Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)

The olfactory organ in decapod crustaceans is represented by the outer antennular flagellum with specialized sensilla called aesthetascs. Characteristic structures of the lateral antennular flagellum with olfactory setae in larvae, juveniles and adults of grass shrimp Pandalus kessleri Czerniavski,...

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Published in:Вестник зоологии
Date:2010
Main Authors: Blinova, N.K., Cherkashin, S.A.
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Language:English
Published: Інститут зоології ім. І.І. Шмальгаузена НАН України 2010
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Online Access:https://nasplib.isofts.kiev.ua/handle/123456789/65719
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Journal Title:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Cite this:Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae) / N.K. Blinova, S.A. Cherkashin // Вестник зоологии. — 2010. — Т. 44, № 5. — С. 413–419. — Бібліогр.: 14 назв. — англ.

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author Blinova, N.K.
Cherkashin, S.A.
author_facet Blinova, N.K.
Cherkashin, S.A.
citation_txt Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae) / N.K. Blinova, S.A. Cherkashin // Вестник зоологии. — 2010. — Т. 44, № 5. — С. 413–419. — Бібліогр.: 14 назв. — англ.
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description The olfactory organ in decapod crustaceans is represented by the outer antennular flagellum with specialized sensilla called aesthetascs. Characteristic structures of the lateral antennular flagellum with olfactory setae in larvae, juveniles and adults of grass shrimp Pandalus kessleri Czerniavski, 1878 are described. Орган обоняния десятиногих ракообразных представлен наружными жгутами антеннул, с расположенными на них специализированными чувствительными щетинками — эстетасками. Описаны особенности строения латерального жгута антеннулы с обонятельными щетинками у личинок, молоди и половозрелых особей травяной креветки — Pandalus kessleri Czerniavski, 1878.
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fulltext UDC 595.384:591.486 ONTOGENETIC DEVELOPMENT OF OLFACTORY ORGANS IN GRASS SHRIMP, PANDALUS KESSLERI (DECAPODA, PANDALIDAE) N. K. Blinovà1, S. A. Cherkashin2 1 Technological Institute of Volodymyr Dahl East Ukrainian National University Sovetskiy pr., 59 a, Severodonetsk, Luhansk oblast, 934000 Ukraine E-mail: sti@sti.lg.ua 2 Pacific Research Fisheries Centre Shevchenko alley, 4, Vladivostok, 690091 Russia E-mail: cherkashin@tinro.ru Received 20 September 2009 Accepted 8 June 2010 Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae). Blinovà N. K., Cherkashin S. A. — The olfactory organ in decapod crustaceans is represented by the outer antennular flagellum with specialized sensilla called aesthetascs. Characteristic structures of the lateral antennular flagellum with olfactory setae in larvae, juveniles and adults of grass shrimp Pandalus kessleri Czerniavski, 1878 are described. Ke y wo r d s: grass shrimp, olfactory organ, development, aesthetasc. Ðàçâèòèå îðãàíîâ îáîíÿíèÿ òðàâÿíîé êðåâåòêè, Pandalus kessleri (Decapoda, Pandalidae), â îíòîãåíåçå. Áëèíîâà Í. Ê., ×åðêàøèí Ñ. À. — Îðãàí îáîíÿíèÿ äåñÿòèíîãèõ ðàêîîáðàçíûõ ïðåäñòàâëåí íàðóæíûìè æãóòàìè àíòåííóë, ñ ðàñïîëîæåííûìè íà íèõ ñïåöèàëèçèðîâàííûìè ÷óâñòâèòåëüíûìè ùåòèíêàìè — ýñòåòàñêàìè. Îïèñàíû îñîáåííîñòè ñòðîåíèÿ ëàòåðàëüíîãî æãóòà àíòåííóëû ñ îáîíÿòåëüíûìè ùåòèíêàìè ó ëè÷èíîê, ìîëîäè è ïîëîâîçðåëûõ îñîáåé òðàâÿíîé êðåâåòêè — Pandalus kessleri Czerniavski, 1878. Êëþ÷åâûå ñ ëîâ à: òðàâÿíàÿ êðåâåòêà, îðãàí îáîíÿíèÿ, ðàçâèòèå, ýñòåòàñê. Introduction Today, the crustaceans olfactory system is the subject of close morpho-functional studies (McClintock et al., 2006). In decapod crustaceans, this organ is studied to a greater extent. The large body size and accessibility of chemosensor organs in such species as Caribbean spiny lobster Panulirus argus, California spiny lobster Panulirus interruptus, and American lobster Homarus americanus allowed their successful use in morphological and neurobiological experiments (McClintock et al., 2006; Schmidt et al., 2006; Derby, Sorensen, 2008). The olfactory organ in decapod crustaceans is represented as the outer antennular flagellum with specialized sensilla called aesthetascs. There are lots of information on aesthetascs morphology in many Decapoda species (Ghiradella et al., 1868; Snow, 1973; Tierney et al., 1986; Blinova, 1988; Steullet et al., 2000). Characteristic structures of olfactory receptors in grass shrimp Pandalus kessleri Czerniavski, 1878 has been already described (Blinova, 1988, 2008). However, data on the ontogenetic development of chemosensor structures in marine decapod crustaceans are still scanty. The aim of the study was description of characteristic structures of olfactory receptors in grass shrimp P. kessleri at different stages of individual development. Material and methods Outer structure of antennules with olfactory setae was studied in larvae of grass shrimp P. kessleri grown in laboratory (Blinova, Cherkashin, 1999). Juveniles and adults for investigations catches in the Bay of Peter the Great in the Sea of Japan. Vestnik zoologii, 44(5): 413–419, 2010 Ìîðôîëîãèÿ Morphometric parameters were studied with using of the scale ruler in MBS–9 binocular and Biola microscope with ocular micrometer. The following parameters were measured: body length, length of the outer antennular flagellum, length of aesthetasc, diameter of proximal and distal parts of antennular flagellum. Body length was measured from the beginning of rostrum till the end of telson; total length of antennular flagellums — from the base of distal annulet; diameter of the distal part of flagellum — at the level of fine appendage without aesthetascs. For the light microscopy, total preparations of the outer flagellum of antennulae stained with methylene blue were used. For scanning electron microscopy, pieces of antennular tissue were fixed in 5% glutaraldehyde in cacodylate buffer at pH 7.4 for 1.5 hours. Post fixation was performed in 1% of OsO4 solution in cacodylate buffer at 4°Ñ for 1 hour. Dehydration was carried out in alcohols of increasing concentrations, material was dried at the critical point, covered with gold and examined under scanning microscope JSM 25S (“JEOL”, Japan). In every size-age group, from 5 to 10 specimens were studied. Totally, 80 animals were studied. Morphometric data of the size-age groups with the number of specimens more than 5 are given with arithmetic mean of error. For existing set of values, with using of MS Excel software, regression equation, significance level of approximation (R2) and Pearson’s correlation coefficient (r) for linear function are calculated. Results Outer structure of antennules with olfactory setae was studied in the early ontoge- nesis of P. kessleri at 4 stages (after Kurata, 1955) of larval development. The transi- tion from one stage to another is associated with moulting. Duration of the period between moults was 4–5 days. Body length of larvae grown under laboratory conditions was 9 mm on average. Antennule unsegmented, its distal part is divided into two branches which further give rise to internal and external flagellums (fig. 1). Internal branch is a short feathery seta, 260 µm long, sitting on a circular prominence. The length of external branch signifi- cantly exceeds that of the inner (650 µm) due to a fine distal process, and on the ven- tral side it has two smooth setae 120 µm in length each. Morphometric data on anten- nules and aesthetascs in grass shrimp are presented in table 1. The average size of the second stage larvae was 10.5 mm. Antennule has annulet- ed structure: stem of three annuli and formed inner and outer flagellums. Outer flagel- lum is divided into three annuli bearing 12 aesthetascs on the ventral side (fig. 2). 414 N. K. Blinovà, S. A. Cherkashin Fig. 1. Antennules of Pandalus kessleri at the I larval stage: OF — outer flagellum; IF — inner flagellum. Magnification õ30. Ðèñ. 1. Àíòåííóëû Pandalus kessleri íà I ñòàäèè ëè÷èíî÷íîãî ðàçâèòèÿ: OF — íàðóæíûé æãóò; IF — âíóòðåííèé æãóò. Óâåëè÷åíèå õ30. Fig. 2. Distal part of àntennules of Pandalus kessleri at the II larval stage: OF — outer flagellum; A — aesthetascs. Magnification õ63. Ðèñ. 2. Äèñòàëüíàÿ ÷àñòü àíòåííóëû Pandalus kessleri íà II ñòàäèè ëè÷èíî÷íîãî ðàçâèòèÿ: OF — íàðóæíûé æãóò; A — ýñòåòàñêè. Óâåëè÷åíèå õ63. Larval aesthetascs are fine, smooth setae 350 µm in length with thickened base and annulated rod. On flagellum, they form transverse rows, 3 hairs in each. One row of olfactory setae is located on the distal annulet of the flagellum, two other rows are on the second annulet and one row of growing aesthetascs (length 50–60 µm) on the prox- imal annulet. Internal antennular flagellum is smaller than the outer one and consists of two annuli (table 1). At stage III of larval development, number of annuli on shrimp internal antennu- lae flagellum increases, as well as all morphometric parameters (body length 12 mm). However, the number of annuli of the outer flagellum and the number of aesthetascs on them remain unchanged. The length of aesthetascs reaches 400 µm. Internal anten- nulae flagellum of the IV stage larvae consists of six annuli. It equalizes in length with the outer flagellum and even becomes larger. Short projection of the distal part of the outer flagellum is isolated in a separate annulet, and the 5th group of growing aesthetascs appears on proximal annulet. By the end of larval development, antennulae of grass shrimp have 15 olfactory setae. Statistical analysis of morphometric data indicated an exponential (for the length of the outer flagellum, number of annuli) and power (for aesthetascs) dependence on larval body length (table 2). 415Ontogenetic Development of Olfactory Organs in Grass Shrimp… Ta b l e 1. Morfometric indices of the olfactory organs in larvae, juveniles and adults of Pandalus kessleri Òàáëèö à 1. Ìîðôîìåòðè÷åñêèå ïàðàìåòðû îðãàíîâ îáîíÿíèÿ ó ëè÷èíîê, þâåíèëüíûõ è ïîëîâîçðåëûõ îñîáåé Pandalus kessleri Larvae 10.5 0.35 3 0.11 — 0.35 12.0 0.46 3 — — 0.40 13.0 1.05 4 — — 0.42 Juveniles 16 ± 0.70 1.5 ± 0.06 — 0.15 ± 0.006 0.096 ± 0.00 0.45 ± 0.020 18 ± 0.02 1.7 ± 0.07 — 0.17 ± 0.009 0.096 ± 0.03 0.47 ± 0.020 37 ± 0.30 5.5 ± 0.20 27 ± 0.4 0.28 ± 0.040 0.130 ± 0.010 0.48 ± 0.018 Adults 55 ± 1.8 8.5 ± 0.58 40 ± 1.1 0.41 ± 0.03 0.31 ± 0.03 0.65 ± 0.060 86 ± 2.2 16.3 ± 0.90 65 ± 0.3 0.61 ± 0.03 0.39 ± 0.02 0.65 ± 0.014 110 ± 1.8 18.1 ± 0.31 82 ± 0.6 0.70 ± 0.01 0.39 ± 0.03 0.68 ± 0.016 131 ± 2.1 19.6 ± 0.50 85 ± 1.3 0.74 ± 0.06 0.39 ± 0.02 0.78 ± 0.050 Body length, mm Length of outer flagellum, mm Number of flagellum’s annuli, psc Diameter of flagellum’s base, mm Diameter of the peak, mm Aesthetasc length, mm Ta b l e 2. Dependence of morphometric parameters of olfactory organ on body length of Pandalus kessleri at different ontogenetic stages Ò à á ëèö à 2. Çàâèñèìîñòü ìîðôîìåòðè÷åñêèõ ïàðàìåòðîâ îðãàíà îáîíÿíèÿ îò äëèíû òåëà Pandalus kess- leri íà ðàçëè÷íûõ ýòàïàõ îíòîãåíåçà Length of outer flagellum. Number of flagellum’s annuli Diameter of flagellum’s foundation Diameter of the peak Aesthetasc length No t e. R2 — significance level of approximation; r — Pearson’s correlation coefficient. Larvae Y =e 0.549 x (R2 = 0.92) Y=2.47 e 0.143x (R2=0.75) — — Y = 0.351X 0.168 (R2 = 0.98) Juveniles Y = 2X — 1.1 (R2 = 0.78) r = 0.99 - Y = 0.065X + 0.07 (R2 = 0.86) r = 0.99 Y = 0.017X+0.73 (R2 = 0.75) r = 0.99 Y = 0.450X 0.059 (R2 = 0.99) Adults Y = 3.51X+6.85 (R2 = 0.84) r = 0.95 Y = 15.2Õ+30 (R2 = 0.90) r = 0.97 Y = 0.108X+0.35 (R2 = 0.89) r = 0.97 – Y = 0.237X–0.06 (R2 = 0.73) r = 0.94 After the next moulting, number of aesthetascs increases in proportion to size of animal’s body. On outer antennular flagellum of juvenile shrimps, thin distal part which bears no olfactory setae is formed. In the proximal part of the flagellum, zone with increased number of growing aesthetascs becomes visible (fig. 3). On annuli of the mid- dle part of the outer flagellum, aesthetascs are ordered in rows of 3 setae each (fig. 4). For determined morphometric parameters, linear dependence on the length of animal’s body was noted (table 2). With increased body length, the number of annuli and the length of outer antennular flagellum increases in direct proportion: Pearson’s coefficient of linear correlation is rather higher, 0.99. The dependence of every morphometric parameter of outer antennular flagellum (Y) on body length (X) of young and adult animals represented linear function. However, the length of the aesthetascs in the young is increasing as well as in the larvae, according to power function. The number of aes- thetascs per annulet of the flagellum remains relatively unchanged. Regression equation reflecting the dependence of morphometric parameters of olfactory organs on shrimp’s body length are given in table 2. Antennules of mature specimens of grass shrimp P. kessleri consisted of foundation divided into three parts, interior and outer flagellum (Blinova, 1988; fig. 1). Outer antennular flagellum is slightly shorter than inner one. In grass shrimps of the size 131 mm in length, antennulae is 37 mm, the length of the outer flagellum — 19.6 mm. Normally, outer flagellum consisted of 85 annuli. At the level of proximal annuli, its diameter is 740 µm, and at the level of 60–70 annuli (in place of the transition to a thin distal) is reduced to 390 µm. Outer antennular flagellum is flattened dorso-ventrally (fig. 5). It has considerable longitudinal groove on the ventral side where aesthetascs are located. This groove is non-uniform, it is pronounced more on the medial side and in the middle of antennu- lae. As a result, the groove has two limiting lateral lobes: larger medial and smaller lat- eral. On approaching the thin distal part of antennulae, groove is evened out. Cuticle inside the groove has numerous folds. Each annulet in the middle part of antennulae (excluding 8–10 proximal and 15–20 distal) has two transverse rows of aesthetascs. One 416 N. K. Blinovà, S. A. Cherkashin Fig. 3. New aesthetascs on proximal annuli of outer antennular flagellum of Pandalus kessleri: OF — outer flagellum; A — aesthetascs. Magnification õ160. Ðèñ. 3. Ðàñòóùèå ýñòåòàñêè íà ïðîêñèìàëüíûõ ÷ëåíèêàõ íàðóæíîãî æãóòà àíòåííóëû Pandalus kessleri: OF — íàðóæíûé æãóò; A — ýñòåòàñêè. Óâåëè÷åíèå õ160. Fig. 4. Outer antennular flagellum with aesthetascs of juvenile Pandalus kessleri: OF — outer flagellum; A — aesthetascs. Magnification õ63. Ðèñ. 4. Íàðóæíûé æãóò àíòåííóëû ñ ýñòåòñêàìè ó þâåíèëüíûõ îñîáåé Pandalus Kessler: OF — íàðóæíûé æãóò; A — ýñòåòàñêè. Óâåëè÷åíèå õ63. row consists of 6 sensory hairs. Proximal 6–8 annuli of the flagellum have no aes- thetascs. Each next annulet contains two rows of 3, then 4, 5, and at last of 6 olfacto- ry setae. Aesthetasc of mature grass shrimp is a fine hairless villus embedded into the cutic- ular fold of antennulae. It is formed by expanded ampoule shaped base and a rod of segmented structure. In specimens with average body length of 131 mm, the total length of hairs in the middle part of antennulae is 780 µm, and the hairs located on the dis- tal and proximal annuli — 620 µm. Diameter of hairs at the base is 30 µm. The height of the rod annuli increases from 20 mm at the base to 40 µm in the middle. The api- cal part of the aesthetascs is characterized by thin seta, 30–35 µm in length. In cutic- ular fold of antennulae, small pores (10 pores in each hair) are located proximally from aesthetasc. In some specimens of P. kessleri with body length of 130–140 mm, special fan- shaped setae were found behind aesthetascs. These setae have rounded base and up to 40 fused elongated «petals», the total size of which does not exceed 35 µm. Discussion Distant perception of chemical stimuli in crustaceans by antennular chemorecep- tors (Antenna 1) is studied. However, antennule of crustaceans is multifunctional sen- sory organ with numerous sensitive structures of different modalities. Among sensory setae of outer antennular flagellum in grass shrimp, as well as in other species of deca- pod crustaceans, the most numerous specific olfactory setae are aesthetascs. Sensory setae appeared on antennules on early ontogenetic stages. Grass shrimp has incomplete metamorphosis — hatched larvae look like adults. Nevertheless, mor- phological studies of olfactory organs on various ontogenetic stages P. kessleri revealed significant differences between the outer antennular structure and olfactory setae in lar- vae, juveniles and adults. During the growth and development of grass shrimp, the structure of olfactory organs is being improved and complicated to meet increasing sen- sory needs of the animal. 417Ontogenetic Development of Olfactory Organs in Grass Shrimp… Fig. 5. Outer antennular flagellum of antennule of Pandalus kessleri with aesthetascs: OF — outer flagellum; A — aesthetascs. Scanning electronogramme. Scale bar 1000 µm. Ðèñ. 5. Íàðóæíûé æãóò àíòåííóëû Pandalus kessleri ñ ýñòåòàñêàìè: OF — íàðóæíûé æãóò; A — ýñòåòàñêè. Ñêàíèðóþùàÿ ýëåêòðîíîãðàììà. Ìàñøòàáíàÿ ëèíåéêà 1000 ìêì. The outer antennular structure with their sensory setae in P. kessleri larvae has been described in detail earlier (Blinova, Cherkashin, 1999). Hatched larvae of grass shrimp have two smooth setae on each ventral outer antennular branch. These setae may be precursors of aesthetascs. Before the first moult, their outer structure is not sim- ilar to that of aesthetascs. The larvae of some Far Eastern species of shrimps on the early stages of development also have sensory setae on their antennules (Ivanov, 1971). In ontogenesis, aesthetascs in P. kessleri appear on the II stage of larval development: 9 morphologically formed setae and 3 young growing setae (Blinova, Cherkashin, 1999). Kurata (1955) also noted that in this period outer antennular flagellum in grass shrimp consists of three annuli with four groups of sense hairs. By the end of larval development, the outer antennular flagellum totally contains 15 aesthetascs. In young animals, newly emerged setae starts functioning after a long time. It is known that in the post-embryonic period larvae of crustaceans complete their organogenesis (Ivanova- Cazas, 1979). The growth and formation of aesthetascs in the young individuals starts in the proximal part of the outer antennular flagellum and then wave of turnover goes distal- ly to fine prominence where aesthetascs destructed. On the outer antennular flagellum of grass shrimp, as well as other decapod crustaceans, from proximal to distal parts, the following zones are seen: proliferation where setae are formed; zone with functionally mature aesthetascs and, finally, senescense zone (Schmidt et al., 2006). Sometimes the transition zone is distinguished between the proliferation zone and zone with mature aesthetascs (McClintock et al., 2006). It covers proximal annuli of the outer flagellum with growing aesthetascs. For P. kessleri, the annuli with functionally mature sensory setae form most part of the outer antennular flagellum (50%). The lifetime of newly appeared setae in juvenile lobster P. argus is not associated with moulting and this is a period of approximately 3 to 6 moults (Steullet et al., 2000). Differentiation and func- tional formation of olfactory sensory neurons in aesthetascs occurs over rather long period of time: from several weeks to several months. Flagellar growth due to increas- ing number of annuli in the growth zone with a constant number of hairs on each annulet of the middle part of antennulae enables the animal to maintain the constan- cy of the receptive field and sensitivity to chemicals. In ontogenesis, in the middle part of the outer antennular flagellum, the number of aesthetascs in one row increases from three to six. In adults, protective and promot- ing perception of chemical stimuli structures and appliances appear. Deepening of aes- thetascs in P. kessleri into the groove with two lateral lobes prevent damaging of setae. For this purpose, lobster P. argus has powerful guard bristles forming two longitudinal rows medially and laterally from aesthetascs (Derby et al., 2001). Possible functions of pores at the foundation of olfactory setae are associated with release of a secret from so-called “aesthetasc tegumental glands” preventing aesthetascs friction and contami- nation (Schmidt et al., 2006). Fan-shaped setae revealed behind the aesthetascs foun- dation in some large specimens of grass shrimp are probably a sign of sexual dimor- phism and participate in the reception of pheromones in females (Blinova, 2008). Fine apical villus of distal part of setae rod may increase probability of interaction with olfac- tory stimulus. Morphometric parameters of the olfactory organ larvae has nonlinear, but expo- nential or power dependence on the total length of the grass shrimp body. The power function was proposed to determine dimensions of different parts of body in P. kessleri larvae at known carapace length (Kurata, 1955). In contrast to obtained power depen- dence between larval body length and antennular morphometric parameters, young and adult animals have mainly simple linear dependence. Changing the nature of morpho- metric data of olfactory organs from the body length during ontogenesis is likely due to the fact that the development of the peripheral part of olfactory system is the most 418 N. K. Blinovà, S. A. Cherkashin intensive during the larval period and completes in mature animals. Based on these data, we can assume that during the larval and juvenile stages of development of the grass shrimp, morphological basis for functioning of olfactory organ and related innate behavioural reactions are formed. Blinova N. K. Structure of aesthetascs of grass shrimp Pandalus latirostris // Zoologicheskiy Zhurnal. — 1988. — 67, N 2. — P. 460–463. — Russian : Áëèíîâà Í. Ê. Ñòðîåíèå ýñòåòàñêîâ òðàâÿíîãî ÷èëèìà Pandalus latirostris // Çîîëîãè÷åñêèé æóðíàë. Blinova N. K. Morphological features of the olfactory system of the grass shrimp Pandalus kessleri (Decapoda. Pandalidae) // Vestnik zoologii. — 2008. — 42, N 1. — P. 57–62. — Russian : Áëèíîâà Í. Ê. Ìîðôîëîãè÷åñêèå îñîáåííîñòè îáîíÿòåëüíîé ñèñòåìû òðàâÿíîé êðåâåòêè Pandalus kessleri (Decapoda, Pandalidae) // Âåñòíèê çîîëîãèè. Blinova N. K., Cherkashin S. A. Antennular development in larvae of grass shrimp Pandalus kessleri // Biologiya morya. — 1999. — 25, N 3. — P. 217–220. — Russian : Áëèíîâà Í. Ê., ×åðêàøèí Ñ. À. Ðàçâèòèå àíòåííóë ó ëè÷èíîê òðàâÿíîé êðåâåòêè Pandalus kessleri // Áèîëîãèÿ ìîðÿ. Ivanov B. G. Larvae of some Far East shrimps in relation to their systematic position. Zoologicheskiy Zhurnal. — 1971. — 50, N 5. — P. 657–665. — Russian : Èâàíîâ Á. Ã. Ëè÷èíêè íåêîòîðûõ äàëüíåâîñòî÷íûõ êðåâåòîê â ñâÿçè ñ èõ ñèñòåìàòè÷åñêèì ïîëîæåíèåì // Çîîëîãè÷åñêèé æóðíàë. Ivanova-Cazas O. M. Comparative embryology of invertebrates. Arthropods. — Moscow : Nauka, 1979. — 224 p. — Russian : Èâàíîâà-Êàçàñ Î.Ì. Ñðàâíèòåëüíàÿ ýìáðèîëîãèÿ áåñïîçâîíî÷íûõ æèâîòíûõ. ×ëåíèñòîíîãèå. Derby C. D., Steullet P., Horner A. J., Cate H. S. The sensory basis of feeding behavior in the Caribbean spiny lobster. Panulirus argus // Mar. Freshwater Res. — 2001. — 52. — P. 1339–1350. Derby C. D., Sorensen P. W. Neural Processing, Perception, and Behavioral Responses to Natural Chemical Stimuli by Fish and Crustaceans // J. Chem. Ecol. — 2008. — 34. — P. 898–914. Ghiradella H., Case J. F., Cronshaw J. Fine structure of the aesthetasc hairs of Pagurus hirsutiusculus Dana // Protoplasma. — 1968. — 66, N 1–2. — P. 1–20. Kurata H. The post-embryonic development of the prawn, Pandalus kessleri // Bull. Hokkaido Reg. Fish. Res. Lab. — 1955. — N 12. — P. 1–15. McClintock T. S., Ache B. W., Derby C. D. Lobster olfactory genomics: Integrative and comparative biology (Symposium “Genomic and proteomic approach to Crustacean Biology”, Orlando, Florida, January 4–8, 2006) — Oxford : Oxford university press, 2006. — P. 1–8. Schmidt M., Chien H., Tadesse T., Johns M. E., Derby C. D. Rosette-type tegumental glands associates with aesthetasc sensilla in the Caribbean spiny lobster, Panulirus argus // Cell Tissue Res. — 2006. — 325. — P. 369–395. Snow P. J. Ultrastructure of the aesthetasc hairs of the littoral decapod, Paragrapsus gaimardii // Z. Zellforsch. — 1973. — 138. — P. 489–502. Steullet P., Cate H. S., Derby C. D. A spatiotemporal wave of turnover and functional maturation of olfactory receptor neurons in the spiny lobsters Panulirus argus // J. Neiroscience. — 2000. — 20, N 9. — P. 3282–3294. Tierney A. J., Tompson C. D., Dunham D. W. Fine structure of the aesthetasc chemoreceptors in the crayfish Orconectes propinquus // Can. J. 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id nasplib_isofts_kiev_ua-123456789-65719
institution Digital Library of Periodicals of National Academy of Sciences of Ukraine
issn 0084-5604
language English
last_indexed 2025-12-07T17:17:08Z
publishDate 2010
publisher Інститут зоології ім. І.І. Шмальгаузена НАН України
record_format dspace
spelling Blinova, N.K.
Cherkashin, S.A.
2014-07-01T05:30:52Z
2014-07-01T05:30:52Z
2010
Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae) / N.K. Blinova, S.A. Cherkashin // Вестник зоологии. — 2010. — Т. 44, № 5. — С. 413–419. — Бібліогр.: 14 назв. — англ.
0084-5604
https://nasplib.isofts.kiev.ua/handle/123456789/65719
595.384:591.486
The olfactory organ in decapod crustaceans is represented by the outer antennular flagellum with specialized sensilla called aesthetascs. Characteristic structures of the lateral antennular flagellum with olfactory setae in larvae, juveniles and adults of grass shrimp Pandalus kessleri Czerniavski, 1878 are described.
Орган обоняния десятиногих ракообразных представлен наружными жгутами антеннул, с расположенными на них специализированными чувствительными щетинками — эстетасками. Описаны особенности строения латерального жгута антеннулы с обонятельными щетинками у личинок, молоди и половозрелых особей травяной креветки — Pandalus kessleri Czerniavski, 1878.
en
Інститут зоології ім. І.І. Шмальгаузена НАН України
Вестник зоологии
Морфология
Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
Развитие органов обоняния травяной креветки, Pandalus kessleri (Decapoda, Pandalidae), в онтогенезе
Article
published earlier
spellingShingle Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
Blinova, N.K.
Cherkashin, S.A.
Морфология
title Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
title_alt Развитие органов обоняния травяной креветки, Pandalus kessleri (Decapoda, Pandalidae), в онтогенезе
title_full Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
title_fullStr Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
title_full_unstemmed Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
title_short Ontogenetic Development of Olfactory Organs in Grass Shrimp Pandalus kessleri (Decapoda, Pandalidae)
title_sort ontogenetic development of olfactory organs in grass shrimp pandalus kessleri (decapoda, pandalidae)
topic Морфология
topic_facet Морфология
url https://nasplib.isofts.kiev.ua/handle/123456789/65719
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AT cherkashinsa ontogeneticdevelopmentofolfactoryorgansingrassshrimppandaluskessleridecapodapandalidae
AT blinovank razvitieorganovobonâniâtravânoikrevetkipandaluskessleridecapodapandalidaevontogeneze
AT cherkashinsa razvitieorganovobonâniâtravânoikrevetkipandaluskessleridecapodapandalidaevontogeneze