Труды сотрудников ИЛ им. В.Н. Сукачева СО РАН

[Text] / Y. N. Krasnoshchekov, I. N. Bezkorovainaya, V. V. Kuz'michenko // Eurasian Soil Sci. - 2007. - Vol. 40, Is. 2. - P149-157, DOI 10.1134/S1064229307020044. - Cited References: 21 . - 9. - ISSN 1064-2293РУБ Soil Science

Аннотация: The results of studying the dynamics of forest litter properties in the loci of a Siberian moth (Dendrolimus sibiricus) mass outbreak are considered. As a fir forest defoliated by this pest burns, the reserves and fractional composition of the forest litter, its actual acidity, and its chemical composition drastically change. Upon the burning out of such forests, the litter complex of invertebrates is fully destroyed and begins restoring only two years after the fire.

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Держатели документа:
Russian Acad Sci, Sukachev Inst Forestry, Siberian Div, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Krasnoshchekov, Y.N.; Bezkorovainaya, I.N.; Kuz'michenko, V.V.

[Text] / W. E. WALLNER [et al.] // J. Econ. Entomol. - 1995. - Vol. 88, Is. 2. - P337-342. - Cited References: 31 . - 6. - ISSN 0022-0493РУБ Entomology

Аннотация: In field studies in the Russian Far East, five types of illuminating devices were evaluated for attracting adult gypsy moth, Lymantria dispar (L.), pink gypsy moth, L. mathura Moore, and nun moth, L. monacha (L.). Our objective was to determine if light from commercial lamps suited to out-of-doors floodlighting could be modified to reduce their attractiveness to moths without a reduction of illumination. During 17 nights of tests, fluorescent blacklight lamps captured significantly more adults than either phosphor mercury or high-pressure sodium lamps, Captures were slightly higher for phosphor mercury than high-pressure sodium lamps but both were unattractive to all three lymantriids after the addition of filters that blocked spectral emissions <480 nm. Daily temporal periodicity, based on adult captures at lights, resulted in distinct activity patterns for the three lymantriids. Peak activity for L. dispar was between 2300 and 0100 hours; for L. mathura, 0100-0300 hours; and 0300-0500 hours for L. monacha. Temporal activity patterns suggest that L. dispar and L. monacha possess nonoverlapping diel rhythms, whereas L. mathura overlaps broadly with both L. dispar and L. monacha.

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Держатели документа:
FORESTRY CANADA,PACIFIC FORESTRY CTR,VICTORIA,BC V8Z 1M5,CANADA
OSRAM SYLVANIA,SALEM,MA 01970
VN SUKACHEV INST FOREST,KRASNOYARSK 660036,RUSSIA
UNIV MASSACHUSETTS,DEPT ENTOMOL,AMHERST,MA 01003

Доп.точки доступа:
WALLNER, W.E.; HUMBLE, L.M.; LEVIN, R.E.; BARANCHIKOV, Y.N.; CARDE, R.T.

[Text] / R. T. Carde [et al.] // Ann. Entomol. Soc. Am. - 1996. - Vol. 89, Is. 5. - P745-753. - Cited References: 53 . - 9. - ISSN 0013-8746РУБ Entomology

Аннотация: Male Asian gypsy moths, Lymantria dispar (L.), were attracted to synthetic pheromone (cis-7R,8S-epoxy-2-methyloctadecane) in the Russian Far East, Central Siberia, and Germany, where this strain has recently been detected. A bimodal pattern of attraction was evident at all 3 sites. One peak of attraction was in early to midafternoon, with a 2nd, usually smaller peak, following sunset. Temperature modulated attraction: warm daytime temperatures increased catch, whereas low nighttime temperatures generally suppressed or eliminated attraction. However, the surge of male attraction to pheromone in the hour after sunset seemed unaffected by falling temperatures. As average temperatures at the 3 sites decreased, the daytime peak of male activity progressively shifted to later in the afternoon. Female eclosion in Germany also followed a bimodal pattern, with a major midmorning to midday peak of emergence and a 2nd, smaller peak, in the afternoon. The timing of male attraction allowed coordination of the ranging flight of the male with the availability of emerging and pheromone-emitting females. The congruence in daily activity patterns suggest that the timing of mating would not be a barrier to the hybridization of the Asian, European, and North American strains of this lymantriid in new areas of sympatry.

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Держатели документа:
UNIV MASSACHUSETTS,DEPT ENTOMOL,AMHERST,MA 01002
KANSAS STATE UNIV,DEPT ENTOMOL,MANHATTAN,KS 66506
US FOREST SERV,NORTHEASTERN CTR FOREST HLTH RES,NORTHEASTERN FOREST EXPT STN,HAMDEN,CT 06514
VN SUKACHEV INST FOREST,KRASNOYARSK 660006,RUSSIA

Доп.точки доступа:
Carde, R.T.; Charlton, R.E.; Wallner, W.E.; Baranchikov, Y.N.

[Text] / A. V. Bogorodskaya, Y. N. Baranchikov, G. A. Ivanova // Eurasian Soil Sci. - 2009. - Vol. 42, Is. 3. - P310-317, DOI 10.1134/S1064229309030089. - Cited References: 37. - This work was supported by the Russian Foundation for Basic Research (project no. 07-04-00562). . - 8. - ISSN 1064-2293РУБ Soil Science

Аннотация: The state of microbial cenoses in the soils of forest ecosystems damaged by fires of different strengths and gypsy moth outbreaks (Central Siberia) was assessed by the intensity of the basal respiration, the content of carbon of the microbial biomass, and the microbial metabolic quotient. The degree of the disturbance of the microbial cenoses in the soils under pine forests after fires was higher than that in the soils under the forests defoliated by gypsy moths. The greatest changes of the microbial complexes were recorded after the fires of high and medium intensity. In the litters, the content of the microbial biomass, the intensity of basal respiration, and the microbial metabolic quotient value were restored on the fifth year after the fires, whereas in the upper (0-10 cm) soil layer, these parameters still differed from those in the control variant, especially after the highly intense fires. After the weak fires, the ecophysiological state of the microbial complexes was restored within two-three years.

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Держатели документа:
[Bogorodskaya, A. V.
Baranchikov, Yu. N.
Ivanova, G. A.] Russian Acad Sci, Siberian Branch, Sukachev Inst Forestry, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Bogorodskaya, A.V.; Baranchikov, Y.N.; Ivanova, G.A.; Russian Foundation for Basic Research [07-04-00562]

/ N. Kirichenko [et al.] // European Journal of Forest Research. - 2011. - Vol. 130, Is. 6. - P1067-1074, DOI 10.1007/s10342-011-0495-3 . - ISSN 1612-4669
Аннотация: The Siberian moth, Dendrolimus sibiricus, Tschtv. is the most harmful defoliator of coniferous forests in North Asia. The pest has already spread over the Urals and continues moving westwards. Recently, it has been recommended for quarantine in member countries by European and Mediterranean Plant Protection Organization (EPPO). The performances of the pest on coniferous species planted in Europe were assessed on a range of potted trees corresponding to the spectrum of economically important conifers in the EU: European larch Larix decidua, Norway spruce Picea abies, Scots pine Pinus sylvestris, European black pine Pinus nigra, and the North American species: Douglas fir Pseudotsuga menziesii and grand fir Abies grandis. Larvae showed a potential to survive and complete the development on all these host tree species. Favorable hosts were grand fir, European larch, and Douglas fir that allowed higher survival, better larval development, and as a result, yielded heavier pupae and adult moths with higher longevity. Black pine was a poor host but, however, could still support larval and pupal development. Norway spruce and Scots pine had an intermediate behavior. If accidentally introduced to Europe, the Siberian moth may become especially damaging in forest stands predominated by European larch and by the North American firs. Norway spruce and especially the two-needle pines will be less prone to intensive defoliation by this species. The fact that the pest may damage the range of economically important coniferous species should be taken into account in the pest risk assessment for Europe and also for North America where the Siberian moth occurrence is considered likely. В© 2011 Springer-Verlag.

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Держатели документа:
Department of Forest Zoology, V. N. Sukachev Institute of Forest SB RAS, Akademgorodok, Krasnoyarsk 660036, Russian Federation
Lutte biologique et Ecologie spatiale (LUBIES), Universite Libre de Bruxelles, CP 160/12, av. F. D. Roosevelt 50, 1050 Bruxelles, Belgium

Доп.точки доступа:
Kirichenko, N.; Flament, J.; Baranchikov, Y.; Gregoire, J.-C.

/ V. G. Sukhovol'skii, T. M. Ovchinnikova, T. A. Vshivkova // Doklady Biological Sciences. - 2000. - Vol. 373, Is. 1-6. - P409-411 . - ISSN 0012-4966

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Держатели документа:
Sukachev Institute of Forestry, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, Russia.

Доп.точки доступа:
Sukhovol'skii, V.G.; Ovchinnikova, T.M.; Vshivkova, T.A.

/ D. L. Grodnitsky, M. V. Kozlov // Biologisches Zentralblatt. - 1991. - Vol. 110, Is. 3. - P199-206 . - ISSN 0006-3304
Аннотация: Examined wing morphology and flight kinematics in 53 species of moths and butterflies. The main pathways of evolution of flapping plane are described. The structure of wing scale covering was studies in 151 species. The most widely spread modifications of the covering are defined, and relationship of wing evolution to that of scale covering is discussed. The main function of scales is supposed to be thermoinsulatory. -from Authors

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Держатели документа:
V.N. Sukachev Inst. of Forest & Wood, Siberian Branch of the USSR, Academy of Sciences, Krasnoyarsk, 66003, Russia

Доп.точки доступа:
Grodnitsky, D.L.; Kozlov, M.V.

[Текст] / D. L. GRODNITSKY // Zhurnal Obshchei Biol. - 1995. - Vol. 56, Is. 4. - С. 438-449. - Cited References: 64 . - 12. - ISSN 0044-4596РУБ Biology

Аннотация: Analogous structures can be considered as a result of the convergence of unrelated organisms formed by selection under the similar living conditions. The data on the analogous morphologlcal structures (distal fusion of anal veins, secondary vein-like sclerotization, some signes of wing planform, wrinkled veins, cover scales and wing eyes) on insect wings in different orders are provided. It is shown that the origin of these structures cannot be completely explained by the similarity of their functions. It seems also impossible to understand morphology only on the basis of a structure's function in art organism's life. The general approach to an organism's structure must include two independent (additive-according to Bohr) factors: selectional (the subject of the functional and ecological morphology) and morphogenetic (the subject of structuralism and constructional morphology).


Доп.точки доступа:
GRODNITSKY, D.L.

[Текст] / D. L. GRODNITSKY // Zool. Zhurnal. - 1991. - Vol. 70, Is. 6. - С. 77-87. - Cited References: 41 . - 11. - ISSN 0044-5134РУБ Zoology

Аннотация: A comparative study of the wings internal and external morphology has been conducted in 39 species of Phryganeida and 57 species of Papilionida. A pronounced reduction of veins begins when the wing length decreases below 3 to 4 mm. The increase in the body size is associated with the development of jugal sclerotization into true veins, which are considered to be a differentiated part of the anal system. In the most primitive moths neither increase nor decrease of the absolute size leads to changes in the wing venation. The vein homology, wing design in the hypothetical ancestor of Amphiesmenoptera, as well as the differentiation of the venation in the wing evolution are discussed.


Доп.точки доступа:
GRODNITSKY, D.L.

[Text] / N. Kirichenko [et al.] // ZooKeys. - 2015. - Is. 473. - P157-176, DOI 10.3897/zookeys.473.8543. - Cited References:44. - We acknowledge the team at the Biodiversity Institute of Ontario,University of Guelph, Ontario, Canada for their assistance in theproduction of DNA barcodes. Funding for DNA barcoding was partlyprovided by the government of Canada through Genome Canada and theOntario Genomics Institute in support of the International Barcode ofLife project, and by NSERC. Sequence analysis was enabled by a grantfrom the government of Canada through Genome Canada and the OntarioGenomics Institute in support of the International Barcode of LifeProject. Our work was also aided by the BOLD informatics platform whosedevelopment is funded by the Ontario Ministry of Economic Developmentand Innovation. Peter Huemer gratefully acknowledges funding frominatura Erlebnis Naturschau (Dornbirn, Austria) and the Promotion ofEducational Policies, University and Research Department of theAutonomous Province of Bolzano - South Tyrol for support of the project"Genetic biodiversity archive - DNA barcoding of Lepidoptera of thecentral Alpine region (South, East and North Tyrol)". Natalia Kirichenkowas supported by a fellowship of LE STUDIUM (R), France. . - ISSN 1313-2989. - ISSN 1313-2970РУБ Zoology

Аннотация: Europe has one of the best-known Lepidopteran faunas in the world, yet many species are still being discovered, especially in groups of small moths. Here we describe a new gracillariid species from the southeastern Alps, Callisto basistrigella Huemer, Deutsch & Triberti, sp. n. It shows differences from its sister species C. coffeella in morphology, the barcode region of the cytochrome c oxidase I gene and the nuclear gene histone H3. Both C. basistrigella and C. coffeella can co-occur in sympatry without evidence of admixture. Two C. basistrigella specimens show evidence of introgression. We highlight the importance of an integrative approach to delimit species, combining morphological and ecological data with mitochondrial and nuclear sequence data. Furthermore, in connection with this study, Ornix blandella Muller - Rutz, 1920, syn. n. is synonymized with C. coffeella (Zetterstedt, 1839).

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Держатели документа:
INRA, Zool Forestiere UR0633, F-45075 Orleans, France.
SB RAS, Sukachev Inst Forest, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Tiroler Landesmuseen Betriebsgesellsch MbH, Nat Wissensch Abt, A-6020 Innsbruck, Austria.
Museo Civ Storia Nat, I-I37129 Verona, Italy.
Museum Natl Hist Nat, ISYEB, UMR7205, F-75005 Paris, France.
ИЛ СО РАН

Доп.точки доступа:
Kirichenko, Natalia; Huemer, Peter; Deutsch, Helmut; Triberti, Paolo; Rougerie, Rodolphe; Lopez-Vaamonde, Carlos; government of Canada through Genome Canada; Ontario Genomics Institutein support of the International Barcode of Life project; NSERC; Ontario Ministry of Economic Development and Innovation; inatura Erlebnis Naturschau (Dornbirn, Austria); Promotion of Educational Policies,University and Research Department of the Autonomous Province of Bolzano- South Tyrolfellowship of LE STUDIUM(R), France

[Text] / N. Kirichenko [et al.] // ZooKeys. - 2016. - Is. 579. - P99-156, DOI 10.3897/zookeys.579.7166. - Cited References:68. - We are grateful to the team at the Biodiversity Institute of Ontario, University of Guelph, Ontario, Canada for their great assistance in the production of DNA barcodes. Funding for DNA barcoding and sequence analysis was partly provided by the Government of Canada through Genome Canada and the Ontario Genomics Institute in support of the International Barcode of Life project, and by NSERC. Genetic analyses were also partly funded by INRA, UR0633 Zoologie Forestiere's core funding. Our work was also aided by the BOLD informatics platform whose development is funded by the Ontario Ministry of Economic Development and Innovation. NK was supported by a fellowship of LE STUDIUM (R), France and the Russian foundation for basic research (grant No 15-29-02645). . - ISSN 1313-2989. - ISSN 1313-2970РУБ Zoology

Аннотация: During a DNA barcoding campaign of leaf-mining insects from Siberia, a genetically divergent lineage of a gracillariid belonging to the genus Micrurapteryx was discovered, whose larvae developed on Caragana Fabr. and Medicago L. (Fabaceae). Specimens from Siberia showed similar external morphology to the Palearctic Micrurapteryx gradatella and the Nearctic Parectopa occulta but differed in male genitalia, DNA barcodes, and nuclear genes histone H3 and 28S. Members of this lineage are re-described here as Micrurapteryx caraganella (Hering, 1957), comb. n., an available name published with only a brief description of its larva and leaf mine. Micrurapteryx caraganella is widely distributed throughout Siberia, from Tyumen oblast in the West to Transbaikalia in the East. Occasionally it may severely affect its main host, Caragana arborescens Lam. This species has been confused in the past with Micrurapreryx gradatella in Siberia, but field observations confirm that M. gradatella exists in Siberia and is sympatric with M. caraganella, at least in the Krasnoyarsk region, where it feeds on different host plants (Vicia amoena Fisch. and Vicia sp.). In addition, based on both morphological and molecular evidence as well as examination of type specimens, the North American Parectopa occulta Braun, 1922 and Parectopa albicostella Braun, 1925 are transferred to Micrurapteryx as M. occulta (Braun, 1922), comb. n. with albicostella as its junior synonym (syn. n.). Characters used to distinguish Micrurapteryx from Parectopa are presented and illustrated. These findings provide another example of the potential of DNA barcoding to reveal overlooked species and illuminate nomenclatural problems.

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Держатели документа:
Sukachev Inst Forest SB RAS, Akademgorodok 50-28, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, 79 Svobodny Pr, Krasnoyarsk 660041, Russia.
INRA, Zool Forestiere UR0633, F-45075 Orleans, France.
Museo Civ Storia Nat, Lungadige Porta Vittoria 9, I-37129 Verona, Italy.
Univ Oulu, Dept Genet & Physiol, POB 3000, FI-90014 Oulu, Finland.
Agr & Agri Food Canada, Ottawa Res & Dev Ctr, Cent Expt Farm, Ottawa, ON K1A 0C6, Canada.
Univ Tours, Inst Rech Biol Insecte, CNRS UMR 7261, UFR Sci & Tech, F-37200 Tours, France.

Доп.точки доступа:
Kirichenko, Natalia; Triberti, Paolo; Mutanen, Marko; Magnoux, Emmanuelle; Landry, Jean-Francois; Lopez-Vaamonde, Carlos; Government of Canada through Genome Canada; Ontario Genomics Institute; NSERC; INRA [UR0633]; Ontario Ministry of Economic Development and Innovation; LE STUDIUM(R), France; Russian foundation for basic research [15-29-02645]

/ A. Kononov [et al.] // BMC Genet. - 2016. - Vol. 17, DOI 10.1186/s12863-016-0463-5 . - ISSN 1471-2156
Аннотация: Background: Moths of genus Dendrolimus (Lepidoptera: Lasiocampidae) are among the major pests of coniferous forests worldwide. Taxonomy and nomenclature of this genus are not entirely established, and there are many species with a controversial taxonomic position. We present a comparative evolutionary analysis of the most economically important Dendrolimus species in Eurasia. Results: Our analysis was based on the nucleotide sequences of COI and COII mitochondrial genes and ITS2 spacer of nuclear ribosomal genes. All known sequences were extracted from GenBank. Additional 112 new sequences were identified for 28 specimens of D. sibiricus, D. pini, and D. superans from five regions of Siberia and the Russian Far East to be able to compare the disparate data from all previous studies. In total, 528 sequences were used in phylogenetic analysis. Two clusters of closely related species in Dendrolimus were found. The first cluster includes D. pini, D. sibiricus, and D. superans; and the second, D. spectabilis, D. punctatus, and D. tabulaeformis. Species D. houi and D. kikuchii appear to be the most basal in the genus. Conclusion: Genetic difference among the second cluster species is very low in contrast to the first cluster species. Phylogenetic position D. tabulaeformis as a subspecies was supported. It was found that D. sibiricus recently separated from D. superans. Integration of D. sibiricus mitochondrial DNA sequences and the spread of this species to the west of Eurasia have been established as the cause of the unjustified allocation of a new species: D. kilmez. Our study further clarifies taxonomic problems in the genus and gives more complete information on the genetic structure of D. pini, D. sibiricus, and D. superans. © 2016 The Author(s).

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Institute of Cytology and Genetics, the Siberian Branch of the Russian Academy of Science, 10 Prospekt Lavrentyeva, Novosibirsk, Russian Federation
USDA-APHIS-PPQ CPHST, Otis Laboratory, Building 1398, Otis Air National Guard Base, Buzzards Bay, MA, United States
Marshall University, Department of Biological Sciences, 1601 5th Avenue, Huntington, WV, United States
V.N. Sukachev Institute of Forest, the Siberian Branch of the Russian Academy of Science, 50/28 Akademgorodok, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Kononov, A.; Ustyantsev, K.; Wang, B.; Mastro, V. C.; Fet, V.; Blinov, A.; Baranchikov, Y.

/ N. I. Kirichenko [et al.] // Far East. Entomol. - 2017. - Is. 346. - P1-12, DOI 10.25221/fee.346.1 . - ISSN 1026-051X
Аннотация: New data on distribution of seven species of the family Gracillariidae in Asian part of Russia are provided. Six species, Phyllonorycter comparella, Ph. dubitella, Ph. medicaginella, Ph. pyrifoliella, Ph. ringoniella and Ph. sorbi, were recorded in Siberia (Krasnoyarsk krai, Novosibirsk and Omsk oblasts) for the first time. Micrurapteryx caraganella is new for Tuva Republic and the Russian Far East (Amur oblast). Phyllonorycter sorbi was collected in Novosibirsk on new host plants: Amelanchier sp., Sorbocotoneaster pozdnjakovii and Prunus virginiana (Rosaceae). Male genitalia are illustrated for the majority of the listed species.

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Sukachev Institute of Forest, Sukachev Institute of Forest Sibirian Branch of the Russian Academy of Sciences, Federal Research Center 'Krasnoyarsk Science Center SB RAS', Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
All-Russian Plant Quarantine Center, Krasnoyarsk branch, Russian Federation
Museo Civico di Storia Naturale, Verona, Italy
Federal Scientific Center of the East Asia Terrestrial Biodiversity Far Eastern Branch, The Russian Academy of Sciences, Vladivostok, Russian Federation
Far Eastern Federal University, Russky Island, Vladivostok, Russian Federation

Доп.точки доступа:
Kirichenko, N. I.; Akulov, E. N.; Triberti, P.; Ponomarenko, M. G.

/ N. Kirichenko [et al.] // ZooKeys. - 2018. - Is. 736. - P79-118, DOI 10.3897/zookeys.736.20739. - Cited References:57. - We thank E.J. van Nieukerken (The Netherlands), H. Kuroko, A. Kawakita, N. Hirano, K. Niimi, M. Murase, S. Yagi, C. Tsuji (Japan), G. Deschka (Austria), M. Jones (USA), A. Lastuvka, Z. Lastuvka (Czech Republic), A. Cama, J. Nel (France) and P. van Wielink (The Netherlands) for providing specimens and / or DNA barcodes of Phyllocnistis spp., J.C. Koster (The Netherlands) for preparing the genitalia slide of P. cornella, C. van den Berg (The Netherlands) for helping with collection of P. cornella in Japan, S.V. Baryshnikova and M.G. Ponomarenko (Russia) for checking the collections of their institutes for Cornus-feeding Phyllocnistis and for their useful remarks. Special thanks to R. Brito and G.R.P Moreira (Brazil) for their careful reading of the latest version of our manuscript, to D. Lees (UK) for checking the English, to the reviewers R. Rougerie (France) and D. Wagner (USA) and to the editor E.J. van Nieukerken for their insightful comments and suggestions. N. Kirichenko was supported by a fellowship of LE STUDIUM (R), Institute for advanced studies - Loire Valley, France (grant No. INRA-URZF-007); French Embassy in Russia, Bourse Metchnikov (grant No. 908981L, Campus France) and by the Russian Foundation for Basic Research (grant No. 15-29-02645). T. Hirowatari. and I. Ohshima were supported by JSPS KAKENHI (grant No. JP16H05766). . - ISSN 1313-2989. - ISSN 1313-2970РУБ Zoology

Аннотация: During an ongoing DNA-barcoding campaign of the leaf-mining moths that feed on woody plants in Northeast Asia, four lineages of the genus Phyllocnistis (Gracillariidae, Phyllocnistinae) were discovered on dogwood (Cornus spp): P. cornella Ermolaev, 1987 on C. controversa Hemsl. (Japan: Hokkaido) and three new species - one feeding on C. controversa, C. florida L. and C. macrophylla Wall. in Japan (Honshu, Shikoku, Kyushu), a second species on C. macrophylla in China (Yunnan) and a third on Siberian dogwood Cornus alba L. in Russia (Siberia). All these species showed differences in morphology, in the barcode region of the cytochrome c oxidase I gene and in two nuclear genes (histone H3 and 28S ribosomal RNA). No correlation was found between the deep mitochondrial splits observed and the Wolbachia infection pattern. Based on both morphological and molecular evidence, the three recently discovered lineages are described here as new species: P. indistincta Kobayashi & Triberti, sp. n. (Japan), P. saepta Kirichenko, Ohshima & Huang, sp. n. (China) and P. verae Kirichenko, Triberti & Lopez-Vaamonde, sp. n. (Russia). In addition, the authors re-describe the adult morphology of P. cornella, provide the first record of this species from Japan and highlight the diagnostic characters that allow these Cornus-feeding Phyllocnistis species to be distinguished.

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RAS, Sukachev Inst Forest, SB, Akademgorodok 50-28, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, 79 Svobodny Pr, Krasnoyarsk 660041, Russia.
INRA, UR0633, Zool Forestiere, F-45075 Orleans, France.
Museo Civ Storia Nat, Lungadige Porta Vittoria 9, I-37129 Verona, Italy.
Osaka Prefecture Univ, Grad Sch Life & Environm Sci, Entomol Lab, Sakai, Osaka 5998531, Japan.
Kyushu Univ, Fac Agr, Entomol Lab, 6-10-1 Hakozaki, Fukuoka 8128581, Japan.
Univ Hawaii, Dept Plant & Environm Protect Sci, 3050 Maile Way, Honolulu, HI 96822 USA.
Nat Biodivers Ctr, POB 9557, NL-2300 RA Leiden, Netherlands.
Kyoto Prefectural Univ, Dept Life & Environm Sci, Kyoto 6068522, Japan.
Hunan Agr Univ, Hunan Prov Key Lab Biol & Control Plant Dis & Ins, Changsha 410128, Hunan, Peoples R China.
South China Agr Univ, Dept Entomol, Guangzhou 510642, Guangdong, Peoples R China.
Univ Francois Rabelais Tours, CNRS, Inst Rech Biol Insecte, UMR 7261,UFR Sci & Tech, F-37200 Tours, France.

Доп.точки доступа:
Kirichenko, Natalia; Triberti, Paolo; Kobayashi, Shigeki; Hirowatari, Toshiya; Doorenweerd, Camiel; Ohshima, Issei; Huang, Guo-Hua; Wang, Min; Magnoux, Emmanuelle; Lopez-Vaamonde, Carlos; LE STUDIUM(R), Institute for advanced studies - Loire Valley, France [INRA-URZF-007]; French Embassy in Russia, Bourse Metchnikov (Campus France) [908981L]; Russian Foundation for Basic Research [15-29-02645]; JSPS KAKENHI [JP16H05766]

[Текст] : материалы временных коллективов / Н. И. Кириченко, П. Триберти [и др.] // Энтомологическое обозрение. - 2019. - Т.: 98, № : 3. - С. 600-631, DOI 10.1134/S0367144519030109 . - Библиогр. в конце ст. . - ISSN 0367-1445
Аннотация: Фауна молей-пестрянок (сем. Gracillariidae) Сибири - региона, который занимает почти половину территории России, до сих пор остается изученной фрагментарно. В ходе выполнения комплексных работ по ДНК-баркодингу молей-пестрянок Сибири, собранных на преимагинальных стадиях из мин, преимущественно на древесных растениях, нами был определен 41 вид. Три представителя этого семейства были диагностированы только до рода: Сaloptilia sp. (кормовое растение Prunus padus ), Parornix sp. ( Malus sp.), Phyllonorycter sp. ( Crataegus sp.) и могут оказаться малоизученными или новыми для науки видами. 600 Шесть видов указаны для Сибири впервые: Callisto insperatella (из Новосибирской и Томской областей), Caloptilia alnivorella (из Бурятии) , Phyllonorycter ermani (из Иркутской обл.), Ph. lantanella (из Новосибирской обл.), Ph. pumilae (из Омской и Иркутской областей) и Ph. viciae (из Красноярского края). Parornix pfaffenzelleri впервые приведен для России по находке в Хакасии. Для прочих 15 видов молей-пестрянок установлены новые регионы обитания в Сибири. Инвазийная липовая моль-пестрянка, Phyllonorycter issikii впервые зарегистрирована на территории Томской области и Красноярского края в 2017-2018 гг. Для 7 видов молей-пестрянок приведены новые кормовые растения, подтвержденные питанием гусениц в минах: Parectopa ononidis впервые обнаружен на Lupinaster pentaphyllus , Sauterina hofmanniella - на Lathyrus gmelinii , Caloptilia stigmatella - на Salix kochiana , Callisto insperatel la - на Prunus virginiana , Parornix scoticella - на Amelanchier , Phyllonorycter ermani - на Alnus alnobetula subsp . fruticosa , Ph. viciae - на Vicia unijuga . Состав фауны Gracillariidae Сибири на 51 % общий с фауной европейской части России и лишь на 38 % - с фауной Российского Дальнего Востока

Статья в РИНЦ
: 660036, Красноярск, Академгородок, 50, стр. 28

Доп.точки доступа:
Кириченко, Наталья Ивановна; Триберти, П.; Акулов, Е.Н.; Akulov Ye.N.; Пономаренко, М.Г.; Лопес-Ваамонде, К.; Lopez-Vaamonde, C.; Kirichenko, Natal'ya Ivanovna

/ N. I. Kirichenko, P. Triberti, E. N. Akulov [et al.] // Entomol. Rev. - 2019. - Vol. 99, Is. 6. - P796-819, DOI 10.1134/S0013873819060083 . - ISSN 0013-8738
Аннотация: The Gracillariidae fauna of Siberia, the region that occupies almost half of the territory of the Russian Federation, remains poorly studied. During a DNA barcoding study of Gracillariidae in Siberia, based on analysis of larvae and pupae collected from their leaf mines on woody plants, we identified 41 species. Three gracillariids were identified only to genus: Caloptilia sp. (host plant Prunus padus), Parornix sp. (Malus sp.), and Phyllonorycter sp. (Crataegus sp.), representing poorly studied or undescribed species. Six species are reported here for the first time for Siberia: Callisto insperatella (from Novosibirsk and Tomsk provinces), Caloptilia alnivorella (Buryatia), Phyllonorycter ermani (Irkutsk Province), Ph. lantanella (Novosibirsk Province), Ph. pumilae (Omsk and Irkutsk provinces), and Ph. viciae (Krasnoyarsk Territory). Parornix pfaffenzelleri, found in Khakassia, is reported as a species new to Russia. Other 15 gracillariid species previously known from Siberia were recorded in new administrative regions. The invasive lime leafminer Phyllonorycter issikii was first documented in Tomsk Province and Krasnoyarsk Territory in 2017 and 2018, respectively. Seven new gracillariid-host plant associations were found: Parectopa ononidis on Lupinaster pentaphyllus, Sauterina hofmanniella on Lathyrus gmelinii, Caloptilia stigmatella on Salix kochiana, Callisto insperatella on Prunus virginiana, Parornix scoticella on Amelanchier sp., Phyllonorycter ermani on Alnus alnobetula subsp. fruticosa, and Phyllonorycter viciae on Vicia unijuga. The Gracillariidae fauna of Siberia has 51% similarity with that of European Russia and only 38% similarity with that of the Russian Far East. © 2019, Pleiades Publishing, Inc.

Scopus

Держатели документа:
Sukachev Institute of Forest, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
INRA, UR0633 Zoologie Forestiere, Orleans, F-45075, France
Museo Civico di Storia Naturale, Verona, 37129, Italy
Russian Plant Quarantine Center, Krasnoyarsk Branch, Krasnoyarsk, 660075, Russian Federation
Federal Research Center of East Asian Terrestrial Biodiversity Far Eastern Branch of Russian Academy of Sciences, Vladivostok, 690022, Russian Federation
Far Eastern Federal University, Vladivostok, 690922, Russian Federation
Institut de Recherche sur la Biologie de l’Insecte, CNRS-Universite de Tours, UMR 7261, Tours, 37200, France

Доп.точки доступа:
Kirichenko, N. I.; Triberti, P.; Akulov, E. N.; Ponomarenko, M. G.; Lopez-Vaamonde, C.

/ C. Lopez-Vaamonde, N. Kirichenko, A. Cama [et al.] // Front. ecol. evol. - 2021. - Vol. 9. - Ст. 626752, DOI 10.3389/fevo.2021.626752 . - ISSN 2296-701X
Аннотация: Gracillariidae is the most species-rich leaf-mining moth family with over 2,000 described species worldwide. In Europe, there are 263 valid named species recognized, many of which are difficult to identify using morphology only. Here we explore the use of DNA barcodes as a tool for identification and species discovery in European gracillariids. We present a barcode library including 6,791 COI sequences representing 242 of the 263 (92%) resident species. Our results indicate high congruence between morphology and barcodes with 91.3% (221/242) of European species forming monophyletic clades that can be identified accurately using barcodes alone. The remaining 8.7% represent cases of non-monophyly making their identification uncertain using barcodes. Species discrimination based on the Barcode Index Number system (BIN) was successful for 93% of species with 7% of species sharing BINs. We discovered as many as 21 undescribed candidate species, of which six were confirmed from an integrative approach; the other 15 require additional material and study to confirm preliminary evidence. Most of these new candidate species are found in mountainous regions of Mediterranean countries, the South-Eastern Alps and the Balkans, with nine candidate species found only on islands. In addition, 13 species were classified as deep conspecific lineages, comprising a total of 27 BINs with no intraspecific morphological differences found, and no known ecological differentiation. Double-digest restriction-site associated DNA sequencing (ddRAD) analysis showed strong mitonuclear discrepancy in four out of five species studied. This discordance is not explained by Wolbachia-mediated genetic sweeps. Finally, 26 species were classified as “unassessed species splits” containing 71 BINs and some involving geographical isolation or ecological specialization that will require further study to test whether they represent new cryptic species. © Copyright © 2021 Lopez-Vaamonde, Kirichenko, Cama, Doorenweerd, Godfray, Guiguet, Gomboc, Huemer, Landry, Lastuvka, Lastuvka, Lee, Lees, Mutanen, van Nieukerken, Segerer, Triberti, Wieser and Rougerie.

Scopus

Держатели документа:
INRAE, URZF, Orleans, France
IRBI, UMR 7261, CNRS-Universite de Tours, Tours, France
Sukachev Institute of Forest, Siberian Branch of Russian Academy of Sciences, Federal Research Center “Krasnoyarsk Science Center SB RAS, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
La Chapelle sur Loire, France
Department of Plant and Environmental Protection Sciences, College of Tropical Agriculture and Human Resources, University of Hawaii, Honolulu, HI, United States
Naturalis Biodiversity Center, Leiden, Netherlands
Department of Zoology, University of Oxford, Oxford, United Kingdom
Department of Biology, The Pennsylvania State University, University Park, PA, United States
Gancani, Beltinci, Slovenia
Tiroler Landesmuseen Betriebsges.m.b.H, Sammlungs- und Forschungszentrum, Hall in Tirol, Austria
Agriculture and Agri-Food Canada, Ottawa Research and Development Centre, Ottawa, ON, Canada
Prostejov, Czech Republic
Faculty of Agronomy, Mendel University, Brno, Czech Republic
Ecology and Genetics Research Unit, University of Oulu, Oulu, Finland
Department of Life Sciences, Natural History Museum, London, United Kingdom
Staatliche Naturwissenschaftliche Sammlungen Bayerns, Zoologische Staatssammlung Munchen (SNSB-ZSM), Munich, Germany
Museo Civico di Storia Naturale, Zoologia, Verona, Italy
Landesmuseum fur Karnten, Abteilung Zoologie, Sammlungs- und Wissenschaftszentrum, Klagenfurt, Austria
Institut de Systematique, Museum national d’Histoire naturelle, CNRS, Sorbonne Universite, EPHE, Universite des Antilles, Paris, France

Доп.точки доступа:
Lopez-Vaamonde, C.; Kirichenko, N.; Cama, A.; Doorenweerd, C.; Godfray, H. C.J.; Guiguet, A.; Gomboc, S.; Huemer, P.; Landry, J. -F.; Lastuvka, A.; Lastuvka, Z.; Lee, K. M.; Lees, D. C.; Mutanen, M.; van Nieukerken, E. J.; Segerer, A. H.; Triberti, P.; Wieser, C.; Rougerie, R.

/ C. Lopez-Vaamonde, N. Kirichenko, A. Cama [et al.] // Front. Ecol. Evol. - 2021. - Vol. 9. - Ст. 626752, DOI 10.3389/fevo.2021.626752. - Cited References:88. - This work was funded by the Studium (France) to both NK and DL to work as research fellows at INRAE Orleans; the Russian Foundation for Basic Research (No. 19-04-01029-a) and the basic project of Sukachev Institute of Forest SB RAS (project No. 0287-2021-0011) to NK; the Region Centre (France) project ENDOFEED (201000047141) to CL-V; the Ministry of Agriculture (France) project PASSIFOR to CL-V and RR; the Academy of Finland (grant number: 277984) to MM and the Kvantum Institute to KL; Kone foundation, Finnish Cultural foundation for financing the FinBOL (Finnish Barcode of Life) 2011-2015, and the Academy of Finland for financing FinBOL through the FinBIF national infrastructure project since 2014; Agriculture & Agri-Food Canada, Science and Technology Branch (projects Nos. J-000977 and J-002279) to J-FL; Promotion of Educational Policies, University and Research Department of the Autonomous Province of Bolzano - South Tyrol and Austrian Federal Ministry of Science, Research and Economics in the framework of ABOL (Austrian Barcode of Life) to PH. CD's salary and all DNA sequencing at Naturalis Biodiversity Center was funded through the Dutch Economic Restructuring Fund (FES). AS was supported by the Bavarian Ministry of Science and Art (Germany) project BFB and the Federal Ministry of Education and Research (Germany) project GBOL. Funding for DNA barcoding was also partly provided by the Government of Canada through Genome Canada, the Ontario Genomics Institute in support of the International Barcode of Life project, and by the National Science and Engineering Research Council of Canada. . - ISSN 2296-701XРУБ Ecology

Аннотация: Gracillariidae is the most species-rich leaf-mining moth family with over 2,000 described species worldwide. In Europe, there are 263 valid named species recognized, many of which are difficult to identify using morphology only. Here we explore the use of DNA barcodes as a tool for identification and species discovery in European gracillariids. We present a barcode library including 6,791 COI sequences representing 242 of the 263 (92%) resident species. Our results indicate high congruence between morphology and barcodes with 91.3% (221/242) of European species forming monophyletic clades that can be identified accurately using barcodes alone. The remaining 8.7% represent cases of non-monophyly making their identification uncertain using barcodes. Species discrimination based on the Barcode Index Number system (BIN) was successful for 93% of species with 7% of species sharing BINs. We discovered as many as 21 undescribed candidate species, of which six were confirmed from an integrative approach; the other 15 require additional material and study to confirm preliminary evidence. Most of these new candidate species are found in mountainous regions of Mediterranean countries, the South-Eastern Alps and the Balkans, with nine candidate species found only on islands. In addition, 13 species were classified as deep conspecific lineages, comprising a total of 27 BINs with no intraspecific morphological differences found, and no known ecological differentiation. Double-digest restriction-site associated DNA sequencing (ddRAD) analysis showed strong mitonuclear discrepancy in four out of five species studied. This discordance is not explained by Wolbachia-mediated genetic sweeps. Finally, 26 species were classified as "unassessed species splits" containing 71 BINs and some involving geographical isolation or ecological specialization that will require further study to test whether they represent new cryptic species.

WOS

Держатели документа:
URZF, INRAE, Orleans, France.
Univ Tours, IRBI, UMR 7261, CNRS, Tours, France.
RAS, SB, Sukachev Inst Forest, Fed Res Ctr,Krasnoyarsk Sci Ctr, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.
Univ Hawaii, Coll Trop Agr & Human Resources, Dept Plant & Environm Protect Sci, Honolulu, HI USA.
Nat Biodivers Ctr, Leiden, Netherlands.
Univ Oxford, Dept Zool, Oxford, England.
Penn State Univ, Dept Biol, University Pk, PA 16802 USA.
Gancani, Beltinci, Slovenia.
Tiroler Landesmuseen BetriebsgesmbH Sammlungs & F, Hall In Tirol, Austria.
Agr & Agri Food Canada, Ottawa Res & Dev Ctr, Ottawa, ON, Canada.
Mendel Univ Brno, Fac Agron, Brno, Czech Republic.
Univ Oulu, Ecol & Genet Res Unit, Oulu, Finland.
Nat Hist Museum, Dept Life Sci, London, England.
Staatliche Nat Wissensch Sammlungen Bayerns, Zool Staatssammlung Munchen SNSB ZSM, Munich, Germany.
Museo Civ Storia Nat, Zool, Verona, Italy.
Landesmuseum Karnten, Abt Zool Sammlungs & Wissensch Zentrum, Klagenfurt, Austria.
Univ Antilles, Inst Systemat Evolut Biodivers ISYEB, Museum Natl Hist Nat, CNRS,Sorbonne Univ,EPHE, Paris, France.

Доп.точки доступа:
Lopez-Vaamonde, Carlos; Kirichenko, Natalia; Cama, Alain; Doorenweerd, Camiel; Godfray, H. Charles J.; Guiguet, Antoine; Gomboc, Stanislav; Huemer, Peter; Landry, Jean-Francois; Lastuvka, Ales; Lastuvka, Zdenek; Lee, Kyung Min; Lees, David C.; Mutanen, Marko; van Nieukerken, Erik J.; Segerer, Andreas H.; Triberti, Paolo; Wieser, Christian; Rougerie, Rodolphe; Studium (France); Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [19-04-01029-a]; basic project of Sukachev Institute of Forest SB RAS [0287-2021-0011]; Region Centre (France) project ENDOFEED [201000047141]; Ministry of Agriculture (France) project PASSIFOR; Academy of FinlandAcademy of FinlandEuropean Commission [277984]; Kone foundation; Finnish Cultural foundationFinnish Cultural Foundation; Agriculture & Agri-Food Canada, Science and Technology Branch [J-000977, J-002279]; Promotion of Educational Policies, University and Research Department of the Autonomous Province of Bolzano - South TyrolPronvincia Autonoma di Bolzano; Austrian Federal Ministry of Science, Research and Economics in the framework of ABOL; Dutch Economic Restructuring Fund (FES); Bavarian Ministry of Science and Art (Germany) project BFB; Federal Ministry of Education and Research (Germany) project GBOL; Government of Canada through Genome CanadaGenome Canada; Ontario Genomics Institute in support of the International Barcode of Life project; National Science and Engineering Research Council of CanadaNatural Sciences and Engineering Research Council of Canada (NSERC); Kvantum Institute; Academy of FinlandAcademy of FinlandEuropean Commission

[Текст] / Н. И. Кириченко, М. А. Рязанова, А. А. Ефременко // Сибирский лесной журнал. - 2023. - № 1. - С. 85-97, DOI 10.15372/SJFS20230108 . - ISSN 2311-1410

ГРНТИ

68

68.47.37

34.33.19

Аннотация: В 2006-2018 гг. в Сибири заметные повреждения растениям (преимущественно древесным) причиняли 13 видов минирующих молей-пестрянок (Gracillariidae), т. е. около шестой части от всего числа видов молей-пестрянок, известных в этой части России. Подъемы численности с сильной (50-75 % листьев с повреждениями) и сплошной (> 75 %) степенью повреждения листьев растений задокументированы для 9 видов молей-пестрянок, среди которых 5 видов - местные вредители тополей ( Populus L.): Phyllonorycter apparella (Herrich-Schäffer) , Ph. comparella (Duponchel), Ph. populifoliella (Treitschke) , Phyllocnistis labyrinthella (Bjerkander) и Ph. unipunctella (Stephens). Три вида молей-пестрянок - дубовая ( Acrocercops brongniardella Fabricius) , сиреневая ( Gracillaria syringella (Fabricius)) и липовая ( Phyllonorycter issikii (Kumata)) - чужеродные для Сибири. Их многочисленные мины отмечены на древесных растениях (дуб ( Quercus L.)), сиренях ( Syringa L.), ясене ( Fraxinus L.) и липах ( Tilia L.)) в Западной Сибири (Омской, Тюменской и Новосибирской областях). Чужеродное происхождение молей люцерновой ( Phyllonorycter medicaginella (Gerasimov)) и калиновой ( Ph. lantanella (Schrank)) в Сибири требует уточнения. Как местные, так и чужеродные виды молей-пестрянок проявляют тенденцию к нанесению заметного вреда древесным растениям в искусственных экосистемах Сибири - в городских насаждениях, парках, дендрариях, ботанических садах, лесопитомниках. Соотношение случаев повышения численности молей-пестрянок к таковым в естественных экосистемах составляет 8 : 2. Основным донором чужеродных видов молей-пестрянок для Сибири выступает Европейская часть России. Чужеродные виды проникают сюда как в результате прямых заносов, так и путем ступенчатых инвазий с запада России
In 2006-2018, 13 species of leaf mining gracillariid moths (Gracillariidae) caused noticeable damage to plants (mainly trees and shrubs) in Siberia, i. e. about six of all moth species known in this part of Russia. Relative damage levels of 50-75 % and > 75 % were recorded for 9 moths, of which 5 species are native pests of poplars ( Populus L.): Phyllonorycter apparella (Herrich-Schäffer), Ph. comparella (Duponchel), Ph. populifoliella (Treitschke), Phyllocnistis labyrinthella (Bjerkander), and Ph. unipunctella (Stephens). Three moth species, namely Acrocercops brongniardella Fabricius, Gracillaria syringella (Fabricius) and Phyllonorycter issikii (Kumata) are alien to Siberia. Their numerous mines were found on leaves of woody plants (oaks ( Quercus L.), lilacs ( Syringa L.), ash ( Fraxinus L.) and lime ( Tilia L.) trees) in Western Siberia (Omsk, Tyumen and Novosibirsk Oblast). Alien origin of Phyllonorycter medicaginella (Gerasimov) and Ph. lantanella (Schrank) in Siberia requires confirmation. Both native and alien moth species showed a tendency to cause significant damage to the plants in artificial (manmade) stands, i. e. in urban green plantings, parks, arboreta, botanical gardens, tree nurseries. Overall 81 % of cases of significant damage by gracillariids was documented in artificial plantings vs. 19 % in forests. The European part of Russia remains the main donor of alien gracillariid species for Siberia. Alien species distribute to Siberia directly or through bridge-effect invasions from the west of Russia

РИНЦ

Держатели документа:
ИЛ СО РАН : 660036, Красноярск, Академгородок, 50, стр. 28

Доп.точки доступа:
Рязанова, Мария Александровна; Ефременко, Антон Андреевич; Kirichenko, Natal'ya Ivanovna