|
KEYWORDS' INDEX, 2005
| 12S rDNA | 1(39), S(90) |
| 16S rDNA | S(90) |
| A |
| Acidification | S(134) |
| Acropodium | S(286) |
| Advertisement calls | S(20, 35) |
| Agama agama (subspecies) complex | 2(143) |
| Agama agama species group | 2(143) |
| Agama finchi sp.nov. | 2(143) |
| Agamidae | 1(69) |
| Agamidae | 2(143) |
| Agamidae | 3(167) |
| Age of maturity | S(176) |
| Age structure | S(176) |
| Age | 2(107), S(187) |
| Agile frog | S(205) |
| Agriculture | S(140) |
| Ailao Shan, China | 1(17) |
| Allozymes | S(57) |
| Alytes obstetricans | S(126) |
| Amphibia | 2(135), 3(195), S(143, 167, 286) |
| Amphibian cryocollection | S(233) |
| Amphibian decline | S(134) |
| Amphibian ecology | S(140) |
| Amphibian | S(193) |
| Amphibians | 1(7), S(126, 130, 146, 150, 153, 164, 219, 238, 301) |
| Anoles | 2(94) |
| Anolis carolinensis | 2(94) |
| Anura | 2(135), 3(195) |
| Anura | S(16, 53, 143, 198, 219) |
| Anuran | 3(161) |
| Artificial crossing | S(193) |
| Astrakhan’ Oblast’, Russia | S(123) |
| Aturia ornata | 2(99) |
| Augrabies National Park | 3(237) |
| Australia | 2(99) |
| Axolotl | 2(113) |
| B |
| Basipodium | S(286) |
| Batrachology | S(13) |
| Behavior | S(143) |
| Bioacoustics | 3(195) |
| Biogeography | 1(17), 3(167), S(47) |
| Bioindication | S(167) |
| Biological diversity | S(126, 164) |
| Biomonitoring | 2(83) |
| Body size differences | S(27) |
| Body size | S(201, 298) |
| Body temperature | S(179) |
| Boidae | 3(223) |
| Boiga barnesi | 3(213) |
| Boiga beddomei | 3(213) |
| Boiga ceylonensis | 3(213) |
| Boiga ocellata | 2(102) |
| Boiga siamensis | 2(102) |
| Boiga sp.nov. | 3(213) |
| Bombina | S(16) |
| Breeding | S(158) |
| Bronchocela vietnamensis, new species | 3(167) |
| Buffer zone | S(209) |
| Bufo | S(16) |
| Bufo bufo | S(130, 134, 150) |
| Bufo viridis | S(183) |
| Bulgaria | S(74, 241) |
| Bungarus | S(307) |
| C |
| Calabria, Italy | S(216) |
| Calliophis | S(307) |
| Captive breeding | S(138, 213) |
| Capture history | S(146) |
| Cardiac electrical activity | S(179) |
| Caucasian species | S(213) |
| Ceylanpinar, Turkey | 3(230) |
| Chamaeleo | 2(151) |
| Chameleons | 2(151) |
| Character | S(29) |
| Chemical elements | S(167) |
| Chemical learning | S(198) |
| China | S(191) |
| China, Ailao Shan | 1(17) |
| China, Yunnan province | 1(17) |
| Chitulia inornata | 2(99) |
| Chromosomal rearrangments | S(47) |
| Chromosome evolutionary rate | S(80) |
| Chromosome structure | S(80) |
| Chromosomes | S(61) |
| Clutch size | S(238) |
| Coelognathus | 1(39) |
| COI | 1(39) |
| Color pattern | S(32) |
| Color polymorphism | S(74) |
| Coloration | S(53) |
| Colubrid snakes | 3(213) |
| Colubridae | 2(102), 2(156), S(29, 74, 93, 252) |
| Colubrinae | 2(156) |
| Colubrini | 1(39) |
| Common adder | S(64) |
| Common lizard | 2(83) |
| Comparative analysis | S(213) |
| Conservation | S(123, 126, 205, 219) |
| Consumers | S(252) |
| Coronellini | 1(39) |
| Cryopreservation of amphibian germinal cells | S(233) |
| Cryopreservation of amphibian spermatozoa | S(233) |
| Cryptic speciation | S(53) |
| Cryptobranchus | S(279) |
| Cycles | 2(94) |
| Cyprus | S(32) |
| Cytogenetics | S(80) |
| D |
| Dendrobates auratus | 3(161) |
| Dendrobates | 1(13) |
| Dentition | S(312) |
| Dermophis mexicanus | S(40) |
| Description | 2(99) |
| Development | S(254, 270) |
| Diagnostic characters | S(77) |
| Discriminant analysis | S(102) |
| Dispersal | S(143, 193) |
| Distribution | 2(111), 3(183, 230), S(64, 117, 241) |
| DNA | S(40) |
| DNA extraction | S(230) |
| DNA flow cytometry | S(16) |
| DNA, microsatellite | S(205) |
| Dnepr River, Ukraine | 1(61) |
| E |
| Early Triassic | S(301) |
| East Africa | 2(143) |
| Eastern Europe | S(57, 64) |
| East-European plain | 1(7) |
| Ecological niche | S(171) |
| Ecology | 3(195), S(143 205, 216) |
| Egg and tadpole translocation | S(183) |
| Egg density | S(130) |
| Egg size | S(238) |
| Eirenis | S(29) |
| Elachistodon westermanni | 2(156) |
| Elapidae | S(307) |
| Embryogenesis | S(130) |
| Embryonic development | S(120) |
| Emys orbicularis | S(40, 245) |
| Eunectes beniensis | 3(223) |
| Europe | S(219) |
| Europe, Eastern | S(57, 64) |
| Evolution | S(47, 304) |
| ex-USSR | S(310) |
| F |
| Far East, Russia | S(117, 191) |
| Faunal evolution | S(301) |
| Fecundity | S(201, 238) |
| Femur bone thickness | S(298) |
| First record | 2(111) |
| Fish introduction | S(140) |
| Form-formation | S(47) |
| Frog | S(176) |
| Frogs | 1(13), S(153) |
| Functional morphology | S(307) |
| G |
| Gekkonidae | 2(155), S(291) |
| Gekkota | S(291) |
| Genetic cryobank | S(233) |
| Genetic differentiation | S(40) |
| Genome size | S(16, 57) |
| Geochemical monitoring | S(167) |
| Geographic variation | 2(127), S(40, 113, 298) |
| Geographical and local variation | S(187) |
| Germany | S(146, 238) |
| Glutamate receptors | S(267) |
| Gonads | S(270) |
| Gonyosoma | 1(39) |
| Green frog | S(20) |
| Growth | S(153) |
| Growth marks | 2(107) |
| Growth rate | S(187) |
| Gymnophiona | S(254, 270) |
| H |
| Habitat assessment | S(219) |
| Habitat differentiation | S(161) |
| Helminths | S(252) |
| Hematological indexes | S(296) |
| Hemidactylus brooki | 2(107) |
| Hemilaelaps | S(310) |
| Hemipenes structure | S(64) |
| Herpetology | S(13) |
| Hierophis viridiflavus | S(113) |
| Home area recognition | 3(161) |
| Home range | S(171) |
| Hormones, thyroid | S(304, 312) |
| Hybrids | S(93) |
| Hydrophiidae | 2(99) |
| Hyla | S(15, 16) |
| Hyla arborea | S(138) |
| Hyla savignyi | S(32) |
| Hylidae | 3(195), S(32) |
| Hynobius | S(279) |
| I |
| Identification key | 3(223) |
| Iguania | S(291) |
| Illegal export | S(191) |
| India, Maharashtra | 2(156) |
| Indonesia | 3(195) |
| Integument | S(291) |
| Interdigital membrane | S(279) |
| Internal transcribed spacers | S(105) |
| Interspecific breeding | S(93) |
| Iran, East | 2(155) |
| Iran, Zagros mountains | 2(127) |
| Irian Jaya (Papua) | 3(195) |
| Italy | S(113) |
| Italy, Calabria | S(216) |
| J |
| Jaw apparatus | S(307) |
| Jersey, UK | S(205) |
| Juveniles | S(193) |
| K |
| Karyotype variations | S(47) |
| Karyotype | S(61) |
| Kenya | 2(143) |
| Kherson Province, Ukraine | 1(61) |
| Kon Tum province, Vietnam | 1(17) |
| L |
| Lacerta agilis | S(100, 109, 241) |
| Lacerta agilis boemica | S(298) |
| Lacerta strigata | S(298) |
| Lacerta vivipara | 2(83) |
| Laelapidae | S(310) |
| Lao Cai province, Vietnam | 1(17) |
| Larval limb development | S(274) |
| Laudakia caucasia | 3(183) |
| Leptobrachium | 1(17) |
| Leptodactylus fuscus | S(90) |
| Leptodactylus pentadactylus species cluster | S(35) |
| Leptoseps | 1(65) |
| Life history | S(143) |
| Life-history characteristics | S(183) |
| Likhvinian age | 1(7) |
| Limb development | S(279) |
| Liming | S(134) |
| Litoria | 3(195) |
| Lizard | S(249) |
| Lizard defenses | 1(69) |
| Lizards | S(105, 171, 298) |
| Local adaptation | S(193) |
| Longevity | S(176) |
| Long-legged forms | S(161) |
| Long-term study | S(146, 150) |
| Lophopus Tschudi, 1838 | S(15) |
| Lygosominae | 1(65) |
| M |
| Macedonia | S(16) |
| Macronyssidae | S(310) |
| Maharashtra, India | 2(156) |
| Mapping | S(219) |
| Maticora | S(307) |
| Mediodactylus spinicauda | 2(155) |
| Mediterranean, Western | S(27) |
| Megophryidae | 1(17) |
| Meiosis | S(61) |
| Mertensiella | S(263) |
| Mesalina brevirostris | 3(230) |
| Mesostigmata | S(310) |
| Metamorphosis | 1(13), S(304, 312) |
| Microsatellite DNA | S(205) |
| Microstructure | S(291) |
| Middle Neopleistocene | 1(7) |
| Migration | S(143) |
| Minimum age | S(146) |
| Minimum survival rates | S(146) |
| Mitosis | S(61) |
| Molecular analyses | S(90) |
| Molecular methods | S(230) |
| Molecular phylogeography | S(40) |
| Monitoring | S(150) |
| Moor frog | S(235) |
| Morphogenesis | S(235) |
| Morphological analysis | S(64) |
| Morphological characters | S(96) |
| Morphological deviations | S(235) |
| Morphological variation | S(77) |
| Morphology | 1(39), 3(183, 195), S(57, 100, 102) |
| Morphometrics | S(53) |
| Mortality | S(130) |
| mtDNA | 1(39) |
| Multivariate analysis | 2(127) |
| N |
| Native pond | S(198) |
| Native pond odor | S(209) |
| Natrix megalocephala | 2(111) |
| ND1 | S(90) |
| Neotype | 2(102) |
| Neurergus | 2(127) |
| Neurergus microspilotus | 1(1) |
| New Guinea | 3(195) |
| New locality | 3(230) |
| New record | 2(156) |
| New species | 1(65), 2(135), 3(195) |
| New species Bronchocela vietnamensis | 3(167) |
| Newt | S(120) |
| Newts | S(140) |
| Ngoc Linh mountain, Vietnam | 1(17) |
| Nikolsky’s viper | S(64) |
| Nomenclature | S(13) |
| North of area | S(87) |
| Norway | S(134) |
| O |
| Olfaction | 3(161) |
| Ontogeny | 2(113) |
| Onychodactylus | S(279) |
| Onychodactylus fisheri | S(274) |
| Ophionyssus | S(310) |
| Oreocryptophis (nomen novum) | 1(39) |
| Oriental racers | 1(39) |
| Orientation | S(193, 209) |
| Osteology | 3(195) |
| P |
| Pachydactylus haackei | 3(237) |
| Palpation | S(245) |
| Papua (Irian Jaya) | 3(195) |
| Parasitic gamasid mites | S(310) |
| Pattern | S(29) |
| Pelobates | S(16) |
| Pelobates fuscus | S(53) |
| Pelodiscus sinensis | S(117, 191) |
| Periods of learning | S(209) |
| Pesticides | S(296) |
| Philautus | 2(135) |
| Philippines | 3(167) |
| Pholidosis | S(29, 100) |
| Phylogenetic analyses | S(90) |
| Phylogeny | 1(39), S(29) |
| Polyploidization | S(61) |
| Pond-type | S(279) |
| Population dynamics | S(150, 205) |
| Population recovery | S(183) |
| Prey selection | 2(151) |
| Q |
| Quinzhyla | S(15) |
| R |
| Radiography | S(245) |
| Radionuclide accumulation | 2(83) |
| Rana | S(16, 258) |
| Rana arvalis | S(161) |
| Rana dalmatina | S(146, 150, 205, 238) |
| Rana dybowskii | S(191) |
| Rana esculenta complex | S(77) |
| Rana kurtmuelleri | S(241) |
| Rana ridibunda | 2(87), S(296) |
| Rana temporaria | S(134, 146, 230, 238) |
| RAPD | S(93) |
| RAPD-PCR | S(40, 230) |
| Rat snake | S(93) |
| Red Data Book | S(164) |
| Refuge use | 1(69) |
| Reintroduction | S(138) |
| Release calls | S(20) |
| Replacement name | S(15) |
| Reproduction | 2(94), S(238, 245) |
| Reproductive biology | S(213) |
| Reproductive characteristics | S(187) |
| Reproductive cycle | 1(1) |
| Reproductive isolation | S(35) |
| Reproductive structures | S(263) |
| Reptiles | 1(7), S(164, 219, 301, 310) |
| Reptilia | 2(102, 107, 143), 3(167, 187, 223), S(286, 307, 310) |
| Reptilian resources | S(123) |
| Republic of South Africa | 3(237) |
| Return rates | S(146) |
| Rhacophoridae | 2(135) |
| Ribosomal DNA | S(105) |
| Russia, Astrakhan’ Oblast’ | S(123) |
| Russia, Far East | S(117, 191) |
| Russia, Volga – Kama Region | S(87, 252) |
| S |
| Salamander larva | S(279) |
| Salamandrella keyserlingii | S(274) |
| Salamandridae | 2(127) |
| Sauria | S(291) |
| Scalation | S(74) |
| Scincidae | 1(65) |
| Seasonal variations | S(249) |
| Sensitive period | S(198) |
| Sequence data | S(90) |
| Serbia and Montenegro | S(16) |
| Serpentes | 2(99, 156), 3(223), S(74, 96, 158, 307) |
| Sex chromosomes | S(47, 80) |
| Sex ratio | S(74) |
| Sexual segment of the kidney | S(249) |
| Sexual size differences | S(298) |
| Short-legged forms | S(161) |
| Sibling species | S(90) |
| Size, genome | S(16) |
| Skeletochronological method | S(230) |
| Skeletochronology | 2(107), S(153, 298) |
| Skin organs | S(291) |
| Skull | 2(113) |
| Speciation | S(35, 47, 80) |
| Sperm storage | 1(1), S(158) |
| Spermatogenesis | 2(94) |
| Spermatozoa | 1(1) |
| Spiny-tailed thin-toed gecko | 2(155) |
| Squamata | 1(69), 2(143), 3(167, 223) |
| Sri Lanka | 3(213) |
| Status | S(219) |
| Stream-type | S(279) |
| Subspecies | S(87, 109) |
| Survival | 1(13) |
| Survivorship | S(187) |
| Sympatry | S(171) |
| Synonymy | 2(102) |
| Systematics | S(57, 64) |
| T |
| Tadpole | S(130) |
| Tadpoles | 1(13) |
| Tanzania | 2(143) |
| Taxonomic key to species | 3(167) |
| Taxonomical position | S(241) |
| Taxonomy | 1(65), 2(143), 3(167, 223), S(13, 96) |
| Temperature influence | S(120) |
| Temperature | 1(13) |
| Teratoscincus | S(291) |
| Testudines | 3(187) |
| Testudinidae | 3(187) |
| Testudo | S(40) |
| Testudo graeca | 3(187) |
| Testudo hermanni | 3(187), S(27) |
| Thailand | 2(102) |
| Thermal habitats | 2(87) |
| Thermopreferenda | S(179) |
| Thiuorea | 2(113) |
| Thrace | 3(187) |
| Threat displays | 1(69) |
| Thumb pad glands | S(258) |
| Thyroid hormone | 2(113) |
| Thyroid hormones | S(304, 312) |
| Toad | S(130) |
| Toadlets | S(209) |
| Trade-off | S(238) |
| Triassic, Early | S(301) |
| Trimeresurus albolabris | S(158) |
| Trimeresurus erythrurus | S(158) |
| Triturus alpestris | S(150, 241) |
| Triturus alpestris inexpectatus | S(120) |
| Triturus cristatus | 1(61), S(146) |
| Triturus dobrogicus | 1(61) |
| Triturus italicus | S(216) |
| Triturus vittatus | S(274) |
| Triturus vulgaris | S(134, 274) |
| Triturus | S(57) |
| Trophic spectrum | 2(87) |
| Truong Son mountains, Vietnam | 1(17), 2(135) |
| Turkey | 3(187) |
| Turkey, Ceylanpýnar | 3(230) |
| Turkey, Çamlýhemþin | 2(111) |
| Typhlonectes compressicauda | S(254, 270) |
| U |
| Uganda | 2(143) |
| Ukraine | S(40, 100, 109) |
| Ukraine, Dnepr River | 1(61) |
| Ukraine, Kherson Province | 1(61) |
| Ultrasonography | S(245) |
| Urban ecology | S(126, 235) |
| Urban growth | S(126) |
| Urodela | S(312) |
| Urodele | 2(113) |
| Urodeles | S(304) |
| Uromasticinae | 1(69) |
| Uromastyx aegyptius | 1(69) |
| USSR, ex- | S(310) |
| V |
| Variability | S(201, 286) |
| Variation | S(32) |
| Variety | S(100) |
| Vibrissaphora | 1(17) |
| Vietnam | 1(65) |
| Vietnam, Hoang Lien mountains | 1(17) |
| Vietnam, Kon Tum province | 1(17) |
| Vietnam, Lao Cai province | 1(17) |
| Vietnam, Ngoc Linh mountain | 1(17) |
| Vietnam, Truong Son mountains | 1(17), 2(135) |
| Vipera berus | S(64, 96, 102, 241) |
| Vipera nikolskii | S(64) |
| Vipera renardi bashkirovi | S(87) |
| Vipera | S(213) |
| Viperidae | S(64, 96, 158) |
| Visual cues | 2(151) |
| Volga – Kama Region, Russia | S(87, 252) |
| W |
| Western Mediterranean | S(27) |
| Wetland features | S(140) |
| Winter | 2(87) |
| X |
| Xenopus laevis tadpoles | S(267) |
| Y |
| Yunnan province, China | 1(17) |
| Z |
| Zagros mountains, Iran | 2(127) |
| Zamenis situla | S(74) |
| Zone of intergradation | S(109) |
| Zootoca vivipara | S(47, 201) |
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