Neurons controlling the gill vasculature in five species of teleosts

Summary A plexus of nerve fibers encompassing neuronal perikarya is present within the gill filament; it surrounds the proximal portion of the efferent filament artery and the efferent lamellar arterioles. This innervation resembles the pattern described for the area around the sphincter of the efferent filament artery: acetylcholinesterase-positive neurons and fibers, fast-fading yellow-fluorescent neurons and fibers, long-lasting green-fluorescent fibers. In addition, synaptic contacts between the different components suggest functional interrelationships. Nerves evidently control the efferent limb of the filament circulation including the sphincter of the efferent filament arteries, the proximal portion of the efferent filament arteries proper, and their corresponding efferent lamellar arterioles. However, the distal portion of this system is poorly innervated.     

Simulation of trait- and density-mediated indirect effects induced by piscivorous predators

The study demonstrates how to use a spatially explicit individual-based model (IBM) to tackle the problem of resolving density-mediated (DMII) and trait-mediated indirect interactions (TMII) when manipulative experimentation is difficult on the scale of community-level interactions in the real word. As an example we simulated predator-induced behavioural changes in a roach (Rutilus rutilus (L.)) population before and after stocking a lake with an additional pelagic predator (Sander lucioperca (L.)). By this it was possible to calculate bioenergetic gains and costs of trait changes as well as the relative proportions of DMIIs and TMIIs in roach consumption on littoral and pelagic resources in the lake food web. Despite higher net activity costs of 64%, roach migrating horizontally over the diel cycle had a net benefit (higher energy intake of 75%) compared to roach that were restricted to the littoral as a behavioural response to the new predator. By separating the components of the indirect predator effects, we demonstrate that a predator-induced modification in prey traits (behaviour, feeding activity) could contribute substantially to the net indirect effect of a predator even when there are strong density effects. When considering the predation pressure by roach on pelagic resources, the net TMIIs due to the behavioural adaptation of the consumer in response to the predator were 13–14 times stronger than the DMIIs alone. When comparing the different effects on littoral resources it can be shown that the TMIIs approximately compensate the DMIIs thus resulting in a nearly zero net effect.

Zusammenfassung

In der vorliegenden Arbeit wurde ein räumlich explizites individuenbasiertes Modell (IBM) verwendet, um dichteabhängige (DMII) und eigenschaftsabhängige (TMII) indirekte Interaktionen zu vergleichen. Da sich dies auf der Ebene der Lebensgemeinschaft unter realen experimentellen Bedingungen als besonders schwierig erwiesen hat, wurden räuberinduzierte Verhaltensänderungen einer Plötzenpopulation (Rutilus rutilus (L.)) vor und nach dem Besatz mit einem zusätzlichen pelagischen Räuber, dem Zander (Sander lucioperca (L.)), simuliert. Dadurch war es möglich, sowohl die energetischen Kosten und Nutzen der räuberinduzierten Verhaltensänderung als auch die relativen Anteile von DMIIs and TMIIs an der Plötzenkonsumtion auf litorale und pelagische Ressourcen innerhalb des Nahrungsnetzes zu kalkulieren. Verglichen mit den Plötzen, welche sich aufgrund des neuen Räubers vor allem im Litoral aufhielten, hatten die täglich (horizontal) wandernden Plötzen trotz höherer Nettoaktivitätskosten von 64% eine größere Energieaufnahme von 75%. Durch die Auflösung der verschiedenen indirekten Räubereffekte konnten wir demonstrieren, dass räuberinduzierte Modifikationen von Beuteeigenschaften (Verhalten, Fraßaktivität) erheblich zu den indirekten Nettoeffekten eines Räubers beitragen können, auch wenn starke dichteabhängige Effekte vorhanden sind. Wenn man die Plötzenkonsumtion auf pelagische Ressourcen betrachtet, so ergeben sich 13-14 fach stärkere TMIIs als DMIIs. Wenn man die verschiedenen Effekte auf litorale Ressourcen vergleicht, zeigt es sich, dass TMIIs die DMIIs kompensieren, wodurch der indirekte Nettoeffekt fast null beträgt.     

Condition and size of the non‐native pikeperch Sander lucioperca (Linnaeus, 1758) in Portuguese river basins

We studied life‐history traits focusing on the growth and condition of the pikeperch Sander lucioperca to evaluate its phenotypic plasticity when introduced to new environments. Pikeperch is a non‐native fish introduced to Iberian freshwater fauna in 1998 that quickly spread to other river basins through human‐mediated activities, occupying now a wide variety of habitats along mainland Portugal. Condition (K and SMI), fork length at age, and length–weight relationships were studied for Portuguese populations. Pikeperch fork length for ages 1, 2, 3, and 4 was different between several populations. We applied generalized linear models (GLM) to study the influence of habitat type, latitude, altitude, time after first detection, and fish prey richness on pikeperch populations size at age 4 and condition. We observed higher condition values on populations from lower altitudes at lentic systems more recently introduced. But higher fork length at age 4 was found in populations from higher altitudes, on older populations with higher prey richness. Habitat type, time since first detection, and fish fauna composition are discussed as the main environmental factors explaining the observed phenotypic plasticity with concerns on predatory impact on native fauna.     

Isolation and characterization of nine microsatellite loci from the pike-perch, Sander lucioperca (Linnaeus, 1758)

In order to facilitate studies on the genetic structure of wild populations as well as to monitor genetic changes in cultured stocks, nine polymorphic microsatellite loci were isolated from pike-perch (Sander lucioperca). Single loci allele numbers varied between two (loci MSL-3 and MSL-7) and six (loci MSL-1 and MSL-2), and observed heterozygosities ranged from 0.36 (locus MSL-2) to 1.00 (locus MSL-9) in a test panel of 25 individuals. Only one pair of loci (MSL-5 and MSL-8) displayed significant linkage disequilibrium after sequential Bonferroni corrections. Hardy-Weinberg tests revealed significant excesses of heterozygotes at three loci (MSL-1, MSL-7, and MSL-9).     

Do benthivory and piscivory result in similar growth in walleye?

Growth and condition of piscivorous and non-piscivorous walleye Sander vitreus classified on the basis of their stomach contents were compared to assess the consequences of their trophic flexibility. Piscivorous males showed a significantly higher growth trajectory than non-piscivorous ones, while there was no difference in the growth of females. No differences were found in the condition of piscivorous and non-piscivorous walleye for either sex. Trophic specialization of males, with some individuals foraging mainly on invertebrates and others including forage fishes in their diets, seems to be the most plausible explanation for the observed growth differences. The results also suggest that invertebrates are an important component in walleye diet throughout its ontogeny.     

Stunted growth of pikeperch Sander lucioperca in Lake Sahajärvi, Finland

Growth of pikeperch Sander lucioperca in the eutrophic and clay-turbid Lake Sahajärvi, Southern Finland, was extremely slow in comparison with other lakes at similar latitudes. The most important food item in July was phantom midge larvae Chaoborus flavicans for all sizes of S. lucioperca (239–423 mm total length L _T), while later, in August and September, the diet of S. lucioperca (149–407 mm L _T) consisted of small (30–100 mm L _T) perch Perca fluviatilis , ruffe Gymnocephalus cernuus and roach Rutilus rutilus .     

Pikeperch habitat use within a canal network in spring

Thirteen pikeperch Sander lucioperca were implanted with acoustic transmitters and 10 were successfully tracked twice a week from March to early July in a drainage canal connected to a brackish lagoon located in the Rhône delta. Pikeperch was found in the main canal and in narrow tributaries, but never in the lagoon. Pikeperch avoided shallow parts of the canal and selected areas with high riparian vegetation (mainly trees). No between sexes differences occurred in habitat selection. At the basin scale, while both sexes remained in the upstream part of the canal during the spawning period, after spawning, females migrated downstream and also into the tributaries. This migration may have been induced by the movement of prey while males remained guarding the nests.     

The effects of meal size, body size and temperature on gastric evacuation in pikeperch

Prey size had no effect on the gastric evacuation rate of pikeperch Stizostedion lucioperca. The gastric evacuation was adequately described applying an exponent of 0·5 in the power model. Applying length instead of weight of pikeperch in the gastric evacuation model resulted in a change of estimated parameters, in accordance with the weight–length relationship of pikeperch.     

Stress and survival of small pike-perch Sander lucioperca (L.) after trawling and chilling

The mortality and stress responses (plasma cortisol concentration) of undersized (total length, L _T, <370 mm) pike-perch Sander lucioperca caught as by-catch in a trawl fishery were assessed. The effects of three different holding methods on pike-perch caught by trawl were compared: (1) fish that were transferred to ambient-temperature water (15·0–21·4° C) immediately after capture and not exposed to chilling water, (2) fish held in chilling water for 10 min and (3) fish exposed to chilling water for 2 h. The sample fish were held and monitored in individual plastic restrainers at ambient-water temperature for 48 h after each of the handling procedures. Total mortality was similar for fish held in chilling tanks for 10 min (27·2% total mortality) compared to fish that were only held in ambient-temperature water (28·2% mortality). Total mortality reached 91·3% when fish were held in chilled water for 2 h. Mortality and plasma cortisol concentrations correlated inversely with size (96–368 mm L _T) and directly with lake-water temperature (15·0–21·4° C) after treatment. In addition, the effect of chilling was observed in elevated cortisol concentration and delayed start of recovery. The results show that quickly removing (<10 min) undersized pike-perch from chilled water could markedly improve the survival of released fish. Due to delayed recovery, however, fish should be allowed to recover (30–40 min) in a deck tank before release.     

Physiological effects of saline waters on zander

Rapid transfer of zander Stizostedion lucioperca to hypoosmotic brackish water (mean osmolality 230 mOsmol kg–1 , c. 8 psu) significantly increased plasma chloride concentrations after 24 h compared to those transferred to fresh water, although plasma osmolality was not significantly affected. After 6 days, plasma osmolality was slightly elevated but stable plasma glucose and cortisol concentrations and blood haematocrit and haemoglobin suggest a lack of hormonal stress responses and resultant secondary effects. Rapid transfer of zander to a more saline environment, hyperosmotic to plasma (mean osmolality 462 mOsmol kg^‐1, c. 16 psu) induced a greater increase in plasma osmolality and chloride concentrations within 24 h, with a further rise after 6 days exposure, but all fish maintained a state of hypo‐osmoregulation both 24 h and 6 days after transfer. The initial osmotic disturbance (at 24 h) was accompanied by increased plasma glucose, blood haematocrit and haemoglobin and a decreased mean cell haemoglobin concentration (MCHC), suggesting an adrenergic stress response, but these parameters fully recovered within 6 days of exposure to this hyperosmotic environment with MCHC rising to exceed the level in freshwater fish. Zander did not survive rapid transfer to more hyperosmotic conditions (750 or 1001 mOsmol kg^‐1, 26‐35 psu), but they did survive exposure to simulated‘tidal cycles’ of rising and declining salinity, peaking after 6 h at c. 29 or 33 psu. Although osmotic disturbance was apparent after 6 h exposure and other physiological parameters suggested both adrenergic and corticosteroid components of a stress response, rapid recovery was apparent after return to fresh water. The results indicate that the zander, a non‐indigenous species in the U.K., has a high level of osmotic tolerance and a degree of hypo‐osmoregulation in saline environments not found in most stenohaline freshwater teleosts. This osmoregulatory ability could enable invasion of new U.K. river systems by using inshore marine environments of low salinity as saltwater bridges.