Ontogeny of the gastrointestinal tract and selected digestive enzymes in cobia Rachycentron canadum (L.)

The ontogeny of the digestive system of cobia Rachycentron canadum from hatching to 22 days post-hatch (dph) (20·1 mm standard length) was examined with light microscopy. The activities of selected pancreatic enzymes were also determined during this period in order to optimize current rearing methods for this species. At hatching (3·6 mm), the digestive tract consisted of a relatively undifferentiated, straight tube positioned dorsally to the yolk sac. The major morphological changes in the digestive tract primarily occurred over the first 1–4 dph (3·6–4·4 mm). During this time, larvae began exogenous feeding (3 dph) and the digestive tract differentiated into five histologically distinct regions: buccopharynx, oesophagus, stomach anlage, anterior intestine and posterior intestine. Yolk reserves were exhausted by 5 dph (4·5 mm) and the oil globule began rapidly decreasing in size disappearing entirely by 9–10 dph (6·3–6·8 mm). Gastric glands differentiated at this time, and by 12 dph (8·1 mm) surface mucous cells of the stomach anlage stained positive for neutral mucosubstances. By 16 dph (11·6 mm), the blind sac (fundic region) of the stomach formed as did the pyloric caecae which initially appeared as a single protrusion of the anterior intestine just ventral to the pyloric sphincter. Generally, enzyme activities (U larva⁻¹) for amylase (0·0–1·8), chymotrypsin (0·0–7902·4), trypsin (0·2–16·6) and lipase (9·3–1319·0) were measurable at or soon after hatching and increased steadily from c. 8–22 dph (5·7–20·1 mm). The results of this study are discussed in terms of current and future weaning practices of this species.     

Feeding behaviour of yearling and older hybrid grass carp

Hybrid grass carp resulting from the cross of a female grass carp, Ctenopharyngodon idella (Val.), and a male bighead carp, Hypophthalmichthys ( Aristichthys ) nobilis Rich., 12–18 months old ( c . 300 mm T.L.) were studied in a two-part experiment to determine feeding preference and total daily consumption fish^-1 on selected species of aquatic plants. Fish were maintained in circular pools with 6840·8 1 of water inside a temperature-controlled greenhouse. Preference tests were conducted at three temperature ranges; 25–28° C, 17–20° C and 12–15° C. Based on the time to complete consumption or the relative quantity consumed, the most preferred plant was Lemna gibba when in combination with six other species. Chara sp., Najas guadalupensis and Potamogeton peciinatus were readily consumed and considered to be of about equal preference. Ceratophyllum demersum and Myriophyllum brasiliense were least preferred. Hybrid grass carp generally consumed as much plant material species^-1 and in the same order of preference at the 12–15°C range as they did at 25–28° C. In the second part, mean daily consumption (g) fish^-1 at 25·7–31·0° C for five plant species tested separately was as follows: Chara sp. 369·8; Lemna gibba 178·2; Najas guadalupensis 172·6; Hydrilla verticillata 106·4 and Ceratophyllum demersum 8·8.     

Characteristics of egg and larval production in captive bluespotted gobies

Spawning of the Hawaiian coral-reef goby Asterropteryx semipunctata was diurnal, occurring at various times throughout the day. Mean length of eggs deposited in nests was 0·76 mm (range 0·67–0·84); mean egg width was 0·47 mm (range 0·41–0·52). Clutch size varied from 296 to 1552 eggs (mean=886±309), and was independent of standard length, total body weight, and body condition. Mean relative clutch size was 1·59 eggs mg^-1 total body weight (range 0·84–2·43). Clutches hatched 4–5 nights after being deposited in a nest. Mean notochord length of newly-hatched larvae was 1·88 mm (range 1·60–2·04). The minimum period of time that elapsed between egg deposition and subsequent growth of a new batch of oocytes to spawning size was 5–6 days, providing a reasonable estimate of minimum spawning interval. Compared with other gobiids, tropical species tend to have shorter incubation periods, smaller eggs and smaller larvae at hatching.     

Early life history strategies of notothenioids at South Georgia

Antarctic notothenioid early life history strategies are examined in general and then for common species at South Georgia. Channichthyids, bathydraconids, artedidraconids and some nototheniids have large eggs 3·0–4·9 mm whereas other nototheniids and arpagiferids have smaller eggs 1·6–2·7 mm. At South Georgia the larvae of species with large eggs hatched between August (late winter) and late November (late spring) at 11–16 mm standard length ( L _s). Larvae of species with small eggs hatched mainly during October and December at 4.5–9 mm L _s. Most of the larvae of all species attain urostyle flexion between October and January, and develop to the end of the larval stage between November and May. The duration of the larval stage varies from 2 months in species with smaller larvae to 6 months for some of the species with larger larvae. Two nototheniid species develop to the early juvenile stage before a channichthyid and a bathydraconid that hatch around 2 months earlier. During their first winter, the early-juveniles of most species with large eggs are pelagic, whereas those of species with small eggs may be pelagic or demersal. Four groups of strategies are proposed based on egg size and the winter ecotype of the early-juvenile stage.     

Post mortem shrinkage of four species of temperate and tropical marine fishes, without freezing or preservation

The present study indicated significant post mortem decreases in length for four Australian teleost species from temperate to tropical habitats: black bream Acanthopagrus butcheri , King George whiting Sillaginodes punctata , summer whiting Sillago ciliata and redthroat emperor Lethrinus miniatus . Shrinkage averaged 5·0 mm after 24 h (range 0–10 mm) for A. butcheri , 4 mm (0–8 mm) for S. punctata , 2·2 mm (0·7–3·7 mm) for S. ciliata and 5·4 mm (−2·5–15·0 mm) for L. miniatus . For A. butcheri held under three different post mortem treatments, the mean length of fish in all treatments decreased but there was no significant effect of treatment type on the extent of shrinkage. The rate of shrinkage of S. ciliata varied with treatment, but the ultimate extent did not. For A. butcheri shrinkage was most rapid (2·5 mm h⁻¹) between 1 and 2 h postcapture. The results from these studies confirm that a post mortem decrease in length is a common phenomenon, even in fishes that are not frozen or preserved. Such shrinkage has implications for the enforcement of minimum legal length legislation, and may cause bias in biological investigations, including growth estimates from tag and recapture studies.     

Osteological development of the vertebral column and of the caudal complex in Dentex dentex

Osteological development of the vertebral column and caudal complex in common dentex was described under extensive larval rearing conditions. Generally, the cartilaginous bones developed prior to the membranous bones. The development of the axial skeleton began with the formation of the hypural 1, the neural arches 2 and 3, as well as the haemal arches 1–8 at 4·8, 4·9 and 5·0 mm total length ( L _T, measured in vivo ), respectively. By 7·5 mm L _T, all the cartilaginous elements were formed, except for the ventral ribs, which formed between the range of 8·4–18·0 mm L _T. The caudal lepidotrichia were the first membranous bones to appear (5·3 mm L _T) and attain their full meristic count (7·4 mm L _T), followed by the vertebral centra, which formed between 6·6 and 9·7 mm L _T. By 25·0 mm L _T, all the elements were fully ossified except for the ventral ribs. The developmental direction and order of all the elements were studied with respect to their formation and ossification. The results were discussed in the contexts of ichthyoplankton, ecology and aquaculture. Compared with other Sparidae species, common dentex followed a pattern of relatively rapid rate of osteological development.     

Influence of different rations and water temperatures on the growth rates of shortfinned eels and longfinned eels

Juvenile (12–152 g) shortfinned eels Anguilla australis and longfinned eels A. dieffenbachia caught in New Zealand streams were fed squid mantle Nototodarus spp. 4 days per week in laboratory experiments. A linear multiple regression equation showed the amount of food eaten (0–2·7% w day⁻¹) explained 77·7% of the variation in specific growth rates (–0·60 to +1·07% w day⁻¹) among individual eels, while previous growth rates, water temperature (10·0–20·6°C), and eel weight (12–152 g) explained a further 5·6, 1·4 and 0·8%, respectively. Growth in length ranged from –0·3 to +0·9 mm day⁻¹. Eels which were starved and then given high rations grew substantially faster than expected. Once growth rates were adjusted for differences in ration and other factors, there were no significant differences in growth rates between species or individual fish. Growth of shortfinned eels fed maximum rations of commercial eel food depended on fish size and water temperatures and ceased below 9·0°C. Growth rates in the wild were substantially less than the maximum possible, after seasonal changes in water temperatures were taken into account, indicating that food supplies and not low water temperatures were controlling growth rates in the wild.     

Life history and distribution of the small south-western Atlantic octopus, Octopus tehuelchus

Although this species has been reported from shallow waters down to 90 m depth, knowledge is almost entirely based on intertidal samples. In this study both intertidal and subtidal samples were taken during 1982–1987, in northern San Matias Gulf (41° S, 63° 30' W). This is a large-egged (eggs: 9–12 mm long ×–5 mm wide, stack of 4–6 mm long) and small-sized (up to 150 g) octopus. Egg laying occurs between autumn and winter. Embryonic development takes about four months (water temperature:–19°C). Large hatchlings (DML: 5·64 mm, TL: 14·23 mm, TW: 0·139 g) emerge over spring and early summer, and development is direct. Maximum size is reached after 17–18 months; mating takes place in summer. Females reduce their feeding activity when they reach maturity, and cease eating while brooding. Mean life-span is two years, but some individuals (mostly females) may live up to three years. Females approaching the beginning of the brooding period move to the subtidal zone, where males outnumber females until the end of summer and females (mostly brooders) then outnumber males. In the intertidal zone sex ratio was 1:1 from December to late March, but in April males outnumber females.
These life-history traits are compared with those of other large-egged octopuses and are discussed in relation to environmental conditions prevailing in the San Matias Gulf.     

Growth rates of juvenile smalltooth sawfish Pristis pectinata Latham in the western Atlantic

The growth rates of juvenile smalltooth sawfish Pristis pectinata collected in Florida waters between 1999 and 2006 were investigated using length-frequency and tag-recapture data. Stretched total length ( L _ST) data from 144 smalltooth sawfish (690–4960 mm) and 28 recaptures (775–2150 mm) were used for the analyses. Both methods indicated that growth was rapid during the first 2 years after birth. The L _ST increased by 650–850 mm in the first year, and by 480–680 mm in the second year. Data for animals >2200 mm were limited, so growth beyond 2 years of age was uncertain. The von Bertalanffy growth parameters estimated from L _ST frequency data were L _∞= 6000 mm, K = 0·140 year⁻¹ and t ₀=−0·863 years. Growth rates over the size range for which tag-recapture data were available were similar to that from L _ST frequency data. The growth rates reported are substantially faster than those previously assumed for this species and may have important implications for the recovery of this endangered species. There are conflicting data regarding the growth rates of older P. pectinata which need to be resolved with more data from the wild population before a complete understanding of the conservation implications can be obtained.     

Structure of the gut of the racer goby Neogobius gymnotrachelus (Kessler, 1857)

The morphological and histological features of the gut of juvenile racer goby Neogobius gymnotrachelus [range of body mass 0·2–0·9 g and standard length ( L _S) 20·0–38·8 mm] were examined in fish collected from the Włocławek Reservoir on the Vistula River, Poland. Evidence is provided of the stomachless nature of the gut of the racer goby. The intestine of the juveniles lacks the intestinal bulb. A particular feature of the racer goby gut is the secretory oesogaster (the transitional region where the secretory oesophagus merges into the intestine) with multicellular alveolar glands that secrete via a common duct to the surface between the mucosal folds. The cells in the secretory oesogaster alveolar glands are periodic-acid-Schiff (PAS) positive indicating the presence of neutral mucopolysaccharides. It is hypothesized that the secretory oesogaster is evidence of the loss of the functional stomach in this species. There are two sphincters: the oesogaster–intestinal and the intestinal–rectal in the racer goby gut. It can be concluded that the oesogaster–intestinal sphincter is functionally related to the gastro-intestinal sphincter described in many fish species having a stomach. Enterocytes with a distinct brush border and only a few goblet cells are observed in the epithelium along the whole intestine. The existence of vacuoles in the supranuclear region of the rectal enterocytes is also confirmed.     

The reproductive biology of the crystal goby with a comparison to that of the transparent goby

A histological analysis of the gonad of the pelagic crystal goby Crystallogobius linearis , from the coastal central area of the Adriatic Sea, showed it to be a truly semelparous species; after the first spawning the mature gonads of both males and females appeared to have lost the capability for further spawning. Mature females had very low fecundity (200–700 mature oocytes) and small egg size (0·2–0·55 mm) similarly to other progenetic species. This reproductive strategy is compared with that of Aphia minuta , and a possible cause for the post-reproductive mortality of the two gobies is suggested and discussed.     

A histological study on the development of the digestive system of Pseudosciaena crocea larvae and juveniles

The ontogenetic development of the gut and accessory organs in large yellow croaker Pseudosciaena crocea was investigated using light microscopy from hatching up to the juvenile stage (40 days post hatch, dph). At 3 dph (mean ±  s . d ., 4·1 ± 0·1 mm total length, L _T), coinciding with the buccopharynx opening, larvae started to feed exogenously, and the gut consisted of a well‐developed buccopharynx, a partially‐differentiated oesophagus and an intestine divided in three regions (anterior intestine, intermediate intestine and rectum). Yolk reserves were not completely depleted at the onset of exogenous feeding, and a period of mixed nutrition was observed up to 6 dph (4·3 ± 0·1 mm L _T), when yolk was definitively exhausted. Important morphological changes occurred at the end of the larval period, coinciding with metamorphosis. At 17 dph (6·8 ± 0·6 mm L _T), pyloric caeca differentiated at the junction of the pyloric stomach and the anterior intestine. Gastric glands were first observed at 21 dph (9·2 ± 1·2 mm L _T), coinciding with the morphological development of the stomach in three different regions (cardiac, fundic and pyloric) according to the histological characteristics of their mucosa. At this age, large longitudinal folds appeared in the median and posterior oesophageal mucosa. These morphological and histological features suggested the achievement of a digestive system characteristic of large yellow croaker juveniles and adults.     

Morphological and mitochondrial DNA divergence validates blackmouth, Galeus melastomus, and Atlantic sawtail catsharks, Galeus atlanticus, as separate species

A total of 60 morphometric traits and nucleotide sequences of the entire mtDNA NADH dehydrogenase subunit 2 (ND2) gene [1047 base pair (bp)] in 23 individuals of blackmouth, Galeus melastomus , and 13 individuals of sawtail catsharks, Galeus atlanticus , caught in Southern Portugal, were examined to test the validity of these two taxa. These sharks closely resemble each other, have overlapping geographical ranges and are difficult to identify by morphological characters. Non-metric multidimensional scaling of morphometric variables indicates a clear separation between the two species, with 10 characters each contributing 2·12–2·45% of the total variability between species. Maximum likelihood, parsimony and neighbour-joining trees revealed two major mtDNA haplotype clades, corresponding to the two species, with an average corrected sequence divergence between them of 3·39 ± 0·56%. Within species divergences between haplotypes averaged 0·27 ± 0·18% in G. melastomus and 0·12 ± 0·08% in G. atlanticus . A total of 35 diagnostic nucleotide site differences and four restriction fragment length polymorphism recognition sites in the ND2 gene can be used to distinguish the two species.     

Phenotypic sex differentiation of blue tilapia under constant and fluctuating thermal regimes and its adaptive and evolutionary implications

Oreochromis aureus exposed during the first 28 days of exogenous feeding to constant 35° C, or fluctuating temperatures (day at 35° C, night at 27° C, and vice versa) showed significantly ( P <0·05) faster growth, least size heterogeneity and better survival rates than siblings under constant 27° C. Constant high temperatures had a strong masculinizing effect (M: F sex ratios of 7·33–19·00: 1·00 v . 0·75–0·82: 1·00 in controls reared at 27° C). Fluctuating temperatures had less masculinizing potential but still produced sex ratios significantly skewed to the detriment of females (M: F sex ratios of 2·33–11·50: 1·00). This suggests that ambient temperature may have represented a sufficient environmental pressure for the selection of thermolabile sex-determinism in this species, and presumably in other Oreochromis spp. The evolutionary advantage of thermosensitivity in Oreochromis spp. is discussed, considering a framework where individual advantages oppose, to some degree, to the population or species interest.     

Elevated red myotomal muscle temperatures in the most basal tuna species, Allothunnus fallai

The present study tested the hypothesis that Allothunnus fallai can elevate its slow-oxidative red myotomal muscle (RM) temperature. Measurements on 30 A. fallai (750–850 mm fork length) captured by hook and line off the coast of southern New Zealand revealed that RM temperatures are elevated by mean ± s . d . 8·1 ± 1·3° C (range 6·7–10·0° C) above the mean ± s . d . ambient sea surface temperature 15·3 ± 0·8° C (range 14·3 to 16·4° C). These data provide evidence that the vascular modifications to the central circulation of A. fallai act as a counter-current heat exchanger and that RM heat conservation is a character state present in all extant tuna species.     

Differences in growth rates among cohorts of Encrasicholina punctifer and Engraulis japonicus larvae in the coastal waters off Tanshui River Estuary, Taiwan, as indicated by otolith microstructure analysis

The hatching dates of Encrasicholina punctifer and Engraulis japonicus larvae collected in the coastal waters off Tanshui River Estuary during the fishing seasons of 1992 and 1993 indicated that these two anchovies had protracted spawning seasons, which resulted in multiple recruitment cohorts. Encrasicholina punctifer larvae recruited to the estuary from October to March, while the majority of E. japonicus larvae came in March-May and to a lesser extent in October and November. The E. punctifer larvae on arrival to the estuary were 17·4–35·6 mm in length, 167ndash;89 days old and had growth rates of 0·4–1·0 mm day⁻¹, E. japonicus larvae were 12·1–32·7 mm in length, 19–62 days old and had growth rates of 0·7–0·9 mm day⁻¹. Growth rates were significantly different among cohorts and positively correlated to water temperature.     

Feeding ecology and growth of O-group flatfish (sole, dab and plaice) on a nursery ground (Southern Bight of the North Sea)

The food composition of O-group sole Solea solea , dab Limanda limanda and plaice Pleuronectes platessa on a nursery ground at Gravelines, France, included 17–25 taxa. Sole (new settlers) fed mainly on harpacticoid copepods and when 50 mm in size, on polychaetes (Terebellidae). Dab (<40 mm) consumed mainly polychaetes (Magelonidae and Spionidae), and later amphipods, polychaetes (Spionidae) and Hydrozoa. O-group plaice diet was dominated by polychaetes (Terebellidae), crustaceans and molluscs at all sizes. O-group sole, dab and plaice did not compete for food resources, each species being specialized in different prey items. Growth rates during May-July 1998 varied between 0·5 and 0·67 mm day⁻¹ for sole, 0·12 and 0·24 mm day⁻¹ for dab and 0·55 and 0·81 mm day⁻¹ for plaice. For sole and plaice, these estimates were similar to those recorded in other nurseries and also close to the maximal growth predicted by experimental models. This suggests that their growth was not limited by food during the first summer of life.     

Larval development of five species of blenny (Teleostei: Blenniidae) from the western central North Atlantic, with a synopsis of blennioid family characters

Light trap collections on oil and gas platforms in the northern Gulf of Mexico off Louisiana from 1995 to 1997 contained young of tessellated blenny Hypsoblennius invemar , freckled blenny Hypsoblennius ionthas , featherduster blenny Hypleurochilus multifilis , molly miller Scartella cristata and seaweed blenny Parablennius marmoreus , which are described. Interspecific differences were: number of dorsal, anal, pelvic and caudal fin elements; number of mandibular pores; presence or absence of canine teeth, hypural 5 and pectoral fin pigment; width of gill openings; length of preopercular spines (in larvae). Size at settlement differed among some taxa, but all five species settled within a narrow size window of c . 1·5 mm standard length ( L _S). Hypsoblennius invemar , H. ionthas , H. multifilis and S. cristata settled at mean sizes between 11·3 and 12·1 mm L _S, whereas P. marmoreus settled at a mean size of 19·3 mm L _S. Sexually dimorphic differences were consistently evident by 17–18 mm L _S in all species but P. marmoreus . The two smallest blennies with external characters normally associated with sexual maturity were a 20 mm male and 21 mm female H. multifilis . Primary caudal fin rays began to bifurcate between 17·0 and 18·3 mm L _S in H. invemar , H. ionthas , H. multifilis and S. cristata . Hypleurochilus multifilis displayed the external characteristics of being sexually mature at 20–21 mm L _S. Thus, bifurcation of primary caudal fin rays was an indicator of approaching sexual maturity in H. multifilis and this may also be true in the other species studied.     

Heat resistance of Cronobacter species (Enterobacter sakazakii) in milk and special feeding formula

Aim:  To determine D - and z -values of Cronobacter species ( Enterobacter sakazakii ) in different reconstituted milk and special feeding formula and the effect of reconstitution of powdered milk and special feeding formula with hot water on the survival of the micro-organism.
Methods and Results:  Five Cronobacter species (four C. sakazakii isolates and C. muytjensii ) were heated in reconstituted milk or feeding formula pre-equilibrated at 52–58°C for various times or mixed with powdered milk or feeding formula prior to reconstitution with water at 60–100°C. The D -values of Cronobacter at 52–58°C were significantly higher in whole milk (22·10–0·68 min) than in low fat (15·87–0·62 min) or skim milk (15·30–0·51 min) and significantly higher in lactose-free formula (19·57–0·66 min) than in soy protein formula (17·22–0·63 min). The z -values of Cronobacter in reconstituted milk or feeding formula ranged from 4·01°C to 4·39°C. Water heated to ≥70°C and added to powdered milk and formula resulted in a > 4 log₁₀ reduction of Cronobacter .
Conclusions:  The heat resistance of Cronobacter should not allow the survival of the pathogen during normal pasteurization treatment. The use of hot water (≥70°C) during reconstitution appears to be an effective means to reduce the risk of Cronobacter in these products.
Significance and Impact of the Study:  This study supports existing data available to regulatory agencies and milk producers that recommended heat treatments are sufficient to substantially reduce risk from Cronobacter which may be present in these products.