Seed shattering, or shedding, is an important fitness trait for wild and weedy grasses. U.S. weedy rice (Oryza sativa) is a highly shattering weed, thought to have evolved from non-shattering cultivated ancestors. All U.S. weedy rice individuals examined to date contain a mutation in the sh4 locus associated with loss of shattering during rice domestication. Weedy individuals also share the shattering trait with wild rice, but not the ancestral shattering mutation at sh4; thus, how weedy rice reacquired the shattering phenotype is unknown. To establish the morphological basis of the parallel evolution of seed shattering in weedy rice and wild, we examined the abscission layer at the flower-pedicel junction in weedy individuals in comparison with wild and cultivated relatives.
Consistent with previous work, shattering wild rice individuals possess clear, defined abscission layers at flowering, whereas non-shattering cultivated rice individuals do not. Shattering weedy rice from two separately evolved populations in the U.S. (SH and BHA) show patterns of abscission layer formation and degradation distinct from wild rice. Prior to flowering, the abscission layer has formed in all weedy individuals and by flowering it is already degrading. In contrast, wild O. rufipogon abscission layers have been shown not to degrade until after flowering has occurred.
Seed shattering in weedy rice involves the formation and degradation of an abscission layer in the flower-pedicel junction, as in wild Oryza, but is a developmentally different process from shattering in wild rice. Weedy rice abscission layers appear to break down earlier than wild abscission layers. The timing of weedy abscission layer degradation suggests that unidentified regulatory genes may play a critical role in the reacquisition of shattering in weedy rice, and sheds light on the morphological basis of parallel evolution for shattering in weedy and wild rice.
Abscission is the process by which plants shed unwanted organs, such as those that have been damaged or diseased, or release ripe seeds and fruits . Seed abscission is an important mechanism for seed dispersal in many wild cereals . During domestication of grass species (e.g. wheat, rye, barley, and rice), a critical shift occurred towards reductions in seed-shedding ability, facilitating the harvesting of grains [2–5]. Seed shattering is costly to farmers, as crop yield is diminished, and lost seeds may lead to persistence of crop volunteers in cultivated fields [5, 6]. However, seeds that require intense labor to harvest are also undesirable, along with those that remain on the plant and germinate (i.e. preharvest sprouting). A balance between ease of shattering and difficult threshing is maintained in crop species, determined in part by specific demands of the harvesting system (e.g. hand vs. machine threshing) [7, 8]. In contrast, in agricultural weeds -- plants that invade cultivated fields -- increased seed dispersal is believed to be favored, much as it is in wild species . Seed shattering is a commonly observed trait in agricultural weedy plants that are related to domesticated species . Seed shattering is thus under opposing selection in crops and weeds inhabiting agricultural complexes.
Domesticated Asian rice (Oryza sativa L.) is one of the world's most important crop species, providing about 20% of the world's caloric intake . Cultivated rice fields worldwide are invaded by a weedy relative of rice known as weedy or red rice (O. sativa) . Weedy rice is costly to farmers in terms of yield losses and removal efforts, as it competes aggressively with cultivated rice and can contaminate harvests [10, 11]. The ability of weedy rice to survive and spread in cultivated rice fields has been attributed in part to its reported capacity to shatter seeds (e.g. [12–15]). High levels of seed shattering are also prevalent in the wild ancestor of cultivated rice, O. rufipogon, which is native to tropical wetlands of South Asia . Cultivated Asian rice, in contrast, shows a wide range of seed threshability levels, from nearly shattering to difficult to thresh, but is generally less shattering than wild and weedy species [17, 18].
Organ abscission in plants depends on the formation of abscission zones, which are morphologically distinct structures generally consisting of one to multiple layers of cells dense with cytoplasm [1, 6]. Swelling and dissolving of the middle lamella between adjacent cell walls in the abscission layer allows for organ release [1, 19]. In many plants, the abscission layer is formed long before the activation of cell separation and breakage occur [19, 20]. Seed shattering in Oryza is dependent on the proper formation and subsequent degradation of an abscission layer between the flower and the pedicel. QTL (quantitative trait loci) associated with loss of shattering have been identified on nearly every rice chromosome, and three loci have been cloned to date: sh4/SHA1, qsh1 and OsCPL1 [8, 21, 22]. Of these loci, sh4, which encodes a nuclear transcription factor, is considered the most important contributor to reduced shattering during rice domestication . A single nonsynonymous substitution (G to T) in the first exon of sh4 leads to reduced function of SH4 and incomplete development of the abscission layer in non-shattering cultivated rice . This non-shattering mutation is fixed in all cultivated rice varieties examined to date [8, 18, 24, 25], spanning the highly differentiated japonica and indica cultivar groups. There is still some controversy whether Asian rice was independently domesticated at least twice from O. rufipogon populations [26–28], or only once [3, 29]. Regardless of the domestication scenario, the ubiquity of the T substitution in cultivated rice suggests very strong selection for loss of shattering (perhaps in combination with introgression) during domestication [8, 24, 25].
Recently, we examined the seed shattering phenotype and the sh4 shattering locus in populations of U.S. weedy rice . Several genetically differentiated populations of weedy rice occur in the U.S., and these can be distinguished by their predominant hull morphology . Main populations include the straw-hulled (SH) group, early flowering weeds characterized by straw-colored hulls and lack of awns, and the black-hulled awned (BHA) group, later flowering weeds with seeds that have predominantly black hulls and long awns [30–32]. Genome-wide data indicate that SH and BHA weedy rice groups share genomic identity with Asian domesticated rice from the indica and aus variety groups, respectively, suggesting weedy origins within these cultivated groups [30, 32, 33]. Minor U.S. weedy rice groups include the brown-hulled (BRH) group, which are putative hybrids between SH and BHA weeds, and the mixed groups (MX), containing individuals likely to be hybrids between weeds and local tropical japonica cultivars . We have found that nearly all U.S. weedy rice readily shatters its seeds to a similar degree as wild rice . However, all populations of U.S. weedy rice share the "non-shattering" sh4 substitution common to cultivated rice, regardless of their propensity to shatter . These results support the evolution of U.S. weedy rice from cultivated ancestors and, since wild and major weedy groups have separate origins, the parallel evolution of the shattering trait among these Oryza groups. Our results further imply that weedy rice re-acquired the shattering trait through the involvement of unidentified loci other than sh4 .
In an effort to understand how weedy rice may have re-evolved the shattering trait after its loss in domesticated ancestors, we investigate here the morphological basis of shattering in U.S. weedy rice groups. Given that wild and weedy rice do not share the ancestral sh4 shattering substitution characteristic of O. rufipogon, it is possible that wild and weedy groups do not share the same morphological shattering mechanism. Moreover, despite sharing the same "non-shattering" mutation at the sh4 locus , the two major U.S. weedy rice populations -- SH and BHA -- have separate origins, and may have acquired the shattering phenotype in mechanistically different ways, representing a separate instance of parallel evolution. To our knowledge, no study to date has investigated the morphological basis of the shattering trait in weedy rice. We examine the abscission layer at the flower-pedicel junction in weedy rice prior to, at and shortly after flowering to determine morphology and level of degradation of this layer in relation to seed shattering ability, and compare these results to those of wild and cultivated Oryza, to gain insight into how traits important to weed fitness can evolve.
Results and Discussion
Abscission Layer Formation Differs in Wild and Cultivated Oryza
We observed the abscission layer at the flower-pedicel junction at flowering in six wild Oryza (Table 1, donated with asterisk): four O. rufipogon, the wild ancestor of cultivated Asian rice, and two O. nivara, an annual ecotype of O. rufipogon . All six wild Oryza show clear abscission layers between the flower and the pedicel at flowering (Figure 1A-F, and data not shown). The layer is slightly curved and occurs on both sides of the vascular bundle. Further magnification (60x) of the abscission layer shows very dark staining of cells at the center of the layer with some cells beginning to swell. This dark staining is most likely due to high lignification of these cells' walls, as abscission layer cells have been shown previously to be highly lignified . Cells surrounding the layer are highly organized into rows and perpendicular to the plane of abscission. (Figure 1B, D, F). No degradation of the abscission layer is yet observed at this stage. The occurrence of well-developed abscission layers upon flowering suggests that all six wild Oryza accessions will shatter their seeds readily, an observation that is consistent with our previous measurement of shattering levels of ripe seeds in these accessions (average Breaking Tensile Strength (BTS) = 0 g, Table 1; also see ).
List of Accessions used for this study.
USDA ID/Common Namec
Mean BTS (gram)d
Khao Dawk Mali -105
Wild Asian rice
a Based on STRUCTURE and identity from Reagon et al, 2010
b Origin for weeds is a U.S. state abbreviation, origins for cultivated and wild rice is country
c Accessions with RA numbers were acquired from Susan McCouch while all others were acquired from IRRI, these ID's were also used in Reagon et al, 2010.
d BTS (Breaking Tensile Strength) corresponds to the maximum weight a seed can hold before releasing; from data reported in Thurber et al, 2010
*-- Individuals used for Microscopy; all others used only for shattering time course
x-- no data available
We also observed the flower-pedicel junction at flowering in four cultivated rice samples (Figure 1G-L and data not shown) belonging to the aus and indica cultivar groups, the putative ancestors of U.S. weedy rice. None of the spikelets (i.e. rice flowers with attached glumes) sampled shows formation of a clear abscission layer upon flowering, although two indica accessions (3A09 and 3A11; Figure 1G, H, K, L) show weak staining in the region of the abscission layer. In these accessions, further magnification shows diffuse staining of cells in the abscission zone, although cellular organization is not as defined as in the wild tissue samples at this stage (Figure 1H, J, L). This further supports the absence of an abscission layer, and, in all cultivated samples, the pedicel blends in easily with the floral tissue at flowering. The lack of an abscission layer at flowering in all three indica cultivated accessions is consistent with their lack of shattering (average BTS = 70 to 137 g, Table 1). The single aus sampled is considered a very easy seed releasing variety (average BTS = 18 g, Table 1), yet it also appears to not possess an abscission layer at flowering (Figure 1G, H), suggesting that formation of this layer may be delayed and incomplete.
Our overall observations of clear abscission layers upon flowering in shattering wild Oryza individuals and lack of abscission layers at this stage in non-shattering cultivated rice are consistent with previous studies (see [8, 17, 21, 25]), and serve as a baseline for comparison to weedy rice. Because our observations do not differ from those published previously for other cultivated and wild rice samples, we concluded that abscission layer traits are robust under our growth conditions, and we did not sample additional time points of abscission layer development. Studies have documented that the abscission layer begins to form at least one week prior to flowering in wild O. rufipogon (and some exceptionally easy threshing indica and aus cultivars), and by flowering is prominent and clearly visible with staining [25, 36–39]. The abscission layer in O. rufipogon begins to degrade at or within a week of pollination, about two weeks after flowering, and continues degradation as the seed begins to form and mature, until the seed is released [37–39]. In contrast, in cultivated rice varieties, the abscission layer (if present) remains intact for at least 12 days after pollination . Both previous studies and ours show that there are dramatic differences in abscission layer formation and degradation between wild and cultivated rice, likely due to selection against shattering during the domestication process.
Degradation of the Abscission Layer is Accelerated in Weedy Rice
To determine the role of abscission layer formation and degradation in the shattering phenotype of weedy rice, we sampled six weedy rice accessions from three separate groups (SH (3), BHA (2), MX (1); Table 1, denoted with asterisk) at each of three time points: prior to, at and after flowering. With the exception of the non-shattering MX accession (MXSH_1B06, average BTS = 35 g, Table 1), all other weedy rice shatter easily, regardless of population identity (average BTS < 8 g, Table 1). We chose the single MX individual, as it was the only accession found in  that did not shatter extensively, and was one of the few accessions identified as a putative hybrid between SH weeds and U.S. tropical japonica . We hypothesized that abscission layer formation and degradation in shattering weedy samples would resemble that observed for O. rufipogon and O. nivara, while the non-shattering weed individual would resemble cultivated rice.
One week prior to flowering, all five shattering weedy rice accessions, including the two shown in Figure 2 (SH_1A08 and BHA_1A05) possess well-defined abscission layers (Figure 2A, G). Inspection with a higher magnification 60× lens shows that the BHA and SH weedy rice abscission layers prior to flowering (Figure 2B, H) are similar in staining and organization to the wild rice at flowering stage (Figure 1B, D, F); the highly lignified cells are darkly stained and starting to swell slightly, while the cells around the region are parallel to the plane of abscission. In contrast, the non-shattering MX weed shows only unbalanced, diffuse staining in the abscission zone with no clear organization of cells surrounding the zone (Figure 2M, N).
At flowering, the abscission layers for all the BHA and SH shattering weeds already show mild to moderate degradation and swollen cells at the abscission zone (Figure 2C, I; Additional File 1). Further magnified images show very swollen cells at the abscission layer with the darkest staining seen on the edges that are now exposed due to breakage (Figure 2D, J). All five shattering weeds already show degradation that is not observed in their shattering wild relatives at the flowering stage, yet there is some variation in the degree of degradation between weed accessions (Figure 1; Additional File 1). In contrast, the non shattering MX still shows only diffuse, weak staining, yet is beginning to form an abscission layer to one side of the vascular bundle (Figure 2O, P). Interestingly, when compared to wild and cultivated spikelets at this developmental stage, MX looks very similar to the non-shattering indica cultivars (Figure 1G, I, K).
A week after flowering has occurred, which is roughly one to two weeks prior to seed set in weedy rice, all SH and BHA shattering weeds sampled show moderate to near complete separation at the abscission layer and are only held together at the tips of the layer and the vascular bundle (Figure 2E, K, and data not shown). Cells that are still attached at the layer are swollen and darkly stained along the plane of breakage. Cells that have already been separated are losing their dark staining, possibly due to rearrangement of cell wall components (Figure 2F, L). A week after flowering, the non-shattering MX individual has developed a complete abscission layer, yet the cells at this layer have not begun to swell or degrade (Figure 2Q). When examined more closely, the cells of the non-shattering weed look very similar to wild abscission layer cells at flowering and to the shattering weeds prior to flowering: the cells are darkly stained and show a clear abscission layer with organized cells in the abscission zone (Figure 2R).
Taken together, our microscopy results demonstrate that shattering weeds display abscission layer developmental differences compared to wild and cultivated rice. Both wild and weedy individuals develop similar looking abscission layers in the same location of the floral-pedicel junction; this similar cellular morphology is consistent with the shared shattering trait of wild and weedy individuals. Moreover, abscission layer formation in shattering weedy rice occurs at least one week prior to flowering, if not earlier, similar to what has been reported for shattering wild rice [25, 36]. However, at flowering, the abscission layer in weedy rice has already begun to degrade, in some cases severely, which is not the case in shattering wild rice or easy threshing varieties of cultivated rice  (Figures 1 and 2; Additional File 1). This suggests that timing of abscission layer degradation, rather than morphological differences, distinguishes the shattering trait in weedy and wild rice groups. Surprisingly, despite their independent origins from separate cultivar groups (aus and indica, respectively), both BHA and SH weeds show similar abscission layer traits and timing. This suggests that both U.S. weedy rice groups may have re-acquired the shattering trait in a similar mechanistic manner, opening the question of whether common genetic elements are involved.
Further investigation of additional developmental stages and a finer scale of developmental series may help identify more precisely when the abscission layer forms in weedy rice and how rapidly after formation it degrades. It is unclear from previous studies how the abscission layer degradation process is activated in rice, yet it is possible that the degradation repertoire is activated only after a certain stage of abscission layer development is complete. While further research is needed, our results indicate that weedy rice may reach this formative stage earlier than wild shattering relatives, and as a result, show earlier degradation. It is also possible that the formation of the abscission layer progresses at the same rate in both weedy and wild rice, with weedy rice abscission activating their degradation repertoire earlier in abscission layer formation than in wild rice.
Seed Shattering Time Course Profiles are Altered in Weedy Rice Compared to the Wild Relatives
The early degradation of U.S. weedy rice abscission layers may confer an earlier shattering phenotype than reported for wild rice. Earlier degradation of the abscission layer suggests that as soon as the weedy seed is mature, or nearly so, it can more readily fall to the ground. The timing of seed release is considered important to weed fitness, as it may be beneficial to disperse seeds prior to harvest ; earlier shattering could thus be a response to rice cultivation practices. Additionally, or alternatively, earlier release may prevent seeds from drying out and losing dormancy, another trait that enhances weediness ; higher moisture content in seeds is known to confer a greater level of dormancy , but desiccation of rice seeds occurs as they mature. Easy shattering may not necessarily always be an advantage, however. Seeds that shatter before they are mature enough to germinate will lower a plant's fitness .
Phenotypically, little is known about the shattering levels in weedy rice groups across floral/seed development. Previous studies in cultivated and wild rice have shown that shattering level increases dramatically after 15 days post flowering in wild rice and in some cultivated rice samples grown in both field and greenhouse settings [17, 36]. In an effort to determine if shattering levels mirror the observed formation and degradation of the abscission layer in U.S. weedy rice groups, we assessed levels of shattering as the amount of weight a grain can hold prior to release from the panicle (breaking tensile strength; BTS) in eight cultivated, five wild and seven weedy rice individuals, at various time points through seed development (Figure 3 and Additional File 2).
To date, we have examined eight cultivated rice varieties from the indica, aus and tropical japonica groups (Additional File 2). Four of these samples are shown in Figure 3A (3A06, 3A11, 2B03 and 3A09). All cultivated rice accessions show consistent high BTS values between 150 g to 250 g from before flowering through ten days after flowering. By 15 days after flowering, BTS values have dropped close to the level previously seen in these cultivars at maturity (between 25 g and 125 g), and remain at these levels through 30 days after flowering, consistent with measurements reported in . The five wild rice individuals surveyed (2F02, 2C12, 2C04, 2C02 and 2C09) show a similar shattering pattern to cultivated rice up through ten days post flowering (Figure 3B and Additional File 2). However, at 15 days post flowering, the BTS levels have dropped dramatically to near 0 g and stay at this level through 30 days post flowering (Figure 3B and Additional File 2). This is consistent with all reported observations of O. rufipogon and O. nivara shattering behavior across floral development [17, 36], and is consistent with the wild rice seed shattering trait at maturity (Table 1).
All six shattering weeds examined (SH_1A08, SH_1A09, BHA1_1B08, BHA1_1A05, BHA1_1C04 and BHA1_1B02) registered BTS values above 150 g five days before through five days after flowering (Figure 3C and Additional File 2). By ten days after flowering, BTS values for three weeds (SH_1A08, BHA1_1C04 and BHA1_1A05) have dropped to below 60 g, while all other weeds are still registering values around 150 g. By fifteen days after flowering, all shattering weeds shown have dropped their BTS values dramatically to nearly 0 g (Figure 3C and Additional File 2). The BTS values thereafter stay at 0 g throughout the remainder of seed maturation for all shattering weeds shown. The single non-shattering weed (MXSH_1B06) shows a different time course as the shattering weeds. The sharpest decreases in BTS values are only seen after 20 days after flowering and instead of dropping to 0 g the BTS values for this individual only go as low as 40 g (Figure 3C and Additional File 2).
The variation in timing of the sharp reduction in BTS values across the weeds surveyed indicates that shattering ability is only partly correlated with abscission layer degradation rates. Though all weedy rice accessions used in our microscopy study displayed earlier degradation of the abscission layer than what is seen in wild rice, a range of degradation severity seems to exist (Figure 2; Additional File 1). Two weed samples that showed reduction in BTS values five days prior to other weeds tested appear to possess the highest degraded abscission layers at flowering (Figure 2). Weeds with drastically reduced BTS values at 15 days, a timing consistent with that of wild rice, seem to have somewhat less-degraded layers at flowering (Additional File 1). Overall the weedy rice individuals that showed the least degradation at flowering have similar shattering time courses to what has been shown previously for wild rice, while those with the most degradation show an earlier drop in BTS values. This indicates that the timing of when shattering is first noticeable in weedy rice is variable, despite the fact that all weeds degrade their abscission layer at an earlier time than wild rice.
Novel mutations likely underlie the parallel evolution of shattering in weedy and wild rice
Previous studies of the sh4 locus in wild and domesticated rice have implicated this gene in both the formation and degradation of the abscission layer at the flower-pedicel junction [8, 25]. A mutation in the sh4 gene, strongly selected upon during rice domestication, is associated with reduction in shattering in cultivated rice varieties due to the formation of a discontinuous abscission layer . Transgenic experiments have further demonstrated that the ancestral sh4 allele (present in wild O. rufipogon) can restore shattering in non-shattering cultivated rice . Our previous work showed that U.S. weedy rice groups carry the derived non-shattering mutation fixed in cultivated rice , demonstrating that the functional mutation identified in the sh4 locus does not result in non-shattering in the weed, and is thus not sufficient for loss of shattering. This suggested that novel loci, perhaps distinct from those acting in wild rice species, are involved in the evolution of shattering in U.S. weedy rice groups.
The distinct developmental profile observed here for weedy rice abscission layers further supports that U.S. weedy rice groups did not acquire the shattering trait through introgression with wild species. Thus, this and our previous work  suggest that parallel evolution of shattering in weedy and wild rice has occurred through both different loci and different developmental mechanisms. Studies in several other systems have shown that parallel evolution between populations can arise from independent mutations in the same gene, as has been shown for body shape characteristics in two independent populations of freshwater stickleback and for two independently evolved populations of melanic Peromyscus rodents [43, 44]. Conversely, studies of independent melanic populations of rock pocket mice have also shown that convergent phenotypes can sometimes be achieved through mutations in different genes [45, 46]. The acquisition of the shattering trait in wild and weedy rice groups further supports the possible role of independent loci in parallel evolution.
Interestingly, the similarities in abscission layer traits (development and shattering time course) between two distinct weedy rice groups, SH and BHA, suggest that the gene(s) involved in reacquiring seed shattering may be the same in both populations. This is surprising, as these groups have been shown to have independent evolutionary origins [30, 32]. The convergence in the mechanistic basis of seed shattering among these weedy rice groups may indicate certain genetic or morphological constraints inherent to re-evolving the shattering trait after its loss through domestication. Future studies into the genes involved in the progression of abscission layer formation and degradation in both weedy and wild rice will be integral to the study of weed evolution.
Our results show that the shattering trait in U.S. weedy rice has a distinct mechanistic basis from that of the shattering wild ancestor of rice, consistent with the re-evolution of this trait in weedy groups from domesticated ancestors. Surprisingly, independently evolved weedy groups have converged on this feature of abscission layer development. In some cases, the altered timing of abscission layer degradation appears to lead to earlier shattering in weedy rice compared to wild rice.
Plant materials for microscopy
All accessions used in this study are a subset of those used in  for which phenotypic and sequence data are available. Five weedy rice accessions, collected in the Southern U.S. rice belt, were generously supplied by David Gealy (USDA) (Table 1). Accessions were chosen to represent the two major weedy rice groups (SH and BHA) based on population structure analysis  and a group of putative weed-crop hybrids (MX) showing some resistance to seed shattering. Additional samples of wild and cultivated Oryza were originally obtained from the International Rice Research Institute (IRRI) (O. rufipogon (4) and O. nivara, a close relative or annual ecotype of O. rufipogon (2)) and Susan McCouch (O. sativa (4)). All plants were grown in a Conviron PGW36 growth chamber at the University of Massachusetts Amherst. One seed per accession was planted in a 4 inch pot and grown as described in . Panicles from wild and cultivated individuals were collected at flowering, while panicles from weedy individuals were harvested at three time points: one week prior to flowering, at flowering and one week after flowering. For observations prior to flowering, panicles were collected when the boot, or flag leaf sheath, was swollen yet before flowers had begun emerging. At flowering, panicles were collected once 50% of the panicle had emerged from the boot. Panicles to be collected after flowering were bagged upon flowering to prevent pollen flow and loss of seeds. At each collection, approximately eight flower-pedicel tissue samples were excised from the flowers at the topmost end of the panicle using a dissecting scope.
Tissue samples were fixed with glutaraldehyde (100 mM) in a solution containing 100 mM PIPES pH 7.0, 100 mM Glutaraldehyde, 0.5 mM CaCl2, and 5.0 mM MgCl2 for 2 hours. Following fixation samples were dehydrated first in an ethanol series then further dehydrated in acetone. Dehydrated samples were infiltrated and embedded in Epon Araldite resin . Samples were sectioned longitudinally using a diamond knife on a rotary microtome (Porter-Blum JB4) to create 2 micrometer sections. Sections were dried onto rectangular microscope slides and subsequently stained for 3 minutes with Toluidine Blue (0.5% solution in 0.1% sodium carbonate, pH 11.1), a metachromatic dye which stains regions with high lignin dark blue-green and regions of unlignified cell wall reddish purple (see ). Bright field images were taken at both 10× and 60× using a Nikon TE 300 Inverted Microscope with an attached CCD camera (Quantix CoolSnap HQ; Roper Scientific).
Time course shattering measurements
Five weedy rice accessions, along with five wild rice accessions and eight cultivated O. sativa accessions (see above) were analyzed for shattering ability during floral and seed development (Table 1). All plants were grown as described above for microscopy. Panicles from each individual were collected ~5 days before flowering (swollen boot with top most flower of panicle approaching emergence), at flowering (50% of panicle emerged from boot), as well as 5, 10, 15, 20, 25, and 30 days after flowering. Upon flowering, panicles to be collected were bagged to prevent pollen flow and loss of seeds. The oldest (topmost) 10 flowers per panicle were analyzed for breaking tensile strength (BTS), or shattering level, using a digital force gauge as described in . BTS is a measure of the maximum amount of weight, in grams, a single flower or grain can hold before releasing; values at or near zero grams (g) are considered highly shattering while values over 100 g represent non-shattering or hard threshing [8, 18, 21]. Average BTS values for the ten measurements are reported for each sample.
Accessions are identical to those used in a previous study  and are grouped by type (weed, wild or cultivar). Identification numbers as well as phenotypic values for seed shattering are reported here as well as in .
A very special thank you to Dr. Caleb Rounds for technical assistance in microscopy. Additional thanks to Dale Callahan at the University of Massachusetts Central Microscope Facility for the use of equipment. This study was funded in part by a grant from the U.S. National Science Foundation Plant Genome Research Program (DBI-0638820) to A.L.C., K.M. Olsen and Y. Jia, and NSF grant MCB-0847876 to P.K.H.
Biology Department, University of Massachusetts
Patterson SE: Cutting Loose. Abscission and Dehiscence in Arabidopsis.Plant Physiology 2001, 126: 494–500.PubMedView Article
Harlan JR, DeWet JM: Some thoughts about weeds.Econ Bot 1965, 19: 16–24.View Article
Fuller DQ, Qin L, Zheng Y, Zhao Z, Chen X, Hosoya LA, Sun GP: The Domestication Process and Domestication Rate in Rice: Spikelet Bases from the Lower Yangtze.Science 2009, 323: 1607–1609.PubMedView Article
Sang T: Genes and Mutations Underlying Domestication Transitions in Grasses.Plant Physiology 2009, 149: 63–70.PubMedView Article
Zhang G, Mergoum M: Molecular mapping of kernel shattering and its association with Fusarium head blight resistance in a Sumai3 derived population.Theoretical and Applied Genetics 2007, 115: 757–766.PubMedView Article
Roberts JA, Whitelaw CA, Gonzalez-Carranza ZH, McManus MT: Cell Separation in Plants--Models, Mechanisms and Manipulation.Annals of Botany 2000, 86: 223–235.View Article
Sang T, Ge S: The Puzzle of Rice Domestication.Journal of Integrative Plant Biology 2007, 49: 760–768.View Article
Li C, Zhou Ailing, Sang Tao: Rice Domestication by Reducing Shattering.Science 2006, 311: 1936–1939.PubMedView Article
Burgos NR, Norsworthy JK, Scott RC, Smith KL: Red rice (Oryza sativa) status after 5 years of imidazolinone-resistant rice technology in Arkansas.Weed Technology 2008, 22: 200–208.View Article
Cao QJ, Lu BR, Xia H, Rong J, Sala F, Spada A, Grassi F: Genetic diversity and origin of weedy rice (Oryza sativa f. Spontanea) populations found in North-eastern China revealed by simple sequence repeat (SSR) markers.Annals of Botany 2006, 98: 1241–1252.PubMedView Article
Delouche JC, Burgos NR, Gealy DR, de San Martín GZ, Labrada R, Larinde M, Rosell C: Weedy rices - origin, biology, ecology and control.FAO PLANT PRODUCTION AND PROTECTION PAPER 2007., 188:
Gealy DR, Mitten DH, Rutger JN: Gene flow between red rice (Oryza sativa) and herbicide-resistant rice (O. sativa): Implications for weed management.Weed Technology 2003, 17: 627–645.View Article
Noldin JA, Chandler JM, McCauley GN: Red rice (Oryza sativa) biology. I. Characterization of red rice ecotypes.Weed Technology 1999, 13: 12–18.
Oard J, Cohn MA, Linscombe S, Gealy D, Gravois K: Field evaluation of seed production, shattering, and dormancy in hybrid populations of transgenic rice (Oryza sativa) and the weed, red rice (Oryza sativa).Plant Science 2000, 157: 13–22.PubMedView Article
Oka HI: Origin of Cultivated Rice. Tokyo: Japan Scientific Societies Press and Elsevier Science Publishers; 1988.
Ji HS, Chu SH, Jiang W, Cho YI, Hahn JH, Eun MY, McCouch SR, Koh HJ: Characterization and Mapping of a Shattering Mutant in Rice That Corresponds to a Block of Domestication Genes.Genetics 2006, 173: 995–1005.PubMedView Article
Thurber CS, Reagon M, Gross BL, Olsen KM, Jia Y, Caicedo AL: Molecular evolution of shattering loci in U.S. weedy rice.Molecular Ecology 2010, 19: 3271–3284.PubMedView Article
Ayeh KO, Lee Y, Ambrose MJ, Hvoslef-Eide AK: Characterization and structural analysis of wild type and a non-abscission mutant at the development funiculus (Def) locus inPisum sativumL.BMC Plant Biology 2009, 9: 76–83.PubMedView Article
Cho SK, Larue CT, Chevalier D, Wang H, Jinn TL, Zhang S, Walker JC: Regulation of floral organ abscission inArabidopsis thaliana.Proc Natl Acad Sci 2008, 105: 15629–15634.PubMedView Article
Konishi S, Izawa T, Lin SY, Ebana K, Fukuta Y, Sasaki T, Yano M: An SNP Caused Loss of Seed Shattering During Rice Domestication.Science 2006, 312: 1392–1396.PubMedView Article
Ji H, Kim SR, Kim YH, Kim H, Eun MY, Jin ID, Cha YS, Yun DW, Ahn BO, Lee MC, Lee GS, Yoon UG, Lee JS, Lee YH, Suh SC, Jiang W, Yang JI, Jin P, McCouch SR, An G, Koh HJ: Inactivation of the CTD phosphatase-like geneOsCPL1enhances the development of the abscission layer and seed shattering in rice.The Plant Journal 2010, 61: 96–106.PubMedView Article
Purugganan MD, Fuller DQ: The nature of selection during plant domestication.Nature 2009, 457: 843–848.PubMedView Article
Zhang LB, Zhu Q, Wu ZQ, Ross-Ibarra J, Gaut BS, Ge S, Sang T: Selection on grain shattering genes and rates of rice domestication.New Phytologist 2009, 184: 708–720.PubMedView Article
Lin Z, Griffith ME, Li X, Zhu Z, Tan L, Fu Y, Zhang W, Wang X, Xie D, Sun C: Origin of seed shattering in rice (Oryza sativa L.).Planta 2007, 226: 11–20.PubMedView Article
Caicedo AL, Williamson SH, Hernandez RD, Boyko A, Fledel-Alon A, York TL, Polato N, Olsen KM, Nielsen R, McCouch S, Bustamante CD, Purugganan MD: Genome-wide patterns of nucleotide polymorphism in domesticated rice.PLoS Genetics 2007, 3: e163.View Article
Londo JP, Chiang YC, Hung KH, Chiang TY, Schaal BA: Phylogeography of Asian wild rice,Oryza rufipogon, reveals multiple independent domestications of cultivated rice,Oryza sativa.Proceedings of the National Academy of Sciences of the United States of America 2006, 103: 9578–9583.PubMedView Article
Fuller D, Sato YI, Castillo C, Qin L, Weisskopf A, Kingwell-Banham E, Song J, Ahn SM, van Etten J: Consilience of genetics and archaeobotany in the entangled history of rice.Archaeological and Anthropological Sciences 2010., 2:
Reagon M, Thurber CS, Gross BL, Olsen KM, Jia Y, Caicedo AL: Genomic patterns of nucleotide diversity in parallel populations of U.S. weedy rice.BMC Evolutionary Biology 2010, 10: 180.PubMedView Article
Gealy DR, Tai TH, Sneller CH: Identification of red rice, rice, and hybrid populations using microsatellite markers.Weed Science 2002, 50: 333–339.View Article
Londo JP, Schaal BA: Origins and population genetics of weedy red rice in the USA.Molecular Ecology 2007, 16: 4523–4535.PubMedView Article
Gealy DR, Agrama HA, Eizenga GC: Exploring Genetic and Spatial Structure of U.S. Weedy Red Rice (Oryza sativaL.) in Relation to Rice Relatives Worldwide.Weed Science 2009, 57: 627–643.View Article
Zheng XM, Ge S: Ecological divergence in the presence of gene flow in two closely relatedOryzaspecies (Oryza rufipogonandO. nivara).Molecular Ecology 2010, X: X.
Tabuchi T, Ito S, Arai N: Anatomical Studies of the Abscission Process in the Tomato Pedicels at Flowering Stage.J Japan Soc Hort Sci 2001, 70: 63–65.View Article
Oba S, Sumi N, Fujimoto F, Yasue T: Association between Grain Shattering Habit and Formation of Abscission Layer Controlled by Grain Shattering genesh-2in Rice (Oryza sativa L.).Japanese Journal of Crop Science 1995, 64: 607–615.
Jin ID: On the formation and development of abscission layer in rice plants,Oryza sativa L.Jpn J Crop Sci 1986, 55: 451–457.
Jin ID, Inouye J: Relation between grain shedding and pedicel morphology near the abscission layer of japonica-indica hybrid rices bred in Korea.Jpn J Crop Sci 1982, 51: 271–275.
Jin ID, Inouye J: On the degree of grain shedding, histological peculiarity of abscission region and esterase isozyme genotype of Bulu and Tjereh rice varieties originated in Indonesia.Jpn J Crop Sci 1985, 54: 373–378.
Shivrain VK, Burgos NR, Scott RC, Gbur EE Jr, Estorninos LE Jr, McClelland MR: Diversity of weedy red rice (Oryza sativa L.) in Arkansas, U.S.A. in relation to weed management.Crop Protection 2010.
Gu XY, Kianian SF, Foley ME: Seed Dormancy Imposed by Covering Tissues Interrelates to Shattering and Seed Morphological Characters in Weedy Rice.Crop Science 2005, 45: 948–955.View Article
Delouche JC, Burgos NR, Gealy DR, Zorrilla de San Martin G, Labrada R, Larinde M, Rosell C: Weedy rices- origin, biology, ecology and control. In Book Weedy rices- origin, biology, ecology and control. Volume 188. City: FAO, Rome, Italy; 2007.
Kinglsey EP, Manceau M, Wiley CD, Hoekstra HE: Melanism in Peromyscus is Caused by Independent Mutations in Agouti.PLoS One 2009, 4: e6435.View Article
Schluter D, Clifford EA, Nemethy M, McKinnon JS: Parallel Evolution and Inheritance of Quantitative Traits.American Naturalist 2004, 163: 809–822.PubMedView Article
Nachman MW, Hoekstra HE, D'Agostino SL: The genetic basis of adaptive melanism in pocket mice.PNAS 2003, 100: 5268–5273.PubMedView Article
Hoekstra HE, Nachman MW: Different genes underlie adaptive melanism in different populations of rock pocket mice.Molecular Ecology 2003, 12: 1185–1194.PubMedView Article
Mollenhauer HH: PLASTIC EMBEDDING MIXTURES FOR USE IN ELECTRON MICROSCOPY.Stain Technology 1964, 39: 111–114.PubMed
O'Brien TP, Feder N, McCully ME: Polychromatic Staining of Plant Cell Walls by Toluidine Blue O.Protoplasma 1964, 59: 367–373.View Article
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.