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Figures 43–49 in A review of the history of the names Hamaticherus Dejean and Plocaederus Dejean and description of a new genus and species (Coleoptera: Cerambycidae: Cerambycinae)

Figures 43–49. Hamaederus glaberrimus (Martins, 1979). 43–48) Holotype female. 43) Dorsal habitus. 44) Ventral habitus. 45) Scape, pedicel, and antennomeres III–V. 46) Scape. 47) Lateral habitus. 48) Prosternal and mesoventral processes. 49) Male, dorsal habitus.

Figures 18–23 in A review of the history of the names Hamaticherus Dejean and Plocaederus Dejean and description of a new genus and species (Coleoptera: Cerambycidae: Cerambycinae)

Figures 18–23. Hamaederus bipartitus (Buquet, 1860), specimens from Bolivia (Santa Cruz). 18–22) Male. 18) Dorsal habitus. 19) Ventral habitus. 20) Lateral habitus. 21) Prosternal and mesoventral processes, lateral view. 22) Prosternal and mesoventral processes. 23) Female, dorsal habitus.

Figures 71–81 in A review of the history of the names Hamaticherus Dejean and Plocaederus Dejean and description of a new genus and species (Coleoptera: Cerambycidae: Cerambycinae)

Figures 71–81. Hamaederus yucatecus (Chemsak and Noguera, 1997). 71) Male from Bolivia, Santa Cruz (Buena Vista), dorsal habitus. 72) Male from Costa Rica, Guanacaste (near Bagaces). 73) Male from Mexico, Chiapas (near Ocozocoautla), dorsal habitus. 74) Male from Mexico, Chiapas (El Chorreodero Canyon), dorsal habitus. 75–76) Plocaederus barauna Martins and Monné, 2002 (= H. yucatecus (Chemsak and Noguera, 1997)), paratypes. 75) Dorsal habitus, female. 76) Antennomeres III–IV, male. 77–81) Scape. 77) Male from Bolivia. 78) Male from Mexico. 79) Male from Mexico. 80) Paratype male of P. confusus from Brazil. 81) Paratype female of P. confusus from Brazil.

Figures 65–70 in A review of the history of the names Hamaticherus Dejean and Plocaederus Dejean and description of a new genus and species (Coleoptera: Cerambycidae: Cerambycinae)

Figures 65–70. Hamaederus confusus Martins and Monné, 2002 (= H. yucatecus (Chemsak and Noguera, 1997)). 65–67) Holotype male. 65) Dorsal habitus. 66) Ventral habitus. 67) Prosternal and mesoventral processes, lateral view. 68) Paratype female, dorsal habitus, from Brazil (São Paulo). 69) Paratype male, dorsal habitus, from Brazil (Rio de Janeiro). 70) Paratype male, dorsal habitus, from Brazil (São Paulo).

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Рис. 2. ПяΑеницы (Geometridae) Ботчинского заповеΑника: A — Ourapteryx maculicaudaria, самка; B — Charissa remmi, самка; C — Charissa creperaria, самка; D — Macaria wauaria, самец. ШкаΛа поΑ бабочками — 10 мм. Figs 2. Geometrid moths (Geometridae) of the Botchinsky Reserve: A — Ourapteryx maculicaudaria, female; B — Charissa remmi, female; C — Charissa creperaria, female; D — Macaria wauaria, male. The scale under the moths — 10 mm in Fauna of the geometrid moths (Lepidoptera, Geometridae) of the eastern Sikhote-Alin in the area of the Botchinsky State Nature Reserve I: History of research and subfamilies Archiearinae, Ennominae, Desmobathrinae, and Geometrinae

Рис. 2. ПяΑеницы (Geometridae) Ботчинского заповеΑника: A — Ourapteryx maculicaudaria, самка; B — Charissa remmi, самка; C — Charissa creperaria, самка; D — Macaria wauaria, самец. ШкаΛа поΑ бабочками — 10 мм. Figs 2. Geometrid moths (Geometridae) of the Botchinsky Reserve: A — Ourapteryx maculicaudaria, female; B — Charissa remmi, female; C — Charissa creperaria, female; D — Macaria wauaria, male. The scale under the moths — 10 mm

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Рис. 1. Пункты сбора материаΛов в районе Ботчинского заповеΑника. Пункты сбора обозначены красными кружками, наибоΛее крупный из которых соответствует основному месту сбора — корΑону «ТепΛый КΛюч». Номера пунктов сбора соответствуют номерам в тексте при их описании. БΛизко распоΛоженные пункты сборов показаны оΑним симвоΛом Fig. 1. Points of collection of materials in the area of the Botchinsky Nature Reserve. Collection points are marked with red circles, the largest of which corresponds to the main collection point — the cordon "Teply Klyuch". The collection point numbers correspond to the numbers in the text when they are described. Closely located collection points are shown with one symbol in Fauna of the geometrid moths (Lepidoptera, Geometridae) of the eastern Sikhote-Alin in the area of the Botchinsky State Nature Reserve I: History of research and subfamilies Archiearinae, Ennominae, Desmobathrinae, and Geometrinae

Рис. 1. Пункты сбора материаΛов в районе Ботчинского заповеΑника. Пункты сбора обозначены красными кружками, наибоΛее крупный из которых соответствует основному месту сбора — корΑону «ТепΛый КΛюч». Номера пунктов сбора соответствуют номерам в тексте при их описании. БΛизко распоΛоженные пункты сборов показаны оΑним симвоΛом Fig. 1. Points of collection of materials in the area of the Botchinsky Nature Reserve. Collection points are marked with red circles, the largest of which corresponds to the main collection point — the cordon "Teply Klyuch". The collection point numbers correspond to the numbers in the text when they are described. Closely located collection points are shown with one symbol

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Fig. 3 in Biology and life history of Atanycolus cappaerti (Hymenoptera: Braconidae), a North American larval parasitoid attacking the invasive emerald ash borer (Coleoptera: Buprestidae)

Fig. 3. Immature stages of Atanycolus cappaerti. (A) Egg on Agrilus planipennis larva at 3× magnification; (B) 1st instar at 3× magnification; (C) 2nd instar at 3× magnification; (D) 3rd instar at 3× magnification; (E) 4th instar at 3× magnification; (F) 5th instar at 1.8× magnification; (G) 6th instar at 1.8× magnification; (H) pupal cocoon at 1.8× magnification; (I) eclosed adult.

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Fig. 2 in Biology and life history of Atanycolus cappaerti (Hymenoptera: Braconidae), a North American larval parasitoid attacking the invasive emerald ash borer (Coleoptera: Buprestidae)

Fig. 2. Diapause behavior of Atanycolus cappaerti progeny when reared in normal rearing conditions (25 ± 2 °C, 65 ± 10% RH, and a photoperiod of 16:8 h L:D).

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Fig. 1 in Biology and life history of Atanycolus cappaerti (Hymenoptera: Braconidae), a North American larval parasitoid attacking the invasive emerald ash borer (Coleoptera: Buprestidae)

Fig. 1. (A) Longevity and (B) realized fecundity and host utilization (parasitism) rate of adults of Atanycolus cappaerti when reared in single mating pairs (n = 16 for both sexes) and continually provided with emerald ash borer larvae on a weekly basis for their lifespan.

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Fig. 2. Florida Entomologist now projects a in A short history of Florida Entomologist in recognition of 100 years of publication

Fig. 2. Florida Entomologist now projects a modern image, and has grown not only in popularity (number of papers printed) but also in physical dimensions. Page size has increased from 11 × 19 cm in the original "Buggist" to 18.5 × 25 cm now. Color has been added to the cover, and is an option for both printed and online articles.

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Fig. 1 in A short history of Florida Entomologist in recognition of 100 years of publication

Fig. 1. Florida Entomologist originated as The Florida Buggist, an interesting but unusual name. The name and content soon changed to reflect a more professional image and scientific content.

Fig. 7 in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 7. Seasonal polyphenism in the dorsal wing color of male Atala, Eumaeus atala. Green (lef photo) is predominantly found in cooler winter and spring southeast Florida temperatures.

Fig. 5 in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 5. Eumaeus atala pupal development time (d) for different seasons is indicated by the different line styles. Two distinct groups of development are present, the warm season (summer to fall) and cool season (winter to spring).

Fig. 6 in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 6. Polyphenism in Atala, Eumaeus atala, pupae. Increased melanization is associated with cooler temperatures. All pupae were 10 d old when the photographs were taken.

Fig. 3 in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 3. Eumaeus atala egg development time (d) for different seasons is indicated by different line styles. A separation in development is starting to show between warm season (summer to fall) and cool season (winter to spring).

Fig. 2 in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 2. Seasonal temperatures as programmed in environmental chambers. A) Temperatures in the chambers were programmed to match Homestead, Miami temperatures as closely as possible (see discussion) and B) degree-day units were analyzed using a Baskerville–Emin adjustment (see discussion). Bars indicate standard error.

Fig. 1. Percival environmental chambers housing Eumaeus atala. A in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 1. Percival environmental chambers housing Eumaeus atala. A) Interior view of fabric housing cages in the Percival chambers and B) plastic 'deli-box' larval cages inside with host plant material and young Eumaeus atala larvae.

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Fig. 1 in Timing of irradiation and male mating history effects on female remating in Anastrepha ludens (Diptera: Tephritidae)

Fig. 1. Interaction between age of pupal irradiation (24, 48, or 72 h before emergence) and male previous sexual experience (virgin, once mated, or twice mated) of the GSS strain of A. ludens (Tapachula-7) males on wild female likelihood to remate (N = 945).

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Fig. 2 in What drives population-level effects of parasites? Meta-analysis meets life-history

Fig. 2. Funnel plot of effect size (Hedges' g) by standard error (SE). The white circles represent studies included in the meta-analysis. The black circles represent missing imputed studies. The white diamond represents overall effect size as calculated in the meta-analysis, and the black diamond represents the corrected effect size.