spermatophore transfer in the hermit crab clibanarius vittatus

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JOURNAL OF MORPHOLOGY 253:166-175 (2002) Spermatophore Transfer in the Hermit Crab Clibanarius vittatus (Crustacea, Anomura, Diogenidae) Gregory S. Hess and Raymond T. Bauer* Department of Biology, University of Louisiana at Lafayette, Lafayette, Louisiana 70504-2451 ABSTRACT Although mating has been described in sev eral hermit crab species, the mechanics of spermatophore transfer have not previously been demonstrated. Evidence from pleopod and gonopore morphology, video observa tions, and inseminated females indicates that in Clibana rius vittatus the male applies a spermatophoric mass di rectly onto the female via the gonopores rather than with modified pleopods 1-2 (gonopods) and/or genital papillae as in many other decapods. The single second pleopod of males of C. vittatus has a simple endopod with no appar ent modifications for sperm transfer. There are no genital papillae extending from the male gonopores. The globular spermatophores are aligned in rows surrounded by a sem inal secretion in the male ducts (vasa deferentia that terminate in ejaculatory ducts opening to the exterior via the gonopores). During copulation, described from time- lapse video recordings, tbe ventral surface of the last thoracic segment of the male, bearing the gonopores, was In decapod crustaceans, the immotile spermato zoa are surrounded by protective and adhesive ma terials when transferred to the female (Subramo- niam, 1993). These sperm-bearing structures (spermatophores), formed prior to or during ejacula tion, vary in size, shape, and complexity. The place ment of spermatophores on the exterior of the fe male or within spermathecae is often achieved with ified anterior pleopods (abdominal appendages) uti lized for sperm transfer in many decapods (Bauer, 1986), such as caridean shrimps (Bauer, 1976), penaeoidean shrimps (Bauer, 1991, 1996a,b), cani- barid crayfishes (Andrews, 1911), nephropid lob sters (Farmer, 1974), and brachyuran crabs (Cronin, 1947; Ryan, 1967). In some decapods, such as ste- nopodid shrimps (Bauer, 1986) and palinurid lob sters (Phillips et al., 1980), the male anterior pleo pods are not modified for sperm transfer. Males of anomuran species, including the hermit crabs of the superfamily Paguroidea (McLaughlin, 1983), produce characteristic spermatophores that apparently are deposited on the external surface of the female (Tudge, 1999a,b). Tudge (1991, 1995, 1999a,b) and Subramoniam (1993) described the predominant spermatophore type encountered in paguroidean crabs as stalked or pedunculate with three distinct components, the distal ampulla, stalk. apposed to the ventral cephalothorax of the female. A massive amount of seminal secretion containing sper matophore ribbons, termed here the spermatophoric mass and described for the first time in a hermit crab species, was observed covering the sternites and coxae of pereo- pods 1-5 of a recently copulated female. It is suggested that during copulation the male emits the contents of the ejaculatory ducts directly onto the female without the aid of gonopods or genital papillae. Although spermatophore transfer is simple in C. vittatus, the presence of modified anterior pleopods or elongate genital papillae (sexual tubes) in other paguroidean species suggests the possibil ity of a more complex insemination process in these other hermit crabs. J. Morphol. 253:166-175, 2002. © 2002 Wiley-Liss. Inc. KEY WORDS: gonopods; gonopores: hermit crab; sper matophore: sperm transfer and proximal pedestal. The spermatozoa are stored within the ampulla, which is composed of two halves joined along their lateral ridges (Tudge, 1999a). The distal ampulla rests atop the stalk, which is under lain by the pedestal or base of the stalk. The pedes tal appears to function as the point of attachment for the spermatophore to the external surface of the female during copulation (Tudge, 1999b). Mouchet (1930, 1931) and Hamon (1937, 1939) suggested that the ampulla splits along this ridge, termed the line of dehiscence (Tudge 1999a) or "ligiie de suture" (Hamon, 1937), thereby releasing the spermatozoa (Tudge 1991, 1995, 1999a,b). Hamon (1937) sug gested tha t mechanical or osmotic forces might cause the ampulla to fracture and release the sper matozoa. Contract grant sponsors: the Graduate Student Organization, Uni versity of Louisiana at Lafayette I DLL), and the Neptune Foundation. 'Correspondence to: Raymond T. Bauer, Department of Biology, University of Louisiana at Lafayette. Lafayette, Louisiana 70504- 2451. E-mail: [email protected]  Published online 20 Ma y 2002 in Wiley InterSeience ( www.interscience.wiley.com)  DOI; 10.1002/jmor.lll8 <D 2002 WILEY-LISS. INC.

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7/27/2019 Spermatophore Transfer in the Hermit Crab Clibanarius Vittatus

http://slidepdf.com/reader/full/spermatophore-transfer-in-the-hermit-crab-clibanarius-vittatus 1/10

JOURNAL OF MORPHOLOGY 253:166-175 (2002)

Clibanarius

(Crustacea, Anomura, D iogenidae)

aymond T. Bauer*

tment of Biology, University of Louisiana at Lafayette, Lafayette, Louisiana 70504-2451

Al though mat ing has been desc r ibed in sev

v e n o t p r e v i o u sl y b ee n d e m o n s t r a t e d . E v i d e n c e

Clibanat h e m a l e a p p l i e s a s p e r m a t o p h o r i c m a s s d i

ma ny o th e r decapo ds . Th e s ing le second p l eopod o fC. vittatus has a s imple endopod wi th no appar

I n d e c a p o d c r u s t a c e a n s , t h e im m o t i l e s p e r m a t o

a r e s u r r o u n d e d b y p r o t e c t i v e a n d a d h e s i v e m a

w h e n t r a n s f e r r e d t o t h e f e m a l e ( S u b r a m o -

, 1 9 9 3) . T h e s e s p e r m - b e a r i n g s t r u c t u r e s

a t o p h o r e s ) , f o r m e d p r i o r t o o r d u r i n g e j a c u l a

v a r y in s i z e , s h a p e , a n d c o m p l e x i t y . T h e p l a c e

e n t o f s p e r m a t o p h o r e s o n t h e e x t e r i o r o f t h e f e

l e o r w i t h i n s p e r m a t h e c a e is o ft en a c h i e v e d w i t h

o r m o r e p a i r s of m a l e g o n o p o d s , w h i c h a r e m o d

e d a n t e r i o r p le o p o d s ( a b d o m i n a l a p p e n d a g e s ) u t i

f or s p e r m t r a n s f e r in m a n y d e c a p o d s ( B a u e r ,

, s u c h a s c a r i d e a n s h r i m p s ( B a u e r , 1 9 7 6 ) ,

a e o i d e a n s h r i m p s ( B a u e r , 1 9 9 1 , 1 9 9 6 a , b ) , c a n i -r i d c r a y f i s h e s ( A n d r e w s , 1 9 1 1 ) , n e p h r o p i d l o b

s ( F a r m e r , 1 9 7 4) , a n d b r a c h y u r a n c r a b s ( C r o n i n ,

R y a n , 1 9 6 7 ) . I n s o m e d e c a p o d s , s u c h a s s t e -

s h r i m p s ( B a u e r , 1 9 8 6 ) a n d p a l i n u r i d l o b

r s ( P h i l l i p s e t a l . , 1 9 8 0 ) , t h e m a l e a n t e r i o r p l e o

s a r e n o t m o d i f i e d fo r s p e r m t r a n s f e r .

M a l e s o f a n o m u r a n s p e c i e s , i n c l u d i n g t h e h e r m i t

o f t h e s u p e r f a m i l y P a g u r o i d e a ( M c L a u g h l i n ,

p r o d u c e c h a r a c t e r i s t i c s p e r m a t o p h o r e s t h a t

p a r e n t l y a r e d e p o s i t e d o n t h e e x t e r n a l s u r f a c e o f

f e m a l e ( T u d g e , 1 9 9 9 a , b ) . T u d g e ( 1 9 9 1 , 1 9 9 5 ,

a n d S u b r a m o n i a m (1 9 9 3 ) d e s c r i b e d t h e

o m i n a n t s p e r m a t o p h o r e t y p e e n c o u n t e r e d i n

r o i d e a n c r a b s a s s t a l k e d o r p e d u n c u l a t e w i t h

e d i s t i n c t c o m p o n e n t s , t h e d i s t a l a m p u l l a , s t a l k .

apposed to t he ven t r a l cepha lo tho rax o f t he f emale . Ama ss ive am ou n t o f sem ina l sec r e t ion con ta in ing spe r m a t o p h o r e r i b b o n s , t e r m e d h e r e t h e s p e r m a t o p h o r i c m a s sand descr ibed for the f i r s t t ime in a hermi t crab species ,was obse rved cover ing the s t e rn i t e s and coxae o f pe r eo -pod s 1-5 of a rece nt ly copu lated fem ale . I t i s sug ges tedtha t du r ing copu la t ion the ma le emi t s t he con ten t s o f t hee j acu la to ry duc t s d i r ec t ly on to the f emale wi thou t t he a ido f gonopods o r gen i t a l pap i l l ae . A l though spe rmatophoret ransfer i s s imple in C. vittatus, the presence of modif ied

an te r io r p l eopods o r e longa te gen i t a l pap i l l ae ( sexua ltubes) i n o the r paguro idean spec i es sugges t s t he poss ib i l i t y o f a more complex insemina t ion p rocess i n t hese o the rh e r m i t c r a b s . J . M o r p h o l . 2 5 3 : 1 6 6 - 1 7 5 , 2 0 0 2 .

© 2002 Wiley-Liss. Inc.

KEY WORDS: gonopods ; gonopores : he rmi t c r ab ; spe r m a t o p h o r e : s p e r m t r a n s f e r

a n d p r o x i m a l p e d e s t a l . T h e s p e r m a t o z o a a r e s t o r e d

w i t h i n t h e a m p u l l a , w h i c h i s c o m p o s e d o f t w o h a l v e s

j o i n e d a l o n g t h e i r l a t e r a l r i d g e s ( T u d g e , 1 9 9 9 a ) . T h e

d i s t a l a m p u l l a r e s t s a t o p t h e s t a l k , w h i c h i s u n d e r

l a i n b y t h e p e d e s t a l o r b a s e o f t h e s t a l k . T h e p e d e s

t a l a p p e a r s t o f u n c t i o n a s t h e p o i n t o f a t t a c h m e n t fo r

t h e s p e r m a t o p h o r e t o t h e e x t e r n a l s u r f a c e of t h e

f e m a l e d u r i n g c o p u l a t i o n ( T u d g e , 19 9 9 b ). M o u c h e t

( 1 9 3 0 , 1 9 3 1 ) a n d H a m o n ( 1 9 3 7 , 1 9 3 9 ) s u g g e s t e d t h a t

t h e a m p u l l a s p l i t s a l o n g t h i s r i d g e , t e r m e d t h e l i n e

o f d e h i s c e n c e ( T u d g e 1 9 9 9 a ) o r "ligiie de suture"

( H a m o n , 1 9 3 7 ) , t h e r e b y r e l e a s i n g t h e s p e r m a t o z o a

( T u d g e 1 9 9 1 , 1 9 9 5 , 1 9 9 9 a , b ) . H a m o n ( 1 9 3 7 ) s u g g e s t e d t h a t m e c h a n i c a l o r o s m o t i c f o rc e s m i g h t

c a u s e t h e a m p u l l a t o f r a c t u r e a n d r e l e a s e t h e s p e r

m a t o z o a .

Contract grant sponsors: the Graduate Student Organization, University of Louisiana at Lafayette I DLL), and the Neptune Foundation.

'Correspondence to: Raymond T. Bauer, Department of Biology,University of Louisiana at Lafayette. Lafayette, Louisiana 70504-

2451. E-mail: [email protected]  

Published online 20 May 2002 inWiley InterSeience (www.interscience.wiley.com) DOI; 10.1002/jmor.lll8

7/27/2019 Spermatophore Transfer in the Hermit Crab Clibanarius Vittatus

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S P E R M A T O P H O R E T R A N S F E R I N A H E R M I T C R A B 1 7 5

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m u r e s e t B r a c h y o u r e s e t c a s t r a t i o n p a r a s i t a i r e c h e z q u e l q u e sP a g u r e s . A n n S t a t O c e a n S a l a m m b o 6 : 1 - 2 0 3 .

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f a m i l i e s P a g u r i d a e a n d P a r a p a g u r i d a e ( P a g u r o i d e a , A n o m u r a ,D e c a poda ) . Inve r t R e p rod D ev 35 :203 - 214 .

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7/27/2019 Spermatophore Transfer in the Hermit Crab Clibanarius Vittatus

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G.S. HE SS AND R.T. BAUER

t h e r s t r u c t u r e s i n a v a r i e t y o f o t h e r d e c a p o d sue r , 1979 , 1998 , 1999) . Th i s b r i s t l i ng a r r a y o f

The gonopores of male Clibanarius vittatus a r er em ar k ab l e ap e r t u r e s gua r ded by f l ap - li ke ope r -

ns ion s of th e e jacula tory duc t s ) , as in se vera l

I n t he penaeo i d sh r i m p Sicyonia dorsalis,

en t o f t h e com pl ex gonopods ( pe t a sm a)ue r , 1996b) . T he lack of gen i ta l pa pi l l ae in m alesC. vittatus i nd i ca t e s t ha t e j acu l a t ed m a t e r i a l s i m

Dur ing the br ie f copula t ion of Clibanarius vittath e gonopo res of th e m ale a re ne ar to or in

tac t wi th th e ve nt r a l sur face of th e female cepha-O u r i n t e r p r e t a t i on i s t h a t w hen e j acu l a

r m a t op hor es i s em i t t ed fr om bo t h m a l e gono

T h e ro w s of s p e r m a t o p h o r e s , n e a t l y a r r a n g e d

ina l secre t ion i s spew ed out onto the fem ale

f e g g s w i t h s p e r m a t o p h o r e s d u r i n g s p a w n i n g

y cause t h e sp l i t t i ng o f t he i r l a t e r a l r i dges sub qu en t re lea se of spe rm atoz oa for fe r t i l i za t ion . Th e

t he m a j o r c l ean i ng and g r oom i ng appendage o f

A l t hough w e conc l ude t ha t t r ans f e r o f spe r m a t o Clibanarius vittatus i s a morphological ly

ods beca use of th e i r comp lex modi f ica t ions

of th e type see n in o th er decap od spec ies in

add i t i on , m any o t he r pagur o i dean spec i e s have p r o nounced gen i t a l pap i l l a e , t e r m ed " sexua l t ubes"( McL augh l i n , 1980; Lem a i t r e and Mc Laug h l i n ,1995) t ha t m i gh t be used t o p l ace spe r m a t ophor i cm asses o r spe r m a t ophor es d i r ec t l y on t he f em a l e i na more complex fashion than tha t observed in C.vittatus. S p e r m a t o p h o r e t r a n s f e r in h e r m i t c r a b s

spec i e s w i t h "gonopods" and s exua l t ubes need s t o bei nves t i ga t ed t o de t e r m i ne i f and how t hese s t r uc t u r e s a r e i nvo l ved i n i n sem i na t i on .

A C K N O W L E D G M E N T S

We t hank D r . F r ank Tr uesda l e f o r g r an t i ng acces sto and ass i s tance a t the col lec t ing s i t e in GrandeTer r e , Lou i s i ana . O ur spec i a l t hanks t o D r s . R a f ae lLem a i t r e and C hr i s t ophe r Tudge f o r sha r i ng t he i rexpe r t i s e i n t he sys t em a t i c s and r ep r oduc t i ve m or pho l ogy o f he r m i t c r abs . We t hank D r s . D a i r y ]Fe l de r , Lew i s D ea t on , and t he anonym ous r ev i ew er so f t he m an usc r i p t fo r he l p fu l co m m ent s and sugges t i o n s . Th i s i s C on t r i bu t i on 80 of t he U LL Lab or a t o r yof C r u s t a c e a n R e s e a r c h .

L I T E R A T U R E C I T E D

Aiken DE, Waddy SL. 1980. Reproduct ive b iology. In : Cobb JS,Ph i l l i p s BF . ed i t o r s . The b i o l ogy and managemen t o f l obs t e r s .New York : Academi c Press , p 215-276 .

Am eyaw -Akfum i C. 1975, Th e breed ing biology of two sym pa t r icspec i es o f t rop i ca l i n t e r t i da l hermi t c r abs , Clibanarius chupini

a n d C. senegalensis. Mar B i o l 29 : 15 -28 .Andre ws EA. 1905 . The sperm - recep t ac l e of Cambarus. J o h n s

H o p k i n s U n i v e r s i t y C i r c u l a r 1 7 8 : 1 - 8 .

Andre ws EA. 1906 . The a nn u l u s ven t r a l i s . P roc Bos t Soc Nat Hi s t3 2 : 4 2 7 - 4 9 7 .

Andre ws EA. 1908 . The sperm - recep t ac l e i n t he c r ay fi shes . Cam-barus CUbetlStS a n d C. paradoxus. Proc Wash Acad Sc i 10 : 167-185 .

And rew s EA. 1911 . Ma l e o rg ans for sperm - t r ans fe r i n t he c r ay fish. Cambarus a/finis: t he i r s t ru c t u re and use . J Morpho l 39 :4 1 9 - 4 3 4 .

Bauer RT. 1976 . Mat i ng behav i o r and spermat ophore t r ans fer i nt h e s h r i m p Heplacarpus piclus (S t i mpson) (Decapoda: Car i dea :Hi ppo l y t i dae) . J Na t Hi s t 10 : 415-4 40 .

Bau er , RT. 1979 . An t i fou l i ng adap t a t i o ns o f m ar i ne sh r i mp (De

capoda: Car i dea) : g i l l c l ean i ng mechan i sms and c l ean i ng o fb rooded embryos . Zoo l J L i nn Soc 65 : 28 1-303 .

Ba ue r RT. 1986 . Phy l oge ne t i c t r en ds i n sperm t r ans fer and s t o r age compl ex i ty i n decapod crus t ace ans . J C rus t ac ean B io l6 : 3 1 3 - 3 2 5 .

B a u e r R T . 1 9 9 1 . S p e r m t r a n s f e r a n d s t o r a g e s t r u c t u r e s i n p e n a e o i d sh r i mps : a func t i ona l and phy l ogene t i c per spec t i ve . In :Bauer RT and Mar t i n JW. ed i t o r s . C rus t acean Sexual B i o l ogy .New York and Oxfo rd : Co l umbi a Un i ver s i t y , p .18 3 -207 .

B a u e r R T . 1 9 9 3 . S p e r m a t o p h o r e s a n d p l u g s u b s t a n c e o f t h e m a r i n e s h r i m p Trachypenaeus sirnilis ( C r u s t a c e a : D e c a p o d a :Peuae i dae l : fo rmat i on i n t he mal e r ep roduct i ve t r ac t and d i s pos i t ion in t he i n sem i na t e d f emal e . B io l Bu ll 18 5 : 174 -18 5 .

Ba ue r RT. 1996a . A t es t o f hypo t heses on mal e mat i ng sys t em s

and f emal e mo l t i ng i n decapod sh r i mp , u s i ng Sicyonia dorsalis( D e c a p o d a : P e n a e o i d e a ) . J C r u s t a c e a n B io l 1 6 : 4 2 9 - 4 3 6 .

Ba uer RT. 1996b . Ro l e o f t he pe t a sm a and a ppend i ce s m ascu l i naedur i n g copu l a t i on and i n sem i na t i on i n t he penaeo i d sh r i m p .Sicyonia dorsalis ( C r u s t a c e a : D e c a p o d a : D e n d r o b r a n c h i a t a ) .I n v e r t e b r R e p r o d D e v 2 9 : 1 7 3 - 1 8 4 .

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SPERMATOPHORE TRANSFER IN A HERMIT CRAB 17 3

Fig . 6 . Clibanarius vittatus. S E M o f t h e s p e r m a t o p h o r i cm a s s o n c o p u l a t e d f e m a l e s ( H M D S d r i e d ) . A , C , E : F e m a l eprese rve d jus t a f te r copula t ion . B , D: Fem ale tha t h ads p a w n e d b e t w e e n c o p u l a t i o n a n d p r e s e r v a t i o n . A : S p e r m a t o

phor i c mass sur rounding the gonopores (gp) and cove r ing thes t e rn i t e s and coxae of pe reopods 1-4 . Note s emina l s ec re t ion( s sl a n d s p e r m a t o p h o r e s ( s p ) w i t h i n t h e s p e r m a t o p h o r i c m a s s .B : R e m n a n t s o f a s p e r m a t o p h o r i c m a s s ( u n l a b e le d a r r o w s ) o na recen t ly spawn ed female , gp , gonopo re . C: H ighe r magni f ica t ion of spe r ma toph or i c m ass f rom A. Note rup tur ing ofs p e r m a t o p h o r e s . s p . s p e r m a t o p h o r e ; s s , s e m i n a l s e c r e t i o n s . D :High er magni f i ca t ion of B show ing rem na nt s o f t he spe rm a top h o r i c m a s s a n d r u p t u r e d s p e r m a t o p h o r e s ( s p ). s s , s e m i n a ls ec re t ion . E : H ig he r magni f i ca t ion of spe rm a top hor e f rom Cshowin g ru p t ur e a long the l i ne of deh i s cence (com pare to Fig .3 E ) . Scale ba r = 1 mm in A and B, 200 urn in C, 100 y.m in Da n d E .

p leo p o d sh o ws n o o b v io u s mo d i f i ca t i o n for t h e ro l e o f f emale p l eo p o d s in i n c u b a t io n o f em -e r m a t o p h o r e t r a n s f e r . A l t h o u g h t h e s e c o n d b r y o s . T h e p l e o p o d s o f f e m a l e s , r e l a t i v e l y l a r g e r

C. vittatus i s s e x u a l l y d i m o r p h i c , t h e a n d m o r e s e t o s e t h a n t h o s e o f m a l e s , s e r v e a sb e t w e e n t h e s e x e s c a n b e a t t r i b u t e d t o a t t a c h m e n t s i t e s fo r e m b r y o s . T h e s e t a e of f e m a l e

"1 ^

-• ' ••' $ > J

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G.S. HE SS AND R.T. BAUER

5. Clibanarius uittatus. P o s i t i o n o f t h e s p e r m a t o p h o r i con the fema le . A : Pho togra ph of a fema le prese rv ed j u s t

spin, s p e r m a t o p h o r i c m a s s . B : D r a w i n g of t h eA d e p i c ti n g s p e r m a t o p h o r i c m a s s ( sp m ) c o v e ri n g t h e

pi—5, pereopods 1—6. C:

ra luc ida dra wi ng of a fema le th a t had copula t e d 2 .5 h

o n a n d p r e s e r v a t i o n . N o t e t h e r e m n a n t s of t h e s p e r m a t o

and 4 (p4) . Scale b ar = 1 cm for B and C.

r o f t h e s p e r m a t o p h o r i c m a s s f ro m t h e m a l e

pos i t ion of the spe rm a top ho r ic ma ss on the fe

the m a le gonopores ra t he r tha n wi th th e a id of go n o p o d s o r o t h e r i n t r o m i t t e n t s t r u c t u r e s .

T he use of modif ied f irst a nd seco nd pleop ods a sg o n o p o d s f or s p e r m a t o p h o r e t r a n s f e r h a s b e e nd e m o n s t r a t e d i n d e c a p o d g r o u p s s u c h a s c a r i d e a ns h r i m p s ( B a u e r , 1 9 7 6 ; B e r g a n d S a n d i f e r , 1 9 8 4 ),

p e n a e o i d e a n s h r i m p s ( B a u e r , 1 9 9 1 , 1 9 9 6 b ) , c a m -b a r i d c r a y f i sh e s ( A n d r e w s , 1 9 1 1 ), n e p h r o p i d l ob s t e r s ( F a r m e r , 1 9 7 4 ) , a n d b r a c h y u r a n c r a b s ( C ro -n in , 1947 ; Ry an , 1967) . M a le s o f Clibanariusvitlatus do no t have f i r s t p l eopods and the s ing le

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S P E RMA T OP HORE T RANS F E R IN A HE RM IT CRAB 171

Fig. 4. Clibanarius vi.ttatus. Copula to r y pos i t ion m ode led f r om v ideo r ecor d ings o f copula t ionand f r om pr ese r v ed spec im e ns p laced in m a t in g pos tu r e . The m a le ( unsha ded , above f em a le ) hasthe gonopor e a r ea n ea r the ven t r a l su r face o f the pos te r io r ceph a lo tho r ax o f the f em a le ( d a r ks h a d i n g ) , a b , a b d o m e n : p l - p 5 , per eopods 1 - 5 .

f th e female in i t s gas t r opo d she l l , a s desc r ibed

t ra l s u r fa c e s o f th e c e p h a lo th o r a x o f

e pos te r io r ve n tr a l su rface of th e pe reopod 1-4e n t s (F ig. 4 ) . T h e m a le a n d fe ma le w a lk in g l e g s

—5 a r e he ld ou tw ard f rom th e ceph a lo th orax a t

c o n ta c t w i th th e f e ma le . In th e th r e e m a t in g

but on ly fo r 5 sec in the th i rd . One of the th reeles f rom the se pa i r s wa s p re se rv ed 2 .5 h a f te r

fem ales , p re se rv ed a t leas t 6 h a f te r co pula t ion ,

S p e r m a t o p h o r i c M a s s

Th e s ing le fema le p res e rve d ju s t a f te r copula t ionh a d a l a rg e o p a q u e g e la t in o u s ma s s c o v e r in g th ev e n t ra l s u r fa c e o f th e c e p h a lo th o ra x f ro m p e re o p o d s1-4 , inc lu d ing the gonopore s (F ig . 5A,B) . Th e adhes iv e s e m in a l s e c re t io n s a t t a c h e d th e s p e rm a to -pho res to th e s te rn i te s and coxae of th e fem ale .Mic ro s c o p ic e x a min a t io n o f th e ma s s p r io r to S E Mre v e a le d lo n g r ib b o n s o f u n ru p tu re d s p e rm a to -p h o re s e mb e d d e d w i th in a m a s s o f s e min a l s e c re t ion . The dehydra t ion p rocess fo r SEM caused theses p e rma to p h o re s to ru p tu re (F ig . 6 A ,C ,E ) . De h y d ra t io n a l s o c a u s e d s o me s h r in k a g e in b o th th e s e min a ls e c r e t i o n a n d s p e r m a t o p h o r e s .

In a n o th e r c o p u la t e d f e ma le , p re s e rv e d 2 .5 h a f t e rc o p u la t io n , s p a wn in g h a d o c c u r re d b u t r e mn a n t s o fa s p e r m a t o p h o r i c m a s s r e m a i n e d , c o v e r i n g t h ecoxae o f pe reo pod s 4 - 5 a s we ll a s th e s te rn i te s ofp e re o p o d s 3 -5 (F ig s . 5 C , 6 B ,D) . Ob s e rv a t io n s ma d ef i r s t w i th a s t e re o mie ro s c o p e a n d th e n S E M s h o we dt h a t r u p t u r e d s p e r m a t o p h o r e s w e r e s t i l l p r e s e n t o nthe coxae o f pe reopods 3 as we l l a s the coxae ands te rn i te s o f pe reopods 4 (F ig . 6B,D).

D I S C U S S I O N

Ha zle t t (1996) f irst no ted th e p rese nce o f a spe rma to p h o r i c ma s s o n re c e n t ly c o p u la t e d f e ma le s o fClibanarius vittatus. In th e p re s e n t s tu d y , we d e s c r ib e th e s p e rm a to p h o r i c m a s s o f a h e rm i t c ra bspecies in deta il for the firs t t ime. I t is composed of

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0 G.S. HESS AND R.T. BAUER

Fig. 3 . Clibanarius vittatus. A: Light micrograph of a r ibbon ofs p e r m a t o p h o r e s ( s p ) s u r r o u n d e d w i t h s e m i n a l s e c r e t i o n s ( s s )wi t h i n t he d i s t a l mo s t r eg i on o f t he va s deferens , ed , e j acu l u t o ryduct . B : En l arg em en t o f A t o show de t a i l of t he sper ma t opho res( sp) and t h e i n t e rcon nec t i ng ba sa l r eg i on (b ) be t we en t wo sper ma t opho res . sz , sperm at ozo a wi t h i n a spe rma t oph ore . C : Confo-ca l mi crog raph o f s i ng l e sper ma t oph ore con t a i n i ng spe rmat o zoa( sz) . D: SEM of t wo HM DS-d r i ed sp erm at oph ores ( sp ) d i s sec t edf rom t he e j acu l a t o ry duc t , s s , semi na l secre t i on . E : SEM of acr i t i ca l -po i n t -d r i ed spe rma t oph ore wi t h cha rac t e r i s t i c l i ne o f dehiscence ( Id) . Scale bar = 500 \t.m in A, 100 |j.m in B, 50 (xm in C,40 |xm in D, and 30 |o.m in E.

en s o f t he va sa de f e r en t i a and e j acu l a t o r y duc t s t hem se l ve s cause d t he l a t t e r t o r u p t u r e a long t he i r

i n a l s e c re t io n or t h e s p e r m a t o p h o r e s

l a t e r a l r i dges .

D e s c r i p t i o n o f C o p u l a t i o n

U pon con t ac t w i t h a r ecep t i ve f em a l e , t he m a l ebeg an p r ecop u l a t o r y behav i o r , a t ap p i n g and r o t a t -

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S P E R M A T O P H O R E T R A N S F E R I N A H E R M I T C R A B 1 69

Fig. 2. Clibanarius villains. Sexua l d imorp hi sm in reproduc t ive morphology of gonop ores and s econd p leopods . A : SEM of ma lepores (gp) and o perc ulum (o) located on the coxae of th e f i fth pere opo ds (HM DS dried ! . B : SE M of female gon opo res (gpl on coxae

th i rd pe reopods (H MD S dr i ed) . C: Ante r io r v i ew of s econd p leopod of ma le ( sh i e ld l eng th = 10 .5 mm ) wi th s e t a e removed , en ,pod; ex, exopod. D: Anterio r view of second pleopod of fema le (shie ld leng th _ 6.3 mm) wi th s e t ae removed , en , endopod; ex ,

SEM of ma le pleopod seta (s t ) and s etu les (su) (cr i t ica l -p oint -d ried) . F : SEM of den se ar ray of female pleo podal 2 se tules ;ind ica t e s m ul t id i g i t a t e s ca l e subse tu l e ( s c ) on s e tu l e (HM DS dr i ed) . G : SE M of a s ing le ma le p l eopod 2 s e tu l e w i th s imp le s ca l e

se tu l e s ( s c) (c r i t ica l -po in t -dr i ed) . H : SEM of fema le s e tu l e w i th mu l t id ig i t a t e s ca l e subse tu l e s ( s c ) (HM DS dr i ed) . Sca le ba r - 1 m m\xm in E, 40 pjm in F, 2 p.m in G, and 4 p.m in H.

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G.S. HESS AND R.T. BAUER

gPvd

Fig. 1. Clibanarius vittatus. Tes tes and vasa de i ' e ren t ia t e rmina t ing wi th in the pereopod 5coxae as e jaeu la to ry d uc t s th a t open to the ex te r io r th ro ugh the gonopores . c, coxa; gp . gonopore ;t , t es t i s ; vd , vas defe rens . Sca le bar = 1 nn t i .

g . 2 B ) . T h e s t e r n u m b e t w e e n t h e t h i r d

ina t io ns o f th e exosk e le ton o r ape r s s u g g e s t i v e of t h e f e m a l e s p e r m - s t o r a g e s t r u c

a n d s p e r m a t h e c a e of p e n a e o i d e a n s h r i m p s

e r , 19 91 , 1993 , 1996a ,b ) , c am bar id c ray f i shesnd rew s , 1905, 1906, 1908; Ho bbs , 1974) , and ne-

( F a r m e r , 1 9 74 ; A i k e n a n d W a d d y ,

st two pair s of pleopod s are modified as go nopodsClibanarius vittatus, as in many

of th e abdo m en. Th e firs t abdo m inal som ite oflacks a p leopod in both males and females

The pleopods ai-e bi ramous , wi th both an endopod

of m ales an d females

and wid th to th e endopod, whi le in male s the exopod islonger and bro ader th an the endopod (Fig . 2C,D). Bothth e endopod an d exopod of fem ale pleopod 2 possess agrea ter number and proport iona l ly longer se tae andse tule s tha n th ose of th e mal e (Fig . 2E,F) . The se tu lesof p leopod 2 se ta e of the ma le a re sparse ly equippedwith s imple scale subsetules (Fig. 2G), wlii le those of

the female a re dense ly covered wi th mul t id ig i ta tesca le subse tules (Fig . 2F.H).

S p e r m a t o p h o r e s a n d S e m i n a l S e c r e t i o n

Sp erm a to ph ore s of th i s spec ie s a re fo rmed p r io r toe jacu la t ion and can be obse rved wi th in the lumensof the vasa d e fe ren t i a a nd e jaeu la to ry duc t s (F igs . 1,3 A , B ) . E a c h n o n p e d u n c u l a t e s p e r m a t o p h o r e i s c o m posed o f two ha lv es me e t in g a t a ra i s e d l ine t e rm edthe " l a t e ra l r idge" o r " l ine o f deh i s cence" (Tudge ,1991 , 1 9 9 9 a ) , f o r m i n g t h e a m p u l l a o f t h e s p e r m a t o phore (F ig . 3D,E) . Spe rma tozoa can be obse rvedwi th in the am pu l l a (F ig . 3B ,C) . Be low the am pu l l ais a basa l region (Fig . 3B) tha t ac ts as a connect ingc o r d a t t a c h i n g a d j a c e n t s p e r m a t o p h o r e s w i t h i n t h e

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SPERMA TOPHORE TRANSF ER IN A HERMIT CRAB 167

Mouche t (1931) . Hamon (1937 , 1939) , Ma thewsG r e e n w o o d ( 1 9 72 ) , a n d U m a a n d S u b r a m o -

Dardanus asper (Diogenidae) form a con

c o n t r a c t i o n s of t h e s u r r o u n d i n g m u s c u l a r

c s h a p e o f t h e s p e r m a t o p h o r e .

A l t h o u g h a s p e c t s of s p e r m a t o p h o r e f o r m a t i o n

; M a th ew s , 1953), the me cha m b y w h i c h s p e r m a t o p h o r e s a r e t r a n s m i t t e d

ma laven i , 1949 ; M a the ws , 1956 ; Haz le t t , 1966 ,Am eyaw-Ak fumi . 1975). The purpo se of th i s

C/ibanarius vittatun.t he an te r io r p leopods of the m a le ,

, s p e r m a t o p h o r e s , a n d s p e r m a t o p h o r i c

A N D M E T H O D S

Live spec imens o f Clibanarius vittatus (Bosc ,w ere col lec ted in Ju ly and A ug us t 1999 from

m a t i n g o b s e r v a t i o n s . T h e h e r m i t c r a b s w e r e

w a t e r t a b l e s y s t e m w i t h w a t e r t e m p e r a t u r e

T e s t e s a n d v a s a d e f e r e n t i a c o n t a i n i n g s p e r m a t o

The crabs were f i rs t anes the t ized by chi l l ing ,

s t r a ig hte n th e abd om ens for ease of d issecan d the n f ixed in 10% form al in . Eja cula tory

the d i s t a lm os t po r t ions o f the vasa de fe ren t i a

g e lec t ron m icroscopy (SEM ). Th e freshly d is rent i a of one m ale wer e p laced in

enated s ea w ate r for 1 h and then placed in 10%

by wa sh i ng wi th s eaw a te r fo r 30 m in , s t a ined wi thFM 464* (Red l ipoph i l i c marke r ) and Sy to 13*(g reen nuc lea r marke r ) fo r 30 min and examinedwith a confoca l microscope (Biorad® MRC 1024 ES).

Dr aw ings of t e s t e s and p leopods were m ad e u s inga camera luc ida moun ted on a s t e reomic roscope .Ma te r i a l pho tographed us ing l igh t mic roscopy wasfirst f ixed in 10% se aw at er form alin for 1 h, wa sh ed

twice wi th seawater for 20 min, s ta ined wi th ac idfuchs in , and c leared wi th CMCP-10 high viscos i tym o u n t a n t .

For obse rva t ion o f morpho logy wi th SE M,fo rm a l in -p re se rved va sa de fe ren t i a , spe rm a to phor es , app end age , and po r t ions of the ceph a lo tho-rax f rom va r ious ind iv idu a l c rabs were wa she d tw icefor 15 min with a 0.2 M PBS (pH 7.2) (Tudge, 1992)to remove re s idua l fo rma l in and then dehydra tedwi th a g raded e thano l s e r i e s (20-100%) . Spec imenswe re e i the r c r i t i c a l -po in t -d r i ed wi th C 0 2 or a i r -dr iedaf te r t rea tment wi th a 1 :1 solut ion of 100% hexam-

e thy ld i s a l i zane (H MD S) and 100% e thano l for 20min fol lowed by im m ers io n in 100% HM DS . Al l specim ens we re spu t t e r -coa te d w i th go ld for 1 -6 minbe fo re v iewing them in a JEOL 6300-FV SEMequipped wi th a d ig i t a l image -cap tu re sys tem.

To a s se s s ova r i an m a tu r i ty for m a t in g obse rva t i o n s , fema le he rmi t c rabs were removed f rom she l l sby gen t ly he a t in g the apex o f the i r ga s t ropod she l l swi t h a bu ta ne c iga re t t e l igh te r . N in e teen fema le sw ith m at ur e ov ar ies ( fu ll of v i te l logenic oocytes ) , butw i t h o u t e m b r y o s or r e m n a n t s of e g g m e m b r a n e s o nthe p leopods , we re ind iv idua l ly pa i red wi th a ma le

in aqu ar ia . Act iv i t ies were recorded for 1 day a t a24-h recording speed (f ive f rames /sec) wi th a t ime-lapse v ideo recor der sys tem a t t ach ed to an infrared -sens i t ive su rve i l l an ce cam era equ ipped wi th a 3 0 -180 m m zoom lens . I l lu m ina t ion cons is ted of two 880nm in f ra red l amps dur ing the n igh t (da rk ) pe r iodan d two 40 -w at t fluorescent lam ps for day (l igh t)obse rva t ions . V ideo tapes were rev iewed da i ly to de t e r m ine if copu la t ion ha d occur red . W hen copu la t ionwa s observe d on a ta pe (3 of 19 pa i r ings ) , th e pa i rswere p re se rved in 10% sea wa te r fo rma l in and th efema le s were l a t e r examined fo r the p re sence o r

absence o f spe rm a top hor es and s em ina l s ec re t ions .One add i t iona l copu la t ion was obse rved on a wa te rt ab le and the ma t ing pa i r was immedia te ly p re s e rved and l a t e r examined a s in the o the r th reep a i r s .

R E S U L T S

G o n o p o r e a n d P l e o p o d M o r p h o l o g y

Th e dis t a l ends of th e va sa deferen t ia , th e e jacula tory du ets , a r e loca ted wi th in the coxae of th e f if th

pereopods of the male and open to the exter ior v iathe gonopores (Figs . 1 , 2A). These openings a regu ard ed by f lap- like oper cula (Fig . 2A). T he femalegonopo res , the e x te rn a l open ings of the ov iduc t s , a r e