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Importance of Physiological Traits Vulnerability in Determine Halophytes Tolerance to Salinity Excess: A Comparative Assessment in Atriplex halimus

Abstract

Many halophytic physiological traits related to the tolerance of plants to salinity excess have been extensively studied, with a focus on biomass and/or gas exchange parameters. To gain a more complete understanding of whether salinity excess affects the physiological performance of halophytes, an experiment was performed using the halophyte Atriplex halimus L. as a model. A. halimus plants were subjected to two salinity treatments (171 and 513 mM NaCl) over 60 days in a controlled environment. After this period, dry biomass, specific stem conductivity, water potential at turgor loss point, osmotic potential, gas exchange parameters, and the fluorescence of chlorophyll a derived parameters were assessed in order to obtain knowledge about the differences in vulnerability that these parameters can show when subjected to salinity stress. Our results showed a decrease in belowground and aboveground biomass. The decrement in biomass seen at 513 mM NaCl was related to photosynthetic limitations and specific stem conductivity. Turgor loss point did not vary significantly with the increment of salinity. Therefore, the parameter that showed less vulnerability to saline stress was the turgor loss point, with only a 5% decrease, and the more vulnerable trait was the stem conductivity, with a reduction of nearly 50%.

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Importance of Physiological Traits Vulnerability in Determine Halophytes Tolerance to Salinity Excess: A Comparative Assessment in Atriplex halimus

Author: Pérez Romero, Jesús Alberto; Mateos Naranjo, Enrique; López Jurado, Javier; Redondo Gómez, Susana; Torres Ruiz, José Manuel
Publisher: MDPI
Year: 2020
DOI: 10.3390/plants9060690
Source: https://idus.us.es/bitstreams/700691f3-90fe-4eac-9030-ca2b5451be9e/download
plan s
A icle
Impo ance o Physiological T ai s Vulne abili y in
De e mine Halophy es Tole ance o Salini y Excess:
A Compa a i e Assessmen in A iplex halimus
Jesús Albe o Pé ez-Rome o 1,* , En ique Ma eos-Na anjo 1, Ja ie López-Ju ado 1,
Susana Redondo-Gómez 1and JoséM. To es-Ruiz 2
1Dp o. de Biología Vege al y Ecología, Facul ad de Biología, Uni e sidad de Se illa, A Reina Me cedes s/n,
41012 Se illa, Spain; [email p o ec ed] (E.M.-N.); [email p o ec ed] (J.L.-J.); [email p o ec ed] (S.R.-G.)
2INRA, PIAF, Uni e si éCle mon -Au e gne, 63000 Cle mon -Fe and, F ance; o es [email p o ec ed]
*Co espondence: jpe [email p o ec ed]; Tel.: +34-95-4557064; Fax: +34-95-4615780
Recei ed: 7 May 2020; Accep ed: 26 May 2020; Published: 28 May 2020


Abs ac :
Many halophy ic physiological ai s ela ed o he ole ance o plan s o salini y excess
ha e been ex ensi ely s udied, wi h a ocus on biomass and/o gas exchange pa ame e s. To gain
a mo e comple e unde s anding o whe he salini y excess a ec s he physiological pe o mance
o halophy es, an expe imen was pe o med using he halophy e A iplex halimus L. as a model.
A. halimus plan s we e subjec ed o wo salini y ea men s (171 and 513 mM NaCl) o e 60 days in a
con olled en i onmen . A e his pe iod, d y biomass, speci ic s em conduc i i y, wa e po en ial a
u go loss poin , osmo ic po en ial, gas exchange pa ame e s, and he luo escence o chlo ophyll a
de i ed pa ame e s we e assessed in o de o ob ain knowledge abou he di e ences in ulne abili y
ha hese pa ame e s can show when subjec ed o salini y s ess. Ou esul s showed a dec ease
in belowg ound and abo eg ound biomass. The dec emen in biomass seen a 513 mM NaCl was
ela ed o pho osyn he ic limi a ions and speci ic s em conduc i i y. Tu go loss poin did no a y
signi ican ly wi h he inc emen o salini y. The e o e, he pa ame e ha showed less ulne abili y o
saline s ess was he u go loss poin , wi h only a 5% dec ease, and he mo e ulne able ai was he
s em conduc i i y, wi h a educ ion o nea ly 50%.
Keywo ds:
halophy e; speci ic conduc i i y; u go loss poin ; pho osyn hesis; chlo ophyll luo escence
1. In oduc ion
Halophy es a e plan species wi h he abili y o comple e hei li e cycles unde a leas 200 mM
NaCl [
1
]. The e a e many physiological mechanisms in ol ed in he capaci y o halophy es o cope
wi h salini y excess, and hese esponses and mechanisms a e species-speci ic in many cases [2].
Among speci ic ole ance mechanisms, i is well ecognized ha halophy es use osmop o ec i e
and ion-de oxi ica ion s a egies [
3
–
5
] o egula e hei issues’ Na concen a ion pa e ns o K/Na a io
a ia ions [
2
]. Many s udies ha e been ca ied ou o e alua e he e ec o sal excess ca boxyla ion
capaci y and ene gy use e iciency in halophy es [
6
–
12
], showing how hese plan s a e able o main ain
me abolic p ocesses despi e being exposed o high sal concen a ion. Howe e , s udies ocused on he
e ec o sal on xylem ana omy and unc ioning, plan –wa e ela ions, and pho osyn he ic capaci y
a e sca ce [
13
], despi e he ele ance o hese ai s o de e mine plan ole ance o en i onmen al
s ess [
14
–
16
]. The e ha e been ew a emp s o assess he e ec o salini y on pa ame e s such as
u go loss poin in halophy e species. These s udies ha e assessed he impo ance o soil-sal wa e
on he wa e s a us o Juncus oeme ianus [
17
] and di e ences in xylem speci ic conduc i i y among
di e en mang o e species, in which L
ó
pez-Po illo e al. [
18
] ound di e en esponses in glycophy e
and halophy e species.
Plan s 2020,9, 690; doi:10.3390/plan s9060690 www.mdpi.com/jou nal/plan s
Plan s 2020,9, 690 2 o 11
Cell u go loss has an impac on cellula s uc u al in eg i y, me abolism, and whole-plan
pe o mance [
19
,
20
], being a ai ha has been adi ionally conside ed an indica o o plan wa e
s ess [
21
]. Due o he simila i ies be ween wa e and Salini y s ess [
22
], s udying how u go loss poin
a ies in halophy es exposed o salini y s ess is impo an o imp o e ou knowledge abou which
mechanisms a ec hese changes. E alua ing how di e en sal concen a ions a ec he ana omical
p ope ies o xylem and i s hyd aulic e iciency would also allow us o be e unde s and he esponse
o halophy es o salini y [13].
In addi ion, i is a e o ind a comple e analysis o hese ai s aking in o accoun plan
pho osyn he ic pe o mance pa ame e s o acqui e a b oade iew o some o he main physiological
esponses o halophy es o excess salini y.
To gain a mo e comple e unde s anding o whe he salini y excess a ec s he physiological
pe o mance o halophy es, he e ec o di e en sal concen a ions on he ana omical and unc ional
p ope ies o xylem, plan wa e s a us, gas exchange, and chlo ophyll luo escence we e e alua ed in
he halophy e A iplex halimus L.
The A iplex genus is composed o mo e han 400 species wo ldwide [
23
]. Se e al species o his
genus a e well adap ed o ex eme en i onmen al condi ions such as A. ho ensis, which is ole an
o high salini y, A. canescens a . angus i olia, which is a d ough - ole an sh ub, o A. len i o mis,
which can li e in seawa e i iga ion and xe ic condi ions [
24
]. A iplex species could se e as ools
o he phy o emedia ion o pollu ed, a id, o semi-a id soils [
22
,
25
–
27
] o as o age species [
27
–
29
].
Among hem, A iplex halimus L. is one o he mos plan ed A iplex species wo ldwide [
22
], and he e o e
ep esen s one o he mos impo an species wi hin his genus. I is a pe ennial sh ub wi h a C4
pho osyn he ic me abolic pa hway ha is able o g ow in a wide ange o salini y condi ions [
22
].
This cha ac e is ic makes i a good candida e o he exhaus i e analysis o he e ec s o salini y excess
on plan physiological pe o mance.
He e, we hypo hesized ha di e en salini y le els would exe a di e en ial e ec on he main
physiological plan ai s ela ed o ole ance o salini y. The e o e, he possible exis ence o di e en
ulne abili y le els o sal s ess in hese ai s should be conside ed when de e mining he salini y
ole ance o his species. Thus, he aim o his wo k was o e alua e how di e en le els o NaCl
concen a ion in g owing solu ion a ec ed he u go loss poin , xylem speci ic heo e ical conduc i i y,
hyd aulic mean diame e , essel densi y, osmo ic po en ial, and he main lea gas exchange and
chlo ophyll luo escence pa ame e s in o de o achie e a mo e global ision o he physiological
pe o mance o A. halimus unde di e en salini y concen a ions. The wo selec ed le els we e 171 mM
NaCl (o 10 g L−1) and a h ee old highe one (i.e., 513 mM o 30 g L−1).
2. Resul s and Discussion
2.1. Plan De elopmen and Xylem Ana omical and Func ional Fea u es
The e we e signi ican e ec s o salini y on he g ow h, xylem speci ic heo e ical conduc i i y,
and hyd aulic mean diame e o A iplex halimus L. a e 60 days o ea men . Mo e speci ically,
ae ial pho osyn he ic, ae ial non-pho osyn he ic, and oo d y mass dec eased by 24%, 51%, and 41%,
espec i ely, in plan s g own in 513 mM NaCl compa ed o he con ol ea men (171 mM NaCl)
(one-way ANOVA, p<0.05; Table 1). Ou esul s ag ee wi h o he o me s udies showing ha
NaCl le els g ea e han 200 mM induce a signi ican dec ease in he biomass o A. halimus [
29
–
31
].
Howe e , no e ec on g ow h has been desc ibed o da e o NaCl concen a ions below 600 mM [
22
,
32
].
These disc epancies be ween s udies ega ding he e ec o NaCl concen a ions on plan g ow h
ha e been asc ibed o in aspeci ic a iabili y in g ow h esponses o salini y excess ac oss A iplex
popula ions, which a e dis ibu ed in di e en habi a s [32–36].
Plan s 2020,9, 690 3 o 11
Table 1.
Pho osyn he ic d y mass, non-pho osyn he ic d y mass, oo d y mass (R ), ne pho osyn he ic
a e (A
N
), s oma al conduc ance (g
s
), in e cellula CO
2
concen a ion, (C
i
), in insic wa e use e iciency
(
i
WUE), and maximum quan um e iciency o pho osys em II (PSII) pho ochemis y (F
/F
m
) and
quan um e iciency o PSII (
ΦPSII
) o A iplex halimus L. in esponse o ea men wi h 171 and 510 mM
NaCl o 60 d. Biomass and physiological pa ame e alues ep esen mean
±
SE, n=16 and n=12,
espec i ely. Di e en le e s indica e means ha a e signi ican ly di e en be ween bo h salini ies
(ANOVA es , p<0.05).
Salini y Concen a ion
Pa ame e s 171 mM 510 mM
Pho osyn he ic d y mass (g) 5.98 ±0.44 a4.55 ±0.53 b
Non-pho osyn he ic d y mass (g) 5.41 ±0.53 a2.73 ±0.44 b
Roo d y mass (g) 1.48 ±0.12 a0.89 ±0.13 b
AN(µmoL m−2s−1)4.35 ±0.67 a2.74 ±0.32 b
gs(mmoL m−2s−1)53.4 ±7.47 a46.6 ±6.49 a
Ci (µmoL mol−1)252.1 ±30.0 a274.6 ±23.5 a
iWUE (µmoL mol−1)84.3 ±12.6 a69.1 ±11.6 a
F /Fm 0.70 ±0.02 a0.70 ±0.02 a
ΦPSII 0.18 ±0.03 a0.14 ±0.02 a
a, b show he signi ican di e ences be ween salini ies
I is well known ha sal s ess can a ec he ana omy o xylem, which can exe a limi a ion on
plan hyd aulic unc ioning [
13
,
37
]. Highe NaCl concen a ion a ec ed he ana omy, educing he
essel diame e (Figu e 1) and p oducing a non-signi ican inc ease o essel densi y (VD) (Figu e 2).
Mo eo e , he pi h and co ex a ea inc eased, and a xylem essel numbe dec ease was seen a 510
mM NaCl (Figu e 1). Thus, no signi ican di e ences in VD we e obse ed be ween he wo NaCl
concen a ions (Figu e 2). Howe e , he e was a signi ican educ ion in hyd aulic mean diame e
(dh) o plan s g own a 513 mM NaCl (one-way ANOVA, p<0.05; Figu e 2). These a ia ions in he
diame e o he xylem essels be ween ea men s also led o a signi ican di e ence in xylem hyd aulic
unc ioning be ween hem. The lowe alues o xylem speci ic heo e ical conduc i i y (K
S
) o hose
plan s exposed o highe NaCl concen a ion (one-way ANOVA, p<0.05; Figu e 2) illus a ed his
di e ence in xylem unc ioning. In line wi h ou esul s, Boughalleb e al. [
13
] obse ed a dec ease in
essel diame e o A. halimus g own a 800 mM NaCl, and L
ó
pez-Po illo e al. [
18
] epo ed highe K
S
alues o halophy e plan s when g own be ween 3 and 253 mM NaCl and lowe alues o plan s
g own beyond ha ange o salini y.
Figu e 1.
T ans e sal sec ions o he main s em o A iplex halimus L. s ained wi h 1% oluidine blue
g own a 171 (
A
) and 513 (
B
) mM NaCl a e 60 d ea men showing E (epide mis), Co (co ex),
Xy (xylem essels), and P (pi h cells).
Plan s 2020,9, 690 4 o 11
Figu e 2.
Xylem speci ic heo e ical conduc i i y, K
S
(
A
), essel densi y, VD (
B
), and hyd aulic mean
diame e , dh (
C
) in andomly selec ed p ima y lea es o A iplex halimus L. in esponse o ea men
wi h wo NaCl concen a ions (171 and 513 mM) a e 60 d o ea men . Values ep esen mean
±
SE,
n=3. Di e en le e s indica e means ha a e signi ican ly di e en om each o he (ANOVA es ,
p<0.05) and ns indica es non-signi ican di e ences.
2.2. Plan –Wa e Rela ions Analysis
The e we e signi ican e ec s o salini y on some plan –wa e ela ions o A iplex halimus L. a e
60 days o ea men , wi h lowe osmo ic po en ial alues (
ΨO
) o highe NaCl ea men . Plan s g own
a 171 and 513 mM NaCl showed
ΨO
alues o
−
4.5 and
−
6.9 MPa, espec i ely (one-way ANOVA,
p<0.05; Figu e 3B), in conco dance wi h p e iously epo ed alues o his species [
33
]. Meanwhile,
lea u go loss poin (
ΨTLP
) did no a y wi h NaCl concen a ion, wi h mean alues o ~
−
1.70 MPa
o bo h ea men s (Figu e 3A).
ΨTLP
has been used o assess physiological abio ic s ess ole ance o
d ough [
21
], wi h lowe alues measu ed in plan s occu ing in high salinized habi a s [
17
]. Lowe
u go loss poin alues indica e a wide ange o lea wa e po en ials wi hin which he lea emains
u gid and main ains i s unc ion [
38
,
39
]. In his sense, lowe
ΨTLP
alues ha e been ela ed o plan
abili y o main ain s oma al conduc ance, pho osyn he ic gas exchange and g ow h a low soil wa e
Plan s 2020,9, 690 5 o 11
po en ial [
38
,
40
–
43
]. The osmo egula o y capaci y ep esen s an impo an adap ion by plan s o sal
s ess since i allows hem o keep aking wa e om he soil e en when exposed o high le els o sal
s ess [
17
]. Thus, he capaci y o A. halimus o main ain he
ΨTLP
while educing
ΨO
a high NaCl
concen a ions e lec s he capaci y o his species o cope wi h high concen a ions o sal .
Figu e 3.
Wa e po en ial o u go loss poin ,
ΨTLP
(
A
) and osmo ic po en ial,
Ψ0
(
B
) in andomly
selec ed p ima y lea es o A iplex halimus L. in esponse o ea men wi h wo NaCl concen a ions
(171 and 513 mM) a e 60 d o ea men . Values ep esen mean
±
SE, n=5. Di e en le e s
indica e means ha a e signi ican ly di e en om each o he (ANOVA es , p<0.05) and ns indica es
non-signi ican di e ences.
2.3. Plan Pho osyn he ic Pe o mance Analysis
Salini y a ec ed some ai s ela ed o gas exchange. Thus, ne pho osyn he ic a e (A
N
) alues
we e signi ican ly lowe in plan s g own a 513 mM NaCl han in he con ol plan s (one-way ANOVA,
p<0.05; Table 1), while simila alues o s oma al conduc ance (g
s
), in e cellula CO
2
concen a ion
(C
i
), and in insic wa e use e iciency (
i
WUE) we e obse ed be ween NaCl concen a ion ea men s
(Table 1). The lack o di e ences in C
i
e en wi h a signi ican dec emen o A
N
could indica e a g ea e
e ec o NaCl inc emen on he ubisco ac i i y a he han plan CO
2
di usion capaci y, as has been
desc ibed o o he halophy es [12,44–46].
I has been epo ed ha he impac o NaCl excess on plan pho osyn he ic pe o mance is ela ed
o al e a ions in pho osys em II (PSII) pho ochemis y machine y e iciency [
47
]. In ac , se e al s udies

Plan s 2020,9, 690 6 o 11
ha e al eady shown how salini y excess dec eased elec on chain e iciency along wi h he abili y o
use he inciden pho ons [
10
,
48
,
49
], which can lead o a signi ican dec ease in he maximum yield o
p ima y pho ochemis y [
50
]. In con as o hese obse a ions, ou luo escence esul s indica ed ha
F
/F
m
and
ΦPSII
alues did no a y signi ican ly be ween salini y le els (ANOVA, p>0.05; Table 1),
indica ing he high in eg i y and unc ionali y o i s pho ochemical appa a us unde sal excess, as has
been p e iously desc ibed o o he halophy ic species [9].
2.4. Analysis o Di e en ial T ai s Vulne abili y o Salini y Excess
The ole ance o halophy es o salini y has been in ensely s udied wo ldwide, and he
cha ac e iza ion o his ole ance has usually been based on speci ic physiological ai s, o en combined
wi h de ailed plan de elopmen analyses [
6
–
12
]. Many s udies ha e based hei ole ance in e ences
on de ailed analyses o plan wa e s a us. In ac , ΨTLP has been widely used o assess physiological
abio ic s ess ole ance, as p e iously men ioned. Based on his, ou
ΨTLP
alues indica ed a a ia ion
o 5% be ween 171 and 513 mM NaCl. Toge he wi h small a ia ions in o he eco ded ai s linked
wi h plan wa e s a us and use e iciency, such as
ΨO,
g
s
and
i
WUE, his indica ed a g ea capaci y o
A. halimus o ole a e salini y. This was also suppo ed by ou esul s on PSII pho ochemis y e iciency,
since F
/F
m
and
ΦPSII
did no a y wi h he inc emen o salini y. Howe e , hese esul s con as ed
wi h a d as ic educ ion in plan g ow h (i.e., almos
−
40%) unde ele a ed NaCl concen a ion.
This g ow h esponse is likely ela ed o he a ia ions obse ed in o he physiological ai s, such as
plan CO
2
assimila ion capaci y. In his sense, we ound ha A
N
dec eased ci ca 30% in plan s g own
a 513 mM NaCl, his pe cen age being simila o ha egis e ed o plan pho osyn he ic and oo
g ow h. Simila ly, he xylem ana omical p ope ies showed a good ela ionship wi h plan g ow h
esponses. Thus, a educ ion in K
S
o almos 50% was obse ed o plan s g own a 513 mM NaCl
compa ed wi h plan s g own a 171 mM NaCl.
The e o e, ou esul s showed di e en esponses o salini y o hose physiological ai s in ol ed
in ca bon assimila ion and hyd aulic unc ioning, which we e e lec ed in di e en g ow h a es o
plan s exposed o he highe NaCl concen a ion. Thus, he capaci y o A. halimus o main ain he
ΨTLP
while educing
ΨO
a high NaCl concen a ion e lec s he capaci y o his species o cope wi h
high concen a ions o sal . Mo e s udies e alua ing di e en halophy e species exposed o di e en
NaCl concen a ions a e he e o e equi ed o ob ain a mo e comp ehensi e unde s anding o how
his abio ic s ess a ec s halophy e pe o mance and o de e mine plan sal ole ance mo e p ecisely.
This is i al o a oid possible masking e ec s ha occu when s udies a e based on assessing a small
numbe o ai s ocusing exclusi ely on ce ain me abolic p ocesses.
3. Ma e ial and Me hods
3.1. Plan Ma e ial
Cu ings o A iplex halimus L. we e collec ed in Ap il 2018 om di e en adul indi iduals
(n=20) ha we e andomly selec ed om a well-es ablished popula ion in Odiel Ma shes (37
◦
15
0
N,
6
◦
58
0
O; SW Spain). Cu ings we e anspo ed o he labo a o y in a e ige a ed chambe (4
◦
C) and
immedia ely plan ed in indi idual plas ic po s (9 cm high
×
11 cm diame e ) using pe li e as subs a e.
Then, po s we e placed in a g eenhouse unde con olled condi ions: empe a u e be ween 21 and
25
◦
C, 40%–60% ela i e humidi y, and na u al dayligh o 250
µ
mol m
−2
s
−1
as he minimum and
1000
µ
mol m
−2
s
−1
as he maximum ligh lux. Po s we e alloca ed o shallow ays and wa e ed wi h
20% Hoagland’s solu ion [
51
] and 171 mM NaCl. Plan s we e kep unde hese condi ions un il he
expe imen al se up.
3.2. Expe imen al T ea men s
In July 2018, a e 3 mon hs o cu ing cul u e, 17 cm high plan s showing a comple ely de eloped
oo sys em we e andomly di ided in o wo blocks o 30 plan s each. Each block was exposed o
Plan s 2020,9, 690 7 o 11
di e en NaCl concen a ions: con ol (171 mM) and ele a ed concen a ion (513 mM) o 60 days.
Chosen salini ies we e based on A. halimus soil salini y concen a ion ole ance, [
29
–
31
] and can be
ound in he na u al dis ibu ion o his species [
7
]. These NaCl concen a ions we e es ablished by
combining Hoagland’s solu ion wi h app op ia e amoun s o NaCl. A he beginning o he expe imen ,
he po s we e placed in plas ic ays con aining app op ia e solu ions o a dep h o 1 cm. Du ing
he expe imen , g eenhouse condi ions we e con olled wi h a empe a u e o 21–25
◦
C, 40%–60%
ela i e humidi y, and na u al dayligh o 250
µ
mol m
−2
s
−1
as he minimum and 1000
µ
mol m
−2
s
−1
as he maximum ligh lux. NaCl concen a ion in he g ow h medium was moni o ed con inuously o
a oid changes caused by wa e e apo a ion om he nu ien solu ion. In addi ion, he en i e solu ion
(including NaCl) in he ays was enewed weekly.
A e 60 days o exposu e o salini y ea men s, an exhaus i e e alua ion o xylem ana omical
and unc ional ea u es we e made. This analysis was complemen ed wi h measu emen s o lea
wa e ela ions and pho osyn he ic appa a us pe o mance. Finally, he emaining plan s (n=16,
six een samples pe ea men ) we e ha es ed, and belowg ound and abo eg ound (pho osyn he ic
and non-pho osyn he ic) ac ions we e sepa a ed, d ied a 80
◦
C o 48 h, and weighed o d y
mass de e mina ion.
3.3. E alua ion o Xylem Speci ic Theo e ical Conduc i i y, Hyd aulic Mean Diame e , and Vessel Densi y
Fo xylem ana omy cha ac e iza ion, 5 cm long b anch samples we e andomly collec ed om
plan s g own in bo h salini y ea men s (n=3, h ee samples pe ea men ). All samples we e collec ed
10 cm abo e he base o he ille and we e w apped in mois pape o keep hem well hyd a ed un il
sample p epa a ion o sec ioning. Samples we e i s ly ixed in FAA (3.7% o maldehyde, 50% e hanol,
5% ace ic acid, and 41.3% wa e ) and hen dehyd a ed h ough a g adual e hanol se ies (50%, 70%, 80%,
and 95%). Then, samples we e p og essi ely embedded in LR Whi e esin (Sigma-Ald ich) o 30 min
a 4
◦
C in di e en esin:e hanol 100% combina ions (1/3:2/3; 1/2:1/2; 2/3:1/3) o 1 h a 4
◦
C in pu e LR
Whi e esin. Finally, samples embedded in he esin we e encapsula ed in gela in capsules (size 4) and
le o 48 h a 50–55
◦
C o achie e he polyme iza ion o he esin. In o de o ob ain hin sec ions (2 and
3
µ
m hick), an OmU2 o a y mic o ome (Reiche , Vienna, Aus ia) equipped wi h a his o diamond
kni e was used. Sec ions we e s ained wi h 1% oluidine blue (w/ ). C oss sec ions we e obse ed unde
an op ical mic oscope ( ansmi ed ligh , Zeiss Axioplan 2, Zeiss, Jena, Ge many) a
×
40 magni ica ion.
Images we e eco ded using a digi al came a (AxioCam HR, Zeiss) wi h AxioVision digi al imaging
so wa e. By using he “mosaic” ool, a single image pe sample was cons uc ed by joining images
wi h he same magni ica ion. A e spa ial calib a ion, ana omical and unc ional measu emen s we e
pe o med by image analysis in o de o de e mine essel densi y (VD), hyd aulically weigh ed essel
diame e (dh), and heo e ical speci ic xylem hyd aulic conduc ance (K
S
) o h ee c oss sec ions pe
sample using ImageJ so wa e [
52
]. K
S
(mmol m
−2
MPa
−1
s
−1
) was calcula ed by adding up he
conduc i i ies o he condui s ound in he c oss sec ion, using he Hagen–Poiseuille equa ion o
calcula e he conduc i i y o e e y single condui :
Ks =
πd4
128η
As
whe e dis he in e nal diame e o he condui ,
η
is he dynamic iscosi y o wa e aken as 10
−9
MPa s
a 20 ◦C and As is he c oss-sec ional a ea.
VD was calcula ed as he quo ien be ween he xylem a ea and he numbe o essels. Hyd aulic
mean diame e (dh) was calcula ed ollowing he Spe y e al. [53] o mula:
dh =
2P 5
P 4
whe e is he a io o he essels.
Plan s 2020,9, 690 8 o 11
3.4. Lea Tu go Loss Poin and Osmo ic Po en ial
To es he e ec o salini y inc emen on plan –wa e ela ions, we quan i ied lea u go loss poin
(
ΨTLP
) and osmo ic po en ial (
ΨO
) (n=5, i e samples pe ea men ). Fo
ΨTLP
, p essu e– olume
cu es we e pe o med on andomly selec ed ully de eloped lea es. Thus, lea es we e collec ed wi h
a azo blade and ully hyd a ed du ing 24 h in he da k a 4
◦
C. A e ha , lea wa e po en ial and
esh lea weigh we e measu ed e e y 3 min using a Scholande - ype chambe (PMS) and a scale
(Me le -Toledo), espec i ely, un il he lea wa e po en ial eached ca.
−
4 MPa. Then, lea es we e
d ied a 80
◦
C o 24 h, and he d y mass was measu ed [
54
]. Lea ela i e wa e con en (RWC) was
de e mined along wi h he measu emen s by he a io be ween he d y and esh weigh acco ding o
Sack and Pasque -Kok [
55
]. The a ea o each indi idual lea was de e mined by using an LI-3100C a ea
me e (LICOR). Finally,
ΨTLP
alues we e ob ained a e plo ing lea wa e po en ial s. 100 RWC
alue o de e mine he poin a which he ansi ion be ween cu ed and linea po ions occu ed.
Lea osmo ic po en ial (
ΨO
) was de e mined by eezing small po ions o lea issue in liquid
ni ogen, le ing hem haw, and cen i uging (12,000
×
g, 10 min) a 4
◦
C in 2 mL ubes. To sepa a e a
minimum o 10
µ
L o lea sap, we inse ed he ops o il e ips in o hese ubes.
ΨO
was measu ed om
he ex ac ed sap using he psych ome ic echnique wi h a apo p essu e osmome e (5600 Vap o,
Wesco , Logan, UT, USA).
3.5. Lea Gas Exchange
Lea gas exchange and chlo ophyll luo escence pa ame e s we e measu ed in ully expanded
lea es (n=12, wel e samples pe ea men ) using an in a ed gas analyze (LI-6400-XT, Li-COR
Inc., Lincoln, NE, USA) and a modula ed luo ime e (FMS-2; Hansa ech Ins umen s L d., King’s
Lynn, UK), espec i ely. Thus, ne pho osyn he ic a e (AN), s oma al conduc ance (gs), in e cellula
CO
2
concen a ion (C
i
), and ins an aneous wa e use e iciency (
i
WUE; a io be ween A
N
and g
s
)
we e ob ained. The ollowing se ings we e applied: lux ligh densi y o 1000
µ
moL pho ons
m
−2
s
−1
(wi h 15% blue ligh o maximize s oma al ape u e), ambien CO
2
concen a ion (C
a
) o
400
µ
moL moL
−1
ai , lea empe a u e o 25
±
2
◦
C, 50%
±
5% ela i e humidi y, and apo p essu e
de ici o 2.0–3.0 kPa. As Sch eibe e al. [
56
] desc ibed, ligh ene gy yields o pho osys em II (PSII)
eac ion cen e s we e de e mined wi h a sa u a ion pulse me hod. Thus, he maximum quan um
e iciency o PSII pho ochemis y (F
/F
m
) and quan um e iciency o PSII (
ΦPSII
) we e ob ained in
ligh and 30 min da k-adap ed lea es a midday (1500
µ
moL pho ons m
−2
s
−1
) using a sa u a ing
ligh pulse o 0.8 s wi h an in ensi y o 10,000
µ
moL m
−2
s
−1
acco ding o he p o ocol ollowed by
Ma eos-Na anjo e al. [25].
3.6. S a is ical Analysis
The e ec o NaCl ea men s on xylem ana omical and unc ional ea u es, as well as on wa e
po en ial measu emen s, pho osyn he ic pe o mance, and g ow h was de e mined by using one-way
analysis o a iance (F- es ). Be o e s a is ical analysis, Kolmogo o –Smi no and Le ene es s we e
used o e i y he assump ions o no mali y and homogenei y o a iances, espec i ely. All he
s a is ical es s we e pe o med using he s a is ical so wa e package R.
Au ho Con ibu ions:
Concep ualiza ion, me hodology, o mal analysis, w i ing—o iginal d a , w i ing— e iew
and edi ing, J.A.P.-R.; concep ualiza ion, me hodology, unding acquisi ion, w i ing— e iew and edi ing, E.M.-N.;
me hodology, o mal analysis, w i ing— e iew and edi ing, J.L.-J.; concep ualiza ion, unding acquisi ion,
w i ing— e iew and edi ing, S.R.-G.; concep ualiza ion, me hodology, o mal analysis, esou ces, w i ing— e iew
and edi ing, J.M.T.-R. All au ho s ha e ead and ag eed o he published e sion o he manusc ip .
Funding:
This wo k was unded by he Minis e io de Econom
í
a y Compe i i idad (MINECO P ojec
CGL2016-75550-R co unded by FEDER). J.A. P
é
ez-Rome o hanks Minis e io de Educaci
ó
n, Cul u a y Depo e
o i s pe sonal inancial suppo (FPU014/03987).
Acknowledgmen s:
We a e g a e ul o he Uni e si y o Se ille G eenhouse Gene al Se ices (CITIUS) o i s
collabo a ion and o he INRA-PIAF Cle mon -Fe and s a .
Plan s 2020,9, 690 9 o 11
Con lic s o In e es : The au ho s ha e no con lic o in e es o decla e.
Re e ences
1. Flowe s, T.J.; Hajibaghe i, M.A.; Clipson, N.J.W. Halophy es. Q. Re . Biol. 1986,61, 313–337. [C ossRe ]
2.
Van Zelm, E.; Zhang, Y.; Tes e ink, C. Sal ole ance mechanisms o plan s. Annu. Re . Plan Biol.
2020
,
403–433. [C ossRe ] [PubMed]
3.
Quin e o, F.J.; Oh a, M.; Shi, H.; Zhu, J.-K.; Pa do, J.M. Recons i u ion in yeas o he A abidopsis SOS
signaling pa hway o Na+homeos asis. P oc. Na l. Acad. Sci. USA
2002
,99, 9061–9066. [C ossRe ]
[PubMed]
4.
Flowe s, T.J.; Munns, R.; Colme , T.D. Sodium chlo ide oxici y and he cellula basis o sal ole ance in
halophy es. Ann. Bo . 2015,115, 419–431. [C ossRe ] [PubMed]
5.
Slama, I.; M’Rabe , R.; Ksou i, R.; Talbi, O.; Debez, A.; Abdelly, C. Wa e de ici s ess applied only o
combined wi h salini y a ec s physiological pa ame e s and an ioxidan capaci y in Sesu ium po ulacas um.
Flo a Mo phol. Dis ib. Func . Ecol. Plan s 2015,213, 69–76. [C ossRe ]
6.
Khan, M.A.; Unga , I.A.; Showal e , A.M. E ec s o salini y on g ow h, wa e ela ions and ion accumula ion
o he sub opical pe ennial halophy e, A iplex g i i hii a . s ocksii. Ann. Bo .
2000
,85, 225–232. [C ossRe ]
7.
Redondo-G
ó
mez, S.; Wha mby, C.; Cas illo, J.M.; Ma eos-Na anjo, E.; Luque, C.J.; De Ci es, A.; En ique
Figue oa, M. G ow h and pho osyn he ic esponses o salini y in an ex eme halophy e, Sa coco nia u icosa.
Physiol. Plan . 2006,128, 116–124. [C ossRe ]
8.
Redondo-G
ó
mez, S.; Ma eos-Na anjo, E.; Da y, A.J.; Fe n
á
ndez-Muñoz, F.; Cas ellanos, E.M.; Luque, T.;
Figue oa, M.E. G ow h and pho osyn he ic esponses o salini y o he sal -ma sh sh ub A iplex po ulacoides.
Ann. Bo . 2007,100, 555–563. [C ossRe ]
9.
Redondo-G
ó
mez, S.; Ma eos-Na anjo, E.; Figue oa, M.E.; Da y, A.J. Sal s imula ion o g ow h and
pho osyn hesis in an ex eme halophy e, A h ocnemum mac os achyum. Plan Biol.
2010
,12, 79–87.
[C ossRe ]
10.
Ma eos-Na anjo, E.; Redondo-G
ó
mez, S.; Sil a, J.; San os, R.; Figue oa, M.E. E ec o p olonged looding on
he in ade Spa ina densi lo a B ong. J. Aqua . Plan Manag. 2007,45, 121–123.
11.
Ma eos-Na anjo, E.; P
é
ez-Rome o, J.A.; Redondo-G
ó
mez, S.; Mesa-Ma
í
n, J.; Cas ellanos, E.M.; Da y, A.J.
Salini y alle ia es zinc oxici y in he sal ma sh zinc-accumula o Juncus acu us. Eco oxicol. En i on. Sa .
2018,163, 478–485. [C ossRe ] [PubMed]
12.
P
é
ez-Rome o, J.A.; Idaszkin, Y.L.; Ba cia-Pied as, J.M.; Dua e, B.; Redondo-G
ó
mez, S.; Caçado , I.;
Ma eos-Na anjo, E. Disen angling he e ec o a mosphe ic CO
2
en ichmen on he halophy e Salico nia
amosissima J. Woods physiological pe o mance unde op imal and subop imal saline condi ions. Plan
Physiol. Biochem. 2018,127, 617–629. [C ossRe ] [PubMed]
13.
Boughalleb, F.; Denden, M.; Tiba, B.B. Ana omical changes induced by inc easing NaCl salini y in h ee
odde sh ubs, Ni a ia e usa, A iplex halimus and Medicago a bo ea. Ac a Physiologiae Plan a um
2009
,31,
947–960. [C ossRe ]
14.
Ca ajal, M.; Ce da, A.; Ma inez, V. Does calcium amelio a e he nega i e e ec o NaCl on melon oo
wa e anspo by egula ing aquapo in ac i i y? New Phy ol. 2000,145, 439–447. [C ossRe ]
15.
Li, S.; Liu, J.; An, Y.; Cao, Y.; Liu, Y.; Zhang, J.; Yang, P. MsPIP2; 2, a no el aquapo in gene om Medicago
sa i a, con e s sal ole ance in ansgenic A abidopsis. En i on. Exp. Bo . 2019,165, 39–52. [C ossRe ]
16.
Singh, R.K.; Shwe a, S.; Mu hamila asan, M.; Rani, R.; P asad, M. S udy on aquapo ins o Se a ia i alica
sugges s he in ol emen o SiPIP3; 1 and SiSIP1; 1 in abio ic s ess esponse. Func . In eg . Genom.
2019
,19,
587–596. [C ossRe ]
17.
Touche e, B.W. Sal ole ance in a Juncus oeme ianus b ackish ma sh: Spa ial a ia ions in plan wa e
ela ions. J. Exp. Ma . Biol. Ecol. 2006,337, 1–12. [C ossRe ]
18.
L
ó
pez-Po illo, J.; Ewe s, F.W.; Angeles, G. Sap salini y e ec s on xylem conduc i i y in wo mang o e
species. Plan Cell En i on. 2005,28, 1285–1292. [C ossRe ]
19. K ame , P.J.; Boye , J.S. Wa e Rela ions o Plan s and Soils; Academic P ess: Camb idge, MA, USA, 1995.
20.
McDowell, N.G. Mechanisms linking d ough , hyd aulics, ca bon me abolism, and ege a ion mo ali y.
Plan Physiol. 2011,155, 1051–1059. [C ossRe ]