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Divergence in seed germination patterns among populations of the same species is important for understanding plant responses to environmental gradients and potential plant sensitivity to climate change. In order to test responses to flooding and decreasing water potentials, over 3 years we germinated and grew seeds from three habitats of Euterpe edulis Mart. occurring along an altitudinal gradient. Seed germination and root growth were evaluated under different water availability treatments: control, flood, -0.4 MPa, -0.8 MPa, in the years 2012, 2013 and 2014, and in the final year of the experiment (2014) at -1.0 MPa and -1.5 MPa. Seeds from the montane habitat did not germinate in the flooding treatment. Seed germination of all three habitats decreased in the -1.5 MPa treatment and the montane habitat had lowest germination in this treatment. Time required for half of the seeds to germinate increased up to -0.8 MPa. Seeds from montane habitats germinated more slowly in all treatments. The only difference in seed germination synchrony was an increase in the submontane population under the flooding treatment. However, synchrony decreased at the lowest water potentials. Roots of the montane population were more vigorous in most treatments, except at -0.8 MPa. The unusual ability of these seeds to germinate at low water potentials might be related to early seed germination at the onset of the rainy season, which potentially decreases seed predation pressure. Seeds of the montane population were more sensitive to both types of water stress. A predicted increase in the frequency and intensity of extreme high rainfall or drought events may predispose early stages of this population to adverse factors that might negatively affect population viability with elevational in future climate change scenarios.

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Biological agents and their metabolic activity produce significant changes over the microstructure and properties of composites reinforced with natural fibers. In the present investigation, oil palm empty fruit bunch (OPEFB) fiber-reinforced acrylic thermoplastic composites were elaborated at three processing temperatures and subjected to water immersion, Prohesion cycle, and continuous salt-fog aging testing. After exposition, microbiological identification was accomplished in terms of fungal colonization. The characterization was complemented by weight loss, mechanical, infrared, and thermogravimetric analysis, as well as scanning electron microscopy. As a result of aging, fungal colonization was observed exclusively after continuous salt fog treatment, particularly by different species of Aspergillus spp. genus. Furthermore, salt spray promoted filamentous fungi growth producing hydrolyzing enzymes capable of degrading the cell walls of OPEFB fibers. In parallel, these fibers swelled due to humidity, which accelerated fungal growth, increased stress, and caused micro-cracks on the surface of composites. This produced the fragility of the composites, increasing Young's modulus, and decreasing both elongation at break and toughness. The infrared spectra showed changes in the intensity and appearance of bands associated with functional groups. Thermogravimetric results confirmed fungal action as the main cause of the deterioration.

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[This corrects the article DOI: 10.3389/fphys.2022.867362.].

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Fiber-reinforced composites are among the most investigated and industrially applied materials. Many studies on these composites using fibers, especially with natural fibers, were made in response to an urgent action for ambient preservation. A particularly relevant situation exists nowadays in the area of materials durability. In this respect, no studies on water-immersion-accelerated aging in fique fiber-epoxy composites are reported. This work aimed to fill this gap by investigating the epoxy matrix composites reinforced with 40 vol% fique fabric. The epoxy matrix and the composite, both unaged and aged, were characterized by weight variation, water absorption, morphology, colorimetry (CIELAB method), Fourier transform infrared spectroscopy (FTIR) and dynamic-mechanical analysis (DMA). The main results were that degradation by water presents appearance of complex microfibril structures, plasticization of epoxy resin, and debonding of the fique fiber/epoxy matrix. The most intense color change was obtained for the water-immersion-aged epoxy by 1440 h. Cole-Cole diagrams revealed the heterogeneity of the materials studied.

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Purpose: To investigate the effect of different water immersion temperatures on the kinetics of blood markers of skeletal muscle damage and the main leukocyte subpopulations. Methods: Eleven recreationally trained young men participated in four experimental sessions consisting of unilateral eccentric knee flexion and 90 min of treadmill running at 70% of peak oxygen uptake, followed by 15 min of water immersion recovery at 15, 28 or 38°C. In the control condition participants remained seated at room temperature. Four hours after exercise recovery, participants completed a performance test. Blood samples were obtained before and immediately after exercise, after immersion, immediately before and after the performance test and 24 h after exercise. The number of leukocyte populations and the percentage of lymphocyte and monocytes subsets, as well as the serum activity of creatine kinase and aspartate aminotransferase were determined. Results: Leukocytosis and increase in blood markers of skeletal muscle damage were observed after the exercise. Magnitude effect analysis indicated that post-exercise hot-water immersion likely reduced the exercise-induced lymphocytosis and monocytosis. Despite reduced monocyte count, recovery by 38°C immersion, as well as 28°C, likely increased the percentage of non-classical monocytes in the blood. The percentage of CD25+ cells in the CD4 T cell subpopulation was possibly lower after immersion in water at 28 and 15°C. No effect of recovery by water immersion was observed for serum levels of creatine kinase and aspartate aminotransferase. Conclusions: Recovery by hot-water immersion likely attenuated the leukocytosis and increased the mobilization of non-classical monocytes induced by a single session of exercise combining resistance and endurance exercises, despite no effect of water immersion on markers of skeletal muscle damage. The monocyte response mediated by hot water immersion may lead to the improvement of the inflammatory response evoked by exercise in the skeletal muscle.

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BACKGROUND: Recovery from training is vital as it ensures training and performance to continue at high intensities and longer durations to stimulate the body and cause further adaptations. OBJECTIVE: To evaluate different methods of post-workout recovery in Paralympic powerlifting athletes. METHODS: Twelve male athletes participated (25.4 ± 3.3 years; 70.3 ± 12.1 kg). The presence of muscle edema, pain threshold, plasma cytokines, and performance measurement were evaluated five times. The recovery methods used in this study were passive recovery (PR), dry needling (DN), and cold-water immersion (CWI). RESULTS: The data analysis showed that the maximal force decreased compared to the pretest value at 15 min and 2 h. The results also revealed that CWI and DN increased Interleukin 2 (IL-2) levels from 24 to 48 h more than that from 2 h to 24 h. After DN, muscle thickness did not increase significantly in any of the muscles, and after 2 h, muscle thickness decreased significantly again in the major pectoralis muscle. After CWI, pain pressure stabilized after 15 min and increased significantly again after 2 h for acromial pectoralis. CONCLUSION: The strength training sessions generate several changes in metabolism and different recovery methods contribute differently to maintain homeostasis in Paralympic powerlifting athletes.

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High-intensity interval training (HIIT) induces vascular adaptations that might be attenuated by postexercise cold-water immersion (CWI). Circulating angiogenic cells (CAC) participate in the vascular adaptations and circulating endothelial cells (CEC) indicate endothelial damage. CAC and CEC are involved in vascular adaptation. Therefore, the aim of the study was to investigate postexercise CWI during HIIT on CAC and CEC and on muscle angiogenesis-related molecules. Seventeen male subjects performed 13 HIIT sessions followed by 15 min of passive recovery (n = 9) or CWI at 10 °C (n = 8). HIIT comprised cycling (8-12 bouts, 90%-110% peak power). The first and the thirteenth sessions were similar (8 bouts at 90% of peak power). Venous blood was drawn before exercise (baseline) and after the recovery strategy (postrecovery) in the first (pretraining) and in the thirteenth (post-training) sessions. For CAC and CEC identification lymphocyte surface markers (CD133, CD34, and VEGFR2) were used. Vastus lateralis muscle biopsies were performed pre- and post-training for protein (p-eNOSser1177) and gene (VEGF and HIF-1) expression analysis related to angiogenesis. CAC was not affected by HIIT or postexercise CWI. Postexercise CWI increased acute and baseline CEC number. Angiogenic protein and genes were not differently modulated by post-CWI. HIIT followed by either recovery strategy did not alter CAC number. Postexercise CWI increased a marker of endothelial damage both acutely and chronically, suggesting that this postexercise recovery strategy might cause endothelial damage. Novelty HIIT followed by CWI did not alter CAC. HIIT followed by CWI increased CEC. Postexercise CWI might cause endothelial damage.

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Cold water immersion (CWI) has become a highly used recovery method in sports sciences, which seeks to minimize fatigue and accelerate recovery processes; however, tensiomyography (TMG) is a new method to analyze the muscle mechanical response as a recovery indicator after CWI protocols, this relative new tool of muscle function assessment, can lead to new information of understand fatigue recovery trough CWI. The objective of the study was to compare the effect of two CWI protocols, on neuromuscular function recovery. Thirty-nine healthy males (21.8 ± 2.8 years, 73.2 ± 8.2 kg, 176.6 ± 5.3 cm and body fat 13.5 ± 3.4%) were included in the study. Participants were grouped into a continuous immersion (12 min at 12 ± 0.4°C) group, intermittent immersion (2 min immersion at 12 ± 0.4°C + 1 min out of water 23 ± 0.5°C) group, and a control group (CG) (12 min sitting in a room at 23 ± 0.5°C). Afterward, the participants performed eight sets of 30 s counter movement jumps (CMJs) repetitions, with a 90 s standing recovery between sets. Muscle contraction time (Tc), delay time (Td), muscle radial displacement (Dm), muscle contraction velocity at 10% of DM (V10), and muscle contraction velocity at 90% of DM (V90) in rectus, biceps femoris, and CMJ were measured. Neither CWI protocol was effective in showing improved recovery at 24 and 48 h after training compared with the CG (p > 0.05), in any TMG indicator of recovery in either muscle biceps or rectus femoris, nor was the CMJ performance (F(6,111) = 0.43, p = 0.85, ωp2 = 0). Neither CWI protocol contributed to recovery of the neuromuscular function indicator.

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When exercises are done in intense or exhaustive modes, several acute biochemical mechanisms are triggered. The use of cryotherapy as cold-water immersion is largely used to accelerate the process of muscular recovery based on its anti-inflammatory and analgesic properties. The present study aimed to study the biochemical effects of cold-water immersion treatment in mice submitted to exercise-induced exhaustion. Swiss albino mice were divided into 4 treatment groups: control, cold-water immersion (CWI), swimming exhaustive protocol (SEP), and SEP+CWI. Treatment groups were subdivided into times of analysis: 0, 1, 3, and 5 days. Exhaustion groups were submitted to one SEP session, and the CWI groups submitted to one immersion session (12 min at 12°C) every 24 h. Reactive species production, inflammatory, cell viability, and antioxidant status were assessed. The SEP+CWI group showed a decrease in inflammatory damage biomarkers, and reactive species production, and presented increased cell viability compared to the SEP group. Furthermore, CWI increased acetylcholinesterase activity in the first two sessions. The present study showed that CWI was an effective treatment after exercise-induced muscle damage. It enhanced anti-inflammatory response, decreased reactive species production, increased cell viability, and promoted redox balance, which could decrease the time for the recovery process.

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This study aims to evaluate the effect of regular post-exercise cold water immersion (CWI) on intramuscular markers of cellular stress response and signaling molecules related to mitochondria biogenesis and exercise performance after 4 weeks of high intensity interval training (HIIT). Seventeen healthy subjects were allocated into two groups: control (CON, n = 9) or CWI (n = 8). Each HIIT session consisted of 8-12 cycling exercise stimuli (90-110 % of peak power) for 60 s followed by 75 s of active recovery three times per week, for 4 weeks (12 HIIT sessions). After each HIIT session, the CWI had their lower limbs immersed in cold water (10 °C) for 15 min and the CON recovered at room temperature. Exercise performance was evaluated before and after HIIT by a 15-km cycling time trial. Vastus lateralis biopsies were obtained pre and 72 h post training. Samples were analyzed for heat shock protein 72 kDa (Hsp72), adenosine monophosphate-activated protein kinase (AMPK), and phosphorylated p38 mitogen-activated protein kinase (p-p38 MAPK) assessed by western blot. In addition, the mRNA expression of heat shock factor-1 (HSF-1), peroxisome proliferator-activated receptor gamma coactivator-1α (PGC-1α), nuclear respiratory factor 1 and 2 (NRF1 and 2), mitochondrial transcription factor A (Tfam), calcium calmodulin-dependent protein kinase 2 (CaMK2) and enzymes citrate synthase (CS), carnitine palmitoyltransferase I (CPT1), and pyruvate dehydrogenase kinase (PDK4) were assessed by real-time PCR. Time to complete the 15-km cycling time trial was reduced with training (p < 0.001), but was not different between groups (p = 0.33). The Hsp72 (p = 0.01), p38 MAPK, and AMPK (p = 0.04) contents increased with training, but were not different between groups (p > 0.05). No differences were observed with training or condition for mRNA expression of PGC-1α (p = 0.31), CPT1 (p = 0.14), CS (p = 0.44), and NRF-2 (p = 0.82). However, HFS-1 (p = 0.007), PDK4 (p = 0.03), and Tfam (p = 0.03) mRNA were higher in CWI. NRF-1 decrease in both groups after training (p = 0.006). CaMK2 decreased with HIIT (p = 0.003) but it was not affected by CWI (p = 0.99). Cold water immersion does not alter HIIT-induced Hsp72, AMPK, p38 MAPK, and exercise performance but was able to increase some markers of cellular stress response and signaling molecules related to mitochondria biogenesis.

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Introducción: El dolor y las dificultades técnicas constituyen un problema al realizar la colonoscopia estándar. El empleo de agua en la colonoscopia es una técnica que facilita la inserción del instrumento y se relaciona con mejor tolerabilidad por el paciente. Objetivo: comparar la colonoscopia de inmersión modificada con la colonoscopia estándar como mejor técnica y uso de menos sedación en niños. Pacientes y Método: estudio prospectivo y aleatorizado, desde septiembre de 2012 a marzo de 2013. Grupo A: inmersión con agua e insuflación. Grupo B: con insuflación (estándar). Se evaluó la tasa de intubación cecal y tiempo de intubación cecal, sedación adicional, analgesia y tolerabilidad del paciente considerando la presencia de dolor. Resultados: Grupo A: 10 niños, edad promedio 6,6 años (rango: 2-11), 76,92% varones. Grupo B: 13 niños, edad promedio: 6,3 años (rango: 2-12), 70% varones. La indicación más frecuente del estudio fue rectorragia en ambos grupos. La tasa de intubación del ciego, en el grupo A fue 80% frente a 61,53% del grupo B, OR=2,5 (IC 95%= 0,37-16,89), El tiempo promedio de intubación del ciego en el grupo A fue 9,18 minutos + 3,51 y en el grupo B 13,97 minutos + 4,88, sin diferencia significativa (p=0.2362). Sedación adicional y administración de bromuro de butilhioscina fue requerida en 1/9(10%) del grupo A y en 8/13(61,53%) del grupo B, con una diferencia significativa (p=0.0288), con mejor tolerabilidad del procedimiento en el grupo A. Conclusiones: la técnica de agua e insuflación en la colonoscopia en niños se asoció a menor sedación y mejor tolerabilidad del procedimiento. La aplicación de la técnica en un grupo más numeroso permitirá establecer un mejor tiempo y éxito en la intubación cecal.

Introduction: Pain and technical difficulties are a problem when performing standard colonoscopy. The use of water in colonoscopy is a technique that facilitates insertion of the instrument and is associated with better tolerated by the patient. Objective: To compare the modified immersion colonoscopy versus standard colonoscopy as better technical and use less sedation in children. Patients and Methods: A prospective, randomized study, from September 2012 to March 2013. Group A: immersion in water and air insuffl ation. Group B: with insufflation (standard). We evaluated the rate cecal intubation, cecal intubation time, additional sedation, analgesia and tolerability considering the presence of pain. Results: Group A: 10 children, mean age 6.6 years (range: 2-11), 76.92% males. Group B: 13 children, mean age 6.3 years (range: 2-12), 70% male. The most frequent indication was rectal bleeding in both groups. The cecal intubation rate in group A was 80% compared to 61.53% in group B, OR = 2.5 (95% CI = 0.37 to 16.89), The average cecal intubation in group A was 9,18 minutes + 3,51 y en el grupo B 13,97 minutes + 4,88, without significant difference (p = 0.2362). Additional sedation Butylscopolamine bromide administration was required in 1/9 (10%) in group A and in 8/13 (61.53%) in group B, with a significant difference (p = 0.0288), with better tolerability process in group A. Conclusions: technique of water and air insuffl ation on colonoscopy in children was associated with less sedation and better tolerability of the procedure. The application of the technique in a larger group will establish a better time and cecal intubation success.

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Water may influence the mechanical properties of the acrylic resins. Thus, the effect of water storage on the impact strength (IS) of one denture base (Lucitone 550 - L) and four reline resins (Tokuyama Rebase II - T; UfiGel Hard - U; Kooliner - K; New Truliner - NT) was evaluated. Bars of L were made (60 x 6 x 2 mm) and relined (2 mm) with T, U, K, NT and L. Intact specimens of each material (60 x 6 x 4 mm) were also fabricated for comparative purposes. Specimens were submitted to Charpy impact tests without water storage (control) and after immersion in water for 7, 90 and 180 days. Data (kJ/m²) analyzed by two-way ANOVA and Tukey's test (p=0.05) revealed that after 90 days, U exhibited an increase in the IS (0.93) compared to 7 days (0.58). K (1.48) and L/K (7.21) exhibited a decrease at the 7-day period (1.01 and 3.23, respectively). NT (0.60) showed an increase in the IS after 180 days (1.52), whereas L/NT (7.70) showed a decrease (3.17). Water immersion improved the IS of U and NT, and decreased the IS of K, L/K, and L/NT. Water may affect differently the IS of acrylic resins and, consequently, the resistance to fracture of relined denture bases.

A água pode influenciar as propriedades mecânicas das resinas acrílicas. Assim, o efeito do armazenamento em água na resistência ao impacto (RI) de uma resina para base de prótese (Lucitone 550-L) e quatro materiais reembasadores (Tokuyama Rebase II-T; UfiGel Hard-U; Kooliner-K; New Truliner-NT) foi avaliado. Barras da resina L foram confeccionadas (60 x 6 x 2 mm) e reembasadas (2 mm) com T, U, K, NT e L. Amostras não reembasadas de cada material também foram confeccionadas (60 x 6 x 4 mm) para fins comparativos. As amostras foram submetidas aos testes de impacto tipo Charpy sem armazenamento (controle) e após imersão em água por 7, 90 e 180 dias. Os resultados (kJ/m²) analisados por meio de ANOVA dois fatores e teste de Tukey (p=0,05) revelaram que, após 90 dias, U exibiu aumento na RI (0,93) comparado com 7 dias (0,58). K (1,48) e L/K (7,21) exibiram diminuição no período de 7 dias (1,01 e 3,23, respectivamente). NT (0,60) apresentou aumento na RI após 180 dias (1,52), enquanto L/NT (7,70) apresentou redução (3,17). A imersão em água melhorou a RI de U e NT e diminuiu a RI de K, L/K, e L/NT. A água pode afetar de maneira diversa a RI das resinas acrílicas e, consequentemente, a resistência à fratura das bases de próteses reembasadas.

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O estresse sistêmico induzido pelo exercício libera substâncias bioativas determinantes da mobilização neutrofílica. A crioterapia diminui a reação inflamatória e atenua a elevação da perfusão sanguínea induzida pelo exercício. O objetivo deste trabalho foi analisar a influência da hipotermia decorrente da crioimersão corporal (CIC) imediata ao esforço físico agudo nas concentrações neutrofílicas e linfocíticas no sangue. Os ratos do grupo controle (AI) foram mantidos em repouso enquanto os do grupo AII foram submetidos ao protocolo de CIC a 10ºC por 10 minutos. Enquanto os animais dos grupos BI, BII, BIII e BIV realizaram o esforço físico agudo (EFA) em água a 31ºC durante 100 minutos com sobrecarga corpórea de 5% do peso corporal, os dos grupos CI, CII, CIII e CIV foram submetidos ao EFA seguido imediatamente de CIC. Nos grupos B e C, os animais foram sacrificados nos períodos de 06 (I), 12 (II), 24 (III) e 48 (IV) horas posteriores ao EFA. Através da microscopia óptica realizou-se a contagem dos neutrófilos e linfócitos. Utilizou-se do Teste T Student para análise estatística considerando-se nível de significância p < 0,05. Observou-se uma significativa neutrofilia nos grupos AII, BI, BII, BIII, BIV, CI, CII e CIII em relação a AI, diferentemente do grupo CIV, que apresentou quantidade de neutrófilos igual ao grupo controle. Os valores de linfócitos nos grupos BII, BIII, BIV, CI e CII foram significativamente menores do que AI, e nos grupos AII, BI, CIII e CIV foram iguais a AI. A neutrofilia e a linfopenia posteriores ao intenso exercício agudo são mantidas por 48 horas ou mais, porém, mediante a aplicação da crioimersão corporal imediata ao exercício, são normalizadas em 24 horas.

Systemic stress induced by exercise increases bioactive substances in plasma which leads to neutrophilic mobilization. Cryotherapy causes a decrease in the inflammatory reaction and attenuates high blood perfusion after exercise. The objective of this work was to analyze the influence of cold water immersion (CWI) after acute exercise on neutrophil and lymphocyte mobilization. A control group of rats (AI) was kept at rest and a second group (AII) was submitted to CWI at 10º C for 10 minutes. The animals of Groups BI, BII, BIII and BIV were submitted to acute exercise which consisted in swimming in water at 31º C for 100 minutes with a load equivalent to 5% of the body weight. Groups CI, CII, CIII and CIV were submitted to CWI immediately after acute exercise. The animals were sacrificed at 6 (I), 12 (II), 24 (III) and 48 (IV) hours after the exercise and neutrophil and lymphocyte cells were counted for all groups by optic microscopy. The Student t-test was used for statistical analysis with a significance level of p< 0.05. A significant increase in the number of neutrophils was observed in Groups AII, BI, BII, BIII, BIV, CI, CII and CIII compared to AI. The neutrophil count of the CIV Group was similar to the Control Group. There was a significant drop in the number of lymphocytes in Groups BII, BIII, BIV, CI and CII when compared to Group AI. The lymphocyte count of Groups AII, BI, CIII and CIV were similar to the Control Group. The changes in neutrophil and lymphocyte counts caused by acute exercise were reverted to normal at 24 hours by cold water immersion.

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O objetivo deste estudo foi analisar o efeito da imersão sobre VO2 de repouso (ml/kg/min). A amostra foi composta por 6 mulheres praticantes de hidroginástica (idade: 21,3 ± 1,03 anos, massa corporal: 57 ± 4,29 kg, estatura: 164,5 ± 4,09 cm), avaliadas em diferentes situações experimentais (SE) na seguinte ordem: 20 minutos em repouso em decúbito dorsal fora da água (DD); 5 minutos na posição ortostática fora da água (OF) e 3 minutos em repouso na posição ortostática com imersão ao nível do processo xifóide (OI). Cada SE foi realizada em três dias diferentes, com intervalo de 48 horas, a fim de avaliar o efeito da variação metabólica dos indivíduos. A temperatura da água variou entre 32 e 33 °C. Para a coleta de VO2 foi utilizado o analisador de gases Aerosport KB1- C. Utilizou-se ANOVA para medidas repetidas e ANOVA One Way (Bonferroni) (p<0,05). Não foram encontradas diferenças estatisticamente significativas entre as mesmas SE nos três dias de coleta. Dessa forma, os dados das SE semelhantes foram somadas e suas médias utilizadas para comparação entre diferentes SEs. Encontramos um aumento no VO2 de DD (3,17 ± 0,34) para OF (3,62 ± 0,36) e dessa para a OI (3,98 ± 0,44), entretanto foram encontradas diferenças significativas somente entre a DD e OI. A imersão no processo xifóide na temperatura avaliada provocou aumento significativo do VO2 em repouso nos 3 primeiros minutos de imersão somente com a associação da mudança de posição corporal.

The aim of this study was to analyse the effect of immersion over rest VO2. The sample complised of six women that practice water exercise, aging 21.3 ± 1.03 years, body mass 57 ± 4.29 kg, height 164 ± 4.09 cm, which were evaluated in the following experimental situations: 20 minutes of rest in dorsal decumbant outside the water (DD); 5 minutes of orthostatic position outside the water (OO); and 3 minutes of rest in orthostatic position under immersion at the xyphoid process level (OI). Each experimental situation was procceeded in three days, with intervals of 48 hours, to evaluate the effect of metabolic variation of the individuals. The water temperature varied between 32 and 33oC. The VO2 analyses were done through a KB1-C Aerosport gás analyser. Repeted measurements and One Way ANOVA (Bonferroni) (p<0.05) were used for statistical analysis. There were no statistically significant differences among the same experimental situations. These datas were added and your means used for comparison among different experimental situations. There was a raise of VO2 in DD (3.17 ± 0.36) when compared to OO (3.62 ± 0.34), which was different than the OI (3.98 ± 0.44), but the differences were significant only for the first and third experimental situations. Water immersion of xyphoid process in the temperature used caused a significant raise of VO2 under rest during the three firts minutes of immersion only with the association of a change in body position.

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