ArticlePDF Available

Sea Lamprey Attached to a Greenland Shark in the St. Lawrence Estuary, Canada

Authors:
  • St. Lawrence Shark Observatory (ORS | GEERG)

Abstract and Figures

A Petromyzon marinus (sea lamprey) was observed attached to an approximately 3-m fork length, male Somniosus microcephalus (Greenland shark) on 9 October 2004 in Baie St. Pancrace, St. Lawrence Estuary, PQ. This is the first report of a sea lamprey attached to a member of Somniosidae.
Content may be subject to copyright.
NORTHEASTERN NATURALIST
2006 13(1):35–38
Sea Lamprey Attached to a Greenland Shark in the
St. Lawrence Estuary, Canada
JEFFREY GALLANT
1
, CHRIS HARVEY-CLARK
2
, RANSOM A. MYERS
3
,
AND MICHAEL J.W. STOKESBURY
3,*
Abstract - A Petromyzon marinus (sea lamprey) was observed attached to an
approximately 3-m fork length, male Somniosus microcephalus (Greenland shark) on
9 October 2004 in Baie St. Pancrace, St. Lawrence Estuary, PQ. This is the first
report of a sea lamprey attached to a member of Somniosidae.
Introduction
Petromyzon marinus Linnaeus (sea lamprey) is the largest lamprey spe-
cies (Scott and Crossman 1973). Landlocked sea lampreys have been studied
extensively in fresh water, but little is known of the oceanic and estuarine
portions of the life cycle of anadromous conspecifics (Beamish 1980, Scott
and Scott 1988). Sea lampreys spawn in fresh water and their larvae spend
6–8 years in the substrate (Beamish and Potter 1975) followed by metamor-
phosis (Ooi and Youson 1977) and movement to sea. They remain in the
estuarine and marine environment for a juvenile feeding period lasting 23 to
28 months (Beamish 1980), during which they grow from approximately 4 to
900 g (Beamish 1980). At the end of this period, sea lampreys move into
rivers as adults and reproduce. During the juvenile feeding phase, sea lam-
preys typically are considered predatory, if their feeding kills the animal
they are attacking, or parasitic, if the animal continues to survive (Scott and
Scott 1988). Sea lampreys attach to prey or hosts by suction created using
their buccal funnel. They then use their rasping tongue to grind through the
skin or scales, and they ultimately feed on the flesh and body fluids (Scott
and Scott 1988). Sea lampreys feed on a wide variety of bony fishes
(Beamish 1980, Bigelow and Schroeder 1953, Halliday 1991): Eubalaena
glacialis Borowski (right whale) (Nichols and Hamilton 2004), Cetorhinus
maximus Gunnerus (basking shark) (Bigelow and Schroeder 1953),
Prionace glauca L. (blue shark) (Benz and Bullard 2004), and Carcharhinus
plumbeus Nardo (sandbar shark), and C. obscurus Lesueur (dusky sharks)
(Jenson and Schwartz 1994). Herein we report observation of a sea lamprey
attached to a Somniosus microcephalus (Bloch and Schneider) (Greenland
shark) in Baie St. Pancrace, PQ, Canada.
1
Greenland Shark and Elasmobranch Education and Research Group, PO Box 483,
Drummondville, PQ, Canada J2B 6W3.
2
Animal Care Center, University of British
Columbia, 6199 South Campus Drive, Vancouver, BC, Canada V6T 1W5.
3
Depart-
ment of Biological Sciences, Dalhousie University, 1355 Oxford Street, Halifax, NS,
Canada B3H 4J1. *Corresponding author - mstokesb@dal.ca.
Northeastern Naturalist Vol. 13, No. 1
36
Methods and Results
On 9 October 2004 at 14:23 h, divers using SCUBA observed, photo-
graphed, and videotaped a sea lamprey attached to a Greenland shark in Baie
St. Pancrace (49.288°N, 68.049°W), St. Lawrence Estuary, PQ. The ap-
proximately 3-m fork length, male Greenland shark approached the divers
with the sea lamprey attached to its ventral side between the pelvic fins close
to the base of the claspers. The sea lamprey was approximately 40 cm long
and was bluish-grey (Fig. 1). The shark swam away from the divers, toward
deeper water, as the divers approached to photograph the lamprey. The
encounter between the divers and shark lasted approximately 2 minutes and
was recorded using digital and video cameras. Observations were made at a
water depth of 22 m, 0.5 m above the bottom. Water temperature at 22 m
depth was 4.4 ºC. Three other Greenland sharks were observed on this dive,
however, no other sea lamprey was observed.
Discussion
This is the first record of a sea lamprey attached to a member of
Somniosidae (Squaliformes). Sea lampreys are found from the shallows to
depths in excess of 4000 m (Halliday 1991, Scott and Crossman 1973) and
display an ambient water temperature tolerance from -0.6 to 20 ºC (Beamish
1980). In the western Atlantic Ocean, they range from waters off southwest-
ern Greenland (Scott and Scott 1988) to Florida and the Gulf of Mexico
Figure 1. Sea lamprey attached to a Greenland shark, 9 October 2004, in Bay St.
Pancrace, St. Lawrence Estuary, PQ, Canada.
J. Gallant, C. Harvey-Clark, R.A. Myers, and M.J.W. Stokesbury2006 37
(Flescher and Martini 2002). Greenland sharks have been recorded from the
shallows to depths in excess of 2200 m and display an ambient water
temperature tolerance from approximately -1.5 (Skomal and Benz 2004) to
12 ºC (Bigelow and Schroeder 1948). In the western Atlantic Ocean, they
range from waters off western Greenland (Scott and Scott 1988) in the north,
to deep waters as far south as off Georgia (Herdendorf and Berra 1995).
Thus, sea lampreys and Greenland sharks have similar vertical and horizon-
tal distributions and there is the potential for interaction between these
species. As it is unknown if the sea lamprey reported on here was feeding on
the shark to which it was attached, it remains unknown if sea lampreys use
Greenland sharks as a food resource.
Acknowledgments
Diving was performed by S. Sirois, J.-Y. Forest, and C. Beaudoin under the
supervision of J. Gallant.
Literature Cited
Beamish, F.W.H. 1980. Biology of the North American anadromous sea lamprey,
Petromyzon marinus. Canadian Journal of Fisheries and Aquatic Sciences
37:1924–1943.
Beamish, F.W.H., and I.C. Potter. 1975. The biology of the anadromous sea lamprey
(Petromyzon marinus) in New Brunswick. Journal of Zoology 177:57–72.
Benz, G., and S.A. Bullard. 2004. Metazoan parasites and associates of
chondrichthyans with emphasis on taxa harmful to captive hosts. Pp. 325–416, In
M. Smith, D. Warmolts, D. Thoney, and R. Hueter (Eds.). The Elamobranch
Husbandry Manual: Captive Care of Sharks, Rays, and their Relatives. Ohio
Biological Survey, Columbus, OH. 416 pp.
Bigelow, H.B., and W.C. Schroeder. 1948. Sharks. Pp. 59–546, In J. Tee-Van, C.
Breder, S. Hildebrand, A. Parr, and W. Schroeder (Eds.). Fishes of the Western
North Atlantic: Lancelets, Cyclostomes, and Sharks. Sears Foundation for Ma-
rine Research, Memoir 1, Part 1. Yale University Press, New Haven, CT. 576 pp.
Bigelow, H.B., and W.C. Schroeder. 1953. Fishes of the Gulf of Maine. US Fishery
Bulletin 53:1–577.
Flescher, D., and F.H. Martini. 2002. Lampreys. Order Petromyzontiformes. Pp.
16–19, In B.B. Collette and G. Klein-MacPhee (Eds.). Bigelow and
Schroeder’s Fishes of the Gulf of Maine. Smithsonian Institution Press, Wash-
ington, DC. 748 pp.
Halliday, R.G. 1991. Marine distribution of the sea lamprey (Petromyzon marinus)
in the Northwest Atlantic. Canadian Journal of Fisheries and Aquatic Sciences
48:832–842.
Herdendorf, C.E., and T.M. Berra. 1995. A Greenland shark from the wreck of the
SS Central America at 2200 meters. Transactions of the American Fisheries
Society 124:950–953.
Jensen C., and F.J. Schwartz. 1994. Atlantic Ocean occurrences of the sea lamprey,
Petromyzon marinus (Petromyzontiformes, Petromyzontidae), parasitizing sand-
bar, Carcharhinus plumbeus, and dusky, C. obscurus (Carcharhiniformes:
Carcharhinidae), sharks off North and South Carolina. Brimleyana 21:69–72.
Northeastern Naturalist Vol. 13, No. 1
38
Nichols, O.C., and P.K. Hamilton. 2004. Occurrence of the parasitic sea lamprey,
Petromyzon marinus, on western North Atlantic right whales, Eubalaena
glacialis. Environmental Biology of Fishes 71:413–417.
Ooi, E.C., and J.H. Youson. 1977. Morphogenesis and growth of the definitive
opisthonephric kidney during metamorphosis of anadromous sea lamprey,
Petromyzon marinus L. Journal of Embryology and Experimental Morphology
42:219–235.
Scott, W.B., and E.J. Crossman. 1973. Freshwater fishes of Canada. Fisheries Re-
search Board of Canada Bulletin 184:1–966.
Scott, W.B., and M.G. Scott. 1988. Atlantic fishes of Canada. Canadian Bulletin of
Fisheries and Aquatic Sciences 219:1–731.
Skomal, G.B., and G.W. Benz. 2004. Ultrasonic tracking of Greenland sharks,
Somniosus microcephalus, under Arctic ice. Marine Biology 145:489–498.
... Marine parasitic juvenile Sea Lamprey in the western North Atlantic have been observed on megafaunal hosts including teleosts Schroder 1953, Perlmutter 1962), cetaceans (Nichols and Hamilton 2004, Nichols and Tscherter 2011, Samarra et al. 2011, and selachians (Gallant at al. 2006, Jensen and Schwartz 1994, Wilkie et al. 2004). The occurrence of Sea Lamprey on selachians is noteworthy because the skin of sharks is covered with placoid scales (or dermal denticles). ...
... Our observation coupled with those of Michael (1993), Jensen et al. (1998), and Gallant et al. (2006) suggests that when a Sea Lamprey does adhere to a shark, the region of the cloaca is a common point of attachment. This may be because the placoid scales of that region do not exhibit the same roughness as elsewhere on the body, as has been demonstrated in several shark species (Ankheli et al. 2018, Sayles andHershkowitz 1937). ...
Article
We report an observation of a Petromyzon marinus (Sea Lamprey) adhering to a Prionace glauca (Blue Shark) in pelagic waters off Rhode Island. We compare our observation of lamprey adhesion to previously published accounts of lamprey parasitism on sharks and aspects of interactions between lampreys and elasmobranchs that warrant further study.
... Marine parasitic juvenile Sea Lamprey in the western North Atlantic have been observed on megafaunal hosts including teleosts Schroder 1953, Perlmutter 1962), cetaceans (Nichols and Hamilton 2004, Nichols and Tscherter 2011, Samarra et al. 2011, and selachians (Gallant at al. 2006, Jensen and Schwartz 1994, Wilkie et al. 2004). The occurrence of Sea Lamprey on selachians is noteworthy because the skin of sharks is covered with placoid scales (or dermal denticles). ...
... Our observation coupled with those of Michael (1993), Jensen et al. (1998), and Gallant et al. (2006) suggests that when a Sea Lamprey does adhere to a shark, the region of the cloaca is a common point of attachment. This may be because the placoid scales of that region do not exhibit the same roughness as elsewhere on the body, as has been demonstrated in several shark species (Ankheli et al. 2018, Sayles andHershkowitz 1937). ...
Article
We report an observation of a Petromyzon marinus (Sea Lamprey) adhering to a Prionace glauca (Blue Shark) in pelagic waters off Rhode Island. We compare our observation of lamprey adhesion to previously published accounts of lamprey parasitism on sharks and aspects of interactions between lampreys and elasmobranchs that warrant further study.
... Parasite (blood feeder) Chilean lamprey Unknown N/A Mordacia lapicida Short-headed lamprey Fishes: Black bream (Acanthopagrus butcheri), Yellow-eye mullet (Aldrichetta forsteri), Snoek (Thyrsites atun), Potter et al., 1968;Renaud, 2011 Mordacia mordax Sea lamprey Fishes: Dusky shark (Carcharhinus obscurus), Sandbar shark (Carcharhinus plumbeus), Basking shark (Cetorhinus maximus), Greenland shark (Somniosus microcephalus), Tiger shark (Galeocerdo cuvier), Blue shark (Prionace glauca), Common eagle ray (Myliobatis aquila), Gulf sturgeon (Acipenser oxyrinchus)*, Atlantic sturgeon (Acipenser sturio)*, Blueback shad (Alosa aestivalis), Allis shad (Alosa alosa), Twaite shad (Alosa fallax)*, Alewife (Alosa pseudoharengus), American shad (Alosa sapidissima), Atlantic wolffish (Anarhichas lupus), Garfish (Belone belone), Bogue (Boops boops), Atlantic menhadden (Brevoortia tyrannus), Golden grey mullet (Chelon aurata), Thinlip grey mullet (Chelon ramada), Atlantic herring ( Bird et al. (1994), Gallant et al. (2006), Farmer (1980, Halliday (1991), Heyning (2003), Japha (1910), Jensen and Schwartz (1994), Jensen et al. (1998), Mansueti (1962), McAlpine (2003, Moyer et al. (2020), Miočić -Stošić et al. (2020), Nichols and Hamilton (2004), Nichols and Tscherter (2011), Potter and Beamish (1977), Powell et al. (1999), Samarra et al. (2012), Silva et al. (2013a), Silva et al. (2013b), Silva et al. (2013c), Silva et al. (2014) a discrete wound through the skin and tissue of their host, and the continuous production of lamphredin (an anticoagulant) to prevent their host's blood from clotting, as well as to facilitate tissue breakdown (Khidir and Renaud, 2003;Lethbridge and Potter, 1979;Potter and Hilliard, 1987;Renaud et al., 2009). Although documentation of sea lamprey hosts is growing (Silva et al., 2014; Table 1), there is a need to obtain information on the feeding ecology of the two other blood-feeding lampreys (Chilean and shortheaded lamprey; Table 1). ...
Article
Full-text available
This paper synthesizes information on the at-sea ecology of ten anadromous lampreys, with emphasis on trophic ecology. The at-sea ecology of these lampreys concerns the juvenile stage, in which growth is most rapid. Anadromous lampreys can be categorized into four groups, based on feeding modalities: 1) scavenger (Caspian lamprey, Caspiomyzon wagneri); 2) parasite-predator (Pacific lamprey, Entosphenus tridentatus); 3) predators (western river lamprey, Lampetra ayresii; European river lamprey, L. fluviatilis; Arctic lamprey, Lethenteron camtschaticum; pouched lamprey, Geotria australis; and Argentinian pouched lamprey, G. macrostoma); and 4) parasites (sea lamprey, Petromyzon marinus; Chilean lamprey, Mordacia lapicida; and short-headed lamprey, M. mordax). This paper discusses direct evidence for lamprey feeding ecology, as observed through lamprey-induced wounds on hosts and prey, and lamprey attachments on hosts and prey; and indirect evidence for feeding ecology, via analyses of fatty acids, stable isotopes, contaminants, and bioenergetics modelling. A part of the information presented on feeding ecology is from landlocked sea lamprey, and in some instances this information can be generalizable to anadromous populations. For most anadromous lampreys, but particularly for Southern Hemisphere taxa, little is known about their feeding ecology at sea. Duration of the trophic marine phase and habitat use are still subjects of debate. Species identified as lamprey hosts can be demersal or pelagic, possibly reflecting marine habitat preferences. To unlock understanding of the marine phase of anadromous lampreys, direct evidence of feeding ecology should be coupled with natural (i.e., biomark-ers) and artificial (e.g., biologgers) markers to identify habitat use, movement patterns and dispersal.
... Because metamorphosis is a non-trophic (nonfeeding) phase, energy is primarily provided by the lipid reserves accumulated during the larval phase (Lowe et al., 1973;Kao et al., 1997). Following metamorphosis, juvenile sea lampreys ingest large quantitities of protein-rich blood from large salmonid fishes, other game fishes, sturgeons, as well as sharks and even cetaceans in marine environments (Bigelow and Schroeder, 1948;Beamish and Potter, 1975;Jensen and Schwartz, 1994;Wilkie et al., 2004Wilkie et al., , 2006Gallant et al., 2006;Nichols and Hamilton, 2004;Renaud et al., 2009). The rate of blood ingestion by parasitic juvenile sea lampreys is typically 3-10% of their total body mass per day, but may approach 30% in the latter part of the parasitic life stage (Farmer et al., 1975;Farmer, 1980). ...
Article
The invasion of the Laurentian Great Lakes of North America by sea lampreys (Petromyzon marinus) in the early 20th century contributed to the depletion of commercial, recreational and culturally important fish populations, devastating the economies of communities that relied on the fishery. Sea lamprey populations were subsequently controlled using an aggressive integrated pest-management program which employed barriers and traps to prevent sea lamprey from migrating to their spawning grounds and the use of the piscicides (lampricides) 3-trifluoromethyl-4-nitrophenol (TFM) and niclosamide to eliminate larval sea lampreys from their nursery streams. Although sea lampreys have not been eradicated from the Great Lakes, populations have been suppressed to less than 10% of their peak numbers in the mid-1900s. The ongoing use of lampricides provides the foundation for sea lamprey control in the Great Lakes, one of the most successful invasive species control programs in the world. Yet, significant gaps remain in our understanding of how lampricides are taken-up and handled by sea lampreys, how lampricides exert their toxic effects, and how they adversely affect non-target invertebrate and vertebrates species. In this review we examine what has been learned about the uptake, handling and elimination, and the mode of TFM and niclosamide toxicity in lampreys and in non-target animals, particularly in the last 10 years. It is now clear that the mode of TFM toxicity is the same in non-target fishes and lampreys, in which TFM interferes with oxidative phosphorylation by the mitochondria leading to decreased ATP production. Vulnerability to TFM is related to abiotic factors such as water pH and alkalinity, which we propose changes the relative amounts of the bioavailable un-ionized form of TFM in the gill microenvironment. Niclosamide, which is also a molluscicide used to control snails in areas prone to schistosomiasis infections of humans, also likely works by uncoupling oxidative phosphorylation, but less is known about other aspects of its toxicology. The effects of TFM include reductions in energy stores, particularly glycogen and high energy phosphagens. However, non-target fishes readily recover from sub-lethal TFM exposure as demonstrated by the rapid restoration of energy stores and clearance of TFM. Although both TFM and niclosamide are non-persistent in the environment and critical for sea lamprey control, increasing public and institutional concerns about pesticides in the environment makes it imperative to explore other means of sea lamprey control. Accordingly, we also address possible “next-generation” strategies of sea lamprey control including genetic tools such as RNA interference and CRISPR-Cas9 to impair critical physiological processes (e.g. reproduction, digestion, metamorphosis) in lamprey, and the use of green chemistry to develop more environmentally benign chemical methods of sea lamprey control.
... The trophic ecology of adult lampreys can be evaluated using evidence of lamprey-host interactions, including lampreys still attached to hosts and the wounds left as a result of these encounters. Although lampreys are occasionally observed attached to large-bodied vertebrates, such as whales (Pike 1951;Nichols and Tscherter 2011;Samarra et al. 2012) and sharks (Gallant et al. 2006), teleosts more frequently exhibit evidence of parasitic lamprey interactions-specifically wounds in their skin and muscle. These wounds have been observed on the following groups of teleosts in the North Pacific Ocean: Gadidae, Clupeidae, Salmonidae, Sebastidae, and Pleuronectidae (Sviridov et al. 2007;Orlov et al. 2009;Shevlyakov and Parensky 2010). ...
... Although lampreys are occasionally observed attached to large bodied vertebrates such as whales ( Pike 1951;Nichols and Tscherter 2011;Samarra et al. 2012) and sharks ( Gallant et al. 2006), teleosts more frequently exhibit evidence of parasitic lamprey interactions, specifically wounds in their skin and muscle. These wounds have been observed on the following groups of teleosts in the North Pacific Ocean: Gadidae, Clupeidae, Salmonidae, Sebastidae, and Pleuronectidae ( Sviridov et al. 2007;Orlov et al. 2009;Shevlyakov and Parensky 2010). ...
Article
Arctic Lamprey Lethenteron camtschaticum and Pacific Lamprey Entosphenus tridentatus are ecologically and culturally valuable native species that co-occur in the eastern Bering Sea. Lamprey wounds are often observed on fishes in this region, yet there is a paucity of information on the distribution of anadromous lampreys, lamprey-host interactions, and foraging behavior in the ocean. Our hypothesis was that each lamprey species would be positively associated (distribution and abundance) with their presumed hosts: Arctic Lamprey with smaller fish that could easily be killed, and Pacific Lamprey with larger hosts that would sustain blood feeding. To examine lamprey distribution, abundance, and associations, we utilized data from two fishery-independent surveys, one epipelagic trawl and one benthic trawl, conducted between 2002 and 2012 in the eastern Bering Sea. Distinct distributions of lamprey species were evident in models of their presence and absence by latitude and longitude, where Arctic Lampreys inhabited the northern regions on the inner/middle continental shelf in depths less than 100 m, while Pacific Lampreys inhabited waters deeper than 150 m along the continental slope. Pacific Herring and juvenile salmonids were found in regions with relatively high Arctic Lamprey catches in the epipelagic trawl survey, and catches of lampreys and these potential hosts were positively correlated. Demersal groundfishes were found in regions with relatively high Pacific Lamprey abundance in the benthic trawl survey, though catches of Pacific Lamprey and these hosts were not consistent. We conclude that Arctic and Pacific lampreys are segregated in the eastern Bering Sea, and while differences in their distributions may be explained by species-specific host preferences, alternate explanations include differences in seasonal movements, source river locations, and marine residence times. This study provides an initial baseline of the oceanic ecology of lampreys, which increases our understanding of species-specific differences beyond traditional freshwater studies. Received 25 Apr 2017 accepted 02 Oct 2017 revised 25 Aug 2017
... Lamprey species classified as flesh feeding parasites (Renaud et al. 2009) may also cause enough damage to internal organs during a feeding event as to cause death by massive organ failure (Talabishka et al. 2012). Most lamprey attachments have been observed on teleosts, but attachments to elasmobranchs (Wilkie et al. 2004, Gallant et al. 2006 and cetaceans are also known to occur (Nichols and Tscherter 2011, Bertulli et al. 2012, Ólafsdóttir and Shinn 2013. ...
Article
Full-text available
The Pacific sleeper shark Somniosus pacificus is a large-bodied and broad-ranging squaliform shark that occupies diverse habitats throughout the Pacific Ocean. Despite its large size and occurrence as bycatch in various commercial fisheries, little is known about even the most basic aspects of its biology and ecology. Observed declines in certain parts of its range, coupled with life history characteristics associated with low productivity, have led to conservation concerns for this cryptic but charismatic species. Here, we provide a comprehensive review of the current state of knowledge regarding the distribution, diet, life history, and other aspects of the Pacific sleeper shark and present updated fisheries and survey data for the eastern North Pacific Ocean. The most pressing research gaps identified during the course of this review concern habitat use at different life stages and basic life history information. While work is currently in progress to expand our base of knowledge for this species, we recommend a precautionary approach to management until sufficient information becomes available to ensure its conservation.
Article
This datasheet on Petromyzon marinus covers Identity, Overview, Distribution, Dispersal, Diagnosis, Biology & Ecology, Environmental Requirements, Natural Enemies, Impacts, Uses, Prevention/Control, Further Information.
Chapter
Eighteen of 41 lamprey species worldwide feed post metamorphosis; nine in either marine waters or fresh waters and nine exclusively in fresh waters. Four feeding modes have been identified: blood feeding, flesh feeding, blood and flesh feeding, and carrion feeding. Adaptations to these feeding modes are associated with characteristics of the dentition of the oral disc and tongue-like piston, the oral papillae and fimbriae, the velar tentacles, and the buccal glands. The duration of the adult feeding phase varies from a few months to 4 years and during this time the various species grow either slightly or up to nearly eight times the length that they reached as larvae. The post-metamorphic diet consists usually of fishes but in some cases may include marine mammals. Feeding behavior is complex and highly variable and differs between the two major modes of blood feeding and flesh feeding. Blood feeders tend to selectively attack larger hosts and tend to attach ventrally to them in deep water but dorsally in shallower habitats. Flesh feeders tend to attach dorso-laterally to schooling fishes, and their hosts may be relatively small compared to those used by blood feeders.
Article
The definitive opisthonephros of the adult lamprey, Petromyzon marinus L., develops during metamorphosis from the nephrogenic cord confined within a nephric fold and extending from the posterior tip of the larval opisthonephros to the cloaca. This development is initiated prior to the first signs of external metamorphosis and begins with the simultaneous appearance of clusters of cells scattered along the entire length of the cord. Proliferation of these cell clusters and their elongation to connect to the closely associated archinephric duct results in the formation of rudimentary nephron units. Subsequent development involves the formation of tubular lumina, branching of the tubules, and the participation of the proximal ends of the newly formed tubules in the formation of the single renal corpuscle. Growth in size of the kidney is the result of lengthening of the existing tubules through cell proliferation rather than through the addition of new nephrons. This growth appears to be at the expense of adipose tissue within the nephric fold. During later stages of metamorphosis, cell proliferation is more prevalent in the ventral part of the nephric fold where a parallel system of tubules develops. The development of the definitive opisthonephros during metamorphosis of lamprey may prove to be a useful model for further studies of tissue differentiation and interaction during kidney development in vertebrates.
Article
The three-masted, wooden-hulled steamship Central America sank in 1857 during a hurricane 370 km east of Savannah, Georgia. During a recovery project begun in 1988, the unmanned research submersible Nemo equipped with video and still cameras filmed a 6-m-long, male Greenland shark Somniosus microcephalus at the 2,200-m-deep wreck site. The depth is 1,000 m deeper than the maximum reported depth for this species. The Savannah location is 440 km further south than the previously known North Carolina records for the Greenland shark.
Article
For the past twenty years, the standard reference on the varieties of species native to the Canadian Atlantic region was A.H. Leim and W.B. Scott's Fishes of the Atlantic Coast of Canada. This new work, by W.B. Scott in collaboration with M.G. Scott, now replaces the earlier volume as a comprehensive guide to over 500 species found the region. Arranged in three parts, it offers keys to families, or major categories, and to the members, ot species, within each family. Accounts for each include habitat, reproduction, food, growth, predation, parasites and diseases, distribution, utilization, and physical description. An introduction provides an overview of Canadian Atlantic fisheries and the oceanography of the region. Fully illustrated, this long awaited volume will be indispensable to all those involved in the fisheries resource and allied studies.
Article
Catch data from trawling surveys by the Canadian Department of Fisheries and Oceans and the U.S. National Marine Fisheries Service conducted between Nova Scotia and Cape Hatteras mainly during 1978–90 contained 60 records of sea lamprey (Petromyzon marinus) captures. A further 20 records were obtained from a variety of other sources. These animals ranged in length from 12 to 84 cm. Those less than 39 cm were almost all taken in bottom trawl surveys on the continential shelf or in coastal trap nets whereas most animals 56 cm and larger were caught in midwater trawls primarily along the shelf edge and over the continental slope. The data are consistent with a previously proposed 2.5-yr marine juvenile parasitic period but a 1.5-yr period cannot be ruled out until intermediate-sized animals 39–55 cm are caught. Direct and indirect evidence on host species indicates that feeding on anadromous and small marine fish may be restricted to the first juvenile year and that large pelagic fish and marine mammals are hosts at older ages. Thus, subsequent to the first winter following metamorphosis, sea lampreys are apparently pelagic in habit and possibly wide ranging in distribution in association with large pelagic hosts.
Article
The sea lamprey (Petromyzon marinus) in the western Atlantic Ocean adjacent to North America is usually found within a depth of 200 m between latitudes of 30 and 53°. Spawning size lampreys have been recorded in 116 rivers between 32 and 48° latitude. The upstream spawning migration which may extend to several hundred kilometres, takes place between March and September, the actual time varying directly with latitude. Fecundity of the anadromous P. marinus (approximately 124 000–305 000) is the highest for any lamprey species. Energy requirements for migration and reproduction are discussed in the context of parental investment. The larval phase lasts 6–8 yr and is followed by a highly synchronous period of metamorphosis. On completion of metamorphosis in late autumn some juveniles migrate downstream to the estuary or ocean and commence feeding. In at least some rivers, a portion of the young juveniles overwinter in the natal stream without feeding. Subsequent to a short feeding period in May these young juveniles leave the river for the sea. Sea lampreys attack a variety of marine elasmobranchs and teleosts. Only swordfish, Xiphias gladius, and striped bass, Roccus saxatilis, are reported to eat lampreys. During the marine interval, which lasts from 23 to 28 mo, the calculated instantaneous growth rate is 0.645–0.785 g∙d−1. Lamprey scarring frequency on Atlantic salmon, Salmo salar, in the St. John River, New Brunswick, increased from 2.6 to 15.0% between 1972 and 1975 coincident with a dramatic rise in the number of migrant salmonids. Scars were most prevalent on larger salmon, particularly females. Most scars were recorded on the right side of salmon, particularly in the ventral regions.Key words: sea lamprey, Atlantic Ocean, distribution, life cycle, growth, energetics, fecundity