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Fig. 2. A in Application of allozyme markers for screening of turbot populations along Western Black Sea coast

Fig. 2. A. Electrophoregrams on PROT from turbot (Bulgarian and Romanian coast), using different tissues:1-3 – haemoglobins, 4-5- eye (retina) and 6 – muscle, 0 – origin. B. Electrophoregrams on PROT from turbot Bulgarian and Rumanian coast haemoglobin tissue. PROT-1* and PROT-2* were polymorphic, 0 – origin.

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Fig. 2 in Soluble proteins in Messor structor (Latreille, 1798) (Hymenoptera: Formicidae) populations from Bulgaria - genetic variability and possible usage as population-genetic markers

Fig. 2. Spectrum of soluble proteins of M. structor workers (7.5% PAGE): a. Elenovo population; b. Tsalapitsa population.

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Fig. 3. a in Soluble proteins in Messor structor (Latreille, 1798) (Hymenoptera: Formicidae) populations from Bulgaria - genetic variability and possible usage as population-genetic markers

Fig. 3. a. UPGMA dendrogram (Sneath et al. 1973); b. Neighbour-joining dendrogram (Saitou & Nei 1987).

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Рис. 3. Снижение чисΛенности гусениц при возΑействии разΛичных географических штаммов ВЯП. СтоΛбцы: коΛичество погибших во время эксперимента гусениц поΑ опреΑеΛенной инфекционной нагрузкой. ПоказатеΛи (в процентах) привеΑены в Λевой части табΛицы. СтреΛки: минимаΛьное и максимаΛьное коΛичество погибших во время очереΑного учета гусениц и крестообразные маркеры: среΑнее коΛичество погибших во время очереΑного учета гусениц. ПоказатеΛи (в абсоΛютных значениях) в правой части табΛицы. По горизонтаΛи: номер титра, от боΛьшего к меньшему Fig. 3. Decrease in the number of caterpillars under the influence of various geographical strains of NPV. Columns: number of caterpillars killed during the experiment under a certain infectious load. Indicators (in percent) are shown on the left side of the table. Arrows: the minimum and maximum number of deaths during the next track count and cross markers: the average number of deaths during the next track count. Indicators (in absolute values) on the right side of the table. Horizontal: titre, from highest to lowest in Sensitivity of caterpillars of the gypsy moth (Lymantria dispar, Erebidae) from the South of Khabarovsk Territory to various strains of nuclear polyhedrosis virus

Рис. 3. Снижение чисΛенности гусениц при возΑействии разΛичных географических штаммов ВЯП. СтоΛбцы: коΛичество погибших во время эксперимента гусениц поΑ опреΑеΛенной инфекционной нагрузкой. ПоказатеΛи (в процентах) привеΑены в Λевой части табΛицы. СтреΛки: минимаΛьное и максимаΛьное коΛичество погибших во время очереΑного учета гусениц и крестообразные маркеры: среΑнее коΛичество погибших во время очереΑного учета гусениц. ПоказатеΛи (в абсоΛютных значениях) в правой части табΛицы. По горизонтаΛи: номер титра, от боΛьшего к меньшему Fig. 3. Decrease in the number of caterpillars under the influence of various geographical strains of NPV. Columns: number of caterpillars killed during the experiment under a certain infectious load. Indicators (in percent) are shown on the left side of the table. Arrows: the minimum and maximum number of deaths during the next track count and cross markers: the average number of deaths during the next track count. Indicators (in absolute values) on the right side of the table. Horizontal: titre, from highest to lowest

Fig. 7 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs

Fig. 7. Isotope signatures of the European grapevine moth, Lobesia botrana; error bars are 2 standard deviations of the mean.

Fig. 1 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs

Fig. 1. Percentage of sucrose based on dry weight (DW) in popular artificial diets for mass rearing various moth species, as described by Dyck (2010).

Fig. 3 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs

Fig. 3. Isotope signatures of the African sugarcane borer, Eldana saccharina. Wild moths developed on sugarcane at Eston, and at Tinely Manor, a 3rd group developed on papyrus at Eston and a 4th group was mass reared on an artificial diet. Error bars are 3 standard deviations of the mean.

Fig. 2 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs

Fig. 2. Isotope signatures of cactus, a laboratory formulated diet and of cactus moths, Cactoblastis cactorum, reared on these 2 substrates; error bars are 2 standard deviations of the mean.

Fig. 4 in Stable isotope markers differentiate between mass-reared and wild Lepidoptera in sterile insect technique programs

Fig. 4. Isotope signature of the light brown apple moth, Epiphyas postvittana (LBAM); error bars are 2 standard deviations of the mean.

Fig. 4 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 4. Vizcainocypria viator gen. nov. sp. nov., male (MUVHNZY0011). A: A2. B: Right prehensile palp. C: Left prehensile palp. D: Hemipenis. E: Zenker organ. Scale bars: A–E = 50 µm.

Fig. 2 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 2. Vizcainocypria viator gen. nov. sp. nov., female (MUVHNZY0012). A: A1 (arrow pointing to apical claw on penultimate segment). B: A2. C: Md coxa. D: Md palp. E: Detail of α and β setae. F: Mxl. Scale bars: A–F = 50 µm.

Fig. 3 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 3. Vizcainocypria viator gen. nov. sp. nov., female (MUVHNZY0012). A: T1. B: T2. C: T3. D: CR. E: Caudal attachment. Scale bars: A–E = 50 µm.

Fig. 6 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 6. Male copulatory organs (hemipenes) of different species of Cyclocyprididae. A: Cyclocypris, B: Cypria, C: Physocypria, D: Dentocypria, E: Keysercypria, F: Brasilocypria, G: Claudecypria, H: Vizcainocypria. Redrawn from Almeida et al. (2023): F, G; Karanovic (2011): C (P. bullata), E; Hartmann (1959): H (V. granadae); Meisch (2000): A, B (C. exsculpta, C. ophtalmica), C (P. kraepelini); Savatenalinton (2017): D; Smith and Janz (2008): B (C. matzkeae), C (P. nipponica, P. biwaensis); Wouters (1984): B (C. subsalsa). Scale bars are shown when available: D. smithi = 46 µm; C. ovum, C. ophtalmica, C. subsalsa, P. nipponica, P. biwaensis, D. mesquitai, B. pea, B. alisonae, C. mesquitai, C. rochei, V. viator = 50 µm; C. matzkeae, P. bullata, K. affinis, K. deformis = 100 µm.

Fig. 1 in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 1. Vizcainocypria viator gen. nov. sp. nov., female (A, C–G, I), male (B, H). A: Mature female specimen. B: Mature male specimen. C: CpL from right side (MUVHNZY0020). D: CpF (MUVHNZY0019). E: CpD (MUVHNZY0018). F: LVi (MUVHNZY0016). G: Detail of the internal tooth (MUVHNZY0016). H: RVi (MUVHNZY0011). I: Detail of the tubercles on RV margin (MUVHNZY0017). Scale bars: A–F, H = 200 µm; G = 10 µm; I = 5 µm.

Fig. 5. Maximum likelihood tree for 28S in Fig. 1 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 5. Maximum likelihood tree for 28S (A) and COX1 (B) genes. Red branches indicate the presence of tubercles on the RV margin.

Fig. 8. The IL-6 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 8. The IL-6 expression levels of Japanese eel and giant mottled eel reared in different spectra. W: white light; B: blue light; G: green light; R: red light; black: dark. Different letters indicate significant differences between different spectra groups of the same eel species (p <0.05).

Fig. 7 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 7. The LZM expression levels of Japanese eel and giant mottled eel reared in different spectra. W: white light; B: blue light; G: green light; R: red light; black: dark. Different letters indicate significant differences between different spectra groups of the same eel species (p <0.05).

Fig. 6 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 6. The SOD expression levels of Japanese eel and giant mottled eel reared in different light spectra. W: white light; B: blue light; G: green light; R: red light; black: dark. Different letters indicate significant differences between different spectra groups of the same eel species (p <0.05).

Fig. 5 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 5. The body weight of giant mottled eel reared in different light spectra for 12 weeks. W: white light; Black: dark; B: blue light; G: green light; R: red light. Different letters indicate significant differences between groups of the same week (p <0.05).

Fig. 3 in Fig. 4 in Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels ().

Fig. 3. The body weight of Japanese eel reared in different light spectra for 12 weeks. W: white light; Black: dark; B: blue light; G: green light; R: red light.