Ladino clover is a variety of white clover (McLeod, 1982); intermediate types of white clover are more tolerant of heat than are ladino-type white clovers (Miller, 1984c). There are Canadian varieties of white clover that tolerate soil pH as low as 4.5. (Miller, 1984c).
As a perennial legume, this species spreads by stolons (Slayback, pers. comm.).
Leaves, stems, and flower heads of Ladino clover generally are from two to four times as large as common white clover. In shape, color and markings, the leaves and flower heads look like common white clover (Miller et al., 1951).
White clover can develop a taproot 1 m deep, but it dies at the end of the first year, and secondary roots developing from the stolon become the main root system. The roots of white clover are mainly shallow (Miller, 1984c).
White clover grows best under cool, moist conditions (Carlson, et al., 1985) and is about as hardy as Red Clover or Alfalfa (McLeod, 1982). Hofstetter (1988) termed it extremely winter-hardy.
Miller et al. (1951) advised that in districts subject to severe frosts, clover-seed fields should enter winter with at least 6 to 8 inches of growth. Such growth protects the stand against excessive frost damage. With mild climates, the grazing can continue into winter without serious damage ensuing.
Heritability of frost tolerance in white clover is high (0.75-0.93), suggesting that incorporation of frost tolerance into agronomically-suitable, but frost-sensitive cultivars could be successful (Caradus, et al., 1990).
As heat tolerance is concerned, intermediate types of white clover are more resistant than ladino types (Miller, 1984c). Hot dry periods during the summer reduce growth of white clover, but plants will usually survive (McLeod, 1982)
Miller et al. (1951) wrote that seed production usually necessitates irrigation about every 7 to 10 days during summer. With frequent irrigations, to produce good seed on open soils may require from 2 to 3 times that needed on heavier type soils. On heavy clay soils the irrigation interval may range from ten to twenty-one days.
Miller et al. (1951) recommended the strip-check system of land preparation and irrigation. A modified version of the contour check system of irrigation, was also successful for irrigated pastures but was rarely used for Ladino seed production. Immediate and complete drainage following the irrigation is essential to avoid seed damage through germination and drowning of plants. Sprinklers may be used where land cannot be leveled. Clover-seed fields require frequent irrigation, so land preparation should be calculated to minimize labor costs.
Madson (1951) suggested that white clover should be irrigated when leaves begin to cup together. This may occur in sandy or hard spots at first. Field condition in general should be considered. Do not withhold irrigation until the entire field is wilting.
Irrigation should replenish the soil moisture to the depth of the white clover roots. Examine the soil to ascertain the depth of soil and the root zone. From 1 to 3 inches of water per irrigation will usually suffice. Larger applications will be wasteful and perhaps harmful. Ponding in hot weather can drown plants (Miller et al., 1951).
It is customary to withhold water for 4 to 10 days before a field is cut for seed. Miller et al. (1951), however, advised not intentionally drying up a field which has a good developing seed crop, because this would reduce seed yield, cause much seed to shrivel, and reduce germination. Whereas Ladino clover requires frequent irrigation, its annual requirement usually does not exceed that of alfalfa. In most of California, Ladino requires from 3 to 5 acre-feet of water per acre annually. In the interior valleys on open, permeable soils 6 to 9 acre-feet year may be needed.
If water is withheld before harvest, irrigate immediately afterward, to minimize drought damage. This can also increase fall pasturage. Irrigations should be given frequently in the fall until the seasonal rains begin (Miller et al., 1951).
White clover can grow on clays to silty loams if water is available all year (Gibson and Cope, 1985). Ladino clover does well on soils with a high water table or with poor drainage (Miller, 1984c), but it is not suited to dry, swampy, high-alkaline, or highly-saline sites (Gibson and Cope, 1985).
Mixtures of grasses and white clover are difficult to maintain because grasses may shade the clover and because the clover requires high soil moisture levels. If soil nitrogen is high, grasses will tend to predominate, whereas the clover will dominate if nitrogen is low (Miller, 1984c).
White clover responds well to addition of gypsum or flowers of sulfur as sulfur sources. It showed a 63% increase in dry matter production following application to a 2-year-old stand (Bowdler and Pigott, 1990).
Mixtures of grasses and white clover are difficult to maintain because grasses may shade the clover and because the clover requires high soil moisture levels. If soil nitrogen is high, grasses will tend to predominate, whereas the clover will dominate if nitrogen is low (Miller, 1984c).
Kanyama-Phiri et al., (1990) wrote that in strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, the clovers were most productive with 60 kg/ha of N added. Strawberry clover and ladino clover are similar in morphology and growth habit but differ in response to different nutrient and grazing regimes. In strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, with no added nitrogen, ladino clover peaked in dry matter production in October, then fell off during November. Strawberry clover peaked in November. By contrast, when nitrogen was added (60, 120, and 180 kg/ha of N added), these situations were reversed.
Some Canadian varieties of white clover can tolerate soil pH as low as 4.5 (Miller, 1984c), but acid soil should be limed to a pH of 6.0-6.5 before seeding white clover (Carlson et al., 1985).
White clover is not suited to dry, swampy, high-alkaline, or highly-saline sites (Gibson and Cope, 1985).
Ladino clover does well on soils with a high water table or with poor drainage (Miller, 1984c), but it is not suited to dry, swampy, high-alkaline, or highly-saline sites (Gibson and Cope, 1985). White clover can grow on clays to silty loams if water is available all year (Gibson and Cope, 1985).
When grown for seed production, heavier clay or loam soils are best. White clover does well on shallow soil underlain by a tight clay layer or a hardpan, even if this is 18 inches or slightly less of the surface. On deep, open, friable, fertile soils, seed production seldom is good because plants do not produce abundant seed heads. Luxuriant vegetative growth, sparse production of seed heads, and excessive water losses combine to reduce seed production (Miller et al., 1951).
Rogers et al. (1993) rated cultivars of white clover for salinity tolerance as follows: 'Haifa' and 'Irrigation' > 'Tamar' and 'Ladino'. With moderate salinity, highest yields occurred with cultivars that yield the most under non-saline conditions. Varieties that showed little decline with increased salinity yielded poorly in non-saline conditions.
In establishing clover simultaneously with grass, drill grass seed in rows 40 to 50 cm apart, then broadcast white clover seed and cover them using a cultipacker (Gibson and Cope, 1985).
If establishing white clover amid preexisting warm-season grass sod, the clover should be seeded (possibly along with a cool-season grass such as ryegrass) in the fall when the grass is dormant. Mow or graze the grass closely, broadcast the inoculated clover seed, and use a roller to press it into the soil. If establishing the white clover during the spring, grass competition should be reduced by mowing or grazing closely, or by damaging strips of the grass by ploughing or banding herbicide (Gibson and Cope, 1985).
The herbicides propyzamide and carbetamide can be useful in suppressing incumbent grasses during the establishment phase of slot-seeded white clover (Standell, 1990).
Spring seedings are preferable if fields are foul with winter weeds, although the chances of obtaining a satisfactory seed crop are fewer. In areas subject to severe winter frosts, planting should be completed early enough in the fall to insure seedling establishment before the first hard freeze (Miller et al., 1951).
In reestablishing stands in warm regions, white clover seed should always be inoculated before sowing. In cool regions, rhizobia from the preexisting white clover crop will survive in the soil (Duke, 1981).
Animal manures, unless known to be weed-seed free, should not be used on seed fields (Miller et al., 1951).
For seed formation, Ladino clover flowers must be cross-pollinated. 1 to 1.5 beehives per acre is sufficient for complete pollination. Bees should be moved in when blossoming starts, usually 2 to 3 weeks after the spring grazing or cutting is finished. In California, bees are usually moved in about May 10, and are retained through the blooming period, i.e., until late August or September (Miller et al., 1951).
The average production of Ladino clover seed in California is about 100 lbs/acre. Seed yields vary tremendously depending upon management and age of stand. Early fall-planted, well-managed stands may produce 100 to 300 lbs or more of seed per acre the first season. Some spring-planted stands do not produce any seed at all the first year. Second-year stands give peak seed production, and may yield 250 to 5000 lbs per acre. After the third year, seed yields usually decline rapidly, and there is seldom production after the fifth year. Weeds such as ryegrass cause declining seed yields from the third year on (Miller et al., 1951).
The species is low growing with prostrate stems (McLeod, 1982).
White clover grows rapidly, and is a long-lived, true clover, spreading by creeping stems called stolons. These elongate rapidly and root at the joints if soil is moist. Thus, sparse stands may thicken by the end of the first year (Miller et al., 1951).
As related by Turkington (1989), Trifolium repens can reproduce either vegetatively or by seed. In a permanent pasture, the species may display phenotypic plasticity allowing a clone to respond to local conditions (fine-grained environmental variability), and genotypic variability allowing different genets to respond differentially to coarse-grained environmental variability.
Miller et al. (1951) wrote that white clover plants have most roots in the upper 18 to 24 inches of soil. Therefore, Ladino clover does well on soils too shallow for deep-rooted crops like alfalfa, sugar beets, or tree crops. On deep, open soils, roots extend to four or five feet.
White clover taproot can extend to a depth of 1-3 ft (Brinton, 1989).
Kutschera (1960) reported that white clover generally roots to a depth of 61-76 cm.
As noted by Gibson and Cope (1985), white clover clones expand through the adventitious rooting of stolons; nonetheless, establishment is crucial. A good initial stand of white clover outperforms poor stands even after 3 years.
The herbicides propyzamide and carbetamide can be useful in suppressing incumbent grasses during the establishment phase of slot-seeded white clover (Standell, 1990).
Young or thin stands can thicken rapidly. When foliage is removed by grazing or clipping, recovery occurs in from 21 to 28 days (Miller et al., 1951).
White clover performs best under regimes of heavy grazing or mowing (Gibson and Cope, 1985). Heavy accumulation of vegetation is deleterious to white clover because light is reduced, soil moisture may be depleted, and the microclimate predisposes for disease and insect problems. Under such a regime, white clover is prone to have very succulent growth, and is unlikely to survive the microclimatic change that would result from sudden heavy mowing or grazing.
In managing mixed stands, grass height must be controlled to allow white clover to do well (Carlson et al., 1985).
In mixtures of white clover and bermuda grass or another warm- season grass, nitrogen should be applied in the late spring or summer, if the desire is to encourage the grass. If the desire is to encourage cool-season grasses, the nitrogen should be applied in the fall or early spring (Miller, 1984c).
Mixtures of grasses and white clover are difficult to maintain because grasses may shade the clover and because the clover requires high soil moisture levels. If soil nitrogen is high, grasses will tend to predominate, whereas the clover will dominate if nitrogen is low (Miller, 1984c).
In Austria, Danso et al. (1991) conducted a 2-year trial in a triple-species mixed sward of white clover (cv 'Zapican'), birdsfoot trefoil (Lotus corniculatus cv 'Gabriel') and fescue (Festuca arundinacea cv 'Tacuabe'). White clover showed good production for the first harvest of the first year; thereafter, birdsfoot trefoil dominated. In the first year, both legumes contribute about equally to the approximately 130 kg N/ha fixed in the sward. In the second year, white clover only contributed 5% of the 46 kg N/ha fixed in the last two harvests. Mixtures including the two legumes have an advantage because the early production by white clover is complemented by later production and better persistence by birdsfoot trefoil. Stands with multiple legumes often show better livestock weight gains.
Kanyama-Phiri et al. (1990) reported that in strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, close mowing alternating with 30-31 day regrowth periods apparently favored the two clovers and the perennial ryegrass.
Kanyama-Phiri et al. (1990) asserted that Strawberry clover and ladino clover are similar in morphology and growth habit but differ in response to different nutrient and grazing regimes. In strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, with no added nitrogen, ladino clover peaked in dry matter production in October, then fell off during November. Strawberry clover peaked in November. By contrast, when nitrogen was added (60, 120, and 180 kg/ha of N added), these situations were reversed.
As related by Turkington (1989), Trifolium repens can reproduce either vegetatively or by seed. In a permanent pasture, the species may display phenotypic plasticity allowing a clone to respond to local conditions (fine-grained environmental variability), and genotypic variability allowing different genes to respond differentially to coarse-grained environmental variability.
In managing mixed stands of white clover and grasses, grass height must be controlled to allow white clover to do well (Carlson et al., 1985). Frequent mowing will encourage the clover (Miller, 1984c), which revives quickly when cut for hay, because stems are not cut (McLeod, 1982). Four or five cuttings per year, at 35-40 day intervals, can be harvested in some areas (McLeod, 1982).
Miller et al. (1951) advised that first-year stands should not be grazed, except near the end of the season; otherwise, severe injury to the stand can result. By contrast, spring grazing or mowing until mid-May is typical, helps in weed control weeds and promotes more uniform flowering and seed production (Miller et al., 1951).
According to Miller (1984c), white clover is subject to root damage by the fungi Sclerotium rolfsii and Sclerotinia trifoliorum. Root and stolon damage is caused by the fungi Rhizoctonia, Fusarium, Leptodiscus, Curvularia, and Colletotrichum. In the Southeast, the root-knot nematodes, Meloidogyne spp., damage white clover roots. Host plant resistance, crop rotation, soil fertility, and proper cutting schedules can aid in control of these pests.
As noted by Kanyama-Phiri et al., (1990), in strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, close mowing alternating with 30-31 day regrowth periods apparently favors the two clovers and the perennial ryegrass. Strawberry clover and ladino clover are similar in morphology and growth habit but differ in response to different nutrient and grazing regimes. In strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, with no added nitrogen, ladino clover peaked in dry matter production in October, then fell off during November. Strawberry clover peaked in November. By contrast, when nitrogen was added (60, 120, and 180 kg/ha of N added), these situations were reversed.
Miller et al. (1951) recommended harvesting for seed when 90-95% of the visible heads are brown and the flower stems (seed stalks) have started to dry. In the Sacramento and San Joaquin Valleys, this would be in July and August. Withhold irrigation for 4 to 10 days prior to harvest. According to Duke (1981), seed should be harvested when most seed heads are light brown, about 25-30 days after peak blossoming. Mow and cure in swaths or in small windrows and retrieve using combines with pickup attachments. Each handling causes some shattering, so minimize the number of operation. Complete drying of seeds may require artificial means or spreading and turning the covered seed.
White clover revives quickly after mowing because stems are not cut. Four or five cuttings per year, at 35-40 day intervals, can be harvested in some areas (McLeod, 1982).
White clover is widely used as an irrigated pasture plant in California (Finch & Sharp, 1983) and is best adapted to rotational pasture management. As a cover crop, it is suitable in orchards where a perennial ground cover can be maintained (Miller, 1988) and in vineyards of the same description (Finch & Sharp, 1983).
Companion or nurse crops of barley or oat are not recommended for fall seedings, but may be used for spring-sown Ladino on tight soils which seal or cake. Nurse plants lead to better spring-sown stands by shading and reducing surface moisture loss. Therefore, white clover seedlings are better able to establish. Mow the nurse crop promptly once the clover has established, to reduce competition (Miller et al., 1951).
Gibson and Cope (1985) recommended that if establishing clover simultaneously with grass, one should drill grass seed in rows 40 to 50 cm apart, then broadcast white clover seed and cover them using a cultipacker. In establishing white clover amid preexisting warm-season grass sod, the clover should be seeded (possibly along with a cool-season grass such as ryegrass) in the fall when the grass is dormant. Mow or graze the grass closely, broadcast the inoculated clover seed, and use a roller to press it into the soil. If establishing the white clover during the spring, grass competition should be reduced by mowing or grazing closely, or by damaging strips of the grass by ploughing or banding herbicide.
The herbicides propyzamide and carbetamide can be useful in suppressing incumbent grasses during the establishment phase of slot-seeded white clover (Standell, 1990). By contrast, the herbicide 2,4-DB does not injure grass or white clover (Miller, 1984c).
In mixtures of white clover and bermuda grass or another warm-season grass, Gibson and Cope (1985) advised that nitrogen should be applied in the late spring or summer, if the desire is to encourage the grass. If the desire is to encourage cool-season grasses, the nitrogen should be applied in the fall or early spring.
Mixtures of grasses and white clover are difficult to maintain because grasses may shade the clover and because the clover requires high soil moisture levels. If soil nitrogen is high, grasses will tend to predominate, whereas the clover will dominate if nitrogen is low (Miller, 1984c). White clover is a poor competitor with grass for soil P (Mackay et al., 1990).
Woledge (1988) wrote that mixtures of perennial ryegrass (Lolium perenne L.) and white clover (Trifolium repens L.) yield less than heavily fertilized monocultures of the former. Addition of small amounts of nitrogen in the spring leads to reduction of the proportions of clover in the stand. The present study indicated that the relative growth rate of clover is as great as that of the grass when nitrogen is added, and greater when nitrogen is not added. There was no evidence that fertilized grass overtopped clover. Clover showed a smaller ratio of leaf area to total above-ground dry weight, but had a higher proportion of its lamina in the upper, well-lit strata.
In Austria, Danso et al. (1991) conducted a 2-year trial in a triple-species mixed sward of white clover (cv 'Zapican'), birdsfoot trefoil (Lotus corniculatus cv 'Gabriel') and fescue (Festuca arundinacea cv 'Tacuabe'). White clover showed good production for the first harvest of the first year; thereafter, birdsfoot trefoil dominated. In the first year, both legumes contributed about equally to the approximately 130 kg N/ha fixed in the sward. In the second year, white clover only contributed 5% of the 46 kg N/ha fixed in the last two harvests. Mixtures including the two legumes have an advantage because the early production by white clover is complemented by later production and better persistence by birdsfoot trefoil. Stands with multiple legumes often show better livestock weight gains.
Kanyama-Phiri et al. (1990) wrote that in strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, close mowing alternating with 30-31 day regrowth periods apparently favors the two clovers and the perennial ryegrass. The clovers were most productive with 60 kg/ha of N added. Strawberry clover and ladino clover are similar in morphology and growth habit but differ in response to different nutrient and grazing regimes. In strawberry clover - white clover - perennial ryegrass - orchardgrass mixtures, with no added nitrogen, ladino clover peaked in dry matter production in October, then fell off during November. Strawberry clover peaked in November. By contrast, when nitrogen was added (60, 120, and 180 kg/ha of N added), these situations were reversed.
Turkington (1989) reported that Trifolium repens in the same 1-ha old field will diverge genetically through time depending on the grass species with which it is associated. Reciprocal transplant experiments have demonstrated differential success of T. repens from areas dominated by the grasses Lolium perenne or Agrostis capillaris to areas dominated by the original grass or other perennial grasses. The results suggested that, even within a field, white clover clones are genetically adapted to perform better amid stands of particular grasses.
In replicated pot and field trials, Hartl, W. (1989) grew wheat with undersown white clover, black medic, Medicago lupulina L., Persian clover, Trifolium resupinatum L., and various associated weeds. In both pot and field trials, biomass of weeds alive at the time of harvest was reduced substantially (50% or more reduction). The field trials showed reduction of wheat yield, as well, for black medic and Persian clover, but a non-significantly-increased yield when white clover, Trifolium repens, was used.
Studies by McNeill and Wood (1990) in an environmental chamber with an atmosphere enriched by 15N indicated that white clover did not rapidly transfer nitrogen to associated ryegrass. The plants were mycorrhizal.
White and Scott (1991) in New York found that yield of cereal rye was less affected by living mulch of white clover, 'Ladino' clover, or red clover than of crown vetch, birdsfoot trefoil or alfalfa.
Dry matter yield of white clover should equal or exceed that of red clover (1,500 to 2,000 lb/acre) (Hofstetter, 1988). In mid-May, a first-year stand of a fall-sown mixed stand of strawberry and white clover yielded an above-ground dry biomass of 3.9+/-0.9 Mg/ha (Mean +/- S.E.M.) in an organic vineyard in Mendocino County, California. This figure is significantly less than that of the standing biomass for various winter-annual vetches, clovers, and medics sown in the same trial. With weeds including, the corresponding figure is 6.8+/-1.2 Mg/ha (Bugg et al., 1996).
White clover responds well to addition of gypsum or flowers of sulfur as sulfur sources. It showed a 63% increase in dry matter production following application to a 2-year-old stand (Bowdler and Pigott, 1990).
In Austria, Danso et al. (1991) conducted a 2-year trial in a triple-species mixed sward of white clover (cv 'Zapican'), birdsfoot trefoil (Lotus corniculatus cv 'Gabriel') and fescue (Festuca arundinacea cv 'Tacuabe'). White clover showed good production for the first harvest of the first year; thereafter, birdsfoot trefoil dominated. In the first year, both legumes contributed about equally to the approximately 130 kg N/ha fixed in the sward. In the second year, white clover only contributed 5% of the 46 kg N/ha fixed in the last two harvests. Mixtures including the two legumes have an advantage because the early production by white clover is complemented by later production and better persistence by birdsfoot trefoil. Stands with multiple legumes often show better livestock weight gains.
First-year white clover mean nitrogen content is 81 lb/a, according to Brinton (1989). Nitrogen content of white clover averages 3.8%. A good stand should provide 100 lb of N per acre when plowed at bud stage (Hofstetter, 1988).
Haley and Hogue (1990) assessed influence of type of ground cover on apple aphid, Aphis pomi DeGeer (Homoptera: Aphididae), and its predators in a young apple orchard. Four ground cover regimes were compared: (1) fall cereal rye (Secale cereale), herbicided in spring and summer; (2) a mixture of white clover (Trifolium repens) and grass; (3) herbicided tree-row strips and grassed-in alleys; and (4) woven black-plastic strips in the tree row and grassed alleys. The trial was initiated at the beginning of the second year of the orchard. Few aphidophagous insects of interest (e.g., the predatory mirids Deraeocoris brevis and Campylomma verbasci, the predatory midge Aphidoletes aphidimyza, lady beetles, hover flies, or lacewings), were found in the ground covers. In the first year of the study, leaf nitrogen and aphid and predator densities were lower on trees with the white clover-grass mixture. These differences did not occur the second year. Terminal growth was particularly depressed for apple trees with understories of white clover and grass.
McNeill and Wood (1990) conducting studies in an environmental chamber with an atmosphere enriched by 15N indicated that white clover did not rapidly transfer nitrogen to associated ryegrass. The plants were mycorrhizal.
Mackay et al. (1990) evaluated 119 cultivars and lines of white clover for response to P addition. Based on principal components analysis, these were assigned to 8 groups. 26 of the varieties were selected to represent the 8 groups. The varieties that absorbed the most P also accumulated the most N.
In a field study in Uruguay, Mallarino and Wedin (1990) found that N-fixation was more markedly depressed through the application of nitrogen fertilizer (100kg/ha) for birdsfoot trefoil than for white clover or red clover.
In combination with tall fescue (Festuca arundinacea), year diculture stands with birdsfoot trefoil, white clover, and red clover led to respective annual total N fixation of 70-223, 42-200, and 49-277 kg N/ha. White clover-tall fescue mixes did not require legume domination in order to maximize total N fixation. Red clover gave the greatest N fixation among the legumes tested (Mallarino et al., 1990).
In Sweden, Marstorp and Kirchmann (1991) reported the following values for stems and leaves of several legumes harvested from the field 100 days after emergence. and later used as green manure:
% Of Dry Matter Species Carbon Nitrogen Lignin C C/N Red Clover 45.9 2.61 9.08 17.6 White Clover 39.5 3.10 10.26 12.7 Black Medic 42.9 3.12 10.88 13.8 Persian Clover 46.1 3.20 11.38 20.9 Berseem Clover 45.3 2.52 12.47 18.0 Subterranean Clover 42.6 3.02 9.69 14.1
In Wales, Mytton et al. (1993) evaluated the differential effects on soil structure and water infiltration of monocultural swards of white clover and perennial ryegrass and a mixture of the two. The replicated study employed undisturbed soil cores (100 mm i.d. x 180 mm length; silt loam acid brown earth) extracted from the field and arranged in a greenhouse. White clover stands led to greater water infiltration, 43.1g/4h, vs. 32.9 for annual ryegrass, vs. 39.4 for mix. Apparent greater soil friability in the clover cores was not reflected in soil bulk density of % soil aggregates >2mm upon wet sieving. Total porosity was little changed, but air-filled (macroporosity) was as follows: clover > mix > perennial ryegrass.
White clover is very palatable to livestock. In mixture with grasses and other legumes, it provides highly productive, nutritive pasture and is the basic legume in California's irrigated pasture (Miller et al., 1951).
Miller et al. (1951) wrote that cut Ladino clover dries slowly; it is usually ensiled rather than cured for hay. 70 to 80 lbs of cane molasses can be added per ton of green clippings going into the silo; this improves silage quality and feeding value.
Avoid insecticides other than sulfur if bees are working seed-producing stands of white clover (Miller et al., 1951). Duke (1981) wrote that many arthropods attack white clover, including grasshoppers, clover leaf weevil (Hypera punctata), potato leafhopper (Empoasca fabae), meadow spittlebug (Philaenis spumarius), garden fleahopper (Halticus bractatus), spider mites, clover root curculio (Sitona hispidula), green june beetle (Cotinus nitida), lesser clover leaf weevil (Hypera nigrirostris), clover head weevil (Hypera meles), clover seed weevil (Microtrogus picirostris). white clover flower midge (Dasineura gentneri), lygus bugs, clover aphid (Nearctaphis bakeri), green cloverworm (Plathypena scabra), cutworms, lesser cornstalk borer (Elasmopalpus lignocellus), alfalfa weevil (Hypera postica), blister beetles (Epicauta spp.), and the fall armyworm (Spodoptera frugiperda).
Potato leafhopper (Empoasca fabae) is the most important insect pest of white clover. Other pests include meadow spittlebug, clover leaf weevil, alfalfa weevil, lygus bugs, clover seed weevil, and clover seed midge. Crop resistance, weed control, and crop rotation may be important in controlling some insect pests (Miller, 1984c).
Miller et al. (1951) wrote that four species of spider mite (called red spiders) can cause damage, beginning in early May. These include Atlantic mite, brown almond mite, Pacific mite, and the two-spotted mite. These mites are usually found on the undersides of the leaves, and infested leaves become cupped, yellowish and spotted. Heavily infested fields may appear dried-out and reddish-brown. Lygus bugs may build up rapidly in seed fields in late May, June, and July. These damage the flower parts and developing seed. Various grasshopper species may move into Ladino fields in great numbers. Infestations may originate in high, dry checks and borders, and fence rows within fields. Adjacent dry fields may be breeding grounds. Yellow-striped armyworm may damage seed fields,and in some cases may strip a field in 3 or 4 days.
Flexner et al. (1990) related their studies in southern Oregonian pear orchards. Certain understory weeds can harbor high densities of twospotted spider mite, Tetranychus urticae Koch (Acari: Tetranychidae). This mite is mainly a secondary pest and a creature of pesticide-disrupted or stressed agroecosystems. Among the plant species suitable for use as cover crops, white clover appeared particularly prone to outbreaks of the mite. Use of herbicides led to increased movement by mites into trees.
Haley and Hogue (1990) assessed the influence of type of ground cover on apple aphid, Aphis pomi DeGeer (Homoptera: Aphididae), and its predators in a young apple orchard. Four ground cover regimes were compared: (1) fall cereal rye (Secale cereale), herbicided in spring and summer; (2) a mixture of white clover (Trifolium repens) and grass; (3) herbicided tree-row strips and grassed-in alleys; and (4) woven black-plastic strips in the tree row and grassed alleys. The trial was initiated at the beginning of the second year of the orchard. Few aphidophagous insects of interest (e.g., the predatory mirids Deraeocoris brevis and Campylomma verbasci, the predatory midge Aphidoletes aphidimyza, lady beetles, hover flies, or lacewings) were found in the ground covers. In the first year of the study, leaf nitrogen and aphid and predator densities were lower on trees with the white clover-grass mixture. These differences did not occur the second year. Terminal growth was particularly depressed for apple trees with understories of white clover and grass.
White clover is used as a nectar source by Scolia sp. (Scoliidae) and Prionyx sp. (Sphecidae) wasps in pecan orchards of southern Georgia (Bugg, pers. comm.).
Grafton-Cardwell et al. (unpublished manuscript) found that pollen of bell bean, 'Austrian Winter' field pea, and New Zealand white clover sustained longevity and fecundity of the predatory mite Euseius tularensis (Acari: Phytoseiidae) as well as the standard diet of iceplant pollen. By contrast, reduced fecundity was observed for common vetch, woollypod vetch, and crimson clover, and E. tularensis did not survive more than one generation when fed pollen of rose clover or red clover. Inoculation with E. tularensis in early spring led to build-up of the mite by late spring in a cover crop of bell bean, field pea, and woollypod vetch. Most of the mites were found on the bell bean component of the mix. When the cover crop was mowed and the mowings placed in young citrus trees, significantly increased densities of the predatory mite were observed on the citrus foliage.
In England, the nematode Tylenchorynchus dubius is known to damage white clover (Clements and Boag, 1990).
In the Southeast, the root-knot nematodes, Meloidogyne spp. damage white clover roots. Host plant resistance, crop rotation, soil fertility, and proper cutting schedules can aid in control of these pests (Miller, 1984c).
White clover can be attacked by several foliar and root diseases, as well as clover mosaic virus. The latter cause more problems where white clover persists as a perennial and regenerates vegetatively than were it reseeds as an annual (Gibson and Cope, 1985).
Heavy accumulation of vegetation is deleterious to white clover because light is reduced, soil moisture may be depleted, and the microclimate predisposes for disease and insect problems. Under such a regime, white clover is prone to have very succulent growth and is unlikely to survive the microclimatic change that would result from sudden heavy mowing or grazing (Gibson and Cope, 1985).
As of 1951, no serious diseases of economic importance had affected the Ladino crop in California (Miller et al., 1951).
Interspecific hybrids between Trifolium repens and T. ambiguum show resistance to peanut stunt mosaic, clover yellow vein virus, and alfalfa mosaic virus. These resistances could prove valuable if they can be incorporated into adapted white clover varieties (Pederson and McLaughlin, 1989).
For seed production, grazing or mowing by May 15 can reduce weeds. Grazed fields should be mowed thereafter to control weeds and equalize the stand (Miller et al., 1951).
Hartl, W. (1989) reported replicated pot and field trials in which wheat was grown with undersown white clover, black medic, Medicago lupulina L., Persian clover, Trifolium resupinatum L., and various associated weeds. In both pot and field trials, biomass of weeds alive at the time of harvest was reduced substantially (50% or more reduction). The field trials showed reduction of wheat yield, as well, for black medic and Persian clover, but a non-significantly-increased yield when white clover, Trifolium repens, was used.
Bugg et al. (1996) conducted a replicated study of various cover crops (r=4) at Blue Heron Vineyard (Fetzer Vineyards), Hopland, Mendocino County, California. Weed above-ground biomass data (dry) were taken in a replicated Cover crops were seeded in late October, 1990; harvest was on May 15-16, 1991. Dominant winter annual weeds were chickweed, shepherds purse, rattail fescue, and annual ryegrass. In plots sown to a mixture of white and strawberry clovers, weed biomass was 2.8+/-0.7 Mg/ha (Mean +/- S.E.M.). This was 57.5% of the value obtained in weedy control plots. Vegetational cover afforded by the clover mix was 77.50+/-3.23 % Vegetational Cover (Mean +/- S.E.M.).

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