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147 results for “Lures”
Figure 1 in The lure of hidden death: development of an attract-and-kill strategy against Agriotes obscurus (Coleoptera: Elateridae) combining semiochemicals and entomopathogenic nematodes
Figure 1. Proportion of dead wireworms over time after the application of different nematode strains (χ2 = 57.76, p <0.001). Hb stands for Heterorhabditis bacteriophora, Sc stands for Steinernema carpocapsae, and Sf stands for Steinernema feltiae. Control corresponds to absence of EPNs. The stars indicate that the concerned strains are responsible for a significantly higher mortality (Tukey HSD; p <0.05).
Figure 4 in The lure of hidden death: development of an attract-and-kill strategy against Agriotes obscurus (Coleoptera: Elateridae) combining semiochemicals and entomopathogenic nematodes
Figure 4. Proportion of dead wireworms according to nematode populations across time. Light bars correspond to the treatments without potato extract (χ2 = 0.96; p = 0.62), and the dark bars correspond to the treatments with addition of potato extract (χ2 = 6.50; p = 0.01). Error bars represent 95% confidence intervals.
Figure 1 in Mosquito (Diptera: Culicidae) species richness and abundance across a tree-height gradient: does adding CO enhance the BG-Lure?
Figure 1. Study Site and Sampling Setting. (A) Monroe County in Indiana, USA. (B) Hickory Ridge Fire Tower and Nearest Weather Station within Monroe County. (C) BG-pro mosquito trap in CDC style. (D) Tower canopy height gradient. / Figura 1. Sitio de estudio y metodologÍa de muestreo. (A) Condado Monroe, Indiana, Estados Unidos. (B) Torre de avistamiento de incendios y estación meteorológica más cercana dentro del Condado Monroe. (C) Trampa de mosquitos BG-pro configurada en estilo CDC. (D) Gradiente de altitud arbórea.
Fig. 1 in Effect of storage of pheromone lures for Amyelois transitella: field performance and compound ratios
Fig. 1. Cumulative total of males (mean and SE, n = 4) captured by Suterra NOW Biolure acquired in 2013, 2014, or 2015, or by Trécé NOW-L2L or NOWL2H during 4-week periods between lure change. Sets of lures were tested during Mar through Jun of 2015 as follows: (a) 1 Mar to 26 Mar; (b) 26 Mar to 23 Apr; (c) 23 Apr to 21 May; and (d) 21 May to 25 Jun. Means with different super- scripts are significantly different (ANOVA, experiment-wise P <0.05).
Fig. 2 in Effect of storage of pheromone lures for Amyelois transitella: field performance and compound ratios
Fig. 2. Effect of time of storage on emission of C23 pentaene by NOW Biolure. Emission rate of pheromone components was evaluated by GC-MS in Jun 2015 for lures purchased prior to the field season in 2013,2014, and 2015. Lures were stored at –20 °C prior to analysis. The rate of pentaene emission is expressed as a percentage of the rate of emission of Z11,Z13-16:Ald. Means with different letters are significantly different (ANOVA, P <0.05).
Fig. 1 in Evaluation of pheromone traps and lures for trapping male Agriotes sputator (Coleoptera: Elateridae) beetles in eastern Canada
Fig. 1. Vernon beetle trap (A) and Vernon pitfall trap (B) designed for collecting Agriotes obscurus, Agriotes lineatus, and Agriotes sputator click beetles, shown installed for optimum capture in the field.
Fig. 2 in Evaluation of pheromone traps and lures for trapping male Agriotes sputator (Coleoptera: Elateridae) beetles in eastern Canada
Fig. 2. Capture of Agriotes sputator using Vernon pitfall traps baited with commercial and experimental lures throughout the swarming season in 3 fields in Prince Edward Island, Canada. Note the close correspondence between the 2 lure types in 2017, but not in 2016. Primed lures were placed at room temperature 3 wk before deployment, whereas non-primed lures were kept at −20 °C until deployment
Figure 2 in Commercial Lure Comparison for Monitoring of Cryptophlebia spp. (Lepidoptera: Tortricidae) Associated with Macadamia in Hawai'i
Figure 2. Mean ± SEM number of male C. illepida moths captured in traps, baited with different commercially manufactured lures, deployed in Kea'au from November 2021 to January 2022.
Figure 1 in Commercial Lure Comparison for Monitoring of Cryptophlebia spp. (Lepidoptera: Tortricidae) Associated with Macadamia in Hawai'i
Figure 1. Mean ± SEM number of male C. ombrodelta moths captured in traps, baited with different commercially manufactured lures, deployed in Kea'au (A) and Kapa'au (B) from November 2021 to January 2022.
Figure 5 in Trapping Pestiferous Fruit Flies (Diptera: Tephritidae): Additional Studies on the Performance of Solid Bactrocera Male Lures and Separate Insecticidal Strips Relative to Standard Liquid Lures
Figure 5. Captures of Bactrocera cucurbitae males in traps baited with toxicants of variable age. Data for DDVP strips weathered in Arizona and Florida are given in top and bottom plots, respectively. While toxicant age varied among treatments, the lure was fresh (no weathering) in all treatments. All traps were baited with fresh liquid CL, except the Fresh DDVP treatment which employed a fresh CL plug. Height of bar represents mean number of males captured per trap (n = 15 traps per treatment) in a 24-h period; error bars are + 1 SE. No significant variation existed among treatments for either Arizona (F = 2.5, P = 0.07) or Florida (F = 0.5, P = 0.66). Bars sharing a letter did not differ significantly (P> 0.05).
Figure 1 in Trapping Pestiferous Fruit Flies (Diptera: Tephritidae): Additional Studies on the Performance of Solid Bactrocera Male Lures and Separate Insecticidal Strips Relative to Standard Liquid Lures
Figure 1. (A) CL plug contained in two face-to-face perforated baskets along with Plato strip (red object). (B) ME wafer with plastic basket holding DDVP strip affixed. Photos show the lures and DDVP strips only, and when deployed in the field, these were housed in Jackson traps.
Figure 3 in Trapping Pestiferous Fruit Flies (Diptera: Tephritidae): Additional Studies on the Performance of Solid Bactrocera Male Lures and Separate Insecticidal Strips Relative to Standard Liquid Lures
Figure 3. Captures of Bactrocera dorsalis males in traps baited with toxicants of variable age. Data for DDVP strips weathered in Arizona and Florida are given in top and bottom plots, respectively. While toxicant age varied among treatments, the lure was fresh (no weathering) in all treatments. All traps were baited with fresh liquid ME, except the Fresh DDVP treatment which employed a fresh ME wafer. Height of bar represents mean number of males captured per trap (n = 15 traps per treatment) in a 24-h period; error bars are + 1 SE. Significant variation existed among treatments for Arizona (F = 3.7, P = 0.02) but not for Florida (H = 1.8, P = 0.61); bars sharing a letter did not differ significantly (P> 0.05).
Figure 2 in Trapping Pestiferous Fruit Flies (Diptera: Tephritidae): Additional Studies on the Performance of Solid Bactrocera Male Lures and Separate Insecticidal Strips Relative to Standard Liquid Lures
Figure 2. Captures of Bactrocera dorsalis males in traps baited with ME lures of variable age. Data for wafers weathered in Arizona and Florida are given in top and bottom plots, respectively. While lure age varied among treatments, the toxicant was fresh (no weathering) in all treatments. Liquid was applied to a cotton wick; in all other cases ME was presented in a polymeric wafer. Height of bar represents mean number of males captured per trap (n = 15 traps per treatment) in a 24-h period; error bars are + 1 SE. Significant variation existed among treatments for both Arizona (F = 10.5, P <0.001) and Florida (F = 11.0, P <0.001); bars sharing a letter did not differ significantly (P> 0.05).
Figure 4 in Trapping Pestiferous Fruit Flies (Diptera: Tephritidae): Additional Studies on the Performance of Solid Bactrocera Male Lures and Separate Insecticidal Strips Relative to Standard Liquid Lures
Figure 4. Captures of Bactrocera cucurbitae males in traps baited with CL lures of variable age. Data for CL plugs weathered in Arizona and Florida are given in top and bottom plots, respectively. While lure age varied among treatments, the toxicant was fresh (no weathering) in all treatments. Liquid was applied to a cotton wick; in all other cases CL was presented in a polymeric plug. Height of bar represents mean number of males captured per trap (n = 15 traps per treatment) in a 24-h period; error bars are + 1 SE. No significant variation existed among treatments for either Arizona (F = 0.5, P = 0.65) or Florida (F = 1.9, P = 0.15). Bars sharing a letter did not differ significantly (P> 0.05).
Tairua Pearl Shell Lure
Fishing lure made from tropical black-lipped pearl shell ([Pinctada margaritifera](https://en.wikipedia.org/wiki/Pinctada_margaritifera)). It was found in 1964 during an archaeological excavation at Tairua on the Coromandel Peninsula. The lure is highly significant because it was made in East Polynesia (in the early-mid1300s) and brought here, on a waka, with the Polynesian settlers of Aotearoa. Identifier: **AU1785** [Source record](http://www.aucklandmuseum.com/collections-research/collections/record/am_humanhistory-object-592550?k=AU1785&ordinal=0) on Auckland Museum website. #AMCollection Source: Objaverse 1.0 / Sketchfab
Raw data of experiments on the Bisexual lures and their comparison with synthetic sex attractants for trapping Orthosia species (Lepidoptera: Noctuidae)
<p>Raw data of experiments on the manuscript of the "Bisexual lures and their comparison with synthetic sex attractants for trapping Orthosia species (Lepidoptera: Noctuidae)."</p>
Responses of predatory fish to lures
<p>The evolution of bright "warning" colours in nontoxic animals often is attributed to mimicry of toxic species, but empirical tests of that hypothesis are elusive. Populations of a harmless sea snake species (<em>Emydocephalus annulatus</em>) in New Caledonia exhibit colour polymorphism, with around 20% of individuals banded rather than melanic. Stability in that proportion over 20 years has been attributed to Batesian mimicry of deadly snake species by banded morphs of the harmless taxon. This hypothesis requires that banded colours reduce a snake's vulnerability to predation. We tested that idea by pulling flexible snake-shaped models through the water and recording responses by predatory fish. Black and banded lures attracted similar numbers of following fish, but attacks were directed almost exclusively to black lures. Our methods overcome several ambiguities associated with experimental studies on mimicry in terrestrial snakes, and support the hypothesis that banded colour patterns reduce a non-venomous marine snake's vulnerability to predation.</p>
Figure 46 in Males of a new species of Jotus from Australia wave a paddle-shaped lure to solicit nearby females (Araneae: Salticidae: Euophryini)
Figure 46. Field records of predation on ants by a male Jotus remus at Barrington Tops (1), a female Anasaitis canosa from Greenville County, South Carolina (2), and a male Naphrys pulex, also from Greenville County (3). Although found on a different continent, Naphrys is thought to be more closely related to the Australian Jotus than to the Anasaitis that shares its leaf-litter habitat (Zhang & Maddison 2013). 2-3, Scale = 1 mm.
Figure 45 in Males of a new species of Jotus from Australia wave a paddle-shaped lure to solicit nearby females (Araneae: Salticidae: Euophryini)
Figure 45. Take-off sequence by an adult male Jotus remus based on analysis of high-speed (sequential frames at 1000 FPS), low resolution video frames. Note the paddles on legs III. In this sequence, the spider crouched (1-4), then sprung off of the surface in a near-vertical trajectory, extending all four hind legs in about 3 msec.
Figure 43 in Males of a new species of Jotus from Australia wave a paddle-shaped lure to solicit nearby females (Araneae: Salticidae: Euophryini)
Figure 43. Take-off sequence by an adult male Jotus auripes based on analysis of high-speed (1000 FPS) video frames. In this example, legs IV accelerated the spider to ~50 cm/s, then to ~55 cm/s, and extension of legs III brought this up to ~90 cm/s.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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