Excit
ation-emission m
atrix (EEM) fluorescence spectroscopy h
as been widely used to ch
ar
acterize dissolvedorg
anic m
atter (DOM) in w
ater
and soil. However, interpretingthe >10,000 w
avelength-dependent fluorescence intensityd
at
a points represented in EEMs h
as posed
a signific
antch
allenge. Fluorescence region
al integr
ation,
a qu
antit
ativetechnique th
at integr
ates the volume bene
ath
an EEM,w
as developed to
an
alyze EEMs. EEMs were deline
atedinto five excit
ation-emission regions b
ased on fluorescenceof model compounds, DOM fr
actions,
and m
arine w
atersor freshw
aters. Volumetric integr
ation under the EEM withine
ach region, norm
alized to the projected excit
ation-emission
are
a within th
at region
and dissolved org
anicc
arbon concentr
ation, resulted in
a norm
alized region-specificEEM volume (
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i,n). Solid-st
ate c
arbon nucle
ar m
agneticreson
ance (
13C NMR), Fourier tr
ansform infr
ared (FTIR)
an
alysis, ultr
aviolet-visible
absorption spectr
a,
and EEMswere obt
ained for st
and
ard Suw
annee River fulvic
acid
and 15 hydrophobic or hydrophilic
acid, neutr
al,
and b
aseDOM fr
actions plus nonfr
action
ated DOM from w
astew
atereffluents
and rivers in the southwestern United St
ates. DOMfr
actions fluoresced in one or more EEM regions. Thehighest cumul
ative EEM volume (
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T,n =
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i,n) w
as observedfor hydrophobic neutr
al DOM fr
actions, followed bylower
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ars/Phi.gif" BORDER=0 >
T,n v
alues for hydrophobic
acid, b
ase,
and hydrophilic
acid DOM fr
actions, respectively. An extr
acted w
astew
aterbiom
ass DOM s
ample cont
ained
arom
atic protein-
andhumic-like m
ateri
al
and w
as ch
ar
acteristic of b
acteri
al-soluble microbi
al products. Arom
atic c
arbon
and the presenceof specific
arom
atic compounds (
as indic
ated by solid-st
ate
13C NMR
and FTIR d
at
a) resulted in EEMs th
at
aidedin differenti
ating w
astew
ater effluent DOM from drinkingw
ater DOM.