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Habitat loss and fragmentation are growing global threats to natural habitats and their networks, posing significant challenges to biodiversity conservation. Globally, ponds are sharply declining in number because their small size makes them highly vulnerable to land use changes. While it is generally agreed that connectivity in habitat networks is crucial for sustaining biodiversity, the effect of connectivity on biodiversity patterns over small‐scaled habitat networks has so far received less attention given the general assumption that metacommunities lack spatial structuring on small scales. In this study, we tested whether this holds for multiple passively and actively dispersing organism groups in a well‐delineated pond metacommunity of 54 bomb crater ponds situated within 1 km. We investigated the influence of space and environment on species richness and metacommunity structure in these ponds, which share similar age, size, and shape and are subject to strong environmental gradients, making it an ideal study system. We specifically examined the impact of network centrality on taxonomic richness and eigenvector‐based spatial arrangement on metacommunity structure across different organism groups, including prokaryotes, microeukaryotes, zooplankton, macroinvertebrates, and amphibians. We found that while environmental filtering is the primary driver of community dynamics, there is also a significant spatial signal, particularly for passively dispersing groups, demonstrating the role of the central‐peripheral connectivity gradient. These findings highlight the importance of studying and protecting ponds as parts of a network rather than focusing on individual ponds. [ABSTRACT FROM AUTHOR]

Salinity is a major environmental predictor of phytoplankton species richness and composition. We hypothesize that the variation in phytoplankton richness along coastal salinity gradients is reflected in essential ecosystem functions like resource use efficiency (RUE)—the proportion of limiting resource that is converted into biomass. To test the hypothesis, we analyzed time series of phytoplankton and environmental variables from the Chesapeake Bay and the Baltic Sea. We analyzed the relationship among salinity, diversity, and RUE in bivariate and interaction association, and in structural equation model (SEM)—a form of path analysis to resolve multivariate relationships among interrelated variables. We concluded that the intrusion of marine water will lead to rapid change in species diversity on the fresh side. Despite diversity drop, individual community functions, like RUE, remain relatively resilient, reflecting functional redundancy. We propose that the salinity gradient also reflects trophic complexity, allowing stable resource use at reduced diversity. [ABSTRACT FROM AUTHOR]

Chytrid fungal parasites convert dietary energy and essential dietary molecules, such as long‐chain (LC) polyunsaturated fatty acids (PUFA), from inedible algal/cyanobacteria hosts into edible zoospores. How the improved biochemical PUFA composition of chytrid‐infected diet may extend to zooplankton, linking diet quality to consumer fitness, remains unexplored.Here, we assessed the trophic role of chytrids in supporting dietary energy and PUFA requirements of the crustacean zooplankton Daphnia, when feeding on the filamentous cyanobacterium Planktothrix.Only Daphnia feeding on chytrid‐infected Planktothrix reproduced successfully and had significantly higher survival and growth rates compared with Daphnia feeding on the sole Planktothrix diet. While the presence of chytrids resulted in a two‐fold increase of carbon ingested by Daphnia, carbon assimilation increased by a factor of four, clearly indicating enhanced carbon transfer efficiency with chytrid presence.Bulk carbon (δ13C) and nitrogen (δ15N) stable isotopes did not indicate any treatment‐specific dietary effects on Daphnia, nor differences in trophic position among diet sources and the consumer. Compound‐specific carbon isotopes of fatty acids (δ13CFA), however, revealed that chytrids bioconverted short‐chain to LC‐PUFA, making it available for Daphnia. Chytrids synthesised the ω‐3 PUFA stearidonic acid de novo, which was selectively retained by Daphnia. Values of δ13CFA demonstrated that Daphnia also bioconverted short‐chain to LC‐PUFA.We provide isotopic evidence that chytrids improved the dietary provision of LC‐PUFA for Daphnia and enhanced their fitness. We argue for the existence of a positive feedback loop between enhanced Daphnia growth and herbivory in response to chytrid‐mediated improved diet quality. Chytrids upgrade carbon from the primary producer and facilitate energy and PUFA transfer to primary consumers, potentially also benefitting upper trophic levels of pelagic food webs. [ABSTRACT FROM AUTHOR]

Zoosporic fungi of the phylum Chytridiomycota are ubiquitous parasites of phytoplankton in aquatic ecosystems, but little is known about phytoplankton defense strategies against parasitic chytrid attacks. Using a model chytrid-phytoplankton pathosystem, we experimentally tested the hypothesis that the mucilage envelope of a mucilage-forming desmid species provides protection against the parasitic chytrid Staurastromyces oculus. Mucilage-forming Staurodesmu s cells were not accessible to the chytrid, whereas physical removal of the mucilage envelope rendered the same Staurodesmus sp. strain equally susceptible to chytrid infections as the original non-mucilage-forming host Staurastrum sp. Epidemic spread of the parasite only occurred in Staurastrum sp. whereas non-mucilage-bearing Staurodesmus sp. allowed for co-existence of host and parasite, and mucilage-bearing Staurodesmus sp. caused parasite extinction. In addition to the mucilage defense barrier, we also demonstrate the ability of both Staurastrum sp. and Staurodesmus sp. to resist infection by preventing chytrid development while still remaining viable and being able to reproduce and thus recover from an infection. This study extends our knowledge on phytoplankton defense traits and the functional role of mucilage in phytoplankton as a physical barrier against fungal parasites. [ABSTRACT FROM AUTHOR]