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Fig. 6 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 6. Population fluctuation of Frankliniella occidentalis related with tomato crops at Tlayacapan 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 vertical arrow and subsequently between consecutive arrows.

Fig. 2 in Population fluctuations of thrips (Thysanoptera) and their relationship to the phenology of vegetable crops in the central region of Mexico

Fig. 2. Population fluctuation of Frankliniella occidentalis in the cucumber crops at 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. 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.

Fig. 11. A–L in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems

Fig. 11. A–L. Mamatia retracta (Popov). A. Dorsal valve RM Br133828, exterior, × 40. B. Dorsal valve RM Br133829, interior, × 50. C. Ventral valve RM Br133830, exterior, × 32. D. Dorsal valve RM Br133831, interior, × 27. E, H, I, K. Ventral valve RM Br133832, exterior (E, × 75), oblique posterior view (H, × 40), oblique lateral view (I, × 75), detail of larval shell (K, × 162). F. Ventral valve RM Br133833, oblique lateral view, 62. G, J. Ventral valve RM Br133834, interior (G, × 45) and detail of apical process (J, × 195). L. Ventral valve RM Br133835, detail of larval shell, × 150. All specimens from the Tremadoc chalcedonites, Wysoczki.

Fig. 6. A–N in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems

Fig. 6. A–N. Siphonotretella popovi sp. nov. A, N. Dorsal valve RM Br133791, exterior (A, × 26), detail of spines (N, × 100). B. Dorsal valve RM Br133792, exterior, × 32. C. Holotype, ventral valve RM Br133793, exterior, × 26. D, G, L. Dorsal valve RM Br133794, oblique posterior view (D, × 30), exterior (G, × 30), detail of larval shell (L, × 80). E, J. Dorsal valve RM Br133795, exterior (E, × 40) and detail of larval shell (J, × 120). F, H, I, K. Ventral valve RM Br133796, oblique lateral view (F, × 26), oblique posterior view (H, × 32), detail of larval shell and pedicle opening (I, × 80), detail of larval shell and pedicle opening (K, × 90). M. Dorsal valve RM Br133797, interior, × 40. O. Ventral valve RM Br133798, interior, × 23. All specimens from the Tremadoc chalcedonites, Wysoczki.

Fig. 8. A–Q. Semitreta maior Biernat. A in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems

Fig. 8. A–Q. Semitreta maior Biernat. A. Dorsal valve RM Br133807, × 30. B. Dorsal valve RM Br133808, interior, × 40. C, G. Ventral valve RM Br133809, exterior (C, × 13) and oblique lateral view (G, × 13). D, L. Dorsal valve RM Br133812, oblique lateral view (D, × 50), detail of larval shell (L, × 195). E. Dorsal valve RM Br133810, exterior, × 30. F, Q. Ventral valve RM Br133811, oblique lateral view (F, × 75), detail of larval shell (Q, × 195). H. Dorsal valve RM Br133814, oblique lateral view, × 40. I. Dorsal valve RM Br133813, oblique lateral view, × 50). J, K, P, O. Dorsal valve RM Br133815, dorsal interior (J, × 25), oblique lateral view (K, × 50), detail of pseudointerarea (P, 100), detail of pseudointerarea (O, × 60). M, N. Ventral valve RM Br133816, oblique lateral view (M, 32), oblique posterior view (N, × 45). All specimens from the Tremadoc chalcedonites, Wysoczki.

Fig. 4. A–L in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems

Fig. 4. A–L. Siphonobolus uralensis (Lermontova). A, G. Dorsal valve RM Br133779, interior (A, × 15) and oblique lateral view (G, × 23). B. Ventral valve RM Br133780, exterior, × 19. C, D, L. Ventral valve RM Br133781, oblique lateral view of exterior (C, × 33), posterior view (D, × 36) and detail of pedicle opening (L, × 80). E, H, J. Ventral valve RM Br133782, oblique lateral view of interior (E, × 28), detail of posterior margin (H, × 100) and detail of pedicle tube (J, × 70). F. Dorsal valve RM Br133783, oblique lateral view of exterior, × 26. I. Dorsal valve RM Br133784, oblique lateral view of interior, × 37. K. Ventral valve RM Br133785, detail of pedicle tube, × 55. All specimens from the Tremadoc chalcedonites, Wysoczki.

Fig. 2. A–K in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems

Fig. 2. A–K. Elliptoglossa polonica sp. nov. A, H. Dorsal valve RM Br133767, exterior (A, × 45) and oblique lateral view (H, × 45). B, G. Dorsal valve RM Br133768, interior (B, × 32) and oblique lateral view (G, × 40). C. Holotype, ventral valve RM Br133769, exterior, × 45. D. Ventral valve RM Br133770, interior, × 45. E, F, I. Ventral valve RM Br133771, exterior (E, × 38), oblique lateral view (F, × 40) and detail of larval shell (I, × 135). J. Ventral valve RM Br133772, detail of pseudointerarea, × 400. K. Dorsal valve RM Br133773, oblique lateral view of umbonal section of interior, × 100. All specimens from the Tremadoc chalcedonites, Wysoczki.

Fig. 9. A–F in Urban and Peri-urban small and medium-size Enterprise Development for sustainable Vegetable Production and Marketing Systems

Fig. 9. A–F.?Ditreta dividua Biernat. A, D. Dorsal valve RM Br133817, interior (A, × 36), detail of pseudointerarea (D, × 80). B, C, E, F. Ventral valve RM Br133818, oblique lateral view (B, × 32), exterior (C, × 30), oblique posterior view (E, × 30), detail of larval shell (F, × 165). All specimens from the Tremadoc chalcedonites, Wysoczki.

Fig. 3 in Post-fire effect of savannah vegetation on the establishment of new colonies of Atta sexdens rubropilosa (Hymenoptera: Formicidae)

Fig. 3. Characterization of Atta sexdens rubropilosa surviving colonies in burned and unburned areas, afer 120 d of queen reclusion (female), in soils from 2 depths (0.0–10.0 cm and 10.1–20.0 cm). Means (and standard errors) followed by the same letter did not differ from each other (ANOVA, P> 0.05)

Fig. 2 in Post-fire effect of savannah vegetation on the establishment of new colonies of Atta sexdens rubropilosa (Hymenoptera: Formicidae)

Fig. 2. Characterization of Atta sexdens rubropilosa surviving colonies in burned and unburned areas, afer 120 d of queen reclusion (female). Means (and standard errors) followed by the same letter did not differ from each other (ANOVA, P> 0.05).

Fig. 1 in Post-fire effect of savannah vegetation on the establishment of new colonies of Atta sexdens rubropilosa (Hymenoptera: Formicidae)

Fig. 1. Microbial activity (mean and standard error) in soils collected at 2 depths (0.0 to 10.0 cm and 10.1 to 20.0 cm) in areas with burned and unburned vegetation in Ipameri, GO, Brazil. Means followed by the same letter (accumulated CO2 production at 10 d), for each depth where the soil was collected, did not differ from each other (Mann–Whitney U test, P> 0.05).

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Fig. 1. Sample completeness curve for a in Abundance and diversity of beneficial and pest arthropods in buckwheat on blueberry and vegetable farms in north Florida

Fig. 1. Sample completeness curve for a vegetable farm (dark shaded area, 38 samples) and blueberry farm (light shaded area, 19 samples) in Suwannee County, Florida. The solid line is the interpolated insect family-level richness and the dashed line is the extrapolated richness. The shaded areas represent 95% confidence intervals. Sampling effort is standardized based on the sample completeness (the proportion of sampled families to predicted families) at each sampling level, with the circle representing final sampling completeness of 38 samples taken at the vegetable farm and the triangle representing final sampling completeness of 19 samples taken at the blueberry farm.

opencc-by-4.0Aug 2015View details →

Fig. 2 in Elevation and vegetation determine Cryptosporidium oocyst shedding by yellow-bellied marmots (Marmota flaviventris) in the Sierra Nevada Mountains

Fig. 2. Association between Cryptosporidium oocyst shedding by yellow-bellied marmots in the Sierra Nevada Mountains and elevation (using 9,068 ft as the reference), stratified by presence or absence of vegetation at sites where scat samples were collected.

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Fig. 1 in Elevation and vegetation determine Cryptosporidium oocyst shedding by yellow-bellied marmots (Marmota flaviventris) in the Sierra Nevada Mountains

Fig. 1. Locations in the Sierra Nevada Mountains where scat samples from yellow-bellied marmot were collected. The map contains 14 locations, but some locations clustered together due to the shorter distances between them and the scale of the map. The cluster in Yosemite National Park includes Tenaya Creek, Bridaveil Creek, Pothole Dome, and Lembert Dome. The cluster at Mineral King includes Mineral King, Eagle Lake, White Chief Creek, and Elk Kaweah River.

Abb. G 41-G 48 in Zur Kenntnis der Schmetterlingsfauna der Iberischen Halbinsel I. Topografie, Geologie, Klima und Vegetation. Daten der Tagfalter aus den Geländeprotokollen zwischen den Jahren 1970 bis 2013 (Insecta: Lepidoptera, Papilionoidea)

Abb. G 41-G 48: (G 41) Murcia, Jumilla, Sra. del Carche, 1200 m, 2008; (G 42) Murcia, Sra. Seca, Revolcadores, 2001 m, 1984; (G 43) Salamanca, Pena de Francia, 1732 m, 2008; (G 44) Teruel, Maestrazgo, Orgos de Montoro, 1983; (G 45) Toledo, Mtes. de Toldeo, Cistus-Matorral, 1977; (G 46) Valencia, Rincon de Ademuz, 1973; (G 47) P-Beira alta, Sra. da Estrela, Torre, 2005; (G 48) P-Beira alta, Sra. da Estrela, Vale de Zezere, 2005.