Genetics and analysis of quantitative traits

Life history biology sits on the interface between genetics and ecology, and both have made important theoretical and empirical contributions to our understanding. However, the connections between the disciplines have not always been as close as they might have been and this book takes some useful steps towards remedying this. It gives an excellent review of life history theory, and integrates this well with results from the empirical literature. After an 11-page introduction, Roff sets out ‘a framework for analysis’ in which he covers the necessary elements of quantitative and population genetics. This includes clear definitions of fitness in a range of circumstances, from density independent populations in constant environments through to the more complex situations of density and frequency dependence and environments that are spatially or temporally stochastic. Trade-offs are then examined, including a valuable analysis of potential pitfalls in studying them and ways that these can be avoided. The author then deals in turn with evolution in constant environments; stochastic environments and ‘predictable environments’. The last of these covers situations where there is environmental variation, but at least some information is available to allow individuals to make an adaptive response. The final chapter identifies 20 topics for future study. Some will find the book too dominated by theory. Others (but probably not readers of Heredity!) will find it contains too much genetics. But Roff does an excellent job of making the theory accessible, covering the essential issues and pointing to original sources for the details. Theory is related to a significant number of empirical studies, although there is room for another book reviewing the empirical literature on life histories in detail, and Roff’s book would provide a robust skeleton on which to hang this. To make my own assessment, I examined in detail Roff’s discussion of the question of fitness measures for density dependent populations in stochastic environments – an area in which I have been involved. I could not fault him – all the key references were there and the issues were made very clear without the more esoteric mathematics. I also examined some areas that I was less familiar with, and again the text was clear and easy to read. My only real criticism of the book would be that its very long chapters (more than 130 pages in one case) makes it difficult to find things. It would have been simple to address this by including the section headings on the contents pages. A minor personal quibble would be that the book usually expresses problems in terms of the intrinsic rate of increase, r, and the characteristic (Lotka) equation. A matrix formulation is often more tractable and is easier to generalise to density dependent populations and stochastic environments, so expanding on the relationship between the two would have been useful. But overall this is an excellent book. It brings together the key theory in a single place. It gives an invaluable route into the literature, with a bibliography of 1600 or so items. These features, and its identification of topics that need further study should make an important contribution to moving the field forward.

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Life History Evolution

Egg and sperm quality in fish

The measurement of sperm motility and factors affecting sperm quality in cultured fish

Endocrine manipulations of spawning in cultured fish: from hormones to genes

Since the first work of Blaxter in 1953, fish sperm cryopreservation has been attempted on about 30 marine species. The present paper reviews the techniques used and the results published in these species. Particular attention is paid to the handling procedure of sperm before freezing, the problems of semen ageing and semen contamination with urine. The quality of frozen-thawed semen was evaluated using previously standardized biotests, such as a two-step motility activation technique adapted for the different species and fertilization assays using a discriminating insemination technique. Most extenders used in marine fish are saline or sugar solutions. From the investigated cryoprotectants, dimethyl sulphoxide (DMSO) generally leads to the best results. Cooling rates range from 8 °C to 99 °C min-1; the thawing rate is generally high. Compared with freshwater species, a high percentage of spermatozoa survives cryopreservation. Therefore, and because of the simplicity of the techniques, the cryopreservation of marine fish sperm is suited for application in aquaculture.

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Cryopreservation of sperm in marine fish

Summary

This contribution reviews existing literature and some new own findings on teleost sperm motility and factors controlling it, emphasizing selected marine species. In marine teleosts with external fertilization (halibut, turbot, sea bass, hake, cod and tuna serving as examples), mainly the osmolality controls sperm motility: movement is activated by transfer from the seminal fluid into sea water, representing a large upward step in osmolality. The exception are flatfishes (such as halibut or turbot) where CO2 is responsible for flagellar immotility in seminal fluid. In all cases, the duration of motility is short and limited to minutes ranges due to partial exhaustion of the ATP energy and to increase of internal ionic concentration as suggested by studies with de-membranated/ATP reactivated flagellae. In this overview, we compare motility characteristics (percentage of active spermatozoa, velocity, linearity), flagellar waves parameters (wave length and amplitude, number of waves) and energy content (respiration and ATP concentration) within species where these data have been established. All parameters show a rapid decrease after activation; therefore progressive forward movement needed by the sperm to effectively reach the egg surface, is limited to a short initial period following activation. In two species (turbot and sea bass) the rapid decrease of sperm motility is reflected by a corresponding decrease of the fertilizing ability. Exposure to external environments (sea water) at activation also leads to local defects of the sperm flagella posing additional limitations on motility duration. However, minor flagellar damages as well as energetic exhaustion are reversible: after a resting period in a non-swimming solution at the end of the motility period, spermatozoa can be re-activated for a second motility period. From these results and from additional data obtained from de-membranated/ATP re-activated spermatozoa, a paradigm has been developed which establishes a link between external osmolality (sea water), internal ionic concentration and control of axonemal activity.

Studying sperm motility in marine fish: an overview on the state of the art

The development of cheaper technical tools and the availability of well established assay kits provide today the spermatologists with several devices for objective and quantifying assessment of sperm quality. The present paper reviews modern methods on sperm concentration assessment, morphometry, motility processes through flagellum studies, motility objective assessment by computer assisted sperm analysis (CASA), sperm integrity and energetic state measurements.

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Evaluation of fish sperm quality

After a long period of spermatogenesis (several weeks to months), marine fish spermatozoa are delivered at male spawning in seawater (SW) at the same time as ova. In some fish species, as the ova micropyle closes quickly after release, these minute unicells, the spermatozoa, have to accomplish their task of reaching the micropyle within a very brief period (several seconds to minutes), for delivery of the haploid male genetic information to the ova. To achieve this goal, their high-performance motile equipment, the flagellum, must fully activate immediately on contact with the SW and then propel the sperm cell at an unusually high initial velocity. The cost of such ‘hyperactivity’ is a very rapid consumption of intracellular ATP that outstrips the supply. The spermatozoa become rapidly exhausted because mitochondria cannot compensate for this very fast flagellar energy consumption. Therefore, any spermatozoon ends up with two possibilities: either becoming exhausted and immotile or reaching the egg micropyle within its very short period of forward motility (in the range of tens of seconds) before micropyle closure in relation to both contact of SW and cortical reaction. The aim of the present review is to present step by step the successive events occurring in marine fish spermatozoa from activation until their full arrest of motility. The present knowledge of activation mechanisms is summarized, as well as a description of the motility parameters characterizing the motility period. As a complement, in vitro results on axonemal motility obtained after demembranation of flagella bring further understanding. The description of the sperm energetic content (ATP and other high energy compounds) and its evolution during the swimming period is also discussed. A general model aiming to explain all the successive cellular events occurring immediately after the activation is presented. This model is proposed as a guideline for understanding the events governing the sperm lifespan in the marine fish species that reproduce through external fertilization.

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Christian Fauvel

Papers

Cryopreservation of sperm in marine fish

Studying sperm motility in marine fish: an overview on the state of the art

Evaluation of fish sperm quality

Marine fish spermatozoa: racing ephemeral swimmers.

Sperm features in turbot (Scophthalmus maximus): a comparison with other freshwater and marine fish species