Effects of social isolation on aggressiveness in fish with special reference to the swordtail (Xiphophorus helleri)

The attack readiness of socially isolated male swordtails ($\text{Xiphophorus helleri}$) was measured in two different aggression tests: (a) In the standard–opponent test the aggressive responses to a small, rather passive opponent swimming in a small adjacent compartment of the test aquarium were counted. (b) In the mirror test the subjects were confronted with their own mirror image. Social isolation for 4 weeks resulted in a decrease of attack readiness in both test situations. It is concluded that -- similar to cichlids -- external stimuli from conspecifics are essential for maintaining the level of aggression readiness characteristic for socially living males. There are good reasons to propose that the effect of external stimuli is mediated by the pituitary-gonadal axis. On the other hand, it is well known from previous studies that, in escalated encounters between freely swimming males, isolated males fight longer and at higher intensities for rank-order position than non-isolated males. The hypothesis is proposed that the high fighting intensity of previously isolated males could be due to an experience levelling effect of social isolation, i.e. the influence of different agonistic experience is reduced by isolation.A critical review of the literature on isolation-induced decremental and incremental effects on aggression in teleosts is presented. Often it is extremely difficult to compare the results of different authors because the methods of behavioural measurement differ to a large extent. However, it is a striking fact that social isolation of immature fish in all known cases has resulted in an increase of aggressiveness. Probably in mature males, depending on species and circumstances, either an incremental or a decremental effect of social isolation may be adaptive. On the one hand, a spontaneous increase of attack readiness may be advantageous for defence of a territory or a position in the social hierarchy and improves the ability of a single individual to join a group of strange conspecifics. On the other hand, it may be economic to lower the level of androgenic hormones to some extent in the absence of conspecifics, and this could lead to a reduction of the aggression level.     

Temporal relationships between shock treatment and intermale fighting behaviour in laboratory mice. Effects of modifying testicular and adrenal functions

The three experiments of this series were conducted to (1) examine subsequent effects of electric shock on intermale fighting in previously isolated mice, and (2) determine to what extent post-shock fighting is affected by manipulations of the pituitary-gonadal and pituitary-adrenocortical axes. In experiment 1 it was found that shock treatment significantly increases fighting $\text{1}\text{2}$ to 1 h later. Experiment 2 showed that castration alone does not affect post-shock fighting, whereas adrenalectomy and castration combined with adrenalectomy both inhibit such fighting. Experiment 3 showed that pretreatment with testosterone increases fighting in intact males, but fails to restore post-shock fighting in adrenalectomized and castrated-adrenalectomized males. These findings suggest that (1) the pituitary-adrenocortical axis plays an important role in controlling post-shock fighting in mice, and (2) the inhibition of post-shock fighting by adrenalectomy and castration combined with adrenalectomy is not a result of the loss of adrenal testosterone which accompanies these operations.     

What do fish make of mirror images?

Fish act aggressively towards their mirror image suggesting that they consider it another individual, whereas in some mammals behavioural response to mirrors may be an evidence of self-recognition. Since fish cannot self-recognize, we asked whether they could distinguish between fighting a mirror image and fighting a real fish. We compared molecular, physiological and behavioural responses in each condition and found large differences in brain gene expression levels. Although neither levels of aggressive behaviour nor circulating androgens differed between these conditions, males fighting a mirror image had higher immediate early gene (IEG) expression in brain areas homologous to the amygdala and hippocampus than controls. Since amygdalar responses are associated with fear and fear conditioning in other species, higher levels of brain activation when fighting a mirror suggest fish experience fear in response to fights with a mirror image. Clearly, the fish recognize something unusual about the mirror image and the differential brain response may reflect a cognitive distinction.     

Agonistic experience and individual recognition in male Quelea quelea

Male $\text{Quelea}$ were moved between groups to assess whether experience of winning or losing in new groups was correlated with their success in competition over food when they were returned to their original groups. No such effect was found. However, differences in time spent feeding after deprivation and in aggressive behaviour were found between groups depending on whether they were made up from high- or low-ranking individuals. In paired encounters there was no evidence that birds threatened unfamiliar individuals more than familiar ones or that they avoided sitting next to them more than familiar birds. This suggests that individual recognition, if it exists at all in these groups, is not important in their agonistic relationships. The rank birds occupied was correlated with beak colour, a probable measure of androgen levels, and with the amount of food consumed after deprivation. The latter result suggests that the same period of deprivation may affect some individuals more than others and this in turn may lead them to compete more for food.     

Eye colour and aggression in juvenile guppies, Poecilia reticulata peters (Pisces: Poeciliidae)

A series of four related experiments on guppy, Poecilia reticulata, juveniles indicates that eye colour is related to motivational state. In juveniles of this species two distinct eye colour states are easily discernible, with a transient intermediate state infrequently seen. These states are dark, light, and intermediate. In aggressive interactions involving both both dark- and light-eyed fish, dark-eyed fish won 98.6% of the encounters (N=222 encounters). Eye colours are significantly correlated with bout lengths of certain behaviours (aggressive encounters, swimming, substrate biting); total time spent in certain behaviours (swimming, aggressive encounters); and type and intensity of aggressive encounters. Eye colour appears to be related to motivational state and may serve a signal function.     

The effects of mate separation on pair re-formation in the Texas cichlid fish (Cichlasoma cyanoguttatum)

This study tested whether mated pairs of Texas cichlid ($\text{Cichlasoma cyanoquttatum}$) would reform and continue rearing their offspring after being separated for either one, four, or ten days. All pairs successfully re-formed after one day, while only 50% re-formed after 4 days. No pair re-formed after 10 days of separation. In successfully re-formed pairs, the female was always more aggressive than her mate, irrespective of whether the female was the resident or the returning individual. Aggressiveness seemed related to the female's attempt to control the male's parental behavior. For pairs which did not re-form, the resident parent, either the male or female, violently and continously attacked the returned mate.     

Winning fights elevates testosterone levels in California mice and enhances future ability to win fights

The 'winner effect' has been studied in a variety of species, but only rarely in mammals. We compared effects of winning three, two, one, or zero resident-intruder encounters on the likelihood of winning a subsequent aggressive encounter in the California mouse (Peromyscus californicus). During the training phase, we ensured that resident males won all encounters by staging contests with mildly sedated, smaller intruders. During the test phase, the resident male encountered an unfamiliar, more evenly matched intruder that had experience winning an encounter and was larger than the resident. Testosterone (T) plasma levels significantly increased after the final test when they had experienced two prior winning encounters, and the probability of winning a future encounter increased significantly after three prior wins independent of intrinsic fighting ability. We hypothesize a 'winner-challenge' effect in which increased T levels serve to reinforce the winner effect in male California mice.     

A teleost (Tilapia mossambica) gonadotropin that resembles luteinizing hormone.

A purified gonadotropin preparation was obtained from pituitaries of a teleost fish ($\text{Tilapia}$$\text{mossambica}$). This gonadotropin was found to resemble LH in that it behaved identically to mammalian and non-mammalian LHs in several chromatographic systems, and stimulated testerone production in isolated rat Leydig cells. In this assay, specific for LH, the $\text{Tilapia}$ gonadotropin was less potent than mammalian LHs but significantly more active than avian, reptilian or amphibian LHs. The $\text{Tilapia}$ gonadotropin was found to be a glycoprotein; preliminary amino acid composition data show resemblances to both mammalian and non-mammalian LHs.     

Distinguishing kinds of prior dominance and subordination experiences in males of green swordtail fish (Xiphophorus helleri)

In experiments, there are usually two general ways of obtaining dominants and subordinates to test for the effect of recent experience upon ulterior behavior and dominance. One is to ‘impose’ such an experience on the contestants by a priori deciding which individual of the pair will become the dominant and which will become the subordinate through the use of rigged contests. The second technique is to let contestants ‘self-select’ the winner and loser by waiting for the spontaneous outcome of dyadic encounters between two usually well matched opponents. These two techniques of obtaining dominants and subordinates probably represent extreme cases on a single continuum of investment made by animals to settle dominance. To test this, we compared dominants and subordinates obtained from these two techniques in Xiphophorus fish males. It was found that pairs obtained through rigged contest (R) were much more aggressive in subsequent encounters than pairs in which the dominant and subordinate could self-select (S). They recuperated more rapidly from handling, initiated contact earlier, took more time to assess each other, and fought for a longer period of time. Prior-winners and prior-losers of the R condition more frequently relied on aggressive behavior during contest than that of the S condition. As a consequence, prior-winners and prior-losers of the R condition won equally the subsequent contest. On the contrary, prior-winners of the S condition defeated their prior-loser opponent in a majority of cases. These results can be tentatively explained by the following principle, winning or losing against a well matched opponent would leave more ‘experience’ than winning over a much weaker opponent, or losing to a much stronger one. This reinforces the hypothesis that prior-experiences are not qualitative states but come in various degrees.     

Inhibition of spider mite ATPases by plictran and three organochlorine acaricides

The ATPase enzyme system from two-spotted spider mites, $\text{Tetranychus}$$\text{urticae}$ (Koch) was sensitive, in vitro, to four acaricides. Tricyclohexylhydroxytin (Plictran^R) was an outstanding inhibitor of oligomycin-sensitive (mitochondrial) Mg²⁺ATPase from fish brain and spider mite homogenates. The I₅₀ values were 6.6×10^?11M and 6.2×10^?10M, respectively. Less effective were chlorbenside, chlorfenethol and ovotran. Plictran at a higher concentration (2×10^?7M) was also more effective on Na⁺-K⁺ATPase both in mites and fish brain homogenates as compared to chlorfenethol, chlorbenside and ovotran. Plictran inhibited oligomycin-insensitive Mg²⁺ATPase at concentrations of 10^?8M but stimulated at high concentrations (5×10^?6M and higher).     

Male Siamese fighting fish use gill flaring as the first display towards territorial intruders

The Siamese fighting fish (Betta splendens) is well known as an aggressive fish with unique spawning and parental care behavior. During reproduction, male fish construct a bubble nest, court females, protect the brood, and defend the territory through aggressive displays. Aggression in male Siamese fighting fish has long been the subject of investigation; however, the kinematics of aggression during contests have been largely overlooked. Here we investigated how nest-holding, male Siamese fighting fish use two different types of displays, gill flaring and fin spreading, towards intruders during various reproductive phases; before (BB) and after bubble nest building, and after spawning (AS), and hatching (AH). Males were more aggressive towards male than female intruders and the level of aggression changed significantly between reproductive phases. Gill flaring, the more energetically costly display, was the dominant initial display towards male and female intruders in BB, AS, AH phases. However, defending males switched to fin spreading after prolonged exposure to intruders. The results suggest that Siamese fighting fish use gill flaring as an acute response in order to defend their territory; this response may be replaced by fin spreading as a chronic response, probably to reduce the energetic costs during the contest.     

Variation in aggressive behaviour in the poeciliid fish Brachyrhaphis episcopi: Population and sex differences

Aggression is often positively correlated with other behavioural traits such as boldness and activity levels. Comparisons across populations can help to determine factors that promote the evolution of such traits. We quantified these behaviours by testing the responses of wild-caught poeciliid fish, Brachyrhaphis episcopi, to mirror image stimuli. This species occurs in populations that experience either high or low levels of predation pressure. Previous studies have shown that B. episcopi from low predation environments are less bold than those that occur with many predators. We therefore predicted that fish from high predation populations would be more aggressive and more active than fish from low predation populations. However, we found the opposite - low predation fish approached a mirror and a novel object more frequently than high predation fish suggesting that ‘boldness’ and aggression were higher in low predation populations, and that population-level boldness measures may vary depending on context. When tested individually, low predation fish inspected their mirror image more frequently. Females, but not males, from low predation sites were also more aggressive towards their mirror image. Variation in female aggression may be driven by a trade-off between food availability and predation risk. This suggests that the relationship between aggression and boldness has been shaped by adaptation to environmental conditions, and not genetic constraints.     

The influence of sex, line, and fight experience on aggressiveness of the Siamese fighting fish in intrasexual competition

We examined the influence of sex, line, i.e., broods from different parents, and previous fight experience on the aggressiveness of the Siamese fighting fish Betta splendens in intrasexual competition. The innate aggressiveness of the fish against their mirror images was measured on the day prior to the direct fight with other individuals, and it was found to be influenced by the line type but not by the sex. In the direct fight with other individuals, the males invested more effort in the fight than the females. In addition, the individuals of a particular line that exhibited a lower innate aggressiveness spent less time in the direct fight and were often losers when compared with those of other lines. After the direct fight with other individuals, the aggressiveness of the fish against their mirror images was remarkably influenced by the outcome of the direct fight, i.e., the winners exhibited more aggressive behavior, whereas the losers exhibited a lesser degree of aggressive behavior. This influence of the previous fight experience on subsequent aggressiveness was the greatest in the individuals of the line that have exhibited the lowest innate aggressiveness. However, the positive effect of the winning experience or the negative effect of the losing experience on subsequent aggressiveness decreased following several days after the previous fight increased.     

Studies on the purification and properties of teleost prolactin

A protein fraction containing prolactin activity from the pituitary tissue of a teleost fish, $\text{Tilapia mossambica}$, has been purified by a combination of ion-exchange and exclusion chromatographic procedures. The purified $\text{Tilapia}$ prolactin was characterized by disc gel electrophoresis, amino-terminal group identification, and amino acid analysis. Its amino acid composition was found to be similar to ovine prolactin. The purified fish prolactin was found to be 40–50 times more potent than ovine prolactin in the $\text{Tilapia}$ sodium-retaining bioassay. However, it was found to be devoid of $\text{Gillichthys}$ yellow pigment-dispersing activity which was previously thought to be a property of teleost prolactin.     

Changes in behaviour associated with pair formation in the polychaete Harmothoë imbricata (L.)

Spacing between individuals in populations of Harmothoë imbricata has been investigated both on the shore and in the laboratory. Males tend to occur closer together than females, and the mean male‐male individual distance measured was less than the mean distance between females; male—female distances for immature worms were intermediate. When worms mature they pair: the male mounts the female and lies across her dorsal surface. There is evidence that after spawning the members of a pair separate. Contact responses between worms have been investigated in the laboratory. Most encounters between immature worms lead to separation, as a result of one or both worms moving rapidly away from the other or fighting; females show more marked avoidance behaviour than males. The majority of male‐male and female‐female encounters between mature worms also lead to separation but in male‐female encounters the male usually mounts the female. A male which has mounted a female becomes highly aggressive and will attack intruding males but not females.     

Repeated Recent Aggressive Encounters Do Not Affect Behavioral Consistency in Male Siamese Fighting Fish

Consistent individual differences in behavior suggest that individuals respond in a predictable and repeatable manner in a specific situation while differing from other individuals. Male Siamese fighting fish exhibit consistent individual differences in decision‐making strategies when they encounter a receptive female and a rival male simultaneously. However, whether these differences are altered by recent experience is unknown. We examined the influence of repeated aggressive encounters on behavioral consistency and decision‐making. Males were presented with paired female–male dummies prior to any aggressive experiences to obtain a baseline measure. Next, males either won or lost three consecutive contests against rivals and then received the paired female–male dummies after each of these encounters. Overall levels of highly aggressive behaviors were affected by contest outcome, while levels of female‐directed were not. Not surprisingly, winning a fight led to an increase in male‐directed bites, an overtly aggressive behavior that only occurs after fights have escalated. Fighting a male before encountering the dummies caused males to perform more tail beats to the dummy male, perhaps as a result of increased motivation. Males exhibited similar levels of repeatability and used the same strategies when faced with conflicting stimuli regardless of fighting experience. Thus, while winning or losing a fight impacts overall aggression, it does not influence behavioral consistency. This study demonstrates that consistent individual differences and decision‐making strategies may be resistant to recent aggressive experiences, even over a period of days.     

Does dehydration contribute to retarded fetal growth in rats exposed to alcohol during gestation?

An earlier study showed that pregnant rats given ethanol in drinking water exhibited a significant degree of dehydration. The objective of the present study was to determine whether dehydration alone contributes to fetal growth retardation in alcohol treated rats. Female Sprague-Dawley rats were divided into 4 dietary groups. Group 1 (alcohol) received 20% ethanol in drinking water for four weeks prior to mating and 30% alcohol in drinking water throughout pregnancy and a stock diet $\text{ad libitum}$. Group 2 (pair-fed) was given an amount of food equal to that consumed by the alcohol group with the alcohol isocalorically substituted by corn starch. Water was available $\text{ad libitum}$. Group 3 (pair-water) was given an amount of food and water equal to that consumed by the alcohol animals. Group 4 ($\text{ad libitum}$) was given food and water $\text{ad libitum}$. On day 21 of gestation body weights of the alcohol exposed fetuses were significantly lower than those of the other three treatment groups. The difference in fetal body weights between the pair-fed and pair-water groups was not significant. Placentas were significantly heavier in the alcohol group than in the pair-fed and pair-water groups. Maternal plasma osmolality was significantly higher in the alcohol treated rats when compared to the pair-fed and $\text{ad libitum}$ controls but not the pair-water group. No significant differences were seen in fetal plasma osmolality among the four treatment groups. It is concluded that dehydration does not contribute significantly to retarded fetal growth in rats given alcohol in drinking water as the sole source of fluid prior to and during gestation.     

Puberty in the male pony: Plasma gonadotropin concentrations and the effects of castration

Ten male ponies were studied from 17 December 1978 through 9 August 1979. Six of the colts were born the previous spring (1978) and four were born during the previous summer. Three of the spring-born colts had been castrated at 4 months of age. Based on the presence of spermatozoa in the epididymis, all spring-born colts ($\text{3}\text{3}$), but only one summer-born colt ($\text{1}\text{4}$) had reached puberty by the end of the project (August). Spermatogenesis was significantly more advanced in the spring-born colts than in the summer-born colts.Concentrations of FSH and LH in the intact males remained constant from December through August, and levels were significantly lower than for the long-term castrated males throughout this period. In the long-term castrates, concentrations of FSH and LH increased from late winter and early spring to the highest levels during late spring and summer.On 9 August, the three spring-born colts (approximately 16 months of age) were castrated. The four summer-born colts (approximately 12–13 months old) were randomly assigned to either castrate (n=2) or hemicastrate (n=2) groups, and surgery was done on all colts on the same day. Both gonadotropins increased following castration in spring-born males. Concentrations of FSH and LH did not change following hemicastration.     

Vocalization during Agonistic Behaviour in Cottus gobio L. (Cottidae): An Acoustic Threat Display

Agonistic behaviour in the river bullhead C. gobio consists of visual (raising gill covers and fins, lowering the head, darkening) and acoustic (single knock sounds and trains of knock sounds) threat displays, rarely followed by attacks and bites. This study investigates the relationship of vocalizations with size, dominance, territory dimensions and sex of the opponents. Four groups, each consisting of a big male, a small male and a female, were each investigated for three different days. The number of won contests of each individual, the numbers of each sound produced during these encounters and the tank part where encounters took place were determined. Subordinate fish emit fewer sounds but relatively far more trains of knock sounds than dominant ones. They produce relatively more sounds under shelters whereas dominants do this on uncovered areas. α-fish produce more calls during agonistic encounters with β-fish than Ω fish. In β-individuals no such difference was noted. Basically no sex related behaviour could be observed. In each area of the tank one individual won most contests (= territory). Dimensions of territories differed significantly between individuals in each tank (α-, β-, Ω-fish). In no case were all three individuals able to maintain territories. Relative sizes of fish correlate significantly with relative numbers of successful encounters and with territory dimensions. Furthermore, both parameters are positively correlated with the numbers of sounds emitted by an individual. Sound production in C. gobio functions as an acoustical threat display. Because of the high energy costs of sound emission underwater it might be a very effective method of assessing the fighting ability of an opponent.     

Anestrus in cycling beef heifers experimentally inoculated with Anaplasmamarginale

Normal estrous cycles were established for twenty beef heifers. Ten heifers were inoculated with blood from a known $\text{Anaplasma}$$\text{marginale}$ carrier. The inoculated heifers experienced anemia, anorexia, and positive $\text{Anaplasma}$$\text{marginale}$ complement-fixing antibody titers, and $\text{A}$. $\text{marginale}$ was observed on the erythrocytes while uninoculated control heifers remained normal. Further observation following inoculation revealed that five of ten inoculated heifers experienced anestrus while controls continued to cycle normally. Anestrus coincided with clinical signs of acute anaplasmosis. Normal estrus patterns returned following treatment and recovery. This study provides evidence that acute anaplasmosis in beef heifers may cause anestrus and therefore lead to reproductive inefficiency.