Cost of reproduction and the evolution of deferred breeding in the western gull

Survival patterns in a population of western gulls (Larus occidentalis)of known age of first breeding, a, indicate a cost of reproductionrelated to the age of initial breeding. Among both sexes, birdsthat commenced breeding at the earliest ages (3 years in malesand 4 years in females) had higher annual mortality than thosethat deferred breeding one or more years. In addition, females(but not males) evidenced a cumulative cost of reproduction:holding age constant, females with more annual breeding attemptsdemonstrated poorer survival. These patterns of -specific survivalwere statistically significant after controlling for interannualvariation in food availability and are not explained simplyby variation in the intrinsic quality of individuals. To assessthe effects of these sex-specific costs on fitness, we combinedthe observed survival patterns with data on prebreeding survivorshipand -specific reproductive success to estimate rates of populationgrowth and lifetime reproductive success for different agesat first reproduction. Males showed a clearly defined fitnessoptimum at = 4 years, which coincided with the modal for malesin the population. Females showed no clear optimum, except thatbreeding at age 4 was suboptimal, hence females benefited fromdeferring breeding to ages 5-7 years. Observed age of firstbreeding also showed no clear mode for females, with slightpeaks at ages 5 and 7. As a result, in both sexes, the fitnesssurface for corresponded well with observed frequencies of. We suggest that stabilizing selection has acted to shape thephenotypic distribution of in males but, due to trade-offsbetween survival and early reproduction, stabilizing selectionis weak or absent in females     

Optimal surveillance and eradication of invasive species in heterogeneous landscapes

Cost-effective surveillance strategies are needed for efficient responses to biological invasions and must account for the trade-offs between surveillance effort and management costs. Less surveillance may allow greater population growth and spread prior to detection, thereby increasing the costs of damages and control. In addition, surveillance strategies are usually applied in environments under continual invasion pressure where the number, size and location of established populations are unknown prior to detection. We develop a novel modeling framework that accounts for these features of the decision and invasion environment and determines the long term sampling effort that minimises the total expected costs of new invasions. The optimal solution depends on population establishment and growth rates, sample sensitivity, and sample, eradication, and damage costs. We demonstrate how to optimise surveillance systems under budgetary constraints and find that accounting for spatial heterogeneity in sampling costs and establishment rates can greatly reduce management costs.     

The rising cost of warming waters: effects of temperature on the cost of swimming in fishes

Understanding the effects of water temperature on the swimming performance of fishes is central in understanding how fish species will respond to global climate change. Metabolic cost of transport (COT)-a measure of the energy required to swim a given distance-is a key performance parameter linked to many aspects of fish life history. We develop a quantitative model to predict the effect of water temperature on COT. The model facilitates comparisons among species that differ in body size by incorporating the body mass-dependence of COT. Data from 22 fish species support the temperature and mass dependencies of COT predicted by our model, and demonstrate that modest differences in water temperature can result in substantial differences in the energetic cost of swimming.     

Life span and reproductive cost explain interspecific variation in the optimal onset of reproduction

Fitness can be profoundly influenced by the age at first reproduction (AFR), but to date the AFR–fitness relationship only has been investigated intraspecifically. Here, we investigated the relationship between AFR and average lifetime reproductive success (LRS) across 34 bird species. We assessed differences in the deviation of the Optimal AFR (i.e., the species‐specific AFR associated with the highest LRS) from the age at sexual maturity, considering potential effects of life history as well as social and ecological factors. Most individuals adopted the species‐specific Optimal AFR and both the mean and Optimal AFR of species correlated positively with life span. Interspecific deviations of the Optimal AFR were associated with indices reflecting a change in LRS or survival as a function of AFR: a delayed AFR was beneficial in species where early AFR was associated with a decrease in subsequent survival or reproductive output. Overall, our results suggest that a delayed onset of reproduction beyond maturity is an optimal strategy explained by a long life span and costs of early reproduction. By providing the first empirical confirmations of key predictions of life‐history theory across species, this study contributes to a better understanding of life‐history evolution.     

Economic evaluation of water loss saving due to the biological control of water hyacinth at New Year’s Dam,Eastern Cape province,South Africa

Water hyacinth Eichhornia crassipes is considered the most damaging aquatic weed in the world. However, few studies have quantified the impact of this weed economically and ecologically, and even fewer studies have quantified the benefits of its control. This paper focuses on water loss saving as the benefit derived from biological control of this plant between 1990 and 2013 at New Year’s Dam, Alicedale, Eastern Cape, South Africa. Estimates of water loss due to evapotranspiration from water hyacinth vary significantly; therefore, the study used three different rates, high, medium and low. A conservative raw agriculture value of R 0.26 per m³ was used to calculate the benefits derived by the water saved. The present benefit and cost values were determined using 10% and 5% discount rates. The benefit/cost ratio at the low evapotranspiration rate was less than one, implying that biological control was not economically viable but, at the higher evapotranspiration rates, the return justified the costs of biological control. However, at the marginal value product of water, the inclusion of the costs of damage to infrastructure, or the adverse effects of water hyacinth on biodiversity, would justify the use of biological control, even at the low transpiration rate.     

Energy requirement for foliage construction depends on tree size inyoung Picea abies trees

 The relationship between stand biomass production, and tree age and size is generally a curve with a maximum. To understand why wood production decreases in the final stages of stand development, the influence of increasing tree size on foliage chemical composition and substrate requirement for foliage construction in terms of glucose [CC, g glucose (g dry mass)^{–  1}] was investigated in the evergreen conifer Picea abies (L.) Karst. Because it was already known that irradiance affects both foliage morphology and chemistry in this species, and it was expected that the foliage in large overstory trees would intercept on average more light than that in saplings in understory, irradiance was measured in the sampling locations and included in the statistical models. CC of needles increased with increasing total tree height (TH) and was independent of relative irradiance. A major reason for increasing CC with increasing TH was a greater proportion of carbon-rich lignin in the needles in large trees. However, lignin did not fully account for the observed changes in CC, and it was necessary to assume that certain other carbon-rich secondary metabolites such as terpenes also accumulate in the foliage of large trees. Enhanced requirements for needle mechanical strength as evidenced by greater lignin concentrations in large trees were attributed to increased water limitations with increasing tree height. Because water relations may also control the sink capacities for assimilate usage, apart from the mechanical requirements, they may provide an explanation for the accumulation of other energetically expensive compounds in the needles as well. Biomass partitioning within the shoot was another foliar parameter modified in response to increasing tree size. The proportion of shoot axes, which serve to provide needles with mechanical support and to supply them with water, decreased with increasing TH. This may limit water availability in the needles, and/or manifest a lower water requirement of the needles containing proportionally more supporting and storage substances, and consequently, less physiologically active compounds such as proteins. Probably the same factors which caused CC of the needles to depend on TH, were also responsible for greater CC of the shoot axes in larger trees. These results collectively suggest that increasingly more adverse water relations with increasing tree size may provide a mechanistic explanation for the decline in foliar biomass and its functional activity during stand ageing. Received: 9 April 1996 / Accepted: 14 January 1997     

Sink-limitation and the size-number trade-off of organs: production of organs using a fixed amount of reserves

To analyze the nature of size-number trade-off of organs, we develop models in which the effects of sink-limitation in the growth of organs and the loss of resources by maintenance respiration are taken into consideration. In these models, the resource absorption rate of an organ is proportional to either its absolute size or its surface area and either the initial size of an organ or the total initial size of the organs produced is fixed. In all models, organs are produced using a fixed amount of reserved resources and no additional resources become newly available for their growth. We theoretically show that size-number trade-offs are nonlinear if the resource absorption rate of an organ is proportional to the absolute size of the organ and the initial size of the individual organs is fixed or if the resource absorption rate of an organ is proportional to the surface area of the organ. In these nonlinear size-number trade-offs, the size of individual organs increases less rapidly than in linear trade-offs with a decrease in the number of organs and the total size of organs is an increasing function of the number of organs produced. This implies that increasing the number of organs produced is advantageous in terms of resource-use efficiency. In contrast, size-number trade-off is linear if the resource absorption rate of an organ is proportional to the absolute size of the organ and there is a linear trade-off between the initial size of organs and their number. To exemplify the effects of those size-number trade-offs on the life-history evolution, we calculate the optimal offspring sizes that maximize the number of offspring successfully being established. In the case of nonlinear size-number trade-offs, the optimal offspring sizes are smaller than the optimal offspring size in the case of linear size-number trade-offs, namely, that in the model of Smith and Fretwell (1974). Our optimal offspring size depends on the metabolism of organ development; the optimal offspring size decreases with an increase in maintenance respiration rate relative to the growth coefficient of organs.     

The worm re-turns: hiding behavior of a tube-dwelling marine polychaete, Serpula vermicularis

The polychaete worm Serpula vermicularis (Serpulidae) filterfeeds at the mouth of its calcareous tube, but retreats intothe tube when startled by mechanical stimuli likely to be associatedwith predators. While in its tube, a worm is safe but cannotfeed. Thus, hiding has a lost-opportunity cost. We show thatthis cost can be substantial, given that food in the naturalhabitat appears in pulses, and good feeding conditions may notlast long or recur frequently. We expect that a worm's hidingtime will be sensitive to the lost-opportunity cost, and wepresent data from a series of experiments that support thisprediction. The worms seem able to track relatively short-termchanges in food availability, and some evidence suggests thatthey assess food availability on a relative basis, comparingcurrent feeding conditions to those recently experienced. Hidingand other types of cryptic behavior are common antipredatortactics, and animals may commonly adjust the durations of suchbehaviors to current benefits and costs (including lost opportunity),as they perceive them