Processing of insect larvae
11930803 ยท 2024-03-19
Assignee
Inventors
- Kees Wilhelmus Petrus Aarts (Vught, NL)
- Maurits Petrus Maria Jansen (Bavel, NL)
- Anne Louise Mia Jacobs (Dongen, NL)
- Mark C. Mescher (Zurich, CH)
- Robert Prentner (Zollikon, CH)
- Alexander MATHYS (Zurich, CH)
- Consuelo M. de Moraes (Zurich, CH)
Cpc classification
A23J1/00
HUMAN NECESSITIES
A01M1/2094
HUMAN NECESSITIES
International classification
Abstract
The present invention provides a method and system for processing insect larvae in an ethical manner and without imposing unnecessary stress on them. The method involves anaesthetising the insects by cooling and then cutting them, thereby destroying the nervous system of the insects. Thus, an energy-saving method of processing insects with minimal stress is provided.
Claims
1. A method of processing insect larvae comprising the steps of: anaesthetising the insect larvae by cooling, wherein the insect larvae are stored in cold water before or after the anaesthetising step, followed by cutting the insect larvae into pieces to effect destruction of a nervous system of the insect larvae while the insect larvae are anaesthetized.
2. The method according to claim 1, wherein the insect larvae are cooled by mixing them with a fluid.
3. The method according to claim 2, wherein a cooling temperature of the fluid is below 15? C.
4. The method according to claim 2, wherein a cooling temperature of the fluid is below 7?.
5. The method according to claim 1, wherein a cooling temperature of the insect larvae is below 15? C.
6. The method according to claim 1, wherein a cooling temperature of the insect larvae is below 10? C.
7. The method according to claim 1, wherein cutting the insect larvae into pieces comprises cutting at least 90% of the insect larvae into at least 5 pieces each.
8. The method according to claim 1, wherein the insect larvae are processed to powder comprising protein and/or fat and/or chitin.
9. The method according to claim 1, wherein the insect larvae are separated from rearing residue before the anaesthetising step.
10. The method according to claim 1, wherein during storing, the insect larvae are agitated.
11. A system for processing insect larvae according to claim 1 comprising means for cooling the insect larvae, and means for cutting the insect larvae, wherein the system is also configured to store and cool the insect larvae in cold water before processing.
12. The system according to claim 11, wherein the cooling means are configured to maintain a temperature below 15? C.
13. The system according to claim 11, wherein the insect larvae are separated from rearing residue by separating means.
14. The system according to claim 11, wherein the cutting means are configured to cut the insect larvae in at least 5 pieces at once.
15. The system according to claim 11, wherein the system is configured to agitate the insect larvae during storing.
16. The system according to claim 11, wherein the cooling means are configured to maintain a temperature below 10? C.
17. The method according to claim 1, wherein the insect larvae are cooled by mixing them with water.
18. The method according to claim 1, wherein a cooling temperature of the insect larvae is below 7?.
Description
BRIEF DESCRIPTION OF THE DRAWING
(1)
DETAILED DESCRIPTION OF THE INVENTION
(2) In order to assess the stress level of insect larvae during rearing and processing, research has been done to identify a way to inactivate insects with minimal stress levels.
(3) Stress might correlate to the various steps in processing such as anaesthetising, washing, transport, storage, and inactivation of larvae. The presence of potentially stressful conditions was assessed by measuring physiological responses to the corresponding stimuli.
(4) To assess physiological response to stress, levels of the stress-related hormone Octopamine (OCT) was measured. In invertebrates, Octopamine regulates muscle activity and flight-or-fight behavior. Concentrations of Octopamine can be used as proxy for physiological responses to stressful conditions. After exposing larvae to various stimuli, increases or decreases in OCT are measured relative to unexposed control larvae.
(5) In the course of the research, the following stimuli were tested: Chilling of the larvae for 5-15 minutes at 4-15? C., immersed in water. Exposure to heat without inducing permanent damage to the insect larvae Storage in a 50:50 mixture of water/larvae at 4? C. and 10? C. Gassing the larvae with CO.sub.2.
(6) Abruptly cooling the insect larvae by immersing them in water of 4? C. immediately rendered the major part of the insect larvae immobile. The OCT level thereby decreased and did not rise back to the control level measured before the treatment while being chilled. After exposing the insect larvae to room temperature, the OCT level again reached the control level. As an aside it has to be noted, that OCT level does not always correlate with visible behaviour, rendering OCT a more reliable indicator for relaxation/arousal.
(7) Exposure to severe heat, but without effectively harming the insect larvae, lead to curling behaviour which is considered as being painlike behaviour. The heat exposure clearly resulted in increased OCT levels indicating that any method involving heat without prior anaesthetising or inactivation of larvae should be avoided.
(8) Spraying with water did not result in any visual behavioural response of the larvae.
(9) Two stimuli that most likely have an anaesthetic effect on larvae were investigated: Chilling larvae in cold water and gassing larvae with CO.sub.2. Putting larvae into cold water of 4? C. instantly rendered most larvae immobile and no movement was observed after one minute. After 10 minutes, larvae were removed from the water and put on a dry surface. From there on, the time was recorded until larvae exhibited visible signs of activity. Onset of movement was visible after approximately 5 minutes, and normal movement was recovered after approximately 12 minutes.
(10) Due to the fact that insects are poikilothermic, for anaesthetising the insect larvae and stopping their metabolism, temperatures of 15? C. or less, preferably 10? C. or less, are sufficient. Cooling has no effect on the animals' physiology and they can be stored up to 4 days and reactivated if desired without causing any harm.
(11) When being gassed with CO.sub.2, on the other hand, movement was slowly beginning to decrease only after approximately 2 minutes with widespread loss of movement only after around 8 minutes of exposure. After 10 minutes, treatment was stopped and larvae were put again on a dry surface. First slow movements already set in after 1-2 minutes, and after 5 minutes, normal behaviour was recovered. These qualitative findings indicate, first, that chilling using cold water is more effective in anaestethising larvae compared to gassing, and secondly, recovery after chilling is slower than after gassing.
(12) While the above described research was focused on non-lethal stimuli, in further evaluations, different processing methods were assessed. Those involved cutting, boiling and ripping with the use of heat. Consequently, the curling or escape behaviour after the lethal process was observed. With reference to table 1 it was thereby noticed that cutting lead to a very weak response, boiling induced a medium response and heat ripping caused a strong or long lasting curling behaviour in more cases compared to the other processing methods. Hence, inactivation methods that involve heat are comparatively slow and tend to increase response intensity, while methods using an effective cutting technique are recommended for processing purposes. Methods involving gassing of the animals are acceptable in terms of stress level and pain but are comparatively slow.
(13) TABLE-US-00001 TABLE 1 Response Processing method total weak medium strong cutting 50 28 17 5 boiling 50 21 19 10 ripping/heat 50 16 20 14
(14) The state of the art relies on freezing techniques involving either shock-freezing by liquid nitrogen or freezing larvae at ?20? C., which is a slightly slower process than shock-freezing.
(15) While both are lethal and do not evoke behaviour that would indicate pain or stress, they, however, are very energy intensive.
(16)
(17) Further research showed that stunning or anaesthetising the animals, respectively, by cooling or gassing both lead to a decrease in stress level, whereby cooling is preferred since it acts faster and yields better results. Therefore, anaesthetising the animals before processing them is recommended. Storage in cold water did not impose additional stress to the insect larvae but slightly lowered OCT concentration. Thus, water can be used both for storing and for anaesthetising insect larvae. When processing the animals, fast methods such as cutting or shock-freezing are recommended since they do not increase the stress level as much as methods involving heat.
(18) Thus, a processing method for appropriate inactivation of the animals with minimal stress should consider the above presented results.
(19) The method according to the invention involves anaesthetising the insect larvae by cooling them, followed by inactivation the insect larvae by cutting, thereby destroying their nervous system.
(20) The cooling step may be performed by mixing water with larvae. The water/insect larvae mixture may thereby have a ratio of 50:50 or may have any other suitable ratio.
(21) Preferably, the target temperature of the cooling process is be 15? C. or lower. The target temperature of the cooling process may also be 10? C., 7? or lower.
(22) In a preferred embodiment, the cutting process may cut each insect larva in at least 5 pieces at once. The insect larvae may be processed to protein powder thereafter.
(23) By using a method as specified in the claims, an appropriate procedure of processing insect larvae is presented. After anaesthetising the larvae via cooling below at least about 15? C., the insect larvae are separated from rearing residue, e.g. by sieving or a washing step. A fast and efficient cutting technique leads to an immediate deactivation of the insect larvae. Furthermore, the presented method is significantly less cost and energy intensive since the freezing step is replaced by anaesthesia by cooling and successive cutting. By performing cooling and inactivating of the insect larvae, two objectives can be achieved. Firstly, the animal welfare is ensured since the process involves anaesthesia and a quick destruction of the nervous system. Secondly, the product quality is consistent since the current status of the insect larvae is preserved by cooling them and thereby stopping their metabolism.
(24) The method may also be applied for living insects of all life cycle stadia.