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2,567 results for “Leafhoppers”

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zenodo28/100

Figure 16 from: Stiller M (2021) New macropterous leafhopper genera and species within the tribe Bonaspeiini from the Fynbos biome of South Africa (Insecta, Hemiptera, Auchenorrhyncha, Cicadellidae). African Invertebrates 62(1): 1-45. https://doi.org/10.3897/afrinvertebr.62.54721

Figure 16 Flavorubivolatus tensiverpus gen. nov. & sp. nov. male genitalia and ovipositor A aedeagus, lateral, Clanwilliam B aedeagus, lateral, Doltuin C aedeagus, lateral, Clanwilliam D aedeagus, ventral, Clanwilliam E style F connective, Doltuin G connective, Clanwilliam H genital capsule, dorsal I pygofer lobe, lateral J subgenital plate K pygofer lobe, caudal L pygofer lobe, lateral M sternite 7 N pygofer lobe, caudal.

opencc-by-4.0Jan 2021View details →
zenodo28/100

Figure 5 from: Stiller M (2021) New macropterous leafhopper genera and species within the tribe Bonaspeiini from the Fynbos biome of South Africa (Insecta, Hemiptera, Auchenorrhyncha, Cicadellidae). African Invertebrates 62(1): 1-45. https://doi.org/10.3897/afrinvertebr.62.54721

Figure 5 Retevolatus subspiniverpus gen. nov. & sp. nov. ovipositor, specimen from Nuwerus A valvula 1 B valvifer 1 C valvula 1, sculpture, subapex D valvula 1, sculpture, midsection E valvula 2 F valvula 3, apex G valvula 2, sculpture, midsection. Scale bars: 0.5 mm (A, E); 0.05 mm (B–D, F, G).

opencc-by-4.0Jan 2021View details →
zenodo28/100

Figure 6 from: Stiller M (2021) New macropterous leafhopper genera and species within the tribe Bonaspeiini from the Fynbos biome of South Africa (Insecta, Hemiptera, Auchenorrhyncha, Cicadellidae). African Invertebrates 62(1): 1-45. https://doi.org/10.3897/afrinvertebr.62.54721

Figure 6 Retevolatus flexiverpus gen. nov. & sp. nov. male genitalia and female ovipositor A aedeagus, lateral, Brakwater B aedeagus, lateral, Garies C aedeagus, lateral, Ceres D aedeagus, apex, Ceres E aedeagus, gonopore, lateral, Ceres F aedeagus, gonopore, anterior, Ceres G connective H style I subgenital plate J pygofer, Clanwilliam K pygofer, Clanwilliam L sternite 7, Garies M sternite 7, Piketberg N sternite 7, Garies O valvifer 1, left, Garies, specimen #99 P valvifer 1, right, Garies, specimen #99 Q valvifer 1, left Garies, specimen #92 R valvifer 1, right, Garies, specimen #92.

opencc-by-4.0Jan 2021View details →
dryad28/100

Data from: Jumping without slipping: leafhoppers (Hemiptera: Cicadellidae) possess special tarsal structures for jumping from smooth surfaces

Many hemipteran bugs can jump explosively from plant substrates, which can be very smooth. We therefore analysed the jumping performance of froghoppers (Philaenus spumarius, Aphrophoridae) and leafhoppers (Aphrodes bicinctus/makarovi, Cicadellidae) taking off from smooth (glass) and rough (sandpaper, 30 µm asperity size) surfaces. On glass, the propulsive hind legs of Philaenus froghoppers slipped, resulting in uncontrolled jumps with a fast forward spin, a steeper angle and only a quarter of the velocity compared with jumps from rough surfaces. By contrast, Aphrodes leafhoppers took off without their propulsive hind legs slipping, and reached low take-off angles and high velocities on both substrates. This difference in jumping ability from smooth surfaces can be explained not only by the lower acceleration of the long-legged leafhoppers, but also by the presence of 2–9 soft pad-like structures (platellae) on their hind tarsi, which are absent in froghoppers. High-speed videos of jumping showed that platellae contact the surface briefly (approx. 3 ms) during the acceleration phase. Friction force measurements on individual hind tarsi on glass revealed that at low sliding speeds, both pushing and pulling forces were small, and insufficient to explain the recorded jumps. Only when the tarsi were pushed with higher velocities did the contact area of the platellae increase markedly, and high friction forces were produced, consistent with the observed jumps. Our findings show that leafhoppers have special adhesive footpads for jumping from smooth surfaces, which achieve firm grip and rapid control of attachment/detachment by combining anisotropic friction with velocity dependence.

opencc-zeroDec 2016View details →
dryad28/100

Data from: Mammalian herbivores affect leafhoppers associated with specific plant functional types at different timescales

1. Theory predicts that mammalian herbivores affect the quantity and quality of plants on which they preferentially feed in the short term. In the longer term, they can promote either preferred or less preferred plants, depending on whether preferred plants are adapted or sensitive to grazing. Less clear are the short- and long-term responses of herbivorous insects to mammalian herbivory, and how these responses depend on the specific plants or plant functional types on which the insects feed. 2. We progressively excluded large, medium, and small mammals for five growing seasons in two subalpine vegetation types with long-term differences in mammalian grazing intensity. Short-grass vegetation has a history of intensive grazing, while tall-grass vegetation has been grazed less intensively. We tested whether mammals altered the abundance and body size of leafhoppers specialized on specific plant functional types (grasses, sedges, forbs, or legumes/forbs), distinguishing between short-term (exclosures) and long-term (vegetation types) differences in mammalian grazing pressure. Furthermore, we assessed whether leafhoppers' responses were explained by changes in biomass or quality of the plant functional types on which they feed. 3. In the short term, mammal exclosures increased the abundance of grass- and forb-feeding leafhoppers via increases in the biomass of grasses and forbs, regardless of vegetation type. Both grasses and forbs are preferred food plants of mammals. In the long term, the biomass of sedges, which are less preferred by mammals, increased in the less intensively grazed tall-grass vegetation. This resulted in a higher abundance of sedge-feeding leafhoppers. The small size of these sedge feeders lowered the average leafhopper body size in the tall-grass vegetation. Plant nutritional quality did not explain any effects of exclusions or vegetation types. 4. Our results demonstrate that both short- and long-term effects of mammalian herbivores on the biomass of specific plant functional types caused concurrent changes in the abundance of specialized herbivorous insects, which scaled up to community-wide shifts in insect body size, a key life-history trait. A plant-functional-type approach can thus help to predict how overabundance or extinction of mammalian herbivores impacts on other components of the food web at various timescales.

opencc-zeroDec 2016View details →
zenodo28/100

FIGURE 25 in Minucella, a new leafhopper genus from China (Hemiptera: Cicadellidae: Stegelytrinae)

FIGURE 25. Minucella leucomaculata Variations of male pygofer, lateral view.

opennotspecifiedDec 2008View details →
zenodo28/100

FIGURE 28 in Minucella, a new leafhopper genus from China (Hemiptera: Cicadellidae: Stegelytrinae)

FIGURE 28. Minucella leucomaculata Variations of aedeagus, lateral view.

opennotspecifiedDec 2008View details →
zenodo28/100

FIGURES 27 in Minucella, a new leafhopper genus from China (Hemiptera: Cicadellidae: Stegelytrinae)

FIGURES 27. Minucella leucomaculata Variations of aedeagus, dorsal view.

opennotspecifiedDec 2008View details →
zenodo28/100

FIGURES 7, 8 in Morphological and molecular differentiation of the Anagrus epos species complex (Hymenoptera: Mymaridae), egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in North America

FIGURES 7, 8. Anagrus daanei female (Washington). 7. Antenna. 8. Forewing. Scale bars = 0.1 mm.

opennotspecifiedDec 2010View details →
zenodo28/100

FIGURES 9, 10 in Morphological and molecular differentiation of the Anagrus epos species complex (Hymenoptera: Mymaridae), egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in North America

FIGURES 9, 10. Anagrus epos female (Minnesota). 9. Antenna. 10. Forewing. Scale bars = 0.1 mm.

opennotspecifiedDec 2010View details →
zenodo28/100

FIGURES 1, 2 in Morphological and molecular differentiation of the Anagrus epos species complex (Hymenoptera: Mymaridae), egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in North America

FIGURES 1, 2. Anagrus tretiakovae female (Arizona). 1. Antenna. 2. Forewing.

opennotspecifiedDec 2010View details →
zenodo28/100

FIGURES 5, 6 in Morphological and molecular differentiation of the Anagrus epos species complex (Hymenoptera: Mymaridae), egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in North America

FIGURES 5, 6. Anagrus daanei female (Colorado). 5. Antenna. 6. Forewing. Scale bars = 0.1 mm.

opennotspecifiedDec 2010View details →
zenodo28/100

FIGURES 11, 12 in Morphological and molecular differentiation of the Anagrus epos species complex (Hymenoptera: Mymaridae), egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in North America

FIGURES 11, 12. Anagrus vulneratus female (paratype, Colorado). 11. Antenna. 12. Wings.

opennotspecifiedDec 2010View details →
zenodo28/100

FIGURES 3, 4 in Morphological and molecular differentiation of the Anagrus epos species complex (Hymenoptera: Mymaridae), egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in North America

FIGURES 3, 4. Anagrus daanei female (California). 3. Antenna. 4. Forewing.

opennotspecifiedDec 2010View details →
zenodo28/100

FIGURE 8 in Revision of the Oriental leafhopper genus Parallygus Melichar (Hemiptera: Cicadellidae: Deltocephalinae) with description of new species

FIGURE 8. Map showing distribution of species of Parallygus in India, Sri Lanka and China.

opennotspecifiedDec 2012View details →
zenodo28/100

FIGURE 1 in Review of the Australian leafhopper genus Trocnada with notes on related genera (Hemiptera: Cicadellidae: Iassinae)

FIGURE 1. Dorsal and lateral habitus of Trocnada dorsigera Walker [(A –H) female; (I–J) male].

opennotspecifiedDec 2012View details →
zenodo28/100

FIGURES 1–3 in A new species of the leafhopper genus Neoreticulum Dai in China (Hemiptera: Cicadellidae: Deltocephalinae), with a key to species

FIGURES 1–3. Neoreticulum attenuatum sp. nov. 1. 3, dorsal view; 2. 3, face; 3. 3, lateral view.

opennotspecifiedDec 2012View details →
zenodo28/100

FIGURES 5–7 in Egg parasitoids (Hymenoptera: Mymaridae and Trichogrammatidae) of the gall-making leafhopper Scenergates viridis (Hemiptera: Cicadellidae) from Uzbekistan, with taxonomic notes on the Palaearctic species of Aphelinoidea

FIGURES 5–7. Aphelinoidea sariq female (holotype). 5. Antenna. 6. Wings. 7. Body.

opennotspecifiedDec 2013View details →
zenodo28/100

FIGURES 1–3 in First record of the leafhopper genus Soractellus Evans, 1966 (Hemiptera: Cicadellidae: Deltocephalinae) from China, with description of a new species

FIGURES 1–3. Soractellus jianfengensis sp. nov.: 1, ♂,dorsal view; 2, face; 3, ♂,lateral view.

opennotspecifiedDec 2014View details →
zenodo28/100

FIGURE 12 in Key to species of the leafhopper genus Membranacea Qin & Zhang (Hemiptera, Cicadellidae, Typhlocybinae, Empoascini), with a new species from China

FIGURE 12. Map showing the distribution of all species of genus Membranacea Qin & Zhang.

opennotspecifiedDec 2014View details →

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