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Preservation methodology and stable isotope composition in sea stars: Can museum collections be useful for trophic ecology studies?

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(1)

Preservation methodology and stable

isotope composition in sea stars:

Can museum collections be useful for

trophic ecology studies?

(2)

Context

Objectives Methodology Results ConclusionsSummary

PhD project

● Study of trophic ecology of Antarctic sea stars using stable

isotopes

(3)

Context

Objectives Methodology Results ConclusionsSummary

PhD project

(4)

● Museum specimens in food web studies?

→ Samples for past periods

● Museum samples are stored/fixed with preservative fluids

(formaldehyde, ethanol) or dried instead of frozen

● Impact of preservation method on stable isotopes ratios?

→ No studies on sea stars Context

(5)

Objectives

δ

13

C

δ

15

N

Drying Freezing Formaldehyde Ethanol

?

To assess the temporal evolution of stable isotope ratios in sea

star samples preserved with four preservation treatments: Context

(6)

Marthasterias glacialis (Atlantic Ocean), n = 20

Context

(7)

Marthasterias glacialis (Atlantic Ocean), n = 20

● Arm 1 = control T0 (dissection, drying and grounding)

Context

(8)

Marthasterias glacialis (Atlantic Ocean), n = 20

● Arm 1 = control T0 (dissection, drying and grounding)

● Other arms = treatments: drying (control), freezing at -28°C, 3.4%

formaldehyde, 99.8% ethanol)

Context

(9)

Marthasterias glacialis (Atlantic Ocean), n = 20

● Arm 1 = control T0 (dissection, drying and grounding)

● Other arms = treatments: drying (control), freezing at -28°C, 3.4%

formaldehyde, 99.8% ethanol)

six sections per arm → time effect (1 to 24 months)

Context

(10)

Context

Objectives Methodology Results ConclusionsSummary

● Comparison of mean δ13C and δ15N between T0 and preserved

samples

● Comparison of SEA

B between T0 and preserved samples

● Estimation of overlap between

T0 and preserved samples

● Good overlap if similar or

higher than the overlap between the T0 of each treatment

(11)

Context

Objectives Methodology Results ConclusionsSummary

● Formaldehyde: sharp decrease of δ13C and then stability ● Ethanol: non-significant and continuous increase of δ13C

(12)

Context

Objectives Methodology Results ConclusionsSummary

(13)

● No consistent

change of SEAB through time.

● Low overlap from 3

to 9 months.

Drying (control)

Context

(14)

● No significant changes of SEAB through time. ● Low overlap at 6 months.

Freezing

Context

(15)

● No consistent

change of SEAB trough time.

● Decrease and then

stability of δ13C → no overlap.

Formaldehyde

Context

(16)

● No consistent change of SEAB through time. ● Low overlap at 6 months.

Ethanol

Context

(17)

Context

Objectives Methodology Results ConclusionsSummary Mean δ13C Mean δ15N SEA

B Overlap

Drying NS NS NS NS

Freezing NS NS NS < T0

Formaldehyde Decrease NS NS Low

Ethanol NS NS Inconsistent < T0

● Non-consistent changes of stable isotope values, ellipse size and

reduction of overlap (6 months)

(18)

● Freezing: Best preservation method ● Ethanol: Beware of lipid content

● Formaldehyde:

+0.8

Context

(19)

Acknowledgements

Samples used in the PhD project provided with the help of: – Camille Moreau (Université Libre de Bruxelles)

– Quentin Jossart (Université Libre de Bruxelles) – Bruno Danis (Université Libre de Bruxelles)

(20)

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