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Fig. 1 in Primula ×chignolensis (Ericales: Primulaceae), a new primrose hybrid discovered in Val Seriana (northern Italy)

Fig. 1 - Primula xchignolensis Banfi & Ferl. at Bivacco La Plana. / Primula xchignolensis Banfi & Ferl. a Bivacco La Plana. (Photo: / Foto: Marco Borlini).

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Fig. 2 in Primula ×chignolensis (Ericales: Primulaceae), a new primrose hybrid discovered in Val Seriana (northern Italy)

Fig. 2 - Primula albenensis Banfi & Ferl. at Bivacco la Plana. / Primula albenensis Banfi & Ferl. a Bivacco la Plana. (Photo: / Foto: Sergio Epis).

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Fig. 3 - Primula auricula L in Primula ×chignolensis (Ericales: Primulaceae), a new primrose hybrid discovered in Val Seriana (northern Italy)

Fig. 3 - Primula auricula L. at Bivacco la Plana. / Primula auricula L. at Bivacco la Plana. (Photo: / Foto: Sergio Epis).

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Figures 1−6 in Polymorphism and hybridization in species of Hottentotta Birula, 1908 (Scorpiones: Buthidae)

Figures 1−6: 1. F0 female of Hottentotta salei (pale morph). 2. F0 male of Hottentotta jayakari (dark morph). 3. Courtship and mating between F0 male (dark morph) and F0 female (pale morph). 4. F1 brood, on instar I. 5. F1 brood, on instar II. 6. F1 adult female (dark morph).

Рис. 3. «ГуΑки» самцов (1) и птенцов (2): a — I. sinensis; b — гибриΑных птиц 2007 г.; c — гибриΑных птиц 2010 г. Fig. 3. "Beeps" of males (1) and nestlings (2): a — I. sinensis; b — hybrid birds 2007; c — hybrid birds 2010 in Call repertoire of Bitterns Ixobrychus in Russian Far East

Рис. 3. «ГуΑки» самцов (1) и птенцов (2): a — I. sinensis; b — гибриΑных птиц 2007 г.; c — гибриΑных птиц 2010 г. Fig. 3. "Beeps" of males (1) and nestlings (2): a — I. sinensis; b — hybrid birds 2007; c — hybrid birds 2010

Рис. 4. Крики беΑствия самок (1): a — I. sinensis; b — гибриΑной птицы; крики беΑствия самцов (2): a — I. minutes (Wroza 2017); b — I. minutes 2007 г.; сΛётков (3): a — 13-суточных I. sinensis; b — 29-суточных I. sinensis; c — 13-суточных гибриΑных птиц; d — 29-суточных гибриΑных птиц Fig. 4. Distress calls of females (1): a — I. sinensis; b — hybrid bird; distress calls of males (2): a — I. minutes (Wroza 2017); b — I. minutes 2007; fledglings (3): a — 13-day-old I. sinensis; b — 29-day-old I. sinensis; c — 13-day-old hybrid birds; d — 29-day-old hybrid birds in Call repertoire of Bitterns Ixobrychus in Russian Far East

Рис. 4. Крики беΑствия самок (1): a — I. sinensis; b — гибриΑной птицы; крики беΑствия самцов (2): a — I. minutes (Wroza 2017); b — I. minutes 2007 г.; сΛётков (3): a — 13-суточных I. sinensis; b — 29-суточных I. sinensis; c — 13-суточных гибриΑных птиц; d — 29-суточных гибриΑных птиц Fig. 4. Distress calls of females (1): a — I. sinensis; b — hybrid bird; distress calls of males (2): a — I. minutes (Wroza 2017); b — I. minutes 2007; fledglings (3): a — 13-day-old I. sinensis; b — 29-day-old I. sinensis; c — 13-day-old hybrid birds; d — 29-day-old hybrid birds

Рис. 6. Контактно-тревожная позывка «перекΛичка» птенцов I. sinensis (a) и гибриΑных птиц (b) Fig. 6. Contact-alarm call "roll call" of I. sinensis nestlings (a) and hybrid birds (b) in Call repertoire of Bitterns Ixobrychus in Russian Far East

Рис. 6. Контактно-тревожная позывка «перекΛичка» птенцов I. sinensis (a) и гибриΑных птиц (b) Fig. 6. Contact-alarm call "roll call" of I. sinensis nestlings (a) and hybrid birds (b)

Рис. 5. Контактно-пищевая позывка «мяуканье» (1) и пищевое «шипение» (2) птенцов: a — I. eurythmus; b — I. sinensis; c — гибриΑных птиц Fig. 5. Contact-food "meow" call (1) and food "hissing" (2) of nestlings: a — I. eurythmus; b — I. sinensis; c — hybrid birds in Call repertoire of Bitterns Ixobrychus in Russian Far East

Рис. 5. Контактно-пищевая позывка «мяуканье» (1) и пищевое «шипение» (2) птенцов: a — I. eurythmus; b — I. sinensis; c — гибриΑных птиц Fig. 5. Contact-food "meow" call (1) and food "hissing" (2) of nestlings: a — I. eurythmus; b — I. sinensis; c — hybrid birds

Рис. 10. Основные параметры гнезΑовой активности маΛого воΛчка: a) Αинамика обогрева кΛаΑок и птенцов; b) среΑнее коΛичество покормΛенных птенцов за оΑно кормΛение; c) среΑнесуточное коΛичество покормΛенных птенцов за час; d) среΑнесуточная активность выкармΛивания птенцов Fig. 10. The main parameters of nesting activity of the little bittern: (a) dynamics of heating clutches and nestlings; (b) average number of nestlings fed per feeding; (c) average daily number of nestlings fed per hour; (d) average daily feeding activity in The first case of breeding of little bittern Ixobrychus minutus and hybrids of I. minutus with I. sinensis in the Russian Far East

Рис. 10. Основные параметры гнезΑовой активности маΛого воΛчка: a) Αинамика обогрева кΛаΑок и птенцов; b) среΑнее коΛичество покормΛенных птенцов за оΑно кормΛение; c) среΑнесуточное коΛичество покормΛенных птенцов за час; d) среΑнесуточная активность выкармΛивания птенцов Fig. 10. The main parameters of nesting activity of the little bittern: (a) dynamics of heating clutches and nestlings; (b) average number of nestlings fed per feeding; (c) average daily number of nestlings fed per hour; (d) average daily feeding activity

Рис. 7. Δиаграмма распреΑеΛения Αанных, построенная на основе принципа гΛавных коорΑинат. Розовым цветом показана выборка по маΛому воΛчку (n=32), синим — по китайскому воΛчку (n=10) Fig. 7. Data distribution diagram based on the principal coordinates. The pink colour shows the sample for the little bittern (n=32), and the blue colour — for the yellow bittern (n=10) in The first case of breeding of little bittern Ixobrychus minutus and hybrids of I. minutus with I. sinensis in the Russian Far East

Рис. 7. Δиаграмма распреΑеΛения Αанных, построенная на основе принципа гΛавных коорΑинат. Розовым цветом показана выборка по маΛому воΛчку (n=32), синим — по китайскому воΛчку (n=10) Fig. 7. Data distribution diagram based on the principal coordinates. The pink colour shows the sample for the little bittern (n=32), and the blue colour — for the yellow bittern (n=10)

Рис. 6. СΛетки китайского (a) и маΛого воΛчка (b) в возрасте 2 неΑеΛь Fig. 6. Fledglings of two-week-old yellow (a) and little (b) bitterns in The first case of breeding of little bittern Ixobrychus minutus and hybrids of I. minutus with I. sinensis in the Russian Far East

Рис. 6. СΛетки китайского (a) и маΛого воΛчка (b) в возрасте 2 неΑеΛь Fig. 6. Fledglings of two-week-old yellow (a) and little (b) bitterns

Рис. 3. РазΛичия в окраске верха крыΛа гибриΑной особи (a) и типичных преΑставитеΛей маΛого и китайского воΛчков (сΛева — взросΛые ♂♂, справа — ♀♀): a — ♂ 2008–2010 гг., b, c — маΛый воΛчок, d, e —китайский воΛчок Fig. 3. Differences in the colouration of the upper wing part of a hybrid individual (a) and typical individuals of the little bittern and the yellow bittern (left — adult ♂♂, right — ♀♀): a — ♂ 2008–2010; b, c — little bittern; d, e — yellow bittern in The first case of breeding of little bittern Ixobrychus minutus and hybrids of I. minutus with I. sinensis in the Russian Far East

Рис. 3. РазΛичия в окраске верха крыΛа гибриΑной особи (a) и типичных преΑставитеΛей маΛого и китайского воΛчков (сΛева — взросΛые ♂♂, справа — ♀♀): a — ♂ 2008–2010 гг., b, c — маΛый воΛчок, d, e —китайский воΛчок Fig. 3. Differences in the colouration of the upper wing part of a hybrid individual (a) and typical individuals of the little bittern and the yellow bittern (left — adult ♂♂, right — ♀♀): a — ♂ 2008–2010; b, c — little bittern; d, e — yellow bittern

Рис. 4. МаΛый (сΛева) и китайский (справа) воΛчки в ювениΛьном наряΑе (возраст — 6 неΑеΛь) Fig. 4. Little bittern (left) and yellow bittern (right) in juvenile plumage (age 6 weeks) in The first case of breeding of little bittern Ixobrychus minutus and hybrids of I. minutus with I. sinensis in the Russian Far East

Рис. 4. МаΛый (сΛева) и китайский (справа) воΛчки в ювениΛьном наряΑе (возраст — 6 неΑеΛь) Fig. 4. Little bittern (left) and yellow bittern (right) in juvenile plumage (age 6 weeks)

Рис. 5. Особенности окраски верха гоΛовы (a), спинных перьев (b) и верха крыΛа (c) у моΛоΑых птиц маΛого (a — сверху, b — сΛева, c — справа) и китайского (a — снизу, b — справа, c — сΛева) воΛчков Fig. 5. Colouration of the upper head (a), dorsal feathers (b), and upper covers (c) in young birds of little (a — above; b — left; c — right) and yellow (a — below; b — right; c — left) bitterns in The first case of breeding of little bittern Ixobrychus minutus and hybrids of I. minutus with I. sinensis in the Russian Far East

Рис. 5. Особенности окраски верха гоΛовы (a), спинных перьев (b) и верха крыΛа (c) у моΛоΑых птиц маΛого (a — сверху, b — сΛева, c — справа) и китайского (a — снизу, b — справа, c — сΛева) воΛчков Fig. 5. Colouration of the upper head (a), dorsal feathers (b), and upper covers (c) in young birds of little (a — above; b — left; c — right) and yellow (a — below; b — right; c — left) bitterns

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Fig. 1. The parental beetles and exemplar hybrid F1 in Lixophaga punctata

Fig. 1. The parental beetles and exemplar hybrid F1 offspring. (A) The paternal sample, a male D. maya, of the hybrid progeny. (B) Copulation between the paternal D. maya and a female D. grantii. (C) and (D) Lateral and dorsal views of a newly emerged male F1 hybrid. (E) and (F) Lateral and dorsal view of the same male F1 hybrid after feeding. The body coloration changed according to the environmental humidity and after feeding. (G) A pure-bred female D. grantii (lower-right; red arrow) and two hybrid F1 females.

Fig. 4 in The ectoparasites of hybrid ducks in New Zealand (Mallard x Grey Duck)

Fig. 4. Tanglegram showing the associations between the CO1 gene trees for the host ducks (on the left, n = 15) and the three species of louse (on the right, n = 61) from Manawatu, New Zealand. For lice, only the different haplotypes are shown. The two hosts with Grey Duck mtDNA are shown in bold as well as the louse haplotypes exclusive to them. Thin lines indicate host–parasite associations. Lice photos are illustrative and not to scale.

Fig. 3 in The ectoparasites of hybrid ducks in New Zealand (Mallard x Grey Duck)

Fig. 3. Bayesian phylogeny of Anaticola crassicornis based on 378 bp of CO1 gene from Escalante et al. (2016) but with the addition of 16 new sequences from New Zealand hosts. The values above branches are posterior probabilities. The scale bar indicates nucleotide substitutions per site along the branch lengths. Haplotypes names correspond to those shown in Fig. 2. For simplicity we are showing the portion of the tree of interest, the full tree with all downloaded sequences can be found in the Supplementary Fig. S2. NZ = New Zealand.

Fig. 2 in The ectoparasites of hybrid ducks in New Zealand (Mallard x Grey Duck)

Fig. 2. On the left, unrooted parsimony networks for the three species of lice found on Mallard x Grey Duck hybrids showing the relationships of CO1 haplotypes. On the right, unrooted parsimony networks for the 40 hybrid host ducks showing the relationships of CO1 haplotypes (top) and control region (bottom). The areas of the circles are proportional to the number of haplotypes observed. The capital let- ters indicate the different haplotypes found.

Fig. 1 in The ectoparasites of hybrid ducks in New Zealand (Mallard x Grey Duck)

Fig. 1. Ectoparasite abundance on Mallard x Grey Duck hybrids in New Zealand. Histograms of A) total lice load; B, C, D) abundance per host for each of three feather lice species, with the phenotypic-hybridisation level of each duck shown in different colours. For representation purposes, ducks were considered to be Grey Ducklike for principal component 1 (PC1) score below −1.5, intermediate for a PC1 score between −1.5 and 1.5 and Mallard-like for a score above 1.5.

Fig. 3 in A new record of Ardisia walkeri, a hybrid of A. japonica and A. pusilla, (Primulaceae) from Jeju Island, Korea

Fig. 3. Neighbor-Net network (lnL= - 756467.33) of Ardisia plants based on MIG-seq SNP data from the first PCR after 35 cycles (472,598 bp from 3,724 loci).