The Czech Academy of Sciences INSTITUTE OF VERTEBRATE BIOLOGY
BIENNIAL REPORT 2017 –2018
BRNO 2019 BIENNIAL REPORT
INSTITUTE OF VERTEBRATE BIOLOGY
the Czech Academy of Sciences
2017 –2018 BIENNIAL REPORT 2017–2018
A periodical continuation of the Institute’s previous bulletins: Vertebratologické zprávy (1969–1987), Zprávy ÚSEB (1988–1991) and the ILE Biennial Report (1993–1994).
Edited by Alena Fornůsková, Josef Bryja, Hana Slabáková and Marcel Honza Published by the Institute of Vertebrate Biology of the Czech Academy of Sciences, Brno, 2019 English editing by Kevin Roche Layout and pre-press by Jiří Kaláček Printed by H.R.G. Litomyšl
© Institute of Vertebrate Biology of the Czech Academy of Sciences.
Front cover: The cuckoo catfishSynodontis ( multipunctatus), the only obligatory brood parasite species among fishes. Photo( by R. Blažek) Back cover: The Institute’s new cuckoo catfish breeding facility, with 24 breeding and 32 experimental tanks housing hundreds of cuckoo catfish and their cichlid hosts. Photo( by M. Vrtílek)
ISBN 978-80-87189-26-9 CONTENTS PREFACE ...... 5
1. BACKGROUND ...... 7 | STRUCTURE OF THE INSTITUTE OF VERTEBRATE BIOLOGY ...... 7 | STAFF AND BUDGET ...... 8 | HEADQUARTERS ...... 11 | RESEARCH FACILITIES ...... 11 | FIELD STATION ...... 11 | MANAGEMENT AND SERVICES ...... 11 | BOARD OF THE INSTITUTE ...... 12 | SUPERVISORY BOARD ...... 12 | RESEARCH STAFF ...... 13
2. RESEARCH PROJECTS ...... 19 Projects supported by the Czech Science Foundation (GA ČR) ...... 19 Projects supported by the Technology Agency of the Czech Republic (TA ČR) ...... 21 Projects supported by the Ministry of Agriculture of the Czech Republic ...... 21 Projects supported by the Ministry of Education, Youth and Sport of the Czech Republic . . 21 International projects ...... 22
3. SCIENTIFIC RESULTS ...... 23 | SUMMARY OF PUBLICATION OUTPUT ...... 23 RESEARCH HIGHLIGHTS ...... 24 Geographical distribution of selected research activities ...... 26 Geographic distribution of the most important international cooperation activities . . . . . 28 Complete list of publications ...... 29 Books, textbooks, edited proceedings ...... 29 Book chapters ...... 29 Papers in journals included in the Web of Science Database ...... 30 Papers in other refereed journals ...... 45 Papers in proceedings ...... 45 Book reviews ...... 46 Popular books and articles ...... 47 Patents, utility models, function samples, verified technologies, certified methodologies ...... 48 | SELECTED SCIENTIFIC ACHIEVEMENTS ...... 49 EVOLUTIONARY ECOLOGY ...... 52 BIODIVERSITY ...... 66 PARASITES AND DISEASES ...... 80
4. OTHER ACTIVITIES ...... 89 | POPULARISATION ACTIVITIES ...... 89 Science exposition 2017 and 2018 ...... 90 Open door days ...... 90 | THE INSTITUTE OF VERTEBRATE BIOLOGY AND STRATEGY AV21 ...... 93 | NATIONAL ANIMAL GENETIC BANK OF THE CZECH REPUBLIC ...... 94 | IVB EXPERIMENTAL BREEDING FACILITIES ...... 97 Studenec experimental breeding facility ...... 97 Brno fish breeding facility ...... 98 | COMMERCIALISATION OF RESEARCH OUTPUTS ...... 98 | OUTREACH PROJECTS ...... 99 Project ATHENE – The Little Owl in danger ...... 99 The 2nd European Mammal Atlas (2017–2023) ...... 100 | MEETINGS ORGANISED BY THE INSTITUTE ...... 101 “Zoological days” Conference 2017 (Brno) and 2018 (Prague) ...... 101 The Czech Congress of Herpetology ...... 103 Hybrid zone workshop ...... 104 Rybikon 2018 – XVI Fisheries and ichthyological conference ...... 104 Lynx and wolf in the Western Carpathians: current population status, ecology and conservation ...... 105 Evolutionary workshop for PhD students ...... 106 | MEMBERSHIP OF EDITORIAL BOARDS ...... 106 | EDUCATION AND TEACHING ACTIVITIES ...... 106 Teaching at universities and supervision of students ...... 106 PhD students working at the Institute and/or supervised by the Institute’s fellows . . . . . 107 PhD theses defended over 2017–2018 and supervised by Institute fellows ...... 110 | EDITORIAL ACTIVITIES – FOLIA ZOOLOGICA ...... 111 | AWARDS ...... 112
OBITUARY ...... 113 post-graduate students (more than 100) studying with us is strong evidence of our Institute´s im- portant position in the Czech educational system, particularly in the fields of zoology, ecology, evo- lutionary biology and biodiversity. Our staff are extremely competitive and have had great success, both in obtaining research grants and in fund-raising from both national and foreign sources. These research grants and other contract funds contributed significantly to the IVB budget, representing an additional 48 and 47 million CZK in 2017 and 2018, respectively. At this point, I would like to express my deepest appreciation to all fellows who successfully applied for research grants and to express a vote of heartfelt thanks for the truly excellent results achieved over the past PREFACE two years. It also gives me great pleasure to announce that, over the past two years, we have completed the Dear reader, construction of a new modern breeding facility at It is my great pleasure to introduce what has already Studenec, at a cost of cca 40 million CZK. become a traditional publication of the Institute of Vertebrate Biology (IVB), the Biennial report. Dear reader, The major goal of this report is to provide both I will finish my 10 year period as Director of the a representative overview of the extensive range Institute in mid-June 2019 and I believe that the of research activities undertaken at the IVB and to new Director will bring new ideas and challenges inform the reader about the most important news for the future progress of the IVB. I sincerely hope and events occurring at the IVB over 2017–2018, that our work will continue to be guided by a spirit all in a style that is fully accessible to the interested of mutual understanding and collaboration. layperson. Finally, I wish to extend my sincere thanks to all Each chapter in this report provides a detailed the colleagues that supported and helped me over summary of the results of work completed over my tenure as Director. the previous two years. The majority of scientific papers were published in high ranking journals With my very best wishes, covered by the Web of Science. Of particular note is the impressive range of international coopera- tion and wide distribution of study sites through- out the world that is now characteristic of our re- search activities. Despite the majority of studies addressed by our fellows being primarily focused toward basic science, I must stress that the results of our work have also significantly contributed to ap- plied problems in the areas of nature conservation, fisheries, forestry, agriculture and epidemiological surveillance. The solid number of foreign students involved in our research is a clear indication that the In- Marcel Honza stitute has a good reputation abroad. In addition, Director of the IVB our huge participation in education at Czech Uni- versities and the amazing number of graduate and March, 2019
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BACKGROUND
1. BACKGROUND
| STRUCTURE OF THE INSTITUTE OF VERTEBRATE BIOLOGY
Supervisory Board Director Board of the Institute
Deputy Directors Scientific Secretary
Research Sector * Services (Brno)
Research Team 1 Administrative Department (headed by group leader 1)
Research Team 2 Scientific Information (headed by group leader 2) Centre and Library
Research Team 3 Secretariat (headed by group leader 3)
Research Team … X * dispersed at three research facilities – Brno, (headed by group leader … X) Studenec, Valtice
The Institute of Vertebrate Biology (IVB) is a relatively small institute of the Czech Academy of Sciences and, as such, is not structured into separate research departments. Senior researchers are usually the Principle Investigators of national and international projects and are responsible for creating and main- taining their teams, predominantly from external funds. Principle Investigators (group leaders) of projects are directly subordinated to the Director. Research teams are highly flexible and are composed of junior researchers, post-doctorates, research assistants, technicians and pre- and post-graduate students (mostly paid from project grants). Research subjects can be divided into three main domains: evolutionary ecology, biodiversity and pathogens and diseases (see below). However, individual projects can cover more topics and researchers often use interdisciplinary approaches.
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
| STAFF AND BUDGET
33 % 44 % 67 % 56 %
Supporting Staff Researchers Institutional Projects
Staff structure over the period 2017–2018 .
The number of employees paid from different sources has remained relatively stable in recent years, but the proportion of employees dependent on short-term projects is still very high .
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BACKGROUND
Increased subsidies from institutional funds have allowed us to employ more full time paid staff .
9 653 32 562
30 044 10 846
46 852 46 094
2017 Own resources 2018 Own resources Subsidies from funds Institutional subsidies Subsidies from funds Institutional subsidies
Budget structure of (numbers are in thousands of CZK) .
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018 Budget (in thousands of CZK)
The total budget of the Institute has increased slightly, partly due to an increase in institutional subsidies over 2017 and 2018 .
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BACKGROUND
ADDRESSES | FIELD STATION
Mohelno field station 675 75 Mohelno 134, | HEADQUARTERS Czech Republic Telephone: +420 543 422 512 Institute of Vertebrate Biology of the Czech Website: http://www.ivb.cz/research-facili- Academy of Sciences ties-field-station-mohelno.html Květná 8 Contact: Pavla Bučková, e-mail: [email protected] 603 65 Brno, Czech Republic Telephone: ++420-543422540 [email protected], [email protected] | MANAGEMENT AND Website: http://www.ivb.cz Contacts: Marcel Honza, e-mail: [email protected] SERVICES (Director) Pavla Bučková, e-mail: [email protected] Director (Head of administrative department) Assoc . Prof . Ing . Marcel Honza, PhD Jitka Novotná, e-mail: [email protected] Telephone: ++420-543211538, (Secretary) ++420-543422554 Fax: ++420-543211346 [email protected] | RESEARCH FACILITIES Deputy directors Brno research facility Ing . Pavel Jurajda, PhD Květná 8 Telephone: ++420-43422523 603 65 Brno, Czech Republic Fax: ++420-543211346 Telephone: ++420-543422523 [email protected] Website: http://www.ivb.cz/research-facilities-re - search-facility-brno.html Prof . RNDr . Jan Zima, DSc † 2019 Contact: Pavel Jurajda, e-mail: [email protected] Telephone: ++420-543422553 (Head of research facility) Fax: ++420-543211346 [email protected] Studenec research facility Studenec 122 Scientific secretary 675 02 Koněšín, Czech Republic Assoc . Prof . Mgr . et Mgr . Josef Bryja, PhD Telephone: ++420560590601 Telephone: ++420-560590601 Website: http://www.ivb.cz/research-facilities-ex- [email protected] ternal-research-facility-studenec.html Contact: Josef Bryja, e-mail: [email protected] PR manager (Head of research facility) Mgr . Alena Fornůsková, PhD Telephone: ++420-560590621 Valtice research facility [email protected] Klášterní 2 691 42 Valtice, Czech Republic Administrative department Telephone: ++420-519352961 & secretariat Website: http://www.ivb.cz/research-facilities-ex- ternal-research-facility-valtice.html Ing . Pavla Bučková (Head of department) Contact: Ivo Rudolf, e-mail: [email protected] [email protected] (Head of research facility)
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
Bohumila Kožnárková (Accountant) Scientific Information Centre and [email protected] Library Ing . Pavlína Březinová (Accountant) Ing . Hana Slabáková (Head) [email protected] [email protected] Marie Brodecká (Accountant) Alena Florianová, (Librarian) [email protected] [email protected] Pavla Denková (Accountant) [email protected] Editorial office of Folia zoologica Kateřina Srnová (Accountant) Prof . RNDr . Jan Zima, DSc (Editor-in-Chief) † 2019 [email protected] [email protected] Věra Pospíšilová (Secretary of administrative Lenka Glosová (Managing Editor) department) [email protected], [email protected] [email protected] Jitka Novotná (Secretary) Collections [email protected] Jiří Chamr (Curator) Vlastimil Hanáček (Technician) [email protected] Anežka Knechtová (Cleaner)
Prof . RNDr . Miloš Macholán, PhD | BOARD (Institute of Animal Physiology and Genetics, OF THE INSTITUTE Czech Academy of Sciences, Brno)
Chairman: | SUPERVISORY BOARD Assoc . Prof . Mgr . et Mgr . Josef Bryja, PhD Telephone: ++420-560590601 [email protected] Chairman: Prof . Ing . Petr Ráb, DSc (until 4. 3. 2018) Vice-chairman: (Institute of Animal Physiology and Genetics, Ing . Pavel Jurajda, PhD Czech Academy of Sciences, Liběchov) Telephone: ++420-43422523 Assoc . Prof . RNDr . Stanislav Kozubek, DSc Fax: ++420-543211346 (Institute of Biophysics, Czech Academy [email protected] of Sciences, Brno) (since 5. 3. 2018) Internal members: Assoc . Prof . Ing . Marcel Honza, PhD Vice-chairman: Assoc . Prof . RNDr . Ivo Rudolf, PhD Ing . Pavla Bučková Assoc . Prof . RNDr . Martin Reichard, PhD (Institute of Vertebrate Biology, Czech Academy Prof . RNDr . Jan Zima, DSc † 2019 of Sciences, Brno)
External members: Members: Prof . RNDr . Michal Horsák, PhD Assoc . Prof . RNDr . Jan Helešic, PhD (until 30. 4. 2017) (Masaryk University, Brno) (Masaryk University, Brno) Assoc . Prof . Mgr . Tomáš Bartonička, PhD Assoc . Prof . RNDr . Jan Kirschner, PhD (until 30. 4. 2017) (Masaryk University, Brno) (Institute of Botany, Czech Academy of Sciences, Průhonice)
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BACKGROUND
PhDr . Mgr . Martin Reissner, PhD (until 30. 4. 2017) Prof . PhDr . Ludvík Kunz, CSc, dr . h . c . (since 1. 5. 2017) (Moravian museum, Brno) (Institute of Physics of Materials, Czech Academy Prof . PhDr . Marek Blatný, DSc (since 1. 5. 2017) of Sciences) (Institute of Psychology, Czech Academy of Ing . Jan Osuský (since 1. 5. 2017) Sciences)
| RESEARCH STAFF
Only people with an employment contract are • population genetics and interspecies hybridisa- shown, i.e. not all PhD students are listed (for tion in deer; a complete list of PhD students see below). Nu- • ecology and conservation of carnivores in frag- merous fellows contracted on the basis of external mented landscapes; grant funding have only part-time jobs (extent not • food ecology of herbivorous mammals and their shown here), often limited to short periods. impact on the environment; • diet and parasites of primates. BRNO RESEARCH FACILITY Head of facility Ing . Pavel Jurajda, PhD The research facilities in Brno include zoological
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
Fellows contracted on the basis of external grant funding: Mgr . Klára Petrželková, PhD
Assoc . Prof . RNDr . Martin Reichard, PhD Mgr . Jan Mendel, PhD
Prof . RNDr . Jan Zima, DSc † 2019 Research assistants
Technicians PhD students Jiří Chamr Mgr . Jitka Fojtů, Milena Koníčková Rita Maria Santos Cameira, MSc Mgr . Zdenka Jurajdová, PhD Laurie Megane Lefebre, MSc Jakub Žák Mgr . Veronika Nezhybová Mgr . Libor Mikl Mgr . Markéta Pravdová Mgr . Tereza Prokopová
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BACKGROUND
Doreen Schulz, MSc Head of facility Mgr . Kateřina Sosnovcová Assoc . Prof . RNDr . Ivo Rudolf, PhD Mgr . Andrea Slaninová
The Valtice research facility is well equipped with Research assistants both state-of-the-art molecular equipment and Mgr . Hana Blažejová a modern animal rearing facility that fulfils all Ing . Lenka Betášová safety requirements needed for the handling of laboratory animals. Research is mainly focused on Technicians ecology and eco-epidemiology of zoonotic micro- Juraj Peško organisms, with a main emphasis on emerging and Ladislava Ševčíková re-emerging pathogens. In particular, research fo- cusses on the role of endotherm vertebrates (hosts to pathogenic agents) and haematophagous ar- STUDENEC thropods (biological vectors) in the circulation of RESEARCH FACILITY zoonotic pathogens, along with the natural and so- cio-economic factors driving emergence of particu- The Studenec research facility is a very dynamic lar infections. The main issues addressed include: part of the Institute that has evolved significantly • isolation and identification of novel microorganisms, over recent years. It houses modern, well equipped including human pathogens (microbe hunting); molecular-genetic, physiological and microscopic • ecology of arthropod-borne microorganisms laboratories, a breeding facility for small mammals, (e.g. West Nile and tick-borne encephalitis birds and amphibians and facilities allowing ex- flaviviruses, spirochaeteBorrelia burgdorferi, perimentation under semi-natural conditions. Em- rickettsiae Anaplasma phagocytophilum, the pirical data from observations, laboratory analysis spotted fever group rickettsiae and Babesia spp. and experiments (supplemented by simulation protozoa); modelling) are used to investigate important evo- • implementing the ‘one health’ concept for studying lutionary questions, mainly at the population level. emerging zoonoses; Research activities are mostly fundamental but may • risk of introduction and establishment of new have applications in biomedicine, species conserva- mosquito invasive vectors and mosquito-borne tion and epidemiology. Examples of research topics diseases into Central Europe; (model organisms given in parentheses) include: • providing expert advice regarding prevention • hybrid zones as barriers against gene flow and their and control of zoonoses (contribution to preven- role in speciation (rodents, amphibians, reptiles); tive human and veterinary medicine); • phylogeography, reconstruction of historical • providing expert opinion on emerging infectious colonisation and mechanisms of biodiversity evo- diseases. lution (mainly African rodents and amphibians);
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
• study of factors affecting population structure, Research assistant conservation genetics (fish, birds, rodents, Mgr . Anna Bryjová carnivores); • mating systems, analysis of reproductive success Technicians and factors affecting fitness (passerine birds); • immunogenetics, links between adaptive genetic Dagmar Šoukalová variation and fitness (rodents, passerine birds); Mgr . Jana Piálková • host-parasite co-evolution, genetic variation in Helena Hejlová pathogens and their hosts (rodents, bats, patho- genic fungi, helminths, RNA-viruses); • mechanisms and evolution of thermal physiolo- Fellows contracted on the basis of gy traits in ectotherms (newts); external grant funding: • functional approaches in the study of morpho- logical adaptation (amphibians and reptiles). Research scientists Head of facility Beate Nurnberger, PhD Assoc . Prof . Mgr . & Mgr . Josef Bryja, PhD Evolutionary biology, population genomics,
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BACKGROUND
Administrative and project assistants Mgr . Pavlína Opatová Dagmar Abrahámová Mgr . Lucie Schmiedová Mgr . Jana Vrbová Komárková Mgr . Jana Těšíková Mgr . Barbora Turbaková PhD students Mgr . Marie Kotasová Adámková Technicians Mgr . Tatiana Aghová Sampath Kumar Anandan, MSc Mgr . Jana Albrechtová Mgr . Barbora Bendová Sanka Baškiera, MSc Mgr . Ondřej Kauzál Mgr . Lukáš Bobek Bc . Anna Kousalová Mgr . Matej Dolinay Lucie Labská Oliver Gast, MSc Luděk Podhájský Mgr . Markéta Harazim Jindřiška Rezková Mgr . Alexandra Hánová Ludmila Rousková Mgr . Martin Janča Bc . František Snítilý Mgr . Tereza Králová Mgr . Jarmila Krásová Mgr . Adéla Petrželková Mgr . Jan Petružela Mgr . Iva Martincová
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
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RESEARCH PROJECTS
2. RESEARCH PROJECTS
Projects supported by the Czech Science Foundation (GA ČR)
GAP505/12/G112ECIP European Centre of Ich- GA15-11782S Biology of ageing: mechanisms thyoparasitology. Recipient: Masaryk University and patterns of senescence in free-living birds. in Brno. Principle Investigator: Milan Gelnar. Recipient: Institute of Vertebrate Biology, Czech Subrecipient: Institute of Vertebrate Biology, Academy of Sciences, Brno. Principle Investiga- Czech Academy of Sciences, Brno. Principle tor: Tomáš Albrecht. Research years: 2015–2017. Co-Investigator: Pavel Jurajda. Research years: 2012–2018. GA15-13265S High resolution genomic analysis of introgression across a species barrier. Recipient: GAP505/13/05872S The effects of non-native Institute of Vertebrate Biology, Czech Academy species on host-parasite relationships. Recipient: of Sciences, Brno. Principle Investigator: Stuart Institute of Vertebrate Biology, Czech Academy J. E. Baird. Research years: 2015–2017. of Sciences, Brno. Principle Investigator: Martin Reichard. Research years: 2013–2017. GJ15-13415Y Amphibian species diversification
across sky-island and lowland rainforests in Research projects GAP505/13/06451S Linking events through the a spatial and ecological context: genome-wide annual cycle: the importance of carry-over effects and continental transect. Recipient: Institute of for the ecology of migratory birds. Recipient: Vertebrate Biology, Czech Academy of Sciences, Institute of Vertebrate Biology, Czech Academy Brno. Principle Investigator: Václav Gvoždík. Re- of Sciences, Brno. Principle Investigator: Petr search years: 2015–2017. Procházka. Research years: 2013–2017. GA15-20229S Evolution of rodents and their GAP506/13/12580S Which mechanisms affect parasites in open habitats of East Africa. the diversity of clones and their coexistence with Recipient: Institute of Vertebrate Biology, Czech sexual species? European loaches of the genus Academy of Sciences, Brno. Principle Investigator: Cobitis as a model. Recipient: Institute of Verte- Josef Bryja. Research years: 2015–2017. brate Biology, Czech Academy of Sciences, Brno. Principle Investigator: Karel Halačka. Research GA16-00291S Ageing in the wild: from demo- years: 2013–2017. graphy to gene expression. Recipient: Institute of Vertebrate Biology, Czech Academy of Sciences, GA15-05180S Genetic diversity and cross-trans- Brno. Principle Investigator: Martin Reichard. missions of strongylid nematodes between Af- Research years: 2016–2018. rican great apes and man. Recipient: Institute of Vertebrate Biology, Czech Academy of Sciences, GA16-20049S Hybrid zones: natural laboratories Brno. Principle Investigator: Klára Petrželková. for the study of pathogen emergence. Recipient: Research years: 2015–2017. Institute of Vertebrate Biology, Czech Academy of Sciences, Brno. Principle Investigator: Joëlle GA15-07140S Thermal niche: evaluation of cur- Goüy de Bellocq. Research years: 2016–2018. rent concepts in ectothermic vertebrates. Re- cipient: Institute of Vertebrate Biology, Czech GA16-20054S Advanced studies on West Nile vi- Academy of Sciences, Brno. Principle Investiga- rus infection pathogenesis towards novel thera- tor: Lumír Gvoždík. Research years: 2015–2017. peutic strategies. Recipient: Institute of Organic Chemistry and Biochemistry, Czech Academy
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
of Sciences. Principle Investigator: Radim Nenc- GA17-20284S Physiology of bat hibernation ka. Subrecipient: Institute of Vertebrate Biology, with respect to multistressor impacts. Recipi- Czech Academy of Sciences, Brno. Principle ent: University of Veterinary and Pharmaceu- Co-Investigator: Zdeněk Hubálek. Research tical Sciences, Brno. Subrecipient: Institute of years: 2016–2018. Vertebrate Biology, Czech Academy of Sciences, Brno. Principle Investigator: Jiří Pikula Principle GA16-23773S Phylogeography, selection and mu- Co-Investigator: Natália Martínková. Research tation rate at the genomic level: Inference from years: 2017–2019. mtDNA sequences of the house mouse. Recipi- ent: Institute of Animal Physiology and Genetics, GA17-12262S Reproductive strategies of an ob- Czech Academy of Sciences, Brno. Subrecipient: ligate brood parasite: host selection, offspring Institute of Vertebrate Biology, Czech Academy sex allocation and individual success. Recipient: of Sciences, Brno. Principle Investigator: Miloš Institute of Vertebrate Biology, Czech Academy Macholán. Principle Co-Investigator: Jaroslav of Sciences, Brno. Principle Investigator: Marcel Piálek. Research years: 2016–2018. Honza. Research years: 2017–2019.
GA16-26714S Genomic dissection of barriers to GA17-24782S Latitudinal and altitudinal pat- gene flow in hybridising fire-bellied toads. Recip- terns in avian pace-of-life syndromes: a study of ient: Institute of Vertebrate Biology, Czech Acad- Afrotropical and European songbirds. Recipient: emy of Sciences, Brno. Principle Investigator: Institute of Vertebrate Biology, Czech Academy Beate Nürnberger. Research years: 2016–2018. of Sciences, Brno. Principle Investigator: Tomáš Albrecht. Research years: 2017–2019. GA17-15480S Freshwater ectotherms under cli- mate change: the role of phenotypic plasticity GA17-25320S Genotypes and phenotypes as- in life histories and trophic interactions. Re- sociated with Y chromosome introgression in cipient: University of South Bohemia in České the European house mouse hybrid zone: com- Budějovice. Subrecipient: Institute of Vertebrate parison among transects. Recipient: Institute of Research projects Research Biology, Czech Academy of Sciences, Brno. Vertebrate Biology, Czech Academy of Sciences, Principle Investigator: David Boukal. Principle Brno. Principle Investigator: Stuart J. E. Baird. Co-Investigator: Lumír Gvoždík. Research years: Research years: 2017–2019. 2017–2019. GA18-14325S The genetic basis of species origin: GA17-09807S Why and how animals abandon What can we learn from organisms with female sex? On the causal role of hrybridization in trig- heterogamety? Recipient: Charles University gering asexual reproduction. Recipient: Institute in Prague. Subrecipient: Institute of Vertebrate of Animal Physiology and Genetics, Czech Acad- Biology, Czech Academy of Sciences, Brno. emy of Sciences, Brno. Subrecipient: Institute of Principle Investigator: Radka Reifová. Princi- Vertebrate Biology, Czech Academy of Sciences, ple Co-Investigator: Tomáš Albrecht. Research Brno. Principle Investigator: Karel Janko. Prin- years: 2018–2020. ciple Co-Investigator: Karel Halačka. Research years: 2017–2019. GA18-17398S Evolution at steep elevational gra- dients: assessing the role of genetic and ecolog- GA17-04364S The role of Prdm9 allelic variations ical factors in speciation processes. Recipient: and activity in hybrid sterility in mice. Recipient: Institute of Vertebrate Biology, Czech Academy Institute of Molecular Genetics, Czech Academy of Sciences, Brno. Principle Investigator: Josef of Sciences. Subrecipient: Institute of Vertebrate Bryja. Research years: 2017–2019. Biology, Czech Academy of Sciences, Brno. Principle Investigator: Emil Parvanov. Principle GA 18-19629S Comparative parasite hybridisa- Co-Investigator: Jaroslav Piálek. Research years: tion genomics controlling for host divergence. 2017–2019. Recipient: Institute of Vertebrate Biology, Czech
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RESEARCH PROJECTS
Academy of Sciences, Brno. Principle Investi- GA18-24345S Epidemiology and pathological gator: Joëlle Goüy de Bellocq. Research years: effects of gastrointestinal helminthiases in crit- 2017–2019. ically endangered mountain gorillas. Recipient: Institute of Vertebrate Biology, Czech Academy GA18-24544S Genomic insights into the evolu- of Sciences, Brno. Principle Investigator: Klára tionary history and contact zones of slow-worm Petrželková. Research years: 2017–2019. lizards (Anguis). Recipient: Institute of Verte- brate Biology, Czech Academy of Sciences, Brno. GA18-26284S Embryo and environment – annual Principle Investigator: Vašk Gvoždík. Research fish as a unique model to study embryo ecology. years: 2017–2019. Recipient: Institute of Vertebrate Biology, Czech Academy of Sciences, Brno. Principle Investiga- GA18-17796Y Consequences of vertebrate micro- tor: Matej Polačik. Research years: 2017–2019. biota changes due to symbiotic associations with humans. Recipient: Institute of Vertebrate Biolo- GA18-00682S A novel system to understand gy, Czech Academy of Sciences, Brno. Principle brood parasitism: the cuckoo catfish parasiting Investigator: Jakub Kreisinger. Research years: African cichlids. Recipient: Institute of Ver- 2017–2019. tebrate Biology, Czech Academy of Sciences, Brno. Principle Investigator: Martin Reichard. Research years: 2017–2019.
Projects supported by the Technology Agency of the Czech Republic Research projects (TA ČR)
TG03010048 Commercialization of results of Principle Investigator: Jan Zukal. Research years: zoological research – applications for nature 2016–2019. conservation. Recipient: Institute of Vertebrate Biology, Czech Academy of Sciences, Brno.
Projects supported by the Ministry of Agriculture of the Czech Republic
QJ1510077 Increasing and more efficient produc- QJ1620240 Application of “top-down” bioma- tion of salmonids in the Czech Republic using nipulation to reduce eutrophication caused by their genetic identification.Recipient: Mendel agriculture in reservoirs. Recipient: Institute of University in Brno, Subrecipient: Institute of Vertebrate Biology, Czech Academy of Sciences, Vertebrate Biology, Czech Academy of Sciences, Brno. Principle Investigator: Karel Halačka. Re- Brno. Principle Investigator: Jan Mareš. Principle search years: 2016–2018. Co-Investigator: Karel Halačka. Research years: 2015–2018.
Projects supported by the Ministry of Education, Youth and Sport of the Czech Republic
OP VVV MEZEK International collaboration in Biology, Czech Academy of Sciences, Brno. Prin- ecological and evolutionary biology of Ver- ciple Investigator: Josef Bryja. Research years: tebrates. Recipient: Institute of Vertebrate 2018–2020.
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
International projects
KONTAKT II LH15175 Functional interaction Interreg V-A SK-CZ Coordination of the man- between host gene regulation and the microbi- agement of Eurasian lynx and grey wolf popu- ome in the primate gut. Recipient: Institute of lations in the Western Carpathians. Recipient: Vertebrate Biology, Czech Academy of Sciences, State Nature Conservancy of the Slovak Repub- Brno. Principle Investigator: Klára Petrželková. lic. Subrecipient: Institute of Vertebrate Biology, Research years: 2015–2017. Managed by: The Czech Academy of Sciences, Brno. Principle In- Ministry of Education, Youth and Sport of the vestigator for the Czech Republic: Jarmila Kro- Czech Republic. jerová-Prokešová. Research years: 2017–2019.
VectorNet European network for sharing data on ATHENE – Care for the largest residual popula- the geographic distribution of arthropod vectors tions of the European Owl. Recipient: Czech transmitting human and animal disease agents. Society for Ornithology. Subrecipient: Institute Principle Investigator for the Czech Republic: of Vertebrate Biology, Czech Academy of Scienc- Zdeněk Hubálek. Research years: 2015–2017. es, Brno. Principle Investigator at IVB: Martin Šálek. Research years: 2014–2020. The ATHENE African and Central European Vertebrates: Dis- project is part of the Czech Republic – Free State coverability of Genomic Samples Located at the of Saxony 2014–2020 cross-border Cooperation Institute of Vertebrate Biology. Provider: GGBN/ Program. This project is supported by the Euro- GGI Award Programme (Global Genome Bio- pean Union under the European Regional De- diversity Network/Global Genome Initiative). velopment Fund. Recipient: Institute of Vertebrate Biology, Czech Academy of Sciences, Brno. Principle Investigator: Petra Hájková. Research years: 2017–2018. Research projects Research
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3. SCIENTIFIC RESULTS
| SUMMARY OF PUBLICATION OUTPUT
Researchers at the IVB produced numerous scientific publications over 2017–2018, mainly in the form of research articles in international peer-reviewed journals. The publication profile and main scientometric criteria are shown below.
Distribution of papers categorized according to the Web of Science database over 2017–2018 . ECOLOGY ECOLOGY ZOOLOGY ZOOLOGY FISHERIES VIROLOGY VIROLOGY FORESTRY FORESTRY Publication Output LIMNOLOGY ENTOMOLOGY ENTOMOLOGY CELL BIOLOGY CELL BIOLOGY IMMUNOLOGY IMMUNOLOGY ORNITHOLOGY ORNITHOLOGY PARASITOLOGY PARASITOLOGY MICROBIOLOGY MICROBIOLOGY ANTHROPOLOGY ANTHROPOLOGY GENETICS HEREDITY TROPICAL MEDICINE VETERINARY SCIENCE VETERINARY INFECTIOUS DISEASES BEHAVIORAL SCIENCES BEHAVIORAL GEOGRAPHY PHYSICAL EVOLUTIONARY BIOLOGY BIOLOGY EVOLUTIONARY ANATOMY MORPHOLOGY MORPHOLOGY ANATOMY PSYCHOLOGY BIOLOGICAL PSYCHOLOGY DEVELOPMENTAL BIOLOGY BIOLOGY DEVELOPMENTAL ENVIRONMENTAL SCIENCES ENVIRONMENTAL MULTIDISCIPLINARY SCIENCES MULTIDISCIPLINARY MARINE FRESHWATER BIOLOGY FRESHWATER MARINE BIOCHEMISTRY MOLECULAR BIOLOGY BIOCHEMISTRY AGRICULTURE DAIRY ANIMAL SCIENCE ANIMAL DAIRY AGRICULTURE BIODIVERSITY CONSERVATION BIOLOGY BIODIVERSITY CONSERVATION BIOTECHNOLOGY APPLIED MICROBIOLOGY APPLIED MICROBIOLOGY BIOTECHNOLOGY PUBLIC ENVIRONMENTAL OCCUPATIONAL HEALTH HEALTH OCCUPATIONAL PUBLIC ENVIRONMENTAL
The IF values of papers published over the last two years confirm the increasingly high quality of IVB publications (source: ASEP Database, Czech Academy of Sciences) .
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
The distribution of article impact factors once again shifted toward higher values over 2017–2018 . Publication Output Publication
Citations of IVB papers over the last two years again confirm the increasing trend seen in previous years (note that the Institute of Vertebrate Biology was founded in 1998) .
RESEARCH HIGHLIGHTS
Many significant results and findings were published deserve special attention or emphasis and we have over 2017–2018. Although we provide a complete list highlighted some of these below. of publication produced over that period, we believe Species thermal requirements are key to our un- that some of the results are so significant that they derstanding of both species distribution and the
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SCIENTIFIC RESULTS impact of climate change on population dynamics. host’s ability to resist catfish parasitism depends on In the review “Just what is the thermal niche?”, both its evolutionary history of coexistence with the Lumír Gvoždík (Oikos 127 (2018): 1701–1710) parasite and individual experience. shows that understanding of this term in the cur- Joëlle Goüy de Beloque and colleagues (Gryseels rent scientific literature is highly variable, which et al. Plos Pathogen 13 (2017): e100673) studied complicates interdisciplinary communication. the role of host genetic background on distribution Accordingly, Gvoždík proposed a new conceptual of particular arenaviruses (they include e.g. Lassa framework that should unify our understanding of virus, highly pathogenic for human). Genetic anal- this ecological term. yses of multimammate mice Mastomys natalensis The team led by Martin Reichard studies the An- showed that each region has its own mice and that nual killifish (genusNothobranchius ), which have de- the regional borders appear sharp. They studied veloped adaptions allowing them to complete their one such contact zone in Tanzania and showed that life cycle in temporary pools of the African savan- the mice on either side carry different members of na. In a series of publications (Vrtílek et al. Current the viral family, which appear unable to cross the Biology 28 (2018): R822-R824, Scientific Reports8 boundary. This pattern would explain why Lassa is (2018): 4774, Science of Nature 105 (2018): 68), it was limited to western Africa. shown that wild killifish reach sexual maturity in just The so-called reticulate evolution combines di- two weeks, and often have complete life cycles rep- vergence and hybridisation. For example, if a species resenting a condensed version of typical vertebrate wants to colonise a higher elevation, it may be ad- ontogeny and lasting just two months. vantageous to receive mitochondrial DNA already Brood parasitism in birds (a reproductive strategy adapted to environments with low oxygen con- in which obligate brood parasites relinquish parental centrations. Josef Bryja and colleagues (Bryja et al. Publication Output care to host species) has been a traditional research Molecular Phylogenetics and Evolution 118 (2018): theme at the IVB since 1992. Recently, Radim Blažek 75–87), working on endemic rodents in the Ethio- published results on a unique fish brood parasite, the pian mountains, recently discovered that Afroalpine Cuckoo catfish, which parasitises African cichlids ecosystems spread down to lower elevations in the (Blažek et al. Science Advances 4 (2018): eaar4380). colder Pleistocene period, allowing specialised taxa In this seminal paper, Blažek demonstrated that the to cross the Rift valley. Once on the opposite side, they hybridised with local species, facilitating their colonisation of mountains at higher elevations. In a series of papers (Forstmeier et al. Jour- nal of Evolutionary Biology 30 (2017): 968–976, Knief et al. Nature Ecology & Evolution 1 (2017): 1177–1184, Tomášek et al. Proc. R. Soc. B Biologi- cal Sciences 284 (2017): 20162444), our research- ers detected a unique mechanism (Z chromo- some inversion) responsible for the maintenance of sub-optimal sperm phenotypes in zebra finch populations, small passerines displaying lifelong social monogamy. They further showed that only heterozygous males (carrying just one copy of the inversion) produce “super sperm” and these have the highest fertilisation success. Furthermore, they identified factors that reduce (inbreeding, oxidative stress) and enhance (carotenoid supplementation) sperm quality in zebra finches. More information Research in Tanzania. Joëlle Goüy de Bellocq is ta- regarding these interesting findings (and many oth- king samples of blood from Mastomys natalensis. ers) can be found below in Section 6 SELECTED (Photo by S. Gryseels) SCIENTIFIC ACHIEVEMENTS.
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
Geographical distribution of selected research activities
BULGARIA (Photo by I. Rudolf) SLOVAKIA (Photo by J. Ksiažek) RUSSIA (Photo by N. Martínková) Publication Output Publication
BRAZIL (Photo by M. Reichard) URUGUAY (Photo by M. Reichard) CHINA (Photo by M. Reichard)
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CAMEROON REPUBLIC OF THE CONGO CENTRAL AFRICAN REPUBLIC (Photo by V. Gvoždík) (Photo by V. Gvoždík) (Photo by D. Modrý) Publication Output
DR OF THE CONGO UGANDA ETHIOPIA (Photo by V. Gvoždík) (Photo by M. McLennan) (Photo by D. Mizerovská)
TANZANIA (Photo by S. Gryseels) ANGOLA (Photo by J. Krásová) MOZAMBIQUE (Photo by M. Polačik)
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
Geographic distribution of the most important international cooperation activities FRANCE • Aix Marseille University, Marseille SWITZERLAND • Muséum National d´Histoire Naturelle, Paris NORWAY • Centre de Biologie pour la Gestion des Populations, • Natural History Museum, University of Oslo, Oslo Montferrier sur Lez cedex • Université Montpellier • Swiss Ornithological Institute, Sempach GERMANY UK • Robert Koch Institute, Berlin • University of Sheffield • Max Planck Institute for Ornithology, Seewiesen • University of St Andrews • Max Planck Institute for Biology of Ageing, Cologne, SPAIN • Humboldt-Universität zu Berlin • University of Barcelona POLAND PORTUGAL • University of Lodz • CIBIO-InBIO, Research Centre in Biodiversity • Wrocław University of Environmental and Life Sciences, Wrocław and Genetic Resources ITALY BRAZIL • Scuola Normale Superiore, Pisa SLOVAKIA • Universidade do Vale do Rio dos Sinos, Sao Leopoldo • Biomedical Research Centre, SAV, Bratislava BULGARIA • Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro • Institute of Biodiversity and Ecosystem Research, Sofia URUGUAY RUSSIA • Universidad de la República, • Ural State Medical University, Yekaterinburg Montevideo • Irkutsk State Medical University, Irkutsk • Far East Branch of Russian Academy of Sciences, Vladivostok • A. N. Severtsov Institute of Ecology and Evolution of the Russian Academy of Sciences, Moscow, Russia Publication Output Publication
JAPAN • Oita University, Dannoharu Oita-shi
VIETNAM • Institute of Ecology and Biological Resources (IEBR), Vietnamese, Academy of Science and Technology, Hanoi
THAILAND • Udonthani Rajabhat University, Mueang Udon Thani District, Udon Thani BELGIUM • University of Antwerp REPUBLIC OF THE CONGO CHINA • Royal Belgian Institute for • National Research Institute of Exact • Institute of Hydrobiology, Chinese Academy Natural Sciences, Brussels and Natural Sciences, Brazzaville of Sciences, Wuhan CANADA ETHIOPIA USA • University of Sherbrooke • University of Mekelle, Tigray • United States Department of Agriculture Forest Service, Columbia, Missouri • Centre for Disease Control and Prevention (CDC), Fort Collins, Colorado TANZANIA • J. Craig Venter Institute, La jolla, California • Sokoine University of Agriculture, Morogoro • Cornell University, Ithaca • University of Colorado, Boulder DEMOCRATIC REPUBLIC OF THE CONGO • Field Museum of Natural History, Chicago • Biodiversity Monitoring Centre, University of Kisangani
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Complete list of publications
Books, textbooks, edited proceedings
BRYJA J, HORSÁK M, HORSÁKOVÁ V, Vtáctvo slovenskej časti Medzibodrožia. ŘEHÁK Z, ZUKAL J (eds), 2017. Zoologické Slovenská ornitologická spoločnosť/ dny Brno 2017. ÚBO AV ČR, Brno, BirdLife Slovensko, Bratislava, 505 pp. 254 pp. ISBN 978-80-87189-21-4. ISBN 978-80-89526-17-8.
BRYJA J, SOLSKÝ M (eds), 2018. Zoologické MODRÝ D, PAFČO B, PETRŽELKOVÁ KJ, dny Praha 2018. ÚBO AV ČR, Brno, 283 pp. HASEGAWA H (eds), 2018. Parasites ISBN 978-80-87189-24-5. of apes: an atlas of coproscopic diagnostics. Chimaira, Frankfurt am Main, 198 pp. BALLA M, ČAPEK M, DANKO Š, FULÍN M, Frankfurter Beiträge zur Naturkunde 78. CHRAŠČ P, KLOUBEC B, LITERÁK I, ISBN 978-3-89973-116-3. MOŠANSKÝ L, PAČENOVSKÝ S, PEŠKE L, REPEL M, ŠIMKOVÁ A, VYHNAL S, 2017.
Book chapters Publication Output ALBRECHT T, 2017. Avian sperm competition. Cognition and Behavior. Springer, Cham: 1-5. In Shackelford TK, Weekes-Shackelford ISBN 978-3-319-47829-6. VA (eds). Encyclopedia of Evolutionary Psychological Science. Springer, Cham: 1-4. REICHARD M, 2018. Fish diversity and ISBN 978-3-319-16999-6. ecology. In Scholz T, Vanhove MPM, Smit N, Jayasundera Z, Gelnar M (eds). A Guide to the ALBRECHT T, 2017. Sperm competition – Parasites of African Freshwater Fishes. RBINS’ Evidence in nonhumans. In Shackelford TK, Scientific Publication Unit, Brussels: 33-40. Weekes-Shackelford VA (eds). Encyclopedia Abc Taxa 18. ISBN 978-9-0732-4238-8. of Evolutionary Psychological Science. Springer, Cham: 1-4. ISBN 978-3-319-16999-6. ROCHE K, ADÁMEK Z, JURAJDA P, 2018. Utilisation of natural food resources by carp HONZA M, CHERRY MI, 2017. Egg in fish ponds. In Rahman MM, Balcombe characteristics affecting egg rejection. In Soler SR (eds). Cyprinus carpio: biological features, M (ed.). Avian brood parasitism. Springer, ecology and diseases and control measures. Cham: 401-419. Fascinating life sciences. Nova Science Publishers, New York: 65- ISBN 978-3-319-73137-7. 101. Marine and Freshwater Biology. ISBN 978-1-53614-024-8. JURAJDA P, 2018. Sampling of fish for parasitological investigation. In Scholz T, ZUKAL J, BERKOVÁ H, BANĎOUCHOVÁ H, Vanhove MPM, Smit N, Jayasundera Z, KOVÁČOVÁ V, PIKULA J, 2017. Bats and Gelnar M (eds). A Guide to the Parasites of caves: activity and ecology of bats wintering African Freshwater Fishes. RBINS’ Scientific in caves. In Karabulut S, Cinku MC (eds). Publication Unit, Brussels: 41-50. Abc Taxa 18. Cave investigation. InTech, Rijeka: 51-75. ISBN 978-9-0732-4238-8. ISBN 978-953-51-3331-5.
OPATOVÁ P, 2018. Peak fertility. In Vonk J, Shackelford T (eds). Encyclopedia of Animal
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Papers in journals included in the Web of Science Database
AGHOVÁ T, KIMURA Y, BRYJA J, BARTONIČKA T, BANĎOUCHOVÁ H, DOBIGNY G, GRANJON L, KERGOAT GJ, BERKOVÁ H, BLAŽEK J, LUČAN R, 2018. Fossils know it best: Using a new set of HORÁČEK I, MARTÍNKOVÁ N, PIKULA J, fossil calibrations to improve the temporal ŘEHÁK Z, ZUKAL J, 2017. Deeply torpid bats phylogenetic framework of murid rodents can change position without elevation of body (Rodentia: Muridae). Molecular Phylogenetics temperature. Journal of Thermal Biology 63: and Evolution 128: 98-111. 119-123.
AGHOVÁ T, ŠUMBERA R, PIÁLEK L, BELL RC, PARRA JL, BADJEDJEA G, MIKULA O, MCDONOUGH MM, BAREJ MF, BLACKBURN DC, BURGER M, LAVRENCHENKO LA, MEHERETU Y, CHANNING A, DEHLING JM, MBAU JS, BRYJA J, 2017. Multilocus GREENBAUM E, GVOŽDÍK V, phylogeny of East African gerbils (Rodentia, KIELGAST J, KUSAMBA C, LÖTTERS S, Gerbilliscus) illuminates the history of the MCLAUGHLIN PJ, NAGY ZT, RÖDEL M-O, Somali-Masai savanna. Journal of Biogeography PORTIK DM, STUART BL, VANDERWAL J, 44: 2295-2307. ZASSI-BOULOU A-G, ZAMUDIO KR, 2017. Idiosyncratic responses to climate-driven forest ARSLAN A, ZIMA J, 2017. Heterochromatin fragmentation and marine incursions in reed distribution and localization of NORs in the frogs from Central Africa and the Gulf of Guinea 2n=48 cytotypes of Nannospalax xanthodon Islands. Molecular Ecology 26: 5223-5244. and N. ehrenbergi. Turkish Journal of Zoology 41: 390-396. BLAŽEJOVÁ H, ŠEBESTA O, RETTICH F, MENDEL J, ČABANOVÁ V, BAIRD SJE, 2017. The impact of high- MITERPÁKOVÁ M, BETÁŠOVÁ L, PEŠKO J, throughput sequencing technology on HUBÁLEK Z, KAMPEN H, RUDOLF I, 2018.
Publication Output Publication speciation research: maintaining perspective. Cryptic species Anopheles daciae (Diptera: Journal of Evolutionary Biology 30: 1482-1487. Culicidae) found in the Czech Republic and Slovakia. Parasitology Research 117: 315-321. BANĎOUCHOVÁ H, BARTONIČKA T, BERKOVÁ H, BRICHTA J, KOKUREWICZ T, BLAŽEK R, POLAČIK M, KAČER P, KOVÁČOVÁ V, LINHART P, PIAČEK V, CELLERINO A, ŘEŽUCHA R, PIKULA J, ZAHRADNÍKOVÁ JR A, METHLING C, TOMÁŠEK O, SYSLOVÁ K, ZUKAL J, 2018. Alterations in the health of TERZIBASI TOZZINI E, ALBRECHT T, hibernating bats under pathogen pressure. VRTÍLEK M, REICHARD M, 2017. Repeated Scientific Reports 8: 6067. intraspecific divergence in life span and aging of African annual fishes along an aridity BARTÁKOVÁ V, BRYJA J, REICHARD M, 2018. gradient. Evolution 71: 386-402. Fine-scale genetic structure of the European bitterling at the intersection of three major BLAŽEK R, POLAČIK M, SMITH C, European watersheds. BMC Evolutionary HONZA M, MEYER A, REICHARD M, 2018. Biology 18: 105. Success of cuckoo catfish brood parasitism reflects coevolutionary history and individual BARTÁKOVÁ V, REICHARD M, 2017. No effect experience of their cichlid hosts. Science of recent sympatry with invasive zebra mussel Advances 4: eaar4380. on the oviposition decisions and reproductive success of the bitterling fish, a brood parasite of unionid mussels. Hydrobiologia 794: 153-166.
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BOSÁKOVÁ T, TOCKSTEIN A, ŠEBKOVÁ N, BURGSTALLER JP, KOLBE T, HAVLICEK V, ŠIMONÍK O, ADAMUSOVÁ H, HEMBACH S, POULTON J, PIÁLEK J, ALBRECHTOVÁ J, ALBRECHT T, STEINBORN R, RÜLICKE T, BREM G, BOSÁKOVÁ Z, DVOŘÁKOVÁ- JONES NS, JOHNSTON IG, 2018. Large-scale HORTOVÁ K, 2018. New insight into sperm genetic analysis reveals mammalian mtDNA capacitation: a novel mechanism of 17 beta- heteroplasmy dynamics and variance increase estradiol signalling. International Journal of through lifetimes and generations. Nature Molecular Sciences 19: 4011. Communications 9: 2488.
BRIESTENSKÁ K, JANÍKOVÁ M, BURGUNDER J, PAFČO B, PETRŽELKOVÁ KJ, KABÁT P, CSEPÁNYIOVÁ D, ZUKAL J, MODRÝ D, HASHIMOTO C, MACINTOSH PIKULA J, KOVÁČOVÁ V, LINHART P, AJJ, 2017. Complexity in behavioural BANĎOUCHOVÁ H, MISTRÍKOVÁ J, 2018. organization and strongylid infection among Bats as another potential source of murine wild chimpanzees. Animal Behaviour 129: gammaherpesvirus 68 (MHV-68) in nature. 257-268. Acta Virologica 62: 337-339. BURGUNDER J, PETRŽELKOVÁ KJ, BRLÍK V, ILIEVA M, LISOVSKI S, VOIGT CC, MODRÝ D, KATO A, MACINTOSH AJJ, PROCHÁZKA P, 2018. First insights into the 2018. Fractal measures in activity patterns: Do migration route and migratory connectivity gastrointestinal parasites affect the complexity of the Paddy field Warbler using geolocator of sheep behaviour? Applied Animal Behaviour
tagging and stable isotope analysis. Journal of Science 205: 44-53. Publication Output Ornithology 159: 879-882. CANNIFF L, DAINSON M, LÓPEZ AV, BRYJA J, KONVIČKOVÁ H, BRYJOVÁ A, HAUBER ME, GRIM T, SAMAŠ P, MIKULA O, MAKUNDI R, HANLEY D, 2018. Probing the limits of egg CHITAUKALI WN, ŠUMBERA R, 2018. recognition using egg rejection experiments Differentiation underground: range- along phenotypic gradients. Jove-Journal wide multilocus genetic structure of the of Visualized Experiments 2018: e57512. silvery mole-rat does not support current taxonomy based on mitochondrial sequences. ČABANOVÁ V, MITERPÁKOVÁ M, Mammalian Biology 93: 82-92. VALENTOVÁ D, BLAŽEJOVÁ H, RUDOLF I, STLOUKAL E, HURNÍKOVÁ Z, BRYJA J, KOSTIN D, MEHERETU Y, DZIDOVÁ M, 2018. Urbanization impact on ŠUMBERA R, BRYJOVÁ A, KASSO M, mosquito community and the transmission MIKULA O, LAVRENCHENKO LA, 2018. potential of filarial infection in central Europe. Reticulate Pleistocene evolution of Ethiopian Parasites & Vectors 11: 261. rodent genus along remarkable altitudinal gradient. Molecular Phylogenetics and Evolution ČAPEK M, PETRUSKOVÁ T, ŠEBELÍKOVÁ Z, 118: 75-87. SERRANO JC, PROCHÁZKA P, HONZA M, POŽGAYOVÁ M, 2017. Great Reed Warbler BRYJA J, ŠUMBERA R, KERBIS singing behavior and conspicuous song PETERHANS JC, AGHOVÁ T, BRYJOVÁ A, structures are not nest-location cues for the MIKULA O, NICOLAS V, DENYS C, Common Cuckoo. Journal of Ornithology 158: VERHEYEN E, 2017. Evolutionary history of 925-933. the thicket rats (genus Grammomys) mirrors the evolution of African forests since late Miocene. Journal of Biogeography 44: 182-194.
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ČERVENÁ B, HRAZDILOVÁ K, VALLO P, DAVID AA, JANÁČ M, 2018. Twenty-year KETZIS J, BOLFA P, TUDOR E, LUX- anniversary of the ICAIS: progress and challenges HOPPE EG, BLANVILLAIN C, MODRÝ D, towards a better understanding of aquatic 2018. Mammomonogamus nematodes in invasions. Aquatic Invasions 13: 433-437. fetid carnivores: a minireview and the first molecular characterization. Parasitology 145: DIMITROV D, ILIEVA M, IVANOVA K, 1959-1968. BRLÍK V, ZEHTINDJIEV P, 2018. Detecting local transmission of avian malaria and related ČERVENÁ B, HRAZDILOVÁ K, haemosporidian parasites (Apicomlexa, VALLO P, PAFČO B, FENYKOVÁ T, Haemosporida) at a Special Protection Area PETRŽELKOVÁ KJ, TODD A, TAGG N, of Natura 2000 network. Parasitology Research WANGUE N, LUX HOPPE EG, 117: 2187-2199. DUARTE MORAES MF, LAPERA IM, SOUZA POLLO A, ALBUQUERQUE DOHERTY-BONE TM, GVOŽDÍK V, 2017. ACA, MODRÝ D, 2018. Diversity of The amphibians of Mount Oku, Cameroon: an Mammomonogamus (Nematoda: Syngamidae) updated species inventory and conservation in large African herbivores. Parasitology review. ZooKeys 643: 109-139. Research 117: 1013-1024. DONROVICH SW, DOUDA K, ČERVENÁ B, VALLO P, PAFČO B, PLECHINGEROVÁ V, RYLKOVÁ K, JIRKŮ K, JIRKŮ M, PETRŽELKOVÁ KJ, HORKÝ P, SLAVÍK O, LIU H-Z, TODD A, TURKALO AK, MODRÝ D, REICHARD M, LOPES-LIMA M, SOUSA R, 2017. Host specificity and basic ecology of 2017. Invasive Chinese pond mussel Mammomonogamus (Nematoda, Syngamidae) Sinanodonta woodiana threatens native mussel from lowland gorillas and forest elephants in reproduction by inducing cross‐resistance of Central African Republic. Parasitology 144: host fish.Aquatic Conservation Marine and 1016-1025. Freshwater Ecosystems 27: 1325-1333. Publication Output Publication ČÍŽKOVÁ D, BAIRD SJE, TĚŠÍKOVÁ J, DOUDA K, LIU H-Z, YU D, ROUCHET R, VOIGT S, ĎUREJE Ľ, PIÁLEK J, GOÜY DE LIU F, TANG Q-Y, METHLING C, SMITH C, BELLOCQ J, 2018. Host subspecific viral REICHARD M, 2017. The role of local strains in European house mice: Murine adaptation in shaping fish-mussel coevolution. cytomegalovirus in the Eastern (Mus musculus Freshwater Biology 62: 1858-1868. musculus) and Western house mouse (Mus musculus domesticus). Virology 521: 92-98. DREWES S, STRAKOVÁ P, DREXLER JF, JACOB J, ULRICH RG, 2017. Assessing the D’AMICO G, ESTRADA-PEÑA A, KALMÁR Z, diversity of rodent-borne viruses: exploring FUH T, PETRŽELKOVÁ KJ, MIHALCA AD, of high-throughput sequencing and classical 2018. Redescription of the adult stages of amplification/sequencing approaches. Ixodes (Afrixodes) rasus Neumann 1899, with Advances in Virus Research 99: 61-108. notes on its phylogenetic position within the genus Ixodes. Ticks and Tick-borne Diseases 9: DREWES S, TURNI H, ROSENFELD UM, 654-659. OBIEGALA A, STRAKOVÁ P, IMHOLT C, GLATTHAAR E, DRESSEL K, PFEFFER M, DANISZOVÁ K, MIKULA O, MACHOLÁN M, JACOB J, WAGNER-WIENING C, POSPÍŠILOVÁ I, VOŠLAJEROVÁ ULRICH RG, 2017. Reservoir-driven BÍMOVÁ B, HIADLOVSKÁ Z, 2017. heterogeneous distribution of recorded human Subspecies-specific response to ACTH Puumala virus cases in South-West Germany. challenge test in the house mouse (Mus Zoonoses and Public Health 64: 381-390. musculus). General and Comparative Endocrinology 252: 186-192.
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EDME A, ZOBAČ P, OPATOVÁ P, FRANCOVÁ K, SEIFERTOVÁ M, ŠPLÍCHALOVÁ P, MUNCLINGER P, BLAŽEK R, GELNAR M, MAHMOUD ZN, ALBRECHT T, KRIST M, 2017. Do ŘEHULKOVÁ E, 2017. Quadriacanthus ornaments, arrival date, and sperm size species (Monogenea: Dactylogyridae) from influence mating and paternity success in the catfishes (Teleostei: Siluriformes) in eastern collared flycatcher?Behavioral Ecology and Africa: new species, new records and first Sociobiology 71: 3. insights into interspecific genetic relationships. Parasites & Vectors 10: 361. ELFEKI M, ELBESTAWY E, TKADLEC E, 2017. Bioconversion of Egypt’s agricultural wastes GAMERO A, BROTONS L, BRUNNER A, into biogas and compost. Polish Journal of FOPPEN R, FORNASARI L, GREGORY RD, Environmental Studies 26: 2445-2453. HERRANDO S, HOŘÁK D, JIGUET F, KMECL P, LEHIKOINEN A, LINDSTRÖM Å, FEDORČÁK J, KOŠČO J, HALAČKA K, PAQUET JY, REIF J, SIRKIÄ PM, MANKO P, 2017. Growth differences in ŠKORPILOVÁ J, VAN STRIEN A, SZÉP T, different biotypes of the hybrid complex TELENSKÝ T, TEUFELBAUER N, of Cobitis elongatoides × Cobitis tanaitica TRAUTMANN S, VAN TURNHOUT (Actinopterygii: Cypriniformes: Cobitidae) in CAM, VERMOUZEK Z, VIKSTRØM T, the Okna River (Danube River basin), Slovakia. VOŘÍŠEK P, 2017. Tracking progress toward Acta Ichthyologica et Piscatoria 47: 125-132. EU Biodiversity Strategy targets: EU policy effects in preserving its common farmland
FEDORČÁK J, PEKÁRIK L, HALAČKA K, birds. Conservation Letters 10: 395-402. Publication Output ŠMIGA Ľ, MANKO P, HAJDÚ J, VETEŠNÍK L, KOŠČO J, 2018. Microhabitat GARCÍA D, LOUREIRO M, MACHÍN E, preferences of triploid Cobitis fish and diploid REICHARD M, 2018. Phenology of three progenitors in two streams in Slovakia coexisting annual fish species: seasonal (Danube River Basin). Limnologica 69: 59-66. patterns in hatching dates. Hydrobiologia 809: 323-337. FERENC M, SEDLÁČEK O, TROPEK R, ALBRECHT T, ALTMAN J, DANČÁK M, GOEBEL J, PROMEROVÁ M, BONADONNA F, DOLEŽAL J, JANEČEK Š, MAICHER V, MCCOY KD, SERBIELLE C, STRANDH M, MAJEVSKÝ L’, MOTOMBI FN, MURKWE M, YANNIC G, BURRI R, FUMAGALLI L, SÁFIÁN S, SVOBODA M, HOŘÁK D, 2017. 100 million years of multigene family 2018. Something is missing at the bottom: evolution: origin and evolution of the avian Importance of coastal rainforests for MHC class IIB. BMC Genomics 18: 1-9. conservation of trees, birds and butterflies in the Mount Cameroon area. African Journal GOÜY DE BELLOCQ J, WASIMUDDIN, of Ecology 56: 679-683. RIBAS A, BRYJA J, PIÁLEK J, BAIRD SJE, 2018. Holobiont suture zones: Parasite FORSTMEIER W, IHLE M, OPATOVÁ P, evidence across the European house mouse MARTIN K, KNIEF U, ALBRECHTOVÁ J, hybrid zone. Molecular Ecology 27: 5214-5227. ALBRECHT T, KEMPENAERS B, 2017. Testing the phenotype-linked fertility GRYSEELS S, BAIRD SJE, BORREMANS B, hypothesis in the presence and absence of MAKUNDI R, LEIRS H, GOÜY DE inbreeding. Journal of Evolutionary Biology 30: BELLOCQ J, 2017. When viruses don’t go 968-976. viral: the importance of host phylogeographic structure in the spatial spread of arenaviruses. PLoS Pathogens 13: e1006073.
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GVOŽDÍK L, 2018. Just what is the thermal HORNÍČEK J, MENCLOVÁ P, POPELKOVÁ A, niche? Oikos 127: 1701-1710. RYMEŠOVÁ D, ZÁRYBNICKÁ M, BRYJA J, SVOBODOVÁ J, 2017. Microsatellite analysis GVOŽDÍK L, KRISTÍN P, 2017. Economic detects low rate of extra-pair paternity in thermoregulatory response explains mismatch Tengmalm’s owl, Aegolius funereus. Folia between thermal physiology and behaviour zoologica 66: 22-28. in newts. Journal of Experimental Biology 220: 1106-1111. HUBÁLEK Z, 2017. How sunrise and weather affect timing of rooks (Corvus frugilegus) HÁJKOVÁ L, HUBÁLEK Z, KOŽNAROVÁ V, morning departure from the winter communal BARTOŠOVÁ L, MOŽNÝ M, 2018. Flowering roost. Folia Zoologica 66: 227-230. of allergenically important plant species in relation to the North Atlantic Oscillation HUBÁLEK Z, JUŘICOVÁ Z, STRAKOVÁ P, system and thermal time in the Czech BLAŽEJOVÁ H, BETÁŠOVÁ L, RUDOLF I, Republic. Aerobiologia 34: 157-169. 2017. Serological survey for West Nile virus in wild artiodactyls, Southern Moravia (Czech HALAČKA K, MUŠKA M, MENDEL J, Republic). Vector-Borne and Zoonotic Diseases VETEŠNÍK L, 2017. A newly discovered 17: 654-657. population of the Balkan spiny loach Sabanejewia balcanica (Karaman, 1922) in the HUBÁLEK Z, KOSINA M, RUDOLF I, River Jihlava, Czech Republic. Folia Zoologica MENDEL J, STRAKOVÁ P, TOMEŠEK M, 66: 163-166. 2018. Mortality of Goshawks (Accipiter gentilis) due to West Nile virus lineage 2. Vector-Borne HAVIERNIK J, ŠTEFÁNIK M, FOJTÍKOVÁ M, and Zoonotic Diseases 18: 624-627. KALI S, TORDO N, RUDOLF I, HUBÁLEK Z, EYER L, RŮŽEK D, 2018. HUBÁLEK Z, RUDOLF I, 2017. Francisella Arbidol (Umifenovir): a broad-spectrum tularensis prevalence and load in Dermacentor
Publication Output Publication antiviral drug that inhibits medically reticulatus ticks in an endemic area in Central important arthropod-borne flaviviruses. Europe. Medical and Veterinary Entomology 31: Viruses 10: 184. 234-239.
HEROLDOVÁ M, MICHALKO R, CHARLES KL, BELL RC, BLACKBURN DC, SUCHOMEL J, ZEJDA J, 2018. Influence of BURGER M, FUJITA MK, GVOŽDÍK V, no-tillage versus tillage system on common JONGSMA GFM, KOUETE MT, vole (Microtus arvalis) population density. Pest LEACHÉ AD, PORTIK DM, 2018. Sky, Management Science 74: 1346-1350. sea, and forest islands: diversification in the African leaf-folding frog Afrixalus paradorsalis HLOUŠKOVÁ M, BALOGOVÁ M, (Anura: Hyperoliidae) of the Lower Guineo- KRŠÁKOVÁ V, GVOŽDÍK L, 2018. No trade- Congolian rain forest. Journal of Biogeography offs in interspecific interference ability and 45: 1781-1794. predation susceptibility in newt larvae. Ecology and Evolution 8: 9095-9104. CHRENKOVÁ M, DOBRÝ M, ŠÁLEK M, 2017. Further evidence of large-scale population HONZA M, POŽGAYOVÁ M, decline and range contraction of the little PETRŽELKOVÁ A, PROCHÁZKA P, owl Athene noctua in Central Europe. Folia 2018. Does host-absent vocalisation of Zoologica 66: 106-116. common cuckoo chicks increase hosts’ food provisioning behaviour? Behavioral Ecology and Sociobiology 72: 121.
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IGIC B, HAUBER ME, MOSKÁT C, GRIM T, JAPA O, MORAND S, SHAWKEY MD, PROCHÁZKA P, KARNCHANABANTHOENG A, HONZA M, 2017. Brood parasite and CHAISIRI K, RIBAS A, 2018. Detection host eggshells undergo similar levels of of Neospora caninum (Toxoplasmatidae) in decalcification during embryonic development. wild small mammals from Thailand.Folia Journal of Zoology 301: 165-173. Parasitologica 65: 018.
JABLONSKI D, NAJBAR B, JELÍNKOVÁ E, KRECHLER I, JURAJDA P, GROCHOWALSKA R, GVOŽDÍK V, PAPEŽÍKOVÁ I, NAVRÁTIL S, STRZAŁA T, 2017. Phylogeography and MARKOVÁ Z, PALÍKOVÁ M, 2018. postglacial colonization of Central Europe by Relationship between seasonal dynamics in Anguis fragilis and Anguis colchica. Amphibia- zooplankton density and ergasilus infection Reptilia 38: 562-569. in two reservoirs. Acta Veterinaria Brno 87: 91-98. JANÁČ M, BRYJA J, ONDRAČKOVÁ M, MENDEL J, JURAJDA P, 2017. GENETIC JIRKŮ M, DOSTÁL D, ROBOVSKÝ J, structure of three invasive gobiid species along ŠÁLEK M, 2018. Reproduction of the golden the Danube-Rhine invasion corridor: similar jackal (Canis aureus) outside current resident distributions, different histories.Aquatic breeding populations in Europe: evidence from Invasions 12: 551-564. the Czech Republic. Mammalia 82: 592-595.
JANÁČ M, ROCHE K, ŠLAPANSKÝ L, JOÓ K, BAKONYI T, SZENCI O, FERENCZI E, Publication Output POLAČIK M, JURAJDA P, 2018. Long-term BARNA M, MALIK P, HUBÁLEK Z, monitoring of native bullhead and invasive FEHÉR O, KUTASI O, 2017. Comparison gobiids in the Danubian rip-rap zone. of assays for the detection of West Nile Hydrobiologia 807: 263-275. virus antibodies in equine serum after natural infection or vaccination. Veterinary JANČA M, GVOŽDÍK L, 2017. Costly Immunology and Immunopathology 183: 1-6. neighbours: heterospecific competitive interactions increase metabolic rates in JURAJDA P, ROCHE K, HALAČKA K, dominant species. Scientific Reports 7: 5177. MRKVOVÁ M, ZUKAL J, 2018. Winter activity of common bream (Abramis brama L.) JANDZIK D, JABLONSKI D, ZINENKO O, in a European reservoir. Fisheries Management KUKUSHKIN OV, MORAVEC J, and Ecology 25: 163-171. GVOŽDÍK V, 2018. Pleistocene extinctions and recent expansions in an anguid lizard of KANKILIÇ T, ARSLAN A, ŞEKER PS, the genus Pseudopus. Zoologica Scripta 47: KANKILIÇ T, TOYRAN K, ZIMA J, 21-32. 2017. A new chromosomal race (2n=44) of Nannospalax xanthodon from Turkey JANKO K, PAČES J, WILKINSON- (Mammalia: Rodentia). Zoology in the Middle HERBOTS H, COSTA RJ, ROSLEIN J, East 63: 181-188. DROZD P, IAKOVENKO N, RÍDL J, HROUDOVÁ M, KOČÍ J, REIFOVÁ R, KIPSON M, ŠÁLEK M, LUČAN R, UHRIN M, ŠLECHTOVÁ V, CHOLEVA L, 2018. MAXINOVÁ E, BARTONIČKA T, Hybrid asexuality as a primary postzygotic ANDREAS M, KIPSON K, PUŠIĆ A, barrier between nascent species: on the RNJAK, D, NAĎO L, HORÁČEK I, 2018. interconnection between asexuality, Foraging habitat, home-range size and diet of hybridization and speciation. Molecular a Mediterranean bat species, Savi’s pipistrelle. Ecology 27: 248-263. Acta Chiropterologica 20: 351-360.
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KLVAŇA P, CEPÁK J, MUNCLINGER P, KOVÁČOVÁ V, KOLAŘÍK M, MICHÁLKOVÁ R, TOMÁŠEK O, BANĎOUCHOVÁ H, BARTONIČKA T, ALBRECHT T, 2018. Around the BERKOVÁ H, HAVELKOVÁ B, Mediterranean: an extreme example of loop HRUDOVÁ E, KOHOUTOVÁ L, migration in a long-distance migratory MARTÍNKOVÁ N, ZUKAL J, PIKULA J, passerine. Journal of Avian Biology 49: e01595. 2018. Recovery of a phytopathogenic bacterium Lonsdalea quercina from a lesser KNIEF U, FORSTMEIER W, PEI Y, IHLE M, horseshoe bat in Moravian karst, Czech WANG D, MARTIN K, OPATOVÁ P, Republic. Forest Pathology 48: e12379. ALBRECHTOVÁ J, WITTIG M, FRANKE A, ALBRECHT T, KEMPENAERS B, 2017. A KOVÁČOVÁ V, ZUKAL J, BANĎOUCHOVÁ H, sex-chromosome inversion causes strong BOTVINKIN AD, HARAZIM M, overdominance for sperm traits that affect MARTÍNKOVÁ N, ORLOV OL, PIAČEK V, siring success. Nature Ecology & Evolution 1: SHUMKINA AP, TIUNOV MP, PIKULA J, 1177-1184. 2018. White-nose syndrome detected in bats over an extensive area of Russia. BMC KOLEČEK J, HAHN S, EMMENEGGER T, Veterinary Research 14: 192. PROCHÁZKA P, 2018. Intra-tropical movements as a beneficial strategy for KRÁLOVÁ T, ALBRECHT T, BRYJA J, Palearctic migratory birds. Royal Society Open HOŘÁK D, JOHNSEN A, LIFJELD JT, Science 5: 171675. NOVOTNÝ M, SEDLÁČEK O, VELOVÁ H, VINKLER M, 2018. Signatures of diversifying KOLEČEK J, PROCHÁZKA P, selection and convergence acting on passerine IERONYMIDOU C, BUFIELD IJ, REIF J, Toll‐like receptor 4 in an evolutionary context. 2018. Non-breeding range size predicts the Molecular Ecology 27: 2871-2883. magnitude of population trends in trans- Saharan migratory passerine birds. Oikos 127: KRASNOVYD V, VETEŠNÍK L, GETTOVÁ L,
Publication Output Publication 599-606. CIVÁŇOVÁ K, ŠIMKOVÁ A, 2017. Patterns of parasite distribution in the hybrids of KONEČNÝ A, POPA O, BARTÁKOVÁ V, non-congeneric cyprinid fish species: is DOUDA K, BRYJA J, SMITH C, POPA LO, asymmetry in parasite infection the result of REICHARD M, 2018. Modelling the limited coadaptation? International Journal for invasion history of Sinanodonta woodiana Parasitology 47: 471-483. in Europe: tracking the routes of a sedentary aquatic invader with mobile parasitic larvae. KREISINGER J, KROPÁČKOVÁ L, Evolutionary Applications 11: 1975-1989. PETRŽELKOVÁ A, ADÁMKOVÁ M, TOMÁŠEK O, MARTIN J, MICHÁLKOVÁ R, KOTSAKIOZI P, JABLONSKI D, ILGAZ Ç, ALBRECHT T, 2017. Temporal stability and KUMLUTAŞ Y, AVCI A, MEIRI S, the effect of transgenerational transfer on ITESCU Y, KUKUSHKIN O, GVOŽDÍK V, fecal microbiota structure in a long distance SCILLITANI G, ROUSSOS SA, JANDZIK D, migratory bird. Frontiers in Microbiology 8: 50. KASAPIDIS P, LYMBERAKIS P, POULAKAKIS N, 2018. Multilocus phylogeny KREISINGER J, SCHMIEDOVÁ L, and coalescent species delimitation in PETRŽELKOVÁ A, TOMÁŠEK O, Kotschy’s gecko, Mediodactylus kotschyi: ADÁMKOVÁ M, MICHÁLKOVÁ R, Hidden diversity and cryptic species. Molecular MARTIN J-F, ALBRECHT T, 2018. Phylogenetics and Evolution 125: 177-187. Fecal microbiota associated with phytohaemagglutinin-induced immune response in nestlings of a passerine bird. Ecology and Evolution 8: 9793-9802.
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KRKAVCOVÁ E, KREISINGER J, KVACH Y, JANÁČ M, NEHRING S, HYÁNKOVÁ L, HYRŠL P, JAVŮRKOVÁ V, ONDRAČKOVÁ M, JURAJDA P, 2017. 2018. The hidden function of egg white Parasite communities and infection levels antimicrobials: egg weight-dependent effects of of the invasive Chinese sleeper Perccottus avidin on avian embryo survival and hatchling glenii (Actinopterygii: Odontobutidae) from phenotype. Biology Open 7: bio031518. the Naab river basin, Germany. Journal of Helminthology 91: 703-710. KROJEROVÁ-PROKEŠOVÁ J, BARANČEKOVÁ M, KAWATA Y, OSHIDA T, KVACH Y, JURAJDA P, BRYJOVÁ A, IGOTA H, KOUBEK P, 2017. Genetic TRICHKOVA T, RIBEIRO F, PŘIKRYLOVÁ I, differentiation between introduced Central ONDRAČKOVÁ M, 2017. European European sika and source populations in distribution for metacercariae of the North Japan: effects of isolation and demographic American digenean Posthodiplostomum events. Biological Invasions 19: 2125-2141. cf. minimum centrarchi (Strigeiformes: Diplostomidae). Parasitology International 66: KROJEROVÁ-PROKEŠOVÁ J, HOMOLKA M, 635-642. HEROLDOVÁ M, BARANČEKOVÁ M, BAŇAŘ P, KAMLER J, MODLINGER R, KVACH Y, MATVIENKO N, BRYJOVÁ A, PURCHART L, ZEJDA J, SUCHOMEL J, ONDRAČKOVÁ M, 2018. Aquaculture 2018. Patterns of vole gnawing on saplings in as a possible vector in the spread of managed clearings in Central European forests. Posthodiplostomum centrarchi (Hoffman,
Forest Ecology and Management 408: 137-147. 1958) (Digenea: Diplostomidae) in Europe. Publication Output BioInvasions Records 7: 427-432. KROPÁČKOVÁ L, TĚŠICKÝ M, ALBRECHT T, KUBOVČIAK J, ČÍŽKOVÁ D, TOMÁŠEK O, KVACH Y, ONDRAČKOVÁ M, BRYJOVÁ A, MARTIN J-F, BOBEK L, KRÁLOVÁ T, JURAJDA P, 2017. Parasites as biological tags PROCHÁZKA P, KREISINGER J, 2017. of divergence in Central European gudgeon Codiversification of gastrointestinal microbiota populations (Actinopterygii: Cyprinidae: and phylogenyin passerines is not explained by Gobioninae). Biologia 72: 671-679. ecological divergence. Molecular Ecology 26: 5292-5304. KVACH Y, ONDRAČKOVÁ M, JANÁČ M, JURAJDA P, 2018. Methodological issues KUNO G, MACKENZIE JS, JUNGLEN S, affecting the study of fish parasites. III. Effect HUBÁLEK Z, PLYUSNIN A, GUBLER DJ, of fish preservation method.Diseases of 2017. Vertebrate reservoirs of arboviruses: Aquatic Organisms 127: 213-224. myth, synonym of amplifier, or reality?Viruses 9: 185. KVACH Y, ONDRAČKOVÁ M, JANÁČ M, JURAJDA P, 2017. The parasite community of KVACH Y, BRYJOVÁ A, SASAL P, round goby Neogobius melanostomus (Pallas, WINKLER HM, 2017. A revision of the genus 1814) (Actinopterygii: Gobiidae) newly Aphalloides (Digenea: Cryptogonimidae), introduced into the upper Elbe. Knowledge and parasites of European brackish water fishes. Management of Aquatic Ecosystems 418: 19. Parasitology Research 116: 1973-1980. KVACH Y, ONDRAČKOVÁ M, KUTSOKON Y, KVACH Y, BRYJOVÁ A, SASAL P, DZYZIUK N, 2018. New record of WINKLER HM, 2018. The taxonomic and monogenean parasites on non-indigenous phylogenetic status of digeneans from the fishes in the Ukrainian Danube Delta. genus Timoniella (Digenea: Cryptogonimidae) BioInvasions Records 7: 65-72. in the Black and Baltic seas. Journal of Helminthology 92: 596-603.
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KVACH Y, ONDRAČKOVÁ M, TRICHKOVA T, MAPUA MI, PAFČO B, BURGUNDER J, DROBINIAK O, ZAMOROV V, JURAJDA P, PROFOUSOVÁPŠENKOVÁ I, TODD A, 2018. Parasitization of monkey goby, Neogobius HASHIMOTO C, QABLAN MA, MODRÝ D, fluviatilis (Pallas, 1814) (Actinopterygii: PETRŽELKOVÁ KJ, 2017. No impact of Gobiidae), at localities with different salinity strongylid infections on the detection of levels. Oceanological and Hydrobiological Plasmodium spp. in faeces of western lowland Studies 47: 376-383. gorillas and eastern chimpanzees. Malaria Journal 16: 175. LANÉS LEK, REICHARD M, DE MOURA RG, GODOY RS, MALTCHIK L, 2018. MARIËN J, BORREMANS B, GRYSEELS S, Environmental predictors for annual fish SOROPOGUI B, DE BRUYN L, assemblages in subtropical grasslands of South NGIALA BONGO G, BECKER-ZIAJA B, America: the role of landscape and habitat GOÜY DE BELLOCQ J, GÜNTHER S, characteristics. Environmental Biology of Fishes MAGASSOUBA N, LEIRS H, FICHET- 101: 963-977. CALVET E, 2017. No measurable adverse effects of Lassa, Morogoro and Gairo LAVRENCHENKO LA, NADJAFOVA RS, arenaviruses on their rodent reservoir host in BEKELE A, MIRONOVA TA, BRYJA J, natural conditions. Parasites & Vectors 10: 210. 2017. Phylogenetic position of a monotypic Ethiopian endemic rodent genus MARIËN J, SLUYDTS V, BORREMANS B, Megadendromus (Rodentia, Nesomyidae). GRYSEELS S, BROECKE BV, SABUNI CA, Mammalia 81: 71-82. KATAKWEBA AAS, MULUNGU LS, GÜNTHER S, GOÜY DE BELLOCQ J, LEHR E, MORAVEC J, CUSI JC, GVOŽDÍK V, MASSAWE AW, LEIRS H, 2018. Arenavirus 2017. A new minute species of Pristimantis infection correlates with lower survival of its (Amphibia: Anura: Craugastoridae) with natural rodent host in a long-term capture-mark- a large head from the Yanachaga-Chemillén recapture study. Parasites & Vectors 11: 90.
Publication Output Publication National Park in central Peru, with comments on the phylogenetic diversity of Pristimantis MARTÍNKOVÁ N, PIKULA J, ZUKAL J, occurring in the Cordillera Yanachaga. KOVÁČOVÁ V, BANĎOUCHOVÁ H, European Journal of Taxonomy 325: 1-22. BARTONIČKA T, BOTVINKIN AD, BRICHTA J, DUNDAROVA H, LINHART P, ŠÁLEK M, 2017. The assessment KOKUREWICZ T, IRWIN NR, LINHART P, of biases in the acoustic discrimination ORLOV OL, PIAČEK V, ŠKRABÁNEK P, of individuals. PLoS ONE 12: e0177206. TIUNOV MP, ZAHRADNÍKOVÁ JR A, 2018. Hibernation temperature-dependent MAHMOUDI A, ZIMA J, KRYŠTUFEK B, Pseudogymnoascus destructans infection intensity DARVISH J, ALIABADIAN M, ARSLAN A, in Palearctic bats. Virulence 9: 1734-1750. 2018. Systematic relationships within the Microtus arvalis (Rodentia: Cricetidae) group MAZOCH V, MIKULA O, BRYJA J, in Iran, inferred from cytogenetic analyses. KONVIČKOVÁ H, RUSSO IR, Zoology in the Middle East 64: 1-8. VERHEYEN E, ŠUMBERA R, 2018. Phylogeography of a widespread sub-Saharan MAPUA MI, FUEHRER H-P, murid rodent Aethomys chrysophilus: the role PETRŽELKOVÁ KJ, TODD A, NOEDL H, of geographic barriers and paleoclimate in the QABLAN MA, MODRÝ D, 2018. Plasmodium Zambezian bioregion. Mammalia 82: 373-387. ovale wallikeri in western lowland gorillas and humans, central African republic. Emerging Infectious Diseases 24: 1581-1583.
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MENDEL J, JÁNOVÁ K, PALÍKOVÁ M, 2018. MIKULA P, PETRUSKOVÁ T, ALBRECHT T, Genetically influenced resistance to stress and 2018. Song complexity—no correlation disease in salmonids in relation to present- between standard deviation of frequency and day breeding practice – a short review. Acta traditionally used song complexity metrics in veterinaria Brno 87: 35-45. passerines: a comment on Pearse et al. (2018). Evolution 72: 2832-2835. METHLING C, DOUDA K, LIU H, ROUCHET R, BARTÁKOVÁ V, YU D, MIKULÍČEK P, JABLONSKI D, PÁLENÍK M, SMITH C, REICHARD M, 2018. Energetic GVOŽDÍK V, JANDZIK D, 2018. costs in the relationship between bitterling and Characterization of microsatellite markers in mussels in East Asia. Biological Journal of the the genera Anguis and Pseudopus (Reptilia: Linnean Society 125: 750-759. Anguidae). Salamandra 54: 158-162.
MIKL L, ADÁMEK Z, ROCHE K, MIRONOV SV, LITERÁK I, SYCHRA O, VŠETIČKOVÁ L, ŠLAPANSKÝ L, ČAPEK M, 2017. Feather mites of the subfamily JURAJDA P, 2017. Invasive Ponto-Caspian Proctophyllodinae (Acari: Proctophyllodidae) gobies in the diet of piscivorous fish in a from passerines (Aves: Passeriformes) in Costa European lowland river. Fundamental and Rica. Zootaxa 4297: 1-105. Applied Limnology / Archiv für Hydrobiologie 190: 157-171. MORAIS PM, REICHARD M, 2018. Cryptic invasions: a review. Science of the Total
MIKL L, ADÁMEK Z, VŠETIČKOVÁ L, Environment 613-614: 1438-1448. Publication Output JANÁČ M, ROCHE K, ŠLAPANSKÝ L, JURAJDA P, 2017. Response of benthic NEZHYBOVÁ V, REICHARD M, BLAŽEK R, macroinvertebrate assemblages to round ONDRAČKOVÁ M, 2017. Metazoan parasites (Neogobius melanostomus, Pallas 1814) and of African annual killifish (Nothobranchiidae): tubenose (Proterorhinus semilunaris, Heckel abundance, diversity, and their environmental 1837) goby predation pressure. Hydrobiologia correlates. Biotropica 49: 229-238. 785: 219-232. NKRUMAH EE, BADU EK, BALDWIN HJ, MIKULA P, DÍAZ M, ALBRECHT T, ANTI P, KLOSE SM, VALLO P, DROSTEN C, JOKIMAKI J, KAISANLAHTI-JOKIMAKI KALKO EKV, OPPONG SK, TSCHAPKA M, M-L, KROITERO G, MØLLER AP, 2017. Flight activity of Noack’s round-leafbat TRYJANOWSKI P, YOSEF R, HROMADA M, (Hipposideros cf. ruber) at two caves in central 2018. Adjusting risk-taking to the annual cycle Ghana, West Africa. Acta Chiropterologica 19: of long-distance migratory birds. Scientific 347-355. Reports 8: 13989. PAFČO B, BENAVIDES JA, PŠENKOVÁ- MIKULA P, DÍAZ M, MØLLER AP, PROFOUSOVÁ I, MODRÝ D, ČERVENÁ B, ALBRECHT T, TRYJANOWSKI P, SHUTT KA, HASEGAWA H, FUH T, HROMADA M, 2018. Migratory and resident TODD AF, PETRŽELKOVÁ KJ, 2017. Do waders differ in risk taking on the wintering habituation, host traits and seasonality have grounds. Behavioural Processes 157: 309-314. an impact on protist and helminth infections of wild western lowland gorillas? Parasitology MIKULA P, HADRAVA J, ALBRECHT T, Research 116: 3401-3410. TRYJANOWSKI P, 2018. Large-scale assessment of commensalistic-mutualistic PAFČO B, ČÍŽKOVÁ D, KREISINGER J, associations between African birds and HASEGAWA H, VALLO P, SHUTT K, herbivorous mammals using internet photos. TODD A, PETRŽELKOVÁ KJ, MODRÝ D, PeerJ 6: e4520. 2018. Metabarcoding analysis of strongylid
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nematode diversity in two sympatric primate site cues by a fish revealed by tests with an species. Scientific Reports 8: 5933. artificial host.Animal Behaviour 126: 187-194.
PAFČO B, TEHLÁROVÁ Z, JIRKŮ- PIKULA J, AMELON SK, BANĎOUCHOVÁ H, POMAJBÍKOVÁ K, TODD A, BARTONIČKA T, BERKOVÁ H, BRICHTA J, HASEGAWA H, PETRŽELKOVÁ KJ, HOOPER S, KOKUREWICZ T, KOLAŘÍK M, MODRÝ D, 2018. Gastrointestinal protists KÖLLNER B, KOVÁČOVÁ V, LINHART P, and helminths of habituated agile mangabeys PIAČEK V, TURNER GG, ZUKAL J, (Cercocebus agilis) at Bai Hokou, Central MARTÍNKOVÁ N, 2017. White-nose African Republic. American Journal of syndrome pathology grading in Nearctic and Primatology 80: e22736. Palearctic bats. PLoS ONE 12: e0180435.
PAKOSTA T, VETEŠNÍK L, ŠIMKOVÁ A, PIRIA M, COPP GH, DICK JTA, DUPLIĆ A, 2018. A Long temporal study of parasitism GROOM Q, JELIĆ D, LUCY FE, in asexual-sexual populations of Carassius ROY HE, SARAT E, SIMONOVIĆ P, gibelio: Does the parasite infection support TOMLJANOVIĆ T, TRICARICO E, coevolutionary Red Queen dynamics? BioMed WEINLANDER M, ADÁMEK Z, Research International 2018: 6983740. BEDOLFE S, COUGHLAN NE, DAVIS E, DOBRZYCKA-KRAHEL A, GRGIĆ Z, PAVLISKA PL, RIEGERT J, GRILL S, ŠÁLEK M, KIRANKAYA SG, EKMEKCI FG, LAJTNER J, 2018. The effect of landscape heterogeneity on LUKAS JAY, KOUTSIKOS N, MENNEN GJ, population density and habitat preferences of the MITIĆ B, PASTORINO P, RUOKONEN TJ, European hare (Lepus europaeus) in contrasting SKÓRA ME, SMITH ERC, ŠPREM N, farmlands. Mammalian Biology 88: 8-15. TARKAN AS, TREER T, VARDAKAS L, VEHANEN T, VILIZZI L, ZANELLA D, PETROVÁ I, PETRILÁKOVÁ M, LOSÍK J, CAFFREY JM, 2017. Tackling invasive alien GOUVEIA A, DAMUGI IED, TKADLEC E, species in Europe II: threats and opportunities
Publication Output Publication 2018. Density-related pattern of variation until 2020. Management of Biological Invasions in body growth, body size and annual 8: 273-286. productivity in the common hamster. Mammalian Biology 91: 34-40. POLAČIK M, JANÁČ M, 2017. Costly defence in a fluctuating environment-sensitivity of annual PETRUŽELA J, ŠUMBERA R, AGHOVÁ T, Nothobranchius fishes to predator kairomones. BRYJOVÁ A, KATAKWEBA AS, Ecology and Evolution 7: 4289-4298. SABUNI CA, CHITAUKALI WN, BRYJA J, 2018. Spiny mice of the Zambezian bioregion POLAČIK M, REICHARD M, VRTÍLEK M, – phylogeny, biogeography and ecological 2018. Local variation in embryo development differentiation within theAcomys spinosissimus rate in annual fish.Journal of Fish Biology 92: complex. Mammalian Biology 91: 79-90. 1359-1370.
PETRŽELKOVÁ A, PÖYSÄ H, KLVAŇA P, POLAČIK M, SMITH C, REICHARD M, 2017. ALBRECHT T, HOŘÁK D, 2017. Egg Maternal source of variability in the embryo morphology fails to identify nests parasitized development of an annual killifish.Journal by conspecifics in common pochard: a test of Evolutionary Biology 30: 738-749. based on protein fingerprinting and including female relatedness. Journal of Avian Biology 48: POŽGAYOVÁ M, PIÁLKOVÁ R, HONZA M, 229-234. PROCHÁZKA P, 2018. Sex-specific nestling growth in an obligate brood parasite: Common PHILLIPS A, REICHARD M, SMITH C, 2017. Cuckoo males grow larger than females. Auk Sex differences in the responses to oviposition 135: 1033-1042.
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PRAVDOVÁ M, ONDRAČKOVÁ M, ROCHE K, KUTA J, SEDLÁČEK I, PŘIKRYLOVÁ I, BLAŽEK R, MAHMOUD Z, ČERVENKA R, TOMANOVÁ K, JURAJDA P, GELNAR M, 2018. Dactylogyrids 2018. First data on uranium uptake in three (Platyhelminthes: Monogenea) from Sudanese nototheniid fishes from Antarctica (James Ross Labeo spp., with a description of Dogielius Island). Chemosphere 211: 510-514. sennarensis n. sp. and a redescription of Dogielius flosculus Guégan, Lambert & Euzet, ROSÀ R, ANDREO V, TAGLIAPIETRA V, 1989. Helminthologia 55: 306-321. BARÁKOVÁ I, ARNOLDI D, HAUFFE HC, MANICA M, ROSSO F, BLAŇAROVÁ L, PROCHÁZKA P, BRLÍK V, YOHANNES E, BONA M, DERDÁKOVÁ M, HAMŠÍKOVÁ Z, MEISTER B, AUERSWALD J, ILIEVA M, KAZIMÍROVÁ M, KRALJIK J, HAHN S, 2018. Across a migratory divide: KOCIANOVÁ E, MAHRÍKOVÁ L, divergent migration directions and non- MINICHOVÁ L, MOŠANSKÝ L, SLOVÁK M, breeding grounds of Eurasian reed warblers STANKO M, ŠPITALSKÁ E, DUCHEYNE E, revealed by geolocators and stable isotopes. NETELER M, HUBÁLEK Z, RUDOLF I, Journal of Avian Biology 49: e01769. VENCLÍKOVÁ K, SILAGHI C, OVERZIER E, FARKAS R, FÖLDVÁRI G, HORNOK S, PROCHÁZKA P, HAHN S, ROLLAND S, VAN TAKÁCS N, RIZZOLI A, 2018. Effect of DER JEUGD H, CSÖRGÖ T, JIGUET F, climate and land use on the spatio-temporal MOKWA T, LIECHTI F, VANGELUWE D, variability of tick-borne bacteria in Europe. KORNER-NIEVERGELT F, 2017. Delineating International Journal of Environmental
large-scale migratory connectivity of reed Research and Public Health 15: 732. Publication Output warblers using integrated multistate models. Diversity and Distributions 23: 27-40. ROUCHET R, SMITH C, LIU H, METHLING C, DOUDA K, YU D, TANG Q, REICHARD M, 2017. Evolutionary perspectives REICHARD M, 2017. Avoidance of host on ageing. Seminars in Cell & Developmental resistance in the oviposition-site preferences Biology 70(SI), 99-107. of rose bitterling. Evolutionary Ecology 31: 769-783. REICHARD M, BLAŽEK R, POLAČIK M, VRTÍLEK M, 2017. Hatching date variability RUDOLF I, BETÁŠOVÁ L, BLAŽEJOVÁ H, in wild populations of four coexisting species VENCLÍKOVÁ K, STRAKOVÁ P, of African annual fishes.Developmental ŠEBESTA O, MENDEL J, BAKONYI T, Dynamics 246: 827-837. SCHAFFNER F, NOWOTNY N, HUBÁLEK Z, 2017. West Nile virus in REICHARD M, JANÁČ M, POLAČIK M, overwintering mosquitoes, central Europe. BLAŽEK R, VRTÍLEK M, 2017. Community Parasites & Vectors 10: 452. assembly in Nothobranchius annual fishes: nested patterns, environmental niche and RUDOLF I, BLAŽEJOVÁ H, STRAKOVÁ P, biogeographic history. Ecology and Evolution 7: ŠEBESTA O, PEŠKO J, MENDEL J, 2294-2306. ŠIKUTOVÁ S, HUBÁLEK Z, KAMPEN H, SCHAFFNER F, 2018. The invasive Asian tiger REICHARD M, LANÉS LEK, POLAČIK M, mosquito Aedes albopictus (Diptera: Culicidae) BLAŽEK R, VRTÍLEK M, GODOY RS, in the Czech Republic: Repetitive introduction MALTCHIK L, 2018. Avian predation events highlight the need for extended mediates size-specific survival in a Neotropical entomological surveillance. Acta Tropica 185: annual fish: a field experiment. Biological 239-241. Journal of the Linnean Society 124: 56-66.
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RYMEŠOVÁ D, KRÁLOVÁ T, PROMEROVÁ M, adaptation to a high-fiber diet?International BRYJA J, TOMÁŠEK O, SVOBODOVÁ J, Journal of Primatology 39: 567-580. ŠMILAUER P, ŠÁLEK M, ALBRECHT T, 2017. Mate choice for major histocompatibility SMITH C, 2017. Bayesian inference supports complex complementarity in a strictly the host selection hypothesis in explaining monogamous bird, the grey partridge (Perdix adaptive host specificity by European perdix). Frontiers in Zoology 14: 9. bitterling. Oecologia 183: 379-389.
SABUNI C, AGHOVÁ T, BRYJOVÁ A, SMITH C SPENCE R, REICHARD M, 2018. ŠUMBERA R, BRYJA J, 2018. Biogeographic Sperm is a sexual ornament in rose bitterling. implications of small mammals from Northern Journal of Evolutionary Biology 31: 1610-1622. Highlands in Tanzania with first data from the volcanic Mount Kitumbeine. Mammalia 82: SMITH P, WILLEMSEN D, POPKES M, 360-372. METGE F, GANDIWA E, REICHARD M, VALENZANO DR, 2017. Regulation of life SAMAŠ P, RUTILA J, HONZA M, span by the gut microbiota in the short-lived KYSUČAN M, GRIM T, 2018. Rearing a African turquoise killifish.eLife 6: e27014. virulent common cuckoo is not extra costly for its only cavity-nesting host. Proceedings of SOSNOVCOVÁ K, KOLEČEK J, the Royal Society B – Biological Sciences 285: POŽGAYOVÁ M, JELÍNEK V, ŠULC M, 20181710. STEIDLOVÁ P, HONZA M, PROCHÁZKA P, 2018. Timing of natal nests is an important SEHONOVÁ P, PLHALOVÁ L, BLAHOVÁ J, factor affecting return rates of juvenile Great DOUBKOVÁ V, MARŠÁLEK P, PROKEŠ M, Reed Warblers. Journal of Ornithology 159: TICHÝ F, SKLÁDANÁ M, FIORINO E, 183-190. MIKULA P, VEČEREK V, FAGGIO C, SVOBODOVÁ Z, 2017. Effects of selected STAROSTOVÁ Z, GVOŽDÍK L,
Publication Output Publication tricyclic antidepressants on early-life stages of KRATOCHVÍL L, 2017. An energetic common carp (Cyprinus carpio). Chemosphere perspective on tissue regeneration: the costs of 185: 1072-1080. tail autotomy in growing geckos. Comparative Biochemistry and Physiology A-Molecular & SEHONOVÁ P, PLHALOVÁ L, BLAHOVÁ J, Integrative Physiology 206: 82-86. DOUBKOVÁ V, PROKEŠ M, TICHÝ F, FIORINO E, FAGGIO C, SVOBODOVÁ Z, STRAKOVÁ P, DUFKOVÁ L, ŠIRMAROVÁ J, 2017. Toxicity of naproxen sodium and its SALÁT J, BARTONIČKA T, KLEMPA B, mixture with tramadol hydrochloride on fish PFAFF F, HÖPER D, HOFFMANN B, early life stages. Chemosphere 188: 414-423. ULRICH RG, RŮŽEK D, 2017. Novel hantavirus identified in European bat species ŞEKER PS, ARSLAN A, SELVI E, KANKILIÇ T, Nyctalus noctula. Infection, Genetics and ZIMA J, 2018. Variation in the conventional Evolution 48: 127-130. and banded karyotypes among populations of Arvicola amphibius (L., 1758) (Mammalia: STRAKOVÁ P, JAGDMANN S, Rodentia) from Turkey. Acta Zoologica BALČIAUSKAS L, BALČIAUSKIENĖ L, Bulgarica 70: 147-152. DREWES S, ULRICH RG, 2017. Puumala virus in bank voles, Lithuania. Emerging SCHULZ D, QABLAN MA, PROFOUSOVÁ- Infectious Diseases 23: 158-160. PŠENKOVÁ I, VALLO P, FUH T, MODRÝ D, PIEL AK, STEWART F, PETRŽELKOVÁ KJ, STRAKOVÁ P, KUBÁNKOVÁ M, FLIEGEROVÁ K, 2018. Anaerobic fungi VAŠÍČKOVÁ P, JUŘICOVÁ Z, RUDOLF I, in gorilla (Gorilla gorilla gorilla) feces: an HUBÁLEK Z, 2018. Hepatitis E virus in
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archived sera from wild boars (Sus scrofa), Ethiopian highlands as a cradle of the African Czech Republic. Transboundary and Emerging fossorial root-rats (genus Tachyoryctes), the Diseases 65: 1770-1774. genetic evidence. Molecular Phylogenetics and Evolution 126: 105-115. STURMBAUER C, BÖRGER C, VAN STEENBERGE M, KOBLMÜLLER S, 2017. TĚŠÍKOVÁ J, BRYJOVÁ A, BRYJA J, A separate lowstand lake at the northern LAVRENCHENKO LA, GOÜY DE edge of Lake Tanganyika? Evidence from BELLOCQ J, 2017. Hantavirus strains in East phylogeographic patterns in the cichlid genus Africa related to Western African hantaviruses. Tropheus. Hydrobiologia 791: 51-68. Vector-Borne and Zoonotic Diseases 17: 278-280.
SVOBODOVÁ J, BAUEROVÁ P, ELIÁŠ J, TKADLEC E, VÁCLAVÍK, T, KUBELOVÁ, M, VELOVÁ H, VINKLER M, ALBRECHT T, ŠIROKÝ, P, 2018. Negative spatial covariation 2018. Sperm variation in Great Tit males in abundance of two European ticks: diverging (Parus major) is linked to a haematological niche preferences or biotic interaction? healthrelated trait, but not ornamentation. Ecological Entomology 43: 804-812. Journal of Ornithology 159: 815-822. TOMÁŠEK O, ALBRECHTOVÁ J, ŚWIDERSKÁ Z, ŠMÍDOVÁ A, BUCHTOVÁ L, NĚMCOVÁ M, OPATOVÁ P, ALBRECHT T, BRYJOVÁ A, FABIÁNOVÁ A, 2017. Trade-off between carotenoid-based MUNCLINGER P, VINKLER M, 2018. Avian sexual ornamentation and sperm resistance to
Toll-like receptor allelic diversity far exceeds oxidative challenge. Proceedings of the Royal Publication Output human polymorphism: an insight from Society B – Biological Sciences 284: 20162444. domestic chicken breeds. Scientific Reports 8: 17878. TRNKA A, POŽGAYOVÁ M, 2017. Does conspicuous colouration of Magpies Pica pica ŠÁLEK M, BAŽANT M, ŻMIHORSKI M, 2018. influence aggressive behaviour in nesting Great Active farmsteads are year-round strongholds Reed Warblers Acrocephalus arundinaceus? for farmland birds. Journal of Applied Ecology Bird Study 64: 108-111. 55: 1908-1918. TRNKA A, SAMAŠ P, GRIM T, 2018. Stability ŠÁLEK M, HULA V, KIPSON M, DAŇKOVÁ R, of a behavioural syndrome vs. plasticity in NIEDOBOVÁ J, GAMERO A, 2018. Bringing individual behaviours over the breeding diversity back to agriculture: smaller fields cycle: Ultimate and proximate explanations. and non-crop elements enhance biodiversity Behavioural Processes 153: 100-106. in intensively managed arable farmlands. Ecological Indicators 90: 65-73. VALLO P, MOTSCH P, BENDA P, MAGANGA GD, BOURGAREL M, 2018. ŠÁLEK M, ŻMIHORSKI M, 2018. Manure heaps Mitochondrial phylogeny and morphological attract farmland birds during winter. Bird variation of the African sheath-tailed bat Study 65: 426-430. (Coleura afra, Emballonuridae). Acta Chiropterologica 20: 73-84. ŠLAPANSKÝ L, JANÁČ M, ROCHE K, MIKL L, JURAJDA P, 2017. Expansion of round gobies VANMECHELEN K, BLETSA M, LAENEN L, in a non-navigable river system. Limnologica LOPES AR, VERGOTE V, BELLER L, 67: 27-36. DEBOUTTE W, KORVA M, AVŠIČ ŽUPANC T, GOÜY DE BELLOCQ J, ŠUMBERA R, KRÁSOVÁ J, GRYSEELS S, LEIRS H, LEMEY P, LAVRENCHENKO LA, MENGISTU S, VRANCKEN M, MAES P, 2018. Discovery BEKELE A, MIKULA O, BRYJA J, 2018. and genome characterization of three new
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Jeilongviruses, a lineage of paramyxoviruses VRTÍLEK M, ŽÁK J, PŠENIČKA M, characterized by their unique membrane REICHARD M, 2018. Extremely rapid proteins. BMC Genomics 19: 617. maturation of a wild African annual fish. Current Biology 28: R822-R824. VLČKOVÁ K, KREISINGER J, PAFČO B, ČÍŽKOVÁ D, TAGG N, HEHL AB, VŠETIČKOVÁ L, MIKL L, ADÁMEK Z, MODRÝ D, 2018. Diversity of Entamoeba PRÁŠEK V, ROCHE K, JURAJDA P, 2018. spp. in African great apes and humans: an The diet of reservoir perch before, during and insight from Illumina MiSeq high-throughput after establishment of non-native tubenose sequencing. International Journal for goby. Knowledge and Management of Aquatic Parasitology 48: 519-530. Ecosystems 419: 4.
VLČKOVÁ K, PAFČO B, PETRŽELKOVÁ KJ, WINTERNITZ JC, ABBATE JL, HUCHARD E, MODRÝ D, TODD A, YEOMAN CJ, HAVLÍČEK J, GARAMSZEGI LZ, 2017. TORRALBA M, WILSON BA, STUMPF RM, Patterns of MHC-dependent mate selection in WHITE BA, NELSON KE, LEIGH SR, humans and non-human primates: a meta- GOMEZ A, 2018. Relationships between analysis. Molecular Ecology 26: 668-688. gastrointestinal parasite infections and the fecal microbiome in free-ranging western lowland WINTEROVÁ B, GVOŽDÍK L, 2018. Influence gorillas. Frontiers in Microbiology 9: 1202. of interspecific competitors on behavioral thermoregulation: developmental or acute VLČKOVÁ K, SHUTT-PHILLIPS KA, plasticity? Behavioral Ecology and Sociobiology HEISTERMANN M, PAFČO B, 72: 169. PETRŽELKOVÁ KJ, TODD A, MODRÝ D, NELSON KE, WILSON BA, STUMPF RM, ZAHRADNÍKOVÁ JR A, KOVÁČOVÁ V, WHITE BA, LEIGH SR, GOMEZ A, 2018. MARTÍNKOVÁ N, ORLOVA MV, Impact of stress on the gut microbiome of free- ORLOV OL, PIAČEK V, ZUKAL J, PIKULA J,
Publication Output Publication ranging western lowland gorillas. Microbiology 2018. Historic and geographic surveillance of 164: 40-44. Pseudogymnoascus destructans possible from collections of bat parasites. Transboundary and VOTÝPKA J, PAFČO B, MODRÝ D, MBOHLI D, Emerging Diseases 65: 303-308. TAGG N, PETRŽELKOVÁ KJ, 2018. An unexpected diversity of trypanosomatids in fecal ZÁRYBNICKÁ M, RIEGERT J, BEJČEK V, samples of great apes. International Journal for SEDLÁČEK F, ŠŤASTNÝ K, ŠINDELÁŘ J, Parasitology: Parasites and Wildlife 7: 322-325. HEROLDOVÁ M, VILÍMOVÁ J, ZIMA J, 2017. Long-term changes of small mammal VRTÍLEK M, POLAČIK M, REICHARD M, communities in heterogeneous landscapes of 2017. The role of energetic reserves during Central Europe. European Journal of Wildlife embryonic development of an annual killifish. Research 63: 89. Developmental Dynamics 246: 838-847. ZIEBA G, DUKOWSKA M, PRZYBYLSKI M, VRTÍLEK M, ŽÁK J, BLAŽEK R, POLAČIK M, FOX MG, SMITH C, 2018. Parental care CELLERINO A, REICHARD M, 2018. compromises feeding in the pumpkinseed Limited scope for reproductive senescence in (Lepomis gibbosus). Science of Nature 105: 26. wild populations of a short-lived fish.Science of Nature 105: 68. ZIEBA G, SMITH C, FOX MG, YAVNO S, ZÁHORSKÁ E, PRZYBYLSKI M, VRTÍLEK M, ŽÁK J, POLAČIK M, BLAŽEK R, MASSON G, CUCHEROUSSET J, REICHARD M, 2018. Longitudinal demographic VERREYCKEN H, VAN KLEEF HH, study of wild populations of African annual COPP GH, 2018. Red operculum spots, body killifish.Scientific Reports 8: 4774. size, maturation and evidence for a satellite
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male phenotype in non-native European into new territory: How Mascarene ridged populations of pumpkinseed Lepomis gibbosus. frogs diversified across Africa and Madagascar Ecology of Freshwater Fish 27: 874-883. to maintain their ecological niche. Molecular Phylogenetics and Evolution 106: 254–269. ZIMKUS BM, LAWSON LP, BAREJ MF, BARRATT CD, CHANNING A, DASH KM, ŽÁK J, REICHARD M, GVOŽDÍK L, 2018. DEHLING JM, DU PREEZ L, GEHRING P-S, Limited differentiation of fundamental thermal GREENBAUM E, GVOŽDÍK V, HARVEY J, niches within the killifish assemblage from KIELGAST J, KUSAMBA C, NAGY ZT, shallow temporary waters. Journal of Thermal PABIJAN M, PENNER J, RÖDEL M-O, Biology 78: 257–262. VENCES M, LÖTTERS S, 2017. Leapfrogging
Papers in other refereed journals
AMBÜHL P, VAN BOHEEMEN S, PIPEK P, balkánský (Sabanejewia balcanica) v České PROCHÁZKA P, EHRENGRUBER MU, 2017. republice – minulost, současnost a budoucnost. Gesangsdialekte der Goldammer Emberiza Lampetra. Bulletin pro výzkum a ochranu citrinella in der Schweiz. Ornithologische biodiverzity vodních toků 8: 90–102. Beobachter 114: 1–10. LUSK S, KOŠČO J, LUSKOVÁ V, HALAČKA K,
BLAŽEK R, POLAČIK M, REICHARD M, 2017. MENDEL J, KOŠÚTH P, 2017. The Publication Output Rasches Wachstum, frühe Reifung und kurze nonindigenous fish Perccottus glenii in the Generationenzeit bei afrikanischen annuellen Tisza River drainage, Eastern Slovakia – I. part: Fischen. DKG Journal 49: 131–141. history of invasion, habitat associations and genetic characteristics (results up to the ČEPELKA L, HEROLDOVÁ M, HOMOLKA M, year 2006). Lampetra. Bulletin pro výzkum PURCHART L, SUCHOMEL J, 2017. a ochranu biodiverzity vodních toků 8: 127–143. Diverzita a početnost drobných savců v lesních výsadbách na podzim 2015. Zprávy lesnického PIKULA J, BANĎOUCHOVÁ H, výzkumu 62: 189–196. KOVÁČOVÁ V, LINHART P, PIAČEK V, ZUKAL J, 2017. Reproduction of rescued JABLONSKI D, HEGNER D, SMOLINSKÝ R, vespertilionid bats (Nyctalus noctula) in 2017. Natrix natrix (Grass Snake). Maximum captivity: veterinary and physiologic aspects. elevation. Herpetological Review 48: 215. Veterinary Clinics of North America: Exotic Animal Practice 20: 665–677. KUTAL M, BELOTTI E, VOLFOVÁ J, MINÁRIKOVÁ T, BUFKA L, POLEDNÍK L, RUDOLF I, BLAŽEJOVÁ H, ŠEBESTA O, KROJEROVÁ J, BOJDA M, VÁŇA M, MENDEL J, PEŠKO J, BETÁŠOVÁ L, KUTALOVÁ L, BENEŠ J, FLOUSEK J, STRAKOVÁ P, ŠIKUTOVÁ S, HUBÁLEK Z, TOMÁŠEK V, KAFKA P, POLEDNÍKOVÁ K, 2018. West Nile virus (linie 2) v komárech POSPÍŠKOVÁ J, DEKAŘ P, MACHCINÍK B, na jižní Moravě – očekávání prvních KOUBEK P, DUĽA M, 2017. Výskyt velkých autochtonních lidských případů. Epidemiologie, šelem – rysa ostrovida (Lynx lynx), vlka Mikrobiologie, Imunologie 67: 44–46. obecného (Canis lupus) a medvěda hnědého (Ursus arctos) – a kočky divoké (Felis silvestris) VALLO P, VAN CAKENBERGHE V, 2017. v České republice a na západním Slovensku Advances in taxonomy of African house bats v letech 2012–2016 (Carnivora). Lynx 48: 93–107. (Scotophilus, Vespertilionidae). African Bat Conservation News 46: 4–9. LUSK S, HALAČKA K, MÁJSKY J, VETEŠNÍK L, MENDEL J, 2017. Sekavčík
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
Papers in proceedings
ADÁMEK Z, JURAJDA P, ZUKAL J, JANÁČ M, nádrží v povodí Moravy. In Účelové rybí MIKL L, ŠLAPANSKÝ L, VŠETIČKOVÁ L, obsádky na vodárenských nádržích: 5–13. PRÁŠEK V, ŠÚTOVSKÝ I, CHYTKA V, ISBN 978-80-7509-573-2. MRKVOVÁ M, 2017. Kvalita prostředí a potravní chování kapra ve vztahu MENDEL J, MAREŠ J, PALÍKOVÁ M, k přikrmování v polointenzivní rybniční HALAČKA K, ABAFFY P, ŠINDELKA R, akvakultuře. In Sborník referátů 4. ročníku 2018. Genetický monitoring aktuálního stavu odborné konference konané v Českých českých chovů pstruha duhového a sivena Budějovicích 9. a 10. února 2017: 43–53. v Evropském kontextu. In Zkušenosti s chovem ISBN 978-80-87699-10-2. lososovitých ryb s využitím jejich genetické identifikace: 12–18. ISBN 978-80-7509-590-9. BLÁBOLIL P, MATĚNA J, HALAČKA K, DURAS J, KUBEČKA J, 2018. Monitoring MENDEL J, MAREŠ J, PALÍKOVÁ M, tohoročních štik obecných a bolenů dravých HALAČKA K, VETEŠNÍK L, 2018. DNA ve vodní nádrži Švihov. In Účelové rybí servis a konkrétní genetické produkty obsádky na vodárenských nádržích: 30–36. pro chovatele nejen lososovitých ryb. ISBN 978-80-7509-573-2. In Zkušenosti s chovem lososovitých ryb s využitím jejich genetické identifikace: 35–39. HALAČKA K, MENDEL J, MAREŠ J, 2018. ISBN 978-80-7509-590-9. Morfologie chovaných skupin lososovitých ryb. In Zkušenosti s chovem lososovitých ryb MENDEL J, MAREŠ J, PALÍKOVÁ S, s využitím jejich genetické identifikace: 40–44. HALAČKA K, VETEŠNÍK L, ABAFFY P, ISBN 978-80-7509-590-9. ŠINDELKA R, 2018. Genetika ve službách biodiverzity a akvakultury – tři aktuální HALAČKA K, MENDEL J, MUŠKA M, případové studie. In Sborník příspěvků
Publication Output Publication MERTA L, VETEŠNÍK L, 2018. Historický z konference RYBIKON 2018: 64–71. a současný stav populací sekavce (Cobitis ISBN 978-80-7509-572-5. sp.) a sekavčíka balkánského (Sabanejewia balcanica) na území České republiky. In MIKL L, ADÁMEK Z, ŠLAPANSKÝ L, Sborník příspěvků z konference RYBIKON 2018: VŠETIČKOVÁ L, JURAJDA P, 2018. 41–45. ISBN 978-80-7509-572-5. Potrava dravých ryb vodárenských nádrží povodí Moravy. In Účelové rybí HALAČKA K, POŠTULKOVÁ E, KOPP R, obsádky na vodárenských nádržích: 20–29. MAREŠ J, VETEŠNÍK L, 2018. Možnosti ISBN 978-80-7509-573-2. značení vysazovaných ryb pomocí ARS – aplikace a detekce. In Účelové rybí ŠKRABÁNEK P, MARTÍNKOVÁ N, 2017. obsádky na vodárenských nádržích: 37–43. Extraction of outliers from imbalanced sets. ISBN 978-80-7509-573-2. In Hybrid Artificial Intelligent Systems, HAIS 2017: 402–412. Lecture Notes in Artificial JURAJDA P, 2018. Nepůvodní druhy ryb v ČR – Intelligence 10334. ISBN 978-3-319-59649-5. vážný problém nebo přehnané obavy? In Sborník příspěvků z konference RYBIKON 2018: VŠETIČKOVÁ L, MIKL L, ADÁMEK Z, 46–50. ISBN 978-80-7509-572-5. VAŠEK M, ŠVECOVÁ H, KOLÁŘOVÁ J, JURAJDA P, 2018. Hlaváč černoústý JURAJDA P, JANÁČ M, ROCHE K, MIKL L, v potravním řetězci našich vod. In Sborník ŠLAPANSKÝ L, KRECHLER I, ADÁMEK Z, příspěvků z konference RYBIKON 2018: 52–57. JURAJDOVÁ Z, HALAČKA K, 2018. ISBN 978-80-7509-572-5. Rybí společenstva pěti vodárenských
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SCIENTIFIC RESULTS
Book reviews
ČAPEK M, 2018: SHIRIHAI H, SVENSSON ZIMA J, 2017. Wilson DE, Lacher Jr TE, L: HANDBOOK OF WESTERN Mittermeier RA (eds): The Mammals of the PALEARCTIC BIRDS. Volume I: Larks to World – Vol. 7, Rodents II. Lynx Edicions, Warblers. Volume II: Flycatchers to Buntings. Barcelona, 1008 pp. ISBN 978-84-16728-04-0. Christopher Helm, London, 2018, 1271 pp. Folia Zoologica 66: 277. ISBN 978-1-4729-3757-5; ISBN 978-1-4729-3737-7. Sylvia 54: 89–96. ZIMA J, 2018. Wilson DE, Mittermeier RA (eds): The Mammals of the World – PROCHÁZKA P, 2017. Mikulica O, Vol. 8, Insectivores, Sloths and Colugos. Grim T, Schulze-Hagen K, Stokke BG: Lynx Edicions, Barcelona, 710 pp. The Cuckoo: the uninvited guest. Wild ISBN 978-84-16728-08-4. Folia Zoologica 67: 61. Nature Press, Plymouth, 2017, 160 pp. ISBN 978-0-9955673-0-6. Sylvia 53: 90–91.
Popular books and articles
BRYJA J, FORNŮSKOVÁ J, ZIMA J, KOLEČEK J, PROCHÁZKA P, 2017. Co nám SLABÁKOVÁ H, HONZA M (eds), 2017. prozradily geolokátory o migraci rákosníků
Biennial report 2015–2016. velkých? Kroužkovatel 23: 10–11. Publication Output ÚBO AV ČR, Brno, 104 pp. ISBN 978-80-87189-22-1. KOUBEK P, 2017. Co nového o muflonovi? Svět myslivosti: 18(1): 18–19. BARANČEKOVÁ M, 2018. Vlk, nebo kříženec? Svět myslivosti 19(7), 28–30. KOUBEK P, 2017. Domácí mazlíček, nebo plyšový vrah? Svět myslivosti 18(7): 23–25. BAŽANT M, ŠÁLEK M, HOŠKOVÁ L, 2018. Co děláme pro sýčka. Ptačí svět 25(1): 26. KOUBEK P, 2017. Tchoř stepní – kriticky ohrožený druh je u nás lovnou zvěří. ČAPEK M, 2017. Významný slovenský ornitológ Svět myslivosti 18(4): 16–19. Štefan Danko jubiloval. Tichodroma 29: 54–61. KOUBEK P, 2018. Africký mor prasat po česku. GVOŽDÍK V, 2018. Jiří Moravec šedesátiletý. Svět myslivosti 19(1): 29–31. Živa: 66(6): CLI. KROJEROVÁ J, 2017. Jelen sika – problematický HEROLDOVÁ M, HOMOLKA M, 2017. druh naší fauny. Veronica 31(2): 35–37. Muflon.Veronica 31(1): 30–31. PROCHÁZKA P, 2018. Sýček už nechce být HOMOLKA M, 2017. Potravní chování velkých poslem špatných zpráv. Ptačí svět 25(1): 9. býložravců v lesních ekosystémech. Veronica 31(1): 7–11. RUDOLF I, ŠEBESTA O, 2017. Invazní a nepůvodní druhy komárů aneb Máme JURAJDA P, 2018. Hlaváči v našich vodách. se u nás bát exotických nákaz? Živa 65(4): Živa 66(5): 269–271. 174–180.
JURAJDA P, 2018. Nepůvodní druhy v našich ŠÁLEK, M, 2018. Jak sýčkům pomoci? vodách. Rybářství 2018(7): 12–17. Ptačí svět 25(1): 18.
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ŠÁLEK M, 2018. Sýček se představuje. ŠÁLEK M, KLVAŇOVÁ A, HOŠEK J, 2018. Za Ptačí svět 25(1): 3–8. sovami lidských sídel. Ptačí svět 25(1): 13–16.
ŠÁLEK M, 2018. Tipy pro hledání sýčka. ŠUMBERA R, BRYJA J, 2018. Obludy vysoko Ptačí svět 25(1): 19. v horách: Evoluce endemických hlodavců v etiopské vysočině. Vesmír 97(12): 734–737. ŠÁLEK M, DOBRÝ P, 2018. Smrtící pasti pro ptáky lidských sídel. Ptačí svět 25(1): 24–25.
Patents, utility models, function samples, verified technologies, certified methodologies
HALAČKA K, POŠTULKOVÁ E, KOPP R, MAREŠ J, POŠTULKOVÁ E, PALÍKOVÁ M, MAREŠ J, 2017. Alternativní značení MENDEL J, 2018. Výsledky chovu vysazovaných ryb pro umožnění jejich lososovitých ryb různého genetického následného sledování. Verified technology původu. Verified technology R22/2018. R17/2017. ISBN 978-80-7509-547-3. ISBN 978-80-7509-625-8.
HALAČKA K, POŠTULKOVÁ E, MAREŠ J, MENDEL J, HALAČKA K, MAREŠ J, 2017. VETEŠNÍK L, 2018. Možnost využití Využití polymerázové řetězové reakce, značení štik pomocí Alizarinové červeně PCR-RFLP techniky a sekvenační analýzy a způsob terénní detekce značených k determinaci homozygotů, vnitrodruhových ryb. Verified technology R18/2018. heterozygotů a mezidruhových hybridů ISBN 978-80-7509-574-9. rodu Salvelinus v chovných zařízeních. Certified methodology R15/2017. HALAČKA K, VETEŠNÍK L, MAREŠ J, 2018. ISBN 978-80-7509-514-5.
Publication Output Publication Příprava a uchování vzorků ryb pro průtokovou cytometrii. Certified methodology R16/2017. MENDEL J, HALAČKA K, VETEŠNÍK L, 2018. ISBN 978-80-7509-582-4. Způsob identifikace evropských sladkovodních ryb a hybridů v biologických materiálech JURAJDA P, BEDNÁŘ R, 2017. Anoda metodou S7iCAPS. Patent UPV 307525. elektrolovného zařízení a elektrolovné zařízení s touto anodou. Utility model 30721. ZUKAL J, 2017. Diagnostická souprava ELISA pro stanovení syndromu bílého nosu u netopýrů. JURAJDA P, BEDNÁŘ R, 2017. Anoda Function sample. elektrolovného zařízení a elektrolovné zařízení s touto anodou. Utility model 30722.
48 | SELECTED SCIENTIFIC ACHIEVEMENTS
Evolutionary Ecology
Biodiversity
Parasites and diseases
SELECTED SCIENTIFIC ACHIEVEMENTS EVOLUTIONARY ECOLOGY
Evolutionary Ecology Evolutionary Ecology
Extremely rapid life history of African annual killifish ...... 52 Embryo adaptations to seasonal and unpredictable habitat in the African annual killifish ...... 53 Coevolution between a brood parasite and its hosts: parasite growth, begging behaviour and rearing costs imposed on hosts...... 54 Brood parasitism in fishes: African cuckoo catfish parasitizing mouthbrooding cichlids...... 54 Post-copulatory sexual selection and sperm phenotypes in songbirds ...... 56 Mate choice for genetic complementarity in grey partridges ...... 57 Bitterling fish ejaculate acts as olfactory sexual ornament...... 58 What is the thermal niche? Conceptual and empirical approaches...... 59 Winter activity of common bream (Abramis brama)...... 60 Population changes and movement ecology of European migratory passerines ...... 62
Photo by R. Blažek51
INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
EVOLUTIONARY ECOLOGY
Extremely rapid life history of African annual killifish
From the moment they leave the egg, annual killifish We discovered that killifish from dry regions live live their lives at incredible speed. African annual kil- shorter lives, and that this is also observed under lifish are found in freshly inundated pools that form laboratory conditions without the risk of habitat across the African savannah at the peak of the rainy desiccation. Shorter-lived populations also aged season, most of which will dry out again in three to more sharply, experiencing more rapid and steep- four weeks, killing all the fish. During our research er physiological deterioration than longer lived on demography and ageing of wild killifish popu- populations. Unexpectedly, this rapid ageing was lations, we found that killifish hatch, grow, reach not mirrored by faster growth and sexual matu- sexual maturity and reproduce in just two weeks. ration, or in a stronger investment into reproduc- In other pools, rainwater may remain for much tion. Further, long- and short-lived populations longer, with some pools containing water for over did not differ in their so-called “pace-of-life” as four months. Indeed, pools in wetter coastal areas neither metabolic activity nor behaviour differed, of Mozambique predictably have water for much perhaps being optimised at some other level than longer than those in the dry interior regions. We between populations. Overall, we demonstrated examined four annual killifish species, whose natu- that inter-population variability in African annual ral distribution includes both wet and dry regions, killifish lifespan and ageing is genetically correlated to assess whether different populations of the same and strongly affected by natural selection. species have evolved different life history optima.
BLAŽEK R, POLAČIK M, KAČER P, CELLERINO A, ŘEŽUCHA R, METHLING C, TOMÁŠEK O, SYSLOVÁ K, TERZIBASI TOZZINI E, ALBRECHT T, VRTÍLEK M, REICHARD M, 2017. Repeated intraspecific divergence in life span and aging of African annual fishes
Evolutionary Ecology Evolutionary along an aridity gradient. Evolution 71: 386–402. VRTÍLEK M, ŽÁK J, PŠENIČKA M, REICHARD M, 2018. Extremely rapid maturation of a wild African annual fish. Current Biology 28: R822-R824. VRTÍLEK M, ŽÁK J, POLAČIK M, BLAŽEK R, REICHARD M, 2018. Longitudinal demographic study of wild populations of African annual killifish. Scientific Reports8: 4774. VRTÍLEK M, ŽÁK J, BLAŽEK R, POLAČIK M, CELLERINO A, REICHARD M, 2018. Limited scope for reproductive senescence in wild populations of a short-lived fish. Science of Nature 105: 68.
A temporary pool in Mozambique, typical habitat 17-18-day-old African annual killifish. of African annual killifish. (Photo by M. Vrtílek) (Photo by M. Vrtílek)
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SELECTED SCIENTIFIC ACHIEVEMENTS EVOLUTIONARY ECOLOGY
Embryo adaptations to seasonal and unpredictable habitat in the African annual killifish
A peculiar group of annual fish has adapted to life to production of slow-developing eggs later. This is in small savannah pools that dry out annually. The an adaptive process as pools occasionally become fish produce drought-resistant eggs that persist in the desiccated but may be re-inundated during the rainy desiccated pool substrate over the dry season, and season. When this happens, the fast-developing eggs hatch as soon as the pool fills with rainwater. How- can give rise to the next generation of fish within ever, it sometimes happens that the first rains of the the same rainy season. In contrast, slow-developing season are not heavy enough to keep the pools full eggs are intended to enter diapause and remain like long enough for fish to grow, mature and reproduce. this throughout the dry season. Since energy con- We studied adaptations and strategies displayed sumption is kept to a minimum during diapause, by the eggs during their embryonic development duration of development is de-coupled from the to cope with such situations. In the wild, the egg amount of energetic reserve provided to the egg by hatch coincides with peak rainfall during the rainy the mother. Despite huge variation in the duration of season, with temporal and spatial synchronisation embryonic development, larger eggs always produce apparently following the geographic rainfall pat- larger juveniles. Over the killifish range, duration tern. The fish typically hatch synchronously, but and predictability of pool inundation varies along occasionally both protracted hatching and multiple a gradient; nevertheless, we found a similar degree age cohorts may also occur. Under laboratory condi- of developmental asynchrony across all areas exa- tions, we documented a strong bet-hedging strategy mined. Further, fish from more arid regions (where in the egg bank, with some eggs developing to the pools often desiccate during the rainy season) pro- pre-hatching stage in just three weeks, while others duced more eggs with short embryo developmental Evolutionary Ecology took many months to reach the pre-hatching stage. times, thereby enhancing the chances of hatching a Weak rainfall (which may be followed by rapid des- second generation within a single season. Our re- iccation) prompts hatching in a fraction of the eggs sults suggest that evolution of African annual fish while others remain in diapause (a resting stage). embryonic development has been remarkably fine- Duration of embryonic development appears to be tuned to the hostile and unpredictable environment under maternal control as, during her life, a female of temporary pools. initially produces fast-developing eggs and switches
POLAČIK M, REICHARD M, VRTÍLEK M, 2018. Local variation in embryo development rate in annual fish. Journal of Fish Biology, 92: 1359–1370. VRTÍLEK M, POLAČIK M, REICHARD M, 2017. The role of energetic reserves during embryonic development of an annual killifish. Developmental Dynamics, 246: 838–847. POLAČIK M, SMITH C, REICHARD M, 2017. Maternal source of variability in the embryo development of an annual killifish. Journal of Evolutionary Biology, 30: 738–749. REICHARD M, BLAŽEK R, POLAČIK M, VRTÍLEK M, 2017. Hatching date variability in wild populations of four coexisting species of African annual fishes. Developmental Dynamics, 246: 827–837.
Early (left) and late (right) annual killifish embryo developmental stages. (Photos by M. Polačik)
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
Coevolution between a brood parasite and its hosts: parasite growth, begging behaviour and rearing costs imposed on hosts
Growth is a key life history trait related to indi- foster parents into increased provisioning using vidual fitness. We studied sex differences in the various begging strategies. Apart from the normal growth of common cuckoo (Cuculus canorus) begging vocalisation produced during host feed- nestlings reared by two warbler hosts (genus ing visits, common cuckoo nestlings use a differ- Acrocephalus) and found that both sexes exhibited ent type of vocalisation in the absence of their fos- similar mass after hatching and grew at a similar ter parents. Our study confirmed experimentally, rate. Nevertheless, males achieved ~10% higher for the first time, that host-absent vocalisation of asymptotic mass than females, while fledging at a parasitic chick may be interpreted by foster par- a similar age as females. These findings imply that ents as a signal of hunger, thereby increasing host male nestlings may have higher needs than female feeding frequency. nestlings. Moreover, parasite chicks can fool their The fundamental brood parasite-host coevolu- tionary paradigm assumes that host care for the parasite is dramatically more costly than care for host’s own progeny. We quantified parasite-rearing costs in common redstarts (Phoenicurus phoenic- urus) raising either common cuckoo or their own chicks throughout the complete breeding cycle using multiple cost parameters, including incu- bation, brooding and feeding effort; length of pa- rental/host care; parent/host body condition and heterophil/lymphocyte ratio as a stress-level indi- cator. Contrary to traditional assumptions, rearing the much larger parasite was not associated with an overall increase in physiological or physical costs to the host but was similarly demanding as Evolutionary Ecology Evolutionary Great Reed Warblers (Acrocephalus arundinaceus) feeding a young parasitic chick. rearing its own brood. (Photo by M. Honza)
POŽGAYOVÁ M, PIÁLKOVÁ R, HONZA M, PROCHÁZKA P, 2018. Sex-specific nestling growth in an obligate brood parasite: Common Cuckoo males grow larger than females. Auk 135: 1033–1042. HONZA M, POŽGAYOVÁ M, PETRŽELKOVÁ A, PROCHÁZKA P, 2018. Does host-absent vocalisation of common cuckoo chicks increase hosts’ food provisioning behaviour? Behavioral Ecology and Sociobiology 72: 121 SAMAŠ P, RUTILA J, HONZA M, KYSUČAN M, GRIM T, 2018. Rearing a virulent common cuckoo is not extra costly for its only cavity- nesting host. Proceedings of the Royal Society. B – Biological Sciences 285: 20181710
Brood parasitism in fishes: African cuckoo catfish parasitizing mouthbrooding cichlids
Brood parasitism is a reproductive strategy where- occurring under a variety of possible scenarios. by parents pass all their care for the offspring onto In contrast, brood parasitism between parents of other hosts, i.e. individuals that act as foster parents different species is rare. The strategy has evolved for the parasitic offspring. This represents a spe- in birds and social insects (ants, bees, wasps and cial case of host-parasite relationship and is not some beetles), where it is termed social parasit- uncommon between parents of the same species, ism. Most of what we know about brood parasitism
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SELECTED SCIENTIFIC ACHIEVEMENTS EVOLUTIONARY ECOLOGY comes from studies on birds, where interspecific of juveniles from which her own progeny has often brood parasitism has evolved seven times with over been entirely eliminated. 100 parasitic species. We conducted the first experimental study on Recently, we began studying brood parasitism cuckoo catfish ever, using a unique technique that in a unique system, i.e. cuckoo catfish parasitising combines in vitro production of parasitic offspring mouth-brooding cichlid fishes in Lake Tanganyika. and experimental parasitism. We found that while Mouth-brooding cichlids incubate their offspring host cichlids can defend against parasitism, their in the mother’s buccal cavity, a widespread parental ability to defend varies due to a shared evolution- care strategy in Lake Tanganyika and other Afri- ary history between the parasitic catfish and host can lakes. The cuckoo catfish intrudes on a cichlid cichlid. Mouth-brooding cichlid species naturally spawning event and lays its own eggs, which are coexisting with cuckoo catfish in Lake Tanganyika mistakenly taken by the female cichlid for incu- can minimise the cost of parasitism by selective bation. The cuckoo catfish hatches quickly inside ejection of parasitic eggs. They also learn to deal the host’s mouth and immediately starts to feed on with the parasite, with females that have experi- its step-siblings (the host’s own offspring). After enced parasitism in the past being more successful 3–4 weeks, the parasitised female releases a clutch at defending themselves the next time. In contrast, Evolutionary Ecology
The cuckoo catfish and its cichlid host. Top left: a 7-day-old cuckoo catfish embryo; top right: a juvenile cuckoo catfish; bottom: Simochromis diagramma from Lake Tanganyika, a common host of the cuckoo catfish. (Photos by Y. Wenjing (top left) and R. Blažek)
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
cichlid species from other African lakes (where example, sometimes mistakenly eject their own they naturally do not coexist with cuckoo catfish) offspring, while this seldom happens to cichlids are unable to defend against parasitism, and are that lack antiparasitic defence abilities. It appears unable to learn from previous experience of incuba- that parasite abundance is the critical factor that tion failure. Nevertheless, such defensive behaviour determines whether it is better to resist or tolerate can be costly. Cichlids from Lake Tanganyika, for the parasite.
BLAŽEK R, POLAČIK M, SMITH C, HONZA M, MEYER A, REICHARD M, 2018. Success of cuckoo catfish brood parasitism reflects coevolutionary history and individual experience of their cichlid hosts. Science Advances 4: eaar4380.
Post-copulatory sexual selection and sperm phenotypes in songbirds
In addition to choosing her social mate, females capacity of carotenoids, as simultaneous carotenoid in socially monogamous birds frequently engage supplementation resulted in fewer sperm abnor- in extra-pair copulations outside their pair bonds. malities and high quality ejaculates. This exposes male gametes (sperm cells) to com- In another study, we demonstrated that inbreed- petition as gametes of more than one male often ing, resulting from close relatives breeding and pro- occur simultaneously in the female reproductive ducing homozygous offspring, has a negative effect tract, and only one sperm can fertilise the ova. on zebra finch sperm quality, resulting specifically Surprisingly little is known about factors affecting in a higher proportion of abnormal sperm in the sperm fertilisation capacity and male fertility in ejaculate. Interestingly, inbreeding also affected vertebrates, and in birds in particular. beak colouration. Taken together, this appears to We focused on two model songbird species, show that male beak colouration could provide the zebra finch Taeniopygia( guttata) and collared information on the quality of a males ejaculate to flycatcher (Ficedula albicollis), to explore associa- choosing females. Finally, our research revealed tions between sperm (ejaculate) quality, male or- that there is yet another, and so far unexplored, Evolutionary Ecology Evolutionary namentation and male fertilisation success. While mechanism associated with quality of ejaculate and we found little evidence for a link between sperm male fertilisation success in zebra finches. Nearly traits and male fertilisation success in collared fly- half of the variance in sperm morphology in this catchers, partner fertility may determine female species is explained by an inversion on the sex lifetime reproductive success in zebra finches, Z chromosome (males are ZZ and females ZW in where males and females form a life-long partner- birds). The sperm of males that are heterozygous ship and never change social partners. We showed for the inversion (ZZ*) have the longest mid-pieces that male ornamentation (carotenoid-based red and the highest velocity (so-called ‘super sperm‘). beaks in zebra finch males) serves as a signal of Furthermore, such males achieve highest fertility sperm quality. Careful experiments manipulating and highest siring success, both within-pair and oxidative stress and carotenoid intake in males extra-pair. In contrast, males homozygous for the revealed that investment in this ‘male showiness’ derived allele (Z*Z*) show detrimental sperm char- is traded-off against sperm resistance to oxidative acteristics and the lowest siring success. Our results challenge. More intense beak colouration predict- suggest that heterozygote advantage as the mecha- ed an increase in sperm velocity under controlled nism that maintains inversion polymorphism, and conditions but a decline under oxidative challenge. hence variance in sperm design and fitness in zebra Interestingly, we confirmed anin vivo antioxidant finches.
EDME A, ZOBAČ P, OPATOVÁ P, ŠPLÍCHALOVÁ P, MUNCLINGER P, ALBRECHT T, KRIST M, 2017. Do ornaments, arrival date, and sperm size influence mating and paternitz success in the collared flycatcher?Behavioral Ecology and Sociobiology 71:3. FORSTMEIER W, IHLE M, OPATOVÁ P, MARTIN K, KNIEF U, ALBRECHTOVÁ J, ALBRECHT T, KEMPENAERS B, 2017. Testing the phenotype-linked fertility hypothesis in the presence and absence of inbreeding. Journal of Evolutionary Biology 30: 968–976.
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KNIEF U, FORSTMEIER W, PEI Y, IHLE M, WANG D, MARTIN K, OPATOVÁ P, ALBRECHTOVÁ J, WITTIG M, FRANKE A, ALBRECHT T, KEMPENAERS B, 2017. A sex-chromosome inversion causes strong overdominance for sperm traits that affect siring success. Nature Ecology & Evolution, 1: 1177–1184. TOMÁŠEK O, ALBRECHTOVÁ J, NĚMCOVÁ M, OPATOVÁ P, ALBRECHT T, 2017. Trade-off between carotenoid-based sexual ornamentation and sperm resistance to oxidative challenge.Proceedings of the Royal Society B – Biological Sciences 284: 20162444.
Zebra finch sperm cell (top) and zebra finch female (left) and male (right). Sperm traits, such as length or speed, are important post-copulatory determinants of male reproductive success, whereas male beak colouration (redness) is associated with male attractiveness. (Photos by J. Albrechtová and O. Kauzál)
Egg
A A Evolutionary Ecology
Inversion AB*
Midpiece B* B*
AB* Flagellum Head
In zebra finches, a large inverted region on the Z chromosome restricts genetic recombination and allows suites of mutations on different genes within the region to accumulate. Heterozygous males AB*( on the picture) pro- duce the most successful sperm, also known as ‘super sperm’. (from: Fisher SH (2017). Supergene yields super sperm, Nature Ecology & Evolution 1: 1064).
Mate choice for genetic complementarity in grey partridges
Our view on bird mating systems has changed over more than one male and extra-pair males are of- recent decades with the advent of novel molecular ten of higher quality than within-pair partners. methods to determine paternity. It is now appar- The grey partridge Perdix( perdix), in contrast, is ent that sexual monogamy is an extremely rare one of just a few avian species for which genetic system in otherwise socially monogamous birds. polyandry has never been documented, i.e. males In most avian species studied to date, females are and females form pairs but females do not cheat on to some extent polyandrous, i.e. they mate with the males. In order to ascertain how this “puritan”
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
avian species chooses its partners, we assessed ge- (self-referential criteria, where mate attractiveness netic mechanisms of mate choice and social pair is determined by the fit of each partner‘s genome forming. Sexual selection has been hypothesised allowing the most viable offspring to be produced) as favouring mate choice resulting in production being used to explain MHC-based mating. Using of viable offspring with genotypes providing high pair formation data from a radio-tracked popula- pathogen resistance. Specific pathogen recognition tion, we found no evidence for absolute mate choice is mediated by genes of the major histocompatibili- criteria in grey partridges; rather, mate choice at the ty complex (MHC) encoding proteins fundamental MHC level was based on self-referential criteria as for adaptive immune response in jawed vertebrates. females preferentially paired with more MHC-dis- MHC genes are known to be involved in mate similar males. Our study thus provided one of the choice in a number of species, with “good genes” first pieces of evidence for MHC-based mate choice (absolute criteria, where certain males are bearers of for genetic complementarity in a strictly monog- beneficial alleles and are attractive to most females amous bird. in the population) and “genetic complementarity”
RYMEŠOVÁ D, KRÁLOVÁ T, PROMEROVÁ M, BRYJA J, TOMÁŠEK O, SVOBODOVÁ J, ŠMILAUER P, ŠÁLEK M, ALBRECHT T, 2017. Mate choice for major histocompatibility complex complementarity in a strictly monogamous bird, the grey partridge (Perdix perdix). Frontiers in Zoology 14: 9.
The grey partridge (Perdix perdix), a strictly monoga- mous galliform. Evolutionary Ecology Evolutionary (Photo by M. E. Šálek)
Bitterling fish ejaculate acts as olfactory sexual ornament
Chemical signals are a frequent component of One mechanism by which odour cues mediate mating systems, acting as pheromones to attract mating preference in vertebrates is through the in- the opposite sex and signalling an individual’s fluence of an individual’s major histocompatibility dominance, health status, genetic constitution or complex (MHC) genotype. The MHC is a family parasite burden. In fishes, olfactory signals elicit of highly polymorphic genes that play a key role specific responses to other individuals and play in resistance to infectious diseases. MHC polymor- a key role in courtship and mating. While we know phism generates a specific odour signature, which that pheromones are involved in mate choice de- is perceived by potential mates and affects their cisions, many aspects of this form of signalling are mating decisions. While our previous work on rose poorly understood, including signalling behaviour bitterling (Rhodeus ocellatus) reproductive behav- and signal structure. iour demonstrated that female mate preferences are
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SELECTED SCIENTIFIC ACHIEVEMENTS EVOLUTIONARY ECOLOGY affected by MHC structure, with females preferring oviposition at high male ejaculation rate. Finally, MHC-dissimilar mates, it is still not known how we demonstrated that female mate choice decisions female bitterling recognise MHC compatibility in were adaptive, with embryo survival being greater potential mates. when females mated with MHC-dissimilar part- We first showed that female oviposition was pos- ners. These results support a non-additive genet- itively stimulated by olfactory cues delivered in the ic basis to the rose bitterling mating system. We form of male sperm solution. We then confirmed propose that sperm acts as a releaser pheromone that females mated more often with MHC-dis- in bitterling, functioning as a sexual ornament sig- similar males and increased the probability of nalling male quality as a mate.
SMITH C, SPENCE R, REICHARD M, 2018. Sperm is a sexual ornament in rose bitterling. Journal of Evolutionary Biology 31: 1610–1622.
Male Chinese rose bitterling (Rhodeus ocellatus). (Photo by M. Reichard) Evolutionary Ecology
What is the thermal niche? Conceptual and empirical approaches
The term “thermal niche” is frequently used in ecol- estimation, even in thermally-challenging aquatic ogy. While the use of “thermal niche” has increased environments. Competing amphibian taxa, used as notably over the last 15 years, its meaning differs a model system, varied in the effectiveness of their between studies. We present a new conceptual uni- behavioural thermoregulation and thermal require- fication model for the term based on the proposition ments, corresponding to differences in their habitat that the choice of commonly used thermal phys- use. Using an optimality approach, indirect thermal iology traits for indirect thermal niche estimates requirement estimates produced similar results to depends on behavioural ability to buffer variation those based on thermal dependence of factorial in thermal environments, during periods of both aerobic scope. Species interactions induced acute, activity and inactivity (diel or seasonal). The result- rather than developmental, plastic responses in be- ing body temperature distribution determines the havioural thermoregulation, suggesting stability relative importance of key thermal physiology traits, of species thermal requirements within ecological thermal tolerance, thermal preferenda and tempera- communities. These results (i) clarify the meaning ture dependence of metabolic rate. This framework of thermal niche, which is a central concept across provides a guide for using the term ‘thermal niche’ various ecological sub-disciplines; (ii) contribute in ecological literature and identifies key areas for to our understanding of interspecific competition further research. among amphibian larvae; and (iii) help predict the Empirical results support the importance of impact of habitat destruction and climate change thermoregulatory behaviour for thermal niche on populations of these threatened vertebrates.
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GVOŽDÍK L, KRISTÍN P, 2017. Economic thermoregulatory response explains mismatch between thermal physiology and behaviour in newts. Journal of Experimental Biology 220: 1106–1111. JANČA M, GVOŽDÍK L, 2017. Costly neighbours: Heterospecific competitive interactions increase metabolic rates in dominant species. Scientific Reports 7: 5177. GVOŽDÍK L, 2018. Just what is the thermal niche? Oikos 127: 1701–1710. HLOUŠKOVÁ M, BALOGOVÁ M, KRŠÁKOVÁ V, GVOŽDÍK L, 2018. No trade-offs in interspecific interference ability and predation susceptibility in newt larvae. Ecology and Evolution 8: 9095–9104. WINTEROVÁ B, GVOŽDÍK L, 2018. Influence of interspecific competitors on behavioral thermoregulation: developmental or acute plasticity? Behavioral Ecology and Sociobiology 72: 169. ŽÁK J, REICHARD M, GVOŽDÍK L, 2018. Limited differentiation of fundamental thermal niches within the killifish assemblage from shallow temporary waters. Journal of Thermal Biology 78: 257–262.
A B C D
E F Evolutionary Ecology Evolutionary
Our research on defining thermal niche was undertaken using horizontal A,B( ) and vertical (C,D) thermal gradi- ents, mesocosm experiments (E) and intermittent respirometry across temperatures (F). (Photo by L. Gvoždík)
Winter activity of common bream (Abramis brama)
It is generally assumed that cyprinid fish overwin- abdominal cavity of the fish), we monitored the ter in reservoirs by forming dense, static shoals in spatial distribution and activity of adult common the deepest sections, their activity levels dropping bream (Abramis brama) during the winter at the 8-m drastically as their metabolisms slow due to the deep Hamry drinking water reservoir in the Bohe- drop in temperature. While this widespread no- mian-Moravian highlands. Surprisingly, we found tion is still a feature of many textbooks, the actual that overwintering bream did not cluster at the deep- behaviour of fish during their overwintering pe- est point of the reservoir; instead, they remained riod has been the subject of relatively little study. relatively active throughout the winter, though less Using radio telemetry (remote monitoring so than during the warmer growing season, with with the use of radio transmitters placed into the significant differences in activity patterns between
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SELECTED SCIENTIFIC ACHIEVEMENTS EVOLUTIONARY ECOLOGY individuals. Night movements were somewhat short- Our study showed that, under certain conditions, er than day movements, confirming the maintenance common bream populations display much higher of day time activity. As physical activity was main- levels of winter activity (and feeding) than previ- tained throughout the winter, it can be assumed that ously assumed, which has implications for both the fish were feeding as their energy reserves would fisheries management and for future studies as re- not have been sufficient to survive the entire winter. gards common bream (and other cyprinid species’) Activity of almost all fish was limited to the middle behavioural patterns, energy budgets and diet in section of the reservoir, coinciding with a 3–5 m deeper lakes and reservoirs. Clearly, there is still zone of warmer, oxygenated water below an inverse much to learn about the behaviour and ecology of thermocline. The fish appeared to avoid colder, shal- fish under natural conditions, especially in relation low zones (<1.5 m) at the inlet and near the banks to behaviour in winter when it is difficult to observe and the deepest zone (5–8 m) near the dam/outlet, fish using classical ichthyological methods. possibly due to poor food availability.
JURAJDA P, ROCHE K, HALAČKA K, MRKVOVÁ M, ZUKAL J, 2018. Winter activity of common bream (Abramis brama L.) in a European reservoir. Fisheries Management and Ecology 25: 163–171. Evolutionary Ecology
Common bream (Abramis brama L.) immediately af- ter implantation with a small radio transmitter in its lower abdominal cavity. (Photo by P. Jurajda)
Individual telemetry readings (black dots) showing the minimum winter activity range (shaded area) Using radio telemetry equipment to pinpoint tagged for one of eight tagged common bream in Hamry common bream (Abramis brama L.) in Hamry reservoir reservoir over 2010. over winter 2010. (Image by K. Roche) (Photo by P. Jurajda)
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Population changes and movement ecology of European migratory passerines
Study of movement ecology is crucial for under- movements across non-breeding grounds, we dis- standing a wide array of evolutionary processes and covered that three-quarters of great reed warblers for planning effective conservation interventions (Acrocephalus arundinaceus) exhibited intra-trop- at both the local and global scales. To address this, ical movements across sub-Saharan Africa. When we investigated the ecology of migratory birds at vegetation conditions deteriorated at the first both population and multi-species levels. First, we sites, migrating birds resided at their second sites, employed light-level geolocators and stable isotopic suggesting that the birds probably benefited from assignments to study patterns in the migration of improved conditions over those at the sites they three species of Acrocephalus warblers and barn had left. Finally, unlike the other species studied, swallows (Hirundo rustica) breeding at several the paddy field warbler Acrocephalus( agricola) oc- European sites. Moreover, we assessed population cupied non-breeding sites in southern Asia. One stability in 36 trans-Saharan migratory passerines individual from a breeding site in Bulgaria retraced at the continental level. We found that the major- recent range expansion and followed a rather con- ity of western European populations of Eurasian servative route instead of migrating directly to In- reed warbler (Acrocephalus scirpaceus) frequent- dia. In addition, evidence from stable hydrogen ly used the western Mediterranean flyway. How- analysis indicated a low degree of migratory con- ever, a higher absolute number of reed warblers nectivity at the non-breeding grounds. used the eastern flyway, with a migratory divide At the multi-species level, magnitude of popu- found in southeastern Central Europe. Individual lation trends grew with decreasing absolute and populations used different stopover areas during relative size of sub-Saharan non‐breeding ranges post‐ and pre‐breeding migration, resulting in an over 2001–2012. After repeating the analysis with anticlockwise loop migration pattern. Loop migra- trend direction, the relationship with non‐breed- tion was also documented in Czech barn swallows, ing range size disappeared, indicating that both with most birds using an eastern route for both population decreases and increases were frequent the spring and autumn migration, but shifted their among species with small non‐breeding range sizes. spring migration eastwards (anti-clockwise loops). Hence, species with small non‐breeding ranges are Evolutionary Ecology Evolutionary The remaining individuals used an eastern or cen- at a higher risk of population decline due to adverse tral route, and shifted their spring migration route factors such as habitat loss or climatic extremes, westwards (clockwise loops), while one individ- though their populations are also more likely to ual utilised both the eastern (autumn) and west- increase when conditions improve. ern (spring) migratory flyway. When evaluating
BRLÍK V, ILIEVA M, LISOVSKI S, VOIGT C, PROCHÁZKA P, 2018. First insights into the migration route and migratory connectivity of the Paddyfield Warbler using geolocator tagging and stable isotope analysis. Journal of Ornithology 159: 879–882. KLVAŇA P, CEPÁK J, MUNCLINGER P, MICHÁLKOVÁ R, TOMÁŠEK O, ALBRECHT T, 2018. Around the Mediterranean: an extreme example of loop migration in a long-distance migratory passerine. Journal of Avian Biology 49: jav-01595. KOLEČEK J, HAHN S, EMMENEGGER T, PROCHÁZKA P, 2018. Intra-tropical movements as a beneficial strategy for Palearctic migratory birds. Royal Society Open Science 5: 171675. KOLEČEK J, PROCHÁZKA P, IERONYMIDOU C, BURFIELD IJ, REIF J, 2018. Non-breeding range size predicts the magnitude of population trends in trans-Saharan migratory passerine birds. Oikos 127: 599–606. PROCHÁZKA P, BRLÍK V, YOHANNES E, MEISTER B, AUERSWALD J, ILIEVA M, HAHN S, 2018. Across a migratory divide: divergent migration directions and non-breeding grounds of Eurasian reed warblers revealed by geolocators and stable isotopes. Journal of Avian Biology 49: e01769. PROCHÁZKA P, HAHN S, ROLLAND S, VAN DER JEUGD H, CSÖRGŐ T, JIGUET F, MOKWA T, LIECHTI F, VANGELUWE D, KORNER- NIEVERGELT F, 2017. Delineating large-scale migratory connectivity of reed warblers using integrated multistate models.Diversity and Distributions 23: 27–40.
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A great reed warbler (Acrocephalus arundinaceus) tagged with a light-level geolocator that records light inten- sity. Light data can be used to ascertain time of local sunset and sunrise, subsequently allowing calculation of geographical position. Evolutionary Ecology (Photo by J. Koleček)
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Biodiversity Biodiversity
Complex speciation processes in Ethiopian rodents...... 66 Dating of the evolution of murid rodents...... 67 MtDNA heteroplasmia dynamics in mammals ...... 69 Evolution and biogeography of anguid lizards...... 70 Diversification in African amphibians ...... 70 Population genetic modelling of the Chinese pond mussels (Sinanodonta woodiana) invasion history ...... 72 Novel research on invasive gobiid fishes...... 73 Conservation genetics of Eurasian lynx in Central Europe...... 74 Genetic consequences of sika deer (Cervus nippon) introduction to Central Europe...... 75 Effective conservation of farmland biodiversity should support habitat heterogeneity and non-farmland habitats...... 76
Photo by V. Gvoždík.65
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BIODIVERSITY
Complex speciation processes in Ethiopian rodents
The Ethiopian highlands are the largest mountainous the highlands into two main parts by the Great Rift complex in Africa and, together with the Great Rift Valley. More recent genetic data, however, provide Valley, provide a wide spectrum of model situations evidence for a more complex speciation process, for evolutionary studies. The highlands have one of often in the form of so-called reticulate evolution the most striking elevational ecological gradients that combines divergence and hybridisation. During on Earth, exactly the kind of place where ecological colder Pleistocene periods, Afroalpine ecosystems speciation associated with complex genetic changes spread to lower elevations, allowing specialised is expected. Multiple steep climatic and vegetational high-elevation taxa to cross the Great Rift Valley gradients are separated by non-negligible migration where they then hybridised with local species, pos- barriers, though close enough to be connected un- sibly facilitating the colonisation of high elevation der different climatic conditions, which could cause mountains, e.g. through adaptive introgression of in situ differentiation to interfere with partial geo- mitochondrial genomes already adapted to high al- graphic isolation. As such, the extant species, often titudes and low oxygen concentrations. One impli- markedly differentiated and endemic, are expected cation of this finding is an inability to use mitochon- to possess complex genetic features whose investiga- drial DNA sequences for simple species barcoding, tion could inform us about the relative importance of at least for Ethiopian rodents. disruptive selection, temporary geographic isolation A further important feature of Ethiopian rodent and introgression in adaptive radiations. diversification is the important role of selection in Researchers from the Institute of Vertebrate Biol- extreme Afroalpine conditions, which is reflected ogy, together with their Ethiopian and Russian col- in the evolution of significantly distinct forms (e.g. leagues, used a unique collection of rodents collected Tachyoryctes macrocephalus, Stenocephalemys albo-
Biodiversity from across the Ethiopian highlands over the last caudata, genus Megadendromus) adapted to life on three decades to reconstruct phylogenetic relation- high plateaus. However, all these taxa are internal ships in selected genera through combined analysis lineages of more widespread congeners and their of multiple nuclear and mitochondrial markers. morphological (and possibly also physiological) ad- Previous models proposed a simple scenario of al- aptations are the result of rapid adaptive processes lopatric diversification following the separation of caused by strong selection.
The genus Stenocephalemys (here S. albipes) is an Ethiopian mountains provide a unique opportu- endemic Ethiopian clade of murid rodents. Six nity for evolutionary research. The Ethiopian Bale species (two not yet scientifically described) have Mountains, east of the Great Rift Valley, have a re- evolved through a combination of ecological and markable elevational gradient that provides highly allopatric diversification followed by hybridisation suitable conditions for studies on adaptation to and (adaptive) introgression of mitochondrial DNA high altitudes. (reticulate evolution). (Photo by J. Hošek) (Photo by M. Polák)
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Root rats of the genus Tachyoryctes are ecologically specialised subterranean/fossorial African rodents. We found that Ethiopia represents a cradle of evolutionary diversity; with the morphologically and ecologically distinct species T. macrocephalus representing an internal lineage of the genus that has evolved under strong selection pressure in the Afro-alpine conditions of the Bale Mountain range. All 12 formally described “morpho- species” in the Kenyan Highlands and the Albertine Rift Mountains are descendants of a single, relatively recent, “out-of-Ethiopia” colonisation event and, as such, should be synonymised. The shaded areas on the right panel represent the distribution of the genus according to the IUCN. (Image by P. Říha and R. Šumbera)
ŠUMBERA R, KRÁSOVÁ J, LAVRENCHENKO LA, MENGISTU S, BEKELE A, MIKULA O, BRYJA J, 2018. Ethiopian highlands as a cradle of
the African fossorial root-rats (genus Tachyoryctes), the genetic evidence. Molecular Phylogenetics and Evolution 126: 105–115. Biodiversity BRYJA J, KOSTIN D, MEHERETU Y, ŠUMBERA R, BRYJOVÁ A, KASSO M, MIKULA O, LAVRENCHENKO LA, 2018. Reticulate Pleistocene evolution of Ethiopian rodent genus along remarkable altitudinal gradient. Molecular Phylogenetics and Evolution 118: 75–87. LAVRENCHENKO L, NADJAFOVA R, BEKELE A, MIRONOVA T, BRYJA J, 2017. Phylogenetic position of a monotypic Ethiopian endemic rodent genus Megadendromus (Rodentia, Nesomyidae). Mammalia 81: 71–82.
Dating of the evolution of murid rodents
Murid rodents (Muridae) are the most diverse mam- mal family, encompassing around 155 genera and more than 800 recognised species, including two major biomedical models, the brown rat (Rattus norvegicus) and the house mouse (Mus musculus). Despite their practical importance, their evolution- ary histories have not yet been sufficiently resolved, and this is especially true for the dating of diver- gence. Researchers from the Institute of Vertebrate Biology, together with French mammalogists and a Japanese palaeontologist, reconstructed a dated complete family phylogeny using a large multilocus dataset (six nuclear and nine mitochondrial gene African Grass rats (genus Arvicanthis) are a highly fragments) encompassing 161 species representing successful group of murid rodents living in various 82 distinct murid genera from four extant sub-fam- types of open habitat in tropical Africa. ilies (Deomyinae, Gerbillinae, Lophiomyinae, and (Photo by T. Aghová) Murinae). Compared with previous studies, this
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INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018 Biodiversity
Dated murid rodent phylogeny based on a large multi-locus analysis and nine fossil constraints reliably placed on the phylogenetic tree (numbers 1–9). Time axis in Million years before present. (Reproduced from Aghová et al. 2018)
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SELECTED SCIENTIFIC ACHIEVEMENTS BIODIVERSITY work stands out for its implementation of multi- sub-families (Deomyinae, Gerbillinae and Lophio- ple fossil constraints within the family thanks to myinae) are inferred to have originated in the Afro- a thorough review of the fossil record, after which tropical region, while the most diverse subfamily, the the fossils were reliably placed on the phylogenetic Murinae, has its origin in the Indomalayan region. tree. Based on nine controlled fossil calibrations, Biogeographic reconstructions also allowed us to the inferred temporal timeframe indicates that the show where and when distinct lineages of the latter murid family likely originated around 20 million- subfamily colonised Africa (at least 3–4 times), the years-ago, and that most major lineages started their Palaearctic region and Australasia. diversification around 10 million-years-ago. Three
AGHOVÁ T, KIMURA Y, BRYJA J, DOBIGNY G, GRANJON L, KERGOAT GJ, 2018. Fossils know it best: Using a new set of fossil calibrations to improve the temporal phylogenetic framework of murid rodents (Rodentia: Muridae). Molecular Phylogenetics and Evolution 128: 98–111.
MtDNA heteroplasmia dynamics in mammals
DNA from mitochondria (mtDNA), the pow- erhouse of the cell, is part of the extra-nuclear
genetic information complex and is passed down Biodiversity from mother to child. In mammals, the maternal mtDNA line is inherited as the embryo is derived from the egg. However, mutations may mean that the mother can have multiple types of mtDNA in her egg (heteroplasmia), and mothers that carry a mtDNA mutation may potentially pass a disease on to their child, such as hereditary diabetes. We assessed heteroplasmic dynamics in moth- ers of different ages and their offspring using two mouse sp. models. Variability in the representa- DNA from mitochondria (mtDNA), the powerhouse tion of different types of mtDNA was dependent of the cell, is passed down from mother to child. on the mouse model (genotype) and increased There are many mitochondria in each cell and dramatically with maternal age. This suggests that these may have different genetic features. If the while the proportion of mtDNA in younger moth- mother carries a mixture of mitochondrial DNA types, this can make it hard to say which features ers is similar, the probability of transmitting more their children will inherit. Family planning and cli- extreme (low and high) levels of a genetic feature nical therapies can also be challenging if mothers increases with the mother’s age as older mothers carry a disease-causing mtDNA mutation. displayed greater mtDNA variability. (Photo by A. Fornůsková)
BURGSTALLER JP, KOLBE T, HAVLICEK V, HEMBACH S, POULTON J, PIÁLEK J, STEINBORN R, RÜLICKE T, BREM G, JONES NS, JOHNSTON IG, 2018. Large-scale genetic analysis reveals mammalian mtDNA heteroplasmy dynamics and variance increase through lifetimes and generations. Nature Communications 9: 2488.
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Evolution and biogeography of anguid lizards
Our studies focus on the evolutionary history, bioge- available in previously published data from Cen- ography and evolutionary-ecological relationships in tral Europe and the northern Balkans. Anguis fra- legless lizards of the anguid family (Anguidae), and gilis was represented by a single haplogroup, while particularly of two genera, the slowworm (Anguis) three haplogroups were recorded for A. colchica, and the glass lizard (Pseudopus). suggesting four independent sources/refugia for A phylogeographic study on Central Europe- the postglacial recolonisation of northern Central an populations of two slowworm species (Anguis Europe. The mitochondrial contact zone appears fragilis, A. colchica) focussed on the situation in to mirror the border between the lowlands of the Poland and the surrounding regions as a mito- North European and East European Plains and the chondrial contact zone was expected to occur be- south-eastern Polish uplands, the River Vistula tween the two species. Haplotypes of both species apparantly not representing a biogeographic bar- were recorded in the study area based on both rier. Our confirmation of two slowworm species new mitochondrial DNA sequences and those in Poland has implications for Polish conservation legislation. A second phylogeographic study was undertak- en on European glass lizards (Pseudopus apodus) from south-eastern Europe and western Asia. Based on analysis of DNA variation, we propose that the European glass lizard has survived historically un- suitable climatic periods in the Anatolian, Levant and Transcaucasian regions. Present low genetic variation indicates population extinctions dur- ing these unsuitable climatic periods, followed by subsequent rapid population expansion into their
Biodiversity present-day range. This finding is in contrast with many other species of Western Palearctic reptile, A male European slowworm (Anguis fragilis). which commonly survived in numerous smaller (Photo by V. Gvoždík) refugia and display more complex spatial genetic variation (phylogeographic pattern).
JANDZIK D, JABLONSKI D, ZINENKO O, KUKUSHKIN OV, MORAVEC J, GVOŽDÍK V, 2018. Pleistocene extinctions and recent expansions in an anguid lizard of the genus Pseudopus. Zoologica Scripta 47: 21–32. MIKULÍČEK P, JABLONSKI D, PÁLENÍK M, GVOŽDÍK V, JANDZIK D, 2018. Characterization of microsatellite markers in the genera Anguis and Pseudopus (Reptilia: Anguidae). Salamandra 54: 158–162. JABLONSKI D, NAJBAR B, GROCHOWALSKA R, GVOŽDÍK V, STRZAŁA T, 2017. Phylogeography and postglacial colonization of Central Europe by Anguis fragilis and Anguis colchica. Amphibia-Reptilia 38: 562–569.
Diversification in African amphibians
The study of species diversification assesses how As part of an international network, we have new species arise, where they originate and how been involved in several research projects study- such species have diversified over time. It is our ing diversification processes in different anuran long-term aim to study the diversification (species (frog) model taxa. There is growing support for formation, diversity and systematics) of amphibians the important role played by forest refugia in driv- within Sub-Saharan Africa. ing intraspecific divergence in the Guineo-Congo- lian rainforest and Gulf of Guinea archipelago of
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Central Africa, particularly in relation to hyperoliid models (Hyperoliidae), particulrly Afrixalus para- dorsalis and three Hyperolius species complexes (H. cinnamomeoventris, H. ocellatus, H. tubercula- tus). It has been demonstrated that fluctuating sea levels periodically expose a land bridge connecting Bioko Island with the mainland Guineo-Congolian forest, and that habitats across the exposed land bridge likely enabled dispersal of some species but not others. To date, there is no evidence that rivers have acted as biogeographic barriers across any of the species complexes. Despite marked differ- ences in the geographic extent of stable climates and temporal estimates of divergence among the A male African leaf-folding frog (Afrixalus paradorsalis). species complexes, we recorded a shared pattern (Photo by V. Gvoždík) of intermittent climatic suitability with recent pop- ulation connectivity and demographic expansion across the Congo Basin. This pattern supports the speciation events took place throughout the Mio- hypothesis that genetic exchange across the Congo cene, including “out-of-Africa” overseas dispersal Basin during humid periods, followed by vicariance events to Madagascar in the east and to Sao Tome during arid periods, has shaped regional diversity. in the west. The bioclimatic niche was remarkably In addition, several distinct lineages were identified well conserved, with most species tolerating similar
among our focal taxa, some of which may reflect temperature and rainfall conditions common to Biodiversity incipient or unrecognised species. the Central African region. TheP. mascareniensis A second model was based on the Mascarene complex provides insights into how the bioclimatic ridged frog (Ptychadena mascareniensis), a species niche shaped current biogeographic patterns, with complex that includes numerous lineages occur- niche conservatism being exhibited by the Central ring mostly in humid savannahs and open forests African radiation and niche divergence shaping of mainland Africa, Madagascar, the Seychelles populations in West Africa and Madagascar. As and the Mascarene Islands. High levels of genet- such, central Africa, including the Albertine Rift ic differentiation yielding ten distinct lineages or region, has been an important centre of diversifi- operational taxonomic units were detected. Most cation for this species complex.
CHARLES KL, BELL RC, BLACKBURN DC, BURGER M, FUJITA MK, GVOŽDÍK V, JONGSMA GFM, TALLA KOUETE M, LEACHÉ AD, PORTIK DM, 2018. Sky, sea, and forest islands: Diversification in the African leaf-folding frog Afrixalus paradorsalis (Anura: Hyperoliidae) of the Lower Guineo-Congolian rain forest. Journal of Biogeography 45: 1781–1794. DOLINAY M, TASSE TABOUE GC, FOKAM EB, GVOŽDÍK V, 2018. Geographic and altitudinal range extension of Arthroleptis palava (Anura: Arthroleptidae) from the Cameroon Volcanic Line. Herpetology Notes 11: 557–560. BELL RC, PARRA JL, BADJEDJEA G, BAREJ MF, BLACKBURN DC, BURGER M, CHANNING A, DEHLING JM, GREENBAUM E, GVOŽDÍK V, KIELGAST J, KUSAMBA C, LÖTTERS S, McLAUGHLIN PJ, NAGY ZT, RÖDEL M-O, PORTIK DM, STUART BL, VANDERWAL J, ZASSI- BOULOU AG, ZAMUDIO KR, 2017. Idiosyncratic responses to climate-driven forest fragmentation and marine incursions in reed frogs from Central Africa and the Gulf of Guinea Islands. Molecular Ecology 26: 5223–5244. ZIMKUS BM, LAWSON LP, BAREJ MF, BARRATT CD, CHANNING A, DASH KM, DEHLING JM, DU PREEZ L, GEHRING P-S, GREENBAUM E, GVOŽDÍK V, HARVEY J, KIELGAST J, KUSAMBA C, NAGY ZT, PABIJAN M, PENNER J, RÖDEL M-O, VENCES M, LÖTTERS S, 2017. Leapfrogging into new territory: How Mascarene ridged frogs diversified across Africa and Madagascar to maintain their ecological niche. Molecular Phylogenetics and Evolution 106: 254–269.
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Population genetic modelling of the Chinese pond mussels (Sinanodonta woodiana) invasion history
Non-native species sometimes rapidly increase their a large part of East Asia. As with many other cur- abundance and distribution, often with associated rently invasive species, S. woodiana persisted in Eu- negative impacts on native species, communities and ropean waters as several isolated populations locally ecosystems. As such, understanding the invasive po- restricted to zones with artificially elevated water tential of species outside their native range is one of temperatures and showed no signs of spreading. the most pressing questions in applied evolution- However, S. woodiana suddenly started to spread ary and ecological research. We know that different rapidly across Europe after 2005 and is now a very species vary in their propensity to become invasive common species across most of the continent. when translocated outside their native ranges, but we We described invasion pathways of S. woodiana are only beginning to understand the characteristics using fine-scale sampling of populations and var- linked to invasiveness. iable genetic markers. We rejected the hypothesis The Chinese pond mussel (Sinanodonta woodi- that the sudden spread of S. woodiana populations ana), easily recognised by its large shell, is native to across Europe was associated with introduction of a new lineage, better adapted to colder waters than the initial European S. woodiana populations. Fish are often parasitised on their fins and gills by the mussel’s larval stage and it appears to have been the repeated transport of fish between regions that established a regular connection (and frequent gene flow) between otherwise isolated populations. These frequent connections have facilitated adap- tation to the colder conditions of European waters, compared with their native habitats in Asia.
Biodiversity Frequent transport of fish juveniles for fisheries purposes has not only helped S. woodiana popula- tions to spread across Europe, but also to greatly increase their adaptive genetic potential, facilitat- ing their adaptation to colder waters. In addition to understanding general patterns of biological A large Chinese pond mussel (Sinanodonta woo- invasion, our study also provides detailed map- diana) collected in Central Moravia. ping of S. woodiana colonisation within Europe, (Photo by R. Hečová) starting from a single isolated Romanian popula- tion in 1979 to its current widespread occurrence.
KONEČNÝ A, POPA O, BARTÁKOVÁ V, DOUDA K, BRYJA J, SMITH C, POPA LO, REICHARD M, 2018. Modelling the invasion history of Sinanodonta woodiana in Europe: tracking the routes of a sedentary aquatic invader with mobile parasitic larvae. Evolutionary Applications 11: 1975–1989.
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Novel research on invasive gobiid fishes
Several Ponto-Caspian gobiid species have ex- suggests high initial propagule pressure, most likely panded their ranges throughout Europe and North connected with transport via shipping. Finally, an America since the 1990s. For these species, rapid increase in the genetic diversity of round goby sam- population explosions in newly colonised areas are ples from non-native areas suggests strong prop- typical. Abundant populations of non-native spe- agule pressure with introductions from multiple cies have the potential to affect recipient systems sources followed by admixture, the latter stressing in a number of ways, including predation on and large inland ports as natural hot-spots for admix- competition with native fishes, predation on native ture of invasive aquatic species and their role in the macroinvertebrates or alterations to food-webs and onward spread of admixed populations to novel host-parasite interactions. Consequently, our team locations. This research provided support for (i) has devoted much effort to studying mechanisms of a Danubian origin for all three goby species in the invasions and impacts on recipient systems. Rhine, (ii) lower genetic diversity in fish colonising Our recent research has focused on tracing non-navigable tributaries, and (iii) provided early gobiid invasive histories in European freshwa- genetic data for a newly established round goby ters. While genetic studies have been widely used population on the River Elbe. to assess the invasion history of gobiids in North While Ponto-Caspian gobiids are believed to America, complex genetic studies involving mul- represent a significant negative threat to native tiple sites and species have been less common fish assemblages, relatively few studies have tried in Europe, severely limiting our understanding to document actual impacts, most being short-term of invasion processes along navigable rivers and and/or laboratory based. To address this, we under-
their tributaries. We used both nuclear and mito- took further research focused on demonstrating Biodiversity chondrial markers to assess genetic diversity and observable in situ impacts on fish assemblages. To structure in native and non-native populations of this end, long-term monitoring studies were con- three gobiids, the Western tubenose goby (Pro- ducted on the middle Danube and its tributaries. terorhinus semilunaris), round goby (Neogobius We observed no negative impacts on native fish melanostomus) and bighead goby (Ponticola kes- diversity or abundance attributable to round goby sleri), sampled from the main areas of their joint in either the middle Danube or its tributaries. Es- distribution, i.e. the lower Danube, middle Danube pecially surprising was the lack of impact on native and lower Rhine. Our research revealed significant European bullhead (Cottus gobio) in the Danube. differences in the invasion histories of these three Though cottids are presently considered to be most species, despite their joint distribution. A founder vulnerable to gobiid invasion, we observed no neg- effect observed in tubenose goby populations sug- ative trend in bullhead abundance over the eight- gests one or very few introduction events and less year dataset, with populations remaining stable and dependence on shipping as a dispersal vector, while at similar abundances to gobiids. In the context no genetic structuring in bighead goby populations of other impact case studies, some of which have
Sampling non-native gobies by electro- fishing along the banks of the lower River Rhine. (Photo by L. Mikl)
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demonstrated severe negative impacts on native round goby on tubenose goby, suggesting antago- fishes, our research suggests that gobiid impacts nistic interactions between the two gobiid invaders on ichthyofauna are region-specific, being driven and providing an alternative exception to the ‘in- by local idiosyncrasies of the invaded systems. The vasional meltdown’ hypothesis. research also revealed potential negative impacts of
Long-term movements of invasive round gobies (Neogobius melanostomus) were assessed using mark-recapture techniques, with individual gobies tagged with colour- and number-specific pit-tags. (Photo by L. Šlapanský)
JANÁČ M, ROCHE K, ŠLAPANSKÝ L, POLAČIK M, JURAJDA P, 2018. Long-term monitoring of native bullhead and invasive gobiids in the Danubian rip-rap zone, Hydrobiologia 807: 263-275. JANÁČ M, BRYJA J, ONDRAČKOVÁ M, MENDEL J, JURAJDA P, 2017. Genetic structure of three invasive gobiid species along the Danube-Rhine invasion corridor: similar distributions, different histories. Aquatic Invasions 12: 551–564. MIKL L, ADÁMEK Z, ROCHE K, VŠETIČKOVÁ L, ŠLAPANSKÝ L, JURAJDA P, 2017. Invasive Ponto-Caspian gobies in the diet of piscivorous fish in a European lowland river. Fundamental and Applied Limnology / Archiv für Hydrobiologie 190: 157–171. ŠLAPANSKÝ L, JANÁČ M, ROCHE K, MIKL L, JURAJDA P, 2017. Expansion of round gobies in a non-navigable river system. Limnologica 67: 27–36. Biodiversity
Conservation genetics of Eurasian lynx in Central Europe
In a unique long-term research programme, we utilised genetic analysis of non-invasively col- lected samples from the Eurasian lynx (i.e. faeces, hair) to study the social structure of this elusive and endangered species. In doing so, we were able to reconstruct the genealogy of individual lynx in a small, partially isolated, population at the edge of their range in the West Carpathians. The results confirmed a low population density (eight adults on average) and a relatively high level of fluctua- tion in the number of individuals (of 40 genotyped individuals, just six were present in the study area for longer than four years). Female offspring usu- ally settled in or near the maternal home range, Two Eurasian lynx (Lynx lynx) kittens photographed in June 2013. which contributed to the formation of two separate family groups comprising closely related animals (Photo by P. Konupka) that mated together (i.e. father-daughter, grandfa- ther-granddaughter). Breeding with close relatives not only significantly decreased the effective pop- variability. Our study confirmed that, even if this ulation size but also decreased population genetic range-edge population were to be connected with
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KROJEROVÁ-PROKEŠOVÁ J, TURBAKOVÁ B, JELENČIČ M, BOJDA M, KUTAL M, SKRBINŠEK T, KOUBEK P, BRYJA J, 2018. Genetic constraints of population expansion of the Carpathian lynx at the western edge of its native distribution range in Central Europe. Heredity 122: 785-799.
Two male adult lynx photographed in March 2015 using the same camera. Genetic analysis confirmed that the male on the left was the son of the male on the right. (Photos from parallel camera-trapping research undertaken in cooperation with Friends of the Earth, Olomouc) Biodiversity
Genetic consequences of sika deer (Cervus nippon) introduction to Central Europe
In the late-nineteenth and early-twentieth centu- lowest variability. Multiple introductions, rapid ry, sika deer were introduced into many countries population growth and possible hybridisation across Eurasia and Australasia and to North Amer- with red deer appear to have helped the successful ica. Subsequently, free-living invasive populations expansion of sika within the Czech Republic. The became established in many countries, including the Czech Republic, where the expanding sika population now causes serious problems through over- grazing, browsing damage and through competition and hybridisation with na- tive red deer. Our research focused on the effect of introduction on the genetic makeup of introduced sika deer in Cen- tral Europe (founder effect). We detect- ed a high level of genetic differentiation between native Japanese sika and the introduced Czech populations. Genet- ic variability was generally low due to recent demographic events (founder effect in the Czech population, bot- tlenecks in Japanese populations); Increasing numbers of Japanese sika deer legally culled per year however, genetic variability differed (1962–2014) confirm expansion of the Czech sika population. greatly between subpopulations, with (Reproduced from Krojerová-Prokešová et al. 2017) the Czech populations not displaying
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results also indicate that male-mediated gene flow between introduced sika and native red deer is now and human-mediated translocations have signifi- being studied intensively in both the Czech Repub- cantly influenced the current genetic structure of lic and the far east of Russia, where distribution native sika populations in Japan. Hybridisation ranges of these species naturally overlap.
KROJEROVÁ-PROKEŠOVÁ J, BARANČEKOVÁ M, KAWATA Y, OSHIDA T, IGOTA H, KOUBEK P, 2017. Genetic differentiation between introduced Central European sika and source populations in Japan: effects of isolation and demographic events. Biological Invasions 19: 2125–2141.
Sika females (left) and a male (right) in winter coat without the typical white spots. (Photo by J. Červený)
Biodiversity Effective conservation of farmland biodiversity should support habitat heterogeneity and non-farmland habitats
Agricultural intensification has substantially re- In our first study, we investigated the effects of duced multi-scale habitat heterogeneity through in- habitat configuration and composition on var- creased field size and loss of semi-natural structures ious taxa in two adjacent, intensively managed, resulting in large-scale deterioration of farmland arable-dominated farmland landscapes. More biodiversity. Within the European Union, substan- specifically, we used data from fine-scale habitat tial resources are currently spent on conservation mapping at two spatial scales and data on abun- measures aimed at halting the decline of farmland dance and species richness of spiders, butterflies, biodiversity; however, the effects of these measures birds and European hare abundance. Our study are usually not clear and several studies have even clearly demonstrated that smaller patch sizes and reported no positive effects. One reason for the larger areas of non-cropped elements were related low effectiveness of such conservation measures to higher farmland biodiversity of different taxo- could be incomplete identification of habitats act- nomic groups. Thus, conservation measures pro- ing as hotspots for farmland biodiversity. However, moting habitat heterogeneity, namely decreasing there is increasing evidence showing that a sub- field size and increasing the availability of non- stantial number of rare and declining farmland cropped elements, may be valuable tools for con- taxa exclusively inhabit non-farmland habitats. In serving declining farmland biodiversity, especially our research, we focused on the effects of habitat in regions with substantial reduction of semi-nat- heterogeneity and non-farmland habitat as regards ural habitats and large crop fields. Furthermore, conservation of farmland biodiversity. promoting structurally diverse farmlands may contribute substantially to ecosystem function and
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SELECTED SCIENTIFIC ACHIEVEMENTS BIODIVERSITY services as many taxa and species from diverse conservation concern. Moreover, the importance ecological guilds are considered important pest of farmsteads increases in winter when many red‐ predators and crop pollinators. listed species and resident farmland birds change In our second study, we investigated the im- from a preference for farmland and abandoned portance of agricultural farmsteads for alpha and farmsteads to active farmsteads producing food. gamma diversity of farmland birds. We demon- Our study shows that there is a need to broaden strated that farmsteads, especially those with an- our approach to conservation of rare and declin- imal and plant production, are hotspots for farm- ing farmland birds by paying more attention to land birds and key habitats for several species of non‐farmland habitats, such as farmsteads.
ŠÁLEK M, HULA V, KIPSON M, DAŇKOVÁ R, NIEDOBOVÁ J, GAMERO A, 2018. Bringing diversity back to agriculture: Smaller fields and non-crop elements enhance biodiversity in intensively managed arable farmlands. Ecological Indicators 90: 65–73. ŠÁLEK M, BAŽANT M, ŻMIHORSKI M, 2018. Active farmsteads are year-round strongholds for farmland birds. Journal of Applied Ecology 55: 1908–1918. Biodiversity
The Northern Lapwing (Vanellus vanellus), a spe- cies typical of agricultural landscapes, has shown a population decline over recent years.Presence Smaller patch sizes and larger areas of non-cropped of marshy patches and/or meadows at breeding elements result in higher biodiversity. grounds has been positively correlated with la- (Photo by M. Šálek) pwing abundance. In addition, our results indicate higher hatching success in ploughed fields and at sites with marshy patches. (Photo by M. Šálek)
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78 Parasites and diseases
Effects of multiple stressors on bat hibernation ...... 80 Evolution of parasites in host secondary contact zones ...... 82 The importance of host phylogeographic structure in spatial spread of viruses: Mastomys natalensis arenaviruses in Tanzania ...... 83 Evolution of innate immunity receptors in passerine birds ...... 84 Differences in evolutionary patterns of bird and mammal gut microbiota ...... 85 Impact of stress and parasite infection on the gastrointestinal microbiome of western lowland gorillas...... 86 West Nile virus in overwintering mosquitoes: implications for its persistence during unfavourable conditions ...... 86 Hepatitis E virus found in archived wild boar samples: established virus circulation and potential risks for the consumer. . . 87
(Photo by A. Ribas)
INSTITUTE OF VERTEBRATE BIOLOGY | THE CZECH ACADEMY OF SCIENCES BIENNIAL REPORT 2017–2018
PARASITES AND DISEASES
Effects of multiple stressors on bat hibernation
Hibernation is an adaptation of temperate zone can mitigate the negative impacts of infection by bats that allows them to survive scarcity of ali- modifying their selection of hibernation site. We mentary resources in winter. With lowered body have shown that bats in hibernacula with lower temperature, the animal’s metabolic functions are environmental temperatures develop less severe suppressed which, together with lowered energet- symptoms of white-nose syndrome, an infectious ic costs for thermoregulation, makes hibernation disease caused by P. destructans. As such, a shift a behavioural adaptation of energy metabolism. by hibernators to lower temperature sites can be The frequency of active euthermic periods during seen as a behavioural adaptation to presence of the torpor is a key factor determining survival during fungus, whose growth is limited by low tempera- hibernation as fat reserves are rapidly depleted with tures. In addition to behaviour promoting energy repeated arousals. In a recent study, we observed conservation during hibernation, we also found active hibernating bats that showed no body tem- that bats have evolved genetic adaptations to skin perature elevation to the euthermic stage (low tem- infection, with genes involved in skin integrity and perature movements). This ability to adjust roosting down-regulation of the immune reaction being un- position (e.g. when microclimatic conditions or der positive selection, indicating that energy con- conspecific disturbances alter roost suitability) servation and the protective role of bodily barriers without body temperature elevation represents act together to improve host survival. an important decrease in energy expenditure and The survival of hibernating bats is affected by significantly changes our understanding of basic multiple endogenous and exogenous factors, in- hibernation principles. cluding fat reserves, torpor length and arousal pat- Infection during hibernation poses a serious terns, hibernation roost temperature, and pathogen threat to animals because of the high energy de- infestation. Our results suggest that hibernating mands of the immune response. Bats infected with bats have evolved skin disease tolerance through the fungal skin pathogen Pseudogymnoascus de- a set of genomic, behavioural and physiology Parasites and Diseases Parasites structans exhibit mild metabolic acidosis, lowered adaptations. blood glucose and eosinophilia. We found that bats
Bats from lower tempera- ture hibernacula exhibit milder symptoms of whi- te-nose syndrome as low temperatures limit fungal growth. (Adopted from Martínková et al. 2018.)
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arousal
Immune response A molecular mechanistic mo- modulation del of white-nose syndrome tolerance in bats, showing im- torpor portant adaptations for survi- ving the skin disease. Disease tolerance is promoted by skin
B2 B2 B2 integrity, suppressed immune B 2 B response during torpor arou- 2 sals and increased wound he- surface cupping neutrophilic lesion necrosis in ammation aling capacity. colonization erosions sequestration healing (Adopted from Harazim et al. 2018). wound healing skin integrity
An example of a low body tempera- ture movement, where a bat moves between clusters from left to right (a, b, c). The upper images were taken
with a thermal camera and the lower Parasites and Diseases images were taken simultaneously using photo traps. White rectangles in the photo-trap images indicate the position of the thermal image, while red circles indicate the moving bat. Tmax = maximum temperature of the thermal image. (Adopted from Bartonička et al. 2018)
BARTONIČKA T, BANĎOUCHOVÁ H, BERKOVÁ H, BLAŽEK J, LUČAN R, HORÁČEK I, MARTÍNKOVÁ N, PIKULA J, ŘEHÁK Z, ZUKAL J, 2017. Deeply torpid bats can change position without elevation of body temperature. Journal of Thermal Biology 63: 119–123. PIKULA J, AMELON SK, BANĎOUCHOVÁ H, BARTONIČKA T, BERKOVÁ H, BRICHTA J, HOOPER S, KOKUREWICZ T, KOLAŘÍK M, KÖLLNER B, KOVÁČOVÁ V, LINHART P, PIACEK V, TURNER GG, ZUKAL J, MARTÍNKOVÁ N, 2017. White-nose syndrome pathology grading in Nearctic and Palearctic bats. PLoS ONE 12: 8. BANĎOUCHOVÁ H, BARTONIČKA T, BERKOVÁ H, BRICHTA J, KOKUREWICZ T, KOVÁČOVÁ V, LINHART P, PIAČEK V, PIKULA J, ZAHRADNÍKOVÁ JR. A, ZUKAL J, 2018. Alterations in the health of hibernating bats under pathogen pressure. Scientific Reports 8: 6067. HARAZIM M, HORÁČEK I, JAKEŠOVÁ L, LUERMANN K, MORAVEC J, MORGAN S, PIKULA J, SOSÍK P, VAVRUŠOVÁ Z, ZAHRADNÍKOVÁ JR. A, ZUKAL J, MARTÍNKOVÁ N, 2018. Natural selection in bats with historical exposure to white-nose syndrome. BMC Zoology 3: 8. KOVÁČOVÁ V, ZUKAL J, BANĎOUCHOVÁ H, BOTVINKIN AD, HARAZIM M, MARTÍNKOVÁ N, ORLOV OL, PIAČEK V, SHUMKINA AP, TIUNOV MP, PIKULA J, 2018. White-nose syndrome detected in bats over an extensive area of Russia. BMC Veterinary Research 14: 192. MARTÍNKOVÁ N, PIKULA J, ZUKAL J, KOVÁČOVÁ V, BANĎOUCHOVÁ H, BARTONIČKA T, BOTVINKIN A, BRICHTA J, DUNDAROVA H, KOKUREWICZ T, IRWIN N, LINHART P, ORLOV O, PIAČEK V, ŠKRABÁNEK P, TIUNOV M, ZAHRADNÍKOVÁ JR. A, 2018. Hibernation temperature-dependent Pseudogymnoascus destructans infection intensity in Palearctic bats. Virulence 9: 1734–1750. ZAHRADNÍKOVÁ JR. A, KOVÁČOVÁ V, MARTÍNKOVÁ N, ORLOVA MV, ORLOV OL, PIAČEK V, ZUKAL J, PIKULA J, 2018. Historic and geographic surveillance of Pseudogymnoascus destructans possible from collections of bat parasites. Transboundary and Emerging Diseases 65: 303–308.
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Evolution of parasites in host secondary contact zones
Hybrid-zone studies of host-parasite systems have vhybrid zone with three different types of para- largely taken a host-centric viewpoint focussing on site, a DNA virus (the murine cytomegalovirus, how parasitism might affect the outcome of host MCMV), a yeast-like fungus (Pneumocystis mu- hybridisation by differentially impacting the fit- rina), and a nematode (Syphacia obvelata). These ness of host taxa vs. their hybrid descendants, the three parasites clearly show host-specific genetic parasites being seen as an homogeneous entity with clustering, with 94% of the genome in the MCMV a single strong effect on hybridvs . parental hosts. model showing host-specific genetic clustering In contrast, the process creating secondary contact while a small part of the genome encoding immune zones in hosts is also likely to give rise to secondary evasion genes showed maintenance of ancestral contact in their intimate parasites. These parasites polymorphism. For the fungal and nematode par- will be two entities, each arising out of co-existence asites, we found clear host-specific genetic cluster- with a different host and having no clear singular ing, with presence of hybrid parasites at the centre effect on hybrids. We showed that this is the case of the host hybrid zone. in the European house mouse (Mus musculus)
GOÜY DE BELLOCQ J, WASIMUDDIN, RIBAS A, BRYJA J, PIÁLEK J, BAIRD SJE, 2018. Holobiont suture zones: Parasite evidence across the European house mouse hybrid zone. Molecular Ecology 27: 5214–5227. ČÍŽKOVÁ D, BAIRD STUART JE, TĚŠÍKOVÁ J, VOIGT S, ĎUREJE Ľ, PIÁLEK J, GOÜY DE BELLOCQ J, 2018. Host subspecific viral strains in European house mice: Murine cytomegalovirus in the Eastern (Mus musculus musculus) and Western house mouse (Mus musculus domesticus). Virology 521: 92–98. Parasites and Diseases Parasites
Anterior part of Syphacia obvelata. (Photo by A. Ribas)
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The importance of host phylogeographic structure in spatial spread of viruses: Mastomys natalensis arenaviruses in Tanzania
Secondary contact between hosts can aid our un- are in direct physical contact, in principle allow- derstanding of the distribution of zoonotic viruses. ing viral exchange, yet neither of two arenaviruses Reservoirs of such viruses are usually equated with (Gairo and Morogoro virus) were found to have a particular wildlife species. However, it has rarely crossed the zone. Such intraspecific genetic barriers been assessed genetic groups below species level to arenavirus spatial spread have important impli- may instead represent the actual reservoir, despite cations for our understanding of the related Lassa this having major implications on estimations arenavirus, another M. natalensis virus potentially of zoonosis spatial distribution. We investigated highly pathogenic to humans. Although Lassa virus whether geographically and genetically distinct appears to infect several secondary hosts, its distri- sub-taxa of the Natal multimammate mouse (Mas- bution is restricted to West Africa and matches that tomys natalensis), a widespread African rodent, car- of another M. natalensis sub-taxon. Hence, our data ry distinct arenaviruses by detailed sampling across suggest that the human Lassa fever endemic area the contact zone of two of these sub-taxa. Ongoing has not expanded to the rest of sub-Saharan Africa hybridisation shows that individuals of the sub-taxa because of M. natalensis intraspecific distinctions.
GRYSEELS S, BAIRD SJE, BORREMANS B, MAKUNDI R, LEIRS H, GOÜY DE BELLOCQ J, 2017. When viruses don’t go viral: the importance of host phylogeographic structure in the spatial spread of arenaviruses. PLoS Pathogens 13: e1006073. Parasites and Diseases
Tanzanian Natal multimamma- te mice (Mastomys natalensis). (Photo by S. Gryseels)
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Evolution of innate immunity receptors in passerine birds
Recent developments in the scientific community In our study, we focused on the ligand-binding calling for more interdisciplinary approaches in region of TLR4 in 55 passerine species adapted answering have given rise to brand new fields of bi- to different climatic conditions. Using structural ological study, e.g. ecoimmunology, which combines bioinformatics, we showed adaptations in the dis- perspectives of classical immunology with ecolo- tribution of electrostatic potential on the surface gy, physiology and evolution, mainly in free-living of the TLR4 molecule, some of which have devel- wild animals. Ecoimmunology focuses on describing oped independently several times in birds (con- and explaining natural variation in immune func- vergent). Even small changes in surface charge on tion, including its causal factors, thereby providing key molecule sites may mean the difference be- a unique and novel point-of-view on the evolution of tween a strong or weak response and inhibition of immunity in the wild. Innate immunity is a complex immune reaction. Although we did not find a con- system providing the first barrier between an organ- nection between these differences and basic eco- ism and its pathogens. Presence of pathogens in an logical characteristics of the selected species (e.g. organism is recognised by various innate immune migration and latitudinal distribution, diet), our receptors, e.g. Toll-like receptors (TLR), which vary results potentially show functionally important greatly between species, possibly mirroring the need sites on the TLR4 surface, and thus contribute to of different species to recognise different pathogens our understanding of host-pathogen co-evolution. correctly.
KRÁLOVÁ T, ALBRECHT T, BRYJA J, HOŘÁK D, JOHNSEN A, LIFJELD JT, NOVOTNÝ M, SEDLÁČEK O, VELOVÁ H, VINKLER M, 2018. Signatures of diversifying selection and convergence acting on passerine Toll-like receptor 4 in an evolutionary context.Molecular Ecology 27: 2871–2883. Parasites and Diseases Parasites
Variability in TLR4 ligand-binding region (LBR) surface charge in four different passerine species. The two species showing greatest distance based on surface electrostatic potential of the whole TLR4 LBR were the Eurasian treecreeper (Certhia familiaris) and the European robin (Erithacus rubecula). The inner (left-hand side) and outer (right-hand side) surface of each TLR4 LBR is displayed with the ligand-binding surface shown in the left-hand view (positive charge highlighted in red and negative charge in blue). (Reproduced from Králová et al. 2018)
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Differences in evolutionary patterns of bird and mammal gut microbiota
The vertebrate digestive tract is inhabited by a tax- microbiota composition appear to differ between onomically and functionally diverse communi- birds and mammals. Unlike mammals, diet com- ty of microorganisms dominated by mutualistic position (and other ecological variables) affects and commensal prokaryotes. This gut microbiota the passerine gut microbiota only marginally. On can interact with a broad range of host physio- the other hand, between-species similarity in pas- logical systems and provides valuable ecosystem serine gut microbiota composition increases with services to the host, including increased diges- their phylogenetic relatedness. This pattern may tion and vitamin synthesis efficiency, protection have arisen if divergence of genes regulating gut against pathogens and immune and nervous sys- microbiota follows passerine phylogeny. At the tem regulation. To date, most attention has been individual level, we observed stochastic fluctua- paid to interactions between the host and its gut tion in passerine gut microbiota composition over microbiota in mammals, knowledge of these time, which again contrasts with some previous interactions in other vertebrates being limited. studies on mammals that report relatively stable Our research on passerines shows that this bird microbiota in individuals over several years. Tak- group has a substantially different gut microbio- en together, our work shows that host and gut mi- ta composition than mammals, which is at least crobiota interactions can vary substantially across partially explained by major differences in their the animal kingdom and that it is not possible to digestive tract physiology and anatomy. Similarly, generalise findings obtained by studying a par- the factors driving interspecific variability in gut ticular taxonomic group. Parasites and Diseases
KREISINGER J, KROPÁČKOVÁ L, PETRŽELKOVÁ A, ADÁMKOVÁ M, TOMÁŠEK O, MARTIN J-F, MICHÁLKOVÁ R, ALBRECHT T, 2017. Temporal stability and the effect of transgenerational transfer on fecal microbiota structure in a long distance migratory bird. Frontiers in Microbiology 8: 50. KROPÁČKOVÁ L, TĚŠICKÝ M, ALBRECHT T, KUBOVČIAK J, ČÍŽKOVÁ D, TOMÁŠEK O, MARTIN J-F, BOBEK L, KRÁLOVÁ T, PROCHÁZKA P, KREISINGER J, 2017. Codiversification of gastrointestinal microbiota and phylogenyin passerines is not explained by ecological divergence. Molecular Ecology 26: 5292–5304. KREISINGER J, SCHMIEDOVÁ L, PETRŽELKOVÁ A, TOMÁŠEK O, ADÁMKOVÁ M, MICHÁLKOVÁ R, MARTIN J-F, ALBRECHT T, 2018. Fecal microbiota associated with phytohaemagglutinin‐induced immune response in nestlings of a passerine bird. Ecology and Evolution 8: 9793–9802.
L. Kropáčková during DNA extraction from the pas- serine gut. (Photo by J. Kreisinger)
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Impact of stress and parasite infection on the gastrointestinal microbiome of western lowland gorillas
Relationships between gastrointestinal microbiome we observed associations between (i) gastroin- (GIM), stress and parasite infection are widely testinal parasites and GIM and (ii) physiological discussed topics across mammalian species due stress and GIM, using next generation sequencing to their possible impact on the host’s health. As (454 pyrosequencing of 16S rRNA bacterial gene part of a long-term monitoring programme of amplicons), coprological methods and measure- western lowland gorillas in the Dzanga Sangha ments of faecal glucocorticoid metabolites using Protected Area in the Central African Republic, enzyme immunoassays. We found that presence of Entamoeba spp. infections were associated with significant differences in the abundance of bacterial taxa that, aside from being characteristic members of the gorilla gut microbiome, likely play impor- tant roles in host nutrition and metabolism. On the other hand, exposure to stressors appears to be associated with minor changes in the gorilla GIM. In particular, members of the family Anaerolin- eaceae, genus Clostridium cluster XIVb and genus Oscillibacter were positively correlated with faecal glucocorticoid metabolite levels. Our results have implications for both conservation biology and for our overall understanding of factors influencing non-human primate GIM VLČKOVÁ K, PAFČO B, PETRŽELKOVÁ K, MODRÝ D, TODD A, YEOMAN CJ, TORRALBA M, WILSON BA, STUMPF RM, WHITE BA, NELSON KE, LEIGH SR, GOMEZ A, 2018. Relationships between gastrointestinal parasite infections
Parasites and Diseases Parasites and the fecal microbiome in free-ranging western lowland gorillas. Frontiers in Microbiology 9: 1202. Adult female with an infant from a habituatuated VLČKOVÁ K, SHUTT-PHILLIPS KA, HEISTERMANN M, PAFČO B, group in a forest clearing in Dzanga Sangha. PETRŽELKOVÁ K, TODD A, MODRÝ D, NELSON KE, (Photo by K. Shutt) WILSON BA, STUMPF RM, WHITE BA, LEIGH SR, GOMEZ A, 2018. Impact of stress on the gut microbiome of free-ranging western lowland gorillas. Microbiology 164: 40–44.
West Nile virus in overwintering mosquitoes: implications for its persistence during unfavourable conditions
West Nile virus (WNV) is currently the most im- were found from 2011 to 2016, though lineage 2 portant mosquito-borne pathogen spreading in WNV RNA was detected in three pools of Culex Europe. Data on overwintering of WNV in mos- pipens mosquitoes collected in 2017 at two study quitoes are crucial for understanding WNV cir- sites. To the best of our knowledge, this is the culation in Europe. A total of 28,287 hibernating first record of WNV in overwintering mosqui- mosquitoes (27,872 Culex pipiens, 73 Anopheles toes in Europe. The data support the hypothesis maculipennis sensu lato, and 342 Culiseta annu- of WNV persistence in mosquitoes throughout lata) caught in February or March between 2011 the winter season in Europe. As an epidemiologi- and 2017 in a WNV-endemic region of South cal consequence, it can be assumed that lineage 2 Moravia, Czech Republic, were screened for the WNV infections in Europe are sustained by virus presence of WNV RNA. No WNV-positive pools persistence in mosquitoes followed by vertical
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SELECTED SCIENTIFIC ACHIEVEMENTS PARASITES AND DISEASES transmission and maintenance of the mosqui- to-bird transmission cycle, without the necessity of virus re-introduction.
RUDOLF I, BETÁŠOVÁ L, BLAŽEJOVÁ H, VENCLÍKOVÁ K, STRAKOVÁ P, ŠEBESTA O, MENDEL J, BAKONYI T, SCHAFFNER F, NOWOTNY N, HUBÁLEK Z, 2017. West Nile virus in overwintering mosquitoes, Central Europe. Parasites & Vectors 10: 452.
Collecting overwintering mosquitoes in a wine cellar. (Photo by I. Rudolf)
Hepatitis E virus found in archived wild boar samples: established virus circulation and potential risks for the consumer Parasites and Diseases Nowadays, hepatitis E, a self-limited disease caused and 2008. Of these, 31 (8.5%) proved seropositive, by the hepatitis E virus (HEV), is considered with nested RT-PCR revealing two distinct sequenc- a worldwide public health threat. The genotypes es, the first (from a boar hunted in 2008) clustered HEV-1 and HEV-2 have been associated with human together with sequences from German and Czech epidemics in developing countries where poor hy- wild boar and the second (from a boar hunted in giene, sanitation and faecal contamination of drink- 1997) clearly differentiated. A positive sample from ing water can increase the risk of HEV outbreak via 1990 is the oldest HEV seropositive sample ever de- the faecal-oral transmission route. The genotypes tected. Our results indicate that the wild boar acts as HEV-3 and HEV-4, characterised as zoonoses, are a reservoir of HEV in the Czech Republic and that not only detected in humans but also in a wide va- this virus has been circulating in the study area for riety of animals, with pigs and wild boar the most more than 20 years. From an epidemiological point important animal reservoirs. In order to determine of view, consumption of undercooked game or pork whether HEV is distributed in South Moravian wild products should continue to be taken as a possible boar populations, 366 sera samples were obtained serious health threat. from archived wild boars collected between 1990
STRAKOVÁ P, KUBÁNKOVÁ M, VAŠÍČKOVÁ P, JUŘICOVÁ Z, RUDOLF I, HUBÁLEK Z, 2018. Hepatitis E virus in archived sera from wild boars (Sus scrofa), Czech Republic. Transboundary and Emerging Diseases 65: 1770–1774.
Our research shows that Czech wild boars (Sus scrofa) act as reservoirs for the Hepatitis E virus. (Photo by J. Drimaj)
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OTHER ACTIVITIES
4. OTHER ACTIVITIES
| POPULARISATION ACTIVITIES
Popularisation of science is an important part of also organise workshops and conferences for uni- the IVBs activities and many seminars, workshops, versity students and for other scientists. In 2017, field excursions, talks and open days are organised our institute participated for the first time in the each year. During such activities, different scien- largest annual scientific exposition in Prague, The tific topics are presented to the wider public and Science Exposition organised by the Czech Acad- students from different levels of education. We emy of Sciences. Other Activites Other
A B
C D
(A-C): PhD students from the IVB present most interesting results of IVB to the wider public at the 2017 and 2018 Science Exposition in Prague, EXPO Letňany, (D): Scientific exposition was also attended by the President of the Czech Academy of Sciences, Prof. RNDr. Eva Zažímalová PhD. (Photo from IVB and CAS archive)
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Science exposition 2017 and 2018
In 2017 (8–10 June), 17,000 people attended the to learn about vacancies in the various research in- Prague Science Fair, while 25,000 attended in 2018 stitutions and companies seeking talented students. (7–9 June). Numerous novelties and attractions The IVB had its own stand where we presented our from the world of science and research were pre- most interesting scientific results. In 2018, the IVB sented by the main research centres of the Czech presented a new popularisation initiative based Academy of Sciences, universities and innovative around six humorous posters covering a range of companies. One such attraction was the Zone for scientific topics, produced in collaboration with Students and Graduates, who had the opportunity Šimon Bryja, a high school student. Other Activites
Examples of humorous posters produced by Šimon Bryja, a high school student, in collaboration with IVB scientists.
Open door days
Over the course of the Czech Republics ‘Science and breeding facilities. In addition, a series of in- and technology Week’ (6–12 November 2017), the teresting lectures were provided, including two at Czech Academy of Sciences opens its doors to the the Brno Observatory and Planetarium in 2017 public in a series of open house events. All IVB entitled ‘The biodiversity of amphibians and rep- research facilities participated in the event and tiles in the Congo and following the footsteps of welcomed a wide selection of the public through a new crocodile species’ by Václav Gvoždík, and their doors. Visitors gained an insight into research ‘Newts – masters of transformation’ presented by taking place at the various facilities and were able Lumír Gvoždík. to see the normal functioning of the laboratories
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OTHER ACTIVITIES
The Studenec Research facility welcomed students from a number of schools during the Science and Technology Week (Photos by A. Bryjová) Other Activites Other
Open house at the Valtice Research Facility (Photo by I. Rudolf)
Visitors also had the possibility of visiting the fish breeding facility in Brno during the Science and Technology Week (Photo by M. Čapek)
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Ústav biologie obratlovců AV ČR, TÝDEN VĚDY A TECHNIKY
Týden vědy a techniky Akademie věd ČR je největší vědecký festival v České republice, který zahrnuje přednášky, výstavy, akce na pracovištích, dokumentární filmy, workshopy, vědecké kavárny a mnohé další aktivity napříč celou republikou i všemi vědeckými obory. Festival je určen jak studentům středních škol, pro které připravujeme především přednášky a exkurze v dopoledních hodinách, tak široké veřejnosti, na kterou cílí program v odpoledních a večerních časech.
PRACOVIŠTĚ BRNO PRACOVIŠTĚ VALTICE PRACOVIŠTĚ STUDENEC Květná 8, 603 65 Brno Klášterní 2, 691 42 Valtice Studenec 122, 675 02 Koněšín
Kdy: 7. 11. 2018, 9:00 – 16:00 Kdy: 7. 11. 2018 Kdy: 7. - 10. 11. 2018 Other Activites Kontakt: Ing. Pavel Jurajda, Dr., tel. 543 422 523, Kontakt: doc. RNDr. Ivo Rudolf, Ph.D., tel. 519 352 961, Kontakt: Jana Vrbová Komárková, tel. 775 049 634, e-mail: [email protected] e-mail: [email protected] e-mail: [email protected]