Elisenda Ballesté

Plastic has introduced a novel and persistent substrate into natural ecosystems, rapidly colonized by microbial biofilms collectively termed the plastisphere. Since its introduction, the concept has catalyzed interdisciplinary research and shaped scientific and public discourse on plastic pollution. Yet, a central question remains unresolved: Do plastisphere communities represent a fundamentally distinct ecological entity, or are they conventional biofilms forming on an unconventional material? Here, we synthesize current evidence across marine and terrestrial systems to argue that plastisphere communities are not consistently taxonomically or functionally unique. Instead, they largely reflect established biofilm assembly processes governed by environmental conditions, source communities, and successional dynamics. Claims of plastic biodegradation, pathogen enrichment, or antimicrobial resistance hotspots remain context-dependent and often lack robust comparative frameworks. We propose that the ecological significance of the plastisphere lies not in microbial novelty, but in the properties of the substrate itself. Plastics are uniquely persistent and, in many environments, highly mobile, enabling microbial communities to disperse across ecosystems and extend residence times beyond those of natural particles. By reframing the plastisphere as a condition of microbial life on durable, mobile substrates, we retain its conceptual value while aligning it with ecological theory and advancing a more precise research agenda.

Soft-bottom areas are among the least explored ecosystems in Antarctica. To improve our understanding of these environments, we performed a preliminary assessment of the marine macrobenthic fauna in False Bay, Livingston Island, near Huntress Glacier (South Shetland Islands, Antarctica). Fourteen Van Veen grabs (0.018 m ² area) were deployed at two stations within the bay at depths of 174–210 m. The samples provided values up to 159 556 individuals m ^-2 within 15 major taxonomic groups. Annelida Polychaeta was predominant (~93%), followed by Ophiuroidea and Bivalvia at the external station and Bivalvia and Amphipoda at the internal site. Maldanid polychaetes, particularly Maldane sarsi antarctica , constituted 84.62–90.74% of the samples. Total biomass was 6673.25 grams of wet weight per square metre, mainly from Ascidiacea, Polychaeta, Holothuroidea and Ophiuroidea. Approximately 12% of the macrofauna inhabited the sediment (epifauna), while 88% lived into the sediments (infauna). Regarding feeding modes, specimens were detritivores (77.91–82.71%), suspension-feeders (7.59–13.37%) and, infrequently, predators (4.07–5.07%) and grazers (4.63–4.65%). According to the compilation of occurrence records in the Southern Ocean, M. sarsi antarctica has a circum-Antarctic distribution. Furthermore, the population of this species in False Bay appears to be stable and undisturbed with a normal distribution in size structure, with a higher proportion of individuals at intermediate sizes (2.85–4.26 cm). This study provides for the first time detailed descriptions of the macrofauna from the soft bottoms of False Bay, representing a preliminary effort to monitor ecological shifts in this critically important and understudied region, which is experiencing rapid environmental changes within Antarctic marine ecosystems.

Microorganisms, including potential pathogens, can colonise plastic surfaces in aquatic environments. This study investigates the colonisation of plastic pellets by Escherichia coli ( E. coli ) as a proxy for faecal pathogens in aquatic environments. Plastic pellets from a polluted beach were placed in seawater aquaria spiked with E. coli . Diverse bacteria, primarily from the Proteobacteria phylum, rapidly colonised the pellets within 24 h, with notable species known for plastic or hydrocarbon degradation. Over 26 days, biofilms formed on the plastic surfaces, reaching bacterial populations of up to 6.8·10 ⁵ gene copies (gc) of the 16S rRNA mm ⁻² . E. coli , was detected in the pellets for up to 7 days using culture methods, exhibiting varying attachment densities regardless of source or environmental factors. The study highlights plastic biofilms as reservoirs for E. coli , contributing to the survival and persistence of faecal bacteria in aquatic systems. These findings deepen our understanding of the risks associated with plastic pollution in marine settings, offering insights into the behaviour of faecal indicators and their implications for water quality assessments, while providing valuable information on potential pathogen dissemination within plastic‐associated microbial communities.

This study investigates the influence of urban pollution and climate dynamics on water quality and the bacterial communities in an Argelian watershed. Twenty-one sampling campaigns were conducted over two years at six sites along the Oued Boussellam, a river impacted by the effluent of a sewage treatment plant, from a low-polluted site to a water reservoir within a 50 km distance. Fecal indicators and the human fecal marker crAssphage were monitored. Illumina 16S rRNA amplicon sequencing was used to assess water microbial populations’ changes. Urban sewage discharge had an impact on the river quality and microbial ecosystem, which was attenuated along the river course. Significant reductions (>4 log₁₀ for E. coli and somatic coliphages, >3 log₁₀ for crAssphage) occurred, particularly during high-temperature periods. crAssphage correlated strongly with somatic coliphages downstream the river. Seasonal differences were observed in the diversity of the bacterial communities, with higher values during the high-temperature period. The genus-level community structure was similar at highly polluted river sites, also displaying seasonal differences. Despite high pollution levels, natural processes reduced fecal indicators to acceptable levels in the reservoir as well as shaped the bacterial communities along the river, highlighting the importance of understanding indicator persistence and microbial community resilience for effective water quality management within the context of the global warming scenario.

Crassvirales (crAss-like phages) are an abundant group of human gut-specific bacteriophages discovered in silico. The use of crAss-like phages as human fecal indicators is proposed but the isolation of only seven cultured strains of crAss-like phages to date has greatly hindered their study. Here, we report the isolation and genetic characterization of 25 new crAss-like phages (termed crAssBcn) infecting Bacteroides intestinalis, belonging to the order Crassvirales, genus Kehishuvirus and, based on their genomic variability, classified into six species. CrAssBcn phage genomes are similar to ΦCrAss001 but show genomic and aminoacidic differences when compared to other crAss-like phages of the same family. CrAssBcn phages are detected in fecal metagenomes around the world at a higher frequency than ΦCrAss001. This study increases the known crAss-like phage isolates and their abundance and heterogeneity open the question of what member of the Crassvirales group should be selected as human fecal marker.