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Рис. 1. Карта-схема р. Амазар. Цифрами обозначены: I — места Αобычи россыпного зоΛота; II — участки иссΛеΑования в 2018–2019 гг.: 1 — реки Амазар и БоΛьшая Чичатка в районе пгт. Амазар, 2 — воΑохраниΛище, 3 — р. Крестовая, 4 — р. Амазар в нижнем течении Fig. 1. Schematic map of the Amazar River. Legend: I — placer gold mining areas; II — survey areas in 2018–2019: 1 — the Amazar and the Bolshaya Chichatka Rivers in the area of Amazar urban-type settlement, 2 — water storage reservoir, 3 — the Krestovaya River, 4 — the lower reaches of the Amazar River in Dynamics and current status of the Amazar River ichthyofauna after the construction of the PPM «Polyarnaya» hydroelectric complex

Рис. 1. Карта-схема р. Амазар. Цифрами обозначены: I — места Αобычи россыпного зоΛота; II — участки иссΛеΑования в 2018–2019 гг.: 1 — реки Амазар и БоΛьшая Чичатка в районе пгт. Амазар, 2 — воΑохраниΛище, 3 — р. Крестовая, 4 — р. Амазар в нижнем течении Fig. 1. Schematic map of the Amazar River. Legend: I — placer gold mining areas; II — survey areas in 2018–2019: 1 — the Amazar and the Bolshaya Chichatka Rivers in the area of Amazar urban-type settlement, 2 — water storage reservoir, 3 — the Krestovaya River, 4 — the lower reaches of the Amazar River

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Рис. 3. Останки пятнистого оΛеня — жертвы воΛков на ΛьΑу р. Бикин в верхнем течении, 29 января 2019 г. Fig. 3. Remains of a sika deer (wolves' prey) on the ice in the upper reaches of the Bikin River, January 29, 2019 in Documented Evidence Of Habitation For The Sika Deer, The Amur Leopard Cat And The Striped Field Mouse In The Bikin National Park (Russia)

Рис. 3. Останки пятнистого оΛеня — жертвы воΛков на ΛьΑу р. Бикин в верхнем течении, 29 января 2019 г. Fig. 3. Remains of a sika deer (wolves' prey) on the ice in the upper reaches of the Bikin River, January 29, 2019

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Рис. 4. РаспреΑеΛение рыб в верхнем и нижнем бьефе в периоΑ осенней миграции 2018 г. (а) и верхнем бьефе в весеннюю миграцию 2019 г. (б). Точками показаны места фиксации рыб эхоΛотом Fig. 4. Distribution of fish upstream and downstream of the reservoir during the autumn migration of 2018 (а) and upstream of the reservoir during the spring migration of 2019 (b). Points indicate the locations where fish were registered by echosounder in Dynamics and current status of the Amazar River ichthyofauna after the construction of the PPM «Polyarnaya» hydroelectric complex

Рис. 4. РаспреΑеΛение рыб в верхнем и нижнем бьефе в периоΑ осенней миграции 2018 г. (а) и верхнем бьефе в весеннюю миграцию 2019 г. (б). Точками показаны места фиксации рыб эхоΛотом Fig. 4. Distribution of fish upstream and downstream of the reservoir during the autumn migration of 2018 (а) and upstream of the reservoir during the spring migration of 2019 (b). Points indicate the locations where fish were registered by echosounder

Fig. 2 in A report of 43 unrecorded bacterial species within the phyla Bacteroidetes and Firmicutes isolated from various sources from Korea in 2019

Fig. 2. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences, showing the relationship between the isolates and their relatives of the phylum Bacteroidetes. Bootstrap values (>70%) are shown. Filled circles indicate that both maximum-likelihood and maximum-parsimony trees obtained the same node arrangement, while empty circles indicate either only maximum-likelihood or maximum-parsimony obtained the same corresponding nodes. Escherichia coli ATCC 11775T (X80725) was used as an outgroup. Bar, 0.05 substitutions per nucleotide position.

Fig. 5 in A report of 43 unrecorded bacterial species within the phyla Bacteroidetes and Firmicutes isolated from various sources from Korea in 2019

Fig. 5. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences, showing the relationship between the isolates and their relatives of the orders Clostridiales and Lactobacillales. Bootstrap values (>70%) are shown. Filled circles indicate that both maximum-likelihood and maximum-parsimony trees obtained the same node arrangement, while empty circles indicate either only maximum-likelihood or maximum-parsimony obtained the same corresponding nodes. Escherichia coli ATCC 11775T (X80725) was used as an outgroup. Bar, 0.02 substitutions per nucleotide position.

Fig. 3 in A report of 43 unrecorded bacterial species within the phyla Bacteroidetes and Firmicutes isolated from various sources from Korea in 2019

Fig. 3. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences, showing the relationship between the isolates and their relatives of the family Bacillaceae. Bootstrap values (>70%) are shown. Filled circles indicate that both maximum-likelihood and maximum-parsimony trees obtained the same node arrangement, while empty circles indicate either only maximum-likelihood or maximum-parsimony obtained the same corresponding nodes. Escherichia coli ATCC 11775T (X80725) was used as an outgroup. Bar, 0.02 substitutions per nucleotide position.

Fig. 1 in A report of 43 unrecorded bacterial species within the phyla Bacteroidetes and Firmicutes isolated from various sources from Korea in 2019

Fig. 1. Transmission electron micrographs of cells. Strains: 1, LPB0329; 2, SO92; 3, FS31; 4, BT243; 5, F-49; 6, HMF9403; 7, SS28; 8, HMF6110; 9, HMF6096; 10, HMF6964; 11, R20; 12, 19D1S38; 13, LPB0288; 14, CAU 1601; 15, LPB0313; 16, BT246; 17, JBTF-M5; 18, LPB0275; 19, 19D1F21; 20, DN10; 21, 19D1C9; 22, LPB0284; 23, N17; 24, BT366; 25, BT245; 26, CAU 1600; 27, BSSK_R2A22; 28, FS120; 29, CAU 1604; 30, DS-19; 31, NC2; 32, CAU 1557; 33, CAU 1563; 34, CAU 1572; 35, CAU 1562; 36, LPB0311; 37, LPB0214; 38, YG19; 39, AM8; 40, AM13; 41, LPB0309; 42, LPB0308; 43, LPB0307.

Fig. 4 in A report of 43 unrecorded bacterial species within the phyla Bacteroidetes and Firmicutes isolated from various sources from Korea in 2019

Fig. 4. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences, showing the relationship between the isolates and their relatives of the families Paenibacillaceae, Planococcaceae and Staphylococcaceae. Bootstrap values (>70%) are shown. Filled circles indicate that both maximum-likelihood and maximum-parsimony trees obtained the same node arrangement, while empty circles indicate either only maximum-likelihood or maximum-parsimony obtained the same corresponding nodes. Escherichia coli ATCC 11775T (X80725) was used as an outgroup. Bar, 0.02 substitutions per nucleotide position.

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Figs. 1-2 in Eublemma baccatrix Hacker, 2019 (Lepidoptera: Erebidae: Boletobiinae: Eublemmini): recurrent immigrant or rapidly expanding species throughout the Iberian south area? Eublemma baccatrix Hacker, 2019 (Lepidoptera: Erebidae: Boletobiinae: Eublemmini): inmigrante recurrente o especie en rápida expansión por el sur ibérico?

Figs. 1-2.- Eublemma baccatrix Hacker, 2019. 1.- Casa Athene, Vejer de la Frontera, Cádiz, 10-11-2023, leg. & phot. Stephen Knapp, coll. José Luis Yela. 2.- Duquesa Fairways, San Luis de Sabinillas, Manilva, Málaga, phot. Richard Banham.

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Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) in Call repertoire of Bitterns Ixobrychus in Russian Far East

Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016)

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Рис. 2. Сезонная Αинамика чисΛенности и биомассы зоопΛанктона оз. Арейское в 2019– 2020 гг. Fig. 2. Seasonal dynamics of the zooplankton abundance and biomass in the Areiskoye Lake in 2019–2020 in Zooplankton of the Areiskoye Lake (Ingoda River basin, Trans-Baikal Territory)

Рис. 2. Сезонная Αинамика чисΛенности и биомассы зоопΛанктона оз. Арейское в 2019– 2020 гг. Fig. 2. Seasonal dynamics of the zooplankton abundance and biomass in the Areiskoye Lake in 2019–2020

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Рис. 1. Карта-схема распоΛожения станций отбора проб в оз. Арейское в 2019–2020 гг. Fig. 1. Schematic map of the sampling station locations in the Areiskoye Lake in 2019–2020: 1 — N 50°59.8657ʹ, E 111°14.1410ʹ; 2 — N 50°59.8836ʹ, E 111°15.4172ʹ; 3 — N 50°58.7316ʹ, E 111°15.0106ʹ; 4 — N 50°58.7474ʹ, E 111°14.1384ʹ; 5 — N 50°59.0378ʹ, E 111°13.9848ʹ; 6 — N 50°59.3193ʹ, E 111°14.0639ʹ in Zooplankton of the Areiskoye Lake (Ingoda River basin, Trans-Baikal Territory)

Рис. 1. Карта-схема распоΛожения станций отбора проб в оз. Арейское в 2019–2020 гг. Fig. 1. Schematic map of the sampling station locations in the Areiskoye Lake in 2019–2020: 1 — N 50°59.8657ʹ, E 111°14.1410ʹ; 2 — N 50°59.8836ʹ, E 111°15.4172ʹ; 3 — N 50°58.7316ʹ, E 111°15.0106ʹ; 4 — N 50°58.7474ʹ, E 111°14.1384ʹ; 5 — N 50°59.0378ʹ, E 111°13.9848ʹ; 6 — N 50°59.3193ʹ, E 111°14.0639ʹ

Fig. 5. Maximum Likelihood tree, produced with Cytochrome oxidase subunit I in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.

Fig. 5. Maximum Likelihood tree, produced with Cytochrome oxidase subunit I (COI) sequences of Dipturus argentinensis, D. lamillai, Zearaja brevicaudata, Z. chilensis, Z. nasuta and Amblyraja doellojuradoi as outgoup. Barcode Index Number assigned by Barcode of Life Datasystem (A) and the results of species delimitation analyses using bPTP (B) and ABGD (C) algorithms are shown as vertical bars on the right. Dipturus lamillai sequences are marked in bold.

Fig. 6. Maximum Likelihood tree produced with NADH dehydrogenase subunit 2 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.

Fig. 6. Maximum Likelihood tree produced with NADH dehydrogenase subunit 2 (NADH2) sequences of Dipturus argentinensis, D. lamillai, Zearaja brevicaudata, Z. chilensis, Z. nasuta and D. olseni as outgroup. Dipturus lamillai sequences are marked in bold and sequences corresponding to the description of the species (Concha et al. 2019) are indicated with *.

Fig. 4 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.

Fig. 4. External components of the clasper of a mature male of Zearaja brevicaudata (RM 186, 783 mm TL). Cl: cleft, Dl: distal lobe, P: pocket, Pr: pseudorhiphidion, Rh: rhiphidion, Sh: shield, Sl: slit, Sp: Spike, Sr: spur, Tb: terminal bridge. Scale bar = 30 mm.

Fig. 1 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.

Fig. 1. Principal component analysis based on morphological data expressed as percentage of total length. a) PC1 vs PC2 b) PC2 vs PC3. PC1: first principal component, PC2: second principal component, PC3: third principal component. ▲, ellipse with whole line: Zearaja brevicaudata; ■, holotype of Raia brevicaudata; ●, ellipse with dotted line: Z. chilensis; ◊, ellipse with dashed line: Dipturus lamillai.

Fig. 3 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.

Fig. 3. Female specimen of Zearaja brevicaudata (RM 317, 427 mm TL) showing the same coloration pattern as female paratype of Dipturus lamillai (cf. Concha et al., 2019, fig. 7B). Scale bar = 50 mm.

Fig. 2 in Morphological and Molecular Evidence Reveals the Longnose Skate (Marini, 1933) to be a Senior Synonym of Concha, Caira, Ebert & Pompert 2019.

Fig. 2. Dorsal spinulation pattern of an adult female of Zearaja brevicaudata (RM 170, 943 mm TL). White arrows point the dorsal thorns. Scale bar = 50 mm.

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Fig. 10 in Hylomus saiyans Nguyen & Nguyen & Nguyen & Phung 2019, sp. nov.

Fig. 10. Distribution of stranded/bycaught sea turtles in different towns in Yilan County. Location of each coastal township in Yilan County is showed in the upper right figure.