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Albatrossia
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| Giant grenadier | |
|---|---|
| |
Scientific classification 
| |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Class: | Actinopterygii |
| Order: | Gadiformes |
| Suborder: | Macrouroidei |
| Family: | Macrouridae |
| Genus: | Albatrossia Jordan & Gilbert, 1898 |
| Species: | A. pectoralis
|
| Binomial name | |
| Albatrossia pectoralis (Gilbert, 1892)[1]
| |
| Synonyms[1] | |
Albatrossia pectoralis, the giant grenadier or giant rattail, is a very large rattail,[1] and the only member of the genus Albatrossia.[2] It is found in the north Pacific from northern Japan to the Okhotsk and Bering Seas, east to the Gulf of Alaska, and south to northern Baja California in Mexico. It is found at depths between 140 and at least 4,250 m,[3] but typically between 700 and 1100 m.[1] The giant grenadier has the usual greatly elongated, pointed tail of the rattails.
Ecology
[edit]Giant grenadiers are among the most abundant species from 400–1,000 m in the North Pacific Ocean.[4] Giant grenadiers are apex predators on the upper continental slopes of the northern Pacific. Their main prey are Octopoteuthis deletron squid and Vampyroteuthis infernalis vampire squid.[5]
Description
[edit]It can grow to 2.1 m (6 ft 11 in) total length.[2]
Otoliths
[edit]Giant grenadier have two otolith shapes that have been observed to date, and there is a third shape that seems to be a mixture of the two distinct shapes.[4]
Fishery
[edit]
Giant grenadier are of low commercial value but are caught as by-catch.[4] Because of their great abundance, several attempts have been made to develop a fishery for giant grenadier. However, the fish is categorized as "unpalatable" because of its soft texture, high moisture content, and low protein content.[6]
References
[edit]- ^ a b c d Froese, Rainer; Pauly, Daniel (eds.). "Albatrossia pectoralis". FishBase. February 2024 version.
- ^ a b Froese, Rainer; Pauly, Daniel (eds.). "Species in genus Albatrossia". FishBase. February 2024 version.
- ^ NOAA Ocean Explorer Video
- ^ a b c Rodgveller, Cara J.; Hutchinson, Charles E.; Harris, Jeremy P.; Vulstek, Scott C.; Guthrie, Charles M. (2017). "Otolith shape variability and associated body growth differences in giant grenadier, Albatrossia pectoralis". PLOS ONE. 12 (6) e0180020. Bibcode:2017PLoSO..1280020R. doi:10.1371/journal.pone.0180020. PMC 5489205. PMID 28658326.
- ^ Drazen, Jeffrey C; Buckley, Troy W; Hoff, Gerald R (2001). "The feeding habits of slope dwelling macrourid fishes in the eastern North Pacific". Deep-Sea Research Part I: Oceanographic Research Papers. 48 (3): 909–935. Bibcode:2001DSRI...48..909D. doi:10.1016/S0967-0637(00)00058-3.
- ^ "The Abundant—But Not So Tasty—Giant Grenadier". The Abundant—But Not So Tasty—Giant Grenadier. NOAA Fisheries. Retrieved 5 January 2017 – via LegiStorm.
 | This Gadiformes-related article is a stub. You can help Wikipedia by adding missing information. |
Albatrossia
View on Grokipediafrom Grokipedia
Taxonomy
Classification
Albatrossia is a monotypic genus of deep-sea fishes belonging to the family Macrouridae, known as grenadiers or rattails, within the order Gadiformes.[1] However, some recent taxonomic revisions, including Eschmeyer's Catalog of Fishes (as of 2025), have synonymized the genus with Coryphaenoides, though it remains recognized as distinct in sources like FishBase and WoRMS.[3][1][4] The sole species is Albatrossia pectoralis, and the genus's taxonomic hierarchy follows the standard classification for ray-finned fishes: Kingdom Animalia, Phylum Chordata, Class Actinopterygii, Order Gadiformes, Suborder Macrouroidei, Family Macrouridae, Genus Albatrossia.[4][5] Phylogenetically, Albatrossia (or Coryphaenoides pectoralis in some classifications) is positioned within the subfamily Macrourinae of the Macrouridae, distinguished from closely related genera such as Coryphaenoides by morphological traits including six branchiostegal rays, a low snout slightly protruding beyond the large mouth, and the absence of a spinous terminal scute on the snout.[5] This separation reflects adaptations suited to its deep-water habitat, though some molecular studies have suggested closer affinities to Coryphaenoides subgenera; recent genetic analyses, including DNA barcoding, support synonymy with Coryphaenoides based on molecular data, while combined morphological and genetic evidence from earlier studies maintained its monotypic status.[6][7] The species A. pectoralis was first described by Charles H. Gilbert in 1892 under the name Macrourus pectoralis, based on specimens collected during the U.S. Fish Commission steamer Albatross expeditions in the North Pacific.[3] In 1898, David Starr Jordan and Charles Henry Gilbert described the genus Albatrossia in the publication by Jordan and Barton Warren Evermann, recognizing its unique features within the Macrouridae.[5][8] Junior synonyms of A. pectoralis include Coryphaenoides pectoralis, Chalinura pectoralis, and Dolloa pectoralis, reflecting historical taxonomic reassignments before its stabilization in Albatrossia.[4][9]Etymology
The genus name Albatrossia, established by David Starr Jordan and Charles Henry Gilbert in 1898, derives from the suffix -ia (Latin, belonging to) combined with Albatross, honoring the USS Albatross, a groundbreaking U.S. fisheries research vessel launched in 1882 and active until 1921, renowned for its deep-sea expeditions in the Pacific Ocean where early specimens of this grenadier were collected.[10] The etymology explicitly recalls "the good ship Albatross, in remembrance of her splendid contributions to our knowledge of the life of the deep sea," reflecting the vessel's role in advancing marine biology through systematic dredging and sampling during the late 19th and early 20th centuries.[10] The species epithet pectoralis, originally assigned by Charles Henry Gilbert in 1892 when describing the fish as Macrurus pectoralis, originates from Latin pectoralis, meaning "of or pertaining to the breast or chest," in reference to the species' distinctive long and narrow pectoral fins.[10] This naming occurred amid the USS Albatross's expeditions, which significantly contributed to ichthyological discoveries by providing the first comprehensive collections of deep-sea fauna from the North Pacific, thereby laying foundational knowledge for the taxonomy of macrourid fishes.[10]Description
Morphology
Albatrossia pectoralis exhibits an elongated, tapering body form typical of rattail fishes in the family Macrouridae, with an oval cross-section and a muscular trunk adapted to deep-sea pressures.[11] The head is large and robust, featuring a low, pointed snout that slightly protrudes beyond the terminal mouth, which is equipped with a broad upper jaw extending past the eye orbit.[11][5] Scales are small and slightly oblong, covering the body with a moderate median ridge and few weak spinules.[11] The species reaches a maximum total length of 210 cm, with common lengths around 85 cm, and a maximum published weight of 86 kg; females exhibit sexual dimorphism by attaining larger sizes than males.[11] The fins include a single dorsal fin with 2 spines and 7–9 soft rays, a reduced anal fin with 131 soft rays and no spines, and long, narrow pectoral fins that extend beyond the base of the pelvic fins, which have 6–8 rays.[11][5] Luminous organs are present as rows of photophores and cirri along the ventral surface, with those on the head underside forming a U-shaped pattern.[12] Coloration is uniform gray-brown over the head and body, with each scale bearing a prominent dark posterior border; the fins and lateral line are darker, the mouth lining and gill cavity blackish, and the peritoneum pale.[11] Internally, a reduced swim bladder is present, featuring two retia mirabilia, supporting buoyancy in deep-water environments.[11]Otoliths
The sagittal otoliths of Albatrossia pectoralis are large relative to head size and exhibit notable morphological variability, typically appearing thin and elongate with distinct anterior and posterior features that vary by individual. These otoliths are characterized by three primary shapes: hatchet-shaped, with a narrow posterior and fanning anterior margin accompanied by slight ventral crenulation; comb-shaped, featuring rounded ends and a deeply crenulated ventral side; and mixed-shaped, which combines elements of both.[13] This structure facilitates age validation through the counting of annual growth increments, or annuli, which form translucent zones separated by opaque bands, reflecting periodic growth patterns influenced by environmental factors.[13] Otolith shape variability in A. pectoralis is closely linked to differences in body growth rates and may indicate potential stock structure across its North Pacific distribution. For instance, fish with hatchet-shaped otoliths demonstrate faster growth, attaining larger pre-anal fin lengths at given ages compared to those with comb-shaped otoliths, with shape classifications derived from elliptical Fourier descriptors and principal component analysis achieving up to 69% accuracy for hatchet forms.[13] Studies have also identified sexual dimorphism in otolith size, with females exhibiting larger otoliths correlating to their greater overall body dimensions, though detailed shape analyses have primarily focused on females due to their predominance in deep-water samples.[14] In research applications, otoliths of A. pectoralis enable precise age estimation, with validated counts reaching up to 56 years through annuli interpretation, supporting assessments of longevity in this slow-growing species.[2] These data are integral to fisheries management, informing growth models such as the von Bertalanffy growth function, where parameters for total length include an asymptotic length (L∞) of approximately 150 cm and growth coefficient (K) of about 0.02 year−1, highlighting the species' extended maturation timeline.[14] Otoliths are collected by extracting the paired sagittae from the inner ear during specimen processing from trawl or longline surveys, typically at depths of 400–800 m, and preserved either dry with glycerin-thymol or in ethanol to maintain integrity.[13] For analysis, they undergo thin-sectioning by grinding the distal surface to expose the core and annuli, enhancing readability of growth zones under reflected light microscopy, a method refined for macrourids to address their opaque outer layers.[15]Distribution and habitat
Geographic range
Albatrossia pectoralis is endemic to the North Pacific Ocean, with its range extending from northern Baja California, Mexico (approximately 25°N), northward to the Bering Sea, and eastward to approximately 140°E off Japan.[16][5] The species inhabits continental slopes around the arc of the North Pacific, encompassing both eastern and western sectors, though populations exhibit some discontinuity between these regions.[15][13] The fish is particularly abundant in key areas such as the waters off Alaska, including the Gulf of Alaska and Aleutian Islands, as well as off British Columbia, Canada, where it forms a significant component of deep-sea bycatch.[2][17] In Alaskan waters, it dominates biomass on continental slopes at depths exceeding 500 m, reflecting high local densities.[17] Off British Columbia, records confirm its presence along the coastal slope, contributing to regional grenadier assemblages. The latitudinal distribution of A. pectoralis primarily spans 25°N to 65°N, aligned with temperate to subarctic waters of the North Pacific.[16] Abundance shows seasonal variations, potentially linked to sex-specific migrations, with females and males occupying separate areas at times.[14] Historical records indicate that A. pectoralis was first collected during late 19th-century expeditions by the U.S. Fish Commission steamer Albatross in 1888–1889, leading to its formal description in 1892.[4] Recent surveys, including those in the Gulf of Alaska and Russian Far East, confirm the stability of this range, with no significant shifts observed despite ongoing deep-sea fisheries.[15][18]Environmental preferences
Albatrossia pectoralis is a bathydemersal species primarily inhabiting the continental slopes of the North Pacific Ocean at depths ranging from 140 m to 3,500 m. Peak abundances are typically recorded between 700 m and 1,500 m, with variations by region; for instance, in the Gulf of Alaska, biomass concentrations are highest at 1,000–1,500 m, while in the eastern Bering Sea, they occur at 400–1,000 m.[19][20][21] The species prefers cold deep waters with temperatures between 1°C and 4°C, avoiding warmer surface layers and showing densest distributions in regions where bottom temperatures range from 1.8°C to 3.7°C. It is often associated with oxygen minimum zones (OMZs), where dissolved oxygen levels are low but do not limit its distribution, reflecting physiological tolerance to hypoxic conditions typical of mid-depth slopes.[20][5][22] A. pectoralis occurs over soft sediment substrates such as mud or sand on steep continental slopes and seamounts, where it is commonly captured using bottom trawls and longlines. The species is non-migratory in a horizontal sense but may exhibit vertical shifts in distribution to align with prey availability in the water column. As a deep-sea inhabitant, it demonstrates adaptations to high hydrostatic pressures inherent to bathydemersal environments, and its range is influenced by major oceanographic features like the cold, upwelling-driven California Current system.[20][23][19][24]Ecology
Diet and feeding
Albatrossia pectoralis is primarily an active predator that targets midwater nekton, with its diet dominated by fishes such as lanternfishes (Myctophidae) and cephalopods including squids of the genus Gonatus.[25][26] Stomach content analyses from trawl surveys reveal that fishes comprise the bulk of the diet, typically 50–70% by weight, followed by cephalopods at 25–45%, with minor contributions (less than 5%) from benthic invertebrates such as shrimps, amphipods, and echinoderms.[27] The species' food spectrum encompasses over 50 prey taxa, reflecting opportunistic foraging within the water column.[26] As a benthopelagic forager, A. pectoralis employs its terminal mouth and large eyes to hunt actively in the midwater, often ascending to shallower depths nocturnally to exploit vertically migrating prey.[25] This behavior aligns with observed patterns of higher abundance in upper water layers at night, facilitating access to epipelagic resources while residing on the continental slope during the day.[28] Its trophic level is estimated at approximately 4.0, positioning it as a secondary consumer in deep-sea food webs.[29] Ontogenetic shifts in diet occur as individuals grow; juveniles, which exhibit bathypelagic tendencies up to 50–60 cm in length, consume smaller planktonic prey including copepods and small crustaceans, transitioning to larger midwater fishes and squids in adulthood.[26][1] This progression from nektobenthophagy to nektophagy supports the species' role as a key mesopredator in slope ecosystems.[26]Reproduction and development
Albatrossia pectoralis displays sexual dimorphism in size at maturity, with males reaching sexual maturity at total lengths (TL) of 65–70 cm and females at 70–80 cm TL.[30] Females typically achieve 50% maturity at approximately 23 years of age (95% CI: 21–27 years), based on otolith-derived age estimates.[15][2] Males mature slightly earlier, though precise ages for males are less documented. The species is oviparous with external fertilization and exhibits a protracted, year-round spawning season, peaking in spring (April–May) and late summer to early autumn (August–October).[30] It is a batch spawner, releasing multiple clutches of eggs annually.[15] Fecundity varies widely, ranging from 35,000 to 231,000 oocytes per female (mean ≈106,761), with mature oocytes averaging 1.26 mm in diameter; oocytes develop in a group-synchronous pattern.[15] Eggs are pelagic and found above depths of 400 m.[1] Early life stages are planktonic: larvae (≤10 cm TL) occupy meso- to bathypelagic zones at 160–300 m, while juveniles (10–40 cm TL) range from 250–800 m before transitioning to benthic habitats at >40 cm TL.[30] Growth is slow throughout the life cycle, modeled using otolith annuli, with a maximum reported lifespan of 56 years.[2] Natural mortality is low at 0.05–0.08 year⁻¹, though total mortality increases with fishery impacts.[15] Catches of A. pectoralis often exhibit a female-biased sex ratio (≈2:1 to 91% females), potentially reflecting deeper habitat preferences by females during maturation and spawning.[30]Human interactions
Fishery
Albatrossia pectoralis, commonly known as the giant grenadier, is primarily encountered as bycatch in deep-sea commercial fisheries targeting sablefish (Anoplopoma fimbria) and Pacific halibut (Hippoglossus stenolepis) across the North Pacific. These operations occur at depths of 800–1,500 m on the continental slope, employing bottom trawls, longlines, and pots, with major fleets operating from Alaska and Russia's Far East. In Alaskan waters, the species constitutes a significant portion of bycatch in sablefish longline and pot fisheries, as well as Greenland turbot (Reinhardtius hippoglossoides) trawls, where it comprises up to 98% of grenadier catches in surveyed areas. Russian vessels also capture it incidentally in trawl and experimental trap fisheries in regions like the western Bering Sea and southeastern Kamchatka. Recent research indicates intensification of the fishery in Russian Far East waters, with estimates of maximum sustainable yield and increased catches as of 2024.[21][31][22][30] Annual catches of A. pectoralis in the North Pacific, predominantly as bycatch, have ranged from 11,000 to 21,000 metric tons between 1997 and 2008 in the Gulf of Alaska, Bering Sea, and Aleutian Islands, with a mean of approximately 16,000 metric tons; however, nearly all were discarded at sea due to high mortality from pressure changes and poor flesh quality. In Russian waters, experimental trap fisheries in 2011 across southeastern Kamchatka, the western Bering Sea, Shirshov Ridge, and the Aleutian-Commander region yielded an estimated exploitable biomass of 11,882 metric tons, though actual landings remained limited. Utilization varies by region: in Alaska, the gelatinous, watery flesh limits commercial interest, leading to full discards, while Russian catches are processed into fishmeal from the flesh, liver oil rich in vitamins A and D, and canned eggs for added value. Some grenadier species, including A. pectoralis, have been processed into surimi or dried products for niche markets, though direct landings for these purposes are minimal.[21][22][14][32] Bottom trawls and longlines used in these mixed-species fisheries contribute to habitat damage on sensitive deep-sea substrates like corals and sponges, exacerbating vulnerability in the slow-growing species' environment. Historical data from the 1990s onward show increasing bycatch rates correlating with expanded fishing effort on the continental slope, particularly in sablefish and halibut operations. Economically, A. pectoralis holds low direct value due to processing challenges and limited consumer demand, but it plays a notable role in overall fishery yields through bycatch management and secondary products like liver oil and eggs, with Russian exports supporting regional processing industries.[31][21][22]Conservation status
Albatrossia pectoralis, commonly known as the giant grenadier, has not been formally assessed by the International Union for the Conservation of Nature (IUCN) Red List, where it is categorized as Not Evaluated, reflecting significant data deficiencies in its population dynamics and life history traits.[1] However, its biological characteristics, including slow growth rates, late maturity (females around 23 years), and longevity up to 56 years, render it potentially vulnerable to overexploitation and environmental perturbations in its deep-sea habitat.[2] In Alaskan waters, it is classified as an Ecosystem Component species under the North Pacific Fishery Management Council's groundfish fishery management plans for the Gulf of Alaska (GOA) and Bering Sea/Aleutian Islands (BSAI), indicating no directed fishery but recognition of its role in the ecosystem.[20] The primary threats to A. pectoralis stem from human activities, particularly bycatch in commercial fisheries. Giant grenadiers constitute a substantial portion of bycatch, averaging nearly 20% of total bycatch in Alaskan groundfish fisheries, with most encounters occurring in the sablefish longline fishery where they are almost entirely discarded at sea with a 100% mortality rate.[33][34] Bottom trawling further exacerbates risks through direct habitat disruption on the continental slope, where this species resides at depths of 700–1,100 meters.[1] Climate change poses an emerging threat by altering ocean oxygenation and temperature profiles, potentially compressing suitable habitat as oxygen minimum zones expand, thereby increasing physiological stress on this oxygen-sensitive deep-sea species.[35] Management efforts focus on mitigating incidental mortality rather than direct harvest, as there is no targeted fishery for giant grenadiers. Under the North Pacific Fishery Management Council, an 8% maximum retainable allowance applies in relevant groundfish fisheries, with observer programs deployed to monitor bycatch rates and ensure compliance.[20] While no specific quotas or overfishing levels (OFL) are set, the species benefits from broader ecosystem-based approaches, including prohibitions on retention in certain areas and integration into stock assessments for associated fisheries like sablefish. These measures have contributed to declining catches since 2012, averaging 3,078 metric tons annually in the BSAI from 2013–2019 compared to 6,401 metric tons from 2003–2012.[20] Recent stock assessments indicate stable but relatively low biomass levels in Alaskan waters, with estimates of 369,618 metric tons in the GOA (2019) and 1,055,348 metric tons in the BSAI (2020), reflecting a decline from peaks in 2016.[20] Post-2020 research, including age and growth studies, underscores the need for comprehensive stock assessments to address gaps in understanding larval and juvenile habitats, deep-water distribution, and fishery-induced mortality rates.[2] Enhanced monitoring and modeling of climate impacts are also recommended to inform adaptive management strategies.References
- https://species.wikimedia.org/wiki/Albatrossia