plant breeding

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Apriums and Plumcots and Pluots, Oh My!

I was once a teenage paper carrier in small town Idaho. One of my stops was an apartment complex, and for much of the year, this was an uneventful stop. But for a few weeks in the summer, the purple-leaved plum trees out front had ripe fruit on them, and each time I was there, I would stop and take a few. In general, I don’t get that excited about fruit, but I enjoyed eating these plums. This variety of plum is typically planted for its looks rather than its fruit, and it may even be the tree that recently received a pitifully low score on an episode of Completely Arbortrary. Ornamental plum or not – and low cone score or not – I thought the fruit was good.

Many of the things we eat are a result of crosses between two related species, and plums are a great example of this. Species are species because they are reproductively isolated. A species does not typically mate with a member of another species and create viable offspring, except this happens all the time both naturally and artificially. In many cases, the offspring isn’t actually viable, but there is offspring nonetheless, and in the case of plants, that offspring can then reproduce asexually – by leaf, stem, or root cuttings or by some other means – and the resulting hybrid can exist indefinitely. One species mating with another species (specifically two species that are members of the same genus) is called interspecific hybridization, and there is a good chance that you’ve eaten something recently that is a result of this.

One of the most widely grown species of plum, Prunus domestica (commonly known as European plum), is a result of interspecific hybridization that occurred many centuries ago. A paper published in Horticulture Research (2019) confirmed that P. domestica originated as a cross between Prunus cerasifera and Prunus spinosa, the latter of which may have also been a result of interspecific hybridization. There are over 400 species in the genus Prunus that are distributed across temperate regions in the northern hemisphere. Within this genus is the subgenus Prunus (or Prunophora), a group that includes dozens of familiar species such as the plums, apricots, peaches, and almonds. Due to their close relationship, both natural and artificial hybridization among members of this subgenus is common, which explains the origin of Prunus domestica, as well as the majority of the plums we grow today.

Current commercial production of plums in North America is largely thanks to work done by Luther Burbank in the late 19th to early 20th centuries. Burbank was obsessed with plant breeding and released hundreds of new varieties of all kinds of different plants during his decades long career. He seemed particularly interested in plums, developing 113 different cultivars, which account for more than half of all his fruit releases. Probably his most well known plum variety is ‘Santa Rosa,’ which thanks to modern day genetics has been determined to be a cross between at least four different species of plum.

apriums

Early colonizers to the American continent were mainly growing varieties of the European plum they had brought over from Europe. North America is also home to several species of plums, which are used by indigenous populations. Shortly before Burbank began working with plums on his farm in California in 1881, Asian plum species were imported to the U.S., and breeders began using them in crosses with both European and North American plum species. Burbank became particularly engulfed in these efforts. In an article published in HortScience (2015), David Karp writes, “In the history of horticulture it is rare to find an individual who almost single-handedly created a new commercial industry based on a novel fruit type as Luther Burbank did for Asian-type plums in the United States.” Most Asian-type plums sold in stores today are hybrids of several different plum species due to the numerous complex crosses that Burbank made.

Burbank is also said to be the first to cross plums and apricots, creating the first of many cultivars of the plumcot. Plum and apricot crosses didn’t really catch on for a few more decades, and when they did, it was thanks to the work of Floyd Zaiger of Zaiger Genetics who developed and released numerous varieties. Apriums and Pluots are Zaiger Genetics trademarks, along with a few other unlikely crosses with plums and their related counterparts.

plumcots

A plumcot is the simplest cross. It is said to be 50% Asian plum (Prunus salicina) and 50% apricot (Prunus armeniaca). However, due to all the breeding of Asian plums carried out by Burbank and others, the Asian plum involved in the cross is typically a hybrid with other plum species, as discussed in a recent paper published in Plants (2022). An aprium is the result of a cross between a plumcot and an apricot, making it 75% apricot and 25% plum, while a pluot is a cross between a plumcot and a plum, making it 75% plum and 25% apricot. There is typically much more that goes into making these crosses, but that’s the general idea. If you’re lucky, you can find all three of these intraspecific crosses in a produce section near you, but it may not be clear what cultivar you’re purchasing. Myriad cultivars have been released of each of these hybrids – each one varying in color, size, flavor, disease resistance, etc. – and unfortunately most grocery stores don’t include cultivar names on their products, so it’s difficult to know what you’re getting.

At Awkward Botany Headquarters, there is a plum tree growing in our front yard. We didn’t plant it, so at this point I have no idea what species or cultivar it is. The plums are delicious though, and the leaves aren’t purple like the plums I used to eat on my paper route. Considering all of the intraspecific crossing that has gone on with plums, it’s quite likely that it is a combination of different species, which isn’t going to make it easy to figure out. But I’ll do my best.

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Dispersal by Open Sesame!

In certain instances, “open sesame” might be something you exclaim to magically open the door to a cave full of treasure, but for the sesame plant, open sesame is a way of life. In sesame’s case, seeds are the treasure, which are kept inside a four-chambered capsule. In order for the next generation of plants to have a chance at life, the seeds must be set free. Sesame’s story is similar to the stories of numerous other plant species whose seeds are born in dehiscent fruits. But in this instance, the process of opening those fruits is fairly unique.

Sesamum indicum is a domesticated plant with a 5000 plus year history of cultivation. It shares a genus with about 20 other species – most of which occur in sub-Saharan Africa – and belongs to the family Pedaliaceae – the sesame family. Sesame was first domesticated in India and is now grown in many other parts of the world. It is an annual plant that is drought and heat-tolerant and can be grown in poor soils and locations where many other crops might struggle. However, the best yields are achieved on farms with fertile soils and adequate moisture.

image credit: wikimedia commons

Depending on the variety and growing conditions, sesame can reach up to 5 feet tall and can be unbranched or highly branched. Its broad lance-shaped leaves are generally arranged directly across from each other on the stem. The flowers are tubular, similar in appearance to foxglove, and are typically self-pollinated and short-lived. They come in shades of white, pink, blue, and purple and continue to open throughout the growing season as the plant grows taller, even as fruits formed earlier mature. The fruits are deeply-grooved capsules with at least four separate chambers called locules. Rows of tiny, flat, teardrop shaped seeds are produced in each chamber. The seeds are prized for their high oil content and are also used in numerous other ways, both processed and fresh. One of my favorite uses for sesame seeds is tahini, which is one of the main ingredients in hummus.

The fruits of sesame are dehiscent, which means they naturally split open upon reaching maturity. Compare this to indehiscent fruits like acorns, which must either rot or be chewed open by an animal in order to free the seeds. Dehiscence is also called shattering, and in many domesticated crop plants, shattering is something that humans have selected against. If fruits dehisce before they can be harvested, seeds fall to the ground and are lost. Selecting varieties that hold on to their seed long enough to be harvested was imperative for crops like beans, peas, and grains. In domesticated sesame, the shattering trait persists and yield losses are often high.

Most of the world’s sesame crop is harvested by hand. The plants are cut, tied into bundles, and left to dry. Once dry, they are held upside down and beaten in order to collect the seeds from their dehisced capsules. When harvested this way, naturally shattering capsules may be preferred. But in places like the United States and Australia, where mechanical harvesting is desired, it has been necessary to develop new, indehiscent varieties that can be harvested using a combine without losing all the seed in the process. Developing varieties with shatter-resistant seed pods, has been challenging. In early trials, seed pods were too tough and passed through threshers without opening. Additional threshing damaged the seeds and caused the harvest to go rancid. Mechanically harvested varieties of sesame exist today, and improvements in these non-shattering varieties continue to be made.

In order to develop these new varieties, breeders have had to gain an understanding of the mechanisms behind dehiscence and the genes involved in this process. This research has helped us appreciate the unique way that the capsules of the sesame plant dehisce. As in the seed bearing parts of many other plant species, the capsules of sesame exhibit hygroscopic movements. That is, their movements are driven by changes in humidity. The simplest form of hygroscopic movement is bending, which can be seen in the opening and closing of pine cone scales. A more complex movement can be seen in the seed pods of many species in the pea family, which both bend and twist as they split open. In both of these examples, water is evaporating from the plant part in question. As it dries it bends and/or twists, thereby releasing its contents.

dehisced capsules of sesame (Sesamum indicum); photo credit: wikimedia commons (Dinesh Valke)

The cylindrical nature and cellular composition of sesame fruits leads to an even more complex form of hygroscopic movement. Initially, the capsule splits at the top, creating an opening to each of the four locules. The walls of each locule bend outward, then split and twist as the seed falls from the capsule. In a study published in Frontiers in Plant Science (2016), researchers found that differences in the capsule’s inner endocarp layer and outer mesocarp layer are what help lead to this interesting movement. The endocarp layer is composed of both transvere (i.e. circumferential) and longitudinal fiber cells, while the mesocarp is made up of soft parenchyma cells. The thicknesses of these two layers gradually changes along the length of the capsule. As the mesocarp dries, the capsule initially splits open and starts bending outwards, but as it does, resistance from the fiber cells in the endocarp layer causes further bending and twisting (see Figure 1 in the report for an illustration). As the researchers write, “the non-uniform relative thickness of the layers promotes a graded bi-axial bending, leading to the complex capsule opening movement.”

All this considered, a rock rolling away from the entrance of a cave after giving the command, “Open sesame!” almost seems simpler than the “open sesame” experienced by the fruit of the sesame plant.

See Also: Seed Shattering Lost – The Story of Foxtail Millet

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Maize Anatomy and the Anatomy of a Maze

Commonly known as corn throughout much of North America, maize is a distinctive emblem of the harvest season. It is one of the most economically important crops in the world (the third most important cereal after rice and wheat) and has scads of uses from food to feed to fuel. The story of its domestication serves as a symbol of human ingenuity, and its plasticity in both form and utility is a remarkable example of why plants are so incredible.

The genus Zea is in the grass family (Poaceae) and consists of five species: Z. diploperennis, Z. perennis, Z. luxurians, Z. nicaraguensis, and Z. mays. Maize is the common name of Zea mays subsp. mays, which is one of four Z. mays subspecies and the only domesticated taxon in the genus. All other taxa are commonly and collectively referred to as teosintes.

The domestication of maize, apart from being an impressive feat, has long been a topic of research and a challenging story to tease apart. The current understanding is that maize was first domesticated around 9000 years ago in the Balsas River valley in southern Mexico, the main progenitor being Zea mays subsp. parviglumis. It is astonishing how drastically different in appearance teosintes are from modern day maize, but it also explains why determining the crop wild relative of maize was so difficult.

Teosinte, teosinte-maize hybrid, and maize - photo credit: wikimedia commons

Teosinte, teosinte-maize hybrid, and maize – photo credit: wikimedia commons

Teosintes and maize both have tall central stalks; however, teosintes generally have multiple lateral branches which give them a more shrubby appearance. In teosinte, each of the lateral branches and the central stalk terminate in a cluster of male flowers; female flowers are produced at the nodes along the lateral branches. In maize, male flowers are borne at the top of the central stalk, and lateral branches are replaced by short stems that terminate in female flowers. This is where the ears develop.

Ears – or clusters of fruits – are blatantly different between teosintes and maize. To start with, teosinte produces a mere 5 to 12 fruits along a short, narrow cob (flower stalk). The fruits are angular and surrounded in a hard casing. Maize cobs are considerably larger both in length and girth and are covered in as many as 500 or more fruits (or kernels), which are generally more rounded and have a softer casing. They also remain on the cob when they are ripe, compared to teosinte ears, which shatter.

Evolutionary biologist, Sean B. Carroll, writes in a New York Times article about the amazing task of “transform[ing] a grass with many inconvenient, unwanted features into a high-yielding, easily harvested food crop.” These “early cultivators had to notice among their stands of plants variants in which the nutritious kernels were at least partially exposed, or whose ears held together better, or that had more rows of kernels, and they had to selectively breed them.” Carroll explains that this “initial domestication process which produced the basic maize form” would have taken several hundred to a few thousand years. The maize that we know and love today is a much different plant than its ancestors, and it is still undergoing regular selection for traits that we find desirable.

Female inflorescence (or "ear") of Zea mays subsp. mays - photo credit: wikimedia commons

Female inflorescence (or “ear”) of Zea mays subsp. mays – photo credit: wikimedia commons

To better understand and appreciate this process, it helps to have a basic grasp of maize anatomy. Maize is an impressive grass in that it regularly reaches from 6 to 10 feet tall and sometimes much taller. It is shallow rooted, but is held up by prop or brace roots – adventitious roots that emerge near the base of the main stalk. The stalk is divided into sections called internodes, and at each node a leaf forms. Leaf sheaths wrap around the entirety of the stalk, and leaf blades are long, broad, and alternately arranged. Each leaf has a prominent midrib. The stalk terminates in a many-branched inflorescence called a tassel.

Maize Anatomy 101 - image credit: Canadian Goverment

Maize Anatomy 101 – image credit: Canadian Government

Maize is monoecious, which means that it has separate male and female flowers that occur on the same plant. The tassel is where the male flowers are located. A series of spikelets occur along both the central branch and the lateral branches of the tassel. A spikelet consists of a pair of bracts called glumes, upper and lower lemmas and paleas (which are also bracts), and two simple florets composed of prominent stamens. The tassel produces and sheds tens of thousands of pollen grains which are dispersed by wind and gravity to the female inflorescences below and to neighboring plants.

Female inflorescences (ears) occur at the top of short stems that originate from leaf axils in the midsection of the stalk. Leaves that develop along this reduced stem wrap around the ears forming the husk. Spikelets form in rows along the flower stalk (cob) within the husk. The florets of these spikelets produce long styles that extend beyond the top of the husk. This cluster of styles is known as the silk. When pollen grains land on silk stigmas, pollen tubes grow down the entire length of the silks to reach the embryo sac. Successful fertilization produces a kernel.

The kernel – or fruit – is known botanically as a caryopsis, which is the standard fruit type of the grass family. Because the fruit wall and seed are fused together so tightly, maize kernels are commonly referred to as seeds. The entire plant can be used to produce feed for animals, but it is the kernel that is generally consumed (in innumerable ways) by humans.

There is so much more to be said about maize. It’s a lot to take in. Rather than delve too much further at this point, let’s explore one of the other ways that maize is used by humans to create something that has become another feature of the fall season – the corn maze.

Entering the corn maze at The Farmstead in Meridian, Idaho

Exploring the corn maze at The Farmstead in Meridian, Idaho

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Developing Perennial Grain Crops from the Ground Up

This is the fourteenth in a series of posts reviewing the 17 articles found in the October 2014 Special Issue of American Journal of Botany, Speaking of Food: Connecting Basic and Applied Science.

Useful Insights from Evolutionary Biology for Developing Perennial Grain Crops by Lee R. DeHaan and David L. Van Tassel

The environmental impacts of modern agriculture are diverse and extensive. Our growing population needs to be fed; however, practices that have long-term negative effects on soil, water, and air quality are unsustainable. It is imperative that we find better alternatives. Developing perennial grain crops is one way that plant breeders are working to address this issue.

Moving from annual to perennial grain crops could potentially “increase water quality, reduce soil erosion, increase soil carbon, and improve habitat for wildlife.” It may also help “address the looming challenges of land degradation, food security, energy supply, and climate change.” Sounds like a major win if we can do it, right? And maybe we will, but first we must domesticate perennial grain varieties that perform on a similar level with annual ones. Most plant breeding today involves “improvement of previously domesticated species;” however, new perennial grain crops must be developed “de novo” (i.e. from wild species) in a matter of “decades rather than centuries to millennia.”

The roots of perennial grasses are considerably more extensive than annual grasses. (photo taken from an article about perennial grain crops at nationalgeographic.com)

The roots of perennial grasses are considerably more extensive than annual grasses, which helps reduce erosion and limits the need for fertilizer applications. (photo taken from an article about perennial grain crops at nationalgeographic.com)

Little has been published concerning “strategies for the wholesale remodeling of plants,” and so the authors reviewed findings in other fields, such as evolutionary biology and population genetics, in order to devise strategies for developing perennial grain crops. In this article, the authors summarize the published research they reviewed and describe how it relates to breeding perennial grains. It is a dense and lengthy article, so rather than offering a thorough review, I will briefly describe some of the main areas explored by the authors and then summarize their conclusions.

  • Trade-offs – This occurs when “resources allocated to one trait are unavailable for other traits.” Can perennial grain crops achieve yields comparable to annual varieties when faced with “trade-offs between seed and perennial organs?” Are such yields only attainable by “sacrificing longevity?” Strategies must be devised to “create herbaceous perennial crops with abundant seed production.”
  • Genetic Loads – This is simply defined as “the presence of deleterious alleles in a population.” In perennials, compared to annuals, “highly recessive deleterious alleles can arise at a rate faster than they can be efficiently eliminated.” Low seed set, among other things, may be a result of genetic load, so breeders of perennial grains must “account for and actively reduce genetic load.”
  • Bottlenecks – This refers to the loss of genetic diversity that occurs when population size is reduced. During a bottleneck, “previously rare deleterious recessive genes” can accumulate; however, some models indicate that “inbreeding and the associated bottlenecks may be useful in accelerating domestication.” If the population is isolated and introduced to a new environment simultaneously, “the newly exposed variation could now be adaptive.” Also, “if additional genetic diversity is required,” crosses can be made with wild populations.
  • Pleiotropy – This means that “a single gene [is] affecting multiple traits.” When domesticating wild species, “it would be useful to predict the prevalence of pleiotropy and whether to expect positive or negative pleiotropy to dominate.”
  • Epistatsis – This occurs when the effect of one gene is dependent on the presence of another gene or genes. This is particularly important if “large-effect genes” (pleiotropy) are dependent on a “particular genetic background to function optimally,” because “removing one critical element will severely impact the whole structure.” Perennial grain crops will have to undergo “many generations of plant breeding” in order to ensure that desired genes are found “within a genetic background where their benefits can be used without negative side effects.”
  • Cryptic Variation – Genetic variation is cryptic when “the inheritance of a particular mutated allele has no effect on phenotype and thus is hidden from natural and artificial selection.” New environments or mutations can release cryptic variation. “Ranking candidate species for their likely domesticability” may be an effective approach to cryptic variation. “The best candidates for domestication” originate from areas where conditions are highly favorable for growth and reproduction as opposed to areas that are “resource-limited,” because they have experienced periods of “selective enrichment” that make them suitable for agriculture settings.
  • Past Domestication – Domestication involves a series of “evolutionary changes that may decrease the fitness of a species in the wild but increase it under human management.” Historically this was “likely driven by unconscious selection pressures,” but currently it is “driven by conscious selection.” Studies of past domestication events reveal “somewhat predictable stages” in the process. Even though “current domestication efforts might not follow historical precedent,…the order in which traits are subjected to strong selection may be important.” Investigation into domestication also suggests that “dramatic changes” in plant morphology can be accomplished by selection for a “small number of major-effect genes,” so breeding programs are advised to “first search for useful major genes and evaluate their effects before moving on to strategies designed to accumulate genes of small effect.”
  • Selection – The authors describe “four major limits to selection.” 1.) Desired traits “may only exist in our imagination.” 2.) “The necessary genetic variation may not exist in the population,” and so waiting for or inducing mutations may be required. 3.) There may be “negative genetic correlations between characters being selected,” which will slow response to selection. This can be addressed by subdividing the population, evaluating the population in a new environment, or crossing with other populations. 4.) Conversely, “insufficient genetic correlation between traits may reduce the response to selection.” This makes “finding superior genotypes challenging,” so the authors suggest breeding plants in a “uniform environment,” and then later the plants can “accumulate genes for tolerance to specific stresses in separate populations.”

Intermediate wheatgrass (Thinopyrum intermedium) "produces much larger seeds in the greenhouse during the winter than ever seen in the field during the summer," an example of phenotypic plasticity. (photo credit: www.eol.org)

Intermediate wheatgrass (Thinopyrum intermedium) “produces much larger seeds in the greenhouse during the winter than ever seen in the field during the summer,” an example of phenotypic plasticity. (photo credit: www.eol.org)

The authors determined that the best candidates for perennial grain breeding programs are plant populations that have high diversity between and within individual plants, plastic phenotypes (i.e. adaptable to changes in the environment), and “an evolutionary history that includes adaptation to high resource environments.” They also suggest that breeders “focus more on the required functions [like nonshattering fruits] than on morphological traits” because it will increase the feasibility of evaluating “very large experimental populations.” The ideal experimental set-up would consist of very large populations of widely spaced plants that are subdivided in order to perform evaluations from various angles. Lastly, the authors encourage breeders to embrace new plant forms and breeding strategies and be open to the possibility that perennial grain crops may not “look like modern annual grains.”

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Your Food Is a Polyploid

This is the seventh in a series of posts reviewing the 17 articles found in the October 2014 Special Issue of American Journal of Botany, Speaking of Food: Connecting Basic and Applied Science.

Doubling Down on Genomes: Polyploidy and Crop Plants by Simon Renny-Byfield and Jonathan F. Wendel

This is another fascinating but dense article about genetics. The major theme, as the title suggests, is polyploidy and its role in crop domestication and future crop improvements – a sub-theme being that by studying polyploidy in crop plants, we can gain insights into polyploidy generally as it relates to non-crop plants. Polyploidy – or whole genome duplication – is “where an organism possesses more than a diploid complement of chromosomes.” Typically, chromosomes come in sets of two, one set from each parent. Organisms with this type of an arrangement are called diploids. Polyploids are organisms with more than two sets of chromosomes. In general terms, this can occur as a result of two species hybridizing (interspecific hybridization), which is called allopolyploidy, or it can occur as a result of spontaneous genome doubling in a single species, which is called autopolyploidy. This article deals mainly with allopolyploid as polyploidy in crop plants is largely a result of hybridization.

Much of what we know about polyploidy has been discovered relatively recently during what is referred to as the “genomics era.” Traditionally, identifying polyploids was done by examining the number of chromosomes in a cell. Today, technological advances such as next generation sequencing have brought new insights into polyploidy and allowed us to identify evidence of it in organisms that cannot be observed simply by counting chromosomes. Plants that are now considered diploids went through periods of whole genome duplication in the distant past; however, due to genome downsizing and other events, they present themselves as diploids. This historical polyploidy is called paleopolyploidy. Evidence now suggests that all seed plants and flowering plants (angiosperms) are “rightly considered to have a paleopolyploidy ancestry.”

As I did with past articles that were very genetics heavy, I will use the bullet point method to list some of the main things that I learned from the article rather than offering a full review. As with any article that I review, my goal is to present the information in a digestible manner for as wide of an audience as possible without misrepresenting or oversimplifying the science and the research. This seems to be one of the main struggles faced by all who write about science for a general audience – a topic to be explored another time, perhaps.

  • The recent discovery that the genomes of all seed plants and angiosperms have “experienced multiple rounds of whole genome duplication” is “one of the most significant realizations to emerge from the genomics era.” In the past decade, “the ubiquity and scope of whole genome duplication has truly come to light,” and we no longer need to ask, “Is this species a polyploid?,” but rather “how many rounds of whole genome duplication occurred in the ancestral lineage of this taxon, and when was the most recent polyploidy?”
  • Recently formed polyploids are not stable and experience a period of “genomic shock.” They must “overcome an initial fitness cost associated with genomic [deviations].” These “large-scale perturbations [events that alter the function of a biological system] have the potential to add novel genetic material to the genome, potentially useful in the context of domestication and selection.”
  • Plants that appear to be diploids are actually paleopolyploids that have undergone a process called diploidization “in which the genome of a polyploidy is pruned, often by poorly understood mechanisms, such that it returns to a diploid-like condition.” Over time, duplicated genes are removed, DNA is eliminated, chromosome numbers decrease, etc. The organism then presents itself as a diploid, however traces of its polyploidy past remain detectable.
  • It has long been understood that hybrids can exhibit what is known as hybrid vigor (or heterosis) wherein they express traits that are superior to their parents, such as faster growth and higher yields. This is the reason plant breeders make such crosses. Debate continues concerning the “precise causes of heterosis.” Current research is focused on the epigenetic variability that is “induced by hybridization and polyploidy.” Epigenetics, which concerns variation that is not a result of alterations to DNA, is an emerging field that can be advanced through the study of polyploidy. Additionally, “the utilization of epigenetic diversity within crop species will provide a novel avenue for crop improvement in the coming years.”
  • While polyploids have great potential to increase our understanding of genomics and greatly improve “targeted breeding efforts,” they are historically difficult to study mainly due to the large size of their genomes compared to diploids. “Larger genomes are more expensive to sequence and require greater computational finesse.” To date, “only a single example of a ‘complete’ polyploidy genome exists, that of autotetraploid potato.” The authors “anticipate that these methodological challenges will soon be overcome by advances in genome sequencing technologies,” and along with “other powerful approaches,” continued insights into polyploidy will be attained.

Upland cotton (Gossypium hirsutum) is the most widely cultivated species of cotton in the United States. It is an allopolyploid that produces fibers that are "considerably longer, stronger, and whiter than are possible to obtain from any diploid." (photo credit: www.eol.org)

Upland cotton (Gossypium hirsutum) is the most widely cultivated species of cotton in the United States. It is an allopolyploid, and it produces fibers that are “considerably longer, stronger, and whiter than are possible to obtain from any diploid.” (photo credit: www.eol.org)