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17 pages, 14686 KiB  
Article
New Record of Encarsia protransvena and Confirmed Occurrence of Encarsia hispida (Hymenoptera: Aphelinidae) as Parasitoids of Singhiella simplex (Hemiptera: Aleyrodidae) in Italy
by Giuliano Cerasa, Luigi Tomasello, Gianluca Melone, Elia Russo, Gaetano Siscaro, Carmelo Cavallaro, Annamaria Ienco, Francesca Laudani, Vincenzo Palmeri, Orlando Campolo, Francesca Garganese, Francesco Porcelli, Paolo A. Pedata, Vittorio Farina, Giovanni Gugliuzza, Roberto Rizzo, Stefania Laudonia and Gabriella Lo Verde
Insects 2025, 16(1), 40; https://doi.org/10.3390/insects16010040 - 3 Jan 2025
Viewed by 772
Abstract
Encarsia protransvena (Hymenoptera: Aphelinidae) is recorded here for the first time in Italy as a parasitoid of the whitefly Singhiella simplex (Hemiptera: Aleyrodidae), one of the most invasive alien pests of exotic Ficus species. Singhiella simplex, originating from the Oriental region, has established [...] Read more.
Encarsia protransvena (Hymenoptera: Aphelinidae) is recorded here for the first time in Italy as a parasitoid of the whitefly Singhiella simplex (Hemiptera: Aleyrodidae), one of the most invasive alien pests of exotic Ficus species. Singhiella simplex, originating from the Oriental region, has established a global presence. Monitoring of the whitefly and its parasitoids was conducted in the southern areas of Italy, providing crucial insights into their distribution and interactions. The taxonomic identity of E. protransvena, was confirmed by scrutiny of morphological and molecular taxonomic characters. At the time of writing, we also obtained some specimens of Encarsia hispida from the host collected in Campania. We reserve the right to provide bio-ethological information on the species in the future. Comprehensive illustrations and diagnostic features are provided for the host and the parasitoids. An identification key is included for all Encarsia species associated with S. simplex, which provides a valuable tool to distinguish these aphelinid wasps for future research and applications in biological control programs. Full article
(This article belongs to the Collection Hymenoptera: Biology, Taxonomy and Integrated Management)
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Figure 1
<p><span class="html-italic">Singhiella simplex</span>: (<b>A</b>) slide-mounted adult female, arrows show eggs retained in the abdomen; (<b>B</b>–<b>F</b>) whitefly eggs.</p>
Full article ">Figure 2
<p>Immature stages of <span class="html-italic">Singhiella simplex</span>: (<b>A</b>) whitefly first instar; (<b>B</b>–<b>E</b>) second to fourth instar; (<b>F</b>–<b>I</b>) prepupa and pupa.</p>
Full article ">Figure 3
<p><span class="html-italic">Singhiella simplex</span>: (<b>A</b>,<b>B</b>) emerging adults; (<b>C</b>) exuvia (pupal case); (<b>D</b>–<b>G</b>) adults in dorsal, lateral and ventral view (scale bar: 300 µm, except in (<b>D</b>)).</p>
Full article ">Figure 4
<p><span class="html-italic">Singhiella simplex</span>, microscope slide mounted: (<b>A</b>) first instar; (<b>B</b>,<b>C</b>) pupal case and enlargement shows vasiform orifice and caudal furrow; (<b>D</b>) antenna of male; (<b>E</b>) antenna of female; (<b>F</b>) needle-like mouthparts; (<b>G</b>) genital capsule, claspers and aedeagus of the male; (<b>H</b>) female genitalia (scale bar: 50 µm, except in (<b>B</b>)).</p>
Full article ">Figure 5
<p><span class="html-italic">Encarsia protransvena</span>: (<b>A</b>–<b>C</b>) larvae; (<b>D</b>) pupa; (<b>E</b>), pupa ready to emerge; (<b>F</b>,<b>G</b>) dissection showing the emerging adult and pupal remains; (<b>H</b>,<b>I</b>) puparia cases of <span class="html-italic">S. simplex</span> with <span class="html-italic">E. protransvena</span> emerging hole; (<b>J</b>) meconium of <span class="html-italic">E. protransvena</span> (scale bar: 300 µm, except in (<b>J</b>)).</p>
Full article ">Figure 6
<p><span class="html-italic">Encarsia protransvena</span>: (<b>A</b>) forewing and hindwing, the black arrow indicating the presence of two large setae on the submarginal vein and the white arrow a bare area just above the stigmal vein; (<b>B</b>) scutellar sensillae (black arrows) closely placed or touching, ovoid and separated by less than their maximum diameter, rarely by a full diameter (left-right black arrow indicates the distance between the sensilla).</p>
Full article ">Figure 7
<p><span class="html-italic">Encarsia protransvena</span>: (<b>A</b>) body, dorsal view, mid-lobe of mesosoma with 4 pairs of setae, preapical pair not reaching the base of apical pair; (<b>B</b>) head, ventrolateral view; (<b>C</b>) body, lateral view; (<b>D</b>) stemmaticum, reticulate; (<b>E</b>) apex of middle tibia and tarsus.</p>
Full article ">Figure 8
<p><span class="html-italic">Encarsia protransvena</span>: (<b>A</b>) ovipositor slender and with straight tip; (<b>B</b>) body, ventral view, the arrows indicate ovipositor, antennal clava and middle tibia length; (<b>C</b>) seventh metasomal tergum (Mt7) with 6 setae, 4 long setae medial to cerci; (<b>D</b>) basal seta (BS) of third valvula (TVL) not reaching base of subapical seta (SB); subapical seta located beyond halfway (0.65) between basal seta of third valvula and apex.</p>
Full article ">Figure 9
<p><span class="html-italic">Encarsia hispida</span> (<b>A</b>–<b>F</b>) and <span class="html-italic">Encarsia protransvena</span> (<b>G</b>): (<b>A</b>) adult female, dorsal view; (<b>B</b>) ovipositor, middle and hind tibia; (<b>C</b>) antenna; (<b>D</b>) forewing, the black arrow indicates the absence of a bare area around the stigmal vein; (<b>E</b>) apex of middle tibia, showing mid tarsus segments and the spur-to-basitarsus relative length; (<b>F</b>) pupa of <span class="html-italic">E. hispida</span> and (<b>G</b>) pupa of <span class="html-italic">E. protransvena</span>.</p>
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17 pages, 4655 KiB  
Article
Reproductive Biology and Rearing Improvements of Apanteles opuntiarum, Potential Biocontrol Agent of the Argentine Cactus Moth, Cactoblastis cactorum
by Laura Varone, Nicole Benda, Mariel Eugenia Guala, Juan José Martínez and Octavio Augusto Bruzzone
Insects 2024, 15(8), 604; https://doi.org/10.3390/insects15080604 - 10 Aug 2024
Cited by 1 | Viewed by 1295
Abstract
The cactus moth, Cactoblastis cactorum (Berg) (Lepidoptera: Pyralidae) is native to South America and has been used as a biocontrol agent of Opuntia (Cactaceae) in Australia and South Africa. Its invasion in North America has raised concerns for the native Opuntia in the [...] Read more.
The cactus moth, Cactoblastis cactorum (Berg) (Lepidoptera: Pyralidae) is native to South America and has been used as a biocontrol agent of Opuntia (Cactaceae) in Australia and South Africa. Its invasion in North America has raised concerns for the native Opuntia in the USA and Mexico. We investigated the reproductive biology and rearing procedures of a host-specific potential biocontrol agent, Apanteles opuntiarum Martínez and Berta (Hymenoptera: Braconidae). Given the gregarious nature of the parasitoid larvae, we studied the morphology of the immature stages and evaluated evidence of polyembryony and superparasitism. We also investigated the effects of host exposure arena and host density on parasitism rates and wasp production. The morphological descriptions provide a basis for comparison with other species. Early larval instars of A. opuntiarum are similar to other microgastrine immature stages. However, the mature larva exhibits placoid sensilla in the epistomal region, a unique character not previously reported. We provide evidence that A. opuntiarum eggs are not polyembryonic; females frequently superparasitize and have an oviposition preference for larvae parasitized 1–2 d previously. Exposing larvae of C. cactorum to wasps while inside the cactus resulted in lower parasitism and fewer offspring from each host than exposing larvae in the arena without the cactus. Parasitism and mortality rates were higher at lower host densities, possibly due to reduced host group defensive behavior. These results suggest that preference for superparasitism, host defensive behavior, and interactions with the cactus may play an important role in per-host wasp production under laboratory conditions. Full article
(This article belongs to the Special Issue Insect Rearing: Reserve Forces with Commercial and Ecological Values)
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Figure 1
<p>Immature stages of <span class="html-italic">Apanteles opuntiarum</span>: (<b>a</b>) egg 2 h after oviposition; (<b>b</b>) egg 24 h after oviposition; (<b>c</b>) first larval instar; (<b>d</b>) second larval instar with short tail; (<b>e</b>) third larval instar. References: asp I-VII., abdominal spiracles on segments I to VII; tsp., thoracic spiracle.</p>
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<p>Slide mount of instars of <span class="html-italic">Apanteles opuntiarum:</span> (<b>a</b>) mandibles of the first instar in ventral view; (<b>b</b>) mandibles of second instar in ventral view; (<b>c</b>) mandible of third instar in ventral view; (<b>d</b>) placoid sensilla in the epistomal areas of third instar. References: mda., mandibular apex; pl., placoid sensilla.</p>
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<p>Distribution of measurements of head and mandible of larvae of <span class="html-italic">Apanteles opuntiarum,</span> evidencing 3 size categories, and hence, three instars (L1–L3).</p>
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<p>Cephalic structures of the third instar of <span class="html-italic">Apanteles opuntiarum:</span> (<b>a</b>) SEM image of the mouthparts; (<b>b</b>) scheme of mouthparts. References: h., hipostoma; hsp., hipostomal spur; lbp., labial palp; lbs., labial sclerite; md., mandible; pl., placoid sensilla; sp., silk press; sts., stipital sclerite; mxp., maxillary palp.</p>
Full article ">Figure 5
<p>Host attractiveness to <span class="html-italic">Apanteles opuntiarum</span> on a Thurstone scale of attractiveness as a function of the number of days since the first oviposition by the parasitoid. The blue circles are the measurements, the solid line is the interpolated mean, and the gray area between the dotted lines are the confidence intervals.</p>
Full article ">Figure 6
<p>Mean parasitism rate ± SE (<b>a</b>) and mortality rate ± SE (<b>b</b>) at different host densities of <span class="html-italic">C. cactorum</span> exposed within cacti and in a Petri dish. Sample sizes are listed on the bars. Bars with the same letter above them are not significantly different at α ≤ 0.05 using a Bonferroni-corrected post-hoc <span class="html-italic">t</span>-test for multiple comparisons.</p>
Full article ">Figure 7
<p>Mean number of wasps emerging per parasitized host ± SE (<b>a</b>) and total number of wasps emerging from each exposure jar ± SE (<b>b</b>) at different host densities of <span class="html-italic">C. cactorum</span> exposed within cacti and in a Petri dish. Sample sizes are listed directly on the bars. Bars with the same letter above them are not significantly different at α ≤ 0.05 using a Bonferroni-corrected post-hoc <span class="html-italic">t</span>-test for multiple comparisons.</p>
Full article ">
22 pages, 2495 KiB  
Review
Current and Future Insect Threats to Oaks of the Midwest, Great Lakes, and Northeastern United States and Canada
by Amanda J. Stump, Katie Bershing, Tara L. Bal and Carsten Külheim
Forests 2024, 15(8), 1361; https://doi.org/10.3390/f15081361 - 4 Aug 2024
Viewed by 2925
Abstract
Increasing temperatures, prolonged drought, the increased severity and intensity of storms, and other effects of climate change are being felt globally, and long-lived forest tree species may struggle in their current ranges. Oaks (Quercus spp.) have evolved a range of adaptations to [...] Read more.
Increasing temperatures, prolonged drought, the increased severity and intensity of storms, and other effects of climate change are being felt globally, and long-lived forest tree species may struggle in their current ranges. Oaks (Quercus spp.) have evolved a range of adaptations to dry and hot conditions and are believed to be a “climate change winner” by increasing their suitable habitat. However, a mixture of life history traits and increasing susceptibility to herbivores and xylovores as well as secondary pathogen infections still put oaks at risk of decline. Oak species found in the Midwestern, Great Lakes, and Northeastern United States and Canada are important keystone species with high ecological and economical importance. They are also vulnerable to existing, new, and emerging threats that have the potential to cause mortality across entire stands quickly. Current examples of insect threats include the Lymantria dispar (spongy moth), Agrilus bilineatus (twolined chestnut borer), and Nitidulidae (sap beetles) as disease vectors. Examples of emerging insects of concern include Cynipidae (oak gall wasps) and Enaphalodes rufulus (red oak borer). This study describes these insects, explains their mechanisms of action and the effects on oaks, and explores mitigation strategies for each. Full article
(This article belongs to the Special Issue Forest Pathology and Entomology—Series II)
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Figure 1
<p>Examples of existing and potential insect (<b>a</b>) threats to <span class="html-italic">Quercus</span> include (<b>b</b>: A: <span class="html-italic">Lymantria dispar</span> A1: male; A2: female (widespread defoliation), B: <span class="html-italic">Curculio glandium</span> (acorn fruit destruction), C: gall wasps (twig node disruption and crown dieback), D: Nitidulidae (spreading oak wilt via fungal hyphae), E: <span class="html-italic">Agrilus bilineatus,</span> and F: <span class="html-italic">Enaphalodes rufulus</span> (wood boring and girdling) (scale bar = 1.0 mm).</p>
Full article ">Figure 1 Cont.
<p>Examples of existing and potential insect (<b>a</b>) threats to <span class="html-italic">Quercus</span> include (<b>b</b>: A: <span class="html-italic">Lymantria dispar</span> A1: male; A2: female (widespread defoliation), B: <span class="html-italic">Curculio glandium</span> (acorn fruit destruction), C: gall wasps (twig node disruption and crown dieback), D: Nitidulidae (spreading oak wilt via fungal hyphae), E: <span class="html-italic">Agrilus bilineatus,</span> and F: <span class="html-italic">Enaphalodes rufulus</span> (wood boring and girdling) (scale bar = 1.0 mm).</p>
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<p>The cycle of oak wilt infection and Nitidulidae. (<b>A</b>): Nitidulidae carrying the oak wilt fungal pathogen <span class="html-italic">Bretzeilla fagacearum</span> spreads the fungus to healthy oak trees, (<b>B</b>): oaks displaying characteristic signs of oak wilt: widespread crown dieback and leaf tissue necrosis, (<b>C</b>): further example of oak crown dieback and fungal hyphae mats under the outer bark layer, (<b>C1</b>): oak trees with oak wilt can spread the pathogen to adjacent stand trees via underground root grafts causing healthy trees (<b>C2</b>) to become infected (<b>C3</b>) and continue spreading the infection to other adjacent trees (<b>C4</b>), (<b>D</b>): Nitidulidae beetles attracted by the fermenting scent of oak wilt hyphae mats congregate to feed and mate, (<b>E</b>): Nitidulidae carrying the oak wilt fungal pathogen <span class="html-italic">Bretzeilla fagacearum</span> spread it to additional trees and the infection cycle continues.</p>
Full article ">
17 pages, 7202 KiB  
Article
Future Range Expansions of Invasive Wasps Suggest Their Increasing Impacts on Global Apiculture
by Xueyou Zhang, Peixiao Nie, Xiaokang Hu and Jianmeng Feng
Insects 2024, 15(7), 546; https://doi.org/10.3390/insects15070546 - 19 Jul 2024
Cited by 2 | Viewed by 1074
Abstract
Until now, no study has examined the future range dynamics of major invasive wasp species to assess their future impacts on global apiculture. Here, we developed 12 species distribution models to calibrate the future range dynamics of 12 major invasive Vespidae wasp species [...] Read more.
Until now, no study has examined the future range dynamics of major invasive wasp species to assess their future impacts on global apiculture. Here, we developed 12 species distribution models to calibrate the future range dynamics of 12 major invasive Vespidae wasp species under a unified framework. An increase in their habitat suitability was identified in more than 75% of global land. Substantial range expansions were detected for all 12 species, and they were primarily induced by future climate changes. Notably, Polistes dominula and Vespa crabro had the largest potential ranges under all scenarios, suggesting their greater impact on global apiculture. Polistes chinensis and Vespa velutina nigrithorax had the highest range expansion ratios, so they warrant more urgent attention than the other species. Polistes versicolor and P. chinensis are expected to exhibit the largest centroid shifts, suggesting that substantial shifts in prioritizing regions against their invasions should be made. Europe and the eastern part of the USA were future invasion hotspots for all major invasive wasp species, suggesting that apiculture might face more pronounced threats in these regions than in others. In conclusion, given their substantial range shifts, invasive wasps will likely have increasingly negative impacts on global apiculture in the future. Full article
(This article belongs to the Section Insect Ecology, Diversity and Conservation)
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Figure 1
<p>Occurrences of the 12 major invasive wasp species. Occurrences were retrieved from the Global Biodiversity Information Facility (<a href="http://www.gbif.org" target="_blank">www.gbif.org</a>, accessed on 7 September 2023). A total of 19,196 occurrences were retrieved after spatial thinning.</p>
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<p>The importance of each predictor in the baseline models. Topographical, climatic, and land-use factors are shown in green, blue, and orange fonts, respectively. For each species, importance values were standardized according to the max–min method. The grayscale shading indicates the relative importance of each of the predictors, and the blanks indicate that the predictors were not inputted into the final models for the species.</p>
Full article ">Figure 3
<p>Overlap indices of habitat suitability of the 12 major invasive wasp species: (<b>a</b>) current scenario; (<b>b</b>) scenario of F126; (<b>c</b>) scenario of F585; (<b>d</b>) scenario of M126; (<b>e</b>) scenario of 585. High habitat suitability overlap indices in the five scenarios was detected in Europe, the eastern and western parts of the USA, and the southeastern part of Australia.</p>
Full article ">Figure 4
<p>Changes in overlap indices of habitat suitability of 12 major invasive wasps. (<b>a</b>) F126; (<b>b</b>) F585; (<b>c</b>) M126; (<b>d</b>) M585. Considerable increases of overlap indices of habitat suitability under F126 and M126 were mainly detected in eastern coastline regions and the eastern part of USA, North Europe, East China, Nepal, New Zealand and southeastern coastlines of Australia. Large increases in the overlap indices of habitat suitability under the scenarios of M585 and F585 were primarily identified in the eastern part of North America, western coastline regions of the North America, North Europe, western part of Russia, Nepal, India, East China and the far-east regions of Russia.</p>
Full article ">Figure 5
<p>Potential ranges and range dynamics of the 12 major invasive wasp species under future scenarios. The potential ranges are shown in grayscale. The range dynamics are indicated by expanding ranges in redscale, the range expansion ratios in bluescale, and the range similarity indices in yellowscale. Under most scenarios, <span class="html-italic">Polistes dominula</span>, <span class="html-italic">Vespa crabro</span>, and <span class="html-italic">Vespula germanica</span> were projected to show larger potential ranges than the other species; <span class="html-italic">Vespa velutina nigrithorax</span> and <span class="html-italic">Polistes chinensis</span> were projected to have the higher range expansion ratios; <span class="html-italic">Polistes versicolor</span> and <span class="html-italic">P. chinensis</span> were projected to have lower range similarity indices; and <span class="html-italic">Vespa velutina</span> and <span class="html-italic">Polistes dominula</span> were projected to have larger expanding ranges.</p>
Full article ">Figure 6
<p>Overlap indices of potential ranges of the 12 major invasive wasp species: (<b>a</b>) overlap indices of potential ranges under the current scenario; (<b>b</b>) range overlap indices under F126; (<b>c</b>) range overlap indices under F585; (<b>d</b>) range overlap indices under M126; (<b>e</b>) range overlap indices under M585. High overlap indices of potential ranges were mainly projected in Europe, the eastern part of the USA, a region to the west of the Cascade Mountain Range in the USA, the eastern part of China, Japan, the southeast part of Australia, New Zealand, Argentina, and the southeastern part of Brazil.</p>
Full article ">Figure 7
<p>Overlap indices of expanding ranges of the 12 major invasive wasps. (<b>a</b>) overlap indices of expanding ranges of expanding ranges under F126 scenarios; (<b>b</b>) overlap indices of expanding ranges of expanding ranges under F585 scenarios; (<b>c</b>) overlap indices of expanding ranges under M126 scenarios; (<b>d</b>) overlap indices of expanding ranges under M585 scenarios. High values of overlapping indices of expanding ranges in Europe, northeastern and northwestern parts of the United States of America, southeastern and southwestern parts of Canada, Southeast China, New Zealand, southeastern coastline regions of Australia, Japan and southern part of Chile.</p>
Full article ">
19 pages, 6128 KiB  
Article
Identifying Morphs of the Yellow-Legged Hornet (Vespa velutina) and Other Pests of Quarantine Importance with Geometric Morphometrics
by Allan Smith-Pardo, P. David Polly and Todd Gilligan
Diversity 2024, 16(7), 367; https://doi.org/10.3390/d16070367 - 26 Jun 2024
Viewed by 1489
Abstract
We assess the accuracy of geometric morphometrics (GMM) for determining the origin of insects of quarantine importance using the Asian hornet (Vespa velutina Lep.1836) as a case study. This species is highly variable, has an extensive natural distribution, and has been transported [...] Read more.
We assess the accuracy of geometric morphometrics (GMM) for determining the origin of insects of quarantine importance using the Asian hornet (Vespa velutina Lep.1836) as a case study. This species is highly variable, has an extensive natural distribution, and has been transported to many regions of the world. Forewing landmarks were applied to a large sample of regionally specific color morphs (previously considered “subspecies”) from across the species’ native Asian range. We reconfirm that GMM can statistically distinguish geographic variants independent of the color patterns that have heretofore been used for provenance, but which have been suspected of being unreliable. Almost all morphs in our analyses were statistically different except the centrally located V. v. variana, whose range lies between the continental V. v. auraria Smith, 1852, and V. v. nigrithorax du Buysson, 1905 morphs, and the Malaysian and Indonesian morphs. Even with moderate-sized training samples, discriminant function analysis (DFA) was able to classify geographic morphos with about 90% accuracy (ranging from 60% to 100%). We apply these results to determine the origin of a dead wasp recently intercepted in a mail parcel in Utah. Both DFA and continuous-trait maximum-likelihood clustering suggest that the Utah specimen belongs to the nigrithorax morph, which is native to southern China but now invasive in Europe, Japan, and Korea. These results are also supported by DNA barcode analysis, which groups the Utah individual with nigrithorax populations in South Korea and Japan. The relationship between variation in wing shape and genetic differentiation deserves further study, but molecular data are consistent with the GMM results suggesting that morphometric comparisons may be able to identify and provenance intercepted specimens quickly and inexpensively when molecular sequences and taxonomic specialists are unavailable. Full article
(This article belongs to the Special Issue Ecology and Management of Invasive Vespidae)
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<p>Distribution map. Map showing the approximate distribution of named color morphs of the Asian hornet, <span class="html-italic">Vespa vetulina</span> (following [<a href="#B7-diversity-16-00367" class="html-bibr">7</a>]). Base map generated from World Bank Official Boundaries shapefile data under a CC-BY 4.0 license.</p>
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<p>Numbered geometric morphometric landmarks on the forewing.</p>
Full article ">Figure 3
<p>Mean shapes of the forewings of the color morphs, all of which are named subspecies of <span class="html-italic">Vespa velutina</span>, and the specimen intercepted in Utah. Labels indicate the name of the color morph and the location of our sample. Warped grids show the difference between the morph and the average wing shape in our data set. Differences were multiplied by a factor of 5 to make them easier to see. The color scheme is the same as in <a href="#diversity-16-00367-f001" class="html-fig">Figure 1</a>.</p>
Full article ">Figure 4
<p>Principal components morphospace of forewing shape in <span class="html-italic">Vespa velutina</span>. The first four dimensions of this space are shown (<b>A</b>–<b>C</b>). The degree of separation is illustrated by plotting the individual scores and group mean for each of the morphs on PC 1 (<b>D</b>). The color scheme is the same as in <a href="#diversity-16-00367-f001" class="html-fig">Figure 1</a>.</p>
Full article ">Figure 5
<p>Shape models illustrate the differences represented by each of the first four principal components. The shape at the negative end of each axis is shown in orange landmarks and the shape at the positive end of the axis is shown by the wireframe. The arrows and thin plate spline show the transformation from the negative to the positive end. Differences were multiplied by a factor of 5 to make them easier to see.</p>
Full article ">Figure 6
<p>Canonical variates plot showing the first two canonical axes.</p>
Full article ">Figure 7
<p>Phenotypic similarity of the intercepted hornet from Utah and the color morphs. (<b>A</b>) Continuous trait maximum-likelihood tree based on mean forewing shape of the color morphs. (<b>B</b>) Morphospace of the Utah hornet and mean forewing shapes of the morphs with the tree projected into it.</p>
Full article ">Figure 8
<p>Barcoding tree. Neighbor-joining (distance) trees constructed under the Kimura 2 parameter model (K2P) showing barcode similarity between the Utah specimen and <span class="html-italic">nigrithorax</span> from South Korea and Japan. Color coding matches <a href="#diversity-16-00367-f001" class="html-fig">Figure 1</a>; numbers show provenance in <a href="#app1-diversity-16-00367" class="html-app">Figure S7</a>.</p>
Full article ">
23 pages, 4517 KiB  
Article
Aroplectrus dimerus (Hymenoptera: Eulophidae), Ectoparasitoid of the Nettle Caterpillar, Oxyplax pallivitta (Lepidoptera: Limacodidae): Evaluation in the Hawaiian Islands
by Juliana A. Yalemar, Walter T. Nagamine, Renato C. Bautista, Dexter Y. Cho, Larry M. Nakahara and Mohsen M. Ramadan
Life 2024, 14(4), 509; https://doi.org/10.3390/life14040509 - 15 Apr 2024
Viewed by 1853
Abstract
The stinging nettle caterpillar, Oxyplax (syn. Darna) pallivitta (Lepidoptera: Limacodidae), is a serious invasive pest of agricultural products and a health hazard on the Hawaiian Islands first discovered in 2001. Nursery workers and homeowners have been stung by the caterpillars while handling [...] Read more.
The stinging nettle caterpillar, Oxyplax (syn. Darna) pallivitta (Lepidoptera: Limacodidae), is a serious invasive pest of agricultural products and a health hazard on the Hawaiian Islands first discovered in 2001. Nursery workers and homeowners have been stung by the caterpillars while handling their plants, especially rhapis palms (Rhapis sp.). Throughout its invaded range, it causes widespread damage, including the many cultivated and native palm species that have grown in Hawaii. Larvae contain urticating hairs that secrete a toxin, causing painful skin swelling and irritation on contact. Horticulture and nursery products impacted by the limacodid pest are estimated at $84.3 million (2018 value). Suppression efforts with pesticides and lure traps were ineffective, and the moth population continued to spread to major Hawaiian Islands (Hawaii, Kauai, Maui, Oahu). The introduction of specific biological control agents from the native region was thought to be the long-term solution for this invasive pest. Initial exploration in Indonesia and Thailand resulted in the introduction of a pupal ectoparasitoid, Nesolynx sp. (Hymenoptera: Eulophidae: Tetrastichinae), that was not specific. The oriental wasp, Aroplectrus dimerus Lin (Hymenoptera: Eulophidae: Eulophinae), idiobiont gregarious ectoparasitoid of the stinging nettle caterpillar, was introduced from Taiwan in 2004 for host specificity studies and biocontrol in Hawaii. Host range testing showed the parasitoid attacked only limacodid species, and it was approved for field release in 2010. The parasitoid identity, host specificity under containment facility conditions, reproductive performance, and colonization on the major infested sites were assessed. A total of 13,379 parasitoids were colonized on 162 release sites on four Hawaiian Islands. Evaluations were conducted using field surveys of larvae, pupal counts, and male lure traps. Field parasitism was thoroughly investigated on Oahu Island, averaging 18.9 ± 5.6% of 3923 collected larvae during 2010–2023. The numbers of male moths caught/trap/month were significantly reduced on Oahu Island (p < 0.05). Recently, the hyperparasitoid, Pediobius imbreus Walker (Hymenoptera: Eulophidae: Entedoninae), was detected, reducing the efficiency of A. dimerus in the field. The mean hyperparasitism of A. dimerus pupae was 27.3 ± 7.6% on Oahu Island. There was no detailed biological assessment for A. dimerus or its field evaluation available in scientific literature. Results were discussed regarding the potential use of A. dimerus in biocontrol elsewhere if the stinging nettle caterpillar was invaded in the future. Full article
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<p>Map of major infestation sites, parasitoid colonization, and establishment on the Hawaiian Islands (sizes of the islands are not in scale). Sampling locations with GPS coordinates are shown in Tables. (Oahu Island GPS coordinates of 21°18′56.1708″ N, 157°51′29.1348″ W; Hawaii Island with the GPS coordinates of 19°44′30.3180″ N, 155°50′39.9732″ W; Kauai Island with GPS coordinates of 22°6′30.7548″ N, 159°29′48.3540″ W.; Maui Island with GPS coordinates of 20°47′54.1068″ N and 156°19′54.9264″ W. [<a href="https://www.latlong.net" target="_blank">https://www.latlong.net</a> (accessed on 13 December 2023)].</p>
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<p><span class="html-italic">Aroplectrus dimerus</span> (<b>A</b>) female side habitus, curved down mesosoma in profile along the dorsal margin, overall body color yellow and reddish, scape longer than eye, head narrower than mesosoma, smooth hind coxae; (<b>B</b>) scutellum finely granulate with longitudinal carinae, propodeum, median carina weak, submedian areola divided completely into two sectors by a continuous oblique carina; (<b>C</b>) forewing hyaline, densely pilose veins brownish wing post-marginal vein longer than stigmal vein; (<b>D</b>) elongate metatibial spur longer than basitarsus, not reaching apex of second tarsal segment; (<b>E</b>) gaster, female metasoma shorter and narrower than mesosoma, oblong-ovate in dorsal view unicolor, gaster showing dark bands and black ovipositor sheath, ovipositor exerting beyond abdominal apex, smooth hind coxae (pictures taken using MMR).</p>
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<p><span class="html-italic">Aroplectrus dimerus</span> (<b>A</b>) female antenna, funicle 4 segmented and a clava, F1 4X longer than broad, antenna with reddish scape, darker on funicle, female antenna, clava as long as F4; (<b>B</b>) male antenna showing slender funicle and shorter clava, antennae more slender, club broader than funicle 1; (<b>C</b>) showing vertex and yellow pronotum, head dorso-posterior view showing occipital carina feature, and quadrate pronotum with two side-long sitae in the middle; (<b>D</b>) dorso frontal view of head showing scape longer than eye and facial epistomal suture distinct straight, vertex with few black sitae and sparse cilia, malar space smooth shorter than eye, antenna with scape much longer than eye; (<b>E</b>) head frontal facial view showing head wider than head length (pictures taken using MMR).</p>
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<p><span class="html-italic">Pediobius imbreus</span>, (<b>A</b>) side habitus of female, has a body mostly dark with less metallic reflections, antennae inserted at the lower level of eyes, coxae, trochanters, femora black, tibiae, and tarsus coloration varied between specimens in HDOA collection, some specimens with all dark or all white, with or without metallic bluish reflections; (<b>B</b>) exit holes from pupae of <span class="html-italic">Aroplectrus dimerus</span> (red arrows on exit holes anterior with hyper pupal molt, and posterior of pupa); (<b>C</b>) head front view showing transverse frontal suture extended close to compound eyes; (<b>D</b>) scutum reticulate, scutellum with longitudinal reticulate sculpture having a median narrow, smooth band, broad head pronotum, and reticulate sculptured mesothorax; (<b>E</b>) propodium with divergent middle carina and lateral propodeal plicae. Propodeum short, with submedian carinae diverging posteriorly (pictures taken using MMR).</p>
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<p>(<b>A</b>) female <span class="html-italic">Aroplectrus dimerus</span> on the host larva; (<b>B</b>) female dorsal view showing color peculiarity; (<b>C</b>) eggs laid on host larva between scolli; (<b>D</b>) first instars <span class="html-italic">A. dimerus</span> migrate to the underside of host larva (arrows point at first instars, black marks are female stinging marks to paralyze the host before oviposition not the feeding wounds by larvae); (<b>E</b>) mature larvae consume the host still with uncharged prepupal meconia; (<b>F</b>) pupae of the parasitoid underneath the host‘ cadaver, dark material between pupae are the vacated meconia. Photos credited to MMR and WTN.</p>
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<p>Survivorship of male and female <span class="html-italic">Aroplectrus dimerus</span> under laboratory conditions. All wasp categories fed honey and had access to water, except starved wasps. Different letters on top of bars indicate significant differences (ANOVA, <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Mean number of <span class="html-italic">Oxyplax pallivitta</span> lured into male pheromone traps per month on the Hawaiian Islands before parasitoid release during 2007, 2009, and after parasitoid establishment during 2011, 2021–2023 on Oahu Island. Different letters on top of bars indicate significant differences (ANOVA, <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p><span class="html-italic">Oxyplax pallivittus</span>: (<b>A</b>) female habitus; (<b>B</b>) male habitus see bipectinate antennae and end of abdomen; (<b>C</b>) flat eggs (1.6 mm length); (<b>D</b>) stinging larvae (L6–L10); (<b>E</b>) spherical cocoons collected from Oahu nursery in thousands in 2007 (6.5 mm Ø); (<b>F</b>) male pupa removed from the cocoon. Photos taken using MMR, WTN.</p>
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2 pages, 129 KiB  
Abstract
Exploring the Role of N-WASP in Breast Cancer Metastasis through Mass Spectrometry and Potential Signalling Pathway Analysis
by Rhiannon Yannan Yu, Wenguo Jiang and Tracey Martin
Proceedings 2024, 103(1), 17; https://doi.org/10.3390/proceedings2024103017 - 12 Apr 2024
Viewed by 551
Abstract
Background: Neural Wiskott–Aldrich Syndrome Protein (N-WASP) is a key regulator of the actin cytoskeleton and is implicated in various cellular processes, including cell motility and invasion. In cancer biology, the role of N-WASP in cell motility and metastasis is of particular interest, yet [...] Read more.
Background: Neural Wiskott–Aldrich Syndrome Protein (N-WASP) is a key regulator of the actin cytoskeleton and is implicated in various cellular processes, including cell motility and invasion. In cancer biology, the role of N-WASP in cell motility and metastasis is of particular interest, yet its specific functions in breast cancer remain to be fully understood. Method: To investigate the impact of N-WASP on breast cancer cell behaviour, we employed siRNA to knock down N-WASP expression in the MDA-MB-231 breast cancer cell line. After the knockdown, proteomic changes in the cells were analysed using mass spectrometry. Notable alterations in the genes present in both total and phosphorylated proteins were further analysed. Results: The proteomic data analysis ranked 50 genes that exhibited the most up-regulation and down-regulation in total and phosphorylated proteins. These 200 genes were further examined using the REACTOME database to identify affected signalling pathways. Knockdown of N-WASP led to significant changes in the RHOD, RHOF, and RHOG GTPase cycles (p = 0.015, p = 0.01, and p = 0.027), pathways closely associated with cell motility and actin cytoskeleton organisation. These cycles are crucial in modulating cellular dynamics, impacting a range of processes from immune response to neuronal development, wound healing, and, particularly, cancer metastasis. Furthermore, the findings highlighted the role of non-integrin membrane–ECM interactions in cell motility and cytoskeleton dynamics (p = 0.021). The altered protein expression patterns suggest a link between N-WASP, non-integrin membrane–ECM interactions, and the cytoskeletal changes essential for cell migration and invasion—key factors in cancer metastasis. Conclusions: Our findings reinforce the critical role of N-WASP in regulating the cytoskeleton and influencing cell motility, invasion, and metastasis in breast cancer. This study not only provides deeper insights into the molecular mechanism of breast cancer progression but also highlights N-WASP as a potential therapeutic target for intervention strategies in breast cancer treatment. Full article
(This article belongs to the Proceedings of The 3rd International Electronic Conference on Biomolecules)
19 pages, 3439 KiB  
Article
Reproductive Parameters and Host Specificity of Eurytoma erythrinae (Hymenoptera: Eurytomidae), a Biological Control Agent of the Erythrina Gall Wasp, Quadrastichus erythrinae (Hymenoptera: Eulophidae)
by Walter T. Nagamine, Juliana A. Yalemar, Mark G. Wright and Mohsen M. Ramadan
Insects 2023, 14(12), 923; https://doi.org/10.3390/insects14120923 - 3 Dec 2023
Viewed by 1688
Abstract
Eurytoma erythrinae Gates & Delvare (Hymenoptera: Eurytomidae) is an important biological control agent of the erythrina gall wasp (EGW), Quadrastichus erythrinae Kim (Hymenoptera: Eulophidae), an invasive species likely originating in eastern Africa that is a threat to Erythrina trees in Hawaii and worldwide. Thousands [...] Read more.
Eurytoma erythrinae Gates & Delvare (Hymenoptera: Eurytomidae) is an important biological control agent of the erythrina gall wasp (EGW), Quadrastichus erythrinae Kim (Hymenoptera: Eulophidae), an invasive species likely originating in eastern Africa that is a threat to Erythrina trees in Hawaii and worldwide. Thousands of Erythrina trees in Hawaii have succumbed to EGW since 2005 and died within a few years of infestation. The endemic wiliwili tree, Erythrina sandwicensis, an important component of Hawaii’s dry forests and one of few deciduous native trees, were severely impacted by this wasp. Early during the invasion by EGW it became evident that the endemic species may be driven to extinction, and exploration programs for natural enemies of the EGW started in December 2005. East Africa was selected as the starting point for natural enemy exploration owing to high native Erythina species richness. Several gall formers were found in Tanzania and a putative color variant type of Q. erythrinae was detected in association with three ectoparasitoids. During January 2006, the dominant parasitoid of this gall former was introduced to Hawaii and described as the new species, E. erythrinae. It was found in Ghana and South Africa attacking other gall wasp species on Erythrina. Eurytoma erythrinae was a voracious ectoparasitoid feeding as a predator on 1–5 adjacent EGW immatures to complete its development. Host specificity studies that included seven nontarget gall-forming species showed no evidence of attraction or parasitism by this parasitoid. Mean ± SEM longevity of host-deprived females (40.4 ± 2.2 days) was significantly higher than males (20.5 ± 1.1 days). Host feeding enhanced longevity of ovipositing females (51.3 ± 1.5 days). Female E. erythrinae is synovigenic, with high egg-maturation rate. Peak fecundity (105–239 offspring/female), host feeding biology, short life cycle (18.4 ± 0.1 days), and synchronization with the host were additional desirable attributes of this species. The parasitoid was approved for field release in Hawaii in November 2008. A total of 3998 wasps were distributed on six Hawaiian Islands, with establishment in less than a year. Impacts on high density infestations of EGW were sufficient to prevent tree deaths. Limited rates of parasitism on low-density galled leaves, flowers, and seedpods necessitated the consideration for releasing a second parasitoid, Aprostocetus nitens Prinsloo & Kelly (Hymenoptera: Eulophidae). We report on the reproductive characteristics and host specificity of E. erythinae that could be of importance for classical biocontrol programs in areas with an EGW problem. Full article
(This article belongs to the Section Insect Pest and Vector Management)
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<p>(<b>A</b>) EGW early infestation of <span class="html-italic">Erythrina variegata</span>; (<b>B</b>) massive infestation on <span class="html-italic">E. variegata</span>; (<b>C</b>) <span class="html-italic">Erythrina variegata</span> tree at original site of EGW detection in Manoa, Oahu Island, April 2005; (<b>D</b>) same <span class="html-italic">E. variegata</span> tree in Manoa, dead after heavy EGW infestation, December 2006; (<b>E</b>) dead native infested trees of <span class="html-italic">Erythrina sandwicensis</span>, Koko Head, Oahu; (<b>F</b>) dead infested trees of tall variety <span class="html-italic">Erythrina variegata</span>, Oahu Island.</p>
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<p>(<b>A</b>) EGW dissected from infested swollen plant tissue with numerous EGW pupae in closeness of gall chambers. Inset: an egg (red arrow) of the parasitoid on a parasitized larva; (<b>B</b>) female <span class="html-italic">Eurytoma erythrinae</span> ovipositin on a gall; (<b>C</b>) larva of the parasitoid devouring EGW immatures in the tunnels; (<b>D</b>) pupa of the parasitoid in a chewed chamber.</p>
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<p>Comparison of front wing lengths (measured from tigula to tip of wing) of <span class="html-italic">Eurytoma erythrinae</span>, <span class="html-italic">Aprostocetus nitens</span>, and their host EGW, as indication of wasp’s size. Except for <span class="html-italic">A. nitens</span> (thelytokous laboratory colony), species and sex are wild type collected from <span class="html-italic">Erythrina variegata</span> on Oahu Island (12 October 2023). Bars topped by the same letter indicate no significant differences among wing lengths at the 5% level according to Tukey test.</p>
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<p>Average immature developmental period (days) and male–female emergence patterns of <span class="html-italic">Eurytoma erythrinae</span> under laboratory conditions; data were obtained at 21.8 ± 0.12 °C.</p>
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<p>(<b>A</b>) Dried wiliwili forest <span class="html-italic">Erythrina sandwicensis</span> O.Deg, Lahaina Lua, Maui Island, December 2008; (<b>B</b>) massive infestation on Ulupalakua Maui Island, December 2008; (<b>C</b>) lateral habitus of <span class="html-italic">Eurytoma erythrinae</span> released, female (upper), male (lower); (<b>D</b>) infestation on flowers and seedpods of wiliwili still needs higher parasitism, reason for release of a second parasitoid; (<b>E</b>) wiliwili recovery after wasp establishment at Koko Head crater, Oahu Island, 8 December 2015; (<b>F</b>) wiliwii yellow flowering tree at Koko Head crater, Oahu Island, December 2020 photo. Photos credited to Mach Fukada, Maui Island Entomologist (<b>A</b>,<b>B</b>), Walter Nagamine (<b>C</b>), and Juliana Yalemar (<b>D</b>–<b>F</b>).</p>
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12 pages, 2058 KiB  
Article
Co-Occurrence of Wing Deformity and Impaired Mobility of Alates with Deformed Wing Virus in Solenopsis invicta Buren (Hymenoptera: Formicidae)
by Godfrey P. Miles, Xiaofen F. Liu, Esmaeil Amiri, Michael J. Grodowitz, Margaret L. Allen and Jian Chen
Insects 2023, 14(10), 788; https://doi.org/10.3390/insects14100788 - 27 Sep 2023
Cited by 3 | Viewed by 3288
Abstract
Deformed wing virus (DWV), a major honey bee pathogen, is a generalist insect virus detected in diverse insect phyla, including numerous ant genera. Its clinical symptoms have only been reported in honey bees, bumble bees, and wasps. DWV is a quasispecies virus with [...] Read more.
Deformed wing virus (DWV), a major honey bee pathogen, is a generalist insect virus detected in diverse insect phyla, including numerous ant genera. Its clinical symptoms have only been reported in honey bees, bumble bees, and wasps. DWV is a quasispecies virus with three main variants, which, in association with the ectoparasitic mite, Varroa destructor, causes wing deformity, shortened abdomens, neurological impairments, and colony mortality in honey bees. The red imported fire ant, Solenopsis invicta Buren, is one of the most-invasive and detrimental pests in the world. In this study, we report the co-occurrence of DWV-like symptoms in S. invicta and DWV for the first time and provide molecular evidence of viral replication in S. invicta. Some alates in 17 of 23 (74%) lab colonies and 9 of 14 (64%) field colonies displayed deformed wings (DWs), ranging from a single crumpled wing tip to twisted, shriveled wings. Numerous symptomatic alates also exhibited altered locomotion ranging from an altered gait to the inability to walk. Deformed wings may prevent S. invicta alates from reproducing since mating only occurs during a nuptial flight. The results from conventional RT-PCR and Sanger sequencing confirmed the presence of DWV-A, and viral replication of DWV was confirmed using a modified strand-specific RT-PCR. Our results suggest that S. invicta can potentially be an alternative and reservoir host for DWV. However, further research is needed to determine whether DWV is the infectious agent that causes the DW syndrome in S. invicta. Full article
(This article belongs to the Collection Biology of Social Insect Diseases)
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<p><span class="html-italic">Solenopsis invicta</span> specimens displaying the normal wing (NW) and deformed wing (DW) phenotype. (<b>A</b>) Normal wing (NW) adult male alate collected from Colony 8. (<b>B</b>) DW male alate from Colony 2021, which was the first DW alate identified. (<b>C</b>) Wing tip deformity of a DW male alate collected from Colony 11. (<b>D</b>) Two melanized male pupae with DW (bottom) and NW (top), both collected from Colony NBCL-1 collected directly from the ground. All images were captured using a Keyence VHX 5000 (Itasca, IL, USA). Scale bars are 1 mm for all images except Image C, which represents 0.5 mm.</p>
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<p><span class="html-italic">Solenopsis invicta</span> specimens displaying the normal wing (NW) and deformed wing (DW) phenotype. (<b>A</b>) Normal wing (NW) adult female alate collected from Colony 8. (<b>B</b>) DW female alate with a moderate level of wing deformity, also collected from Colony 8. (<b>C</b>) Female DW alate with severe wing deformity, from Colony NBCL-14. (<b>D</b>) The same female alate as C under higher magnification. All images were captured using a Keyence VHX 5000 (Itasca, IL, USA). Scale bars are set at 1 mm for all images, except Image D, which represents 0.5 mm.</p>
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<p>Replicative form of DWV. (<b>A</b>) Representative DNA agarose gel image showing detection of replicative form of DWV using primers specific to the RNA-dependent RNA polymerase (RdRp) gene of DWV in <span class="html-italic">Solenopsis invicta</span>. Lane order is as follow: (L) 100 bp ladder, (Lane 1) adult workers, (Lane 2) worker pupae, (Lane 3) deformed wing (DW) male alates (pooled, <span class="html-italic">n</span> = 5), and (Lane 4) male DW alate (different colony than Lane 3). Lanes 5–8 represent a 1/10 dilution of Lanes 1–4, respectively, (9) DWV-symptomatic Western honey bee (<span class="html-italic">Apis mellifera</span>), (C1) NTC, (C2) no primer, (C3) no transcriptase, and (C4) PCR-NTC. Red dots represent the location where a portion of the band (plug) was removed for reamplification. Amplicon length is 451 bp, 1.5% gel. (<b>B</b>) Reamplification of 1/10 dilution samples. Sanger sequencing results of the 1/10 diluted samples were all positive for the DWV RdRp gene; see <a href="#app1-insects-14-00788" class="html-app">Supplementary Materials Dataset S1</a>.</p>
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14 pages, 303 KiB  
Article
Analysis of Genes Related to Invadopodia Formation and CTTN in Oral Squamous Cell Carcinoma—A Systematic Gene Expression Analysis
by Immanuel Desel, Susanne Jung, Nikolai Purcz, Yahya Açil, Christoph Sproll, Johannes Kleinheinz and Sonja Sielker
Curr. Issues Mol. Biol. 2023, 45(8), 6927-6940; https://doi.org/10.3390/cimb45080437 - 18 Aug 2023
Cited by 1 | Viewed by 1695
Abstract
Successful treatment for any type of carcinoma largely depends on understanding the patterns of invasion and migration. For oral squamous cell carcinoma (OSCC), these processes are not entirely understood as of now. Invadopodia and podosomes, called invadosomes, play an important role in cancer [...] Read more.
Successful treatment for any type of carcinoma largely depends on understanding the patterns of invasion and migration. For oral squamous cell carcinoma (OSCC), these processes are not entirely understood as of now. Invadopodia and podosomes, called invadosomes, play an important role in cancer cell invasion and migration. Previous research has established that cortactin (CTTN) is a major inducer of invadosome formation. However, less is known about the expression patterns of CTTN and other genes related to it or invadopodia formation in OSCC during tumor progression in particular. In this study, gene expression patterns of CTTN and various genes (n = 36) associated with invadopodia formation were analyzed to reveal relevant expression patterns and give a comprehensive overview of them. The genes were analyzed from a whole genome dataset of 83 OSCC samples relating to tumor size, grading, lymph node status, and UICC (Union for Internatioanl Cancer Control). The data revealed significant overexpression of 18 genes, most notably CTTN, SRC (SRC proto-onocogene, non-receptor tyrosine kinase), EGFR (epidermal growth factor receptor), SYK (spleen associated tyrosine kinase), WASL (WASP like actin nucleation promotion factor), and ARPC2 (arrestin beta 1) due to their significant correlation with further tumor parameters. This study is one of the first to summarize the expression patterns of CTTN and related genes in a complex group of OSCC samples. Full article
(This article belongs to the Special Issue Advances in Molecular Pathogenesis Regulation in Cancer)
17 pages, 2127 KiB  
Article
Combining Irradiation and Biological Control against Brown Marmorated Stink Bug: Are Sterile Eggs a Suitable Substrate for the Egg Parasitoid Trissolcus japonicus?
by Gerardo Roselli, Gianfranco Anfora, Raffaele Sasso, Livia Zapponi, Sergio Musmeci, Alessia Cemmi, David Maxwell Suckling, Kim Alan Hoelmer, Claudio Ioriatti and Massimo Cristofaro
Insects 2023, 14(7), 654; https://doi.org/10.3390/insects14070654 - 22 Jul 2023
Cited by 3 | Viewed by 1765
Abstract
The brown marmorated stink bug (BMSB), Halyomorpha halys, is a phytophagous invasive pest native to south-eastern Asia, and it is now distributed worldwide. This species is considered to be one of the most damaging insect pests in North America and in Europe. [...] Read more.
The brown marmorated stink bug (BMSB), Halyomorpha halys, is a phytophagous invasive pest native to south-eastern Asia, and it is now distributed worldwide. This species is considered to be one of the most damaging insect pests in North America and in Europe. In agriculture, the predominant approach to managing BMSB is based on the use of insecticides, specifically pyrethroids and neonicotinoids. Unfortunately, the biology of the species and its facility to develop mechanisms of resistance to available pesticides has induced farmers and scientists to develop different, least-toxic, and more effective strategies of control. In a territorial area-wide approach, the use of a classical biological control program in combination with other least-toxic strategies has been given prominent consideration. Following exploratory surveys in the native range, attention has focused on Trissolcus japonicus, a small scelionid egg parasitoid wasp that is able to oviposit and complete its larval development in a single egg of H. halys. A common method for detecting egg parasitoids in the native range involves the placement of so-called ‘sentinel’ egg masses of the pest in the environment for a short period, which are then returned to the laboratory to determine if any of them are parasitized. Outside of the area of origin, the use of fertile sentinel eggs of the alien species may lead to the further release of the pest species; an alternative is to use sterile sentinel eggs to record the presence of new indigenous egg parasitoids or to detect the dispersal of alien species (in this case, T. japonicus) released in a new environment to control the target insect pest species. This study evaluated the performance of three types of sterile sentinel eggs as a suitable substrate for the oviposition and larval development of the egg parasitoid T. japonicus in a context of combining classical biological control with a Sterile Insect Technique (SIT) approach. Full article
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<p>Average (±95% confidence interval) proportion of emergence (%) for the egg mass type (I, Irradiated; R, Refrigerated; S, SIT) at different egg age.</p>
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<p>Estimated smooth functions for the generalized additive models (GAMs), according to egg mass type (I, Irradiated; R, Refrigerated; S, SIT). Smoothing parameters estimated using restricted maximum likelihood (REML). Different letters indicate different parameters: (<b>a</b>), Proportion of emergence; (<b>b</b>), Sex ratio; (<b>c</b>), Fecundity—0 days; (<b>d</b>), Fecundity—12 days; (<b>e</b>), Dry weight; (<b>f</b>), Longevity.</p>
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15 pages, 2786 KiB  
Article
Efficacy of Protein Baits with Fipronil to Control Vespa velutina nigrithorax (Lepeletier, 1836) in Apiaries
by Jesús F. Barandika, Omaira de la Hera, Roberto Fañanás, Arrate Rivas, Eugenia Arroyo, Rosa M. Alonso, M. Luz Alonso, Egoitz Galartza, Aitor Cevidanes and Ana L. García-Pérez
Animals 2023, 13(13), 2075; https://doi.org/10.3390/ani13132075 - 23 Jun 2023
Cited by 5 | Viewed by 2047
Abstract
The yellow-legged hornet (Vespa velutina nigrithorax), outside its natural range, has become a major threat to domestic bees. Several control methods have been used to fight against V. velutina, but the results achieved are not satisfactory. The use of protein [...] Read more.
The yellow-legged hornet (Vespa velutina nigrithorax), outside its natural range, has become a major threat to domestic bees. Several control methods have been used to fight against V. velutina, but the results achieved are not satisfactory. The use of protein baits with biocides has shown to be an effective method to control invasive wasp populations, but they have not been used to control V. velutina. Thus, the efficacy of protein baits containing fipronil to reduce the presence of hornets in apiaries was evaluated in this study. After laboratory determination of the optimal efficacy of a protein bait at a 0.01% concentration of fipronil, field trials were conducted involving 222 beekeepers. The data reported by the 90 beekeepers who completed the requested questionnaire demonstrated that in the groups of apiaries with the highest pressure of hornets (groups with 10–30 and >30 hornets), there was a significant decrease in the presence of V. velutina, lasting at least two weeks. The reduction in the number of hornets was positively correlated with bait consumption, and bait consumption was positively correlated with the number of hornets present at the time of treatment. Although the method used has shown good efficacy and the concentration of fipronil used was very low; possible negative effects on the environment should also be evaluated. Full article
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<p>Color changes observed in the <span class="html-italic">Vespa velutina</span> larvae (<b>A</b>), and aspect of swollen larva in comparison with control larva (<b>B</b>,<b>C</b>) within 48 h after feeding with fipronil.</p>
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<p>Counts of hornets in front of the hives on the day of treatment (<b>A</b>) and the amount of bait consumed in each apiary (<b>B</b>) over the three months in which the trials were carried out. The black dots represent the mean. Orange and blue dots represent individual observations.</p>
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<p>Overall mean evolution of the number of hornets during the field trial [*, <span class="html-italic">p</span> &lt; 0.05].</p>
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<p>Correlation between the number of hornets in the apiaries and the bait consumed on Day 0 (<b>A</b>). Correlation between the bait consumption on Day 0 and the percentage of reduction (RE%) on days +2 (<b>B</b>), +7 (<b>C</b>) and +14 (<b>D</b>) post-baiting; R = Spearman’s rank correlation rho. The shaded area corresponds to the 95% confidence interval of the regression line (in blue).</p>
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13 pages, 5563 KiB  
Article
Host Range Expansion of Nest-Parasitic Moths Pyralis regalis and Hypsopygia mauritialis in Social Wasp Nests: New Findings and Implications for Biological Control
by Young-Min Shin, Heung Sik Lee, Il-Kwon Kim, Chang-Jun Kim and Moon Bo Choi
Diversity 2023, 15(6), 789; https://doi.org/10.3390/d15060789 - 19 Jun 2023
Viewed by 2504
Abstract
Parasitic moths are common in social wasp (Hymenoptera) nests, attacking many species of Polistinae and a few species of Vespinae. In the Republic of Korea, two moth species are known to parasitize the brood of Polistes rothneyi koreanus: Pyralis regalis (Pyralidae) and [...] Read more.
Parasitic moths are common in social wasp (Hymenoptera) nests, attacking many species of Polistinae and a few species of Vespinae. In the Republic of Korea, two moth species are known to parasitize the brood of Polistes rothneyi koreanus: Pyralis regalis (Pyralidae) and Anatrachyntis japonica (Cosmopterigidae). Although previously reported elsewhere, a novel case of parasitization was recently documented in the Republic of Korea, in which Hypsopygia mauritialis (Pyralidae) was identified in the nests of social wasps. Pyralis regalis is the most common parasitic moth in the Republic of Korea, feeding on the nests of 11 species of social wasps, mostly the Korean Vespa species. To that list of hosts, we add a species of Dolichovespula and two species of Polistes. Parasitism of Vespa velutina nigrithorax, an invasive alien hornet, by both P. regalis and H. mauritialis, was observed for the first time. However, their potential to control invasive alien hornets is expected to be low. This study provides new insights into the diversity of nest-parasitic moths in social wasp nests and their hosts in the Republic of Korea, and highlights the potential for these moths to impact pest populations. Full article
(This article belongs to the Special Issue Ecology and Management of Invasive Vespidae)
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Figure 1
<p><span class="html-italic">Hypsopygia mauritialis</span>. (<b>A</b>) Adult male; (<b>B</b>) adult female; (<b>C</b>) male genitalia (slide no. KNAEYM181); (<b>D</b>) female genitalia (slide no. KNAEYM182); (<b>E</b>) detail of signum. &lt;Scale bar: 1 mm&gt;.</p>
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<p>Neighbor-joining tree of the genus <span class="html-italic">Hypsopygia</span>. The divergence was calculated using the Kimura 2-parameter model on the basis of 280–658 bp COI sequences. Bootstrap values below 50 are not shown. The sequences of the <span class="html-italic">P. regalis</span>, which includes Pyralini, were used as an outgroup.</p>
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<p>A nest-parasitic moth, <span class="html-italic">P. regalis</span> (arrow), appeared in the nests of the <span class="html-italic">Vespa</span> species in the Republic of Korea. (<b>A</b>) Traces of silk bundles generated by <span class="html-italic">P. regalis</span> in the nest of <span class="html-italic">V. analis parallela</span>; (<b>B</b>) larvae of <span class="html-italic">P. regalis</span> developed from the nest of <span class="html-italic">V. simillima simillima</span>; (<b>C</b>) <span class="html-italic">P. regalis</span> adults emerged from the nest of <span class="html-italic">V. mandarinia</span>; (<b>D</b>) larvae of <span class="html-italic">P. regalis</span> developed in the nest of <span class="html-italic">V. dybowskii.</span></p>
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<p>Nest-parasitic moths from the nests of <span class="html-italic">P. rothneyi koreanus</span>. (<b>A</b>,<b>B</b>) Adult (<b>A</b>) and larvae (<b>B</b>) of <span class="html-italic">P. regalis</span> occurred in the nests; (<b>C</b>) excreta filled in most cells of the nest by <span class="html-italic">P. regalis</span> larvae feeding inside (28 September, Nest 24); (<b>D</b>) adult of <span class="html-italic">A. japonica</span> emerging from nest; (<b>E</b>) entire nest infected by <span class="html-italic">A. japonica</span>; (<b>F</b>) holes (red circle) made by <span class="html-italic">A. japonica</span> larvae feeding through the nest.</p>
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<p><span class="html-italic">H. mauritialis</span> from nests of <span class="html-italic">P. rothneyi koreanus</span>. (<b>A</b>) Entire nest infested by <span class="html-italic">H. mauritialis</span>; (<b>B</b>) <span class="html-italic">H. mauritialis</span> adults newly emerged from a nest.</p>
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<p>Nest-parasitic moths from the nests of the invasive alien hornet, <span class="html-italic">V. velutina nigrithorax</span>. (<b>A</b>) The primary nest of <span class="html-italic">V. velutina nigrithorax</span> infected by <span class="html-italic">P. regalis</span> (Andong, Nest 11), with wasp workers remaining until early August; (<b>B</b>) adult <span class="html-italic">P. regalis</span> from Nest 11; (<b>C</b>) Nest 11, where most of the comb was parasitized by <span class="html-italic">P. regalis</span>; (<b>D</b>) <span class="html-italic">P. regalis</span> larvae occurred from Nest 10, of which most of the cells were covered by a silk web of the larvae; (<b>E</b>) the primary nest parasitized by <span class="html-italic">H. mauritialis</span> (Jinju, Nest 38), there were no workers in the nest in early August; (<b>F</b>,<b>G</b>) <span class="html-italic">H. mauritialis</span> larvae and adults found in Nest 37 (found dead in nests kept indoors). See <a href="#diversity-15-00789-t001" class="html-table">Table 1</a> for the nest numbers.</p>
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13 pages, 4703 KiB  
Article
Climatic Niche Differentiation between the Invasive Hornet Vespa velutina nigrithorax and Two Native Hornets in Europe, Vespa crabro and Vespa orientalis
by Simone Lioy, Luca Carisio, Aulo Manino and Marco Porporato
Diversity 2023, 15(4), 495; https://doi.org/10.3390/d15040495 - 28 Mar 2023
Cited by 9 | Viewed by 3293
Abstract
The introduction and expansion of the Asian yellow-legged hornet (Vespa velutina nigrithorax) in Europe poses concern for multiple reasons, including biodiversity conservation. In addition to the predation of native insects (e.g., bees and wasps), this species may compete with native hornets [...] Read more.
The introduction and expansion of the Asian yellow-legged hornet (Vespa velutina nigrithorax) in Europe poses concern for multiple reasons, including biodiversity conservation. In addition to the predation of native insects (e.g., bees and wasps), this species may compete with native hornets due to an overlap of their climatic and trophic niches. The aim of this study is to investigate the realised climatic niche of V. v. nigrithorax and its response to climatic conditions and to evaluate the degree of overlap with the niches of the two native Vespa species present in Europe, Vespa crabro and Vespa orientalis. The niches of both native species partially overlap with the niche of the invasive species (Schoener’s D, 0.43 for V. crabro and 0.28 for V. orientalis), although some differences can be detected. V. crabro appears to be more adapted to cold and dry conditions than the invasive species, and V. orientalis is more adapted to arid climates. These differences may provide a competitive advantage to both native species in areas with a lower environmental suitability for V. v. nigrithorax, in the probable event that this species continues to spread, reaching all areas predicted to be suitable in Europe and in the Mediterranean basin. Full article
(This article belongs to the Special Issue Ecology and Management of Invasive Vespidae)
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<p>Global distribution of <span class="html-italic">Vespa velutina</span> (blue), <span class="html-italic">V. crabro</span> (red) and <span class="html-italic">V. orientalis</span> (orange). The temporal range of the data is 1990–2021.</p>
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<p>Distribution of <span class="html-italic">Vespa velutina nigrithorax</span> (<b>a</b>), <span class="html-italic">V. crabro</span> (<b>b</b>) and <span class="html-italic">V. orientalis</span> (<b>c</b>) in the western palearctic and saharo-arabian zoogeographic region (violet area of the map). The temporal range of the data is 1990–2021.</p>
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<p>Distribution of <span class="html-italic">Vespa crabro</span>, <span class="html-italic">V. orientalis</span> and <span class="html-italic">V. v. nigrithorax</span> records along the latitudinal gradient of the study area, after considering the sampling bias.</p>
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<p>Results of the climatic niche analysis (PCA-env) at the study area level. (<b>a</b>,<b>c</b>) show the realised climatic niches of <span class="html-italic">Vespa velutina nigrithorax</span> (red) and the one of the two native species (green), respectively <span class="html-italic">V. crabro</span> and <span class="html-italic">V. orientalis</span>. Niche overlap is highlighted in blue. The solid and dashed contour lines illustrate, respectively, 100% and 50% of the available (background) environment. Arrows represent how the centre of the niche (red solid lines) and of the background (blue dashed line) change between species. (<b>b</b>,<b>d</b>) represent the variables plot of the PCA-env analysis along the first two principal components (PC1 and PC2).</p>
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<p>Density plots of the first two components (PC1 and PC2) of the PCA-env analyses between <span class="html-italic">Vespa velutina nigrithorax</span> (blue) and the two native <span class="html-italic">Vespa</span> species, respectively <span class="html-italic">V. crabro</span> (red, <b>a</b>,<b>b</b>) and <span class="html-italic">V. orientalis</span> (yellow, <b>c</b>,<b>d</b>).</p>
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<p>Results of the climatic niche analysis (PCA-occ) in the areas of co-occurrence of <span class="html-italic">Vespa velutina nigrithorax</span> and <span class="html-italic">V. crabro</span>. (<b>a</b>) shows the realised climatic niches of <span class="html-italic">V. v. nigrithorax</span> (red) and <span class="html-italic">V. crabro</span> (green). Niche overlap is highlighted in blue. The solid and dashed contour lines illustrate, respectively, 100 and 50% of the available (background) environment. The red arrow represents how the centre of the niche changes between species. (<b>b</b>) show the variables plot of the PCA-occ analysis along the first two principal components (PC1 and PC2). (<b>c</b>,<b>d</b>) report the density plots of the PCA-occ along the first two components, respectively, PC1 and PC2.</p>
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18 pages, 3238 KiB  
Article
Occurrence, Distribution, Damage Potential, and Farmers’ Perception on Fall Armyworm, Spodoptera frugiperda (J.E. Smith): Evidence from the Eastern Himalayan Region
by Satyapriya Singh, Mahadevan Raghuraman, Manikyanahalli Chandrashekara Keerthi, Anup Das, Saswat Kumar Kar, Biswajit Das, Hidangmayum Lembisana Devi, Sunil Kumar Sunani, Manas Ranjan Sahoo, Ryan Casini, Hosam O. Elansary and Gobinda Chandra Acharya
Sustainability 2023, 15(7), 5681; https://doi.org/10.3390/su15075681 - 24 Mar 2023
Cited by 7 | Viewed by 3045
Abstract
The fall armyworm (FAW), Spodoptera frugiperda (J.E. Smith), is a polyphagous non-native pest identified as a serious threat to crop production and food security globally, including in India. Its unintentional introduction and quick coverage in large areas is a serious concern to millions [...] Read more.
The fall armyworm (FAW), Spodoptera frugiperda (J.E. Smith), is a polyphagous non-native pest identified as a serious threat to crop production and food security globally, including in India. Its unintentional introduction and quick coverage in large areas is a serious concern to millions of farmers in the eastern Himalayan region. However, detailed understanding of farmers’ perceptions and the biological attributes associated with the meteorological factors for FAW is limited. The present investigation, which aimed to create baseline data on this pest, concurs with the idea that the FAW is widely dispersed throughout the maize ecosystems of Tripura, with an average infestation rate of 21.33 percent. The severity ranged from 0 to 1.40, with an average leaf damage score of 1 on a 0–4 categorical scale. The findings indicate that pheromone trap catch was significantly correlated with the evaporation rate as other meteorological factors influenced variably. The biological attributes imply that the life cycle was completed in 32.82 ± 0.08 days, with a high fecundity potential (1068.57 ± 4.35 numbers) in controlled conditions (25 ± 1 °C, 70 ± 5% RH). Indigenous natural enemies, such as entomopathogens, spiders, and wasps, were found to be the first defence against this invasive pest. A minority of the population (17.51%) was aware of the incidence of FAW. Furthermore, respondents’ socio-demographic variables were associated significantly with FAW status. This is the first scientific report from the eastern Himalayan region about farmers’ knowledge and awareness of the invasiveness of FAW. This finding enumerates a detailed understanding of FAW from diverse perspectives. Further, the concerted data provide an important baseline that could help the development of holistic management strategies for FAW. Full article
(This article belongs to the Special Issue Causes and Impacts of Biological Invasions in the Anthropocene)
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<p>Location of the study. The collection sites are magnified, and respective regions are denoted by circumferences of different colours. The elevation is distinctly coloured. The collection sites are marked with (▲). Damaged field and FAW larvae are depicted graphically.</p>
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<p>Biology, damage and natural enemies of fall armyworm; (<b>a</b>) egg stage; (<b>b</b>) larval stage; (<b>c</b>) pupal stage; (<b>d</b>) adult female; (<b>e</b>) adult male; (<b>f</b>) larva feeding in whorl region of the maize plant with production of frasses and faecal matter; (<b>g</b>) <span class="html-italic">Eocanthecona furcellata</span> adult; (<b>h</b>). Ichneumonid pupae; (<b>i</b>,<b>j</b>) attack by entomopathogen (fungal infection and NPV infection); (<b>k</b>) <span class="html-italic">Campoletis chloridae</span>; (<b>l</b>) spiders; (<b>m</b>) wasp. All the images were captured by the corresponding author, Satyapriya Singh.</p>
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<p>Severity of <span class="html-italic">S. frugiperda.</span> Violin and box plots showing the distribution of severity of <span class="html-italic">S. frugiperda</span> in each of the 15 locations. Points are jittered along the <span class="html-italic">x</span>-axis to ease visualization.</p>
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<p>Leaf damage rating for infestation by <span class="html-italic">S. frugiperda.</span> Violin and box plots showing the distribution of damage rating of <span class="html-italic">S. frugiperda</span> in each of the 15 locations. Points are jittered along the <span class="html-italic">x</span>-axis to ease visualization.</p>
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<p>Percentage of insect intensity for <span class="html-italic">S. frugiperda.</span> Violin and box plots show the distribution of percentages of insect intensity for <span class="html-italic">S. frugiperda</span> in each of the 15 locations. Points are jittered along the <span class="html-italic">x</span>-axis to ease visualization.</p>
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<p>Correlation analysis between the insect caught in the trap and the weather factor. Significance level; ns <span class="html-italic">p</span> ≥ 0.05, * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Natural mortality factor. Box plot; the middle line gives the median value, Upper and lower bar represents 75 and 25% quartile. Different letters above bars represent significant difference.</p>
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