Growth and population studies on Tilapia galilaea in Lake Kinneret

SUMMARY. Between 1967 and 1977, catches of Tilapia galilaea in Lake Kinneret fell from an annual average of about 200 tonnes to a low of 70 tonnes in 1974, and then returned to their former level. Total yearly mortality ( Z ) was estimated at 1.84 between 1970 and 1976. Assuming a natural mortality ( M ) of 0.94, total stock size averaged 300–700 tonnes in that period, while recruitment averaged < 0.7–3 million per year. Three broods hatched in years of relatively high water levels (1970, 1971 and 1972) yielded especially low recruitment.
The Von Bertalanffy growth coefficient ( K ) was estimated at 0.67, and final length (L∞) at 25–36cm total length. First year's growth, 23–152mm, was closely related to final length, which appeared to be affected by genetic variation in the population. Yearly fluctuations in size distribution were attributed to changes in the proportions of fast- and slow-growers, as well as in the abundance of year-classes. Recruitment to the fishery, at 17–20cm, occurred between ages l+and3+.
The highest growth rates for age-1 T, galilaea , 1–2% mean weight per day, occurred in April and May, the Peridinium season. However, only a small proportion of age-1 fish reached marketable size by July, when their food supply began to diminish. During the autumn months, there was hardly any length increment, and all T. galilaea became lean, especially the age-0 group. It is surmised that recruitment of stocked fish could be increased by introduction in December and by use of fingerlings which are potentially able to grow to marketable size in less than two seasons.     

Borings produced by brachiopod pedicles, fossil and Recent

Bromley, R. G. & Surlyk, F.: Borings produced by brachiopod pedicles, fossil and Recent.
Characteristic etching traces are produced in hard calcareous substrates by the pedicles of brachiopods belonging to several groups. It was previously unsuspected that the ability to bore was widespread within the brachiopod phylum. Five species were investigated from the Norwegian Sea: Terebratulina retusa and T. septentrionalis (Terebratulacea), Hemithyris psittacea (Rhynchonellida), and Macandrmia cranium and Dallina septigera (Terebratellacea). Fossil traces with closely similar morphology occur in the Cretaceous and are probably also the work of brachiopods. The most characteristic form is designated Podichnus centrifugalis n. ichnogen., n. ichnosp.     

Some aspects of the biology of the red bass, Lutjanus bohar (Forsskal), from the Tigak Islands, Papua New Guinea

The growth rate, food, reproduction and mortality rates of the red bass, Lutjanus bohar , are described for fish associated with coral reefs in the Tigak Islands of Papua New Guinea. Spawning intensity by month was investigated by examination of gonad maturation stages. The length–at–maturity of female L. bohar was estimated from the relationship between changes in gonad index with increasing size. Female fish matured at about 45–0 cm fork length. The Petersen method was used to obtain age–at–length data from length frequency data of L. bohar captured by hook–and–line fishing. The growth of L. bohar was described by a von Bertalanffy growth curve with the parameters AT=0.27 and L_∞ = 81.7 cm. There was a positive correlation between water depth (D) and the length of L. bohar (L) that was described by L = 318–8+ 3.050 D . The mortality rates ( Z ) of L. bohar from shallow (≤30m) and deep (≤80m) water were estimated from length converted catch curves and were 1–181 and 0–64 respectively. The high Z value for the shallow water population of L. bohar was ascribed to the migration of larger specimens into deeper water. The deep water population of L. bohar remains unfished and the estimate of Z was believed to be equivalent to the natural mortality rate ( M ). An empirical method of calculating M gave an estimate of 0.59. Lutjanus bohar is a carnivorous piscivore that feeds throughout the water column.     

On Argyripnus atlanticus, Maul 1952 (Pisces, Stomiatoidei), with a description of post-larval forms

Twelve specimens standard length 16·8–53·0 mm, including 2 post-larvae (hitherto unknown to the genus), of Argyripnus atlanticus Maul 1952 are reported. The external characteristics of adults are summarized and the internal features of 2 specimens described. A swimbladder is present. The post-larvae are described and their distinction from other maurolicid genera given. Development of the species is considered in terms of morphometric growth changes and increase with age of photophore number. A relatively longer tail and shorter preventral length is characteristic of juveniles and post-larvae, but other body proportions remain approximately constant at all growth stages. A full complement of photophores is attained at approximately 43 mm standard length. Morphological examination of the ovaries of 7 females indicate that first full maturation has not been reached. Development, geographic variation and habits of the species are discussed.     

Magnesium and sulphur in the calcite shells of two brachiopods, Terebratulina retusa and Novocrania anomala

This study determines the distribution of magnesium and sulphur in the shells of two species of brachiopod from the same environment to highlight environmental and biological influences on shell composition. In Terebratulina retusa there are differences in magnesium concentration between the primary layer and the outer and inner regions of the secondary layer. In contrast, Novocrania anomala has a shell composed of high magnesium calcite and there is no significant difference in magnesium concentration between the primary and the secondary shell layers. Sulphur provides an indication of the distribution of sulphated organic matrix within the shells of T. retusa and N. anomala . In T. retusa the distribution of magnesium and sulphur correlates across the shell; however, there is no evidence for a relationship between magnesium and sulphur distribution in N. anomala . The relationship between magnesium and sulphur in T. retusa indicates that a proportion of the magnesium content of the shell is associated with the sulphated fraction of the organic matrix. In these two species of brachiopod, from the same environment, magnesium and organic concentration and distribution are very different, emphasizing the importance of fully understanding the factors that control biomineral composition before the application of these biominerals to environmental studies.     

Morphogenetic regulation in the shells of bivalves and brachiopods: evidence from the geometry of the spiral

Ackerly. S. C. 1992 07 15: Morphogenetic regulation in the shells of bivalves and brachiopods: evidence from the geometry of the spiral.
Analyses of the spiral geometry in shells of the mollusc Pecten maximus and the brachiopod Terebratulina retusa indicate a relative reduction in morphological variability within the population during growth. The spiral, as measured by a model of exponential radial expansion, tends to converge on a particular adult form, irrespective of irregularities during early growth phases. The recurrence of this pattern of variability in populations from two separate phyla (molluscs and brachiopods) suggests a common mechanism controlling shell form. Brachiopoda. Mollusca, coiling, spiral. morphogenetic regulation, growth .     

Hunger, light level and body size affect refuge use by post-settlement lingcod Ophiodon elongatus

Using experimental methods, body size, nutritional state (hunger) and light level were investigated as possible determinants of the extent to which juvenile lingcod Ophiodon elongatus used structural refuges. In the laboratory, older, larger individuals (134–162 mm total length, L _T) exhibited a higher propensity for structure use than did smaller juvenile fish (78–103 mm L _T). In fish of both body sizes, increasing hunger levels caused fish to emerge more readily from refuges than satiated individuals, with this effect most prominent for smaller fish. Diel patterns of ambient illumination were simulated in the laboratory, and refuge use by large individuals decreased significantly in response to lower nocturnal light levels, a pattern that was not observed in the smaller size class. These results indicate an ontogenetic shift in refuge use. During the summer, as post-settlement fish grew larger, they tended to increase affinity for structurally complex habitat, and also showed divergent patterns of behaviour in relation to hunger and light level.     

Disturbance and contrasting patterns of population structure in the brachiopod Terebratulina septentrionalis (Couthouy) from two subtidal habitats

The population structures of Terebratulina septentrionalis (Couthouy) from exposed upper rock surface and semi-cryptic rock wall habitats at 33 m depth in the Gulf of Maine differ. Over a 3-yr period, population densities were consistently higher in rock wall habitats. Although both populations were dominated by juveniles (1–4 mm shell length), size-frequency distributions constructed from upper rock surface and rock wall populations were significantly different, as a result of a greater frequency of large brachiopods (> 20 mm shell length) in rock wall populations. Prominent modes occurred at 14–15 mm shell length in upper surface populations and at 19–20 mm length in rock wall populations. Recruitment was higher in rock wall habitats where ambient light intensities were significantly lower than on upper rock surfaces. Differences in recruitment are either the result of larval selection for shaded rock walls or differential juvenile mortality between habitats. The larvae of Terebratulina settle on a diverse array of substrata. These include bedrock, sandy polychaete tubes and algae in upper surface habitats and bedrock, calcareous polychaete tubes, and ascidians in rock wall habitats. Individuals attached to polychaete tubes and algae in upper surface habitats do not attain large body size (> 13 mm shell length). It is suggested that these differences in population structure reflect the greater intensity of disturbance in upper surface habitats. For example, the cod, Gadus morhua (Linnaeus), ingests brachiopods attached to algae and polychaete tubes in this habitat. Gastropod predation affects brachiopods in upper surface habitats but not in rock wall habitats. Predation by gastropods and asteroids is not size-specific. These results are consistent with the hypothesis that predation contributed to the decline in the abundance and diversity of articulate brachiopods since the Mesozoic, and suggest that the restriction of recent populations to semi-cryptic rock wall and crevice habitats is, in part, controlled by disturbance.     

Optimal resource allocation of the marine bivalve Yoldia notabilis: The effects of size-limited reproductive capacity and size-dependent mortality

The effects of the morphological constraint of maximum reproductive output (reproductive capacity) and the size at which individuals can avoid heavy mortality (refuge size) on the resource allocation pattern between growth and reproduction are investigated using a dynamic modelling approach for a population of Yoldia notabilis (Mollusca: Bivalvia) in Otsuchi Bay, northeastern Japan. A state variable model is developed using field data on shell length, somatic weight, production, survivorship and reproductive capacity of the bivalve. The optimal allocation pattern is characterized by sudden switching from growth to reproduction without the assumption of reproductive capacity, while simultaneous investment in growth and reproduction becomes optimal when maximum reproductive output is limited by reproductive capacity. Size-specific reproductive effort, size at maturity and the growth curve predicted by the latter model fit more closely to the field data, suggesting that size-limited reproductive capacity can play an important role in the evolution of the observed resource allocation pattern. The mortality pattern affects optimal size at maturity, but not size-specific reproductive effort after maturity. When refuge size is fixed, optimal size at maturity increases with survivorship above refuge size. Optimal size at maturity changes in a more complex way with changes in refuge size. Size at maturity remains constant when refuge size is small, increases when it is intermediate, and decreases when it is large. The results suggest that refuge size is an important factor in the evolution of size at maturity, although its contribution varies depending on the values of other factors, such as size-dependent production and survivorship above refuge size. This revised version was published online in July 2006 with corrections to the Cover Date.     

ONTOGENETIC NICHE SHIFT IN THE BRACHIOPOD TEREBRATALIA TRANSVERSA: RELATIONSHIP BETWEEN THE LOSS OF ROTATION ABILITY AND ALLOMETRIC GROWTH

Abstract: Many articulated brachiopods experience marked life habit variations during ontogeny because they experience their fluid environment at successively higher Reynolds numbers, and they can change the configuration of their inhalant and exhalant flows as body size increases. We show that the extant brachiopod Terebratalia transversa undergoes a substantial ontogenetic change in reorientation governed by rotation around the pedicle. T. transversa′s reorientation angle (maximum ability to rotate on the pedicle) decreases during ontogeny, from 180 degrees in juveniles to 10–20 degrees in individuals exceeding 5 mm, to complete cessation of rotation in individuals larger than 10 mm. Rotation ability is substantially reduced after T. transversa achieves the adult lophophore configuration and preferred orientation with respect to ambient water currents at a length of 2.5–5 mm. We hypothesize that the rotation angle of T. transversa is determined mainly by the position of ventral and dorsal points of attachment of dorsal pedicle muscles relative to the pedicle. T. transversa shows a close correlation between the ontogenetic change in reorientation angle and ontogeny of morphological traits that are related to points of attachment of dorsal pedicle muscles, although other morphological features can also limit rotation in the adult stage. The major morphological change in cardinalia shape and the observed reduction of rotation affect individuals 2.5–10 mm in length. The position of ventral insertions of dorsal pedicle muscles remains constant, but contraction of dorsal pedicle muscles is functionally handicapped because dorsal insertions shift away from the valve midline, rise above the dorsal valve floor, and become limited by a wide cardinal process early in ontogeny (<5 mm). The rate of increase of cardinal process width and of distance between dorsal pedicle muscle scars substantially decreases in the subadult stage (5–10 mm), and most of the cardinalia shell traits grow nearly isometrically in the adult stage (>10 mm). T. transversa attains smaller shell length in crevices than on exposed substrates. The proportion of small‐sized individuals and population density is lower on exposed substrates than in crevices, indicating higher juvenile mortality on substrates prone to grazing and physical disturbance. The loss of reorientation ability can be a consequence of morphological changes that strengthen substrate attachment and maximize protection against biotic or physical disturbance (1) by minimizing torques around the pedicle axis and/or (2) by shifting energy investments into attachment strength at the expense of the cost involved in reorientation.     

No evidence of nonlinear effects of predator density,refuge availability,or body size of prey on prey mortality rates

Predator density, refuge availability, and body size of prey can all affect the mortality rate of prey. We assume that more predators will lead to an increase in prey mortality rate, but behavioral interactions between predators and prey, and availability of refuge, may lead to nonlinear effects of increased number of predators on prey mortality rates. We tested for nonlinear effects in prey mortality rates in a mesocosm experiment with different size classes of western mosquitofish (Gambusia affinis) as the prey, different numbers of green sunfish (Lepomis cyanellus) as the predators, and different levels of refuge. Predator number and size class of prey, but not refuge availability, had significant effects on the mortality rate of prey. Change in mortality rate of prey was linear and equal across the range of predator numbers. Each new predator increased the mortality rate by about 10% overall, and mortality rates were higher for smaller size classes. Predator–prey interactions at the individual level may not scale up to create nonlinearity in prey mortality rates with increasing predator density at the population level.     

Use of streambed substrate as refuge by steelhead or rainbow trout Oncorhynchus mykiss during simulated freshets

A flume was used to estimate the carrying capacity of streambed substrates for juvenile steelhead or rainbow trout Oncorhynchus mykiss seeking refuge from simulated freshets. The simulated freshets had mean water column velocities of c. 1·1 m s^?1. The number of O. mykiss finding cover within the interstices of the substrate was documented for different substrate sizes and levels of embeddedness. The availability of suitable refuges determined the carrying capacity of the substrate for O. mykiss. For the size of the O. mykiss tested [mean ± s.d. fork length (L_F) = 122 ± 12·6 mm], the number of interstices with depths ≥200 mm measured with a 14·0 mm diameter flexible plastic tube was the best predictor of the number of O. mykiss able to find cover (r² = 0·75). Oncorhynchus mykiss seeking refuge from freshets may need deeper interstices than those seeking concealment at autumn or winter base flows. The availability of interstices suitable as refuge from high flows may determine autumn and winter carrying capacity.     

Disturbance regime and limits on benefits of refuge use for fishes in a fluctuating hydroscape

Refuge habitats increase survival rate and recovery time of populations experiencing environmental disturbance, but limits on the ability of refuges to buffer communities are poorly understood. We hypothesized that importance of refuges in preventing population declines and alteration in community structure has a non‐linear relationship with severity of disturbance. In the Florida Everglades, alligator ponds are used as refuge habitat by fishes during seasonal drying of marsh habitats. Using an 11‐year record of hydrological conditions and fish abundance in 10 marshes and 34 alligator ponds from two regions of the Everglades, we sought to characterize patterns of refuge use and temporal dynamics of fish abundance and community structure across changing intensity, duration, and frequency of drought disturbance. Abundance in alligator ponds was positively related to refuge size, distance from alternative refugia (e.g. canals), and abundance in surrounding marsh prior to hydrologic disturbance. Variables negatively related to abundance in alligator ponds included water level in surrounding marsh and abundance of disturbance‐tolerant species. Refuge community structure did not differ between regions because the same subset of species in both regions used alligator ponds during droughts. When time between disturbances was short, fish abundance declined in marshes, and in the region with the most spatially extensive pattern of disturbance, community structure was altered in both marshes and alligator ponds because of an increased proportion of species more resistant to disturbance. These changes in community structure were associated with increases in both duration and frequency of hydrologic disturbance. Use of refuge habitat had a modal relationship with severity of disturbance regime. Spatial patterns of response suggest that decline in refuge use was because of decreased effectiveness of refuge habitat in reducing mortality and providing sufficient time for recovery for fish communities experiencing reduced time between disturbance events.     

Growing large in a low grade environment: size dependent foraging gain and niche shifts to cannibalism in Arctic char

Arctic char ( Salvelinus alpinus ) living in allopatry in lakes often show a distinct size dimorphism where the large char prey upon small char. We studied the relationship between size scaling of energy intake, total metabolic costs and levels of storage energy related to the niche shift from invertebrate feeding to cannibalism in an alpine Arctic char population. Gill-net samples consisted of two distinct size modes, small invertebrate feeding char (92–172 mm total length) and large cannibalistic char (265–606 mm total length). Food consumption was estimated for a one year period using a radioactive tracer (¹³⁷Cs). The energy intake followed a hump-shaped relationship with fish size for invertebrate feeding char and increased monotonically with size for cannibalistic char. Total metabolic costs increased exponentially with size for both groups. Char feeding in the invertebrate niche had a maximum net energy gain at 140 mm total length with an upper size limit for positive net energy gain at 180 mm. For cannibals the relationship between size and net energy gain formed a hump shaped function with maximum net energy gain at 400 mm and a lower size limit for positive net energy gain at 230 mm. The size at maturation for both small and large char was close to the size for maximum energy gain in their respective niches. Immature individuals close to the upper size limit for positive net energy gain in the invertebrate niche had low levels of storage lipids but tended to have high mass specific growth rates. This may imply a reallocation from reversible (stored) energy to structural (length) growth as a strategy to transform into the size-range where the cannibalistic niche successfully could be exploited.     

The growth and mortality of larval herring, Clupea harengus L., in the River Blackwater Estuary, 1978–1980

Herring larvae were sampled in the Outer Thames Estuary and the River Blackwater Estuary in the springs of 1978, 1979 and 1980. Data were collected on larval stage, yolk sac and post yolk sac, larval length and total larval numbers. Newly hatched larvae were 6.8±0.5 mm long and the growth rate of yolk sac larvae was estimated at 0.18 mm d⁻¹ ( L = 6.8±0.186 t ). The growth rate of post yolk sac larvae increased to 0.43mm d⁻¹ ( L = 11±48.0±43 t ). Mortality estimates, derived from total numbers in the summed estuary segments, varied between the years and the cohorts within the year. In 1979 the mortality rates were 0.061 d⁻¹ and 0.074 d⁻¹ for the two cohorts. The mean size of the larval population was estimated at 2.48×10⁹ (1.63–3.77 × 10⁹) which agreed well with population size estimates from egg laying and from catch in numbers at age together with estimated fishing mortality rates.     

The growth rates of the estuarine mollusc Musculista arcuatula Yamamoto and Habe (Bivalvia: Mytilidae)

The pattern of growth of the total population of Musculista arcuatula over a period of thirteen months was built up plotting length-percentage frequency histograms each month. From the shifting of the modes it was noticed that the increase in size from November to December was 2 mm, the growth during December to January 3 mm. In February the growth was nil. In March the size increasing by 6 mm and in April by 1 mm, when mortality of the largest size groups started to get completed in May. In June a conspicuous mode appeared at 9 mm, grew 1 mm in July, 2 mm in August and 3 mm in September. Growth remained stationary in October and November. The rate of increase in length was found to follow exponential law. The growth rate of this bivalve goes on increasing at a steady pace, the rate being 1.086 mm per month. The mean size of the females was found to be significantly larger than that of the males. The proportion of the males in the size group 3 mm to 10 mm was found to be significantly larger than in the entire population. But in the larger size groups there was no difference in the number of males and females and the proportion was almost 1:1. Throughout the year only one age class was recognizable in the natural population. There appears to be an excessive post reproductive mortality of adults rendering the population during most of the year of a single age class recruited through the various months of spawning. The maximum longevity was found to be at the most 18 months.     

Changes in population structure and reproduction during a 3-yr population cycle of voles

Cyclic changes in population growth rate are caused by changes in survival and/or reproductive rate. To find out whether cyclic changes in reproduction are an important part of the mechanism causing cyclic fluctuations in small mammal populations, we studied changes in the population structure and reproduction of field voles ( Microtus agrestis ), sibling voles ( M. rossiaemeridionalis ), bank voles ( Clethrionomys glareolus ), and common shrews ( Sorex araneus ) in western Finland during 1984–1992, in an area with 3-yr vole cycles. We also modelled the population growth of voles using parameter values from this study. The animals studied were collected by snap trapping in April, May, June, August, September, and, during 1986–1990, also in October. We found several phase-related differences in the population structure (age structure, sex ratio, proportion of mature individuals) and reproduction (litter size, length of the breeding season) of voles. In non-cyclic common shrews, the only significant phase-related difference was a lower proportion of overwintered individuals in the increase phase. According to the analyses and the vole model, phase-related changes in litter size had only a minor impact on population growth rate. The same was true for winter breeding in the increase phase. The length and intensity of the summer breeding season had an effect on yearly population growth but this impact was relatively weak compared to the effect of cyclic changes in survival. The population increase rates of Microtus were delayed dependent on density (8–12-month time lag). Our results indicate that cyclic changes in reproduction are not an important part of the mechanism driving cyclic fluctuations in vole populations. Low survival of young individuals appeared to play an important role in the shift from the peak to the decline phase in late summer and early autumn.     

The biology of the West African shad Ethmalosa fimbriata (Bowdich) in the Lagos Lagoon, Nigeria

The biology of the population of Ethmalosa fimbriata occurring in the Lagos lagoon was investigated. Three size groups, 35–69 mm (Yoyo), 70–169 mm (Efolo) and 170 mm and above (Agbodo) occur in the lagoon and the spatial distribution of these size groups and the length frequency distribution of the species is given. The relationship between length, weight, age and growth is discussed and the food and feeding intra-relationship of the size groups is shown. Information on the fecundity and possible spawning periods is discussed.     

Mechanical strength of shells of selected extant articulate brachiopods: Implications for paleozoic morphologic trends

Dried shells of Terebratalia transversa, Laqueus californianus, Hemithyris psittacea, and T. unguicula and alcohol‐soaked, tissue‐lined shells of Terebratulina retusa, Dallina septigera, Cryphus vitreus, and Liothyrella uva were crushed in an apparatus that facilitated measurement of the force (newtons) against the valves at the instant of fracture. The results revealed that the costate shells of T. transversa and T. retusa were the strongest. Force is correlated with valve thickness, but not with size (length). When normalized for valve thickness, the force required to fracture shells is correlated with shell biconvexity (height/length) among pooled species of dried specimens. Geniculate specimens of T. retusa were not stronger than the intraspecific variants with a constant radius of curvature to their valves.

The percent‐frequency of plicate, spinose, lamellose and rugate genera increase significantly in the successive stages, Caradocian (Late Ordovician) through Famennian (Late Devonian) at the expense of smooth to costellate genera. The percent‐frequency of rectimarginate (central fold lacking) genera also decreases appreciably in this time frame. These morphologic trends, in combination with the experimental crushing data, support the hypothesis that selection favored species with such anti‐predatory adaptations during a time of escalation of shell‐crushing predators.