Sex Differentiation in Meloidogyne incognita and Anatomical Evidence of Sex Reversal

Sex differentiation was studied by examining the cellular structure of gonad primordia extracted from second-stage juveniles developing under different environmental conditions. In female jnveniles, divisions of the two somatic cells of the primordium occurred in mid-sccond stage and resulted in 12 cells. Two of them were differentiated as cap cells, two occupied the anterior central and eight the posterior central part of the V-shaped primordium. The two germinal cells divided at the 6-8 somatic-cell stage of the primordium; i.e., earlier than in any other plant-parasitic nematode. In male juveniles of similar developmental stage, divisions of somatic cells resulted in 10 cells: one cap cell at the posterior tip and nine cells at the anterior part of the rod-shaped primordium. Germinal cells divided at the 6-8 sontatic-cell stage. On the basis of gonad anatomy it was concluded that some female juveniles undergo sex reversal and proceed with further development as males. The degree of expression of intersexual features depends on the period at which sex reversal occurs. Sex reversal at an early period gives rise to males with one testis, almost indistinguishable front true males. Sex reversal at mid-second stage involves degeneration of the nucleus of one of the cap cells resulting in males with an atrophied testis and a well-developed testis. More delayed sex reversal results in males with two testes of approximately equal size. To explain these patterns of development, it is assumed that sex differentiation is hormonally controlled and that the environment influences hormonal balance by affecting gene expression.     

Influence of Temperature on Embryogenesis in Meloidogyne javanica

The optimum temperature for embryogenesis in Meloidogyne javanica lies between 25 and 30 C. Embryogenesis is slightly more rapid at 30 C (9-10 days), but more eggs complete development at 25 C (11-13 days). At temperatures of 25, 27.5, and 30 C, embryogenesis is about twice as rapid as at 20 C (23-25 days), and about four times as rapid as at 15 C (46-48 days). Time-lapse studies showed that the thermal optimum is similar throughout the different stages of embryonic development.     

Influence of Low Temperature on Rate of Development of Meloidogyne incognita and M. hapla Larvae

Development of Meloidogyne incognita and M. hapla larvae in clover roots was studied at 20, 16, 12, and 8 C in growth chambers and in the field from fall through spring, in North Carolina. Larvae of both species invaded roots and developed at 20, 16, and 12 C, but not at 8 C. The time necessary to complete the larval stages at each temperature was determined. The minimal temperature for development of M. incognita larvae was 10.08 C and 8.8 C for M. hapla larvae. In the field, soil temperature at 10 cm deep was favorable for development of larvae until the end of November, and again from February on. All stages of the nematodes survived freezing temperatures in the roots. Reproduction of both species was evident in March or Apri1 after inoculation and accumulation of 8,500 to 11,250 degree-hours.     

Influence of Photoperiod and Temperature on Migrations of Meloidogyne Juveniles

Photoperiod influences the migration of M. incognita juveniles toward tomato roots. Approximately 33% migrated vertically 20 cm in 7 days to roots when 12 h dark were alternated with 12 h light. Only 7% migrated when light was constant for 24 h. Vertical migration of M. incognita juveniles was studied at 14, 16, 18, 20, and 22 C. The migration of M. incognita juveniles begins at about 18 C and reaches its maximum at 22 C. The migration of M. hapla and M. incognita juveniles were compared at 14, 18, and 22 C. Juveniles of M. hapla were able to migrate at a lower temperature than those of M. incognita. With M. hapla, there was no significant difference in migration between 18 and 22 C.     

Population Behavior of Meloidogyne graminis in Field-grown 'Tifgreen' Bermudagrass

The vertical distribution and overwintering potential of Meloidogyne graminis on field-grown Cynodon sp (var. ''Tifgreen'' bermudagrass) was measured. Total populations of M. graminis were found to be lowest in March and highest in May. Larvae were most abundant in the top 5-cm of soil during periods favoring bermudagrass growth and least numerous during periods of host dormancy. Throughout the year, more t h a n 50% of the nematodes recovered each month were in roots within the top 5-cm of the soil profile. Both eggs and larvae of M. graminis overwinter in eastern Virginia.     

Pathogenicity and Histopathology of Meloidogyne graminis Infecting 'Tifdwarf' Bermudagrass Roots

In a greenhouse experiment Meloidogyne graminis was pathogenic to ''Tifdwarf'' bermudagrass, causing significant reduction in plant weight. Roots and tops of inoculated grass weighed 28.4% less than non-inoculated grass 8 months after inoculation. Clipping weight of nematode-infected turf weighed 68.9% less than clippings from non-infected turf. Histopathological studies showed that the head of the female nematode penetrated the vascular system and resulted in giant cell formation in the feeding area. The nematode body remained in the cortex parallel to the vascular system. Eggs were deposited at the posterior of the nematode in a gelatinous matrix in the cortex. M. graminis fed with its anterior end oriented toward the growing root tip. M. incognita had no set body orientation pattern when feeding on bermudagrass.     

Influence of Low Temperature on Development of Meloidogyne incognita and M. hapla Eggs in Egg Masses

Egg masses of Meloidogyne incognita and M. hapla were placed in soil at 10, 12, 16, and 20 C. At regular intervals, eggs from samples of egg masses were released from the gelatinous matrices and their developmental stages recorded. The number of days necessary to complete each stage from gastrulation to hatch is given for each temperature. The minimal temperature threshold for the development of eggs was computed by linear regression to be 8.26 C for M. incognita and 6.74 C for M. hapla.     

甲壳动物性别分化的遗传决定及外界因素的影响(英文)

本文综述了甲壳动物的性别决定机理及外界因素对性别分化的影响。绝大多数甲壳动物没有明显的性染色体 ,促雄腺被认为是甲壳动物性别分化的最主要的决定因子 ,其作用已得到了广泛的证明。由于甲壳动物幼体在早期发育过程中具有向两性发育的潜能 ,促雄腺可以决定个体未来发育的性别 ,并且通过人为摘除或移植促雄腺的方法可以使性别已经分化的个体发生性逆转 ,从而改变幼体的性别。虽然甲壳动物的性别是由遗传决定的 ,但外界的因素比如寄生、光周期、温度或激素可以改变其性比 ,其中以寄生的影响研究比较多 ,并认为是影响某些甲壳动物性别分化的主要外界因子。由于大多数养殖的甲壳动物雌雄性之间有体重和体长的差异 ,在水产养殖中可以利用这些特征进行全雌或全雄种苗的生产 ,以提高产量和效益。     

Effects of Temperature on Resistance in Phaseolus vulgaris Genotypes and on Development of Meloidogyne Species

Phaseolus vulgaris lines with heat-stable resistance to Meloidogyne spp. may be needed to manage root-knot nematodes in tropical regions. Resistance expression before and during the process of nematode penetration and development in resistant genotypes were studied at pre- and postinoculation temperatures of 24 °C and 24 °C, 24 °C and 28 °C, 28 °C and 24 °C, and 28 °C and 28 °C. Resistance was effective at all temperature regimes examined, with fewer nematodes in roots of a resistant line compared with a susceptible line. Preinoculation temperature did not modify resistance expression to later infections by root-knot nematodes. However, postinoculation temperatures affected development of Meloidogyne spp. in both the resistant and susceptible bean lines tested. The more rapid development of nematodes to adults at the higher postinoculation temperature of 28 °C in both bean lines suggests direct temperature effects on nematode development instead of on resistance expression of either of two gene systems. Also, resistance was stable at 30 °C and 32 °C.     

Preferred Temperature of Meloidogyne incognita

In laboratory thermal gradients, newly hatched infective juveniles of the plant-parasitic root-knot nematode Meloidogyne incognita migrated toward a preferred temperature that was several degrees above the temperature to which they were acclimated. After shifting egg masses to a new temperature, the preferred temperature was reset in less than a day. Possible functions of this type of thermotaxis are discussed, including the use of thermal gradients around plant roots to locate hosts and to maintain a relatively straight path while ranging in the absence of other cues (a collimating stimulus).     

Influence of Meloidogyne incognita on Fusarium Wilt of Tomato at or below the Minimum Temperature for Wilt Development

''Bonny Best'' tomato plants were grown at 16, 21, or 24 C for 28 d in soil infested with either of two isolates of Fusarium oxysporum f. sp. lycopersici race 1 and Meloidogyne incognita. Significant levels of fusarium wilt occurred at all temperatures including 16 C, which has not been reported previously. One Fusarium isolate resulted in the highest levels of disease incidence at 21 and 24 C in the presence of root-knot nematodes, and at 24 C when the nematodes were not present. At 16 C there was no significant difference in the number of plants infected by the second Fusarium isolate alone or in combination with root knot nematodes, although the presence of nematodes resulted in a significant increase in the percentage of disease occurrence and vessel infection at 21 C.     

Effect of Temperature on Attachment,Development, and Interactions of Pasteuria penetrans on Meloidogyne incognita

The effect of temperature (10, 20, 25, 30, and 35 C) on attachment and development of Pasteuria penetrans on Meloidogyne arenaria race 1 was elevated in growth chambers. The greatest attachment rate of endospores of P. penetrans occurred on second-stage juveniles at 30 C. The bacterium developed more quickly within its host at 30 and 35 C than at 25 C or below. The development of the bacterium within the nematode female was divided into nine recognizable life stages, which ranged from early vegetative thalli to mature sporangia. Mature sporangium was the predominant life stage observed after 35, 40, 81, and 116 days at 35, 30, 25, and 20 C, respectively. The body width and length of M. arenaria females infected with P. penetrans were smaller initially than the same dimensions in uninfected females, but became considerably larger over time at 25, 30, and 35 C. This isolate of P. penetrans also parasitized and completed its life cycle in males of M. arenaria.     

The Development and Influence of Meloidogyne incognita and M. javanica on Wheat

The effects of soil temperature and initial inoculum density (Pi) of Meloidogyne incognito and M. javanica on growth of wheat (Triticum aestivum cv. Anza) and nematode reproduction were studied in controlled temperature baths in the glasshouse. Nematode reproduction was directly proportional to temperature between 14 and 30 C for M. incognita and between 18 and 26 C for M. javanica. Reproduction rates (Pf/Pi, where Pf = final number of eggs) for Pi''s of 3,000, 9,000, and 30,000 eggs/plant were greatest at each temperature when Pi = 3,000. Maximum M. incognita reproduction rate (Pf/Pi = 51.12) was at 30 C. At 26 C, M. javanica reproduction (Pf/Pi = 14.82, 9.02, and 4.23 for Pi = 3,000, 9,000, and 30,000, respectively) was about half that of M. incognita when Pi = 3,000 or 9,000 but similar when Pi = 30,000. Reproduction of both species was depressed between 14 and 18 C. Shoot and root growth and head numbers were inversely related to soil temperature between 14 and 30 C but were not affected by the Pi of M. incognita when 7 d old seedlings were inoculated. When newly germinated seedlings were inoculated with M. incognita or M. javanica, the Pi did not affect shoot and root fresh weights, shoot/root ratio, and tillering, but it did reduce root dry weight (M. javanica at 26 C) and increase shoot dry weight (M. incognita at 18-22 C). The optimum temperature range is lower for wheat growth than for nematode reproduction. Wheat cv. Anza is a good host for M. incognita and M. javanica, but it is tolerant to both species.     

线虫的性别分化和决定

线虫（Caeborhabditis elegans)是十分重要的模式生物。在遗传学,发育生物学以及神经生物学中有着广泛的应用。就线虫性别分化和性别决定相关基因的特性和功能进行了详细介绍,并在此基础上初步概括了其性别决定的分子机制。     

Development of Meloidogyne arenaria on Peanut and Soybean under Two Temperature Cycles

Florunner peanut and three soybean cultivars, Centennial, Gasoy 17, and Wright, were inoculated with 48-hour age cohorts of Meloidogyne arenari race 1 second-stage juveniles and placed in a growth chamber set to simulate early season (low temperature) and midseason (high temperature) conditions. Percentages of the initial inoculum penetrating roots 4 and 8 days after inoculation were 2-3 times higher in soybean cultivars than in peanut; 25% on susceptible soybean and 9% on peanut. Penetration and early development of M. arenaria were greater in the higher temperature environment. Penetration percentages were expressed as a function of cumulative degree-days by regression models. Development of M. arenaria 10, 20, and 30 days after inoculation was more rapid on peanut than on soybean. The resistant soybean cultivar Wright had slower development rates than did the other two soybean cultivars. Nematode growth and development were dependent on temperature. In greenhouse experiments, production of eggs by M. arenaria was more than 10 times greater on peanut than on susceptible soybean. The reproductive factor for Wright soybean was less than one, but plant growth parameters indicated that this cultivar was intolerant of M. arenavia.