Global inventory of species categorized by known underwater sonifery.

A working group from the Global Library of Underwater Biological Sounds effort collaborated with the World Register of Marine Species (WoRMS) to create an inventory of species confirmed or expected to produce sound underwater. We used several existing inventories and additional literature searches to compile a dataset categorizing scientific knowledge of sonifery for 33,462 species and subspecies across marine mammals, other tetrapods, fishes, and invertebrates. We found 729 species documented as producing active and/or passive sounds under natural conditions, with another 21,911 species deemed likely to produce sounds based on evaluated taxonomic relationships. The dataset is available on both figshare and WoRMS where it can be regularly updated as new information becomes available. The data can also be integrated with other databases (e.g., SeaLifeBase, Global Biodiversity Information Facility) to advance future research on the distribution, evolution, ecology, management, and conservation of underwater soniferous species worldwide.

The importance of context in the acoustic behaviors of marine, subtropical fish speciesa).

Despite the importance of acoustic signaling in fishes, the prevalence of the behavioral contexts associated with their active (i.e., intentional) sound production remains unclear. A systematized review was conducted to explore documented acoustic behaviors in marine, subtropical fishes and potential influences affecting their relative pervasiveness. Data were collected on 186 actively soniferous fish species studied across 194 publications, identified based on existing FishSounds and FishBase datasets. Disturbance was the most common behavioral context associated with active sound production-reported for 140 species or 75% of the species studied-and then aggression (n = 46 species, 25%) and reproduction (n = 34 species, 18%). This trend, however, somewhat differed when examined by research effort, study environment, and fish family, such as reproductive sounds being more commonly reported by studies conducted in the wild. The synthesis of fish sound production behaviors was in some ways stymied by the fact that many species' sound production did not have discernible associated behavioral contexts and that some investigations did not clearly identify the study environments in which active sound production was observed. These findings emphasize the importance of context-behavioral or otherwise-when studying acoustic behaviors in fishes.

The sound production of Aplodinotus grunniens in the presence of boat sounds.

Archived soundscape data from Lake Champlain, New York, were used to examine the effect of anthropogenic sounds produced by recreational boating on freshwater drum (Aplodinotus grunniens) soniferous behavior. Drum progressed from sporadic calling during the day to calls that increasingly overlapped culminating in a chorus in the late afternoon and evening. The response of drum to boat noise appeared to differ among these states, perhaps reflecting differences in the underlying behaviors. In response to boat noise, freshwater drum spawning choruses occurred later in the day, thus avoiding the noisiest periods. The peak frequency and knock rate of calls also increased in the presence of boat noise. Of the acoustical adjustments observed, the most strongly shown were those which increased the likelihood of signal reception, suggesting a Lombard effect response. Therefore, these data suggest freshwater drum have plasticity in their acoustical behavior, potentially shifting chorusing time, and altering sound characteristics to optimize communication in the presence of anthropogenic noise. However, additional work is needed to further clarify the response of freshwater drum to anthropogenic noise.

Acoustic homogeneity in the piranha Serrasalmus maculatus.

Different studies suggest some social calls could be used in fish identification if their specificity is unambiguously assessed. Sounds of different populations of piranhas Serrasalmus maculatus Kner, 1858 were recorded to determine their homogeneity between rivers inside a single basin (Araguari and Grande River, upper Paraná River basin) and between separated basins (Amazon and Paraná basins). All fish from the different populations produced sounds with similar acoustic features. Consequently, the populations were not discernible based on individual sound characteristics. This high homogeneity between sounds from different populations indicates their usefulness for conservation projects using passive acoustic monitoring in piranhas. Moreover, it supports the use of acoustic features as complementary key characteristics in taxonomic studies.

Sablefish (Anoplopoma fimbria) produce high frequency rasp sounds with frequency modulation.

Sablefish sounds, named rasps, were recorded at two captive facilities in British Columbia and Washington State. Rasps consisted of highly variable broadband trains of 2 to 336 ticks that lasted between 74 and 10 500 ms. The 260 rasps that were measured contained frequencies between 344 and 34 000 Hz with an average peak frequency of 3409 Hz. The frequency structure of ticks within rasps was highly variable and included both positive and negative trends. This finding makes sablefish one of the few deep-sea fish for which sounds have been validated and described. The documentation of sablefish sounds will enable the use of passive acoustic monitoring methods in fisheries and ecological studies of this commercially important deep-sea fish.

Temperate freshwater soundscapes: A cacophony of undescribed biological sounds now threatened by anthropogenic noise.

The soundscape composition of temperate freshwater habitats is poorly understood. Our goal was to document the occurrence of biological and anthropogenic sounds in freshwater habitats over a large (46,000 km2) area along the geographic corridors of five major river systems in North America (Connecticut, Kennebec, Merrimack, Presumpscot, and Saco). The underwater soundscape was sampled in 19 lakes, 17 ponds, 20 rivers and 20 streams, brooks and creeks that were grouped into broad categories (brook/creek, pond/lake, and river). Over 7,000 sounds were measured from 2,750 minutes of recording in 173 locations over a five-week period in the spring of 2008. Sounds were classified into major anthropophony (airplane, boat, traffic, train and other noise) and biophony (fish air movement, also known as air passage, other fish, insect-like, bird, and other biological) categories. The three most significant findings in this study are: 1) freshwater habitats in the New England region of North America contain a diverse array of unidentified biological sounds; 2) fish air movement sounds constitute a previously unrecognized important component of the freshwater soundscape, occurring at more locations (39%) and in equal abundance than other fish sounds; and 3) anthropogenic noises dominate the soundscape accounting for 92% of the soundscape by relative percent time. The high potential for negative impacts of the anthropophony on freshwater soundscapes is suggested by the spectral and temporal overlap of the anthropophony with the biophony, the higher received sound levels of the anthropophony relative to the biophony, and observations of a significant decline in the occurrence, number, percent time, and diversity of the biophony among locations with higher ambient received levels. Our poor understanding of the biophony of freshwater ecosystems, together with an apparent high temporal exposure to anthropogenic noise across all habitats, suggest a critical need for studies aimed at identification of biophonic sound sources and assessment of potential threats from anthropogenic noises.

New High-Tech Flexible Networks for the Monitoring of Deep-Sea Ecosystems.

Increasing interest in the acquisition of biotic and abiotic resources from within the deep sea (e.g., fisheries, oil-gas extraction, and mining) urgently imposes the development of novel monitoring technologies, beyond the traditional vessel-assisted, time-consuming, high-cost sampling surveys. The implementation of permanent networks of seabed and water-column-cabled (fixed) and docked mobile platforms is presently enforced, to cooperatively measure biological features and environmental (physicochemical) parameters. Video and acoustic (i.e., optoacoustic) imaging are becoming central approaches for studying benthic fauna (e.g., quantifying species presence, behavior, and trophic interactions) in a remote, continuous, and prolonged fashion. Imaging is also being complemented by in situ environmental-DNA sequencing technologies, allowing the traceability of a wide range of organisms (including prokaryotes) beyond the reach of optoacoustic tools. Here, we describe the different fixed and mobile platforms of those benthic and pelagic monitoring networks, proposing at the same time an innovative roadmap for the automated computing of hierarchical ecological information on deep-sea ecosystems (i.e., from single species' abundance and life traits to community composition, and overall biodiversity).

Air movement sound production by alewife, white sucker, and four salmonid fishes suggests the phenomenon is widespread among freshwater fishes.

We sought to describe sounds of some of the common fishes suspected of producing unidentified air movement sounds in soundscape surveys of freshwater habitats in the New England region of North America. Soniferous behavior of target fishes was monitored in real time in the field in both natural and semi-natural environments by coupling Passive Acoustic Monitoring (PAM) with direct visual observation from shore and underwater video recording. Sounds produced by five species including, alewife (Alosa pseudoharengus, Clupeidae), white sucker (Catastomus commersonii, Catostomidae), brook trout (Salvelinus fontinalis, Salmonidae), brown trout (Salmo trutta, Salmonidae), and rainbow trout (Oncorhynchus mykiss, Salmonidae) were validated and described in detail for the first time. In addition, field recordings of sounds produced by an unidentified salmonid were provisionally attributed to Atlantic salmon (Salmo salar, Salmonidae). Sounds produced by all species are of the air movement type and appear to be species specific. Our data based on fishes in three distinct orders suggest the phenomenon may be more ecologically important than previously thought. Even if entirely incidental, air movement sounds appear to be uniquely identifiable to species and, hence, hold promise for PAM applications in freshwater and marine habitats.

Cataloging fish sounds in the wild using combined acoustic and video recordings.

Although many fish are soniferous, few of their sounds have been identified, making passive acoustic monitoring (PAM) ineffective. To start addressing this issue, a portable 6-hydrophone array combined with a video camera was assembled to catalog fish sounds in the wild. Sounds are detected automatically in the acoustic recordings and localized in three dimensions using time-difference of arrivals and linearized inversion. Localizations are then combined with the video to identify the species producing the sounds. Uncertainty analyses show that fish are localized near the array with uncertainties < 50 cm. The proposed system was deployed off Cape Cod, MA and used to identify sounds produced by tautog (Tautoga onitis), demonstrating that the methodology can be used to build up a catalog of fish sounds that could be used for PAM and fisheries management.

Sounds of Arctic cod (Boreogadus saida) in captivity: A preliminary description.

Sounds produced by Arctic cod were recorded for the first time and suggest passive acoustic monitoring (PAM) can be an effective additional tool for the study and management of the species. Each of the 38 calls detected in three different aquatic facilities consisted of a single grunt with 6 to 12 pulses and a mean duration of 289 ms. Call frequency ranged between 59 and 234 Hz, with a mean peak frequency of 107 Hz. These preliminary data suggest Arctic cod can be distinguished from other gadids, but additional studies of sympatric species are needed before PAM can be confidently adopted.

Mapping the Acoustic Soundscape off Vancouver Island Using the NEPTUNE Canada Ocean Observatory.

NEPTUNE Canada is a cabled ocean observatory system containing five nodes located in the northeast Pacific Ocean. Using passive acoustic data recorded at two nodes (Folger Passage Deep and Barkley Canyon Axis) between June 2010 and May 2011, we sought to quantify the levels of vessel traffic and the occurrence of biological sounds to determine the potential impact of anthropogenic sound in masking acoustic communication. The results from a comparison of the relative amplitude and occurrence of low-frequency biotic sounds to broadband sounds resulting from vessel traffic are presented. Additional contributions to the marine soundscape from self-generated instrument noise are discussed.

Functional morphology of the sonic apparatus in the fawn cusk-eel Lepophidium profundorum (Gill, 1863).

Recent reports of high frequency sound production by cusk-eels cannot be explained adequately by known mechanisms, i.e., a forced response driven by fast sonic muscles on the swimbladder. Time to complete a contraction-relaxation cycle places a ceiling on frequency and is unlikely to explain sounds with dominant frequencies above 1 kHz. We investigated sonic morphology in the fawn cusk-eel Lepophidium profundorum to determine morphology potentially associated with high frequency sound production and quantified development and sexual dimorphism of sonic structures. Unlike other sonic systems in fishes in which muscle relaxation is caused by internal pressure or swimbladder elasticity, this system utilizes antagonistic pairs of muscles: ventral and intermediate muscles pull the winglike process and swimbladder forward and pivot the neural arch (neural rocker) above the first vertebra backward. This action stretches a fenestra in the swimbladder wall and imparts strain energy to epineural ribs, tendons and ligaments connected to the anterior swimbladder. Relatively short antagonistic dorsal and dorsomedial muscles pull on the neural rocker, releasing strain energy, and use a lever advantage to restore the winglike process and swimbladder to their resting position. Sonic components grow isometrically and are typically larger in males although the tiny intermediate muscles are larger in females. Although external morphology is relatively conservative in ophidiids, sonic morphology is extremely variable within the family.