Speed breeding is a powerful tool to accelerate crop research and breeding

The growing human population and a changing environment have raised significant concern for global food security, with the current improvement rate of several important crops inadequate to meet future demand1. This slow improvement rate is attributed partly to the long generation times of crop plants. Here, we present a method called ‘speed breeding’, which greatly shortens generation time and accelerates breeding and research programmes. Speed breeding can be used to achieve up to 6 generations per year for spring wheat (Triticum aestivum), durum wheat (T. durum), barley (Hordeum vulgare), chickpea (Cicer arietinum) and pea (Pisum sativum), and 4 generations for canola (Brassica napus), instead of 2–3 under normal glasshouse conditions. We demonstrate that speed breeding in fully enclosed, controlled-environment growth chambers can accelerate plant development for research purposes, including phenotyping of adult plant traits, mutant studies and transformation. The use of supplemental lighting in a glasshouse environment allows rapid generation cycling through single seed descent (SSD) and potential for adaptation to larger-scale crop improvement programs. Cost saving through light-emitting diode (LED) supplemental lighting is also outlined. We envisage great potential for integrating speed breeding with other modern crop breeding technologies, including high-throughput genotyping, genome editing and genomic selection, accelerating the rate of crop improvement. Fully enclosed, controlled-environment growth chambers can accelerate plant development. Such ‘speed breeding’ reduces generation times to accelerate crop breeding and research programmes, and can integrate with other modern crop breeding technologies.

For most crop plants, the breeding of new, advanced cultivars, takes several years. Following crossing of selected parent lines, 4-6 generations of inbreeding are typically required to develop genetically stable lines for evaluation of agronomic traits and yield. This is particularly timeconsuming for field-grown crops that are often limited to only 1-2 generations per year. Here, we present flexible protocols for "speed breeding" that use prolonged photoperiods to accelerate the developmental rate of plants [2], thereby reducing generation time. We highlight the opportunity presented by speed breeding and detail protocols to inspire widespread adoption as a state-of-theart breeding and research tool.
To evaluate speed breeding as a method to accelerate applied and basic research on cereal species, standard genotypes of spring bread wheat (T. aestivum), durum wheat (T.  Table 1). A light/dark period was chosen over a continuous photoperiod to support functional expression of circadian clock genes [3]. Growth Table 5) and both wheat and barley plants   produced a healthy number of spikes per plant, despite the rapid growth (Supplementary Table 6).
Viability of mature seeds was unaffected by speed breeding with similar seed germination rates observed for all species (Supplementary Table 7). Moreover, crosses made between wheat cultivars under speed breeding conditions produced viable seed, including crosses between tetraploid and hexaploid wheat (Supplementary Table 8 In an alternative, yet similar protocol for rapid generation cycling, we evaluated a collection of spring wheat, barley, canola and chickpea varieties in Queensland, Australia, in a temperature-controlled glasshouse fitted with high pressure sodium lamps to extend the photoperiod to a day-length of 22 hours. A control treatment in a glasshouse used a natural 12hour control photoperiod. Both used the same temperature regime (22/17°C; Fig. 1 Tables 11-14 SD), an important feature, as synchronous flowering across genotypes is desirable for crossing. Additionally, wheat seed was harvested before maturity: 14 days post-anthesis in speed breeding conditions and following a 4-day cold treatment seed viability was high (Supplementary Table 21) indicating generation time can be further reduced by harvesting premature seed without the need for labour intensive embryo rescue [5]. Seed viability of all other species under Speed breeding II conditions were either unaffected or improved compared with day-neutral conditions (Supplementary Tables 22-24). Since temperature greatly influences the rate of plant development [6], generation time may be further accelerated by elevating temperature.
This may however induce stress and affect plant performance.
Seed production (g/plant) of canola and chickpea was similar between speed breeding and day-neutral conditions (Supplementary Tables 25, 26). Considering the time taken to produce viable seed under speed breeding in the glasshouse, wheat, barley, canola and chickpea could produce 5.7, 5.4, 3.8 and 4.5 generations per year, respectively (Supplementary Table 27). These results highlight the opportunity to apply speed breeding across several important crop species without jeopardising the production of subsequent generations. The application of speed breeding conditions in a glasshouse fitted with supplementary lighting exemplifies the flexibility of the approach and may be preferred over growth chambers if rapid generation advance is to be applied to large populations, such as in breeding programmes.
Single seed descent (SSD) is commonly used in breeding programs and research to facilitate development of homozygous lines following a cross [7]. This process only requires one  Tables 28, 29). This was likely caused by stress or plant competition as a result of the higher density, which is known to hasten flowering [8]. In most cases, each plant produced a single viable tiller containing on average 19.0 ± 1.3 and 18.6 ± 1.8 seeds for wheat and barley, respectively. Seed viability was 80% for wheat at two weeks post-anthesis and 100% for both wheat and barley at four weeks post anthesis (Supplementary Tables 28, 29). Therefore, integrating speed breeding and SSD techniques can effectively accelerate the generation of inbred lines for research and plant breeding programs.
In an additional protocol (Supplementary Table 1; Speed breeding III), we successfully implemented a low cost speed breeding growth room design, lit exclusively by LEDs (lightemitting diode) to reduce the operational cost of lighting and cooling, which permits 4-5 generations a year, depending on genotype and crossing plans ( Supplementary Fig. 2). These results highlight the flexibility of tailoring the speed breeding 'recipe' to suit the local purpose and resources.
Besides exploring the various ways in which speed breeding can be used to accelerate generation time, we also evaluated the ability to phenotype some key adult plant phenotypes of wheat and barley. We observed that phenotypes associated with the EMS-induced mutation of the awn suppressor B1 locus [9] and the Green Revolution Reduced height (Rht) genes in wheat [10] could be accurately recapitulated in the controlled environment room conditions (Fig. 3a,b). We also evaluated the effects that speed breeding might have on disease by inoculating resistant (Sumai 3) and susceptible (Timstein) wheat spikes with Fusarium graminearum, the causal agent of fusarium head blight (FHB). Consistent with expectations, we found clear signs of FHB progression in the susceptible cultivar, and little to no disease progression in the resistant cultivar ( Fig. 3c; Supplementary Table 30). Previously, it has been shown that adult plant resistance (APR) to wheat leaf rust (caused by Puccinia triticina f. sp. tritici) and wheat stripe rust (Puccinia striiformis f. sp. tritici) can also be scored accurately under speed breeding conditions [11,12].
We also evaluated the effect of loss-of-function of FLOWERING LOCUS T-B1 in the F6 RIL of Paragon x W352 under speed breeding conditions. We observed the expected late flowering phenotype in the RIL, albeit within fewer days and with fewer leaves produced ( Fig. 3d; Supplementary Table 31). To study the effect of speed breeding on cuticular -diketone wax production in barley, we grew wild type and Eceriferum mutants [13]. The mutant leaf sheaths exhibited a clear, decreased glaucous appearance in the flag leaf stage, compared to the control ( Fig. 3e). We also studied polyploid wheat chromosome pairing at metaphase I in meiosis in the presence and absence of the PAIRING HOMOEOLOGOUS 1 (Ph1) locus [14]. We grew wheat carrying Ph1 and wheat-rye hybrids either carrying or lacking Ph1 in speed breeding and control conditions, and observed no major differences in chromosome pairing and recombination in meiocytes at metaphase I (Supplementary Table 32). The chromosome behavior suggests that both wheat and wheat-rye hybrids are cytologically stable under speed breeding conditions ( Supplementary Fig. 3). In summary, all the above adult plant phenotypes could be recapitulated accurately and much faster than in the corresponding glasshouse conditions. We further investigated the potential for using speed breeding in conjunction with genetic transformation. Seeds of barley (cv. Golden Promise) were sown and immature embryos harvested and transformed ( Supplementary Fig. 4). The transformation efficiency of speed grown and normal plants was comparable (Supplementary Table 33). Moreover, we observed that transformed barley explants could be grown under speed breeding conditions and viable seed obtained >6 weeks earlier than in standard control conditions (Supplementary Table 34; Supplementary Fig. 5).
We investigated the ability to phenotype canola, grown under glasshouse speed breeding, conditions for pod shattering resistance, a significant factor causing yield loss in the field. Using an established method which measures the energy absorbed by each pod when shattered by a pendulum [15] (Supplementary Fig. 6) we tested five canola cultivars considered susceptible to shattering. All displayed varying degrees of pod strength comparable to measures obtained from field-grown pods (Supplementary Table 35). Due to the lack of shatter resistance in cultivars, new alleles from related Brassica species could be transfered to canola [16]. Our results suggest that speed breeding could accelerate this objective.
Speed breeding is likely to reduce generation time for other crop species, such as sunflower (Helianthus annuus), pepper (Capsicum annuum), and radish (Raphanus sativus), which have been shown to respond well to extended photoperiod [2]. Speed breeding methods have already been successfully applied to accelerate breeding objectives for amaranth (Amaranthus spp.) [17] and peanut (Arachis hypogaea) [18]. For species that require short days to trigger the reproductive phase, such as rice (Oryza sativa) and maize (Zea mays), the speed breeding technique could be used to promote rapid vegetative growth prior to reducing the photoperiod.
Recent advances in genomic tools and resources [19][20][21][22][23] and the decreasing cost of sequencing have enabled plant researchers to shift their focus from model to crop plants. Despite such advances, the slow generation times of many crop plants continue to impose a high entry barrier. We envisage that combining these tools and resources with speed breeding will provide a strong incentive for more plant scientists to perform research on crop plants directly, thus further accelerating crop improvement research. In a breeding context, rapid generation advance to homozygosity following crossing will facilitate genetic gain for key traits and allow more rapid production of improved cultivars by breeding programs.   In the left panel, the parents flower while the F6 is just beginning to boot at 44 days; in the right panel, the F6 hybrid is shown with developed spikes at 67 days when the parents have moved into senescence. e, Reduced glaucousness of Eceriferum (Cer) mutants in H. vulgare cv. Bonus.

Speed breeding I -Controlled environment chamber speed breeding conditions
A Conviron BDW chamber (Conviron, Canada) was programmed to run a 22-hour photoperiod, with a temperature of 22 C during the photoperiod, and 17 C during the 2-hour dark period. Light and temperature were set to ramp up and down for 1 hour 30 minutes to mimic natural dawn and dusk conditions (as illustrated in Fig. 1). Humidity was set to 70%. Lighting was supplied by a mixture of white LED bars (Valoya; 6 units per 3.67 m 2 ), far red LED lamps (Valoya; 12 units per 3.67 m 2 ) and metal HQI lamps (Valoya; 32 units per 3.67 m 2 ). Light intensity was adjusted to 360-380 µmol m -2 s -1 (highest value after ramping) at bench height, where the pots were kept, and 490-500 µmol m -2 s -1 (highest value after ramping) at adult plant height (with reference to wheat cv. Supplementary Fig. 7.  Supplementary Fig. 8.

Sowing, harvesting, and germination rate evaluation for speed breeding in a controlled environment room chamber
Wheat, barley and Brachypodium seeds were imbibed on filter paper wetted with sterile water containing 0.5 ppm gibberellic acid, stratified at 4 C for 3 days and then germinated at room temperature for 2 days before sowing in 1.33 L pots containing 900 mL of soil (one seed per pot).
The soil used was the John Innes Centre (JIC) cereal mix, the composition of which is outlined in Supplementary Table 36. Seeds were harvested ~2.5-3 weeks post anthesis. The plants were not watered in the last week leading up to harvest in order to accelerate the grain ripening. The harvested spikes were kept in paper bags and dried at 28-30 C for 3-5 days to reduce the moisture content. The grain was threshed and stored at room temperature. To measure germination rates, seeds were placed in Petri dishes lined with filter paper, and wetted with sterile water. The seeds were stratified for 4 C for 3 days, and then placed at room temperature, with periodic rehydration of the filter paper lining to maintain moisture levels. Seeds were observed for germination at daily  Table 10). At six weeks and nine weeks, respectively, the plants in the cabinet and glasshouse were no longer watered. Mature, dry seed were chipped and placed on moist filter paper for 5 days at room temperature in the dark to estimate percentage germination.
The number of seeds where the radicle and shoot had not emerged were counted as not germinated.
Wild-type M. truncatula (genotype Jemalong A17) seeds were scarified with glasspaper, surface-sterilized for 3 minutes in 10% sodium hypochlorite and washed five times with distilled water. Seeds were left to imbibe for 2 hours before being transferred to agar plates for 72 hours at 4 C. Seedlings were sown in JIC Cereal Compost Mix in 24-cell trays (each cell containing 80 mL of soil) and transferred to 1 L pots after 14 days. The number of days after sowing for the first flower to appear was recorded. Watering stopped following maturation of ~90% of the pods. Pods were harvested 14 days later and the resulting seeds subjected to germination tests similar to pea.

Speed breeding II -Glasshouse speed breeding conditions
A temperature-controlled glasshouse fitted with high pressure sodium vapour lamps (Philips SON-T 400W E E40 in Sylvan High Bay housing with glass diffuser) was programmed to a 17/22 C temperature regime with a 12-hour turnover and 22-hour photoperiod (Supplementary Fig. 9). The 2-hour period without lamps operating and 17 C cycle occurred during the night. Light intensity was 440-650 µmol m -2 s -1 at adult plant height (approximately 45 cm above bench height). Light and temperature changes did not include a ramping up/down procedure. Light quality (spectral composition) is shown in Supplementary Fig. 10.

Sowing, harvesting, and germination rate evaluation for speed breeding in a lightsupplemented glasshouse
Wheat, barley, canola and chickpea seeds were imbibed by placing on water-moistened filter paper in agar plates overnight at room temperature. The imbibed seeds were chilled at 4 °C for 4 days to break any dormancy and support uniform germination. Seeds were then left at room temperature for 5 days. All seedlings were sown singly into 1.4 L pots. Soil media consisted of the CGS20 compost mix (Supplementary Table 37) with the addition of Scotts Osmocote R Plus trace elements (2 g/L soil) and a final pH of 5.5-6.5. Pots were placed in pot racks in complete randomized block designs and hand-watered daily. Plants were supplemented with a weekly foliar spray of calcium nitrate diluted in filtered water (1 g/L) to mitigate any calcium deficiency, which is common with such rapid growth [24].
Anthesis date was recorded for wheat, canola and chickpea while awn peep was recorded for barley. One spike was harvested from wheat and barley at 2 and 4 weeks post-anthesis. Three pods per plant of canola and chickpea were harvested 6 weeks post-anthesis. All harvested seeds were placed in paper bags and immediately dried in an air-forced oven for 5 days at 35 °C, threshed by hand, then weighed. Germination tests were carried out as per the pre-sowing treatments described above. Percentage germination was calculated following 5 days at room temperature.
At approximately 4-6 weeks following anthesis, water supply was reduced to every second day for one week, then twice per week for one week, followed by complete withholding of water.
When plants were fully senesced, all spikes or pods were harvested, counted, dried, threshed and weighed to determine yield. Grain number per spike of wheat and barley plants was counted following threshing of each individual spike.
One cultivar each of wheat (cv. Westonia) and barley (cv. Commander) was sown in a 100cell tray (length, 350 mm; width, 290 mm; height 45 mm; each cell approximately 18 ml) to demonstrate the potential of high density planting. Three spikes were harvested at 2 and 4 weeks post-anthesis and percentage germination determined, as above. The watering regime was also as above. Following complete senescence, all grain was harvested, dried, threshed and weighed to determine yield.
As a control, an identical protocol was carried out on the same species/cultivars in a similar glasshouse maintained at the same temperature settings but with no supplemental lighting. The lighting was set to run a 12-hour photoperiod (12 hours darkness) for 4 weeks and then increased to an 18-hour photoperiod (6 hours darkness). The lights did not ramp up and down during the switch between light and dark periods in the 24-hour cycle. The air-conditioner was set to run at 18 C in darkness and 21 C when the LED lights were on, with fluctuation being no more than ± 1 C. measures were adjusted for variation in pod length to calculate RELSQ (rupture energy per length squared), as per [25]. The five canola cultivars were also grown in field row plots at the experimental farm of WWAI in two replicates [16], and evaluated for shattering resistance using the same technique, where 10 fully mature pods were sampled per plot.

Wheat crossing and evaluation of crossing efficiency
Newly emerged spikes were emasculated to remove all immature anthers. The emasculated spikes were bagged for up to 3 days to allow for maturation of the stigma and then pollinated by anthers from a separately selected parent. The spikes were checked for seed setting 3-5 days post pollination. Crossing efficiency was calculated as the percentage of emasculated ovaries that successfully set seed.

Wheat flowering time
For measurement of flowering time of the wheat cultivars Paragon, Watkins landrace W352 [26], and the late flowering Paragon x W352 F6 recombinant inbred line, the number of days taken to reach heading was recorded for each replicate of each line. At the same time, the leaves on the main tiller were counted (starting from the 3-leaf stage) until the time of heading.

Wheat seed count
Seeds were manually counted in each spike. Images were obtained using a Nikon DSC D90 camera (HFX-DX, Melville, NY) and processed using ViewNX 2 software, produced by Nikon (Nikon, Surrey, UK) ( Supplementary Fig. 12). Details are given in Supplementary   Information.

Fusarium Head Blight infections
The test undertaken was for type II resistance, which is resistance to spread from floret to floret within the head. A suspension of 1x10 6 conidiaspores per ml of Fusarium graminearum, which had been cultured in a mungbean liquid media, was used for point inoculations [27]. The isolate was a mix of two aggressive deoxynivalenol-producing F. graminearum UK isolates (K1-4/K1-

Transformation of barley
Immature embryos of the barley cv. Golden Promise were inoculated with Agrobacterium strain AGL1 and transformed plants were recovered following the protocol of Harwood [28]. Constructs from the pBRACT series [29] containing selection cassettes conferring resistance to the antibiotic hygromycin were introduced.

Wheat meiosis studies
The anthers used for this study came from hexaploid wheat (T. aestivum cv. Chinese Spring (CS)) carrying the Ph1 locus and crosses between rye (Secale cereale cv. Petkus) and hexaploid wheat (CS) either carrying or lacking the Ph1 locus (ph1b deletion) [30].
Seeds were stratified on wet filter paper in the dark for 5 days at 4 °C, followed by a period of germination for 24 hours at 25 °C. The seedlings were vernalized for 3 weeks at 5 °C and then transferred to different controlled environment rooms until meiosis. Three seedlings from each genotype were transferred to the Conviron speed breeding chamber and an additional three were transferred to a glasshouse with no supplementary lighting or heating, as a control. From each plant, one spike was collected for the determination of meiotic stability in pollen-mother cells.
For meiosis studies, suitable young spikes were excised and fixed in ethanol:acetic acid (3:1).
The samples were kept at room temperature, for at least one week, until slide preparation. Each floret has three synchronous anthers, and so one anther per floret was squashed in 45% acetic acid in water and assigned at metaphase I in meiosis by observation under a Leica DM2000 microscope (Leica Microsystems Ltd., Heerbrug, Germany; http://www.leica microsystems.com). The two remaining anthers were stained following the Feulgen procedure [31]. The present observations were limited to this stage. Images were collected using the Leica DM2000 microscope equipped with a Leica DFC450 camera (Leica Microsystems) and