Description: It has been suggested that non-native species are more tolerant towards abiotic stress than ecologically comparable native species. Furthermore, non-native marine macroalgae should be under lower grazing pressure than native seaweeds, because they left their co-evolved enemies behind. As a consequence, they generally need to allocate less energy to defences and can invest more into compensating the negative effects of abiotic stress or, assuming that grazing pressure is low but not zero, to defensive reactions following grazer attack. This, in turn, should make them more stress tolerant and less susceptible to herbivory. However, empirical evidence for both concepts is still scarce and very little is known about whether enemy release is commonly associated with an enhanced tolerance towards abiotic or biotic stress. We therefore ran an experimental study that (a) assessed attractiveness for grazers, (b) verified whether short-term low-light stress impairs growth and (c) investigated whether light limitation and previous grazing interactively affect the consumption of two macroalgae from Madeira Island, the native brown alga Stypopodium zonale and the non-native red alga Grateloupia imbricata by the sea urchin Paracentrotus lividus. To come to ecologically meaningful low-light stress levels, pilot studies were performed in order to determine the light compensation point of photosynthesis for each algal species and then we established six light regimes around this point by reducing the amount of incoming light. Simultaneously, we let one sea urchin graze on each algal individual to stimulate a chemical defence in the seaweeds if present. In parallel to this, we kept the same number of algal replicates in the absence of sea urchins. After 21 days, we compared algal growth in the absence of grazers as well as the attractiveness of previously grazed and non-grazed algal material for P. lividus across all light regimes. Algal attractiveness was assessed in no-choice feeding assays. The observation that the non-native alga was less consumed by the grazer than the native species generally confirms the concept of enemy release. However, light limitation reduced growth in the non-native but not in the native seaweed, while previous grazing reduced consumption of the native but enhanced it in case of the non-native alga. These findings do not corroborate the assumption that enemy release can, through the re-allocation of energy, enhance tolerance to abiotic (light limitation) or biotic (grazing) stressors in non-native marine macroalgae.

Description: Highlights: • Sea urchin food consumption and gonad index followed thermal performance curves. • Body size and sex interacted with temperature and influenced food consumption rates. • Only body size, not sex, in addition to temperature influenced gonad indices. • Larger sea urchins were impacted to a greater extent by warmer temperatures. Rising sea surface temperatures affect the feeding behaviour and reproductive success of many coastal benthic invertebrates. This experimental study investigated the effects of ocean warming on macroalgal food consumption rates in the sea urchins Arbacia lixula and Paracentrotus lividus from Madeira Island to assess how the feeding pressure they exert may change under warmer ocean conditions. Additionally, in A. lixula, the relationship between temperature and the gonad index was examined to estimate potential future reproductive output. Over the course of 25 days, 180 individuals of each species were exposed to temperatures between 22 degrees C and 31 degrees C. After 20 days, consumption rates were assessed in 48-h feeding trials. Gonad indices of A. lixula were determined on the last day of the experiment. In the thermal range investigated, both traits were found to be unimodal functions of temperature. In addition to temperature, consumption rates in both species and the gonad indices in A. lixula were influenced by body size, while feeding in A. lixula also varied between sexes. Maximum food consumption rates (A. lixula and P. lividus) as well as maximum gonad indices (only A. lixula) were observed between 25 degrees C and 26 degrees C. These values are at the upper end of the temperature range that currently prevails around Madeira, and may become average summer temperatures by the year 2100. Consequently, both sea urchin species may thrive during future warm summers and may enhance their top-down control on local macroalgal populations.

Description: Seagrass meadows are globally recognized as important coastal habitats due to the various ecological functions and ecosystem services they provide. Substantial global decline of seagrass habitats has been recorded over the last decades, underlining the need for extensive studies, including monitoring and mapping these habitats across their distributional range. Cymodocea nodosa (Ucria) Ascherson is the only seagrass species reported in the archipelago of Madeira (NE Atlantic) and systematic or reliable information of its occurrence is very scarce and mostly anecdotal. This study reports the discovery of a yearly-persistent patch of C. nodosa in the southeast coast of Madeira and provides insights into key ecological and biological aspects (e.g. density, leaf length, associated fauna and flora). Seasonal monitoring surveys over a 3-year period, indicate that (1) the patch has increased in size and shoot density over the study period, and (2) leaf lengths follow a typical seasonal pattern over the year. Accounts of past destruction of seagrass meadows in the island, underline the importance of continuous monitoring of the patch and adjacent areas to reveal how the current seagrass patch develops (i.e. patch continuity and/or disappearance), if it integrates a larger meadow and whether anthropogenic pressures as coastal development and/or associated terrigenous sediment runoff events will affect its resilience.

Description: Experiments were conducted from 4 June to September 2007 inside laboratory facilities at the south coast of Madeira (32°38'N, 16°54'W). The organisms used for this study were the sea urchin Paracentrotus lividus collected at Doca do Cavacas (32° 38'06 N; 16° 56'52 W), the red seaweed Grateloupia imbricata collected from the marina of Funchal (32° 38'41 N; 16° 54'46 W) at 0.5 m water depth, and the brown seaweed Stypopodium zonale collected from boulders at Reis Magos, Caniço (32° 83'45 N; 16° 49'25 W) in water depths of 3-7 m. The study consisted of three sequential stages: (i) assessing algal light compensation points, (ii) inducing light limitation and grazing, (iii) assessing grazer consumption rates in no-choice feeding assays after light limitation and grazer impact. For the latter we used the algal material from stage (ii) (see additional file 1). Pilot studies were carried out in June 2007 to identify the Light Compensation Point (LCP) for both algal species, i.e. the light intensity at which the rate of photosynthesis (measured as oxygen production) equals respiration. For this, we reduced the amount of incoming light by placing various layers of black plastic gauze material with a mesh size of 1 mm on top of each aquarium. For both macroalgae, we had a total of 12 aquaria (3.5 L each) of with each was loaded with 30 - 40 g wet weight of seaweed material. We randomly assigned two aquaria to each of six different light regimes. The number of gauze layers used was 0, 1, 2, 3, 4 and 5. After we recorded the concentration of dissolved oxygen with an oxymeter (Oxi 197, WTW Wissenschaftlich-Technische Werkstätten GmbH, Weilheim, Germany) twice a day (9am and 5pm) for the following 4 days (see additional file 2). Experiments were carried out in July 2007 for G. imbricata, and in September 2007 for S. zonale. We conducted a two-factorial experiment for each of the species in which we crossed two levels of grazing ("grazed" and "non-grazed") with six levels of light intensities (0-5 layers of gauze material) and each treatment combination was replicated eight times (n=8). Consequently, we had 6 x 8 = 48 aquaria of which each contained one sea urchin, while another 48 aquaria had no sea urchins. The latter were used to determine total algal growth rates under the different light regimes in the absence of grazers and to provide non-grazed algal material for the feeding assays. In total we had 96 aquaria for each of the two seaweed species in the study and the respective treatments, i.e. light limitation and grazing, were imposed simultaneously for 21 days. We tested for possible effects of the previously applied light limitation and grazing (see stage (ii)) on grazer consumption rates in no-choice feeding assays that lasted for 24 h. Hence, the number of replicates for the assays at stage (iii) was the same as at stage (ii). Grazer consumption rates of algal material were determined as the grazers' total consumption, which was calculated using the equation suggested by Cronin and Hay (1996-a): [Ai x (Cf / Ci) - Af ] where Ai and Af were the initial and final weight of the algae portions used in the feeding assays; Ci and Cf are the equivalent weights of the growth control algal pieces before and after the assays (Sotka et al., 2002). Finally, consumption rates were standardised for grazer wet biomass (g alga/g grazer). Negative consumption was recorded in case algal growth rates during the assays exceeded consumption rates (see additional file 3 raw data).

Description: This experimental study investigated the effects of ocean warming on food consumption rates in the sea urchins Paracentrotus lividus from Madeira Island to assess how the feeding pressure they exert may change under warmer ocean conditions. Over the course of25 days, 180 individuals of each species were exposed to temperatures between 22 °C and 31 °C in the laboratory. After 20 days, consumption rates were assessed in 48-h feeding trials. Data contain information about place and time of the animal collection as well as laboratory experiment and information about temperature regimes, and food consumption rates of Paracentrotus.

Description: This experimental study investigated the effects of ocean warming on food consumption rates in the sea urchins Arbacia lixula from Madeira Island to assess how the feeding pressure they exert may change under warmer ocean conditions. Additionally, in A. lixula, the relationship between temperature and the gonad index was examined to estimate potential future reproductive output. Over the course of25 days, 180 individuals of each species were exposed to temperatures between 22 °C and 31 °C in the laboratory. After 20 days, consumption rates were assessed in 48-h feeding trials. Gonad indices of A. lixula were determined on the last day of the experiment. Data contain information about place and time of the animal collection as well as laboratory experiment and information about temperature regimes, food consumption rates of Arbacia and information about gonad indices and the sex of the animals.