Observations on the reproduction and postlarval morphology of pourtalesiid sea urchins in the Rockall Trough area (N.E. Atlantic Ocean)

Gametogenesis was studied histologically in the deep-sea species Pourtalesia jeffreysi (Wyville Thomson), P. miranda (A. Agassiz) and Echinosigra phiale (Wyville Thomson) collected during 1973–1983 from various positions at depths of 1 040 to 2 921 m in the Rockall Trough. The gonads are small and no synchrony in terms of the stage of gametogenic development was evident in females of the latter two species collected at different times of the year, indicating nonseasonal breeding. Males appear to be ripe at all times of the year. Follicle cells were well developed around the developing oocytes. Both the size range of the yolky ripe eggs (173 to 357 m diam) and potential fecundity within the range of 1 000 to 4 000 oocytes per individual, are indicative of an abbreviated, indirect, lecithotrophic mode of development occurring in all three species. Pourtalesiid postlarvae occurred also in fine-meshed trawl hauls, and their morphology is described. It was not possible to distinguish between P. miranda and E. phiale at sizes <3 mm in length.     

Natural growth bands and growth variability in the sea urchin Echinus esculentus: results from tetracycline tagging

Growth of the European edible sea urchin Echinus esculentus L. was studied in a population held for 2 yr in cages on the sea bed, after labelling with the skeletal growth marker tetracycline. The final position of the tetracycline tag on the genital plates agreed with an annual periodicity in natural growth zones; two such growth zones appeared beyond the position of the tag on the ground surface of the plate as light-reflecting bands separated by narrow dark lines in the middle layer. Individual and group (pooled data) growth parameters were estimated from the growth increment shown in the genital plate, whose lateral growth displayed a linear relationship to the diameter of the urchin test within the size range of these measurements. Von Bertalanffy growth parameters (asymptotic size and growth-rate function K) fitted to the growth increment on each individual were highly significantly correlated to those fitted to the natural growth lines, assuming an annual periodicity. The inferred growth pattern agrees well with conclusions based on H. B. Moore's growth-band data. The caged urchins can be assumed to have experienced exactly similar conditions, yet the growth curves fitted to individuals showed considerable variability. The good agreement between estimated growth function parameters of individuals obtained by the two methods indicate that this reflects real variability in growth between individuals that probably is genetically rather than environmentally determined. The growth of E. esculentus, and the adaptational significance of high growth variability in the population is briefly discussed.     

Skeletal growth zones as age-markers in the sea urchinPsammechinus miliaris

Growth of the inshore sea urchinPsammechinus miliaris (Gmelin) was studied in Loch Creran, western Scotland, using the skeletal growth-marker tetracycline in order to test the validity of natural growth-banding in the coronal test plates as annual age-markers. In order to test whether tetracycline affected the growth ofP. miliaris, an injected and a control group of urchins were held in identical conditions in running sea water aquaria for 21 mo from 1989 to 1991 and measured periodically. A small but significant difference in mean size of injected compared to controls was recorded at 12 mo, but none during subsequent measurements. Size measurements during the trial were consistent with an annual growth cycle, with a maximum in spring and slowing or cessation of growth during autumn/winter. Tetracycline-labelled juveniles were recovered up to 18 mo after initial tagging in mark/recapture experiments undertaken from 1987 to 1989 at two intertidal marked quadrats in Loch Creran. Large numbers ofP. miliaris were also marked with tetracycline and held for 1 yr at 10 m depth in seabed cages in Loch Creran during 1988–1990. All of the intertidal recoveries, and about 69% of the caged specimens that had been successfully labelled, showed a consistent relationship between the position of the tetracycline tag and the pattern of natural growth zones. The remainder were mostly large, slow-growing urchins with the tag positioned near the plate margin. In these the outer growth bands were closely spaced and, particularly if major growth bands seemed to be broken up into double or multiple lines, the major bands were impossible to resolve at the margin. The results support the assumption that in wild populations the dark bands visible with reflected light (translucent in transmitted light) after charring the plate are formed when skeletal growth has stopped or slowed in winter. These lie between wider, lighter coloured (opaque in transmitted light) zones of active plate growth in spring/summer. The dark band formed beyond the tag usually was made up of several closely spaced fine lines, or sometimes of two closely spaced dark bands. The wide growth zones beyond the tag, like those formed previously, usually were broken by fine, dark lines that may represent brief discontinuities in growth. From tagging, the double dark bands can be related to growth over one year; but such anomalous bands, along with the general presence of fine, dark lines interrupting the growth zones, make it difficult reliably to estimate age from the closely spaced peripheral banding on older, slow-growing urchins.     

Effect of sunlight intensity and albinism on the covering response of the Caribbean sea urchin<Emphasis Type="Italic"> Tripneustes ventricosus</Emphasis>

At Discovery Bay, Jamaica, Tripneustes ventricosus lives in beds of the turtle grass Thalassia testudinum. Especially during daylight hours, it covers its aboral surface with fragments of this plant and other objects. Normally pigmented, wild-type sea urchins covered themselves significantly less with Thalassia when sunlight was experimentally decreased to 66% or 32% ambient intensity. Consistent with this result, naturally occurring sea urchins exhibited significantly less covering at a deep (3.5 m) site than at a shallow (1 m) site, where light intensities at the bottom were 619 and 946 mol s^–1 m^–2, respectively. The graded covering response to light intensity suggests that covering is a defense against damaging solar radiation. Albino sea urchins covered themselves significantly more with Thalassia than wild-type sea urchins in both full and 66% sunlight. In addition, at the shallow site where they accounted for about 4% of the population, they showed significantly greater covering than wild-type urchins. The greater covering response of albino sea urchins suggests a greater susceptibility to solar radiation.Communicated by P. W. Sammarco, Chauvin     

Diet,behaviour and reproduction of the whelk Buccinum undatum in the northern Gulf of St. Lawrence,eastern Canada

A laboratory experiment was used to examine whether a decrease in the width of sutures is the basis for shrinking of the test in echinoids under conditions of low food availability and whether the body condition of sea urchins is likely to be retained when shrinking occurs. This experiment was performed with H. erythrogramma specimens collected in January 1987 from Pt. Lillias in Corio Bay, Australia. Suture widths in the test and gonad volume were significantly less (relative to body volume) in Heliocidaris erythrogramma (Val.) in the low food treatment than the high food treatment after 4 mo. These results imply that sea urchins which shrink may have a poorer body condition and be less able to reproduce than sea urchins that do not shrink. A comparison of the expected to the observed changes in suture width showed that a decrease in suture width is involved in the shrinking of the test in H. erythrogramma and may be of sufficient magnitude to fully explain the observed reduction in test size. This suggests that the amount a sea urchin may shrink under low food conditions is constrained by the degree to which the sutures can be reduced in width.     

Selective accumulation of mycosporine-like amino acids in ovaries of the green sea urchin Strongylocentrotus droebachiensis is not affected by ultraviolet radiation

Field sampling and laboratory experiments examined whether ultraviolet radiation (UVR) affects the reproduction or the accumulation of mycosporine-like amino acids (MAAs) and ascorbic acid in ovaries of the green sea urchin Strongylocentrotus droebachiensis (Müller). Ovaries of sea urchins sampled across a depth gradient (0.5–10 m) in March 1998 did not differ in their gonadal index, or in concentrations of MAAs, or ascorbic acid. Concentrations of MAAs and ascorbic acid in ovaries were higher in sea urchins collected from a kelp bed compared with those collected from a community of crustose coralline algae. The concentrations of MAAs in ovaries varied seasonally, peaking in March, when sea urchins had high gonadal indices just before spawning. Ovaries of sea urchins maintained on controlled diets from October 1997 to April 1998 accumulated significantly higher concentrations of MAAs when fed a diet rich in MAAs than did ovaries of sea urchins fed an alga lacking MAAs, but the gonadal indices did not differ between diets. Sea urchins accumulated principally one MAA, shinorine, but not others that were available in high concentrations in their diet. Neither the gonadal index nor the ovarian concentrations of MAAs were affected by daily exposure of adult urchins to UVR for 6 months. Concentrations of ascorbic acid in ovaries did not differ among diets or UV-treatments. The percentages of nutritive phagocytes and gametic cells were not affected by diet or UVR, and did not co-vary with concentrations of MAAs or ascorbic acid in ovaries. These data support previous demonstrations that female sea urchins accumulate MAAs from their diet of macroalgae, but further show that the accumulation is selective for specific MAAs, particularly shinorine, and that adult S. droebachiensis do not accumulate MAAs in their ovaries or eggs in response to UV-exposure. These are also the first experimental studies to address whether MAAs are affected by or regulate gametogenesis, and indicate that they do not. Received: 5 May 2000 / Accepted: 29 September 2000     

Growth and reproduction of Loxechinus albus (Echinodermata: Echinoidea) at the southerly peripheries of their species range, Falkland Islands (South Atlantic)

Sea urchins Loxechinus albus were collected from an unfished population inhabiting inshore areas of the eastern part of the Falkland Islands (Southwest Atlantic) at bimonthly intervals between January 2005 and March 2006. The gonads of 491 specimens were sampled to ascertain GSI, and a subsample was examined microscopically in order to determine sex and maturity stage. Age was determined by ring counts on genital plates of 349 specimens with the annual periodicity of ring deposition validated by marginal increment analysis. This investigation suggests that the study population spawns at the warmest time of the year thus allowing for greater growth in their pelagic larvae and newly settled juveniles. Size at age data were found to be asymptotic and out of three growth functions tested the von Beralanffy growth model best described the data. The relatively short period of optimal water temperatures around the Falkland Islands does not enable L. albus to grow as fast as in other regions with higher seasonal temperatures (central Chilean coasts) resulting in relatively small adult sizes.     

Differences in somatic and gonadic growth of sea urchins ( Stronglyocentrotus droebachiensis ) fed kelp ( Laminaria longicruris ) or the invasive alga Codium fragile ssp. tomentosoides are related to energy acquisition

The rocky subtidal community off the Atlantic coast of Nova Scotia has historically undergone a cyclical transition between Laminaria-dominated kelp beds and sea urchin-dominated barrens. Since the introduction of the invasive alga Codium fragile ssp. tomentosoides, a third community state has emerged: Codium-dominated algal beds. We conducted a 42-week feeding experiment in the laboratory, which mimicked the quantity and quality of food available to urchins (Strongylocentrotus droebachiensis) in each of these community states. Feeding rate, growth, reproduction, and survival of urchins fed either Laminaria longicruris or C. fragile ad libidum, or L. longicruris 2 days per month, were measured. Although the ad libidum feeding rate on C. fragile was higher than that on kelp, energy intake was lower. Urchins in the ad libidum kelp treatment were larger and had larger gonads than those in the C. fragile treatment. Urchins fed kelp infrequently exhibited little somatic and gonadic growth over the course of the experiment. Regression analysis revealed that urchin performance on these diets was strongly related to energy intake. Diet treatment had no effect on survival or gonad maturation. Although urchins can consume substantial amounts of C. fragile, it appears that they cannot, or do not, feed quickly enough to compensate for its lower nutritional value. Our results suggest that, although urchins feeding on C. fragile are capable of surviving, growing, and reproducing, the replacement of kelp by C. fragile in some areas might negatively affect urchin populations as they continue to repopulate the shallow subtidal zone.     

Diel foraging patterns of the sea urchin Centrostephanus coronatus as a predator avoidance strategy

During the day, the diadematid sea urchin Centrostephanus coronatus occupies holes and crevices in shallow subtidal rocky substrata. Individuals emerge from these after sunset and forage on organisms attached to the surrounding rock surface. Each urchin travels <1 m from its shelter and returns to the same one before sunrise. The sheephead wrasse Pimelometopon pulchrum does not remove urchins from their shelters, but will attack and consume urchins placed in normal feeding locations during the daytime. The active periods of the sheephead and the urchin do not overlap; urchins begin foraging about 20 min after the diurnal sheephead retire in the evening and return to their shelters 1 to 2 h before sheephead resume feeding in the morning. We infer that the urchin's daytime crevice-dwelling and nocturnal foraging habits have evolved as a response to sheephead predation. Moreover, because shelters are limited in supply, shelter fidelity may have evolved to insure refuge from sheephead.     

Plasticity of biometrical and mechanical properties of Echinocardium cordatum spines according to environment

We investigated the plasticity of spines of the burrowing heart urchin Echinocardium cordatum inhabiting sandy beaches. This urchin has very specialized spines which play specific roles in feeding and locomotion. Biometrical and mechanical properties of the spine skeleton of individuals from a wave-exposed intertidal site and a protected subtidal site (Brittany, France) were compared and related to sediment grain size, food supply and urchin small-scale distribution and burrowing depth. The intertidal site was characterized by coarser sand; the urchins were more scattered and more deeply buried than in the subtidal site. Intertidal urchins were bigger than subtidal urchins but showed similar resource allocation. Spines of intertidal urchins were longer than those of subtidal urchins, their architecture was reinforced and they presented a higher fracture force and stiffness. These spine differences would be essentially due to passive plasticity, but could also be adaptative at a certain extent.     

Resource allocation and growth rates in the sea urchin Evechinus chloroticus (Echinoidea: Echinometridae)

The morphometry of the sea urchin Evechinus chloroticus from habitats of contrasting algal abundance but of similar urchin density was examined at two localities in southern New Zealand during 1993. Populations from habitats of high algal abundance (Dusky Sound) had similar relationships of demipyramid (jaws) to test diameter, but individuals had significantly smaller jaws relative to their test diameter than those from a locality where algal abundance was low (Arapawa Island). The body wall mass (in relation to total wet weight) was similar for populations from both localities but, for Dusky Sound populations, individuals from exposed sites had greater relative body mass than those from sheltered sites. The ratios of gonad weight:total weight were similar between localities. However, E. chloroticus from Arapawa Island reached reproductive maturity at a smaller size than those from Dusky Sound. Growth rates of E. chloroticus varied among localities in Dusky Sound. Growth was modelled by the Tanaka function, which allows for rapid early growth until reproductive maturity is reached and declining growth rates thereafter. The results show that sea urchins respond to low resource availability by increasing the size of the food-gathering apparatus, maturing at a smaller size, and growing to a smaller size than individuals from food-rich habitats. Received: 3 December 1996 / Accepted: 29 January 1997     

Morpho-functional defences of Mediterranean sea urchins,<Emphasis Type="Italic"> Paracentrotus lividus</Emphasis> and<Emphasis Type="Italic"> Arbacia lixula</Emphasis>, against fish predators

Morpho-functional features potentially involved in defence mechanisms against fish predators (i.e. attachment tenacity, spine length, and test robustness and thickness) have been assessed in two Mediterranean sea urchins, Paracentrotus lividus and Arbacia lixula. All four morpho-functional features were significantly and positively related to individual size for both species of sea urchins. Test robustness (i.e. static load needed to break sea urchin tests) was significantly greater for A. lixula (from 3,450 to 15,000 g depending on size) than for P. lividus (1,180–11,180 g). Attachment tenacity (i.e. force needed to dislodge sea urchins from the rocky substrate) was greater in A. lixula (280–3,300 g) than in P. lividus (110–1,450 g), and the difference tended to decrease in relation to smaller sea urchin size. Spine length was greater in A. lixula (1.5–2.9 cm) than in P. lividus (0.5–2.3 cm), but the difference decreased for larger sea urchin size. Test thickness was slightly greater (but not significantly) in A. lixula (0.35–1.10 mm) than in P. lividus (0.12–0.90 mm). These results provide evidence that morpho-functional features of sea urchins could be involved in affecting predation rates by fishes upon P. lividus and A. lixula, with potential implications for the population structure and distribution patterns of the two sea urchins in shallow rocky reefs.Communicated by R. Cattaneo-Vietti, Genova     

Changes in sea urchin populations after the destruction of kelp beds

In St. Margaret's Bay, Nova Scotia, Canada, there are large areas in which sea urchins (Strongylocentrotus droebachiensis) have eliminated beds of kelp (Laminaria spp.). Sites were identified where destruction of kelp beds had taken place 1, 2, 3, 3.5 and 4 years ago. With increase of time since kelp disappearance, the sea urchins showed decreased growth rate, reduced gonad size, but an increase in numbers resulting from high recruitment rates in the first two years after kelp bed destruction. These sea urchin populations, by their browsing, effectively prevent the regeneration of kelp. There is, as yet, no evidence of the sea urchin populations being starved out to allow the kelp to return.     

Population dynamics of the sea urchin Strongylocentrotus purpuratus in a Central California kelp forest: recruitment,mortality, growth,and diet

The population dynamics of Strongylocentrotus purpuratus inhabiting dense mats of geniculate coralline algae in a shallow central California Macrocystis pyrifera forest was examined. Sea otters had occupied the area for over two decades. Sea urchin density and size distribution were sampled during 1984–1986 to determine recruitment and mortality patterns. Growth rates were obtained from tetracycline-labeled individuals and changes in sizefrequency modes. Periodic collections were made to examine gut contents and the relationship of diet to food availability. The interaction of recruitment and mortality resulted in a dynamic population structure. Mean densities ranged from 6.5 to 12.7 urchins 0.25 m^-2. The population consisted primarily of urchins up to 40 mm in test diameter in a size distribution which changed from unimodal to bimodal and back over the 2 yr study. Mortality was temporally variable and related to test diameter. Growth rates were somewhat lower than most previous reports for the species and suggested that most of the population was made up of 1 and 2 yr-old individuals. Diet consisted largely of geniculate coralline algae, with fleshy brown algae becoming important when available as drift. This study showed high densities of small urchins can exist in a California kelp forest inhabited by sea otters, but regular recruitment may be necessary to maintain such populations.     

Allocation of45calcium to body components of starved and fed purple sea urchins (Strongylocentrotus purpuratus)

Several lines of evidence in the literature indicate that environmental stress such as starvation may initiate reallocation of sea urchin endoskeletal tissue. For example, Aristotle's lantern enlarges under conditions of starvation, and sea urchins tagged with tetracycline and then fed develop a distinct growth line, while starved individuals develop a diffuse pattern. We designed anin vivo system to examine stress-related changes in calcification in the purple sea urchinStrongylocentrotus purpuratus. SmallS. purpuratus (ca. 2 cm test diam) were collected from the Mission Bay jetty or Imperial Beach (San Diego, California, USA) in 1987.⁴⁵Ca was incorporated from seawater into all body fractions including the organic tissue/coelomic fluid. In an initial experiment, sea urchins were fed or starved for 4 wk and then post-incubated in isotope. Overall, starved individuals deposited new calcite more slowly than did fed individuals; however, allocation was very different and calcification of teeth of starved sea urchins was nearly as great as in fed individuals. In a second experiment,S. purpuratus were first pre-labeled with isotope and then treated by feeding or starving. More of the labeled calcium was mobilized from the soft tissues and coelomic fluid into calcite in fed than in starved individuals. Growth of the teeth in starved sea urchins was significantly greater than in those fed. We conclude that starvation changes the metabolism of calcium in order to preferentially build teeth. However, we also found no evidence that calcium was resorbed from old skeletal calcite in order to build new skeleton.     

Incidence,occurrence and distribution of the nematode Echinomermella matsi in its echinoid host,Strongylocentrotus droebachiensis,in northern Norway

The incidence, occurrence and distribution of the nematode Echinomermella matsi (Jones and Hagen) in its host, the echinoid Strongylocentrotus droebachiensis Müller, were examined in Norwegian waters from Nordmre (63° N) to the Russian border (70° N) in a range of habitats (e.g. kelp cover and community type) from 1982 to 1992. The results are used to examine the likely influence of the parasite on fitness (individual growth and gonad production) and its potential in regulating the population size of its echinoid host. The nematode infections are restricted to areas between Vikna (Vega) and middle Troms, with the highest prevalence (40 to 88% infected) in the Bodø area, the focus of the distribution. The prevalence rates are similar on kelp beds and barren grounds. No difference in growth rates between infected and noninfected sea urchins was found. Nematode-infected sea urchins in kelp bed populations had gonads weighing about one-sixth of those of equivalent uninfected individuals. This indicates that nematodes are really parasites causing reduced reproductive capacity. Areas with high prevalence (>40% infected) of nematodes had low sea urchin densities. High nematode intensities were found in the areas with high prevalence. The mean abundance in high prevalence areas was highest (eight nematodes) in the 4-to 7-yr-old age group and decreased to zero among the oldest age groups. The ratio of variance/mean abundance was also highest among 5-to 8-yr-old sea urchins. At highly and slightly infected locations, the relationships between the log of the variance and the log of the mean abundance of parasites were 1.35 and 1.69, respectively. Measurements of the frequency distribution of nematodes in sea urchins and the corresponding estimates of the negative binomial distribution showed significantly higher counts in estimated than observed subpopulations exceeding 20 nematodes per sea urchin. These results may explain nematode-induced sea urchin mortality. The low density of the host in the Bodø area, which had high prevalence, may be a result of increased host mortality caused by nematodes, by lower recruitment because of reduced gonad production, or by other factors. Low prevalence among older sea urchins may be caused by nematodeinduced host mortality or by cycles in infection. However, studies on the life cycle of the nematode and long term investigations of host density and nematode intensity/prevalence will be needed before any true conclusions can can be drawn.     

Reef-basel herbivores and the distribution of two seagrasses (Syringodium filiforme and Thalassia testudinum) in the San Blas Islands (Western Caribbean)

Two seagrasses, manatee grass (Syringodium filiforme) and turtle grass (Thalassia testudinum), predominated in the areas bordering Ukkup Tupo, San Blas Islands, Western Caribbean. These seagrasses occupied the following three concentric zones extending outward from the reef: a near-reef turtle grass zone, an intermediate manatee grass zone and an off-reef turtle grass zone. Feeding experiments between January and March 1980 indicate that the absence of manatee grass close to the reef resulted from grazing by reef-associated herbivores, mainly day-active fishes and night-active sea urchins (Diadema antillarum). Grazing on manatee grass by fishes was approximately six times greater than grazing by sea urchins; thus, it appears that herbivorous fishes restrict the near-reef distribution of manatee grass at the study area. Where grazing was heaviest, the inner boundary of the manatee grass zone was farthest from the reef. The volume of manatee grass grazed during experiments was five times the volume of turtle grass consumed, strongly suggesting that the former species is a preferred food item. This is the first evidence for selective grazing on seagrasses.     

Fish predators and scavengers of the sea urchin Paracentrotus lividus in protected areas of the north-west Mediterranean Sea

Direct observations of predation on 436 individuals of the sea urchin Paracentrotus lividus (Lamarck) were carried out in infralittoral rocky bottoms (between 5 and 20 m deep) in three Mediterranean marine reserves. The predator guild was composed of six fish species, the sparids Diplodus sargus and D. vulgaris being the main predators, and the labrid Coris julis a major predator of juvenile sea urchins. Four species attempted but failed to open sea urchins. The scavenger guild was most rich in species, with 17 species observed. Predation was size-dependent; the size of predators increased with increasing size of the sea urchins. The presence of two feeding guilds is suggested, one composed of sparids (Diplodus spp.), able to kill juvenile and adult sea urchins, and the other composed of labrids (mainly C. julis), which feed on juvenile sea urchins. To avoid the extension of overgrazed, barren areas created by P. lividus populations, fisheries' regulations should focus on major sea-urchin predators, chiefly D. sargus, D. vulgaris and C. julis. Received: 23 April 1997 / Accepted: 30 May 1997     

Food preferences and related behavior of the browsing sea urchin <Emphasis Type="Italic">Tripneustes gratilla</Emphasis> (Linnaeus) and its potential for use as a biological control agent

The short-spined toxopneustid sea urchin Tripneustes gratilla feeds on a wide variety of algal species and on sea grasses. However, the urchin does show preferences when offered a selection of macroalgal species, which it encounters in nature. Preferences among macroalgae were evident in field-collected urchins exposed to pair-wise tests where the variable was either the consumption rate of the algae or observation of which algal species the urchins chose to touch with their lantern teeth. Exposure of lab-housed urchins to one of five species of macroalgae for 5 months did not seem to alter preferences of urchins in three of the exposure groups, but those exposed to Padina sanctae-crucis seemed to show an enhanced preference for this species when offered a choice of the five species of macroalgae at the end of the exposure period, and those exposed to Gracilaria salicornia seemed to avoid the species when offered the choice of the five species. Perhaps more ecologically important than their preferences were two other observations on these urchins: first, when offered only a single species of algae, the urchins on four of five diets ate the same quantity per day. Second, when simultaneously offered the choice among the five macroalgal species, the urchins consumed more macroalgae per day than when offered only one species. These urchins move about a meter a day. They probably encounter food resources in a relatively coarse-grained fashion and have evolved to eat what is available. Because of their limited movements, their habitat overlap with grazing fishes, their acceptance of a wide variety of macroalgae and their preference for macroalgae, these native urchins are thought to have the potential to serve as biological control agents of alien and invasive macroalgae, which have come to dominate some reef zones normally occupied by corals in Hawaii.     

On the place of origin of deep-sea lsopods

Biogeographic and phylogenetic data on the deep-sea isopod family Ilyarachnidae (Paraselloidea) document its origin and evolutionary radiation in the deep sea. The distribution of eyes among paraselloidean families suggests an in situ evolution for all those families which have primarily deep-sea distributions. Present-day distributions of paraselloidean isopods provide no hints to their ultimate sources in shallow water. These findings contrast to recent suggestions in the literature that the deep-sea isopod fauna has been derived from shallow Antarctic waters.