Pochazia shantungensis (Chou & Lu, 1977)
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https://dx.doi.org/10.3897/zookeys.880.32810 |
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lsid:zoobank.org:pub:EFFE7128-E4A2-42F6-84CE-0BDDD5E0A447 |
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https://treatment.plazi.org/id/5804BA4F-6A42-5552-B3FD-23F12459D9A2 |
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scientific name |
Pochazia shantungensis (Chou & Lu, 1977) |
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Pochazia shantungensis (Chou & Lu, 1977)
Description.
The mature spermatozoa of P. shantungensis are held together (totally 128 spermatozoa per spermatodesm) in the form of coiled sperm bundles in the seminal vesicles. Anterior ends of heads are embedded in a homogenous matrix that forms the spermatodesmata ( Fig. 1A, B, D View Figure 1 ). The spermatozoon is long and filiform when it is separated from the bundles and exposed to a 0.9% saline solution ( Fig. 1C View Figure 1 ). It is approximately 127 µm in mean length and has an elongate single head (about 16 µm) and a conventional single flagellum (about 111 µm).
The head is formed by the nucleus and the acrosome. The acrosome has an irregular saccular acrosomal vesicle and a perforatorium, both located anterior to the nucleus ( Figs 1E View Figure 1 , 2A, B View Figure 2 , 3A, B View Figure 3 ). Between the base of the perforatorium and the anterior portion of the nucleus is a noticeable transition ( Figs 1E View Figure 1 , 2B View Figure 2 , 3 C–E View Figure 3 ). The acrosome gradually invaginates posteriorly to form a subacrosomal space in which the anterior part of the elongated nucleus is inserted ( Figs 2B View Figure 2 , 3C, D View Figure 3 ). The nuclei, different in shape ( Figs 2B View Figure 2 , 3 B–N View Figure 3 ), are full of homogeneous condensed chromatin and are separated from each other by a cell membrane ( Fig. 1D View Figure 1 ). The ovoid nucleus measures approximately 0.94 µm in diameter in cross-section; in longitudinal-section, it turns into a cylinder-shape ( Fig. 2A, B View Figure 2 ).
The nucleus-flagellum transition region has a centriole and centriolar adjunct ( Fig. 2B, C View Figure 2 ). The centriole starts near the terminal incurvation of the nucleus and terminates anterior of the axoneme ( Fig. 2B, C View Figure 2 ); it is parallel to the moderately electron-dense centriole adjunct ( Fig. 2B View Figure 2 ). The centriole adjunct contains dense granules between the accessory bodies and mitochondrial derivatives in longitudinal profile ( Fig. 2B, C View Figure 2 ); in cross-section the centriole adjunct arises near the end of the nucleus and terminates anterior to the mitochondrial derivatives ( Fig. 3 I–K View Figure 3 ). The nucleus is wrapped by the centriolar adjunct ( Figs 2B, C View Figure 2 , 3 I–M View Figure 3 ). In several transverse profiles of spermatozoa, the posterior nucleus region overlaps the different regions of accessory bodies and mitochondrial derivatives ( Fig. 3 G–L View Figure 3 ).
The flagellum region contains an axoneme, two mitochondrial derivatives and two accessory bodies ( Fig. 4 A–D View Figure 4 ); they are parallel to each other throughout most of the length of the flagellum ( Fig. 2 B–D View Figure 2 ). The axoneme arises from the centriole ( Fig. 2C View Figure 2 ). It is composed of two innermost microtubules, nine outermost accessory microtubules, and nine doublets, showing the typical 9 + 9 + 2 microtubules arrangement in insects ( Fig. 4D, G View Figure 4 ). The mitochondrial derivatives and accessory bodies are symmetrical in size and diameter in cross-section ( Fig. 4 A–D View Figure 4 ). Each mitochondrial derivative is made up of one serrated electron-dense area, one small oval electron-lucid portion and one mitochondrial cristae region ( Fig. 4C View Figure 4 ). In longitudinal-section, the mitochondrial derivatives are positioned lateral to the axoneme and are initiated near the extreme base of the centriole adjunct ( Fig. 2 B–D View Figure 2 ). The cristae are perpendicular to the longitudinal axis, bearing regular intervals (42 nm) between adjacent derivatives ( Fig. 2E View Figure 2 ). The accessory bodies are fishhook-shaped; they originate from the centriolar adjunct between the axoneme and mitochondrial derivatives ( Fig. 4 B–D View Figure 4 ).
Close to the posterior sperm tip, the axoneme becomes disorganized step by step, and the accessory bodies gradually taper to a cone-shape, while the mitochondrial derivatives disappear ( Fig. 4E, F View Figure 4 ). At the terminal region of the flagellum, the doublet microtubules are the last to disappear ( Fig. 4H View Figure 4 ).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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