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East Asian finless porpoise
East Asian finless porpoise
from Wikipedia

East Asian finless porpoise
At Miyajima Public Aquarium
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Artiodactyla
Infraorder: Cetacea
Family: Phocoenidae
Genus: Neophocaena
Species:
N. sunameri
Binomial name
Neophocaena sunameri
Pilleri & Gihr, 1975

The East Asian finless porpoise (Neophocaena sunameri) is a species of porpoise native to the East China Sea, Yellow Sea, and the seas around Japan. The Yangtze finless porpoise (N. asiaeorientalis) was formerly considered a subspecies but is now thought to be a distinct species.[2]

Name

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The Korean communities of the porpoise are sometimes known as sanggwaengi (Korean: 상괭이) and the Japanese communities, particularly the subspecies N. p. sunameri, as sunameri (Japanese: 砂滑)(Japanese: スナメリ).

Distribution

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In the Namhae

The species inhabits the coastal areas off mainland China (e.g., Chongming Island)[3] south to the Penghu Islands. The Matsu Islands are thought to be their northern limit, and the local population in this area is physically smaller than the Indo-Pacific finless porpoise. These two species overlap in the Matsu region.[4] The population in coastal waters around Japan is geographically isolated by the deep waters between Japan and continental Asia. Vagrant animals can reach the Ryukyu Islands.[citation needed]

Habitat

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A young porpoise in Tokyo Bay

Throughout their range, the porpoises stay in shallow waters, up to 50 m (160 ft) deep, close to the shore, in waters with soft or sandy seabed, or in estuaries and mangrove swamps. In exceptional cases, they have been encountered as far as 135 km (84 mi) off-shore in the East China and Yellow Seas, albeit still in shallow water.[5]

Description

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Finless porpoises can grow to as much as 2.27 m (7 ft 5 in) in length, and can weigh up to 72 kg (159 lb), although most are smaller. Adults grow more than 1.55 m (5 ft) in length and up to 30–45 kg (65–100 lb) in weight.[6] The flippers are moderately large, reaching up to 20% of the total body length. Adults are typically a uniform, light grey color, although some may have lighter patches of skin around the mouth, or darker patches in front of the flippers. Newborn calves of the central and eastern subspecies are mostly black with grey around the dorsal ridge area, becoming fully grey after four to six months. However, newborn calves of the western subspecies are a light creamy grey and become darker as they age.[6][7]

Anatomy

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The anatomy of finless porpoises has been relatively well studied, compared with that of some other cetacean species. The tubercles along the dorsal ridge are known to contain numerous nerve endings that have a sensory function. The auditory system also appears well-developed, with numerous nerve fibers specialized for rapid communication between the ears and the brain. Sight is relatively poor, however, due to the overall cloudiness of the Yangtze River; they have a reduced lens and a limited number of fibers in the optic nerve and to the muscles moving the eyes compared to the Indo-Pacific finless porpoise. It is speculated that their vision is somewhat better than that of the Yangtze river dolphin.[6]

The skeleton is light, accounting for only 5% of the total weight of the animal. There are between 58 and 65 vertebrae, about half of them in the tail, and with the first three cervical vertebrae fused into a single structure. This reduces flexibility of the neck while increasing stability in the water. There are ten to fourteen pairs of ribs in the chest, and an additional set of vestigial ribs has sometimes been reported in the neck, in association with the seventh cervical vertebra.[6] There are 44 sets of spinal nerves. Like all porpoises, they have spade-shaped teeth well suited for catching small fish and shrimp.[8] Their skeletal design allows them to leap from the water and perform "tail stands".[6]

The nasal passage contains nine or ten air sacs, which are capable of sealing off all air within the passage. Behind these are an additional set of vomeronasal sacs.[9] The trachea, however, is short, with only four cartilaginous rings.[6] The stomach has three chambers, with no caecum, and no distinct difference between the small and large intestines.[10][11]

Sexual maturity is thought to occur at around six years, with only one calf born at a time. The gestation period is approximately one year long and lactation lasts for over six months.[7][6]

Behavior

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In Chinese coastal waters, finless porpoises are generally found in groups of three to six,[12] although aggregations of up to about fifty have been reported.[13] In Japanese waters, groups appear to be smaller, with pairs being typical, and even rare aggregations being no larger than thirteen individuals.[13]

Diet

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The species consumes fish, shrimp and squid in the Yellow Sea/Bohai area.[14]

Conservation

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Off the coast of South Jeolla Province

The primary danger to the species is environmental degradation. Except for being briefly hunted after World War II due to the lack of seaworthy fishing boats, finless porpoises have never been widely hunted in Japan. It is a species protected since 1930 at the area around Awajima Island, Takehara and this coverage had since been extended to all Japanese coastal waters. [clarification needed] A decline of over 50% over the last three generations has been noted in the species, and it is thus classified as Endangered. This decline is largely thought to be a consequence of intensified fishing activity, which has caused large amounts of porpoises to be entangled in gillnets. Habitat loss and pollution are also thought to be major threats.[1]

Local conservation groups in Korea, such as at Yeosu, have started campaigning for the protection of the local populations.[15] It is classed as a protected species in the country.[16]

In captivity

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Finless porpoises have commonly been kept in Japan, as well as China and Indonesia. Ninety-four in total have been in captivity in Japan, eleven in China, and at least two in Indonesia. Japan has had three establishments designated for breeding them, and there have been five recorded births. Three, however, died moments after birth, but two survived for several years.

See also

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
The East Asian finless porpoise (Neophocaena asiaeorientalis sunameri), also known as the narrow-ridged finless porpoise, is a small odontocete cetacean endemic to the shallow coastal waters of , distinguished by the absence of a and the presence of a narrow dorsal bearing small tubercles. Adults typically reach lengths of 1.5 to 1.9 meters and exhibit a uniform light gray coloration, often with lighter patches near the mouth and eyes. The species inhabits nearshore environments, including estuaries and bays, ranging from the and southward to the and seas surrounding and Korea, preferring depths less than 50 meters where it forages on small , cephalopods, and crustaceans using echolocation. Classified as Endangered on the , the East Asian finless porpoise faces population declines driven primarily by incidental capture in fisheries, particularly stow nets and gillnets, which account for the majority of documented mortality. degradation from coastal industrialization, , and increased vessel traffic exacerbates these pressures, fragmenting populations and reducing prey availability through and . Conservation efforts include bycatch mitigation through gear modifications and protected areas, though enforcement challenges in high-fishing-pressure zones limit efficacy, underscoring the need for data-driven management informed by acoustic surveys and stranding records. Distinct from the critically endangered freshwater (N. a. asiaeorientalis), the coastal East Asian form maintains some connectivity across its range but remains vulnerable to cumulative anthropogenic impacts without intensified regulatory measures.

Taxonomy and nomenclature

Scientific classification

The East Asian finless porpoise is classified in the genus Neophocaena within the family Phocoenidae. Its full taxonomic hierarchy is as follows:
  • Kingdom: Animalia
  • : Chordata
  • Class: Mammalia
  • Order: Artiodactyla
  • Infraorder: Cetacea
  • Parvorder: Odontoceti
  • Family: Phocoenidae
  • Genus: Neophocaena
  • : N. asiaeorientalis (narrow-ridged finless porpoise)
  • : N. a. sunameri
This classification reflects the 2010 taxonomic revision recognizing N. asiaeorientalis as a distinct from the (N. phocaenoides), based on differences in skull morphology, vertebral counts, and genetic markers. Previously treated as a of N. phocaenoides since its description in 1972, N. asiaeorientalis was elevated due to evidence of and adaptive divergence in coastal East Asian waters versus broader Indo-Pacific ranges. The sunameri, described in 1975, is distinguished by narrower ridges on the rostrum and is restricted to marine habitats in the , , and waters off and Korea, separate from the freshwater-adapted N. a. asiaeorientalis in the Yangtze River. Although some genetic studies propose full status for sunameri based on divergence exceeding 2%, the IUCN and most cetacean authorities maintain rank pending further nuclear genome analysis.

Etymology and common names

The genus name Neophocaena derives from the Greek roots neo- (new) and phocaena (porpoise), signifying a genus newly differentiated from established taxa when first described in 1829 by for the related N. phocaenoides. The specific epithet sunameri for the East Asian finless porpoise is taken directly from the Japanese vernacular name sunameri (スナメリ), written in kanji as 砂滑, where suna () and nari or meri (to slide or be smooth) evoke the animal's sleek, finless dorsal ridge and slippery skin texture. In English, it is commonly called the East Asian finless porpoise, emphasizing its regional distribution and lack of , a trait shared with congeners but diagnostic for the . Regional names include sunameri (スナメリ) in Japanese and sang-gwaeng-i (상괭이) in Korean, both rooted in local observations of its appearance and in coastal East Asian waters.

Physical description

Anatomical features

The East Asian finless porpoise (Neophocaena asiaeorientalis) displays a compact, body optimized for maneuverability in coastal and riverine environments, with adults typically reaching lengths of 1.3 to 2.3 meters and weights of 30 to 72 kilograms. A hallmark feature is the complete absence of a , substituted by a narrow, elevated dorsal along the back's midline, measuring 0.2 to 1.2 centimeters in width—occasionally extending to 2-4 centimeters—and lined with small, rounded tubercles that enhance sensory perception and reduce drag. This , narrower and higher than in related species, distinguishes the narrow-ridged form and supports rapid turns and surfacing in shallow waters. The head is bulbous and rounded, featuring a short, blunt rostrum without a distinct , small laterally positioned eyes, and a single blowhole slightly displaced to the left. Coloration is predominantly uniform dark gray to blackish dorsally, often paling to grayish-white ventrally, with occasional lighter patches near the mouth. Pectoral flippers are broad, curved, and paddle-shaped, extending up to 20% of total body length to provide stability and control, while the tail stock narrows into broad, triangular flukes lacking a notch, aiding in powerful undulatory swimming. Dentition consists of small, spade-shaped teeth suited for grasping prey, with 16-21 teeth in each upper half and 15-20 in each lower, totaling fewer than in many porpoises; the condylobasal length ranges from 210 to 295 millimeters, reflecting a compact cranial structure adapted for echolocation in turbid waters. thickness varies regionally, with stratified layers (outer, middle, inner) observed via , thicker dorsally (up to several centimeters) for insulation and .

Morphological variations and subspecies

The East Asian finless porpoise (Neophocaena phocaenoides), also known as the , is currently regarded as monotypic, with no formally recognized under modern taxonomic revisions. Earlier classifications proposed such as N. p. phocaenoides (coastal populations from the northward) and N. p. sunameri (Korean and Japanese waters), distinguished tentatively by minor differences in and fidelity, but these have been synonymized into the single due to insufficient genetic and morphological divergence to warrant subspecific status. The narrow-ridged form, previously N. p. asiaeorientalis, was elevated to full status (N. asiaeorientalis) in 2008 based on consistent differences in dorsal ridge morphology, vertebral counts, and genetic markers, separating it from the wide-ridged N. phocaenoides. Morphological variations within N. phocaenoides primarily manifest as geographic differences in external measurements, cranial dimensions, and body coloration patterns, reflecting adaptations to local environmental conditions such as water depth and prey availability. Adult body length ranges from 1.2 to 2.3 meters, with males averaging smaller than females; populations in enclosed bays like Japan's and Ariake Sound exhibit shorter total lengths (up to 1.8 meters) compared to open coastal groups in the , where individuals reach 2.0 meters or more. Cranial morphometrics show significant variation, including rostrum length, zygomatic width, and braincase proportions; for instance, skulls from Japanese Pacific coast populations have relatively broader rostra and larger temporal fossae than those from the , as quantified through of 20+ measurements from stranded specimens collected between 1970 and 1990. Coloration varies ontogenetically and regionally, with neonates born dark gray dorsally and lighter ventrally, darkening to uniform gray-black in adults; individuals from subtropical southern ranges (e.g., ) retain subtler spotting longer than northern temperate populations, potentially linked to against varying levels. The defining trait—a low, wide dorsal ridge spanning 15–25% of body width with 3–6 rounded s—shows minor intraspecific variation in tubercle count and height, with higher counts (up to 7) in deeper-water populations, but these do not correlate strongly with genetic clusters. These variations, while statistically significant in morphometric studies of over 100 specimens, fall within the range of intraspecific plasticity observed in other phocoenids and do not indicate . ![Neophocaena phocaenoides at Miyajima Aquarium, illustrating dorsal ridge morphology][float-right]

Distribution and habitat

Geographic range

The (Neophocaena asiaeorientalis sunameri) inhabits shallow coastal marine waters across , primarily in regions with depths under 50 meters. Its confirmed range spans from the northward along China's eastern seaboard, including the and , extending to the in the north. This distribution encompasses key areas such as the and coastal zones near . Populations also occur off the western and southern coasts of and , reaching as far east as the Pacific waters adjacent to Japan's and islands, with records in the and northern Aki coastal areas. Sightings are concentrated within 15-20 km of shorelines, reflecting its preference for nearshore habitats, though no confirmed occurrences exist beyond these margins or into deeper offshore waters. The species does not overlap with the freshwater-adapted Yangtze subspecies (N. a. asiaeorientalis) or the more southerly (N. phocaenoides).

Environmental preferences and adaptations

The East Asian finless (Neophocaena asiaeorientalis) primarily inhabits shallow coastal waters less than 50 m deep, including estuaries, bays, mangrove swamps, and large rivers, with a strong preference for areas shallower than 20 m. The marine subspecies (N. a. sunameri) occupies temperate coastal zones from the northward to and Korea, while the Yangtze subspecies (N. a. asiaeorientalis) is restricted to freshwater riverine systems, favoring sandy substrates, gentle slopes, and vegetated shallows. Depth preferences vary seasonally and with ; in the , suitable depths range from 4–8 m during low water levels to 7–20 m during high levels, with optimal zones at 7–12 m featuring flat benthic . Environmental selectivity extends to hydrodynamic features, with individuals exhibiting a for low (0.001–0.0015 s⁻¹), likely aiding efficient and in turbulent riverine or estuarine flows. temperature influences distribution, particularly in wet seasons, where warmer conditions correlate with higher densities in ex situ reserves mimicking natural variability around 27°C. tolerance spans brackish to fully marine (up to 33‰) for coastal populations and near-zero for the subspecies, reflecting capabilities. Key adaptations include evolved osmoregulatory systems in the freshwater population, involving genetic modifications for ion balance and kidney function to counter hypotonic stress absent in marine cetaceans. morphology varies ontogenetically and regionally, with thicker layers in cooler temperate waters enhancing insulation and control in shallow dives typically under 20 m. These traits, combined with high reliance on echolocation in turbid habitats, enable persistence in structurally complex, low-visibility environments where visual cues are limited.

Ecology and behavior

Social structure and daily patterns

East Asian finless porpoises typically occur in small, loose groups, with the most common sizes ranging from 1 to 3 individuals, though sightings of up to 10 animals have been recorded in coastal surveys. Mother-calf pairs form a frequent unit, reflecting the species' reproductive strategy, while larger aggregations of 6-8 individuals are occasionally reported by fishers, potentially linked to opportunistic feeding near trawlers. Limited observations indicate minimal complex social interactions, such as alliance formation or hierarchical structures, distinguishing them from more gregarious odontocetes; their elusive nature and reliance on acoustic cues suggest fluid associations driven by habitat patchiness rather than stable pods. Daily activity patterns exhibit diel variation, with biosonar emissions—click trains and buzzes associated with —occurring at significantly lower rates during daylight (1.44 ± 0.19 click trains and 0.06 ± 0.02 buzzes per 10 minutes) compared to evening, night, and crepuscular periods, where rates increase to 2.49 ± 0.70 and 0.23 ± 0.10, respectively. This pattern correlates positively with prey density, which peaks in low-light conditions (e.g., 4.56 ± 1.30 fish/m³ in evening versus 1.79 ± 0.33 during day), indicating crepuscular and nocturnal peaks adapted to prey behavior in shallow coastal waters. Boat traffic shows no strong influence on these rhythms, underscoring prey availability as the primary driver, though porpoises may adjust ranging by migrating upstream in evenings to exploit aggregated resources. Echolocation encounters remain predominantly solitary (89.3% of 168 detections), aligning with their generally low group cohesion during routine activities.

Diet and foraging strategies

The East Asian finless porpoise (Neophocaena asiaeorientalis) exhibits an opportunistic diet dominated by demersal and benthic prey, reflecting its adaptation to shallow coastal and estuarine habitats. Stomach content analyses from specimens in the reveal consumption of 24 fish species, three species, and two species, with Japanese sand shrimp (Crangon affinis) comprising the primary prey by . In western waters, prey diversity includes various fishes (e.g., gobies and flatfishes), cephalopods like octopuses and squids, and crustaceans such as , with caloric intake estimated at approximately 18,051 kJ per day for an average weighing 32.49 kg. Metabarcoding of fecal samples from Korean populations confirms broad prey diversity, underscoring flexibility in response to local availability rather than strict specialization. Foraging strategies emphasize bottom-oriented hunting in waters typically shallower than 50 meters, leveraging passive listening to choruses for prey localization and active echolocation for precise targeting of small, schooling and . Juveniles preferentially consume smaller and cephalopods, while mature individuals, including lactating females, shift toward larger prey to meet higher energetic demands. Habitat selection favors areas of elevated —regions of turbulent water flow that aggregate prey —enhancing encounter rates without extensive migration. Seasonal dietary shifts occur, with stable analyses indicating variations in and prey sources tied to prey migrations and environmental productivity in the . This benthic focus contrasts with pelagic foraging in other cetaceans, aligning with the porpoise's lack of a for streamlined swimming in open waters and its reliance on near-shore ecosystems.

Reproduction and development

The East Asian finless porpoise (Neophocaena phocaenoides) has a reproductive cycle spanning 1-2 years, with gestation lasting 10-11 months and typically producing one calf per birth. Births occur seasonally between and in coastal waters. Observations of mating behavior, including males attempting to mount females in the presence of calves, have been recorded in , such as May. Females attain between 4 and 5 years of age, with the youngest documented pregnant female at 5 years and the oldest at 19 years. Males reach maturity around 4-6 years, varying slightly by population such as those in the or , where minimum ages are estimated at 5-6 growth layer groups (GLGs) via . Parturition timing, inferred from fetal body lengths, aligns with spring to summer months in some populations. Calf development includes around 10-11 months post-birth, after which juveniles grow to sizes of approximately 135-145 cm for females and similar for males. is evident, particularly in captive studies of related , indicating hormonal peaks tied to environmental cues. Population-specific variations in maturity age and size, such as 137-150 cm for females in southern , underscore adaptive differences across habitats.

Human interactions

Fisheries bycatch and incidental mortality

Fisheries constitutes a primary anthropogenic threat to the East Asian finless porpoise (Neophocaena phocaenoides), occurring predominantly through entanglement in gillnets, set nets, and trawls within coastal and nearshore operations. These incidents lead to drowning due to the porpoise's inability to surface for air, with entire pods sometimes affected in high-density gear areas. Incidental mortality is exacerbated by the species' preference for shallow, turbid waters overlapping with small-scale fisheries targeting fish and crustaceans. In Japanese waters, particularly Ariake Sound and Tachibana Bay, annual estimates reached 250 individuals during 2007–2008, far exceeding the potential biological removal level of 27 porpoises per year. viability modeling indicates that sustained at observed rates could result in annual declines of 0.671% to 3.87%, projecting quasi-extinction risks (fewer than 100 individuals) of up to 64.6% within 100 years and rendering the at least Vulnerable under IUCN criteria. These estimates derive from models incorporating historical abundance data from 1993–1994 (approximately 3,093 individuals) and corrected rates accounting for underreporting. Along China's , public reports documented 326 events and 203 strandings involving finless porpoises from 2000 to 2018, totaling 606 individuals across 240 incidents. Events increased rapidly from 2010 to 2017, averaging about 30 per year, with hotspots in Laizhou Bay, the Yantai-Weihai region, and Qingdao-Rongcheng area; predominated in the northern , while strandings were more common in the southern . Gear entanglement, particularly in gillnets and set nets amid extensive and 38,410 registered fishing vessels, alongside vessel strikes, drove mortality, which occurred year-round but peaked in spring and early summer (). Younger porpoises (mean length 127 cm) were disproportionately affected in compared to strandings (137 cm), suggesting selective impacts on juveniles. Such data likely underestimate true mortality, as they rely on voluntary reporting and fisher observations, which may omit unobserved deaths or illegal discards. Across the species' East Asian range, remains unregulated in many areas, contributing to ongoing population declines without evidence of reduction despite awareness of gear overlaps.

Cultural and historical significance

The East Asian finless porpoise (Neophocaena asiaeorientalis) has been documented in historical Chinese records primarily through poetry, reflecting its visibility as a common aquatic feature in rivers and coastal waters before significant population declines. Analysis of 724 poems spanning over 1,400 years, from the (618–907 CE) onward, reveals frequent references to the species, particularly the Yangtze subspecies (N. a. asiaeorientalis), indicating a historical range that has since contracted by approximately 65%. These poems, including one by Qianlong in describing encounters during a Yangtze River voyage, portray the porpoise as a familiar sight rather than a central mythological figure, with mentions often tied to direct observations rather than symbolic reverence. In Chinese cultural contexts, the lacks the deep symbolic roles attributed to other cetaceans like dolphins in broader but holds local significance as an endearing element of riverine , colloquially known as "jiangtun" or "river piglet" in Mandarin, emphasizing its pig-like and playful demeanor. This and poetic documentation underscore its integration into everyday environmental awareness among historical literati and communities, linking to ecological history without of ritualistic or medicinal uses. Recent interdisciplinary studies using these texts highlight how such records provide verifiable baselines for conservation, connecting millennia of observation to modern assessments. In , sightings of the narrow-ridged (N. a. sunameri) in coastal areas like the have inspired local legends, such as tales of Buddhist monks' shaved heads bobbing in the water, interpreted as misidentifications of the porpoise's smooth, finless profile. These anecdotes reflect the species' familiarity to coastal inhabitants as a benign marine presence, though without broader national or historical exploitation documented in primary sources. Korean records similarly note the porpoise's coastal prevalence but lack distinct cultural motifs, focusing instead on incidental interactions in narratives.

Conservation status

In coastal Chinese waters of the Bohai and Yellow Seas, regional population estimates indicate thousands of individuals, though comprehensive range-wide totals remain undetermined due to fragmented survey efforts. In Bohai Bay, the population is estimated at approximately 5,000 individuals based on recent assessments. Along the coast, estimates range up to 15,000 individuals. A dedicated line-transect survey conducted from 2018 to 2021 in a 23,530 km² area off the yielded an abundance of 3,978 individuals (CV = 22.39%, 95% CI: 2,561–6,180), with a density of 0.169 individuals/km² concentrated nearshore. In Japanese waters, the Seto Inland Sea supports an estimated 7,600 to 9,200 individuals, representing one of the larger known subpopulations, though the species is classified as vulnerable there with evidence of declines in enclosed bays due to bycatch and pollution. Surveys have identified five discrete coastal populations in Japan, often in small groups, but abundance has decreased in areas like the Inland Sea consistent with fishery impacts. Korean coastal waters, particularly the west coast, historically hosted one of the largest subpopulations, with an estimate of approximately 36,000 individuals in 2005 derived from sighting surveys. However, subsequent assessments, including a dedicated west coast study, signal a , attributed primarily to incidental entanglement in fisheries and habitat degradation, though exact recent abundances are not fully quantified in available data. Local ecological knowledge surveys in shared Chinese-Korean areas like the southern corroborate downward trends, with over 50% of fishers reporting reduced sightings linked to prey depletion and . Across the range, trends are predominantly negative, with inferred declines of around 30% over three generations in monitored areas, driven by anthropogenic factors rather than natural variability, though data gaps persist in less-surveyed regions like the . No evidence of recovery is documented without targeted interventions, and subpopulations exhibit fragmentation, limiting and resilience.

Primary threats and causal factors

The primary threats to the East Asian finless porpoise (Neophocaena asiaeorientalis) stem from intense anthropogenic pressures in its coastal and riverine habitats, with in gear identified as the leading cause of direct mortality. Entanglement in non-selective nets, such as gillnets and stow-nets, accounts for significant incidental deaths, particularly along coastlines like Shandong Province in , where activities overlap with porpoise distribution. This is exacerbated by unregulated or unselective fisheries that deplete prey species through , leading to food shortages and reduced , as porpoises rely on small fish and that have declined sharply in overexploited waters. Habitat degradation further compounds these risks, driven by coastal industrial expansion, dredging, and that alter shallow, nearshore environments preferred by the . In regions like the Yangtze River and adjacent seas, from chemical effluents and vessel traffic introduces toxins that bioaccumulate in porpoise tissues, impairing and increasing vulnerability to . Underwater noise from shipping and disrupts echolocation and , while vessel strikes cause traumatic injuries, with these factors collectively accelerating declines observed since the 1990s. Causal factors trace to rapid in , where high human population densities and fisheries output—exceeding 15 million tons annually in the Yellow and Seas—prioritize short-term resource extraction over , without adequate enforcement of gear restrictions or protected areas. Although direct hunting has diminished, opportunistic take from persists, underscoring the need for causal interventions targeting practices rather than symptomatic conservation alone.

Mitigation efforts and outcomes

Efforts to mitigate threats to the East Asian finless (Neophocaena asiaeorientalis) have primarily focused on reducing in coastal fisheries, the ' leading cause of mortality. Acoustic pingers, devices emitting high-frequency to deter porpoises from gillnets and set nets, have been tested in since the early . A long-term study in Ise Bay demonstrated that AQUAmark 100 pingers (operating at 20-160 kHz) initially reduced porpoise encounter rates by prompting avoidance behavior, achieving near-100% efficacy in short-term trials. However, effectiveness diminished after 3-6 months due to , with porpoises resuming approaches to netted areas, necessitating strategies like pinger rotation or combined deterrents to sustain benefits. Regulatory measures include bans on direct exploitation and trade. In the Republic of Korea, the 2017 Marine Protection Law prohibited the capture, trade, and consumption of finless porpoises, targeting incidental and intentional mortality in stow-net fisheries, which account for the majority of . In , habitat protection initiatives, such as identifying priority coastal zones in the and for spatial conservation planning, aim to limit fishing intensity and ; surveys from 2018-2022 informed these by mapping high-density areas off . Enforcement of seasonal fishing moratoria has also reduced effort in key s, correlating with localized decreases in strandings along coasts post-2020. Outcomes remain limited, with no of population recovery despite interventions. The ' IUCN status was upgraded to Endangered in recent assessments, reflecting ongoing declines driven by persistent exceeding rates in fragmented coastal populations estimated at under 10,000 individuals range-wide. Pingers and bans have averted some mortality—e.g., Korean trade cessation reduced documented intentional kills—but widespread adoption lags due to fisher compliance issues and economic costs, while degradation from coastal development continues unabated. Integrated monitoring, including acoustic surveys, underscores the need for adaptive, multi-national enforcement to achieve measurable stabilization.

Captivity and reintroduction programs

East Asian finless porpoises (Neophocaena asiaeorientalis sunameri) are held in mainly in Japanese aquariums, where they serve purposes of , conservation , and exhibition. Facilities including Aquarium have observed natural parturition events, typically occurring between and May, demonstrating under captive conditions. Breeding outcomes include documented births, such as two calves—one male and one female—born between late May and early June 2022 at an aquarium in central , with one promptly entering public display. Other establishments, like those maintaining multi-generational lineages, have achieved successful propagation, as evidenced by offspring and grandchildren of earlier captives surviving in facilities as of 2023. These programs contribute to behavioral and physiological studies but face challenges in scaling due to the species' specialized needs and echolocation-dependent . Reintroduction initiatives for the East Asian subspecies remain ad hoc, centered on rehabilitating stranded animals rather than population augmentation. In one documented instance, a female stranded in Bohai Bay, , on March 30, 2008, was rescued, treated for injuries including and skin lesions, and released after 45 days of care, showing post-release adaptations like increased activity and feeding. Unlike the intensive ex situ breeding and semi-wild releases for the critically endangered Yangtze subspecies (N. a. asiaeorientalis), no equivalent large-scale reintroduction programs exist for sunameri, reflecting its comparatively stable coastal populations and lower extinction risk. Success in individual releases underscores potential for such interventions, though broader threats like necessitate protections over reliance on captivity-derived reinforcements.

References

  1. ./assets/Neophocaena_phocaenoides_-Miyajima_Aquarium_-Japan-8a.jpg
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