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The microbial contribution to carbon and nutrient cycling across a variable tropical landscape Madeleine M. Stone Dissertation Defense November 21, 2014

M Stone- Dissertation Defense

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Page 1: M Stone- Dissertation Defense

The microbial contribution to carbon

and nutrient cycling across a variable

tropical landscape

Madeleine M. Stone

Dissertation Defense

November 21, 2014

Page 2: M Stone- Dissertation Defense

Tropical forests dominate carbon fluxes in the

terrestrial biosphere

Amazon Basin

Page 3: M Stone- Dissertation Defense

Soils are largest terrestrial carbon pool

(1500 — 2000 Pg C)

Tropical forests contribute disproportionately to

subsoil C stocks, which have high potential for

long-term C stabilization

Page 4: M Stone- Dissertation Defense

Dissertation Proposal | October 19, 2012

Most carbon in soils exists as soil organic matter

Schmidt et al. 2011, Nature

Page 5: M Stone- Dissertation Defense

Soil is the most biologically diverse habitat on Earth (thousands — millions species per gram)

Soil microbial communities produce, maintain and

decompose soil organic matter

Page 6: M Stone- Dissertation Defense

Substrate

signaling

Catabolic repression

Product formation

Enzyme

production

Exo-enzymes link microbial ecology and soil biogeochemistry

Page 7: M Stone- Dissertation Defense

Substrate

signaling

Catabolic repression

P

P

N

N

C

C

C

C

C

C

C

C

C

Product formation

Microbial stoichiometry links carbon, nitrogen and phosphorus cycling

60 : 7 : 1

“Redfield ratio” for soil

microbes?

Enzyme

production

Page 8: M Stone- Dissertation Defense

In their search for energy and nutrients,

microbes drive biogeochemical cycles of

carbon, nitrogen and phosphorus.

But what controls the microbes?

Page 9: M Stone- Dissertation Defense
Page 10: M Stone- Dissertation Defense

Luquillo Mountains, Puerto Rico

Oxisol Inceptisol

Page 11: M Stone- Dissertation Defense

Gradients in climate, vegetation

Pre-montane forest

(Colorado)

Lowland forest

(Tabonuco) ridge

slope

valley

ridge

slope

valley

Page 12: M Stone- Dissertation Defense

Environmental gradients with depth

High resource

surface soils

Low resource subsoils

Δ C, Nutrients,

pH, moisture,

oxygen

Page 13: M Stone- Dissertation Defense

110 cm

20 cm

50 cm

80 cm

Page 14: M Stone- Dissertation Defense

What controls the

biogeochemical capacity of soil

microbes throughout the Luquillo

Critical Zone?

Page 15: M Stone- Dissertation Defense

1. Patterns in soil resourcesStone, M.M., DeForest, J.L., Plante, A.F. (2014), Soil Biology &

Biochemistry (Dissertation Chapter 3)

Stone, M.M., Hockaday, W.C., Plante, A.F. In Preparation.

(Dissertation Chapter 6)

2. Patterns in soil microbesStone, M.M., DeForest, J.L., Plante, A.F. (2014), Soil Biology &

Biochemistry (Dissertation Chapter 3)

Stone M. M., Plante, A.F. (2014) Soil Biology and Biochemistry

(Dissertation Chapter 5)

Stone, M.M., Plante, A.F. In preparation.

Page 16: M Stone- Dissertation Defense

Sample Set

Variable Forest Types Soil Types Landscape

Positions

Depths

Basic soil

characterization

Colorado,

Tabonuco

Oxisol (VC),

Inceptisol (QD)

Ridge,

(Slope x3),

Valley

0-140 cm

(300 samples)

Carbon

Chemistry

Colorado,

Tabonuco

Oxisol (VC),

Inceptisol (QD)

Ridge, Slope,

Valley

Various [C] >

1%

(34 samples)

Microbial

Biomass,

Activity &

Community

Structure

Colorado,

Tabonuco

Oxisol (VC),

Inceptisol (QD)

Ridge, Slope,

Valley

0, 20, 50, 80,

110 & 140 cm

(72 samples)

Page 17: M Stone- Dissertation Defense

1. Patterns in soil resourcesStone, M.M., DeForest, J.L., Plante, A.F. (2014), Soil Biology &

Biochemistry (Dissertation Chapter 3)

Stone, M.M., Hockaday, W.C., Plante, A.F. In Preparation.

(Dissertation Chapter 6)

2. Patterns in soil microbesStone, M.M., DeForest, J.L., Plante, A.F. (2014), Soil Biology &

Biochemistry (Dissertation Chapter 3)

Stone M. M., Plante, A.F. (2014) Soil Biology and Biochemistry

(Dissertation Chapter 5)

Stone, M.M., Plante, A.F. In preparation.

Page 18: M Stone- Dissertation Defense

High resource

surface soils

Low resource subsoils

Plant inputs

Increased decomposition,

Mineral association

1. Carbon and nutrient concentrations will decline rapidly from

the surface

2. Shifts in SOM chemistry from plant — microbial

Page 19: M Stone- Dissertation Defense

1. Leaf litter chemistry (forest) will be important in determining

surface soil organic matter composition

Plant inputs

Increased decomposition,

Mineral association

2. Mineral associations (soil type) will be important in

determining subsoil organic matter composition

Page 20: M Stone- Dissertation Defense

Basic soil characterization

• Total C and N measured by combustion

analysis

• “Labile” P quantified using partial

sequential Hedley fractionation (NaHCO3

& NaOH-extractable)

• Soil pH measured in DI water

Page 21: M Stone- Dissertation Defense

Exponential declines in carbon and nutrients…

mg g-1 soil mg g-1 soil mg kg-1 soil

Page 22: M Stone- Dissertation Defense

More carbon in higher elevation

forest

Carbon and nitrogen along the upper 80 cm of soil profiles

Page 23: M Stone- Dissertation Defense

13C Nuclear magnetic resonance spectroscopy (NMR)

Page 24: M Stone- Dissertation Defense

• High O-alkyl C in soils, plant and microbial tissues

• Enrichment in N-alkyl and amide C in fungal biomass

• Enrichment in Alkyl C in SOM

Page 25: M Stone- Dissertation Defense

Carbon Chemistry Distinct Across Forests

−0.2 −0.1 0.0 0.1 0.2

−0.2

−0

.10.0

0.1

0.2

PC1 42 %

PC

2 3

2 %

−4 −2 0 2 4

−4

−2

02

4

Alkyl

Nalkyl

Oalkyl

DiOAlkyl

Amide

ColDys5

Fungi

Root

Litter

Phenolic Aromatic

Alkyl

DiOAlkyl

Oalkyl

RootLitterFungiColorado Forest SoilTabonuco Forest Soil

Distinct Alkyl: O-alkyl ratios

Root: 0.3 ± 0.0

Fungi: 0.4 ± 0.2

Litter: 0.6 ± 0.0

Tabonuco: 0.7 ± 0.1

Colorado: 2.1 ± 0.3

Page 26: M Stone- Dissertation Defense

Depth trends in

carbon chemistry

observed at the

individual soil profile

level

But different

patterns were

observed in each

pit.

AlkylO-AlkylAromaticAmide

Oxisol Valley Depth Profile

Page 27: M Stone- Dissertation Defense

Greater amounts of poorer quality C in Colorado forest

No differences across soil types!

Changes in SOM chemistry with depth are observable at the level

of individual profiles

Alkyl C (lipids) may be particularly important for long-term tropical

C storage

Page 28: M Stone- Dissertation Defense

1. Patterns in soil resourcesStone, M.M., DeForest, J.L., Plante, A.F. (2014), Soil Biology &

Biochemistry (Dissertation Chapter 3)

Stone, M.M., Hockaday, W.C., Plante, A.F. In Preparation.

(Dissertation Chapter 6)

2. Patterns in soil microbesStone, M.M., DeForest, J.L., Plante, A.F. (2014), Soil Biology &

Biochemistry (Dissertation Chapter 3)

Stone M. M., Plante, A.F. (2014) Soil Biology and Biochemistry

(Dissertation Chapter 5)

Stone, M.M., Plante, A.F. In preparation.

Page 29: M Stone- Dissertation Defense

High resource

surface soils

Low resource subsoils

1. Soil microbial biomass and activity will decline with

depth, tracking declines in C and nutrients

2. Specific metabolic activities will shift with depth,

reflecting shifts in resource allocation

3. Microbial community structure will shift with depth,

tracking changing environment

Page 30: M Stone- Dissertation Defense

In surface soils, microbial

abundance, activity and

structure will relate to vegetation

In subsoils, microbial

abundance, activity and

structure will relate to the

physiochemical environment

(soil type)

Page 31: M Stone- Dissertation Defense

Phospholipid Fatty Acid Analysis

Wikimedia

Commons

Page 32: M Stone- Dissertation Defense

Extract and quantify

phospholipids for :

1. Viable biomass

2. Broad microbial

community structure

Fungi

Actinobacteria

Page 33: M Stone- Dissertation Defense

Soil Respiration

CO2 evolution

measured during

90-day respiration

experiment

Respiration rate

normalized to soil

C and microbial C

concentrations to

determine specific

metabolic activity

Page 34: M Stone- Dissertation Defense

Natural process

Fluorimetric assay

Fluorimetric Enzyme Assaysα – glucosidase (starch)

β-glucosidase (cellulose dimers)

β-xylosidase (hemicellulose)

cellobiohydrolase (cellulose oligomers)

N-acetyl glucosaminidase (chitin)

acid phosphatase (organic phosphate)

Total Potential Activity

Specific Activity

(Per carbon or biomass)

Page 35: M Stone- Dissertation Defense

No substantial differences among landscape

units (3-way ANOVA):

Microbial

biomass

Cumulative

respiration

Total Enzyme

Activity

P value

Soil parent material

(VC vs. QD)

0.85 0.39 0.27

Forest type (Col vs.

Tab)

0.65 0.16 0.13*

*2/4 carbon cycle enzymes significantly higher in Colorado forest

Page 36: M Stone- Dissertation Defense

20 %

P < 0.01

Page 37: M Stone- Dissertation Defense

Dep

th (

cm

)

140

110

80

50

20

0

0 2 4 6

Resp rate per unit soil

µg CO2g-1

day-1

−1 0 1

Resp rate per unit soil C

µg CO2mg C-1

day-1

0.2 0.4 0.6

Resp rate per unit microbial C

µg CO2mg Cmic-1

day-1

Dep

th (

cm

)

140

110

80

50

20

0

0 2 4 6

Resp rate per unit soil

µg CO2g-1

day-1

−1 0 1

Resp rate per unit soil C

µg CO2mg C-1

day-1

0.2 0.4 0.6

Resp rate per unit microbial C

µg CO2mg Cmic-1

day-1

7.8 x

P = 0.07

Dep

th (

cm

)

140

110

80

50

20

0

0 2 4 6

Resp rate per unit soil

µg CO2g-1

day-1

−1 0 1

Resp rate per unit soil C

µg CO2mg C-1

day-1

0.2 0.4 0.6

Resp rate per unit microbial C

µg CO2mg Cmic-1

day-1

Page 38: M Stone- Dissertation Defense

19 x

P < 0.01

Page 39: M Stone- Dissertation Defense

20 x

P < 0.01NSD(Mostly)

NSD

High variability in deep soil enzyme activity

Increased specific activity with depth driven largely by phosphatase

Page 40: M Stone- Dissertation Defense

Substrate

signaling

Catabolic repression

Product formation

Enzyme

production

Why high specific metabolic activity in resource

limited subsoils?

Page 41: M Stone- Dissertation Defense

Substrate

signaling

Catabolic repression

Product formation

Enzyme

production

Stress due to resource scarcity?

Page 42: M Stone- Dissertation Defense

Microbes strongly driven by energy availability

Page 43: M Stone- Dissertation Defense

Substrate

signaling

Catabolic repression

Product formation

Enzyme

production

Decreased enzyme turnover rates?

Page 44: M Stone- Dissertation Defense

High enzyme activity following sorption

Page 45: M Stone- Dissertation Defense

Substrate

signaling

Catabolic repression

Product formation

Enzyme

production

Community shift?

Page 46: M Stone- Dissertation Defense

Evidence for this!

Depth P < 0.001

66 %

P = 0.01

Page 47: M Stone- Dissertation Defense

1.7

60.0

40%

P = 0.01

80%

P = 0.01

Increased phosphatase activity relative to C and N cycle enzymes suggests

microbes at depth invest more in P acquisition

Why?

What’s up with phosphatase?

Page 48: M Stone- Dissertation Defense

Phosphatase activity driven by microbial carbon demand?

Page 49: M Stone- Dissertation Defense

Energy availability drives microbial activity—much more than landscape differences

Microbial biogeochemical capacity remains similar or increases with depth, per unit biomass

High specific metabolic activity could be a stress response, decreased enzyme turnover, or community shifts

Prevalence of phosphatase suggests a special role for this enzyme

Page 50: M Stone- Dissertation Defense

Starving – survival lifestyle?

Microbes retain metabolic capacity for biogeochemical

processes in low—energy subsoils

“Stability” of deep soil carbon—microbial starvation?

Implications

Page 51: M Stone- Dissertation Defense

Future Directions

IPCC October, 2014

Page 52: M Stone- Dissertation Defense

Thank you!

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