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The inaudible impact: physiological stress responses to ultrasonic exposure in the solitary ascidian Ciona intestinalis

Our take

The increasing prevalence of ultrasonic technologies in coastal environments raises critical questions about their impact on marine life. A recent study investigated the physiological stress responses of the solitary ascidian, *Ciona intestinalis*, to continuous and pulsed ultrasound exposure. Findings reveal that continuous ultrasound significantly impairs antioxidant defenses, induces cell death, disrupts filter-feeding, and damages mechanosensory structures—effects potentially more impactful than peak intensity alone. This research underscores the need to consider emission patterns in the environmental assessment of ultrasonic technologies, informing eco-design strategies.
The inaudible impact: physiological stress responses to ultrasonic exposure in the solitary ascidian Ciona intestinalis

The escalating deployment of ultrasonic technologies in marine environments, while promising advancements in antifouling, sonar, and other applications, demands a more rigorous understanding of their ecological consequences. Recent research, highlighted in a new study on the solitary ascidian *Ciona intestinalis*, underscores this need. We’ve previously explored the challenges of biofouling in aquaculture settings [What is this pink mass that develops on the tank walls?] and the insidious impact of persistent pollutants on marine mammal health [‘Forever chemicals’ could be aging dolphins beyond their years], demonstrating the complex interplay of anthropogenic stressors impacting ocean ecosystems. This new study adds a critical dimension to that understanding, revealing subtle but significant physiological damage induced by even low-intensity ultrasonic exposure, and demonstrating that the *way* sound is delivered may be as important as the intensity itself.

The investigation meticulously examined the effects of continuous (CUES) and pulsed (PUES) ultrasonic waves on *Ciona intestinalis*, a widely used model organism in marine biology. The researchers employed a comprehensive suite of biomarkers – assessing oxidative stress, filter-feeding performance, apoptosis, and even ultrastructural changes within the ascidian’s sensory organs – to paint a detailed picture of the biological response. The key finding is that continuous ultrasonic exposure, even at relatively low intensities, induced a cascade of detrimental effects, including suppressed antioxidant defenses, cell death in branchial tissue (gills), impaired filter-feeding, and neurological dysfunction. Strikingly, despite a significantly higher peak intensity, pulsed ultrasound caused considerably less damage, suggesting that the intermittent nature of the emission limits the accumulation of cellular stress. This distinction is crucial and highlights a critical gap in current environmental assessments of ultrasonic technologies.

The implications of these findings extend beyond the solitary ascidian. *Ciona intestinalis*, while a simple organism, shares fundamental biological mechanisms with more complex marine invertebrates, suggesting that similar vulnerabilities may exist across a broader range of species. Sessile invertebrates, like sponges, corals, and barnacles, are foundational components of many marine ecosystems, providing habitat and food for countless other organisms. Disruptions to these populations, even at the physiological level, can trigger cascading effects throughout the food web. The study’s emphasis on the temporal structure of ultrasonic emissions—the difference between continuous and pulsed delivery—is particularly noteworthy. Current environmental impact assessments often focus primarily on peak intensity, potentially overlooking the cumulative effects of prolonged exposure, even at lower power levels. Integrating emission mode into eco-design practices, as the authors advocate, is a vital step toward minimizing unintended consequences.

Moving forward, the challenge lies in developing standardized and ecologically relevant testing protocols to evaluate the impact of ultrasonic technologies on marine organisms. While this study provides valuable insights into the mechanisms of ultrasonic-induced stress, further research is needed to determine the long-term consequences of these effects on population dynamics and ecosystem function. Furthermore, understanding how different species and life stages respond to varying ultrasonic parameters will be essential for informed decision-making. A key question worth watching is whether similar effects are observed in more complex marine organisms, and whether these physiological disruptions translate into demonstrable ecological impacts within natural environments.

Ultrasonic technologies are increasingly deployed in coastal and marine environments for antifouling, sonar, underwater communication, and ballast water treatment; however, their biological effects on sessile invertebrates remain poorly understood. This study investigated the physiological responses of the solitary ascidian Ciona intestinalis to continuous (CUES) and pulsed (PUES) ultrasound exposure at 30 kHz using a biochemical, behavioral, histological, and ultrastructural multi-biomarker approach. Animals were exposed for 15 min, 30 min, 1 h, 2 h, 5 h, and 24 h. Oxidative stress biomarkers assessed in visceral tissue included superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase (GST), acetylcholinesterase (AChE), and the GSH/GSSG ratio. Filter-feeding performance, apoptosis in branchial tissue, and ultrastructural integrity of the coronal organ — a mechanosensory structure on the oral tentacles homologous to vertebrate inner ear hair cells — were also evaluated. CUES induced a time-dependent functional impairment of antioxidant defenses, with progressive suppression of SOD, CAT, and non-Se GPx activities and severe depletion of the reduced glutathione pool. These changes were accompanied by branchial cell death, documented by histochemical markers of early and late apoptosis, and by a significant reduction in filter-feeding performance, consistent with loss of ciliated branchial epithelium. CUES also triggered progressive cholinergic dysregulation, manifested as persistent siphon opening and complete loss of the touch-evoked siphon withdrawal reflex after 24 h. Ultrastructural analysis revealed time-dependent reduction in ciliary coverage of coronal organ sensory hair cells, most severe under CUES. Despite delivering instantaneous peak intensities nearly 38-fold higher than CUES, PUES caused comparatively milder and more transient effects, likely because the intermittent emission pattern limited the accumulation of mechanically induced cellular stress. These findings suggest that the temporal structure of ultrasonic emissions may play a more important role than instantaneous peak intensity in determining biological impact. They also provide an experimental basis for incorporating emission mode into the environmental assessment and eco-design of ultrasonic technologies, supporting the development of devices that minimize unintended effects on non-target benthic organisms.

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