Daucus carota (carrot)
Datasheet Types: Pest, Crop, Invasive species, Host plant
Abstract
This datasheet on Daucus carota covers Identity, Overview, Associated Diseases, Pests or Pathogens, Distribution, Dispersal, Hosts/Species Affected, Diagnosis, Biology & Ecology, Natural Enemies, Impacts, Uses, Prevention/Control, Management, Genetics and Breeding, Food Quality, Food Safety, Economics, Further Information.
Identity
- Preferred Scientific Name
- Daucus carota L.
- Preferred Common Name
- carrot
- Other Scientific Names
- Daucus gingidium L
- Daucus sativus Hoffm.
- International Common Names
- Englishbird's nestbishop's laceQueen Anne's lacewild carrot
- Spanishzanahoria
- Frenchcarotte
- Arabicgazar
- Portuguesecenoura-brava
- Local Common Names
- GermanyKarottenMohren
- Italycarota selvatica
- Japannoraninjin
- Netherlandswilde peen
- Swedenvild morot
- EPPO code
- DAUCA (Daucus carota)
Pictures

Flowering umbel
Daucus carota (wild carrot, Queen Anne's lace). flowering umbel. Kula, Maui, Hawaii, USA. April, 2009.
©Forest & Kim Starr-2009 - CC BY 3.0

Field crop
Daucus carota (carrot); field crop. Israel. February 2011.
©Oren Peles/via the PikiWiki/Israel free image collection project - CC BY 2.5

Flowering umbels
Daucus carota (wild carrot, Queen Anne's lace). flowering umbels. Kula, Maui, Hawaii, USA. April, 2009.
©Forest & Kim Starr-2009 - CC BY 3.0

Fruiting umbel
Daucus carota (wild carrot). fruiting umbel. Southern Heath Nature Park, Lower Saxony, Germany.
©Hajotthu/via wikipedia - CC BY-SA 3.0

Fruiting umbel
Daucus carota (wild carrot). dry, fruiting umbel. Southern Heath Nature Park, Lower Saxony, Germany.
©Hajotthu/via wikipedia - CC BY-SA 3.0

Field crop
Daucus carota (carrot); field crop. Haßloch (Pfalz), Germany. October 2004.
©Georg Slickers/via wikipedia - CC BY-SA 2.5

Field crop
Daucus carota (carrot); field crop. José Francisco da Silva, responsible for fertilization and planting, cleans organic carrots from the Mokiti Okada Association (MOA). Brasil. April 2005.
©José Cruz/Agência Brasil (ABr)/via wikipedia - CC BY 3.0 BR

Carrot diversity
Daucus carota (carrot); carrot diversity in both shape and colour.
Public Domain - Released by the United States Dept of Agrculture/Agricultural Research Service (USDA-ARS)

Harvested carrots
Daucus carota (carrot); harvested and washed carrots at a weekly market. Rhineland-Palatinate, Germany. September 2009.
©4028mdk09/via wikipedia - CC BY-SA 3.0

Seeds
Daucus carota (carrot); seeds. Scale 5mm grid.
©Sarefo/via wikipedia - CC BY-SA 4.0

Seedlings
Daucus carota (carrot); two-leaf seedlings. Stow, Masschusetts, USA. July 2008.
©Dwight Sipler, Stow, MA, USA/via wikipedia - CC BY 2.0

Field crop
Daucus carota (carrot); field crop. Companion planting of carrots and onions. Germany. August 2008.
©Manfred Sause/via wikipedia - CC BY-SA 3.0

Harvested carrots
Daucus carota (carrot); harvested carrots on a market stall. Tamil Nadu India. October 2011.
©Prof Thamizhpparithi Maari, Tamil Nadu, India/via wikipedia - CC BY-SA 3.0

Harvested carrots
Daucus carota (carrot); harvested and bunched carrots on a market stall. Granville Island Public Market, Vancouver, British Columbia, Canada. September 2013.
©Christof46 (CHK46)/via wikipedia - CC BY-SA 4.0

Selectively bred carrots
Daucus carota (carrot); selectively bred carrots with greatly varied pigmentation.
Public Domain - Released by the United States Dept of Agriculture/Agricultural Research Service (USDA-ARS)/original image by Stephen Ausmus

Harvested carrots
Daucus carota (carrot); harvested carrots, in sacks. Afghanistan. March 2003.
Public Domain - Released by the United States Agency for International Development (USAID)
Overview
Progressing from its initial use as a medicinal plant, carrot has become a major world vegetable and is one of the most widely grown and important vegetables in the family Apiaceae. The modern carrot probably evolved from the wild carrot Daucus carota subsp. carota. Carrot is a cool-season, biennial dicot, whose fleshy axis is the edible tissue consumed as food. Carrot plants form a rosette of leaves and a large fleshy storage taproot during the first year. The stem is very compressed like a plate during the first year of growth, with foliage height generally ranging between 25-60 cm. The leaves or tops are inedible. The primary reason for selling carrots with tops is to show freshness of product, since the leaves are discarded and not consumed. Bunched carrots are more expensive because extra effort is required to keep the tops looking fresh without wilting. Bunched carrots have been largely replaced by roots sold in plastic bags. As a carrot flowers, anthers mature and fall before pistils become receptive. This characteristic is called protandry, and is a strategy to increase cross-pollination by insects, primarily bees. Pollen must come from different plants or from later maturing umbels on the same plant for successful pollination. Therefore, carrot seeds are a mixture of self- and cross-pollination, which increases variability. There is more diversity of carrot root shapes and sizes then usually seen in commercial markets. Preferences for carrot root shape and colour vary regionally. Carrot cultivars are sometimes grouped into two broad classes: eastern or Asian and western or European. European cultivars are firm, sweet, highly flavoured, yellow-orange to strongly orange in colour, slow bolting, and adapted to cool temperatures. Asian cultivars tend to have a softer texture, are less sweet, less flavoured, adapted to warm temperatures, bolt easily, and may be red or red-orange coloured.
Principal sources: Welbaum (2015)
Summary of Invasiveness
Wild carrot, the progenitor of the cultivated carrot, is a biennial weed native to Europe, southwestern Asia and North Africa. Being a prolific seed producer, it can spread rapidly, and in its introduced range in North America and Australia it invades open grasslands, meadows, roadsides, abandoned fields, waste areas and degraded prairies, competing with and displacing native plants. Wild carrot can also negatively affect commercial carrot cultivation through genetic introgression in seed crops.
Taxonomic Tree
Notes on Taxonomy and Nomenclature
Daucus carota is a complex, very variable species comprising wild and cultivated carrots, resulting in a confused taxonomy. The complex is subdivided into 13 subspecies, 12 for wild taxa and one for the cultivated taxon (subsp. sativus (Hoffm.) Arc.). However, for cultivated carrot it is better to classify directly at cultivar level below the species level.
There are two main groups of cultivated carrot: the eastern (anthocyanin) and western (carotene) carrot. The eastern carrot has branched roots, is yellow, reddish-purple to purple-black, rarely yellowish-orange; leaves slightly dissected, greyish-green, pubescent; flowering in the first year. The western carrot has unbranched roots and is yellow, orange or red, occasionally white; leaves strongly dissected, bright green, sparsely hairy; normally biennial, but often annual in tropical regions. At present the western carrot is by far the most important, although the eastern carrot is still cultivated in some Asian countries. Three main groups of western (carotene) carrot cultivars arose by selection in the 19th and early 20th centuries in western Europe and the USA from the Dutch landraces 'Long Orange' and 'Horn'.
Cultivated carrots cross readily with the wild carrot taxon D. carota subsp. carota, which is very common in Europe and South-West Asia and has been introduced and naturalized elsewhere, notably to North America and Australia. In America it is known as 'Queen Anne’s Lace'. The modern carrot probably evolved from a wild plant resembling Queen Anne’s Lace. There are several other wild carrot taxa and Daucus species occurring in the Mediterranean area and South-West Asia, most of which are crossable with the cultivated carrot.
Plant Type
Annual
Biennial
Herbaceous
Seed propagated
Description
Annual or biennial erect herb, 20-50 cm tall at the mature vegetative stage and 120-150 cm tall when flowering. Taproot fleshy, straight, conical to cylindrical, 5-50 cm long and 2-5 cm in diameter at top, orange (most common), reddish-violet, yellow or white; the core (xylem) of mature roots is usually somewhat lighter in colour than the phloem, and the top of the root is often green. Leaves 8-12, growing in a rosette, glabrous, green, with long petiole often sheathed at its base; leaf-blade 2-3-pinnate, the segments divided into often linear ultimate lobes. Flowering stalks few to several, branched, each branch ending in a compound umbel (inflorescence); each umbel comprising 50 or more umbellets, each of which has up to ca. 50 flowers; involucral bracts more or less pinnatipartite; primary rays 2-25 cm, secondary rays 1-6 cm, pedicels 0.5-1.5 cm long; flowers mainly bisexual in primary umbels, in umbels of higher order an increasing number of male flowers may occur in addition to bisexual flowers; a few purple-red sterile flowers may be present in the central umbellets, especially in wild plants; flower small, 2 mm in diameter, epigynous, white, 5-merous but with 2 carpels and 2 styles. Fruit an oblong-ovoid schizocarp, 2-4 mm long, at maturity splitting into 2 mericarps, primary ridges ciliate, secondary ridges with hooked spines. Seed (inside the mericarp) with a long embryo embedded in endosperm. Seedling with long, thin taproot, cordate cotyledons and pinnate first true leaves.
Distribution
It is generally assumed that the purple (anthocyanin-containing) carrot originated in Afghanistan in the region where the Himalayan and Hindu Kush mountains are confluent, and that it was domesticated also in Afghanistan and adjacent regions of Russia, Iran, India, Pakistan and Anatolia. Purple carrot, together with a yellow variant, spread to the Mediterranean area and Western Europe in the 11-14th centuries, and to China, India and Japan in the 14-17th centuries. The orange (carotene-containing) carrot probably arose in Europe or in the western Mediterranean region through gradual selection within yellow carrot populations. The Dutch landraces Long Orange and the finer Horn types were the basis for the orange carrot cultivars grown at present all over the world. In Asia they have now largely replaced the purple and yellow types because of superior yield and changing fashion.
The wild carrot, D. carota subsp. carota, is very common in Europe and South-West Asia and has been introduced to North America, Australasia and elsewhere.
Distribution Map
Distribution Table
History of Introduction and Spread
Wild carrot, also known as bird’s nest, bishop’s lace and (in North America) Queen Anne’s lace, is native to temperate regions of Europe, southwestern Asia and North Africa, and is naturalized in North America, Japan, New Zealand and Australia (NatureWatch NZ, 2015). It was probably introduced to North America from Europe as a weed seed contaminant in imported grain by the earliest colonists in the early 17th century. Cultivated carrots could also have escaped from gardens to become naturalized. Wild carrot now occurs at different levels of weediness in most eastern and southern Canadian provinces and all 48 contiguous states of the USA (USDA-NRCS, 2015), with reports also from Alaska and Hawaii (NatureWatch NZ, 2015). In Australia wild carrot is thought to have originated in the carrot seed that was imported from the UK to the colony of Sydney between 1786 and 1798 for food production; it is now present in every state and is commonly found naturalized in coastal regions around heavily populated areas, particularly in the south east of the country and Tasmania (Weeds in Australia, 2015).
Risk of Introduction
Wild carrot already occurs in many temperate regions of the world. Although cultivated carrot is harvested before it produces seeds, escapes from cultivation do occur, allowing the establishment of wild populations.
Means of Movement and Dispersal
Natural Dispersal
Wild carrot seed can be dispersed by wind, but this is usually less than 3 m from the source plant (Umehara et al., 2005). However, the umbel curls up into a ball, hence one of its common names bird’s nest, which acts as a seed disperser when detached from the host plant (‘tumbleweed’ effect).
Vector Transmission
The commonest means of dispersal is by attachment to animal fur or human clothing. Manzano and Malo (2006) showed that wild carrot seeds adhering to wool could be transported 400 km by transhumant sheep flocks, with 7% remaining attached for up to 6 months.
Accidental Introduction
Seed of wild carrot can be transported attached to people’s clothing or via mud attached to the undersides of vehicles (Schmidt, 1989). It can also be transported as a seed contaminant of seed and grain shipments.
Pathway Causes
Pathway cause | Notes | Long distance | Local | References |
---|---|---|---|---|
Crop production (pathway cause) | Wild carrot seed introduced as seed or grain contaminant | Yes | Yes | |
Escape from confinement or garden escape (pathway cause) | Yes | |||
Seed trade (pathway cause) | Wild carrot occurs as seed or grain contaminant | Yes | Yes |
Pathway Vectors
Pathway vector | Notes | Long distance | Local | References |
---|---|---|---|---|
Clothing, footwear and possessions (pathway vector) | Yes | |||
Land vehicles (pathway vector) | Seed can adhere via mud to underside of vehicles | Yes | Yes | |
Livestock (pathway vector) | Can attach to sheep wool for up to 6 months | Yes | Yes | |
Plants or parts of plants (pathway vector) | Seed or grain contaminant | Yes | Yes | |
Wind (pathway vector) | Yes |
Plant Trade
Plant parts liable to carry the pest in trade/transport | Pest stages | Borne internally | Borne externally | Visibility of pest or symptoms |
---|---|---|---|---|
True seeds (inc. grain) | weeds/seeds | Yes |
Plant parts not known to carry the pest in trade/transport |
---|
Bark |
Bulbs/Tubers/Corms/Rhizomes |
Flowers/Inflorescences/Cones/Calyx |
Fruits (inc. pods) |
Growing medium accompanying plants |
Leaves |
Roots |
Seedlings/Micropropagated plants |
Stems (above ground)/Shoots/Trunks/Branches |
Wood |
Hosts/Species Affected
In Australia, wild carrot invades open ground and competes with native grasses and herbs for resources. The plant poses a threat to recovering grasslands, as it matures faster and grows larger than many native plants (Weeds in Australia, 2015). In the USA, where it is listed as a noxious weed in the states of Iowa, Michigan, Ohio and Washington (USDA-NRCS, 2015), it is one of many alien species to invade the prairies in the west of the country, displacing native plant species, such as Sidalcea nelsoniana (US Fish and Wildlife Service, 1998). Throughout its range, where it occurs in the vicinity of cultivated carrots, especially those being grown for seed production, it can cross pollinate, resulting in a genetically contaminated seed crop (Grzebelus et al., 2011).
Host Plants and Other Plants Affected
Host | Family | Host status | References |
---|---|---|---|
Citrus | Rutaceae | Unknown | |
Hordeum vulgare (barley) | Poaceae | Unknown | |
Medicago sativa (lucerne) | Fabaceae | Unknown | |
Solanum lycopersicum (tomato) | Solanaceae | Unknown | |
Triticum aestivum (wheat) | Poaceae | Unknown |
Similarities to Other Species/Conditions
Similar in appearance to Conium maculatum, the deadly poison hemlock, D. carota is distinguished by a mix of tri-pinnate leaves, fine hairs on its leaves and slender, solid, green stems, a root that smells like carrots, occasionally a single dark red flower in the centre of the umbel, shorter stature and summer rather than late spring flowering. Poison hemlock has purple-spotted, smooth, hollow and relatively stout stems and hairless leaves. Another wild carrot-like highly toxic plant is spotted waterhemlock (Cicuta maculata), and this has a cluster of enlarged roots that smell like parsnip, rather than a single taproot that smells of carrot. Wild parsnip (Pastinaca sativa) is not poisonous and can be distinguished from wild carrot by coarsely toothed rather than feathery leaves, and yellowish rather than white flowers (Penn State Extension, 2015).
The domesticated carrot (D. carota subsp. sativus) is easily differentiated from wild carrot (D. carota subsp. carota) by its highly pigmented, fleshy, edible, brittle, non-fibrous roots. In wild carrots, fresh roots are generally yellowish, flexible and fibrous, becoming tough and woody due to high xylem content. Also, the transition from shoot to storage organ is indistinct externally (abrupt in cultivated carrot), rosette foliage is often prostrate (usually conspicuously erect in domesticated forms), and umbels often have one or several purple central flowers (rarely in domesticated forms) (Encyclopedia of Life, 2015).
Habitat
Wild carrot can be found growing in rough grassland, along coastal cliffs and in dunes, as well as in overgrown thickets, weedy meadows, along railroads and roadsides, abandoned fields, degraded prairies and waste lands. In some situations, wild carrot can spread aggressively, its deep taproot making it difficult to extirpate by mowing or hand-pulling (Hilty, 2015).
Habitat List
Category | Sub category | Habitat | Presence | Status |
---|---|---|---|---|
Terrestrial | ||||
Terrestrial | Terrestrial – Managed | Cultivated / agricultural land | Secondary/tolerated habitat | Harmful (pest or invasive) |
Terrestrial | Terrestrial – Managed | Cultivated / agricultural land | Secondary/tolerated habitat | Natural |
Terrestrial | Terrestrial – Managed | Disturbed areas | Secondary/tolerated habitat | Natural |
Terrestrial | Terrestrial – Managed | Rail / roadsides | Secondary/tolerated habitat | Natural |
Terrestrial | Terrestrial ‑ Natural / Semi-natural | Natural grasslands | Principal habitat | Natural |
Terrestrial | Terrestrial ‑ Natural / Semi-natural | Scrub / shrublands | Secondary/tolerated habitat | Harmful (pest or invasive) |
Terrestrial | Terrestrial ‑ Natural / Semi-natural | Scrub / shrublands | Secondary/tolerated habitat | Natural |
Littoral | Coastal areas | Principal habitat | Natural | |
Littoral | Coastal dunes | Principal habitat | Natural |
Biology and Ecology
Cultivated Carrot
Growth and Development
Carrot seed will remain viable (70-80% germination) for 6-7 years when stored dry (moisture content 9%) at temperatures below 18°C. Germination is epigeal with first appearance of seedlings 9-12 days after sowing. The first four true leaves are formed at 4 to 5-day intervals, starting 3-4 weeks after sowing, but then the interval increases gradually to 15-18 days for subsequent leaves. A thin taproot grows down vertically to 20-25 cm, and 30-40 days after germination it starts swelling and gradually turning orange (in carotene carrots) from the hypocotyl stem downwards. About 80% of all carbohydrates produced in the plant are diverted to the root during this stage of development. The roots are mature 70-120 days after sowing according to the type of cultivar and growing conditions. The generative phase is induced by low temperatures. Carrot plants become sensitive to vernalization after the formation of at least eight leaves. The bolting-resistant cultivars of higher latitudes require 5- 12 weeks at 2-6°C to induce bolting. Local cultivars grown in the tropics show bolting when the night temperatures drop below approximately 16°C. The generative phase is accelerated by long days after devernalization (20°C). First a new rosette of leaves is formed, followed by elongation of the flowering stalk and first flowering 3 months later. Flowers are arranged in spirals and development is centripetal: the first mature flowers are on the outer edges of the outer umbellets. Flowering may last for one month, starting with the primary umbel. Initially the umbels are flat and concave. At anthesis the umbellets turn downwards progressively from the outside towards the centre, so that by the time the central flowers are mature, the umbels are more or less convex to conical. After pollination the umbellets turn upwards again. Carrot is predominantly outbreeding due to protandry. Insects such as bees and flies, attracted by abundant nectar, effect cross-pollination. The stigma becomes receptive 2-3 days after pollen dehiscence. Petals drop soon after fertilization and the seeds (mericarps) are mature 40-50 days later.
Ecology
In their adaptation to the northern latitudes of Europe, carrots became biennial and tolerant of long days (non-bolting) during the vegetative phase. They require subsequent vernalization at low temperatures to induce flowering. Carrots adapted to tropical and subtropical latitudes respond to long days by bolting even before the roots have properly thickened. Carrots are mostly cultivated as a cool season crop. High soil temperatures, in excess of 25°C, induce slow growth rates, fibrous roots and low carotene content. For economic yields, carrots should be grown in tropical regions at altitudes above 700 m. Early-maturing carrot cultivars may grow in the lowlands, but yields will be low and roots will have a poor colour. Optimum air temperatures are 16-24°C. Soils should be well-drained, fertile and of a sandy texture. Heavy clay soils may induce malformed and twisted roots and harvesting will be difficult. Optimum pH is 6.0-6.5. A regular supply of water is essential to obtain smooth and even roots. Flowering and seed set are successful only in climates with mean day temperatures below 20°C.
Carrot seed will remain viable (70-80% germination) for 6-7 years when stored dry (moisture content 9%) at temperatures below 18°C. Germination is epigeal with first appearance of seedlings 9-12 days after sowing. The first four true leaves are formed at 4 to 5-day intervals, starting 3-4 weeks after sowing, but then the interval increases gradually to 15-18 days for subsequent leaves. A thin taproot grows down vertically to 20-25 cm, and 30-40 days after germination it starts swelling and gradually turning orange (in carotene carrots) from the hypocotyl stem downwards. About 80% of all carbohydrates produced in the plant are diverted to the root during this stage of development. The roots are mature 70-120 days after sowing according to the type of cultivar and growing conditions. The generative phase is induced by low temperatures. Carrot plants become sensitive to vernalization after the formation of at least eight leaves. The bolting-resistant cultivars of higher latitudes require 5- 12 weeks at 2-6°C to induce bolting. Local cultivars grown in the tropics show bolting when the night temperatures drop below approximately 16°C. The generative phase is accelerated by long days after devernalization (20°C). First a new rosette of leaves is formed, followed by elongation of the flowering stalk and first flowering 3 months later. Flowers are arranged in spirals and development is centripetal: the first mature flowers are on the outer edges of the outer umbellets. Flowering may last for one month, starting with the primary umbel. Initially the umbels are flat and concave. At anthesis the umbellets turn downwards progressively from the outside towards the centre, so that by the time the central flowers are mature, the umbels are more or less convex to conical. After pollination the umbellets turn upwards again. Carrot is predominantly outbreeding due to protandry. Insects such as bees and flies, attracted by abundant nectar, effect cross-pollination. The stigma becomes receptive 2-3 days after pollen dehiscence. Petals drop soon after fertilization and the seeds (mericarps) are mature 40-50 days later.
Ecology
In their adaptation to the northern latitudes of Europe, carrots became biennial and tolerant of long days (non-bolting) during the vegetative phase. They require subsequent vernalization at low temperatures to induce flowering. Carrots adapted to tropical and subtropical latitudes respond to long days by bolting even before the roots have properly thickened. Carrots are mostly cultivated as a cool season crop. High soil temperatures, in excess of 25°C, induce slow growth rates, fibrous roots and low carotene content. For economic yields, carrots should be grown in tropical regions at altitudes above 700 m. Early-maturing carrot cultivars may grow in the lowlands, but yields will be low and roots will have a poor colour. Optimum air temperatures are 16-24°C. Soils should be well-drained, fertile and of a sandy texture. Heavy clay soils may induce malformed and twisted roots and harvesting will be difficult. Optimum pH is 6.0-6.5. A regular supply of water is essential to obtain smooth and even roots. Flowering and seed set are successful only in climates with mean day temperatures below 20°C.
Wild Carrot
Genetics
D. carota is an outcrossing diploid species with 2n = 18 chromosomes. Wild carrot is considered a source of genes for traits such as cytoplasmic male sterility required in domesticated carrot breeding. However, gene flow from wild carrot can be a problem for carrot seed producers; pollination with pollen from wild carrot can result in genetically impure seed lots. As pollen can be transported long distances by insects and pollen remains viable for 10 days, a minimum distance of at least 1 km is required between cultivated fields and wild carrot habitats, with at least 5 km being required in some cases (Grzebelus et al., 2011).
Reproductive Biology
Each flower in a wild carrot umbel has five irregularly shaped petals. The flowers on the outer edge of the umbel often have larger petals, perhaps to make the umbel more conspicuous to pollinators. Each flower has five tiny thread-like stamens and most also have two pistils. Although the flowers in each umbel have both male and female parts, the inner flowers are functionally male only. In the centre of many wild carrot umbels there is often a purple, sterile flower, the function of which is unknown (Stokes and Stokes, 1985). Like the cultivated form, wild carrot exhibits a protandrous dichogamous reproductive strategy, with anthers maturing before stigma development. Pollination is by insects. After flowering and going to seed at the end of the growing season, the whole plant dies, but the flower stems often remain, dispersing seeds through the winter.
Physiology and Phenology
As in cultivated carrot, seed germination in wild carrots is epigeal. After emergence, the plant grows to a height of around 60-120 cm. In the first year it typically grows just a basal rosette with a deep taproot. Although wild carrot is often referred to as a biennial (growing as a rosette of basal leaves in the first growing season, then growing upward, flowering and dying the next), in fact its life history depends on environmental conditions (e.g., what time of year the seed germinated, nutrient and light availability, competition etc.). Under good conditions, germination may occur in the spring and the plant may flower in late summer of the same year. Under poor conditions, the rosette may grow for several years before the plant flowers. When flowering occurs, the top-most flowers in the umbel generally mature and develop seeds first. New flower stems are produced from the basal rosette throughout the growing season, which makes wild carrot unusually resilient to mowing. Once the flowers are pollinated, the umbel closes in on itself and dries out as the seeds mature (Stokes and Stokes, 1985).
Longevity
Wild carrot, like the domesticated form, is a biennial, producing seed in its second year. Research on the persistence of the seedbank in Oregon prairie showed that 28% of seeds survived the first winter, with most going on to germinate in the following spring, but 40% of the surviving seed germinated in the second year. No seeds survived beyond the second year (Grzebelus et al., 2011).
Associations
In North America, the nectar and pollen of wild carrot flowers attract small bees, wasps, flies and beetles, including wild carrot wasps (Gasteruption spp.). The foliage, roots and other parts are food for other insects. Seeds are eaten by the ring-necked pheasant (Phasianus colchicus), ruffed grouse (Bonasa umbellus) and pine mouse (Microtus spp.). The aromatic and somewhat bitter foliage is browsed sparingly by mammalian herbivores (Hilty, 2015).
Environmental Requirements
Wild carrots require vernalization at low temperatures to induce flowering. Optimum air temperatures for growth are 16-24°C. Flowering and seed set are successful only in climates with mean day temperatures below 20°C. High soil temperatures (in excess of 25°C) induce slow growth rates. The preference is for full sunlight, mesic to dry conditions, and soil that contains either loam or clay-loam with a slightly acidic to alkaline pH. However, wild carrot will also adapt to partial sun, moist conditions, and other kinds of soil (Hilty, 2015).
Notes on Pests
Pests
The most noxious pest of carrot in temperate areas is carrot root fly (Psila rosae), whose larvae burrow in the roots, mainly in the lower two thirds of the root. Some degree of resistance has been found in the Nantes-type cultivar 'Sitan' and in the wild species D. capillifolius. The carrot weevil (Listronotus oregonensis) is also as significant problem in temperate areas, and creates feeding tunnels in the upper one third of the root. Field slugs (Deroceras reticulatum) and the turnip moth (Agrotis segetum) also attack carrot roots. The carrot aphid Semiaphis dauci, the willow-carrot aphid (Cavariella aegopodii) and the carrot sucker (Trioza apicalis) damage the leaves and vector virus diseases. Thrips (Frankliniella tritici and F. occidentalis), flea beetles (Systena blanda), and in tropical areas whiteflies (Bemisia and Trialeurodes spp.) also feed on foliage. The lygus bug (Lygushesperus and L. elisus) feeds on seed crops, reducing seed yield and quality. Affected plants may exhibit a virus-like foliage disorder or premature bolting. The leafhopper (Macrosteles quadrilineatus) is vector of aster yellows. In South-East Asia, the army worm Spodoptera exigua causes serious crop losses; larvae feed on leaves and roots (Welbaum, 2015).
Another pest of carrot roots is nematodes. Some nematodes that affect carrot include the lance nematode (Hoplolaimus uniformis), lesion nematode (Pratylenchus penetrans and Pratylenchus spp.), sting nematode (Belonolaimus longicaudatus), carrot cycst nematode (Heterodera carotae) – a principal European pest, and the root knot nematode (Meloidogyne hapla). Crop loss by root-knot nematodes may be kept under control by crop rotation, for example, with cereals, and by the application of organic manure (Welbaum, 2015),
Diseases
Bacterial leaf blight (Xanthomonas campestris pv. carotae) is a common disease in most growing areas. First symptoms are angular, yellow leaf spots which later become irregular, brown or black, water-soaked spots with yellow halos. The organism is seedborne and survives in crop debris. It is spread by water splash and is worst in wet conditions. Control is by clean seed, hot-water treatment of seed and crop rotation. Seed production without irrigation helps. Copper sprays can reduce disease severity (Koike et al., 2006).
Southern blight, caused by Athelia rolfsii, is most damaging in the tropics and subtropics and affects many crops including carrots, celery and parsley. It can cause water-soaked lesions if foliage is in contact with the soil, followed by wilting. Roots attacked directly develop a pale brown soft rot with a white mycelium which spreads to neighbouring plants. Soil fumigation and heat treatment can be effective controls (Koike et al., 2006).
Cavity spot, caused by Pythium spp., particularly P. violae, P. sulcatum and P. intermedium. For many years the causal organism was unknown because the cavities often have secondary colonists. This is an important disease in Europe, Australia, USA and other temperate regions. The pathogen enters roots early in crop life although symptoms are often not seen until maturity or develop in store. Cavity spot can be partially controlled by a lengthy rotation, fungicides or liming.
Alternaria leaf blight (Alternaria dauci) has a worldwide distribution. The brown spots are initially angular and can spread rapidly, especially in humid weather. The damage looks similar to that of bacterial leaf blight and Cercospora blight. Control is by avoidance of planting close to older crops likely to pass on disease, and through fungicide programmes based on weather conditions and experiences of the disease in the area. Some varieties have tolerance or resistance (Koike et al., 2006).
Viral diseases include Carrot mottle virus, an Umbravirus that can also be responsible for the symptoms of carrot motley dwarf disease. There are many other virus and viroid diseases of carrots which can become severe when early season aphids are not controlled (Koike et al., 2006; Welbaum, 2015). Carrot red leaf virus (CtRLV) is another important viral disease.
Other diseases of carrot are Phytophthora root rot (Phytophthora medicaginis) black rot (Alternaria radicina), violet root rot (Helicobasidium brebissonii), white rot (Sclerotinia sclerotiorum), crown and root rot (Thanatephorus cucumeris), grey mold (Botrytis cinerea), licorice rot (Mycocentrospora acerina). Some primarily affect the foliage including Cercospora leaf blight (Cercospora carotae), powdery mildew (Erysiphe heraclei and Leveillula spp.) and white rust (Aecidium foeniculi or Uromyces graminis). Bacterial disease include soft rot (Dickeya chrysanthemi, Pectobacterium carotovorum subsp. carotovorum), carrot bacteriosis (Xanthomonas campestris), hairy root (Rhizobium rhizogenes), milky disease (Paenibacillus popilliae) and scab (Streptomyces scabiei) (Koike et al., 2006; Welbaum, 2015).
Powdery mildew (Erysiphe betae), white rust (Albugo candida) and bacterial blight (Xanthomonas hortorum pv. carotae) are also diseases of carrot. The major problems in tropical carrot production are leaf blights/spots (A. dauci and C. carotae) and root-knot nematodes (M. hapla).
Local Indonesian cultivars (for example 'Cipanas') have strong foliage with a remarkable field tolerance to Alternaria leaf blight, which often completely destroys the foliage of cultivars introduced from Europe.
Fungi responsible for root diseases are the most serious: Phytophthora root rot (P. medicaginis), violet root rot (H. brebissonii) and white rot (S. sclerotiorum). Rotations with a minimal duration of 5 years, liming and draining of the soil, are the conditions necessary to maintain carrot crops in a state of good health. Root diseases are more severe in heavy soils with a poor structure. Various root rots occur before or during storage, often after mechanical damage or as secondary pathogens (Botrytis cinerea, Fusarium spp., S. sclerotiorum, P. violae and other species, Pectobacterium carotovorum subsp. carotovorum).
Each carrot-growing area has its own locally most important diseases, though in general soil-borne fungal pathogens are responsible for the greatest yield losses. Where decisions have to be made on whether a crop will be stored for later sale growers typically conduct numerous test digs towards the end of the season to determine levels of root disease or blemish (Koike et al., 2006).
Molecular techniques are starting to be used to determine whether certain genes have been activated which would indicate the likelihood of disease developing during crop storage (http://www.nsure.eu/webshop/en/47/carrot.html).
List of Pests
Non-Infectious Disorders
Carrots are susceptible to root splitting/cracking/breakage. Widely spaced carrots and large roots are more likely to exhibit early splitting and produce more secondary roots. Variations in growth rate and soil moisture availability are suspected causes. Shatter cracking is initiated by mechanical damage. High root turgidity appears to increase susceptibility.
Splitting, cracking and root breakage during harvest and subsequent handling are more common when soils are cold and susceptibility is highest in early morning. Early morning harvesting and careful handling during harvesting can decrease the damage.
Root forking is often due to early damage or obstruction of the taproot apical meristem, by stones or hard pans in the soil, which leads to distortion and multiple-rooting. Nematodes, fungi and insect-feeding can also cause deformed and forked roots.
Air pollution, e.g. high ozone, can cause bleached stippling to the upper leaf surfaces of carrot plants. Sulfur dioxide and ethylene can also cause plant injuries.
Principal sources: Rubatzky et al. (1999)
Notes on Natural Enemies
The best known natural enemy of wild carrot in eastern North America is the black swallowtail (Papilio polyxenes), the caterpillars of which feed on the leaves of a range of plants in the family Apiaceae. In temperate regions, pests attacking cultivated carrot crops often attack wild carrot. The most noxious pest of carrot in temperate areas is carrot root fly (Psila rosae), whose larvae burrow into the roots. Other insects feeding destructively on the plant’s parts include root-feeding larvae of Listronotus oregonensis and Ligyrus gibbosus, and foliage-eating larvae of the moth Melanchra picta (Wagner, 2005; Hilty, 2015). Wild carrot is a summer host for such aphids as Cavariella aegopodii, Dysaphis apiifolia, Hyadaphis foeniculi and H. passerinii (Blackman and Eastop, 2013). Another principal European pest is the root-damaging carrot cyst nematode (Heterodera carotae).
In North America, seeds are eaten by the ring-necked pheasant, ruffed grouse and pine mouse. The aromatic and somewhat bitter foliage is browsed sparingly by mammalian herbivores, such as deer and rabbits (Hilty, 2015).
The ability of wild carrots to act as reservoirs of disease for cultivated carrot crops is sparsely documented, even though fungi responsible for diseases in cultivated carrot are likely pathogenic on wild carrot. For example, wild carrots were identified as sources of Alternaria dauci infection in New Zealand carrot crops (Soteros, 1979), while Sherf and MacNab (1986) identified wild carrot as a reservoir of Carrot mottle virus.
The ability of wild carrots to act as reservoirs of disease for cultivated carrot crops is sparsely documented, even though fungi responsible for diseases in cultivated carrot are likely pathogenic on wild carrot. For example, wild carrots were identified as sources of Alternaria dauci infection in New Zealand carrot crops (Soteros, 1979), while Sherf and MacNab (1986) identified wild carrot as a reservoir of Carrot mottle virus.
Natural enemies
Natural enemy | Type | Life stages | Specificity | References | Biological control in | Biological control on |
---|---|---|---|---|---|---|
Alternaria dauci (leaf blight of carrot) | Pathogen | Leaves | to genus | Soteros (1979) | ||
Bonasa umbellus (ruffed grouse) | Herbivore | Seeds | not specific | |||
Carrot mottle virus (motley dwarf of carrot) | Pathogen | Leaves | not specific | |||
Cavariella aegopodii (carrot-willow aphid) | Herbivore | Stems Leaves | not specific | |||
Dysaphis apiifolia | Herbivore | Stems Leaves | not specific | |||
Heterodera carotae (carrot cyst nematode) | Parasite | Roots | not specific | |||
Hyadaphis foeniculi (honeysuckle, aphid (England)) | Herbivore | Stems Leaves | not specific | |||
Hyadaphis passerinii | Herbivore | Leaves Roots | not specific | |||
Ligyrus gibbosus | Herbivore | Roots | not specific | |||
Listronotus oregonensis (carrot weevil) | Herbivore | Roots | not specific | |||
Melanchra picta | Herbivore | Leaves | not specific | |||
Microtus | Herbivore | Seeds | not specific | |||
Papilio polyxenes (black swallowtail) | Herbivore | Leaves | not specific | |||
Phasianus colchicus (common pheasant) | Herbivore | Seeds | not specific | |||
Psila rosae (carrot root fly) | Herbivore | Roots | not specific |
Impact Summary
Category | Impact |
---|---|
Economic/livelihood | Negative |
Environment (generally) | Negative |
Human health | Positive |
Impact: Economic
Wild carrots appear to be an important source of Carrot mottle virus infection in cultivated carrot crops (Sherf and MacNab, 1986). They may harbour other pests and diseases that will attack commercial crops. Hybridization with the commercial plant can result in poor seed production.
Impact: Environmental
In its introduced range, wild carrot as an invasive weed can displace native plants. In Oregon in the USA, Nelson's checker-mallow (Sidalcea nelsoniana) was federally listed as threatened without critical habitat in 1993. A recovery plan was published in 1998 (US Fish and Wildlife Service, 1998) and updated in the 2010 Recovery Plan for the Prairie Species of Western Oregon and Southwest Washington (US Fish and Wildlife Service, 2010). It is a perennial herb in the family Malvaceae with tall, lavender to deep pink flowers, and occurs mainly in open areas with little or no shade (US Fish and Wildlife Service, 2015). It is threatened throughout its range by encroaching successional species, primarily resulting from suppression or elimination of natural disturbance regimes including periodic flooding and fires. Populations in Oregon’s Willamette Valley are extremely imperilled, as agricultural and urban development have modified and depleted habitats, fragmenting populations into mostly small, widely scattered patches. Extirpation is an ongoing threat to many Nelson’s checker-mallow occurrences on private lands, roadsides, undeveloped lots and otherwise vulnerable sites. In addition to land use threats, populations are particularly subject to competitive exclusion by exotic species (US Fish and Wildlife Service, 1998). Some 111 plant species are associated with Nelson’s checker-mallow, with about half of them being non-native. Most sites in the Willamette Valley have been densely colonized by invasive weeds, including wild carrot, but Nelson’s checker-mallow appears to be the listed prairie species most readily recoverable. Several recovery actions for habitat restoration have been implemented, including obtaining seeds and establishing plants, and evaluating the efficacy of habitat management techniques and ways to reduce the competition threat from non-native plants. Nelson’s checker-mallow plants have responded well to various management activities such as out-planting, transplanting, mowing and burning (US Fish and Wildlife Service, 2012).
Threatened Species
Threatened species | Where threatened | Mechanisms | References | Notes |
---|---|---|---|---|
Sidalcea nelsoniana | Oregon | Competition |
Risk and Impact Factors
Invasiveness
Proved invasive outside its native range
Has a broad native range
Abundant in its native range
Tolerates, or benefits from, cultivation, browsing pressure, mutilation, fire etc
Tolerant of shade
Has high reproductive potential
Has propagules that can remain viable for more than one year
Impact outcomes
Changed gene pool/ selective loss of genotypes
Ecosystem change/ habitat alteration
Negatively impacts agriculture
Negatively impacts livelihoods
Reduced native biodiversity
Threat to/ loss of endangered species
Threat to/ loss of native species
Likelihood of entry/control
Highly likely to be transported internationally accidentally
Difficult to identify/detect as a commodity contaminant
Uses
Carrots are one of the most popular vegetables worldwide. The swollen taproot of carrot is eaten and is an important market vegetable, even in tropical areas. The roots are consumed raw or cooked, alone or in combination with other vegetables (for example, peas), as an ingredient of soups, sauces, salads and in dietary compositions. Carrots are often canned, dehydrated, or quick frozen. Large quantities are also processed into infant food, juice or as an ingredient of soups, sauces and stews. A part of production is used as fodder. Young leaves are sometimes eaten raw or are also used as fodder (Elzebroek and Wind, 2008).
Uses List
Medicinal, pharmaceutical > Traditional/folklore
Human food and beverage > Vegetable
Animal feed, fodder, forage > Fodder/animal feed
Genetic importance > Gene source
Prevention and Control
Due to the variable regulations around (de)registration of pesticides, your national list of registered pesticides or relevant authority should be consulted to determine which products are legally allowed for use in your country when considering chemical control. Pesticides should always be used in a lawful manner, consistent with the product's label.
Eradication
Fire is not very effective in removing wild carrot plants from natural areas, although they tend to decline spontaneously in such areas when there is an absence of disturbance (Hilty, 2015).
Cultural Control and Sanitary Measures
Crop rotations can be used to reduce wild carrot infestations. In particular incorporating wheat into the rotation can reduce or even prevent wild carrot seed production as wheat harvest occurs when wild carrot is flowering.
Physical/Mechanical Control
Mowing wheat stubble to 10 cm in late August will cut off any wild carrot flowers, as will mowing in pastures and non-crop areas, where mowing as close to the ground as possible when 75% of plants have begun flowering is advocated.
Chemical Control
Control of wild carrot using herbicides requires application to over-wintered plants early in spring, to established plants in autumn, and/or to seedlings using pre- or post-emergence herbicides. Herbicides are most effective when applied at the seedling stage.
Ecosystem Restoration
In the Willamette Valley of Oregon, several recovery actions for prairie habitat restoration have been implemented, including obtaining seed of native species and establishing plants, habitat management and reducing the competition threat posed by non-native plants. Management activities have included out-planting, transplanting, mowing and burning (US Fish and Wildlife Service, 2012).
Agronomic Aspects
Propagation and PlantingSeed multiplication at high latitudes with cold winters is based on stored and vernalized mature or young roots (stecklings) replanted in the field in spring (the root-seed method). In areas with mild winters and early snow cover, seeds are sown in late summer and the plants are left to overwinter in the field. These will bolt in spring and the seed-seed cycle is completed in 12-13 months. Carrot cultivars adapted to tropical regions have low vernalization requirements and are propagated in highland regions above 1200 m. Highland carrot growers often maintain their cultivars by selecting the best mature roots and replanting them at one end of the field. Bolting and seed set soon follow. Seeds are sown, often mixed with sand, 1-2 cm deep in drills 10-15 cm apart in finely prepared soils previously cultivated to a depth of at least 30 cm. Seedlings are thinned to 5-8 cm in the rows. Seed requirements (200 plants/m²and 70% germination) for the dominant half-long carrot cultivars used in Asia, are 4-5 kg/ha. For bigger carrots, the density may be reduced to about 100 plants/m².HusbandryCrop rotation is essential to reduce soilborne diseases and pests. Mulching (rice straw) after sowing is recommended to encourage germination. Radish seedlings may be grown to protect carrot seedlings in the winter. Seedlings may be earthed-up when roots start swelling to keep them cool and prevent green tops. 15 to 20°C is optimal for seed development. In hot weather, light overhead shade is beneficial. Irrigation during dry spells is necessary to prevent irregular root development. Nutrient requirements of carrots are particularly high for K (200-300 kg/ha), low to medium for N (100-150 kg/ha), normal for P, Ca, Mg and other elements. Carrots are sensitive to high Cl concentrations and more susceptible to diseases at very high soil pH. Liming or the use of Ca-containing fertilizers is recommended when pH is below 5.5. Well-decomposed organic manures are beneficial when applied moderately (10-20 t/ha). Fresh organic matter, for example, from a leguminous crop, can be detrimental to the carrot crop.HarvestingCarrot is mostly harvested manually by pulling up the roots at the leaves. This requires strong and healthy foliage. Mechanical harvesting (in Europe, USA) is also based on pulling up by the foliage, or first topping the leaves and then lifting the carrots as in potato harvesting. In Asia carrots are usually ready for harvesting 70-85 days after sowing. Mature roots should be orange-coloured internally down to the blunt tip.In Europe and the USA, yields of 30-120 t/ha can be reached, depending on the type of cultivar and culture. In Asia yields vary from 8-20 t/ha; higher yields are possible above 800 m altitude. Marketable yield is much influenced by plant density and time of harvest. Root weight and uniformity are closely related to seed size and quality. Seed yields are 200-500 kg/ha.Carrots bunched with leaves will store up to 3 weeks in a cool place, but can remain in good condition for 100-150 days when topped (foliage removed) and stored at 1-4 C with 95-100% relative humidity. Carrots should be stored separately from other vegetables to prevent a bitter flavour induced by ethylene. Generally carrots store better when the dry matter content is high, when they are grown on soils with low organic matter content, when they are mature and harvested under moist conditions, and undamaged and free of diseases and pests. Carrots may be graded according to weight A <50 g), B (50-200 g), C (200-400 g) and D (>400 g).
Cultivation
Site preparation and planting
The crop should be produced on raised beds if waterlogging is likely to occur. The crop can be produced in beds or as a row crop. Weed control is an important issue and when possible the stale seedbed technique should be applied, although the seed normally germinates in approximately 10 days, assuming seed of acceptable vigour and germination has been used.
Care must be taken in the preparation of carrot seedbeds to produce a satisfactory tilth of final particle size ranging from rice grain to pea in sizes. If the final tilth is too fine it will pan and form a crust and if too coarse there will be seedling emergence problems; a poorly prepared seedbed can result in malformed roots.
Soil management
Carrots are most successful in a deep loam; root production in well-drained sandy soils can also be very successful provided there is sufficient available water throughout the crop’s life. Stony soils should be avoided as much as possible. Carrots do not tolerate acid conditions: the optimum pH is 6.0-7.0, but carrots are grown commercially between 5.5-7.5 pH, soils with a lower pH should have an application of a liming material during preparations. Recently manured land should not be used for carrot production as it tends to cause misshapen roots (often referred to as ‘fanging’) However, sites which received bulky organic manures for a previous crop, such as onions are suitable.
Mulching (rice straw) after sowing is recommended to encourage germination when sowing in cool soils. Radish seedlings may be grown to protect carrot seedlings in the winter. On soils subject to wind erosion barley is sometimes sown in rows between the carrot rows. It has to be killed by herbicide before it becomes competitive with the carrot crop. Alternatively, organic stabilising materials can be sprayed to protect the soil after sowing the crop. Seedlings may be earthed-up when roots start swelling to keep them cool and prevent green tops. 15°C to 20°C is optimal for seed development. In hot weather, light overhead shade is beneficial.
Irrigation
Uniform soil moisture is essential because water stress will slow growth and result in thickened, woody cells, reduced sugar content, and bitter flavour. Carrot crops require approximately 30–50 mm of water per week or from 450–600 mm for a cropping season depending on soil type and evapotranspiration. Water should be applied whenever about 40% of available moisture has been depleted from the root zone. Crops are often established with overhead irrigation before switching to furrow or drip irrigation after emergence. Overhead irrigation may be used the entire season. Excessive soil moisture can cause root splitting or cracking and may inhibit proper colour development.
Fertilizers and manures
The uptake of nutrients per hectare varies; depending on yield it can be 140-150 kg N, 20-35 kg P, 265-330 kg K, 60-130 kg Ca and 12-21 kg Mg. Carrots are sensitive to high Cl concentrations and more susceptible to diseases at very high soil pH. Liming or the use of Ca-containing fertilizers is recommended when pH is below 5.5. Where soils are low in boron, this nutrient should be applied in the seedbed to prevent brownheart. Boron deficiency is particularly problematic when soil pH values are high and/or the soil is light and sandy. Where soil analysis indicates a deficiency, apply boron to the seedbed (2 kg/ha B) or as a foliar spray according to manufacturers recommendations as soon as leaf cover allows (Litterick, et al. 2013). Well-decomposed organic manures are beneficial when applied moderately (10-20 t/ha). Fresh organic matter, for example from a leguminous crop, can be detrimental to the carrot crop.
In the seedling stage, high concentrations of nutrients in the soil may cause damage to the plants, so application of fertilizer is best done before ploughing. During ploughing, the fertilizer will then get mixed well through the upper layer of the soil. Application of manure immediately before planting must be avoided, because it may cause roughness and branching of the taproots. Application of fertilizer can be based on soil fertility and the removal of nutrients at harvest. Forty-five tonnes of harvested fresh carrot roots removes about 100 kg N, 15 kg P and 120 kg K from the soil.
Cropping systems
Crop rotations are an important management practice to limit disease, nematodes, insect pests, and weed infestations. Soil maintenance and improvement are other benefits of rotations. Generally root crops should not follow root crops as they are often hosts to carrot pests and diseases (e.g. sugar beet and potatoes); this makes design of crop rotations more difficult especially if cropping area is limited. There are exceptions were carrots have been grown repeatedly on the same soil for consecutive years, but such situations are dependent on soil fumigation practices which are expensive and not always desirable.
Harvesting
Carrots take approximately 3 months to mature in the tropics; the earlier, short-rooted cultivars take less time to reach maturity than the longer rooted cultivars. Subsistence farmers should use the crop from the ground as required, unless there is a niche market locally to justify a bulk harvest. The root crop does not store well except at lower temperatures and this is not normally economic in the tropics.
Many cultivars exist, which makes it possible to sow carrots in all seasons except the winter. When carrots can be harvested depends on cultivar, desired size and growing conditions. Full-grown carrots require up to 125 days to mature, baby carrots require 60-80 days. However, it is possible to harvest carrots any time when they have a usable size, maturing is not necessary. In Asia carrots are usually ready for harvesting 70-85 days after sowing.
Mechanical harvesting is routinely used for large scale commercial production. There are two main types of machine, top lifters and share lifters; each of which may be tractor drawn or self-propelled. In a top lifter the roots are undercut while belts simultaneously grasp the foliage, lifting the entire plant from the soil. Top lifters are used where the tops remain strong up till harvest, with the crop commonly sold fresh rather than going into store. Share lifters are used where the tops senesce, due to maturity, disease or cold. Where foliage remains dense prior to use of a share lifter it is topped first and the foliage removed, a share is then used to get the carrots out of the ground from underneath. Hand harvesting remains common in subsistence and very small scale commercial production.
Yield
Average world yield in 2013 (carrot and turnip) was 30 t/ha. In Europe and the USA, yields of 30-120 t/ha can be reached, depending on the type of cultivar and culture. In 2013, average yields in the USA reached 42 t/ha, and in Europe average yields were 33 t/ha. In California, where over half of the USA carrot production occurs, yields reached 41 t/ha in 2013. Within Europe, during 2013, yields in the UK reached 66 t/ha, yields in Poland 39 t/ha and in Italy 45 t/ha. In Asia average yields are reported as 30 t/ha for 2013. Yields in China, the biggest producer of carrot, reached 41 t/ha, whilst in Uzbekistan they peaked at 60 t/ha, in Japan average yields were 33 t/ha. The Russian Federation, another significant carrot producer, achieved yields of 24 t/ha during 2013. . Marketable yield is much influenced by plant density and time of harvest. Seed yields are 200-500 kg/ha.
‘Mechanical harvesting is routinely used for large scale commercial production. There are two main types of machine, top lifters and share lifters; each of which may be tractor drawn or self-propelled. In a top lifter the roots are undercut while belts simultaneously grasp the foliage, lifting the entire plant from the soil. Top lifters are used where the tops remain strong up till harvest, with the crop commonly sold fresh rather than going into store. Share lifters are used where the tops senesce, due to maturity, disease or cold. Where foliage remains dense prior to use of a share lifter it is topped first and the foliage removed. Hand harvesting remains common in subsistence and very small scale commercial production.
Postharvest Treatment
A part of the carrot production for the fresh market is bunched with leaves, washed to clean the roots and hydrocooled or iced to reduce temperature and respiration. Most carrots are topped, which means that the leaves and sometimesthe top of the ‘root’ are removed.
Storage
For fresh-market use, carrots are usually mechanically dug, washed, and stored at 0°C and 95% RH during shipment and marketing. At low temperatures (0°C), film-packaged carrots can maintain high quality for 6-7 weeks. Carrot quality deteriorates during long-term storage due to a loss of sugars to respiration. Root respiration rates are relatively low compared with other vegetables and decline further with refrigeration. Soluble sugars increase slightly during cold storage. However, bunched carrots store poorly and roots lose firmness rapidly because moisture is lost through the tops, significantly reducing shelf life to as little as 7 days. Bunched carrots are generally shipped packed in crushed ice to keep the tops looking fresh, which increases shipping costs. Postharvest storage of “minimally processed”, film-packaged, cut, and peeled small carrot sections is usually limited to approximately 20 days.
Carrots are stored for longer periods in areas where production is possible for only a few months per year. Carrot roots are generally not washed before placement into long-term storage at 0°C and high relative humidity. Controlled atmosphere storage (CA) increases long-term carrot storage. Controlled atmosphere storage of 1°C with 2–6% O2 and 3–4% CO2 reduces respiration rates and the loss of sugar in roots compared to conventional storage. However, deviations from these O2 and CO2 ranges may reduce carrot quality. Well-managed refrigerated storage is simpler to manage and may produce results similar to CA. In some areas with mild winters such as Britain and Ireland carrots are stored in the ground over winter, the soil being covered with straw for insulation.
Generally carrots store better when the dry matter content is high, when they are grown on soils with low organic matter content, when they are mature and harvested under moist conditions, and undamaged and free of diseases and pests.
Carrots are processed by freezing, drying and canning. They are increasingly processed into ready meals, batons, salads and other formats for sale through a chill chain, either raw or cooked.
Postharvest problems
During handling and distribution of fresh carrots from field to consumer, a less desirable taste can often develop. Bitterness and harshness are two usual sensory characteristics mentioned in connection with less desirable taste and flavour of carrots. Part of the reduction in taste quality could be due to exposure of carrots to ethylene during transport or storage. Ethylene induces the formation of isocoumarin, which leads to biterness. Therefore, carrots should not be stored with ethylene-producing commodities, such as apples and melons. Carotenoid content declines during long-term storage.
Falcarindiol may be the chemical causing bitterness. An expert on this subject is Dr Kirsten Brandt of the University of Newcastle.
Genetic Resources and Breeding
Genetic Resources
Carrot is an outcrossing diploid species with 2n = 18 chromosomes. It is speculated that mutation and selection were more responsible for the development of the cultivated carrot than hybridization with the wild germplasm. The genetic basis of modern orange carrot cultivars is rather narrow;they are all derived from a few 18th Century Dutch cultivars. Wild carrot is considered a source of genes for traits such as cytoplasmic male sterility required in domesticated carrot breeding. Exploitation of the genetic variation existing in wild Daucus germplasm in the Mediterranean and South-West Asian regions started comparatively recently. Small working collections of D. carota and related species are available in Europe (UK, France, the Netherlands), USA and Japan. However, gene flow from wild carrot can be a problem for carrot seed producers; pollination with pollen from wild carrot can result in genetically impure seed lots.
In 2016 the carrot genome was published, the results will will help facilitate biological discovery in carrot and other closely related crops (Iorizzo et al., 2016).
Breeding
Before 1960, breeding methods were based on mass selection in open-pollinated populations, but F1 hybrids with greater uniformity are now increasingly replacing the older cultivars, particularly in Europe, the USA and Japan. Seed production of F1 hybrid cultivars is based on cytoplasmic male sterility (cms) of one of the parent inbred lines. Two types of cms are used: the brown anther type, in which the anthers degenerate before anthesis, based on S-cytoplasm and at least two recessive genes with complementary action,; and the petaloid type, in which the anthers are replaced by five additional petals, based on S-cytoplasm and at least two dominant genes with complementary action. The development and maintenance of inbred lines are complicated by severe loss of plant vigour after a few generations of inbreeding. Main breeding objectives are improvements in total yield, growth rate and earliness, uniformity of root size and shape (cylindrical), dark orange external and internal colour (uniform in xylem and phloem), smooth periderm, resistance to cracking and breaking of the root during harvesting and post-harvest handling, flavour, texture, carotene content, strong foliage, non-bolting, resistance to diseases and pests. The most popular cultivars are somewhat conical, as these break less easily during harvesting.
Major Cultivars
There is more diversity of carrot root shapes and sizes than usually seen in commercial markets, and preferences vary regionally. Carrot cultivars are sometimes grouped into two broad classes: eastern or Asian and western or European., Eastern (anthocyanin) carrots have an annual habit. The root is branched, yellow, reddish-purple to purple-black, rarely yellowish-orange. Leaves are slightly dissected and are pubescent giving them a gray-green colour; they are adapted to warm temperatures and bolt easily; some tropical Asian cultivars can be induced to bolt at temperatures less than 15°C. The greatest diversity of these carrots is found in Afghanistan, Russia, Iran and India. Western (carotene) carrots have strong biennial characteristics but are often annual in tropical regions. The root is unbranched, yellow, orange or red, occasionally white. The leaves are strongly dissected, bright green and sparsely hairy. They are more tolerant of low temperatures that induce bolting. European cultivars are firm textured, sweet, highly flavoured, yellow-orange to strongly orange in colour. Most likely these carrots derived from the first group by selection among hybrid progenies of yellow Eastern carrots, white carrots and wild subspecies grown in the Mediterranean (http://www.carrotmuseum.co.uk/atoz.html).
At present, the western carrot is by far the most important, although the eastern carrot is still cultivated in some Asian countries. Therefore, the majority of world breeding efforts focus on this type because of their large market share and crop value. Cultivars are often grouped into types that reflect similar morphology or horticultural characteristics. Western cultivars are often classified into three categories based on root shape and length. Short-rooted cultivars, which mature quickly (50–60 days) for early season fresh-market production, include ‘Oxheart’, ‘Early Mokum’, ‘Parisian Market’, ‘Early Nantes’, and ‘Amsterdam Forcing’. Medium-rooted cultivars are used for main-season production for both fresh market and processing. Cultivars mature in 60–75 days from seeding, and include ‘Mokum’, ‘Flakkee’, ‘Autumn King’, ‘Danvers’, and ‘Royal Chantenay’. Long-rooted cultivars such as ‘Imperator’ are usually grown in thoroughly tilled deep loam or muck soils and mature 60–75 days from seeding. The tropical Asian cultivars also vary by root shape ‘Kuroda’ resemble the ‘Danvers’ or ‘Chatenay’ types, while ‘Brasilia’ and ‘Southern Nantes’ resemble ‘Nantes’.
Some of the major commercial carrot types or classes of carrot roots are described as follows:
•
‘Nantes’ is nearly cylindrical in shape, blunt, and rounded at both the top and tip. Its length is from 18 to 23 cm. The cultivar was developed in the late 1800s in the vicinity of Nantes, France. Shorter cultivars ‘Nantes Half Long’ and ‘Early Nantes’ followed. ‘Nantes’ cultivars are known for their sweet and pleasing carrot flavour. ‘Nantes’ cultivars have a high sugar content and tenderness and therefore have a greater tendency to split under certain climates and suffer mechanical damage. In Europe the ‘Nantes’ types predominate for fresh market sales.
•
‘Chantenay’ have broad shoulders and taper towards a blunt, rounded tip. ‘Chantenay’ carrots are shorter than other cultivars with average length of 15-20 cm, but have greater girth, sometimes growing up to 8 cm in diameter. They are most commonly processed into diced and other prepared foods. They grow better on heavy soils than many other cultivars.
•
‘Danvers’ was developed in the late 1800s in a town in Massachusetts, USA of the same name. Danvers carrots have a conical shape, having well-defined shoulders and tapering to a point at the tip similar to ‘Chantenay’ but not as broad. The average ‘Danvers’ root length is 15-20 cm and up to 5 cm in diameter. ‘Danvers’ cultivars are somewhat tolerant of heavy soil and are often processed as baby food or other canned and frozen products. Growth is largely restricted to the USA.
•
‘Imperator’ is a result of a cross between ‘Nantes’ and ‘Chantenay’ and was introduced in the 1920s. ‘Imperator’ roots are 25-30 cm, longer than other cultivars and taper to a point. They are very durable and withstand mechanical damage well, so they are popular for long-distance shipping . However, they have sometimes been criticised for lacking the flavour and eating quality of ‘Nantes’. ‘Imperator’ are most commonly sold whole in the USA or are sliced and peeled for sale as “Baby Cut” carrots, a lightly processed product that is sold fresh in bags as snack food and a cheaper alternative to true baby or small-rooted cultivars.
•
‘Oxheart’ or ‘Guerande’ is an introduction from France. This nearly round cultivar grows well on shallow heavier soils.
All cultivars can be used for fresh market, but some are better suited for processing. For processing, larger-rooted cultivars like ‘Danvers’ or ‘Chantenay’ are preferred. Different cultures prefer specific root colours and shapes, so additional types are also grown. In Japan, where carrots are seldom eaten raw, long reddish orange carrots, like ‘Kuroda’, or even red or purple cultivars with a thick cylindrical shape are preferred. In contrast, there is a preference for relatively short, slender, yellow-orange ‘Nantes’ and ‘Nantes’-like cultivars in Europe, while in North America the long, deep orange ‘Imperator’ and related cultivars predominate.
Researchers have developed new cultivars of carrots with novel traits through traditional breeding methods. Cultivar development involves initial crosses between root type classes, especially with in the western and eastern types. Crosses between carrots form these two climatic regions are also made, but less frequently. There is enough genetic diversity among these classes to easily allow ‘Danvers’ types to be derived from ‘Chantenay’ x ‘Imperator’, or ‘Nantes’, and even allow ‘Imperator’ types to be derived from ‘Chantenay’ x ‘Danvers’. Hence the effective germplasm pool for carrot root shape modification by breeding is very large. Furthermore, crosses of domesticated x wild carrot can be used to derive satisfactory domesticated types, although larger populations, more time and considerable backcrossing to domesticated stocks is required. Transgenic carrots produced through genetic engineering have not had an impact on world markets as of 2013. Novel yellow, white and red cultivars are gaining popularity in some markets because they add variety and variation to salads and other foods containing carrots.
There has been a gradual conversion to F1 carrot cultivars since the 1970s in the USA and Europe because of their greater uniformity and productivity. There is little variation among individual plants in a high quality carrot cultivar. Cytoplasmic male sterility (CMS) is used to ensure that inbred lines are cross-pollinated to produce seeds of hybrid cultivars. Open-pollinated cultivars remain popular for certain applications where the extra cost of F1 seeds is not worth the investment, such as for processing into cut products.
Principal sources: Welbaum (2015)
Propagation
Carrots are propagated from seed. Because of the seed shape and the presence of spines, seeds are often pelleted. Seed is mostly drilled with a precision seeder to a depth of 1-2 cm. Seed rate depends primarily on the size of roots required.and can range from1.0 to 4.5 kg (unpelleted) per hectare. Good seedbed preparations are essential because carrot seed germinates slowly and irregularly, and the seedling is rather weak. Seeds are sown, often mixed with sand, 1-2 cm deep in drills 10-15 cm apart in finely prepared soils previously cultivated to a depth of at least 30 cm. A light mulch of chopped straw or similar material should be applied after sowing to prevent soil capping and also assist the reduction of subsequent soil temperatures. Seed requirements (200 plants/m2 and 70% germination) for the dominant half-long carrot cultivars used in Asia, are 4-5 kg/ha. For bigger carrots, the density may be reduced to about 100 plants/m2. At germination the soil therefore has to crumble easily. Seedlings are thinned to 5-8 cm in the rows. The spacing in the row depends on the desired root size at time of harvest; the rows may be 15-40 cm apart. Too dense spacing must be avoided because that often results in deformed roots. The minimum temperature for germination is 4°C. The first appearance of seedlings is 10-15 days after sowing. In the juvenile stage the plant develops a leaf rosette and starts thickening the taproot; the hypocotyl is drawn into the soil by root contraction. Using coated or pelleted seed assists in obtaining an even seedling stand and should minimize the need for post emergence thinning. Erecting a lightweight shade structure over the crop can improve quality in high temperature environments.
Seed production in the temperate regions requires two growing seasons. Carrots have to be vernalized at low temperatures to induce flowering. However, during the winter the plants must be covered to prevent frost damage. Seed multiplication at high latitudes with cold winters is based on stored and vernalized mature or young roots (stecklings) replanted in the field in spring (the root-seed method). In areas with mild winters and early snow cover, seeds are sown in late summer and the plants are left to overwinter in the field. These will bolt in spring and the seed-seed cycle is completed in 12-13 months. Carrot cultivars adapted to tropical regions have low vernalization requirements and are propagated in highland regions above 1200 m. Highland carrot growers often maintain their cultivars by selecting the best mature roots and replanting them at one end of the field. Bolting and seed set soon follow.
As wild carrots are widely distributed in the temperate regions, they can become a real threat where cultivated carrot seed is produced. The wild plants hybridize easily with the cultivated plants, resulting in a crop with valueless seed.
Principal sources: Elzebroek and Wind (2008)
Nutritional Value
Carrot is one of the richest vegetables in fibres and carotenoids. It also contains vitamin E (0.52 mg /g), vitamin C (0.07 mg/g) and polyphenols such as p-coumaric, chlorogenic and caffeic acids. Fresh carrots contain approximately 90% water, 1% protein, 7% carbohydrates (mainly sugar) and 1% fibre, furthermore Ca, Fe and vitamin C; the orange roots contain b-carotene, which is a prolific source of provitamin A. Carrots are especially rich in carotenoids. a-Carotene and b-carotene are the principal carotenoids in carrots, while lutein is a minor component. There is recent evidence that polyacetylenes in carrots and related members of the Apiaceae have anti-cancer properties, (Saleh et.al., 2013, Xu Xin et al., 2014).
Phytosanitary Issues/Food Safety
Phytosanitary issues
Australia introduced emergency biosecurity measures in 2014 for Candidatus Liberibacter solanacearum, a disease affecting carrots in Europe causing leaf curling and yellowing, stunting and root abnormalities. The emergency quarantine measures include heat treatment or molecular testing of carrot seeds and screening in post-entry quarantine facilities. The carrot industry in Australia is worth $190 million a year and most Australian carrot crops are grown from imported seed.
Taiwan has quarantine controls in place in 2014 on the importation of fresh carrots from Australia where burrowing nematode (Radopholus similis) is known to occur. Controls are also in place for stem nematode (Ditylenchus dipsaci) and white fringed beetle (Naupactus leucoloma).
Food safety
Particularly an issue for carrots, which are subject to minimal processing for convenience of the consumer, is biological contamination. Contamination by Salmonella, Yersinia, Shigella and Norovirus may be caused by use of contaminated irrigation water and/or equipment, access by animals to vegetable growing areas and the proximity of farmyards (EFSA, 2014).
Carrots have been subjected to widespread monitoring and, in general, are only lightly contaminated with pesticide residues, nitrate and heavy metals. Cases of non-compliance with maximum levels have declined. Peeling has been shown to reduce levels of heavy metal contaminants (Norton et al., 2013) which tend to be concentrated within 2 mm of the root surface. Processing using blunt blades has been shown to enhance the penetration of E.coli into tissues and their subsequent survival when stored at 8°C (O'Beirne et al., 2014).
The 2011 European Union Report on Pesticide Residues in Food (EFSA 2014) found that the most frequent maximum residue levels exceedances (in %) for carrot were recorded for chlorpyrifos, fipronil and linuron.
Production and Trade
Total world production of carrots and turnips was 37.2 million metric tonnes for 2013. China was by far the largest producer with a production level of 1.69 million tonnes accounting for 45.4% of the world total. The area harvested was 0.48 million ha and the average yield was 39.2 t/ha. After China, the top producers in 2013 were: Uzbekistan (1.6 million t), Russian Federation (1.6 million t) and USA (1.3 million t). All other countries combined produce account for around 42% of total carrots worldwide, reflecting the widespread production of this crop (FAOSTAT).
In China, the main producing provenances are Shandong and Henan in north central China. Export of carrots is predominately fresh although frozen exports are on the increase. Carrots are one of China's leading fresh vegetable exports. In 2005 the export value was $107 million compared to just $16 million in 2000. The main markets are Japan, ASEAN countries and South Korea (Dede, 2008).
Trends in carrot consumption reflect changes in product availability and improved information about the nutritional benefits from eating carrot. For example, after remaining constant for many years, US carrot consumption increased dramatically to a peak in 1990. This increase was likely caused by scientific information showing that carrots are an excellent source of dietary fibre and carotenoids, two factors known to be important for human nutrition. The available of convenience-packaged carrot items such as lightly processed baby-peeled carrots and shredded carrots in salad mixes also helped to increase consumption during the period. Since 1990, total carrot consumption has declined, with frozen carrot consumption declining sharply (Welbaum, 2015). In 2013, fresh per capita consumption was reported as 3.4 kg/person (FPP, 2015).
For current information on crop production, see FAO Statistics.
Principal sources: Welbaum (2015)
Prospects
Carrot will continue to be an important vegetable worldwide, but adaptation to hot climates will remain limited. Resistance to important diseases and pests is becoming an increasingly important aspect of carrot breeding.
Links to Websites
Name | URL | Comment |
---|---|---|
GISD/IASPMR: Invasive Alien Species Pathway Management Resource and DAISIE European Invasive Alien Species Gateway | https://doi.org/10.5061/dryad.m93f6 | Data source for updated system data added to species habitat list. |
Global register of Introduced and Invasive species (GRIIS) | http://griis.org/ | Data source for updated system data added to species habitat list. |
Bibliography
Banga O, 1963. Main types of western carotene carrot and their origin. Zwolle, the Netherlands: Tjeenk Willink.
Banga O, de Bruyn JW, 1968. Effect of temperature on the balance between protein synthesis and carotenogenesis in the roots of carrots. Euphytica, 17:168-172.
Finch S, 1993. Integrated pest management of the cabbage root fly and the carrot fly. Crop Protection,12(6):423-430.
Baudoin WO, 1988. Vegetable production under arid and semi-arid conditions in tropical Africa. FAO Plant Production and Protection Paper, 89.
Heywood VH, 1983. Relationships and evolution in the Daucus carota complex. Israel Journal of Botany, 32:51-65.
Howard RJ, Garland JA, Seaman WL, 1994. Diseases and pests of vegetable crops in Canada: an illustrated compendium. Ottawa, Canada: Entomological Society of Canada & Canadian Phytopathological Society.
Namesny Vallespir A, 1996. Postharvest vegetable treatment. Volume 2 - Bulbs,tubers, rhizomes. Compendio de Horticultura, 2. Spain, S.L. Reus.
NIAB, 1999. Vegetable variety handbook. NIAB descriptive lists of vegetables 1999. UK, National Institute of Agricultural Botany.
Norman JC, 1992. Tropical vegetable crops. Ilfracombe, UK: Arthur H. Stockwell Ltd.
Peterson CE, Simon PW, 1986. Carrot breeding. In: Bassett MJ ed.: Breeding vegetable crops. Westport, Connecticut, USA: Avi Publishing Company, 321-356.
Quagliotti L,1967. Effects of different temperatures on stalk development, flowering habit and sex expression in the carrot. Euphytica, 16:83-103.
Shinohara S, 1984. Vegetable seed production technology of Japan. Volume 1. Tokyo, Japan: Shinohara's Authorized Agricultural Consulting Engineer Office.
Schoneveld JA, 1991. The cultivation of carrot [Dutch]. PAGV series No 36. Lelystad, the Netherlands: Proefstation voor de Akkerbouw en de Groenteteelt in de Vollegrond (PAGV).
Stein M, Nothnagel, T, 1995. Some remarks on carrot breeding (Daucus carota sativus Hoffm.). Plant Breeding, 114(1):1-11.
Swaider JM, Ware GW, McCollum JP, 1992. Illinois, USA: Producing vegetable crops.
Villeneuve F, Leteinturier J, 1992. La carotte. Tom 1. Guide Pratique. Paris, France: Centre Technique Interprofessionel des Fruits et Legumes.
Banga O, de Bruyn JW, 1968. Effect of temperature on the balance between protein synthesis and carotenogenesis in the roots of carrots. Euphytica, 17:168-172.
Finch S, 1993. Integrated pest management of the cabbage root fly and the carrot fly. Crop Protection,12(6):423-430.
Baudoin WO, 1988. Vegetable production under arid and semi-arid conditions in tropical Africa. FAO Plant Production and Protection Paper, 89.
Heywood VH, 1983. Relationships and evolution in the Daucus carota complex. Israel Journal of Botany, 32:51-65.
Howard RJ, Garland JA, Seaman WL, 1994. Diseases and pests of vegetable crops in Canada: an illustrated compendium. Ottawa, Canada: Entomological Society of Canada & Canadian Phytopathological Society.
Namesny Vallespir A, 1996. Postharvest vegetable treatment. Volume 2 - Bulbs,tubers, rhizomes. Compendio de Horticultura, 2. Spain, S.L. Reus.
NIAB, 1999. Vegetable variety handbook. NIAB descriptive lists of vegetables 1999. UK, National Institute of Agricultural Botany.
Norman JC, 1992. Tropical vegetable crops. Ilfracombe, UK: Arthur H. Stockwell Ltd.
Peterson CE, Simon PW, 1986. Carrot breeding. In: Bassett MJ ed.: Breeding vegetable crops. Westport, Connecticut, USA: Avi Publishing Company, 321-356.
Quagliotti L,1967. Effects of different temperatures on stalk development, flowering habit and sex expression in the carrot. Euphytica, 16:83-103.
Shinohara S, 1984. Vegetable seed production technology of Japan. Volume 1. Tokyo, Japan: Shinohara's Authorized Agricultural Consulting Engineer Office.
Schoneveld JA, 1991. The cultivation of carrot [Dutch]. PAGV series No 36. Lelystad, the Netherlands: Proefstation voor de Akkerbouw en de Groenteteelt in de Vollegrond (PAGV).
Stein M, Nothnagel, T, 1995. Some remarks on carrot breeding (Daucus carota sativus Hoffm.). Plant Breeding, 114(1):1-11.
Swaider JM, Ware GW, McCollum JP, 1992. Illinois, USA: Producing vegetable crops.
Villeneuve F, Leteinturier J, 1992. La carotte. Tom 1. Guide Pratique. Paris, France: Centre Technique Interprofessionel des Fruits et Legumes.
References
Blackman RL, Eastop VF, 2006. Aphids on the world's herbaceous plants and shrubs. Volume 1: host lists and keys. Volume 2: the aphids [ed. by Blackman, R. L.\Eastop, V. F.]. Chichester, UK: John Wiley & Sons, vii + 1415 pp.
Clark L, Mason JR, 1985. Use of nest material as insecticidal and anti-pathogenic agents by the European starling. Oecologia, 67(2):169-176.
Dede, M., 2008. Ministry of Agriculture, Nature and Food Quality of the Netherlands. 49 pp.
EFSA, 2014. 123937. http://www.efsa.europa.eu/en/efsajournal/doc/3937.pdf
Elzebroek, T., Wind, K., 2008. CABI. vii-xi + 516 pp.
Encyclopedia of Life, 2015. Daucus carota subsp. sativus. Domesticated carrot. http://eol.org/pages/1278046/overview
George, R. A. T., 2009. CABI. viii + 320 pp. http://www.cabi.org/cabebooks/ebook/20093330163
Grzebelus D, Baranski R, Spalik K, Allender C, Simon PW, 2011. Daucus. In: Wild crop relatives: genomic and breeding resources. Vegetables [ed. by Chittaranjan Kole]. Berlin, Germany: Springer-Verlag, 91-113.
Hilty J, 2015. Wild carrot: Daucus carota, carrot family (Apiaceae). Illinois wildflowers. http://www.illinoiswildflowers.info/weeds/plants/wild_carrot.htm
Iorizzo, M., Ellison, S., Senalik, D. et al., 2016. 48657-666.
Koike, S. T., Gladders, P., Paulus, A. O., 2006. Manson Publishing Ltd. 448 pp.
Litterick, A., Sinclair, A., Rahn, C., 2008. 10 pp.
Manzano P, Malo JE, 2006. Extreme long-distance seed dispersal via sheep. Frontiers in Ecology and the Environment, 4(5):244-248.
NatureWatch NZ, 2015. Queen Anne's lace (Daucus carota). http://naturewatch.org.nz/taxa/76610-Daucus-carota#cite_note-9
Norton, G., Deacon, C., Mestrot, A., Feldmann, J., Jenkins, P., Baskaran, C., Meharg, A. A., 2013. 476164-6172. http://pubs.acs.org/doi/abs/10.1021/es400720r
O'Beirne, D., Gleeson, E., Auty, M., Jordan, K., 2014. 4071-77. http://www.sciencedirect.com/science/journal/09567135
Penn State Extension, 2015. Wild carrot. University Park, PA, USA: Penn State College of Agricultural Sciences. http://extension.psu.edu/pests/weeds/weed-id/wild-carrot
Rubatzky, V. E., Quiros, C. F., Simon, P. W., 1999. CABI Publishing. ix + 294 pp.
Saleh, H., Garti, H., Carroll, M., Brandt, K., 2013. 72E183.
Schmidt W, 1989. Plant dispersal by motor cars. Vegetatio, 70:147-152.
Sherf AF, MacNab AA, 1986. Vegetable diseases and their control. Second edition. Chichester, UK: John Wiley & Sons, 736 pp.
Soteros JJ, 1979b. Pathogenicity and control of Alternaria radicina and A. dauci in carrots. New Zealand Journal of Agricultural Research, 22(1):191-196
Stokes D, Stokes L, 1985. A guide to enjoying wildflowers. Boston, USA: Little, Brown and Company.
Terry, L. A., 2011. CABI. x + 417 pp. http://www.cabi.org/cabebooks/ebook/20113328619
US Fish and Wildlife Service, 1998. Recovery plan for the threatened Nelson's checker-mallow (Sidalcea nelsoniana). Portland, Oregon, USA: US Fish and Wildlife Service, 61 pp. http://www.fws.gov/ecos/ajax/docs/recovery_plans/1998/980930e.pdf
US Fish and Wildlife Service, 2010. Recovery plan for the prairie species of western Oregon and southwest Washington. Portland, Oregon, USA: US Fish and Wildlife Service, 255 pp. https://www.fws.gov/pacific/ecoservices/documents/100629.pdf
US Fish and Wildlife Service, 2012. Nelson's checker-mallow (Sidalcea nelsoniana), 5-year review: summary and evaluation. Portland, Oregon, USA: US Fish and Wildlife Service, 44 pp. http://ecos.fws.gov/docs/five_year_review/doc4004.pdf
US Fish and Wildlife Service, 2015. Species fact sheet: Nelson's checker-mallow, Sidalcea nelsoniana. Portland, Oregon, USA: US Fish and Wildlife Service. http://www.fws.gov/oregonfwo/Species/Data/NelsonsCheckerMallow
USDA-ARS, 2015. Germplasm Resources Information Network (GRIN). Online Database. Beltsville, Maryland, USA: National Germplasm Resources Laboratory. https://npgsweb.ars-grin.gov/gringlobal/taxon/taxonomysearch.aspx
USDA-NRCS, 2015. The PLANTS Database. Baton Rouge, USA: National Plant Data Center. http://plants.usda.gov/
Umehara M, Eguchi I, Keneko D, Ono M, Kamada H, 2005. Evaluation of gene flow and its environmental effects in the field. Plant Biotechnology, 22(5):497-504.
Wagner DL, 2005. Caterpillars of eastern North America. Princeton, New Jersey, USA: Princeton University Press, 512 pp.
Weeds in Australia, 2015. Daucus carota. Canberra, Australia: Australian Government, Department of the Environment. http://www.environment.gov.au/biodiversity/invasive/weeds/index.html
Welbaum, G. E., 2015. CABI. ix + 476 pp.
Whitson TD, Burrill LC, Dewey SA, Cudney DW, Nelson BE, Lee RD, Parker R, 1991. Weeds of the West. Laramie, WY82071, USA; University of Wyoming College of Agriculture, 630 pp.
Xu Xin, Cheng YunJiu, Li ShiQi, Zhu Yi, Xu XiangLai, Zheng XiangYi, Mao Qiqi, Xie LiPing, 2014. 531615-1623. http://link.springer.com/article/10.1007%2Fs00394-014-0667-2
Hassannejad, S., Ghafarbi, S. P., 2013. Weed flora survey of Tabriz wheat (Triticum aestivum L.) fields.Journal of Biodiversity and Environmental Sciences (JBES), 3(9) 118-132. http://www.innspub.net/wp-content/uploads/2013/09/JBES-Vol3No9-p118-132.pdf
Hassannejad, S., Ghafarbi, S. P., 2014. Weed flora survey in alfalfa (Medicago sativa L.) fields of Shabestar (northwest of Iran).Archives of Agronomy and Soil Science, 60(7) 971-991.
Hassannejad, S., Ghafarbi, S. P., Abbasvand, E., Ghisvandi, B., 2014. Quantifying the effects of altitude and soil texture on weed species distribution in wheat fields of Tabriz, Iran.Journal of Biodiversity and Environmental Sciences (JBES), 5(1) 590-596. http://www.innspub.net/wp-content/uploads/2014/07/JBES-Vol5No1-p590-596.pdf
Celepcİ, E., Uygur, S., Kaydan, M. B., Uygur, F. N., 2017. Mealybug (Hemiptera: Pseudococcidae) species on weeds in Citrus (Rutaceae) plantations in Çukurova Plain, Turkey.Türkiye Entomoloji Bülteni, 7(1) 15-21. http://dergipark.gov.tr/download/article-file/315531
Milanova, S., Boneva, P., Grigorova, P., Valkova, M., 2007. Weed survey in central north Bulgaria. In: European Weed Research Society, 14th EWRS Symposium, Hamar, Norway, 17-21 June 2007 [European Weed Research Society, 14th EWRS Symposium, Hamar, Norway, 17-21 June 2007.], [ed. by Fløistad, E.]. Doorwerth, Netherlands: European Weed Research Society. 217. http://www.ewrs-symposium2007.com
Stobbs, L. W., Greig, N., Weaver, S., Shipp, L., Ferguson, G., 2009. The potential role of native weed species and bumble bees (Bombus impatiens) on the epidemiology of Pepino mosaic virus.Canadian Journal of Plant Pathology, 31(2) 254-261. http://www.tandfonline.com/doi/abs/10.1080/07060660909507599
Pala, F., 2020. Observation of weed species, frequency and density in common barley (Hordeum vulgare L.) fields of Diyarbakir, Turkey: a case study.Tarim Bilimleri Dergisi, 26(2) 164-172.
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