LANGUAGE AND COGNITIVE PROCESSES, 2000, 15 (4/5), 421–444 Effects of prime word frequency and cumulative root frequency in masked morphological priming ` ne Giraudo Héle University of Provence, Aix-en-Provence, France Jonathan Grainger CNRS and University of Provence, Aix-en-Provence, France Four visual lexical decision experiments using the masked priming paradigm tested for effects of prime word frequency and cumulative root frequency with primes varying in degree of morphological and orthographic overlap with free root targets in French. Experiments 1 and 3 showed that only high frequency morphologically related primes produce signicantly faster response times compared to orthographic control primes. On the other hand, no signicant orthographic priming effects were observed in the present study, except in Experiment 2 where the most frequent orthographic primes produced signicantly more errors than the other priming conditions. In Experiment 4 similar levels of morphological priming were obtained to free root targets with high and low cumulative root frequencies. These ndings are interpreted within the framework of a supralexical representation of morphological information in memory. Over the last decade the masked prime paradigm has gradually been adopted as an important tool for uncovering the fast and highly automatised processes that underlie printed word perception. Masked priming combined with the lexical decision task (Forster & Davis, 1984) has helped dene the relative role played by orthographic, phonologic, morphologic, and semantic information in the process. One interesting ` ne Giraudo, Behavioural Sciences Unit, Requests for reprints should be addressed to Héle Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK. Email: [email protected]; [email protected] The authors thank two anonymous reviewers for criticism of a rst version of this work. ` ne Giraudo is currently post-doctoral research fellow at the Institute for Child Health, Héle Behavioural Sciences Unit, University College London. Part of the present research was supported by a Fyssen Foundation (Paris) award to the rst author. c 2000 Psychology Press Ltd http://www.tandf.co.uk/journals/pp/01690965.html 422 GIRAUDO AND GRAINGER dissociation has been observed in prior studies using prime exposures of around 60 ms: whereas morphologically related primes facilitate processing relative to unrelated word primes (e.g., Drews & Zwitserlood, 1995; Forster, Davis, Shocknecht, & Carter, 1987; Frost, Forster & Deutsch, 1997; Grainger Colé & Segui, 1991), orthographically related primes tend to inhibit target word processing, generating longer response times (RTs)) and/or more errors (Drews & Zwitserlood, 1995; Grainger & Ferrand, 1994; Segui & Grainger, 1990). What specic architecture for lexical processing would predict this observed dissociation? Grainger et al. (1991) and Drews and Zwitserlood (1995) have argued that the inhibitory effects of orthographic priming reect competitive processes acting across whole-word representations (via within-level inhibition in an interactive activation network, McClelland & Rumelhart, 1981, for example). On the other hand, according to these authors morphological facilitation is hypothesised to arise via shared morpheme units located above the level of whole-word form representations (a supralexical architecture for morphological processing as schematised in the lefthand panel of Figure 1; Giraudo & Grainger, in press; Grainger et al., 1991).1 When primes and targets share the same root, the activation of the root representation by the prime stimulus facilitates processing of the target word via excitatory connections between morphemic representations and appropriate whole-word representations. Thus, according to the above account, a morphologically related prime generates two conicting effects: within-level inhibition acting across simultaneously activated word forms, and top-down facilitation from shared morphemic representations. Since form overlap across morphologically related items is generally much lower than in situations where form-related inhibitory priming is observed (Segui & Grainger, 1990), this allows the facilitatory morphological component to dominate (Grainger et al., 1991). Keeping target frequency as high as possible will further help morphological facilitation to dominate over form-level inhibition. The higher the surface frequency of the target word, the greater its resistance to within-level inhibition. All the targets tested in the present experiment were relatively high frequency free roots. Using free roots as targets in a masked prime paradigm has the added advantage that participants are never consciously exposed to 1 The ‘‘supra’’ in supralexical refers to a general framework for studying language comprehension where information ows from lower-level, form-centred representations to higher-level, meaning-centred representations. The ‘‘lexical’’ in supralexical refers to the assumption that representations for whole-word forms (orthography and phonology) are part of this processing hierarchy. PRIME WORD FREQUENCY 423 Figure 1. Two possible locations for morphemic representations in a hierarchically organised processing framework that moves from low-level stimulus analysis to high-level semantic representations. The architectures differ with respect to where in this processing hierarchy morphemic representations are situated relative to whole-word (orthographic or phonological) representations. Furthermore, in the sublexical model morphemic representations are form-based (orthographic and phonological codes for roots and affixes) and used to parse the stimulus input, whereas in the supralexical model they are form and modality-independent. morphologically complex stimuli, and therefore cannot adopt strategies that might be particular to this type of stimulus.2 One key manipulation in the present study involves varying the printed frequency of morphologically complex prime words (their surface frequency) while maintaining both target frequency and cumulative root frequency (the summed frequency of all derived words sharing the same root) constant. According to the supralexical model of morphological representation, more frequent morphologically related primes should enhance effects of morphological priming. In this model, morpheme unit activation is a function of the activation of all whole-word representations that share that morpheme. During prime word processing under the brief temporal conditions of masked priming, the only signicantly activated word unit is the prime word itself whose activation level is a function of its surface frequency (McClelland & Rumelhart, 1981). Thus the activation level of supralexical morphemic representations will be a function of the surface frequency of the prime word. Grainger et al. (1991) found that prime word frequency (medium or low) did not interact with effects of morphological priming. However, target word frequency covaried with 2 This also avoids the delicate issue of deciding what are the appropriate nonword stimuli to use in a lexical decision experiment with morphologically complex target words. The choice is vast: simple nonwords, singly complex nonwords (root + nonafx; nonroot + afx), doubly complex nonwords (illegal combination of root + afx). This choice is highly likely to inuence participants’ lexical decision strategies, and therefore merits a fuller investigation on behalf of researchers in this eld. 424 GIRAUDO AND GRAINGER prime frequency in this experiment (medium frequency targets were primed with low frequency words, while low frequency targets were primed by medium frequency words). In Experiment 1 of the present study, prime frequency is varied while maintaining target frequency constant. At a more general level of theorising, the present study aims to test two different accounts of masked morphological priming, both expressed within the framework of a hierarchical activation model of language comprehension that includes whole-word form representations and morphemic representations that intervene between lower-level form analyses and higher-level semantic representations (Figure 1). Both of these accounts propose morphemic representations as the locus of masked morphological priming effects. Thus, all words that share the same morphological root (i.e., belong to the same morphological family) are hypothesised to be linked to a common representation that corresponds to the shared root. Prime stimuli that contain the same root as target stimuli (i.e., morphologically related primes) generate facilitatory priming via preactivation of the root representation. Prime presentation leads to growth of activation in a given morphemic representation thus conferring an advantage in the processing of target stimuli that contain the same morpheme. Here we assume that the size of morphological priming effects are proportional to the activation level of the critical morpheme after prime word presentation. The critical distinction between the two accounts concerns where, in the processing hierarchy from form to meaning, the morphemic representations are hypothesised to be located. According to the supralexical hypothesis, morphemic representations are located directly after wholeword representations in the processing hierarchy that moves from lowerlevel form analysis of the stimulus to higher-level semantics (lefthand panel of Figure 1). The predictions of this type of model have been discussed above. According to the sublexical hypothesis on the other hand, morphemic representations are located immediately before whole-word representations (righthand panel of Figure 1). The latter hypothesis is embodied in all models that invoke a prelexical morphological parsing mechanism whereby morphemic representations are extracted from the stimulus without reference to whole-word representations. Taft (1994), has described one possible implementation of this hypothesis within the interactive-activation framework. In the sublexical approach, morphemic representations are contacted before whole-word representations, and their activation level during prime processing in the masked prime paradigm will not depend on the surface frequency of the prime stimulus. One critical point here is the assumption that the temporal constraints imposed by masked priming do not allow PRIME WORD FREQUENCY 425 potential feedback mechanisms to have signicantly modied the activation level of processing units at target word onset (after 57 ms of prime processing in the present study). In other words, sublexical morphemic representations will not have received signicant feedback from wholeword representations within this brief time interval. Interactivity is assumed to inuence processing in later stages of target word recognition as the system settles into a stable pattern of activation across orthographic, phonological, morphemic, and semantic units. It is important to note that priming effects obtained in prior experimentation using the masked prime procedure of the present study can be captured with purely feedforward mechanisms. For example, phonological priming effects (e.g., Ferrand & Grainger, 1992) can be explained by prime stimuli activating sublexical phonological representations that are then used in the processing of the target word. This could explain why effects that may require feedback mechanisms, such as semantic priming effects with the lexical decision task, are particularly elusive with such short prime exposure durations (e.g., Rastle, Davis, Marslen-Wilson, & Tyler, this issue). Thus, assuming no signicant topdown inuences from whole-word representations to morphemic representations, the sublexical hypothesis depicted in the righthand panel of Figure 1 predicts that the surface frequency of morphological primes should not affect priming. This is examined in Experiment 1. EXPERIMENT 1 Experiment 1 was designed to test for effects of prime word surface frequency in masked morphological priming. Free roots were primed either by a high frequency morphologically related sufxed word prime, a low frequency morphologically related sufxed word prime, or by a medium frequency orthographically related word. Method Participants Thirty-six psychology students at the University of Provence (France) participated in the experiment. In this and the following experiments all participants were native speakers of French and reported normal or corrected-to-normal vision. Design and stimuli. Thirty free roots were selected as targets (see Appendix A). Each target word was tested in three priming conditions dening the three levels of the Prime type factor (high frequency sufxed word, low frequency sufxed word, and orthographic control). Thus each sufxed word target was primed by the following word primes: (1) a high frequency sufxed word sharing the same root (e.g., amitié–ami); (2) a low 426 GIRAUDO AND GRAINGER frequency sufxed word sharing the same root (e.g., amiable–ami) and (3) a monomorphemic word with the same initial letter sequence as the target (e.g., amidon–ami where [ami-] in amidon does not constitute a root morpheme in French). Targets were 4.7 letters long on average and primes 7.8 letters long. Free root targets had a printed frequency of 663 occurrences per million on average. High frequency sufxed word primes had a printed frequency of 160 occurrences per million on average, low frequency sufxed word primes had a printed frequency of 13 occurrences per million on average and orthographic control primes had a printed frequency of 19 occurrences per million on average (Imbs, 1971). Primetarget pairings were counterbalanced across three experimental lists associated with three independent groups of participants, such that each participant was tested in all three priming conditions but saw a given target word once only. Thirty morphologically simple nonwords were added for the purposes of the lexical decision task. The nonword targets resembled real roots and were primed either by nonwords formed by the target plus a derivation sufx (e.g., moureur–moure), or by unrelated nonwords. Procedure The masked priming procedure by Forster and Davis (1984) was used. Each trial consisted of the following sequence of three stimuli: A forward pattern mask composed of hash marks (#) presented for 500 ms, followed by the prime-stimulus presented for 57 ms, which in turn was immediately replaced by the target string (word or nonword) which remained on the screen until participants responded. Primes were presented in upper case and targets in lower case (with the necessary accents in French). The pattern mask was the same length as the primeword. Participants were instructed to respond as rapidly and accurately as possible whether the letter string in lower case was or was not a French word. Participants responded ‘‘yes’’ by pressing one of two response buttons with the forenger of their preferred hand and ‘‘no’’ by pressing the other response button with the forenger of the other hand. Participants were not informed of the presence of prime-words. Results Mean RTs and percent errors for each experimental condition for word targets are given in Table 1. ANOVAs by participants (F1) and items (F2) were performed on these data. The analysis showed a signicant effect of prime type that was signicant by participants but only marginally so by items (F1(2, 66) = 4.97, p < .01; F2(2, 58) = 3.10, p = .05). Planned comparisons showed that only high frequency morphological primes facilitated target processing relative to orthographic control primes (F1(1, 33) = 11.88, p < .0025; F2(1, 29) = 5.46, p < .05). Low frequency PRIME WORD FREQUENCY 427 TABLE 1 Mean lexical decision latencies for correct responses, percentage of errors (in parentheses), standard deviations to word targets and net morphological priming effects relative to the orthographic control condition in Experiment 1 Prime type High frequency morphological primes Low frequency morphological primes Orthographic control primes RT SD Net effect 596 (1.4) 611 (1.7) 621 (5.0) 78.0 81.8 88.2 25* 10 Note. * p < .05 by participants and items. morphologically related primes did not differ signicantly from orthographic controls (F1(1, 33) = 1.18, p > .10; F2(1, 29) = 1.42, p > .10). There was a marginally signicant different between the high frequency and low frequency morphological prime conditions in the analysis by participants (F1(1, 33) = 3.81, p = .05; F2(1, 29) = 1.84, p > .10). An analysis of the error rates to word targets showed a signicant effect of prime type by both participants and items (F1(2, 66) = 4.16, p < .025; F2(2, 58) = 5.28, p < .01). Planned comparisons showed that both high and low frequency primes inuenced target processing relative to orthographic primes (F1(1, 33) = 4.20, p < .05; F2(1, 29) = 7.64, p < .01 and F1(1, 33) = 7.54, p < .01; F2(1, 29) = 5.12, p < .05, respectively). The difference between high and low frequency primes was not signicant (Fs < 1). An analysis of RTs and error rates to nonword targets showed no signicant effects. EXPERIMENT 2 The results of Experiment 1 t with the predictions of a supralexical architecture where morphemic units are situated above the whole-word representations such that morphemic representations only receive activation from low-level stimulus analysis via whole-word representations. Experiment 2 was designed to examine effects of the same frequency manipulation with primes having similar degrees of form overlap with targets as in the morphological conditions of Experiment 1, without being morphologically related to targets. To this end, the free root targets tested in Experiment 1 were primed either by a high frequency orthographically related prime, a low frequency orthographically related prime, or an unrelated medium frequency prime (e.g., chaume–ami). Method Participants. Thirty psychology students at the University of Provence participated in Experiment 2. They had not participated in Experiment 1. 428 GIRAUDO AND GRAINGER Design and stimuli. The 30 free roots used in Experiment 1 served as targets (see Appendix B). Each target word was tested in three priming conditions dening the three levels of the prime type factor: (1) a high frequency word sharing the same initial letter sequence as the target (e.g., amiral–ami where [ami-] in amiral is not a root); (2) a low frequency word sharing the same initial letter sequence as the target (e.g., amidon–ami, where [ami-] in amidon is not a root, and (3) a monomorphemic unrelated word (e.g., chaume–ami). Targets were 4.7 letters long on average and primes 6.9 letters long. Free root targets had a printed frequency of 663 occurrences per million in average. High frequency orthographic primes had an average printed frequency of 60 occurrences per million (due to constraints in stimulus selection this value could not be any higher), low frequency orthographic primes had an average printed frequency of 4 occurrences per million, and unrelated control primes had an average printed frequency of 32 occurrences per million (Imbs, 1971). Prime-target pairings were counterbalanced across three experimental lists associated with three independent groups of participants, such that each participant was tested in all three priming conditions but saw a given target word only once. The 30 morphologically simple nonwords tested in Experiment 1 were primed either by nonwords sharing the same initial letters as the target (e.g., mountes–moure), or by unrelated nonwords. Procedure. This was the same as in Experiment 1. Results and discussion Mean RTs and percent errors for each experimental condition for word targets are given in Table 2. ANOVAs by participants (F1) and items (F2) were performed on these data. The analysis showed that the effect of prime type was not signicant, neither by participants nor by items (Fs < 1). An analysis of the error rates to word targets was performed and showed a signicant effect of prime type by both participants and items (F1(2, 54) = 3.90, p < .05; F2(2, 58) = 3.41, p < .05). Planned comparisons showed TABLE 2 Mean lexical decision latencies for correct responses, percentage of errors (in parentheses), standard deviations to word targets and net orthographic priming effects relative to the unrelated condition in Experiment 2 Prime type High frequency orthographic primes Low frequency orthographic primes Unrelated primes RT SD Net effect 659 (6.7) 662 (2.3) 673 (3.3) 60.4 76.9 83.3 14 11 PRIME WORD FREQUENCY 429 that high frequency orthographically related primes interfered marginally with target processing relative to unrelated primes (F1(1, 27) = 3.06, p < .08; F2(1, 29) = 2.96, p < .09) and produced signicantly more errors than low frequency orthographic primes (F1(1, 27) = 7.57, p < .025; F2(1, 29) = 4.62, p < .05). The difference between low frequency orthographic and unrelated primes was not signicant (Fs < 1). An analysis of RTs and error rates to nonword targets showed no signicant effects. The results of Experiment 2 provide a partial replication of prior work showing that high frequency orthographically related primes tend to produce interference (rather than facilitation) in target word processing. In the present experiment this interference effect was evident in the error rates, but not in RTs. The lack of an effect in RTs could be due to several reasons. First the degree of orthographic overlap is much smaller than in previous studies, and second, we tested relatively high-frequency target words. Prior work has shown that inhibitory effects of orthographic priming are strongest with low-frequency targets (Grainger, 1992; Segui & Grainger, 1990). The critical result, however, is that varying prime word frequency in conditions of form overlap similar to the morphological prime-target pairs of Experiment 1, we found that, if anything, high frequency primes tend to inhibit, and not facilitate, target word recognition. This suggests that prime word frequency differentially inuences the processing of form information and morphological information. Experiment 3 was designed to replicate the inuence of prime word frequency on morphological priming using frequency-matched orthographic and unrelated primes and a larger stimulus set than in Experiment 1. EXPERIMENT 3 Method Participants. Sixty psychology students from the University of Provence participated in the experiment. They had not participated in the previous experiments. Design and stimuli. Sixty free roots were selected as targets (see Appendix C). Each target word was tested in six priming conditions dening the combination of the three levels of the prime type factor (morphologically related sufxed word, orthographically related word, and unrelated word) and the two levels of the prime frequency factor (high or low printed frequency). Thus each sufxed word target was primed by the following word primes: (1) a high frequency sufxed word sharing the same root (e.g., amitié–ami); (2) a low frequency sufxed word sharing the same root (e.g., amiable–ami), (3) a high frequency orthographically related 430 GIRAUDO AND GRAINGER monomorphemic word (e.g. amiral–ami where [ami-] in amiral is not a root morpheme in French), (4) a low frequency orthographically related monomorphemic word (e.g., amidon–ami where [ami-] in amidon is not a root morpheme in French), (5) a high frequency unrelated monomorphemic word (e.g., juillet–ami), and (6) a low frequency monomorphemic word (e.g., morpion–ami). Targets were 5 letters long on average and primes 7.6 letters long. Free root targets had a printed frequency of 549 occurrences per million on average. High frequency sufxed word primes had a printed frequency of 109 occurrences per million on average, low frequency sufxed word primes had a printed frequency of 9 occurrences per million on average, high frequency orthographic word primes had a printed frequency of 104 occurrences per million on average, low frequency orthographic word primes had a printed frequency of 3 occurrences per million on average, high frequency unrelated word primes had a printed frequency of 112 occurrences per million on average and low frequency unrelated word primes had a printed frequency of 8 occurrences per million on average (Imbs, 1971). Prime-target pairings were counterbalanced across six experimental lists associated with six independent groups of participants, such that each participant was tested in all six priming conditions (Prime type Prime frequency) but saw a given target word once only. Sixty morphologically simple nonwords were included for the purposes of the lexical decision task. As in the previous experiments, the nonword targets resembled real roots and were primed either by nonwords formed by the target plus a derivational sufx (e.g., moureur– moure), by an orthographically related nonword (e.g., mountes–moure), or by unrelated nonwords. Each participant received a total of 120 experimental trials: 60 word trials and 60 nonword trials. Procedure. This was the same as in Experiments 1 and 2. Results and discussion Table 3 provides the mean correct RTs and percentage of errors in the different experimental conditions for word targets. An analysis of variance was performed on these data using participants (F1) and items (F2) as random variables. The main effect of prime type was signicant by both participants and items (F1(2, 108) = 7.18, p < .0025; F2(2, 118) = 3.56, p < .05) while the effect of prime frequency was not signicant (F1 < 1; F2 < 1). The Prime type Prime frequency interaction was signicant by subjects (F1(2, 108) = 5.88, p < .005; F2(2, 118) = 1.74, p > 10). The effect of prime type was signicant for targets preceded by high frequency primes (F1(2, 108) = 13.12, p < .0003; F2(2, 118) = 4.61, p < .025), while there was no effect PRIME WORD FREQUENCY 431 TABLE 3 Mean correct lexical decision latencies, percentage of errors (in parentheses) and standard deviations of RTs to word targets in each priming condition. Net morphological priming effects relative to the unrelated condition are given for each prime frequency in Experiment 3 Prime type Morphological Prime frequency High frequency primes Low frequency primes Orthographic Unrelated RT SD RT SD RT SD Net effects 622 (1.3) 640 (3.5) 97 89 648 (4.2) 642 (4.2) 98 84 655 (3.8) 645 (4.0) 100 90 33* 5 Note. * p < .05 by participants and items. of the prime type for targets preceded by low frequency primes (F1 < 1; F2 < 1). Planned comparisons showed that high frequency morphologically related primes produced faster RTs than high frequency unrelated primes (F1(1, 54) = 14.45, p < .001; F2(1, 59) = 6.54, p < .025) and high frequency unrelated primes (F1(1, 54) = 22.21, p < .0003; F2(1, 59) = 8.73, p < .005). No signicant difference was observed between the high frequency orthographic and high frequency unrelated prime conditions (F1(1, 54) = 1.01, p > .010; F2 < 1). Finally, planned comparisons showed that no signicant differences were observed between the three low frequency prime conditions (Fs < 1). An analysis of the error rates showed no main or interaction effects. An analysis of the RTs and error rates to nonword targets showed no signicant effects. The results of Experiment 3 once again demonstrate that prime word frequency inuences the size of masked morphologically priming effects with free root targets in the lexical decision task. On the other hand, the orthographic prime condition did not differ signicantly from the unrelated prime condition in either the RT or the error analyses, and prime word frequency did not modulate this absence of priming effects. As noted in the discussion of Experiment 2, the absence of an inhibitory effect of orthographically related primes is likely due to two factors: target word frequency and degree of orthographic relatedness. All targets had high printed frequencies in the present study, and the degree of orthographic relatedness was on average lower than in prior work showing inhibitory effects (e.g., Grainger, 1992; Segui & Grainger, 1990). EXPERIMENT 4 The fact that morphological priming is observed with high frequency free root targets in Experiments 1 and 3, is problematical for any dual-route 432 GIRAUDO AND GRAINGER account of morphological processing according to which target surface frequency determines the relative involvement of morphological representations (via a sublexical morphological parsing route). A dual-route theorist could argue, however, that by preactivating sublexical morphological representations, the masked priming paradigm articially increases the use made of the morphological parsing route, hence generating morphological priming effects. By preactivating the appropriate sublexical morphological representation, speed of processing via the morphological route becomes faster than via the whole-word route, even for very high frequency target words. If this were to be the case, then since cumulative root frequency (the summed frequency of all words that contain a given root) is assumed to increase the speed of morphological processing in such models (e.g., Burani & Caramazza, 1987), then morphological priming effects should interact with the cumulative root frequency of target words. Smaller priming effects should be obtained with targets having low cumulative root frequencies. This is examined in Experiment 4. Method Participants. Thirty psychology students from the University of Provence participated in the experiment. They had not participated in the previous experiments. Design and stimuli. Thirty free roots with a low cumulative frequency (the sum of the printed frequencies of the free root and all words derived from this root) and small family size3 (e.g., ours) and 30 free roots with a high cumulative frequency and large family size (e.g., cire) were selected as targets (see Appendix C). These two stimulus sets dene the target type factor. The average cumulative frequencies were 125 and 211 occurrences per million (Imbs, 1971) for the two groups of targets, and the average family size 3.3 and 17.8. Targets in the low and high cumulative frequency group were matched for length in letters (5.3 and 5.0 respectively) and surface frequency (114 and 107 occurrences per million respectively). Each target word was primed by (1) a sufxed word sharing the same root (e.g., ourson–ours; cireur–cire), (2) an orthographic control word (e.g., ourlet– ours; cirrus–cire), and (3) an unrelated word (e.g., agenda–ours; goyave– cire). These conditions dene the three levels of the prime type factor. Primes for the low and high cumulative frequency targets were matched 3 We did not attempt to separate out effects of type and token counts of cumulative root frequency. Furthermore, since word frequency was matched across the two sets of targets which were free roots, our cumulative frequency manipulation is equivalent to what de Jong et al. (this issue) refer to as family frequency. PRIME WORD FREQUENCY 433 for surface frequency (10 occurrences per million) and length (between 6 and 10 letters long). All participants were tested in all six experimental conditions (Prime type Target type) but saw each target once only. Sixty morphologically simple nonwords were included for the purposes of the lexical decision task. As in the previous experiments, the nonword targets resembled real roots and were primed either by nonwords formed by the target plus a derivational sufx (e.g., moureur–moure), or by unrelated nonwords. Each participant was tested in a total of 120 experimental trials: 60 word trials and 60 nonword trials. Procedure. This was the same as in the previous experiments. Results and discussion Table 4 provides the mean correct RTs and percentage of errors in the different experimental conditions for word targets. An analysis of variance was performed on these data using participants (F1) and items (F2) as random variables. The main effect of prime type was signicant by both participants and items (F1(2, 54) = 17.40, p < .0001; F2(2, 116) = 11.43, p < .001) while the effect of target type was not signicant (F1 < 1; F2 < 1). The Target type Prime type interaction was not signicant (F1 < 1; F2 < 1). There were signicant effects of prime type for both free root targets with low cumulative frequencies (F1(2, 54) = 9.49, p < .001; F2(2, 58) = 8.11, p < .01) and free root targets with high cumulative frequencies (F1(2, 54) = 9.38, p < .001; F2(2, 58) = 3.57, p < .05). Planned comparisons showed that morphologically related primes produced faster RTs than orthographic primes (F1(1, 27) = 13.81, p < .0025; F2(1, 58) = 8.62, p < .01) and unrelated primes (F1(1, 27) = 23.02, p < .0003; F2(1, 58) = 32.85, p < TABLE 4 Mean correct lexical decision latencies, percentage of errors (in parentheses) and standard deviations to word targets with low and high morphemic frequencies. Net morphological priming effects relative to the unrelated condition are given for each type of target in Experiment 4 Type of primes Morphological Type of target Low cumulative frequency High cumulative frequency Orthographic Unrelated RT SD RT SD RT 653 (4.4) 652 (3.1) 77 62 682 (6.4) 673 (5.3) 80 60 691 (5.6) 698 (3.6) Note. * p < .05 by participants and items. SD Net effects 64 66 38* 46* 434 GIRAUDO AND GRAINGER .0001). An analysis of the error rates showed no main or interaction effects, and an analysis of RTs and error rates to nonword targets showed no signicant effects. The results of Experiment 4 show that cumulative root frequency does not inuence the size of morphological priming on free root targets. Sufxed word primes facilitated the processing of free root targets with low and high cumulative frequencies. Thus, a manipulation designed to modulate the involvement of morphological processing (according to a generic dual-route model), did not lead to variations in morphological priming. No main effect of cumulative frequency was observed to the high frequency free root targets in Experiment 4. Prior studies demonstrating cumulative root frequency effects have used targets with relatively low surface frequencies (e.g., Burani & Caramazza, 1987; Colé, Segui, & Taft, 1997; Meunier & Segui, 1999).4 Furthermore, effects of morphological family size have so far only been reported for words with relatively low surface frequencies (de Jong et al., this issue; Schreuder & Baayen, 1997). GENERAL DISCUSSION First, the present study shows that masked morphological priming can be obtained with derived word primes and free root targets with high surface frequencies. Obtaining masked morphological priming with free root targets is a particularly important result in that it demonstrates that morphological priming can be observed in conditions where participants have no conscious contact with morphological information during the experiment: primes are not identiable, and targets are morphologically simple words. Furthermore, using free roots as targets has the advantage of avoiding the delicate problem of deciding which type of nonword target is appropriate in lexical decision experiments examining morphological processing. At a theoretical level, the fact that high frequency free root targets were shown to be sensitive to morphological priming (Experiments 1, 3, and 4) is evidence against any form of dual-route model of morphological processing where morphological inuences should only be observable in words of low printed frequency (e.g., Caramazza, Laudanna, & Romani, 1988; Schreuder & Baayen, 1995). Second, the present study demonstrates that the surface frequency of morphological primes affects the size of morphological priming. In Experiments 1 and 3, high surface frequency derived word primes showed signicant facilitation relative to form control primes, whereas low 4 Note that the average surface frequency of the high frequency targets in Meunier and Segui’s (1999) study, was only 18 occurrences per million, which is quite low compared to the frequencies of target words in the present study. PRIME WORD FREQUENCY 435 frequency primes did not. This particular result was predicted by a supralexical model of morphological representation, where effects of morphology necessarily depend on processing of a whole-word form that gives rise to effects of surface frequency. In Experiments 2 and 3 a similar frequency manipulation with form-related primes showed no effects relative to unrelated primes in the RT data. However, in the error analysis the high frequency form primes produced an inhibitory effect relative to unrelated primes, but only in Experiment 2. So the general picture that is conrmed by the present study, and already envisaged in the work of Grainger et al. (1991) and Drews and Zwitserlood (1995), is one in which pure form overlap across words tends to generate competitive processes, the strength of which depend on the frequency of the prime and target stimuli and the degree of orthographic overlap between them (Grainger, 1992), while morphological overlap engenders facilitation (via positive resonance between morphemic representations and whole-word representations) that increases as a function of the frequency of the morphologically related prime. As noted in the discussion of Experiment 3, the high printed frequency of the target words tested in the present study, plus the relatively low level of orthographic overlap across primes and targets, are two possible reasons why there was little evidence of inhibitory form priming. Finally, Experiment 4 demonstrated that variations in cumulative root frequency did not inuence the size of masked morphological priming effects obtained with free root targets. Within a dual-route framework, reducing the cumulative frequency of free root targets was expected to reduce involvement of the morphological processing route, hence diminishing morphological priming effects obtained with high frequency targets. Surface frequency and pseudomorphemes The fact that only the high frequency derived word primes produced signicant morphological priming in Experiment 1 is taken as support for a supralexical model of morphological representation. Further support for such a model has been obtained in experiments showing an absence of priming from pseudoroots and pseudoafxes in the masked prime paradigm (Giraudo & Grainger, 2000). In these studies, primes containing pseudoroots or pseudoafxes produced effects that did not differ signicantly from unrelated primes, while true derived word primes sharing a root or an afx with derived word targets produced signicantly faster RTs. Using the same line of argument as used to interpret the effects of prime surface frequency in the present study, we suggested that only a supralexical representation of morphology could accommodate these 436 GIRAUDO AND GRAINGER results. A sublexical account of morphological representation would predict no difference between primes containing a true morpheme or a pseudomorpheme that is shared with the target, since morphemes must be rapidly extracted from the stimulus without consideration of the compatibility of remaining information. On the other hand, morphemic representations that only receive activation (from bottom-up processes) via whole-word forms that contain that morpheme will not be sensitive to stimuli containing pseudomorphemes, and will show effects of prime word surface frequency as observed in Experiments 1 and 3 of the present study. There is evidence, however, that pseudoprexed stimuli are harder to classify as words than matched monomorphemic controls (e.g., Pillon, 1998). This is typically taken as prime facie evidence against a supralexical account of the morphological representation, since the cost in processing caused by a pseudoprex is assumed to arise via some form of prelexical morphological parsing process. As Pillon (1998) points out, there are a number of problems in selecting the appropriate control words in these experiments, a fact that might help explain divergences in the results obtained in prior studies, and a point that certainly calls for caution when interpreting such effects. These problems in stimulus selection are partly obviated by the use of a priming paradigm (Giraudo & Grainger, 2000). Furthermore, a recent study in Finnish (Laine, Vainio, & Hyönä, 1999) did not nd any processing cost for pseudosufxes and pseudostems, thus suggesting that the pseudomorpheme effect, if it exists independently of other factors, is limited to prexes. Cumulative root frequency No main effect of cumulative root frequency was observed in lexical decision times to free root targets in Experiment 4. As noted in the discussion of this experiment, prior work showing effects of cumulative frequency have used words with relatively low surface frequencies (e.g., Burani & Caramazza, 1987), so the use of high frequency targets in the present study may explain the observed absence of an effect. Research showing facilitatory effects of cumulative root frequency with low frequency words and not with high frequency words, has often been used in support of so-called dual-route models of morphological processing where the surface frequency of the complex target word determines the relative involvement of morphological decomposition in the recognition of this word. However, the fact that morphological priming is obtained with high-frequency free root targets in the present study is evidence against this frequency-biased dual-route conception of morphological processing. Two recent sets of results suggest that prior observations of cumulative root frequency effects may in fact reect the correlation of this variable PRIME WORD FREQUENCY 437 with other more relevant variables. Thus, the work of Schreuder and Baayen (1997; see also de Jong et al., this issue) has pinpointed one hitherto unexpected critical variable: a type count of morphological family size. This measure simply provides the number of derived words in a given morphological family (i.e., that share the same root) independently of their surface frequencies and their inected forms. These authors have demonstrated that, while controlling for other relevant variables, increasing the family size of target words leads to faster lexical decision responses to these words. Another critical line of evidence has recently been provided by Meunier and Segui (1999) who demonstrated that the relative frequency ranking of the target word within its morphological family determines lexical decision performance to sufxed derived words. Increasing the number of family members whose surface frequency is greater than that of the target word, leads to poorer performance in an auditory lexical decision task. Combining this observation in the auditory modality with the family size effect reported by Schreuder and Baayen (1997) in the visual modality, it appears that it may well be the frequency distribution of the morphological family that is the critical variable here. In other words, it might not be the total number of family members (family size) that is critical, but rather the presence or not of members that have a relatively high surface frequency. When family frequency is controlled (see de Jong et al., this issue) then manipulations of family size imply that words with a low family size must have some members with relatively high surface frequencies in the family, while words with a high family size are likely to have morphological families composed of words all having relatively low surface frequencies. Thus, the family size effect that is observed when family frequency is controlled, may at least partly reect an inhibitory inuence of the presence of family members with high surface frequencies in the words having a low family size (Meunier & Segui, 1999). Morphology, form and meaning The present results therefore add to the already impressive amount of evidence arguing for the explicit representation of morphological information in memory (e.g., Deutsch, Frost & Forster, 1998; Drews & Zwitserlood, 1995; Feldman, 1994; Frost et al., 1997; Grainger et al., 1991; Laudanna, Badecker, & Caramazza, 1992; Marslen-Wilson, Komisarjevsky-Tyler, Waksler, & Older, 1994). Of course, when morphological relations across words are learned in the absence of explicit instruction (as is generally the case for derivational morphology), then it is the systematic co-occurrence of form and meaning overlap that must be detected by the learner. At the outset, therefore, morphology is nothing other than a 438 GIRAUDO AND GRAINGER combination of form and meaning overlap across words. We argue, however, that the learning process derives explicit representations corresponding to morphemes, and that these morphemes act as a partial interface between whole-word form representations and the representation of semantics, at least as far as French derivational morphology is concerned. The present study provides converging evidence in favour of this hypothesised supralexical representation of derivational morphology. This may well turn out to be a language-specic solution to the processing and representation of morphology. Given large variations in factors such as average word length, the salience of cues to word boundaries in speech, and the transparency and productivity of morphological structures, languages are likely to differ with respect to the relative weight that is assigned to whole-word versus morpheme-sized representations in parsing the stimulus input. Only systematic cross-linguistic comparisons will allow us to clarify this important issue. REFERENCES Burani, C. & Caramazza, A. (1987). Representation and processing of derived words. Language and Cognitive Processes, 2, 217–227. Caramazza, A., Laudanna, A., & Romani, C. (1988). Lexical access and inectional morphology. Cognition, 28, 297–332. Colé, P., Segui, J., & Taft, M. (1997). Words and morphemes as units for lexical access. Journal of Memory and Language, 37, 312–330. Deutsch, A., Frost, R., & Forster, K.I. (1998). Verbs and nouns are organized and accessed differently in the mental lexicon: Evidence from Hebrew. 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Language and Cognitive Processes, 9, 271–294. 440 GIRAUDO AND GRAINGER APPENDIX A Stimuli used in Experiment 1 High surface frequency Low surface frequency Orthographic morphological primes morphological primes controls Targets pureté artiste amitié rêveur bonté maladie muraille grossier hauteur jeunesse nalement justement richesse terrain criminel changement couverture difculté liberté longueur sanglant tardif tournant blancheur froideur gardien gravité imaginaire romantique nesse puriste artisan amiable rêveusement bonnement maladif muret grossiste hautement jeunot naliste justesse richement terreau criminalité changeur couvreur difcilement librement longuet sanguin tardivement tourneur blanchâtre froidure garderie gravement imagerie romanesque nement purin artichaut amidon revêche bonze malabar ` ne mure groseille havane jeudi nnois jument richelieu terrible crinoline chandail couvent dilemme libellule lombric sanglier tarentule tournesol blaireau froment gardon gravas impôt romanichel nance pur art ami rêve bon malade mur gros haut jeune n juste riche terre crime changer couvrir difcile libre long sang tard tourner blanc froid garde grave image roman n PRIME WORD FREQUENCY APPENDIX B Stimuli used in Experiment 2 High surface frequency Low surface frequency orthographic primes orthographic primes Unrelated controls Targets pupille article amiral revers bonnet malabar murmur nance grotte hanche jeudi jument ricochet terrible critique chantier couvent diamant libraire loisir sanglot tartine tourment blague fromage garage gravier impôt romaine ssure banane manteau chaume lustre farine caribou casque crapaud laurier square ` re bie amende mascotte décembre obstacle ardoise épingle graisse ambassade chêvre horloge pastille sommaire ampoule lessive cognac biscuit citron casserole ûte pur art ami rêve bon malade mur n gros haut jeune juste riche terre crime changer couvrir difcile libre long sang tard tourner blanc froid garde grave image roman n purin artichaut amidon revêche bonze malaga ` ne mure nnois groseille havane jeun jujube richelieu terrier crinoline chandail couenne dilemme libellule lombric sanglier tarentule tournesol blaireau froment gardon gravas impact romanichel rme 441 442 GIRAUDO AND GRAINGER APPENDIX C Stimuli used in Experiment 3 High frequency primes: Prime type Low frequency primes: Prime type Morphological Orthographic Unrelated Morphological Orthographic Unrelated Targets purement artiste amitié rêveur bonté tardif tournant blancheur froideur gardien gravité imaginaire jeunesse justement richesse terrain criminel changement couverture difculté liberté romantique nalement maladie magique coupure mineur collier laideur louange chanson vitrine métallique armement menteur misérable penseur passage ` re barrie drapeau chevalier banquier bataillon bâtiment pupille article amiral revers bonnet tartine tourment blague fromage garçon gravier impôt jeudi jument ricaner terrible critique champagne couvent diamant libraire romaine nance malice magasin coupole mince colline laisser louche chantier vitesse métairie araignée menton mission pension passion baraque dragon cheville banquette beteau bâton insecte domaine juillet secours culture ampoule essence caserne coussin théâtre pendule rancune origine sauvage sourcil octobre logique victime automne novembre occasion vestibule assiette couloir appétit platane cahier taureau chambre colombe réexe bouquet vaisselle faisseau galerie obstacle auberge science ` ge colle urgence manuscrit médaille régulier mercredi puriste artisan amiable rêveusement bonnement tardivement tourneur blanchâtre froidure garderie gravement imagerie jeunot justesse richement terreau criminalité changeur couvreur difcilement librement romanesque naliste maladif magicien couperet minier collerette laideron louable chanteur vitrier métallurgie armurier menterie miséreux pensable passeur barrette drapier chevalin bancaire batailleur bâtisse purin artichaut amidon revêche bonze tarentule tournesol blaireau froment gardon gravats impact jeun jujube richelieu termite crinoline chamois couenne dilemme libellule romanichel nnois malaga magnum couperose minet collyre laiton loulou chancre vitriol métacarpe armagnac menthe misogyne pentagone pastel barrique dragée chevrotine banquise bâtard batracien amazone ` ne oxyge morpion biscuit gazelle alvéole guépard carotte vanille cricket bistrot cigogne gouache éclipse pruneau cocaõ¨ne embolie génisse basilic anecdote cantique chronique astrakan chignon sardine ` re hate boléro ` ze trape cagoule épinard binoche javelle codicille dialecte chardon réglisse beignet météor arlequin pommade phosphate aspirine stigmate alphabet pur art ami rêve bon tard tourner blanc froid garder grave image jeune juste riche terre crime changer couvrir difcile libre roman n malade mage couper mine col laid louer chant vitre métal arme mentir ` re mise penser passer barre drap cheval banque bataille bâtir PRIME WORD FREQUENCY APPENDIX CÐ 443 cont. Stimuli used in Experiment 3 High frequency primes: Prime type Low frequency primes: Prime type Morphological Orthographic Unrelated Morphological Orthographic Unrelated Targets modestie communauté équipage formation mollement glacial grandeur guérison lucidité mouchoir musculaire modeste commun équipe former mou glace grand guérir lucide moucher muscle moderne commissaire équivoque formidable mollusque glaive grange guéridon lucarne mouette museau fauteuil cathédrale tonnerre ` re cimetie cartouche écaille appareil paquebot sommaire chocolat labyrinthe modestement communard équipier formateur mollasse glaçon grandement guérisseur lucidement moucheture musculature module commissure équinoxe formol molleton glaõ¨eul granule guérite luciole mouon muscade almanach salamandre marabout clavicule catapulte fenouil seringue nénuphur balustre cervoise naphtaline 444 GIRAUDO AND GRAINGER APPENDIX D Stimuli used in Experiment 4 Low cumulative frequency Prime type High cumulative frequency Targets Morphological Orthographic Unrelated ourson policier toiture bergerie orageux billeterie plagiste juteux mairie ruelle jupon ` re tabatie saladier bijoutier aubergiste ordurier sudiste montagnard trésorier trajectoire futurisme périodique fruitier saisonnier astucieux dattier chandelier bustier théière démomiaque ourlet ploisson toison bergamote oracle billion plagiat jujube maille ruban judas tabasser salamandre bigorneau aubergine ordinal sufxe ` re monaste tresse tramontane funiculaire permanence frusques saindoux astrakan daurade chancelier bufe théorème démocrate agenda immeuble gazette cocktail foulard cataclysme arlequin baobab agneau chêvre lilas bourrique perruche chevreuil prospectus escalope lombric périphérie groseille controverse cellulose champignon morphine cataplasme synagogue tétanos apostrophe giroe chamois escadrille Prime type Targets Morphological Orthographic Unrelated ours police toit berger orage billet plage jus maire rue jupe tabac salade bijou auberge ordure sud montagne trésor trajet futur période fruit saison astuce datte chandelle buste thé démon cireur menteur laitier cassure vitrage briseur pliable gelure barrette muraille poterie louable hachure copier balançoire plâtrier lage couchette cordelette alcoolique ` re glacie chanteur réglable plunage collage crêperie chauffage lavage rondelle bandeau cirrus menton laitue cassoulet vitriole bristol plinthe gelule barrique murmur potence loutre hachisch copeau balalaõ¨ka platine lou couleuvre corbillard alcôve gladiateur chantier réglisse pluriel collyre crecelle chaumière larynx ronchon bandit goyave abeille gorille pharaon bécasse houblon anchois basket cerfeuil scrupule gazelle caniche luciole brioche coquelicot insuline coccyx sacerdoce mayonnaise millimètre acropole anecdote autruche baleine fenouil éléphant escargot cactus capucine corbeau cire mentir lait casser vitre briser plier gel barre mur pot louer hache copie balance plâtre l coucher corde alcool glace chant règle plume coller crêpe chauffer laver rond bande
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