Within the context of global climate change and overfishing of fish stocks, there is some evidence that cephalopod populations are benefiting from this changing setting. These invertebrates show enhanced phenotypic flexibility and are found from polar regions to the tropics. Yet, the global patterns of species richness in coastal cephalopods are not known. Here, among the 370 identified-species, 164 are octopuses, 96 are cuttlefishes, 54 are bobtails and bottletails, 48 are inshore squids and 8 are pygmy squids. The most diverse ocean is the Pacific (with 213 cephalopod species), followed by the Indian (146 species) and Atlantic (95 species). The least diverse are the Southern (15 species) and the Arctic (12 species) Oceans. Endemism is higher in the Southern Ocean (87%) and lower in the Arctic (25%), which reflects the younger age and the “Atlantification” of the latter. The former is associated with an old lineage of octopuses that diverged around 33 Mya. Within the 232 ecoregions considered, the highest values of octopus and cuttlefish richness are observed in the Central Kuroshio Current ecoregion (with a total of 64 species), followed by the East China Sea (59 species). This pattern suggests dispersal in the Central Indo-Pacific (CIP) associated with the highly productive Oyashio/Kuroshio current system. In contrast, inshore squid hotspots are found within the CIP, namely in the Sunda Shelf Province, which may be linked to the occurrence of an ancient intermittent biogeographic barrier: a land bridge formed during the Pleistocene which severely restricted water flow between the Pacific and Indian Oceans, thereby facilitating squid fauna differentiation. Another marked pattern is a longitudinal richness cline from the Central (CIP) toward the Eastern Indo-Pacific (EIP) realm, with central Pacific archipelagos as evolutionary dead ends. In the Atlantic Ocean, closure of the Atrato Seaway (at the Isthmus of Panama) and Straits of Gibraltar (Mediterranean Sea) are historical processes that may explain the contemporary Caribbean octopus richness and Mediterranean sepiolid endemism, respectively. Last, we discuss how the life cycles and strategies of cephalopods may allow them to adapt quickly to future climate change and extend the borealization of their distribution.

The warming of Arctic waters over the last decades has been confirmed by the results of numerous studies. New data on distribution of cephalopods in the Arctic were obtained from the research cruises of PINRO (Russia) and IMR (Norway) during 2006–2011. Teuthowenia megalops and Todaropsis eblanae were found in the Arctic for the first time, at distances of more than 1000 km and 2500 km outside of their ranges, respectively. The demersal species T. eblanae inhabiting the lower shelf and upper continental slope has presumably spread into the Barents Sea by the eastern branch of the Norwegian Current, and further by the southern branch of the North Cape coastal current, as far as the Murman shelf. The bathypelagic species T. megalops is carried to the Arctic evidently by the deep-water warm Atlantic Currents. The new spreading areas of both species are obviously the non-reproductive zones of their ranges. Foraging shoals of Todarodes sagitatus were recorded in the Arctic in 2010 for the first time in the last 25 years, which can be related to not only the warming of Arctic waters, but also the fluctuation of Todarodes levels in the main part of the range in the Northern Atlantic. The native Arctic species Gonatus fabricii has expanded its range to the eastern part of the Barents Sea and to the adjacent part of the Kara Sea. In these areas of Arctic waters, warming is particularly noticeable and the ongoing climatic changes are leading to boreal cephalopods spreading into the Polar Basin. This may impact species relations in vulnerable Arctic ecosystems.

Vampyroteuthis infernalis Chun, 1903, is a widely distributed deepwater cephalopod with unique morphology and phylogenetic position. We assessed its habitat and trophic ecology on a global scale via stable isotope analyses of a unique collection of beaks from 104 specimens from the Atlantic, Pacific and Indian Oceans. Cephalopods typically are active predators occupying a high trophic level (TL) and exhibit an ontogenetic increase in δ¹⁵N and TL. Our results, presenting the first global comparison for a deep-sea invertebrate, demonstrate that V. infernalis has an ontogenetic decrease in δ¹⁵N and TL, coupled with niche broadening. Juveniles are mobile zooplanktivores, while larger Vampyroteuthis are slow-swimming opportunistic consumers and ingest particulate organic matter. Vampyroteuthis infernalis occupies the same TL (3.0–4.3) over its global range and has a unique niche in deep-sea ecosystems. These traits have enabled the success and abundance of this relict species inhabiting the largest ecological realm on the planet.

The first observation of the common bobtail squid Sepietta oweniana has been made in the Barents Sea (Tromsø Bank; 70°54′N 19°46.8′E). It is the northernmost area of this species distribution. No changes were found in the reproductive system structure. But the food spectrum was changed, particularly, juvenile fish of the Lotidae family was found. The bobtail squid of the Sepiolinae subfamily have never been recorded as fish eaters previously. The expansion of boreo-subtropical species of cephalopods into the Arctic during the last decade can be divided into two groups: (1) a foraging migration happening relatively regularly; and (2) a range expansion due to the ongoing Arctic warming. The case of S. oweniana obviously belongs to the second group.

The squid Gonatus fabricii (Lichtenstein, 1818) is the most abundant pelagic cephalopod in the Arctic and the only squid to spend all of its life cycle in this region. Despite being highly abundant, its reproductive biology remains poorly known, and data on large maturing and mature specimens are especially rare. This study, based on extensive material (51 large specimens and >35,000 specimens in all), fills major gaps in the knowledge of the reproductive biology and ecology of G. fabricii. The fecundity of females ranged from 8,862 to 16,200 oocytes, with mature and late maturing specimens having between 8,862 to c. 10,000 and 11,402 oocytes, respectively. Oogenesis was synchronous, and oocyte resorption was observed; resorbed oocytes constituted up to 23.5% of fecundity. Between two to five ripe oocytes were observed, and these were 4.0–5.5 mm in diameter (maximum dimension). Males possessed between 77 and 257 spermatophores (length = 5.8–10.8 mm). Spermatophores were characterized by a cement body with well-developed collar and discs at the oral end, an ejaculatory apparatus longer than the cement body and the lack of a tapered, sharp tip to the cement body. Spermatophore size showed a uniform increase in relation to increasing male size. In newer spermatophores, the length, width and volume of the seminal reservoir also increased. Females possessed between 62 and 84 spermatangia (length = 1.8–2.6 mm); the spermatangia were present on the buccal membranes and lacked special attachment structures. Seminal receptacles were not found on the buccal membranes of females. Our findings are consistent with the hypothesis of geographically restricted spawning in G. fabricii. The study found evidence for one new breeding area in south-eastern Greenland. No differences in sizes at maturity were found between the breeding areas. Such geographically localized reproduction is relatively common in non-deep-water squids, but is much less common in deep-water squids. Localized reproduction may be especially important for G. fabricii because increased food availability in the epipelagic layers would likely increase the survival of epipelagic juveniles, with surface currents potentially aiding in their dispersal.