emi13134-sup-0001-si.doc

advertisement
Table S1; Environmental detection of ananmmox bacterial populations and activities. n.d; not determined, n.a.; not applicable, u.d; under
detection limit. ra: contribution of the anammox process to total N2 gas production.
Environments
Genus
Anammox activities
ra (%)
Methodology†
References
Marine
Sediment
<91.2 nmol
d-1
<23 ± 3 µmol NH4+
g-protein-1 min-1
Gullmar fjord
Scalindua
Gullmar fjord
Scalindua
Gullmar fjord
n.d
33.6-84 µmol L-1 d-1
Gullmar fjord
Scalindua
<0.084 µmol cm-3 d-1
Brofjorden
n.d
Skagerrak
g-1-sediment
0.3-2.4 fmol cell-1
day-1
23-47%
15N
n.d
23-40%
15N
n.d
15N
26.4 µmol L-1 d-1
18%
15N
n.d
<24.1 µmol m-2 d-1
<77%
15N
Skagerrak
n.d
13.2 µmol L-1 d-1
79%
15N
Skagerrak
n.d
<99 µmol L-1 d-1
<67%
15N
Skagerrak
n.d
<0.06 µmol cm-3 d-1
<74%
15N
Skagerrak
Scalindua
0.0206 µmol cm-3 d-1
n.d
15N
Kattegat
n.d
0.0384 µmol cm-3 d-1
15%
15N
Aarhus Bay
n.d
83 µmol L-1 d-1
<2%
15N
0.57-0.98 fmol
cell-1 day-1
0.26 fmol cell-1
day-1
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
FISH
Lipid
FISH
Lipid
FISH
PCR
(rrn)
PCR
(rrn)
FISH
Enrich
ment
Brandsma et al.,
(2011)
van de Vossenberg
et al. (2008)
Engström et al.,
(2005)
Schmid et al.,
(2007)
Engström et al.,
(2005)
Trimmer et al.,
(2013)
Engström et al.,
(2005)
Thamdrup &
Dalsgaard (2002)
Dalsgaard &
Thamdrup (2002)
Schmid et al.,
(2007)
Engström et al.,
(2005)
Thamdrup &
Dalsgaard (2002)
Environments
Methodology†
Genus
Anammox activities
ra (%)
Smeerenburg
fjorden
n.d
23-40.5 µmol cm-3 d-1
(15NH4+ cores)
5-8%
15N
Gihring et al., (2010)
Kongsfjorden
n.d
<8.5 µmol cm-3 d-1
(15NH4+ cores)
23%
15N
Gihring et al., (2010)
Kongsfjorden
Scalindua
n.d
n.d
Scalindua
0.0053 µmol cm-3 d-1
Scalindua
n.d
n.d
n.d
0.0076 µmol cm-3 d-1
10.2%
15N
n.d
5-15 µmol m-2 d-1
10-15%
15N
Disko Bay
Scalindua
0.0151 µmol cm-3 d-1
n.d
15N
Disko Bay
n.d
0.0027-0.181 µmol
cm-3 d-1
18.5-26.
7%
15N
East coasts
of Greenland
n.d
0.0018-0.0285 µmol
cm-3 d-1
1.3-34.9
%
15N
Young Sound
Scalindua
0.0122 µmol cm-3 d-1
n.d
15N
Barents Sea
Scalindua
0.0192 µmol cm-3 d-1
n.d
15N
Barents Sea
Scalindua
n.d
Greenland
Sea
Greenland
Sea
Greenland
Sea
Gulf of
Finland
0.23 fmol cell-1
day-1
0.23 fmol cell-1
day-1
0.32 fmol cell-1
day-1
0.24 fmol cell-1
day-1
n.d
n.d
15N
References
PCR
(rrn)
PCR
(rrn)
PCR
(hzs)
FISH
PCR
(rrn)
FISH
Tian et al., (2009)
Schmid et al.,
(2007)
Harhangi et al.,
(2012)
Rysgaard et al.,
(2004a)
Hietanen and
Kuparinen (2008)
Schmid et al.,
(2007)
Rysgaard et al.,
(2004a)
Rysgaard et al.,
(2004a)
PCR
(rrn)
PCR
(rrn)
PCR
(hzs)
FISH
FISH
Schmid et al.,
(2007)
Schmid et al.,
(2007)
Harhangi et al.,
(2012)
Environments
Genus
Irish Sea
Scalindua
Irish Sea
n.d
Methodology†
Anammox activities
2.1-25.7 nmol mL-1 wet
sediment
ra (%)
n.d
15N
<30.1 µmol m-2 d-1
< 61%
15N
n.d
15N
mL-1
1.3-2.8 nmol
sediment
wet
Celtic Sea
Scalindua
Celtic Sea
n.d
<18 µmol m-2 d-1
< 65%
15N
North Sea
Scalindua
n.d
n.d
15N
North Sea
n.d
2.4-68.4 µmol m-2 d-1
10-20%
15N
North Sea
n.d
<0.0528 µmol cm-3 d-1
< 32%
15N
North Sea
Scalindua
0.006-0.036 µmol cm-3
d-1
< 29%
15N
North Sea
Scalindua
n.d
n.d
Sourth Ionian
Sea
Northwest
Africa
Long Island
Sound
Scalindua
n.d
n.d
unidentifie
d
n.d
n.d
n.d
21.9-28.8 µmol L-1 d-1
4-7%
15N
Block Island
and
Rhode Island
sounds
n.d
<0.104 µmol ml-1
sediment d-1
8-42%
15N
Hanna Shoal
Scalindua
n.d
PCR
(rrn)
PCR
(rrn,
hzs)
PCR
(rrn,
hzs)
PCR
(rrn)
PCR
(rrn)
FISH
Lipid
FISH
Lipid
FISH
References
Jaeschke et al.,
(2009)
Trimmer & Nicholls
(2009)
Jaeschke et al.,
(2009)
Trimmer & Nicholls
(2009)
Schmid et al.,
(2007)
Neubacher et al.,
(2011)
Neubacher et al.,
(2013)
Lipid
Bale et al., (2014)
Lipid
Lipsewers et al.,
(2014)
Lipid
Polymenakou et al.,
(2005)
Jaeschke et al.,
(2010)
Engström et al.,
(2005)
Brin et al., (2014)
PCR
(rrn)
Penton et al., (2006)
Environments
Soledad
basin
Soledad
basin
Gulf of
California
Magdalena
margin
Lesser
Antilles
Cascadia
Basin
Genus
Anammox activities
ra (%)
n.d
n.d
n.d
Scalindua
0.17-0.675 mmol m-2
d-1
57±21%
n.d
n.d
n.d
n.d
n.d
n.d
Scalindua
n.d
0.00045-0.00521 µmol
g-1 d-1
0.00078-0.0204 µmol
mL-1d-1
13-57%
12-51%
Saanich Inlet
Scalindua
n.d
n.d
Puget Sound
Scalindua
n.d
n.d
Scalindua
n.d
n.d
Scalindua
n.d
n.d
Scalindua
n.d
n.d
Golfo Dulce
Scalindua
<0.0216 µmol cm-3 d-1
South Pacific
ocean
Scalindua
n.d
n.d
Equatorial
Pacific
Ocean
Scalindua
n.d
n.d
Washington
Margin
Juan de Fuca
Ridge
East Pacific
Rise
0.08-0.23 fmol
cell-1 day-1
n.d
Methodology†
15N
S
PCR
15N
(rrn,
hdh)
15N
S
15N
S
PCR
15N
(rrn)
References
Prokopenko et al.,
(2006)
FISH
Prokopenko et al.,
(2006)
Prokopenko et al.,
(2006)
Song et al., (2014)
Engström et al.,
(2009)
15N
15N
Prokopenko et al.,
(2013)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn,
hdh)
Walsh et al., (2009)
Penton et al., (2006)
Penton et al., (2006)
Penton et al., (2006)
Santelli et al., (2008)
FISH
Schmid et al.,
(2007)
Durbin & Teske
(2011)
Hong et al., (2011a)
Environments
Genus
Anammox activities
ra (%)
Great Barrier
Reef lagoon
n.d
<117.6 µmol m-2 d-1
< 70%
Jiaozhou Bay
Scalindua
n.d
n.d
Bohai Sea
Scalindua
n.d
n.d
Yellow Sea
Scalindua
n.d
n.d
Scalindua
n.d
n.d
Scalindua
n.d
n.d
South China
Sea
Scalindua
n.d
n.d
South China
Sea
Scalindua
n.d
n.d
South China
Sea
Scalindua
n.d
n.d
South China
Sea
Scalindua
n.d
n.d
Scalindua
n.d
n.d
Scalindua
n.d
n.d
South China
Sea
South China
Sea
South China
Sea
South China
Sea
Methodology†
15N
References
Erler et al., (2013)
PCR
(rrn,
hdh)
PCR
(rrn,
hdh)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn,
hdh,
nirS)
PCR
(rrn,
hdh)
PCR
(nirS)
PCR
(rrn,
hdh)
PCR
(rrn)
PCR
(rrn)
Dang et al., (2010)
Dang et al., (2013)
Hong & Cho (2012)
Li, T. & Wang (2013)
Shu & Jiao (2008)
Li, M. et al., (2013)
Hong et al., (2011b)
Li, M. et al., (2011a)
Li, M. et al., (2010)
Han & Gu (2013)
Han et al. (2013)
Environments
East China
Sea
East China
Sea
Methodology†
Genus
Anammox activities
ra (%)
n.d
n.d
n.d
n.d
<0.12 µmol cm-3 d-1
28%
Okhotsk Sea
Scalindua
n.d.
n.d
Sagami Bay
n.d
0.21 mmol m-2 d-1
37%
Ago Bay
Scalindua
n.d
n.d
Ago Bay
Scalindua
n.d
n.d
15N
Hiroshima
Bay
Scalindua
15 µmol NH4+
g-protein-1 min-1
n.d
15N
Osaka Bay
unidentifie
d
n.d
n.d
Ryukyu
trench
Scalindua
n.d
n.d
Ogasawara
Trench
Scalindua
n.d
n.d
15N
S
Black Sea
n.d
< 11 nmol L-1 d-1
n.d
15N
Black Sea
unidentifie
d
n.d
n.d
Black sea
Scalindua
n.d
References
Lipid
Zhao et al., (2013)
15N
Song et al., (2013)
PCR
(rrn,
hdh)
Shao et al. (2014)
15N
Glud et al., (2009)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
Enrich
ment
Enrich
ment
FISH
FISH
Enrich
ment
FISH
PCR
(rrn)
PCR
(rrn)
PCR
(hdh,
hzs)
Enrich
ment
Nakajima et al.,
(2008a)
Nakajima et al.,
(2008b)
Kindaichi et al.,
(2011)
Awata et al., (2013)
Kawagoshi et al.,
(2012)
Li, L. et al., (1999)
Nunoura et al.
(2013)
Anoxic water
column
3-4 fmol-NH4+
cell-1 d-1
nearly
100%
15N
Jensen et al., (2008)
PCR
(rrn)
FISH
Lipid
FISH
Lipid
Wakeham et al.
(2007)
Kuypers et al.,
(2003)
Schmid et al.,
(2007)
Environments
Genus
Anammox activities
ra (%)
Black sea
Scalindua
10.55 nmol L-1 d-1
n.d
Black sea
Scalindua
n.d
n.d
Black sea
Scalindua
n.d
n.d
Black sea
Scalindua
n.d
n.d
Black sea
Scalindua
n.d
n.d
Baltic sea
Scalindua
0.005-0.05 µmol L-1 d-1
Arabian Sea
n.d
Arabian Sea
<2.3 fmol-NH4+
cell-1 d-1
Methodology†
References
15N
Lam et al., (2007)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(nirS)
Kirkpatrick et al.,
(2006)
Woebken et al.,
(2008)
Fuchsman et al.,
(2012)
Kirkpatrick et al.
(2013)
n.d
15N
<0.00432 µnmol L-1 d-1
< 13%
15N
PCR
(rrn,
nirS)
Scalindua
< 0.038 µmol L-1 d-1
41-77%
15N
PCR
(nirS)
Arabian Sea
Scalindua
n.d
n.d
PCR
(rrn)
Woebken et al.,
(2008)
Arabian Sea
Scalindua
n.d
n.d
PCR
(nirS)
Bowen et al., (2015)
nearly
100%
15N
PCR
(rrn)
FISH
15N
PCR
FISH
4.5 fmol-NH4+ cell-1
d-1
Namibian
OMZ
Scalindua
n.d
Namibian
OMZ
n.d
< 0.248 µmol L-1 d-1
n.d
Namibian
Scalindua
n.d
n.d
FISH
Hannig et al., (2007)
Ward et al., (2009)
FISH
Jensen et al., (2011)
Lipid
Kuypers et al.,
(2005)
Schmid et al.,
(2007)
Kalvelage et al.,
(2011)
Woebken et al.,
Environments
OMZ
Methodology†
(rrn)
Genus
Anammox activities
ra (%)
Namibian
OMZ
Scalindua
n.d
n.d
PCR
(rrn)
Off southern
Mexico-Costa
Rica OMZ
unidentifie
d
n.d
n.d
PCR
(rrn)
Off southern
Mexico-Costa
Rica OMZ
unidentifie
d
n.d
n.d
Colombian
OMZ
Scalindua
n.d
n.d
Golfo Dulce
n.d
21-30.5 mmol m-2 d-1
19-35%
15N
Golfo Dulce
Scalindua
0.36 nmol cm-3 d-1
n.d
15N
Scalindua
16 mmol-NO2- m-2 d-1
Peruvian
OMZ
Peruvian
OMZ
Peruvian
OMZ
Peruvian
OMZ
Peruvian
OMZ
Peruvian
ODZ
Peruvian-Nort
hern Chilean
OMZ
Scalindua
<17 mmol m-2 d-1
n.d
< 0.054 µmol L-1 d-1
Scalindua
n.d
<0.1135 µmol L-1 d-1
Scalindua
n.d
n.d
<0.0216 µmol L-1 d-1
<2.4 fmol-N
d-1
15N
n.d
15N
< 35%
Lipid
15N
15N
PCR
(rrn)
PCR
(nirS)
PCR
(rrn)
PCR
(rrn)
PCR
(hdh)
PCR
(nirS)
Rush et al., (2012)
Podlaska et al.,
(2012)
PCR
(rrn)
nearly10
0%
< 100%
Woebken et al.,
(2008)
FISH
15N
cell-1
References
(2007)
Castro-González et
al. (2014)
Dalsgaard et al.,
(2003)
Schmid et al.,
(2007)
FISH
Lam et al., (2009)
FISH
Lipid
Hamersley et al.,
(2007)
Kalvelage et al.,
(2011)
Woebken et al.,
(2008)
Kalvelage et al.,
(2013)
Bowen et al., (2015)
Dalsgaard et al.,
(2012)
Environments
Northern
Chilean OMZ
Northern
Chilean OMZ
Northern
Chilean OMZ
Northern
Chilean OMZ
Hypersaline
basins
Mediterranea
n Sea
ra (%)
nearly
100%
Methodology†
Genus
Anammox activities
n.d
<0.0168 µmol L-1 d-1
Scalindua
<0.00575 µmol L-1 d-1
n.d
15N
n.d
0.6-1.47 mmol m-2 d-1
82-90%
15N
Scalindua
n.d
n.d
Scalindua
n.d
n.d
Mediterranea
n Sea
Scalindua
0.00252-0.04965 µmol
L-1 d-1
<85.5%
15N
Hydrothermal
vent
Mid-Atlantic
Ridge
Juan de Fuca
Ridge
Guaymas
basin
Kuenenia,
Scalindua
unidentifie
d
<0.03 µmol L-1 d-1
n.d
15N
< 0.0025 µmol L−1 d-1
<1%
15N
Scalindua
n.d
n.d
West coast of
Norway
Scalindua
0.0015 µmol
cm-3-sponge d-1
3.2%
Conch Reef
Kuenenia
n.d
n.d
n.d
1.5-2.5 µmol m-2 d-1
<7%
References
Thamdrup et al.,
(2006)
15N
PCR
(rrn)
FISH
Galán et al., (2009)
Brabandere et al.,
(2014)
Stevens & Ulloa
(2008)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn,
hzs)
PCR
(rrn)
PCR
(rrn)
PCR
(hzs)
van der Wielen et
al., (2005)
FISH
Lipid
Borin et al., (2013)
Lipid
Byrne et al., (2009)
Bourbonnais et al.,
(2012)
Lipid
Russ et al., (2013)
Marine sponge
15N
PCR
(rrn)
PCR
(rrn)
Hoffmann et al.,
(2009)
Mohamed et al.,
(2010)
Sea ice
Young
Sound,
15N
Rysgaard et al.,
(2008)
Environments
Franklin Bay,
Greenland
Sea, Disco
Bay, Arctic
ocean
Young
Sound,
Greenland
Sea
Marine
Aquaculture
marine
recirculating
aquaculture
system
Methodology†
Genus
Anammox activities
ra (%)
n.d
<1.15 µmol m-2 d-1
<19%
Brocadia
2.352 µM-NH3 bead-1
d-1
<10%
Scalindua
<0.132 µmol cm-3 d-1
5-26.4%
15N
n.d
undetectable
<1%
15N
n.d
3.09-10.
93%
15N
Scalindua
< 37%
15N
Colne estuary
n.d
0.7-7.85
%
15N
Colne estuary
Scalindua
<30%
15N
<7.82%
15N
<82%
15N
References
Rysgaard & Glud
(2004b)
15N
PCR
(rrn)
FISH
PCR
(rrn)
FISH
Tal et al., (2006)
Brackish water
Randers fjord
Norsminde
Fjord
Medway
estuary
Medway
estuary
Thames
estuary
Thames
estuary
n.d
n.d
<1884 µmol m-2 d-1
<0.24 µmol
ml-1-sediment d-1
<2.6 nmol ml-wet
sediment-1
FISH
Risgaard-Petersen
et al., (2004)
Risgaard-Petersen
et al., (2004)
Nicholls & Trimmer
(2009)
Rooks et al., (2012)
Nicholls & Trimmer
(2009)
PCR
(rrn)
Dong et al., (2009)
Trimmer et al.,
(2003)
Trimmer et al.,
(2005)
Environments
Thames
estuary
Swale
estuary
Roach
estuary
Crouch
estuary
Blackwater
estuary
Stour estuary
Orwell
estuary
Cavado River
estuary
Lake
Rassnitzer
Gulf of Fos
Plum Island
Sound
estuary
Great
Sippewissett
marsh
Chesapeake
Bay tidal
Choptank
River estuary
New River
Estuary
Genus
Anammox activities
ra (%)
1.45-7.4
4%
1.57-2.4
1%
0.57-1.9
%
1.37-2.9
2%
0.45-7.3
2%
1.55-8.0
3%
0.89-3.5
7%
n.d
n.d
n.d
n.d
n.d
n.d
n.d
Scalindua
<0.04 µmol cm-3 d-1
Brocadia,
Scalindua
0.504 µmol L-1 d-1
n.d
Methodology†
15N
15N
15N
15N
15N
15N
15N
PCR
(rrn)
PCR
(rrn)
References
Nicholls & Trimmer
(2009)
Nicholls & Trimmer
(2009)
Nicholls & Trimmer
(2009)
Nicholls & Trimmer
(2009)
Nicholls & Trimmer
(2009)
Nicholls & Trimmer
(2009)
Nicholls & Trimmer
(2009)
Teixeira et al.,
(2012)
Hamersley et al.,
(2009)
Minjeaud et al.,
(2009)
< 72%
15N
<50%
15N
<36.3 µmol L-1 d-1
<39%
15N
n.d
<0.0024 µmol
g-1-sediment d-1
< 3%
15N
Koop-Jakobsen &
Giblin (2009)
n.d
<0.0006 µmol
g-1-sediment d-1
<1%
15N
Koop-Jakobsen &
Giblin (2009)
Scalindua
<0.0038 µmol cm-3 d-1
< 22%
15N
n.d
<0.0011 µmol cm-3 d-1
< 10%
15N
Jettenia
0.02 – 1.4 nmol
g-sediment -1 h-1
<14.1%
15N
0.04-0.3 fmol cell-1
d-1
PCR
(rrn)
PCR
(rrn)
PCR
(hdh)
FISH
Rich et al., (2008)
Rich et al., (2008)
Lisa et al., (2014)
Environments
Baltimore
Inner Harbor
Cape Fear
River estuary
Providence
River estuary
and
Narragansett
Bay
Satilla River
and Okatee
River estuary
Logan and
Albert River
Genus
unidentifie
d
Kuenenia,
Jettenia,
Scalindua,
Brocadia
n.d
ra (%)
0.00156-0.0158 µmol
g-1-sediment d-1
3.8-16.5
%
15N
<0.024 µmol ml-1
sediment d-1
<4%
15N
Brin et al., (2014)
>2.2%
15N
Porubsky et al.,
(2009)
<9%
15N
Meyer et al., (2005)
<0.096 nmol cm-3 d-1
Yellow River
estuary
Scalindua
n.d
Pearl River
estuary
Kuenenia,
Brocadia,
Jettenia
<31.2 nmol cm-3 d-1
n.d
Tai O
n.d
n.d
n.d
Mandovi and
Chapora river
estuaries
Van Uc and
Lach Tray
River
estuaries
Methodology†
PCR
15N
(rrn)
Anammox activities
0.2 µmol g-sediment-1
d-1
<0.58 fmol cell-1 d-1
< 7%
15N
<2.42 µmol g-1 d-1
< 67%
15N
Scalindua,
Brocadia,
Kuenenia
<0.0168 µmol cm-3 h-1
<2.6%
15N
Scalindua
n.d
n.d
PCR
(rrn)
PCR
(rrn,
hdh)
PCR
(rrn,
hzs)
References
FISH
Tal et al., (2005)
Dale et al., (2009)
Dang et al., (2013)
Wang S.Y. et al.,
(2012)
Fernandes et al.,
(2012)
PCR
(rrn)
Amano et al., (2011)
PCR
(rrn)
Wang, Y.F. & Gu
(2013)
Environments
Mai Po
Nature
Reserve
Mai Po
Nature
Reserve
Methodology†
PCR
(rrn,
hdh)
Genus
Anammox activities
ra (%)
Scalindua
n.d
n.d
Scalindua,
Kuenenia
n.d
n.d
PCR
(nirS)
Li, M. et al., (2011a)
Mai Po
Nature
Reserve
Scalindua,
Kuenenia,
Brocadia,
Jettenia
n.d
n.d
PCR
(rrn,
hdh)
Li, M. et al., (2011b)
Mai Po
Nature
Reserve
Scalindua,
Kuenenia
n.d
n.d
PCR
(rrn,
hdh)
Li, M. et al., (2011c)
Mai Po
Nature
Reserve
Scalindua,
Brocadia,
Kuenenia
n.d
n.d
PCR
(rrn)
Han et al. (2013)
Mai Po
Nature
Reserve
Scalindua,
Brocadia,
Kuenenia,
Jettenia
n.d
n.d
PCR
(rrn)
Han & Gu (2013)
Mai Po
Nature
Reserve
Scalindua,
Kuenenia
n.d.
n.d
PCR
(rrn,
hdh)
Wang, Y.F. et al.
(2014)
Yodo river
estuary
Scalindua,
Kuenenia,
Brocadia
< 16.6 µmol L-1 slurry
d-1
n.d
PCR
(rrn)
Amano et al., (2007)
Freshwater
Lake, river, ditch
15N
References
Li, M. et al., (2010)
Environments
River Leith;
sediments in
hyporheic
zone
Boerenlandp
ad and
Leeuwsweidj
e ditches
Lake Lugano;
stratified
water column
Genus
Anammox activities
ra (%)
n.d
< 2%
Methodology†
Lansdown et al.,
(2012)
15N
Brocadia,
Jettenia
n.d
n.d
Lake
Lugano
cluster
< 0.0145 µmol L- 1 d-1
<30%
Lake
Zwischenahn
er Meer
Brocadia
n.d
n.d
PCR
(rrn)
Manure pond;
sediment
Jettenia
n.d
n.d
PCR
(rrn)
Scalindua
<0.24 µmol L-1 d-1
n.d
undetectable
Wintergreen
lake sediment
Scalindua
n.d
Sheriff’s
marsh
sediment
Scalindua
n.d
Honghe
freshwater
mars
Kuenenia,
Scalindua
n.d
Lake
Tanganyika;
water column
Patuxent
River
<18 fmol-NH4+
cell-1 d-1
References
15N
PCR
(hzs)
Harhangi et al.,
(2012)
PCR
(rrn)
Wenk et al., (2013)
FISH
Enrich
ment
Musat et al., (2010)
Sher et al., (2012)
15N
PCR
(rrn)
15N
PCR
(rrn)
Rich et al., (2008)
n.d
PCR
(rrn))
Penton et al., (2006)
n.d
PCR
(rrn)
Penton et al., (2006)
< 13%
PCR
(rrn,
hdh)
FISH
Schubert et al.,
(2006)
Environments
Fuhe River;
sediments in
hyporheic
zone
Baiyangdian
Lake;
sediments in
riparian
zones
Lake
Baiyangdian;
sediment
Dongjiang
River;
sediments
Dongjiang
River; water
column
Lake Kitaura;
sediments
Koisegawa
river;
sediment
Methodology†
Genus
Anammox activities
ra (%)
Brocadia,
Jettenia
n.d
n.d
Brocadia,
Kuenenia
<0.082-0.238 µmol g-1
d-1
<19-24 fmol-N
cell-1 d-1
< 35%
(locally
up to
94%)
15N
PCR
(rrn,
hzs)
Zhu et al., (2013)
Brocadia
<0.22 µmol g-1 d-1
0.73-2.25 fmol
cell-1 d-1
n.d
15N
PCR
(rrn)
Wang, Z.Y. et al.,
(2013)
Brocadia
n.d
n.d
PCR
(rrn,
hdh)
Sun et al., (2014a)
n.d
n.d
PCR
(rrn,
hdh)
Sun et al., (2014b)
<0.36 µmol cm-3 d-1
<40%
15N
PCR
(rrn)
Yoshinaga et al.,
(2011)
<0.048 µmol g-1 slurry
d-1
n.d
15N
Jettenia,
Brocadia,
Kuenenia,
Scalindua
Brocadia,
Kuenenia,
Jettenia/A
nammoxo
globus-line
age
relating
anammox
bacteria
n.d
PCR
(rrn)
References
FISH
Wang, Z. et al.,
(2012)
Zhou et al., (2014)
Environments
Methodology†
Genus
Anammox activities
ra (%)
Brocadia
n.d
n.d
PCR
(rrn)
Hirayama et al.,
(2005)
Marshes and
lakeshores;
sediments
Kuenenia,
Scalindua
n.d
n.d
PCR
(rrn)
Humbert et al.,
(2010)
natural
wetland
Kuenenia,
Scalindua,
Brocadia,
Jettenia,
Anammox
oglobus
n.d
n.d
PCR
(rrn)
Humbert et al.,
(2012)
Florida
everglades
water
conservation
area
Scalindua
n.d
n.d
PCR
(rrn)
Penton et al., (2006)
freshwater
marsh
Kuenenia,
Scalindua
n.d
n.d
PCR
(rrn,
hdh)
Lee et al., (2014)
n.d
n.d
PCR
(rrn)
Dong & Reddy
(2010)
Hishikari gold
mine
References
Wetland
Constructed
wetland
Constructed
wetland
Constructed
wetland
planctomy
cete
JMK-1
Jettenia,
Brocadia,
Anammox
oglobus
Scalindua
19.2-216 nmol g-1-soil
d-1
n.d
5.1-12.8 fmol cell-1
d-1
< 33%
15N
PCR
(rrn)
PCR
(rrn)
Enrich
ment
Zhu et al., (2011a)
Wang, Y.F. & Gu
(2013)
Environments
Anammox activities
Constructed
wetland
n.d
n.d
PCR
(hzs)
Jasper et al., (2014)
Constructed
wetland
Brocadia,
Kuenenia
Not found
PCR
(hzs)
Coban et al., (2015)
Constructed
wetland
n.d
n.d
PCR
(rrn)
Zhi et al., (2015)
PCR
(rrn)
Zhu et al., (2011b)
paddy soil
paddy soil
paddy soil
Brocadia,
Kuenenia,
Anammox
oglobus,
Jettenia
Brocadia,
Kuenenia
Anammox
oglobus,
Jettenia
<0.006-0.0348 µmol
g-1 d-1
<1.68 µmol g-VS-1 d-1
ra (%)
Methodology†
Genus
2.9-21 fmol cell-1
d-1
4-37%
15N
<5%
15N
paddy soil
Scalindua
n.d
n.d
paddy soil
n.d
n.d
n.d
Kuenenia,
Brocadia
Kuenenia,
Brocadia
Kuenenia,
Brocadia
0.0056-0.0227 µmol
g-1 d-1
0.0032-0.063 µmol g-1
d-1
0.0019-0.015
µmol g-1 d-1
paddy soil
paddy soil
paddy soil
15N
0.6-15%
2-41%
15N
15N
PCR
(rrn)
PCR
(rrn,
hzs)
PCR
(rrn,
hdh)
PCR
(hdh)
PCR
(rrn)
PCR
(hzs)
PCR
(rrn)
References
Sato et al., (2012)
FISH
Enrich
ment
Hu et al., (2013)
Wang, J. & Gu
(2013)
Wang, J. et al.,
(2014)
Shen et al., (2014)
Yang X.R. et al.,
(2015)
FISH
Nie, S. et al., (2015)
Environments
Genus
Anammox activities
ra (%)
Kuenenia,
Brocadia
n.d
n.d
Jettenia
<0.074 nmol g-1 d-1
32.177.9%
n.d
n.d
0.0021-0.023 µmol g-1
d-1
5.920.5%
n.d
Methodology†
References
Soil
agricultural
soil
agricultural
soil
agricultural
soil
agricultural
soil
glassland soil
rhizosphere
and
non-rhizosph
ere
sediments
peat soil
permafrost
soil
Siberian
permafrost
sediments
mesothermic
oil field
Brocadia,
Kuenenia,
Anammox
oglobus,
Jettenia
Brocadia,
Kuenenia,
Anammox
oglobus,
Jettenia
Kuenenia,
Brocadia
15N
PCR
(rrn)
PCR
(hdh)
Humbert et al.,
(2010)
Long et al., (2013)
PCR
(rrn,
hzs)
Shen et al., (2013)
PCR
(rrn)
Shen et al., (2015)
n.d
PCR
(rrn)
Humbert et al.,
(2010)
n.d
n.d
PCR
(rrn)
Chu et al., (2015)
Jettenia,
Brocadia
Kuenenia,
Brocadia,
Jettenia
22.56 mmol-NH4+
g-dry-1 d-1
n.d
PCR
(rrn)
n.d
n.d
PCR
(rrn)
Humbert et al.,
(2010)
Scalindua
n.d
n.d
PCR
(rrn)
Penton et al., (2006)
Kuenenia,
Brocadia
n.d
n.d
PCR
(rrn)
Shartau et al.,
(2010)
Kuenenia,
Brocadia,
Jettenia
15N
FISH
Lipid
Enrich
ment
Hu et al., (2011)
Environments
petroleum
reservoirs
Genus
Scalindua,
Brocadia,
Kuenenia,
Jettenia
Anammox activities
ra (%)
n.d
n.d
319-751 nmol L-1 d-1
< 36%
n.d
n.d
Methodology†
References
PCR
(rrn)
Li, H. et al., (2010)
PCR
(rrn)
Moore et al., (2011)
PCR
(rrn)
Smits et al., (2009)
PCR
(rrn)
Robertson et al.,
(2012)
Groundwater
ammonium-c
ontaminated
aquifer
ammonium-c
ontaminated
aquifer
septic system
plume
contaminated
municipal
aquifer
porous
aquifer
Activated sludge
(AS)
Brocadia,
Scalindua,
Kuenenia,
Jettenia
Kuenenia,
Brocadia,
Jettenia
Brocadia,
Jettenia
n.d
15N
n.d
15N
S
n.d
15N
S
Brocadia
n.d
AS
Jettenia,
Brocadia
1.2-336 µmol g-VSS
d-1
< 15%
15N
AS
n.d
<619 µmol g-VSS-1 d-1
<100%
15N
AS
Brocadia
540 µmol g-1-VSS d-1
8.7%
15N
AS
Brocadia
n.d
AS
Brocadia
1.6 kgN m-3 d-1
Clark et al, (2008)
PCR
(rrn)
Humbert et al.,
(2010)
PCR
(rrn)
Yamagishi et al.,
(2013)
Waki et al., (2010)
PCR
(rrn)
PCR
(hzs)
PCR
(rrn)
Waki et al., (2009)
Harhangi et al.,
(2012)
FISH
Enrich
ment
Lopez et al., (2008)
Environments
Genus
Anammox activities
AS
Brocadia
n.d
AS
Brocadia
11.7 kgN m-3 d-1
AS
Brocadia
n.d
AS
Brocadia,
Kuenenia
n.d
Brocadia,
Kuenenia
Brocadia,
Kuenenia
<1.08 mmol g-1-VSS
d-1
AS
Kuenenia
<2 kgN m-3 d-1
AS
Kuenenia
AS
Kuenenia
AS
Kuenenia,
Jettenia
<9.2 kgN m-3 d-1
AS
Jettenia
n.d
AS
AS
AS
AS
AS
Jettenia,
Anammox
oglobus
Kuenenia,
Brocadia
Anammox
oglobus
Scalindua
n.d
<1.4 kgN m-3 d-1
13 mmol-NH4+ g-VSS-1
d-1
26.5 µmol g-protein-1
min-1
ra (%)
Methodology†
PCR
(rrn)
PCR
(rrn)
FISH
FISH
PCR
(rrn,
hdh)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
<0.16 gN g-VSS-1 d-1
PCR
(rrn)
Araujo et al., (2011)
Tang et al., (2010)
Toh et al., (2002)
Hu et al., (2010)
Enrich
ment
Enrich
ment
Enrich
ment
FISH
<1.5 kgN m-3 d-1
5.0 µmol g-protein-1
min-1
References
Enrich
ment
Enrich
ment
Enrich
ment
FISH
FISH
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Sun et al., (2011)
Tao et al., (2012)
Tao et al., (2013)
Dapena-Mora et al.,
(2004)
Egli et al., (2001)
Wang, T. et al.,
(2013)
Bae et al., (2010)
Viancelli et al.,
(2011)
FISH
Enrich
ment
Shen et al., (2012)
Enrich
ment
Schmid et al.,
(2003)
Environments
Genus
Anammox activities
ra (%)
Methodology†
References
AS
n.d
<2.09 kg m-3 d-1
AS
n.d
13.6 mmol-NH4+ L-1 d-1
FISH
AS
n.d
25 mmol g-VSS-1 d-1
FISH
AS
n.d
AS
Brocadia,
Kuenenia
AS
Brocadia
AS
n.d
0.0146 kg-N NH4
d-1
+
m-3
n.d
FISH
6.24 mmol-NH4+ g-1 h-1
2.3 µmol g-protein-1
min-1
<36 mmol-NH4+ g-VS-1
d-1
n.d
AS
n.d
AS
Brocadia
AS
Brocadia
AS
n.d
AS
n.d
AS
Brocadia
45 µmol NH4+
g-protein-1 min-1
25 µmol NH4+
g-protein-1 min-1
8.01-8.3 mmol-NH4+
g-VSS-1 d-1
<26 kgN m-3 d-1
75 µmol-NH4+
g-protein-1 min-1
<57.1 kgN m-3 d-1
<32.3 mmol-NH4+
g-VSS-1 d-1
<76.7 kgN m-3 d-1
<400 mmol g-VSS-1 d-1
15 µmol NH4+
g-protein-1 min-1
Enrich
ment
FISH
PCR
(rrn)
>0.8 kg-NO2--N m-3 d-1
AS
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
Enrich
ment
FISH
2-20 fmol N cell-1
day-1
PCR
(rrn)
PCR
(rrn)
PCR
(rrn)
FISH
FISH
Lipid
Tang et al., (2013)
Wang, T. et al.,
(2011)
Wang, T. et al.,
(2009)
Liao et al., (2007)
Chamchoi &
Nitisoravut (2007)
Third et al., (2005)
van de Graaf et al.,
(1996)
van der Star et al.,
(2008)
Strous et al., (1998)
Strous et al., (1999)
Puyol et al., (2013)
Enrich
ment
Tsushima et al.,
(2007)
Oshiki et al., (2011)
Enrich
ment
Chen et al., (2011)
Enrich
ment
Enrich
ment
Tang et al., (2011)
Kartal et al. (2008)
Environments
AS
†
15
Genus
Anammox
oglobus
Anammox activities
15 µmol NH4+
g-protein-1 min-1
15
ra (%)
Methodology†
PCR
(rrn)
References
FISH
Lipid
Enrich
ment
Kartal et al., (2007)
15N; N isotope pairing techniqes, NS; isotopic signature analysis, FISH; fluorescence in-situ hybridization analysis, PCR;
polymerase chain reaction, genes are indicated with parentheses.
1
References.
2
Amano, T., Yoshinaga, I., Okada, K., Yamagishi, T., Ueda, S., Obuchi, A. et al. (2007)
3
Detection of anammox activity and diversity of anammox bacteria-related 16S
4
rRNA genes in coastal marine sediment in Japan. Microbes Environ. 22: 232-242.
5
Amano, T., Yoshinaga, I., Yamagishi, T., Chu, V.T., Pham, T.T., Ueda, S. et al. (2011)
6
Contribution of anammox bacteria to benthic nitrogen cycling in a mangrove forest
7
and shrimp ponds, Haiphong, Vietnam. Microbes Environ. 26: 1-6.
8
9
10
11
Araujo, J.C., Campos, A.C., Correa, M.M., Silva, E.C., Matte, M.H., Matte, G.R. et al.
(2011) Anammox bacteria enrichment and characterization from municipal
activated sludge. Water Sci. Technol. 64: 1428-1434.
Bae, H., Park, K.S., Chung, Y.C. and Jung, J.Y. (2010) Distribution of anammox
12
bacteria in domestic WWTPs and their enrichments evaluated by real-time
13
quantitative PCR. Process Biochem. 45: 323-334.
14
Bale, N.J., Villanueva, L., Fan, H., Stal, L.J., Hopmans, E.C., Schouten, S. and
15
Sinninghe Damsté, J.S. (2014) Occurrence and activity of anammox bacteria in
16
surface sediments of the southern North Sea. FEMS Microbiol. Ecol. 89: 99-110.
17
Borin, S., Mapelli, F., Rolli, E., Song, B., Tobias, C., Schmid, M.C. et al. (2013)
18
Anammox bacterial populations in deep marine hypersaline gradient systems.
19
Extremophiles 17: 289-299.
20
Bourbonnais, A., Juniper, S.K., Butterfield, D.A., Devol, A.H., Kuypers, M.M.M.,
21
Lavik, G. et al. (2012) Activity and abundance of denitrifying bacteria in the
22
subsurface biosphere of diffuse hydrothermal vents of the Juan de Fuca Ridge.
23
Biogeosciences 9: 4661-4678.
24
Bowen, J.L., Weisman, D., Yasuda, M., Jayakumar, A., Morrison, H.G. and Ward, B.B.
25
(2015) Marine oxygen-deficient zones harbor depauperate denitrifying
26
communities compared to novel genetic diversity in coastal sediments. Microb.
27
Ecol. 70: 311-321.
28
Brabandere, L.D., Canfield, D.E., Dalsgaard, T., Friederich, G.E., Revsbech, N.P., Ulloa,
29
O. et al. (2014) Vertical partitioning of nitrogen-loss processes across the
30
oxic-anoxic interface of an oceanic oxygen minimum zone. Environ. Microbiol.
31
16: 3041-3054
32
Brandsma, J., van de Vossenberg, J., Risgaard-Petersen, N., Schmid, M.C., Engstrom, P.,
33
Eurenius, K. et al. (2011) A multi-proxy study of anaerobic ammonium oxidation
34
in marine sediments of the Gullmar Fjord, Sweden. Environ. Microbiol. Rep. 3:
35
360-366.
36
Brin, L.D., Giblin, A.E. and Rich, J.J. (2014) Environmental controls of anammox and
37
denitrification in southern New England estuarine and shelf sediments. Limnol.
38
Oceanogr. 59: 851-860.
39
Byrne, N., Strous, M., Crepeau, V., Kartal, B., Birrien, J.L., Schmid, M. et al. (2009)
40
Presence and activity of anaerobic ammonium-oxidizing bacteria at deep-sea
41
hydrothermal vents. ISME J. 3: 117-123.
42
43
44
Chamchoi, N. and Nitisoravut, S. (2007) Anammox enrichment from different
conventional sludges. Chemosphere 66: 2225-2232.
Chen, C.J., Huang, X.X., Lei, C.X., Zhu, W.J., Chen, Y.X. and Wu, W.X. (2012)
45
Improving Anammox start-up with bamboo charcoal. Chemosphere 89:
46
1224-1229.
47
Chu, J., Zhang, J., Zhou, X., Liu, B. and Li, Y. (2015) A comparison of anammox
48
bacterial abundance and community structures in three different emerged
49
plants-related sediments. Curr. Microbiol. doi 10.1007/s00284-015-0851-5.
50
Clark, I., Timlin, R., Bourbonnais, A., Jones, K., Lafleur, D. and Wickens, K. (2008)
51
Origin and fate of industrial ammonium in anoxic ground water 15N evidence for
52
anaerobic oxidation (anammox). Ground Water Monit. R. 28: 73-82.
53
Castro-González, M., Molina, V., Rodríguez-Rubio, E. and Ulloa, O. (2014) The first
54
report of a microdiverse anammox bacteria community in waters of Colombian
55
Pacific, a transition area between prominent oxygen minimum zones of the eastern
56
tropical pacific. Environ. Microbiol. Rep. 6: 595-604.
57
Coban, O., Kuschk, P., Kappelmeyer, U., Spott, O., Martienssen, M., Jetten, M.S.M. et
58
al. (2015) Nitrogen transforming community in a horizontal subsurface-flow
59
constructed wetland. Water Res. 74: 203-212.
60
Dale, O.R., Tobias, C.R. and Song, B.K. (2009) Biogeographical distribution of diverse
61
anaerobic ammonium oxidizing (anammox) bacteria in Cape Fear River Estuary.
62
Environ. Microbiol. 11: 1194-1207.
63
Dalsgaard, T., Canfield, D.E., Petersen, J., Thamdrup, B. and Acuña-González, J. (2003)
64
N2 production by the anammox reaction in the anoxic water column of Golfo
65
Dulce, Costa Rica. Nature 422: 606-608.
66
Dalsgaard, T., Thamdrup, B., Farias, L. and Revsbech, N.P. (2012) Anammox and
67
denitrification in the oxygen minimum zone of the eastern South Pacific. Limnol.
68
Oceanogr. 57: 1331-1346.
69
Dang, H., Chen, R., Wang, L., Guo, L., Chen, P., Tang, Z. et al. (2010) Environmental
70
factors shape sediment anammox bacterial communities in hypernutrified Jiaozhou
71
Bay, China. Appl. Environ. Microbiol. 76: 7036-7047.
72
Dang, H., Zhou, H., Zhang, Z., Yu, Z., Hua, E., Liu, X. et al. (2013) Molecular detection
73
of Candidatus Scalindua pacifica and environmental responses of sediment
74
anammox bacterial community in the Bohai sea, China. PLoS One 8: e61330.
75
Dapena-Mora, A., Hulle, S.W.H.V., Campos, J.L., Mendez, R., Vanrolleghem, P.A. and
76
Jetten, M. (2004) Enrichment of Anammox biomass from municipal activated
77
sludge: experimental and modelling results. J. Chem. Technol. Biotechnol. 79:
78
1421-1428.
79
Dong, L.F., Smith, C.J., Papaspyrou, S., Stott, A., Osborn, A.M. and Nedwell, D.B.
80
(2009) Changes in benthic denitrification, nitrate ammonification, and anammox
81
process rates and nitrate and nitrite reductase gene abundances along an estuarine
82
nutrient gradient (the Colne estuary, United Kingdom). Appl. Environ. Microbiol.
83
75: 3171-3179.
84
Dong, X.L. and Reddy, G.B. (2010) Soil bacterial communities in constructed wetlands
85
treated with swine wastewater using PCR-DGGE technique. Biores. Technol. 101:
86
1175-1182.
87
Durbin, A.M. and Teske, A. (2011) Microbial diversity and stratification of South
88
Pacific abyssal marine sediments. Environ. Microbiol. 13: 3219-3234.
89
Egli, K., Fanger, U., Alvarez, P.J.J., Siegrist, H., van der Meer, J.R. and Zehnder, A.J.B.
90
(2001) Enrichment and characterization of an anammox bacterium from a rotating
91
biological contactor treating ammonium-rich leachate. Arch. Microbiol. 175:
92
198-207.
93
Engström, P., Dalsgaard, T., Hulth, S. and Aller, R.C. (2005) Anaerobic ammonium
94
oxidation by nitrite (anammox): Implications for N2 production in coastal marine
95
sediments. Geochim. Cosmochim. Acta 69: 2057-2065.
96
97
Engström, P., Penton, C.R. and Devol, A.H. (2009) Anaerobic ammonium oxidation in
deep-sea sediments off the Washington margin. Limnol. Oceanogr. 54: 1643-1652.
98
Erler, D.V., Trott, L.A., Alongi, D.M. and Eyre, B.D. (2013) Denitrification, anammox
99
and nitrate reduction in sediments of the southern Great Barrier Reef lagoon. Mar.
100
101
Ecol. Prog. Ser. 478: 57-70.
Fernandes, S.O., Michotey, V.D., Guasco, S., Bonin, P.C. and Bharathi, P.A.L. (2012)
102
Denitrification prevails over anammox in tropical mangrove sediments (Goa,
103
India). Mar. Environ. Res. 74: 9-19.
104
Galán, A., Molina, V., Thamdrup, B., Woebken, D., Lavik, G., Kuypers, M.M.M. et al.
105
(2009) Anammox bacteria and the anaerobic oxidation of ammonium in the oxygen
106
minimum zone off northern Chile. Deep Sea Res. Part 2 Top Stud. Oceanogr. 56:
107
1021-1031.
108
Gihring, T.M., Lavik, G., Kuypers, M.M.M. and Kostka, J.E. (2010) Direct
109
determination of nitrogen cycling rates and pathways in Arctic fjord sediments
110
(Svalbard, Norway). Limnol. Oceanogr. 55: 740-752.
111
Glud, R.N., Thamdrup, B., Stahl, H., Wenzhoefer, F., Glud, A., Nomaki, H. et al. (2009)
112
Nitrogen cycling in a deep ocean margin sediment (Sagami Bay, Japan). Limnol.
113
Oceanogr. 54: 723-734.
114
Hamersley, M.R., Lavik, G., Woebken, D., Rattray, J.E., Lam, P., Hopmans, E.C. et al.
115
(2007) Anaerobic ammonium oxidation in the Peruvian oxygen minimum zone.
116
Limnol. Oceanogr. 52: 923-933.
117
Hamersley, M.R., Woebken, D., Boehrer, B., Schultze, M., Lavik, G. and Kuypers,
118
M.M.M. (2009) Water column anammox and denitrification in a temperate
119
permanently stratified lake (Lake Rassnitzer, Germany). Syst. Appl. Microbiol. 32:
120
571-582.
121
122
Han, P. and Gu, J.D. (2013) More refined diversity of anammox bacteria recovered and
distribution in different ecosystems. Appl. Microbiol. Biotechnol. 97: 3653-3663.
123
Han, P., Huang, Y.T., Lin, J.G. and Gu, J.D. (2013) A comparison of two 16S rRNA
124
gene-based PCR primer sets in unraveling anammox bacteria from different
125
environmental samples. Appl. Microbiol. Biotechnol. 97: 10521-10529.
126
Harhangi, H.R., Le Roy, M., van Alen, T., Hu, B.L., Groen, J., Kartal, B. et al. (2012)
127
Hydrazine synthase, a unique phylomarker with which to study the presence and
128
biodiversity of anammox bacteria. Appl. Environ. Microbiol. 78: 752-758.
129
Hirayama, H., Takai, K., Inagaki, F., Yamato, Y., Suzuki, M., Nealson, K.H. et al.
130
(2005) Bacterial community shift along a subsurface geothermal water stream in a
131
Japanese gold mine. Extremophiles 9: 169-184.
132
Hoffmann, F., Radax, R., Woebken, D., Holtappels, M., Lavik, G., Rapp, H.T. et al.
133
(2009) Complex nitrogen cycling in the sponge Geodia barretti. Environ. Microbiol.
134
11: 2228-2243.
135
136
Hong, J.K. and Cho, J.C. (2012) High level of bacterial diversity and novel taxa in
continental shelf sediment. J. Microbiol. Biotechnol. 22: 771-779.
137
Hong, Y.G., Yin, B. and Zheng, T.L. (2011a) Diversity and abundance of anammox
138
bacterial community in the deep-ocean surface sediment from equatorial Pacific.
139
Appl. Microbiol. Biotechnol. 89: 1233-1241.
140
Hong, Y.G., Li, M., Cao, H. and Gu, J.D. (2011b) Residence of habitat-specific
141
anammox bacteria in the deep-sea subsurface sediments of the South China Sea:
142
analyses of marker gene abundance with physical chemical parameters. Microb.
143
Ecol. 62: 36-47.
144
Hu, B.L., Zheng, P., Tang, C.J., Chen, J.W., van der Biezen, E., Zhang, L. et al. (2010)
145
Identification and quantification of anammox bacteria in eight nitrogen removal
146
reactors. Water Res. 44: 5014-5020.
147
Hu, BL., Rush, D., van der Biezen, E., Zheng, P., van Mullekom, M., Schouten, S. et al.
148
(2011) New anaerobic, ammonium-oxidizing community enriched from peat soil.
149
Appl. Environ. Microbiol. 77: 966-971.
150
Hu, B.L., Shen, L.D., Liu, S., Cai, C., Chen, T.T., Kartal, B. et al. (2013) Enrichment of
151
an anammox bacterial community from a flooded paddy soil. Environ. Microbiol.
152
Rep. 5: 483-489.
153
154
155
Humbert, S., Zopfi, J. and Tarnawski, S.E. (2012) Abundance of anammox bacteria in
different wetland soils. Environ. Microbiol. Rep. 4: 484-490.
Humbert, S., Tarnawski, S., Fromin, N., Mallet, MP., Aragno, M. and Zopfi, J. (2010)
156
Molecular detection of anammox bacteria in terrestrial ecosystems: distribution
157
and diversity. ISME J. 4: 450-454.
158
159
Jasper, J.T., Jones, Z.L., Sharp, J.O. and Sedlak, D.L. (2014) Nitrate removal in shallow,
open-water treatment wetlands. Environ. Sci. Technol. 48: 11512−11520.
160
Jaeschke, A., Rooks, C., Trimmer, M., Nicholls, J.C., Hopmans, E.C., Schouten, S. et al.
161
(2009) Comparison of ladderane phospholipid and core lipids as indicators for
162
anaerobic ammonium oxidation (anammox) in marine sediments. Geochim.
163
Cosmochim. Acta 73: 2077-2088.
164
Jaeschke, A., Abbas, B., Zabel, M., Hopmans, E.C., Schouten, S. and Sinninghe Damsté,
165
J.S. (2010) Molecular evidence for anaerobic ammonium-oxidizing (anammox)
166
bacteria in continental shelf and slope sediments off northwest Africa. Limnol.
167
Oceanogr. 55: 365-376.
168
Jensen, M.M., Kuypers, M.M.M., Lavik, G. and Thamdrup, B. (2008) Rates and
169
regulation of anaerobic ammonium oxidation and denitrification in the Black Sea.
170
Limnol. Oceanogr. 53: 23-36.
171
Jensen, M.M., Lam, P., Revsbech, N.P., Nagel, B., Gaye, B., Jetten, M.S.M. et al. (2011)
172
Intensive nitrogen loss over the Omani Shelf due to anammox coupled with
173
dissimilatory nitrite reduction to ammonium. ISME J. 5: 1660-1670.
174
Kalvelage, T., Jensen, M.M., Contreras, S., Revsbech, N.P., Lam, P., Gunter, M. et al.
175
(2011) Oxygen sensitivity of anammox and coupled N-cycle processes in oxygen
176
minimum zones. PLoS One 6: e29299.
177
Kalvelage, T., Lavik, G., Lam, P., Contreras, S., Arteaga, L., Loscher, C.R. et al. (2013)
178
Nitrogen cycling driven by organic matter export in the South Pacific oxygen
179
minimum zone. Nat. Geosci. 6: 228-234.
180
Kartal, B., van Niftrik, L., Sliekers, O., Schmid, M.C., Schmidt, I., van de
181
Pas-Schoonen, K. et al. (2004) Application, eco-physiology and biodiversity of
182
anaerobic ammonium-oxidizing bacteria. Rev. Environ. Sci. Biotechnol. 3:
183
255-264.
184
Kartal, B., Rattray, J., van Niftrik, L.A., van de Vossenberg, J., Schmid, M.C., Webb, R.I.
185
et al. (2007) Candidatus ‘Anammoxoglobus Propionicus’ a new propionate
186
oxidizing species of anaerobic ammonium oxidizing bacteria.. Syst. Appl.
187
Microbiol. 30: 39-49.
188
Kawagoshi, Y., Fujisaki, K., Tomoshige, Y., Yamashiro, K. and Qiao, Y.W. (2012)
189
Temperature effect on nitrogen removal performance and bacterial community in
190
culture of marine anammox bacteria derived from sea-based waste disposal site. J.
191
Biosci. Bioeng. 113: 515-520.
192
Kindaichi, T., Awata, T., Suzuki, Y., Tanabe, K., Hatamoto, M., Ozaki, N. et al. (2011)
193
Enrichment using an up-flow column reactor and community structure of marine
194
anammox bacteria from coastal sediment. Microbes Environ. 26: 67-73.
195
Kirkpatrick, J., Oakley, B., Fuchsman, C., Srinivasan, S., Staley, J.T. and Murray, J.W.
196
(2006) Diversity and distribution of Planctomycetes and related bacteria in the
197
suboxic zone of the Black Sea. Appl. Environ. Microbiol. 72: 3079-3083.
198
Koop-Jakobsen, K. and Giblin, A.E. (2009) Anammox in tidal marsh sediments: the role
199
of salinity, nitrogen loading, and marsh vegetation. Estuar. Coast. 32: 238-245.
200
Kuypers, M.M., Sliekers, A.O., Lavik, G., Schmid, M., Jorgensen, B.B., Kuenen, J.G. et
201
al. (2003) Anaerobic ammonium oxidation by anammox bacteria in the Black Sea.
202
Nature 422: 608-611.
203
Kuypers, M.M.M., Lavik, G., Woebken, D., Schmid, M., Fuchs, B.M., Amann, R. et al.
204
(2005) Massive nitrogen loss from the Benguela upwelling system through
205
anaerobic ammonium oxidation. Proc. Natl. Acad. Sci. U. S. A. 102: 6478-6483.
206
Lahav, O., Bar Massada, I., Yackoubov, D., Zelikson, R., Mozes, N., Tal, Y. et al. (2009)
207
Quantification of anammox activity in a denitrification reactor for a recirculating
208
aquaculture system. Aquaculture 288: 76-82.
209
Lam, P., Jensen, M.M., Lavik, G., McGinnis, D.F., Muller, B., Schubert, C.J. et al.
210
(2007) Linking crenarchaeal and bacterial nitrification to anammox in the Black
211
Sea. Proc. Natl. Acad. Sci. U.S.A. 104: 7104-7109.
212
Lansdown, K., Trimmer, M., Heppell, C.M., Sgouridis, F., Ullah, S., Heathwaite, A.L. et
213
al. (2012) Characterization of the key pathways of dissimilatory nitrate reduction
214
and their response to complex organic substrates in hyporheic sediments. Limnol.
215
Oceanogr. 57: 387-400.
216
Lee, K.H., Wang, Y.F., Zhang, G.X. and Gu, J.D. (2014) Distribution patterns of
217
ammonia-oxidizing bacteria and anammox bacteria in the freshwater marsh of
218
Honghe wetland in Northeast China. Ecotoxicology 23:1930-1942.
219
220
Liao, D.X., Li, X.M., Yang, Q., Zhao, Z.H. and Zeng, G.M. (2007) Enrichment and
221
granulation of Anammox biomass started up with methanogenic granular sludge.
222
World J. Microbiol. Biotechnol. 23: 1015-1020.
223
224
225
Li, L., Kato, C. and Horikoshi, K. (1999) Bacterial diversity in deep-sea sediments from
different depths. Biodivers. Conserv. 8: 659-677.
Li, M., Hong, Y., Klotz, M.G. and Gu, J.D. (2010a) A comparison of primer sets for
226
detecting 16S rRNA and hydrazine oxidoreductase genes of anaerobic
227
ammonium-oxidizing bacteria in marine sediments. Appl. Microbiol. Biotechnol.
228
86: 781-790.
229
Li, H., Chen, S., Mu, B.Z. and Gu, J.D. (2010b) Molecular detection of anaerobic
230
ammonium-oxidizing (anammox) bacteria in high-temperature petroleum
231
reservoirs. Microb. Ecol. 60: 771-783.
232
Li, M., Ford, T., Li, X. and Gu, J.D. (2011a) Cytochrome cd1-containing nitrite
233
reductase encoding gene nirS as a new functional biomarker for detection of
234
anaerobic ammonium oxidizing (anammox) bacteria. Environ. Sci. Technol. 45:
235
3547-3553.
236
Li, M., Hong, Y.G., Cao, H.L. and Gu, J.D. (2011b) Mangrove trees affect the
237
community structure and distribution of anammox bacteria at an
238
anthropogenic-polluted mangrove in the Pearl River Delta reflected by 16S rRNA
239
and hydrazine oxidoreductase (HZO) encoding gene analyses. Ecotoxicology 20:
240
1780-1790.
241
Li, M., Cao, H., Hong, Y.G. and Gu, J.D. (2011c) Seasonal dynamics of anammox
242
bacteria in estuarial sediment of the Mai Po Nature Reserve revealed by analyzing
243
the 16S rRNA and hydrazine oxidoreductase (hzo) genes. Microbes Environ. 26:
244
15-22.
245
Li, M., Hong, Y., Cao, H. and Gu, J.D. (2013) Community structures and distribution of
246
anaerobic ammonium oxidizing and nirS-encoding nitrite-reducing bacteria in
247
surface sediments of the south China sea. Microb. Ecol. 66: 281-296.
248
Li, T. and Wang, P. (2013) Biogeographical distribution and diversity of bacterial
249
communities in surface sediments of the South china sea. J. Microbiol. Biotechnol.
250
23: 602-613.
251
Lipsewers, Y.A., Bale, N.J., Hopmans, E.C., Schouten, S., Sinninghe Damsté, J.S. and
252
Villanueva, L. (2014) Seasonality and depth distribution of the abundance and
253
activity of ammonia oxidizing microorganisms in marine coastal sediments (North
254
Sea). Front. Microbiol. 5: 472.
255
Lisa, J.A., Song, B.K., Tobias, C.R. and Duernberger, K.A. (2014) Impacts of
256
freshwater flushing on anammox community structure and activities in the New
257
River Estuary, USA. Aquat. Microbiol. Ecol. 72: 17-31.
258
Long, A., Heitman, J., Tobias, C., Philips, R. and Song, B. (2013) Co-occurring
259
anammox, denitrification, and codenitrification in agricultural soils. Appl. Environ.
260
Microbiol. 79: 168-176.
261
Lopez, H., Puig, S., Ganigue, R., Ruscalleda, M., Balaguer, M.D. and Colprim, J.
262
(2008) Start-up and enrichment of a granular anammox SBR to treat high nitrogen
263
load wastewaters. J. Chem. Technol. Biotechnol. 83: 233-241.
264
Meyer, R.L., Risgaard-Petersen, N. and Allen, D.E. (2005) Correlation between
265
anammox activity and microscale distribution of nitrite in a subtropical mangrove
266
sediment. Appl. Environ. Microbiol. 71: 6142-6149.
267
Minjeaud, L., Michotey, V.D., Garcia, N. and Bonin, P.C. (2009) Seasonal variation in
268
di-nitrogen fluxes and associated processes (denitrification, anammox and nitrogen
269
fixation) in sediment subject to shellfish farming influences. Aquat. Sci. 71:
270
425-435.
271
Mohamed, N.M., Saito, K., Tal, Y. and Hill, R.T. (2010) Diversity of aerobic and
272
anaerobic ammonia-oxidizing bacteria in marine sponges. ISME J. 4: 38-48.
273
Moore, T.A., Xing, Y.P., Lazenby, B., Lynch, M.D.J., Schiff, S., Robertson, W.D. et al.
274
(2011) Prevalence of anaerobic ammonium-oxidizing bacteria in contaminated
275
groundwater. Environ. Sci. Technol. 45: 7217-7225.
276
Musat, F., Wilkes, H., Behrends, A., Woebken, D. and Widdel, F. (2010) Microbial
277
nitrate-dependent cyclohexane degradation coupled with anaerobic ammonium
278
oxidation. ISME J. 4: 1290-1301.
279
Nakajima, J., Sakka, M., Kimura, T. and Sakka, K. (2008a) Detection of anaerobic
280
ammonium-oxidizing bacteria in Ago Bay sediments. Biosci. Biotechnol. Biochem.
281
72: 2195-2198.
282
Nakajima, J., Sakka, M., Kimura, T., Furukawa, K. and Sakka, K. (2008b) Enrichment
283
of anammox bacteria from marine environment for the construction of a
284
bioremediation reactor. Appl. Microbiol. Biotechnol. 77: 1159-1166.
285
286
Nicholls, J.C. and Trimmer, M. (2009) Widespread occurrence of the anammox reaction
in estuarine sediments. Aquat. Microb. Ecol. 55: 105-113.
287
Nie, S., Li, H., Yang, X., Zhang, Z., Weng, B., Huang, F. et al. (2015) Nitrogen loss by
288
anaerobic oxidation of ammonium in rice rhizosphere. ISME J. 9: 2059-2067.
289
Nunoura, T., Nishizawa, M., Kikuchi, T., Tsubouchi, T., Hirai, M., Koide, O. et al.
290
(2013) Molecular biological and isotopic biogeochemical prognoses of the
291
nitrification-driven dynamic microbial nitrogen cycle in hadopelagic sediments.
292
Environ. Microbiol. 15: 3087-3107.
293
Penton, C.R., Devol., A.H. and Tiedje, J.M. (2006) Molecular evidence for the broad
294
distribution of anaerobic ammonium-oxidizing bacteria in freshwater and marine
295
sediments. Appl. Environ. Microbiol. 72: 6829-6832.
296
Podlaska, A., Wakeham, S.G., Fanning, K.A. and Taylor, G.T. (2012) Microbial
297
community structure and productivity in the oxygen minimum zone of the eastern
298
tropical North Pacific. Deep Sea Res. Part 1 Oceanogr. Res. Pap. 66: 77-89.
299
Polymenakou, P.N., Bertilsson, S., Tselepides, A. and Stephanou, E.G. (2005) Bacterial
300
community composition in different sediments from the Eastern Mediterranean
301
Sea: a comparison of four 16S ribosomal DNA clone libraries. Microb. Ecol. 50:
302
447-462.
303
Porubsky, W.P., Weston, N.B. and Joye, S.B. (2009) Benthic metabolism and the fate of
304
dissolved inorganic nitrogen in intertidal sediments. Estuar. Coast. Shelf Sci. 83:
305
392-402.
306
Prokopenko, M.G., Hammond, D.E., Berelson, W.M., Bernhard, J.M., Stott, L. and
307
Douglas, R. (2006) Nitrogen cycling in the sediments of Santa Barbara basin and
308
Eastern Subtropical North Pacific: Nitrogen isotopes, diagenesis and possible
309
chemosymbiosis between two lithotrophs (Thioploca and Anammox)—“briding on
310
a glider”. Earth Planet. Sci. Lett. 242: 186-204.
311
Prokopenko, M.G., Hirst, M.B., De Brabandere, L., Lawrence, D.J.P., Berelson, W.M.,
312
Granger, J. et al. (2013) Nitrogen losses in anoxic marine sediments driven by
313
Thioploca-Anammox bacterial consortia. Nature 500: 194-198.
314
Rich, J.J., Dale, O.R., Song, B. and Ward, B.B. (2008) Anaerobic ammonium oxidation
315
(Anammox) in Chesapeake Bay sediments. Microb. Ecol. 55: 311-320.
316
Risgaard-Petersen, N., Meyer, RL., Schmid, M., Jetten, MSM., Enrich-Prast, A.,
317
Rysgaard, S. et al. (2004) Anaerobic ammonium oxidation in an estuarine sediment.
318
Aquat. Microb. Ecol. 36: 293-304.
319
Robertson, W.D., Moore, T.A., Spoelstra, J., Li, L., Elgood, R.J., Clark, I.D. et al.
320
(2011) Natural attenuation of septic system nitrogen by anammox. Ground Wat.
321
50: 541-553.
322
Rooks, C., Schmid, M.C., Mehsana, W. and Trimmer, M. (2012) The depth-specific
323
significance and relative abundance of anaerobic ammonium-oxidizing bacteria in
324
estuarine sediments (Medway Estuary, UK). FEMS Microbial. Ecol. 80: 19-29.
325
Rush, D., Wakeham, S.G., Hopmans, E.C., Schouten, S. and Damste, J.S.S. (2012)
326
Biomarker evidence for anammox in the oxygen minimum zone of the Eastern
327
Tropical North Pacific. Org. Geochem. 53: 80-87.
328
Russ, L., Kartal, B., op den Camp, H.J.M., Sollai, M., Bruchec, J.L., Caprais, J.C. et al.
329
(2013) Presence and diversity of anammox bacteria in cold hydrocarbon-rich seeps
330
and hydrothermal vent sediments of the Guaymas basin. Front. Microbiol. 4: 219.
331
Rysgaard, S., Glud, R.N., Risgaard-Petersen, N. and Dalsgaard, T. (2004)
332
Denitrification and anammox activity in Arctic marine sediments. Limnol.
333
Oceanogr. 49: 1493-1502.
334
335
336
Rysgaard, S. and Glud, R.N. (2004) Anaerobic N2 production in Arctic sea ice. Limnol.
Oceanogr. 49: 86-94.
Rysgaard, S., Glud, R.N., Sejr, M.K., Blicher, M.E. and Stahl, H.J. (2008)
337
Denitrification activity and oxygen dynamics in Arctic sea ice. Polar Biol. 31:
338
527-537.
339
Santelli, C.M., Orcutt, B.N., Banning, E., Bach, W., Moyer, C.L., Sogin, M.L.,
340
Staudigel, H. and Edwards, K.J. (2008) Abundance and diversity of microbial life
341
in ocean crust. Nature 453: 653-656.
342
Sato, Y., Ohta, H., Yamagishi, T., Guo, Y., Nishizawa, T., Rahman, M.H. et al. (2012)
343
Detection of anammox activity and 16S rRNA genes in ravine paddy field soil.
344
Microbes Environ. 27: 316-319.
345
Schmid, M., Walsh, K., Webb, R., Rijpstra, W.I.C., van de Pas-Schoonen, K.,
346
Verbruggen, M.J. et al. (2003) Candidatus “Scalindua brodae”, sp nov.,
347
Candidatus “Scalindua wagneri”, sp nov., two new species of anaerobic
348
ammonium oxidizing bacteria. Syst. Appl. Microbiol. 26: 529-538.
349
Schmid, M.C., Risgaard-Petersen, N., van de Vossenberg, J., Kuypers, M.M.M., Lavik,
350
G., Petersen, J. et al. (2007) Anaerobic ammonium-oxidizing bacteria in marine
351
environments: widespread occurrence but low diversity. Environ. Microbiol. 9:
352
1476-1484.
353
Schubert, C.J., Durisch-Kaiser, E., Wehrli, B., Thamdrup, B., Lam, P. and Kuypers,
354
M.M. (2006) Anaerobic ammonium oxidation in a tropical freshwater system
355
(Lake Tanganyika). Environ. Microbiol. 8: 1857-1863.
356
Shao, S., Luan, X., Dang, H., Zhou, H., Zhao, Y., Liu, H. et al. (2014) Deep-sea
357
methane seep sediments in the Okhotsk Sea sustain diverse and abundant
358
anammox bacteria. FEMS Microbiol. Ecol. 87: 503-516.
359
Shartau, S.L.C., Yurkiw, M., Lin, S.P., Grigoryan, A.A., Lambo, A., Park, H.S. et al.
360
(2010) Ammonium concentrations in produced waters from a mesothermic oil field
361
subjected to nitrate injection decrease through formation of denitrifying biomass
362
and anammox activity. Appl. Environ. Microbiol. 76: 4977-4987.
363
Shen, L.D., Hu, A.H., Jin, R.C., Cheng, D.Q., Zheng, P., Xu, X.Y. et al. (2012)
364
Enrichment of anammox bacteria from three sludge sources for the startup of
365
monosodium glutamate industrial wastewater treatment system. J. Hazard. Mater.
366
199: 193-199.
367
Shen, L.D., Liu, S., Lou, L.P., Liu, W.P., Xu, X.Y., Zheng, P. et al. (2013) Broad
368
distribution of diverse anaerobic ammonium-oxidizing bacteria in Chinese
369
agricultural soils. Appl. Environ. Microbiol. 79: 6167-6172.
370
Shen, L.D., Liu, S., Huang, Q., Lian, X., He, Z.F., Geng, S. et al. (2015) Evidence for
371
the cooccurrence of nitrite-dependent anaerobic ammonium and methane oxidation
372
processes in a flooded paddy field. Appl. Environ. Microbiol. 80: 7611-7619.
373
Shen, L.D., Wu, H.S., Gao, Z.Q., Xu, X.H., Chen, T.X., Liu, S. et al. (2015) Occurrence
374
and importance of anaerobic ammonium-oxidising bacteria in vegetable soils. Appl.
375
Microbiol. Biotechnol. 99: 5709-5718.
376
Sher, Y., Baram, S., Dahan, O., Ronen, Z. and Nejidat, A. (2012) Ammonia
377
transformations and abundance of ammonia oxidizers in a clay soil underlying a
378
manure pond. FEMS Microbial. Ecol. 81: 145-155.
379
Shu, Q.L. and Jiao, N.Z. (2008) Profiling Planctomycetales diversity with reference to
380
anammox-related bacteria in a South China Sea, deep-sea sediment. Mar. Ecol. 29:
381
413-420.
382
Smits, T.H.M., Huttmann, A., Lerner, D.N. and Holliger, C. (2009) Detection and
383
quantification of bacteria involved in aerobic and anaerobic ammonium oxidation
384
in an ammonium-contaminated aquifer. Biorem. J. 13: 41-51.
385
386
387
Stevens, H. and Ulloa, O. (2008) Bacterial diversity in the oxygen minimum zone of the
eastern tropical South Pacific. Environ. Microbiol. 10: 1244-1259.
Suneethi, S. and Joseph, K. (2011a) Batch culture enrichment of ANAMMOX
388
populations from anaerobic and aerobic seed cultures. Biores. Technol. 102:
389
585-591.
390
Suneethi, S. and Joseph, K. (2011b) ANAMMOX process start up and stabilization with
391
an anaerobic seed in Anaerobic Membrane Bioreactor (AnMBR). Biores. Technol.
392
102: 8860-8867.
393
Sun, W., Xu, M., Wu, W.M., Guo, J., Xia, C., Sun, G. et al. (2014a) Molecular diversity
394
and distribution of anammox community in sediments of the Dongjiang River, a
395
drinking water source of Hong Kong. J. Appl. Microbiol. 116: 464-476.
396
Sun, W., Xia, C., Xu, M., Guo, J., Wang, A. and Sun, G. (2014b) Diversity and
397
distribution of planktonic anaerobic ammonium-oxidizing bacteria in the
398
Dongjiang River, China. Microbiol. Res. 169: 897-906.
399
Sun, W.J., Banihani, Q., Sierra-Alvarez, R. and Field, J.A. (2011) Stoichiometric and
400
molecular evidence for the enrichment of anaerobic ammonium oxidizing bacteria
401
from wastewater treatment plant sludge samples. Chemosphere 84: 1262-1269.
402
Tal, Y., Watts, J.E.M. and Schreier, H.J. (2005) Anaerobic ammonia-oxidizing bacteria
403
and related activity in Baltimore inner Harbor sediment. Appl. Environ. Microbiol.
404
71: 1816-1821.
405
Tal, Y., Watts, J.E.M. and Schreier, H.J. (2006) Anaerobic ammonium-oxidizing
406
(anammox) bacteria and associated activity in fixed-film biofilters of a marine
407
recirculating aquaculture system. Appl. Environ. Microbiol. 72: 2896-2904.
408
Tang, C.J., Zheng, P., Zhang, L., Chen, J.W., Mahmood, Q., Chen, X.G. et al. (2010)
409
Enrichment features of anammox consortia from methanogenic granules loaded
410
with high organic and methanol contents. Chemosphere 79: 613-619.
411
Tang, C.J., Zheng, P., Chai, L.Y. and Min, X.B. (2013) Characterization and
412
quantification of anammox start-up in UASB reactors seeded with conventional
413
activated sludge. Int. Biodeterior. Biodegradation 82: 141-148.
414
Tao, Y., Gao, D.W., Fu, Y., Wu, W.M. and Ren, N.Q. (2012) Impact of reactor
415
configuration on anammox process start-up: MBR versus SBR. Biores. Technol.
416
104: 73-80.
417
Tao, Y., Gao, D.W., Wang, H.Y., de Kreuk, M. and Ren, N.Q. (2013) Ecological
418
characteristics of seeding sludge triggering a prompt start-up of anammox. Biores.
419
Technol. 133: 475-481.
420
Teixeira, C., Magalhaes, C., Joye, S.B. and Bordalo, A.A. (2012) Potential rates and
421
environmental controls of anaerobic ammonium oxidation in estuarine sediments.
422
Aquat. Microb. Ecol. 66: 23-32.
423
Thamdrup, B. and Dalsgaard, T. (2002) Production of N2 through anaerobic ammonium
424
oxidation coupled to nitrate reduction in marine sediments. Appl. Environ.
425
Microbiol. 68: 1312-1318.
426
Thamdrup, B., Dalsgaard, T., Jensen, M.M., Ulloa, O., Farias, L. and Escribano, R.
427
(2006) Anaerobic ammonium oxidation in the oxygen-deficient waters off northern
428
Chile. Limnol. Oceanogr. 51: 2145-2156.
429
Third, K.A., Paxman, J., Schmid, M., Strous, M., Jetten, M.S.M. and Cord-Ruwisch, R.
430
(2005) Enrichment of anammox from activated sludge and its application in the
431
CANON process. Microb. Ecol. 49: 236-244.
432
Tian, F., Yu, Y., Chen, B., Li, H.R., Yao, Y.F. and Guo, X.K. (2009) Bacterial, archaeal
433
and eukaryotic diversity in Arctic sediment as revealed by 16S rRNA and 18S
434
rRNA gene clone libraries analysis. Polar Biol. 32: 93-103.
435
Toh, S.K., Webb, R.I. and Ashbolt, N.J. (2002) Enrichment of autotrophic anaerobic
436
ammonium-oxidizing consortia from various wastewaters. Microb. Ecol. 43:
437
154-167.
438
Trimmer, M., Nicholls, J.C. and Deflandre, B. (2003) Anaerobic ammonium oxidation
439
measured in sediments along the Thames estuary, United Kingdom. Appl. Environ.
440
Microbiol. 69: 6447-6454.
441
Trimmer, M., Nicholls, J.C., Morley, N., Davies, C.A. and Aldridge, J. (2005) Biphasic
442
behavior of anammox regulated by nitrite and nitrate in an estuarine sediment.
443
Appl. Environ. Microbiol. 71: 1923-1930.
444
Trimmer, M. and Nicholls, J.C. (2009) Production of nitrogen gas via anammox and
445
denitrification in intact sediment cores along a continental shelf to slope transect in
446
the North Atlantic. Limnol. Oceanogr. 54: 577-589.
447
Trimmer, M., Engström, P. and Thamdrup, B. (2013) Stark contrast in denitrification
448
and anammox across the deep Norwegian Trench: The Skagerrak. Appl. Environ.
449
Microbiol. 79: 7381-7389.
450
Tsushima, I., Kindaichi, T. and Okabe, S. (2007) Quantification of anaerobic
451
ammonium-oxidizing bacteria in enrichment cultures by real-time PCR. Water Res.
452
41: 785-794.
453
Van de Graaf, A.A.V., de Bruijn, P., Robertson, L.A., Jetten, M.S.M. and Kuenen, J.G.
454
(1996) Autotrophic growth of anaerobic ammonium-oxidizing micro-organisms in
455
a fluidized bed reactor. Microbiology 142: 2187-2196.
456
van de Vossenberg, J., Rattray, J.E., Geerts, W., Kartal, B., van Niftrik, L., van
457
Donselaar, E.G. et al. (2008) Enrichment and characterization of marine anammox
458
bacteria associated with global nitrogen gas production. Environ. Microbiol. 10:
459
3120-3129.
460
van der Wielen, P.W., Bolhuis, H., Borin, S., Daffonchio, D., Corselli, C., Giuliano, L.
461
et al. (2005) The enigma of prokaryotic life in deep hypersaline anoxic basins.
462
Science 307: 121-123 .
463
van Kessel, M.A.H.J., Harhangi, H.R., van de Pas-Schoonen, K., van de Vossenberg, J.,
464
Flik, G., Jetten, M.S.M. et al. (2010) Biodiversity of N-cycle bacteria in nitrogen
465
removing moving bed biofilters for freshwater recirculating aquaculture systems.
466
Aquaculture 306: 177-184.
467
Viancelli, A., Kunz, A., Esteves, P.A., Bauermann, F.V., Furukawa, K., Fujii, T. et al.
468
(2011) Bacterial biodiversity from an anaerobic up flow bioreactor with
469
ANAMMOX activity inoculated with swine sludge. Braz. Arch. Biol. Technol. 54:
470
1035-1041.
471
Waki, M., Yasuda, T., Yokoyama, H., Hanajima, D., Ogino, A., Suzuki, K. et al. (2009)
472
Nitrogen removal by co-occurring methane oxidation, denitrification, aerobic
473
ammonium oxidation, and anammox. Appl. Microbiol. Biotechnol. 84: 977-985.
474
Waki, M., Yasuda, T., Suzuki, K., Sakai, T., Suzuki, N., Suzuki, R. et al. (2010) Rate
475
determination and distribution of anammox activity in activated sludge treating
476
swine wastewater. Biores. Technol. 101: 2685-2690.
477
Walsh, D.A., Zaikova, E., Howes, C.G., Song, Y.C., Wright, J.J., Tringe, S.G. et al.
478
(2009) Metagenome of a versatile chemolithoautotroph from expanding oceanic
479
dead zones. Science 326: 578-582.
480
Wang, J. and Gu, J.D. (2013a) Dominance of Candidatus Scalindua species in
481
anammox community revealed in soils with different duration of rice paddy
482
cultivation in northeast China. Appl. Microbiol. Biotechnol. 97: 1785-1798.
483
Wang, J., Dong, H., Wang, W. and Gu, J.D. (2014) Reverse-transcriptional gene
484
expression of anammox and ammonia-oxidizing archaea and bacteria in soybean
485
and rice paddy soils of Northeast China. Appl. Microbiol. Biotechnol. 98: 2675-86.
486
Wang, S.Y., Zhu, G.B., Peng, Y.Z., Jetten, M.S.M. and Yin, C.Q. (2012) Anammox
487
bacterial abundance, activity, and contribution in riparian sediments of the Pearl
488
River estuary. Environ. Sci. Technol. 46: 8834-8842.
489
Wang, T., Zhang, H.M., Yang, F.L., Liu, S.T., Fu, Z.M. and Chen, H.H. (2009) Start-up
490
of the Anammox process from the conventional activated sludge in a membrane
491
bioreactor. Biores. Technol. 100: 2501-2506.
492
Wang, T., Zhang, H.M., Gao, D.W., Yang, F.L., Yang, S.A., Jiang, T. et al. (2011)
493
Enrichment of Anammox bacteria in seed sludges from different wastewater
494
treating processes and start-up of Anammox process. Desalination 271: 193-198.
495
Wang, T., Zhang, H.M., Yang, F.L., Li, Y.F. and Zhang, G.Y. (2013b) Start-up and
496
long-term operation of the Anammox process in a fixed bed reactor (FBR) filled
497
with novel non-woven ring carriers. Chemosphere 91: 669-675.
498
Wang, Y.F. and Gu, J.D. (2013) Higher diversity of ammonia/ammonium-oxidizing
499
prokaryotes in constructed freshwater wetland than natural coastal marine wetland.
500
Appl. Microbiol. Biotechnol. 97: 7015-7033.
501
Wang, Y.F., Li, X.Y. and Gu, J.D. (2014) Differential responses of
502
ammonia/ammonium-oxidizing microorganisms in mangrove sediment to
503
amendment of acetate and leaf litter. Appl. Microbiol. Biotechnol. 98:3165-3180.
504
Wang, Z., Qi, Y., Wang, J. and Pei, Y. (2012) Characteristics of aerobic and anaerobic
505
ammonium-oxidizing bacteria in the hyporheic zone of a contaminated river. World
506
J. Microbiol. Biotechnol. 28: 2801-2811.
507
Wang, Z.Y., Wang, C.H., Wang, Z.X. and Pei, Y.S. (2013) Enhancement of anaerobic
508
ammonium oxidation in lake sediment by applying drinking water treatment
509
residuals. Biores. Technol. 142: 745-749.
510
Ward, B.B., Devol, A.H., Rich, J.J., Chang, B.X., Bulow, S.E., Naik, H. et al. (2009)
511
Denitrification as the dominant nitrogen loss process in the Arabian Sea. Nature
512
461: 78-U77.
513
Wenk, C.B., Blees, J., Zopfi, J., Veronesi, M., Bourbonnais, A., Schubert, C.J. et al.
514
(2013) Anaerobic ammonium oxidation (anammox) bacteria and sulfide-dependent
515
denitrifiers coexist in the water column of a meromictic south-alpine lake. Limnol.
516
Oceanogr. 58: 1-12.
517
Woebken, D., Fuchs, BM., Kuypers, M.M.M. and Amann, R. (2007) Potential
518
interactions of particle-associated anammox bacteria with bacterial and archaeal
519
partners in the Namibian upwelling system. Appl. Environ. Microbiol. 73:
520
4648-4657.
521
Woebken, D., Lam, P., Kuypers, M.M.M., Naqvi, S.W.A., Kartal, B., Strous, M. et al.
522
(2008) A microdiversity study of anammox bacteria reveals a novel Candidatus
523
Scalindua phylotype in marine oxygen minimum zones. Environ. Microbiol. 10:
524
3106-3119.
525
Yang, X.R., Li, H., Nie, S.A., Su, J.Q., Weng, B.S., Zhu, G.B. et al. (2015) The
526
potential contribution of anammox to nitrogen loss from paddy soils in Southern
527
China. Appl. Environ. Microbiol. doi:10.1128/AEM.02664-14.
528
Yamagishi, T., Takeuchi, M., Wakiya, Y. and Waki, M. (2013) Distribution and
529
characterization of anammox in a swine wastewater activated sludge facility. Water
530
Sci. Technol. 67: 2330-2336.
531
532
Yoshinaga, I., Amano, T., Yamagishi, T., Okada, K., Ueda, S., Sako, Y. et al. (2011)
Distribution and diversity of anaerobic ammonium oxidation (anammox) bacteria
533
in the sediment of a eutrophic freshwater lake, Lake Kitaura, Japan. Microbes
534
Environ. 26: 189-197.
535
Zhao, Z.S., Cao, Y.L., Li, L., Song, G.D., Yang, H.M., Liu, S.M. et al. (2013)
536
Sedimentary ladderane core lipids as potential indicators of hypoxia in the East
537
China Sea. Chin. J. Oceanol. Limnol. 31: 237-244.
538
Zhi, W., Yuan, L., Ji, G. and He, C. (2015) Enhanced long-term nitrogen removal and
539
its quantitative molecular mechanism in tidal flow constructed wetlands. Environ.
540
Sci. Technol. 49: 4575-4583.
541
Zhu, G.B., Wang, S.Y., Feng, X.J., Fan, G.N., Jetten, M.S.M. and Yin, C.Q. (2011a)
542
Anammox bacterial abundance, biodiversity and activity in a constructed wetland.
543
Environ. Sci. Technol. 45: 9951-9958.
544
Zhu, G.B., Wang, S.Y., Wang, Y., Wang, C.X., Risgaard-Petersen, N., Jetten, M.S.M. et
545
al. (2011b) Anaerobic ammonia oxidation in a fertilized paddy soil. ISME J. 5:
546
1905-1912.
547
Zhu, GB., Wang, SY., Wang, WD., Wang, Y., Zhou, LL., Jiang, B. et al. (2013) Hotspots
548
of anaerobic ammonium oxidation at land-freshwater interfaces. Nat. Geosci. 6:
549
103-107.
Download