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Arboleda, E.

Publications and source records attributed to Arboleda, E..

3 recordsLinked to original sources

BiOS: An Open-Source Framework for the Integration of Heterogeneous Biodiversity Data

The era of Big Data has reshaped biodiversity research, yet the potential of this information is frequently constrained by data heterogeneity, incompatible schemas, and the fragmentation of resources. Whilst standards such as Darwin Core have improved interoperability, significant barriers persist in harmonising multi-typology datasets ranging from taxonomy and genetics to species distribution. Here, we present the Biodiversity Observatory System (BiOS), a comprehensive, open-source software stack designed to address these impediments through a modular, community-driven architecture. BiOS departs from monolithic database designs by decoupling the back-end data management from the front-end presentation layer. This architectural separation supports a dual-access model tailored to diverse stakeholder needs. For researchers and developers, the system offers a comprehensive Application Programming Interface (API) that exposes all back-end functionalities, enabling seamless programmatic access, automated data retrieval, and integration with external analytical workflows. Simultaneously, the platform features a user web interface designed to lower the technical barrier to entry. This interface facilitates intuitive data exploration through agile taxonomic navigation, advanced geospatial map viewers for species occurrence filtering, and dedicated dashboards for visualising genetic markers and legislative status. Strictly adhering to the FAIR principles (Findable, Accessible, Interoperable, Reusable), BiOS acts as a relational engine capable of integrating heterogeneous data streams. By providing a flexible, interoperable core that supports the "seven shortfalls" framework of biodiversity knowledge, BiOS offers a turnkey solution to overcome data fragmentation and enhance collaborative conservation efforts.

bioinformatics↗

A Cryptochrome adopts distinct moon- and sunlight states and functions as moonlight interpreter in monthly oscillator entrainment

The moons monthly cycle synchronizes reproduction in countless marine organisms. The mass-spawning bristle worm Platynereis dumerilii uses an endogenous monthly oscillator to phase reproduction to specific days. Classical work showed that this oscillator is set by full moon. But how do organisms recognize such a specific moon phase? We uncover that the light receptor L-Cryptochrome (L-Cry) is able to discriminate between different moonlight durations, as well as between sun- and moonlight. Consistent with L-Crys function as light valence interpreter, its genetic loss leads to a faster re-entrainment under artificially strong nocturnal light. This suggests that L-Cry blocks "wrong" light from impacting on the monthly oscillator. A biochemical characterization of purified L-Cry protein, exposed to naturalistic sun- or moonlight, reveals the formation of distinct sun- and moonlight states characterized by different photoreduction- and recovery kinetics of L-Crys co-factor Flavin Adenine Dinucleotide. In vivo, L-Crys sun-versus moonlight states correlate with distinct sub-cellular localizations, indicating different signalling. In contrast, r-Opsin1, the most abundant ocular opsin, is not required for monthly oscillator entrainment. Our work reveals a new concept for correct moonlight interpretation involving a "valence interpreter" that provides entraining photoreceptor(s) with light source and moon phase information. These findings advance our mechanistic understanding of a fundamental biological phenomenon: moon-controlled monthly timing. Such level of understanding is also an essential prerequisite to tackle anthropogenic threats on marine ecology.

neuroscience↗

Differential impacts of the head on Platynereis dumerilii peripheral circadian rhythms

BackgroundThe marine bristle worm Platynereis dumerilii is a useful functional model system for the study of the circadian clock and its interplay with others, e.g. circalunar clocks. The focus has so far been on the worms head. However, behavioral and physiological cycles in other animals typically arise from the coordination of circadian clocks located in the brain and in peripheral tissues. Here we focus on peripheral circadian rhythms and clocks, revisit and expand classical circadian work on the worms chromatophores, investigate locomotion as read-out and include molecular analyses.\n\nResultsWe establish that different pieces of the trunk exhibit synchronized, robust oscillations of core circadian clock genes. These circadian core clock transcripts are under strong control of the light-dark cycle, quickly losing synchronized oscillation under constant darkness, irrespective of the absence or presence of heads. Different wavelengths are differently effective in controlling the peripheral molecular synchronization. We have previously shown that locomotor activity is under circadian clock control. Here we show that upon decapitation it still follows the light-dark cycle, but does not free-run under constant darkness. We also observe the rhythmicity of pigments in the worms individual chromatophores, confirming that chromatophore size changes follow a circadian pattern. These size changes continue under constant darkness, but cannot be re-entrained by light upon decapitation.\n\nConclusionsHere we provide the first basic characterization of the peripheral circadian clock of Platynereis dumerilii. In the absence of the head, light is essential as a major synchronization cue for peripheral molecular and locomotor circadian rhythms. Circadian changes in chromatophore size can however continue for several days in the absence of light/dark changes and the head. Thus, the dependence on the head depends on the type of peripheral rhythm studied. These data show that peripheral circadian rhythms and clocks should be considered when investigating the interactions of clocks with different period lengths, a notion likely also true for other organisms with circadian and non-circadian clocks.

physiology↗