287 results on '"Boukal, David S."'
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2. Combined effects of climate warming and pharmaceuticals on a tri-trophic freshwater food web
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Duchet, Claire, Grabicová, Kateřina, Kolar, Vojtech, Lepšová, Olga, Švecová, Helena, Csercsa, Andras, Zdvihalová, Barbora, Randák, Tomáš, and Boukal, David S.
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- 2024
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3. Bioaccumulation of chemical elements at post-industrial freshwater sites varies predictably between habitats, elements and taxa: A power law approach
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Carreira, Bruno M., Kolář, Vojtěch, Chmelová, Eliška, Jan, Jiří, Adašević, Josip, Landeira-Dabarca, Andrea, Vebrová, Lucie, Poláková, Martina, Horká, Petra, Otáhalová, Šárka, Musilová, Zuzana, Borovec, Jakub, Tropek, Robert, and Boukal, David S.
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- 2023
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4. Muddying the unexplored post-industrial waters: Biodiversity and conservation potential of freshwater habitats in fly ash sedimentation lagoons
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Kolar, Vojtech, Chmelová, Eliška, Bílková, Martina, Borovec, Jakub, Carreira, Bruno M., Černý, Martin, Ditrich, Tomáš, Horká, Petra, Hrivniak, Ľuboš, Hrubý, František, Jan, Jiří, Landeira-Dabarca, Andrea, Lepšová-Skácelová, Olga, Musilová, Zuzana, Otáhalová, Šárka, Poláková, Martina, Polášková, Vendula, Sacherová, Veronika, Špaček, Jan, Sroka, Pavel, Vebrová, Lucie, Boukal, David S., and Tropek, Robert
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- 2023
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5. Somatic growth of pikeperch (Stizostedion lucioperca) in relation to variation in temperature and eutrophication in a Central Europe Lake
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Tesfaye, Million, Souza, Allan T., Soukalová, Kateřina, Šmejkal, Marek, Hejzlar, Josef, Prchalová, Marie, Říha, Milan, Muška, Milan, Vašek, Mojmír, Frouzová, Jaroslava, Blabolil, Petr, Boukal, David S., and Kubečka, Jan
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- 2023
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6. Widespread long-term declines of littoral areas in protected and unprotected Czech fishponds
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Kolar, Vojtech, Francová, Kateřina, Vrba, Jaroslav, Grill, Stanislav, and Boukal, David S.
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- 2023
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7. Effects of a microplastic mixture differ across trophic levels and taxa in a freshwater food web: In situ mesocosm experiment
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Yıldız, Dilvin, Yalçın, Gülce, Jovanović, Boris, Boukal, David S., Vebrová, Lucie, Riha, Derya, Stanković, Jelena, Savić-Zdraković, Dimitrija, Metin, Melisa, Akyürek, Yasmin Naz, Balkanlı, Deniz, Filiz, Nur, Milošević, Djuradj, Feuchtmayr, Heidrun, Richardson, Jessica A., and Beklioğlu, Meryem
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- 2022
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8. Differences in Tri‐Trophic Community Responses to Temperature‐Dependent Vital Rates, Thermal Niche Mismatches and Temperature‐Size Rule.
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Dijoux, Samuel, Smalås, Aslak, Primicerio, Raul, and Boukal, David S.
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GLOBAL warming ,VITAL statistics ,ALLEE effect ,ECOLOGICAL disturbances ,ECOSYSTEM dynamics - Abstract
Warming climate impacts aquatic ectotherms by changes in individual vital rates and declines in body size, a phenomenon known as the temperature‐size rule (TSR), and indirectly through altered species interactions and environmental feedbacks. The relative importance of these effects in shaping community responses to environmental change is incompletely understood. We employ a tri‐trophic food chain model with size‐ and temperature‐dependent vital rates and species interaction strengths to explore the role of direct kinetic effects of temperature and TSR on community structure along resource productivity and temperature gradients. We find that community structure, including the propensity for sudden collapse along resource productivity and temperature gradients, is primarily driven by the direct kinetic effects of temperature on vital rates and thermal mismatches between the consumer and predator species, overshadowing the TSR‐mediated effects. Overall, our study enhances the understanding of the complex interplay between temperature, species traits and community dynamics in aquatic ecosystems. [ABSTRACT FROM AUTHOR]
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- 2024
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9. The influence of successional stage on local odonate communities in man-made standing waters
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Kolar, Vojtech, Vlašánek, Petr, and Boukal, David S.
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- 2021
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10. Ecological consequences of body size reduction under warming.
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Sentis, Arnaud, Bazin, Simon, Boukal, David S., and Stoks, Robby
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BODY size ,ECOLOGICAL impact ,BIOENERGETICS ,COLD-blooded animals ,GENERALIZATION - Abstract
Body size reduction is a universal response to warming, but its ecological consequences across biological levels, from individuals to ecosystems, remain poorly understood. Most biological processes scale with body size, and warming-induced changes in body size can therefore have important ecological consequences. To understand these consequences, we propose a unifying, hierarchical framework for the ecological impacts of intraspecific body size reductions due to thermal plasticity that explicitly builds on three key pathways: morphological constraints, bioenergetic constraints and surface-to-volume ratio. Using this framework, we synthesize key consequences of warming-induced body size reductions at multiple levels of biological organization. We outline how this trait-based framework can improve our understanding, detection and generalization of the ecological impacts of warming. [ABSTRACT FROM AUTHOR]
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- 2024
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11. Changing environmental conditions underpin long-term patterns of phytoplankton in a freshwater reservoir
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Znachor, Petr, Nedoma, Jiří, Hejzlar, Josef, Seďa, Jaromír, Komárková, Jaroslava, Kolář, Vojtěch, Mrkvička, Tomáš, and Boukal, David S.
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- 2020
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12. Species interactions under climate change: connecting kinetic effects of temperature on individuals to community dynamics
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Boukal, David S, Bideault, Azenor, Carreira, Bruno M, and Sentis, Arnaud
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- 2019
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13. Length–mass allometries of the larvae of aquatic dipterans: differences between taxa, morphological traits, and methods
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Mocq, Julien, primary, Dekanová, Vladimíra, additional, and Boukal, David S, additional
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- 2024
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14. Combined effects of climate warming and pharmaceuticals on a tri-trophic freshwater food web
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Duchet, Claire, primary, Grabicová, Kateřina, additional, Kolar, Vojtech, additional, Lepšová, Olga, additional, Švecová, Helena, additional, Csercsa, Andras, additional, Zdvihalová, Barbora, additional, Randák, Tomáš, additional, and Boukal, David S., additional
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- 2023
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15. Sex Determination in Bonellia viridis (Echiura: Bonelliidae): Population Dynamics and Evolution
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Berec, Ludek, Schembri, Patrick J., and Boukal, David S.
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- 2005
16. Implications of Mate Search, Mate Choice and Divorce Rate for Population Dynamics of Sexually Reproducing Species
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Berec, Luděk and Boukal, David S.
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- 2004
17. Body size and trophic position determine the outcomes of species invasions along temperature and productivity gradients
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Dijoux, Samuel, primary, Pichon, Noémie A., additional, Sentis, Arnaud, additional, and Boukal, David S., additional
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- 2023
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18. Optimal gillnet sampling design for the estimation of fish community indicators in heterogeneous freshwater ecosystems
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Blabolil, Petr, Boukal, David S., Ricard, Daniel, Kubečka, Jan, Říha, Milan, Vašek, Mojmír, Prchalová, Marie, Čech, Martin, Frouzová, Jaroslava, Jůza, Tomáš, Muška, Milan, Tušer, Michal, Draštík, Vladislav, Šmejkal, Marek, Vejřík, Lukáš, and Peterka, Jiří
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- 2017
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19. Meta-analysis of multidecadal biodiversity trends in Europe
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Pilotto, Francesca, Kühn, Ingolf, Adrian, Rita, Alber, Renate, Alignier, Audrey, Andrews, Christopher, Bäck, Jaana, Barbaro, Luc, Beaumont, Deborah, Beenaerts, Natalie, Benham, Sue, Boukal, David S., Bretagnolle, Vincent, Camatti, Elisa, Canullo, Roberto, Cardoso, Patricia G., Ens, Bruno J., Everaert, Gert, Evtimova, Vesela, Feuchtmayr, Heidrun, García-González, Ricardo, Gómez García, Daniel, Grandin, Ulf, Gutowski, Jerzy M., Hadar, Liat, Halada, Lubos, Halassy, Melinda, Hummel, Herman, Huttunen, Kaisa-Leena, Jaroszewicz, Bogdan, Jensen, Thomas C., Kalivoda, Henrik, Schmidt, Inger Kappel, Kröncke, Ingrid, Leinonen, Reima, Martinho, Filipe, Meesenburg, Henning, Meyer, Julia, Minerbi, Stefano, Monteith, Don, Nikolov, Boris P., Oro, Daniel, Ozoliņš, Dāvis, Padedda, Bachisio M., Pallett, Denise, Pansera, Marco, Pardal, Miguel Ângelo, Petriccione, Bruno, Pipan, Tanja, Pöyry, Juha, Schäfer, Stefanie M., Schaub, Marcus, Schneider, Susanne C., Skuja, Agnija, Soetaert, Karline, Spriņģe, Gunta, Stanchev, Radoslav, Stockan, Jenni A., Stoll, Stefan, Sundqvist, Lisa, Thimonier, Anne, Van Hoey, Gert, Van Ryckegem, Gunther, Visser, Marcel E., Vorhauser, Samuel, and Haase, Peter
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- 2020
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20. Predicting asp and pikeperch recruitment in a riverine reservoir
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Blabolil, Petr, Ricard, Daniel, Peterka, Jiří, Říha, Milan, Jůza, Tomáš, Vašek, Mojmír, Prchalová, Marie, Čech, Martin, Muška, Milan, Seďa, Jaromír, Mrkvička, Tomáš, Boukal, David S., and Kubečka, Jan
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- 2016
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21. An evolutionary explanation of female-biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L
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Mollet, Fabian M., Enberg, Katja, Boukal, David S., Rijnsdorp, Adriaan D., Dieckmann, Ulf, Mollet, Fabian M., Enberg, Katja, Boukal, David S., Rijnsdorp, Adriaan D., and Dieckmann, Ulf
- Abstract
Sexual size dimorphism (SSD) is caused by differences in selection pressures and life-history trade-offs faced by males and females. Proximate causes of SSD may involve sex-specific mortality, energy acquisition, and energy expenditure for maintenance, reproductive tissues, and reproductive behavior. Using a quantitative, individual-based, eco-genetic model parameterized for North Sea plaice, we explore the importance of these mechanisms for female-biased SSD, under which males are smaller and reach sexual maturity earlier than females (common among fish, but also arising in arthropods and mammals). We consider two mechanisms potentially serving as ultimate causes: (a) Male investments in male reproductive behavior might evolve to detract energy resources that would otherwise be available for somatic growth, and (b) diminishing returns on male reproductive investments might evolve to reduce energy acquisition. In general, both of these can bring about smaller male body sizes. We report the following findings. First, higher investments in male reproductive behavior alone cannot explain the North Sea plaice SSD. This is because such higher reproductive investments require increased energy acquisition, which would cause a delay in maturation, leading to male-biased SSD contrary to observations. When accounting for the observed differential (lower) male mortality, maturation is postponed even further, leading to even larger males. Second, diminishing returns on male reproductive investments alone can qualitatively account for the North Sea plaice SSD, even though the quantitative match is imperfect. Third, both mechanisms can be reconciled with, and thus provide a mechanistic basis for, the previously advanced Ghiselin–Reiss hypothesis, according to which smaller males will evolve if their reproductive success is dominated by scramble competition for fertilizing females, as males would consequently invest more in reproduction than growth, potentially implying lower surv
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- 2023
22. An evolutionary explanation of female-biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
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Mollet, F.M., Enberg, Katja, Boukal, David S., Rijnsdorp, Adriaan, Dieckmann, Ulf, Mollet, F.M., Enberg, Katja, Boukal, David S., Rijnsdorp, Adriaan, and Dieckmann, Ulf
- Abstract
Sexual size dimorphism (SSD) is caused by differences in selection pressures and life-history tradeoffs faced by males and females. Proximate causes of SSD may involve sex-specific mortality, energy acquisition, and energy expenditure for maintenance, reproductive tissues, and reproductive behavior. Using a quantitative, individual-based, eco-genetic model parameterized for North Sea plaice, we explore the importance of these mechanisms for female-biased SSD, under which males are smaller and reach sexual maturity earlier than females (common among fish, but also arising in arthropods and mammals). We consider two mechanisms potentially serving as ultimate causes: (1) male investments into male reproductive behavior might detract energy resources that would otherwise be available for somatic growth, and (2) diminishing returns on male reproductive investments might lead to reduced energy acquisition. In general, both of these can bring about smaller male body sizes. We report the following findings. First, higher investments into male reproductive behavior alone cannot explain the North Sea plaice SSD. This is because such higher reproductive investments require increased energy acquisition, which would cause a delay in maturation, leading to male-biased SSD contrary to observations. When accounting for the observed differential (lower) male mortality, maturation is postponed even further, leading to even larger males. Second, diminishing returns on male reproductive investments alone can qualitatively account for the North Sea plaice SSD, even though the quantitative match is imperfect. Third, both mechanisms can be reconciled with, and thus provide a mechanistic basis for, the previously advanced Ghiselin-Reiss hypothesis, according to which smaller males will evolve if their reproductive success is dominated by scramble competition for fertilizing females, as males would consequently invest more into reproduction than growth, potentially implying lower survival r
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- 2023
23. Body size and trophic position determine the outcomes of species invasions along temperature and productivity gradients.
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Dijoux, Samuel, Pichon, Noémie A., Sentis, Arnaud, and Boukal, David S.
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BODY size ,TOP predators ,POLITICAL stability ,SPECIES ,PLANT invasions ,TEMPERATURE ,COEXISTENCE of species - Abstract
Species invasions are predicted to increase in frequency with global change, but quantitative predictions of how environmental filters and species traits influence the success and consequences of invasions for local communities are lacking. Here we investigate how invaders alter the structure, diversity and stability regime of simple communities across environmental gradients (habitat productivity, temperature) and community size structure. We simulate all three‐species trophic modules (apparent and exploitative competition, trophic chain and intraguild predation). We predict that invasions most often succeed in warm and productive habitats and that successful invaders include smaller competitors, intraguild predators and comparatively small top predators. This suggests that species invasions and global change may facilitate the downsizing of food webs. Furthermore, we show that successful invasions leading to species substitutions rarely alter system stability, while invasions leading to increased diversity can destabilize or stabilize community dynamics depending on the environmental conditions and invader's trophic position. [ABSTRACT FROM AUTHOR]
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- 2024
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24. An evolutionary explanation of female‐biased sexual size dimorphism in North Sea plaice, Pleuronectes platessa L.
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Mollet, Fabian M., primary, Enberg, Katja, additional, Boukal, David S., additional, Rijnsdorp, Adriaan D., additional, and Dieckmann, Ulf, additional
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- 2023
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25. Life-history implications of the allometric scaling of growth
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Boukal, David S., Dieckmann, Ulf, Enberg, Katja, Heino, Mikko, and Jørgensen, Christian
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- 2014
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26. The effect of habitat structure on prey mortality depends on predator and prey microhabitat use
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Klecka, Jan and Boukal, David S.
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- 2014
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27. On the use of functional responses to quantify emergent multiple predator effects
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Sentis, Arnaud and Boukal, David S.
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- 2018
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28. Seasonality and weather conditions jointly drive flight activity patterns of aquatic and terrestrial chironomids
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Vebrová, Lucie, van Nieuwenhuijzen, Andre, Kolář, Vojtěch, and Boukal, David S.
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- 2018
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29. The utility of predatory fish in biomanipulation of deep reservoirs
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Vašek, Mojmír, Prchalová, Marie, Peterka, Jiří, Ketelaars, Henk A.M., Wagenvoort, Arco J., Čech, Martin, Draštík, Vladislav, Říha, Milan, Jůza, Tomáš, Kratochvíl, Michal, Mrkvička, Tomáš, Blabolil, Petr, Boukal, David S., Duras, Jindřich, and Kubečka, Jan
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- 2013
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30. Foraging and vulnerability traits modify predator–prey body mass allometry: freshwater macroinvertebrates as a case study
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Klecka, Jan and Boukal, David S.
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- 2013
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31. Stock–catch analysis of carp recreational fisheries in Czech reservoirs: Insights into fish survival, water body productivity and impact of extreme events
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Boukal, David S., Jankovský, Martin, Kubečka, Jan, and Heino, Mikko
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- 2012
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32. Elmidae of Sarawak: the genus Potamophilus Germar, 1811, with a description of P. kelabitensis sp. nov. (Insecta: Coleoptera)
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Kodada, Ján, Boukal, David S., Vďačný, Peter, Goffová, Katarína, and Ondrejková, Kamila
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Coleoptera ,Elmidae ,Insecta ,Arthropoda ,ddc:590 ,Animalia ,Biodiversity ,Taxonomy - Abstract
Potamophilus kelabitensis sp. nov., a new riffle beetle (Coleoptera, Elmidae) discovered in the Kelabit Highlands (northern Sarawak) and Sapulut environment (southern Sabah), is described. Illustrations of the habitus and diagnostic characters of the new species are presented. Differences from the type species P. acuminatus (Fabricius, 1792) from the Palaearctic region, based on DNA barcodes and morphological characters, are discussed. Selected morphological characters of all known species of Potamophilus from Vietnam, Myanmar, and Papua New Guinea are also compared with the new species. The systematic position of the genus relative to other sympatric genera of the subfamilies Larainae LeConte, 1861 and selected Elminae Curtis, 1830 belonging to three tribes is discussed based on phylogenetic trees inferred from the mitochondrial COI and nuclear ArgK as well as 18S rRNA gene sequences.
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- 2022
33. Potamophilus kelabitensis Kodada & Boukal & Vďačný & Goffová & Ondrejková 2022, sp. nov
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Kodada, Ján, Boukal, David S., Vďačný, Peter, Goffová, Katarína, and Ondrejková, Kamila
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Coleoptera ,Elmidae ,Insecta ,Potamophilus ,Arthropoda ,Potamophilus kelabitensis ,Animalia ,Biodiversity ,Taxonomy - Abstract
Potamophilus kelabitensis sp. nov. urn:lsid:zoobank.org:act: D801EBA4-C36A-4569-B495-7792B4B58F9D Figs 2–5 Type locality Malaysia, Sarawak, Miri district, Ramudu. Adults were collected at light in the Pa’Kelapang river environment in the Ramudu settlement (Fig. 5). Diagnosis Potamophilus kelabitensis sp. nov. is an elongated, parallel-sided, medium-sized (PEL: 5.3–7.3 mm), predominantly black species with reddish-brown antennal segments 1–4, distal portion of femora, trochanters, anterior face of mesofemora, and claws. The pronotum is about 1.5 × as wide as long, gradually expanded posteriad, widest in front of posterior margin, and deeply excised in hind angles. Pronotal sides are moderately arcuate, finely crenate, and explanate, on each side with conspicuous blunt tooth posteriorly; posterior angles are nearly rectangular. Pronotal surface bears dual punctuation. Large punctures are moderately larger than facets, nearly confluent or separated by distances up to 1.5× a puncture diameter, punctures appear to be denser laterally. Small punctures are intermixed within larger ones and are moderately larger than those on the head. Elytron with ten punctate striae and one accessory basal stria between the sutural and second stria. Strial punctures on the disc are more prominent than those on the pronotum, separated by one puncture diameter, punctures becoming smaller posteriorly; punctures in striae 6–10 are more prominent, appearing subquadrate and more closely arranged. Intervals are flat, finely punctured; sutural interval moderately raised; elytral apices are slightly deflected and not meeting at the suture, separated by a gap, narrowly rounded and not protruding. The aedeagus is trilobate, symmetrical; parameres in the apical portion are narrowed, flattened, abruptly bent ventrad, and less sclerotised; apices do not reach the apex of the penis. Differential diagnosis The new species differs from all other described species of Potamophilus by the following combination of external characters: – a relatively small size (separating it from P. feae); – distinctly crenate lateral margins of the pronotum (separating it from P. acuminatus, P. albertisii, P. feae, P. papuanus, and P. spinicollis); – deeply excised hind angles of the pronotum (separating it from P. albertisii); – lack of impression on the pronotal disc in front of the scutellum (separating it from P. acuminatus and P. spinicollis); – flat elytral intervals except the sutural one (separating it from P. acuminatus, P. feae, and P. spinicollis); – coarse strial punctures on the elytra (separating it from P. albertisii); – subquadrate and not rounded strial punctures in intervals 6–10 (separating it from P. acuminatus, P. feae, P. papuanus, and P. spinicollis); – evenly rounded elytral apices in both sexes (separating it from P. acuminatus, P. albertisii, P. feae, and P. papuanus); – the absence of a distinct, well-separated median tubercle on the meso- and metatibia in males (separating it from P. albertisii, P. feae, P. papuanus, and P. spinicollis). For the sake of convenience, brief diagnoses of the described species are given below. In P. acuminatus (PEL: ca 6.1–7.7 mm), the hind angles of the pronotum are deeply excised, pronotal sides are smooth, not crenate; pronotal disc with a wide, distinct depression in front of the scutellum. Strial punctures on the elytra are moderately coarse, sharply impressed, rounded, and separated by about their diameter. Elytra are long and narrow (ca 3.6–4.0 × as long as pronotum), with the first interval raised in the posterior 0.8 of its length, distinctly convex intervals 3 and 5, and other intervals flat to feebly convex. The apex of each elytron is produced, angulate in males while acuminate and more protruding with divergent apices in females. Meso- and metatibia are weakly sinuous; mesotibia in males is usually more strongly enlarged distally with an indistinct median tubercle. In P. albertisii (PEL: ca 6.8–7.1 mm), the hind angles of the pronotum are at most slightly emarginated, with the emargination at most half as wide as scutellum; pronotal sides are smooth, not crenate; pronotal disc is flat or at most indistinctly impressed in front of the scutellum. Strial punctures on the elytra are moderately fine to fine, conspicuously sharply impressed, elongate, and separated by about 1–2 × their length. The first elytral interval is raised, and the remaining intervals are flat or at most slightly convex, similarly as in P. kelabitensis sp. nov. The apex of each elytron is produced, angulate in males and acuminate in females, with subparallel apices. Meso- and metatibia are weakly sinuous, usually more strongly so and always with a distinct, acute median tubercle at the distal end of both tibiae in males. In P. feae (PEL: ca 9.5–10.4 mm), the hind angles of the pronotum are deeply excised; pronotal sides are smooth, not crenate; pronotal disc is at most indistinctly impressed in front of the scutellum. Strial punctures on the elytra are moderately coarse, more delicate on the declivity, moderately sharply impressed and rounded, separated by about 1–2 × their diameter; first and third interval in the posterior half are distinctly raised, other intervals at most feebly convex. The apex of each elytron is produced, more or less angulate, the angle acute (ca 60°), with an almost identical shape in both sexes. Mesotibia is weakly sinuous, and the distal end bears a stout median tubercle in males; metatibia is almost straight in both sexes. In P. papuanus (PEL: ca 5.4–5.9 mm), the hind angles of the pronotum are deeply excised; pronotal sides are smooth, not crenate; pronotal disc is evenly convex to flat in front of the scutellum. Pronotal disc is densely and finely punctate with the punctures smaller than the eye facets, i.e., the punctuation is finer than in P. kelabitensis sp. nov. Elytral intervals are more or less flat, and only the first interval is raised in about the posterior half; strial punctures are rounded, moderately large (slightly larger than eye facets), well and sharply impressed, separated by about 1–2 × their diameter. Elytral apices have an acute angle in males and are angulate to acuminate in females. Mesotibia and metatibia are distinctly curved/sinuate with a blunt tubercle on the mesal face of the distal part in males, nearly straight or only weakly sinuate in females. In P. spinicollis (PEL: ca 7.0 mm), the hind angles of the pronotum are deeply excised; pronotal sides are smooth to indistinctly and irregularly crenate, especially in the posterior half; pronotal disc with a distinct subtriangular depression in front of the scutellum. Elytral intervals are convex on the disc, with the first interval raised in the posterior 0.8 of its length. Strial punctures are rounded and conspicuously coarse, larger than those on the pronotum and much larger than eye facets, well and sharply impressed, separated by at most their diameter on the disc, smaller and sparser towards the lateral sides and posterior declivity. Male with the apex of each elytron separately rounded (female unknown) and with a rather prominent, pointed tubercle on the mesal face of the distal part of meso- and metatibia. Etymology The species is named after the Kelabit Highlands, an isolated highland plateau in the interior of the Sarawak State (Malaysia) and bordering the Kalimantan Province (Indonesia). Type material Holotype MALAYSIA • ♂; “ Malaysia, Sarawak, Miri distr., Ramudu, 26.06.2018, (15) 3°33′17.0″ N 115°29′38.5″ E 921 m a.s.l., Pa’Kelapang riv. env., J. Kodada & D. Selnekovič lgt., at light ”; CFDS. Paratypes MALAYSIA • 11 ♂♂, 7 ♀♀; same collection data as for holotype; CFDS, CKB • 1 ♀; “ Malaysia, Sarawak, Miri distr., Bario, 19.– 23.6.2018, Lian Labang Garden, at light, J. Kodada & D. Selnekovič lgt.”; CKB JK540 • 2 ♂♂, 2 ♀♀; “ Malaysia, Sabah, Batu Punggul Resort env., river in primary forest, 25.Vi. 1990 ”; NHMW. Measurements (all values in mm) PEL: ♂♂ 5.31–5.46 (5.39 ± 0.06, n = 11), ♀♀ 5.77–6.93 (6.18 ± 0.36, n = 7); PL: ♂♂ 1.31–1.36 (1.32 ± 0.03, n = 11), ♀♀ 1.46–1.51 (1.51 ± 0.07, n = 7); PW: ♂♂ 1.91–1.97 (1.97 ± 0.09, n = 11), ♀♀ 2.07–2.57 (2.24 ± 0.16, n = 7); EL: ♂♂ 4.09–4.19 (4.14 ± 0.04, n = 11), ♀♀ 4.39–5.30 (4.76 ± 0.28, n = 7); EW: ♂♂ 2.12–2.22 (2.18 ± 0.03, n = 11), ♀♀ 2.42–3.14 (2.61 ± 0.23, n = 7); HW: ♂♂ 1.21–1.26 (1.25 ± 0.03, n = 11), ♀♀ 1.31–1.51 (1.37 ± 0.06, n = 7); ID: ♂♂ 0.71–0.80 (0.76 ± 0.27, n = 11), ♀♀ 0.81–0.91 (0.84 ± 0.05, n = 7). Description Holotype The description of the holotype is completed by figures of the holo- and paratype specimens (Fig. 2). BODY (Fig. 2A). Elongated, about 2.5× as long as wide (PEL/EW), parallel-sided, and moderately convex. Length including head 5.90 mm, maximal width across elytra 2.1 mm. Overall colour black; antennal segments 1–4, ventral mouthparts, distal portion of femora, trochanters, anterior face of mesofemora, and claws reddish-brown. Vestiture consists of longer, more or less erect setae and short, strongly recumbent, hair-like setae. Longer setae acute, in narrow sockets; dorsal ones moderately dense, brownish. Ventral setae yellowish, denser on lateral portion of thorax, posterior and lateral portion of ventrites, mainly on ventrites 3–5 and on coxae and trochanters (Fig. 2C). Short setae in narrow sockets (micropunctures), moderately densely to densely arranged, especially ventrally very dense. HEAD (Fig. 2D). Moderately wider than long, large (HW: 1.2 mm), moderately declined dorsally, arched laterally and flattened ventrally; slightly retracted into prothorax; frontoclypeal suture finely marked. Labrum transverse, lateral angles rounded, anterior margin feebly emarginated in middle; very dense yellowish setae in close rows along anterior margin and laterally; surface finely punctured, with numerous longer setae. Anterior margin of clypeus straight, bordered by a row of longer setae, clypeus moderately shorter than labrum. Frons without sublateral depressions, surface densely punctured, puncture diameter slightly larger than a facet diameter, punctures separated by 0.5–1.5 × puncture diameter; interstices shiny, with micropunctures. Eyes large and strongly protuberant (ID: 0.7 mm), nearly circular in lateral view, without interfacetal setae, dorsally surrounded by long conspicuous setae. Antennal insertions exposed from above, close to eye margin; subantennal groove vaguely indicated only, shallow and short. Genae without anterolateral process, with numerous longer setae anteriorly. Gula as wide as long, not in the same plane with mentum, with cavity surrounded by dense hair-like setae; gular sutures straight; submentum short, transverse, densely punctured. Cervical sclerites large, wide and strongly sclerotised. Antenna 11-segmented, serrate, reaching slightly behind anterior margin of pronotum. Scape half as long as ID, moderately curved; posterior face flattened, lacking setae. Pedicel 0.5 × as long as scape, both with conspicuously long, hair-like sensilla; combined length of antennomeres 3–11 moderately longer than combined length of previous antennomeres.Antennomeres 6–10 transverse and more tightly aligned than previous antennomeres. Length/width of antennomeres 1–11 (in mm) as follows: 0.36/0.16: 0.18/0.99: 0.12/0.09: 0.06/0.08: 0.08/0.09: 0.81/0.09: 0.06/0.09: 0.06/0.09: 0.06/0.09: 0.06/0.09: 0.08/0.08. Maxillary palpus four-segmented, shorter than ID; terminal palpomere short, apically enlarged and truncate, with large sensory field; palpomeres 2 and 3 subequal in length, widened distally, with numerous moderately long hair-like sensilla. Mentum flat, short and wide, setose, with sides subparallel; palpigers strongly sclerotised, free, and unfused mesally. Labial palpus three-segmented, half as long as maxillary palpus; first segment short; second segment longer, with short and long hair-like sensilla around apical margin; third segment slightly longer than preceding, with apical sensory field similar to that on maxillary palpus. Ligula short and wide, more strongly sclerotised mesally than anterolaterally; anterior angles rounded, produced laterad. THORAX. Pronotum 1.47 × as broad as long, PW: 1.95 mm, PL: 1.30 mm, gradually expanded posteriad, widest in front of posterior angles and deeply excised in hind angles. Pronotal sides moderately arcuate, finely crenate and explanate, on each side with conspicuous blunt tooth (projection) posteriorly; posterior angles almost rectangular; anterior angles not protruding. Anterior margin straight, sides with collar-like thickening; posterior margin trisinuate. Disc moderately convex, with two small prescutellar foveae, strongly deflexed laterad and anteriad. Surface with dual punctuation; large punctures moderately larger than facets, nearly confluent or separated by distances up to 1.5 × puncture diameter, appear to be denser laterally. Small punctures moderately larger than those on head, intermixed within larger ones. Hypomeron with ventral outline trisinuate, deepest emargination at level of procoxae. Width of hypomeron subequal in middle third, moderately narrowed anteriad and posteriad; anterior depression for reception of antennal tip small. Prosternum in front of coxae very short, distinctly shorter than prosternal process, transverse and not concealing head in repose. Prosternal process about twice as long as wide, subtriangular, posterior half distinctly narrowed, sides raised; mesal portion with longitudinal keel. Procoxae transverse, countersunk; procoxal cavities open posteriorly, moderately widely separated; postcoxal projection absent. Mesoventrite moderately shorter than prosternal process, separated by sutures from surrounding sclerites, posterior angles more or less produced posteriad and overlapping metaventrite; mesoventrite divided by fine discrimen; groove for reception of prosternal process deep, present along entire length, posteriorly widened. Mesocoxae large and prominent, subglobular; mesally separated by distance twice as wide as procoxae. Scutellary shield (scutellum) small, subtriangular, as wide as long, sides arcuate. Metaventrite twice as long as mesoventrite; anterior edge of metaventrite not carinate between mesocoxal cavities, anterolateral portion flat; exposed portion of anepisternum 3 moderately wide and long. Metaventral disc convex on sides, with sizeable medial depression extending from anterior third to posterior margin and with small medial depression anteriorly; discrimen fine, present along entire length of metaventrite; metakatepisternal suture subtle, hardly visible; surface finely punctured. Metacoxae large, transverse, oblique, almost reaching elytra, separated from metaventrite by a suture, posteriorly excavate for reception of femora. Elytra 4.05 mm long (EL) and 2.15 mm wide (EW), subparallel-sided, moderately convex; each elytron with ten punctate striae and one accessory basal stria between sutural and second stria. Strial punctures on disc moderately larger than those on pronotum, separated by ca distance of puncture diameter, punctures becoming smaller posteriorly; punctures in striae 6–10 larger, appearing subquadrate and more closely arranged; intervals flat, finely punctured; sutural interval moderately raised. Humeri rounded and prominent; lateral margin moderately explanate, inflected at level of metacoxae; anterior margin smooth; elytral apices slightly deflected and not meeting at suture, separated by a gap, narrowly rounded and simple. Epipleura strongly inflected at the level of metacoxae, their width subequal along entire length, oblique and received in deep grooves on meso- and metathorax; posteriorly relatively tightly fitted to abdomen. Hind wing large, darkly pigmented, fully developed. Legs nearly as long as elytra; femoral pubescence short; tibial groove shallow, present on ca distal 0.66. Tibiae moderately longer than femora, slightly curved, nearly straight; pro- and metatibiae with dense short pubescence; mesotibia flattened and lacking dense pubescence, extended and slightly bent at apex with a trace of tubercle. Tarsi fivesegmented, ca half as long as tibiae (except claws), pro- and metatarsi densely pubescent; claws simple, similar in form and angle of inclination. ABDOMEN. Five strongly sclerotised ventrites present, all well separated by sutures; first three ventrites connate, remaining two separated by thin membrane, movable; ventrites moderately convex, shallowly depressed along midline; first ventrite not entirely divided by metacoxae, admedian carinae absent; lengths of ventrites 1–5 (in mm): 0.75: 0.50: 0.35: 0.30: 0.45. Intercoxal process wide, subtriangular, acute anteriorly; lateral margins moderately raised; fifth ventrite truncate posteriorly and shallowly emarginate in middle. Surface of ventrites finely punctured and densely setose; third and fourth ventrites bears conspicuous longer, narrowly spaced, flattened setae near posterior margin; numerous flattened setae also on central and apical portion of fifth ventrite. Male sternite VIII symmetrical, deeply emarginate posteriorly and with numerous dense, long setae; anterior median struts short and thin (Fig. 4D). Tergite VIII dark, well sclerotised, narrowly rounded posteriorly, with dual punctuation and setation. Male sternite IX asymmetrical, anterior median strut long; posterior portion well sclerotised, semitubular, surrounding phallobase; posterior edge shallowly emarginated (Fig. 4C). AEDEAGUS.Trilobate, symmetrical (Fig. 3A–B), ca 1.30 mm long; phallobase including anterior projection ca 0.7 × as long as parameres, nearly tubular, lateral portions sclerotised, ventral and dorsal portions membranous. Parameres individually articulated with phallobase, dorsally fused near base, ventrally free along whole length; parameres narrowed, flattened, abruptly bent and less sclerotised in apical portion (Fig. 3C), apices do not reach the apex of penis. Penis symmetrical, basal portion expanded ventrally nearly in the form of a ʻbellʼ; dorsal portion flattened with lateral sides explanate in basal 0.6 and further gradually narrowed apicad, thus penis nearly round in cross-section, with apex bent ventrad; ventral sac membranous without fibula, corona present. Female terminalia Posterior margin of female sternite VIII widely rounded; surface with numerous long, dense dark setae (Fig. 4E); anterior margin with robust, subtriangular median strut, the latter subequal in length to posterior portion of sternite. Tergite VIII wider and widely rounded posteriorly; punctuation and setation similar to that of ma
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34. Potamophilus kelabitensis Kodada & Boukal & V��a��n�� & Goffov�� & Ondrejkov�� 2022, sp. nov
- Author
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Kodada, J��n, Boukal, David S., V��a��n��, Peter, Goffov��, Katar��na, and Ondrejkov��, Kamila
- Subjects
Coleoptera ,Elmidae ,Insecta ,Potamophilus ,Arthropoda ,Potamophilus kelabitensis ,Animalia ,Biodiversity ,Taxonomy - Abstract
Potamophilus kelabitensis sp. nov. urn:lsid:zoobank.org:act: D801EBA4-C36A-4569-B495-7792B4B58F9D Figs 2���5 Type locality Malaysia, Sarawak, Miri district, Ramudu. Adults were collected at light in the Pa���Kelapang river environment in the Ramudu settlement (Fig. 5). Diagnosis Potamophilus kelabitensis sp. nov. is an elongated, parallel-sided, medium-sized (PEL: 5.3���7.3 mm), predominantly black species with reddish-brown antennal segments 1���4, distal portion of femora, trochanters, anterior face of mesofemora, and claws. The pronotum is about 1.5 �� as wide as long, gradually expanded posteriad, widest in front of posterior margin, and deeply excised in hind angles. Pronotal sides are moderately arcuate, finely crenate, and explanate, on each side with conspicuous blunt tooth posteriorly; posterior angles are nearly rectangular. Pronotal surface bears dual punctuation. Large punctures are moderately larger than facets, nearly confluent or separated by distances up to 1.5�� a puncture diameter, punctures appear to be denser laterally. Small punctures are intermixed within larger ones and are moderately larger than those on the head. Elytron with ten punctate striae and one accessory basal stria between the sutural and second stria. Strial punctures on the disc are more prominent than those on the pronotum, separated by one puncture diameter, punctures becoming smaller posteriorly; punctures in striae 6���10 are more prominent, appearing subquadrate and more closely arranged. Intervals are flat, finely punctured; sutural interval moderately raised; elytral apices are slightly deflected and not meeting at the suture, separated by a gap, narrowly rounded and not protruding. The aedeagus is trilobate, symmetrical; parameres in the apical portion are narrowed, flattened, abruptly bent ventrad, and less sclerotised; apices do not reach the apex of the penis. Differential diagnosis The new species differs from all other described species of Potamophilus by the following combination of external characters: ��� a relatively small size (separating it from P. feae); ��� distinctly crenate lateral margins of the pronotum (separating it from P. acuminatus, P. albertisii, P. feae, P. papuanus, and P. spinicollis); ��� deeply excised hind angles of the pronotum (separating it from P. albertisii); ��� lack of impression on the pronotal disc in front of the scutellum (separating it from P. acuminatus and P. spinicollis); ��� flat elytral intervals except the sutural one (separating it from P. acuminatus, P. feae, and P. spinicollis); ��� coarse strial punctures on the elytra (separating it from P. albertisii); ��� subquadrate and not rounded strial punctures in intervals 6���10 (separating it from P. acuminatus, P. feae, P. papuanus, and P. spinicollis); ��� evenly rounded elytral apices in both sexes (separating it from P. acuminatus, P. albertisii, P. feae, and P. papuanus); ��� the absence of a distinct, well-separated median tubercle on the meso- and metatibia in males (separating it from P. albertisii, P. feae, P. papuanus, and P. spinicollis). For the sake of convenience, brief diagnoses of the described species are given below. In P. acuminatus (PEL: ca 6.1���7.7 mm), the hind angles of the pronotum are deeply excised, pronotal sides are smooth, not crenate; pronotal disc with a wide, distinct depression in front of the scutellum. Strial punctures on the elytra are moderately coarse, sharply impressed, rounded, and separated by about their diameter. Elytra are long and narrow (ca 3.6���4.0 �� as long as pronotum), with the first interval raised in the posterior 0.8 of its length, distinctly convex intervals 3 and 5, and other intervals flat to feebly convex. The apex of each elytron is produced, angulate in males while acuminate and more protruding with divergent apices in females. Meso- and metatibia are weakly sinuous; mesotibia in males is usually more strongly enlarged distally with an indistinct median tubercle. In P. albertisii (PEL: ca 6.8���7.1 mm), the hind angles of the pronotum are at most slightly emarginated, with the emargination at most half as wide as scutellum; pronotal sides are smooth, not crenate; pronotal disc is flat or at most indistinctly impressed in front of the scutellum. Strial punctures on the elytra are moderately fine to fine, conspicuously sharply impressed, elongate, and separated by about 1���2 �� their length. The first elytral interval is raised, and the remaining intervals are flat or at most slightly convex, similarly as in P. kelabitensis sp. nov. The apex of each elytron is produced, angulate in males and acuminate in females, with subparallel apices. Meso- and metatibia are weakly sinuous, usually more strongly so and always with a distinct, acute median tubercle at the distal end of both tibiae in males. In P. feae (PEL: ca 9.5���10.4 mm), the hind angles of the pronotum are deeply excised; pronotal sides are smooth, not crenate; pronotal disc is at most indistinctly impressed in front of the scutellum. Strial punctures on the elytra are moderately coarse, more delicate on the declivity, moderately sharply impressed and rounded, separated by about 1���2 �� their diameter; first and third interval in the posterior half are distinctly raised, other intervals at most feebly convex. The apex of each elytron is produced, more or less angulate, the angle acute (ca 60��), with an almost identical shape in both sexes. Mesotibia is weakly sinuous, and the distal end bears a stout median tubercle in males; metatibia is almost straight in both sexes. In P. papuanus (PEL: ca 5.4���5.9 mm), the hind angles of the pronotum are deeply excised; pronotal sides are smooth, not crenate; pronotal disc is evenly convex to flat in front of the scutellum. Pronotal disc is densely and finely punctate with the punctures smaller than the eye facets, i.e., the punctuation is finer than in P. kelabitensis sp. nov. Elytral intervals are more or less flat, and only the first interval is raised in about the posterior half; strial punctures are rounded, moderately large (slightly larger than eye facets), well and sharply impressed, separated by about 1���2 �� their diameter. Elytral apices have an acute angle in males and are angulate to acuminate in females. Mesotibia and metatibia are distinctly curved/sinuate with a blunt tubercle on the mesal face of the distal part in males, nearly straight or only weakly sinuate in females. In P. spinicollis (PEL: ca 7.0 mm), the hind angles of the pronotum are deeply excised; pronotal sides are smooth to indistinctly and irregularly crenate, especially in the posterior half; pronotal disc with a distinct subtriangular depression in front of the scutellum. Elytral intervals are convex on the disc, with the first interval raised in the posterior 0.8 of its length. Strial punctures are rounded and conspicuously coarse, larger than those on the pronotum and much larger than eye facets, well and sharply impressed, separated by at most their diameter on the disc, smaller and sparser towards the lateral sides and posterior declivity. Male with the apex of each elytron separately rounded (female unknown) and with a rather prominent, pointed tubercle on the mesal face of the distal part of meso- and metatibia. Etymology The species is named after the Kelabit Highlands, an isolated highland plateau in the interior of the Sarawak State (Malaysia) and bordering the Kalimantan Province (Indonesia). Type material Holotype MALAYSIA ��� ♂; ��� Malaysia, Sarawak, Miri distr., Ramudu, 26.06.2018, (15) 3��33���17.0��� N 115��29���38.5��� E 921 m a.s.l., Pa���Kelapang riv. env., J. Kodada & D. Selnekovič lgt., at light ���; CFDS. Paratypes MALAYSIA ��� 11 ♂♂, 7 ♀♀; same collection data as for holotype; CFDS, CKB ��� 1 ♀; ��� Malaysia, Sarawak, Miri distr., Bario, 19.��� 23.6.2018, Lian Labang Garden, at light, J. Kodada & D. Selnekovič lgt.���; CKB JK540 ��� 2 ♂♂, 2 ♀♀; ��� Malaysia, Sabah, Batu Punggul Resort env., river in primary forest, 25.Vi. 1990 ���; NHMW. Measurements (all values in mm) PEL: ♂♂ 5.31���5.46 (5.39 �� 0.06, n = 11), ♀♀ 5.77���6.93 (6.18 �� 0.36, n = 7); PL: ♂♂ 1.31���1.36 (1.32 �� 0.03, n = 11), ♀♀ 1.46���1.51 (1.51 �� 0.07, n = 7); PW: ♂♂ 1.91���1.97 (1.97 �� 0.09, n = 11), ♀♀ 2.07���2.57 (2.24 �� 0.16, n = 7); EL: ♂♂ 4.09���4.19 (4.14 �� 0.04, n = 11), ♀♀ 4.39���5.30 (4.76 �� 0.28, n = 7); EW: ♂♂ 2.12���2.22 (2.18 �� 0.03, n = 11), ♀♀ 2.42���3.14 (2.61 �� 0.23, n = 7); HW: ♂♂ 1.21���1.26 (1.25 �� 0.03, n = 11), ♀♀ 1.31���1.51 (1.37 �� 0.06, n = 7); ID: ♂♂ 0.71���0.80 (0.76 �� 0.27, n = 11), ♀♀ 0.81���0.91 (0.84 �� 0.05, n = 7). Description Holotype The description of the holotype is completed by figures of the holo- and paratype specimens (Fig. 2). BODY (Fig. 2A). Elongated, about 2.5�� as long as wide (PEL/EW), parallel-sided, and moderately convex. Length including head 5.90 mm, maximal width across elytra 2.1 mm. Overall colour black; antennal segments 1���4, ventral mouthparts, distal portion of femora, trochanters, anterior face of mesofemora, and claws reddish-brown. Vestiture consists of longer, more or less erect setae and short, strongly recumbent, hair-like setae. Longer setae acute, in narrow sockets; dorsal ones moderately dense, brownish. Ventral setae yellowish, denser on lateral portion of thorax, posterior and lateral portion of ventrites, mainly on ventrites 3���5 and on coxae and trochanters (Fig. 2C). Short setae in narrow sockets (micropunctures), moderately densely to densely arranged, especially ventrally very dense. HEAD (Fig. 2D). Moderately wider than long, large (HW: 1.2 mm), moderately declined dorsally, arched laterally and flattened ventrally; slightly retracted into prothorax; frontoclypeal suture finely marked. Labrum transverse, lateral angles rounded, anterior margin feebly emarginated in middle; very dense yellowish setae in close rows along anterior margin and laterally; surface finely punctured, with numerous longer setae. Anterior margin of clypeus straight, bordered by a row of longer setae, clypeus moderately shorter than labrum. Frons without sublateral depressions, surface densely punctured, puncture diameter slightly larger than a facet diameter, punctures separated by 0.5���1.5 �� puncture diameter; interstices shiny, with micropunctures. Eyes large and strongly protuberant (ID: 0.7 mm), nearly circular in lateral view, without interfacetal setae, dorsally surrounded by long conspicuous setae. Antennal insertions exposed from above, close to eye margin; subantennal groove vaguely indicated only, shallow and short. Genae without anterolateral process, with numerous longer setae anteriorly. Gula as wide as long, not in the same plane with mentum, with cavity surrounded by dense hair-like setae; gular sutures straight; submentum short, transverse, densely punctured. Cervical sclerites large, wide and strongly sclerotised. Antenna 11-segmented, serrate, reaching slightly behind anterior margin of pronotum. Scape half as long as ID, moderately curved; posterior face flattened, lacking setae. Pedicel 0.5 �� as long as scape, both with conspicuously long, hair-like sensilla; combined length of antennomeres 3���11 moderately longer than combined length of previous antennomeres.Antennomeres 6���10 transverse and more tightly aligned than previous antennomeres. Length/width of antennomeres 1���11 (in mm) as follows: 0.36/0.16: 0.18/0.99: 0.12/0.09: 0.06/0.08: 0.08/0.09: 0.81/0.09: 0.06/0.09: 0.06/0.09: 0.06/0.09: 0.06/0.09: 0.08/0.08. Maxillary palpus four-segmented, shorter than ID; terminal palpomere short, apically enlarged and truncate, with large sensory field; palpomeres 2 and 3 subequal in length, widened distally, with numerous moderately long hair-like sensilla. Mentum flat, short and wide, setose, with sides subparallel; palpigers strongly sclerotised, free, and unfused mesally. Labial palpus three-segmented, half as long as maxillary palpus; first segment short; second segment longer, with short and long hair-like sensilla around apical margin; third segment slightly longer than preceding, with apical sensory field similar to that on maxillary palpus. Ligula short and wide, more strongly sclerotised mesally than anterolaterally; anterior angles rounded, produced laterad. THORAX. Pronotum 1.47 �� as broad as long, PW: 1.95 mm, PL: 1.30 mm, gradually expanded posteriad, widest in front of posterior angles and deeply excised in hind angles. Pronotal sides moderately arcuate, finely crenate and explanate, on each side with conspicuous blunt tooth (projection) posteriorly; posterior angles almost rectangular; anterior angles not protruding. Anterior margin straight, sides with collar-like thickening; posterior margin trisinuate. Disc moderately convex, with two small prescutellar foveae, strongly deflexed laterad and anteriad. Surface with dual punctuation; large punctures moderately larger than facets, nearly confluent or separated by distances up to 1.5 �� puncture diameter, appear to be denser laterally. Small punctures moderately larger than those on head, intermixed within larger ones. Hypomeron with ventral outline trisinuate, deepest emargination at level of procoxae. Width of hypomeron subequal in middle third, moderately narrowed anteriad and posteriad; anterior depression for reception of antennal tip small. Prosternum in front of coxae very short, distinctly shorter than prosternal process, transverse and not concealing head in repose. Prosternal process about twice as long as wide, subtriangular, posterior half distinctly narrowed, sides raised; mesal portion with longitudinal keel. Procoxae transverse, countersunk; procoxal cavities open posteriorly, moderately widely separated; postcoxal projection absent. Mesoventrite moderately shorter than prosternal process, separated by sutures from surrounding sclerites, posterior angles more or less produced posteriad and overlapping metaventrite; mesoventrite divided by fine discrimen; groove for reception of prosternal process deep, present along entire length, posteriorly widened. Mesocoxae large and prominent, subglobular; mesally separated by distance twice as wide as procoxae. Scutellary shield (scutellum) small, subtriangular, as wide as long, sides arcuate. Metaventrite twice as long as mesoventrite; anterior edge of metaventrite not carinate between mesocoxal cavities, anterolateral portion flat; exposed portion of anepisternum 3 moderately wide and long. Metaventral disc convex on sides, with sizeable medial depression extending from anterior third to posterior margin and with small medial depression anteriorly; discrimen fine, present along entire length of metaventrite; metakatepisternal suture subtle, hardly visible; surface finely punctured. Metacoxae large, transverse, oblique, almost reaching elytra, separated from metaventrite by a suture, posteriorly excavate for reception of femora. Elytra 4.05 mm long (EL) and 2.15 mm wide (EW), subparallel-sided, moderately convex; each elytron with ten punctate striae and one accessory basal stria between sutural and second stria. Strial punctures on disc moderately larger than those on pronotum, separated by ca distance of puncture diameter, punctures becoming smaller posteriorly; punctures in striae 6���10 larger, appearing subquadrate and more closely arranged; intervals flat, finely punctured; sutural interval moderately raised. Humeri rounded and prominent; lateral margin moderately explanate, inflected at level of metacoxae; anterior margin smooth; elytral apices slightly deflected and not meeting at suture, separated by a gap, narrowly rounded and simple. Epipleura strongly inflected at the level of metacoxae, their width subequal along entire length, oblique and received in deep grooves on meso- and metathorax; posteriorly relatively tightly fitted to abdomen. Hind wing large, darkly pigmented, fully developed. Legs nearly as long as elytra; femoral pubescence short; tibial groove shallow, present on ca distal 0.66. Tibiae moderately longer than femora, slightly curved, nearly straight; pro- and metatibiae with dense short pubescence; mesotibia flattened and lacking dense pubescence, extended and slightly bent at apex with a trace of tubercle. Tarsi fivesegmented, ca half as long as tibiae (except claws), pro- and metatarsi densely pubescent; claws simple, similar in form and angle of inclination. ABDOMEN. Five strongly sclerotised ventrites present, all well separated by sutures; first three ventrites connate, remaining two separated by thin membrane, movable; ventrites moderately convex, shallowly depressed along midline; first ventrite not entirely divided by metacoxae, admedian carinae absent; lengths of ventrites 1���5 (in mm): 0.75: 0.50: 0.35: 0.30: 0.45. Intercoxal process wide, subtriangular, acute anteriorly; lateral margins moderately raised; fifth ventrite truncate posteriorly and shallowly emarginate in middle. Surface of ventrites finely punctured and densely setose; third and fourth ventrites bears conspicuous longer, narrowly spaced, flattened setae near posterior margin; numerous flattened setae also on central and apical portion of fifth ventrite. Male sternite VIII symmetrical, deeply emarginate posteriorly and with numerous dense, long setae; anterior median struts short and thin (Fig. 4D). Tergite VIII dark, well sclerotised, narrowly rounded posteriorly, with dual punctuation and setation. Male sternite IX asymmetrical, anterior median strut long; posterior portion well sclerotised, semitubular, surrounding phallobase; posterior edge shallowly emarginated (Fig. 4C). AEDEAGUS.Trilobate, symmetrical (Fig. 3A���B), ca 1.30 mm long; phallobase including anterior projection ca 0.7 �� as long as parameres, nearly tubular, lateral portions sclerotised, ventral and dorsal portions membranous. Parameres individually articulated with phallobase, dorsally fused near base, ventrally free along whole length; parameres narrowed, flattened, abruptly bent and less sclerotised in apical portion (Fig. 3C), apices do not reach the apex of penis. Penis symmetrical, basal portion expanded ventrally nearly in the form of a ��bell��; dorsal portion flattened with lateral sides explanate in basal 0.6 and further gradually narrowed apicad, thus penis nearly round in cross-section, with apex bent ventrad; ventral sac membranous without fibula, corona present. Female terminalia Posterior margin of female sternite VIII widely rounded; surface with numerous long, dense dark setae (Fig. 4E); anterior margin with robust, subtriangular median strut, the latter subequal in length to posterior portion of sternite. Tergite VIII wider and widely rounded posteriorly; punctuation and setation similar to that of ma, Published as part of Kodada, J��n, Boukal, David S., V��a��n��, Peter, Goffov��, Katar��na & Ondrejkov��, Kamila, 2022, Elmidae of Sarawak: the genus Potamophilus Germar, 1811, with a description of P. kelabitensis sp. nov. (Insecta: Coleoptera), pp. 1-18 in European Journal of Taxonomy 806 (1) on pages 6-15, DOI: 10.5852/ejt.2022.806.1695, http://zenodo.org/record/6373905
- Published
- 2022
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35. Evolution of Growth in Gulf of St Lawrence Cod?
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Heino, Mikko, Baulier, Loïc, Boukal, David S., Dunlop, Erin S., Eliassen, Sigrunn, Enberg, Katja, Jørgensen, Christian, and Varpe, Øystein
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- 2008
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36. The Role of Fisheries-Induced Evolution [with Response]
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Browman, Howard I., Law, Richard, Marshall, C. Tara, Kuparinen, Anna, Merilä, Juha, Jørgensen, Christian, Enberg, Katja, Dunlop, Erin S., Arlinghaus, Robert, Boukal, David S., Brander, Keith, Ernande, Bruno, Gårdmark, Anna, Johnston, Fiona, Matsumara, Shuichi, Pardoe, Heidi, Raab, Kristina, Silva, Alexandra, Vainikka, Anssi, Dieckmann, Ulf, Heinno, Mikko, and Rijnsdorp, Adriaan D.
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- 2008
37. Lazy ecologist's guide to water beetle diversity: Which sampling methods are the best?
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Klečka, Jan and Boukal, David S.
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- 2011
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38. Managing Evolving Fish Stocks
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Jørgensen, Christian, Enberg, Katja, Dunlop, Erin S., Arlinghaus, Robert, Boukal, David S., Brander, Keith, Ernande, Bruno, Gårdmark, Anna, Johnston, Fiona, Matsumura, Shuichi, Pardoe, Heidi, Raab, Kristina, Silva, Alexandra, Vainikka, Anssi, Dieckmann, Ulf, Heino, Mikko, and Rijnsdorp, Adriaan D.
- Published
- 2007
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39. Elmidae of Sarawak: the genus Potamophilus Germar, 1811, with a description of P. kelabitensis sp. nov. (Insecta: Coleoptera)
- Author
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Kodada, Ján, primary, Boukal, David S., additional, Vďačný, Peter, additional, Goffová, Katarína, additional, and Ondrejková, Kamila, additional
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- 2022
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40. Environmental stressors alter multiple determinants of individual reproductive output in the acid‐tolerant mayfly Leptophlebia vespertina
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Šupina, Jan, primary, Bojková, Jindřiška, additional, and Boukal, David S., additional
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- 2022
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41. Evolutionary Regime Shifts in Age and Size at Maturation of Exploited Fish Stocks
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de Roos, André M., Boukal, David S., and Persson, Lennart
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- 2006
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42. Caught between two Allee effects: Trade-off between reproduction and predation risk
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Pavlová, Viola, Berec, Lude˘k, and Boukal, David S.
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- 2010
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43. Valuable Secondary Habitats or Hazardous Ecological Traps? Environmental Risk Assessment of Minor and Trace Elements in Fly Ash Deposits across the Czech Republic
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Chmelová, Eliška, Kolar, Vojtech, Jan, Jiří, Carreira, Bruno M., Landeira-Dabarca, Andrea, Otáhalová, Šárka, Poláková, Martina, Vebrová, Lucie, Borovec, Jakub, Boukal, David S., Tropek, Robert, and Repositório da Universidade de Lisboa
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coal combustion waste ,Environmental sciences ,Environmental effects of industries and plants ,fungi ,human-made habitats ,TJ807-830 ,GE1-350 ,biodiversity conservation ,energy industry ,environmental pollution ,heavy metals ,TD194-195 ,Renewable energy sources - Abstract
Deposits of coal combustion wastes, especially fly ash, are sources of environmental and health risks in industrial regions. Recently, fly ash deposits have been reported as habitat surrogates for some threatened arthropods in Central Europe. However, the potential environmental risks of fly ash have not yet been assessed in the region. We analysed concentrations of 19 minor and trace elements in 19 lignite combustion waste deposits in the Czech Republic. We assessed their environmental risks by comparison with the national and EU legislation limits, and with several commonly used indices. Over 50% of the samples exceeded the Czech national limits for As, Cu, V, or Zn, whilst only V exceeded the EU limits. For some studied elements, the high-risk indices were detected in several localities. Nevertheless, the measured water characteristics, the long-term presence of fly ash, previous leaching by acid rains, and the low amount of organic matter altogether can infer low biological availability of these elements. We presume the revealed high concentrations of some heavy metals at some studied sites can be harmful for some colonising species. Nevertheless, more ecotoxicological research on particular species is needed for final decision on their conservation potential for terrestrial and freshwater biota.
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- 2021
44. From individuals to communities: Habitat complexity affects all levels of organization in aquatic environments
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Soukup, Pavel R., primary, Näslund, Joacim, additional, Höjesjö, Johan, additional, and Boukal, David S., additional
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- 2021
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45. Linking the Allee Effect, Sexual Reproduction, and Temperature‐Dependent Sex Determination Via Spatial Dynamics
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Berec, Luděk, Boukal, David S., and Berec, Michal
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- 2001
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46. Are non-sexual models appropriate for predicting the impact of virus-vectored immunocontraception?
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Deredec, Anne, Berec, Luděk, Boukal, David S., and Courchamp, Franck
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- 2008
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47. Modelling mate-finding Allee effects and populations dynamics, with applications in pest control
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Boukal, David S. and Berec, Luděk
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- 2009
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48. A simple fish-based approach to assess the ecological quality of freshwater reservoirs in Central Europe
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Blabolil Petr, Říha Milan, Ricard Daniel, Peterka Jiří, Prchalová Marie, Vašek Mojmír, Čech Martin, Frouzová Jaroslava, Jůza Tomáš, Muška Milan, Tušer Michal, Draštík Vladislav, Sajdlová Zuzana, Šmejkal Marek, Vejřík Lukáš, Matěna Josef, Boukal David S., Ritterbusch David, and Kubečka Jan
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Artificial lakes ,eutrophication ,fish indicators ,gillnets ,index sensitivity ,WFD ,Aquaculture. Fisheries. Angling ,SH1-691 - Abstract
The assessment of ecological quality in freshwater ecosystems is a key issue in many countries, but conditions for the development of assessment methodologies are often country-specific. This study proposes a simple methodology for the assessment of the ecological potential of reservoirs based on fish communities using a dataset covering major environmental and pressure gradients in reservoirs in the Czech Republic. Fish data obtained by gillnet sampling were correlated with a proxy of eutrophication as a key indicator of anthropogenic pressure for selecting appropriate fish-based indicators, establishing scoring criteria and developing the index of ecological quality. Expert judgement was also used to select potential fish indicators. Nine indicators were selected for the final fish-based index, fulfilling the criteria required by the Water Framework Directive. Two steps were used to validate the fish-based index quantification of its inter annual stability and sensitivity analysis of individual indicators. Finally, the index was compared to a previously developed general index for Central and Western Europe. Our study demonstrates that a combination of expert judgement and strict validation methods can result in an informative assessment of the ecological conditions, which can help identify conservation and restoration priorities.
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- 2017
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49. Community structure and collapses in multichannel food webs: Role of consumer body sizes and mesohabitat productivities
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Dijoux, Samuel, primary and Boukal, David S., additional
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- 2021
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50. How predator functional responses and Allee effects in prey affect the paradox of enrichment and population collapses
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Boukal, David S., Sabelis, Maurice W., and Berec, Luděk
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- 2007
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