Embryological stages of oviparous elasmobranch during development can be difficult to identify, requiring magnification and/or fixation of an anaesthetized embryo. These restrictions are poorly suited for monitoring the development of living elasmobranchs inside their egg cases. There are two major aims of this study. The first was to observe elasmobranch embryonic development non-invasively and produce a non-invasive developmental key for identifying the life stages for an elasmobranch inside the egg case. To this end, 7 key developmental stages were identified for the greater spotted catshark, Scyliorhinus stellaris, and are provided here with diagrams from multiple perspectives to demonstrate the key features of each stage. The physiological and ecological relevance of each stage are discussed in terms of structure and function for embryonic survival in the harsh intertidal zone. Also discussed is the importance of the egg case membrane and the protective embryonic jelly. The second aim of the study was to understand the applicability of the 7 developmental stages from S. stellaris to other oviparous elasmobranchs. Thus, changes in embryonic body size and egg yolk volume at each stage were measured and compared with those of the closely related, lesser spotted catshark, Scyliorhinus canicula. We find nearly identical growth patterns and yolk consumption patterns in both species across the 7 developmental stages. Thus, although the 7 developmental stages have been constructed in reference to the greater spotted catshark, we suggest that it can be applied to other oviparous elasmobranch species with only minor modification.

As global biodiversity declines, there is an increasing need to create an educated and engaged society. Having people of all ages participate in measuring biodiversity where they live helps to create awareness. Recently, the use of environmental DNA (eDNA) for biodiversity surveys has gained momentum. Here, we explore whether sampling eDNA and sequencing it can be used as a means of rapidly surveying urban biodiversity for educational purposes. We sampled 2 × 1 L of water from each of 15 locations in the city of Trondheim, Norway, including a variety of freshwater, marine, and brackish habitats. DNA was extracted, amplified in triplicate targeting the barcoding fragment of COI gene, and sequenced. The obtained data were analyzed on the novel mBRAVE platform, an online open‐access software and computing resource. The water samples were collected in 2 days by two people, and the laboratory analysis was completed in 5 days by one person. Overall, we detected the presence of 506 BINs identified as belonging to 435 taxa, representing at least 265 putative species. On average, only 5.4% of the taxa were shared among six replicates per site. Based on the observed diversity, three distinct clusters were detected and related to the geographic distribution of sites. There were some taxa shared between the habitats, with a substantial presence of terrestrial biota. Here we propose a new form of BioBlitz, where with noninvasive sampling effort combined with swift processing and straightforward online analyses, hundreds of species can be detected. Thus, using eDNA analysis of water is useful for rapid biodiversity surveys and valuable for educational purposes. We show that rapid eDNA surveys, combined with openly available services and software, can be used as an educational tool to raise awareness about the importance of biodiversity.

Safeguarding marine ecosystems is essential for maintaining ecosystem function and biodiversity, but effective monitoring of marine habitats can be logistically challenging, costly, and difficult to regularly implement. Environmental DNA-based biomonitoring is a rapidly growing tool that is non-destructive, cost-effective, and reliable. However, discrepancies in eDNA sampling protocols and methodology persist, which can greatly impact the interpretations of biomonitoring results, particularly across highly diverse ecosystems with historically elevated biodiversity. The South African coastal system is a unique and highly diverse ecoregion consisting of two ocean boundary currents creating one of the most diverse biological regions on the planet.Here, we present the first eDNA-based metabarcoding assessment of South African coastal fishes while also providing key management insights into study and sample design. We observed strong ecological associations with fish species richness across the extent of the South African coast, along with weaker associations with seasonality. We detected 466 operational taxonomic units across 112 of the 270 families described previously from the region, with greater species richness on the eastern subtropical coast compared to the western coast, which follows expected species richness patterns. Additionally, we provide evidence that biological replication is necessary to detect intra-site fish diversity and that three biological replicates are sufficient for capturing species diversity dynamics. Our work highlights the value of eDNA biomonitoring across space and time enabling biodiversity characterizations for the management of a gradient of coastal marine environments.

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