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14 June 2019 Biological Studies of the Oligonychus litchii (Trombidiformes:Tetranychidae) on Four Commercial Litchi Cultivars
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Abstract

Litchi is one of the most important pillars of the fruit industry in Southeast Asia and mainland China. The litchi spider mite, Oligonychus litchii Lo & Ho (Prostigmata: Tetranychidae), is a major pest of litchi. To determine the influence of different litchi cultivars on the life cycle, fecundity, and longevity of O. litchii, life tables of O. litchii on 4 popular commercial litchi cultivars in China (‘Baili,’‘Fezixiao,’‘Sanyuehong,’ and‘Nuomici’) were constructed under laboratory conditions at 25 ± 1 °C, 65 to 80% RH, and photoperiod of 14: 10 h (L: D). Life stages of O. litchii consist of egg, larva, protonymph, deutonymph, and adult, with distinct body sizes and colors. The life table parameters were significantly influenced by litchi cultivars. Our results showed that the developmental time of immature O. litchii was significantly longer on Baili than on the other 3 litchi cultivars. The immature survival rates of O. litchii varied from 21.74% to 68.42%. Oligonychus litchii laid significantly more eggs on Nuomici (64.84 eggs per female) than on other cultivars. The population doubling time of O. litchii ranged from 4.56 to 22.42 d, and a significant varietal effect was seen. The mites feeding on Nuomici showed the lowest intrinsic rate of natural increase per d (rm = 0.14 female per female per d). In addition, the net reproductive rate (R0) and finite rate of increase (λ) of O. litchii had the highest value on Nuomici (22.86 female per female per generation, and 1.16 female per female per d, respectively). The comparison of rm, R0, and immature survival rate of O. litchii on host plants revealed that Nuomici is the most suitable cultivar, suggesting that Nuomici is more susceptible to the litchi spider mite than the other 3 litchi cultivars.

Litchi (Litchi chinensis Sonn) (Sapindaceae) originated in the moist tropical and subtropical forests of southern China, and has a long history according to unofficial Chinese records going back to about 2000 BC (Huang et al. 2005). It is principally cultivated in Asia-Pacific regions, such as India, South Africa, Mauritius, Mexico, Australia, and Hawaii for its popular fruit (Menzel 2002; Wall 2006). The largest producer in Asia-Pacific regions is China, and the litchi is one of the most important pillars of the fruit industry in Southeast Asia and mainland China (Wei et al. 2015). The cultivated area of litchi and commercial litchi production in mainland China are estimated to exceed 635,524 ha and 1.42 million metric tons, respectively (Houbin 2017).

Litchi is susceptible to a range of pests and diseases (Menzel 2002). The litchi spider mite, Oligonychus litchi Lo & Ho (Prostigmata: Tetranychidae) is one of the most damaging mite pests of litchi (Chyi-chen 2000). Reportedly, O. litchii has become the principal pest of Dimocarpus longan Lour (Sapindaceae), Psidium guajava Linn (Myrtaceae), Eriobotrya japonica (Thunb.) Lindl (Rosaceae), and Syzygium samarangense Merr. et Perry (Myrtaceae) in Taiwan (Ho 2004). Also, it was found recently to cause damage in other litchi-producing areas, such as Guangdong, Hainan, Guangxi, Yunnan, and Fujiang provinces in mainland China (Shu et al. 2014b; Wenhua et al. 2016). Their mouthparts (chelicerae) are specifically designed for puncturing the epidermal cells of leaves, producing characteristic reddish brown spots on the upper surface of mature leaves (Shu et al. 2014a). High population density of O. litchii leads to leaf defoliation and nutrition accumulation reduction of the host plants, further resulting in severe crop loss (Chyi-chen 2004; Shu et al. 2014b).

The impacts of host plant morphological and chemical features on teranychid mite species has been noted repeatedly (Awmack& Leather 2002; Vasquez et al. 2008). Host plant species or cultivars are among the most important extrinsic factors that affect development rate, longevity, and fecundity of mites (Van et al. 2003). For example, the adult longevity of Oligonychus afrasiaticus (McGregor) (Prostigmata: Tetranychidae) differed among 4 date palm cultivars with values ranging from 4.70 to 18.10 d (Ben et al. 2011). In a comparative study of Panonychus ulmi (Koch) (Prostigmata: Tetranychidae) on different apple cultivars, the total fecundity per female was significantly different among 4 apple cultivars (Dongyin et al. 2013). Furthermore, the egg hatchability of Tetranychus urticae Koch (Prostigmata: Tetranychidae) range from 88.25 to 94.20% on 6 common bean cultivars (Najafabadi et al. 2014).

In recent years, several important fruit trees, including litchi, guava, and loquat in southern China were attacked by O. litchii, among which litchi is the most important host plant for this mite pest. However, little is known about the occurrence of susceptible cultivars, or the development, survival, reproduction, and life table parameters of O. litchii. Hence, the purpose of this study was to better understand the influence of litchi cultivars on life-history parameters of O. litchii, by constructing the life tables of this spider mite on 4 popular commercial litchi cultivars in China.

Materials and Methods

MITE COLONY AND MAINTENANCE

Oligonychus litchii used in these experiments were originally collected at litchi orchards in Conghua city (northeast of Guangdong Province, China, a region dominated by a subtropical monsoon climate) in Mar 2013. A stock O. litchii colony was started on healthy litchi leaflets in a rearing chamber at 25 ± 1 °C, 65 to 80% RH, and a 14: 10 h (L: D) photoperiod. The mites were cultured on leaflets of 4 litchi cultivars (Baili, Fezixiao, Sanyuehong, Nuomici) for at least 4 generations before being used as the test materials in this study.

LEAF DISCS

New litchi leaflets (30–40 d old) in the mature stage were obtained from a litchi orchard of the Institute of Plant Protection, Guangdong Academy of Agricultural Sciences, China, for leaf disc preparation. All host plants were irrigated at the same time and no fertilizers or pesticides were used during the experiments. A modified leaf-disc method was used to rear O. litchii in this study (Perumalsamy et al. 2010; Rahman et al. 2013). A sheet of cotton wool gauze was set in a large Petri dish (46 cm in diam), and distilled water was added to the Petri dish to keep the gauze water-saturated. The edge of all experimental litchi leaflets was wrapped with moist filter paper to prevent the escape of the tested mites and to keep the leaves fresh. Then each of the leaf discs was placed on the wetted gauze in the Petri dish with the top side facing upward. The new leaf discs were prepared and the mites transferred every 6 d.

DEVELOPMENT TIME, SURVIVAL OF IMMATURE STAGES, ADULT FECUNDITY, AND LONGEVITY

To obtain synchronized eggs for the experiments, 5 mated females from each colony were moved to a leaf disc with the same cultivars as those from which they were collected. The females were allowed to lay eggs for 12 h, and then only 1 egg was retained on the leaf disc after removing females and other eggs. In all, 60 to 70 eggs were tested for each litchi cultivar. The egg was observed each d until it hatched. The newly emerged larva was transferred to a fresh leaf disc, and observed under a binocular microscope (Olympus, SZ4045, Olympus (China) Co. Ltd., Shanghai, China) at 50× every d until they reached maturity. The presence of exuviae was used as the criterion of successful molting to the next development stage. The development time and survival of larvae, protonymphs, deutonymphs, males, and females were recorded. Each mature female that had emerged within the last 24 h was supplied with an additional adult male from each colony to ensure mating. The additional adult males were removed after mating with females. The remainder of the females and males were reared individually. To estimate the preoviposition period, observation was made at 8 h intervals until the first egg was deposited. To calculate the oviposition period, fecundity, and longevity, the number of eggs laid by each female on 4 litchi cultivar leaflets were checked and removed daily. All experiments were carried out in a rearing chamber with the same rearing conditions mentioned above.

LIFE TABLE CONSTRUCTION

The raw data obtained in the studies of developmental time, survival of immature stages, adult fecundity, and longevity were used for a time-specific life table construction of O. litchii under laboratory conditions. The life table parameters were estimated from a life-fecundity table according to the equation given by Birch (1948) and Southwood and Henderson (2000):

e01_418.gif

where x is the age class, l x is the possibility of survival at age x, and m x is the daily number of female offspring at age x. The net reproductive rate R 0 is represented by R 0 =, the intrinsic rate of increase by r m= lnR 0 /T 0, the mean generation time T 0 (in d) by T=lnR 0 /r m, and the finite rate of increase (λ) by λ=. The doubling time (DT) by DT = ln2/ r m was calculated as described by Deevey (1947), Birch (1948), and Mackauer (1983). The life table study is extremely time-consuming; thus, experimental replication is impractical in this study (Jih-Zu et al. 2005). Based on the bias corrected and accelerated bootstrap (BCaWW method) (Wyatt & White 1977), the life history parameters and 95% confidence limit (CI) were estimated using 1,000 bootstrap samples (Lawo & Lawo 2011).

STATISTICAL ANALYSIS

The data of developmental duration, immature survival rate, sex ratio, and effects of different litchi cultivars on female lifespan and fecundity of O. litchii were evaluated using 1-way analysis of variance (ANOVA), and means were separated by Tukey's test.

Results

BIOLOGICAL AND BEHAVIORAL OBSERVATION

Life stages of O. litchii consist of egg, larva, protonymph, deutonymph, and adult (Fig. 1). The O. litchii went through 3 molts between the egg and adult stages. During each molt, the mites attached themselves to the surface of the host plant and underwent a quiescent period, in the same manner as other spider mites (Goldarazena et al. 2004; Negm et al. 2014; Oku 2016). Mating occurred within 24 h after the adult female reached sexual maturation. Gravid females move around slowly and prefer to spin visible webs near the midrib of host leaves, on which they walk and lay eggs. The newly deposited eggs are translucent, oval in shape, with a sticky surface, and become cream colored before hatching. The newly hatched larva has 3 pairs of legs, whereas the protonymph, deutonymph, and adult of O. litchii have 4 pairs of legs, as well as larger body size, darker brownish body color, and faster mobility than larvae. Gender can be easily identified in the adult stage, because the adult female is larger in body size and has a more rounded posterior margin of the abdomen than the adult male.

DEVELOPMENT AND SURVIVAL OF IMMATURE MITES

The development time of different stages (before maturation) of O. litchii is given in Table 1. Egg incubation period of O. litchii was significantly longer on Nuomici than on the other 3 cultivars (P < 0.05; Table 1). On the contrary, the deutonymph period of O. litchii on Nuomici was the shortest (1.94 ± 0.20 d) among the 4 litchi cultivars. Total development time ranged from 12.26 ± 0.32 to 14.56 ± 0.20 d (mean ± SE), but no significant difference was observed among Feizixiao, Sanyuehong, and Nuomici. In addition, due to the different development rates among individuals as well as between sexes, there were significant overlaps between different stages. The age-stage survival rate (s xj) of O. litchii was the probability that a newly hatched larva will survive to age x and stage j (Fig. 2). Except for the overlaps between different stages, these curves also showed the stage differentiation and survivorship of O. litchii. The probability that a newly laid egg survives to adult stage was similar on Baili and Feizixiao (0.15, 0.17 for females, and 0.06, 0.07 for males, respectively), whereas survival was lower than that on Sanyuehong and Nuomici (0.48, 0.51 for females, and 0.15, 0.18 for males, respectively). The female adults emerged earlier and survived longer than males on all 4 tested litchi cultivars.

Fig. 1.

Life stages of Oligonychus litchi: (A) egg; (B) larva; (C) protonymph; (D) deutonymph; (E) adult male; (F) adult female.

f01_418.jpg

ADULT FEMALE LONGEVITY AND FECUNDITY

The longest female lifespan of O. litchii was 32.67 d on Nuomici, whereas the shortest female longevity was 25.95 d on Sanyuehong. In addition, different litchi cultivars had different impacts on fecundity of adult female mites. The longest preoviposition period and oviposition period were registered on Baili and Nuomici, respectively (P < 0.05; Table 2). Total fecundity of O. litchii was significantly different among the tested litchi cultivars, and was highest on Nuomici (64.84 ± 3.57 eggs per female). The progeny sex ratio [/( + )] on Nuomici and Sanyuehong was female-biased as shown in Table 2. Figure 3 illustrates m x and l x of O. litchii. The first eggs on Baili, Feizixiao, Sanyuehong, and Nuomici were laid at the d-age (from egg to the first eggs laid by female) of 11, 11, 10, and 12 d, respectively. The maximal daily oviposition per female on Nuomici and Sanyuehongwas significantly higher than on Feizixiao and Baili. Maximum egg production was observed on Nuomici. Moreover, the age-specific survival rate (l x) of O. litchii reared on 4 litchi cultivars decreased sharply before the protonymph stage, and resulted in a plateau in the survivorship curve; subsequently, survival continued to decrease until death (Fig. 3). However, the survival rate (the probability that a newly laid egg will survive to the sexual maturation stage) varied significantly among different litchi cultivars, with a range from 21.74 ± 1.30% on Baili to 68.42 ± 2.80% on Nuomici (Table 1). The l x curve also showed that O. litchii survived and reproduced most successfully on Nuomici among the 4 tested litchi cultivars.

Table 1.

Duration of the development stages and immature survival rate (ISR) of Oligonychus litchii mites on 4 litchi cultivars under laboratory conditions.

t01_418.gif

EFFECTS OF DIFFERENT LITCHI CULTIVARS ON THE LIFE TABLE PARAMETERS

Variation of life table parameters of O. litchii on 4 litchi cultivar leaves is presented in Table 3. These parameters were strongly affected by host plant cultivars. The intrinsic rate of population increase (r m) showed a similar pattern to finite rate of increase (λ), in which the highest value occurred on Nuomici and Sanyuehong, followed by Feizixiao, whereas the lowest value was on Baili. The net reproductive rate (R 0) value was the highest on Nuomici and the lowest on Baili. The mean generation time (T) is the required time for the population of O. litchii to multiply, where R 0 and the T value varied from 27.19 ± 2.13 d (on Nuomici) to 18.93 ± 1.01 d (on Baili). The values of population doubling time (DT) ranged from 22.42 ± 2.67 (on Baili) to 4.56 ± 1.02 (on Sanyuehong).

Fig. 2.

Age-stage-specific survival rate of O. litchii reared on different litchi cultivars at 25 ± 1 °C, 65 to 80% RH, and a photoperiod of 14: 10 h (L: D).

f02_418.jpg

Discussion

In this study, biological characteristics of O. litchii were investigated on 4 important commercial litchi cultivars. The 4 litchi cultivars tested varied in their date of fruit maturity: the early-maturing cultivar Sanyuehong, the mid-maturing cultivar Feizixiao, the mid-to-late-maturing cultivar Nuomici, and the late-maturing cultivar Baili. The results showed that O. litchii fed, survived, and developed on all 4 litchi cultivars. The development of O. litchii consists of 5 life stages with distinct biological characteristics, and it is only after the deutonymphal stage that the male and female litchi spider mites may be identified. The population growth parameters of O. litchii, such as the developmental duration of the egg, larva, protonymph, and deutonymph, varied in response to changes in litchi cultivars as show in Table 1. The differences in population growth parameters could be ascribed to the variations in host plant quality and availability of nutrition for the mite pests (Awmack & Leather 2002; Van et al. 2003). In previous studies of other spider mites, Vasquez et al. (2008) reported that the average longevity of Oligonychus punicae (Prostigmata: Tetranychidae) females ranged from 8.10 to 17.50 d on 6 different grapevine cultivars. Dongyin et al. (2013) observed that the duration of development of P. ulmi was slightly different on 3 apple cultivars with a range from 10.70 to 11.70 d, and Najafabadi et al. (2014) reported that the duration of development of T. urticae was highly affected by different bean cultivars, with a range from 12.00 to 24.74 d. Thus, different host plant cultivars have a decisive impact on the duration of development in spider mites. In our study, the total development time of O. litchii on Baili(14.56 ± 0.20 d) was significantly longer than that for the other 3 cultivars, and this was predominantly due to longer larva, protonymph, and deutonymph duration on Baili cultivar. Furthermore,the survival rate of immature stages of O. litchii on litchi cultivars ranged from 21.74% to 68.42%, and the lowest immature survival rate of O. litchii was observed on Baili cultivar (Table 1, Fig. 3). These results suggested that the Baili cultivar was less suitable to immature development of the litchi spider mite, and different litchi cultivars had significant impacts on the developmental duration of litchi spider mite. A possible explanation is the differences in the characteristics among the 4 litchi cultivars, and include nutritional components, secondary metabolites, and morphology of the leaf surface. Baili is a late-maturing cultivar, with light-green leaf color that results in lower levels of nutrient accumulation in leaves as compared to the other 3 litchi cultivars tested.

Table 2.

Effects of different litchi cultivars on lifespan and fecundity of female Oligonychus litchii.

t02_418.gif

Fig. 3.

Age-specific survival rate (l x), age-specific fecundity (m x) of O. litchii reared on different litchi cultivars at 25 ± 1 °C, 65 to 80% RH, and a photoperiod of 14: 10 h (L: D).

f03_418.jpg

Female lifespan, preoviposition and oviposition period, and total fecundity were highly affected by host plant cultivars. Previous studies suggested that the increase of female longevity is an important adaptation for insects to maintain a population when nutrition supply is limited or food quality is low (Uçkan & Ergin 2002; Najafabadi et al. 2014). In the comparative demography study of O. afrasiaticus on palm cultivars, the adult longevity on Deglet Noor cultivar (13.46 d) was significantly longer than that on Bessr cultivar (7.6 d), whereas no statistically significant differences were found in egg hatchability among the experimental cultivars (Ben et al. 2011). A range of different total fecundity values from 20.62 to 34.12 was observed in the study of P. ulmi on 4 apple cultivars (Dongyin et al. 2013). In our study, the longest lifespan of female mites was registered on Nuomici (32.67 d), followed by that on Feizixiao (29.70 d) and Baili (29.50 d), and the shortest one was recorded on Sanyuehong (25.95 d) (Table 2). Intriguingly, total fecundity of female O. litchii on Sanyuehong (38.55 eggs per female) was significantly higher than on Feizixiao (22.30 eggs per female) and Baili (14.78 eggs per female). Shorter duration of development together with higher total fecundity of tetranychid species indicates greater suitability of a host plant (Awmack & Leather 2002). Our results showed that the shortest female lifespan of O. litchii was observed on Sanyuehong, but the maximal daily oviposition per female and the highest total fecundity were observed on Nuomici (Table 2, Fig. 3). Thus, it is difficult to evaluate the suitability of these 4 litchi cultivars for litchi spider mites in our study according to lifespan and fecundity parameters.

Table 3.

Life table parameters of Oligonychus litchii reared on 4 litchi cultivars under laboratory conditions.

t03_418.gif

Life table study is a powerful tool to describe information on development, fecundity, and population dynamics of insects (Mahmood 1997; Hongsen et al. 2014). Previous studies have demonstrated cultivar effects on life table parameters of tetranychid species. The study of O. punicae on 6 grapevine cultivars showed the r m value ranged from 0.14 to 0.31, the R 0 value ranged from 3.85 to 18.47, and the T value ranged from 14.13 to 17.96 (Vasquez et al. 2008). The life parameters of T. urticae varied significantly on 6 bean cultivars with a r m value range from 0.13 to 0.27, a bigger R 0 value range from 26.11 to 62.38, a λ value varied from 1.13 to 1.30, and a DT value varied from 2.54 to 5.33 (Najafabadi et al. 2014). Among all the life-history parameters, the intrinsic rate of natural increase per d (r m) and the net reproductive rate (R 0) are the most important demographic indicators to predict and evaluate the tetranychid population dynamics under given environmental conditions. Comparisons of these 2 indicators could provide more comprehensive insight than independent analysis of individual life table parameters (Mahmood 1997; Kasap 2003; Vasanthakumar & Babu 2013). In the current study, the r m and R 0 of the litchi spider mite were highly affected by litchi cultivars. The r m value varied from 0.04 to 0.14 females per female per d. Hence, the population development of O. litchii was the shortest on Sanyuehong and Nuomici. These results were probably due to short immature duration and high total fecundity on those 2 litchi cultivars. The highest R 0 value was observed on Nuomici (22.86 per d), followed by Sanyuehong (17.80 per d) and Feizixiao (3.76 per d), and the shortest was on Baili (1.79 per d) (Table 3). A significant difference in R 0 values could induce remarkable difference in population growth over time. Furthermore, the higher r m and R 0 value indicated the susceptibility of a litchi cultivar to O. litchii, whereas the lower value of the 2 indicators indicate the resistance of a litchi cultivar to litchi spider mite. However, our findings have revealed that Nuomici is the most suitable and susceptible cultivar for O. litchii, whereas Baili is the most resistant cultivar to O. litchii among these 4 important commercial litchi cultivars.

Spider mites are recognized as a major secondary pest and a threat to agricultural production (Chyi-chen 2000; Perumalsamy et al. 2010), because natural enemies of mites are suppressed by the broad usage of pesticides. Currently, the litchi spider mite has become a serious pest, damaging over 70 plant species, including some very important fruit crops including litchi, guava, loquat, and wax apple in southern China and Taiwan (Ho 2004; Shu et al. 2014b; Wenhua et al. 2016). Basic information on the developmental duration, female longevity, and fecundity and life history parameters would be helpful to better understand the occurrence and population dynamics of O. litchii. This information, together with further field research in litchi orchards would provide comprehensive information for elucidating the nature of host suitability and improving the integrated pest management of O. litchii.

Acknowledgments

We are grateful to K. Lu (College of Life Sciences, Fujian Agriculture and Forestry University, Fujian, China) for his suggestions for the manuscript. This study received financial support from the National Science Foundation of China (Grant No. 31801800), the Natural Science Foundation of Guangdong Province (Grant No. 2017A030310095), the Pearl River Nova Program of Guangzhou (Grant No. 201710010180), and the China Litchi and Longan Research System Foundation (CARS-32-12).

References Cited

1.

Awmack CS, Leather SR. 2002. Host plant quality and fecundity in herbivorous insects.Annual Review of Entomology47: 817–844. Google Scholar

2.

Ben Chaaban S, Chermiti B, Kreiter S. 2011. Comparative demography of the spider mite, Oligonychus afrasiaticus, on four date palm varieties in southwestern Tunisia.Journal of Insect Science11: 136. https://doi.org/10.1673/031.011.13601 Google Scholar

3.

Birch LC. 1948. The intrinsic rate of natural increase of an insect population.Journal of Animal Ecology17: 15–26. Google Scholar

4.

Chyi-chen H. 2000. Spider-mite problems and control in Taiwan.Experimental and Applied Acarology24: 453–462. Google Scholar

5.

Chyi-chen H. 2004. Litchi spider mite (Oligonychus litchii) has become an important agricultural spider mite in Taiwan.The Plant Protection Bulletin31: 927–930. (in Chinese). Google Scholar

6.

Deevey J. 1947. Life tables for natural populations of animals.The Quarterly Review of Biology22: 283–314. Google Scholar

7.

Dongyin W, Guisheng Q, Wentao Y, Lina S, Huaijiang Z, Chunsen M, Adaobi UP. 2013. Age-stage two-sex life tables of Panonychus ulmi (Acari: Tetranychidae), on different apple varieties.Journal of Economic Entomology106: 2118–2125. Google Scholar

8.

Goldarazena A, Aguilar H, Kutuk H, Childers CC. 2004. Biology of three species of Agistemus (Acari: Stigmaeidae): life table parameters using eggs of Panonychus citri or pollen of Malephora crocea as food.Experimental and Applied Acarology32: 281–291. Google Scholar

9.

Ho CC. 2004. Litchi spider mite (Oligonychus litchii) has become an important agricultural spider mite in Taiwan.Plant Protection Bulletin46: 299–302. Google Scholar

10.

Houbin C. 2017. A survey on lychee and longan industry in China, pp. 3–4 In Annual Meeting for Work Reports of China Litchi and Longan Research System.Guangzhou, China, 27–30 Dec 2017. (in Chinese). Google Scholar

11.

Huang X, Zeng L, Houbin C. 2005. Lychee and longan production in China.Acta Horticulturae665: 27–36. Google Scholar

12.

Hongsen P, Bing L, Yanghui L, Desneux N. 2014. Life table parameters of three mirid bug (Adelphocoris) species (Hemiptera: Miridae) under contrasted relative humidity regimes.PloS One9: e115878. https://doi.org/10.1371/journal.pone.0115878 Google Scholar

13.

Jih-Zu Y, Hsin C, Bing-Huei C. 2005. Life table and predation of Lemnia biplagiata (Coleoptera: Coccinellidae) fed on Aphis gossypii (Homoptera: Aphididae) with a proof on relationship among gross reproduction rate, net reproduction rate, and preadult survivorship.Annals of the Entomological Society of America98: 475–482. Google Scholar

14.

Kasap I. 2003. Life history of hawthorn spider mite Amphitetranychus viennensis (Acarina: Tetranychidae) on various apple cultivars and at different temperatures.Experimental and Applied Acarology31: 79–91. Google Scholar

15.

Lawo JP, Lawo NC. 2011. Misconceptions about the comparison of intrinsic rates of natural increase.Journal of Applied Entomology135: 715–725. Google Scholar

16.

Mackauer M. 1983. Quantitative assessment of Aphidius smithi (Hymenoptera: Aphidiidae): fecundity, intrinsic rate of increase, and functional response.Canadian Entomologist115: 399–415. Google Scholar

17.

Mahmood F. 1997. Life-table attributes of Anopheles albimanus (Wiedemann) under controlled laboratory conditions.Journal of Vector Ecology22: 103–108. Google Scholar

18.

Menzel C. 2002. Major pests and diseases. The lychee crop in Asia and the Pacific.Publication 2002/16. Food and Agriculture Organization of the United Nations Regional Office for Asia and the Pacific, Bangkok, Thailand.  http://www.fao.org/docrep/005/ac681e/ac681e00.htm (last accessed 4 Jan 2019). Google Scholar

19.

Najafabadi SS, Shoushtari RV, Zamani AA, Arbabi M, Farazmand H. 2014. Life parameters of Tetranychus urticae (Acari: Tetranychidae) on six common bean cultivars.Journal of Economic Entomology107: 614–622. Google Scholar

20.

Negm MW, Alatawi FJ, Aldryhim YN. 2014. Biology, predation, and life table of Cydnoseius negevi and Neoseiulus barkeri (Acari: Phytoseiidae) on the old world date mite, Oligonychus afrasiaticus (Acari: Tetranychidae).Journal of Insect Science14: 177. doi.org/10.1093/jisesa/ieu039 Google Scholar

21.

Oku K. 2016. Precopulatory mate guarding influences the development of quiescent deutonymph females in the two-spotted spider mite (Acari: Tetranychidae).Experimental and Applied Acarology68: 33–38. Google Scholar

22.

Perumalsamy K, Selvasundaram R, Roobakkumar A, Rahman VJ, Muraleedharan N. 2010. Life table and predatory efficiency of Stethorus gilvifrons (Coleoptera: Coccinellidae), an important predator of the red spider mite, Oligonychus coffeae (Acari: Tetranychidae), infesting tea.Experimental and Applied Acarology50: 141–150. Google Scholar

23.

Rahman VJ, Babu A, Roobakkumar A, Perumalsamy K. 2013. Life table and predation of Neoseiulus longispinosus (Acari: Phytoseiidae) on Oligonychus coffeae (Acari: Tetranychidae) infesting tea.Experimental and Applied Acarology60: 229–240. Google Scholar

24.

Shu X, Kaige C, Qiong Y, Yizhi D, Binxu C. 2014a. Sublethal effects of pyridaben on Oligonychus litchii.Journal of Fruit Science31: 927–930. (in Chinese). Google Scholar

25.

Shu X, Yao Y, Kaige C, Tao J, Binxu C. 2014b. Toxicity test and field efficacy of 5 kinds of acaricides against Oligonychus litchii.Guangdong Agriculture Science14: 83–85. (in Chinese). Google Scholar

26.

Southwood TRE. 2000. Age-grouping, time-specific life tables, and predictive population models, pp. 404–454 In Southwood TRE, Henderson PA [eds.], Ecological Methods, 3rd edition. Blackwell Science Press, Oxford, United Kingdom. Google Scholar

27.

Uçkan F, Ergin E. 2002. Effect of host diet on the immature developmental time, fecundity, sex ratio, adult longevity, and size of Apanteles galleriae (Hymenoptera: Braconidae).Environmental Entomology31: 168–171. Google Scholar

28.

Van BC, Van-beek TA, Dicke M. 2003. Differences among plant species in acceptance by the spider mite Tetranychus urticae Koch.Journal of Applied Entomology127: 177–183. Google Scholar

29.

Vasanthakumar D, Babu A. 2013. Life table and efficacy of Mallada desjardinsi (Chrysopidae: Neuroptera), an important predator of tea red spider mite, Oligonychus coffeae (Acari: Tetranychidae).Experimental and Applied Acarology61: 43–52. Google Scholar

30.

Vasquez C, Aponte O, Morales J, Sanabria ME, Garcia G. 2008. Biological studies of Oligonychus punicae (Acari: Tetranychidae) on grapevine cultivars.Experimental and Applied Acarology45: 59–69. Google Scholar

31.

Wall MM. 2006. Ascorbic acid and mineral composition of longan (Dimocarpus longan), lychee (Litchi chinensis) and rambutan (Nephelium lappaceum) cultivars grown in Hawaii.Journal of Food Composition and Analysis19: 655–663. Google Scholar

32.

Wyatt IJ, White PF. 1977. Simple estimation of intrinsic increase rates for aphids and tetranychid mites.Journal of Applied Entomology14: 757–766. Google Scholar

33.

Wei L, Zhidan X, Xiuli B, Xiaoyang Y, Jing F, Xiang X. 2015. Identifying litchi (Litchi chinensis Sonn.) cultivars and their genetic relationships using single nucleotide polymorphism (SNP) markers.PloS One10: e0135390. https://doi.org/10.1371/journal.pone.0135390 Google Scholar

34.

Wenhua C, Chaoyu LY, Tsuiying C. 2016. Temperature-dependent development and life history of Oligonychus litchii (Acari: Tetranychidae), on wax apple.Journal of Asia-Pacific Entomology19: 173–179. Google Scholar
Qiong Yao, Linfa Quan, Haiming Xu, Tao Jia, Wenjing Li, and Bingxu Chen "Biological Studies of the Oligonychus litchii (Trombidiformes:Tetranychidae) on Four Commercial Litchi Cultivars," Florida Entomologist 102(2), 418-424, (14 June 2019). https://doi.org/10.1653/024.102.0220
Published: 14 June 2019
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