Dynamics of soil organic matter in primary and secondary forest succession on sandy soils in The Netherlands: An application of the ROMUL model

We applied the simulation model ROMUL of soil organic matter dynamics in order to analyse and predict forest soil organic matter (SOM) changes following stand growth and also to identify gaps of data and modelling problems. SOM build-up was analysed (a) from bare sand to forest soil during a primary succession in Scots pine forest and (b) on mature forest soil under Douglas fir plantations as an example of secondary succession in The Netherlands. As some of the experimental data were unreliable we compiled a set of various scenarios with different soil moisture regime, initial SOM pools and amount and quality of above and below ground litter input. This allowed us to find the scenarios that reflect the SOM dynamics more realistically. In the Scots pine forest, total litter input was estimated as 0.50 kg m⁻² year⁻¹. Two scenarios were defined for the test runs: (a) forest floor moisture regimes—‘dry, mesic and hydric’ and (b) augmenting a root litter pool with three ratios of needles and branches to roots: 1:1, 1:1.5 and 1:2.0. The scenario finally compiled had the following characteristics: (a) climate for dry site with summer drought and high winter moisture of forest floor; (b) a litter input of 0.25 kg m⁻² year⁻¹ above ground and 0.50 kg m⁻² year⁻¹ below ground; (c) a low nitrogen and ash content in all litter fall fractions. The test runs for the estimation of the initial SOM pools and the amount and proportion of above and below ground litter fall were also performed in the Douglas fir plantation. The inputs of above ground litter tested in various combinations were 0.30 and 0.60 kg m⁻² year⁻¹, and below ground litter 0.30, 0.60 and 0.90 kg m⁻² year⁻¹. The scenario that fitted the experimental data had an SOM pool of 20–25 kg m⁻², an aboveground litter input of 0.6 kg m⁻² year⁻¹and a below ground litter input of 0.9 kg m⁻² year⁻¹. The long-term simulation corresponded well with the observed patterns of soil organic matter accumulation associated with the forest soil development in primary and secondary succession. During primary succession in Scots pine forest on dry sand there is a consistent accumulation of a raw humus forest floor. The soil dynamics in the Douglas fir plantation also coincide with the observed patterns of SOM changes during the secondary succession, with SOM decreasing significantly under young forest, and SOM being restored in the older stands.     

Using the expert model PERPEST to translate measured and predicted pesticide exposure data into ecological risks

An important topic in the registration of pesticides and the interpretation of monitoring data is the estimation of the consequences of a certain concentration of a pesticide for the ecology of aquatic ecosystems. Solving these problems requires predictions of the expected response of the ecosystem to chemical stress. Up until now, a dominant approach to come up with such a prediction is the use of simulation models or safety factors. The disadvantage of the use of safety factors is a crude method that does not provide any insight into the concentration–response relationships at the ecosystem level. On the other hand, simulation models also have serious drawbacks like that they are often very complex, lack transparency, their implementation is expensive and there may be a compilation of errors, due to uncertainties in parameters and processes. In this paper, we present the expert model prediction of the ecological risks of pesticides (PERPEST) that overcomes these problems. It predicts the effects of a given concentration of a pesticide based on the outcome of already performed experiments using experimental ecosystems. This has the great advantage that the outcome is more realistic. The paper especially discusses how this model can be used to translate measured and predicted concentrations of pesticides into ecological risks, by taking data on measured and predicted concentrations of atrazine as an example. It is argued that this model can be of great use to evaluate the outcome of chemical monitoring programmes (e.g. performed in the light of the Water Framework Directive) and can even be used to evaluate the effects of mixtures.     

Population biology and life strategies of Chlorophthalmus agassizii Bonaparte, 1840 (Pisces: Osteichthyes) in the Mediterranean Sea

The population biology and life strategies of Chlorophthalmus agassizii were studied in the Ionian Sea (eastern–central Mediterranean) using the data collected during the experimental trawl surveys carried out from 1995 to 2000. Depth-related trends of both density and size were found. With depth the former decreased while the latter increased. A typical bigger–deeper phenomenon was detected: young-of-the-year individuals occur on the shelf during autumn–winter months and move towards bathyal bottoms as they grow. The sampled population was made up of several size–age groups. The maximum age of 8 years was identified by means of otolith readings. The Von Bertalanffy growth parameters were estimated from the age–length key (L _∞=189.04±5.401 mm; k=0.24±0.021; t _o=−1.20±0.132; φ′=3.94) and modal progression analysis (L _∞=218.33±18.397 mm; k=0.164±0.028; t _o=−1.694±0.171; φ′=3.89). Reproduction of this monoecious fish was observed during summer–early autumn. Considering the female portion of the gonad, the size at attainment of 50% maturity was 115 mm TL. The corresponding age is within the third year of life. The simultaneous occurrence of oocytes in different development stages was shown in the ovary. Both the asynchronous ovary and oocyte size distribution indicate that C. agassizii spawns more than once during a reproductive season (batch spawner). Functional fecundity (on average 3,018 hydrated oocytes) was between 37 and 69% of the absolute fecundity and increased significantly with the individual size. Since adult specimens are mostly distributed on the slope, eggs and larvae develop in epipelagic waters and migrate in-shore where juvenile forms recruit on the shelf. Juveniles migrate ontogenetically towards deeper bottoms and after 2–3 years start to reproduce annually within a life span greater than 10 years.     

A test of reproductive skew models in a field population of a multiple-queen ant

Determining the evolutionary basis of variation in reproductive skew (degree of sharing of reproduction among coexisting individuals) is an important task both because skew varies widely across social taxa and because testing models of skew evolution permits tests of kin selection theory. Using parentage analyses based on microsatellite markers, we measured skew among female eggs (n=32.3 eggs per colony, range=20–68) in 17 polygynous colonies from a UK field population of the ant Leptothorax acervorum. We used skew among eggs as our principal measure of skew because of the high degree of queen turnover in the study population. Queens within colonies did not make significantly unequal contributions to queen and worker adult or pupal offspring, indicating that skew among female eggs reflected skew among daughter queens. On average, both skew among female eggs (measured by the B index) and queen–queen relatedness proved to be low (means±SE=0.06±0.02 and 0.28±0.08, respectively). However, contrary to current skew models, there was no significant association of skew with either relatedness or worker number (used as a measure of productivity). In L. acervorum, predictions of the concession model of skew may hold between but not within populations because queens are unable to assess their relatedness to other queens within colonies. Additional phenomena that may help maintain low skew in the study population include indiscriminate infanticide in the form of egg cannibalism and split sex ratios that penalize reproductive monopoly by single queens within polygynous colonies.     

Structure of a Mediterranean cryptobenthic fish community and its relationships with habitat characteristics

In the last 10 years, several studies have been carried out on the fish fauna of the Ustica Island marine reserve, yet no investigation was specifically addressed to the cryptobenthic fish assemblage. The first task of this study, conducted along the shallow rocky reefs of Ustica, was to determine the species composition, diversity and relative density of the resident cryptobenthic fishes. Furthermore, we aimed to assess the effects of some macro- and microscale habitat characteristics on the distribution pattern of fishes. In particular, the effect of predator density was indirectly evaluated by comparing density data collected within and outside the integral reserve zone. Overall, 20 species belonging to Blenniidae, Gobiidae, Tripterygiidae, Scorpaenidae and Gobiesocidae were recorded. Gobius bucchichi, Scorpaena maderensis, Tripterygion delaisi, T. melanurus and T. tripteronotus were the numerically dominant and most common species. The effects of zone (i.e. of predator density), bottom type and depth on species richness, diversity and evenness were not significant. A greater total fish density was observed on stones compared with rocky cliff and plateau, but only in the shallowest depth range. At level of single species, G. bucchichi was more abundant inside than outside the integral reserve, but only on stones and at 0–2 m depth range. Density of G. bucchichi was generally higher on stones than on rocky cliffs or plateau and between 0 and 5 m depth, although these differences were not always significant. T. delaisi was conversely more abundant in the deepest stratum (7–10 m). Canonical analyses demonstrated that bottom type and depth influenced significantly the fish assemblage structure. The observed differences in the assemblage structure relied mainly upon the dominant species. T. tripteronotus was mainly associated with rocky plateau and the intermediate depth range (3–5 m), whereas S. maderensis, T. melanurus and Lipophrys trigloides inhabited preferentially the rocky cliffs. At microscale level, the habitat choice of the investigated species was almost entirely based on whether the substrate was either vegetated or composed of bare rock. T. delaisi and T. tripteronotus were associated with substrata covered by algae, whilst G. bucchichi, S. maderensis and T. melanurus preferred bare rock bottoms. In some species, the electivity indices for the less abundant type of cover, measured at different spatial scale, changed accordingly. For instance, the smaller the size of the sampled area, the higher was the intensity of the association between G. bucchichi and Anemonia viridis.     

Variability in grazer-mediated defensive responses of green and red macroalgae on the south coast of South Africa

Variabilities in the responses of several South African red and green macroalgae to direct grazing and the responses of one green alga to cues from grazers were tested. We used two feeding experiments: (1) testing the induced responses of three red and one green algae to direct grazing by mesograzers and (2) a multi-treatment experiment, in which the direct and indirect effects of one macrograzer species on the green alga Codium platylobium were assessed. Consumption rates were assessed in feeding assays with intact algal pieces and with agar pellets containing non-polar extracts of the test algae. Defensive responses were induced for intact pieces of Galaxaura diessingiana, but were not induced in pellets, suggesting either morphological defence or chemical defence using polar compounds other than polyphenols. In contrast, exposure to grazing stimulated consumption of Gracilaria capensis and Hypnea spicifera by another grazing species. In the multi-treatment experiment, waterborne cues from both grazing and non-grazing snails induced defensive algal traits in C. platylobium. We suggest that inducible defences among macroalgae are not restricted to brown algae, but that both the responses of algae to grazers and of grazers to the defences of macroalgae are intrinsically variable and complex.     

On the Estimation of Dispersal Kernels from Individual Mark-Recapture Data

We present a new method for estimating a distribution of dispersal displacements (a dispersal kernel) from mark-recapture data. One conventional method of calculating the dispersal kernel assumes that the distribution of displacements are Gaussian (e.g. resulting from a diffusion process) and that individuals remain within sampled areas. The first assumption prohibits an analysis of dispersal data that do not exhibit the Gaussian distribution (a common situation); the second assumption leads to underestimation of dispersal distance because individuals that disperse outside of sampling areas are never recaptured. Our method eliminates these two assumptions. In addition, the method can also accommodate mortality during a sampling period. This new method uses integrodifference equations to express the probability of spatial mark-recapture data; associated dispersal, survival, and recapture parameters are then estimated using a maximum likelihood method. We examined the accuracy of the estimators by applying the method to simulated data sets. Our method suggests designs for future mark-recapture experiments. Received: January 2004 / Revised: July 2005     

Modeling the beta diversity of coral reefs

Quantifying the beta diversity (species replacement along spatiotemporal gradients) of ecosystems is important for understanding and conserving patterns of biodiversity. However, virtually all studies of beta diversity focus on one-dimensional transects orientated along a specific environmental gradient that is defined a priori. By ignoring a second spatial dimension and the associated changes in species composition and environmental gradients, this approach may provide limited insight into the full pattern of beta diversity. Here, we use remotely sensed imagery to quantify beta diversity continuously, in two dimensions, and at multiple scales across an entire tropical marine seascape. We then show that beta diversity can be modeled (0.852 > or = r2 > or = 0.590) at spatial scales between 0.5 and 5.0 km2, using the environmental variables of mean and variance of depth and wave exposure. Beta diversity, quantified within a "window" of a given size, is positively correlated to the range of environmental conditions within that window. For example, beta diversity increases with increasing variance of depth. By analyzing such relationships across seascapes, this study provides a framework for a range of disparate coral reef literature including studies of zonation, diversity, and disturbance. Using supporting evidence from soft-bottom communities, we hypothesize that depth will be an important variable for modeling beta diversity in a range of marine systems. We discuss the implications of our results for the design of marine reserves.