A western flower thrips passes through six stages on its way to being a problem: egg, two larval stages, a prepupa, a pupa, and an adult that flies.
Cucumeris kills one of them.
Not "prefers" one of them. Not "is most effective against" one of them. In a study that watched individual attacks under a microscope, second-instar larvae of three different thrips species were never successfully attacked at all across the observation windows. The eggs are inserted into plant tissue. The prepupa and pupa are in the soil. The adult is too large and it flies.
Almost everything people find disappointing about this animal falls out of that one sentence — the weeks of lag, the counts that rise before they fall, the reservoir that keeps producing adults, and the reason it is sold as prevention rather than as a cure. It also explains why the usual upgrade advice is wrong, which is the part that surprised us.
The constraint, in numbers
- Stages in a thrips life
- Six
- Stages cucumeris kills
- One — the first instar
- First instars killed per day
- About 6 at 77 °F (25 °C); 4.3 at 68 °F (20 °C)
- Second instars killed
- None observed, in 15-minute attack trials
- What the second instar does back
- Destroys predatory mite eggs
- Time to visible control
- 5–9 weeks, per Ontario's agriculture ministry
- Where the rest of the population is
- 92–98% of prepupae and pupae are in the substrate
It isn't refused. It's attacked, and it fails
The distinction matters because it changes what you expect to see.
A predator that declines to attack large prey is making a choice, and choices can be pushed — starve it, remove the alternatives, and it takes what's there. That is not what happens here.
The foundational work is from 1989. Predatory mites were offered first- and second-stage Thrips tabaci larvae, and capture success was measured against both the predator's hunger and the larva's size. Starved predators attacked more readily — and on contact with a starved predator, second-stage larvae still incurred a lower death risk than first-stage ones. The mechanism was visible: the larvae jerked their abdomens and produced a drop of rectal fluid.
The clever part of that study is the control. When the researchers suppressed the defensive behaviour with anaesthesia, attack success went up — but it did not level out the difference between the two stages. Behaviour explains part of the refuge. Something else, size or handling, explains the rest, and the authors said so rather than papering over it.
Thirty-five years later a different group repeated the logic with a different predator and three thrips species, watching individual attacks in fifteen-minute windows. The result was starker: no second-instar larva of any species was successfully attacked. First instars of two species were sometimes taken — specifically when the predator got to them before they could mount a defence.
Read that carefully. Even the stage cucumeris is sold against sometimes wins. What makes first instars catchable is not that they're defenceless; it's that they're slower to react.
And the second instar doesn't just survive
In the same study, second-instar larvae and adults of two thrips species destroyed predatory mite eggs.
So the larger stages are not merely out of reach. They impose losses on the predator population while they're out of reach — which is a considerably worse position than "can't eat them".
One thing to be precise about: there is no published record of a thrips larva killing or injuring a mobile mite. The documented harm runs entirely through the eggs. Trade writing tends to overstate this.
The droplet is a signal, not just a shield
The defensive droplet is more interesting than it first appears. It contains decyl acetate and dodecyl acetate, and it works as an alarm pheromone — larvae exposed to it, natural or synthetic, produce their own droplet faster when subsequently attacked.
Which means a patch of plant with an active predatory mite in it is a patch of primed thrips. The refuge isn't a fixed property of the prey; it strengthens where the hunting is happening.
It is a small piece of chemistry with an unwelcome implication: the harder the predator works, the better the larvae get at surviving it.
The size argument nobody has actually measured
The standard explanation is that second instars are simply too big. That is almost certainly part of it, and it is worth being straight about how well established it is.
An adult cucumeris is 0.5–1.0 mm long. The first-instar larvae used in the standard predation assay were 0.5–0.6 mm long — already about the predator's own body length. Second instars are larger again, and the first larval stage lasts roughly half as long as the second, so the animal spends most of its larval life at the bigger size.
But: no published study measures thrips larval width or mass by instar alongside phytoseiid body size and computes a predator-to-prey size ratio for this pair. The size argument is asserted universally and, as far as we can find, has never been quantified.
The handling-time literature has the same hole from the other side. Handling times for phytoseiids on first-instar thrips are published — between about 1.8 and 5.2 hours depending on species. There is no handling time for any phytoseiid on a second instar, which is unsurprising when successful attacks are too rare to time. The gap is itself the finding.
How much of a thrips population is even reachable
This is the question the whole subject turns on, and nobody has published the answer. So here is the arithmetic, with the workings visible, because a number you can check beats a number you have to trust.
Measured stage durations for western flower thrips at 77 °F (25 °C): egg 4.1 days, the two larval stages together 7.8 days, prepupa 1.3, pupa 2.8 — about sixteen days egg to adult. Adult females live around 26 days. The first larval stage is roughly a third of the combined larval period.
A caveat that ought to be better known
The most-cited temperature and development study for this thrips could not tell first instars from second instars. In the authors' words, emergence of second-instar larvae was not recorded "due to difficulty in discriminating late first and early second instar when exuviae were not visible."
For a subject built entirely on the boundary between those two stages, that is worth knowing before anyone quotes a stage duration to three significant figures.
Run those durations two ways and the answer forks — which is the actual finding:
| Stage | In a stable population | In a population that's exploding |
|---|---|---|
| Egg | 9.8% | 49.4% |
| First instar | 6.2% | 17.8% |
| Second instar | 12.4% | 19.0% |
| Prepupa | 3.1% | 2.7% |
| Pupa | 6.7% | 4.2% |
| Adult | 61.9% | 6.9% |
These are our calculation from published parameters, not a published result. They assume the measured stage durations, the one-third to two-thirds larval split, an adult lifespan taken from a different temperature to the development times, and no stage-specific mortality — which is a real simplification. Treat them as an order of magnitude.
The spread is the story. In a population growing fast, first instars are a large minority of everything alive and cucumeris is well placed. In a stable or declining population, first instars are around six percent of individuals, three-fifths of which are adults, and the predator is reaching almost nothing.
Which is a strange and slightly beautiful result: cucumeris is at its best against a population that is getting worse. Its window is the exact moment when a grower would say the problem is escalating, and its worst case is a stable population that has been sitting there for a month.
Why nothing happens for three weeks
Ontario's agriculture ministry puts control with cucumeris or swirskii at five to nine weeks, against three to five for a predatory bug that eats every stage. That gap is not a difference in quality. It's the queue.
Kill a first instar today and you have removed an adult that would have emerged in about ten days. You have not touched the second instars, which will pupate regardless, or the pupae in the substrate, or the adults currently laying. Every one of those completes on schedule while the predator works. The count you are watching — adults on a sticky card — is the last stage in the chain, and it responds last.
There is a real gap in the literature here and it is worth flagging plainly. We could not find a published time series of adult thrips counts following a cucumeris-only release against an untreated control. The best available trial reports larval counts only, at thirty days. So the lag is inferred — from stage durations, from the soil reservoir, and from trials showing that adding a soil agent shortens it — rather than measured in the form everyone implies.
The practical version: judging a cucumeris release at week one is judging a queue by its last position.
What it does instead of killing them
The single most useful thing in this literature is buried in a 2006 nematode paper, and it reframes the whole relationship.
Researchers combining predatory mites on the foliage with entomopathogenic nematodes in the soil observed that the presence of mites on the plants caused large numbers of second-instar thrips larvae to drop off the plants and pupate in the soil — thereby increasing the number of hosts available for the nematodes to attack. Combined, the two agents gave up to 83% control, significantly better than either alone.
So cucumeris does not fail to deal with second instars. It moves them. It cannot kill them, and it makes the plant unpleasant enough that they leave it early and go somewhere else — which happens to be the one place where a different agent is waiting.
That is a much better argument for pairing a foliar mite with a soil agent than the usual one, because it isn't about covering a gap in a table. It's a mechanism: the predator on the leaves is actively delivering prey to the predator in the pot.
How big the soil reservoir actually is
Most of a thrips population leaves the plant to pupate, and "most" is doing some work:
| Measured | Crop and conditions |
|---|---|
| 98% went to soil | French bean, microcosms with emergence traps |
| 92–93% in soil | Non-flowering potted chrysanthemum and mini rose |
| 87% in soil | Flowering mini rose |
| 60% in soil | Flowering chrysanthemum — 40% stayed on the plant |
Two things follow. First, the flowering state of the crop changes the answer by more than thirty points, so a soil agent is worth much more on some crops than others. Second, there is an unresolved disagreement in the literature — one study reports 60% for flowering chrysanthemum where a review reports 92% for the same crop at the same growth stage. We are not going to pretend that is settled.
And the fraction moves with humidity rather than being a property of the species. Above 80% humidity was necessary for late second instars to survive to pupation, with 90% optimal — and the humidity at which larvae switch to dropping off the plant rather than staying on it was measured at around 81%. Drier air pushes them down. Which means humidity management changes the size of your reservoir, and therefore how much a soil agent is worth to you.
The contradiction we are obliged to include
The pairing argument is not unanimous. A 2009 review reports that simultaneous release of foliage and soil predators did not reduce thrips beyond what the foliage predators achieved alone.
A cucumber trial found the same shape: cucumeris alone and cucumeris plus a soil mite performed similarly, a non-additive result the authors put down to competition between the two predators.
Against that, a cyclamen trial found nematodes in the soil plus mites in the canopy produced a more prompt reduction of thrips in flowers than either alone. The mechanism is well-evidenced; the crop-level payoff is not consistent.
What reaches the stages it can't
The adults
Nothing in the soil and nothing on the leaves touches adult thrips. Orius does — it takes every mobile stage including adults, and Ontario puts its time to control at three to five weeks rather than five to nine. It is also slow to establish, up to eight or ten weeks by some accounts, and it will eat cucumeris.
The soil stages
Entomopathogenic nematodes are the cleanest complement on the evidence: prepupae and pupae were the most susceptible stages, larvae were killed only at very high rates and even then at 28–37%, and no significant mortality was observed for adults. The stage coverage is almost exactly the inverse of cucumeris's.
It would rather eat pollen, and that's the point
Cucumeris is an omnivore that will complete its entire life cycle on pollen. That is normally presented as a convenience — it survives between pest events — and it is also the thing that makes the whole preventive strategy possible.
It goes further than survival. In a study comparing several supplemental foods against thrips larvae as the reference diet, the supplements produced shorter development times and higher survival than thrips did. Apple and cattail pollen were the best of them; maize was the worst.
A predator that develops better on pollen than on its target pest is not a defective predator. It's a predator you can establish before the pest arrives, which is the only strategy that works given everything above.
The catch is in the other article. Pollen in the crop cut cucumeris predation on thrips by 55% in one study — the mites stay, the mites breed, and they kill fewer thrips. Supplemental food raises predator numbers and lowers per-mite predation at the same time, and whether the net is positive has been demonstrated for swirskii and not for cucumeris.
One more caution worth carrying: pollen quality is not transferable between studies. Two laboratories tested castor bean pollen and one recorded 100% juvenile mortality while the other ranked it the best of seven. They also disagree about maize, where one found the lowest but positive growth rate and the other found no egg-laying at all. "Cucumeris can live on pollen" is true. "Cucumeris can live on this pollen" is a separate question nobody can answer for your crop.
The upgrade argument is wrong
Here is where the research changed our mind, and it is the reason this article exists.
The standard advice — including in comparison tables we have published ourselves — is that swirskii and limonicus are better thrips predators because they take first and second instars where cucumeris takes only first. It is in nearly every table on the internet.
It does not survive contact with the primary literature.
- The canonical source for the idea is a 1995 paper which states that second instars defend themselves well and were therefore not measured. It reports a pilot experiment with no data table.
- The 2024 attack-observation study found Amblyseius swirskii — the species sold as the upgrade — unsuccessful against every second-instar larva of all three thrips species tested.
- The one quantitative second-instar figure we could find is for limonicus: 0.60 second instars per day against 3.10 first instars, and in a choice test it fed on first instars exclusively.
- A peer-reviewed species review of swirskii lists first-instar thrips only. The manufacturer-side review of why swirskii succeeded commercially does not mention prey-stage range at all — it cites multi-pest range, pollen feeding, and cheap mass rearing.
Ontario's ministry does state that swirskii feeds to a lesser extent on second instars. It gives no citation, and the behavioural study directly contradicts it.
So what is the real difference between them?
Per-capita predation on first instars is close to identical: 6.0 per day for cucumeris against 6.9 for limonicus in the same experiment; 2–3.5 per day for all four species in a more recent one.
The differences that are well evidenced are no diapause, better establishment, higher equilibrium populations, and a broader non-prey diet. Those are population properties, not prey-stage properties.
In one greenhouse trial the two species ate the same 2.7 larvae a day in a leaf-disc assay, and in the crop one held thrips below one per leaf while the other allowed 36. The gap was establishment, not appetite.
We would rather correct this than keep repeating it. The case for the other species is real; it is just not the case that gets made.
What follows
- Release before you have a problem. Not as a platitude — as the direct consequence of six stages and one reachable one. A predator present when the first eggs hatch is working on a growing population, which is the situation it is good at.
- Read the trend at weeks three and four, not week one. The adult count is the last link in a chain the predator is working on at the front.
- Pair it with something that reaches the soil — and understand the reason. It isn't that a table has a gap. It's that your mites are actively pushing second instars off the plant, and something should be waiting for them.
- Add sticky cards, always. Nothing you put on the plant or in the pot touches adult thrips. Cards are not monitoring equipment here; they are the only thing acting on that stage at all.
- Don't switch species expecting second-instar coverage. You will not get it. Switch for diapause, establishment or temperature range — those differences are real.
- Watch what stage is on your leaves. Small translucent larvae mean the predator has something to work with. Mostly larger yellowish ones mean it doesn't, and no rate increase fixes that.
Common questions
Why doesn't cucumeris eat bigger thrips larvae?
It tries. Second-instar larvae swing their abdomens and produce a droplet of rectal fluid, and the attack fails — in one study watching individual attacks, no second instar of any of three thrips species was successfully attacked. Part of the refuge is that behaviour and part is size, and the study that separated the two showed suppressing the behaviour did not close the gap entirely.
Does swirskii or limonicus eat second instars?
On the published evidence, essentially no. Swirskii was unsuccessful against every second instar tested in the same behavioural study. Limonicus managed 0.60 per day against 3.10 first instars, and fed exclusively on first instars when offered a choice. The claim that these species cover the second instar is repeated everywhere and traces back to a pilot experiment that published no data. Their genuine advantages are elsewhere — no diapause, better establishment, higher populations.
How long before I should expect to see fewer adult thrips?
Ontario's agriculture ministry puts it at five to nine weeks for cucumeris or swirskii, against three to five for Orius, which eats adults directly. The lag is structural: killing a first instar removes an adult that would have appeared about ten days later, while every second instar, pupa and adult already present completes on schedule regardless.
If it only reaches one stage, why does anyone use it?
Because that stage is the throat of the bottle in a growing population, and because cucumeris can be established on pollen before the pest arrives — it develops faster on pollen than on thrips. Used preventively it intercepts each new cohort as it hatches. Used as a rescue on an established population it is reaching about six percent of what is alive, which is why it disappoints in exactly that situation.
Do I really need a soil agent as well?
The mechanism is good: 87–98% of prepupae and pupae are in the substrate depending on crop, and mites on the foliage have been observed driving second instars off the plant and into the soil early, which increases what a soil agent can reach. But the crop-level evidence is genuinely mixed — one review reports foliage plus soil predators did no better than foliage alone, while a cyclamen trial found the combination reduced thrips in flowers faster. Flowering crops keep more thrips on the plant, so the value of a soil agent is not constant.
References
- Bakker, F.M. & Sabelis, M.W. (1989). How larvae of Thrips tabaci reduce the attack success of phytoseiid predators. Entomologia Experimentalis et Applicata 50(1): 47–51.doi.org
- Beretta, G.M., Zandbergen, L., Deere, J.A., Messelink, G.J., Muñoz Cárdenas, K. & Janssen, A. (2024). Predator–prey interactions: how thrips avoid predation. Biological Control 188: 105437.doi.org
- de Bruijn, P.J.A., Egas, M., Janssen, A. & Sabelis, M.W. (2006). Pheromone-induced priming of a defensive response in western flower thrips. Journal of Chemical Ecology 32: 1599–1603.doi.org
- van Houten, Y.M., van Rijn, P.C.J., Tanigoshi, L.K., van Stratum, P. & Bruin, J. (1995). Preselection of predatory mites to improve year-round biological control of western flower thrips in greenhouse crops. Entomologia Experimentalis et Applicata 74: 225–234.
- Cao, J. & Zhang, Z.-Q. (2026). Stage-specific predation and functional response of predatory mites to greenhouse thrips on avocado. Experimental and Applied Acarology 96(4): 53.
- McDonald, J.R., Bale, J.S. & Walters, K.F.A. (1998). Effect of temperature on development of the western flower thrips. European Journal of Entomology 95: 301–306. eje.cz
- Reitz, S.R. (2009). Biology and ecology of the western flower thrips: the making of a pest. Florida Entomologist 92(1): 7–13.
- van Rijn, P.C.J., Mollema, C. & Steenhuis-Broers, G.M. (1995). Comparative life history studies of Frankliniella occidentalis and Thrips tabaci on cucumber. Bulletin of Entomological Research 85: 285–297.
- Ebssa, L., Borgemeister, C. & Poehling, H.-M. (2006). Simultaneous application of entomopathogenic nematodes and predatory mites to control western flower thrips. Biological Control 39: 66–74.doi.org
- Buitenhuis, R. & Shipp, J.L. (2008). Influence of plant species and plant growth stage on Frankliniella occidentalis pupation behaviour in greenhouse ornamentals. Journal of Applied Entomology 132: 86–88.
- Berndt, O., Meyhöfer, R. & Poehling, H.-M. (2004). The edaphic phase in the ontogenesis of Frankliniella occidentalis. Biological Control 30: 17–24.
- Steiner, M.Y., Spohr, L.J. & Goodwin, S. (2011). Relative humidity controls pupation success and dropping behaviour of western flower thrips. Australian Journal of Entomology 50: 179–186.
- Buitenhuis, R. & Shipp, J.L. (2005). Efficacy of the entomopathogenic nematode Steinernema feltiae as influenced by Frankliniella occidentalis developmental stage and host plant stage. Journal of Economic Entomology 98: 1480–1485.doi.org
- Pozzebon, A., Boaria, A. & Duso, C. (2014). Single and combined releases of biological control agents against canopy- and soil-dwelling stages of Frankliniella occidentalis in cyclamen. BioControl 60: 341–350.
- Cloyd, R.A. (2009). Western flower thrips management on ornamental crops grown in greenhouses: have we reached an impasse? Terrestrial Arthropod Reviews 2: 241–267.
- Delisle, J.F., Brodeur, J. & Shipp, L. (2015). Evaluation of various types of supplemental food for two species of predatory mites. Experimental & Applied Acarology 65: 483–494.
- Ranabhat, N.B., Goleva, I. & Zebitz, C.P.W. (2014). Life tables of Neoseiulus cucumeris exclusively fed with seven different pollens. BioControl 59(2): 195–203.
- Yazdanpanah, S., Fathipour, Y. & Riahi, E. (2021). Pollen grains are suitable alternative food for rearing the commercially used predatory mite Neoseiulus cucumeris. Systematic and Applied Acarology 26(5).
- Messelink, G.J., van Steenpaal, S.E.F. & Ramakers, P.M.J. (2006). Evaluation of phytoseiid predators for control of western flower thrips on greenhouse cucumber. BioControl 51: 753–768.
- Arthurs, S., McKenzie, C.L., Chen, J., Dogramaci, M., Brennan, M., Houben, K. & Osborne, L. (2009). Evaluation of Neoseiulus cucumeris and Amblyseius swirskii as biological control agents of chilli thrips on pepper. Biological Control 49(1): 91–96.
- Ontario Ministry of Agriculture, Food and Agribusiness. Thrips in greenhouse crops — biology, damage and management. ontario.ca
The rest of the cucumeris series
- Cucumeris: Why It Works (and Why It Fails)The species, what it eats, the conditions it needs, and which format to buy.
- Slow Release Is a Placement, Not a Product.What to release, what is inside a sachet, and where to hang it.
- The Mites Are Alive. The Thrips Are Winning.Eleven failure modes, each with the fingerprint that tells it apart.
- Two of These Four Columns Are Guesses.The comparison table, checked cell by cell against the primary literature.
All of Mite MattersEvery organism we sell, written up against the literature rather than the label.
