Isotopic and ionic changes in a snow cover at different ... · PETER RABEN Geologisk Institut,...

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Annals of Glaciology 19 1994 © International Glaciological Societyz Isotopic and ionic changes in a snow cover at different altitudes: observations at Austre Okstindbreen in 1991 PETER RABE N Geologisk Institut, Aarhus Universitet , Ny Munk egade bygn. 521, 8000 Arhus C, Denmark WILFRED H. THEAKSTO NE Geograph y Depart me nt , University cif Man chester, Manchester M1 39PL , England ABSTRACT. Ioni c and is oto pic a naly ses of snow samp les co ll ected at four sit es at the Norwegian glacier Au stre Oks tindbr een during two fi eld seasons in 1991 showed that, before meltin g started, the snowp ack was vert ica ll y inhom ogeneous. Pa tt e rn s of variation with depth of both ions and oxygen isotop es were maintain ed throu g hout the pre-melt period. Horizontal variations of ionic concen tration were smaller than vertical ones. Th e stra tigraphi c patt e rn of ionic con cent ra ti ons in the pack at lo wer a ltitud es re fle cted the influence of me lting-r ef reez in g processes, as we ll as o ri ginal var iations in the falling snow. Th e mea n ionic co nt e nt of the first se t of sam pl es collected at the lowes t site was mu ch lower than that at the others, indi cat ing th at ions had alread y been re moved by me ltwat er. Mu ch liquid water was present in th e snowpack when drainage started, and ions were removed qui c kl y with the first me ltwat er. During the melting phase , co mparativ e rat es of loss of ions r es ultin g from differential movem ent through the pa ck were S04 2 - > N a + > Cl . At 1475 m, only 1 3% of the winter accumulation melted between 6June an d 9July , but at least 88% of the Na + ,89% of the Cl- and a bout 100 % of the SO/ was lost. Initi a ll y, there was no a ltitudinal tr e nd in the mea n 8 18 0 values of the sn owpac k. Wa rmin g of the pa ck was accompanied by a tend ency toward s homog enisation. At the thr ee sit es at which snow remained in Jul y, considerable I 0 e nrichm e nt had occ urr ed since the middle of June . INTRODUCTION Seasonal snow cover ca n be significant in the chemi cal dynami cs of ecosystems in man y te mperat e, a lpine and subar ctic region s, but less is known about the chemi ca l co mposition and dynamics of seasonal snowpacks than about physi ca l pro cesses (D av i es and others , 1991 ) . Th e contribution of melting snow to river disc harge varies seasonally, with consequ ent effects on wat er qualit y. Early in the summer, melting snow makes a substantial co ntribution to the discharge of the river which iss u es from the Norwegian glacier Austr e Okstindbreen, a nd the water is relatively depleted of the h eavy isotope of oxygen, 18 0 (Theakstone, 1988). La ter , as the 18 0 co nt e nt increa ses, the chemical composition of the riv er wat er is cha ra cterised by systematic patterns of variation, upon which are s up er impo sed some apparently random d evia tions (Th ea kstone a:nd Knud sen, 1989). Concen- . fN + K + C 2+ d M 2+· hi ' . tratlons 0 a , ,a an g 111 t e g aCler rIver vary from year to yea r, as well as within a particular summ er, a lthough they generally decrease through the summer (Knud se n, 1990). Th e co ncentrations of ionic species in the accumulated snow at Austre Ok st indbr een reflect the pr eva iling clima ti c co ndi tions, as does the isotopic com posi tion of the snow (H e a nd Th ea kstone, this vo lum e). However, ion ic conce ntr at ions in the snow chan ge with tim e; even when the te mp era tur e is below O°C, chemi ca l dynamics in the pack are not totally suppr e sed. In or der to ob tain data relating to the chemi cal evolution of the snow pack in both the pre-melt and meltin g stages, the snow cover at Austre Oks tindbreen was sa mpl ed between late April a nd mid-July 199 1 at sit es along the glac ier's ce ntr e line, ranging from 1475 m to 810 m a.s. l. The start of the melt seaso n was l ate r th an usual: a sh ar p rise of a ir temperat ur e on 2 Jun e was followed by a p er iod of war mer cond itions and the onset of melting. Perso nnel were not ava ilable to ma intain th e programme between the end of the late wint er field season, in mid-J une, a nd a s umm er fi eld season Ouly- August ). At eac h of the st ud y sit es , s now temperature a nd density were measu red wh en ever sa mpl es were collected, a nd the liquid water con te nt of the pack was d etermined by a dielectric tec hniqu e. Anions (Cr , NO g- , S04 2 -) were dete rmin ed by hig h-pr ess ur e liquid chrom atogra phy , cations (Na +, Ca 2 +, Mg2+, K +) by atomic abso rption spec troph oto - 85

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Page 1: Isotopic and ionic changes in a snow cover at different ... · PETER RABEN Geologisk Institut, Aarhus Universitet, Ny Munkegade bygn. 521, 8000 Arhus C, Denmark WILFRED H. THEAKSTONE

Annals of Glaciology 19 1994

© International Glaciological Societyz

Isotopic and ionic changes in a snow cover at different altitudes: observations at Austre Okstindbreen

in 1991

PETER RABEN Geologisk Institut, Aarhus Universitet, Ny Munkegade bygn. 521, 8000 Arhus C, Denmark

WILFRED H. THEAKSTONE

Geography Department, University cif Manchester, Manchester M139PL, England

ABSTRACT. Ionic and isotopic analyses of snow samples collected a t four sites at the Norwegian glacier Austre Okstindbreen during two fi eld seasons in 1991 showed tha t, before melting started, the snowpack was vertically inhomogeneous. Pa tterns of variation with depth of both ions and oxygen iso topes were maintained throughout the pre-melt period. Horizontal variations of ionic concen tration were smaller than vertical ones. The stra tigraphic pattern of ionic concentra ti ons in the pack at lower altitudes reflected the influence of melting-refreezing processes, as well as ori ginal variations in the falling snow. The mean ionic content of the first se t of samples collected at the lowes t site was much lower than that at the others , indicating th at ions had already been removed by meltwater. Much liquid water was present in the snowpack when drainage started, and ions were removed quickl y with the first meltwater. During the melting phase, comparative rates of loss of ions res ulting from differential movement through the pack were S042- > N a + > Cl . At 1475 m, onl y 13% of the winter accumulation melted between 6June and 9July, but at least 88% of the Na + ,89% of the Cl- a nd a bout 100% of the SO/ was lost. Initia lly, there was no a ltitudinal trend in the mean 8180 values of the snowpack. W a rming of the pack was accompanied by a tendency towards i soto~i c homogenisa tion . At the three sites at which snow remained in July, considerable I 0 enrichment had occurred since the middle of June.

INTRODUCTION

Seasonal snow cover can be significant in the chemical dynamics of ecosystems in many temperate, a lpine and subarctic regions, but less is known about the chemical composition and dynamics of seasonal snowpacks than about physical processes (D avies and others, 1991 ) . The

contribution of melting snow to river discharge varies seasonally, with consequent effects on water quality. Early in the summer, melting snow makes a substantial contribution to the discha rge of the river which iss ues from the Norwegian glacier Austre Okstindbreen, and the water is rela tively d epleted of the heavy isotope of oxygen, 180 (Theakstone, 1988) . La ter, as the 180 content increases, the chemical composition of the river water is characterised by systematic patterns of variation, upon which a re superimposed some apparently random deviations (Theakstone a:nd Knudsen, 1989) . Concen-

. fN + K + C 2+ d M 2+· hi ' . tratlons 0 a , ,a an g 111 t e g aCler rIver vary from year to year, as well as within a particular

summer, a lthough they generally decrease through the summer (Knudsen, 1990).

The concentrations of ionic species in the accumulated

snow a t Austre Okstindbreen reflect the prevailing clima tic condi tions , as does the isotopic com posi tion of the snow (H e and Theakstone, this volume). However, ionic concentrations in the snow change with time; even when the tempera ture is below O°C, chemical dynamics in the pack are not totally suppre sed. In order to ob ta in d a ta relating to the chemical evolution of the snow pack in

both the pre-melt and melting stages, the snow cover at Austre Okstindbreen was sampled between la te April a nd mid-July 199 1 a t sites a long the glacier's centre line, ra nging from 1475 m to 810 m a .s. l. The start of the melt seaso n was late r th an usual: a sharp rise o f a ir temperature on 2 June was followed by a period of warmer conditions and the onset of melting. Personnel were not available to maintain th e programme between the end of the la te winter field season , in mid-J une, and a summer fi eld season O uly- August) . At each of the stud y sites, snow temperature a nd density were measu red whenever samples were collected , and the liquid water con tent of the pack was determined by a dielectric technique. Anions (Cr, NO g- , S042

-) were determined by high-pressure liquid chromatography, cations (Na +, Ca2 +, Mg2+ , K + ) by a tomic abso rption spectrophoto-

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Raben and Theakstone: Isotopic and ionic changes in snow cover with altitude

m etry a t the Aarh us U nive rsi ty Geological Insti tute. O xygen iso tope a na lyses were und er taken at th e Co penhagen U niversi ty G eophysical I sotope L abora­tory.

SAMPLE COLLECTION

Austr e Okst indb reen heads at a bo ut 15 10m a nd termina tes a t 730 m (H e Yuanqing and Theakstone, this

volume, fi gure I). T he local topogra ph y inOu ences acc umula tion patte rns a t the glacier. In la te April and ea rly M ay 199 1 pits were excavated in the snow cove r. A t 1475 m th e dirty 1990 summer surface was a t a dep th of 5.0 m; the pi t was extended slightly into the und erl ying firn . A t 1240 m, 1000 m and 8 10 m, glacier ice was

covered by snow to d epths of 3.0 m , 2.95 m and 2.7 m, res pectively. Samples collected at 1475 m (three sets) and 1240 m (fi ve sets) rep resented pre-melt conditions (Fig. I ).

E ci B-c: .'2 '§ C Q) 0 c: 0 '-'

E ci B-c: . '2 '§ C Q) 0 c: 0 '-'

3 CI -1475m

2

0

Ci ,., ,., os os

< ::::i; ::::i; ~ ~ ~ :::> :::> :::> ..., ..., ...,

co on on 0> I'- ~ (\j (\j

3 1240m

2

1

SO!-

0 ,., ,., ,., ,., Q) Q)

os os os os c: c: ::::i; ::::i; ::::i; ::::i; :::> :::> ..., ..., ~ I'- ~ ~ '" 0

N ~

Fig. 1. Mean ionic concentrations in the snowpack at the two highest sites at Austre Okstindbreen were higher

during the pre-melt phase than during the later melting phase.

During the la te wi nter fi eld season, which ended in mid-June, some heavy snowfalls occurred: at 1240 m the thi ckness of the pack increased by abou t 0.7 m between 7 M ay and I June. Additiona l samples were coll ected during a summer field season (6 July- I August). In early July no snow remained a t 8 10m, onl y 0.4 m a t 1000m, and 1. 2 m at 1240 m . A t 1475m the pack still was some 4 m deep .

Samples, each 0. 24 m long, were coll ec ted from pit

walls which were not exposed to direct so la r radiation.

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On each visit, snow which had fallen, or drifted into, the pits was removed , a nd the pits then were extended la terally by 0.5- 1.0 m before anoth er set of sam pIes was collected from the surface d ownwards. At some si tes it was

not easy to esta blish a sampling datum a t the base of the snowpack, because the und erl ying glacier ice surface was no t hori zonta l. New snow fell between sampling d a tes, and samples taken at differen t tim es a t a pa rti cul a r site therefore were not invari ably from the same pa r t of the pack: a snow layer contained within a single sample on one occasion might have been split between two adj acent samples on ano ther.

During sampling, protective clothing was worn to avoid contamina tion . Samples were allowed to melt in sealed polythene bags before being transferred to pre­cleaned polyethylene Oasks and via ls. U nti l they were

analysed , they were kept a t a tempera ture close to O°C. Because of the low par ticulate content of the snow, filt ra tion was no t carried out; ana lyses of snow samples fro m o th e r remote, hig h-altitud e sites have been conducted in a simila r ma nner (Puxba um and others, 199 1) .

SNOW TEMPERATURES AND LIQUID WATER CONTENT

When samples were first coll ec ted a t 810 m (27 April ) the

snowpack was already almos t isothermal at O°C. At 1000 m on 2 M ay, sub-zero te mpera tures were presen t in the uppermos t 0.75 m, bu t the res t of the pac k was close to O°C . At the higher sites, tempera tures were lower , with means of - 2.6°C and - 6.7°C a t 1240 m and 1475 m,

respec tively. Near-iso thermal conditons were no t a ttained a t 1240 m until 10 June. At 14 75 m , melting-poin t temperatures we re not recorded at depth before the end of the late winter fi eld season (13 June) . Pre-melt conditions prevailed wh en five sets of samples were

collected a t 1240 m and three se ts a t 1475 m .

At the 1000 m pi t, the snow surface gradient was a bou t 10°. Immed ia tely up-glac ier, it was steeper. H orizonta l movement of water would become slower where the gradi en t decreased , at and down-glacier of the site. During the first stage of melting, impermeable ice layers proba bly facilita ted horizonta l movem ent of water

whilst hindering verti cal movement. After th e onset of melting, the number of ice layers in the pack increased . A few days la ter, however, the snow took on a more homogeneous a ppearance. Before 1 June, a li q uid water content in excess of 2% was detected only in the highest pa rt of the pack. Between I a nd 7 June, the liquid wa ter

content rose from 0.50% to 5. 75%, equivalent to an increase of 0.1 7 m water, and the mean d ensity increased fro m 0.52 M g m 3 to 0.57 Mg m 3, a lthough the snow de pth was the same (3.32 m) on bo th d a tes (Fig. 2) . Between 7 and 12 June, the mean liq uid water content did not cha nge significantly, but the snow thickn ess d ecreased by 0.32 m (equivalent to 0. 18m wa ter ) of which 0.2 1 m (0.1 2 m w.e. ) was the result of melting and 0.1 1 m (0.06 m w.e. ) of compaction. Varia tions of liquid water content a t different dep ths indica ted that vertical movement of wa ter was not consta nt, but occurred in a

pulsating manner.

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~ .c;

Q. co

"0

ii:

~ .c;

Q. co

"0

ii:

~ .c;

Q.

'" "0

ii:

Raben and T heakstone: lsoto/lie and ionic changes in snow cover with aLL itllde

b " 0 (%.)

-12 -8 -12 -8 -12 L-L...L..JY--'-'-'-+O L-L.-'--'-'-,--+

-12

2 Cl:

:=:"":"::'---l.1.3

2 2

3 3

2 2

3 3

Na+(p.p .m.)

1 2

CI-(p.p .m.)

o 2 o -hr'---'----'

2

3

4

2

3

Liquid water content (%)

o o

1

2

4 0 o

2

4 0 4 8 12 o +--'---'--;--L-L-J

2

3 3 3 a 1n~ 1 ~ a 1n~"1

o 4 8 12 o +--,---,---<=--L-L-J

2

Fig . 2. Varia tions oJ snow/lack thickness, c/zemist1Y and liquid water content at IOOO m, Austre Okstindb reell , 1991.

RESULTS OF IONIC ANALYSES: THE PRE-MELT PHASE

I oni c concentra tions 111 snow which fell during th e la te winter field season were lower th a n those in th e snow which had acc umula ted previo usly. Their spa ti a l vari ­a ti ons confirmcd th a t a parti cul a r precipita tion event d oes not p rov id e equa l concentra ti ons of ions to a ll pa rts of th e ca tchment.

Sa mples ob ta ined a t th e two hig hes t sites ( 14 75 m a nd 1240 m ) represe n ted pre-melt conditi ons. Th e snowpac k was \"(~ rtica ll y inho mogeneo us, with ma rked differences of ioni c concentra ti ons be tw een adj acent samples. Th e stra ti gra phic " a ri a ti ons re fl ected th e diffe ring chemistry

of snow whi ch had acc umula ted in success ive ep isod es . Sn o,,' d riftin g ha d ca used som e va ri a ti ons o f io ni c concentra ti o n , but hori zonta l differences were sm a ll er th a n vertica l ones: a t 1240 m, the vertica l pa ttern in th e c. 3 m d ee p pack ba re ly cha nged as the pit was extend ed la tera ll y by 2.l m during the peri od of sampling (Fig . 3) . Th e stra tigra phic va ri a ti ons of ionic compos ition of th e snowpac k were re ta ined th ro ugh th e pre-melt phase a t bo th 1475 m and 1240 m .

The highes t measu red concen tra ti ons of N a + a nd C l , a nd th e second highes t of SO l2 , were in the samp le collec ted at th e 1475 m pit on 28 A pril a t a d epth of 0.72-

0 .96 m (c. 4 .2 m a bove th e lirn ) . Concentra ti ons still were hig h a t this pa rt of th e pack on 5 M ay a nd 15 M ay, but th e max imum was bare ly recogni sa ble when th e las t se t of winter season sa mples was co ll ec ted , on 6 June. I ts a ppa rent disappea ra nce m ay have resulted from it hav ing bee n split be twee n two samples . Pa rti c ul a rly hi g h concentra ti o ns of N a +, cr a nd S042 were reg iste red

a t a level coincident with 58% of th e winter acc umul a ti on a t th e two hig hes t sampling sites (a bout 2.5 m a bove th e firn surface a t 1475 m , and 1. 7 m a bove th e glacier ice a t 1240 m) .

RESUL TS OF IONIC ANALYSES: THE MELTING PHASE

A t 1000 m, surface mel ting a nd meltwa ter percola ti on occ urred during th e period of sample coll ec tion. The

co rrela ti on coeffi cien ts lo r th e concen tra tions of N a + and

Cl a nd for C l a nd S042 from 1000 m we re lower th a n th ose for sa m ples coll ec ted during th e pre-mel t phase a t 1240 m (T a ble I ) . This i nd icates th a t some of th e orig ina l ioni c " a ria ti ons in p recipita ti on a t 1000 m cha nged as a res ul t of mcl ting/refreezing processes . The co rrela ti on

coe ffi cients for th e 68 samples co ll ected during th e ea rl y

visi ts to the 1000 m si te, be tween 2 M ay a nd I June, were m a rkedl y hig her th a n th ose for th e 27 samples coll ec ted on 7 and 12 J Lin e, a fte r the onset or melting . This reOec ted d ifferenti a l movement of ions in the melting pack. An increase of m ean ionic concentra ti ons a t 1000 m during

th e first ha lf of Jun e res ul ted fro m sub-horizonta l

mo, 'em ent of wa ter thro ug h th e snowpac k. The propor­ti on or samples a t thi s site in whi ch SO/ was below th e d etecti on limit (0 .25 ppm ) increased from 3 1 % before 2 June to 78% after th a t d a te, indica ting r a pid eluti on a nd / or tra nsport. Th e rela ti o nship be tween N a + a nd C l a lso

cha nged , th e co rrela ti on coeffi cien t fa lling from 0.55 to

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Raben and Theakstone: Isotopic and ionic changes in snow cover with altitude

-15

E 1

.c C. Cl> "0

Cl. 2

- 12

2

-9 0

2

3

4

3 ~----L---------

4 o o +--+--~~--~~-

8

E 1

.c C. Cl> "0

Cl. 2

3

0

E 1

.c C. ID "0

;;: 2

3

0 0 2 0

910513

2

3

-15

3

910524

b" O ('!Ml

-15 -12 -15 -12

-12 -15 -12

."

c-o. "0

2 2 :;--12 -9

2 2

~iJ 3

3 3

3 3

Glacier ice

Na+ (p .p.m .l

0 2 4 2 4

2 4 0 2 910524

2 2 0 1

2

~[,o", 3 3

3

CI- (p .p .m .l

0 4 8 4

4 8 0 4 8 910524

2 J,...----..... 2J----..... o 2

3 3 3

~~'"712

2-S04 (p.p.m.l

2 0 2 0

0 2 910603 0

910610

2

2

3

3

Fig. 3. Variations of snowpack thickness and chemistry at 1240 m, Austre Okstindbreen, 1991. (S0 42- was not detectable in the samples collected from the pack on 12 July .)

0.44. This indicated that a + was removed sligh tl y more quickly than Cl- . Comparative rates of loss were SO/ - > Na+ > CC

samples, collected on 27 April, was much lower than that at the higher sites, indicating that ions already had been removed by meltwater. On each subsequent sampling, the mean concentrations of Na +, Cl- and S042

- varied At 810 m the mean ionic content of the first set of

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Raben and Theakstone: Isotopic and ionic changes in snow cover with aLtitude

Table 1. Correlation coifficients Jor concentrations if three ions in the snowpack at Jour sites, A ustre Okstindbreen, 1991. Separate coefficients Jor the pre-melt and melting phases at 1000 m are shown (N, number if sam/Jles)

N a+ : cr Na + : 5042

1475 m 0 .86 0.7 3 1240m 0.95 0.75

1000m 0.55 0. 78 1000m 0.44 0 .40 810m 0 .75 0 .5 1

markedly; the variations were not synchronous. The correlation be tween N a + and CI- in all the samples from

this site was much poorer tha n that for th e samples collected during th e pre-melt ph ase at 1240 m (Table I ) . On 3 M ay particularly high con centrations of a ll three ions coincided with a n increa se of the liquid wa ter content of the pack at a d epth of 0 .96- 1.20 m. Concentra tions a lso

were h igh in the lowest 0.02 m of the pack, where a water content of 5% showed that meltwa ter was running within the snow immediately above the glacier surface .

Only 0. 36 m w.e. (13% of th e winter accumula tion) m elted a t the 1475 m site between 6 J une and 9July, but the loss of ions totalled 88 % (Na +), 89 % (C I- ) and

c. 100% (SO/-) . Since precipitation must have suppli ed som e ions to the pack duri ng the melting phase, losses of N a + and Cl- must have been still higher. None of th e 40 samples co llec ted a t 1475 m in J uly had a n S042

concentration above the d etection limit.

RESUL TS OF ISOTOPIC ANALYSES

Stratigraphic variations of the isotope content of th e snowpack in late winter reflect th e isotopic composition of

discre te snowfalls, a nd th e amo unt of snow which has

accumulated at different rates at different times. 8180

~ ? .0

-9 1000m

-10

- 11

-12

Apr Ma:y June July

Fig. 4. M ean 8/80 values in the snowpack at Austre Okstindbreen in Late winter 1991 did not vary system­aticaLly with aLtitude. VaLues increased during the melting phase, as a result if the relative enrichment in the heavy isotope. ( Open symbols indicate that a sample was lost, and that the mean was determined J or the remaining samples.)

cr : 50 42- N Sampling period

0 .75 86 28 A pril- 6 June 0 .80 70 1 M ay- 3 June

0. 62 68 2 M ay- I June 0 . 14 27 7 June- 12 June 0.62 8 1 27 Apri l- I 1 June

va lue in fa lling snow d epend in pa rt on tempera ture. H owever, th e influence of topogra ph y on snow accum­ula tion ra tes, a nd on th e d epth of th e pack, may modify altitude- related pa tte rns (H e Yua nqing a nd Theakstone, this vo lum e). There was no a ltitudin al trend in th e mean 8180 values of the snow pack when samples were first collected in la te win ter (Fig . 4 ) . V erti cal inhomoge neity

was cha racteristic a t each site, a nd th e distinc t stra ti ­gra phic varia tions rem a ined evid ent fo r seve ra l weeks.

On 27 Apri l th e mean 8180 va lue of the accumu la ted snow a t 1475 m was - 11 .8 7%0. Th e und erl ying firn was ri cher in 180 th a n was most of the snow . The composition

of new snow which had acc umulated during the la te

winter period va ried : th a t which fell be twee n 5 a nd 15 M ay was stro ngly d eple ted of IBa , but th a t which acc umul a ted la te r was 180_rich when sampled on 6 June. W a rming of th e pack was accompa nied by a tendency towa rds iso topic homogenisa tion. In J u ly 8180

values were less va ri a bl e th a n in la te winter; th e mean for

th e 3.4m of snow remaining on 17 Ju ly was - 11.03%0. At 1240 m , th e iso topic profile refl ected th e presence of

two ice layers, 2.2 m a nd 1.2 m a bove the g lacier surface . Their 8180 values differed ; o n 13 M ay, th a t of th e higher layer was - 11 .29%0, whilst th a t of th e lower one was - 9.26%0. N ew snow sampled on 24 M ay was IBO-dep leted

(8180 value: - 15 .66%0), but on I June th e 8180 value of th e top sample was - 9.92%0. As littl e snow fell during the intervening period , th e cha nge is likely to have resulted principa lly from evaporatio n . Between I a nd 10June, th e snowpack became 0. 3 m thinner, more ice layers becam e

visible, a nd th e central pa rt of th e pack becam e more

homogeneous (Fig. 3) . On 12 July, the mean 8180 value of th e 1. 2 m of snow wh ich rem a ined (- 10.76%0) indica ted th a t considera ble 180-enri chment had occurred as surface melting occurred during the preceding 32 d ays.

At 1000 m , a 8180 maximum a t a bo ut 2 m above th e

glacier ice was a prominent fea ture of the iso tope profi le

for much of M ay (Fig . 2) . The lowes t part of th e pack was rela tively ri ch in ISO. Wh en the first se t of samples was collec ted , isoto pic va ri a tions in th e top metre were rela ti vely sm a ll. Between 2 a nd 8 May a n increase in th e number of visible ice layers was accompa nied by ch a nges of 81S0 valu es. Althou g h th e snow-cove r

th ickness d ec reased by 0 .32 m between 7 a nd 12 June, th e influence of th e ice layer res ponsible for th e 81S0 m aximum remained ; below it, th e 180 content of th e pack tended to increase towards th e bo ttom . On 14 Ju ly th e thin snow cove r was ISO-rich.

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Raben and Theakstone: Isotopic and ionic changes in snow cover with altitude

DISCUSSION

The liquid water content of th e pack throws light on processes occurring during melting. At 1000 m, before melting became widespread , water was dra ining slowly in ce rt a in strata within the pac k, where hig h ionic concentrations coincided with a high liquid water

content. In parts of the pack beneath a sloping snow surface th e re was more than 10 % liquid water, appa rentl y because wa ter arriving from high er-l ying areas was unable to drain freely to lower a reas . As the first meltwa ter was released , variations of the amount of free water within the pack resulted from res tri ction

imposed on vertical dra inage by ice layers, some of which had form ed a t non-hori zonta l discontinuities within the pack. lv[any smaller ice laye rs disappeared as melting proceeded, but others became thi cker. As the ice layers changed , the liquid ,·va ter content of the snow and

fim varied in a ma nner which sugges ted that drainage

occurred in "waves". Before melting started , la rge vertical vari a ti ons of

ionic concentra tions were prcsent in thc snow cove r: a t particul a r levels, concentrations were high. Such var­ia tions in the accumulated snow result principa ll y from varying concentrations in falling snow. There was no marked dependence of concentrations on a ltitud e and , with the exception of snow which fell on 4 May, altitudinal gradients and high ionic concentrations were not ev ident in late winter snowfall s.

Compared with vertical variations of ionic concen­trations, horizonta l vari at ions at each site were relatively small. Stra tigraphic differences persisted during lateral extension of pi ts over di stances eq ui va len t to, or greater than , the depth of th e snowpack. During the pre-melt phase at 1475 m and 1240 m, th e coeffi cients of varia tion of individual ion concentra tions were moderate. When melting occ urred , metamorphism and melting/ refreez ing

processes caused ion s to beco me co nce ntrated at particular horizons. At 1475 m, warming of the deep (c. 5 m) cold (c. - 7°C ) snowpack to the melting point, largely by hea t transfer from the upper surface, resulted in downward migration of ions at the melting front. Ions were particularly a bundant where the tempera ture

gradient within the pack was steep, and downward perco lation of wa ter was slow . As the tempera lUre of a snowpack ri ses to the melting point, it is likely that ions with high mobility, displaced from the upper pa rt , become concentrated in the snow immediately a bove the level to which melting has penetra ted .

High co rrela tions between Na + , Cl and S042 in a vertical profile refl ec t their common origin. At Austre Okstindbreen the correla ti on between la + and C l was stronger than those between S042 and the other ions, because abou t 50% of the S04 2 transported to the surface of the glacier during the 1990- 91 winter had a

non-marine origin. At 810 m where some ions probabl y were removed during winter periods of melting, a nd thawing/refreezing processes began to operate before th ey did a t grea ter altitud e, ionic concentrations were lower than a t the higher sites.

Pre-melt stratigraphic variations of iso topic compos­ition of the snowpack refl ec t the discrete na ture of snow acc umulation events. 'vVh en melting starts, percola tion of

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meltwater into the pack results at first in onl y slight changes of 8180 values; major stratig ra phic dilTerences a re retained for some time after temperatures rise to the melting point. Eventu all y, however, reactions between phases lead to a more homogeneous sta te (Stichler, 1987 ) . The rate of change of the original ve rti cal variations of the 180 / 160 ratio at a site depends on the thermal

conditions, and on the form ation , g rowth and decay of ice layers within th e pack. The changes a re much greater during the melt season than during th e pre-melt phase.

CONCLUSIONS

Large a mounts of liquid water a re prese nt in the snowpack when drainage starts, and ions are t-emoved qui ckly with the first meltwater. The order of elution, SO/ > Na + > Cl , agrees with previous investigations elsewhere (Tranter, 1991 ) . At 1475 m, in 1991 , more than

85% of the ions had been removed after only 13% of the meltwa ter had left the pack, indicating tha t ions a re exposed to remova l with the first meltwater as a consequence of metamorphism which accompa ni es th aw­ing and refreezing ep isodes during slow warming. Ions dra ining from the inhomogeneous snow pack at 1475 m

were removed more quickly than pred icted by a model of a homogeneous pack (Ba les , 199 1) .

M elting of the snow pac k is accompanied by 180_ enri chment and a trend towards a more homogeneous iso topic com posi tion. As iso th ermal condi ti ons develop a nd ice laye rs have a more prono unced effect on meltwa ter perco la tion , the composition of the ice laye rs cha nges. Combined studi es of ions, iso topes and liquid wate r content provid e more information a bout the evo luti on of th e snowpack during the pre-melt and early melting phases than does a single-pa rameter investig­a tion.

ACKNOWLEDGEMENTS

W e th ank Niels Tvis Knudsen for his cons id erab le assista nce in the fi eld and for many discuss ions abo ut th e st udi es at Okstind a n, Niels Haakensen , Fran k

J acobsen a nd Hugo R a ben for help during the fi eld­work, and D av id Collins fo r fruitful discussions abo ut glacia l h ),drochemistry. 'vVe are grateful to personnel at the Copenhagen University Geophysical I sotope Labor­a tory for underta king the num erous iso tope analyses. The

studies were carri ed out whilst Theakstone was in receipt of a R esea rch Grant (GR3/ 7253) from th e U.K. Natural Environment R esearch Council.

REFERENCES

Bales, R. C. 1991. 1\lodelling in-pack chemical transform a tions. 111 Davies, T. D. , M. Tranter and H . G. J ones, eds. Seasollal slIowpacks.

Pmcesses oJ composilional change. Berlin , Springer-Verlag, 139 163. (NATO AS I Series G: Ecological Sciences 28. )

D avies, T. D., M. Tranter and H. G. J ones, eds. 199 1. Seasonal snow/){Icks.

Processes oJ comjJosilio71al chan,~e . Berlin , Spri nge r-Vcrl ag, vii ix. (l\ATO ASI Series G: Ecologica l Sciences 28. )

He, Y. and W. H . Theakstone. 1994. Climatic influ ence on the com position of the snow cover at Austre Okstindbreen, Norway,

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Raben and Theakstone: Isotopic and ionic changes in snow cover with aLtitude

1989 and 1990. Alln. Glaciol., 19 (see paper in this volume. ) Knudse n, N. T. 1990. Dissolved load ill glacier river waler, Auslre

Okslilldbreen , Okstindan, Norway. Manchester, University or Man­chester. (Okstindan Glacier Projec t Report 90.2. )

Puxbaum , H ., A. Kovar and :vl. Kalina. 1991. Chemica l composition a nd Ouxes of wet depos ition at elevated sites (700-3015 m a.s. l. ) in the eastern Alps, Austria. III Davies, T. D. , 1"1. Tral1ler and H. C. jones, eds. Seasonal S1lowpacks. Processes tif compositional change. Berlin , Springer­Verlag, 273- 297. (NATO AS! Series G: Ecologica l Sciences 28. )

Stichler, Iv". 1987. Snowcover and snowmel t processes studied by means or environmental iso topes. 111 J ones, H. G. a nd W.]. Orvilie-Thomas, eds. Seasollal snOWCOVfrS: physics, chemisl1y, h)'drology. Dordrecht , etc., D. Reidel Publish ing Company, 673- 726.

Theakstone, W. H. 1988. Temporal va riations of isotopi c composition of g lacier-river waleI' during summe r: observations at Austre Okstind-

breen , Okslindan, Norway. J. Glaciol., 34( 11 8), 309- 317. Theakston e, W. H. and K. T. Knudsen. 1989. Temporal changes or

glacie r hydrolog ica l sys tems indica ted by iso topic and related observations a t Austre Okstindbreen , Okstindan, Norwa y, 1976-87. Ann. Glaciol. , 13, 252- 256.

Tramer, ~r. 1991. Controls of the composition of snowl11elt. In Dm'ies, T. D. , \11. Tranter and H. C. Jones, eds. Seasonal sllow/Jacks. Processes of compositional change. Berlin , Springer- Verlag, 241 271. (NATO ASI Series G: Ecologica l Sciences 28. )

The accuracy rif references w the text and in this List is the responsibiLity oJ the authors, to whom queries shouLd be addressed.

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