially, thus creating mosaic-like patterns of local adaptations. Here, we investigated natural variation in floral morphology, flower volatile emission, and phenology in four accessions of a self-compatible wild tobacco, &lt;em&gt;Nicotiana attenuata&lt;/em&gt;, to assess how these traits match the sensory perception of a known pollinator, the hawkmoth &lt;em&gt;Manduca sexta&lt;/em&gt;. These accessions differ in floral traits and also in their habitat altitudes. Based on habitat temperatures, the accession occurring at the highest altitude (California) is less likely to be visited by&lt;em&gt; M. sexta&lt;/em&gt;, while the others (Arizona, Utah 1, and Utah 2) are known to receive &lt;em&gt;M. sexta&lt;/em&gt; pollinations. The accessions varied significantly in flower morphologies, volatile emissions, flower opening, and phenology, traits likely important for &lt;em&gt;M. sexta&lt;/em&gt; perception and floral handling. In wind tunnel assays, we assessed the seed set of emasculated flowers after &lt;em&gt;M. sexta&lt;/em&gt; visitation and of natural selfed and hand-pollinated selfed flowers. After moth visitations, plants of two accessions (Arizona and Utah 2) produced more capsules than the other two, consistent with predictions that accessions co-occurring with &lt;em&gt;M. sexta&lt;/em&gt; would benefit more from the pollination services of this moth. We quantified flower and capsule production in four accessions in a glasshouse assay without pollinators to assess the potential for self-pollination. The two Utah accessions set significantly more seeds after pollen supplementation compared with those of autonomous selfing flowers, suggesting a greater opportunistic benefit from efficient pollinators than the other two. Moreover, emasculated flowers of the accession with the most exposed stigma (Utah 2) produced the greatest seed set after &lt;em&gt;M. sexta&lt;/em&gt; visitation. This study reveals intraspecific variation in pollination syndromes that illuminate the potential of a plant species to adapt to local pollinator communities, changing environments, and altered pollination networks.&amp;quot;&lt;/p&gt;
</style></abstract><section><style face="normal" font="default" size="100%">680463</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yamamoto, R. T.</style></author><author><style face="normal" font="default" size="100%">Fraenkel, G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Assay of the principal gustatory stimulant for the Tobacco Hornworm, {IProtoparce sexta}, from solanaceous plants</style></title><secondary-title><style face="normal" font="default" size="100%">Annals of the Entomological Society of America</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">FOODPLANT SPECIFICITY</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">PHYSIOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1960</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1960</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">53</style></volume><pages><style face="normal" font="default" size="100%">499-503</style></pages><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yamamoto, R.T.</style></author><author><style face="normal" font="default" size="100%">Fraenkel, G.S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">The specificity of the Tobacco Hornworm, Protoparce sexta, to solanaceous plants</style></title><secondary-title><style face="normal" font="default" size="100%">Annals of the Entomological Society of America</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">FOODPLANT</style></keyword><keyword><style  face="normal" font="default" size="100%">FOODPLANT SPECIFICITY</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1960</style></year><pub-dates><date><style  face="normal" font="default" size="100%">07/1960</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://academic.oup.com/aesa/article-abstract/53/4/503/28955</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">53</style></volume><pages><style face="normal" font="default" size="100%">503-507</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">4</style></issue><section><style face="normal" font="default" size="100%">503</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Yamamoto, R.T.</style></author><author><style face="normal" font="default" size="100%">Fraenkel, G.S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Assay of the principal gustatory stimulant for the tobacco hornworm, Protoparce sexta, from solanaceous plants</style></title><secondary-title><style face="normal" font="default" size="100%">Annals of the Entomological Society of America</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">FOODPLANT CHEMISTRY</style></keyword><keyword><style  face="normal" font="default" size="100%">FOODPLANT SPECIFICITY</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">PHYSIOLOGY</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1960</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1960</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1093/aesa/53.4.503</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">53</style></volume><pages><style face="normal" font="default" size="100%">499-503</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;Oviposition and feeding of the tobacco hornworm arc almost entirely restricted to plants of the family Solinaceae. Oviposition appears to be initiated by olfactory stimuli widely distributed in this plant family, and consequently it, is largely suppressed in the absence of host plants or after excision of the antennae. Both in the field and laboratory, the moths preferred tomato foliage over other solanaceous plants for oviposition. Larval feeding appears to be governed by gustatory stimuli common to plants of this family. On certain ones, such as &lt;em&gt;Nicandra&lt;/em&gt; and &lt;em&gt;Petunia&lt;/em&gt;, feeding and growth are limited by the presence of repellents or toxins. Some limited feeding occurred on certain nonsolanaceous plants after various periods of starvation.&amp;quot;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><section><style face="normal" font="default" size="100%">499</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Winz, R. A.</style></author><author><style face="normal" font="default" size="100%">Baldwin, I. T.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Molecular interactions between ... Manduca sexta (Lepidoptera, Sphingidae) and its natural host Nicotiana attenuata. IV. Insect-induced ethylene reduces jasmonate-induced nicotine accumulation by regulating putrescine N-methyltransferase transcripts</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Physiology</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">FOODPLANT</style></keyword><keyword><style  face="normal" font="default" size="100%">FOODPLANT CHEMISTRY</style></keyword><keyword><style  face="normal" font="default" size="100%">HERBIVORY</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2001</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2001</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">125</style></volume><pages><style face="normal" font="default" size="100%">2189-2202</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Full title: Molecular interactions between the specialist herbivore Manduca sexta (Lepidoptera, Sphingidae) and its natural host Nicotiana attenuata. IV. Insect-induced ethylene reduces jasmonate-induced nicotine accumulation by regulating putrescine N-methyltransferase transcripts.&lt;/p&gt;
</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Williams, E. L.</style></author><author><style face="normal" font="default" size="100%">Howe, G. 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size="100%">AGRIUS</style></keyword><keyword><style  face="normal" font="default" size="100%">APIS</style></keyword><keyword><style  face="normal" font="default" size="100%">CACTACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">DATURA</style></keyword><keyword><style  face="normal" font="default" size="100%">FLORAL SCENT</style></keyword><keyword><style  face="normal" font="default" size="100%">HYLES</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">NECTAR COMPOSITION</style></keyword><keyword><style  face="normal" font="default" size="100%">PENIOCEREUS</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATION</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATOR SPECIFICITY</style></keyword><keyword><style  face="normal" font="default" 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font="default" size="100%">SPAIN</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">1977</style></year><pub-dates><date><style  face="normal" font="default" size="100%">1977</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">87</style></volume><pages><style face="normal" font="default" size="100%">95-96</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><section><style face="normal" font="default" size="100%">95</style></section></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nattero, J.</style></author><author><style face="normal" font="default" size="100%">Moré, M.</style></author><author><style face="normal" font="default" size="100%">Sérsic, A.N.</style></author><author><style face="normal" font="default" size="100%">Cocucci, A.A.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Possible tobacco progenitors share long-tongued hawkmoths as pollen vectors</style></title><secondary-title><style face="normal" font="default" size="100%">Plant Systematics and Evolution</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AGRIUS</style></keyword><keyword><style  face="normal" font="default" size="100%">BATS</style></keyword><keyword><style  face="normal" font="default" size="100%">HYBRIDS</style></keyword><keyword><style  face="normal" font="default" size="100%">MANDUCA</style></keyword><keyword><style  face="normal" font="default" size="100%">NICOTIANA</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATION</style></keyword><keyword><style  face="normal" font="default" size="100%">POLLINATOR SPECIFICITY</style></keyword><keyword><style  face="normal" font="default" size="100%">SOLANACEAE</style></keyword><keyword><style  face="normal" font="default" size="100%">SPHINGIDAE</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2003</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2003</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">241</style></volume><pages><style face="normal" font="default" size="100%">47-54</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;&amp;quot;The putative ancestors of the allopolyploid hybrid &lt;i&gt;Nicotiana tabacum&lt;/i&gt; have distinct flower features, apparently suited either for hawkmoth or bat pollination. This suggests that progenitors were reproductively isolated by mechanical and ethological barriers. However, the present data show that in natural populations pollen vectors could be shared by two of the possible progenitors. Pollen vectors of one of the possible male progenitors (&lt;i&gt;N. otophora&lt;/i&gt;) were short- and long-tongued hawkmoths and a nectar-feeding bat, while those of the female ancestor (&lt;i&gt;N. sylvestris&lt;/i&gt;) were only long-tongued hawkmoths. The latter are then the most likely vectors responsible for the presumed spontaneous hybridization. These data also suggest that interspecific pollen transfer occurred more likely in one direction.&amp;quot;&lt;/p&gt;
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