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Fig. 7 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 7. Population fluctuation of Frankliniella occidentalis in the tomatillo crops at Tlayacapan, Morelos, and Tepeojuma, Puebla, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.

Fig. 4 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 4. Population fluctuation of Frankliniella occidentalis in the zucchini crops at Tlayacapan, Tepalcingo and Atlatlahucan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st red vertical arrow and between consecutive red arrows.

Fig. 5 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 5. Population fluctuation of Frankliniella occidentalis in the pepper crops at Izucar de Matamoros and Tepeojuma, Puebla, and Tlayacapan, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.

Fig. 1 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 1. Population fluctuation of Frankliniella occidentalis in the cucumber crops at Atlatlahucan and Tepalcingo, Morelos, Mexico, 2010–2011. Sufficient thermal units (195 degree days) occurred to support 1 life cycle of F. occidentalis from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.

Fig. 10 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 10. Population fluctuation of Thrips tabaci in the onion crops at Tilapa and Tepeojuma, Puebla, Mexico, 2010–2011. Sufficient thermal units (180 degree days) occurred to support 1 life cycle of T. tabaci from transplantation until the 1st vertical arrow and subsequently between consecutive arrows.

opencc-by-4.0Mar 2015View details →

Figs. 1 and 2. 1 in Problems in Costa Rican thrips taxonomy and systematics (Insecta: Thysanoptera)

Figs. 1 and 2. 1. Maxillary stylets of genus Kolia [Fig. 1B from Soto-Rodriguez et al (2013)]. 2. Head and antennae of Jessicathrips cubensis [Fig. 1a from Gonzalez et al. (2010)].

opencc-by-4.0Mar 2015View details →

Figs. 3–9 in Problems in Costa Rican thrips taxonomy and systematics (Insecta: Thysanoptera)

Figs. 3–9. [3–7 provided by Olman Alvarado Rodríguez of CIEMIC, University of Costa Rica]. 3–5. Holotype females of Arthrips madresalvensis, Kolia lilianae and Kolia zaidae. 6–7. Mouth cone of Kolia guanacastenis and Kolia zaidae, with protruding maxillary stylets indicated. 8. Tergite VIII posterior margin of Frankliniella fortissima female labelled "type" with microtrichial comb interrupted medially. 9. Head of Frankliniella caribae holotype (Fig. 2 from Retana-Salazar 2010a).

Fig. 2 in Brazilian collections and laboratory biology of the thrips Pseudophilothrips ichini (Thysanoptera: Phlaeothripidae): a potential biological control agent of the invasive weed Brazilian peppertree (Sapindales: Anacardiaceae)

Fig. 2. Life history stages of the thrips Pseudophilothrips ichini reared on leaves of Schinus terebinthifolia in quarantine at the United States Department of Agriculture, Agricultural Research Service, Invasive Plant Research Laboratory (horizontal bars = 0.5 mm).

Fig. 1 in Brazilian collections and laboratory biology of the thrips Pseudophilothrips ichini (Thysanoptera: Phlaeothripidae): a potential biological control agent of the invasive weed Brazilian peppertree (Sapindales: Anacardiaceae)

Fig. 1. Map showing the distribution of the host Brazilian peppertree, Schinus terebinthifolia, in its native range (black dots) and the thrips Pseudophilothrips ichini (red dots). Thrips introduced to quarantine for life history studies were collected from a population near Ouro Preto, Minas Gerais, Brazil.

Fig. 2 in Examining the relationship between flower thrips (Thysanoptera: Thripidae) spatial distribution and blueberry (Ericales: Ericaceae) flower density

Fig. 2. Graph of percentage of open blueberry flowers vs. log10 thrips per trap from the Windsor farm on 18 Mar 2010. The black line represents a regression line fitted by least squares regression.

Fig. 1 in Examining the relationship between flower thrips (Thysanoptera: Thripidae) spatial distribution and blueberry (Ericales: Ericaceae) flower density

Fig. 1. Graphs showing percentage of open blueberry flowers vs. thrips per trap from the Inverness farm on a) 30 Jan and b) 5 Feb 2009. The black lines represent regression lines fitted by Theil regression.

Fig. 1 in New findings of thrips (Thysanoptera: Thripidae) on plants in Brazil

Fig. 1. Thrips and damage to cultivated plants. a,b,c: Damage from Dinurothrips hookeri to Mentha sp. leaves; d: Frankliniella insularis (adult); e, f, g: damage from F. insularis to rose flowers; h: Heliothrips haemorrhoidalis (adult); i: H. haemorrhoidalis (pupa); j: damage from H. haemorrhoidalis to Plumeria sp. leaves (upper side); k: damage from H. haemorrhoidalis to Plumeria sp. leaf (underside); l: Retithrips syriacus (adult); m: R. syriacus (immatures); n: damage from R. syriacus on Terminalia catappa leaves; o: damage from R. syriacus on Rosa sp. leaf; p: Selenothrips rubrocinctus (adult and immatures) on Calophyllum brasiliense leaf; q, r: damage from S. rubrocinctus on C. brasiliense; s, t: damage from S. rubrocinctus on Liquidambar styraciflua.

opencc-by-4.0Sep 2016View details →

Fig. 2 in Development of Thripastichus gentilei (Hymenoptera: Eulophidae) in the thrips Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae)

Fig. 2. Survivorship function [S(t)] for Thripistichus gentilei adults provisioned with a sugar water solution, distilled water, or no food (starved) along with thrips hosts. Median survival time was greater for wasps provided sugar water compared with survival for those given either water or starved. Bars represent the standard error [SE S(t)].

opencc-by-4.0Sep 2016View details →

Fig. 1 in Development of Thripastichus gentilei (Hymenoptera: Eulophidae) in the thrips Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae)

Fig. 1. Two immatures of Gynaikothrips uzeli: the upper individual is a normal larva, and the lower one displays the transparent, swollen appearance of a parasitized larva. The parasitoid, Thripistichus gentilei, develops with a polarity that is reverse relative to the host.

opencc-by-4.0Dec 2022View details →

Рис. 1. Новые виΑы чешуекрыΛых ΑΛя Новосибирской обΛасти. Имаго, общий виΑ: A — Hepialus humuli, ♂, ШагаΛовский, 08.07.2009; B — Hepialus humuli, ♀, ШагаΛовский, 22.06.2008; C — Paracossus thrips, ♂, ПоΛьяново, 15.08.2021; D — Chelis maculosa, ♂, ПоΛьяново, 07.07.2021; E — Eucarta virgo, ♂, ШагаΛовский, 22.06.2008; F — Actinotia polyodon, Березовские скаΛы, 07.06.2021; G — Conisania suaveola, СокоΛиный камень, 02.06.2020; H — Actebia praecox, Огурцово, 15.08.2014 Fig. 1. New species of Lepidoptera for the Novosibirsk region. Imago, general view: A — Hepialus humuli, ♂, Shagalovsky, 08.07.2009; B — Hepialus humuli, ♀, Shagalovsky, 22.06.2008; C — Paracossus thrips, ♂, Polyanovo, 15.08.2021; D — Chelis maculosa, ♂, Polyanovo, 07.07.2021; E — Eucarta virgo, ♂, Shagalovsky, 22.06.2008; F — Actinotia polyodon, Berezovskie rocks, 07.06.2021; G — Conisania suaveola, Falcon stone, 02.06.2020; H — Actebia praecox, Ogurtsovo, 15.08.2014 in New records of rare and local butterflies and moths (Insecta, Lepidoptera) in Omsk and Novosibirsk regions

Рис. 1. Новые виΑы чешуекрыΛых ΑΛя Новосибирской обΛасти. Имаго, общий виΑ: A — Hepialus humuli, ♂, ШагаΛовский, 08.07.2009; B — Hepialus humuli, ♀, ШагаΛовский, 22.06.2008; C — Paracossus thrips, ♂, ПоΛьяново, 15.08.2021; D — Chelis maculosa, ♂, ПоΛьяново, 07.07.2021; E — Eucarta virgo, ♂, ШагаΛовский, 22.06.2008; F — Actinotia polyodon, Березовские скаΛы, 07.06.2021; G — Conisania suaveola, СокоΛиный камень, 02.06.2020; H — Actebia praecox, Огурцово, 15.08.2014 Fig. 1. New species of Lepidoptera for the Novosibirsk region. Imago, general view: A — Hepialus humuli, ♂, Shagalovsky, 08.07.2009; B — Hepialus humuli, ♀, Shagalovsky, 22.06.2008; C — Paracossus thrips, ♂, Polyanovo, 15.08.2021; D — Chelis maculosa, ♂, Polyanovo, 07.07.2021; E — Eucarta virgo, ♂, Shagalovsky, 22.06.2008; F — Actinotia polyodon, Berezovskie rocks, 07.06.2021; G — Conisania suaveola, Falcon stone, 02.06.2020; H — Actebia praecox, Ogurtsovo, 15.08.2014

opencc-by-4.0Jun 2016View details →

Fig. 1 in Thrips species (Thysanoptera: Thripidae) in Brazilian papaya (Brassicales: Caricaceae) orchards as potential virus vectors

Fig. 1. Location of the 20 papaya orchards sampled in the main Brazilian papaya-producing and -exporting region, Espírito Santo State, Brazil.

Figs. 20–22. Plate IX in A photo-based key of thrips (Thysanoptera) associated with horticultural crops in Florida

Figs. 20–22. Plate IX: Larval antennal, sternite and pronotal characteristics. 20a. Antennal segments with smooth margins, lacking annulations (larval Tubulifera: Phlaeothripidae). 20b. Antennal segments with margins interrupted by annulations, microtrichia arise from these annulations (white arrows) (larval Terebrantia). 21a. Two setae present on each sternite (white arrows) (larva I). 21b. Six setae present on each sternite (white arrows) (larva II). 22a. Twelve setae (6 pairs, D1–D6) on pronotum (Larva I). 22b. Fourteen setae (7 pairs, D1–D7) on pronotum (Larva II).

Figs. 27–30. Plate XI in A photo-based key of thrips (Thysanoptera) associated with horticultural crops in Florida

Figs. 27–30. Plate XI: Larval abdominal characteristics. 27a. Teeth (black arrow) on posterior margin of abdominal segment IX large, prominent (larval Chaetanaphothrips). 27b. Teeth (black arrow) on posterior margin of abdominal segment IX small but longer than basal width of D1 setae; base of D1 seta (white arrow) (larval Frankliniella bispinosa). 27c. Teeth (black arrow) on posterior margin of abdominal segment IX small and equal to or shorter than basal width of D1 setae; base of D1 seta (white arrow) (larval Frankliniella schultzei). 28. Campaniform sensilla (white arrows) on abdominal segment IX separated by 2.0 times the distance (long white line) as compared with the distance (short white line) between D1 setae (larval Frankliniella). 29a. Setae arising from tergites on abdominal segment IX pointed (black arrows) (adult Frankliniella occidentalis). 29b. Setae arising from tergites on abdominal segment IX blunt (black arrows) (adult Frankliniella bispinosa or Frankliniella schultzei). 30. Plaques with well-defined microtrichia (white arrows) on abdominal segment VIII (larval Frankliniella occidentalis or Frankliniella bispinosa).

Fig. 12. Plate VI in A photo-based key of thrips (Thysanoptera) associated with horticultural crops in Florida

Fig. 12. Plate VI: Comb of microtrichia on Tergite VIII. 12a. Comb on abdominal segment VIII posterior margin present and uninterrupted (black arrows) (adult Frankliniella occidentalis). 12b. Comb on abdominal segment VIII posterior margin present but interrupted medially (black arrows) (adult Frankliniella insularis). 12c. Comb on abdominal segment VIII posterior margin present (black arrows) (adult Anaphothrips obscurus). 12d. Comb on abdominal segment VIII posterior margin weakly developed (white arrows) (adult Frankliniella fusca). 12e. Comb on abdominal segment VIII absent (black arrows) (adult Caliothrips phaseoli).

Figs. 16–19 in A photo-based key of thrips (Thysanoptera) associated with horticultural crops in Florida

Figs. 16–19. Plate VIII: Tergal, metanotal and discal characteristics. 16. Lateral thirds of abdomen greatly reticulated (white arrows) (adult Caliothrips phaseoli). 17. Posterior margin of each tergum with a toothed craspedum (white arrows) (adult Microcephalothrips abdominalis). 18a. Metanotal setae arising at anterior margin (white arrows) (adult Thrips florum or Thrips hawaiiensis). 18b. Metanotal setae arising posterior to anterior margin (white arrows) (other adult Thrips). 19a. Discal setae present (black arrows) (adult Thrips australis). 19b. Discal setae absent (adult Thrips tabaci or Thrips palmi).