| Podarcis depressa CAMERANO, 1878 Lacerta depressa var. rudis BEDRIAGA, 1886 Lacerta depressa WERNER, 1904 Lacerta saxicola rudis MEHELY, 1909 Lacerta muralis var. rudis BOULENGER, 1920 Lacerta rudis ENGELMANN et al, 1993 Darevskia rudis ARRIBAS, 1997 |
| rudis: Lectotype: MRSN (= MSNTO = MZUT) 2737:1 (Museo ed Istituto di Zoologia Sistematica, Torino), designated by Böhme and Budak 1977.
bischoffi: Holotype: ZDEU 183/977, 05.1977. Coll.: A. Budak.
bolkardaghica: Holotype: ZDEU 144/2009.6, 19.07.2009. Coll.: Y. Kumlutas.
chechenica: Holotype: NMW 33504.1, 6.08.1965; ZISP 17882:1, male fide Böhme 2014: 150; Coll.: I.S. Darevsky; Paratypes: ZFMK, ZIL, NMW.
lantzicyreni: Lectotype (designated by Darevsky & Eiselt 1967): GNM 2459, female.
macromaculata: Holotype: ZISP 17940.6 (Figs. 8-9 in Doronin 2017), 24.06.1961. Coll.: I.S. Darevsky.
obscura: Lectotype: ZISP 17171.1, designated by Doronin 2017 (Fig. 7 in Doronin 2017), 30.05.1914. Coll.: L.A. Lantz; paralectotypes: BMNH 1918.11.21.5–7.
svanetica: Holotype: ZISP 17875.1 (Fig. 10 in Doronin 2017), 13.08.1965. Coll.: I.S. Darevsky. |
| rudis: Type locality: Batumi (Republic of Georgia) and Trabzon (Turkey).
bischoffi: Type locality: Turkey, Artvin Province, 6 km to the southwest Arhavi, rocky exits along the automobile route, 41°19 ́15 ́ ́N 41°14 ́41 ́ ́E.
bolkardaghica: Type locality: Karagöl, Ulukışla, Niğde, Central Anatolia; “Turkey, Mersin Province, rocks vicinity of Karagöl Lake, 37°24 ́13 ́ ́N 34°33 ́27 ́ ́E” fide Doronin 2017.
chechenica: Type locality: Russia, Chechnya Shatoysky District, gorge of the Argun River 4 km higher (north) of the Sovetskoye (= Shatoy) village, 1500 m asl, 42°54 ́41 ́ ́N 45°42 ́56 ́ ́E; paratypes: NMW; paratype locality: Südabfall des zentralen Kaukasus, Pasanauri, Georgien.
lantzicyreni: Type locality: Erciyes Dað, ca. 1900 asl.” [Erciyes (= Erdschias) Dagh in Kayseri, Central Anatolia, Turkey].
macromaculata: Type locality: Georgia, Samtskhe-Javakheti Region, vicinity of Akhalkalaki, about 1800 m asl, 41°23 ́N 43°29 ́E.
obscura: Lectotype locality: Georgia, Samtskhe-Javakheti, Borjomi, Road to Akhaltsikhe.
svanetica: Type locality: Georgia, Samegrelo-Zemo Svaneti Region, vicinity of Mestia, 43°03 ́N, 42°45 ́E, 1700 m asl; Paratype locality: Pari in the Inguri Valley, Svaneti.
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Bedriaga, J. von (1886) - Description of Darevskia rudis rudis. - In: “Beiträge zur Kenntnis der Lacertiden-Familie (Lacerta, Algiroides, Tropidosaura, Zerzumia, Bettaia)”. Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft, 14: 17-444. Ryabinina, N.L. & Bannikova, A.A. & Kosushkin , S.A. & Ciobanu, D.G. & Milto, D.A. & Tuniyev, B.S. Orlova, V.F. & Grechko, V.V. & Darevsky, I.S. (2002) - Estimation of the subspecies level of differentiation in Caucasian lizards of the genus Darevskia (syn. Lacerta saxicola complex, Lacertidae, Sauria) using genome DNA markers. - Russian Journal of Herpetology, Moscow, 9 (3): 185–194. × The taxonomic categories such as population and subspecies were studied on the example of three Caucasian lizard species of genus Darevskia - D. praticola, D. derjugini, and D. rudis by comparing the morphological data and results inferred from nuclear DNA markers. RAPD and new inter-MIR-PCR (IM-PCR) methods were used. The IM-PCR was used to characterize the lacertid DNA fragments located between dispersed SINE type repeats which occurred to be ortologous to mammalian repeats of the same type. It was shown that separation of the Northern population of D. derjugini (subspecies silvatica) is supported by the comparison with two Southern populations (derjugini and barani). The latter ones, in their turn, are very similar and hardly can be considered as good subspecies by the genetic distance. The subspecific division of D. praticola (praticola and pontica) also requires more specification. For example, several populations from North Caucasus (ssp. praticola) occurred to be heterogeneous. The level of differences between ssp. praticola and pontica is of the same order as in some of the praticola populations. Low level of molecular differences between two subspecies of D. rudis (obscura and bischoffi) does not confirm their validity as a full subspecies. Bischoff, W. (2003) - Die Eidechsenfauna Georgiens. Teil II. Die Gattung Darevskia. - Die Eidechse, Bonn, 14 (3): 65-93. × In Georgia, 16 species of rock lizards of the Genus Darevskia are occuring (D. alpina, D.
„armeniaca`, D. brauneri, D. caucasica, D. clarkorum, D. daghestanica, D. „dahli`, D.
derjugini, D. mixta, D. nairensis, D. parvula, D. portschinskii, D. praticola, D. rudis, D.
„unisexualis` and D. Valentini). Besides short presentations of the single species and hints on their distribution and habitats, also some systematic remarks are given. Ciobanu, D.G. & Grechko, V.V. & Darevsky, I.S. (2003) - Molecular Evolution of Satellite DNA CLsat in Lizards from the Genus Darevskia (Sauria: Lacertidae): Correlation with Species Diversity. - Russian Journal of Genetics, Moscow, 39 (11): 1292-1305. × The structure and evolution of a satellite DNA family was examined in lizards from the genus Darevskia(family Lacertidae). Comparison of tandem units of repeated DNA (satDNA), CLsat, in all species from the genus Darevskiahas shown that their variability is largely explained by single-nucleotide substitutions, which form about 50 diagnostic positions underlying classification of the family into three subfamilies. Maximum differences between the subfamilies reached 25%. At this level of tandem unit divergence in the subfamilies, no cross-hybridization between them was observed (at 65°C). The individual variability within one subfamily within the species was on average 5% while the variability between species consensuses within a subfamily was 10%. The presence of highly conserved regions in all monomers and some features of their organization show that satellites of all Darevskia species belong to one satDNA family. The organization of unit sequences of satellites CLsat and Agi160 also detected by us in another lizard genus, Lacerta s. str. was compared. Similarity that was found between these satellites suggests their relatedness and common origin. A possible pathway of evolution of these two satDNA families is proposed. The distribution and content of CLsat repeat subfamilies in all species of the genus was examined by Southern hybridization. Seven species had mainly CLsatI (83 to 96%); three species, approximately equal amounts of CLsatI and CLsatIII (the admixture of CLsatII was 2–5%); and five species, a combination of all three subfamilies in highly varying proportions. Based on these results as well as on zoogeographic views on the taxonomy and phylogeny of the Darevskia species, hypotheses on the evolution of molecular-genetic relationships within this genus are advanced. Чобану Д.Г., Гречко В.В., Даревский И.С. (2003) - Молекулярная эволюция сателлитной ДНК CLSAT ящериц рода Darevskia (Sauria: Laeertidae): корреляция с видовым разнообразием. - Генетика, 39 (11): 1527-1541. × Исследовали структуру и эволюцию семейства сателлитной ДНК ящериц рода Darevskia сем. Lac-ertidae. При сравнительном анализе последовательностей мономеров тандемных повторов ДНК (сатДНК) - CLsat - всех видов ящериц р. Darevskia показано, что вариабельность повторов обусловлена главным образом однонуклеотидными заменами, которые образуют около 50 диагностических позиций, на основании которых выделены три подсемейства повторов. Максимальные значения различий между подсемействами достигают 25%. При такой степени дивергенции мономеров трех подсемейств перекрестной гибридизации (при 65°С) между ними не наблюдается. Индивидуальная вариабельность мономеров одного подсемейства внутри вида в среднем составляет 5%, а вариабельность между видовыми консенсусами внутри подсемейства - 10%. Наличие высококонсервативных областей во всех мономерах и ряд особенностей их организации позволяют рассматривать сателлиты всех видов р. Darevskia как единое семейство сатДНК. Приведено сравнение организации последовательности мономеров сателлита CLsat и обнаруженного нами Agi160 из другого рода ящериц -Lacerta s. str. Выявлено сходство, свидетельствующее о родстве этих сателлитов и об их общем происхождении, предложен вероятный путь эволюции этих двух семейств сатДНК. Методом Саузерн-гибридизации изучено распространение и содержание подсемейств повторов CLsat во всех видах рода. Семь видов содержат в основном CLsatl (от 83 до 96%), три вида - примерно равные количества CLsatl и CLsatIII (примесь CLsatII составляет 2-5%), а пять видов - сумму всех трех подсемейств в сильно отличающихся соотношениях. На основе этих данных, в совокупности с зоогеографически-ми представлениями о родстве видов р. Darevskia, предложены гипотезы эволюции молекулярно-генетического родства видов этого рода. Arribas, O. & Candan, K. & Kornilios, P. & Ayaz, D. & Kumlutas, Y. & Gül, S. & Yilmaz, C. & Yildirim Caynak, E. & Ilgaz, C. (2022) - Revising the taxonomy of Darevskia valentini (Boettger, 1892) and Darevskia rudis (Bedriaga, 1886) (Squamata, Lacertidae): a Morpho-Phylogenetic integrated study in a complex Anatolian scenario. - Zootaxa, 5224 (1): 1-68. × Revealing biodiversity allows the accurate determination of the underlying causes of many biological processes such as speciation and hybridization. These processes contain many complex patterns, especially in areas with high species diversity. As two of the prominent zoogeographic areas, Anatolia and Caucasus are also home to the genus Darevskia, which has a complex morphological structure and parthenogenetic speciation. Darevskia valentini and D. rudis are two largely distributed taxa of this genus, both of which have a controversial taxonomic delimitation. Here we performed both a highly detailed morphological comparison and a molecular evaluation for the populations in both species groups. The most comprehensive taxonomic revision of this complex was carried out to determine the cases where the data obtained were compatible or not with each approach. As a result of the obtained outputs, it seems that D. spitzenbergerae stat. nov., D. mirabilis stat. nov. and D. obscura stat. nov. should be accepted as the species level, this later with subspecies D. o. bischoffi comb. nov. and D. o. macromaculata comb. nov.. Also, we propose two new taxa: D. josefschmidtleri sp. nov. and D. spitzenbergerae wernermayeri ssp. nov.. It has also been shown that “lantzicyreni” subspecies belong to D. rudis instead of D. valentini. The extensive revision has contributed to subsequent studies to more accurately understand the past histories of species in the genus Darevskia.
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