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76 results for “invasive insect”
FIGURE 4 in New scale insect (Hemiptera: Sternorrhyncha: Coccoidea) records from Fiji: three new species, records of several new invasive species and an updated checklist of Coccoidea
FIGURE 4. Adult female Pseudaulacaspis pyrrosiae Hodgson & Łagowska, sp. n. Where A = small dorsal 2-barred ducts; B = large dorsal 2-barred ducts; C = dorsal view of posterior end of pygidium; D = ventral view of posterior end of pygidium; E = gland spine; F = variation in shape of median lobes; G = ventral microduct; H = ventral small 2-barred duct; J = anterior spiracle, and K = antenna.
FIGURE 2 in New scale insect (Hemiptera: Sternorrhyncha: Coccoidea) records from Fiji: three new species, records of several new invasive species and an updated checklist of Coccoidea
FIGURE 2. Adult female Paracoccus boumaensis Hodgson & Łagowska, sp. n. Where A = dorsal trilocular pore; B = dorsal oral-rim duct; C = dorsal setae; D = dorsal discoidal pore; E = dorsal multilocular pore; F = dorsal view of anal lobe; G = ventral view of anal lobe; H = ventral multilocular pore; J = claw; K = metatibia; L = larger oral-collar duct; M = smaller oral collar duct; N = metacoxa; P = ventral discoidal pore; Q = ventral trilocular pore.
FIGURE 1. Adult female Icerya imperatae Rao. Where A in New scale insect (Hemiptera: Sternorrhyncha: Coccoidea) records from Fiji: three new species, records of several new invasive species and an updated checklist of Coccoidea
FIGURE 1. Adult female Icerya imperatae Rao. Where A = anterior dorsal loculate pore; B = area of dorsum showing density of pores and setae; C = sclerotised dorsal pore; D = dorsal setae; E = abdominal spiracle; F = posterior dorsal loculate pore; G = anal tube; H = ventral seta near vulva; J = vulva area; K = claw; L = area of derm within ovisac band showing density of pores and setae; M = ventral loculate pore; P = sclerotised ventral pore; Q = area of ventral derm showing density of pores and setae; R = trochanter of prothoracic leg; S = antenna; T = loculate pores in ovisac band, and X = loculate pore near anus and vulva.
Light pollution affects invasive and native plant traits important to plant competition and herbivorous insects
<p>Dataset that goes with our accepted publication in Biological Invasions entitled "Light pollution affects invasive and native plant traits important to plant competition and herbivorous insects"</p>
Data from: Evolution of starvation resistance in an invasive insect species, Aethina tumida (Coleoptera: Nitidulidae)
<p>Starvation resistance, or the ability to survive periods without food, can shed light on selection pressure imposed by food scarcity, including chances to invade new regions as a result of human transport. Surprisingly little information is known about starvation resistance for invasive insect species. Given that native and invasive populations differ in starvation resistance, this would suggest different selection scenarios and adaptive shifts fostering invasion success. Here, we show striking differences in starvation resistance of adult small hive beetles Aethina tumida (SHB) between native and invasive populations. In the laboratory, starvation resistance of freshly-emerged laboratory-reared and field-collected adult females and males was evaluated in the beetle's native African range and in their invasive North American range. SHB in their native African range survived longer than SHB in their invasive North American range. Across ranges, females survived longer than males. Field-collected SHB survived in Africa longer than freshly-emerged ones, but not in the invasive range. This suggests no selection for starvation resistance in the invasive range, possibly due to differences between African and European-derived honey bee hosts facilitating a tradeoff scenario between reproduction and starvation resistance. The ability of adult females to survive up to two months without food appears to be one factor contributing to the invasion success of this species. Assuming food availability is usually high in the invasive ranges, and trade-offs between starvation resistance and fecundity/reproduction are common, it seems as if selection for starvation resistance during transport could set up potential trade-offs that enhance reproduction after invasion. It would be interesting to see if this is a possible general pattern for invasive insect species.</p>
Data and code for "Insect and plant invasions follow two waves of globalization"
<p>Data and code for "Insect and plant invasions follow two waves of globalization", Ecology Letters</p>
Data and code for "Insect and plant invasions follow two waves of globalization"
<p>Data and code from: <span>Bonnamour, A.</span>, <span>Gippet, J.M.W.</span>& <span>Bertelsmeier, C.</span> (<span>2021</span>) <span>Insect and plant invasions follow two waves of globalisation</span>. <em>Ecology Letters</em>, <span>24</span>, <span>2418</span>–<span>2426</span>. <a href="https://doi.org/10.1111/ele.13863">https://doi.org/10.1111/ele.13863</a></p>
Figure 3 in Seasonality and abundance of Metamasius callizona (Coleoptera: Dryophthoridae), an invasive insect herbivore, on two species of Tillandsia (Bromeliaceae) in Florida
Figure 3. Average monthly values (¡ two standard errors) for: (A) rainfall (cm); (B) lowest temperature (°C); (C) health ratings for Tillandsia fasciculata; and (D) health ratings for Tillandsia utriculata.
Figure 4 in Seasonality and abundance of Metamasius callizona (Coleoptera: Dryophthoridae), an invasive insect herbivore, on two species of Tillandsia (Bromeliaceae) in Florida
Figure 4. The average weevil count per fallout (wc:fo) per month (¡ two standard errors) for: (A) T. fasciculata; and (B) T. utriculata from June 2001 to June 2005. Note: The weevil count was the number of living weevil adults and living or dead weevil larvae and pupae found in fallout.
Supplementary material 2 from: Brockerhoff EG, Gresham BA, Meurisse N, Nahrung HF, Perret-Gentil A, Pugh AR, Sopow SL, Turner RM (2023) Pining away and at home: global utilisation of Pinus radiata by native and non-native insects. In: Jactel H, Orazio C, Robinet C, Douma JC, Santini A, Battisti A, Branco M, Seehausen L, Kenis M (Eds) Conceptual and technical innovations to better manage invasions of alien pests and pathogens in forests. NeoBiota 84: 137-167. https://doi.org/10.3897/neobiota.84.95864
Statistics for Table 2. Statistical tests of proportions out of all species among feeding types for impacts, establishments and interceptions.
Supplementary material 3 from: Brockerhoff EG, Gresham BA, Meurisse N, Nahrung HF, Perret-Gentil A, Pugh AR, Sopow SL, Turner RM (2023) Pining away and at home: global utilisation of Pinus radiata by native and non-native insects. In: Jactel H, Orazio C, Robinet C, Douma JC, Santini A, Battisti A, Branco M, Seehausen L, Kenis M (Eds) Conceptual and technical innovations to better manage invasions of alien pests and pathogens in forests. NeoBiota 84: 137-167. https://doi.org/10.3897/neobiota.84.95864
Numbers (and percentages) of species by impact class, and whether or not they have been intercepted (based on the international interceptions dataset covering the period 1995–2021) or established in a region outside their native range.
Supplementary material 4 from: Brockerhoff EG, Gresham BA, Meurisse N, Nahrung HF, Perret-Gentil A, Pugh AR, Sopow SL, Turner RM (2023) Pining away and at home: global utilisation of Pinus radiata by native and non-native insects. In: Jactel H, Orazio C, Robinet C, Douma JC, Santini A, Battisti A, Branco M, Seehausen L, Kenis M (Eds) Conceptual and technical innovations to better manage invasions of alien pests and pathogens in forests. NeoBiota 84: 137-167. https://doi.org/10.3897/neobiota.84.95864
Percentages of species native to a region in each feeding guild, regardless of impact. Those in the "Native country: other" category are species native to other regions but not to Australia or New Zealand.
Data from: Implementing an evolutionary framework for understanding genetic relationships of phenotypically defined insect biotypes in the invasive soybean aphid (Aphis glycines)
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Data from: Biological invasion modifies the co-occurrence patterns of insects along a stress gradient
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Data from: Evolution of starvation resistance in an invasive insect species, Aethina tumida (Coleoptera: Nitidulidae)
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Data from: The interactive effects of photoperiod and future climate change may have negative consequences for a wide-spread invasive insect
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Data from: Genome-wide transcriptional signatures of migratory flight activity in a globally invasive insect pest
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Data from: Contrasted invasion processes imprint the genetic structure of an invasive scale insect across southern Europe
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Data from: The effects of insects, nutrients, and plant invasion on community structure and function above- and belowground
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Data from: The ecological implications of rubber-based agroforest: insect conservation and invasion control
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.