Does paternity or paternal investment determine the level of paternal care and does female choice explain egg stealing in the fifteen-spined stickleback?

An earlier field study on the fifteen-spined stickleback (Spinachia spinachia) showed that frequent male—male interactionsresult in high frequencies of sneaking and egg stealing. Moreover,sneaking behavior was performed not only by males adoptingalternative mating strategies, but also by males with theirown nests. The advantage of sneaking is easily understood, but it is more difficult to explain the evolutionary benefitof stealing eggs from other males. I investigated whether malessuffering from sneaking adjust their paternal effort in relationto their degree of paternity. I also examined whether femalesprefer males that have more eggs in their nests, as this couldexplain egg stealing. There was no relationship between thedegree of paternity and fanning activity, hatching success,or nest defense. However, the older the eggs become, the morethe males increase their attack rate toward potential egg predators(goldsinny wrasse and shore crabs). Thus, males adjusted theirlevel of defense to the amount of energy and time already investedin the clutch. Females did not prefer males with more eggs intheir nests. On the contrary, females preferred males withreduced clutches over males with enlarged clutches. Therefore,female choice is unlikely to be a driving force behind eggstealing in this species.     

First report on egg deposition and egg morphology of the endangered endemic Romanian perch

The surface of the whitish translucent egg of Romanichthys valsanicola is sculptured in an irregular honeycomb–like pattern. The micropyle consists only of a type I micropylar channel.     

A Novel Rhamnose-binding Lectin Family from Eggs of Steelhead Trout (Oncorhynchus mykiss) with Different Structures and Tissue Distribution

An L-rhamnose-binding isolectin named STL3 (subunit Mr, 21.5 k) was isolated from eggs of the steelhead trout (Oncorhynchus mykiss) in addition to STL1 (subunit Mr, 31.4 k) and STL2 (subunit Mr, 21.3 k) that had been already isolated. STLs were composed of non-covalently linked subunits. The primary structures of STL1 and STL3 were analyzed by the combined use of protein sequencing and cDNA sequencing. A cDNA encoding STL2, of which the protein sequence had been previously studied, was also analyzed. The STL1 subunit (289 amino acid residues) had different structural properties compared to those of the STL2 subunit (195 amino acid residues) and the STL3 subunit (195 amino acid residues); e.g., the number of repeated domain (three for STL1, and two for STL2 and STL3), although all of them were composed of tandemly repeated homologous domains (40 to 53% identities).

The lectin levels in various tissues and during the embryonic development showed that STL1 had different distribution and expression profiles from those of STL2 and STL3. Although STL1 could be detected in several tissues and serum of both male and female steelhead trout, STL2 and STL3 were only abundant in the ovary. STL2 and STL3 levels dramatically decreased just after hatching, however, the STL1 level increased temporarily. These results indicate that the multiple lectins from eggs of the steelhead trout form a novel rhamnose-binding lectin family with different structures and tissue distribution to share distinct functions in eggs.     

The role of oxygen availability in the embryonation of Heterakis gallinarum eggs.

The importance of oxygen availability in the embryonation of the infective egg stages of the gastrointestinal nematode parasite Heterakis gallinarum was studied in the laboratory. Unembryonated H. gallinarum eggs were kept under either aerobic conditions by gassing with oxygen, or anaerobic conditions by gassing with the inert gas nitrogen, under a range of constant temperatures. Oxygenated eggs embryonated at a rate influenced by temperature. Conversely, eggs treated with nitrogen showed no embryonation although when these eggs were transferred from nitrogen to oxygen gas after 60 days of treatment, embryonation occurred. This demonstrated that oxygen is an essential requirement for H. gallinarum egg development, although undeveloped eggs remain viable, even after 60 days in low oxygen conditions. The effects of climate on the biology of free-living stages studied under constant laboratory conditions cannot be applied directly to the field where climatic factors exhibit daily cycles. The effect of fluctuating temperature on development was investigated by including an additional temperature group in which H. gallinarum eggs were kept under daily temperature cycles between 12 and 22°C. Cycles caused eggs to develop significantly earlier than those in the constant mean cycle temperature, 17°C, but significantly slower than those in constant 22°C suggesting that daily temperature cycles had an accelerating effect on H. gallinarum egg embryonation but did not accelerate to the higher temperature. These results suggest that daily fluctuations in temperature influence development of the free-living stages and so development cannot be accurately predicted on the basis of constant temperature culture.     

Estimating cladoceran birth rate: use of the egg age distribution to estimate mortality of ovigerous females and eggs

The birth rate of natural cladoceran populations can change rapidly (during 2–3 days), reflecting rapid changes in their environment. If the egg ratio is calculated on the basis of egg age distribution, the birth rate can be estimated at short sampling intervals (shorter than egg stage duration) by modified Paloheimo's (1974) formula. When female size structure and age of eggs in clutches at the beginning and the end of a sampling interval are known, death rates of ovigerous females and eggs in separate size classes can be determined and incorporated in birth rate estimates. All these methods have been employed using the data on the population of Diaphanosoma brahyurum from the lake Obsterno (North-Western Belarus) in July–August, 1992. The birth rate values computed by the proposed methods and Poloheimo's formula differed significantly in many cases. The accuracy of birth rate estimations from various calculation methods was tested using a computer simulation. The model contains the essential features of cladoceran life history: distinct egg, juvenile and adult stages, development of eggs and reproduction. The population was divided into 25 age classes, each of 1 day duration. Durations of the egg, juvenile and adult stages were set at 3, 6 and 20 days, respectively. The embryogenesis was divided into three egg stages, each of 1 day duration. Survivorship was set from 0.2 up to 1.0 for each age class. The survivorship and brood size were changed through each of five time intervals (days) that allowed to simulate an increase or reduction of population density. Fecundity, survivorship and egg stage duration remained constant during each of 5 days that assumed stability of an environment (this does not occur in nature). Nevertheless, the egg ratio, proportion of juveniles and birth rates were variable even under these circumstances. Computer simulations showed that Poloheimo's formula evaluates birth rate with the relative error of 62% and usually overestimates its values. We propose methods to decrease errors of birth rate estimations by 3.5–5.5 times.