As important as this process is to the determination of grain yield, it is surprising how little some folks know about the whole thing. Rather than leaving you to learn about such things "on the streets", I've developed this article and the accompanying one on silking (Nielsen, 2020) that describe the ins and outs of sex in the corn field.
Remember that corn has both male flowers and female flowers on the same plant (a flowering habit called monoecious for you trivia fans.) Interestingly, both flowers are initially bisexual (aka "perfect" flowers), but early in their development the female components (gynoecia) of the male flowers and the male components (stamens) of the female flowers abort, resulting in tassel (male) and ear (female) floral development.
Portions of the tassel may be visible before the plant technically reaches its final leaf stage (uppermost, final visible leaf collar) has occurred. By definition, growth stage VT occurs when the last branch of the tassel emerges from the whorl (Abendroth et al., 2011). This source furthermore states that growth stage VT is "...initiated when the last branch of the tassel is completely visible and the silks have not yet emerged." Once upon a time, that exact developmental sequence may have been true, but today's hybrids tend to behave differently. It is not uncommon for silk emergence (growth stage R1) to begin not only prior to the last tassel branch appearing from the whorl, but sometimes prior to the exsertion of anthers and the beginning of pollen shed (Nielsen, 2018).
Maximum plant height occurs at or shortly after growth stage VT as the final stalk internodes complete their elongation. The corn plant is most vulnerable to hail damage at growth stage VT/R1 because all of its leaves are exposed. Complete (100 %) leaf loss at growth stage VT will usually result in complete (100 %) yield loss by harvest. Even if the ovules on the ears are successfully fertilized by the pollen, severe defoliation at growth stage VT/R1 often causes entire ear shoots to die because so few leaves remain to produce the necessary carbohydrates (by photosynthesis) to sustain ear and kernel development.
Approximately 1,000 individual spikelets form on each tassel and each one bears two florets encased in two large glumes. Each floret contains three anthers. An anther and its attached filament comprise the stamen of the male flower. The anthers are those "thingamajigs" that hang from the tassel during pollination. Under a magnifying lens, individual anthers look somewhat like the double barrel of a shotgun. Do the math and you will realize that an individual tassel produces approximately 6,000 pollen-bearing anthers, although hybrids can vary greatly for this number.
As the florets mature, elongation of the filaments allows the anthers to emerge ("exsert" for you trivia fans) from the glumes. Pollen is dispersed through pores at the tips of the anthers that open ("dihisce" for you trivia fans) as the anthers exsert from the glumes. Anther exsertion and pollen shed usually begin in the mid-portion of the central tassel spike and then progresses upward, downward and outward over time. Anthers typically emerge from the upper floret of a pair first, while those from lower floret typically emerge later the same day or on following days. After its pollen is shed, "spent" anthers eventually drop from the tassel and are sometimes mistaken for the pollen when observed on the leaves or ground.
The yellow or white “dust-like” pollen that falls from a tassel represents millions of individual, nearly microscopic, spherical, yellowish- or whitish translucent pollen grains. Estimates of the total number of pollen grains produced per tassel range from 2 to 25 million (yes, they are difficult to count). Each pollen grain contains the male genetic material necessary for fertilizing the ovary of one potential kernel.
The outer membrane of a pollen grain is very thin. Once dispersed into the atmosphere, pollen grains remain viable for only a few minutes before they desiccate. Yet, with only a 15 mph wind, pollen grains can travel as far as 1/2 mile within those couple of minutes.
Therein lies the concern of the potential for pollen “drift” from a transgenic corn field to an adjacent non-transgenic corn field and the risk of transgenic “contamination” of grain intended for non-transgenic markets. The good news is that research suggests that the overwhelming majority of a corn field’s pollen load is shed in the field itself.
All of the pollen from a single anther may be released in as little as three minutes. All the anthers on an individual tassel may take as long as seven days to finish shedding pollen, although the greatest volume of pollen is typically shed during the second and third day of anther emergence. Because of natural field variability in plant development, a whole field may take as long as 14 days to complete pollen shed.
Peak pollen shed usually occurs in mid-morning. Some research indicates that pollen shed decreases after temperatures surpass 86F. A second “flush” of pollen often occurs in late afternoon or evening as temperatures cool. Pollen shed may occur throughout most of the day under relatively cool, cloudy conditions.
Weather conditions influence pollen shed. If the anthers are wet, the pores will not open and pollen will not be released. Thus, on an average Indiana summer morning following a heavy evening dew, pollen shed will not begin until the dew dries and the anther pores open. Similarly, pollen is not shed during rainy conditions. Cool, humid temperatures delay pollen shed, while hot, dry conditions hasten pollen shed.
Extreme heat stress (100F or greater) can kill corn pollen, but fortunately the plant avoids significant loss of pollen viability by virtue of two developmental characteristics. First of all, anthers do not mature at the same time up and down the tassel, nor does complete pollen shed occur on a single day. Anther maturation and pollen shed occur over several days and up to two weeks. Therefore, a day or two of extreme heat usually does not affect the entire pollen supply. More importantly, the majority of daily pollen shed occurs in the morning hours when air temperature is much more moderate.
Traditional seed corn production involves the planting of two fully fertile inbred lines of corn. One is designated to be the seed-bearing parent (i.e., female inbred) and the other is designated to be the pollen donor (i.e., male inbred) for the seed-bearing plants. Tassels are manually removed from the female inbred plants in the field (i.e., detasseling) to avoid those plants from pollinating themselves, therefore restricting the available pollen in the field to only that from the male inbred plants. Seed is harvested from the rows of female inbred plants for sale as seed corn to farmers in subsequent years. Plants of that seed corn are fully fertile, tassels and ears.
An alternative seed corn production strategy involves the development (breeding) of female inbreds that contain cytoplasmic male sterility (CMS) which results in sterile tassels. Use of such CMS inbreds in hybrid seed corn production eliminates the need for costly detasseling (Wych, 1988). Seed corn production based on CMS methodologies was used widely up to 1970 when more than 85% of hybrids grown contained cytoplasmic Texas male sterile (cms-T) genetics and, as it turned out, was extremely susceptible to a mutation in the disease southern corn leaf blight (Bipolar maydis T.) that resulted in average yield losses ranging from 35 and 50% (Bruns, 2017). Use of CMS methodologies for seed production subsequently waned until the availability of alternative, resistant, CMS-C and CMS-S cytoplasms in the late 70s and early 80s (Wych, 1988).
The tassels of CMS inbreds do not produce functional anthers or pollen. According to Rogers & Edwardson (1952), "Normal tassels have well-filled spikelets and produce an abundance of pollen. Partially sterile tassels have somewhat flatter spikelets, while anthers emerge from only a few spikelets of both the lateral branches and main axis. The entire staminate inflorescence of the sterile plants has a slender flattened appearance, and the anthers within the spikelets are shriveled and shrunken. Anthers may occasionally emerge, although very little pollen, if any at all, is shed." See image below for an example of a sterile tassel.
Seed harvested from CMS female parent inbreds is itself male sterile unless the male parent inbred (aka the pollen donor) contained "restorer" genetics (Wych, 1988). Consequently, production of marketable seed corn using CMS methodologies without "restorer" genetics requires the physical blending of male sterile seed from CMS hybrid production fields with male fertile seed of the same hybrid from normal (detasseled) production fields (Wych, 1988). The industry standard for such blending is reportedly 50:50 fertile:sterile but seed companies are not required to report that information on the seed labels. Consequently, about half of the plants in fields planted to such hybrids will exhibit sterile tassels. Not to worry, though, because such blends are perfectly capable of producing enough pollen to adequately pollinate all the silks on ears in the field.
Abendroth, L.J., R.W Elmore, M.J. Boyer, and S.K. Marlay. 2011. Corn Growth and Development. Iowa State Univ. Extension Publication #PMR-1009. https://shop.iastate.edu/extension/farm-environment/crops-and-soils/agronomic-crops/pmr1009.html [Accessed June 2025].
Bruns, H.A. 2017. Southern Corn Leaf Blight: A Story Worth Retelling. Agronomy Journal, 109: 1218-1224. https://doi.org/10.2134/agronj2017.01.0006 [Accessed June 2025].
Nielsen, RL (Bob). 2018. Unusually long silks in corn. Corny News Network, Purdue Univ. [online] http://www.kingcorn.org/news/timeless/LongSilks.html [Accessed June 2025].
Nielsen, RL (Bob). 2020. Silk Emergence. Corny News Network Purdue Univ. [On-Line]. Available at http://www.kingcorn.org/news/timeless/Silks.html [Accessed June 2025].
Nielsen, RL (Bob). 2022. A Fast & Accurate Pregnancy Test for Corn. Corny News Network, Purdue Univ. [On-Line]. Available at http://www.kingcorn.org/news/timeless/EarShake.html [Accessed June 2025].
Rogers, J.S. and Edwardson, J.R. 1952. The Utilization of Cytoplasmic Male-Sterile Inbreds in the Production of Corn Hybrids. Agron. J., 44: 8-13. https://doi.org/10.2134/agronj1952.00021962004400010004x [Accessed June 2025].
Russell, W.A. and A.R. Hallauer. 1980. Corn. (a chapter in Hybridization of Crop Plants. American Soc. of Agronomy-Crop Science Soc. of America. Madison, WI.
Strachan, Stephen. (date unknown). Relating Silk Emergence at Pollination to Kernel Set at Harvest. Crop Insights, Pioneer/Corteva. https://www.pioneer.com/us/agronomy/emergence.html [Accessed June 2025].
Wiebold, William. 2012. Corn Pollination, the Good, the Bad, and the Ugly, Part 1: The Male Role. Integrated Pest & Crop Management, Univ. Missouri. https://ipm.missouri.edu/cropPest/2012/7/Corn-Pollination-the-Good-the-Bad-and-the-Ugly-Pt-1 [Accessed June 2025].
Wych, Robert D. 1988. Production of Hybrid Corn. In Corn and Corn Improvement (eds G.F. Sprague and J.W. Dudley). https://doi.org/10.2134/agronmonogr18.3ed.c9 [Accessed June 2025].
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