Reproductive success is an individual's production of offspring per breeding event or lifetime. This is not limited by the number of offspring produced by one individual, but also the reproductive success of these offspring themselves.
Reproductive success is different from fitness in that individual success is not necessarily a determinant for adaptive strength of a genotype since the effects of chance and the environment have no influence on those specific genes. Reproductive success turns into a part of fitness when the offspring are actually recruited into the breeding population. If offspring quantity is not correlated with quality this holds up, but if not then reproductive success must be adjusted by traits that predict juvenile survival in order to be measured effectively.
Quality and quantity is about finding the right balance between reproduction and maintenance. The disposable soma theory of aging tells us that a longer lifespan will come at the cost of reproduction and thus longevity is not always correlated with high fecundity.
Parental investment is a key factor in reproductive success since taking better care to offspring is what often will give them a fitness advantage later in life. This includes mate choice and sexual selection as an important factor in reproductive success, which is another reason why reproductive success is different from fitness as individual choices and outcomes are more important than genetic differences. As reproductive success is measured over generations, longitudinal studies are the preferred study type as they follow a population or an individual over a longer period of time in order to monitor the progression of the individual(s). These long term studies are preferable since they negate the effects of the variation in a single year or breeding season.
Nutritional contribution
Nutrition is one of the factors that influences reproductive success. For example, different amounts of consumption and more specifically carbohydrate to protein ratios. In some cases, the amounts or ratios of intake are more influential during certain stages of the lifespan. For example, in the Mexican fruit fly, male protein intake is critical only at eclosion. Intake at this time provides longer lasting reproductive ability. After this developmental stage, protein intake will have no effect and is not necessary for reproductive success. In addition, Ceratitis capitata males were experimented on to see how protein influence during the larval stage affects mating success. Males were fed either a high protein diet, which consisted of 6.5g/100mL, or a no protein diet during the larval stage. Males that were fed protein had more copulations than those that weren't fed protein, which ultimately correlates with a higher mating success. Protein-deprived black blow fly males have been seen to exhibit lower numbers of oriented mounts and inseminate fewer females than more lively fed males. In still other instances, prey deprivation or an inadequate diet has been shown to lead to a partial or complete halt in male mating activity. Copulation time lasted longer for sugar-fed males than protein-fed flies, showing that carbohydrates were more necessary for a longer copulation duration.
In mammals, amounts of protein, carbohydrates, and fats are seen to influence reproductive success. This was evaluated among 28 female black bears evaluated by measuring the number of cubs born. Using different foods during the fall including corn, herbaceous, red oak, beech, and cherry, nutritional facts of protein, carbohydrate, and fat were noted, as each varied in percent compositions. Seventy-percent of the bears who had high fat and high carbohydrate diets produced cubs. Conversely, all 10 females who had low carbohydrate diets did not reproduce cubs, deeming carbohydrates a critical factor for reproductive success where fat was not a hindrance.