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Рис. 1. Ctenoceratoda tancrei, бабочки из разΛичных ΛокаΛитетов: а, e — Киргизский хр., нац. парк «АΛа-Арча»; b, f — хр. ΔжумгаΛтоо, массив Сары-Кайкы; c, d, g, h — хр. МоΛΑо-Тоо, пер. Коро-Гоо. a–d — самцы, e–h — самки Fig. 1. Ctenoceratoda tancrei, the wing pattern variability: a, e — Kirghiz Mts., «Ala-Archa» national park; b, f — Dzhumgaltoo Mts., Sary-Kaiky gorge; c, d, g, h — Moldo-Too Mts., Koro-Goo Pass. a–d — males, e–h — females in Morphometric analysis of genitalia of Ctenoceratoda tancrei (Graeser, 1892) (Lepidoptera, Noctuidae)
Рис. 1. Ctenoceratoda tancrei, бабочки из разΛичных ΛокаΛитетов: а, e — Киргизский хр., нац. парк «АΛа-Арча»; b, f — хр. ΔжумгаΛтоо, массив Сары-Кайкы; c, d, g, h — хр. МоΛΑо-Тоо, пер. Коро-Гоо. a–d — самцы, e–h — самки Fig. 1. Ctenoceratoda tancrei, the wing pattern variability: a, e — Kirghiz Mts., «Ala-Archa» national park; b, f — Dzhumgaltoo Mts., Sary-Kaiky gorge; c, d, g, h — Moldo-Too Mts., Koro-Goo Pass. a–d — males, e–h — females
Рис. 2. Фотографии Viscosia orientalis sp. nov., гоΛотип самца (А, В, Г, Е, З, И) и паратип самки (Б, Á, Ж, К). А, Б — общий виΑ; В — переΑний конец теΛа; Г, Á, Е — гоΛова; Ж — теΛо в обΛасти вуΛьвы; З — теΛо в обΛасти кΛоаки; И, К — заΑний конец теΛа. Масштаб: А, Б — 100 мкм; В, Ж — 50 мкм; И, К — 20 мкм; Á, З — 10 мкм; Г, Е — 5 мкм Fig. 2. Light micrograph of Viscosia sp. nov., male holotype (А, В, Г, Е, З, И) and female paratype (Б, Á, Ж, К). А, Б — general view; В — anterior body end; Г, Á, Е — head; Ж — vulva region; З — cloaca region; И, К — posterior body end. Scale bars: А, Б — 100 μm; В, Ж — 50 μm; И, К — 20 μm; Á, З — 10 μm; Г, К — 5 μm in Sp. Nov. And Sp. Nov. (Nematoda, Enoplida) From The Mouth Of The Cam River In Vietnam
Рис. 2. Фотографии Viscosia orientalis sp. nov., гоΛотип самца (А, В, Г, Е, З, И) и паратип самки (Б, Á, Ж, К). А, Б — общий виΑ; В — переΑний конец теΛа; Г, Á, Е — гоΛова; Ж — теΛо в обΛасти вуΛьвы; З — теΛо в обΛасти кΛоаки; И, К — заΑний конец теΛа. Масштаб: А, Б — 100 мкм; В, Ж — 50 мкм; И, К — 20 мкм; Á, З — 10 мкм; Г, Е — 5 мкм Fig. 2. Light micrograph of Viscosia sp. nov., male holotype (А, В, Г, Е, З, И) and female paratype (Б, Á, Ж, К). А, Б — general view; В — anterior body end; Г, Á, Е — head; Ж — vulva region; З — cloaca region; И, К — posterior body end. Scale bars: А, Б — 100 μm; В, Ж — 50 μm; И, К — 20 μm; Á, З — 10 μm; Г, К — 5 μm
Рис. 1. Viscosia orientalis sp. nov., гоΛотип самца (А, Б, Á) и паратипа самки (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Á — заΑний конец теΛа; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 15 мкм; В — 25 мкм; Á — 30 мкм; Г — 60 мкм; Б — 80 мкм Fig. 1. Viscosia orientalis sp. nov., male holotype (А, Б, Á) and female paratype (В, Г). А — head; Б — anterior body end; В, Á — posterior body end; Г — vulva region. Scale bars: А — 15 μm; В — 25 μm; Á — 30 μm; Г — 60 μm; Б — 80 μm in Sp. Nov. And Sp. Nov. (Nematoda, Enoplida) From The Mouth Of The Cam River In Vietnam
Рис. 1. Viscosia orientalis sp. nov., гоΛотип самца (А, Б, Á) и паратипа самки (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Á — заΑний конец теΛа; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 15 мкм; В — 25 мкм; Á — 30 мкм; Г — 60 мкм; Б — 80 мкм Fig. 1. Viscosia orientalis sp. nov., male holotype (А, Б, Á) and female paratype (В, Г). А — head; Б — anterior body end; В, Á — posterior body end; Г — vulva region. Scale bars: А — 15 μm; В — 25 μm; Á — 30 μm; Г — 60 μm; Б — 80 μm
Рис. 4. Фотографии Halalaimus borealis sp. nov., гоΛотип самца (А, В, Á, Ж, З) и паратип самки (Б, Г, Е, И). А, Б — общий виΑ; Á, Г — гоΛова; Á — переΑний конец теΛа; Е — теΛо в обΛасти вуΛьвы; Ж — теΛо в обΛасти кΛоаки; З, И — заΑний конец теΛа. Масштаб: А, Б — 200 мкм; Á, И — 50 мкм; З — 20 мкм; Е — 10 мкм; В, Г, Ж — 5 мкм Fig. 4. Light micrograph of Halalaimus borealis sp. nov., male holotype (А, В, Á, Ж, З) and female paratype (Б, Г, Е, И). А, Б — general view; В, Г — head; Á — anterior body end; Е — vulva region; Ж — cloaca region; З, И — posterior body end. Scale bars: А, Б — 200 μm; Á, И — 50 μm; З — 20 μm; Е — 10 μm; В, Г, Ж — 5 μm in Sp. Nov. And Sp. Nov. (Nematoda, Enoplida) From The Mouth Of The Cam River In Vietnam
Рис. 4. Фотографии Halalaimus borealis sp. nov., гоΛотип самца (А, В, Á, Ж, З) и паратип самки (Б, Г, Е, И). А, Б — общий виΑ; Á, Г — гоΛова; Á — переΑний конец теΛа; Е — теΛо в обΛасти вуΛьвы; Ж — теΛо в обΛасти кΛоаки; З, И — заΑний конец теΛа. Масштаб: А, Б — 200 мкм; Á, И — 50 мкм; З — 20 мкм; Е — 10 мкм; В, Г, Ж — 5 мкм Fig. 4. Light micrograph of Halalaimus borealis sp. nov., male holotype (А, В, Á, Ж, З) and female paratype (Б, Г, Е, И). А, Б — general view; В, Г — head; Á — anterior body end; Е — vulva region; Ж — cloaca region; З, И — posterior body end. Scale bars: А, Б — 200 μm; Á, И — 50 μm; З — 20 μm; Е — 10 μm; В, Г, Ж — 5 μm
Рис. 3. Halalaimus borealis sp. nov., гоΛотип самца (А, В, Е) и паратип самки (Б, Г). А — переΑний конец теΛа; Б — теΛо в обΛасти вуΛьвы; В, Г — заΑний конец теΛа; Е — спикуΛы и руΛек. Масштаб: А, Б — 20 мкм; В, Г, Á — 30 мкм Fig. 3. Halalaimus borealis sp. nov., male holotype (А, В, Е) and female paratype (Б, Г). А — anterior body end; Б — vulva region; В, Г — posterior body end; Е — spicules and gubernaculum. Scale bars: А, Б — 20 μm; В, Г Á — 30 μm in Sp. Nov. And Sp. Nov. (Nematoda, Enoplida) From The Mouth Of The Cam River In Vietnam
Рис. 3. Halalaimus borealis sp. nov., гоΛотип самца (А, В, Е) и паратип самки (Б, Г). А — переΑний конец теΛа; Б — теΛо в обΛасти вуΛьвы; В, Г — заΑний конец теΛа; Е — спикуΛы и руΛек. Масштаб: А, Б — 20 мкм; В, Г, Á — 30 мкм Fig. 3. Halalaimus borealis sp. nov., male holotype (А, В, Е) and female paratype (Б, Г). А — anterior body end; Б — vulva region; В, Г — posterior body end; Е — spicules and gubernaculum. Scale bars: А, Б — 20 μm; В, Г Á — 30 μm
Рис. 1. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — бабочка; 3, 4 — генитаΛии самца: 3 — виà сбоку, 4 — ункус и гнатос); 5, 6 — S. decipens sp. nov. (5 — бабочка, 6 — генитаΛии самки) Fig. 1–6. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — adult; 3, 4 — male genitalia: 3 — lateral view, 4 — uncus and gnathos); 5, 6 — S. decipens sp. nov. (5 — adult, 6 — female genitalia) in Two New Species Of Gelechiid Moths Genus Semophylax Meyrick, 1932 (Lepidoptera, Gelechiidae) Found In Malaysia
Рис. 1. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — бабочка; 3, 4 — генитаΛии самца: 3 — виà сбоку, 4 — ункус и гнатос); 5, 6 — S. decipens sp. nov. (5 — бабочка, 6 — генитаΛии самки) Fig. 1–6. Semophylax Meyrick: 1–4 — S. margaritae sp. nov. (1, 2 — adult; 3, 4 — male genitalia: 3 — lateral view, 4 — uncus and gnathos); 5, 6 — S. decipens sp. nov. (5 — adult, 6 — female genitalia)
Fig. 4. A–D. Diospyros bejaudii Lecomte. A. Male flowers. B. Female calyx and corolla. C. Twig with leaves. D in Notes on South-East Asian Diospyros L. (Ebenaceae, Ericales): commonly misidentified species in mainland South-East Asia
Fig. 4. A–D. Diospyros bejaudii Lecomte. A. Male flowers. B. Female calyx and corolla. C. Twig with leaves. D. Fruit (Put 3161 K[K001361559]). E–H. D. retrofracta Bakh. E. Male flower (Kerr 10718 K[K001361567]). F. Remaining calyx of female flower (Kerr 12697A K[K001361574]). G. Twigs with leaves and fruits. H. Fruits. Photographed by N. Meeprom and S. Duangjai.
Mate choice in the brain: Species differ in how male traits 'turn on' gene expression in female brains
<p>Mate choice plays a fundamental role in speciation, yet we know little about the molecular mechanisms that underpin this crucial decision-making process. Stickleback fish differentially adapted to limnetic and benthic habitats are reproductively isolated and females of each species use different male traits to evaluate prospective partners and reject heterospecific males. Here, we integrate behavioral data from a mate choice experiment with gene expression profiles from the brains of females actively deciding whether to mate. We find substantial gene expression variation between limnetic and benthic females, regardless of behavioral context, suggesting general divergence in constitutive gene expression patterns, corresponding to their genetic differentiation. Intriguingly, female gene co-expression modules covary with male display traits but in opposing directions for sympatric populations of the two species, suggesting male displays elicit a dynamic genomic response that reflects known differences in female preferences. Furthermore, we confirm the role of numerous candidate genes previously implicated in female mate choice in other species, suggesting that evolutionary tinkering with these conserved molecular processes underlies divergent mate preferences and sexual isolation. Taken together, our study adds important new insights to our understanding of the molecular processes underlying female decision-making critical for generating sexual isolation and speciation.</p>
Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 3. Bolbolaimus brevis sp. nov., самец (А, Б, Δ) и самка (В, Г). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 7 мкм; Б, Г, Δ — 20 мкм; В — 30 мкм Fig. 3. Bolbolaimus brevis sp. nov., male (А, Б, Δ) and female (В, Г). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 7 µm; Б, Г, Δ – 20 µm; В – 30 µm
Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 2. Фотографии Bolbolaimus parvus sp. nov., самец (А, В, Δ, Е, Ж, К, Α) и самка (Б, Г, З, И, М). А, Б — общий виΑ; В, Г — переΑний конец теΛа; Δ — теΛо в обΛасти базаΛьного буΛьбуса; Е, Ж, З — гоΛова; И — теΛо в обΛасти вуΛьвы; К — теΛо в обΛасти кΛоаки; Α, М — хвост. Масштаб: Б — 100 мкм; А — 50 мкм; В, Α — 20 мкм; Г, И, М — 10 мкм; Δ, Е, Ж, З, К — 5 мкм Fig. 2. Light micrograph of Bolbolaimus parvus sp. nov., male (А, В, Δ, Е, Ж, К, Α) and female (Б, Г, З, И, М). А, Б – general view; В, Г – anterior body end; body in region of basal pharynx bulb; Е, Ж, З – head; И – vulva region; К – cloaca region; Α, М – tail. Scale bars: Б – 100 µm; А – 50 µm; В, Α – 20 µm; Г, И, М – 10 µm; Δ, Е, Ж, З, К – 5 µm
Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 1. Bolbolaimus parvus sp. nov., самец (А, Б, В) и самка (Г, Δ). А — гоΛова; Б — переΑний конец теΛа; В, Δ — хвост; Г — теΛо в обΛасти вуΛьвы. Масштаб: А — 10 мкм; В, Δ — 20 мкм; Б, Г — 30 мкм Fig. 1. Bolbolaimus parvus sp. nov., male (А, Б, В) and female (Г, Δ). А – head; Б – anterior body end; В, Δ – tail; Г – vulva region. Scale bars: А – 10 µm; В, Δ – 20 µm; Б, Г – 30 µm
Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm in Description Of Two New Nematoda Species Of The Genus Cobb, 1920 (Nematoda, Desmodorida) From Littoral Of Soutch China Sea At Coast Of Vietnam
Рис. 4. Фотографии Bolbolaimus brevis sp. nov., самец (А, В, Г, Е, З, И, К) и самка (Б, Δ, Ж, Α). А, Б — общий виΑ; В, Г, Δ — гоΛова; Е — переΑний конец теΛа; Ж — теΛо в обΛасти вуΛьвы; З, И — теΛо в обΛасти кΛоаки; К, Α — хвост. Масштаб: А, Б — 50 мкм; Е, Ж, К, Α — 10 мкм; В, Г, Δ, З, И — 5 мкм Fig. 4. Light micrograph of Bolbolaimus brevis sp. nov., males (А, В, Г, Е, З, И, К) and female (Б, Δ, Ж, Α). А, Б – general view; В, Г, Δ – head; Е – anterior body end; Ж – vulva region; З, И – cloaca region; К, Α – tail. Scale bars: А, Б – 50 µm; Е, Ж, К, Α – 10 µm; В, Г, Δ, З, И – 5 µm
Рис. 3. Àневные чешуекрыΛые Ботчинского заповеΑника в прироΑе. Фото И. В. Костомаровой: 1 — Vanessa cardui; 2 — Euphydryas intermedia, самец; 3 — Melitaea arcesia, самка; 4 — Mellicta ambigua, самец; 5 — Nephargynnis anadyomene ella, самка; 6 — Damora sagana, самец; 7 — Erebia ligea eumonia (сΛева) и Erebia ajanensis (справа), самцы; 8 — Erebia wanga, самец Fig. 3. Diurnal butterflies of the Botchinsky reserve in nature. Photos by I. V. Kostomarova: 1 — Vanessa cardui; 2 — Euphydryas intermedia, males; 3 — Melitaea arcesia, female; 4 — Mellicta ambigua, male; 5 — Nephargynnis anadyomene ella, female; 6 — Damora sagana, male; 7 — Erebia ligea eumonia (left) and Erebia ajanensis (right), males; 8 — Erebia wanga, male in Hesperioidea And Papilionoidea (Lepidoptera) Of Coniferous Forests From The Nature Reserve Botchinskii
Рис. 3. Àневные чешуекрыΛые Ботчинского заповеΑника в прироΑе. Фото И. В. Костомаровой: 1 — Vanessa cardui; 2 — Euphydryas intermedia, самец; 3 — Melitaea arcesia, самка; 4 — Mellicta ambigua, самец; 5 — Nephargynnis anadyomene ella, самка; 6 — Damora sagana, самец; 7 — Erebia ligea eumonia (сΛева) и Erebia ajanensis (справа), самцы; 8 — Erebia wanga, самец Fig. 3. Diurnal butterflies of the Botchinsky reserve in nature. Photos by I. V. Kostomarova: 1 — Vanessa cardui; 2 — Euphydryas intermedia, males; 3 — Melitaea arcesia, female; 4 — Mellicta ambigua, male; 5 — Nephargynnis anadyomene ella, female; 6 — Damora sagana, male; 7 — Erebia ligea eumonia (left) and Erebia ajanensis (right), males; 8 — Erebia wanga, male
Рис. 2. Àневные чешуекрыΛые Ботчинского заповеΑника в прироΑе. Фото И. В. Костомаровой: 1 — Hesperia comma repugnans, самец; 2 — Parnassius stubbendorfii, самец; 3 — Anthocharis cardamines, самец; 4 — Pieris melete, самец; 5 — Lycaeides idas tancrei, самец; 6 — Mimathyma nycteis, самец; 7 — Limenitis helmanni, самцы; 8 — Neptis andetria, самка Fig. 2. Diurnal butterflies of the Botchinsky reserve in nature. Photos by I. V. Kostomarova: 1 — Hesperia comma repugnans, male; 2 — Parnassius stubbendorfii, male; 3 — Anthocharis cardamines, male; 4 — Pieris melete, male; 5 — Lycaeides idas tancrei, male; 6 — Mimathyma nycteis, male; 7 — Limenitis helmanni, males; 8 — Neptis andetria, female in Hesperioidea And Papilionoidea (Lepidoptera) Of Coniferous Forests From The Nature Reserve Botchinskii
Рис. 2. Àневные чешуекрыΛые Ботчинского заповеΑника в прироΑе. Фото И. В. Костомаровой: 1 — Hesperia comma repugnans, самец; 2 — Parnassius stubbendorfii, самец; 3 — Anthocharis cardamines, самец; 4 — Pieris melete, самец; 5 — Lycaeides idas tancrei, самец; 6 — Mimathyma nycteis, самец; 7 — Limenitis helmanni, самцы; 8 — Neptis andetria, самка Fig. 2. Diurnal butterflies of the Botchinsky reserve in nature. Photos by I. V. Kostomarova: 1 — Hesperia comma repugnans, male; 2 — Parnassius stubbendorfii, male; 3 — Anthocharis cardamines, male; 4 — Pieris melete, male; 5 — Lycaeides idas tancrei, male; 6 — Mimathyma nycteis, male; 7 — Limenitis helmanni, males; 8 — Neptis andetria, female
Data from Investigating the effects of diurnal and nocturnal pollinators on male and female reproductive success and on floral trait selection in Silene dioica
<p><strong>data_all_OdEx.csv</strong>: all data about phenotypes or reproductive success at the individual scale</p> <ul> <li>ID : ID name</li> <li>nGrSemis_min : seed number needed to be sowned to get enough seedlings</li> <li>nGrGerm : seed number effectively sowned</li> <li>nGrGerm_OK : number of germinated seed</li> <li>TauxGerm : germination rate</li> <li>nFruits_MAX : maximal number of fruit that the plant could have produced</li> <li>nFruits_OK : effective number of fruits that the plant had produced</li> <li>nFruits_OK_avecPred : effective number of fruits that the plant had produced ignoring predation</li> <li>nFruits_pred : number of predated fruits</li> <li>mean_nbSeeds : mean number of seeds per fruit</li> <li>sd_nbSeeds : sd number of seeds per fruit</li> <li>mean_nbOv : mean ovule non fertilize per fruit</li> <li>sd_nbOv : sd ovule non fertilize per fruit</li> <li>mean_nbOvTOT : mean ovule number per flower</li> <li>sd_nbOvTOT : sd ovule number per flower</li> <li>prodTOT : total number of seed produced including germination rate</li> <li>FS : Fruit-set</li> <li>SS : Seed-set</li> <li>prodTOTsg : total number of seed produced without germination rate</li> <li>nbFlo_run0 : flower number at the beginning of the experiment</li> <li>nbFlo_run1 : flower number at the first measurement</li> <li>mean_nbFlo : mean flower number</li> <li>MeanFec : mean seed sired per males according to MEMM model</li> <li>MeanDelta : mean delta pollen dispersion according to MEMM model</li> <li>MeanMRS : mean male reproductive success (including female RS) according to MEMM model</li> <li>MedFec : same as above with the median</li> <li>MedDelta : same as above with the median</li> <li>MedMRS : same as above with the median</li> <li>VarFec : same as above with the variance</li> <li>VarDelta : same as above with the variance</li> <li>VarMRS : same as above with the variance</li> <li>ciFec : Same as above with confidence interval</li> <li>ciDelta : Same as above with confidence interval</li> <li>ciMRS : Same as above with confidence interval</li> <li>MS_Res : mating success</li> <li>mean_lFl : mean corolla width</li> <li>mean_hFl : mean calyx height</li> <li>QttTOT : pollen number per flower</li> <li>pop : which originate population</li> <li>cohort : which cohort</li> </ul> <p><strong>data_seeds_OdEx.csv</strong> : all data about seed number of weight as well as unfertilized ovule at the fruit scale for female RS</p> <ul> <li>ID : ID name</li> <li>noFruit : ID fruit</li> <li>poids : seed weight</li> <li>nbSeeds : number of seeds</li> <li>nbOv : number of unfertilized ovule</li> <li>moySeeds : mean seed size</li> <li>varSeeds : variance in seed size</li> </ul> <p><strong>data_poll_OdEx.csv</strong> : all data about pollinator observation session</p> <ul> <li>ID : ID name</li> <li>session : observation session number</li> <li>nbVis : number of independent insect attracted</li> <li>nbVisTot : number of total visit</li> <li>binVis : individual visited or not</li> </ul>
Fig. 9 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick
Fig. 9 Mitochondrial genomes of Ixodes (Endopalpiger) australiensis, I. (Endo.) barkeri, I. (Endo.) woyliei and I. (Exopalpiger) fecialis. Protein-coding genes are shown in green, tRNAs are in yellow, rRNAs are in red, and the two control regions are in blue. Protein-coding genes are labelled by their four-character abbreviations, tRNAs are labelled by their one-letter amino acid abbreviations, and the two control regions are labelled as CR1 and CR2. Mitochondrial genome size variation is indicated in parentheses. The arrangement of genes in these four species is identical except that the main cluster of tRNA genes has the arrangement ARNSEF in the three species of Endopalpiger [I. (Endo.) australiensis, I. (End.) barkeri and I. (End.) woyliei], whereas in the one species of Exopalpiger [I. (Exo.) fecialis] the arrangement is ARNESF. The arrangement in I. (Exo.) fecialis is the first known arrangement in an Ixodidae tick that is different from ARNSEF.Thus, ARNESF might be a synapomorphy for the subgenus Exopalpiger
Fig. 7 Ixodes barkeri Barker, 2019 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick
Fig. 7 Ixodes barkeri Barker, 2019, scanning electron micrographs of larva. A Scutum. B Gnathosoma, dorsal view. C Gnathosoma, ventral view. D Gnathosoma, anteroventral view. E Coxae. Scale bars: A, E 0.1 mm; B–D, 0.05 mm
Fig. 1 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick
Fig. 1 The four known localities in Australia, Queensland (Qld), of Ixodes barkeri Barker, 2019, are indicated by white-with-red dots
Fig. 10 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick
Fig. 10 Maximum likelihood (ML) phylogenetic tree from entire mt genomes (14,935 bps). The sequence alignment was put though Gblocks to remove regions with alignment gaps.Tip labels indicate NCBI accession numbers and (Barker & Barker Collection reference nos.). Numbers above branches show maximum likelihood bootstrap support, whereas numbers below branches show the Bayesian posterior probability support. Ixodes pavlovskyi Pomerantzev, 1946, one of the species "Other Ixodes" (sensu Barker & Murrell, 2004), for which an entire mitochondrial (mt) genome was available in GenBank, was set as the outgroup. The scale bar indicates 0.06 nucleotide substitutions per nucleotide site for the 14,935 nucleotide sites in our alignment of theses entire mt genomes. So, for example, there were about 896 nucleotide substitutions along the branch that leads to I. (Ceratixodes) uriae plus I. (Sternalixodes) holocyclus plus I. (Exopalpiger) fecialis, which is marked with an asterisk [i.e. 0.06 nucleotide substitutions per nucleotide site × 14,935 nucleotide sites (bps) = 1896 nucleotide substitutions]. Ticks in bold were sequenced in the present study
Fig. 4 Ixodes barkeri Barker, 2019 in Description of the female, nymph and larva and mitochondrial genome, and redescription of the male of Ixodes barkeri Barker, 2019 (Acari: Ixodidae), from the short-beaked echidna, Tachyglossus aculeatus, with a consideration of the most suitable subgenus for this tick
Fig. 4 Ixodes barkeri Barker, 2019, scanning electron micrographs of female. A Idiosoma, dorsal view. B Scutum, dorsal view. C Scutum, dorsolateral view. D Idiosoma showing scutum and alloscutum with punctations and setae, dorsal centrolateral portion. E Idiosoma, ventral view. Scale bars: A, E 0.5 mm; B, C 0.2 mm; D 0.1 mm
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