Orientador: Márcia Ortiz Mayo Marques / Resumo: A Lippia alba (Verbenaceae), popularmente conhecida como erva-cidreira, é uma planta originaria da América do Sul e considerada um recurso genético vegetal de altíssimo valor para estudos de bioprospecção pela sua potencial importância econômica, ecológica e propriedades do seu óleo essencial. A irrigação de sistemas de produção agrícola depende da disponibilidade dos recursos hídricos da demanda de água em cada etapa do cultivo, requerendo um manejo criterioso e sustentável. Estudos em plantas aromáticas têm mostrado que o manejo da água por meio da irrigação e as condições climáticas do local de cultivo são fatores abióticos determinantes na produção de biomassa, rendimento de óleo essencial e síntese de princípios ativos de interesse para a indústria de cosméticos, perfumes e fragrâncias. O objetivo deste estudo foi avaliar o efeito de diferentes lâminas de irrigação na biomassa, rendimento, produção e composição química do óleo essencial da espécie Lippia alba, de clones selecionados de quimiotipo linalol, pertencentes ao Banco de Germoplasma do Instituto Agronômico (IAC). As mudas foram obtidas por propagação assexuada e o cultivo conduzido em casa de vegetação em sistema orgânico de produção. Os tratamentos foram representados pelo manejo da irrigação com base na evapotranspiração de referência (50%, 75%, 100% ET0 e 125% da ET0). Os cortes foram efetuados aos 90, 180, 270 e 360 dias após a poda de formação (DAPF). As plantas foram avaliadas quanto à produção total de ma... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Lippia alba (Verbenaceae), popularly known as lemon balm, is a plant originally from South America and considered a highly valuable plant genetic resource for bioprospecting studies due to its potential economic, ecological and essential oil properties. The irrigation of agricultural production systems depends on the availability of water resources for water demand at each stage of cultivation, requiring careful and sustainable management. Studies on aromatic plants have shown that water management through irrigation and the climatic conditions of the place of cultivation are abiotic factors determining biomass production, essential oil yield and synthesis of active principles of interest to the cosmetics, perfumes industry and fragrances. The objective of this study was to evaluate the effect of different irrigation depths on biomass, yield, production and chemical composition of the essential oil of the species Lippia alba, from selected clones of the linalool chemotype, belonging to the Germplasm Bank of the Agronomic Institute (IAC). The seedlings were obtained by asexual propagation and cultivation was carried out in a greenhouse in an organic production system. The treatments were represented by irrigation management based on reference evapotranspiration (50%, 75%, 100% ET0 and 125% ET0). The cuts were made at 90, 180, 270 and 360 days after the formation pruning (DAPF). Plants were evaluated for total leaf dry matter production (PTMSF), total stem dry matter production... (Complete abstract click electronic access below) / Doutor

Constitutive and alternative splicing of pre-mRNAs from multiexonic genes controls the diversity of the proteome; these precisely regulated processes also fine-tune responses to cues related to growth, development, and biotic and abiotic stresses. Recent work showed that AS is pervasive across plant species, with more than 60% of intron-containing genes producing different isoforms. Mammalian cell-based assays have discovered various AS small-molecule inhibitors that perturb splicing and thereby provide invaluable tools for use as chemical probes to uncover the molecular underpinnings of splicing regulation and as potential anticancer compounds. Here, I show that the macrolide Pladienolide B (PB) and herboxidiene (GEX1A) inhibits both constitutive and alternative splicing, mimics an abiotic stress signal, and activates the abscisic acid (ABA) pathway in plants. Moreover, PB and GEX1A activate genome-wide transcriptional patterns involved in abiotic stress responses in plants. PB and GEX1A treatment triggered the ABA signaling pathway, activated ABA-inducible promoters, and led to stomatal closure. Interestingly, PB and GEX1A elicited similar cellular changes, including alterations in the patterns of transcription and splicing, suggesting that these compounds might target the same spliceosome complex in plant cells. This work establishes PB and GEX1A as potent splicing inhibitors in plants that can be used to probe the assembly, dynamics, and molecular functions of the spliceosome and to study the interplay between splicing stress and abiotic stresses, as well as having potential biotechnological applications.

Bacterial volatile organic compounds (VOCs) are signal molecules that may have beneficial roles in the soil-plant-microbiome ecosystem. In this Ph.D. thesis, I aimed to assess and characterize the role of bacterial VOCs in plant tolerance to drought and in the biocontrol of fungal pathogens. I started by studying two root endophytic bacteria isolated from pepper plants cultivated under desert farming conditions. They showed an enhancement of pepper tolerance to drought stress and an amelioration of its physiological status. Moreover, they induced the expression of a vacuolar pyrophosphatase proton pump (V-PPase), implicated in the regulation of the vacuolar osmotic pressure, facilitating water uptake. Besides, the exposure of Arabidopsis thaliana plants, grown under salinity stress, to the volatile 2,3-butanediol, described for its plant growth promotion (PGP) potential, enhanced the plants tolerance to salinity, proving the potential involvement of this volatile in the osmotic stress resistance mechanism. Then, I studied VOCs released by three bacteria associated to healthy rice plants. Their released VOCs mixtures modified the color pattern of Magnaporthe oryzae, the agent of the rice blast disease, and protected rice from the pathogen infection. A significant reduction of melanin production, sporulation and appressoria formation was measured in presence of the bacterial VOCs, without major effects on mycelial proliferation. 1-butanol-3-methyl, one of the nine VOCs co-produced by the studied bacteria, proved its potential of reducing M. oryzae melanin in vitro. In vivo tests confirmed the infection inhibition effects mediated by the rice-bacterial VOCs, with a reduction of 94% of the disease incidence. Lastly, I compared the genomes of the five bacteria considered in the previous experimental studies. The PGP traits and the VOCs pathways identified from the genome analyses confirmed the effects observed with the in vitro and in vivo assays, revealing a complex mode of promotion and protection offered by the studied plant-associated bacteria. In conclusion, plant-associated bacterial VOCs can play potentially important roles in modulating plant drought tolerance and reducing fungal virulence. Such biological resources represent novel tools to counteract the deleterious effects of abiotic and biotic stresses and have the potential to be exploited for sustainable approaches in agriculture.

One of the major challenges for agricultural research in the 21st century is to increase crop productivity to meet the growing demand for food and feed. Biotic (e.g. plant pathogens) and abiotic stresses (e.g. soil salinity) have detrimental effects on agricultural productivity, with yield losses being as high as 60% for major crops such as barley, corn, potatoes, sorghum, soybean and wheat, especially in semi-arid regions such as Saudi Arabia. Plant growth promoting bacteria isolated from pioneer desert plants could serve as an eco-friendly, sustainable solution for improving plant growth, stress tolerance and health. In this dissertation, culture-independent amplicon sequencing of bacterial communities revealed how native desert plants influence their surrounding bacterial communities in a phylogeny-dependent manner. By culture-dependent isolation of the plant endosphere compartments and a number of bioassays, more than a hundred bacterial isolates with various biochemical properties, such as nutrient acquisition, hormone production and growth under stress conditions were obtained. From this collection, five phylogenetically diverse bacterial strains were able to promote the growth of the model plant Arabidopsis thaliana under salinity stress conditions in a common mechanism of inducing transcriptional changes of tissue-specific ion transporters and lowering Na+/K+ ratios in the shoots. By combining a number of in vitro bioassays, plant phenotyping and volatile-mediated inhibition assays with next-generation sequencing technology, gas chromatography–mass spectrometry and bioinformatics tools, a candidate strain was presented as a multi-stress tolerance promoting bacterium with potential use in agriculture. Since recent research showed the importance of microbial partners for enhancing the growth and health of plants, a review of the different factors influencing plant-associated microbial communities is presented and a framework for the successful application of microbial inoculants in agriculture is proposed. The presented work demonstrates a holistic approach for tackling agricultural challenges using microbial inoculants from desert plants by combining culturomics, phenomics, genomics and transcriptomics. Microbial inoculants are promising tools for studying abiotic stress tolerance mechanisms in plants, and they provide an eco-friendly solution for increasing crop yield in arid and semi-arid regions, especially in light of a dramatically growing human population and detrimental effects of global warming and climate change.

L'oxydase terminale plastidiale (PTOX) est présente uniquement chez les organismesphotosynthétiques. PTOX oxyde le plastoquinol (PQH2) et réduit l'oxygène en eau.PTOX est impliquée dans la synthèse des caroténoïdes, dans le transportphotosynthétique d'électrons et dans la chlororespiration. De plus, son activité estconsidérée comme pouvant jouer un rôle en tant que soupape de sécurité, permettant de maintenir oxydé le pool de plastoquinones (PQ) et d'éviter la surréduction duchloroplaste et ainsi la photoinhibition. Chez la majorité des plantes testées, les niveaux de PTOX sont plus élevés dans des conditions de stress (une exposition à forte intensité lumineuse, par exemple). D'autre part, la surexpression de PTOX chez Arabidopsis thaliana n'a pas rendu les plantes moins sensibles à la photoinhibition. Par ailleurs, il semble que PTOX surexprimée chez Nicotiana tabacum a induit la génération des espèces réactives de l'oxygène (ERO) et une photoinhibition importante sous forte lumière.Le but de cette thèse était la caractérisation de l'activité enzymatique de PTOX enutilisant la protéine purifiée et de comprendre pourquoi PTOX protège du stressphotooxydant dans certaines conditions et pourquoi elle augmente ce stress quand elle est surexprimée in planta.L'analyse biochimique de PTOX recombinante purifiée a démontré que l'enzymeexiste principalement sous forme tétramérique. Cette forme se dissocie partiellement,principalement en dimères. Le turnover maximal de l'enzyme purifié correspond à 320électrons par seconde et par molécule de PTOX. Nous avons démontré que PTOXgénère des ERO dans une réaction secondaire dépendante de la concentration dusubstrat (PQH2) et du pH de la solution. À pH 8 (représentant le pH du stroma deschloroplastes actifs), PTOX a une activité antioxydante quand la concentration de PQH2 est basse et prooxydante quand cette concentration est élevée.En mesurant la fluorescence de la chlorophylle a, nous avons démontré quePTOX est active lorsqu'elle est ajoutée aux membranes enrichies en PSII.L'attachement aux membranes dépend du pH et de cations de la solution: lorsque le pHdiminue ou lorsque la solution est riche en cations monovalents, la quantité de PTOXattachée à la membrane diminue.L'activité de PTOX in planta et son effet sur le transport des électronsphotosynthétiques ont été analysés en utilisant Arabidopsis thaliana surexprimant laphytoène désaturase bactérienne (CRTI) et Nicotiana tabacum surexprimant PTOX1 deChlamydomonas reinhardtii. Arabidopsis thaliana surexprimant CRTI a un niveau plusimportant de PTOX et de production d'ERO et le transport cyclique des électrons estsupprimé chez les transformants. Cela implique que PTOX est en compétition avec letransfert cyclique pour les électrons du pool PQ et que PTOX joue un rôle importantdans le contrôle de l'état rédox de ce pool. En utilisant Nicotiana tabacum surexprimant PTOX1, nous avons démontré que PTOX fait concurrence au transfert linéaire d'électrons photosynthétique, mais que PTOX est inactivée quand le pH du stroma est neutre. Grâce aux résultats obtenus, nous proposons un modèle où l'association de PTOX avec la membrane est contrôlée par le pH du stroma. Quand le pH est neutre, PTOX est soluble et n'est pas active, ce qui évite l'interférence avec le transfert linéaire d'électrons. Quand le pH du stroma est alcalin et la chaîne des transporteurs photosynthétiques est surréduite (lors des conditions du stress), PTOX s'attache à la membrane, devient active et joue le rôle de soupape de sécurité. / The plastid terminal oxidase PTOX is encoded by higher plants, algae and some cyanobacteria. PTOX is a plastid-localized plastoquinol (PQH2) oxygen oxidoreductase. PTOX was shown to be implicated in plant carotenoid biosynthesis, photosynthetic electron transport and chlororespiration and may act as a safety valve protecting plants against photo-oxidative stress. PTOX protein levels increase during abiotic stress indicating a function in stress acclimation. But overexpression of PTOX in Arabidopsis did not attenuate the severity of photoinhibition or, when overexpressed in tobacco, even increased the production of reactive oxygen species (ROS) and exacerbated photoinhibition.Biochemical analysis of recombinant purified PTOX (PTOX from rice fused to the maltose-binding protein) showed that the enzyme exists mainly as a tetramer, which dissociated to a certain extent during electrophoresis, mainly into a dimeric form. The PTOX activity was 320 electrons s−1 PTOX−1. It was also shown that PTOX generates ROS in a side reaction in a substrate (decylPQH2) and pH-dependent manner when liposomes were used: at the basic stromal pH of photosynthetically active chloroplasts, PTOX was antioxidant at low decylPQH2 gaining prooxidant properties with increasing quinol concentrations. It is concluded that PTOX can act as a safety valve when the steady state [PQH2] is low while a certain amount of ROS is formed at high light intensities.It was shown by chlorophyll a fluorescence that recombinant purified PTOX is active when added to photosystem II (PSII)-enriched membrane fragments. PTOX attached tightly to the PSII-enriched membrane fragments. The amount of PTOX attaching to the membrane depended on pH and salts: an alkaline pH and monovalent compared to divalent cations increased PTOX attachment.PTOX activity in planta and its effect on photosynthetic electron transport were investigated using Arabidopsis expressing bacterial phytoene desaturase and tobacco expressing PTOX1 from Chlamydomonas. Arabidopsis expressing bacterial phytoene desaturase (CRTI lines) showed a higher PTOX content and increased PTOX related ROS generation. Furthermore, cyclic electron flow was suppressed in these lines. This implicates that PTOX competes efficiently with cyclic electron flow for PQH2 in the CRTI-expressing lines and that it plays a crucial role in the control of the reduction state of the plastoquinone pool. Using tobacco expressing PTOX1 from Chlamydomonas, it was shown that PTOX competes efficiently with photosynthetic electron flow, but gets inactive when the stromal pH is neutral. Based on the in vitro and in vivo results, a model is proposed, where the association of PTOX to the membrane is controlled by the stromal pH: When the stromal pH is neutral, PTOX exists as a soluble form and is enzymatically inactive avoiding the interference of PTOX with linear electron flow. When the stromal pH is alkaline and the photosynthetic electron chain is highly reduced under stress conditions as high light, PTOX binds to the membrane, gets enzymatically active and can serve as safety valve.

La photorespiration est un processus essential chez tous les organismes photosynthétiques. Elle est déclenchée par l’activité oxygénase de la Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase (RuBisCO) menant à la production d’une molécule de 3-phosphoglycerate and une molécule de 2-phosphoglycolate (2PG). Le 2PG est toxique et sera recyclé par la photorespiration qui implique huit principales enzymes et prend place dans les chloroplastes, les peroxysomes, les mitochondries et le cytosol. Bien que la photorespiration aboutisse à une efficacité réduite de l’assimilation du CO₂ photosynthétique et soit considérée comme un processus inutile, le phénotype de croissance des mutants d’enzymes photorespiratoires (croissance réduite, chlorose) reflète l’importance de ce processus dans la croissance et le développement normal car il interagit avec plusieurs voies métaboliques primaires. Les données actuelles montrent que sept des huit principales enzymes photorespiratoires pourraient être phosphorylées et qu’ainsi la phosphorylation pourrait être un élément régulateur essentiel du cycle photorespiratoire. Afin de mieux comprendre la régulation du cycle photorespiratoire, nous avons étudié l’effet d’une phosphorylation/ absence de phosphorylation sur la sérine hydroxyméthyltransférase 1 mitochondriale (SHMT1) et de l’hydroxypyruvate réductase peroxisomale en utilisant des versions de ces enzymes mimant une phosphorylation (sérine ou la thréonine mutée en acide aspartique) ou une absence de phosphoryaltion (sérine ou thréonine mutée en alanine).Deux sites sont phosphorylés chez HPR1: S229 et T335. La mutation de ces sites montre que seule la version mimant une phosphorylation sur le site T335 (HPR1 T335D) entraîne une activité réduite de la protéine recombinante HPR1. Ce résultat a été confirmé in vivo puisque le mutant Arabidopsis hpr1 exprimant HPR1 T33D était incapable de totalement complémenter le phénotype photorespiratoire du mutant hpr1.Par complémentation du mutant d’Arabidopsis shm1-1 par une forme sauvage de SHMT1, d’une version mimant (S31D) ou non (S31A) une phosphorylation, les résultats ont montré que toutes les formes de SHMT1 pouvaient presque totalement complémenter le phénotype de croissance de shm1-1. Cependant, chaque ligne transgénique n'avait que 50% de l'activité de SHMT normale. En réponse à un stress dû au sel ou à la sécheresse, les lignées Compl-S31D ont montré un déficit de croissance plus accentué que les autres lignées transgéniques. Cette sensibilité au sel semble refléter les quantités réduites de protéines SHMT1-S31D ainsi qu’une activité plus faible ayant un impact sur le métabolisme des feuilles, entraînant une sous-accumulation de proline et une suraccumulation de polyamines. La mutation S31D de la protéine SHMT1 a également entraîné une réduction de la fermeture stomatique induite par le sel et l'ABA. Ainsi, nos résultats soulignent l’importance du maintien de l’activité du SHMT1 photorespiratoire dans des conditions de stress dû au sel et à la sécheresse et indiquent que la phosphorylation de SHMT1 S31 pourrait être impliquée dans la modulation de la stabilité de la protéine SHMT1. / Photorespiration is an essential process in oxygenic photosynthetic organisms, and it is triggered by the oxygenase activity of Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase (RuBisCO) to produce one molecular 3-phosphoglycerate and one molecular 2-phosphoglycolate. The toxic 2-PG is recycled by the photorespiratory pathway which includes eight core enzymes and takes place in chloroplasts, peroxisomes and metochondria and cytosol. Although the photorespiration leads to a reduced efficiency of the photosynthetic CO₂ assimilation and thereby is considered as a wasteful process, the growth phenotype of the photorespiratory enzymes can reflect the importance of this process in normal growth and development of air-grown plants. Normally, for most photorespiratory enzyme mutants, they exhibit small, chlorotic plants sometimes non-viable in air which are not observed when the mutants are grown under high CO₂ condition that limit the photorespiration by reducing the RuBisCO oxygenase activity. Photorespiratory cycle interacts with several major primary metabolic pathways, thus is a highly regulated and extensive works. Current data show that seven of eight core photorespiratory enzymes could be phosphorylated and the protein phosphorylation seems to be a critical regulatory component of the photorespiratory cycle. In order to better understand the regulation of the photorespiratory cycle, we explored the effect of SHMT1 and HPR1 phosphorylation/non-phosphorylation events on plant physiology and metabolism by several methods: Site-directed mutagenesis assay, complementation assay, activity assay, stomatal aperture assays, plant salt/drought resistance assays, metabolites measurement, gas exchange measurement. The results show the phosphorylation mimicking version of HPR1 at T335 results to a less HPR1 activity and retarded growth at the ambient air condition. For the phosphorylation mimicking version of SHMT1 at S31 resulted in a less stability leading to a reduced resistance to drought and salt stress. The decline of resistance against abiotic stress was mainly due to impairment in the closure of stomata which were unable to respond properly to ABA probably because of a default in the PLC pathway. So there results indicate that the phosphorylation of SHTM1 leads to a negative effect for the plant growth especially under stress condition. Thus, we propose that the SHMT1 can be phosphorylated at a basic level under normal growth conditions, once the photorespiratory flux is increased such under salt stress condition, the SHMT1 should be dephosphorylated to stabilize SHMT1 and sustain a high photorespiration flux to cope with reduced CO₂ availability.

Fresh fruits and vegetables (FFVs) are the most frequently wasted foods because of their perishability and handling requirements. However, there is a lack of information on how much each step of the supply chain impacts FFVs quality, particularly on tomatoes, and what measures need to be taken for an immediate and effective impact on waste reduction. There is also no information on how the supply chain affects the proteome of the tomato and what proteins are differentially regulated by the most impactful steps of the supply chain. The objectives of the work presented on this thesis were to evaluate the decline in the overall quality and quantify tomato waste at each step of the supply chain, from the farm to consumer; and to determine what proteins are impacted by the decline in quality that is associated with temperature abuse. To determine overall quality and tomato waste, light-red tomatoes were exposed to an optimum temperature (13 °C) and eighteen different time-temperature scenarios, normally encountered during supply chain, and sensory and physicochemical attributes measured at each step. To determine the impact of chilling and non-chilling temperatures normally encountered during tomato supply chain, on the proteome, light-red tomatoes were exposed to an optimum temperature (13 °C) and to two time and temperature supply chain scenarios (2 °C and 25 °C) that showed the most negative impact on tomato overall quality, and physicochemical and proteomic attributes were measured at each step. For the first tomato harvest, the steps with the highest impact on quality and waste were shipping to distribution center (DC; 20°C), cooling at the grower (25°C) and storing at the consumer (4°C). For the second tomato harvest, shipping to the store (2°C), cooling at the farm (10°C) and displaying at the store (20°C) negatively impacted quality. High temperatures during cooling, shipping and store display impacted sensory quality and resulted in increased weight loss, and decreased sugar, carotenoids, and ascorbic acid contents. Although low temperatures during shipping, cooling and consumer did not impact tomato sensory quality, they contributed to a decline in sugar, carotenoids and ascorbic acid contents. Overall, the most impactful steps on tomato quality and waste, regardless of the temperature, were shipping to DC, cooling, shipping to stores, displaying at the store, and consumer storage. Analysis of the differentially expressed proteins in the tomato showed that metabolic proteins were greatly impacted by temperature abuses such as phosphomannomutase, heme oxygenase 1, and MAP kinase; and that proteins regulating cellular membrane integrity such as vacuolar protein sorting-associated protein were also impacted.

Keywords: Arabidopsis thaliana, phytoremediation, abiotic stress, ibuprofene, doxorubicin, two-dimensional electrophoresis Nowadays, develop of the pharmaceutical industry is very fast. Reason of this trend is ever-increasing number of diseases, lifestyle and still increasing demand for the drugs. With this trend growing interest in the analysis of the residues of pharmaceuticals in the environment which is result of incomplete wastewater treatment. This diploma thesis is studying effect of cytostatic drugs, specifically doxorubicin and one of the most widely used analgesics - ibuprofen, at the proteome level of the model plant Arabidopsis thaliana. Proteins isolated from plants exposed to the drugs were separated by two-dimensional electrophoresis. Comparing of protein maps by PDQest program (Bio-Rad, USA) was found several proteins whose expression was affected by the presence of drugs in the culture medium. Selected proteins were identified by LC - MS / MS.

Arid and semi-arid regions, mostly found in developing countries with exponentially increasing populations, are in chronic lack of water thereby severely limiting agricultural production. Irrigation with saline water, which is available in large quantities, could be an obvious solution, but current crops are all salt sensitive. Although major efforts are underway to breed salt tolerant crops, no breakthrough results have yet been obtained. One alternative could rely on plant-interacting microbiota communities. Indeed, rhizophere and endosphere microbial communities are distinct from those of the surrounding soils, and these specific communities contribute to plant growth and health by increasing nutrient availability or plant resistance towards abiotic and biotic stresses. Here we show that plant microbe interactions induce plant tolerance to multiple stresses. From a collection of strains isolated from the desert plant Indigofera argentea, we could identify at least four different strategies to induce salt stress tolerance in Arabidopsis thaliana. A deep analysis of Enterobacter sp. SA187 showed that it induces Arabidopsis tolerance to salinity through activation of the ethylene signaling pathway. Interestingly, although SA187 does not produce ethylene as such, the association of SA187 with plants induces the expression of the methionine salvage pathway in SA187 resulting in the conversion of bacterially produced 2-keto-4-methylthiobutyric acid (KMBA) to ethylene. In addition, a metabolic network characterization of both SA187 and Arabidopsis in their free-living and endophytic state revealed that the sulfur metabolic pathways are strongly upregulated in both organisms. Furthermore, plant genetic experiments verified the essential role of the sulfur metabolism and ethylene signaling in plant salt stress tolerance. Our findings demonstrate how successful plant microbes of a given community can help other plants to enhance tolerance to abiotic stress, and reveal a part of the complex molecular communication process during beneficial plant-microbe interaction.

Movement increases the probability for an individual to find food resources, but also increase the metabolic costs and exposure to predators. Hence, swimming behavior of fish is strongly coupled to fitness. Even though swimming activity has been studied in numerous laboratory settings, less is known about in situ activity and its dependence on abiotic factors (temperature, light conditions and barometric pressure). In this study I hypothesized that the activity increases with 1) increasing temperature and decrease with 2) barometric pressure variability and 3) average light conditions (h/day). In order to test the universality of the three hypotheses I also searched for size dependent effects. Fish activity (km/day) was measured in three lakes on individual fish (N=14-21 per lake) using acoustic telemetry providing tracking of fish at a time resolution from seconds to hours. A positive correlation between temperature and swimming activity in line with my first hypothesis was only observed in one of the lakes. The activity decreased with increased variability in barometric pressure in two of the lakes, a finding supporting my second hypothesis. Meanwhile increased light conditions (h/day) decreased activity in one of the lakes, as predicted by my third hypothesis. Nevertheless, none of my hypotheses were valid in all three of the lakes and perch reacted differently to the abiotic factors. One of the possible explanations for this is the importance of size differences as I noticed that the swimming activity differed between bigger and smaller individuals. My findings suggest that not only the temperature, barometric pressure and light conditions alone predict the activity in perch, but also the fish individual size, predation and the metabolic costs linked to thermoregulation.