Sweet corn (Zea mays L. rugosa 'Seneca Scout’) and soybeans (Glycine max L. Merr. ‘Kanrich’) were grown in nutrient solutions containing alachlor [2-chloro-2′,6-diethyl-N-(methoxymethyl)acetanilide] at 2.36 × 10-5 M, polyethylene glycol MW 6000 (PEG6000) at −2.5 bars osmotic potential, alachlor at 2.36 × 10-5 M plus PEG6000 at −2.5 bars osmotic potential or with no additions. Sweet corn and soybean roots exposed to alachlor plus PEG6000 accumulated significantly more PEG6000 than roots exposed to PEG6000 alone; increased shoot uptake occurred only in soybean. Alachlor was also shown to significantly increase root osmotic potential and decrease root electrolyte leakage.

H+-pyrophosphatases (H+-PPases) are integral membrane proteins that couple pyrophosphate energy to an electrochemical gradient across biological membranes and promote the acidification of cellular compartments. Eukaryotic organisms, essentially plants and protozoan parasites, contain various types of H+-PPases associated with vacuoles, plasma membrane and acidic Ca+2 storage organelles called acidocalcisomes. We used Lysotracker Red DND-99 staining to identify two acidic cellular compartments in trophozoites of the marine scuticociliate parasite Philasterides dicentrarchi: the phagocytic vacuoles and the alveolar sacs. The membranes of these compartments also contain H+-PPase, which may promote acidification of these cell structures. We also demonstrated for the first time that the P. dicentrarchi H+-PPase has two isoforms: H+-PPase 1 and 2. Isoform 2, which is probably generated by splicing, is located in the membranes of the alveolar sacs and has an amino acid motif recognized by the H+-PPase-specific antibody PABHK. The amino acid sequences of different isolates of this ciliate are highly conserved. Gene and protein expression in this isoform are significantly regulated by variations in salinity, indicating a possible physiological role of this enzyme and the alveolar sacs in osmoregulation and salt tolerance in P. dicentrarchi.

Sallow-skin horseshoe crabs (late juvenile Tachypleus tridentatus) from 30‰ salinity seawater were subjected to salinities ranging from 0‰ to 70‰ at 5‰ intervals for 7 days. They were returned to 30‰ salinity for 3 days for recovery. During this period, the survival rate, feeding rate, and body mass of the horseshoe crabs were measured. The sallow-skin horseshoe crabs survived well at 15‰–60‰ salinity, fed well at 30‰–55‰ salinity, gained mass at 0‰–25‰ salinity, lost mass at 45‰–70‰ salinity, and maintained mass at 30‰–40‰ salinity during salinity challenge. During the recovery period, the dehydrated (mass lost) horseshoe crabs rapidly gained mass, whereas the water-retaining (mass gained) horseshoe crabs rapidly lost mass. These results indicate that the sallow-skin T. tridentatus horseshoe crabs are osmoconformers and can tolerate a wide range of salinity changes, adapting gradually from inshore low salinity to offshore high salinity.

The salivary glands are the organs of osmoregulation in ticks and, as such, are critical to the biological success of ticks both during the extended period off the host and also during the feeding period on the host. Absorption of water vapour from unsaturated air into hygroscopic fluid produced by the salivary glands permit the tick to remain hydrated and viable during the many months between blood-meals. When feeding, the tick is able to return about 70% of the fluid and ion content of the blood-meal into the host by salivation into the feeding site. This saliva also contains many bioactive protein and lipid components that aid acquisition of the blood-meal. The salivary glands are the site of pathogen development and the saliva the route of transmission. The importance of the multifunctional salivary glands to tick survival and vector competency makes the glands a potential target for intervention. Here we review the cell biology of tick salivary glands and discuss the application of new approaches such as expressed sequence tag projects and RNA interference to this important area in the field of tick and tick-borne pathogen research.

The effects of nitrite (NO2–) on the Nile tilapia (Oreochromis niloticus) were investigated, due to their relevance to worldwide aquaculture. Hematological parameters – functional haemoglobin (oxy+deoxy-Hb, %), methaemoglobin (MetHb%), and hematocrit (Hct) – and – plasma osmolality, plasma chloride ([Cl−]) and magnesium ([Mg2+]) concentrations – were analysed. Two experiments were conducted, each with its own non-contaminated control, 8 tilapias for each group. In experiment 1 (48 hours), and the first 48 hours of experiment 2, fish were contaminated with 0.4 mM NO2– (added as NaNO2). In experiment 2, ambient NaNO2– was removed for the second 48 hours. NaNO2– exposure increased plasma [NO2–] to 0.4 mM, which increased MetHb from 10.8 ± 2.5% to 46.8 ± 8.0%, and consequently decreased functional Hb from 89.2 ± 2.5% to 53.2 ± 8.0%. NaNO2 removal led to recovery of both parameters. Both Hct and plasma Mg2+ were lowest in fish recovering from nitrite exposure. Thus, these parameters did not show recovery. Plasma osmolality and [Cl−] were not affected by NaNO2–, probably due to the moderate rise in plasma [NO2–]. O. niloticus was thus sensitive to 48 hours of exposure to 0.4 mM NaNO2, and partially recovered from its effects after 48 hours in sodium nitrite-free water. Cultivators of Nile tilapia should thus consider the toxicity of nitrite, especially in aquaculture systems using recirculating water.

The ultrastructural changes taking place in Dunaliella bioculata after chronic exposure to a sodium chloride-induced stress were examined. Hyperosmotic shock was induced by raising the sodium chloride concentration of the culture medium from 0·3 to 1·3 M, which affected a number of cellular organelles during the initial stages of the stress period, i.e. 24, 48 and 72 h. Changes in whole-cell volume were recorded, as well as alterations in the size of the following components: starch grains and sheath, lipid and plastoglobuli, chloroplast, pyrenoid, nucleus, mitochondria, cytoplasm, Golgi apparatus and endoplasmic reticulum. Cells were examined using transmission electron microscopy and changes to their fine structure quantified via image analysis of the electron micrographs. The image analysis program was designed to measure various geometric parameters for all the cell components within individual algal cells. Quantitative image analysis of cells subjected to a chronic salt stress revealed marked increases in the cross-sectional areas of the Golgi apparatus and the endoplasmic reticulum. The enhanced production of the Golgi apparatus within the algal cells was thought to be the direct result of a salt-stress-induced endoplasmic reticulum production within the cells. The increase in the endoplasmic reticulum was manifested as extensive networks of cortical endoplasmic reticulum. It is suggested that the endoplasmic reticulum serves both physiological and structural roles during chronic salt stress by providing the driving force behind increased synthetic/Golgi apparatus activities of the cells, and by providing a type of ‘cellular scaffolding’ to limit the degree of cell contraction in the face of long-term salt stress.

Betaine, a donor of labile methyl groups, can spare choline and methionine but cannot replace these compounds in poultry diets. Betaine is synthesized from choline by choline oxidase and it can donate methyl groups to homocysteine to form methionine. Physiologically, betaine is one of several compounds used by cells to regulate osmotic pressure. Among the potential benefits of its inclusion in poultry feeds are sparing choline, carcass fat reduction and aiding cell osmoregulation. Some feed ingredients are natural sources of betaine per se. This review considers the metabolism, functions and applications of betaine in poultry.

La gestion de la reproduction du saumon atlantique nécessite généralement un transfert des géniteurs en eau douce avant la phase finale de la maturation sexuelle pour obtenir des gamètes de bonne qualité. Afin d'analyser l'impact de l'environnement marin, des géniteurs de saumon atlantique âgés de 2 ans (2+) ont été, soit maintenus en mer en cage (EM) jusqu'à la période de reproduction, soit transférés en eau douce (ED), en juin (EDP) ou en octobre (EDT). Les dates d'entrée en spermiation et d'ovulations ont été notées grâce à des observations hebdomadaires. La qualité des gamètes a été évaluée par le taux d'embryonnement au stade œillé après insémination de lots de 200 œufs par du sperme dilué à 10−3 avec du DIA 532®. Les femelles EDP et EDT ont ovulé entre novembre et décembre alors que les femelles EM présentaient un retard et un étalement des ovulations : 67 % des femelles EM avaient ovulé à la fin de l'expérience en avril. La fécondité relative des femelles EDP était significativement plus basse que celle des femelles maintenues en mer au moins jusqu'à l'automne. En dépit des cinétiques d'ovulation et des osmolantés des liquides coelomiques plus élevées, les œufs de femelles EM présentaient une qualité similaire à ceux des femelles ED lorsqu'ils sont utilisés moins d'une semaine après l'ovulation.

Les mâles ED et EM présentent des courbes similaires d'entrée en spermiation. Les spermes des mâles EM présentaient une qualité hétérogène et en moyenne médiocre. L'osmolarité des plasmas séminaux des mâles EM était significativement plus élevée (347 ± 13 mOsmol/l pour EM contre 265 ± 23 mOsmol/l pour ED). Les spermes EM de mauvaise qualité donnaient des résultats médiocres quelle que soit l'osmolarité des dilueurs d'insémination utilisés et comprises entre 150 et 450 mOsmol/l. De plus, aucune relation n'a été mise en évidence entre l'osmolarité individuelle des plasmas séminaux et la mauvaise qualité des spermes. D'un point de vue appliqué, l'osmolarité du plasma séminal ne peut être retenue comme critère qualitatif et le vieillissement des ovules après ovulation dans la cavité abdominale doit être strictement évité pour les femelles EM.

Osmoregulation and salinity tolerance were studied in zoeae 1 and instar IX juveniles of Chionoecetes opilio. In zoeae 1, the lower and upper lethal salinities for 50% of the animals (LS 50) at 14 °C were about 10 and 42‰ at 24 h, 18 and 41‰ at 48 h, 25 and 38‰ at 96 h. In juveniles, the approximate 48 h LS 50 s at 6 °C were 13.5 and 46‰. Both developmental stages are able to withstand relatively ample but brief variations of salinity. Their short-term euryhalinity is discussed in relation to the salinity of their habitat. Zoeae were hyper-osmoconformers. Juveniles were osmoconformers and isoionic to the external medium except for Mg++ which was hypo-regulated. Isosmotic and isoionic regulation in post-metamorphic stages are presumably an attribute of the family Majidae. The pattern of osmoregulation in zoeae 1 and juveniles relate C. opilio to the first of three groups of species previously characterized by their pattern of ontogeny of osmoregulation.

Tilapia species are generally characterized by a large tolerance to salinity; however, such capacity to adapt to brackish or seawater may be modulated by environmental factors. The major osmoregulatory mechanisms involved in salinity adaptation are presented. Most of the available data concern the role of gills in salt or water exchange. The importance of different factors (environmental or endogenous) in such adaptation is also discussed. The second part presents a survey of the endocrine control of osmoregulation in tilapia. Both fast-acting (e. g. glucagon, urotensins, catecholamines) and long-acting (e.g. prolactin, cortisol) hormones have been studied. In conclusion, several areas of osmoregulatory physiology potentially interesting for aquaculture are discussed.

Examples of the mechanisms involved in body fluid regulation by present-day crustaceans inhabiting variable salinity habitats are described using amphipod gammarids and the isopod Mesidotea (Saduria) entomon as models. Appropriately the species inhabiting the most demanding habitats have the greatest range and most sophisticated regulatory responses. Behaviour, micromorphology and physiology are all involved to a variable degree and, in the examples discussed, responses to salinity change seem finely tuned to countering the problems generated by particular environments. This applies both in the rapid responses to sudden alteration in salinity and to the longer term changes associated with acclimation to a new steady state condition. The isolation of populations and features of derived freshwater races are considered and the implications for the presumed physiological mechanisms of fossil forms discussed.

The modes of life and environments of the extant agnathans (cyclostomes) are discussed in relation to their adaptations to temperature, light, oxygen and salinity. As their antitropical distribution indicates, both hagfishes and lampreys are cold water groups. Since hagfishes live in deeper waters than lampreys, they are not exposed to the marked seasonal changes in temperature and light which influence major events in the lamprey life cycle. Both groups tend to be nocturnally active, either burrowing during daylight as in the case of larval lampreys (ammocoetes) and most hagfishes, or showing cryptic behaviour as in the case of adult lampreys. Olfaction plays a major part in the location of prey, presumably aided in adult lampreys by their eyes and sensitive electrosensory system. Rates of standard oxygen consumption, ventilatory frequency and heart rate of adult lampreys increase at night. Standard oxygen consumption is relatively low in ammocoetes (as it also is in hagfishes) but increases markedly during metamorphosis into the adult lamprey. Ammocoetes and hagfishes, and to a lesser extent adult lampreys, are resistant to reduced environmental oxygen tensions. Differences in the oxygen dissociation curves of ammocoetes, adult lampreys and hagfishes can be related to differences in the characteristics of their monomeric haemoglobins and their environments and modes of life. The extraordinary tolerance of the hagfish heart to hypoxia is a reflection of a robust capacity for glycolysis, an LDH isozyme geared towards anaerobic functioning and a low work output. The hagfishes, which are restricted to marine waters, are osmoconformers. The osmolality of their blood, which is almost wholly attributable to inorganic ions, is virtually identical to that of full strength sea water (c. 1000 mOsmkg−1). By contrast, the osmolality of the blood of larval and adult lampreys when in fresh water is only 205-260 mOsm kg−1, i.e. about one quarter to one fifth of those of hagfish, and these rise only to 240-270 mOsm kg−1 in the adults of anadromous lampreys in sea water. The regulation of ions by adult lampreys is achieved by mechanisms similar to those adopted by teleosts. The implications of the contrasting ionic and osmotic physiology of the two living groups of agnathans are discussed in relation to their possible environmental history and against the background of their Carboniferous fossil representatives.

Although many physiological characteristics are very labile, it is proposed that some are stable enough to provide evidence concerning the routes by which terrestrial animals moved on to land. Osmotic tolerance and osmoregulatory ability are investigated first. Marine littoral invertebrates tolerate wide osmotic changes but osmoregulate little. Freshwater invertebrates osmoregulate well, but over a narrow range. Terrestrial prosobranchs of the family Pomatiasidae, which have wide tolerance, may have originated directly from the sea. The Cyclophoridae, which are intolerant, may have moved to land from fresh water. Isopods and talitrid amphipods may all have had direct marine origins with no freshwater phase. Secondly, terrestrial animals of marine origin may have blood with higher osmotic pressures than those passing through fresh water. In prosobranchs, isopods and amphipods, the evidence agrees with the conclusions suggested from character one. Thirdly, the production of hypo-osmotic urine in terrestrial animals may be evidence of freshwater origin. The evidence again supports the initial suggestions about prosobranchs and amphipods. It is concluded that because there is little selection pressure acting on these characters on land, they can be used as evidence of ancestry. Possible use of further characters is discussed.

Chez deux espèces de crevettes pénéides, Penaeus japonicus et P. chinensis, les conditions de survie en fonction de la température et de la salinité ont été déterminées sur les post-larves P20, P40 et P60. Les SL50, 96 heures moyennes pour les trois stades sont respectivement de 19,3 ‰ à 10 °C, 12,1 ‰ à 14 °C, 6,4 ‰ à 18 °C et 5,4 ‰ à 25 °C pour P. japonicus et de 11,3 ‰ à 14 °C, 7,2 ‰ à 18 °C et 11,1 ‰ à 25 °C pour P. chinensis. L'abaissement de la température de 18-25 °C à 10-14 °C diminue fortement la tolérance des post-larves de P. japonicus aux faibles salinités alors que pour P. chinensis ce phénomène est beaucoup moins marqué. Quelle que soit la température, la mortalité est minimum dans les milieux à peu près isosmotiques à l'hémolymphe. Des essais de survie à long terme (35 jours) ont été effectués sur les post-larves des deux espèces. La régulation osmotique des post-larves et des adultes des deux espèces est hyper-osmotique en milieu dilué et hypo-osmotique en eau de mer et 900 mosm.kg−1. Chez P. japonicus il n'y a pas de différence significative entre les courbes de régulation osmotique des P20, P40 et P60 en milieu dilué. Par contre les capacités osmorégulatrices des adultes sont inférieures à celles des post-larves. Chez P. chinensis l'intensité de la régulation en milieu dilué augmente avec l'âge des post-larves et les adultes présentent une capacité hyper-régulatrice supérieure à celle des P60. L'étude de l'action de la température sur l'osmorégulation des P40 de P. japonicus a montré que l'abaissement de la température de 18 à 10 °C pendant 8 jours modifie fortement la régulation qui devient isosmotique en eau de mer. Les différents résultats obtenus permettent de définir les conditions optimales de température et de salinité pour les élevages de post-larves et les ensemencements en bassins ou lagunes.