Malpighian Tubule Cells in Overwintering Cave Crickets Troglophilus cavicola (Kollar, 1833) and T. neglectus Krauss, 1879 (Rhaphidophoridae, Ensifera).

During winter, cave cricket larvae undergo dormancy in subterranean habitats; this dormancy is termed diapause in second year Troglophilus cavicola larvae because they mature during this time, and termed quiescence in T. neglectus, because they mature after dormancy. Here we used electron microscopy to analyze ultrastructural changes in the epithelial cells in the Malpighian tubules (MTs) of T. cavicola during diapause, in order to compare them with previous findings on T. neglectus. Moreover, the autophagosomes were studied with immunofluorescence microscopy in both species. Although the basic ultrastructure of the cells was similar, specific differences appeared during overwintering. During this natural starvation period, the nucleus, rER, the Golgi apparatus and mitochondria did not show structural changes, and the spherites were exploited. The abundances of autophagic structures in both species increased during overwintering. At the beginning of overwintering, in both species and sexes, the rates of cells with autophagic structures (phagophores, autophagosomes, autolysosomes and residual bodies) were low, while their rates increased gradually towards the end of overwintering. Between sexes, in T. cavicola significant differences were found in the autophagosome abundances in the middle and at the end, and in T. neglectus at the end of overwintering. Females showed higher rates of autophagic cells than males, and these were more abundant in T. cavicola. Thus, autophagic processes in the MT epithelial cells induced by starvation are mostly parallel in diapausing T. cavicola and quiescent T. neglectus, but more intensive in diapausing females.

Introduction

The rhaphidophoridan cave crickets (Rhaphidophoridae, Ensiphera) are scotophilic, nocturnal Ensifera inhabiting tropical, subtropical and temperate regions [1-6]. Many of them seek for shelters in caves and other subterranean habitats, or they overwinter there, and a few are adapted for permanent living in subterranenan habitats. In Europe the family is represented by the genera Dolichopoda and Troglophilus, with about 70 species described to date [7, 8]. Only the genus Troglophilus Krauss, 1879 extends its range to central Europe, with two of the 19 species described until recently: T. neglectus Krauss, 1879 and T. cavicola (Kollar, 1833) [8-17]. They are among the most numerous invertebrates, with the largest fresh and dry mass bulk among invertebrates overwintering in central European caves [18].

During overwintering, the larvae of both cave cricket species do not feed, as is typical in insects during dormancy, which is a state of temporarily reduced metabolic activity during unfavorable conditions [19]. The larvae of T. cavicola hatch in May and live in epigean habitats until the late autumn. The younger larvae enter hypogean habitats (in the following text: caves) and overwinter there in quiescence from November until March. Then they live outside until the next autumn when they return, as older larvae, to the caves for the second time. During the second overwintering, they carry out a diapause reaching their maturity, mate and lay eggs in March, and die by June [10, 13, 20, 21]. These conditions are similar in T. neglectus, but these enter caves 2–4 weeks later and leave them 2–4 weeks earlier, carrying out a quiescence during both overwintering periods [11, 20, 21]. Older T. neglectus larvae mature, mate and lay eggs in late June or July. Thus, both Troglophilus species are convenient subjects for studying the influences of stress conditions caused by natural starvation.

The Malpighian tubules (MTs) are the most important excretory and osmoregulatory organs in many myriapods, arachnids and insects [22]. As for their function, the MTs can be compared with the vertebrate kidney tubules, since both transport organic solutes, break down and remove or excrete toxic substances, and maintain ionic balance and immune defenses [23, 24]. MTs actively and passively absorb water and ions from the hemolymph inside the coelom and convert waste metabolites into urine compounds, which move towards the hindgut. The rectum performs osmoregulation within the body by reuse of water and ions [25]. MTs are blind-end tubular organs which extend from the midgut–hindgut junction into the hemocoel. The MT is composed by a single-layered epithelium and individual muscle cells, which are thought to mix the contents of the MT and displace the MT in the haemolymph [22]. The plasma membrane of the epithelial cell is characterized by numerous apical microvilli and numerous prominent infoldings in its basal part. These cells transport fluid and solutes and have a storage role [26].

Autophagy is an evolutionarily conserved self-digestive process in eukaryotic cells adapted to nutrient starvation [27, 28]. It is a common response in starving invertebrates providing cells with needed nutrients [29-32]. The LC3 protein is specifically associated with autophagosomes; consequently, an increase in the amount of the LC3 protein correlates well with an increased number of autophagosomes [33].

Because the two closely related cave cricket species, Troglophilus cavicola and T. neglectus, implement different overwintering strategies during the second year, they are of special interest for comparison to find eventual differences between diapause and quiescence on the cell level. During overwintering, cave crickets do not feed.

Changes in the following two organs are best representative for understanding this natural starvation period. The fat body is the central storage depot for excess nutrients [34] intensively supplying energy for maintaining overwintering insects alive. Besides, MTs show the final products of the cell homeostasis processes during this period. They maintain constant internal environment through the elimination or segregation of waste substances [35, 36]. The MT epithelial cells are appropriate for this study because they contain the final compounds prior to excretion. Consequently, these two organs were of major interest in our research. The fat body had previously been studied in both T. cavicola and T. neglectus [37, 38] and the MT epithelial cells had been researched in T. neglectus [21]. In this study we complete the previous research on the MTs of T. cavicola. We asked how epithelial MT cells respond in the diapausing T. cavicola. Our aim was to analyze the ultrastructure of these cells, and to estimate the number of autophagosomes within these cells in both species during overwintering. For this purpose, autophagic structures in the MT epithelial cells were examined in both species. It was hypothesized that the abundance of the autophagic structures will increase from the beginning until the end of overwintering in both species. A higher number of autophagosomes was expected in diapausing T. cavicola with respect to quiescent T. neglectus. Finally, we summarize the findings in the fat body and MT epithelial cells in diapausing T. cavicola vs. quiescent T. neglectus.

Material and Methods

Material

The cave crickets T. cavicola and T. neglectus were collected from four caves in central northern Slovenia (locality centroid 46°24´55˝ N, 15°10´31˝ E, altitudes 600–740 m), in the territory of the Republic Slovenia with a state permission to one of the co-authors for such researches. These species are neither endangered nor protected. In previous studies on MTs and the fat body it was found that individual differences in the MT cells structure are very limited, and their ultrastructures are comparable [21, 37]. In the pre-study on 30 individuals of each species and sex we found a unified ultrastructure within the cells. Therefore, for the current study, seven T. cavicola and T. neglectus of each sex were analyzed microscopically just before the beginning (November) (in the following text: beginning), in the middle (January) and at the end (March) of overwintering. In each individual 25 MTs were analyzed by light microscopy and transmission electron microscopy (TEM) and 25 MTs by immunofluorescence microscopy (IFM). In each time frame/species/sex at least 300 cells were examined, and representative images are shown here.

Methods

The middle section of MTs, embracing about 90% of a MT, with typical epithelial cells was investigated. The structure of the MTs epithelial cells in T. cavicola was examined by light microscopy and transmission electron microscopy (TEM), as had been done in T. neglectus [21], and both species were examined by immunofluorescence microscopy (IFM) for LC3 localization in autophagosomes at the three time frames during overwintering. We used the marker LC3B primary antibody, commonly used in studies of autophagy [33].

Light and transmission electron microscopy (TEM)

The MTs were fixed in 2.45% glutaraldehyde and 2.45% paraformaldehyde in a 0.1 M sodium cacodylate buffer (pH 7.4) at room temperature for 2 hrs and at 4°C for 12 hrs. The tissue was washed in a 0.1 M sodium cacodylate buffer (pH 7.4) at room temperature for 3 hrs and postfixed with 2% OsO4 at room temperature for 2 hrs. The samples were dehydrated in a graded series of ethanol (50%, 70%, 90%, 96%, 100%, each for 30 minutes at room temperature) and embedded in TAAB epoxy resin (Agar Scientific Ltd., Essex, England). For light microscopy, semi-thin sections (5 μm) were used stained with 0.5% toluidine blue in aqueous solution. For TEM, ultra-thin sections (70–75 nm) of the MTs were transferred onto copper grids, stained with uranyl acetate and lead citrate and analyzed with a Zeiss EM 902 transmission electron microscope.

Ultra-thin sections have been used in order to estimate the ratios of epithelial cells containing autophagic structures−phagophores, autophagosomes, autolysosomes and residual bodies−to the total number of cells in the sample. For this measurement, 100 MT epithelial cells for each time frame and each sex were randomly selected. Random counting was carried out at 3000x magnification.

Immunofluorescence microscopy (IFM) for LC3 localization

The MTs were dissected in phosphate buffered saline (PBS) and fixed in 3.7% formaldehyde (in PBS as diluent) for 20 min at room temperature. The tissue was rinsed with PBS-Tx (PBS containing 0.2% Triton X 100) three times for 5 min each, and permeabilized in 0.2% Triton X 100 in PBS for 20 min at room temperature. To block possible non-specific binding, the tissue was incubated in BlockAid™ Blocking Solution (Molecular Probes) for 1 hour at room temperature. Afterwards, the samples were rinsed with PBS-Tx three times for 5 min each and treated with primary antibodies LC3B (rabbit polyclonal antibody, Molecular Probes, Cat. Nr. L10382) diluted in PBS-Tx (1:250) for 14 hours at 4°C. The tissue was washed with PBS-Tx three times for 5 min each, incubated with secondary goat anti-rabbit IgG antibodies (Molecular Probes) diluted in PBS-Tx (1:100) for 2 hours at room temperature, and washed with PBS-Tx three times for 5 min each. The epithelial cells of the MTs were examined under an inverted confocal laser scanning fluorescence microscope Leica TCS SP5 II. The samples were excited with Argon laser line at 488 nm. Quantification of autophagosomes in the MT cells was performed on unitary image areas [39] in November, January and March. We used the images of immunofluorescence microscopy acquired with a 40x oil immersion objective (NA 1.30) at 800x magnification after applying LC3 to localize the autophagosomes. To control for potential false-positive signals from the immunofluorescence analyses, the pieces of the MTs were incubated with secondary antibodies without the primary antibody.

Statistical analysis

The abundances of autophagosomes in the MTs epithelial cells were tested for normality of distribution using the Kolmogorov-Smirnov test. The distribution of autolysosome abundance was not normal in November, but normal in January and March. Therefore, the differences between the abundances of autophagosomes at different time frames, between the sexes and between the two species were tested using the The Mann-Whitney U test, which does not require normal distributions.

Results

Malpighian tubules

About 50–60 MTs (Fig 1) extended from the midgut-hindgut junction in T. cavicola (Fig 2a) and T. neglectus (Fig 2b). These were unevenly scattered in the haemocoel between the digestive tract and the body wall. In the MTs, three morphologically distinct regions could be distinguished: the proximal, the middle and the distal region. The middle part of the MT occupied its major portion, while the proximal and the distal regions each measured less than 10% of the MT length. The outer diameters of the proximal and the distal regions were about 50 μm and that of the middle portion 60–80 μm. The MTs were composed of the epithelium and individual muscle cells attached to the outer MT surface. The epithelium of the middle part of the MT consisted of columnar cells and the basal lamina (Fig 2a and 2b).

Fig 1

A part of the Malpighian tubule (MT) of T. cavicola at the beginning of overwintering.

Light microsccopy allows to see the general appearance of a MT composed of the epithelium (EP), and the lumen (LU).

Fig 2

Semithin cross-section of the Malpighian tubule (MT) in T. cavicola (a) and T. neglectus (b) at the beginning of overwintering.

The epithelium is composed of columnar epithelial cells (EC) and underlying basal lamina (BL). The apical plasma membrane of the ECs is differentiated into the brush border (BB). The cytoplasm is filled with numerous spherites (S). LU, lumen of the MT; MC, individual muscle cells; N, nucleus of the epithelial cell. Note that this figure shows an oblique transection of the MT.

The general structure of the MT epithelial cells was comparable throughout overwintering, but showed some changes in the structure of spherites, and in the presence of autophagic structures. In January and March, various autophagic structures were present in the cells.

Beginning of overwintering

The apical plasma membrane of the epithelial MT cells of T. cavicola was differentiated into microvilli of up to 5 μm in length, forming a brush border in the tissue observed by light microscopy (Figs 2 and 3a). The apical and the perinuclear cytoplasm were rich in mitochondria and spherites (Fig 3a). The spherites were composed of various concentric layers of electron-lucent and electron-dense material (Fig 3b). In the basal part of the epithelial cell, numerous mitochondria and spherites were seen (Fig 3c). The multiple infoldings of the basal plasma membrane included a few mitochondria in between (Fig 3c). The epithelium was underlayed by muscle cell (Fig 3c). The perinuclear cytoplasm additionally contained the rER and Golgi apparatus (Fig 3d). With IFM, autophagic structures were rarely observed (Fig 4a, Table 1).

Fig 3

Ultrathin cross-section of the Malpighian tubule (MT) in T. cavicola at the beginning of overwintering.

(a) The apical part of the epithelial cell with numerous mitochondria (M) and spherites (S). The apical plasma membrane is differentiated into microvilli of up to 5 μm long (MV). LU, lumen of the MT. (b) The perinuclear cytoplasm containing many mitochondria (M) and spherites (S). (c) The basal part of the epithelial cell with spherites (S) and mitochondria (M). The basal plasma membrane with typical multiple infoldings and a few mitochondria. Muscle cell (MC) beneath the epithelium of the MT. BL, basal lamina. (d) Golgi apparatus (GA) and mitochondria (M) in the perinuclear region of the epithelial cell. Scale bar: 2 μm (a, b, c) and 500 nm (d).

Fig 4

IFM-Visualization of autophagosomes labelled with antiserum against LC3.

Immunofluorescent images show autophagosomes (arrows) in the epithelial cells of the Malpighian tubules of T. cavicola at the beginning of the overwintering (a), in the middle (b) and at the end of overwintering (c).

Table 1

Rates (in %) of the Malpighian tubule epithelial cell samples containing autophagic structures in Troglophilus cavicola and T. neglectus during overwintering, observed by TEM.

Species	Sex	Time frame of overwintering
		Beginning	Middle	End
T. cavicola	Male	7	52	70
	Female	0	64	82
T. neglectus	Male	7	48	70
	Female	0	55	75

Middle of overwintering

The compartments such as rER, Golgi apparatus, mitochondria apparently did not change in T. cavicola. In the perinuclear cytoplasm, spherites were as abundant as at the beginning of overwintering, but most of them contained fewer electron-dense and more electron-lucent layers than at the beginning of overwintering (compare Fig 5a–5d, with Fig 3b). By this time various autophagic structures−the phagophores, autophagosomes, autolysosomes and residual bodies−were present in some cells. The phagophores (Fig 6a, inset) were composed of short fragments of the membrane partly engulfing the cytoplasm. Autophagosomes (Fig 6a), were also detectable using IMF (Fig 4b). These contained material of varying electron density. The autophagosomes were composed of electron-dense granules and electron-lucent material enveloped by a double-membrane (Fig 6a). The autolysosomes (Fig 6b), which can be recognized by electron-dense contents enveloped by a single membrane, were also found, showing the disintegration processes of the engulfed material. Residual bodies were recognized by an undegraded, electron-dense remnant material enveloped by a single membrane.

Fig 5

Ultrathin cross-section of the Malpighian tubule (MT) in T. cavicola in the middle of overwintering.

(a) Apical part of the cell with numerous mitochondria (M). Spherites (S) containing electron-lucent concentric layers. MV, microvilli. Scale bar: 2 μm. (b) Perinuclear region of the epithelial cell with mitochondria (M) and spherites (S). Scale bar: 1 μm. (c) The basal part of the epithelial cell with the nucleus (N), spherites (S) and mitochondria (M). MC, muscle cell. Scale bar: 2 μm. (d) A spherite (S) composed of electron-lucent and electron-dense concentric layers. Scale bar: 500 nm.

Fig 6

Ultrathin cross-section of the Malpighian tubule (MT) in T. cavicola in the middle (a, b) and at the end of overwintering (c, d).

(a) Autophagosome (AP) composed of granular electron-dense material and fragments of the membranes. Scale bar: 500 nm. Inset: the phagophore (arrow). Scale bar: 500 nm. (b) Autolysosome (AL). Scale bar: 500 nm. (c) Autophagosome (AP), a spherite (S) and a mitochondrium (M) in the perinuclear cytoplasm. Scale bar: 500 nm. (d) Autophagosome (AP) containing material of variable electron density. Scale bar: 500 nm. Inset: a residual body (RB) and a mitochondrium (M). Scale bar: 500 nm.

End of overwintering

The morphology of compartments such as rER, Golgi apparatus, mitochondria apparently did not change in T. cavicola. The material of many spherites was partly or completely exploited (Fig 7a). Most spherites in the perinuclear cytoplasm contained electron-lucent layers (Fig 7b). Autophagic structures were present in many cells (Table 1). Among these, autophagosomes (Fig 6c and 6d) and the residual bodies (Fig 6d) were most abundant (Fig 6c and 6d). Using IFM, the high abundance of autophagosomes was also visible (Fig 4c).

Fig 7

Ultrathin cross-section of the Malpighian tubule (MT) in T. cavicola at the end of overwintering.

(a) Epithelial cells (EC) and a muscle cell (MC). Fully-formed spherite in which the dense core is in a contact with the membrane (1). Cases of gradually exploited spherites (2–5). In 2 and 3 the dense spherital cores lost the contact with the membrane. In 4, only one concentric ring of the spherite material and the membrane could be recognized. In 5, the dense core of the spherite is completely exploited; only the membrane is present. LU, lumen of the MT; S, spherite. Scale bar: 2 μm. (b) The perinuclear region of the EC with spherites (S). Scale bar: 1 μm. (c) Apical part of the EC. LU, lumen of the MT; M, mitochondrium; S, spherite. Scale bar: 2 μm. (d) Basal part of the EC and the basal lamina (BL). S, spherite. Scale bar: 2 μm.

Morphometric analysis

Before overwintering, in both sexes in both species the percentage of MT epithelial cells with autophagic structures were low, but these gradually increased until the end of overwintering, as found by TEM (Table 1) and IFM (Table 2, Fig 8). In both sexes of T. cavicola, the numbers of autophagosomes increased between the beginning and the end of overwintering (Table 2). At the beginning of overwintering, there were no significant differences between sexes in any of the species under investigation, while significant differences appeared in T. cavicola in the middle of overwintering and at the end of overwintering (Table 2) and in T. neglectus at the end of overwintering. When males and females were compared separately between species, there were no significant differences in autophagosome abundances in November and January for both sexes (Table 3). A significant difference was found only in females in March, when the abundance of autophagosomes was larger in T. cavicola than in T. neglectus (Table 3, Fig 8).

Table 2

Descriptive statistics (mean ± StD; min − max) of autophagosome abundances per 100 μm2 in the epithelial cells of the Malpighian tubules in Troglophilus cavicola and T. neglectus, and Mann-Whitney U test between the sexes.

Significant differences in bold.

Species	Time frame of overwintering	Male	Female	Mann-Whitney U test between sexes,
		x¯ ± StD	x¯ ± StD	df = 398
		Min—Max	Min—Max
T. cavicola	Beginning	0.9 ± 1.0	0.9 ± 1.2	Z = 0.49; p = 0.625
		0–4	0–6
	Middle	10.9 ± 4.0	12.7 ± 3.5	Z = 4.66; p < 0.001
		0–21	3–21
	End	21.0 ± 5.1	24.8 ± 4.9	Z = 6.75; p < 0.001
		6–29	10–37
T. neglectus	Beginning	0.9 ± 1.2	0.9 ± 1.3	Z = 0.07; p = 0.944
		0–6	0–7
	Middle	11.6 ± 3.3	12.3 ± 3.8	Z = 1.38; p < 0.169
		4–22	4–21
	End	20.4 ± 4.2	23.8 ± 4.4	Z = 6.95; p < 0.001
		9–29	14–34

Fig 8

Abundances of autophagosomes per 100 μm2 in the epithelial cells of the Malpighian tubules in Troglophilus cavicola and T. neglectus during three time frames of overwintering, as determined using IFM.

Table 3

Differences in autophagosome abundances per 100 μm2 in the epithelial cells between each sex of Troglophilus cavicola and T. neglectus using Mann-Whitney U test.

Significant differences in bold.

	Mann-Whitney U test between species
	df = 398
Time frame of overwintering	Male	Female
Beginning	Z = 1.03	Z = 0.35
	P = 0.302	P = 0.729
Middle	Z = 1.83	Z = 1.52
	P = 0.068	P = 0.128
End	Z = 1.82	Z = 2.25
	P = 0.069	P = 0.025

Discussion

In both cave crickets under study, T. cavicola and T. neglectus, the MT epithelial cells were typically shaped and structured, as described in MTs of other insects, e.g. Schistocerca gregaria [40], Acheta domesticus [41] and Sarcophaga ruficornis [42].

Overwintering is a natural starvation period when many metabolic processes occur in cells to maintain the basal organismic metabolism. At the beginning of overwintering, cells are considered to be normally fed and, consequently, characterized by their usual shape and structure [40, 42–44]. In the MT epithelial cells in both cave cricket species and both sexes, the nuclei and compartments such as rER, Golgi apparatus, mitochondria did not show ultrastructural changes during overwintering. Besides, abundant mitochondria in the apical and the perinuclear cytoplasm denote that both are engaged in energy-consuming processes: probably, the apical cell part is mostly engaged in active transport, and the perinuclear part in intensive synthesis in rough and smooth ER [45]. The Golgi apparatus and rER are abundant in the perinuclear part in accordance with their functions [46]. Numerous spherites close to the nucleus reveal that they abundantly support nutrient-consuming processes in this part of the cell.

During overwintering, in both Troglophilus species the most conspicuous were gradually mounting structural changes of the spherites and autophagic structures, as it was also observed in the fat body cells of overwintering T. neglectus [38], and in the cells of the midgut diverticula in overwintering Gyas annulatus [47]. In both Troglophilus species, the abundance of the spherites did not change during overwintering, but they gradually showed much more electron-lucent material, which reveals their intensive exploitation [48]. A previous study of the chemical elements contained in spherites of T. neglectus, showed that Mg, Fe, S and Zn were completely exploited during overwintering [21]. Mg and Fe are thought to be used in the respiratory chain in the inner mitochondrial membrane [49]. S is an essential compound of cysteine, methionine and many enzymes which handle acyl-containing biochemical, e.g. the Co-A, and Zn is an important part of many enzymes, including phospholipases involved in the metabolism of lipids [50]. This study showed that gradually, four types of autophagic structures appeared: the phagophores, the autophagosomes, the autolysosomes and the residual bodies. This is the usual order in the self-metabolizing processes within a cell [30, 33].

As in the fat body of T. neglectus [38], TEM and IFM provided congruent results in the MTs. All these autophagic structures have been found in both the fat body and the MTs of starved T. cavicola and T. neglectus, in each case more and more autophagic structures were found during the course of overwintering (see [38] and this study), suggesting that in these species the autophagic processes in the the fat body and the MTs are parallel and have a very similar sequence. The autophagic processes in T. neglectus are quite comparable with those in T. cavicola. However, as had been expected, in T. neglectus, the autophagic cells are more abundant in the fat body [38], which is in accordance with its central metabolic role during overwintering. It is expected that the same will be found in T. cavicola. Although T. cavicola show a more glycogen dependent metabolism and T. neglectus a more lipid dependent one [37], this does not influence the other metabolic processes within the cells of the fat body and the MTs during overwintering.

This study shows that autophagosomes accumulated significantly in the apical and the perinuclear areas of the MT epithelial cells during quiescence in T. neglectus and during diapause in T. cavicola. The abundance of the autophagic structures gradually augmented during overwintering. An explanation may be that trafficking to lysosomes may be reduced [33], so autophagosomes are not being degraded. The greater extent of autophagy in diapausing T. cavicola in comparison to quiescent T. neglectus, on the one hand, and a greater extent in T. cavicola females than in males, on the other hand, suggests a higher level of the basal metabolism in T. cavicola. The most common mode of reproduction in insects is by yolked eggs, when females accumulate large amounts of proteins and lipids [51]. In female T. cavicola only, at the end of overwintering, abundant ER in the adipocytes prove their biosynthetic activity, which most probably refers to the egg production during diapause (unpublished personal observation; [37]). Therefore the major quantitative differences found in diapausing T. cavicola females in March are most likely because of oogenesis, as compared to quiescent T. neglectus females. This is congruent with the expectation that diapause is a more energy- and nutrient-consuming process than quiescence, and that oogenesis is a more energy- and nutrient-consuming process than spermatogenesis.

Conclusion

In the dormant cave crickets Troglophilus cavicola and the closely related T. neglectus, the main changes in the MT epithelial cells, as well as the fat body cells in both species and sexes are parallel and similar. In these two species, quantitative differences refer to various overwintering strategies, i.e., diapause vs. quiescence. The major quantitative differences affect diapausing T. cavicola females in March because of oogenesis, as compared to quiescent T. neglectus females.