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Article

Densities of Eggs and Nymphs and Percent Parasitism of Bemisia tabaci (Hemiptera: Aleyrodidae) on Common Weeds in West Central Florida

by
Hugh A. Smith
1,*,
Curtis A. Nagle
1 and
Gregory A. Evans
2
1
University of Florida, IFAS, Gulf Coast Research and Education Center, 14625 C.R. 672, Wimauma, FL 33598, USA
2
United States Department of Agriculture, 10300 Baltimore Avenue, BARC-West, Bldg 005, Rm. 09A, Beltsville, MD 20705, USA
*
Author to whom correspondence should be addressed.
Insects 2014, 5(4), 860-876; https://doi.org/10.3390/insects5040860
Submission received: 8 September 2014 / Revised: 23 October 2014 / Accepted: 26 October 2014 / Published: 10 November 2014
(This article belongs to the Special Issue Integrated Pest Management)
Versions Notes

Abstract

:
The density of eggs and nymphs of Bemisia tabaci (Gennadius) biotype B and the percent parasitism of the nymphs were measured from specimens collected on nine species of weeds, commonly found in west central Florida during the spring and summer of 2012 and 2013. The weeds were direct seeded in 2012 and grown as transplants in 2013 for Randomized Complete Block design experiments. The leaf area of each whole-plant sample was measured and the B. tabaci density parameters were converted to numbers per 100 cm2. In June and July, 2013, whole-plant samples became too large to examine entirely, thus a representative portion of a plant totaling about 1000 cm2 was sampled. Egg and nymph densities and percent parasitism varied greatly among weed species, and were higher overall in 2012 than in 2013. The highest densities of eggs and nymphs were measured on Abutilon theophrasti, Cassia obtusifolia and Emilia fosbergii each year. Lower densities of immature B. tabaci were measured on most dates for Amaranthus retroflexus, Bidens alba, Ipomoea lacunosa, Sesbania exaltata and Sida acuta. Nymph to egg ratios of 1:4 were observed on A. theophrasti and S. exaltata in 2012, while less than one nymph per ten eggs was observed overall on A. retroflexus, E. fosbergii and I. lacunosa. In 2012, parasitism rates of 32.3% were measured for B. alba, 23.4% for C. obtusifolia and 17.5% for S. acuta. Of the 206 parasitoids reared out over two seasons, 96.6% were Encarsia spp. and the remainder Eretmocerus spp. The role of weeds in managing B. tabaci is discussed.

1. Introduction

Bemisia tabaci (Gennadius) biotype B (Hemiptera: Aleyrodidae), formerly known as Bemisia argentifolii (Bellows and Perring) or as the Middle East-Asia Minor 1 (MEAM1) genetic group of Bemisia tabaci, attacks a broad range of horticultural, ornamental and row crops [1]. The species causes damage through removal of sap, by producing honeydew, which serves as a substrate for sooty molds that reduce quality [2], and by causing crop disorders, such as irregular ripening of tomato [3]. It is known to transmit over 100 plant viruses in the families Geminiviridae, Closteroviridae and Potyviridae [4] including Tomato yellow leaf curl virus (TYLCV), which is the most important pest problem afflicting tomato production in Florida and many other tomato producing regions [5]. Florida is one of the foremost producers of fresh tomato in the United States [6]. Bemisia tabaci is the only whitefly pest of significance attacking tomato in Florida [7].
In addition to developing on many horticultural crops, B. tabaci can develop on many species of weeds [8,9]. Weeds may enhance B. tabaci problems by serving as hosts for B. tabaci near crops and between cropping seasons [10]. In addition, weeds may serve as alternate hosts for whitefly-transmitted viruses [11,12,13,14,15]. Surveys of weeds in Florida have not detected TYLCV in common weed hosts of B. tabaci [16]. However research in Latin America and the Mediterranean indicates that weeds species (including species present in Florida) are hosts of TYLCV [13,14,15]. Weeds have been identified as hosts for Bemisia tabaci-transmitted viruses affecting other horticultural crops in Florida, including bean golden mosaic, cucurbit leaf crumple and squash vein yellowing viruses [17].
Weeds may contribute to the regulation of populations of B. tabaci by providing a habitat for its predators and parasitoids [18,19,20,21]. Stansly et al. [20] quantified the densities of B. tabaci and its parasitoids on weeds in southwest Florida and found relatively high percentages of parasitism on Bidens sp. and Lantana sp. At least thirteen species of parasitoid have been reared from B. tabaci in Florida [22]. Encarsia pergandiella Howard (Hymenoptera: Aphelinidae), Encarsia nigricephala Dozier (Hymenoptera: Aphelinidae) and Eretmocerus spp. (Hymenoptera: Aphelinidae) predominated, comprising 62%, 17% and 12% respectively of species collected [23]. In west central Florida, tomatoes are transplanted in late winter/early spring (January–March) and late summer/early fall (August–October), with harvest carried out 90–120 days after transplanting, depending on weather and market conditions. Populations of B. tabaci in Florida typically decrease markedly during the cooler winter months, but can be sustained at high levels on alternate hosts and abandoned or improperly destroyed tomato fields during the climatically favorable months of summer. For this reason, it is important to characterize the importance of summer weeds as hosts of B. tabaci, and reservoirs of TYLCV and whitefly parasitoids.
Currently, research is being conducted at the University of Florida’s Gulf Coast Research and Education Center (GCREC) to determine the role of summer weeds in regards to the management of B. tabaci and TYLCV in the west central Florida tomato growing region. The weeds being evaluated include: Abutilon theophrasti Medik (Malik) (Malvaceae), Amaranthus retroflexus L. (Amaranthaceae), Bidens alba L. (Asteraceae), Cassia (Senna) obtusifolia L. (Irwin & Barneby) (Fabaceae), Emilia fosbergii Nicolson (Asteraceae), Ipomoea lacunosa L. (Convolvulaceae), Sesbania exaltata (Raf.) Cory (Fabaceae), Sida acuta Burm. F. (Malvaceae), and Solanum americanum Mill. (Solanaceae). These weeds, and in some cases other species in the same genera, are common on the edges and in irrigation ditches of agricultural fields in west central Florida as well as other parts of the state [24]. With the exception of B. alba, which is present year round, these weed species are most abundant during the spring and through the summer. In addition to being common in the field, B. alba, E. fosbergii and S. acuta are also common in and around the nurseries and screen houses where seedlings of tomato and other horticultural crops are produced.
The objective of the study was to improve understanding of the relative importance of these weeds as summer hosts for B. tabaci and its parasitoids. Large scale commercial production of tomato in Florida largely ceases during the hottest summer months, July and August. Therefore information on the relative importance of these weeds as alternate hosts of B. tabaci when crops are not present is of value. Here we report comparative information on the densities of B. tabaci eggs, nymphs and percent parasitized nymphs on key weeds. Weeds that are determined in the future to be non-hosts of TYLCV would essentially be “dead ends” for the virus. Bemisia tabaci developing on non-virus hosts will be virus-free. Therefore weeds which demonstrate a high percentage of parasitism and do not serve as reservoirs for TYLCV may play a positive role in the suppression of viruliferous B. tabaci populations.

2. Experimental Section

2.1. Field Study Establishment

Abutilon theophrasti, Amaranthus retroflexus, Bidens alba, Cassia obtusifolia, Emilia fosbergii, Ipomoea lacunosa, Sesbania exaltata, Sida acuta, and Solanum americanum were studied at the University of Florida, GCREC, Wimauma FL (N27°45.599', W82°13.446') during the spring and summer of 2012 and 2013. Seed of A. theophrasti, C. obtusifolia and Sesbania exaltata was purchased from Azlin Weed Seed Service (Leland, MS, USA). Seed of A. retroflexus, and Ipomoea lacunosa was purchased from V and J Seed Farms, Inc. (Woodstock, IL, USA). Seed of the remaining weed species in the study was collected from plants growing at GCREC. Weeds were direct seeded into the experimental plots on 27 April 2012 using 2–3 seeds per plant hole, and thinned to one plant per hole after germination. Because of differences in germination and growth rate of the direct seeded plants, comparisons between some host plants were difficult. To avoid this in 2013, each weed species was grown from seed in a growth room with 12:12 (L:D) h at 26–30 °C and then transplanted 10 April, three to four weeks post germination. By transplanting all weeds at the same phenological stage, side by side comparison was facilitated.
The weeds were maintained in 20 cm high and 81 cm wide beds of Myakka fine sand, spaced on 1.5 m centers, covered with white, virtually impermeable plastic mulch and irrigated with drip irrigation without the injection of liquid fertilizer. Each year the experiment was arranged in a Randomized Complete Block design. Each treatment consisted of different weed species replicated four times and planted in a single row of ten plants with 0.3 m between the plants. Plots were spaced 3 m apart, with an unplanted bed between the plots. The plants were infested naturally with B. tabaci from populations that occurred around the study site.

2.2. Sampling

In 2012, sampling began on 8 May and was carried out nearly every week through 17 July. Samples consisted of one whole plant per plot from each replication. Weed species emerged and grew at different rates, with the result that not all species were sampled on each sampling date. A. theophrasti, C. obtusifolia, I. lacunosa, and S. exaltata were sampled during the entire period. Sampling for B. alba was initiated 16 May; sampling for A. retroflexus and E. fosbergii began 25 May. S. acuta and S. americanum emerged weeks after other species and initially grew very slowly. These species were sampled on 11 and 17 July only. Plant samples were brought to the laboratory at GCREC and the underside of all leaves was examined using a dissecting microscope. From the 8th of May to the 7th of June, the number of eggs and nymphs of B. tabaci and the total leaf area per plant were recorded. Leaf area was measured with a LI-COR Portable Area Leaf Meter LI-3000 (LI-COR, Lincoln, NE, USA). By mid-season, most plants had become very large; therefore after the 7th of June, leaf area was not measured and only the number of non-parasitized and parasitized nymphs per plant was recorded. In 2013, sampling occurred from 17 April through 1 July. Numbers of eggs, non-parasitized and parasitized nymphs and leaf area per sample were recorded. When plants became too large for entire whole plant samples to be examined (3 June–1 July), a portion of the plant consisting of one third lower, one third mid and one third upper stratum foliage was selected. These later samples consisted of a total of approximately 1000 cm2 per plant.
Parasitized nymphs were observed on three sample dates in 2012 (2–17 July) and on six sample dates in 2013 (30 April–1 July). The focus of the late-season samples in both years was to determine the suitability of weeds as hosts for parasitoids by comparing the proportion of parasitized nymphs to non-parasitized nymphs on each species.

2.3. Parasitoid Collection

Leaves from a plant sample possessing parasitized nymphs were maintained on moistened filter paper in 60 × 15 mm petri dishes (Fisher Scientific, Waltham, MA, USA; cat. no. 08-757-13A) inside 1.4 liter food service containers (Sterilite Corporation, Ennis, TX, USA) in a growth room with 14:10 (L:D) h at 26–30 °C. Foliage with parasitized nymphs was placed in the food service container with moistened paper to maintain humidity and a yellow sticky card (Olson Products, Medina OH) on the inner cover to attract emerged parasitoids. Emerged parasitoids were removed from the sticky card using Histo-Clear (National Diagnostics, Atlanta, GA, USA) and were sent to the USDA lab in Beltsville MD for identification by Gregory A. Evans.

2.4. Statistical Analysis

Egg and nymph data were converted to number per 100 cm2 when a leaf area measurement accompanied the data and transformed using log10(x + 1) to meet assumptions of normality before analysis using PROC ANOVA with SAS 9.2 software [25]. Percent parasitized nymphs were transformed using arcsine [√(%x/100)] and analyzed similarly to the egg and nymph data.. All means were separated by Fisher’s Protected LSD test (p ≤ 0.05). Means are reported in the original scale.

3. Results and Discussion

3.1. 2012

There were significant differences in the densities of B. tabaci eggs observed across weed species from 16 May–11 June (Table 1). No egg data were recorded after 11 June.
Table
Table 1. Mean (±SE) B. tabaci egg densities on selected weeds in 2012. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Table 1. Mean (±SE) B. tabaci egg densities on selected weeds in 2012. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
B. tabaci Eggs per 100 cm2 Leaf Area (Mean ± SE)
Weed Species8 May16 May25 May4 June11 June
A. retroflexus--42.8de (14.0)40.1c (3.9)85.8cd (21.2)
A. theophrasti159.8a (64.9)540.6a (225.5)296.1c (53.0)328.5a (105.4)448.0b (218.4)
B. alba-6.2c (3.0)28.4ef (9.8)48.7c (5.7)73.0d (15.5)
C. obtusifolia230.3a (125.6)70.7b (25.3)661.6b (104.6)262.3ab (111.1)402.9ab (105.1)
E. fosbergii--1914.8a (62.2)292.9a (13.3)730.4a (117.5)
I. lacunosa133.3a (34.0)32.5b (14.2)64.7d (11.2)162.7b (54.0)152.3c (23.6)
S. exaltata59.3a (35.2)21.5bc (6.3)13.6f (4.1)11.1d (4.0)3.7e (1.5)
F-value1.00 (F3,9)10.33 (F4,12)61.58 (F6,18)23.11 (F6,18)44.60 (F6,18)
p-value0.43750.0007<0.0001<0.0001<0.0001
Egg densities were highest on E. fosbergii, C. obtusifolia and A. theophrasti. Expressed per 100 cm2 foliage, the highest egg densities measured on each species were 1914.8 ± 62.2 on E. fosbergii (25 May), 661.6 ± 104.6 on C. obtusifolia (25 May) and 540.6 ± 225.5 on A. theophrasti (16 May). Egg densities peaked on I. lacunosa at 162.7 ± 54, on A. retroflexus at 85.8 ± 21.2, and on B. alba at 73.0 ± 117.5. Egg densities on young S. exaltata were 59.3 ± 35.2/100 cm2 (8 May), but declined over subsequent weeks and were in the lowest group statistically 25 May–11 June.
Nymph densities overall were much lower than egg densities (Table 2). Nymph densities on E. fosbergii were highest on 25 May (64.6 ± 2.9 per 100 cm2) which was not statistically different from densities on A. theophrasti. Nymph densities on E. fosbergii declined over subsequent weeks, while densities on A. theophrasti and C. obtusifolia increased, reaching 180.1 ± 42.3 per 100 cm2 on A. theophrasti and 171.4 ± 60.2 on C. obtusifolia (not statistically different from each other). Densities on B. alba and I. lacunosa remained below 21 nymphs per 100 cm foliage and did not separate statistically on any sample date. Nymph densities were lowest on A. retroflexus and S. exaltata, not surpassing 6.8 ± 1.7 per 100 cm2 on any sample date.
Table
Table 2. Mean (±SE) B. tabaci nymph densities on whole plants of selected weeds in 2012. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Table 2. Mean (±SE) B. tabaci nymph densities on whole plants of selected weeds in 2012. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
B. tabaci Nymphs per 100 cm2 Leaf Area (Mean ± SE)
Weed Species16 May25 May4 June11 June
A. retroflexus-1.1d (0.9)4.3d (3.2)5.9d (2.2)
A. theophrasti33.2a (27.3)60.4ab (23.2)166.8a (31.8)180.1a (42.3)
B. alba0.4a (0.4)4.2cd (2.5)9.4cd (3.9)10.3cd (4.9)
C. obtusifolia17.9a (5.5)17.5b (3.2)53.7b (11.0)171.4a (60.2)
E. fosbergii-64.6a (2.9)22.8bc (6.9)38.3b (4.4)
I. lacunosa7.3a (2.5)6.7c (2.7)18.0c (8.5)20.6bc (9.0)
S. exaltata5.2a (1.7)2.2cd (1.2)6.8cd (1.7)6.6d (5.4)
F6,182.68 (F4,12)14.6414.3322.36
p-value0.0834<0.0001<0.0001<0.0001

3.2. 2013

Egg and nymph densities were much lower overall in 2013 than 2012. Egg densities were very low in all weed species prior to April 30 (<7 eggs per 100 cm2). Egg densities on A. theophrasti, E. fosbergii and S. acuta peaked between 15 May and 3 June (Table 3). The greatest egg densities were observed on A. theophrasti on 28 May (147.0 ± 47.7 per 100 cm2); the highest egg densities observed on both E. fosbergii and S. acuta were ~53 per 100 cm2 foliage. As in 2012, egg densities were highest on most dates on A. theophrasti and comparable on some dates on E. fosbergii. Egg densities on C. obtusifolia were low relative to these two species in 2013. Egg densities on C. obtusifolia peaked on 17 May (17.0 ± 4.3 per 100 cm2). Egg densities on S. americanum increased till 10 June, peaking at 28.5 ± 9.7 per 100 cm2. Unlike egg densities on other species that increased to a point then declined, densities on A. retroflexus, B. alba and I. lacunosa remained constant and low throughout the trial, similar to what was observed in 2012. Egg densities averaged less than 11 per 100 cm2 on I. lacunosa, less than 9 per 100 cm2 on A. retroflexus, and less than 4 per 100 cm2 on B. alba. Eggs were rarely observed on S. exaltata in 2013.
There were no statistical differences in the density of nymphs among weed species prior to May 28 (Table 4). Nymph densities were highest on A. theophrasti and E. fosbergii during most of the sample period (28 May–1 July). Nymph densities on S. americanum were not statistically different from densities on A. theophrasti or E. fosbergii on a number of sample dates between 28 May and 1 July. Nymph densities peaked on S. acuta on May 28 (33.9 ± 3.2 per 100 cm2) when they were not statistically different from densities on A. theophrasti, E. fosbergii or S. americanum. Nymph densities on C. obtusifolia also peaked on 28 May, averaging 16.1 per 100 cm2. Nymph densities on A. retroflexus, B. alba and I. lacunosa remained low (<6 per 100 cm2) throughout the trial.
Table
Table 3. Mean (±SE) B. tabaci egg densities on whole plants of selected weeds in 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Table 3. Mean (±SE) B. tabaci egg densities on whole plants of selected weeds in 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Weed SpeciesB. tabaci Eggs per 100 cm2 Leaf Area (Mean ± SE)
30 April15 May28 May3 June10 June17 June1 July
A. retroflexus1.8b (0.8)6.4cd (2.8)3.0d (1.0)2.0c (0.8)8.8cd (3.3)4.6bc (3.0)-
A. theophrasti1.3bc (1.0)72.1a (20.6)147.0a (47.7)99.6a (28.8)140.9a (20.2)31.5a (6.9)5.6ab (2.1)
B. alba0.1c (0.1)1.4d (0.2)1.2d (0.6)2.0c (0.6)3.4de (1.3)0.4c (0.2)0.7cd (0.5)
C. obtusifolia1.4bc (0.8)17.0b (4.3)6.3cd (2.8)2.6c (0.6)1.4e (0.6)0.4c (0.2)0.0d (0.0)
E. fosbergii1.6b (0.3)9.6bc (5.7)17.3bc (4.3)52.3a (14.1)44.8b (11.2)6.3b (4.0)14.1a (6.9)
I. lacunosa0.2c (0.1)10.2bc (3.1)6.5cd (3.0)6.1c (4.2)4.0de (1.7)0.4c (0.2)0.4cd (0.3)
S. acuta5.6a (1.5)52.9a (14.9)28.1b (2.2)17.4b (2.5)28.2bc (16.9)4.1b (1.3)1.8cd (1.1)
S. americanum0.6bc (0.2)8.8bc (3.6)7.3cd (4.0)19.6b (7.9)28.5b (9.7)7.2b (3.3)2.2bc (0.8)
F7,215.2410.239.7617.1321.269.198.19 (F6,18)
p-value0.0014<0.0001<0.0001<0.0001<0.0001<0.00010.0002
Table
Table 4. Mean (±SE) B. tabaci nymph densities on whole plants of selected weeds in 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Table 4. Mean (±SE) B. tabaci nymph densities on whole plants of selected weeds in 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Weed SpeciesB. tabaci Nymphs per 100 cm2 Leaf Area (Mean ± SE)
30 April15 May28 May3 June10 June17 June1 July
A. retroflexus0.1a (0.1)0.8a (0.4)4.9c (1.3)2.2d (0.2)3.6c (1.1)5.9cd (0.7)-
A. theophrasti0.9a (0.9)12.7a (11.0)50.2ab (42.3)47.4a (7.1)23.8ab (10.2)58.6a (14.4)12.5a (0.8)
B. alba0.1a (0.0)0.3a (0.1)4.4c (0.5)2.4d (0.7)2.5c (0.4)4.2c–e (1.6)2.9bc (0.9)
C. obtusifolia0.4a (0.3)2.1a (0.8)16.1b (3.7)7.6c (2.6)3.1c (1.1)3.1de (0.5)0.6c (0.2)
E. fosbergii0.3a (0.1)1.6a (0.6)49.5a (7.8)42.4a (5.9)41.4a (6.8)31.3ab (9.5)25.8a (10.7)
I. lacunosa0.1a (0.1)0.9a (0.2)4.5c (2.2)2.2d (1.5)2.4c (1.0)1.4e (0.2)0.5c (0.4)
S. acuta0.6a (0.4)5.3a (1.5)33.9ab (3.2)15.5b (1.2)15.5b (6.7)9.4c (2.3)2.2c (0.3)
S. americanum0.0a (0.0)0.7a (0.1)20.1ab (6.6)11.5bc (1.3)17.8b (4.6)34.1b (14.1)8.5ab (3.2)
F7,210.642.056.3827.8211.5418.779.34 (F6,18)
p-value0.71990.09540.0004<0.0001<0.0001<0.0001<0.0001
Table
Table 5. Mean (±SE) B. tabaci egg and nymph densities and nymph:egg ratio averaged over samples in 2012 and 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Table 5. Mean (±SE) B. tabaci egg and nymph densities and nymph:egg ratio averaged over samples in 2012 and 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Weed Species8 May–11 June, 201215 May–10 June, 2013
B. tabaci per 100 cm2 (Mean ± SE)Nymphs per Egg (Mean ± SE)B. tabaci per 100 cm2 (Mean ± SE)Nymphs per Egg (Mean ± SE)
EggsNymphsEggsNymphs
A. retroflexus56.2d (10.3)3.8d (1.1)0.07bc (0.02)5.1d (1.7)2.9d (0.4)0.68cd (0.15)
A. theophrasti354.6b (66.0)88.1a (16.6)0.25a (0.00)114.9a (20.2)33.5a (13.0)0.29e (0.09)
B. alba39.1d (7.2)6.1cd (1.7)0.15a–c (0.03)2.0e (0.5)2.4d (0.3)1.34a (0.24)
C. obtusifolia325.6b (54.5)52.1ab (12.9)0.16ab (0.03)6.8d (0.4)7.2c (1.2)1.11ab (0.26)
E. fosbergii979.4a (43.3)41.9b (2.7)0.04c (0.00)31.0b (3.4)33.7a (2.7)1.11ab (0.11)
I. lacunosa109.1c (5.3)10.5c (3.2)0.09bc (0.02)6.7d (1.3)2.5d (0.6)0.37de (0.04)
S. acuta---31.6b (7.0)17.5b (2.1)0.61cd (0.09)
S. americanum---16.0c (1.7)12.5b (1.8)0.80bc (0.11)
S. exaltata21.8e (7.6)4.2d (1.4)0.25a (0.11)---
F6,1873.4635.534.31
F7,21 63.07 41.509.16
p-value<0.0001<0.00010.0072<0.0001<0.0001<0.0001

3.3. Nymph to Egg Ratios

There were significant differences among weed species in the ratio of nymphs to eggs each season (Table 5). In 2012, the highest nymph to egg ratio was observed in A. theophrasti and S. exaltata (1:4), followed by B. alba and C. obtusifolia (about 1: 6.5). Less than one nymph per ten eggs was observed in A. retroflexus, E. fosbergii and I. lacunosa. In 2013, overall numbers of eggs and nymphs were much lower across weed species compared to 2012. However the ratio of nymphs to eggs tended to be higher, indicating a higher proportion of surviving nymphs relative to the number of eggs. Densities of nymphs on B. alba, C. obtusifolia, and E. fosbergii were slightly higher than egg densities from May 15 to June 10. Female B. tabaci may have responded to senescing of the other host plants during this time period by ovipositing fewer eggs on these weeds, resulting in the highest nymph to egg ratio on these three species in 2013.
To determine if differences in nymph densities across weed species were related to differences in the number of nymphs successfully completing development, data were collected in 2013 on the number of B. tabaci nymphs in first, mid (2nd–3rd) and fourth instars. (The previous year we simply recorded nymph numbers without regard to instar.) Fourth instar nymphs were first observed on B. alba and S. acuta on 30 April, and on all other weeds except A. retroflexus and A. theophrasti by 15 May. Fourth instar nymphs were observed on A. retroflexus and A. theophrasti by 28 May. Exuviae were also observed on each weed species, but were in some cases too damaged to determine if they presented an adult B. tabaci exit hole, a parasitoid exit hole, or if they had been fed upon by a predator. For this reason the fourth instar was used as evidence that a certain percentage of nymphs were completing their life cycle on the host. Overall, the percentage of fourth instar nymphs was not statistically different among weed species when nymph counts from all sample dates are pooled (Table 6). This suggests that the proportion of nymphs completing development was similar for each weed species. The overall percentage of fourth instar nymphs was generally low for most species, ranging from around 4% for A. theophrasti and S. americanum to around 10 percent for A. retroflexus, B. alba and C. obtusifolia.
Table
Table 6. Mean (±SE) B. tabaci non-parasitized nymphs, 4th instar nymphs and % 4th instar nymphs per sample in 20table13. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Percent 4th instars were transformed arcsine [√(x/100)], other data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Table 6. Mean (±SE) B. tabaci non-parasitized nymphs, 4th instar nymphs and % 4th instar nymphs per sample in 20table13. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Percent 4th instars were transformed arcsine [√(x/100)], other data were transformed log10(x + 1) prior to ANOVA; non-transformed means are presented.
Weed SpeciesAverage of 24 Apr–1 July
B. tabaci per Sample (Mean ± SE)% 4th Instars
1st–4th Instars4th Instars(Mean ± SE)
A. retroflexus11.6d (3.6)1.4d (0.5)10.35a (4.31)
A. theophrasti205.3ab (37.5)11.7b (4.8)3.85a (1.36)
B. alba24.7c (4.9)2.9c (0.7)10.31a (1.26)
C. obtusifolia144.2b (71.2)7.6b (2.2)10.28a (1.80)
E. fosbergii275.8a (23.3)26.6a (4.7)7.39a (2.00)
I. lacunosa18.8cd (2.7)1.9cd (0.6)8.60a (3.29)
S. acuta94.8b (14.2)7.8b (2.6)5.96a (0.65)
S. americanum140.5ab (35.2)7.4b (1.6)4.40a (0.69)
F6,1819.6922.591.61
p-value<0.0001<0.00010.1863

3.4. Parasitism

Because of slow germination and growth, S. acuta and S. americanum were only sampled on 11 and 17 July 2012. By contrast, all I. lacunosa plants had senesced in 2012 before parasitism was observed. Higher levels of parasitism were observed for each species in 2012 than 2013 with the exception of S. americanum, which supported about 1% parasitism each year (Table 7). The highest percent of parasitism in 2012 was observed on B. alba (32.3%), followed by C. obtusifolia (23.4%) and S. acuta (17.5%) when sample dates in July were pooled. The highest percent parasitism observed for these species on a given week in 2012 was 58.6 (±15.9) % for B. alba (11 July), 36.8 (±17.6) for C. obtusifolia (2 July) and 28.8 (±24.0) % for S. acuta (17 July). In 2013, there were no statistical differences among weed species with regard to percent parasitism, which ranged from 0.4% in A. theophrasti to 2.8% in C. obtusifolia. The highest percent parasitism measured on a given week in 2013 was 14.6% on C. obtusifolia on 10 June, which was not statistically different from parasitism on E. fosbergii (7.8%) or S. americanum (7.2%) (F7,21 = 5.72, p = 0.0008). Percent parasitism was never greater than 10% on any given week for I. lacunosa in 2013. It was never greater than 7% on any week for S. acuta or 6% for B. alba that year. Percent parasitism was consistently less than 2% for A. retroflexus and A. theophrasti in 2013.
Of the 206 parasitoids reared out over the two seasons, 199 (96.6%) were Encarsia spp. and less than 4% were Eretmocerus spp (Table 8). Fourteen percent of Encarsia were identified as E. sophia and 12.5% were identified as E. tabacivora.

4. Conclusions

4.1. Colonization of Weed Hosts

Densities of B. tabaci were generally lower in 2013 than in 2012. A cause for the apparent differences between the two trials may have been weather conditions. The average temperature in May of 2013 was 23 °C, which as 2° C lower than that in May of 2012. [26]. Total rainfall for April and May were 3.4 cm and 4.7 cm respectively in 2012 compared to 10.6 cm and 9.0 cm for the same months in 2013.
Exposure to intense rain events can reduce whitefly populations [27] but non-severe rain events do not typically increase mortality of B. tabaci compared to B. tabaci protected conditions [28]. We do not expect that the increase in rain alone in 2013 reduced populations relative to 2012. Rather, plant establishment conditions in 2013 were generally cooler and wetter than in 2012, and we suspect that this slowed the build-up of B. tabaci populations during the second season. In 2013, all weed seedlings were transplanted into the field on the same day at a similar phenological stage to avoid the varied development times that occurred when weeds were grown from seed in the field in 2012. Most weeds were in the field for similar numbers of weeks each year, so we do not believe the overall difference in B. tabaci numbers in the two years was due to differences in exposure time to the pest.
Table
Table 7. Mean (±SE) B. tabaci nymph densities and % parasitism on whole plants of selected weeds in 2012 and 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Nymph densities were transformed, log10(x + 1), and % parasitism transformed arcsine [√ (%x/100)] prior to ANOVA; non-transformed means are presented.
Table 7. Mean (±SE) B. tabaci nymph densities and % parasitism on whole plants of selected weeds in 2012 and 2013. Means within a column followed by the same letter are not significantly different (p < 0.05) by Fisher’s Protected LSD. Nymph densities were transformed, log10(x + 1), and % parasitism transformed arcsine [√ (%x/100)] prior to ANOVA; non-transformed means are presented.
Weed SpeciesMean B. tabaci Nymphal Densities Averaged over Samples & % Parasitism (Mean ± SE)
-------------------- 2012, July (per Plant) --------------------------------- 2013, April-July (per Plant) -------------
TotalParasitized% ParasitismTotalParasitized% Parasitism
A. retroflexus3.7d (1.6)0.3d (0.2)7.9cd (6.5)13.5d (4.2)0.2c (0.1)1.1ab (0.7)
A. theophrasti16.9cd (8.9)0.4cd (0.3)6.2cd (4.0)235.4ab (43.3)1.2bc (1.1)0.4b (0.4)
B. alba37.6bc (7.3)11.3a (1.8)32.3a (5.6)28.6c (5.8)0.6bc (0.2)2.1a (0.5)
C. obtusifolia124.5ab (51.9)19.6a (4.2)23.4ab (7.2)166.9b (81.7)2.2b (0.5)2.8a (1.7)
E. fosbergii119.5ab (71.9)3.7b (0.8)6.8b–d (2.5)322.5a (25.5)7.6a (1.2)2.5a (0.6)
I. lacunosaa---22.0cd (3.3)0.5c (0.2)2.2a (0.6)
S. acuta14.8cd (4.9)3.4b–d (2.1)17.5a–c (7.3)109.6b (17.0)1.5bc (0.9)1.1ab (0.6)
S. americanum243.0a (43.3)2.9bc (1.6)1.0d (0.4)161.9ab (40.1)1.4bc (0.5)1.1ab (0.6)
F6,1810.2012.094.0219.86 (F7,21)6.95 (F7,21)1.83 (F7,21)
p-value<0.0001<0.00010.0100<0.00010.00020.1344
a I. lacunosa had senesced before parasitism was observed.
Table
Table 8. Parasitoids reared from Bemisia tabaci on weeds at GCREC, Balm, Florida in 2012 and 2013.
Table 8. Parasitoids reared from Bemisia tabaci on weeds at GCREC, Balm, Florida in 2012 and 2013.
Weed SpeciesParasitoid Taxa and No. of Specimens Identified
Encarsia spp.E. citrellaE. luteolaE. sophiaE. tabacivoraEretmocerus spp.
A. retroflexus0-1122
A. theophrasti19-14102
B. alba361-6--
C. obtusifolia55--1193
E. fosbergii6--34-
I. lacunosa221-1--
S. acuta1-----
S. americanum---2--
Total1422228257
In 2012, egg densities were highest on A. theophrasti, C. obtusifolia and E. fosbergii relative to other weed hosts. Egg densities tended to be highest on these three weeds in 2013 also, although not to the same degree as in the previous year. Choice studies have demonstrated that Bemisia tabaci will preferentially settle on and colonize some weed hosts in greater numbers than others [18,29,30]. Once the host plant has been accepted, oviposition by Bemisia tabaci is influenced by a number of host plant characteristics including type and density of trichomes, leaf waxiness, and secondary plant compounds, as well as the nutritional status and age of the plant [31]. Densities of several hundred eggs per 100 cm2 measured during some weeks on these hosts are comparable to densities measured on favored economic hosts such as cantaloupe [32].
Egg densities on A. theophrasti, C. obtusifolia and E. fosbergii were also high relative to nymph densities. Nymph to egg ratios may vary on different species because of a number of factors. Gachoka et al. [30] observed that percent egg hatch of B. tabaci varied significantly among different weed species, ranging from as low as 0% on A. retroflexus and Malvastrum coromandelianum L. (Garcke) to 63.6% on Desmodium tortuosum (Sw.) DC. Researchers have noted that B. tabaci mortality tends to be highest in the first instar, particularly the crawler stage [30,33,34]. Key predators of whiteflies, including coccinellids and predatory mites, feed preferentially on B. tabaci eggs and early instars [35]. The same leaf characteristics that influence host acceptance and oviposition by whiteflies, such as type and density of trichomes, degree of pubescence, waxiness, and leaf texture, can also effect searching and the degree of mortality inflicted by predators and parasitoids [36,37]. Additional studies are needed to determine whether differential survival of nymphs on distinct weed hosts is due to differences in host suitability, differences in predation rates, including host feeding by parasitoids, or a combination of factors.
Unlike other studies which have evaluated colony-reared B. tabaci host choice and development on weeds under controlled conditions [28,30,38], we measured egg and nymph densities produced by naturally occurring whitefly populations under field conditions. Our data indicate that oviposition by B. tabaci can be high on A. theophrasti, E. fosbergii and C. obtusifolia, and that these weeds can support significant B. tabaci populations.
Compared to these hosts, Bidens alba supported moderate to low densities of whitefly nymphs, but at least in 2012, comparatively high levels of parasitism. Our findings are consistent with those of Stansly et al. [20] who measured up to 52% parasitism on the closely related B. pilosa. Whether B. alba has a primarily positive or negative effect on managing B. tabaci in the region may depend on its as yet undetermined role as a reservoir for TYLCV.
Amaranthus retroflexus has been described as a poor and possibly even a non-host of Bemisia tabaci in other studies [18,28,30,38]. While egg densities were relatively high in 2012 on A. retroflexus, they were very low in 2013, and nymph densities were consistently very low, not surpassing 6 nymphs per 100 cm2 (11 June 2012 and 17 June 2013). Percent parasitism on A. retroflexus was 7.9 in 2012, not significantly different from percent parasitism on A. theophrasti, E. fosbergii, and S. americanum, although these weed hosts had significantly higher nymph densities than A. retroflexus on most weeks in 2012 and 2013. As a poor host of B. tabaci which supports levels of parasitism similar to levels observed on heavily infested weeds, A. retroflexus may play a mitigating role in the development of B. tabaci populations. Papayiannis et al. [13] detected TYLCV in field collected A. retroflexus on Cyprus. The influence of A. retroflexus on whitefly-related pest problems in Florida may depend on its as yet undetermined role in the epidemiology of TYLCV.
In addition to being a host of B. tabaci, S. americanum is a host of pepper weevil (Anthonomus eugenii Cano) [39]. Its congener, Solanum nigrum L., has been identified as a host of TYLCV in several studies [40]. Stansly et al. [20] observed 26.5% parasitism of B. tabaci on S. americanum, which was higher than what we observed in either year. Stansly et al. [20] recorded 34.9% parasitism B. tabaci on S. acuta. We observed 28.8% parasitism in S. acuta during the week of July 17, 2012, and 17.5% parasitism overall for the season. Sida acuta has been identified as a host of Tomato yellow leaf curl Tanzania virus [41].
As its common name implies, the sweetpotato whitefly has a long documented association with plants in the genus Ipomoea [42,43,44] and other genera in the Convolvulaceae [10,12]. Whitefly-transmitted geminiviruses of Ipomoea are distributed globally [45]. We consistently detected moderate or low levels of eggs and nymphs on I. lacunosa during each season of study. Ipomoea lacunosa germinated and grew rapidly when planted from seed in 2012, but senesced just as rapidly, with no parasitism recorded that year. Percent parasitism was generally low on I. lacunosa in 2013, with the highest level (9.5%) measured on 17 June.
Densities of B. tabaci eggs and nymphs were consistently low on S. exaltata in 2012, and whiteflies were extremely rare on this host in 2013 with the result that sampling of this was abandoned that year. Leaflets on S. exaltata are small—8 mm × 3.5 cm or less [46], providing a limited substrate for whitefly to oviposit on or for the completion of nymphal development.

4.2. Parasitoids

Consistent with other surveys of whitefly parasitoids in Florida, we recovered primarily Encarsia spp. parasitoids and a low number of Eretmocerus [23,47,48]. Of the Encarsia species that could be identified to species, 14% were E. sophia, and 12.5% were E. tabacivora. Further investigation is required to determine if differences in percent parasitism on weeds was influenced by leaf characteristics of different hosts. For example, McAuslane et al. [47] determined that leaf hairiness influenced percentage parasitism of whitefly on soybean (Glycine max L (Merr.)) in Florida, with E. nigricephala and E. transvena (a synonym of E. sophia) more common on glabrous than hirsute soybean, while the opposite was true of E. pergandiella and Er. nr. californicus. Tests on collards (Brassica oleracea var. acephala L.) in Florida demonstrated that while waxiness did not affect parasitism by Eretmocerus sp., more than 4.5 times as many E. pergandiella individuals emerged from collards with glossy leaves versus those with normal wax [49].
Although B. tabaci densities were much lower in 2013 than 2012, a similar pattern with regard to weed colonization was revealed each year. Oviposition on A. theophrasti, C. obtusifolia and E. fosbergii indicated that these three weed species can support high densities of B. tabaci under favorable conditions. By contrast B. tabaci densities on B. alba, A. retroflexus and I. lacunosa were consistently moderate or low, and numbers on S. exaltata were negligible each season. Among these weed species, B. alba tends to dominate uncultivated areas in parts of west central Florida to a greater extent than other species. The high numbers of parasitized nymphs observed on some dates in 2012 confirm that some weeds can support significant parasitism of B. tabaci and provide alternate parasitism sites for key parasitoids of B. tabaci in Florida, primarily Encarsia and Eretmocerus spp.
Our data indicate that the proportion of B. tabaci completing development from egg to adult on most species was often low. Additional studies are needed to reveal the primary factors affecting survival of immature B. tabaci on different weed hosts. Weeds with characteristics that are moderately favorable for whiteflies, such as B. alba and A. retroflexus, but suitable for significant levels of parasitism, may play a positive role in mitigating over-summering populations of whitefly. However it must first be confirmed that these and other weeds do not play a significant role in the epidemiology of Tomato yellow leaf curl and other plant viruses in central and south Florida.

Acknowledgments

Steven Kalb, Yankai Li, Tim Cummings, Bryan Hammons, Deborah Farr and Justin Carter assisted with this research.

Author Contributions

Hugh Smith and Curtis Nagle collaborated on experimental design, data collection, data analysis and manuscript preparation. Greg Evans identified whitefly parasitoids and helped prepare the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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MDPI and ACS Style

Smith, H.A.; Nagle, C.A.; Evans, G.A. Densities of Eggs and Nymphs and Percent Parasitism of Bemisia tabaci (Hemiptera: Aleyrodidae) on Common Weeds in West Central Florida. Insects 2014, 5, 860-876. https://doi.org/10.3390/insects5040860

AMA Style

Smith HA, Nagle CA, Evans GA. Densities of Eggs and Nymphs and Percent Parasitism of Bemisia tabaci (Hemiptera: Aleyrodidae) on Common Weeds in West Central Florida. Insects. 2014; 5(4):860-876. https://doi.org/10.3390/insects5040860

Chicago/Turabian Style

Smith, Hugh A., Curtis A. Nagle, and Gregory A. Evans. 2014. "Densities of Eggs and Nymphs and Percent Parasitism of Bemisia tabaci (Hemiptera: Aleyrodidae) on Common Weeds in West Central Florida" Insects 5, no. 4: 860-876. https://doi.org/10.3390/insects5040860

APA Style

Smith, H. A., Nagle, C. A., & Evans, G. A. (2014). Densities of Eggs and Nymphs and Percent Parasitism of Bemisia tabaci (Hemiptera: Aleyrodidae) on Common Weeds in West Central Florida. Insects, 5(4), 860-876. https://doi.org/10.3390/insects5040860

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