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Algae and fungi found inside the coelenterons. (A) Oedogonium sp. (B) Epithemia sorex. (C) Cosmarium formosulum. (D) and (Ñ) Synedra acus. (E) Navicula sp. (F) Synedra ulna. (G) Class Hyphomycetes. (H) Nitzschia tryblionella. (I) Scenedesmus quadricauda. (J) Nitzschia filiformis. (K) Cocconeis placentula and Rhoicosphenia abbreviata. (L) Gomphonema constrictum. (LL) Scenedesmus falcatus. (M) C. placentula, Cyclotella meneghineana and Navicula zanoni. (N) Order Zygnematales. 

Algae and fungi found inside the coelenterons. (A) Oedogonium sp. (B) Epithemia sorex. (C) Cosmarium formosulum. (D) and (Ñ) Synedra acus. (E) Navicula sp. (F) Synedra ulna. (G) Class Hyphomycetes. (H) Nitzschia tryblionella. (I) Scenedesmus quadricauda. (J) Nitzschia filiformis. (K) Cocconeis placentula and Rhoicosphenia abbreviata. (L) Gomphonema constrictum. (LL) Scenedesmus falcatus. (M) C. placentula, Cyclotella meneghineana and Navicula zanoni. (N) Order Zygnematales. 

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... The medusae are generally planktonic; however, some colonies of polyps are also, for example, members of the family Porpitidae, genus Porpita (Calder 2010). These hydrozoans in marine and freshwater ecosystems are predators of phytoplankton and zooplankton groups (Wintzer et al. 2011, Deserti et al. 2017, Di Camillo et al. 2017. The presence of these hydrozoans can be helpful in nature and human wellbeing because they reflect the conservation status of the marine ecosystem and are bioindicators of hydrographic conditions (Bieri 1977, Edwards 2012, Yilmaz et al. 2020. ...
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... Another major lesson from the hydra experiments comes from wild individuals, since this experiment in fact simulated a dietary evolutionary mismatch. Indeed, hydras in the wild consume freshwater crustaceans [55], but not artemia which live in brackish ecosystems. Moreover, it is unlikely that a similar high-abundance and frequent diet as the one we used would be found in the wild. ...
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... Because of the presence of these asexual individuals, H. oligactis can reach huge population densities during late winter and early summer (Bryden, 1952; J.T. personal observation). This, in turn, could have major consequences for the population dynamics of their prey (mainly cladocerans and copepods, but also small fish; Cuker & Mosley, 1981;Deserti et al., 2017;Elliot et al., 1997;Massaro et al., 2013;Rivera-de la Parra et al., 2016;Schwartz et al., 1983) in a manner that amplifies with climate change. However, whether warming temperatures affect sexual or asexual fitness, and thereby population dynamics in hydra is still unclear. ...
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... Also, given that microbiota is altered in the tumorous polyps, and that the microbiota alters the behavior of hydras (Murillo-Rincon et al., 2017), we cannot exclude that a modified neuronal activity and feeding behavior might be responsible for the more efficient predation of tumorous polyps. We particularly emphasize here that the higher predation capacity of tumorous hydras was observed in both feeding conditions, ad libitum and restricted feeding, whereby the limited food supply is likely the more natural condition for hydras (Deserti et al., 2017). In any case, these results suggest that the level of resources could influence the coexistence between tumorous and non-tumorous individuals in a non-expected manner. ...
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... Also, given that microbiota is altered in the tumorous polyps, and that the microbiota alters the behavior of hydras (Murillo-Rincon et al., 2017), we cannot exclude that a modified neuronal activity and feeding behavior might be responsible for the more efficient predation of tumorous polyps. We particularly emphasize here that the higher predation capacity of tumorous hydras was observed in both feeding conditions, ad libitum and restricted feeding, whereby the limited food supply is likely the more natural condition for hydras (Deserti et al., 2017). In any case, these results suggest that the level of resources could influence the coexistence between tumorous and non-tumorous individuals in a non-expected manner. ...
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Se describe la presencia de cuatro taxones de hidras de agua dulce (Cnidaria, Hydrozoa: Hydridae) en zonas someras epicontinentales de la cuenca del Duero (NO de España). En la subcuenca del Tera se encontraron individuos aislados sobre macrófitos sumergidos de tres taxones: Hydra vulgaris Pallas, 1766, Hydra (Pelmatohydra) oligactis Pallas, 1766 e Hydra (Chlorohydra) viridissima Pallas, 1766, y además en el Carrión grupos coloniales sobre bloques de cuarcita de la forma H. vulgaris var. aurantiaca Ehrenberg, 1838. En todos los casos se corresponde con ecosistemas de media montaña de aguas frías, transparentes y oligotróficas, de pH ligeramente ácido y con escasa mineralización. Todas las especies fueron localizadas en simpatría estricta, aunque en el lago de Sanabria se pudo citar tres taxones en diferentes hábitats. Se documenta la predación en cautividad de H. oligactis sobre gusanos oligoquetos y los periodos de formación de pólipos por gemación.
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The feeding upon large animals—even larger than the predator—by benthic cnidarians has been reported from many ecosystems but never exhaustively studied to date. By reviewing 38 papers on this topic, this review aims to recap the observations on the predatory behaviour of polyps, to establish feeding plasticity boundaries and to understand the contribute of this trophic strategy to the benthic–pelagic coupling. The reviewed documents published increasingly during the last two decades mostly reported observations on heterotrophic Anthozoa in shallow ecosystems collected through photo/video records. The main prey items are represented by gelatinous zooplankton and echinoderms. The lexical discordance in the considered papers highlights the need to standardize the terminology to describe the feeding behaviour of benthic Cnidaria, opportunistic and characterized by a strong plasticity. Given the importance of large prey in cnidarian trophism, we proposed an unambiguous terminology that will help the online search of literature and address future studies. We suggest identifying micro-predation (predator/prey size ratio ≥ 5:1) and macro-predation (predator/prey size ratio is ≤ 1:1) as distinct feeding modalities, because the capture of large prey involves peculiar movements of polyps, such as stretching and retracting of column and tentacles to pull the prey towards the mouth.