A mycological baseline study based on a multidisciplinary approach in a coastal area affected by contaminated torrent input.

Fungi include a vast group of eukaryotic organisms able to colonise different natural, anthropised and extreme environments, including marine areas contaminated by metals. The present study aims to give a first multidisciplinary characterisation of marine bottom sediments contaminated by metals (Cd, Co, Cr, Cu, Ni, and Zn), originating in the water leakage from an abandoned Fe-Cu sulphide mine (Libiola, north-western Italy), and evaluate how the chemical and physical parameters of water and sediments may affect the benthic fungal communities. Our preliminary results showed the high mycodiversity of the marine sediments studied (13 genera and 23 species of marine fungi isolated), and the great physiological adaptability that this mycobiota evolved in reaction to the effects of the ecotoxic bottom sediment contamination, and associated changes in the seawater parameters.

Environmental complexity of a port: Evidence from circulation of the water masses, and composition and contamination of bottom sediments.

Ports are complex environments due to their complicated geometry (quays, channels, and piers), the presence of human activities (vessel traffic, shipyards, industries, and discharges), and natural factors (stream and torrent inputs, sea action, and currents). Taking these factors into consideration, we have examined the marine environment of a port from the point of view of the circulation of the water masses, hydrological characteristics, distribution of the sediment grain-size, mineralogical characteristics, and metal concentrations of the bottom sediments. Our results show that, in the case of the Port of Genoa (north-western Italy), the impact of human activities (such as a coal power-plant, oil depots, shipyards, dredging of the bottom sediments, etc.), natural processes (such as currents, fresh water and sediment inputs from the torrents), and the morphology of the basin, are important factors in the sediment, water, and metal distributions that have given rise to a complex environment.

Marine sediment contamination and dynamics at the mouth of a contaminated torrent: The case of the Gromolo Torrent (Sestri Levante, north-western Italy).

In this study we have examined the currents and hydrological characteristics of the water column off the mouth of the Gromolo Torrent (north-western Italy) in relation to the grain-size, mineralogical characteristics and metal distribution in the marine sediment sampled. Our purpose was to quantify and map the contamination that was carried out to sea from the abandoned Libiola Fe-Cu sulphide mine that has heavily impacted the torrent. Our results show high concentrations of Cu and Zn, and relatively high concentrations of Cd and Ni inside the bay into which the Gromolo Torrent flows. However, high concentrations of As, Cr, Hg, Mn, Pb, and V found in the northern and/or eastern parts of the study area originated from other sources. The subdivision of study stations in terms of metal and mineral contents in the bottom sediments highlighted the clear influence of the currents on their dispersion and distribution in the area.

Effect of temperature on the release and remobilization of ecotoxic elements in AMD colloidal precipitates: the example of the Libiola copper mine, Liguria, (Italy).

Due to their characteristics, colloidal particles are able to control the dispersion of many organic and inorganic pollutants in soils and streams. Colloidal precipitates generated by acid mine drainage (AMD) process are usually amorphous or nanocrystalline materials, and their stability plays a crucial role in controlling the fate of metals released by sulphide oxydation. This paper describes a study of elements release (Fe, Al, Mn, Cd, Co, Cr, Cu, Ni, S, Zn) due to desorption or destabilization of three different colloidal precipitates, two ochreous and a greenish-blue precipitate, sampled at the Libiola mine site (northwest Italy). The samples were heated at high temperature in order to verify this treatment as inertization process. At room temperature, the most easily extracted element was S (with released percentages from 8.39 to 29.17 %), but considerable amounts of Cu, Zn and Mn (up to 16.6, 610.6 and 595.6 mg/kg, respectively) were also observed in the leachates for greenish-blue precipitates. The highest release of elements (S > Cu, Zn, Mn, Cd > Co, Ni > Al, Fe, Cr), with minor differences depending on the mineralogical composition of the samples, was observed for heat-treated samples obtained through moderate heating and mainly formed by anhydrous phases. Samples treated at high temperature had the lowest release, with only Cu showing a significant concentration in the leachate of greenish-blue precipitates. The results showed that dissolution/desorption is limited from ochreous natural colloidal precipitates occurring at the Libiola mine site but also that high amounts of some metals can be remobilized from greenish-blue precipitates. The destabilization of all percipitates through dehydratation-dehydroxylation can further remobilize important amounts of ecotoxic elements. Heat treatment at high temperature could be a definitive, although expensive, way to fix heavy metals in the solid fraction, preventing their dispersion in the surrounding environment.

Evaluation of the boundary condition influence on PAH concentrations in the water column during the sediment dredging of a port.

The mobilisation of sediments and related contaminants connected to dredging activities is one of the most critical issues to the environmental risk and exposure assessment of a dredging project. The aim of this paper was an investigation of the mobilisation of polycyclic aromatic hydrocarbons (PAHs) due to the dredging of the Port of Genoa (Italy) to identify the temporal and spatial extent of the contaminant transport, and the influence of the dredging and the boundary conditions on it. The results showed relatively low background PAH concentrations in the water column and confirmed the dredging as the primary rising factor of concentrations in the water column, but also showed a complex scenario in which the different environmental and dredging factors forced the concentrations at different levels and moments. The post dredging phase showed PAH values close to the background conditions and the concentrations remained relatively high only for a few PAHs.

The Effect of Hydrofluoric Acid Concentration on the Bond Strength and Morphology of the Surface and Interface of Glass Ceramics to a Resin Cement.

The purpose of this study was to evaluate the influence of various concentrations of hydrofluoric acid (HF) on the surface/interface morphology and µ-shear bond strength (µSBS) between IPS Empress Esthetic (EST) (Ivoclar Vivadent) and IPS e.max Press (EMX) (Ivoclar Vivadent) ceramics and resin cement. Ceramic blocks were divided into 12 groups for each kind of ceramic. Six different HF concentrations were evaluated: 1%, 2.5%, 5%, 7.5%, 10%, and 15%. All groups were silanated after etching, and half of the specimens within each group received a thin layer of unfilled resin (UR). Three resin cement cylinders were prepared on each ceramic block for µSBS testing. The specimens were stored in distilled water at 37°C for 24 hours. The µSBS test was carried out in a universal testing machine at a crosshead speed of 0.5 mm/min until fracture. The data were submitted to three-way analysis of variance and multiple comparisons were performed using the Tukey post hoc test (p<0.05). The etched surfaces and bonded interfaces were evaluated using scanning electron microscopy. µSBS means (MPa) for 1%, 2.5%, 5%, 7.5%, 10%, and 15% HF concentrations were, respectively, 25.2, 27.2, 30.1, 31.4, 33.3, and 31.8. µSBS means with or without UR application measured 32.24 and 27.4, respectively; EST and EMX measured 29.8 and 29.9, respectively. For the HF concentrations, 10% and 15% showed higher µSBS means than did 1% and 2.5% (p<0.05); 7.5% was higher than 1% (p<0.05); and no statistical differences were found among the other concentrations (p>0.05). When evaluating UR, µSBS mean was significantly higher and better infiltration was observed on the etched surfaces. No statistical difference was found between the ceramics. The HF concentration and UR influenced the bond strength and surface/interface morphology.

Effect of simulated microwave disinfection on the linear dimensional change, hardness and impact strength of acrylic resins processed by different polymerization cycles.

AIM: This study investigated the effect of simulated microwave disinfection (SMD) on the linear dimensional changes, hardness and impact strength of acrylic resins under different polymerization cycles. METHDOS: Metal dies with referential points were embedded in flasks with dental stone. Samples of Classico and Vipi acrylic resins were made following the manufacturers' recommendations. The assessed polymerization cycles were: A) water bath at 74 ºC for 9 h; B) water bath at 74 ºC for 8 h and temperature increased to 100 ºC for 1 h; C) water bath at 74 ºC for 2 h and temperature increased to 100 ºC for 1 h; and D) water bath at 120 ºC and pressure of 60 pounds. Linear dimensional distances in length and width were measured after SMD and water storage at 37 ºC for 7 and 30 days using an optical microscope. SMD was carried out with the samples immersed in 150 mL of water in an oven (650 W for 3 min). A load of 25 gf for 10 s was used in the hardness test. Charpy impact test was performed with 40 kpcm. Data were submitted to ANOVA and Tukey's test (5%). RESULTS: The Classico resin was dimensionally steady in length in the A and D cycles for all periods, while the Vipi resin was steady in the A, B and C cycles for all periods. The Classico resin was dimensionally steady in width in the C and D cycles for all periods, and the Vipi resin was steady in all cycles and periods. The hardness values for Classico resin were steady in all cycles and periods, while the Vipi resin was steady only in the C cycle for all periods. Impact strength values for Classico resin were steady in the A, C and D cycles for all periods, while Vipi resin was steady in all cycles and periods. CONCLUSION: SMD promoted different effects on the linear dimensional changes, hardness and impact strength of acrylic resins submitted to different polymerization cycles when after SMD and water storage were considered.

Effect of simulated microwave disinfection on the linear dimensional change, hardness and impact strength of acrylic resins processed by different polymerizing cycles.

AIM: This study investigated the effect of simulated microwave disinfection (SMD) on the linear dimensional changes, hardness and impact strength of acrylic resins under different polymerization cycles. METHODS: Metal dies with referential points were embedded in flasks with dental stone. Samples of Classico and Vipi acrylic resins were made following the manufacturers' recommendations. The assessed polymerization cycles were: A-- water bath at 74ºC for 9 h; B-- water bath at 74ºC for 8 h and temperature increased to 100ºC for 1 h; C-- water bath at 74ºC for 2 h and temperature increased to 100ºC for 1 h;; and D-- water bath at 120ºC and pressure of 60 pounds. Linear dimensional distances in length and width were measured after SMD and water storage at 37ºC for 7 and 30 days using an optical microscope. SMD was carried out with the samples immersed in 150 mL of water in an oven (650 W for 3 min). A load of 25 gf for 10 sec was used in the hardness test. Charpy impact test was performed with 40 kpcm. Data were submitted to ANOVA and Tukey's test (5%). RESULTS: The Classico resin was dimensionally steady in length in the A and D cycles for all periods, while the Vipi resin was steady in the A, B and C cycles for all periods. The Classico resin was dimensionally steady in width in the C and D cycles for all periods, and the Vipi resin was steady in all cycles and periods. The hardness values for Classico resin were steady in all cycles and periods, while the Vipi resin was steady only in the C cycle for all periods. Impact strength values for Classico resin were steady in the A, C and D cycles for all periods, while Vipi resin was steady in all cycles and periods. CONCLUSION: SMD promoted different effects on the linear dimensional changes, hardness and impact strength of acrylic resins submitted to different polymerization cycles when after SMD and water storage were considered.

Comparison between two methods to evaluate temperature changes produced by composite light curing units and polymerization techniques.

AIM: This study evaluated the temperature change into the pulp chamber during the light curing of composite resin by direct (bovine tooth) and indirect (matrix) methods. METHODS: Direct method: fifty standardized cavities (2x2x2 mm) were prepared in bovine incisors, which were randomly assigned to evaluation of the temperature changes in the pulp chamber. Indirect method: temperature changes were evaluated through a dentine slice of 1.0 mm thickness in a elastomer cubic mold (2x2x2 mm). Filtek Z250 composite resin (3M/ESPE) was photo-activated using three light curing units: quartz-tungsten-halogen (QTH) by continuous, soft-start or intermittent light modulations; light emitting diode (LED); and plasma arc-curing (PAC). Ten groups (N.=10) were established according to technique evaluation and photo-activation methods. All experiments were carried out in a controlled environment (37 °C and 50 ± 10% relative humidity). The temperature changes were recorded using a digital thermometer attached to a type-K thermocouple in contact with the dentin slice (indirect method) or in contact with the axial wall (dentin) of pulp chamber (direct method). The results were submitted to ANOVA and Tukey's test (α=0.05). RESULTS: Temperature changes were statistically higher for the matrix indirect method (2.56 ºC) than bovine teeth direct method (1.17ºC). The change temperature was statistically higher for the PAC (1.77 ºC) when compared to other photo-activation modes in bovine teeth direct method. CONCLUSION: The two methods of temperature evaluation were different, however indirect method detected the higher temperature increase. Higher energy density arising from the light curing units and polymerization techniques promoted higher temperature increase.

Assessment of the polymerization contraction stress of composites photoactivated by halogen light and light-emitting diode.

AIM: The aim of this study was to compare the polymerization contraction stress of composites photoactivated by two light sources: quartz tungsten halogen light (QTH) and light emitting diode (LED). METHODS: Glass rods were fabricated (5.0 mm X 5.0 cm) and one of the surfaces was air abraded with aluminum oxide. An adhesive was applied to this surface and photoactivated by LED. The glass rods were assembled to a Universal Testing machine (Instron - 5565) and the composite were applied to the lower rod using a manual instrument. The upper rod was placed closer, at 2 mm, and an extensometer was attached to the rods. The twenty composites were polymerized by either by QTH (N.=10) or LED (N.=10). Polymerization was carried out using two apparatuses positioned in opposite sides, which were simultaneously activated for 30 seconds. Contraction stress was analyzed twice: shortly after polymerization (t30s) and 30 minutes later (t30min). RESULTS: The contraction stress for all composites was higher at t30min than at t30s, regardless of the activation source. Z100 showed lower contraction stress values (P<0.05) compared to the other composites. Regarding to Charisma and TPH, the photoactivation source had no influence on contraction stress, except for Z100 at t30min. CONCLUSIONS: It was concluded that composite composition is the factor that most influence the polymerization contraction stress.

Radiopacity of root filling materials using digital radiography.

AIM: To evaluate radiopacity of root filling materials using digital radiography. METHODOLOGY: The sealers tested were AH Plus, Endofill, EndoREZ and Epiphany. Gutta-percha (Dentsply Maillefer) and Resilon cones were also tested. Acrylic plates, containing six wells, measuring 1 mm in depth and 5 mm in diameter, were prepared for the test, and filled with the materials. The test samples were radiographed together with an aluminium stepwedge calibrated in millimetres, according to ANSI/ADA Specification 57. For the radiographic exposures, digital imaging plates and an X-ray machine at 70 kVp and 8 mA were used. The object-to-focus distance was 30 cm, and the exposure time, 0.2 s. After the laser optic reading process, the software determined the radiopacity of the standardized areas, using grey-scale values, calculating the average radiographic density for each material. RESULTS: The decreasing values of radiopacity of the studied materials, expressed in millimetres of aluminium equivalent, were: Resilon (13.0), AH Plus(TM) (11.2), gutta-percha (9.8), Epiphany (8.0), Endofill (6.9) and EndoREZ (6.6). CONCLUSION: All materials had radiopacity values above 3 mm of aluminium recommended by ANSI/ADA Specification 57.

Influence of flask closure and flask cooling methods on tooth movement in maxillary dentures.

PURPOSE: This study investigated the tooth movement of standardized simulated dentures processed by traditional closure or the new Rafael Saide (RS) tension system when cooled in the curing water itself or in curing water followed by bench storage for 3 hours. MATERIALS AND METHODS: Forty stone casts were formed from a mold of an edentulous maxillary arch. The wax denture record bases were made on the casts; the height of the wax rim occlusion was 20 mm in the labial sulcus of the cast and 10 mm in the posterior region. The upper stone cast was mounted on a Mondial 4000 semi-adjustable articulator with wax rim interocclusal references in relation to the lower stone cast teeth. Metallic pins were placed in the incisal border of the maxillary central incisors (I), labial cusp of the first premolars (PM), and mesiolabial cusp of the second molars (M). The incisor-to-incisor (I-I), premolar-to-premolar (PM-PM), and molar-to-molar (M-M) transversal distances and left incisor-to-left molar (LI-LM), and right incisor-to-right molar (RI-RM) anteroposterior distances were measured before and after denture polymerization with an optical microscope with a tolerance of 0.0005 mm. For traditional closure, the dentures were flasked conventionally in standard metallic flasks, which were afterward placed in spring clamps. For the new RS system closure, the flasks were pressed between the metallic plates of the tension system after the final closure. The Clássico heat-polymerizing acrylic resin dough was packed in the flasks under a final packing pressure of 1.250 kg f. Twelve hours after flask closure, the dentures were polymerized in a moist heat-polymerizing cycle for 9 hours at 74 degrees C. The denture was deflasked after cooling in the water of the polymerizing cycle (groups A and C) or in the water of the polymerizing cycle and then bench-stored for 3 hours (groups B and D). Collected data were analyzed with analysis of variance and Tukey's test (p< 0.05). RESULTS: There was no statistically significant difference (p> 0.05) between the conventional and new RS system closure methods for the transversal distances after polymerization in all studied groups. The anteroposterior distances did not change with deflasking after water bath cooling. There were statistically significant differences (p< 0.05) in the anteroposterior distances with deflasking after water bath cooling and then bench storage for 3 hours. CONCLUSION: Tooth movement was similar in dentures processed by traditional closure and by the new RS tension system, with the exception of the anteroposterior distances when the flasks were cooled in their own curing water and bench-stored for 3 hours.

Halogen and LED light curing of composite: temperature increase and Knoop hardness.

This study assessed the Knoop hardness and temperature increase provided by three light curing units when using (1) the manufacturers' recommended times of photo-activation and (2) standardizing total energy density. One halogen--XL2500 (3M/ESPE)--and two light-emitting diode (LED) curing units--Freelight (3M/ESPE) and Ultrablue IS (DMC)--were used. A type-K thermocouple registered the temperature change produced by the composite photo-activation in a mold. Twenty-four hours after the photo-activation procedures, the composite specimens were submitted to a hardness test. Both temperature increase and hardness data were submitted to ANOVA and Tukey's test (5% significance). Using the first set of photo-activation conditions, the halogen unit produced a statistically higher temperature increase than did both LED units, and the Freelight LED resulted in a lower hardness than did the other curing units. When applying the second set of photo-activation conditions, the two LED units produced statistically greater temperature increase than did the halogen unit, whereas there were no statistical differences in hardness among the curing units.

Influence of number and position of flasks in the monomer release, Knoop hardness and porosity of a microwave-cured acrylic resin.

Simultaneous irradiation of multiple flasks may have deleterious effects on the polymerization of microwave cured-acrylic resins. This study evaluated the effect of the number and position of flasks in the monomer release, Knoop hardness and porosity of a microwave-cured acrylic resin. Samples were made of Acron MC(R) (AMC, GC Dent. Ind. Corp.) processed at 500 W. The following associations of the number and position of the flasks were tested: one simple flask centrally placed on the turning plate (I, control); two flasks, one in the centre (IIa) and the other peripherally placed in the plate (IIb); two flasks centrally, one above (IIIa) and the other below (IIIb). The processing time varied according to the number of flasks: 3 or 4.5 min for one or two flasks, respectively. For monomer release, each specimen (n = 12) was put in an assay glass tube containing 6 mL of deionized water that was changed daily. Monomer levels were obtained by spectrophotometry at 206 nm. For hardness test (n = 10), 12 indentations were made in the surface of each specimen. Immersing the polished specimens in permanent ink and counting the porous in a stereo light microscope verified the porosity. Monomer release was significant before 24 h: GI = 263.1(153.3)a, GIIa = 236.9(180.2)a, GIIb = 441.5(446.2)a, GIIIa = 1216.6(857.9)b. Tukey test showed no statistically significant differences among the groups for porosity and hardness. Monomer release was affected by the position of the flask (P < 0.05).

Effect of the photo-activation method on polymerization shrinkage of restorative composites.

This study measured the gap that resulted from polymerization shrinkage of seven restorative resin composites after curing by three different methods. Contraction behavior, according to the specimen region, was also characterized. The materials used for this study were Alert (Jeneric/Pentron, Wallingford, CT 06492, USA), Surefil (Dentsply Caulk, Milford, DE 19963, USA), P60 (3M Dental Products, St Paul, MN 55144, USA), Z250 (3M), Z100 (3M), Definite (Degussa-Hüls, Hanau, Germany) and Flow-it (Jeneric/Pentron). The composite was placed in a circular brass mold 7 mm in diameter and 2 mm in height. Photo-activation was performed by a) continuous light (500 mW/cm2) for 40 seconds; b) stepped light with low intensity (150 mW/cm2) for 10 seconds and high intensity (500 mW/cm2) for 30 seconds and c) intermittent light (450 mW/cm2) for 60 seconds. The top and bottom surfaces were then polished and after 24 +/- 1 hours, the contraction gap was measured by SEM at variable pressure (LEO 435 VP, Cambridge, England). Results were analyzed by ANOVA and the means compared by Tukey's test (5%). The results demonstrated 1) the continuous light method presented the greatest gap values (15.88 microm), while the other methods demonstrated lower polymerization shrinkage values (stepped light, 13.26 microm; intermittent light, 12.79 microm); 2) restorative composites shrunk more at the bottom surface (15.84 microm) than at the top surface (12.11 microm) and (3) the composites Alert (12.02 microm), Surefil (11.86 microm), Z250 (10.81 microm) and P60 (10.17 microm) presented the least contraction gaps, followed by Z100 (15.84 microm) and Definite (14.06 microm) and finally Flow-it (23.09 microm) low viscosity composite, which had the greatest mean value.

Effect of refrigeration on tensile bond strength of three adhesive systems.

The purpose of this study was to investigate the tensile bond strengths of three adhesive systems applied to dentin at refrigerated and room temperatures. Ninety bovine incisor teeth were obtained, embedded in self-cured acrylic resin, abraded on a lathe under water spray and polished to 400 and 600 grit to form standardized dentin surfaces before randomly assigning to six groups (n = 15). The adhesive systems Scotchbond Multi-Purpose, Single Bond and Prime & Bond NT were applied to dentin according to the manufacturers' instructions at refrigerated temperature (4 degrees C) and at room temperature (23 degrees C), before bonding resin-based composite (Z 100). The specimens were stored in distilled water at 37 degrees C for 24 hours and submitted to tensile bond strength tests on a universal testing machine (EMIC DL-2000) at a crosshead speed of 0.5 mm/min. The resulting data were statistically analyzed using analysis of variance and Tukey's test. No statistical differences were found when the adhesive systems were applied at refrigerated and room temperatures. Scotchbond Multi-Purpose and Single Bond had significantly stronger tensile bond strengths than Prime & Bond NT at room and refrigerated temperatures (p < 0.01). Scotchbond Multi-Purpose and Single Bond were statistically similar. No adverse effects upon tensile bond strength were observed when adhesive systems were taken directly from refrigerated storage.

Influence of loading types on the shear strength of the dentin-resin interface bonding.

Small differences in the shear bond test can make critical differences in the bonding strength values. The purpose of this study was to compare the influence of the orthodontic-looped wire, stainless steel tape and chisel systems used in shear bonding tests to verify the resistance in the dentin-resin interface. Forty-eight human teeth were used and divided in three groups. The teeth were ground until a flat smooth surface was achieved, that was delimited with an adhesive tape containing a hole of 4 mm diameter. After, the dentine surface was treated with Scotchbond Multi Purpose and the composite Z-100 was applied in layers, through a stainless steel mold. The samples were stored at 37 degrees C and 100% of relative humidity for 24 h and, then, submitted to 500 thermal cycles. After, they were taken to an universal test machine (Otto Wolpert) with crosshead speed of 6 mm/min. The results were statistically analyzed using a Tukey's test (p\lt 0.05). The orthodontic-looped wire determined the highest values of shear bond (13.33 MPa), following by chisel (7.81 MPa) and stainless steel tape (4.87 MPa). The debonding values depend on a complex stress combination produced during the loading of the samples. Small variations in test methodologies give statistically different values for shear bond strength. Different shear strength methods in vitro make the comparative clinical performance of the resin filling materials difficult.

Correlation between light intensity and exposure time on the hardness of composite resin.

This study evaluated the correlation between light intensity emitted by the curing units and exposure time on the of degree polymerization of dental composites by measured Knoop hardness. Specimens with 5 mm diameter and 2 mm height were prepared in a copper mold, covered with a mylar strip and polymerized for 30 sec by curing units with 50, 130, 180, 220, 280 and 520 mW/cm(2), respectively. The output for all units was measured using a Curing Radiometer (Demetron). Other specimens were polymerized for 45, 60, 75, 90, 105, 120, 135, 150, 165 and 180 sec utilizing units of 130, 220 and 280 mW/cm(2). Knoop hardness values of the top and bottom surfaces were measured after 24 h. The results indicate that the curing units with higher light intensity presented improved values of Knoop hardness on the top and bottom regions. As expected, the top surface always presented improved Knoop hardness values in relation to the bottom, after exposure for 30 sec. The values obtained on the surface were statistically superior compared to the values on the bottom (p<0.05) for the intensity of 130, 220 and 280 mW/cm(2) after 30, 45 and 60 sec of exposure.

Influence of curing tip distance on composite Knoop hardness values.

The purpose of this paper was to study the influence of curing tip distance on Knoop hardness values, at different depths, of two composites, Z100 and Silux Plus. Specimens (5 mm in diameter and 2.5 mm in height) were prepared in a copper mold, covered with mylar strip and polymerized for 40 s, at 3 tip-to-composite surface distances: 0 mm (surface contact), 6 and 12 mm, utilizing an XL 3000 curing unit, with 750 mW/cm2 power. The specimens were then stored at 37 degrees C for 24 h. Knoop hardness values were measured using a microhardness tester, with a load of 50 g for 30 s for each indentation. Four specimens were made for each distance and composite and eighteen indentations were made of each specimen. The results were submitted to analysis of variance and Tukey test at 5% significance level. The results indicated that 1) composite Z100: the larger the curing tip distance in relation to the composite, the lower the Knoop hardness values; 2) Silux Plus: increasing the curing tip distance did not produce a statistically significant difference in the Knoop hardness values; however, at 6 and 12 mm, the deeper layers showed lower Knoop hardness values in relation to the surface; 3) Z100: statistically superior in relation to Silux Plus at all three curing tip distances and at all depths (P < 0.05).