Growth, development and condition of Dendraster excentricus (Eschscholtz) larvae reared on natural and laboratory diets

Feeding invertebrate larvae may be food limited while developingin the ocean. If they are, then their time in the plankton isprolonged, which likely increases mortality. Food limitationcould be due to the quantity and/or quality of the food available.In an effort to answer how food type influences larval nutrition,we compared growth, development and lipid deposition for Dendrasterexcentricus larvae reared in natural seawater from two depths(1 and 20 m) and in filtered seawater on a monoculture laboratorydiet of 6 cells µL^–1 of the green alga Dunaliellatertiolecta (Butcher). Five days post-fertilization, larvaereared on the laboratory diet had developed to the latest stage,were the largest and had lipid deposits. Larvae reared on naturalsurface water were intermediate in size and developmental stage,and larvae reared in the water from 20 m depth were the smallestand developed the slowest. This trend continued at 8 days post-fertilizationwhen surface water diet larvae were similar in size to laboratorydiet larvae, but their juvenile rudiments were significantlysmaller. To assess food availability in each food treatment,we compared the concentration of chlorophyll (Chl) a, b andc in natural seawater from each depth and in D. tertiolectaculture in filtered seawater. Natural seawater collected fromthe surface had the highest concentration of Chl a and c, whereasChl b was not significantly different between treatments. IncreasedChl concentrations in the surface water are likely due to higherconcentrations of diatoms and dinoflagellates, which are typicallynot high-quality food items for echinoid larvae. Our resultssupport a hypothesis that echinoid larvae in the water columnmay be limited by food quality.     

The role of amino acids in the chemosensory swarming and feeding of marine copepods

Behavioural observations were made on two copepods, Eurytemoraherdmani and Acartia hudsonica, presented with 18 dissolvedL-amino acids the concentrations of which ranged from 10^–8M to 10^–2 M. The onset and duration of the swarming behaviourwere determined by the structure and concentration of a restrictednumber of molecules, which differed depending on the copepodspecies. Dicarboxylic amino acids were the most stimulatoryagent for E. herdmani, whereas A. hudsonica responded preferentiallyto aliphatic amino acids. Both the feeding and swarming of A.hudsonica could be induced by the same kind of molecules. Thethreshold sensitivity of the copepods appeared to be compatiblewith the natural concentrations of the dissolved free aminoacids measured at sea. These findings are discussed with referenceto the chemically mediated interactions between phytoplanktonand zooplankton.     

The Development of Fast-Start Performance in Fishes: Escape Kinematics of the Chinook Salmon (Oncorhynchus tshawytscha)

C-starts are high acceleration swimming movements critical forpredator avoidance by fishes. Since larval fishes are particularlyvulnerable to predation, C-start behavior is likely to be especiallyimportant during early life history stages. This paper examinesthe developmental changes in C-start performance with kinematicdata on immature chinook salmon (Oncorhynchus tshawytscha) (eleuthroembryostage, sensu Balon, 1975). The scaling of C-start kinematicsof immature fishes differs from that of adults. Adult C-startdurations increase with increasing body length while C-startdurations of immature fishes decrease (e.g., adult stage 1 duration[sec] = 0.0019.length [L] [cm] $ 0.026 [R² = 0.77] [Webb, 1978];eleuthroembryos stage 1 duration [sec] = –0.026L [cm]$ 0.100 [R² = 0.81]). Distance traveled during stage 2 alsodiffers between adult and immature fishes. Adult distance traveledscales directly with length (distance [cm] = 0.38L^1.01 [cm],R² = 0.96 [Webb, 1978]) while chinook eleuthroembryo distancetraveled is positively allometric with length (distance [cm]=0.37L¹³¹ [cm], R² = 0.83). There are similarities in the developmentof C-starts and burst swimming. For example, mean velocity scalessimilarly between the two locomotor modes (For burst swimming:U_mean [cm/sec] = 8.1 ± 1.1L [cm] $ 4.89 [R² = 0.86] [Webband Corolla, 1981]. For C-start stage 2: U_mean [cm/sec] = 10.96L[cm] - 14.09 [R² = 0.70]). This study demonstrates that C-startescape performance improves during early post-hatching development.Comparisons of immature chinook salmon fast-starts with dataon larval burst swimming and on adult C-starts suggest thatchanges specific to developing fish affect the scaling of kinematicparameters.     

LARVAL GROWTH AND THE INDUCTION OF METAMORPHOSIS OF A TROPICAL SPONGE-EATING NUDIBRANCH

The Hawaiian dorid nudibranch Hypselodoris infucata (Rppell& Leuckart, 1828) was reared to metamorphosis in the laboratory.Egg diameter averaged 88 µm and veligers hatched, afterabout 5 days at 25°C, with a coiled shell averaging 149µm in length. Larvae fed on phytoplankton grew to a maximumshell length of 306 µm in about 15 days. Larval growthwas affected by both quality and quantity of the algal diet.Some larvae were competent to metamorphose 16 days post-hatchingat 26°C, and competence could be retained for at least oneweek. Metamorphosis is complete within 24 hours of exposureto an inducer. At least three species of sponge, Halichondriacoerulea, Sig-modocia sp., and Tedania macrodactyla, in additionto the nudibranch's adult prey species, Dysidea sp., inducedmetamorphosis of competent larvae. Primary films grown on glassslides also induced metamorphosis in some larvae, as did 20µM excess potassium ions in seawater. These data suggestthat nonspecific induction of metamorphosis occurs in this specieseven though the adult nudibranchs are highly prey specific.This implies that in the field, H. infucata find Dysidea sp.after settlement and metamorphosis Present address: Dept of Genetics and Development, College ofPhysicians and Surgeons of Columbia Univeisity, 701 West 168thStreet, NewYork, 10032, USA (Received 22 June 1987; accepted 3 March 1988)     

The Regulation of Proton/Amino Acid Symport in Riccia fluitans L. by Cytosolic pH and Proton Pump Activity

In the aquatic liverwort Riccia fluitans the regulation of theplasma membrane H⁺/amino acid symport has been investigated.Cytosolic pH (pH_c), membrane potential (E_m) and membrane conductancehave been measured and related to transport data, (i) The releaseof [¹⁴C]amino acids is strongly stimulated by cytosolic acidification,induced by the external addition of acetic acid, a decreasein external K⁺, and in the change from light to dark. On average,a decrease in pHc of 0.5 to 0.6 units corresponded with a 4-foldstimulation in amino acid efflux. (ii) External pH changes havefar less effect on substrate transport than the cytosolic pHshifts of the same order. (iii) The inwardly directed positivecurrent, induced by amino acids, is severely inhibited by cytosolicacidification. (iv) Fusicoccin (FC) stimulates amino acid uptakewithout considerable change in proton motive force. (v) Whenthe proton motive force is kept constant, the uptake of aminoacids into Riccia thalli is much lower than when the pump isdeactivated. It is suggested that both the proton pump activityand cytosolic pH are the dominant factors in the regulationof the H⁺/amino acid symport across the plasma membrane of Ricciafluitans, and it is concluded that the proton motive force isnot a reliable quantity to predict and interpret transport kinetics. Key words: Amino acid, cytosolic pH, pH-sensitive electrode, proton motive force, regulation, Riccia fluitans     

Length changes in herring (Clupea harengus) larvae: effects of capture and storage in formaldehyde and alcohol

The effects on standard length of storing laboratory-rearedlarval herring (9–19 mm live length) in 4% buffered formaldehydeor 70% buffered ethanol with and without simulated capture bytowed net were assessed. Lengths during storage were consideredstable after 15 days for larvae placed directly in formaldehyde,and after 30 days for larvae placed directly into alcohol orfor larvae treated by net-capture simulation before storage.The following linear regressions described the relationshipsbetween live length and the stored lengths of larvae after thesetimes: for larvae stored directly in formaldehyde, L = 1.765+ 0.867 x X₁ for larvae stored directly in alcohol, L = 0.564+ 0.971 x X₁; for larvae subjected to net-capture simulationthen stored in formaldehyde, L = 0.984 + 0.993 x X₁; and forlarvae subjected to net-capture simulation then stored in alcohol,L = 0.532 + 0.989 x X₁ where L = live standard length and X₁= standard length after storage. The non-linear regression formulaparameterized by Theilacker (Fish. Bull US, 78,685–692,1980) for northern anchovy larvae provided a good fit to thedata for herring larvae subjected to net-capture simulationand then stored in formaldehyde. However, the model had to bere-parameterized to provide a good fit for larvae stored inalcohol. The precision achieved in length measurements usinga computer-aided measuring system is also discussed.     

Behavioral responses of the brittle star Ophiura ophiura to amino acids, acetylcholine and related low-molecular-weight compounds

Feeding behavior of the brittle star Ophiura ophiura includesorienting posture, orienting movements, arm ‘walking’,changing the direction of ‘walking’ arm coilingand ingestion. All sequential behavior patterns were releasedor enhanced by single low-molecular-weight compounds. Stimuliwhich released ‘walking’ behavior at high concentrations(10^–4 M) in all the test animals are listed in decreasingorder of sensitivity: sarcosine, glycine, urea, L-valine, L-leucine,L-methionine, L-homocysteine, L-norvaline, L-norleucine, L-threonine,L-serine, S-methyl-L-cysteine, L-proline. Threshold values forsingle amino acids were as much as 100 times different in differentindividuals and ranged from 3 x 10^–9 to 3 x 10^–7M for the most effective stimulus, sarcosine, and from 10^–6to 10^–4 M for proline. Above 10^–5 M, only L-prolineregularly released a second behavior pattern, the arm coilingresponse, which temporarily inhibited the ‘walking’behavior. Behavioral thresholds for the ‘walking’behavior for L(+)-lactate and L-alanine were higher than thosefor the orienting movements. Thyoglycolic acid and ß-alaninereleased tube feet walking, which is not part of the feedingbehavior. Structure—activity comparisons were studied at estimated10^–5 M concentrations. Gycline, sarcosine, L-valine, L-norvaline,L-leucine, L-isoleucine, DL-norleucine and DL-homocysteine releasedarm ‘walking’ behavior in more than 75% of all thetests. With the exceptions of S-methyl-and S-ethyl-cysteine,and glycine methylester, derivatives of amino acids were noteffective behavioral stimuli in Ophiura ophiura. L-Isomers ofvaline and leucine regularly stimulated the ‘walking’behavior while their D-isomers were effective in some testsand ineffective in others. Acetylcholine iodide, acetyl-ß-methylcholine chloride and choline phosphate chloride regularly released‘walking’ behavior at concentrations above 10^–5M.     

Grazing of echinoderm larvae (Paracentrotus lividus and Arbacia lixula) on naturally occurring particulate matter

Larvae (72 hr old) of P. lividus and A. lixula grazed on varioussuspensions of natural particulate matter with a size rangeof 2 to 30 microns, and on two species of algae (Phaeodactylumtricor-nutum and Nitzschia sp.) — Larvae graze most in the size range where the particleconcentration is highest. — If larvae deplete certain size categories of particlesthey then graze other size ranges in which the concentrationis still high. — The grazing rate of the two species varied between 988and 91.949 µm³ per pluteus per hour. — For A. lixula larvae the grazing rate increases withincreasing temperature to a maximum at 22°C.     

Cloning and functional characterization of a new subtype of the amino acid transport system N

We have cloned a new subtype of theamino acid transport system N2 (SN2 or second subtype of system N) fromrat brain. Rat SN2 consists of 471 amino acids and belongs to therecently identified glutamine transporter gene family that consists ofsystem N and system A. Rat SN2 exhibits 63% identity with rat SN1. Italso shows considerable sequence identity (50-56%) with themembers of the amino acid transporter A subfamily. In the rat, SN2 mRNA is most abundant in the liver but is detectable in the brain, lung,stomach, kidney, testis, and spleen. When expressed in Xenopus laevis oocytes and in mammalian cells, rat SN2 mediatesNa⁺-dependent transport of several neutral amino acids,including glycine, asparagine, alanine, serine, glutamine, andhistidine. The transport process is electrogenic, Li⁺tolerant, and pH sensitive. The transport mechanism involves the influxof Na⁺ and amino acids coupled to the efflux ofH⁺, resulting in intracellular alkalization. Proline,-(methylamino)isobutyric acid, and anionic and cationic amino acidsare not recognized by rat SN2.

     

The Partitioning of Photosynthetically Assimilated 14C into Amino Acids in Wheat 1. Partitioning During Transport to the Grain

When ¹⁴CO₂ was fed to flag leaf laminae at 20 d post-anthesis,the transport organs between the leaf and the grains containedappreciable ¹⁴C in glutamine, glutamate, serine, alanine, threonineand glycine. Smaller amounts of ¹⁴C were present in gamma-aminobutyricacid (GABA), aspartate and cysteine. Other amino acids whichwere labelled in the source leaf were not labelled in the transportorgans. The export of labelled glutamine, serine, glycine andthreonine from the source leaf was favoured in comparison tothe other amino acids mentioned. Threonine accumulated, andwas subsequently metabolised, in the rachis. [¹⁴C]GABA alsoaccumulated in the rachis. In the grains, the relative amountof soluble [¹⁴C]alanine increased with chase time. This wasprobably due to de novo synthesis and reflected the specialrole of alanine in grain nitrogen metabolism. Wheat, Triticum aestivum, ¹⁴CO₂, amino acids, transport, carbon metabolism     

The influence of individual variation on length-biomass regressions in three crustacean zooplankton species

Length-biomass regressions were established for the cladoceranBosmina longispina maritima and for the copepods Euryremoraaffinis hirundoides and Limnocalanus macrurus, all common inthe Baltic Sea. Biomass was analysed as individual organic carboncontent. For Bosmina, length was a weak estimator of biomass;only 51% of the variation in carbon content was explained bylength. For pre-adult stages of copepods length was a rathergood estimator of biomass. For Euryremora nauplii. the length-carbonrelationship was best described by linear equations (r² wasbetween 0.49 and 0.69), and for copepodite stages (CI-V) byexponential functions (r² = 0.81). The regressions for two differentsampling areas (Baltic proper and Bothnian Bay) did not showstatistically significant differences. Among the copepodites(CI-V) of Limnocalanus there was a linear relationship betweenlength and carbon content (r² = 0.76). In both copepod speciesthere was no or a weak correlation between length and biomassamong adults.     

Some Experimental and Theoretical Observations Concerning Mass Flow in the Vascular Bundles of Heracleum

The theory and practice of applying the thermodynamics of irreversibleprocesses to mass-flow theories is presented. Onsager coefficientswere measured on cut and uncut phloem and cut xylem strandsof Heracleum muntegazzimum. In 0.3 N sucrose + 1 mN KC1 theyare as follows. In phloem, L_EE = 5 ? 10–⁴ mho cm^–1,L_pE = 9 ? 10^–6 cm³ s^–1 cm^–2 volt^–1 cm,and L_PP = 0.16 cm³ s^–1 cm^–2 (J cm^–3)^–1cm. In uncut phloem strands L_EE is about 1 ? 10^–3 mhocm^–1. In xylem in 2 x 10^–3 N KCI, L_pp = 50 to 225,L_PE = 2 ? 10^–4, and L^EE = 4 ? 10^–3. The measurementsare tentative since the blockage of the sieve plates is an interferingfactor, but if they are valid they lead to the conclusion thatneither a pressure-flow nor an electro-kinetic mechanism envisaginga ‘long distance’ current pathway can be the majormotive ‘force’ for transport in mature phloem. Measurementsof biopotentials along conducting but laterally detached phloembundles of Heracleum suggest, nevertheless, that there may bea small electro-osmotic component of at least 0.1 mV cm^–1endogenous in the phloem.     

Effect of Potassium on Sucrose and Amino Acid Release from the Seed Coat of Developing Seeds of Pisum sativum

After removal of the embryo from developing seeds of Pisum sativum,the ‘empty’ ovules (seed coats without enclosedembryo) were filled with a solution (pH 5.5) containing mannitol(usually 400 mM) to which various salts were added. A solutioncontaining two isotopes ((a) [²H]-sucrose/[–¹⁴C]aminoisobutyricacid (AIB) or (b) [³H]valine/[₁₄C]asparagine mixture) was administeredto the plant via the petiole subtending the fruiting node, and[²H]solute and [¹⁴C]solute unloading from the seed coat wasmeasured, in pulse-labelling experiments of about 5 h. The presenceof 25 or 50 mM K⁺ in the ‘empty’ ovule enhancedthe release of sucrose from the seed coat particularly duringthe first hours of the experiment, but the stimulating effectof K⁺ on the release of labelled solutes derived from aminoacids was much smaller. The presence of 25 mM CaCl₂ did notaffect the release of sucrose or amino acids from the seed coat.The effect of K⁺ on sucrose and amino acid release is explainedas an inhibition of sucrose and amino acid resorption from theseed coat apoplast into seed coat cells, after unloading fromthe seed coat unloading sites. It is suggested that amino acidrelease is much less affected by K⁺ than sucrose release, becausefar less resorption of amino acids by seed coat parenchyma cellstakes place during amino acid transport into the seed coat cavity. Pisum sativum, pea, assimilate transport, assimilate unloading, seed-coat exudate, seed development, sucrose resorption, surgical treatment     

Transnodal Transport of 14C in Nitella flexilis: III. FURTHER STUDIES ON DISSOLVED INORGANIC CARBON MOVEMENTS IN TANDEM CELLS

Using NaH ¹⁴CO₃ (0.1 to 3.0 mol m ^–3) fed to 5.0 mm ofan internodal cell of Nitella flexilis in artificial pond waterat pH 6.8 and 19–25 °C, we have found that the carbohydrates(lactose, xylose, mannose, galactoseand sucrose) are formedby photo-assimilation from ¹⁴C-DIC (dissolved organic carbon)in 1 h and are carried in the cytoplasm with amino acids (glutamineand alanine in particular) to the node attached to a tandeminternodal cell. These small sacchandes and some amino acidspassed, apparently unchanged, across the node into the sinkcell. Influx of DIC was highly sensitive to inhibitors of photosystemsI and II (at concentrations around 1.0 mol m^–3) and touncouplers of phosphorylation. Most influx inhibitors, exceptfor NaN₃, also reduced % transnodal transport. NH₄⁺ (1.0 to5.0 mol m^–3) appeared to reduce % transport in light (butnot in dark) with much less effect on influx. Dinitrophenoland Na citrate (at pH 8.2) also strongly reduced apparent %transport without altering cytoplasmic streaming rates. Someof the apparent reduction of transport could be due to an alterationof metabolism or of sequestering in the feed cell, but withNH₄⁺ the latter was not detectable. Our findings support thehypothesis that transnodal transport, including that via theplasmodesmata, is at least partly ‘active’ and requiresmetabolic energy to sustain it. Key words: Inhibitors, influx, plasmodesmata, nodal transport, ¹⁴C, ³⁶Cl     

Structure, function, and genomic organization of human Na(+)-dependent high-affinity dicarboxylate transporter

We have clonedand functionally characterized the human Na⁺-dependenthigh-affinity dicarboxylate transporter (hNaDC3) from placenta. ThehNaDC3 cDNA codes for a protein of 602 amino acids with 12 transmembrane domains. When expressed in mammalian cells, the clonedtransporter mediates the transport of succinate in the presence ofNa⁺ [concentration of substrate necessary for half-maximaltransport (K_t) for succinate = 20 ± 1 µM]. Dimethylsuccinate also interacts with hNaDC3. TheNa⁺-to-succinate stoichiometry is 3:1 and concentration ofNa⁺ necessary for half-maximal transport(K^Na+_0.5) is 49 ± 1 mM as determined by uptake studies withradiolabeled succinate. When expressed in Xenopuslaevis oocytes, hNaDC3 induces Na⁺-dependent inwardcurrents in the presence of succinate and dimethylsuccinate. At amembrane potential of 50 mV,K^Suc_0.5 is 102 ± 20 µM andK^Na+_0.5 is 22 ± 4 mM as determined by the electrophysiological approach. Simultaneous measurements of succinate-evoked charge transfer andradiolabeled succinate uptake in hNaDC3-expressing oocytes indicate acharge-to-succinate ratio of 1:1 for the transport process, suggestinga Na⁺-to-succinate stoichiometry of 3:1. pH titration ofcitrate-induced currents shows that hNaDC3 accepts preferentially thedivalent anionic form of citrate as a substrate. Li⁺inhibits succinate-induced currents in the presence of Na⁺.Functional analysis of rat-human and human-rat NaDC3 chimeric transporters indicates that the catalytic domain of the transporter lies in the carboxy-terminal half of the protein. The humanNaDC3 gene is located on chromosome20q12-13.1, as evidenced by fluorescent in situ hybridization. Thegene is >80 kbp long and consists of 13 exons and 12 introns.

     

Effects of load and tone on the mechanics of isolated human bronchial smooth muscle

Isotonic and isometric properties of nine human bronchial smoothmuscles were studied under various loading and tone conditions. Freshlydissected bronchial strips were electrically stimulated successively atbaseline, after precontraction with10⁷ M methacholine (MCh),and after relaxation with10⁵ M albuterol (Alb).Resting tension, i.e., preload determining optimal initial length(L_o) atbaseline, was held constant. Compared with baseline, MCh decreasedmuscle length to 93 ± 1%L_o(P < 0.001) before any electricalstimulation, whereas Alb increased it to 111 ± 3%L_o(P < 0.01). MCh significantlydecreased maximum unloaded shortening velocity (0.045 ± 0.007 vs.0.059 ± 0.007 L_o/s), maximalextent of muscle shortening (8.4 ± 1.2 vs. 13.9 ± 2.4%L_o), and peakisometric tension (6.1 ± 0.8 vs. 7.2 ± 1.0 mN/mm²). Alb restored all thesecontractile indexes to baseline values. These findings suggest that MChreversibly increased the number of active actomyosin cross bridgesunder resting conditions, limiting further muscle shortening and activetension development. After the electrically induced contraction,muscles showed a transient phase of decrease in tension below preload.This decrease in tension was unaffected by afterload levels but wassignificantly increased by MCh and reduced by Alb. These findingssuggest that the cross bridges activated before, but not during, theelectrically elicited contraction may modulate the phase of decrease intension below preload, reflecting the active part of resting tension.     

Relationship between biomass and enzymatic activity of a bloom-forming dinoflagellate (Dinophyceae) in southern Chile (41{degrees} S): a field approach

In a coastal area of southern Chile (41° S), the major ammoniumassimilating enzyme glutamine synthetase (GS) was detected ina green dinoflagellate bloom during April 2003. High chlorophylla concentrations (1000 µg L^–1) attributable to Gymnodiniumcf. chlorophorum in surface waters were associated with highand very low nitrate reductase activities. Coincident with thebloom, dissolved inorganic nitrogen concentrations were nearthe detection limit (NO₃^– + NH₄⁺ <0.5 µM). SinceGS correlates with the use of ammonium as an external nitrogensource, we suggest that GS activity seems to be a good indicatorof ammonium utilization in a period dominated by a single dinoflagellatespecies.     

Quantitative Analysis of Intercellularly-Transported Photoassimilates in Chara corallina

Using a thin-layer chromatographic technique, we have identifiedthe photoassimilates that are transported intercellularly frombranchlets to internodes in Chara corallina. An internode-branchletcomplex having a primary apex was used in these experiments.After feeding 1 mol m³ NaH¹⁴CO₃ to a branchlet for 10 min, the¹⁴C-labelled photoassimilates (¹⁴C-photoassimilates) found inthe sol endoplasm of the branchlet were composed of sucrose,amino acids, malate, and sugarphosphates. The composition ofthe ¹⁴C-photoassimilates transported from the source branchletto the sink internode in 10 min was the same as that in thesol endoplasm of the source branchlet. From the proportion ofeach ¹⁴C-photoassimilate in both the source branchlet and thesink internode, it was deduced that the main photoassimilatesinvolved in the intercellular transport were sucrose and aminoacids. We found previously that polar transport of photoassimilatesoccurs from a branchlet to an internode with an apex. Determinationof the amount of sucrose, amino acids, glucose-6-phosphate,and malate in both branchlet and internode with or without anapex revealed that there were gradients in the concentrationsof sucrose, serine, and glutamic acid between the sol endoplasmof the two cells. The levels were higher in the branchlet andlower in the internode and the gradients decreased when theapex was detached. Therefore, it is concluded that sucrose andthese amino acids are the compounds involved in the polar intercellulartransport. Key words: Chara corallina, intercellular transport, photoassimilates, ¹⁴C     

ASPECTS OF THE BIOLOGY OF THE GIANT FORM OF STHENOTEUTHIS OUALANIENSIS CEPHALOPODA: OMMASTREPHIDAE) FROM THE ARABIAN SEA

An investigation was carried out on the recently discovered‘giant’ extra large (XL) form of the squid Sthenoteuthisoualaniensis from the Arabian Sea. The sample consisted of 2males, which have not been previously described, and 13 females.Diet composition, parasite loading, sucker ring dentition, biolumi-nescenceand sexual dimorphism were examined and compared to known parametersof the medium (M) form. Reproductive strategy, potential fecundity,egg size distribution in the ovary and oviducts were examinedin mature XL females. Evidence of multiple spawning in the giantform was also investigated. Overall body shape, bioluminescentstructures and coloration of the giant form were similar tothe M form, though the XL form had a smaller fin angle thanthe M form. The mature female XL form has a dorsal mantle lengthabout twice that of a mature female M form. Adult females ofthe XL form have a dorsal mantle length about twice that ofadult males of the same form. Differences between males andfemales were found in arm sucker ring dentition and parasiteload, suggesting a difference in diet. This could be linkedto size differences between the sexes. A strong correlationbetween ovary mass and mantle length was found (r² = 0.64).Poor correlation was found between mantle length and oviductmass (r² = 0.128) and potential fecundity (r² = 0.07). Potentialfecundity ranged between 2–5 million eggs and the holdingcapacity of the oviducts was approximately 300, 000 eggs. Thiscombined with the presence of spermatangia and the presenceof food in the stomach suggest that the XL form is a multiplespawner. S. oualaniensis appears to have a plastic phenotypeand has adapted to the Arabian Sea conditions by evolving thecapacity to grow to a giant size. (Received 6 November 1996; accepted 15 February 1997)     

Effect of concentration on albumin diffusion in lung interstitium

The transport of macromolecules through the lung interstitiumdepends on both bulk transport of fluid and diffusion. In the presentstudy, we studied the diffusion of albumin. Isolated rabbit lungs wereinflated with silicon rubber via airways and blood vessels, and twochambers were bonded to the sides of a 0.5-cm-thick slab that encloseda vessel with an intersititial cuff. One chamber was filled with eitheralbumin solution (2 or 5 g/dl) containing tracer¹²⁵I-albumin or with tracer¹²⁵I-albumin alone; the other wasfilled with Ringer solution. Unbound ¹²⁵I was removed from the tracerby dialysis before use. The chamber with Ringer solution was placed inthe well of a NaI(Tl) scintillation detector. Diffusion oftracer through the interstitium was measured continuously for 60 h.Tracer mass (M) showed a time(t) delay followed by an increase toa steady-state flow(dM/dtconstant). Albumin diffusion coefficient(D) was given byL²/(6T),where T was the time intercept of thesteady-stateM-t line at zero M, andL was interstitial length.Interstitial cuff thickness-to-vessel radius ratio(Th₀/R)was estimated by using Fick's law for steady-state diffusion. BothD andTh₀/Rwere independent of albumin concentration.D averaged 6.6 × 10⁷cm²/s, similar to the freeD for albumin. Values ofTh₀/Raveraged 0.047 ± 0.024 (SD), near the values measuredhistologically. Thus pulmonary interstitial constituents offered norestriction to the diffusion of albumin.