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Table 2 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany
<p><b>Table 2</b> Maximum temperature of water (°C) in the mosquito-positive ovitraps during the field studies at the different study sites</p><table><tbody><tr><th>Study</th><th>Site</th><th><i>Ae. japonicus japonicus</i></th><th><i>Cx.pipiens</i> s.l.</th><th><i>An. plumbeus</i></th><th><i>Ae. geniculatus</i></th></tr></tbody><tbody><tr><th>2017</th><td>Alfter</td><td>26.8</td><td>34.7</td><td>31.3</td><td>20.3</td></tr><tr><th></th><td>Dormagen</td><td>22.1</td><td>27.2</td><td>17.3</td><td>21.7</td></tr><tr><th>2018</th><td>Alfter</td><td>22.6</td><td>19.8</td><td>20.6</td><td>n.n.</td></tr><tr><th></th><td>Bonn SÜd</td><td>24.7</td><td>24</td><td>17.3</td><td>n.n.</td></tr><tr><th></th><td>Heimerzheim</td><td>24.3</td><td>24.6</td><td>23.2</td><td>22.7</td></tr><tr><th></th><td>Lohmar</td><td>28.6</td><td>25.8</td><td>28.6</td><td>16.6</td></tr><tr><th></th><td>Siegburg</td><td>25.8</td><td>30</td><td>27</td><td>23.1</td></tr><tr><th></th><td>Troisdorf</td><td>26.8</td><td>27.7</td><td>25.2</td><td>n.n.</td></tr></tbody></table><p><i>n.n.</i> Species not present</p>
Table 1 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany
<p><b>Table 1</b> Total number and percentages of positive samples and occurrence of mosquito species per trap</p><table><tbody><tr><th>Study</th><th></th><th><i>Aedes japonicus japonicus</i></th><th><i>Culex pipiens</i> s.l.</th><th><i>Anopheles plumbeus</i></th><th><i>Aedes geniculatus</i></th><th>Total</th></tr></tbody><tbody><tr><th>2017</th><td>Total positive traps (<i>n</i>)</td><td>97</td><td>199</td><td>47</td><td>38</td><td>381</td></tr><tr><th></th><td>Positive traps/analysable traps (%)</td><td>15.4</td><td>31.7</td><td>7.5</td><td>6.1</td><td>60.7</td></tr><tr><th></th><td>Traps multiple species (<i>n</i>)</td><td>56</td><td>58</td><td>39</td><td>25</td><td>80</td></tr><tr><th></th><td>Multiple species/positive traps (%)</td><td>57.7</td><td>29.1</td><td>83</td><td>65.8</td><td>21</td></tr><tr><th>2018</th><td>Total positive traps (<i>n</i>)</td><td>441</td><td>285</td><td>137</td><td>19</td><td>882</td></tr><tr><th></th><td>Positive traps/analysable traps (%)</td><td>20.3</td><td>13.1</td><td>6.3</td><td>0.9</td><td>40.7</td></tr><tr><th></th><td>Traps multiple species (<i>n</i>)</td><td>180</td><td>139</td><td>113</td><td>11</td><td>206</td></tr><tr><th></th><td>Multiple species/positive traps (%)</td><td>40.8</td><td>48.8</td><td>82.5</td><td>57.9</td><td>23.4</td></tr></tbody></table><p>Calculations based on a total of 628 samples in 2017 and 2168 samples in 2018.The number of positive ovitraps with more than one species divided by the total number of positive ovitraps represents the portion of positive ovitraps with multiple species.See Additional file 1: Table S1 for all combinations of species and Additional file 2: dataset S1 for all samplings</p>
Table 3 in Oviposition of AedeS japoNiCUS japoNiCUS (Diptera: Culicidae) and associated native species in relation to season, temperature and land use in western Germany
<p><b>Table 3</b> Coefficients and statistically significant output of predictor variables as calculated by the generalised linear model</p><table><tbody><tr><th></th><th>Estimate</th><th>SE</th><th><i>Z</i> -value</th><th><i>P</i></th></tr></tbody><tbody><tr><th>(Intercept)</th><td>− 29.890</td><td>15.100</td><td>− 19.790</td><td>0.0478*</td></tr><tr><th>Temp_mean</th><td>0.2126</td><td>0.0933</td><td>22.800</td><td>0.0226*</td></tr><tr><th>Cxbin</th><td>0.2732</td><td>0.3148</td><td>0.868</td><td>0.3854</td></tr><tr><th>Plbbin</th><td>0.5999</td><td>0.2253</td><td>26.630</td><td>0.0077*</td></tr><tr><th>F100</th><td>0.4931</td><td>0.4826</td><td>10.220</td><td>0.3068</td></tr><tr><th>F10</th><td>0.7486</td><td>0.4127</td><td>18,140</td><td>0.0697</td></tr><tr><th>F/S</th><td>0.8715</td><td>0.3728</td><td>23.380</td><td>0.0194*</td></tr><tr><th>S10</th><td>10.770</td><td>0.3347</td><td>32.170</td><td>0.0013*</td></tr><tr><th>Ngbi</th><td>0.0412</td><td>0.1157</td><td>0.356</td><td>0.722</td></tr><tr><th>Nhbu</th><td>0.0001</td><td>0.0251</td><td>0.003</td><td>0.9972</td></tr><tr><th>Ngki</th><td>0.0295</td><td>0.0432</td><td>0.684</td><td>0.4941</td></tr><tr><th>Nsei</th><td>− 0.0362</td><td>0.0609</td><td>− 0.594</td><td>0.5528</td></tr><tr><th>Ntei</th><td>− 0.0845</td><td>0.0917</td><td>− 0.922</td><td>0.3566</td></tr><tr><th>Ngfi</th><td>0.1002</td><td>0.0832</td><td>12.050</td><td>0.2283</td></tr><tr><th>Nrbu</th><td>0.0648</td><td>0.0456</td><td>14.200</td><td>0.1557</td></tr></tbody></table><p>Characteristics:negative binomial,link = log, <i>z</i> -values calculated by Wald-test. Response variable:total of <i>Ae. japonicus japonicus</i> -positive ovitraps per location Predictors:Temp_mean = Mean water temperature,binary native taxa occurrence:Cxbin = <i>Cx. pipiens</i> s.l., <i>Plbbin An. plumbeus</i>, land use data: percentage forest:F100 = 100% forest,F10 = 60% forest,F/S = 50% forest,S10 = 40% forest,number of tree species in a 10 m radius of the trap locations (the tree species occurred in more than five transects):Nrbu: <i>Fagus sylvatica</i>, Nhbu: <i>Carpinus betulus</i>, Ngbi: <i>Betula pendula</i>, Nsei: <i>Quercus robur</i>, Ntei: <i>Quercus petreae</i>, Ngfi: <i>Picea abies</i>, Ngki: Pinus sylvestris</p>
Figure 16. Conoaxima affinis ovipositing through a in Biology of Lissoderes Champion (Coleoptera, Curculionidae) in Cecropia saplings inhabited by Azteca ants
Figure 16. Conoaxima affinis ovipositing through a prostoma into an Azteca queen.
Fig. 1 in Dependence of daily oviposition activity and total fecundity on body mass in the house cricket Acheta domesticus (L.) (Insecta: Orthoptera)
Fig. 1: Biological traits demonstrably influenced by body mass in orthopterans (WITHMAN 2008).
Figure 2 in Predation and oviposition rates of Gaeolaelaps aculeifer and Parasitus bituberosus (Acari: Laelapidae and Parasitidae) on pre-pupae/pupae of Thrips tabaci (Thysanoptera: Thripidae)
Figure 2 Daily oviposition of Gaeolaelaps aculeiferandParasitus bituberosus on different densities
Fitness landscapes reveal context-dependent benefits of oviposition behaviour
<p><span>Resource choice behaviour has enormous fitness consequences and can drive niche expansion. However, individual behavioural choices are often mediated by context, determined by past experience. Do such context-dependent behaviours reflect maladaptive variation, or are they locally adaptive? Using Tribolium castaneum (the red flour beetle), we demonstrate that context-dependent oviposition behaviour reflects distinct, context-specific local fitness peaks. We measured offspring fitness to generate fitness landscapes as a function of all possible oviposition behaviours (i.e., combinations of fecundity and resource preference) in a habitat containing optimal and suboptimal resource patches. We did this by experimentally manipulating female egg allocation across patches, which allowed us to assess behaviours not typically observed in the laboratory. We found that females from different age and competition contexts exhibit distinct behaviours which optimize different fitness components, linked in a tradeoff. With prior exposure to strong competition and increasing age, females produce few but fast-developing offspring that are advantageous under high resource competition. In contrast, young naïve females produce significantly more (but slower-developing) offspring, which is beneficial under weak competition. Systematically mapping complete context-dependent fitness landscapes is thus critical to infer behavioural optimality and offers predictive power in novel contexts. </span></p>
Multiscale assessment of oviposition habitat associations and implications for management in the spotted lanternfly (Lycorma delicatula), an emerging invasive pest
<p>1. Control of incipient invaders—established invasive species in the early stages of spreading—can be inhibited by incomplete knowledge of the species' habitat use. By identifying consistent habitat associations for incipient invaders early, control efforts can be more effective. Yet, because habitat associations are the result of multiscale processes, approaches are needed for integrating data collected across scales to identify them.</p> <p>2. We employed a hierarchical, multiscale approach to identify oviposition habitat associations in the spotted lanternfly (<em>Lycorma</em> <em>delicatula</em>), an incipient invasive species of high concern in the United States. We targeted four oviposition habitat spatial scales most likely to be used by lanternflies and the spatial scales of explanatory habitat variables most easily used by managers to locate egg masses to control.</p> <p>3. Spotted lanternflies exhibited oviposition habitat associations at the landscape, site, and tree scales. Overall, lanternflies oviposited more frequently at sites and on trees with low canopy cover in the surrounding landscape indicating higher use of human-impacted habitat. Additionally, they oviposited more frequently on trees from the <em>Acer</em> genus and in the crowns of larger trees beyond the reach of managers without special equipment. The duration a site had been invaded had opposing effects on oviposition at the site and tree scales.</p> <p>4. Despite high variation in the number of eggs per egg mass, no habitat variables explained this variation, suggesting more work is needed to understand spotted lanternfly reproductive output.</p> <p>5. Synthesis and applications. Our results indicate a multiscale approach is needed for spotted lanternfly control with unique strategies for locating egg masses at sites and on trees that vary in invasion duration. Specifically, at younger sites at the invasion edge, managers should expect patchy colonization of sites, yet when a site is colonized, many trees will have egg masses. Comparatively, older sites at the invasion core are more likely to have egg masses present, yet often at a lower density, which may make them difficult to find on individual trees. Based on our results, we assert that multiscale investigations of habitat associations would likely inform the control of other incipient invasive species as well. </p>
Oviposition and olfactometry response of codling moth (Cydia pomonella) to quince (Cydonia oblonga) cultivars
<p>Behavioral data of codling moth (Cydia pomonella) mated females and larvae against quince (Cydonia oblonga) cultivars in laboratory assays. </p>
Data on female oviposition behaviour of the Pararge aegeria butterfly in outdoor cages (2019–2020)
<p><span>We studied oviposition behavior in a butterfly (</span><em><span>Pararge aegeria</span></em><span>)</span><span> that used to be confined to forest, but recently colonized anthropogenic areas too. This provides an ideal study system when trying to understand the underlying processes of niche expansion and colonisation success. The dataset produced allows us to test to what extent ecotype origin (agricultural vs. forest landscape types) and larval developmental conditions (open field vs. canopy-covered forest floors) affect multiple features of oviposition behahaviour. We also performed multiple behavioural trials per individual and considered changes in oviposition site preference within and over trials. </span></p> <p>The two provided files contain all behavioral or independent variables that were obtained during behavioural tracking of the oviposition behaviour of the Speckled Wood butterfly (<em>Pararge aegeria</em>) in an outdoor cage in 2019 and 2020.</p> <p>In the<strong> 'femdata' </strong>file, each line contains all dependent (e.g., proportion of time spent active) and independent variables (e.g. ecotype) that apply for a single observation trial of 30 minutes of a single individual.In total, 211 observation trials were performed, by 110 different female individuals. </p> <p>In the <strong>'ovimdata' </strong>file, each line contains all variables for a single oviposition bout (i.e., if a butterfly curls its abdomen on a surface and lays eggs). Examples include number of eggs per bout, the height above ground where an egg was laid and temperature at the egg laying site. These data were for example used to track changes over consecutive bouts within a single trial. In total 275 oviposition bouts were observe, laid by 85 different female individuals.</p> <p>Data of the ovimdata file were also implemented in the femdata file. For example, in the femdata file information can be obtained about the properties of the first oviposition bout an individual made during that trial (starting with 'b1').</p>
Growth rate and oviposition preference of Oc. togoi & Ae. albopictus in salinity stress
<p><em><span>Ochlerotatus togoi</span></em><span><em> </em>is a salt-tolerant euryhaline mosquito that lays its eggs in rock pools. Although it is a pest that transmits flaviviruses and filarial worms to humans, ecological studies have not been actively conducted because of its limited habitat. Rising sea levels have created a favorable environment for <em>Oc. togoi</em> to survive; additionally, the incidence of <em>Oc. togoi</em>-borne diseases may increase with an increase in population of <em>Oc. togoi</em>. We examined oviposition and growth rates in the range of 0–35 psu to obtain ecological data for <em>Oc. togoi</em>. <em>Ochlerotatus togoi</em> exhibited the highest oviposition preference at 0 psu; however, the hatching rate was highest at 10 psu, the pupation rate was highest at 25 psu, and the emergence rate was highest at 5 psu. <em>Ochlerotatus togoi</em> showed the highest rate of growth into adults at 25 psu. The results were verified for statistical significance using Mann–Whitney U and Kruskal–Wallis H tests (post hoc test: Bonferroni), and a regression equation was generated for the incidence of adult <em>Oc. togoi</em> based on the change in salinity (y = −14.318 + 9.821x; y = adult incidence rate; x = salinity). The oviposition habits and developmental conditions of <em>Oc. togoi</em> were confirmed and the number of <em>Oc. togoi </em>was predicted based on the changes in sea level and ocean salinity. The results of this study are expected to be used for controlling salt-tolerant vectors and responding to vector-borne diseases.</span></p>
Oviposition behaviour is not affected by ultraviolet light in a butterfly with sexually-dimorphic expression of a UV-sensitive opsin
<p>Animal vision is important for mediating multiple complex behaviours. In <em>Heliconius</em> butterflies, vision guides fundamental behaviours such as oviposition, foraging and mate choice. Colour vision in <em>Heliconius</em> involves ultraviolet (UV), blue and long- wavelength sensitive photoreceptors (opsins). Additionally, <em>Heliconius</em> possess a duplicated UV opsin, and its expression varies widely within the genus. In <em>Heliconius</em> <em>erato</em>, opsin expression is sexually dimorphic; only females express both UV-sensitive opsins, enabling UV wavelength discrimination. However, the selective pressures responsible for sex-specific differences in opsin expression and visual perception remain unresolved. Female <em>Heliconius</em> invest heavily in finding suitable hostplants for oviposition, a behaviour heavily dependent on visual cues. Here, we tested the hypothesis that UV vision is important for oviposition in <em>H</em>. <em>erato</em> and <em>Heliconius</em> <em>himera</em> females by manipulating the availability of UV in behavioural experiments under natural conditions. Our results indicate that UV does not influence the number of oviposition attempts or eggs laid, and the hostplant, <em>Passiflora</em> <em>punctata</em>, does not reflect UV wavelengths. Models of <em>H. erato</em> female vision suggest only minimal stimulation of the UV opsins. Overall, these findings suggest that UV wavelengths do not directly affect the ability of <em>Heliconius</em> females to find suitable oviposition sites. Alternatively, UV discrimination could be used in the context of foraging or mate choice, but this remains to be tested.</p>
Plant water limitation and its impact on the oviposition preferences of the monarch butterfly, Danaus plexippus (Lepidoptera: Nymphalidae)
<p>Intensifying drought conditions across the western United States due to global climate change are altering plant-insect interactions. Specialist herbivores must find their host plants within a matrix of nonhosts, and thus often rely upon specific plant secondary chemistry for host location and oviposition cues. Climate-induced alterations to plant chemistry could thus affect female selection of larval food-plants. Here, we investigated whether host-plant water limitation influenced oviposition preference in a threatened invertebrate: the monarch butterfly (<em>Danaus plexippus</em>). We found that females deposited more eggs on reduced-water than on well-watered narrowleaf milkweed plants (<em>Asclepias fascicularis</em>), but we could not attribute this change to any specific change in plant chemistry. Specialist herbivores, such as the monarch butterfly, which are tightly linked to specific plant cues, may experience a shift in preferences under global-change conditions. Understanding oviposition preferences will be important to directing ongoing habitat restoration activities for this declining insect.</p>
Quantifying species traits related to oviposition behavior and offspring survival in two important disease vectors
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Effects of oviposition in a non-host species on foraging behaviour of the parasitoid Cotesia glomerata
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Asymmetric oviposition behaviour between Drosophila suzukii and D. subpulchrella suggests competition for the shared niche in their native range
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Data for: Oviposition fluids mediate larval competition
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Data from: The oviposition of unfertilized eggs depends on the presence of potential mates in a kissing bug
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Data from: Adult nutritional stress decreases oviposition choosiness and fecundity in female butterflies
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Data from: Oviposition strategies of Pieridae butterflies in nature and the role of an egg-killing plant trait therein
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