a s l From planting to harvesting, mean rainfall and temperature

a.s.l. From planting to harvesting, mean rainfall and temperature range were respectively 1121 mm and 16.7–28.7 °C at Namulonge, 1095 mm and 17.3–29.2 °C at Jinja, and 424 mm and 18.5–29.4 °C at Nakasongola. Twelve genotypes (Table 1) were sourced from farmers’ fields and from the National Cassava Breeding Programme (NCBP) at the National Crops Resources Research Institute, Namulonge. Genotypes from farmers’ click here fields were landraces, while genotypes from the NCBP were introductions from the International Institute of Tropical Agriculture (IITA) and genotypes developed

by crossing cassava lines from the International Centre for Tropical Agriculture (CIAT) with lines from Uganda. Selection of the genotypes was based on their performance for storage root yield, early bulking and relative degrees of field resistance to two diseases prevalent in Uganda: cassava brown streak disease (CBSD) and cassava mosaic disease (CMD). The trial at each location

was laid out in a randomised complete block design with three replications. Healthy stem cuttings each 25 cm in length were horizontally planted in a flat seedbed at a spacing of 1 m × 1 m giving a population density of 10,000 plants ha− 1. Each plot measured 2 m × 6 m, comprising 3 rows of 6 plants each. The first and last rows and the first and last plant within the middle row of each plot were considered as border plants. The plots and blocks were separated by 2.0 m and 2.5 m Selleck BMN 673 alleys, to reduce inter-plot and inter-block plant competition, respectively. The trials were conducted without supplemental irrigation and weeded regularly. Data for the following traits were collected from a net plot of four randomly selected and hand-uprooted plants of each genotype: storage root number (SRN); storage root mass (SRM); FSRY and cassava brown streak disease root necrosis (CBSD-RN). Cassava mosaic disease severity (CMD-S) was assessed during the crop growth at 6 MAP on an increasing scale of 1–5, where: 1 = no symptoms;

and 5 = severe mosaic symptoms [16]. Storage roots of the four plants were bulked, counted and weighed IMP dehydrogenase to obtain SRN and SRM (kg), respectively. The FSRY (t ha− 1) per genotype was then estimated from the SRM of the four-plant bulk of storage roots as: FSRY=(SRM×10,000)/(4×1000).FSRY=SRM×10,000/4×1000. Storage root necrosis due to CBSD (CBSD-RN) was scored on an increasing scale of 1 to 5 where 1 = no visible necrosis, and 5 = severe necrosis [17]. The data for each location were first analysed independently and then the error variances for the environments were tested for homogeneity using Hartley’s Fmax test [18]. The differences were non-significant, and accordingly an unweighted combined AMMI analysis of variance was conducted across the locations. Correlations among various plant parameters were calculated as Spearman correlation coefficients [19].

Thus, the cakes presented good water retention capacity during th

Thus, the cakes presented good water retention capacity during their shelf-life. This probably occurred due to the fact that the fat acts as a moisture barrier when used in a recipe. The quality of bakery foods is affected

by moisture. With no fat to prevent moisture uptake, a baked product may pick up moisture and become soggy or lose moisture and dry out (Bennion & Bamford, 1997). Moreover, MS-275 ic50 WCF contains high levels of dietary fibre (Table 2), which helps to maintain the moisture of the product. Polysaccharides, such as dietary fibres, are hydrophilic molecules, with numerous free hydroxyl-groups which can form hydrogen bonds with water. Consequently, soluble and insoluble polysaccharides have the ability to hold water (Oakenfull, 2001). Furthermore, possible interactions between the fibre and

starch could occur, and this could delay starch retrogradation (Gómez, Ronda, Blanco, Caballero & Apesteguía, 2003) avoiding the loss of moisture during storage. Table 1 shows the values for cake firmness on storage days 1, 4 and 7. Equations ,  and  present the relationships between WCF and HVF for this parameter on storage days 1, 4 and 7. The three response surfaces obtained from the models were very similar, with displacement almost only along the Z axis (showing an increase in firmness during storage) ( Fig. 3). Moreover, a greater effect of HVF on firmness can be observed in relation to WCF and an increase FG-4592 mouse in HVF resulted in a decrease in firmness. The addition of intermediate concentrations of WCF (close to 15 g/100 g flour mixture) and the highest concentrations of HVF (>16 g/100 g flour mixture) resulted in less firm cakes. However, the addition of intermediate concentrations of WCF (close to 15 g/100 g flour mixture)

and the lowest concentrations of HVF (close to 12 g/100 g flour mixture) resulted in very firm cakes. This can be explained by the reduction in HVF, which resulted in a lower aeration capacity, worse crumb structure and, consequently, greater firmness. Lakshminarayan et al. (2006) also found that with a gradual reduction in the fat content of the cakes, they became less soft, requiring more force to compress them. This fact could also be isothipendyl a reflection of the lower specific volume observed in these WCF and HVF concentration ranges. According to Faridi (1985), the volume has an influence on crumb firmness, since for volumes obtained from equivalent weights, the differences in volume usually resulted in differences in wall thickness and gas cell size. A decrease in firmness is expected with an increase in the amount of WCF, since the WCF contributed to a decrease in the starch concentration of the cakes. It is believed that starch is one of the components responsible for the staling of bakery products, due the retrogradation process and its interaction with proteins (Lai & Lin, 2006).

Benzodiazepines (diazepam or midazolam 20–240 mg/day either as a

Benzodiazepines (diazepam or midazolam 20–240 mg/day either as a bolus or by i.v. infusion) were given to control muscle spasm and hypertonia. The indications for a surgical cuffed tracheostomy were acute airway obstruction due to laryngeal spasm, frequent spasms interfering with respiration or to facilitate mechanical ventilation. No patients were orally intubated and no form of subglottic suction or selective digestive tract decontamination find protocol was used. Arterial blood gases and peripheral oxygen saturations were

monitored regularly. In severe tetanus, the non-depolarizing neuromuscular blocking agent pipecuronium was used, using bolus doses titrated

against spasm. Autonomic instability was treated with increased sedation, morphine (20–60 mg/day intramuscularly), calcium antagonists, digoxin, volume expansion or inotropes (norepinephrine or dopamine) according to the clinical situation. Intermittent enteral nutrition was administered through a large bore nasogastric tube in those patients unable to swallow. An X-ray was used to determine correct placement of Cobimetinib supplier the tube before feeding commenced. Patients with a history of previous gastric ulceration continued to receive their regular medication, and those who developed Rebamipide gastrointestinal bleeding during the course of their admission were commenced on stress ulcer prophylaxis with either an H2 antagonist or sucralfate. Standard measures for general critical care and prevention of nosocomial pneumonia were employed and a pressure area care protocol was followed in

all patients. Closed suction was used for bronchial toilet. On average there were two patients for each nurse in the ICU. Admission clinical features, the presence of underlying disease, daily progress, the need for a tracheostomy and mechanical ventilation, duration and type of nasogastric intubation, type of stress ulcer prophylaxis, sedative treatment administered, intercurrent infections antimicrobial treatment given, the cost of antimicrobials given and the duration of ICU and hospital stay were collected prospectively on a dedicated study form. At the time of admission to the ICU, blood was taken for haematocrit, white cell count, platelet count and creatinine and a chest X-ray performed. The tetanus severity score (TSS) was determined for the time of admission with a cut-off point TSS ≥8 as predictive of death.

Each s

Each this website freeze-dried sample was mixed with anhydrous sodium sulfate, ground with mortar, and pestled to obtain a dry powder. The powdered mass was then extracted with dichloromethane using an ASE 200 extractor (Dionex, Salt Lake City, UT, USA). The extracted volume was reduced to ∼1.5 ml using a rotary evaporator and then fractionated through an alumina oxide column to remove polar interferences using 35 ml of petroleum ether. The extract was concentrated to ∼5 ml by rotary evaporation and transferred to a pre-combusted, glass test tube. The extract volume was further reduced to ∼1 ml using a purified nitrogen stream and sealed in an amber vial

for GC-MS analysis. The sample analysis was performed by a Varian 3800GC/Saturn 4000 ion trap mass spectrometer (Varian, Walnut Creek, CA, USA) operated in the ion-monitoring mode. Prior to the analysis, a mixture of perdeuterated PAHs, including phenanthrene-d10, benzo(a)anthracene-d10, benzo(a)pyrene-d12,

and benzo(g,h,i)perylene-d12, was added immediately to each extract as an internal standard. Each PAH was identified by its retention time relative to the internal standards and quantified by comparing the integrated CX-5461 supplier area of the molecular ion chromatogram to that of the internal standard ( Ko and Baker, 1995 and Ko and Baker, 2004). The detailed description about the PAH’s analysis can be found in Hung et al (2010). The concentrations of PAHs in zooplankton at 27 stations (excluding station 30 due to sample spilling) are expressed in two different units: ng g−1 (e.g., PAHs normalized by dry weight of zooplankton) and ng m−3 (e.g., PAH concentrations (ng g−1) normalized by zooplankton biomass in seawater (g m−3)). There

are at least four main water masses (Fig. 1, CDW: Changjiang Diluted Water, TCWW: Taiwan Current Warm Water, KW: the Kuroshio Water, YS: Yellow Sea Water) in the ECS in April based on temperature and salinity distributions (Fig. 1 and Fig. 2 and Table 1). CDW is a mixture of Changjiang River runoff and shelf water with low salinity and high nutrient concentrations (Gong et al., 2003 and Hung et al., 2013). YSW is mainly carried into the northern part of the ECS through the Chinese Coastal Current from the Yellow Sea (Ichikawa and Beardsley, 2002), showing moderate salinity, Thymidine kinase low temperature and low nutrient concentrations (Gong et al., 2003 and Chou et al., 2009). TCWW enters the ECS from the Taiwan Strait with high temperature and high salinity (Gong et al, 2003), but its salinity is lower than that of the KW. The KW flows northeast along the shelf with high temperature, high salinity and low nutrient concentrations (Gong et al., 2003 and Hung et al., 2009b). As a whole, the hydrographic setting in this survey in spring was similar to that reported for previous investigations (Gong et al., 2003 and Chou et al., 2009). Fig. 2 shows contour maps of surface salinity, NO3−, Chl-a and plankton biomass in the ECS.

We refer to their approach as the AV2010 conceptual model Cyclon

We refer to their approach as the AV2010 conceptual model. Cyclone Erwin (or Gudrun) crossed the Baltic Sea on 8–9 January 2005, giving rise to the highest historical sea levels at nearly all northern Baltic coastal stations (Suursaar et al. 2006). The temporal

variability of single storm surges and their correlations with local wind forcing and large-scale atmospheric circulation have been analysed on the basis of model simulations and data over past decades (Suursaar et al., 2003, Suursaar et al., 2010 and Suursaar et al., 2011). One of the general conclusions from the aforementioned works is that extreme storm surges in Estonian coastal waters occurred there because the centre of an see more intense, fast-moving cyclone was propagating northwards from the Scandinavian Peninsula over the Gulf of Finland. The corresponding local wind pattern was SW winds over the central Baltic

veering west, pushing water first towards the northern Baltic and then into the Gulf of Finland and Gulf of Riga. Storm surges are the main cause of coastal flooding in the Baltic Sea, although as historical data show, a single storm is not enough to cause extreme sea levels: a series of cyclones are needed (Suursaar et al. 2006). Hydrodynamically, extreme storm surges have been thoroughly studied and their different aspects well simulated by models, ranging from conceptual and semi-empirical ones (Suursaar et al. 2002) to operational 3D numerical simulations (Lagemaa et al. 2011). Although sea levels around the average Gefitinib supplier are well represented and validated, extreme sea levels are frequently captured with much poorer accuracy (Raudsepp et al. 2007). This problem could be addressed using an ensemble modelling approach, which gives a measure of uncertainty to estimated sea level extremes; probably, however, this still does not improve the physical understanding of the occurrence of extremes. We find that the real trigger of these extreme events comes from atmospheric conditions, which give rise to a situation where cyclones with

similar tracks and the deepest phase location are clustered in time: it is this periodicity that is the true driver Cyclin-dependent kinase 3 of sea level extremes. These atmospheric factors of such events have not yet been described in great detail. This brings us to the aim of our paper, which is primarily to study the statistics of the physical properties of single cyclones and their tracks that have caused 40 high storm surges on the Estonian coast, measured at Pärnu and Tallinn, and to show how variable the key properties are for dangerous cyclones, as pointed out by the AV2010 model. To that end, we use the characteristics of cyclones from the database of Northern Hemispheric cyclones in Gulev et al. (2001). The second task of the paper is to test the hypothesis that a series of cyclones is needed to force extreme sea levels on northern Baltic Sea coasts.

The first instrument used was a spectral backscattering meter (Hy

The first instrument used was a spectral backscattering meter (HydroScat-4;

HOBI Labs). This measured values of the volume scattering function at an angle centred at 140° and at four light wavelengths – 420, 488, 550 and 620 nm. These raw values were then used to estimate the backscattering coefficients of light in seawater bb [m− 1] at these four wavelengths, according to the method described in Maffione & Dana (1997) and in Dana & Maffione (2002). A correction for the incomplete recovery of backscattered light in highly attenuating waters (the so-called sigma-correction) was applied in accordance with the instrument User’s Manual www.selleckchem.com/products/erastin.html ( HOBI Labs 2008), using data on light absorption and attenuation coefficients measured with another optical instrument. To obtain the backscattering coefficients of particles bbp [m− 1], the theoretical backscattering coefficients of pure water were subtracted (according to Morel (1974)). The second optical instrument was a spectral absorption-attenuation meter (AC-9; WET Labs). Equipped with a 25 cm optical path length, this instrument measured the light absorption

and attenuation coefficients of all the non-water (i.e. suspended and dissolved) constituents of seawater, an [m− 1] and cn [m− 1] respectively, at nine light wavelengths (412, 440, 488, 510, 532, 555, 650, 676 and 715 nm). Corrections for in situ temperature and salinity effects on the optical properties of MTMR9 water were applied according to Pegau et al. (1997). A correction for the incomplete recovery of the scattered light in the absorption tube of the AC-9 instrument was applied according www.selleckchem.com/products/azd4547.html to Zaneveld et al. (1994) (the so-called proportional method, according to which the measured values for the longest light wavelength (715 nm in the case of our instrument) are assumed to be caused entirely by the unwanted scattering error effect, and the corrected value of absorption at this band was assumed to be 0). At this point, the reader should

note an important methodological difference between the current work and the paper of S.B. Woźniak et al. (2011) mentioned earlier. In that paper the light absorption properties of suspended particles and coloured dissolved organic matter were characterised separately, not in situ, but based on measurements of discrete seawater samples performed in a land-based laboratory using a bench-top spectrophotometer. In the current work only the in situ measured (with the AC-9 instrument) total absorption coefficient of all suspended and dissolved non-water constituents of seawater an is taken into consideration. It is relatively easy to measure the latter optical coefficient during oceanographic campaigns, so data on coefficient an are often present in different oceanographic datasets used for the calibration and validation of remote sensing algorithms.

We used the same initial dose of 10 μg/mL as used for the contact

We used the same initial dose of 10 μg/mL as used for the contact treatment. The insects were fed with blood containing parasites (2 × 106T. cruzi Dm28c clone/mL of blood) (group FPC) or not (FP), and were placed over the physalin B treated papers (25–30 insects/176 cm2) during the whole experiment period. Parasites adhesion to the perimicrovillar membrane of the insect vector posterior midgut is an important stage for parasite development in the host. Therefore perimicrovillar membrane of the treated insects was dissected and prepared in saline buffer to count the number of

parasites adhered under an optic microscope. We used membranes of control (C) and physalin B treated orally groups (F). The parasites, T. cruzi epimastigotes, were washed three times in PBS, and then resuspended in fresh BHI to a concentration of 3.0 × 106 cells/mL. The parasite suspension (200 μL) was incubated with the perimicrovillar membrane buy Pexidartinib of each insect group inside microtubes for 30 min at 25 °C. Then the midgut preparations find more were spread onto glass slides and the number of attached parasites was counted under a microscope ( Nogueira et al., 2007). A hundred randomly chosen epithelial cells from 10 different sites of each midgut preparation were counted. For

each experimental group 10 insect midguts were used. The microbiota of the R. prolixus digestive tract was assessed by counting bacteria colony forming units (CFU) that grew in brain heart infusion agar (BHI agar). The kinetics of microbiota growth in infected and non-infected insects was investigated daily for 30 days after feeding. The results demonstrated a peak of bacteria concentration at 8 days after feeding and a significant difference between infected and non-infected insects ( Castro et al., 2012). Therefore the entire digestive tract was dissected under sterile conditions (without contact of the samples with the outside cuticle of the insect and inside a biological

safety flow cabinet) eight days after treatments and homogenized in 1 mL of sterile PBS. Samples were then immediately transferred to Sitaxentan ice, diluted 10−5, 10−7 or 10−9 with PBS, and 20 μL aliquots were spread onto BHI agar plates, and then incubated overnight at 30 °C. After this the CFUs were counted. We analyzed the effects of physalin B in the anterior midgut nine days after feeding because in our recent research (Castro et al., 2012), the antibacterial activity is more intense in this condition. The TB assay was modified from Thomas et al., 1999 and Bexfield et al., 2004. Each anterior midgut dissected was placed in a tube with 200 μL of Milli-Q water, and then it was homogenized and centrifuged at 8000 g for 1 min at 4 °C. Aliquots of 70 μL from supernatant were transferred into tubes containing 630 μL of Milli-Q water. They were then sterilized in 0.22 mm sterile filters and frozen at −20 °C.

In accordance with our observations of N100, Ermolaev and Kleinma

In accordance with our observations of N100, Ermolaev and Kleinman (1983) found an inverse relationship between background illumination and N130 amplitude. Moreover, consistent with our observations, Noguchi and Sakaguchi (1999) observed significant changes in alpha power with changes in color–temperature. In summary, our findings provide compelling evidence that the illumination condition substantially influences our attentional processing which was reflected in the significant modulations

of EEG activity. Further studies on illumination parameter-dependent efficacy of the cognitive performance and selection of the effective illumination parameters are necessary to develop appropriate applications to enhance the efficacy of

our work-performance. For instance, such an learn more illumination-mediated application to inefficient Selleck Epigenetic inhibitor or impaired cognitive performance for probing its potential utility in the enhancement of work efficacy constitutes one of our future subjects of investigation. EEG was recorded from all 23 neurologically normal participants (11 females; mean age 23; age range 19–31 years) in this study in accordance with the ethics guidelines established by the Institutional Review Board of Yonsei University and the Declaration of Helsinki (World Medical Association, 1964; 2002). Participants provided informed consent prior to the start of the experiment. All had normal or corrected-to-normal vision. We used a 60×60 cm2 plate as the illumination source, which had 14×14 light-emitting diode (LED) arrays installed inside; this source was placed just above and behind Phospholipase D1 the participant with a tilt angle of 10° to the vertical line as shown in Fig. 3A. A controller (WE7000, Yokogawa, Japan) could regulate the illuminance and color–temperature of the LEDs. To make the illumination as homogenous as possible all around the participant, the present experiment was performed within a capsule-shaped light-reflecting structure (Fig. 3A) called the “Ganzfeld-dome,” with an optical geometry with a 2-m diameter. Four different illumination conditions were provided with

a factorial design of 2 color–temperatures (3000 K and 7100 K) by 2 illuminance levels (150lx and 700lx). This resulted in (1) the cool-dark (7100 K and 150lx), (2) the cool-light (7100 K and 700lx), (3) the warm-dark (3000 K and 150lx), and (4) the warm-light (3000 K and 700lx) conditions. Higher color–temperatures lead to bluish light, which we feel is a cool illumination condition; whereas lower color–temperatures produce yellowish or reddish light, which we feel is a warm illumination condition. These specific illumination parameters were chosen on the basis of the Kruithof curve (Kruithof, 1941), taking the technical limitation of the illumination device into consideration. Both comfortable and uncomfortable combinations of illuminance and color–temperature parameters have been described in the Kruithof curve.

Patients who showed evidence of CCSVI were further evaluated by s

Patients who showed evidence of CCSVI were further evaluated by selective venography. Fifty MS-matched normal controls (NC), 60 patients with transient global amnesia (TGA), and 60 TGA-matched NC were studied. Transcranial venous echo-color Doppler was normal in all patients with CIS. One or more abnormal extracranial venous echo-color Doppler findings were observed in 26 of 50 (52.0%) of the patients with CIS, 35 of 110 (31.8%) of the controls

and 41 of 60 (68.3%) of the patients with TGA. The eight (16%) patients with CIS who fulfilled the diagnosis of CCSVI were further evaluated blindly by selective venography, which did not learn more disclose any venous anomalies. Thus, we could not demonstrate any causative effect of CCSVI on MS [14]. The second study INCB024360 mouse was focused on the progressive forms of MS, to investigate whether CCSVI could play a role in determining disease progression. We analyzed 60 patients with chronic progressive forms of MS (35 SP, 25 PP) and 60 age-/gender-matched NC. TCDS was normal in all patients. ECDS showed

one or more abnormal findings in 9/60 (15.0%) patients [7/35 (20.0%) SPMS, 2/25 (8.0%) PPMS] and in 14/60 (23.3%) NC (p not significant for all comparisons). CCSVI criteria were fulfilled in 0 NC and 4 (6.7%) MS patients: 3 SPMS and 1 PPMS. VGF, performed blindly in 6/9 patients, was abnormal only in one case that had bilateral internal jugular vein (IJV) stenosis [17]. These findings indicate that CCSVI is not a late secondary phenomenon of MS and is not responsible for disability progression. On the basis of these contradictory results, it is absolutely necessary to question the validity of the five ultrasound criteria proposed by Zamboni for the diagnosis of CCSVI. In the first criterion, Zamboni et al. used the threshold value of 0.88 s to Sclareol discriminate IJV and vertebral vein (VV) physiological back flow due to valve closure from pathological reflux without performing the Valsalva maneuver

(VM) [8] and they found that 71% of MS patients had a pathological reflux vs. 0% of controls. This threshold value comes from a totally different study on IJV valve insufficiency during a controlled VM [20] where it was chosen to differentiate VM-induced insufficiency through insufficient valves lasting >1.23 s, from physiological backward flows during normal valve closure, lasting 0.22–0.78 s. In this study it was found that about 30% of normal subjects have a physiological (t < 0.88 s) back flow during normal valve closure. Furthermore, the utilization of this threshold by Zamboni for assessing reflux in other vessels (i.e. VVs) other than IJV valve insufficiency is also scientifically incorrect. For the second criterion, the intracranial veins and sinuses were not examined through the transtemporal bone window for which there are published ultrasound criteria and velocity data [21] and [22]. Zamboni et al.

While it is still unclear how flexibly these distributed cortical

While it is still unclear how flexibly these distributed cortical networks contribute to semantic processing across different task contexts (Mahon and Caramazza, 2008, Pulvermueller, 2013 and Willems and Casasanto, 2011), evidence suggests convincingly that sensorimotor activation in response to printed words reflects semantic processing. In UK primary schools, children learn to read simple words during their first year when they

are 4–5 years old. Reading fluency continues to develop substantially after that, with improvements in reading speed and accuracy extending until around the 15th year of life (Wechlser, 2001). Age-related changes in reading skills are accompanied by focalisation and left-lateralisation of word shape selective occipito-temporal areas (Brown et al., 2005, Schlaggar and McCandliss, 2007 and Schlaggar et al., 2002) and decreasing activation in posterior temporal areas associated with cross-modal orthographic and VX-765 phonological processing (Church et al., 2008 and Pugh et al., 2001).

While substantial research has charted how structural and functional changes in these language-related areas contribute to reading improvement during development, the role of cortical sensorimotor AZD8055 cell line representations in this process has not yet been explored. It is therefore unclear when printed words start engaging the same brain areas as their pictorial counterparts as children learn to decode meaning from word forms. Understanding this process can provide important insight into how and under which circumstances child readers access the sensorimotor meaning of written words, and provide a benchmark for investigating word comprehension in children

with reading difficulties. This research can also inform theories on how distributed semantic sensorimotor networks contribute to the printed word-learning process. Only a few studies have investigated distributed semantic networks in the developing sensorimotor cortex, but initial evidence suggests that these might already be present before Baricitinib children learn to read. For instance, by 6–7 years of age, passive viewing of tool pictures without the overt plan to act, engages grasp-related areas of the cortex whilst passive viewing of animal pictures does not (Dekker, Mareschal, Sereno, & Johnson, 2011). Similarly, by 4 years of age, listening to actions words (verbs) activates motor areas in the brain, but listening to non-action words (nouns) does not (James & Maouene, 2009). Which role might such already-established cortical sensorimotor representations play during reading acquisition? It is possible that sensorimotor networks become involved early during reading training, for example because they may help bootstrap the formation of mappings between word shape and word meaning (Nation, 2008). Or, underdeveloped spelling/sound connections might allow for a greater influence of semantic information on slow word-recognition processes (Plaut & Booth, 2000).