A cosmopolitan deep diver of continental slopes and submarine canyons, this discreet ziphiid holds the known diving records among mammals and is found mainly in waters > 800-1,000 m, far from steep coasts.
Size & mass. Adult 5-7 m; streamlined body, small falcate dorsal fin set in the last third of the back. Highly variable coloration (slate grey to reddish brown), with a head that is often pale in old males and a body covered in linear scars and oval marks (bites from cookie-cutter sharks). Two throat grooves in a “V”. In the male, two teeth emerge at the tip of the lower jaw.
Global distribution. A species widely distributed in temperate to tropical oceans, absent only from polar waters; in the Mediterranean, regular occurrence and high densities around the canyons (Ligurian, Corsica-Sardinia, etc.).
Identification refs: NOAA Fisheries; WDC; identification guides (Sea Watch/MARLIN).
It can be confused at sea with the mesoplodont beaked whales (e.g. Mesoplodon densirostris): Ziphius is told apart by its shorter beak, its sloping head, the whitish head of the males, the very posterior position of the dorsal fin and the two pronounced throat grooves. The presence of two apical teeth (male) differs from the mesoplodont beaked whales, in which the position of the teeth varies with the species.
Statuses & conventions: global IUCN LC (2018 update covering most of the ziphiids); Mediterranean subpopulation VU; CITES Appendix II; CMS Appendix II (species) and Appendix I (Mediterranean, COP11 decision 2014). Identifiers WoRMS AphiaID 137127; Wikidata Q623173.
A species with a vast biogeographical amplitude, Cuvier’s beaked whale is present in most of the world’s oceans and seas, from tropical waters to temperate zones, with a marked absence only at high polar latitudes. In all likelihood it is the beaked odontocete with the most extensive range.
In the Mediterranean, occurrence is regular in deep-water sectors close to the continental slope and the canyons. The main documented areas of high density are: the Alboran Sea, the Genoa Canyon (Ligurian Sea), the central Tyrrhenian (Caprera sector), the southern Adriatic and the Hellenic Trench. The Pelagos Sanctuary alone holds two of the five highest-density cores identified at basin scale.
The ecological core of the species is associated with deep oceanic waters in the immediate vicinity of continental slopes and canyons, where the topography concentrates prey and currents. Aerial and boat-based surveys show occurrence mostly along these features, rather than offshore over uniform abyssal plains.
At the regional scale, stranding and monitoring data do not indicate any marked seasonal migration; presence appears to be year-round in favourable sectors, with movements along the slope and between canyons.
Main sources: NOAA Fisheries (species profile), Pelagos Sanctuary (species profile), ACCOBAMS & IMMA (technical reports), Cañadas et al. 2018; Podestà et al. 2016 (syntheses and habitat-use maps).
Cuvier’s beaked whale shows a bimodal dive profile: deep dives (often > 800 m) devoted to feeding alternate with shallow dives for recovery. In the eastern Pacific (California), the median of the deep dives is ~1,456 m for ~59 min, the shallow dives ~275 m for ~21 min, with very short surface intervals (often 2-8 min). The species holds the records among mammals: 2,992 m in depth and 222 minutes in duration (3 h 42 min).
Typical sequences group one deep dive followed by several shallow dives, with little diel variation documented in the activity pattern. The mean foraging depth observed around California is ~1,182 m, reflecting a meso-/bathypelagic trophic zone.
Like the other ziphiids, the species emits FM upsweep pulses (≈25-60 kHz, peak ~32-40 kHz, IPI ~0.25-0.5 s) during search phases near the bottom; these turn into rapid buzzes as it closes on prey. This high-frequency sonar is suited to detecting small prey in dark conditions and at long range, with high directivity.
The diet is dominated by mesopelagic cephalopods (histioteuthids, onychoteuthids, etc.), supplemented by fish (myctophids in particular) and, more rarely, crustaceans; the composition varies between ocean basins. Worldwide analyses of stomach contents confirm the predominance of deep-sea squid.
Sightings at sea describe mostly groups of 2 to 7 individuals, sometimes solitary animals. Males use their two apical teeth as weapons in intrasexual interactions, leaving characteristic linear rake marks on other individuals; the hypopigmented oval marks come from the bites of cookie-cutter sharks (Isistius). Differences in pigmentation and marking help determine the sex in adults.
A species that is particularly sensitive to mid-frequency military sonar (2-10 kHz), Cuvier’s beaked whale has repeatedly been involved in atypical mass strandings in the Mediterranean (Greece 1996; Crete 2014) and elsewhere. Experimental work shows changes in behaviour (prolonged dives, rapid movement away, acoustic silence) during exposures. The regional bodies (ACCOBAMS, Pelagos) have issued mitigation recommendations for key habitats.
Key refs: Schorr et al. 2014 (PLOS ONE); Barlow et al. 2020-2021; Royal Society Open Science 2019; NOAA Fisheries; ACCOBAMS & Pelagos; reviews of the diet.
Streamlined body (typically 5-7 m), small dorsal fin set well back, two “V”-shaped throat grooves. Marked sexual dimorphism: in the male, two teeth emerge at the tip of the lower jaw and the head becomes largely whitish; the body carries numerous linear rake marks from intrasexual fights and oval scars from cookie-cutter sharks. Adult mass estimated at up to ~3 t depending on the population.
Sexual maturity at around 7-11 years (males ~5.5-6 m; females ~6 m). Cycle apparently continuous (births all year round, with a spring peak in some regions). Gestation ~12 months; litter of a single calf; interval between births ~2-3 years. Newborn ~2-2.7 m for ~250-300 kg (≈550-660 lb). Lactation duration poorly documented (probably ≥12 months).
Linear growth is rapid in the first years, then slows until maturity. Estimated maximum longevity reaches ~60-62 years, with a likely mean > 30 years.
As in the other great divers, most of the usable oxygen is stored in the blood (haemoglobin) and in the muscles (myoglobin), rather than in the lungs. Myoglobin concentrations in cetaceans are exceptionally high (≈1.8-5.8 g/100 g of wet muscle depending on the species), giving the muscles a very dark red tint and a large local autonomy.
Deep dives are accompanied by a marked bradycardia and a peripheral vasoconstriction that give priority to perfusion of the brain and the heart, while the muscles draw on their myoglobin store; the intensity of this “dive response” is modulated according to the effort and the expected duration. These mechanisms, documented in several odontocetes, are consistent with the record durations reached in Ziphius (> 3 h).
Thoracic compression and pulmonary compliance favour the transfer of air from the alveoli towards the conducting airways at depth, inducing a progressive alveolar collapse that limits exchange and the dissolved nitrogen load. Models and measurements suggest a collapse threshold typically between ~30 and 100 m (varying with initial lung volume and species), then a growing pulmonary shunt that protects against supersaturation.
In the great divers (including Ziphius), the combination of bradycardia, vasoconstriction and alveolar collapse, the optimisation of O2 stores and the kinematics of the dive reduce the risk of inert gas desaturation. Work on related species shows high PN2 at the end of the dive with no evidence of an increased risk of decompression sickness under natural conditions; bubble remnants observed in strandings are interpreted with caution (post-mortem factors).
Main sources: NOAA Fisheries (life cycle), Animal Diversity Web & Azores Whale Watch (reproductive parameters), AnAge (longevity), NHM (O2 stores), JEB/JEB-Open & Frontiers reviews (alveolar collapse, dive response), models and meta-analyses (N2).
Key sources: IUCN/ASCOBANS (statuses), Pelagos (SPAMI, noise studies, 2025), IMO MEPC.380(80) (PSSA 2023), ACCOBAMS (noise guidelines, register), Hellenic Trench IMMA, reviews and notes on sonar-related strandings, NOAA (generic threats).
Would you like an “in the field” box (visual clues, the blow, the look of the animal when surfacing) or a timeline (1823 → 2020 records)? I can add it just below.
According to the open data of the GBIF, 422 georeferenced sightings of Ziphius cavirostris are recorded in our photographic index.
| Country | Notes |
|---|---|
| United States of America | 182 |
| Italy | 70 |
| Spain | 60 |
| Japan | 18 |
| Chinese Taipei | 15 |
| Ecuador | 15 |
| Russian Federation | 14 |
| Mexico | 14 |
| unknown or invalid | 12 |
| Canada | 9 |

Monthly distribution of 492 dated sightings (all years combined): the maximum is reached in August.
| Month | Notes |
|---|---|
| janvier | 36 |
| February | 13 |
| mars | 23 |
| avril | 53 |
| mai | 40 |
| juin | 47 |
| juillet | 74 |
| August | 93 |
| septembre | 32 |
| octobre | 41 |
| novembre | 17 |
| December | 23 |
These figures reflect survey effort (more boaters and more surveys in summer) as much as the actual presence of the species: to be interpreted with caution.












Photographs from GBIF under a Creative Commons licence. The author and the licence of each photograph are given; please respect them if you reuse them.
Automatic selection of the most cited works mentioning the species (source: Crossref).