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1,285 results for “cicada”

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zenodo32/100

Fig. 3 in Giant Cicada Emergence, Protandry and Chorus Centers Formation as Revealed by Studies Using a Sound Trap

Fig. 3 Chorionated oocytes (mean number ± SEM) per Quesada gigas female (columns) and percentage of mature females of Q. gigas (diamonds) captured at different days after the beginning of male emergence in 2015

opennotspecifiedMay 2017View details →
zenodo32/100

Fig. 2 in Giant Cicada Emergence, Protandry and Chorus Centers Formation as Revealed by Studies Using a Sound Trap

Fig. 2 Ovarian maturation status in Quesada gigas captured in 2013 at two dates after cicada emergence. a Immature ovary of Quesada gigas at 15 days after male emergence (DAME). b Mature ovary of Q. gigas with chorionated oocytes inside ovarioles at 30 DAME

opennotspecifiedMay 2017View details →
zenodo32/100

Fig. 4 in Giant Cicada Emergence, Protandry and Chorus Centers Formation as Revealed by Studies Using a Sound Trap

Fig. 4 Number of cicada males (diamonds) or females (squares) collected at different days after the beginning of male emergence using the sound trap in 2015

opennotspecifiedMay 2017View details →
zenodo32/100

Fig. 3 in Thermal adaptation in North American cicadas (Hemiptera: Cicadidae)

Fig. 3. Thermal responses of species with different emergence times in the same habitat. All Magicicada species are active early in the year (May-June) while the Neotibicen species are active in late summer (August-September). ANOVA tests show all thermal responses are significantly different with P <0.001. Species pairs differ significantly (P <0.05 or smaller) except those marked with *, **, ***, †, or †† which have P> 0.05. Maximum voluntary tolerance (MVT) and heat torpor temperatures (HTT) are elevated in species active late in the season when there is the potential exposure to higher temperatures. See text for statistical analysis of each species pair.

opennotspecifiedOct 2017View details →
zenodo32/100

Fig. 2 in Thermal adaptation in North American cicadas (Hemiptera: Cicadidae)

Fig. 2. Thermal responses of the endothermic Neotibicen winnemanna and the sympatric ectothermic N. tibicen tibicen. The minimum flight temperature (MFT) values (*P <0.0001) and maximum voluntary tolerance (MVT) values (**P = 0.0009) differ significantly illustrating the influence of thermoregulatory behavior on the evolution of thermal responses. The heat torpor temperature (HTT) values do not differ significantly (P> 0.05) from one another showing that adaptation to maximum potential habitat temperature is independent of thermoregulatory strategy.

opennotspecifiedOct 2017View details →
zenodo32/100

Fig. 1 in Thermal adaptation in North American cicadas (Hemiptera: Cicadidae)

Fig. 1. Comparison of maximum voluntary tolerance (MVT) and heat torpor temperature (HTT) of Okanagodes gracilis gracilis with species inhabiting different environments and altitudes of Arizona. The MVT and HTT of O. gracilis gracilis is significantly different from all other species at P <0.001.

opennotspecifiedOct 2017View details →
zenodo32/100

Fig. 1 in Virulence of two entomopathogenic nematode species, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), to nymphs of the coffee cicada Dundubia nagarasingna

Fig. 1. Mortality of coffee cicada nymphs, Dundubia nagarasingna, treated with entomopathogenic nematodes, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), at inoculation doses of 100, 200, 300, 400, 500 and 600 infective juveniles (IJ) nymph−1 at A: 24 h, B: 48 h, C: 72 h after inoculation. Values are means ± SE; different letters in each figure represent means that are statistically different between nematode concentrations (Tukey's HSDtest, P <0.05). Thecorrectedcumulative mortality axis indicates nymphal mortality increasing with IJ inoculation doses and exposure time. Mortality data were corrected by Abbott's formula (Abbott, 1925).

opennotspecifiedDec 2018View details →
zenodo32/100

Fig. 4 in Virulence of two entomopathogenic nematode species, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), to nymphs of the coffee cicada Dundubia nagarasingna

Fig. 4. Number of infective juveniles (IJ) (250 ml soil)−1 at the treatment dose of 40 × 103 and 60 × 103 IJ pot−1 10, 20 and 30 days after treatment. A: S-PQ16 strain, B: H-KT3987 strain. Letters indicate significant differences among interval times in each (lower case andupper case) IJdose (one-way ANOVA, P <0.05). Pair-treatmentcomparisonbetweeninitialinoculationsisrepresentedwithlines above thecolumns (Student's t -test, *P <0.05, **P <0.01, ***P <0.001, ns: not significant). Valuesaremeans ± SE.

opennotspecifiedDec 2018View details →
zenodo32/100

Fig. 3 in Virulence of two entomopathogenic nematode species, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), to nymphs of the coffee cicada Dundubia nagarasingna

Fig. 3. Efficacy of entomopathogenic nematodes, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), to coffee cicada nymphs at doses of 40 × 103 and 60 × 103 infective juveniles (IJ) pot−1 after 10, 20 and 30 DAT. A: S-PQ16 strain; B: H-KT3987 strain. Different letters indicate significant differences among interval times in each nematode concentration (One-way ANOVA, P <0.05). Comparisonbetweentwotreateddosesisrepresentedwithlinesabovethecolumns (Student's t -test, *P <0.05, **P <0.01, ***P <0.001, ns: notsignificant). Valuesaremeans ± SE.

opennotspecifiedDec 2018View details →
zenodo32/100

Fig. 2 in Virulence of two entomopathogenic nematode species, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), to nymphs of the coffee cicada Dundubia nagarasingna

Fig. 2. Reproduction yields of entomopathogenic nematodes, Steinernema sp. (strain PQ16) and Heterorhabditis indica (strain KT3987), in coffee cicada nymphs. Values are means ± SE; different letters at the tops of the bars represent means that are statistically differentamong EPNconcentrations (Tukey's HSDtest, P <0.05).

opennotspecifiedDec 2018View details →
zenodo32/100

Figure 6 in Endothermy in African Platypleurine Cicadas: The Influence of Body Size and Habitat (Hemiptera: Cicadidae)

Figure 6. Allometric relationship between maximum calculated ˙Vo2 and body size in cicadas. Values represent the mean value determined for each species (n = 1–8). Filled circles represent endothermic platypleurines, the open circle represents the ectothermic Albanycada albigera, filled squares represent New World endotherms, and open squares represent New World ectotherms. Additional data are from Heath and Wilkin (1970), Heath et al. (1972), Bartholomew and Barnhart (1984), Sanborn (2000), Sanborn et al. (1995a, 1995b, 2003a), and Villet et al. (2003).

opennotspecifiedSep 2004View details →
zenodo32/100

Figure 7 in Endothermy in African Platypleurine Cicadas: The Influence of Body Size and Habitat (Hemiptera: Cicadidae)

Figure 7. Allometric relationship between cooling rate and body size in cicadas. Values represent the mean value reported for each species (n = 1–8). Filled circles represent endothermic platypleurines, the open circle represents the ectothermic Albanycada albigera, filled squares represent New World endotherms, and open squares represent New World ectotherms. Additional data are from Heath and Wilkin (1970), Heath et al. (1972), Bartholomew and Barnhart (1984), Sanborn et al. (1992, 1995a, 1995b, 2002, 2003a), Sanborn (2000), and Villet et al. (2003).

opennotspecifiedSep 2004View details →
zenodo32/100

Figure 4 in Endothermy in African Platypleurine Cicadas: The Influence of Body Size and Habitat (Hemiptera: Cicadidae)

Figure 4. Body temperature as a function of ambient temperature in the endothermic Platypleura plumosa. The slope is significantly different from 1, suggesting thermoregulation. Filled circles represent diurnally calling animals, and open circles represent animals calling without access to solar radiation.

opennotspecifiedSep 2004View details →
zenodo32/100

Figure 3 in Endothermy in African Platypleurine Cicadas: The Influence of Body Size and Habitat (Hemiptera: Cicadidae)

Figure 3. Body temperature as a function of ambient temperature in the endothermic Platypleura capensis. The slope is significantly different from 1, suggesting thermoregulation. Filled circles represent diurnally calling animals; open circles represent animals calling without access to solar radiation.

opennotspecifiedSep 2004View details →
zenodo32/100

Figure 2 in Endothermy in African Platypleurine Cicadas: The Influence of Body Size and Habitat (Hemiptera: Cicadidae)

Figure 2. Body temperature as a function of ambient temperature in the endothermic Platypleura hirtipennis. The slope is significantly different from 1, suggesting thermoregulation. Filled circles represent diurnally calling animals, and open circles represent animals calling without access to solar radiation.

opennotspecifiedSep 2004View details →
zenodo32/100

Figure 1 in Endothermy in African Platypleurine Cicadas: The Influence of Body Size and Habitat (Hemiptera: Cicadidae)

Figure 1. Body temperature as a function of ambient temperature in the ectothermic Albanycada albigera. The slope is not significantly different from 0, suggesting thermoregulation.

opennotspecifiedSep 2004View details →
zenodo32/100

Fig. 5 in An integrated analysis of hyperspectral and morphological data of cicada ovipositors revealed unexplored links to specific oviposition hosts

Fig. 5 Hierarchical cluster cladogram based on 25 morphological characters for each of the 11 cicada species. Ca, Cryptotympana atrata; Hm, Hyalessa maculaticollis; Kc, Karenia caelatata; Kn, Katoa neokanagana; Mm, Meimuna mongolica; Mo, Meimuna opalifera; Ph, Platypleura hilpa; Pk, Platypleura kaempferi; Pl, Pomponia linearis; Sy, Subpsaltria yangi; Tj, Tanna japonensis. Height: the value of the criterion associated with the clustering method for the particular agglomeration

opennotspecifiedJan 2019View details →
zenodo32/100

Fig. 4 in An integrated analysis of hyperspectral and morphological data of cicada ovipositors revealed unexplored links to specific oviposition hosts

Fig. 4 Comparison of morphological characters of ovipositors among different species. a Ovipositor length; b ovipositor height; c basal width of ovipositor; d apical width of ovipositor; e subapical width of ovipositor; f curvature. Data are presented as mean ± SE. Ca, Cryptotympana atrata; Hm, Hyalessa maculaticollis; Kc, Karenia caelatata; Kn, Katoa neokanagana; Mm, Meimuna mongolica; Mo, Meimuna opalifera; Ph, Platypleura hilpa; Pk, Platypleura kaempferi; Pl, Pomponia linearis; Sy, Subpsaltria yangi; Tj, Tanna japonensis

opennotspecifiedJan 2019View details →
zenodo32/100

Fig. 2 in An integrated analysis of hyperspectral and morphological data of cicada ovipositors revealed unexplored links to specific oviposition hosts

Fig. 2 Four major types of sensilla. a Campaniform sensilla; b Basiconica sensilla; c Trichoid sensilla; d Coeloconic sensilla [from Zhong et al. (2017), with kind permission from Springer publishers]. Scale bars: a, b, d 5 µm; c 20 µm

opennotspecifiedJan 2019View details →
ClinicalTrials.gov32/100

Comparing Insomnia Care As Usual to Digital Augmentation (CICADA)

ClinicalTrials.gov study NCT05490550. IPD Sharing: NO. Countries: 1. Publications: 3.

closedIPD-NOFeb 2026View details →

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