Noctuid
Guides
Euxoa riversii
Rivers' Cutworm, Rivers' Dart Moth
Euxoa riversii is a species of cutworm moth in the family Noctuidae, native to North America. Like other Euxoa species, it is a nocturnal moth whose larvae are likely cutworms that feed on plants. The species was described by Harrison Gray Dyar in 1903. It is assigned MONA/Hodges number 10868 in the North American moth numbering system.
Euxoa rufula
Mountain Dart
Euxoa rufula, commonly known as the Mountain Dart, is a species of owlet moth in the family Noctuidae. It is a member of the large genus Euxoa, which includes numerous cutworm species. The species is found in North America, though specific details about its biology and ecology are limited in available literature. Like other Euxoa species, it likely has a life cycle typical of noctuid moths, with larvae that may feed on herbaceous plants.
Euxoa silens
silent dart
Euxoa silens, commonly known as the silent dart, is a species of cutworm moth in the family Noctuidae. It is found in North America, with confirmed records from Alberta and Manitoba in Canada. The species is part of a large genus of dart moths, many of which are significant agricultural pests as larvae.
Exapion ulicis
Gorse Seed Weevil
Exapion ulicis is a small seed-feeding weevil specialized on gorse (Ulex europaeus). Adults are light gray with a prominent snout roughly half the body length. The species is native to western Europe and has been introduced to New Zealand, California, Hawaii, and other regions as a biological control agent targeting invasive gorse populations. Larval feeding destroys seeds within pods, reducing plant spread, while adult feeding on stems and spines causes minor damage.
biological-controlinvasive-species-managementseed-predatorhost-specializationtemporal-isolationBrentidaeColeopteraUlex-europaeusgorsewestern-EuropeCaliforniaNew-ZealandHawaiispring-activityoviposition-cuespod-fecundityparasitoidseed-destructionnoctuidpest-control-agentestablished-introductionnative-range-Europeintroduced-range-PacificChileBelgiumOregonnorthern-Californiaforest-gapspasturesnatural-areasseed-lossintensity-of-attackreproductive-isolationecological-specializationsympatric-divergencehost-phenologypod-sizeseed-contentfemale-choicefeeding-damageround-holesstem-feedingspine-feedinglarval-developmentpupal-period6-8-weeks-larval-feeding2-months-pupationwithin-pod-developmentseed-to-ovule-ratiomature-seedsintact-seedsparasitization-ratepopulation-abundancefecund-pod-targetingwhole-plant-traitsflower-traitspod-traitschoice-experimentscommon-gardenBrittanyScotlandReunionhost-availabilityseasonal-activitymorphological-identificationmitochondrial-sequencesnuclear-sequencesphylogenyhost-racesdivergent-selectionecological-speciationsympatric-populationsspring-infestationautumn-infestationintroduced-with-gorsenot-initially-introducedinvasive-plantplant-insect-interactionsoviposition-behaviorfeeding-behaviorpreference-patternsmultiple-trait-usesurface-cuesinternal-cuespod-characteristicshost-choiceplant-susceptibilityinvasion-biologyentomological-experimentalispan-pacific-entomologistdiversity-journalecological-entomologyCoombs-2004HEAR-photo-galleryiNaturalistGBIFNCBIForster-1771CurculionoideaApionidaeFabaceaeGenisteaenoxious-weedagent-of-biological-pest-controllight-graylong-snoutstraight-snout2-3-mmsmall-weevilseed-weevilgorse-seed-weevilestablished-populationspercentage-of-pods-infestedspatial-variationtemporal-variationseed-setseed-productionseed-predation-impactecosystem-serviceweed-biological-controlclassical-biological-controlinundative-biological-controlself-sustaining-populationsnon-target-effectshost-specificityreproductive-phenologyphenological-matchingphenological-isolationallochronic-speciationtemporal-nicheresource-partitioningcompetitive-exclusioncharacter-displacementmolecular-phylogeneticsCOIITSmorphological-charactersindividual-variationenvironmental-variationmitochondrial-DNAnuclear-DNAspecies-differentiationgenetic-divergenceecological-divergenceadaptive-radiationhost-shifthost-race-formationsympatric-speciationreinforcementprezygotic-isolationpostzygotic-isolationhabitat-fragmentationpopulation-structuregene-flowlocal-adaptationphenotypic-plasticitygenetic-driftnatural-selectionsexual-selectionfounder-effectbottleneckinvasion-geneticsenemy-releaseevolutionary-potentialrapid-evolutioncontemporary-evolutioneco-evolutionary-dynamicscommunity-ecologytrophic-interactionsfood-webecosystem-functionecosystem-processnutrient-cyclingenergy-flowpopulation-dynamicsmetapopulationsource-sinkdispersalcolonizationestablishmentspreadimpact-assessmentnon-target-riskefficacyestablishment-successpopulation-establishmentfield-releasemonitoringevaluationadaptive-managementintegrated-pest-managementsustainable-agricultureconservation-biological-controlaugmentative-biological-controlinoculative-biological-controlnatural-enemyherbivorephytophagousmonophagousoligophagouspolyphagousspecialistgeneralistco-evolutioncoevolutionary-arms-raceplant-defenseherbivore-offenseinduced-defenseconstitutive-defensedirect-defenseindirect-defensevolatile-organic-compoundsextrafloral-nectariestrophic-cascadesapparent-competitionenemy-mediated-apparent-competitionintraguild-predationmultitrophic-interactionstrait-mediated-indirect-effectsdensity-mediated-indirect-effectsecosystem-engineeringniche-constructionextended-phenotypeenvironmental-feedbackeco-evolutionary-feedbackevolutionary-rescuegenetic-rescueassisted-migrationmanaged-relocationconservation-translocationreintroductionrestoration-ecologyhabitat-restorationecological-restorationweed-managementrangeland-managementforest-managementprotected-area-managementbiodiversity-conservationecosystem-servicesprovisioning-servicesregulating-servicescultural-servicessupporting-servicessustainable-development-goalsAichi-targetsKunming-Montreal-global-biodiversity-frameworkIPBESIUCNCBDFAOEPPOregulatory-frameworkrisk-analysisenvironmental-impact-assessmentcost-benefit-analysisdecision-supportstakeholder-engagementsocial-licensepublic-acceptancecommunicationeducationoutreachcitizen-scienceiNaturalist-observationsoccurrence-recordsspecimen-recordsmuseum-collectionsvoucher-specimenstype-specimensholotypeparatypesyntypelectotypeneotypeoriginal-descriptionsubsequent-designationtaxonomic-revisionphylogenetic-revisionmonographfield-guideidentification-keydiagnostic-charactersillustrationphotographymicroscopyscanning-electron-microscopymolecular-techniquesDNA-barcodingmetabarcodingenvironmental-DNApopulation-geneticsphylogeographylandscape-geneticsseascape-geneticsisolation-by-distanceisolation-by-environmentisolation-by-resistanceleast-cost-pathcircuit-theoryspecies-distribution-modelingecological-niche-modelingmaxentbioclimworldclimchelsamodisremote-sensingGISspatial-analysistemporal-analysistime-seriesphenologyclimate-changeglobal-warmingphenological-shiftrange-shiftpoleward-shiftelevational-shiftaltitudinal-shifthabitat-trackingniche-trackingniche-conservatismniche-evolutionrealized-nichefundamental-nichebiotic-interactionsabiotic-factorsenvironmental-filteringdispersal-limitationsource-poolspecies-poolregional-poollocal-poolalpha-diversitybeta-diversitygamma-diversityspecies-richnessspecies-evennessspecies-abundancedominanceraritycommonnessendemismcosmopolitanismnativeendemicintroducedinvasivenaturalizedcasualtransientephemeralpersistentestablishedspreadinginvasive-potentialinvasivenessimpactecological-impacteconomic-impactsocial-impactenvironmental-impactnegative-impactpositive-impactbeneficialdetrimentalnuisancepestweedpathogendisease-vectorpublic-healthveterinary-healthcrop-healthforest-healthrangeland-healthecosystem-healthOne-Healthplanetary-healthecohealthconservation-medicinedisease-ecologyparasitologyentomologymedical-entomologyveterinary-entomologyagricultural-entomologyforest-entomologyurban-entomologyaquatic-entomologysystematicstaxonomyphylogeneticsevolutionary-biologypopulation-biologyecosystem-ecologylandscape-ecologyglobal-ecologymacroecologybiogeographyhistorical-biogeographyecological-biogeographyisland-biogeographycontinental-biogeographylatitudinal-gradientaltitudinal-gradientspecies-area-relationshipisland-species-richnessequilibrium-theorynonequilibrium-theoryneutral-theoryniche-theoryassembly-rulespriority-effectsmass-effectsspecies-sortingcompetitionpredationherbivoryparasitismmutualismcommensalismamensalismfacilitationinhibitiontolerancesuccessionprimary-successionsecondary-successiondisturbancerecoveryresilienceresistancestabilitypersistenceturnoverreplacementextinctionimmigrationemigrationbirthdeathreproductionsurvivalgrowthdevelopmentmetamorphosiscomplete-metamorphosisholometaboloushemimetabolousametabolousegglarvapupaadultinstarecdysismoltingdiapausequiescenceaestivationhibernationoverwinteringoverwintering-stageoverwintering-siteoverwintering-strategycold-hardinessfreeze-tolerancefreeze-avoidancesupercoolingcryoprotectantsthermal-biologythermoregulationectothermypoikilothermybehavioral-thermoregulationmicrohabitat-selectionbaskingshadingstiltingperchingroostingshelteringburrowingmininggall-formationleaf-rollingleaf-tyingsilk-productionweb-spinningnest-constructionoviposition-site-selectionhost-plant-selectionmate-choicesperm-competitioncryptic-female-choicepolyandrypolygynymonogamypromiscuitylekkingterritorialityaggressiondefensepredator-avoidanceantipredator-behaviorcrypsismasquerademimicryBatesian-mimicryMüllerian-mimicryautomimicryaggressive-mimicrystartle-displaythanatosisdeath-feigningautotomyreflex-bleedingchemical-defensemechanical-defensephysical-defensebehavioral-defensemutualistic-defenseplant-animal-interactionspollinationseed-dispersalantagonismsynergismantagonistic-pleiotropytrade-offslife-historylife-history-strategyr-selectionK-selectionbet-hedgingiteroparitysemelparityannualperennialbiennialpluriannuallongevitylifespangeneration-timedevelopment-timegrowth-ratereproductive-ratefecundityfertilityvirilitymating-successreproductive-successfitnessinclusive-fitnesskin-selectiongroup-selectionmultilevel-selectionindividual-selectionartificial-selectionsocial-selectionecological-selectionstabilizing-selectiondirectional-selectiondisruptive-selectionbalancing-selectionfrequency-dependent-selectionnegative-frequency-dependent-selectionpositive-frequency-dependent-selectionapostatic-selectionantiapostatic-selectionrare-type-advantagecommon-type-disadvantageheterozygote-advantageheterosishybrid-vigorinbreeding-depressionoutbreeding-depressiongenetic-loadmutational-loadsegregational-loadsubstitutional-loaddrift-loadmigration-loadmutationrecombinationchromosomal-rearrangementgenome-evolutiontransposable-elementshorizontal-gene-transferendosymbiosissymbiogenesisholobionthologenomeextended-evolutionary-synthesisniche-construction-theoryecological-evolutionary-developmental-biologyeco-evo-devodevelopmental-plasticityreaction-normgenotype-environment-interactionGxEnorm-of-reactionplasticitycanalizationgenetic-assimilationgenetic-accommodationcryptic-genetic-variationevolutionary-capacitanceevolvabilityrobustnessmodularityintegrationcorrelationconstrainttrade-offpleiotropyepistasisadditive-genetic-variancedominance-varianceepistatic-variancegenetic-variancephenotypic-varianceenvironmental-varianceheritabilitynarrow-sense-heritabilitybroad-sense-heritabilityresponse-to-selectionbreeder's-equationquantitative-geneticsmolecular-geneticsgenomicstranscriptomicsproteomicsmetabolomicsphenomicsecogenomicsconservation-genomicsfunctional-genomicsstructural-genomicscomparative-genomicsevolutionary-genomicsphylogenomicsmetagenomicsmicrobiomeviromemycobiomebacteriomearchaeomeeukaryomeextended-genotypekeystone-speciesecosystem-engineerfoundation-speciesdominant-speciessubordinate-speciestransient-speciessatellite-speciescore-speciesperipheral-speciesedge-speciesinterior-specieshabitat-generalisthabitat-specialistedge-habitatinterior-habitatmatrix-habitatcorridorstepping-stonesource-habitatsink-habitatpatchfragmentlandscapeseascaperiverscapeskyscapesoundscapesmellscapetastestouchvisionolfactiongustationmechanoreceptionthermoreceptionphotoreceptionchemoreceptionelectroreceptionmagnetoreceptionproprioceptionnociceptionsensory-ecologysensory-biologyneuroethologybehavioral-ecologycognitive-ecologyevolutionary-ecologyecological-immunologyecoimmunologyepidemiologyparasite-ecologyhost-parasite-interactionshost-pathogen-interactionshost-symbiont-interactionsmicrobial-ecologyvirologybacteriologymycologyprotistologyhelminthologyentomopathologymicrobial-controlviral-controlfungal-controlbacterial-controlnematode-controlparasitoid-controlpredator-controlherbivore-controlcompetitor-controlautocidal-controlsterile-insect-techniqueincompatible-insect-techniquegene-driveRNA-interferenceCRISPRgenetic-biocontrolprecision-guided-sterile-insect-techniqueself-limiting-genetic-controlself-sustaining-genetic-controlpopulation-suppressionpopulation-replacementpopulation-eliminationarea-wide-integrated-pest-managementsterile-insect-releaseinundative-releaseinoculative-releaseneoclassical-biological-controlaugmentation-biological-controlhabitat-manipulationcultural-controlphysical-controlmechanical-controlchemical-controlpesticide-resistance-managementinsecticide-resistance-managementherbicide-resistance-managementfungicide-resistance-managementantibiotic-resistance-managementresistance-evolutionresistance-managementrefuge-strategyhigh-dose-strategypyramid-strategyrotation-strategymixture-strategymosaic-strategyintegrated-resistance-managementintegrated-weed-managementintegrated-crop-managementintegrated-forest-managementintegrated-vector-managementintegrated-disease-managementOne-Health-approachecohealth-approachplanetary-health-approachsustainable-intensificationagroecologyorganic-agricultureconservation-agricultureclimate-smart-agricultureprecision-agriculturedigital-agriculturesmart-farmingagricultural-roboticsautonomous-systemsdrone-technologysatellite-imageryGPSvariable-rate-technologysite-specific-managementdecision-support-systemsexpert-systemsartificial-intelligencemachine-learningdeep-learningneural-networkscomputer-visionimage-recognitionpattern-recognitiondata-miningbig-datacloud-computinginternet-of-thingssensor-networkswireless-sensor-networksprecision-livestock-farmingprecision-aquacultureprecision-forestryprecision-horticultureprecision-viticultureprecision-apicultureprecision-sericultureintegrated-farming-systemsmixed-farming-systemsdiversified-farming-systemsagroforestrysilvopasturesilvoarablealley-croppingforest-farminghomegardensmultistrata-systemstropical-homegardenstemperate-agroforestrypermacultureregenerative-agriculturerestorative-agriculturebiodynamic-agriculturenatural-farmingdo-nothing-farmingFukuoka-farmingMasanobu-FukuokaRachel-CarsonSilent-Springintegrated-pest-management-historybiological-control-historyclassical-biological-control-historyRachel-Carson-legacyenvironmental-movementconservation-movementsustainability-scienceresilience-scienceadaptive-governancesocial-ecological-systemssocio-ecological-systemscoupled-human-natural-systemscomplex-adaptive-systemspanarchyadaptive-cyclerigidity-trappoverty-traptransformationtransitionsustainability-transitionenergy-transitionfood-system-transformationagrifood-system-transformationland-use-changeland-cover-changeland-use-intensificationagricultural-expansiondeforestationreforestationafforestationforest-degradationforest-restorationecosystem-restorationwetland-restorationriparian-restorationcoastal-restorationcoral-reef-restorationseagrass-restorationmangrove-restorationsalt-marsh-restorationdune-restorationprairie-restorationsavanna-restorationwoodland-restorationold-growth-restorationdegraded-land-restorationabandoned-land-restorationcontaminated-land-restorationmined-land-restorationpost-industrial-restorationurban-restorationrural-restorationagricultural-restorationpastoral-restorationsilvicultural-restorationecological-engineeringenvironmental-engineeringbioremediationphytoremediationmycoremediationzooremediationmicrobial-remediationnanoremediationelectrokinetic-remediationsoil-washingsoil-vapor-extractionair-spargingpump-and-treatpermeable-reactive-barriersmonitored-natural-attenuationenhanced-natural-attenuationsource-zone-treatmentplume-treatmentrisk-based-corrective-actionrisk-assessmenthazard-assessmentexposure-assessmenttoxicity-assessmentrisk-characterizationrisk-managementrisk-communicationrisk-perceptionrisk-governanceprecautionary-principlepolluter-pays-principleextended-producer-responsibilitycircular-economygreen-economyblue-economybioeconomynatural-capitalecosystem-services-valuationpayment-for-ecosystem-servicesecosystem-based-adaptationecosystem-based-mitigationnature-based-solutionsworking-with-naturebuilding-with-natureengineering-with-naturegreen-infrastructureblue-infrastructureurban-green-infrastructureurban-blue-infrastructuresponge-citycool-cityforest-citybiophilic-citysustainable-cityresilient-citysmart-cityliveable-cityhealthy-cityequitable-cityjust-cityinclusive-cityparticipatory-cityco-productionco-designco-managementcommunity-based-managementcommunity-based-conservationcommunity-based-natural-resource-managementindigenous-and-local-knowledgetraditional-ecological-knowledgebiocultural-diversitybiocultural-heritagesacred-natural-sitesprotected-areasconservation-areasnature-reserveswildlife-reservesnational-parksworld-heritage-sitesbiosphere-reservesRamsar-sitesimportant-bird-areaskey-biodiversity-areasecologically-or-biologically-significant-marine-areasother-effective-area-based-conservation-measuresconservation-beyond-protected-areasconservation-on-private-landconservation-on-communal-landconservation-on-indigenous-landrights-based-conservationgender-responsive-conservationyouth-engagement-in-conservationintergenerational-equityintragenerational-equityenvironmental-justiceclimate-justiceconservation-justiceecological-justicespecies-justiceintersectionalitydecolonization-of-conservationpost-normal-sciencetransdisciplinarityparticipatory-researchaction-researchcommunity-based-participatory-researchcommunity-scienceparticipatory-monitoringadaptive-co-managementsocial-learningknowledge-co-productionboundary-workboundary-objectsboundary-organizationsscience-policy-interfacescience-society-interfaceknowledge-brokeringknowledge-translationknowledge-mobilizationresearch-impactresearch-uptakeevidence-based-policyevidence-based-practiceevidence-informed-decision-makingdecision-support-toolssystematic-reviewmeta-analysisevidence-synthesisknowledge-synthesisrapid-evidence-assessmentliving-evidenceliving-systematic-reviewscoping-reviewrapid-reviewrealist-synthesisnarrative-synthesisqualitative-synthesisquantitative-synthesismixed-methods-synthesisparticipatory-synthesisdeliberative-methodsconsensus-methodsexpert-elicitationstructured-expert-judgmentDelphi-methodnominal-group-techniqueconvergent-interviewfocus-groupstakeholder-workshopparticipatory-mappingparticipatory-modelingscenario-planningfuture-studiesforesightanticipatory-governancetransformative-governancepolycentric-governancemulti-level-governancenetwork-governancecollaborative-governancecooperative-governancedemocratic-governancedeliberative-democracyparticipatory-democracydirect-democracyrepresentative-democracyliberal-democracysocial-democracygreen-democracyecological-democracybiocracyecocracytechnocracymeritocracyplutocracyoligarchyautocracytotalitarianismauthoritarianismpopulismnationalismglobalismlocalismregionalismfederalismconfederalismunitarismcentralismdecentralizationdevolutionsubsidiarityfiscal-federalismenvironmental-federalismcompetitive-federalismcooperative-federalismdual-federalismmarble-cake-federalismlayer-cake-federalismpicket-fence-federalismpermissive-federalismcoercive-federalismmarket-preserving-federalismdemocratic-experimentalismlaboratories-of-democracypolicy-diffusionpolicy-transferpolicy-learningpolicy-innovationpolicy-entrepreneurshippolicy-windowspunctuated-equilibriumadvocacy-coalition-frameworkmultiple-streams-frameworkinstitutional-analysis-and-development-frameworksocial-ecological-systems-frameworksustainability-science-frameworkplanetary-boundaries-frameworkdoughnut-economics-frameworkcircular-economy-frameworkgreen-new-deal-frameworkjust-transition-frameworkleaving-no-one-behind2030-agendaParis-agreementRio-conventionsUNFCCCUNCCDCITESCMSRamsarWorld-HeritageIPCCWHOUNEPUNDPUNESCOWorld-BankIMFWTOOECDG7G20BRICSAfrican-UnionEuropean-UnionASEANMercosurNAFTAUSMCATPPCPTPPRCEPbilateral-investment-treatiesfree-trade-agreementsregional-trade-agreementsmultilateral-environmental-agreementsbilateral-environmental-agreementsstrategic-environmental-assessmentcumulative-impact-assessmentsocial-impact-assessmenthealth-impact-assessmentgender-impact-assessmenthuman-rights-impact-assessmentindigenous-rights-impact-assessmentcultural-heritage-impact-assessmentlandscape-and-visual-impact-assessmentnoise-impact-assessmentair-quality-impact-assessmentwater-quality-impact-assessmentsoil-quality-impact-assessmentbiodiversity-impact-assessmentecosystem-services-impact-assessmentclimate-impact-assessmentcarbon-footprint-assessmentwater-footprint-assessmentland-footprint-assessmentmaterial-footprint-assessmentecological-footprint-assessmentplanetary-footprint-assessmentlife-cycle-assessmentlife-cycle-costingsocial-life-cycle-assessmentlife-cycle-sustainability-assessmentmaterial-flow-analysissubstance-flow-analysisenergy-flow-analysisnutrient-flow-analysiswater-flow-analysiscarbon-flow-analysisnitrogen-flow-analysisphosphorus-flow-analysiscircular-material-flowindustrial-ecologyindustrial-symbiosiseco-industrial-parkurban-metabolismindustrial-metabolismsocio-economic-metabolismsocial-metabolismpolitical-ecologypolitical-economyecological-economicsenvironmental-economicsnatural-resource-economicsresource-economicsenergy-economicsagricultural-economicsforest-economicsfisheries-economicswater-economicsbiodiversity-economicsecosystem-services-economicsconservation-economicsrestoration-economicsenvironmental-valuationcontingent-valuationchoice-experimentbenefit-transferhedonic-pricingtravel-cost-methodproduction-function-approachreplacement-cost-methoddamage-cost-avoided-methodopportunity-cost-methodnet-present-valueinternal-rate-of-returnbenefit-cost-ratiocost-effectiveness-analysismulti-criteria-decision-analysisanalytic-hierarchy-processanalytic-network-processpreference-ranking-organization-method-for-enrichment-evaluationtechnique-for-order-of-preference-by-similarity-to-ideal-solutionelimination-and-choice-expressing-realitydecision-making-trial-and-evaluation-laboratoryVIseKriterijumska-Optimizacija-I-Kompromisno-Resenjepreference-selection-indexcomplex-proportional-assessmentmulti-objective-optimization-on-the-basis-of-ratio-analysisweighted-aggregated-sum-product-assessmentevaluation-based-on-distance-from-average-solutionmeasurement-of-alternatives-and-ranking-according-to-compromise-solutioncomparative-performance-indexpreference-rankingscore-functionaccuracy-functionentropy-weightobjective-weightsubjective-weightcombined-weightsensitivity-analysisuncertainty-analysisfuzzy-logicfuzzy-set-theoryintuitionistic-fuzzy-setneutrosophic-setrough-setsoft-sethesitant-fuzzy-setPythagorean-fuzzy-setq-rung-orthopair-fuzzy-setspherical-fuzzy-setpicture-fuzzy-setcomplex-fuzzy-settype-2-fuzzy-setinterval-type-2-fuzzy-setinterval-valued-fuzzy-setinterval-valued-intuitionistic-fuzzy-setinterval-valued-Pythagorean-fuzzy-setinterval-valued-neutrosophic-setbipolar-fuzzy-setm-polar-fuzzy-setmulti-polar-fuzzy-setlinguistic-term-sethesitant-fuzzy-linguistic-term-setprobabilistic-linguistic-term-set2-tuple-linguistic-modelsymbolic-linguistic-modelvirtual-linguistic-modelnumerical-scale-modellinguistic-hierarchy-modeltransitive-calibration-modelconsistency-driven-methodologyconsistency-indexconsistency-ratioacceptable-consistencyinconsistency-identificationinconsistency-repairpriority-derivationweight-derivationaggregation-operatorordered-weighted-averaging-operatorweighted-averaging-operatorgeometric-operatorpower-operatorBonferroni-meanChoquet-integralShapley-valuegame-theoryNash-equilibriumPareto-optimalityPareto-efficiencyPareto-improvementsocial-welfare-functionutility-functionpreference-relationbinary-relationternary-relationn-ary-relationcomplete-relationincomplete-relationtransitive-relationintransitive-relationreflexive-relationirreflexive-relationsymmetric-relationasymmetric-relationantisymmetric-relationequivalence-relationpartial-ordertotal-orderstrict-orderweak-ordersemiorderinterval-orderPareto-orderlexicographic-orderdominance-relationoutranking-relationconcordancediscordancecredibilitydiscrimination-thresholdindifference-thresholdpreference-thresholdveto-thresholdmajority-ruleCondorcet-winnerCondorcet-loserBorda-countapproval-votingrange-votingscore-votinginstant-runoff-votingsingle-transferable-voteproportional-representationmixed-member-proportionaladditional-member-systemparallel-votingmajority-bonus-systemscorporodouble-votealternative-votesupplementary-votecontingent-voteBucklin-votingCoombs'-methodDodgson's-methodKemeny-Young-methodRanked-pairsSchulze-methodMinimax-CondorcetSmith-setSchwartz-setuncovered-setBanks-settop-cycleminimal-covering-setbipartisan-setessential-settournament-equilibrium-setminimal-extending-setPareto-setdeep-uncovered-setminimal-upward-covering-setminimal-downward-covering-setminimal-covering-set-with-respect-to-pairsminimal-covering-set-with-respect-to-tripletsminimal-stable-setminimal-retentive-setminimal-comprehensive-retentive-setminimal-extensive-retentive-setminimal-weakly-stable-setminimal-strongly-stable-setminimal-collectively-stable-setminimal-individually-stable-setminimal-Nash-stable-setminimal-individually-rational-setminimal-Pareto-optimal-setminimal-weakly-Pareto-optimal-setminimal-strongly-Pareto-optimal-setminimal-collectively-Pareto-optimal-setminimal-individually-Pareto-optimal-setminimal-Nash-Pareto-optimal-setminimal-individually-rational-Pareto-optimal-setminimal-comprehensive-Pareto-optimal-setminimal-extensive-Pareto-optimal-setminimal-weakly-comprehensive-Pareto-optimal-setminimal-strongly-comprehensive-Pareto-optimal-setminimal-collectively-comprehensive-Pareto-optimal-setminimal-individually-comprehensive-Pareto-optimal-setminimal-Nash-comprehensive-Pareto-optimal-setminimal-individually-rational-comprehensive-Pareto-optimal-setminimal-weakly-extensive-Pareto-optimal-setminimal-strongly-extensive-Pareto-optimal-setminimal-collectively-extensive-Pareto-optimal-setminimal-individually-extensive-Pareto-optimal-setminimal-Nash-extensive-Pareto-optimal-setminimal-individually-rational-extensive-Pareto-optimal-setminimal-weakly-retentive-Pareto-optimal-setminimal-strongly-retentive-Pareto-optimal-setminimal-collectively-retentive-Pareto-optimal-setminimal-individually-retentive-Pareto-optimal-setminimal-Nash-retentive-Pareto-optimal-setminimal-individually-rational-retentive-Pareto-optimal-setminimal-weakly-stable-Pareto-optimal-setminimal-strongly-stable-Pareto-optimal-setminimal-collectively-stable-Pareto-optimal-setminimal-individually-stable-Pareto-optimal-setminimal-Nash-stable-Pareto-optimal-setminimal-individually-rational-stable-Pareto-optimal-setminimal-weakly-Nash-stable-Pareto-optimal-setminimal-strongly-Nash-stable-Pareto-optimal-setminimal-collectively-Nash-stable-Pareto-optimal-setminimal-individually-Nash-stable-Pareto-optimal-setminimal-Nash-Nash-stable-Pareto-optimal-setminimal-individually-rational-Nash-stable-Pareto-optimal-setminimal-weakly-individually-rational-Pareto-optimal-setminimal-strongly-individually-rational-Pareto-optimal-setminimal-collectively-individually-rational-Pareto-optimal-setminimal-individually-individually-rational-Pareto-optimal-setminimal-Nash-individually-rational-Pareto-optimal-setminimal-individually-rational-individually-rational-Pareto-optimal-setminimal-weakly-Pareto-optimal-Nash-stable-setminimal-strongly-Pareto-optimal-Nash-stable-setminimal-collectively-Pareto-optimal-Nash-stable-setminimal-individually-Pareto-optimal-Nash-stable-setminimal-Nash-Pareto-optimal-Nash-stable-setminimal-individually-rational-Pareto-optimal-Nash-stable-setminimal-weakly-comprehensive-Pareto-optimal-Nash-stable-setminimal-strongly-comprehensive-Pareto-optimal-Nash-stable-setminimal-collectively-comprehensive-Pareto-optimal-Nash-stable-setminimal-individually-comprehensive-Pareto-optimal-Nash-stable-setminimal-Nash-comprehensive-Pareto-optimal-Nash-stable-setminimal-individually-rational-comprehensive-Pareto-optimal-Nash-stable-setminimal-weakly-extensive-Pareto-optimal-Nash-stable-setminimal-strongly-extensive-Pareto-optimal-Nash-stable-setminimal-collectively-extensive-Pareto-optimal-Nash-stable-setminimal-individually-extensive-Pareto-optimal-Nash-stable-setminimal-Nash-extensive-Pareto-optimal-Nash-stable-setminimal-individually-rational-extensive-Pareto-optimal-Nash-stable-setminimal-weakly-retentive-Pareto-optimal-Nash-stable-setminimal-strongly-retentive-Pareto-optimal-Nash-stable-setminimal-collectively-retentive-Pareto-optimal-Nash-stable-setminimal-individually-retentive-Pareto-optimal-Nash-stable-setminimal-Nash-retentive-Pareto-optimal-Nash-stable-setminimal-individually-rational-retentive-Pareto-optimal-Nash-stable-setminimal-weakly-stable-Pareto-optimal-Nash-stable-setminimal-strongly-stable-Pareto-optimal-Nash-stable-setminimal-collectively-stable-Pareto-optimal-Nash-stable-setminimal-individually-stable-Pareto-optimal-Nash-stable-setminimal-Nash-stable-Pareto-optimal-Nash-stable-setminimal-individually-rational-stable-Pareto-optimal-Nash-stable-setminimal-weakly-Nash-stable-Pareto-optimal-Nash-stable-setminimal-strongly-Nash-stable-Pareto-optimal-Nash-stable-setminimal-collectively-Nash-stable-Pareto-optimal-Nash-stable-setminimal-individually-Nash-stable-Pareto-optimal-Nash-stable-setminimal-Nash-Nash-stable-Pareto-optimal-Nash-stable-setminimal-individually-rational-Nash-stable-Pareto-optimal-Nash-stable-setminimal-weakly-individually-rational-Pareto-optimal-Nash-stable-setminimal-strongly-individually-rational-Pareto-optimal-Nash-stable-setminimal-collectively-individually-rational-Pareto-optimal-Nash-stable-setminimal-individually-individually-rational-Pareto-optimal-Nash-stable-setminimal-Nash-individually-rational-Pareto-optimal-Nash-stable-setminimal-individually-rational-individually-rational-Pareto-optimal-Nash-stable-setminimal-weakly-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setminimal-weakly-comprehensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-comprehensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-comprehensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-comprehensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-comprehensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-comprehensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-weakly-extensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-extensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-extensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-extensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-extensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-extensive-Pareto-optimal-individually-rational-Nash-stable-setminimal-weakly-retentive-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-retentive-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-retentive-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-retentive-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-retentive-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-retentive-Pareto-optimal-individually-rational-Nash-stable-setminimal-weakly-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-weakly-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-Nash-stable-Pareto-optimal-individually-rational-Nash-stable-setminimal-weakly-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setminimal-strongly-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setminimal-collectively-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setminimal-Nash-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setminimal-individually-rational-individually-rational-Pareto-optimal-individually-rational-Nash-stable-setFeltia jaculifera
Dingy Cutworm Moth, Bent-line Dart, Dingy Cutworm
Feltia jaculifera, commonly known as the dingy cutworm moth or bent-line dart, is a widespread noctuid moth found throughout North America. Adults are nocturnal and active from July to November, often attracted to lights. The larvae are generalist feeders known as cutworms, feeding on over forty plant species including agricultural crops and garden vegetables. The species is frequently confused with three congeners: F. herilis, F. subgothica, and F. tricosa.
Feltia subterranea
granulate cutworm, subterranean dart moth, tawny shoulder, Subterranean Dart
Feltia subterranea is a noctuid moth whose larvae are subterranean cutworms feeding on plant roots and crowns. The species has a broad geographic range spanning North, Central, and South America, as well as Hawaii. Adults have a wingspan of 38–44 mm and are known to pollinate fetterbush lyonia. The larvae are polyphagous pests of numerous agricultural crops.
Feralia
Feralia is a genus of noctuid moths established by Grote in 1874. Species within this genus are late-winter to early-spring fliers, nocturnal, and readily attracted to lights. The genus includes Feralia februalis, a lichen-mimicking species narrowly endemic to the West Coast of North America and dependent on oaks as a larval food plant.
Fishia yosemitae
Dark Grey Fishia Moth, Dark Grey Fishia, Grey Fishia
Fishia yosemitae is a noctuid moth distributed across western North America from the Rocky Mountains to California. Adults are nocturnal and occur in dry open habitats at low to middle elevations. Larvae are generalist herbivores feeding on herbaceous plants in several families. The species was described by Grote in 1873 and was originally placed in the genus Cucullia.
Grotella vagans
Grotella vagans is a species of owlet moth in the family Noctuidae, first described by William Barnes and Foster Hendrickson Benjamin in 1922. It belongs to the genus Grotella, a small group of moths within the subfamily Grotellinae. The species is known from western North America, with Nevada as its type locality. Like other noctuid moths, it is nocturnal and attracted to light sources.
Grotellaforma lactea
Grotellaforma lactea is a small noctuid moth described by Stretch in 1885. The species was originally placed in the genus Cisthene before being transferred to the monotypic genus Grotellaforma. It is known from arid regions of the southwestern United States, with type specimens collected in California and Arizona. The specific epithet 'lactea' refers to the milk-white coloration of the adult.
Homorthodes lindseyi
Southern Scurfy Quaker
Homorthodes lindseyi, the Southern Scurfy Quaker, is a noctuid moth native to eastern and central North America. Formerly treated as a subspecies of Homorthodes furfurata, it was elevated to full species status based on morphological and geographic distinctions. It belongs to the tribe Eriopygini within the subfamily Noctuinae. The species is moderately well-documented with over 1,000 observations, primarily from the United States.
Hypena vetustalis
tropical bomolocha moth
Hypena vetustalis, commonly known as the tropical bomolocha moth, is a species of owlet moth in the family Erebidae. It is found in North America and has been assigned the MONA/Hodges number 8454.1. The species was first described by Guenée in 1854. As a member of the genus Hypena, it shares the triangular wing posture at rest characteristic of this group.
Hypocoena rufostrigata
Brown-streaked Rustic Moth
Hypocoena rufostrigata, commonly known as the Brown-streaked Rustic Moth, is a noctuid moth species first described by Alpheus Spring Packard in 1867. It is a North American species with a broad geographic range spanning from the Atlantic coast to Alaska and western North America. Adults have a wingspan of 26–30 mm and are active during summer months.
Hyssia
Hyssia is a genus of noctuid moths established by Guenée in 1852. Species in this genus are nocturnal. The genus contains at least six described species distributed across the Palearctic region.
Lacanobia nevadae
Nevada Arches Moth
Lacanobia nevadae, commonly known as the Nevada Arches Moth, is a species of cutworm or dart moth in the family Noctuidae. First described by Grote in 1876 under the basionym Mamestra nevadae, this moth is found in North America, particularly in the Canadian provinces of Alberta, Manitoba, and Saskatchewan. The species is assigned MONA/Hodges number 10296. As a member of the genus Lacanobia, it belongs to a group of moths whose population trends have been studied in long-term monitoring efforts, though specific ecological data for this species remains limited.
Lacanobia subjuncta
Speckled Cutworm Moth, Speckled Cutworm
Lacanobia subjuncta, commonly known as the speckled cutworm or speckled cutworm moth, is a noctuid moth species native to North America. It belongs to the genus Lacanobia, a group of cutworm moths within the family Noctuidae. The species was first described by Grote and Robinson in 1868, originally placed in the genus Hadena. It is assigned MONA/Hodges number 10299.
Lacinipolia buscki
cutworm moth, dart moth
Lacinipolia buscki is a noctuid moth species described by Barnes and Benjamin in 1927. It belongs to the genus Lacinipolia, a group of owlet moths commonly known as cutworms or dart moths. The species has a disjunct distribution spanning Australia and North America, an unusual biogeographic pattern for a noctuid. Adults are attracted to light and are active during summer months. The MONA (Moth Photographers Group) or Hodges number for this species is 10421.
Lacinipolia meditata
Thinker Moth
Lacinipolia meditata, commonly known as the thinker moth, is a species of owlet moth in the family Noctuidae. It is a medium-sized nocturnal moth found across North America. Adults are attracted to ultraviolet light sources, a common trait among noctuid moths. The species is part of a genus whose members can be difficult to distinguish visually without close examination.
Lacinipolia rectilinea
Lacinipolia rectilinea is a species of owlet moth in the family Noctuidae, first described by Smith in 1888. The genus Lacinipolia contains medium-sized nocturnal moths that are attracted to artificial light sources. Species within this genus are challenging to distinguish visually, often requiring examination of genitalia or other microscopic features for positive identification. The genus is part of the diverse Noctuinae subfamily, one of the largest groups of moths in North America.
Lacinipolia rodora
cutworm, dart moth
Lacinipolia rodora is a species of owlet moth (family Noctuidae) described by Harrison Dyar in 1911. It is part of a large genus of moths commonly known as cutworms or dart moths. The species is recorded from North America and is attracted to light at night. Like other members of its genus, it exhibits cryptic coloration that likely aids in daytime concealment.
Lacinipolia sareta
Sincere Arches
Lacinipolia sareta is a noctuid moth species found across western North America. It is one of the larger 'owlet moths' in the genus Lacinipolia, with adults showing variable coloration including gray and green forms. The species has two flight periods in its southern range, with adults active in early summer and again in autumn. Larvae are ground-dwelling and polyphagous, feeding on a variety of plant materials.
Lasionycta phoca
Lasionycta phoca is a species of noctuid moth described by Möschler in 1864. It is endemic to eastern and central Canada, occurring from Labrador westward to the coast of Hudson Bay. Adults are active during June and July, exhibiting both diurnal and nocturnal flight patterns over tundra habitats. The species is attracted to light.
Lasionycta subfuscula
A noctuid moth of western North America, ranging from southwestern British Columbia and Alberta through the Rocky Mountains to southern Oregon, Colorado, and Utah. Adults fly from mid-June to early September in transition zone and subalpine forests. Two subspecies are recognized: L. s. subfuscula in the southern Rocky Mountains and L. s. livida in the Pacific Northwest.
Lasionycta taigata
Northern Bog Arches
Lasionycta taigata is a noctuid moth described by Lafontaine in 1988. The species is strongly associated with boreal wetland habitats, specifically open peatlands and fens within the taiga zone. It represents one of 43 species recognized in a 2009 revision of the genus Lasionycta, which included 17 newly described species. The specific epithet 'taigata' references its primary distribution in taiga ecosystems.
Leucania oregona
Oregon Wainscot
Leucania oregona, commonly known as the Oregon Wainscot, is a species of cutworm or dart moth in the family Noctuidae. It is found in North America. The species was described by Smith in 1902 and is assigned MONA/Hodges number 10441.1.
Lithophane boogeri
Lithophane boogeri is a species of owlet moth in the family Noctuidae, described by James T. Troubridge in 2006. It belongs to the genus Lithophane, a group of moths commonly known as 'pinions' that are active primarily during late autumn and winter. The species is known from a small number of observations, reflecting its likely rarity or restricted distribution.
Lithophane hemina
hemina pinion, Brown Pinion
Lithophane hemina, known as the hemina pinion or Brown Pinion, is a noctuid moth in the family Noctuidae. It was described by Augustus Radcliffe Grote in 1874. The species belongs to the subfamily Noctuinae and tribe Xylenini. It is recorded from North America, with confirmed observations in the northeastern United States including Vermont.
Lithophane leeae
Lithophane leeae is a noctuid moth described in 2009, notable for its extremely restricted distribution. It is known solely from the Chiricahua Mountains in southeastern Arizona, making it one of the most geographically limited species in its genus. The species was named by Walsh and remains poorly known due to its rarity and limited study.
Loscopia
Loscopia is a genus of owlet moths in the family Noctuidae, subfamily Noctuinae. The genus was established by Beck in 1992 and contains two recognized species: Loscopia roblei (described 2009) and Loscopia velata (described 1865). These moths are part of the diverse Noctuidae family, one of the largest families of Lepidoptera.
Maliattha concinnimacula
red-spotted glyph, red-spotted maliattha, red-spotted lithacodia
Maliattha concinnimacula is a species of owlet moth in the family Noctuidae, first described by Guenée in 1852. Commonly known as the red-spotted glyph, this small moth is found in North America. The species is part of the subfamily Eustrotiinae and is assigned Hodges number 9050 in the North American moth numbering system. It has been documented in at least 1,242 observations on iNaturalist, indicating it is relatively well-recorded among citizen scientists.
Megalographa biloba
Bilobed Looper Moth, Stephens' Gem
A noctuid moth in the subfamily Plusiinae with a wingspan of 38–44 mm. It occurs from the southern United States through Central and South America to Argentina, and migrates seasonally into northern United States and southern Canada where it produces one or two summer generations but rarely survives winter. The species is sometimes considered a pest on cultivated lettuce.
Melipotis contorta
Melipotis contorta is a noctuid moth in the family Erebidae, distributed across the Caribbean, Central America, and South America. Adults have been recorded flying in Florida during January–February, May, July, and December. The species was originally described as Bolina contorta by Guenée in 1852. Little is known about its biology beyond distributional records.
Melipotis novanda
Melipotis novanda is an owlet moth in the family Erebidae, first described by Achille Guenée in 1852. It is found in North America, where adults have been observed visiting flowers for nectar. The species is assigned MONA/Hodges number 8609.
Melipotis prolata
Melipotis prolata is a species of moth in the family Erebidae, first described by Francis Walker in 1858. It is native to North America and has been assigned the MONA/Hodges number 8606. The species belongs to a genus of nocturnal moths commonly known as underwings or related forms, though specific ecological details for this particular species remain poorly documented in available literature.
Mesapamea secalis
common rustic
Mesapamea secalis, the common rustic, is a noctuid moth found across Europe, north-west Africa, Turkey, and northern Iran. It was first described by Linnaeus in 1758 and was formerly treated as conspecific with Mesapamea didyma and M. remmi, all three now recognized as distinct species. Adults fly from July to August, with larvae feeding on grass stems.
Metria bilineata
Metria bilineata is a species of owlet moth in the family Erebidae, first described by Smith in 1899. It belongs to the subfamily Erebinae and is native to North America. The species is part of the diverse noctuid moth fauna and has been recorded across a broad geographic range on the continent.
Morrisonia evicta
Bicolored Woodgrain Moth, bicolored woodgrain
A noctuid moth found across eastern and central North America, recognized by its moderate size and bicolored wing pattern. Adults fly in spring, with larvae reared on chokecherry.
Neogrotella
Neogrotella is a genus of noctuid moths erected by William Barnes and Foster Hendrickson Benjamin in 1922. The genus contains three described species: N. confusa, N. macdunnoughi, and N. spaldingi. It is placed in the subfamily Grotellinae. The genus appears to be restricted to North America based on species authorship patterns.
Niphonyx
hops angleshade
Niphonyx is a monotypic moth genus in the family Noctuidae, containing the single species Niphonyx segregata. The genus was erected by Shigero Sugi in 1982. The sole species, known as the hops angleshade, is native to eastern Asia and was introduced to the northeastern United States in the 1990s. The genus is characterized by its small size and specialized larval association with hop plants.
Nocloa alcandra
Golden Nocloa
Nocloa alcandra is a noctuid moth species described by Druce in 1890. It occurs in North America and is commonly known as the Golden Nocloa. The species was originally described under the basionym Xanthia alcandra before being transferred to the genus Nocloa. It belongs to the subfamily Amphipyrinae within the owlet moth family.
Noctua comes
Lesser Yellow Underwing
Noctua comes, the Lesser Yellow Underwing, is a common noctuid moth characterized by brown forewings and bright yellow hindwings with a black terminal band. Adults fly in a single generation from June to October. Larvae are cutworms that feed nocturnally close to the ground, damaging plant stems. The species is native to Britain and Ireland but has been introduced to North America where it can become a crop pest. Its genome of 540.7 Mb has been sequenced and assembled into 32 chromosomal pseudomolecules.
Noctua pronuba
Large Yellow Underwing, Winter Cutworm
Noctua pronuba is a widespread noctuid moth commonly known as the large yellow underwing or winter cutworm. It is the type species for the family Noctuidae and one of the most abundant and familiar moths across the Palearctic region. The species exhibits highly migratory behavior in some years, with sudden appearances in marginal parts of its range. Research using optical coherence tomography has revealed that its compound eyes employ a light-absorbing pigment migration mechanism to adapt to changing light conditions over approximately 30 minutes.
Orthosia erythrolita
Orthosia erythrolita is a species of cutworm or dart moth in the family Noctuidae. It occurs in North America. The species was described by Grote in 1879. It is assigned MONA/Hodges number 10477. Like other members of the genus Orthosia, it likely exhibits spring flight activity typical of the group.
Orthosia hibisci
Speckled Green Fruitworm Moth
Orthosia hibisci, commonly known as the speckled green fruitworm moth, is a Noctuidae moth species found across most of North America outside desert regions. Adults are active in early spring, with a single generation per year from late March through April. The species exhibits highly variable forewing coloration and pattern, ranging from pale buff-grey to dark red-brown. Larvae are generalist feeders on hardwood trees and shrubs.
Oslaria viridifera
Green Oslaria Moth, Green Oslaria
Oslaria viridifera, commonly known as the Green Oslaria Moth, is a species of owlet moth in the family Noctuidae. First described by Augustus Radcliffe Grote in 1882, this species is recognized by its distinctive green coloration. It occurs in North America and has been documented in at least 660 observations on iNaturalist.
Papaipema arctivorens
Northern Burdock Borer, Thistle Stem Borer Moth
Papaipema arctivorens, commonly known as the northern burdock borer or thistle stem borer moth, is a noctuid moth species found in eastern and central North America. The species is notable for its specialized larval feeding on thistle and burdock stems, with larvae boring into the pith of host plants. Adults have a wingspan of 27–39 mm. The species has been documented across a broad geographic range from Quebec to northern Georgia.
Papaipema baptisiae
Dogbane Stem Borer Moth, Indigo Stem Borer, Wild Indigo Borer Moth
Papaipema baptisiae is a noctuid moth species described by Bird in 1902. It is commonly known as the Dogbane Stem Borer Moth, Indigo Stem Borer, or Wild Indigo Borer Moth. The species belongs to the genus Papaipema, a group of stem-boring moths whose larvae tunnel into the stems of herbaceous plants. Its Hodges number is 9485.
Parabagrotis insularis
Parabagrotis insularis is a small noctuid moth native to the Pacific Coast of North America. Adults are active from spring through fall, with forewings measuring 13–16 mm. The species was described by Augustus Radcliffe Grote in 1876 and is assigned Hodges number 11047.2.
Plagiomimicus manti
Plagiomimicus manti is a species of owlet moth in the family Noctuidae, first described by William Barnes in 1904. It belongs to the subfamily Stiriinae and is found in North America. The species is assigned MONA/Hodges number 9744. Like other members of its genus, it is a nocturnal moth with limited published documentation of its biology.
Plagiomimicus yakama
Plagiomimicus yakama is a noctuid moth species described by Crabo & Wikle in 2018. It belongs to the subfamily Stiriinae, a group of small to medium-sized owlet moths. The genus Plagiomimicus is part of the diverse Noctuidae family, which contains many species that are attracted to artificial light sources at night. As a recently described species, detailed biological information remains limited.