Pain in crustaceans

Short description: Ethical debate

Close up of the head of a live lobster

There is a scientific debate which questions whether crustaceans experience pain. It is a complex mental state, with a distinct perceptual quality but also associated with suffering, which is an emotional state. Because of this complexity, the presence of pain in an animal, or another human for that matter, cannot be determined unambiguously using observational methods, but the conclusion that animals experience pain is often inferred on the basis of likely presence of phenomenal consciousness which is deduced from comparative brain physiology as well as physical and behavioural reactions.[1]

Definitions of pain vary, but most involve the ability of the nervous system to detect and reflexively react to harmful stimuli by avoiding it, and the ability to subjectively experience suffering. Suffering cannot be directly measured in other animals. Responses to putatively painful stimuli can be measured, but not the experience itself. To address this problem when assessing the capacity of other species to experience pain, argument by analogy is sometimes used.

Crustaceans fulfill several criteria proposed as indicating that non-human animals may experience pain. These fulfilled criteria include a suitable nervous system and sensory receptors; opioid receptors and reduced responses to noxious stimuli when given analgesics and local anaesthetics; physiological changes to noxious stimuli; displaying protective motor reactions; exhibiting avoidance learning; and making trade-offs between noxious stimulus avoidance and other motivational requirements.

In vertebrates, endogenous opioids are neurochemicals that moderate pain by interacting with opioid receptors. Opioid peptides and opioid receptors occur naturally in crustaceans, and although it was concluded in 2005 "at present no certain conclusion can be drawn",[2] more recent considerations suggest their presence along with related physiological and behavioural responses as indicating that crustaceans may experience pain.[3][4] Opioids may moderate pain in crustaceans in a similar way to that in vertebrates. If crustaceans feel pain, there are ethical and animal welfare implications including the consequences of exposure to pollutants, and practices involving commercial and recreational fishing, aquaculture, food preparation and for crustaceans used in scientific research.

## Contents

* 1 Background
* 1.1 Philosophy
* 1.2 Scientific investigation
* 1.2.1 Vertebrates
* 2 Adaptive value
* 3 The experience of pain
* 3.1 Nociception
* 3.2 Emotional pain
* 3.3 Physical pain
* 4 Research findings
* 4.1 Peripheral nervous system
* 4.1.1 Receptors
* 4.1.2 Nerve fibres
* 4.2 Central nervous system
* 4.2.1 Brain
* 4.3 Opioid system and effects of analgesics
* 4.4 Physiological responses
* 4.5 Protective responses
* 4.6 Avoidance learning
* 4.7 Trade-offs in motivation
* 5 Legislation
* 6 Opinions
* 7 Pain during killing
* 8 See also
* 9 References
* 10 Further reading

## Background

The question of whether non-human animals experience pain has a long history. Initially, this was rooted in theoretical and philosophical argument, but more recently, it has also become a topic of scientific investigation.[5]

### Philosophy

Descartes argued that animals could not experience pain

The idea that non-human animals might not feel pain goes back to the 17th-century French philosopher, René Descartes, who argued that animals do not experience pain and suffering because they lack consciousness.[6][7][8] In 1789, the British philosopher and social reformist, Jeremy Bentham, addressed in his book An Introduction to the Principles of Morals and Legislation the issue of our treatment of animals with the following often quoted words: "The question is not, Can they reason? nor, can they talk? but, Can they suffer?"[9]

Peter Singer, a bioethicist and author of Animal Liberation published in 1975, suggested that consciousness is not necessarily the key issue: just because animals have smaller brains, or are 'less conscious' than humans, does not mean that they are not capable of feeling pain. He goes on further to argue that we do not assume newborn infants, people suffering from neurodegenerative brain diseases or people with learning disabilities experience less pain than we would.[10]

Bernard Rollin, the principal author of two U.S. federal laws regulating pain relief for animals, writes that researchers remained unsure into the 1980s as to whether animals experience pain, and veterinarians trained in the U.S. before 1989 were taught to simply ignore animal pain.[11] In his interactions with scientists and other veterinarians, Rollin was regularly asked to "prove" that animals are conscious, and to provide "scientifically acceptable" grounds for claiming that they feel pain.[11]

Continuing into the 1990s, discussions were further developed on the roles that philosophy and science had in understanding animal cognition and mentality.[12] In subsequent years, it was argued there was strong support for the suggestion that some animals (most likely amniotes) have at least simple conscious thoughts and feelings[13] and that the view animals feel pain differently to humans is now a minority view.[6]

### Scientific investigation

Cambridge Declaration on Consciousness (2012)

The absence of a neocortex does not appear to preclude an organism from experiencing affective states. Convergent evidence indicates that non-human animals have the neuroanatomical, neurochemical, and neurophysiological substrates of conscious states along with the capacity to exhibit intentional behaviors. Consequently, the weight of evidence indicates that humans are not unique in possessing the neurological substrates that generate consciousness. Non-human animals, including all mammals and birds, and many other creatures, including octopuses, also possess these neurological substrates.[14]

In the 20th and 21st centuries, there were many scientific investigations of pain in non-human animals. Argument by analogy is sometimes used to assess the capacity of other animals to experience pain. This is based on the principle that if a non-human animal's responses to noxious stimuli are similar to those of humans, they are likely to have had an analogous experience. For example, if a pin is stuck in a chimpanzee's finger and it rapidly withdraws its hand, then argument by analogy indicates that like humans, it felt pain.[15][16][17]

In 2012 the American philosopher Gary Varner reviewed the research literature on pain in animals. His findings are summarised in the following table.[18] Arguing by analogy, Varner claims that any animal which exhibits the properties listed in the table could be said to experience pain. On that basis, he concludes that all vertebrates, including fish, probably experience pain, but invertebrates (e.g. crustaceans) apart from cephalopods probably do not experience pain.[18][19]

#### Vertebrates

Arthritic rats self-select analgesic opiates.[20] In 2014, the veterinary Journal of Small Animal Practice published an article on the recognition of pain which started – "The ability to experience pain is universally shared by all mammals...".[21] Birds with gait abnormalities self-select for a diet that contains carprofen, a human analgesic.[22] In 2005, it was written "Avian pain is likely analogous to pain experienced by most mammals"[23] and in 2014, "it is accepted that birds perceive and respond to noxious stimuli and that birds feel pain."[24] Veterinary articles have been published stating both reptiles[25][26][27] and amphibians[28][29][30] experience pain in a way analogous to humans, and that analgesics are effective in these two classes of vertebrates.

Argument by analogy[18] Property  | Invertebrates  | Vertebrates

|
|

Earth­worms  | Insects  | Leeches/​snails  | Ceph­alopods  | Fish  | Amphib­ians  | Reptiles  | Birds  | Mamm­als
Has nociceptors | ?  | N | Y | ?  | Y | Y | Y | Y | Y
Has brain  | N | N | N | Y | Y | Y | Y | Y | Y
Nociceptors and brain linked  | N | N | N | Y | Y | ? / Y | ? / Y | ? / Y | Y
Has endogenous opioids | Y | Y | ?  | ?  | Y | Y | Y | Y | Y
Analgesics affect responses  | ?  | ?  | ?  | ?  | Y | ?  | ?  | Y | Y
Response to damaging stimuli similar to humans  | N | N | ?  | Y | Y | Y | Y | Y | Y

In the table -

Y denotes Varner believes reliable research indicates the taxon has the attribute
N denotes Varner believes reliable research indicates the taxon does not have the attribute
? denotes Varner believes reliable research has not ascertained whether the taxon has the attribute or varies between species within the taxa.

## Adaptive value

The adaptive value of nociception is obvious; an organism detecting a noxious stimulus immediately withdraws the limb, appendage or entire body from the noxious stimulus and thereby avoids further (potential) injury. However, a characteristic of pain (in mammals at least) is that pain can result in hyperalgesia (a heightened sensitivity to noxious stimuli) and allodynia (a heightened sensitivity to non-noxious stimuli). When this heightened sensitisation occurs, the adaptive value is less clear. First, the pain arising from the heightened sensitisation can be disproportionate to the actual tissue damage caused. Second, the heightened sensitisation may also become chronic, persisting well beyond the tissues healing. This can mean that rather than the actual tissue damage causing pain, it is the pain due to the heightened sensitisation that becomes the concern. This means the sensitisation process is sometimes termed maladaptive. It is often suggested hyperalgesia and allodynia assist organisms to protect themselves during healing, but experimental evidence to support this has been lacking.[31][32]

In 2014, the adaptive value of sensitisation due to injury was tested using the predatory interactions between longfin inshore squid (Doryteuthis pealeii) and black sea bass (Centropristis striata) which are natural predators of this squid. If injured squid are targeted by a bass, they began their defensive behaviours sooner (indicated by greater alert distances and longer flight initiation distances) than uninjured squid. If anaesthetic (1% ethanol and MgCl2) is administered prior to the injury, this prevents the sensitisation and blocks the behavioural effect. The authors claim this study is the first experimental evidence to support the argument that nociceptive sensitisation is actually an adaptive response to injuries.[33]

## The experience of pain

Although there are numerous definitions of pain, almost all involve two key components.

First, nociception is required.[34] This is the ability to detect noxious stimuli which evoke a reflex response that rapidly moves the entire animal, or the affected part of its body, away from the source of the stimulus. The concept of nociception does not imply any adverse, subjective "feeling" – it is a reflex action. An example in humans would be the rapid withdrawal of a finger that has touched something hot – the withdrawal occurs before any sensation of pain is actually experienced. The second component is the experience of "pain" itself, or suffering – the internal, emotional interpretation of the nociceptive experience. Again in humans, this is when the withdrawn finger begins to hurt, moments after the withdrawal. Pain is therefore a private, emotional experience. Nociceptive reflexes act to immediately remove the animal or part of the body from a (potentially) damaging stimulus. However, without learning from this experience, the animal would likely expose itself to the damaging stimulus repeatedly. Pain has the adaptive advantage that it invokes a level of learning, thereby preventing the animal from repeatedly exposing itself to potential injury.[35] Pain cannot be directly measured in other animals, including other humans; responses to putatively painful stimuli can be measured, but not the experience itself. To address this problem when assessing the capacity of other species to experience pain, argument-by-analogy is used. This is based on the principle that if an animal responds to a stimulus in a similar way to ourselves, it is likely to have had an analogous experience.

### Nociception

Main article: Biology:Nociception

Nociception: The reflex arc of a dog with a pin in her paw. Note there is no communication to the brain, but the paw is withdrawn by nervous impulses generated by the spinal cord. There is no conscious interpretation of the stimulus by the dog involved in the reflex itself.

In vertebrates, nociceptive responses involve the transmission of a signal along a chain of nerve fibres from the site of a noxious stimulus at the periphery, to the spinal cord. This process evokes a reflex arc response such as flinching or immediate withdrawal of a limb, generated at the spinal cord and not involving the brain. Nociception is found, in one form or another, across all major animal taxa.[34] Nociception can be observed using modern imaging techniques and both physiological and behavioural responses to nociception can be detected. Many crustacean species, including the rockpool prawn (Palaemon elegans),[36] exhibit the caridoid escape reaction – an immediate, nociceptive, reflex tail-flick response to noxious stimuli (see here[37]).

### Emotional pain

Main article: Medicine:Psychological pain

Sometimes a distinction is made between "physical pain" and "emotional" or "psychological pain". Emotional pain is the pain experienced in the absence of physical trauma, e.g. the pain experienced by humans after the loss of a loved one, or the break-up of a relationship. It has been argued that only primates, including humans, can feel "emotional pain". However, research has provided evidence that monkeys, dogs, cats and birds can show signs of emotional pain and display behaviours associated with depression during painful experience, i.e. lack of motivation, lethargy, anorexia, unresponsiveness to other animals.[10]

### Physical pain

Main article: Medicine:Pain

The nerve impulses of the nociception response may be conducted to the brain thereby registering the location, intensity, quality and unpleasantness of the stimulus. This subjective component of pain involves conscious awareness of both the sensation and the unpleasantness (the aversive, negative affect). The brain processes underlying conscious awareness of the unpleasantness (suffering), are not well understood.

There have been several published lists of criteria for establishing whether non-human animals experience pain, e.g.[38][39] Some criteria that may indicate the potential of another species, including crustaceans, to feel pain include:[39]

1. Has a suitable nervous system and sensory receptors
2. Has opioid receptors and shows reduced responses to noxious stimuli when given analgesics and local anaesthetics
3. Physiological changes to noxious stimuli
4. Displays protective motor reactions that might include reduced use of an affected area such as limping, rubbing, holding or autotomy
5. Shows avoidance learning
6. Shows trade-offs between noxious stimulus avoidance and other motivational requirements
7. High cognitive ability and sentience

## Research findings

File:Shri1000.webm The vast majority of research on pain in crustaceans has used (semi-) aquatic, decapoda species. Animals living in largely different environments are unlikely to have developed the same nociceptive or pain-detecting neural mechanisms. Different environments will result in diverse selection pressures on different animal groups, as well as exposing them to differing types of nociceptive stimuli. For example, crustaceans living in an aquatic world can maintain a certain level of buoyancy, so the risk of collision due to gravity is limited compared with a terrestrial vertebrate. Similarly, noxious chemicals might be diluted considerably in an aquatic environment compared to terrestrial. Therefore, nociceptive and pain systems in aquatic animals may be quite dissimilar to terrestrial animals.[40]

### Peripheral nervous system

The nervous systems of a selection of crustaceans.

#### Receptors

Crayfish (Procambarus clarkii) respond quickly and strongly to high temperatures, however, they show no response to low temperature stimuli, or, when stimulated with capsaicin or isothiocyanate (both are irritants to mammals). Noxious high temperatures are considered to be a potentially ecologically relevant noxious stimulus for crayfish that can be detected by sensory neurons, which may be specialized nociceptors.[41]

The common brown shrimp Crangon crangon and the prawns Palaemon serratus and Palaemon elegans all exhibit a nociceptive sensitivity to both hot and cold temperatures. Both thermal sensitivity levels and nociceptive thresholds change with changes in acclimation temperature.[42]

#### Nerve fibres

Crayfish have peripheral nerve fibres[43] which are responsive to noxious stimuli.[41]

Neurons functionally specialized for nociception have been documented in other invertebrates including the leech Hirudo medicinalis, the nematode Caenorhabditis elegans and the molluscs Aplysia californica and Cepaea nemoralis. Changes in neuronal activity induced by noxious stimuli have been recorded in the nervous centres of Caenorhabditis elegans, Drosophila melanogaster and larval Manduca sexta.[3]

### Central nervous system

When shore crabs (Hemigrapsus sanguineus) have formalin injected into the cheliped (claw), this evokes specific nociceptive behavior and neurochemical responses in the thoracic ganglia and the brain.[3]

#### Brain

Bilaterally symmetrical animals characteristically have a collection of nervous tissue toward the anterior region of their body. This is termed the supraesophageal ganglion and may colloquially be referred to as the "brain". In decapods, the supraesophageal ganglion is divided into three main regions, the protocerebrum, which consists of two optic lobes, and the median protocerebrum.[44]

In 2002, James Rose (University of Wyoming) and more recently Brian Key (University of Queensland) published reviews arguing that fish (and presumably crustaceans) cannot feel pain because they lack a neocortex in the brain and therefore do not have consciousness.[45][46][47] Animal behaviouralist, Temple Grandin, (Colorado State University) argues that animals could still have consciousness without a neocortex because "different species can use different brain structures and systems to handle the same functions."[48] Lynne Sneddon (University of Liverpool) proposes that to suggest a function suddenly arises without a primitive form defies the laws of evolution.[49] Other researchers also believe that animal consciousness does not require a neocortex, but can arise from homologous subcortical brain networks.[14]

### Opioid system and effects of analgesics

Opiates modulate nociception in vertebrates. In vertebrates, morphine is an analgesic and therefore ameliorates the sensation of pain. Naloxone is an opioid-receptor antagonist and therefore blocks the effects of morphine. Opioid modulation of nociception has been demonstrated in several invertebrate species.[50] File:Mantis shrimp in the Philippines.webm The first report of opiate effects in invertebrates is based on the behavioural responses of the crustacean mantis shrimp Squilla mantis. These shrimp respond to an electric shock with an immediate, violent, convulsive-like flexion of the body. If they are injected with morphine-HCL, this produces a dose-dependent analgesia by increasing the intensity threshold to the shock. This effect is fully blocked by naloxone.[51]

Crustaceans have a functional opioid system which includes the presence of opioid receptors similar to those of mammals. Delta- and Kappa-opioid receptors have been described in crustaceans.[52] RT-PCR research on the American lobster (Homarus americanus) has revealed the presence of a Mu-opioid receptor transcript in neural and immune tissues, which exhibits a 100% sequence identity with its human counterpart.[53]

In the American lobster, endogenous morphine is found in the haemolymph and ventral nerve cord. In lobsters which have had a pereiopod (walking leg) cut off or been injected with the irritant lipopolysaccharide, the endogenous morphine levels initially increased by 24% for haemolymph and 48% for the nerve cord.[53]

In vertebrates, opioid peptides (i.e., enkephalins) have been shown to be involved in nociception. Leu-enkephalin and Met-enkephalin are present in the thoracic ganglia of the shore crab, Carcinus maenas.[54]

Both morphine and naloxone affect the estuarine crab (Neohelice granulata) in a similar way to their effects on vertebrates: injections of morphine produce a dose-dependent reduction of their defensive response to an electric shock.[55] However, it has been suggested the attenuated defensive response could originate from either the analgesic or sedative properties of morphine, or both.[56] One study on the effects of a danger stimulus on the crab Chasmagnathus granulatus reported this induces opioid analgesia, which is influenced by naloxone.[57] In American lobsters, the response of endogenous morphine in both haemocytes and neural cells to noxious stimuli are mediated by naloxone.[53]

When the antennae of rockpool prawns Palaemon elegans are rubbed with sodium hydroxide or acetic acid (both are irritants in mammals), they increase grooming and rubbing of the afflicted area against the side of the tank; this reaction is inhibited by benzocaine (a local anaesthetic in mammals), even though control prawns treated with only anaesthetic do not show reduced activity.[36]

The whiteleg shrimp (juvenile shown) has become the preferred species for shrimp farming

Eyestalk ablation is the removal of one or both eyestalks from a crustacean. It is routinely practiced on female prawns in almost every marine shrimp maturation or reproduction facility in the world, both research and commercial. The aim of ablation is to stimulate the female shrimp to develop mature ovaries and spawn.[58] In Macrobrachium americanum, prawns treated with lignocaine (a local anaesthetic in mammals), showed less rubbing, flicking and sheltering than those without the anaesthetic.[59]

One study on reducing the stress of prawns resulting from transportation concluded that Aqui-STM and clove oil (a natural anaesthetic) may be suitable anaesthetic treatments for prawns.[60]

### Physiological responses

Higher levels of stress, as measured by lactate, occur in shore crabs exposed to brief electric shock compared to non-shocked controls. However, shocked crabs showed more vigorous behaviour than controls, possibly indicating it is increased behaviour causing the increased lactate. But, when crabs with the same level of behaviour are matched, shocked crabs still have a stronger stress response compared with controls. The authors suggested that their findings, coupled with previous findings of long-term motivational change and avoidance learning, "fulfils the criteria expected of a pain experience".[4] Others have criticised these findings, including the fact that the lactate levels measured were within the normal range measured for shore crabs, and that any increases in lactate in shocked crabs were possibly due to increased anaerobic activity. They also argued that behavioural "activities that go beyond mere reflex responses" is an inadequate criterion for pain.[61]

In crayfish (Procambarus clarkii), anxiolytic (stress-reducing) drugs made for humans also reduce anxiety.[62]

Injection of formalin into the cheliped of shore crabs (Hemigrapsus sanguineus) evokes specific nociceptive behavior and neurochemical responses in the brain and thoracic ganglion.[63]

### Protective responses

A hermit crab outside of its shell. Note the soft, curved abdomen which is vulnerable to predators.

Most species of hermit crab have long, spirally curved abdomens, which are soft, unlike the hard, calcified abdomens seen in related crustaceans. They protect themselves from predators by entering a salvaged empty seashell, into which they can retract their whole body. As they grow, they must leave their shell and find another larger, more suitable shell.[64] Their shells are therefore highly valuable to them. When hermit crabs (Pagurus bernhardus) are given an electric shock, they leave their shells and subsequently perform prolonged abdominal grooming at the site of where they received the shock.[65]

Male Chasmagnathus granulatus crabs exhibit a "defensive response" to electric shocks.[55] During a study on the ability of shore crabs (Carcinus maenas) learning to avoid an electrical shock, it was observed that many crabs emerged from the dark shelter to avoid the shock thus entering a brightly lit area which would normally be avoided.[66] Immediately after the injection of formalin (an irritant in mammals) or saline into one cheliped (the leg which ends with the claw), shore crabs move quickly into the corner of the aquarium and "freeze" after 2 to 3 seconds. After 1 to 3 minutes, these injected animals are fidgety and exhibit a wide range of movements such as flexion, extension, shaking or rubbing the affected claw. Formalin-treated animals show 20-times more rubbing behaviour during the first minute after injection than saline-treated crabs. Intense rubbing of the claw results in autotomy (shedding) in 20% of animals of the formalin-treated group whereas saline-injected crabs do not autotomise the injected cheliped. During the 10 minutes after injection, crabs in the formalin-treated group tried to use the intact cheliped, guarding the damaged cheliped. The scientists conducting this study commented "the present results obtained in crabs may be indicative of pain experience rather than relating to a simple nociceptive reflex".[3] Other species of crab have been shown to autotomise legs when placed on a hot plate or exposed to a small electric shock.[15]

When the antennae of rockpool prawns (Palaemon elegans) are rubbed with sodium hydroxide or acetic acid (both are irritants), the animals show increased grooming and rubbing of the afflicted area against the side of the tank. Furthermore, this reaction is inhibited by a local anaesthetic, even though control prawns treated with only anaesthetic did not show reduced activity. Other scientists suggested the rubbing may reflect an attempt to clean the affected area[67] as application of anaesthetic alone caused an increase in grooming.

In one study, no behavioural or neural changes in three different crustacean species (red swamp crayfish (Procambarus clarkii), white shrimp (Litopenaeus setiferus) and Palaemonetes sp.) were observed in response to noxious acids or bases.[68]

### Avoidance learning

Shore crabs quickly (within 1 or 2 trials) learn to avoid one of two dark shelters if choosing that shelter consistently results in them receiving an electric shock.[69] The crayfish Procambarus clarkii and the crab Chasmagnathus granulatus learn to associate an electric shock with a light turning on, or with the occupancy of the light compartment of the aquarium, respectively. They quickly learn to respond to these associations by walking to a safe area in which the shock is not delivered (crayfish) or by refraining from entering the light compartment (crab).[15]

### Trade-offs in motivation

A hermit crab

Nociceptive responses are reflexes that do not change regardless of motivational priorities. In contrast, a painful experience may change the motivation for normal behavioural responses, thereby indicating a plastic response to an aversive stimulus, rather than a simple reflex response.[39]

In 2009, Elwood and Mirjam Appel showed that hermit crabs make motivational trade-offs between electric shocks and the quality of the shells they inhabit.[70] In particular, as hermit crabs are shocked more intensely, they become increasingly willing to leave their current shells for new shells, and they spend less time deciding whether to enter those new shells. Moreover, because the researchers did not offer the new shells until after the electrical stimulation had ended, the change in motivational behavior was the result of memory of the noxious event, not an immediate reflex. It was also shown that hermit crabs experiencing increasing electric shocks left their shell at a reduced intensity when the shell was from a less preferred species than did those in shells of a more desirable species. This demonstrates that hermit crabs are willing to risk predator attack by evacuating their shells to avoid a noxious stimulus and that this is dependent upon how valuable the shell is.[40]

A similar study shows that hermit crabs are less likely to leave their shells after electric shock if they are in an environment that contains the odour of predators. This shows the crabs trade-off the motivation to avoid electric shocks and predator avoidance.[71]

Shore crabs (Carcinus maenas) also show motivational trade-offs; they will discard a valuable resource (a preferred shelter) to avoid future encounters with painful stimuli, thereby indicating avoidance learning – a key criterion of the ability to experience pain.[66]

A 2014 study[72] on crayfish (Procambarus clarkii) tested their responses in a fear paradigm, the elevated plus maze in which animals choose to walk on an elevated cross which offers both aversive and preferable conditions (in this case, two arms were lit and two were dark). Crayfish which experienced an electric shock displayed enhanced fearfulness or anxiety as demonstrated by their preference for the dark arms more than the light. Furthermore, shocked crayfish had relatively higher brain serotonin concentrations coupled with elevated blood glucose, which suggests a stress response.[40] A follow-up study using the same species showed the intensity of the anxiety-like behaviour, presumably resulting from the pain, was dependent on the intensity of the electric shock until reaching a plateau. Such a quantitative relationship between stress and anxiety is also a very common feature of human and vertebrate anxiety.[73]

## Legislation

Legislation protects some invertebrates when they are being used in research; the taxa protected varies between countries and regions.

Legislation on the protection of invertebrates in research adapted from[74] Country or
region | Invertebrates protected | Legislation

|
|

Australia
(some states) | Cephalopods | Government National Health and Medical
Research Council's Code of Practice (2004)
Canada | Cephalopods and "some other higher invertebrates" | Canadian Council on Animal Care (1991)[75]
EU | Cephalopods | EU Directive 2010/63/EU[76]
New Zealand | Octopuses, squids, crabs, lobsters, crayfish | Animal Welfare Act (1999)[77]
Norway | Squids, octopuses, decapod crustaceans, honeybees | Norwegian Animal Welfare Act (2009)[78]
Switzerland | Cephalopods, decapod crustaceans | Swiss Animal Welfare Act (2008)[79]

In 2022, the UK Animal Welfare (Sentience) Act recognized the sentience of decapod crustaceans and cephalopods, requiring the government to consider their wellbeing in future policymaking.[80] In December 2025, pursuant to the law, the Department for Environment, Food and Rural Affairs announced its intention to prohibit the live boiling of decapods and cephalopods by 2030.[81]

Jonathan Birch, philosopher of biology at the London School of Economics, argues that we should apply the precautionary principle to animal sentience. Without lowering scientific standards, this principle leads to include in our animal protection laws any species for which we have at least a credible indicator of sentience. If we have good reasons to believe that a species of crab is sentient, it is sufficient to believe that all crabs (more than 4000 species) are sentient. Therefore, it is all the members of the decapod order that should be included in our animal welfare laws.[82]

## Opinions

Advocates for Animals, a Scottish animal welfare group, stated in 2005 that "scientific evidence ... strongly suggests that there is a potential for decapod crustaceans and cephalopods to experience pain and suffering". This is primarily due to "The likelihood that decapod crustaceans can feel pain [which] is supported by the fact that they have been shown to have opioid receptors and to respond to opioids (analgesics such as morphine) in a similar way to vertebrates." Similarities between decapod and vertebrate stress systems and behavioral responses to noxious stimuli were given as additional evidence for the capacity of decapods to experience pain.[83]

In 2005 a review of the literature by the Norwegian Scientific Committee for Food Safety tentatively concluded that "it is unlikely that [lobsters] can feel pain," though they note that "there is apparently a paucity of exact knowledge on sentience in crustaceans, and more research is needed." This conclusion is based on the lobster's simple nervous system. The report assumes that the violent reaction of lobsters to boiling water is a reflex response (i.e. does not involve conscious perception) to noxious stimuli.[2]

A European Food Safety Authority (EFSA) 2005 publication[84] stated that the largest of decapod crustaceans have complex behaviour, a pain system, considerable learning abilities and appear to have some degree of awareness. Based on this evidence, they placed all decapod crustaceans into the same category of research-animal protection as vertebrates.

In 2021, following a review,[85] the United Kingdom officially recognized decapod crustaceans and cephalopods as sentient beings capable of experiencing pain.[86]

## Pain during killing

This tanner crab was cut in half before cooking

The EFSA summarized that the killing methods most likely to cause pain and distress are:[87]

* Any procedures whereby the abdomen is separated from the thorax
* The removal of tissue, flesh, or limbs while the crustacean is alive and fully conscious
* Placing crustaceans in water slowly heated to the boiling point
* Placing crustaceans directly into boiling water
* Placing marine crustaceans in fresh water
* Unfocused microwaving of the body as opposed to focal application to the head

A device called the CrustaStun has been invented to electrocute shellfish, such as lobsters, crabs, and crayfish, before cooking. The device works by applying a 120-volt, 2 to 5 amp electrical charge to the animal. The manufacturer claims it renders the shellfish unconscious in 0.3 seconds and kills the animal in 5 to 10 seconds, compared to 3 minutes to kill a lobster or crab by boiling;[88] however, the source for the claim states that movements detected after 10 seconds were the result of heat's effect on the muscles or escape of air from the branchial chambers, not voluntary movements, and the author declares this measure of 3 minutes "useless" for determining time until death.[89]

## See also

* Animal cognition
* Cruelty to animals
* Declawing of crabs
* Emotion in animals
* Ethics of uncertain sentience
* Moral status of animals in the ancient world
* Pain and suffering in laboratory animals
* Sentience
* Veganism

## References

1. ↑ Abbott, F.V.; Franklin, K.B.J.; Westbrook, R.F. (1995). "The formalin test: Scoring properties of the first and second phases of the pain response in rats". Pain 60 (1): 91–102. doi:10.1016/0304-3959(94)00095-V. PMID 7715946.
2. ↑ 2.0 2.1 Sømme, L. (2005). "Sentience and pain in invertebrates: Report to Norwegian Scientific Committee for Food Safety". Norwegian University of Life Sciences, Oslo.
3. ↑ 3.0 3.1 3.2 3.3 Dyuizen, I.V., Kotsyuba, E.P. and Lamash, N.E. (2012). "Changes in the nitric oxide system in the shore crab Hemigrapsus sanguineus (Crustacea, decapoda) CNS induced by a nociceptive stimulus". Journal of Experimental Biology 215 (15): 2668–2676. doi:10.1242/jeb.066845. PMID 22786644.
4. ↑ 4.0 4.1 Elwood, R.W.; Adams, L. (2015). "Electric shock causes physiological stress responses in shore crabs, consistent with prediction of pain". Biology Letters 11 (11). doi:10.1098/rsbl.2015.0800. PMID 26559514.
5. ↑ "Animal Consciousness". https://plato.stanford.edu/entries/consciousness-animal/.
6. ↑ 6.0 6.1 Carbone, L. (2004). What Animals Want: Expertise and Advocacy in Laboratory Animal Welfare Policy. Oxford University Press. p. 149. ISBN 978-0-19-516196-0. https://books.google.com/books?id=Iheg3hkj99AC&q="What+Animal+Want:+Expertise+and+Advocacy+in+Laboratory+Animal+Welfare+Policy".
7. ↑ Radner, D.; Radner, M. (1989). Animal Consciousness. Prometheus Books: Buffalo.
8. ↑ Harrison, P. (1992). "Descartes on animals". The Philosophical Quarterly 42 (167): 219–227. doi:10.2307/2220217.
9. ↑ "Bentham, J. (1879). An Introduction to the Principles of Morals and Legislation. Clarendon Press.
10. ↑ 10.0 10.1 Sneddon, L.U.. "Can animals feel pain?". The Welcome Trust. http://www.wellcome.ac.uk/en/pain/microsite/culture2.html.
11. ↑ 11.0 11.1 Rollin, B. (1989). The Unheeded Cry: Animal Consciousness, Animal Pain, and Science. Oxford University Press, pp. xii, 117–118, cited in Carbone 2004, p. 150.
12. ↑ Allen, C. (1998). "Assessing animal cognition: Ethological and philosophical perspectives". Journal of Animal Science 76 (1): 42–47. doi:10.2527/1998.76142x. PMID 9464883. https://dl.sciencesocieties.org/publications/jas/abstracts/76/1/42. Retrieved 2016-02-23.
13. ↑ Griffin, D.R.; Speck, G.B. (2004). "New evidence of animal consciousness". Animal Cognition 7 (1): 5–18. doi:10.1007/s10071-003-0203-x. PMID 14658059.
14. ↑ 14.0 14.1 Low, P. (July 7, 2012). "The Cambridge declaration on consciousness". in Jaak Panksepp; Diana Reiss; David Edelman et al.. University of Cambridge. http://fcmconference.org/img/CambridgeDeclarationOnConsciousness.pdf.
15. ↑ 15.0 15.1 15.2 Gherardi, F. (2009). "Behavioural indicators of pain in crustacean decapods". Annali dell'Istituto Superiore di Sanità 45 (4): 432–438. doi:10.1590/s0021-25712009000400013. PMID 20061665.
16. ↑ Sherwin, C.M. (2001). "Can invertebrates suffer? Or, how robust is argument-by-analogy?". Animal Welfare (Supplement) 10: S103–S118. doi:10.1017/S0962728600023551.
17. ↑ Elwood, R.W. (2011). "Pain and suffering in invertebrates?". Institute of Laboratory Animal Resources Journal 52 (2): 175–84. doi:10.1093/ilar.52.2.175. PMID 21709310. http://dels-old.nas.edu/ilar_n/ilarjournal/52_2/PDFs/v5202Elwood.pdf.
18. ↑ 18.0 18.1 18.2 Varner, G.E. (2012). "Chapter 5 - Which animals are sentient?". Personhood, Ethics, and Animal Cognition: Situating Animals in Hare's Two Level Utilitarianism. Oxford University Press. doi:10.1093/acprof:oso/9780199758784.001.0001. ISBN 978-0-19-975878-4. https://books.google.com/books?id=12U6Fr-083YC&q="Personhood,+Ethics,+and+Animal+Cognition". Retrieved 2020-11-07. Table 5.2, page 113.
19. ↑ Kristin, A. (2014). The Animal Mind: An Introduction to the Philosophy of Animal Cognition (section 3.6.2). Routledge. ISBN 978-1-317-67675-1. https://books.google.com/books?id=fiIhBQAAQBAJ&q=fish+pain+philosophy&pg=PT101. Retrieved 2020-11-07.
20. ↑ Colpaert, F.C., Tarayre, J.P., Alliaga, M., Slot. L.A.B., Attal, N. and Koek, W. (2001). "Opiate self-administration as a measure of chronic nociceptive pain in arthritic rats". Pain 91 (1–2): 33–45. doi:10.1016/s0304-3959(00)00413-9. PMID 11240076.
21. ↑ Mathews, K., Kronen, P.W., Lascelles, D., Nolan, A., Robertson, S., Steagall, P.V., Wright, B. and Yamashita, K. (2014). "Guidelines for recognition, assessment and treatment of pain.". Journal of Small Animal Practice 55 (6): E10–E68. doi:10.1111/jsap.12200. PMID 24841489.
22. ↑ Danbury, T.C., Weeks, C.A., Chambers, J.P., Waterman-Pearson, A.E. and Kestin, S.C. (2000). "Self-selection of the analgesic drug carprofen by lame broiler chickens". The Veterinary Record 146 (11): 307–311. doi:10.1136/vr.146.11.307. PMID 10766114.
23. ↑ Machin, K.L. (2005). "Avian analgesia". Seminars in Avian and Exotic Pet Medicine 14 (4): 236–242. doi:10.1053/j.saep.2005.09.004.
24. ↑ Paul-Murphy, J.; Hawkins, M.G. (2014). "Chapter 26 - Bird-specific considerations: recognizing pain in pet birds.". in Gaynor, J.S.. Handbook of Veterinary Pain Management. Elsevier Health Sciences.
25. ↑ Mosley, C.A. (2005). "Anesthesia & Analgesia in reptiles". Seminars in Avian and Exotic Pet Medicine 14 (4): 243–262. doi:10.1053/j.saep.2005.09.005.
26. ↑ Mosley, C. (2011). "Pain and nociception in reptiles". Veterinary Clinics of North America: Exotic Animal Practice 14 (1): 45–60. doi:10.1016/j.cvex.2010.09.009. PMID 21074702.
27. ↑ Sladky, K.K.; Mans, C. (2012). "Clinical analgesia in reptiles". Journal of Exotic Pet Medicine 21 (2): 158–167. doi:10.1053/j.jepm.2012.02.012.
28. ↑ Machin, K.L. (1999). "Amphibian pain and analgesia". Journal of Zoo and Wildlife Medicine 30 (1): 2–10. PMID 10367638.
29. ↑ Machin, K.L. (2001). "Fish, amphibian, and reptile analgesia". The Veterinary Clinics of North America. Exotic Animal Practice 4 (1): 19–33. doi:10.1016/S1094-9194(17)30048-8. PMID 11217460.
30. ↑ Stevens, C.W. (2011). "Analgesia in amphibians: preclinical studies and clinical applications". Veterinary Clinics of North America: Exotic Animal Practice 14 (1): 33–44. doi:10.1016/j.cvex.2010.09.007. PMID 21074701.
31. ↑ Price, T.J.; Dussor, G. (2014). "Evolution: the advantage of 'maladaptive'pain plasticity". Current Biology 24 (10): R384–R386. doi:10.1016/j.cub.2014.04.011. PMID 24845663. Bibcode: 2014CBio...24.R384P.
32. ↑ "Maladaptive pain". Oxford Reference. http://www.oxfordreference.com/view/10.1093/oi/authority.20110803100128206.
33. ↑ Crook, R.J., Dickson, K., Hanlon, R.T. and Walters, E.T. (2014). "Nociceptive sensitization reduces predation risk". Current Biology 24 (10): 1121–1125. doi:10.1016/j.cub.2014.03.043. PMID 24814149. Bibcode: 2014CBio...24.1121C.
34. ↑ 34.0 34.1 Sneddon, L.U. (2004). "Evolution of nociception in vertebrates: comparative analysis of lower vertebrates". Brain Research Reviews 46 (2): 123–130. doi:10.1016/j.brainresrev.2004.07.007. PMID 15464201. https://animalstudiesrepository.org/acwp_vsm/43. Retrieved 2019-08-03.
35. ↑ Elwood, R.W. (2016). "A single strand of argument with unfounded conclusion". Animal Sentience 1 (3): 19. doi:10.51291/2377-7478.1056.
36. ↑ 36.0 36.1 Barr, S., Laming, P.R., Dick, J.T.A. and Elwood, R.W. (2008). "Nociception or pain in a decapod crustacean?". Animal Behaviour 75 (3): 745–751. doi:10.1016/j.anbehav.2007.07.004.
37. ↑ "Crayfish video - tail-flip Response - neur3010". 9 December 2013. https://www.youtube.com/watch?v=CEx_qtN-D7M.
38. ↑ Sneddon, L.U., Elwood, R.W., Adamo, S.A. and Leach, M.C. (2014). "Defining and assessing animal pain". Animal Behaviour 97: 201–212. doi:10.1016/j.anbehav.2014.09.007. http://animalstudiesrepository.org/cgi/viewcontent.cgi?article=1068&context=acwp_arte. Retrieved 2016-02-23.
39. ↑ 39.0 39.1 39.2 Elwood, R.W., Barr, S. and Patterson, L. (2009). "Pain and stress in crustaceans?". Applied Animal Behaviour Science 118 (3): 128–136. doi:10.1016/j.applanim.2009.02.018.
40. ↑ 40.0 40.1 40.2 Sneddon, L.U. (2015). "Pain in aquatic animals". Journal of Experimental Biology 218 (7): 967–976. doi:10.1242/jeb.088823. PMID 25833131.
41. ↑ 41.0 41.1 Puri, S.; Faulkes, Z. (2015). "Can crayfish take the heat? Procambarus clarkii show nociceptive behaviour to high temperature stimuli, but not low temperature or chemical stimuli". Biology Open 4 (4): 441–448. doi:10.1242/bio.20149654. PMID 25819841.
42. ↑ Davies, C.A. (1981). Thermal sensitivity and behaviour in the brown shrimp and some related crustacea (Doctoral dissertation) (Thesis). University College of Swansea.
43. ↑ "Behavioral Neuroscience, Crayfish Circuitry". http://usdbiology.com/cliff/Courses/Behavioral Neuroscience/Crayfish/CrayEscfigs/Crayfishcirc.html.
44. ↑ Sandeman, D. (1990). "Structural and functional levels in the organization of decapod crustacean brains". Frontiers in Crustacean Neurobiology. Birkhäuser Basel. pp. 223–239.
45. ↑ Key, B. (2015). "Fish do not feel pain and its implications for understanding phenomenal consciousness". Biology and Philosophy 30 (2): 149–165. doi:10.1007/s10539-014-9469-4. PMID 25798021.
46. ↑ Rose, J.D. (2002). "The neurobehavioral nature of fishes and the question of awareness and pain". Reviews in Fisheries Science 10 (1): 1–38. doi:10.1080/20026491051668. Bibcode: 2002RvFS...10....1R. http://www.nal.usda.gov/awic/pubs/Fishwelfare/Rose.pdf.
47. ↑ Rose, J.D. (2002). "Do fish feel pain?". http://www.coloradotu.org/do-fish-feel-pain/.
48. ↑ Grandin, T.; Johnson, C. (2005). Animals in Translation. New York: Scribner. pp. 183–184. ISBN 978-0-7432-4769-6. https://archive.org/details/animalsintransla00gran/page/183.
49. ↑ Sneddon, L.U. (2012). "Pain perception in fish: Evidence and implications for the use of fish". Journal of Consciousness Studies 18: 209–229.
50. ↑ Nieto-Fernandez, F., Andrieux, S., Idrees, S., Bagnall, C., Pryor, S.C. and Sood, R. (2009). "The effect of opioids and their antagonists on the nocifensive response of Caenorhabditis elegans to noxious thermal stimuli". Invertebrate Neuroscience 9 (3–4): 195–200. doi:10.1007/s10158-010-0099-5. PMID 20397037.
51. ↑ Maldonado, H.; Miralto, A. (1982). "Effect of morphine and naloxone on a defensive response of the mantis shrimp (Squilla mantis)". Journal of Comparative Physiology 147 (4): 455–459. doi:10.1007/bf00612010.
52. ↑ Hanke, J., Willig, A., Yinon, U. and Jaros, P.P. (1997). "Delta and kappa opioid receptors in eyestalk ganglia of a crustacean". Brain Research 744 (2): 279–284. doi:10.1016/s0006-8993(96)01114-6. PMID 9027387.
53. ↑ 53.0 53.1 53.2 Casares, F.M., McElroy, A., Mantione, K.J., Baggermann, G., Zhu, W. and Stefano, G.B. (2005). "The American lobster, Homarus americanus, contains morphine that is coupled to nitric oxide release in its nervous and immune tissues: Evidence for neurotransmitter and hormonal signaling". Neuro Endocrinol. Lett. 26 (2): 89–97. PMID 15855878.
54. ↑ Lüschen, W., Buck, F., Willig, A. and Jaros, P.P. (1991). "Isolation, sequence analysis, and physiological properties of enkephalins in the nervous tissue of the shore crab Carcinus maenas L.". Proceedings of the National Academy of Sciences 88 (19): 8671–8675. doi:10.1073/pnas.88.19.8671. PMID 11607217. Bibcode: 1991PNAS...88.8671L.
55. ↑ 55.0 55.1 Lozada, M., Romano, A. and Maldonado, H. (1988). "Effect of morphine and naloxone on a defensive response of the crab Chasmagnathus granulatus". Pharmacology Biochemistry and Behavior 30 (3): 635–640. doi:10.1016/0091-3057(88)90076-7. PMID 3211972.
56. ↑ Dyakonova, V.E. (2001). "Role of opioid peptides in behavior of invertebrates". Journal of Evolutionary Biochemistry and Physiology 37 (4): 335–347. doi:10.1023/A:1012910525424.
57. ↑ Valeggia, C., Fernandez-Duque, E. and Maldonado, H. (1989). "Danger stimulus-induced analgesia in the crab Chasmagnathus granulatus". Brain Research 481 (2): 304–308. doi:10.1016/0006-8993(89)90807-x. PMID 2720382.
58. ↑ Uawisetwathana, Umaporn; Leelatanawit, Rungnapa; Klanchui, Amornpan; Prommoon, Juthatip; Klinbunga, Sirawut; Karoonuthaisiri, Nitsara (2011). "Insights into Eyestalk Ablation Mechanism to Induce Ovarian Maturation in the Black Tiger Shrimp". PLOS ONE 6 (9). doi:10.1371/journal.pone.0024427. PMID 21915325. Bibcode: 2011PLoSO...624427U.
59. ↑ Diarte-Plata, G., Sainz-Hernández, J.C., Aguiñaga-Cruz, J.A., Fierro-Coronado, J.A., Polanco-Torres, A. and Puente-Palazuelos, C. (2012). "Eyestalk ablation procedures to minimize pain in the freshwater prawn Macrobrachium americanum". Applied Animal Behaviour Science 140 (3): 172–178. doi:10.1016/j.applanim.2012.06.002.
60. ↑ Coyle, S.D., Dasgupta, S., Tidwell, J.H., Beavers, T., Bright, L.A. and Yasharian, D.K. (2005). "Comparative efficacy of anesthetics for the freshwater prawn Macrobrachiurn rosenbergii". Journal of the World Aquaculture Society 36 (3): 282–290. doi:10.1111/j.1749-7345.2005.tb00332.x. Bibcode: 2005JWAS...36..282C.
61. ↑ Stevens, E.D.; Arlinghaus, R.; Browman, H.I.; Cooke, S.J.; Cowx, I.G.; Diggles, B.K.; Key, B.; Rose, J.D. et al. (2016). "Stress is not pain. Comment on Elwood and Adams (2015) Electric shock causes physiological stress responses in shore crabs, consistent with prediction of pain". Biology Letters 12 (4). doi:10.1098/rsbl.2015.1006. PMID 27048466. PMC 4881339. http://www.fecpl.ca/wp-content/uploads/2016/02/Stevens-et-al.-2015-Biology-Letters.pdf. Retrieved 2016-04-25.
62. ↑ Elwood, R.W. (2016). "Might insects experience pain?". Animal Sentience 1 (9): 18. doi:10.51291/2377-7478.1156.
63. ↑ Dyuizen I.V.; Kotsyuba E.P.; Lamash N.E. (2012). "Changes in the nitric oxide system in the shore crab Hemigrapsus sanguineus (Crustacea, decapoda) CNS induced by a nociceptive stimulus". The Journal of Experimental Biology 215 (15): 2668–2676. doi:10.1242/jeb.066845. PMID 22786644.
64. ↑ "Incredible footage of hermit crab changing shells with anemones!". 13 July 2014. https://www.youtube.com/watch?v=dYFALyP2e7U.
65. ↑ Appel, M.; Elwood, R.W. (2009). "Gender differences, responsiveness and memory of a potentially painful event in hermit crabs". Animal Behaviour 78 (6): 1373–1379. doi:10.1016/j.anbehav.2009.09.008.
66. ↑ 66.0 66.1 Robert W. Elwood; Barry Magee (2013). "Shock avoidance by discrimination learning in the shore crab (Carcinus maenas) is consistent with a key criterion for pain". Journal of Experimental Biology 216 (3): 353–358. doi:10.1242/jeb.072041. PMID 23325857. https://pure.qub.ac.uk/portal/files/130842011/353.full.pdf. Retrieved 2019-09-02.
67. ↑ Ian Sample (November 8, 2007). "Blow for fans of boiled lobster: crustaceans feel pain, study says". The Guardian. https://www.theguardian.com/science/2007/nov/08/animalrights.sciencenews.
68. ↑ Puri, S.; Faulkes, Z. (2010). "Do decapod crustaceans have nociceptors for extreme pH?". PLOS ONE 5 (4). doi:10.1371/journal.pone.0010244. PMID 20422026. Bibcode: 2010PLoSO...510244P.
69. ↑ Magee, B.; Elwood, R.W. (2013). "Shock avoidance by discrimination learning in the shore crab (Carcinus maenas) is consistent with a key criterion for pain". Journal of Experimental Biology 216 (3): 353–358. doi:10.1242/jeb.072041. PMID 23325857.
70. ↑ Robert W. Elwood; Mirjam Appel (2009). "Pain experience in hermit crabs?". Animal Behaviour 77 (5): 1243–1246. doi:10.1016/j.anbehav.2009.01.028. http://www.mbl.edu/research/services/iacuc/pdf/pain_hermit_crabs.pdf.
71. ↑ Magee, B.; Elwood, R.W. (2016). "Trade-offs between predator avoidance and electric shock avoidance in hermit crabs demonstrate a non-reflexive response to noxious stimuli consistent with prediction of pain". Behavioural Processes 130: 31–35. doi:10.1016/j.beproc.2016.06.017. PMID 27374025.
72. ↑ Fossat, P., Bacqué-Cazenave, J., De Deurwaerdère, P., Delbecque, J.-P. and Cattaert, D. (2014). "Anxiety-like behavior in crayfish is controlled by serotonin". Science 344 (6189): 1293–1297. doi:10.1126/science.1248811. PMID 24926022. Bibcode: 2014Sci...344.1293F.
73. ↑ Fossat, P., Bacqué-Cazenave, J., De Deurwaerdère, P., Cattaert, D. and Delbecque, J.P. (2015). "Serotonin, but not dopamine, controls the stress response and anxiety-like behavior in the crayfish Procambarus clarkii". Journal of Experimental Biology 218 (17): 2745–2752. doi:10.1242/jeb.120550. PMID 26139659.
74. ↑ Tonkins, B.B.M. (2016). Why are cephalopods protected in scientific research in Europe?
75. ↑ "Guide To The care and Use Of Experimental Animals". Canadian Council on Animal Care. https://ccac.ca/Documents/Standards/Guidelines/Experimental_Animals_Vol1.pdf.
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81. ↑ Nicolas, Emma (31 December 2025). "UK moves to ban boiling lobsters, shrimp, crabs and langoustines alive, recognizing their capacity for pain". Le Monde. https://www.lemonde.fr/en/environment/article/2025/12/31/uk-moves-to-ban-boiling-lobsters-shrimp-crabs-and-langoustines-alive-recognizing-their-capacity-for-pain_6748952_114.html.
82. ↑ Birch, Jonathan (2017-01-01). "Animal sentience and the precautionary principle". Animal Sentience 2 (16). doi:10.51291/2377-7478.1200. ISSN 2377-7478. https://www.wellbeingintlstudiesrepository.org/animsent/vol2/iss16/1/.
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## Further reading

* Grandin, Temple and Deesing, Mark (2003 update) "Distress in Animals: Is it Fear, Pain or Physical Stress?" American Board of Veterinary Practitioners – Symposium 2002.
* "Consider the Lobster" Essay by David Foster Wallace, published in Gourmet, August 2004.

* v
* t
* e

Animal cognition

Cognition|

* Animal communication
* Animal consciousness
* Animal language
* Cognitive bias in animals
* Cognitive ethology
* Comparative cognition
* Elephant cognition
* Emotion in animals
* Mirror test
* Neuroethology
* Observational learning
* Primate cognition
* Tool use by animals
* Vocal learning

Intelligence|

* Bird
* talking
* Cat
* Cephalopod
* Cetacean
* Dinosaur
* Dog
* Fish
* Hominid
* Swarm

Pain|

* Pain in amphibians
* Pain in animals
* Pain in cephalopods
* Pain in crustaceans
* Pain in fish
* Pain in invertebrates

Relation to brain|

* Brain size
* Brain-to-body mass ratio
* Encephalization quotient
* Neuroscience and intelligence
* Number of neurons

* Category

* v
* t
* e

Animal welfare

Issues|

* Abandoned pets
* Blood sports
* Eating live animals
* Eating live seafood
* Intensive animal farming
* Overview of discretionary invasive procedures on animals
* Puppy mill
* Wild animal suffering

Concepts|

* Abnormal behaviours in animals
* Animal psychopathology
* Animal shelter
* Animal welfare science
* Anthrozoology
* Behavioral enrichment
* Compassionate conservation
* Ethical omnivorism
* Intrinsic value (animal ethics)
* Rescue group

Pain in nonhuman animals|

* Pain in animals
* Pain in amphibians
* Pain in cephalopods
* Pain in crustaceans
* Pain in fish
* Pain in invertebrates
* Grimace scale (animals)

Organisations|

* Animal welfare organizations
* Animal welfare organizations by country
* Animal welfare (journal)
* HSUS
* International Society for Applied Ethology
* List of animal welfare groups
* RSPCA
* Society for the Prevention of Cruelty to Animals
* UFAW
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Animal-welfare scholars|

* Jonathan Balcombe
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Categories|

* Animal advocacy parties
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Legislation|

* Animal testing regulations
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* Animal Welfare Act 1999 (NZ)
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* EU Directive 2010/63/EU (EU)
* EU Directive 1999/74/EC (EU)
* Horse Protection Act of 1970 (US)
* Hunting Act 2004 (US)
* Philippine Animal Welfare Act 1998 (Philippines)

* Category

* v
* t
* e

Animal rights

Topics|

| Overview|

* Animal rights by country or territory
* Abolitionism
* Animal protectionism
* Animal welfare
* Sentientism
* Sentiocentrism
* Speciesism
* Vegaphobia
* Veganism

|

Issues|

* Ahimsa
* Anarchism and animal rights
* Animal cognition
* Animal consciousness
* Animal-free agriculture
* Animal industrial complex
* Animal law
* Animal product
* Animal rights and punk subculture
* Animal rights and the Holocaust
* Animal rights movement
* Animal testing
* Animal testing on non-human primates
* Animals in sport
* Anthrozoology
* Bile bear
* Bioethics
* Blood sport
* Cambridge Declaration on Consciousness
* Carnism
* Testing cosmetics on animals
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* Concentrated animal feeding operation
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* Covance
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* Deep ecology
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* Great ape research ban
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* Huntingdon Life Sciences
* Intensive animal farming
* Ivory trade
* Livestock
* Meat paradox
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* Nafovanny
* Nonviolence
* Open rescue
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* Opposition to hunting
* Pain in animals
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* Pain in fish
* Pain and suffering in laboratory animals
* Qurbani
* International primate trade
* Seal hunting
* Shark culling
* Slaughterhouse
* Toxicology testing
* Veganism
* Vegetarianism
* Western Australian shark cull
* Wild animal suffering
* Wildlife management

Cases|

* Brown Dog affair
* Cambridge University primates
* McLibel case
* Pit of despair
* Silver Spring monkeys
* University of California, Riverside 1985 laboratory raid
* Unnecessary Fuss

Advocates|

| Academics
and writers|

* Carol J. Adams
* James Aspey
* Tom Beauchamp
* Marc Bekoff
* Steven Best
* Paola Cavalieri
* Stephen R. L. Clark
* Alasdair Cochrane
* J. M. Coetzee
* Priscilla Cohn
* Alice Crary
* David DeGrazia
* Sue Donaldson
* Josephine Donovan
* Lawrence Finsen
* Gary L. Francione
* Robert Garner
* Antoine Goetschel
* John Hadley
* Oscar Horta
* Melanie Joy
* Will Kymlicka
* Andrew Linzey
* Dan Lyons
* Charles R. Magel
* Mary Midgley
* J. Howard Moore
* Martha Nussbaum
* Siobhan O'Sullivan
* Clare Palmer
* Tom Regan
* Bernard Rollin
* Mark Rowlands
* Richard D. Ryder
* Peter Singer
* Henry Stephens Salt
* Steve F. Sapontzis
* Gary Steiner
* Cass Sunstein

|

Activists|

* Cleveland Amory
* Greg Avery
* Matt Ball
* Martin Balluch
* Ernest Bell
* Barbi Twins
* Brigitte Bardot
* Bob Barker
* Gene Baur
* Frances Power Cobbe
* Rod Coronado
* Karen Davis
* Chris DeRose
* Alice Drakoules
* Earthling Ed
* Robert Enke
* John Feldmann
* Bruce Friedrich
* Juliet Gellatley
* Tal Gilboa
* Lewis Gompertz
* Jordan Halliday
* Barry Horne
* Ronnie Lee
* Lizzy Lind af Hageby
* Evanna Lynch
* Jo-Anne McArthur
* Bill Maher
* Keith Mann
* Dan Mathews
* Luísa Mell
* Ingrid Newkirk
* Heather Nicholson
* Jack Norris
* Alex Pacheco
* Jill Phipps
* Craig Rosebraugh
* Nathan Runkle
* Henry Spira
* Kim Stallwood
* Marianne Thieme
* Darren Thurston
* Andrew Tyler
* Gary Yourofsky

Movement|

| Groups|

* Animal Aid
* Animal Ethics
* Animal Justice Project
* Animal Legal Defense Fund
* Animal Liberation Front
* Anonymous for the Voiceless
* Centre for Animals and Social Justice
* Chinese Animal Protection Network
* Cruelty Free International
* Direct Action Everywhere
* Farm Animal Rights Movement
* Great Ape Project
* Hunt Saboteurs Association
* In Defense of Animals
* Korea Animal Rights Advocates
* Last Chance for Animals
* Mercy for Animals
* New England Anti-Vivisection Society
* Oxford Centre for Animal Ethics
* Oxford Group
* People for Animals
* People for the Ethical Treatment of Animals
* United Poultry Concerns

|

Parties|

* Animal Justice Party (Australia)
* Animal Protection Party of Canada (Canada)
* Animal Welfare Party (UK)
* Animalist Movement (Italy)
* Human Environment Animal Protection (Germany)
* Italian Animalist Party (Italy)
* Animalist Party Against Mistreatment of Animals (Spain)
* Party for the Animals (Netherlands)
* People–Animals–Nature (Portugal)
* V-Partei³ (Germany)

Media|

| Books|

* Animals' Rights (1892)
* The Universal Kinship (1906)
* Animals, Men and Morals (1971)
* Animal Liberation (1975)
* The Case for Animal Rights (1983)
* The Lives of Animals (1999)
* Striking at the Roots (2008)
* An American Trilogy (2009)

|

Films|

* The Animals Film (1981)
* A Cow at My Table (1998)
* Meet Your Meat (2002)
* Peaceable Kingdom (2004)
* Earthlings (2005)
* Behind the Mask (2006)
* Your Mommy Kills Animals (2007)
* The Cove (2009)
* Forks Over Knives (2011)
* Vegucated (2011)
* Speciesism: The Movie (2013)
* The Ghosts in Our Machine (2013)

Magazines|

* Arkangel
* Bite Back
* Muutoksen kevät
* No Compromise
* Satya

Albums|

* Animal Liberation (1987)
* Tame Yourself (1991)
* Manifesto (2008)
* Salvation of Innocents (2014)
* Onward to Freedom (2014)

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