Showing posts with label in-groups. Show all posts
Showing posts with label in-groups. Show all posts

Tuesday, November 11, 2014

The One Thing that Could Save the World: Why We Need Empathy Now More than Ever

I completely disagree with Paul Bloom (psychologist at Yale) that empathy is a poor moral guide. Bloom sets empathy against rationality, which is a false dichotomy.
George Lakoff: “Empathy is at the heart of real rationality, because it goes to the heart of our values, which are the basis of our sense of justice. Empathy is the reason we have the principles of freedom and fairness, which are necessary components of justice.”
In the article below,

The one thing that could save the world: Why we need empathy now more than ever

Critics say that empathy clouds our judgment and distracts us from true morality. Here's what they're missing.




The one thing that could save the world: Why we need empathy now more than ever 
Gregory Peck and Brock Peters in "To Kill a Mockingbird" 
Empathy is trending. President Obama wants to tackle America’s “empathy deficit,” medical students routinely receive empathy training, and everyone from business gurus to the Dalai Lama have become its champions. The latest neuroscience research shows that 98 percent of us have the capacity to empathize wired into our brains and, like riding a bike, it’s a skill we can learn and develop. No wonder Google searches for the E word have more than doubled  in the past decade. The art of imaginatively stepping into another person’s shoes and seeing the world from their perspective is, it would seem, a most valuable and valued twenty-first century asset.

Not so, says Yale psychologist Paul Bloom, leading the counter-charge against empathy’s popularity surge. It is, he claims, a poor moral guide, lacking the power to inspire us to act on, say, child poverty or humanitarian disasters. “Our public decisions will be fairer and more moral once we put empathy aside,” says Bloom, insisting we should instead, “draw on a reasoned, even counter-empathetic, analysis of moral obligation.” But in doing so, Bloom creates a false – and dangerous – dichotomy between empathy and reason, and misses the long lesson from history: that time and again, empathy has played a crucial role in creating a democratic culture that respects human rights. So where have the critics gone wrong?

The anti-empathy brigade launch their attack with the claim that having too much empathy can lead to what Bloom calls “empathetic distress” or burnout. Yes, identifying closely with someone else’s pain and mirroring their emotions – known as affective empathy – can seem overwhelming. But according to altruism expert Daniel Batson  at the University of Kansas, there is no scientific evidence that those with high levels of affective empathy are less able to respond to other people’s needs: they are not paralyzed by their sensitivity – indeed many may be motivated by it. Moreover, people who need to keep a cool head when the emotional heat is rising – be they doctors, firefighters or social workers – know to draw, instead, on their capacity for cognitive empathy, an ability Bloom too easily sidelines. And there’s a crucial distinction between the two.

If affective empathy is our mirror for reflecting others’ emotions, cognitive empathy is, by contrast, a pair of shoes that invites us to imagine the world from their viewpoint. So the smart doctor aims not to feel her patient’s anxiety, but to understand it, so that she can respond appropriately. Every good parent teaches cognitive empathy to their kids: ‘Imagine how you’d feel if someone did that to you,’ we tell them as a first step in their moral education. Trying to understand others’ perspectives is an essential part of our emotional intelligence toolkit, and it matters all the more if their lives and needs differ from our own. As George Bernard Shaw quipped, ‘Do not do unto others as you would have them do unto you – they might have different tastes.’ Our cognitive empathy enables us to discover those different tastes.

A second charge against empathy is that it fails at a distance: we empathize more easily with people in our backyards, say the critics, so help our neighbors while ignoring earthquake victims overseas. This is muddled thinking. Proximity is clearly no guarantee of care: we can stroll past a homeless person on our street just as we can be stopped in our tracks by a news story about a woman in Japan left homeless by an earthquake. The real question is how to give people a human face, whether they are near or far, so we get beyond abstract statistics and stereotypes and can make an emotional connection with their lived reality. Without empathy, we could never explain the massive rise in humanitarian giving by individuals to developing countries since the end of World War II.

The strongest critique in the empathy wars is the risk of empathic bias: the concern that we are partial towards our in-group – people of a similar socioeconomic or cultural background to our own. Think of the judge who gives a more lenient sentence to a white-collar criminal whose educational background resembles his own. Empathic bias is real and it matters – but it means that we need to deepen, not discard, our empathy, by escaping the boundaries of our peer group. That’s just what the Eton-educated writer George Orwell did when, in the late 1920s, he swapped his natty suit for tramping clothes and lived amongst hobos and beggars on the streets of East London, an empathic immersion described in “Down and Out in Paris and London” that exploded his prejudices about the homeless. We might all learn from his example and get talking to the strangers on our doorsteps, whether it’s your new Afghani neighbor or the heavily tattooed woman who delivers your mail each day.

Our empathy is powerful but it is clearly not perfect. So should the critiques of Bloom and others convince us to cast our innate empathic abilities aside and rely, instead, on reason as our moral compass? This would be a monumental mistake, proving us blind to the lessons of history. Reason divorced from empathy was a specialty of the Nazis, who used reason to argue that Jews were subhuman and then codified it in the Nuremberg Laws. What made the Holocaust possible was the Nazis’ racial ideology that achieved one of the most successful erosions of societal empathy in political history.

There are positive lessons from history too. A growing wave of scholars, from the cultural historian Lynn Hunt to the arch-rational psychologist Steven Pinker, argue that democratic rights have been won when societies have extended their empathy to previously neglected social groups. Look no further than the 18th century humanitarian revolution, which generated the first campaigns to tackle child poverty, the anti-slavery movement and associations to improve working conditions. In “The Better Angels of Our Nature,” Pinker points out it was rooted in ‘the rise of empathy and the regard for human life’, underpinned by the ‘reading revolution’ as literature opened up imaginations to previously hidden lives. When the public became sensitized to the suffering of marginalized groups, it spurred legislative reform. And this story has been repeated in struggles throughout democratic history, from women’s suffrage to gay rights and disability rights.

If there is one lesson that history teaches us, it is this: empathy cracks open the door of our moral concern, and laws and rights wedge that door open. Reason – embodied in laws and rights – and empathy are not, as the critics contend, polar opposites. They are in fact a democratic double act: like knife and fork, ball and socket, Fred and Ginger, they work best when they work together. As the cognitive linguist George Lakoff puts it, “Empathy is at the heart of real rationality, because it goes to the heart of our values, which are the basis of our sense of justice. Empathy is the reason we have the principles of freedom and fairness, which are necessary components of justice.”

Cast empathy aside to lean on reason alone and we would become emotionally tone deaf and politically indifferent. That is not who we want to be and – more importantly – it is not who we are.

Roman Krznaric’s new book is Empathy: Why It Matters, and How to Get It (Perigee/Penguin, on sale Nov. 4). He is a faculty member of The School of Life in London and founder of the world’s first digital Empathy Library. Follow him on Twitter at @romankrznaric.

Friday, May 17, 2013

The Influence of Group Membership on the Neural Correlates Involved in Empathy


This short review article from Frontiers in Human Neuroscience looks at the ways in which affect, cognition, and emotional regulation play together in the formation of empathy. More importantly, they examine how each of the three components is affected by group membership and how that can lead to in-group bias (or an US vs THEM mindset).


Full Citation:
Eres R and Molenberghs P. (2013). The influence of group membership on the neural correlates involved in empathy. Frontiers in Human Neuroscience, 7:176. doi: 10.3389/fnhum.2013.00176

The influence of group membership on the neural correlates involved in empathy


Robert Eres and Pascal Molenberghs
School of Psychology, The University of Queensland, St. Lucia, QLD, Australia  
ABSTRACT: 
Empathy involves affective, cognitive, and emotion regulative components. The affective component relies on the sharing of emotional states with others and is discussed here in relation to the human Mirror System. On the other hand, the cognitive component is related to understanding the mental states of others and draws upon literature surrounding Theory of Mind (ToM). The final component, emotion regulation, depends on executive function and is responsible for managing the degree to which explicit empathic responses are made. This mini-review provides information on how each of the three components is individually affected by group membership and how this leads to in-group bias.

Introduction 

In their Perception-Action Model of empathy, Preston and de Waal (2002)state that “the attended perception of the object's state automatically activates the subject's representations of the state, situation, and object, and that activation of these representations automatically primes or generates the associated autonomic and somatic responses, unless inhibited.” Their view of empathy included various phenomena such as emotional contagion, cognitive empathy, guilt, and helping which according to their model all relied on the perception-action mechanism. While typically empathy has been investigated using behavioral paradigms, more recently it is becoming tangible to investigate the neural architecture that underlies this process (Preston and de Waal, 2002; Boston, 2007; Singer and Lamm, 2009; Decety, 2011; Shamay-Tsoory, 2011; Bernhardt and Singer, 2012). Decety (2011) recently proposed a three component basis for empathic experiences, highlighting affective, cognitive, and emotion regulative components. These components are deemed necessary for experiencing empathy where the affective component is identified as a bottom-up, or automatic, process and the cognitive and emotion regulative components are identified as top-down modulators. That is, sharing the pain of others occurs automatically but behavioral responses are differentiated by cognitive factors (for example, perspective taking) and emotion regulative factors (for example, motivation). Social neuroscience has also begun investigating the modulating factors that interfere with empathic responses such as inter-individual differences (Singer et al., 2004; Hein and Singer, 2008), closeness (Beeney et al., 2011), and groups (Ito and Bartholow, 2009; Chiao and Mathur, 2010). Group membership describes a group of people sharing similar and recognizable characteristics where an individual can categorize others as belonging to that particular social group (Abrams, 2012). The focus of the present review is to identify how group membership affects each of the three components of empathy and to illustrate how this accumulates to a biased view of how we see the world. 

Affective Empathy: the Ability to Share the Affective States of Others


The main problem in understanding empathy from a neuroscience perspective is explaining how we can overcome the physical distance between our brain and that of others. How can we make sure we experience the same emotions as others and how can we understand the emotions of others by just observing their behaviors? Simulation theory suggests that we understand other people's actions and emotions by mirroring their actions and feelings onto our own mind state (Preston and de Waal, 2002; Rizzolatti and Fabbri-Destro, 2008; Keysers and Gazzola, 2009; Rizzolatti and Sinigaglia, 2010). According to the classical view, perception-action coupling of motor actions is supported by mirror neurons located in areas such as the inferior parietal lobule (IPL) and posterior inferior frontal gyrus (Iacoboni et al., 1999; Rizzolatti et al., 2001), however, fMRI studies have shown that additional regions such as superior temporal sulcus (STS), dorsal and ventral premotor cortex and superior parietal lobule are also involved in perception-action coupling of motor actions (Molenberghs et al., 2009, 2010; Caspers et al., 2010).

The human mirror system does not passively respond to the observation of actions but is influenced by the mindset of the observer (Molenberghs et al., 2012c). Crucially for this review, previous studies have shown that group membership can modulate perception-action coupling. For example, a recent fMRI study (Molenberghs et al., 2012b) investigated the effect group membership has on our ability to accurately represent action perception. Participants were randomly divided into red or blue teams and they were told they had to compete against a member of the other team by pressing a button response as quickly as possible. In a subsequent experiment, participants were shown video clips of either in-group or out-group members making button-press responses as quickly as possible in a similar competitive situation, where their job was to identify which team member pressed the button fastest. On average both groups in the video clips pressed the buttons equally fast but behavioral analysis showed that participants responded that their team members pressed the button faster. Additional fMRI analyses showed differential neural activation when presented with actions of in-group members compared with out-group members. That is, for those participants who showed an in-group bias behaviorally (those participants that said their team members were faster), greater activity in the IPL was shown when observing in-group members perform the action compared with members from the out-group (Molenberghs et al., 2012b). The IPL plays an important role in perception action coupling and its modulation by group membership suggests we simulate the actions of in-group members more easily. This is in line with a recent EEG study by Gutsell and Inzlicht (2010), who found larger EEG mu suppression (which has previously been associated with mirror neuron activity) when observing actions of in-group members compared to actions of out-group members. Interestingly, this effect increased with the amount of prejudice toward the out-group (Gutsell and Inzlicht, 2010). This reduced perception-action coupling for out-group members also extends to feelings of empathy. For example in a TMS study, Avenanti and colleagues (2010) found a reduction in motor-evoked potential (MEP) amplitude in the hand of participants (induced by TMS to the contralateral motor cortex) when watching an in-group member being painfully stimulated (compared to touch) but no such effect was found when watching out-group members in pain. This suggests that participants simulated the pain of the in-group member but not the pain of the out-group member.

Though predominantly focused on action-perception, vicarious experiences through mirroring have also been shown to extend to emotion and sensory domains as well (Carr et al., 2003; Keysers et al., 2004, 2010; Keysers and Fadiga, 2008; Keysers and Gazzola, 2009). Observing another person's emotional or sensory state elicits activity in a homologous area in the observer, supporting the notion that we vicariously experience the emotional and sensory states of others and represent these states onto our own emotional and sensory repertoires (Keysers and Gazzola, 2009). Indeed a recent meta-analysis including 125 fMRI studies on the mirror system found that perception-action coupling of emotional expressions through vicarious experience is not limited to the aforementioned mirror areas but also involves brain areas involved in, for example, experiencing pain such as the insula and cingulate cortex (Molenberghs et al., 2009). The role of the mirror system in action understanding and affective empathy is controversial (Saxe, 2005, 2006; Hickok, 2009; Decety, 2010) but our view here is that vicarious responses are at least partially involved in affective empathy through mirroring processes, though we acknowledge that they are only part of the story. For example Decety (2011) views affective empathy more broadly as just mirroring and his model of affective empathy also includes affective arousal which he identifies as “the automatic discrimination of a stimulus as appetitive or aversive, hostile or hospitable, pleasant or unpleasant, threatening or nurturing.”

Neuropsychological evidence suggests that greater vicarious empathic responses are elicited from own-ethnicity members compared with other-ethnicity members (Avenanti et al., 2006, 2010; Ito and Bartholow, 2009;Xu et al., 2009; Chiao and Mathur, 2010; Azevedo et al., 2012; Gutsell and Inzlicht, 2012; Sessa et al., 2013). For example, a recent fMRI study showed that when observing a member of the same ethnicity experiencing painful stimulation, greater activity in the dorsal anterior cingulate cortex (dACC) and anterior insula (AI) were found compared with when a member from a different ethnicity was experiencing pain (Xu et al., 2009). Race, however, is not the only factor to influence empathic responses to in-groups and out-groups. Group membership has also been found to moderate activation of the AI in response to observing painful situations. Hein and Colleagues (2010) showed in their fMRI study that greater activation in the left AI was found when in-group members (those from the same sporting team) received pain compared with out-group members (those from another sporting team). This activity was also found to correlate positively with the willingness to share the pain with an in-group member compared with an out-group member. When and out-group member received pain, rather than an increase in AI activity, more activity occurred in the right ventral striatum [an area typically associated with pleasure and schadenfreude (Singer et al., 2006; Takahashi et al., 2009)], and this activity was negatively correlated with the willingness to share the pain of the out-group member (Hein et al., 2010). In a similar fMRI study, Cikara and colleagues (2011) monitored neural activity when participants watched video clips of two sporting teams (participant favorite vs. other) compete against each other. They found that when the participants' team won, increased activity in the ventral striatum was observed. More importantly, though, when the participants' team lost, greater activity in the AI and dACC were shown suggesting that participants were empathizing with the pain that the players of their favored team felt. However, sharing the emotions with others alone cannot explain the rich experience of empathy. Empathy also involves a cognitive and emotional regulative component. 

Cognitive Empathy or the Ability to Reason About Others' Mental States


Vicariously sharing other people's emotions helps us partially understand how other people are feeling, but to completely understand the beliefs, desires and intentions of others, one must also reason about the mental state of others. This cognitive aspect of empathy is typically associated with regions associated with mental state reasoning or so called Theory of Mind (ToM) and often involves regions such as the medial Prefrontal Cortex (mPFC), Temporoparietal Junction (TPJ), and adjacent posterior Superior Temporal Sulcus (pSTS) (Amodio and Frith, 2006; Saxe, 2006; Decety and Lamm, 2007; Frith, 2007; Keysers and Gazzola, 2007; Uddin et al., 2007;Shamay-Tsoory et al., 2009; Van Overwalle and Baetens, 2009; Cheon et al., 2010; Shamay-Tsoory, 2011).

Cognitive empathy can also be modulated by group membership. Adams et al. (2009) used an fMRI modified version of the “Reading the Mind in the Eyes Test” (Baron-Cohen et al., 2001) in which participants are presented with pictures of just the eyes of people and participants then have to judge what the person in the picture is thinking or feeling. Adams et al. (2009)used pictures of Asian and Caucasian people and then let native Japanese and white Americans judge the mental state of those people. They found a behavioral intra-cultural advantage for understanding the mental state of in-group members compared to out-group members and showed that this in-group bias was associated with increased activity in the posterior STS. In line with Adams et al. (2009), research surrounding ToM has consistently shown the importance of the STS in understanding the mental states of others (Fletcher et al., 1995; Allison et al., 2000; Gallagher and Frith, 2003; Amodio and Frith, 2006). Similarly, Cheon et al. (2011) found that Korean participants showed more empathy for in-group members experiencing emotional pain than out-group members and that this was related to increased activity in the TPJ. Similar studies have also illustrated the importance of the mPFC in in-group bias. For example, Mathur and colleagues (2010) found increased activation in the mPFC when watching in-group members experience emotional pain compared to out-group members and this increase predicted greater empathy and altruistic motivation for one's in-group. Another fMRI study found mPFC activation when participants watched pictures of social groups but not for extreme low-status groups (Harris and Fiske, 2006).

The mPFC also has an important role in social categorization, with increased activation in this region previously associated with in-group concepts compared to out-group concepts in both existing (Morrison et al., 2012) and newly created groups (Molenberghs and Morrison, 2012). Volz and colleagues (2009) also found that during an fMRI modified version of the minimal group paradigm (Tajfel et al., 1971) high in-group favoritism was associated with increased activation in the mPFC. Taken together, the aforementioned findings suggest that increased activation in cognitive empathy regions are associated with increased understanding of the mental state of in-group compared to out-group members (Adams et al., 2009;Mathur et al., 2010; Cheon et al., 2011), in-group minus out-group social categorization (Volz et al., 2009; Molenberghs and Morrison, 2012;Morrison et al., 2012) and in-group favoritism (Volz et al., 2009), suggesting further the modulating role of group membership on empathic experiences. 

Emotional Self-Regulation or the Control of Explicit Emotions


To reiterate, affective empathy is partially supported by simulating the emotional states of others whereas cognitive empathy relies partially on understanding another's mental state through cognitive reasoning. Given this capacity to experience the affective and mental states of others, it seems necessary that an additional network be set to moderate the degree to which we experience these effects or explicitly express these states. Without an emotion regulative network, shared emotional states may inhibit our ability to perform tasks that require emotional distance (e.g., a surgeon operating on a child or a defense lawyer supporting a psychopath) or it may interfere with our ability to hide automatic biases (e.g., a parent being derogative to a teacher of a different racial background). Essentially, there needs to be a neural function that inhibits or facilitates empathic responses more explicitly to allow for appropriate functioning in day-to-day life (Decety, 2011). Areas involved with emotion regulation such as the rostral anterior cingulate cortex (rACC), dorsolateral (dlPFC) and ventromedial (vmPFC) prefrontal cortex have previously been shown to modulate the effects of empathy (Amodio et al., 2006, 2008; Cheng et al., 2007; Beer et al., 2008; Ito and Bartholow, 2009; Decety et al., 2010;Decety, 2011).

For example, Cheng and colleagues (2007) investigated the neural processes underlying expert and naïve populations' reactions to a person experiencing painful (penetrated with acupuncture needles) and non-painful (Q-tip) stimulation. Evidence from their fMRI investigation revealed increased activity for the pain matrix network (dACC, insula, somatosensory cortex) in naïve participants. On the other hand, the experts (physicians with acupuncture experience) provided no activity in these areas, instead neural activity was recorded in vmPFC which is involved in emotion regulation (Decety, 2011) and TPJ which has previously been implicated in self-other differentiation and ToM (Decety and Lamm, 2007). These results suggest that the acupuncturists could influence their vicarious pain experience by down-regulating these responses through emotional regulation and increased self-other differentiation. Using a similar paradigm, Decety et al. (2010) used EEG to identify the time course of empathic responses and the regulation thereof. The authors identified that for naïve participants, early (N110) and late (P3) activity showed differential responses for painful and non-painful stimuli but when the experienced physicians viewed this stimulus set, there were no differences in early or late processes which suggests that emotion regulation can impede on early processing of painful stimulus presentation (Decety et al., 2010).

Relevant to emotion regulation is the ability to inhibit explicit emotional reactions. It is important to regulate explicit emotional expressions to maintain egalitarian status within society. An example of this was shown in an fMRI study by Richeson and colleagues (2003) who argued that people (especially those with high racial bias) during interracial contact must inhibit racial attitudes and this would result in depletion of executive functions (i.e., response inhibition) which in turn would lead to impaired performance on a subsequent task that requires these functions. They tested this hypothesis by measuring White participants internal beliefs toward racial groups (Blacks and Whites) using an Implicit Association Test (IAT). Additionally, they asked participants to comment on a few questions with a Black Experimenter (mixed-race interaction) and then participants completed a Stroop task to measure executive functioning (task inhibition). Results showed that those who scored higher on the IAT for racial bias, also showed more interference effects on the subsequent Stroop task. When followed up with an fMRI task where participants were presented with Black and White faces, they found increased activation in the ACC and the dlPFC when Black faces were presented, suggesting greater response inhibition during these trials. A significant positive relationship was also found between the increase in ACC and dlPFC activation and the IAT and Stroop task, where this increase in the right dlPFC mediated the effect between IAT and Stroop interference. Collating this evidence, it suggests that people who show higher interracial bias try to inhibit automatic stereotypes, ultimately leading to a reduction in cognitive resources.

Another nice example of emotion regulation was shown in an fMRI study by Cunningham and colleagues (2004). They showed White participants pictures of Black (out-group) and White (in-group) faces either very briefly (30 ms) or for a longer duration (525 ms). The authors predicted that when these pictures would be presented very briefly, participants would not have enough time to regulate their emotions (i.e., negative responses to the Black faces). The fMRI results showed there was increased activation in the amygdala for Black faces compared to White faces when the stimuli were presented very briefly but no such effect was found when the stimuli were presented for longer. Instead they found increased activation in the dlPFC and ACC in the long stimulus presentation condition. When correlating the scores of an IAT regarding race bias with that of neural activity, a positive relationship was shown between behavioral data and fMRI activity in the amygdala for Black and White faces. Similarly, Black-White differences in amygdala activity between the short and long image presentations were predicted by frontal activation. Taking these findings together, it suggests that an automatic race bias against Black faces in White participants is moderated using reflective cognitive processes that only take effect after a period of time. Given that it is not socially acceptable to show explicit in-group bias, the authors interpreted this effect as increased emotion regulation of an automatic bias.

However, social categorization can also override automatic biases. For example, Van Bavel et al. (2008) investigated whether arbitrary and temporary novel group membership could override the effects of predominant group memberships within society (i.e., race as described in their study). Therefore, they randomly assigned participants to a mixed-race team. Pairing behavioral paradigms with functional MRI, the authors measured activity in the fusiform face area (FFA), which has previously been shown to be modulated by face perception and visual expertise (Gauthier et al., 1999, 2000; Golby et al., 2001; Van Bavel et al., 2011), when participants were presented with pictures of faces of in-group and out-group members. The results revealed greater activity in bilateral FFA for in-group faces compared to out-group faces. Interestingly this effect was specific to in-group vs. out-group and was not modulated by race (see also Van Bavel and Cunningham, 2009 and Van Bavel et al., 2011 for similar results). This provides evidence that categorizing people from a different race into an in-group can inhibit automatic racial biases. 

Conclusion


The current review aimed to highlight how group membership modulates the affective, cognitive, and regulative components of empathy. We have shown that in-group bias is not only a result of increased vicarious simulation of the actions (Gutsell and Inzlicht, 2010; Molenberghs et al., 2012b) and feelings (Xu et al., 2009) of in-group compared to out-group members but also follows from increased activation in ToM regions (Adams et al., 2009; Mathur et al., 2010; Cheon et al., 2011) when trying to understand the mental state of in-group vs. out-group members. These group biases can be influenced by emotional regulation (Ito and Bartholow, 2009) depending on expertise (Cheng et al., 2007; Decety et al., 2010) and context (Richeson and Shelton, 2003; Cunningham et al., 2004) so that we respond in a socially acceptable way to our environment. Lastly, it seems that arbitrary re-categorization can override automatic biases such as race (Van Bavel et al., 2008). Seeing as group membership modulates responses at each component of empathy, future investigations should identify methods of reversing these biases at each of the three distinguishable levels.


Conflict of Interest Statement


The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


Acknowledgments


This work was supported by an ARC Discovery Early Career Research Award (DE130100120) and ARC Discovery Project Grant (DP130100559) awarded to Pascal Molenberghs.


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